REUSE OF COCONUT RESIDUES AS

ACTIVATED CARBON FOR

DOMESTIC WATER PURIFICATION

IN DEVELOPING REGIONS

 

by

 

 

Paul Indeglia

 

 

 

 

 

A Project

 

Presented to

 

The Faculty of Humboldt State University

 

 

 

 

In Partial Fulfillment

 

of the Requirements for the Degree

 

Master of Science

 

In Environmental Systems:

 

International Development Technology

 

 

 

Fall 1998

 

 

 

 

 

 

REUSE OF COCONUT RESIDUES AS

ACTIVATED CARBON FOR

DOMESTIC WATER PURIFICATION

IN DEVELOPING REGIONS

 

 

 

by

 

Paul Indeglia

 

 

 

Approved by:

 

 

_____________________________________________________________

Robert Gearheart, Major Professor                                     Date

 

 

_____________________________________________________________

Peter Lehman, Committee Member                                     Date

 

 

_____________________________________________________________

Daniel Ihara, Committee Member                                                   Date

 

 

_____________________________________________________________

Charles M. Biles, Graduate Coordinator                                         Date

 

 

_____________________________________________________________

Dean for Research and Graduate Studies                                       Date

 


(i)                 Abstract

 

This work examines the feasibility of incorporating new technologies and strategies for thermally converting coconut residues into useful products. Drawing upon previous documentation, extensive literature reviews, laboratory experimentation and personal experiences, this work analyzes implementing innovative projects involving uses of coconut residues. Laboratory experimentation includes producing activated carbon from coconut shells using technologies similar to those found in developing regions, and examining capacity to remove coliform through filtration. By converting waste from discarded coconuts into activated carbon, water quality and sanitation can be improved, leading to an enhanced physical environment and better public health.


Acknowledgments

 

I wish to express my appreciation to Dr. Robert Gearheart for allowing me the opportunity to study at Humboldt State University, Dr. Daniel Ihara for his direction and advice, both academically and personally, Dr. Peter Lehman, Dr. Margaret Lang, Dr. Thomas Borgers and Mr. Steve Salzman for their technical guidance, and Dr. Howard Stauffer for enhancing my statistical capabilities. I thank my colleagues, Mr. Jeff Detrick, Mr. Erik Nagy and Mr. Michael Harig for their assistance and direction in areas in which I was deficient.  Special appreciation is given to Mr. Tapley Jordan and Mr. Michael McIntyre, who have inspired this project. For allowing me space to conduct my experiments on secure grounds, I am grateful to the City of Arcata Department of Environmental Services.

 

I  would like to offer special thanks and love to my parents for their continued support of their son as he follows his path to internal peace and spiritual fulfillment.

 

This work is dedicated to all life that suffers from the deficiencies of human society, to those eternally searching for truth, and to Jim Richards.


Table of Contents

 

 

Title Page................................................................................................................... i

Signature Page........................................................................................................... ii

Abstract.................................................................................................................... iii

Acknowledgments..................................................................................................... iv

Table of Contents...................................................................................................... v

List of Figures.......................................................................................................... viii

List of Tables............................................................................................................ ix

 

I.                    Introduction................................................................................................... 1

            A.  Overview................................................................................................. 1

            B.  Information Gathering and Methods.......................................................... 2

(2)               Project Background....................................................................................... 3

III.       Identification of Problems............................................................................... 5

A.     Integrated Design..................................................................................... 5

B.     Solid Waste............................................................................................. 6

C.     Water Quantity and Quality...................................................................... 7

D.     The Coconut........................................................................................... 9

IV.       Waste Analysis – Mombasa, Kenya............................................................. 10

A.     Waste Study.......................................................................................... 10

B.     Coconut Consumption and Waste Disposal............................................ 14

C.     Problems............................................................................................... 15

D.     Coconut Survey..................................................................................... 16

E.      Coconut Quantities Available in Mombasa............................................. 17

V.        Adsorptive Capacity of Coconut Waste-Derived Carbon............................. 18

A.     Adsorptive Uses of Carbon................................................................... 18

B.     Parent Material...................................................................................... 19

C.     Production of Carbon for Adsorption..................................................... 20

D.     Adsorption Processes............................................................................ 21

1.      Particle Attachment.................................................................... 21

2.      Chemical Reactivity................................................................... 22

3.      Species Removal from Solution.................................................. 23

VI.       Experiment to Determine Adsorptive Capacity of Coconut Waste-Derived Carbon        27

A.     Experiment Objectives........................................................................... 27

B.     Methods................................................................................................ 28

1.      Indicators.................................................................................. 28

2.      Filter Design.............................................................................. 29

C.     Sample Preparation............................................................................... 31

1.      Coconut Waste-Derived Carbon (CWD-C).............................. 31

2.      Commercially Activated Carbon (CAC)..................................... 33

3.      Sand......................................................................................... 34

D.     Experimentation..................................................................................... 35

E.      Data Collection...................................................................................... 37

F.      Data Analysis........................................................................................ 38

G.     Results.................................................................................................. 39

1.      Raw Water Quality.................................................................... 39

2.      Filtration.................................................................................... 39

a.       Dissolved Oxygen.......................................................... 40

b.      Turbidity........................................................................ 41

c.       Conductivity.................................................................. 42

d.      pH ............................................................................... 44

e.       Flow Rate..................................................................... 45

f.        Coliform........................................................................ 46

H.     Confounding Elements........................................................................... 49

I.        Conclusion of Testing............................................................................. 51

VII.      Alternative: Energy Production..................................................................... 52

VIII.     Conclusions................................................................................................. 54

 

References       ....................................................................................................... 55

 

Appendix A: Analysis of Coconut............................................................................ 59

Appendix B: Production of Activated Carbon........................................................... 66

 

List of Figures

 

3-1: Map of Mombasa, Kenya.................................................................................. 5

4-1: Mombasa Dump – Waste Projections............................................................... 13

4-2: Decomposition Study for Biodegradable, Non-coconut Waste vs.

Coconut Waste at Mombasa Dump.................................................... 14

6-1: Filter Types Used in Testing.............................................................................. 30

6-2: Sand Sieve Analysis......................................................................................... 35

6-3: Comparison of Dissolved Oxygen..................................................................... 40

6-4: Comparison of Turbidity................................................................................... 41

6-5: Comparison of Conductivity............................................................................. 43

6-6: Comparison of pH............................................................................................ 44

6-7: Comparison of Flow Rate................................................................................. 45

6-8:  Comparison of Fecal Coliform......................................................................... 47

6-9:  Comparison of Total Coliform......................................................................... 48

A-1: Uses of Coconuts............................................................................................ 61

 

List of Tables

 

4-1: Summary of Waste Characteristics.................................................................... 11

5-1: Biological Loading for Activated Carbon Filters................................................ 24

5-2: Total Coliform Removal for Activated Carbon.................................................. 24

5-3: Removal Efficiencies for Activated Carbon Filters............................................. 25

6-1: Coliform Removal Efficiencies........................................................................... 46

6-2: Homogeneity of Variance Test.......................................................................... 47

6-3: Summary of Statistical Analysis for Fecal Coliform............................................ 49

6-4: Summary of Statistical Analysis for Total Coliform............................................. 49

A-1: Chemical Composition of Coconut................................................................... 62

B-1: Chemical Reactions for Gasification.................................................................. 70

B-2: Gaseous Fraction from the Gasification Process................................................ 71

B-3: Gas Composition for Pyrolic Emissions............................................................. 72

B-4: Product Yield for Pine Bark and Sawdust Residuals......................................... 73

 

I.          Introduction

 

A.     Overview

 

This proposal began as a design project for a solid waste management course in the spring of 1996. Having spent time on the Kenyan coast as a United States Peace Corps Volunteer, I remembered the numerous vendors of coconut water that discarded their waste, leftover shells and husks, on the ground. Further, I recalled the dump for Mombasa, situated adjacent to the main thoroughfare to the coastal island city. The dump is a breeding ground for a number of illnesses that affect those living in and around the city. It is into this dump that millions of coconuts find their way each year. For this solid waste management project, I decided to study ways to divert coconuts from the Mombasa dump through waste reutilization.

My primary intention for returning to graduate school was to pursue research and study in the field of water quality engineering. I did not need to search long to discover coconut shells are often a parent material for activated carbon, a substance used in water purification. Many residents of developing nations do not have access to safe drinking water and must take precautions to protect themselves against disease. I decided to research processes employed in converting coconut shells to activated carbon for use in domestic water filters, enhancing the quality of water and improving public health. The result of this research is presented within.

Research for this project has expanded to include studies in thermal conversion processes, domestic production of activated carbon from coconuts, and filtration testing. This work is the culminating document for this academic experience, yet additional study is still required and, hopefully, will one day be implemented in Mombasa or any developing region where coconut materials are wasted.

 

B.     Information Gathering and Methodology

 

Information contained in this work has been derived through a variety of sources and methods. The primary source for data was the Humboldt State University library, which includes such resources as current volumes, interlibrary loans and available periodicals. Extensive accounts were obtained on the production of activated carbon and the coconut market internationally from professionals worldwide. The internet was extensively searched, identifying outlets to further documentation and direct, personal contacts. Laboratory experimentation has yielded figures to substantiate the claim that coconut waste-derived carbon is an effective medium for removing biological species from drinking water. The results of these experiments are presented as justification for the implementation of such a project.

 

 

II.                Project Background

 

The world’s population is approximately 5.9 billion persons (U.S. Census Bureau, 1998) with about 2.4 billion people living in coastal countries within the tropics, as calculated by the author using figures from the Central Intelligence Agency (1997). It is estimated by Lester R. Brown of the Worldwatch Institute that at least 60% of the world’s population live within 50 kilometers (30 miles) of the ocean (Brown, 1998). Applying this figure to the population in coastal countries in the tropics, there are, conservatively estimated, 1.4 billion people living in coastal zones in the tropics. As coconuts grow only in these coastal regions (Blaak, 1993; Copeland, 1931), 23.7% of human population has immediate access to coconuts, making them one of the most important resource in the world (Duke, 1989).

Regions in which coconuts flourish are also home to some of the most disadvantaged populations (Okun, 1991). Poor living conditions, inability to access proper water and sanitation, and poverty are very common. Many lack education and employment opportunities due to political and economic circumstances. Furthermore traditional societies have disintegrated primarily due to contact with western civilization.

Public health in developing regions, and specifically in urban centers, is abject. Although there has been an increase in the number of people with access to clean water and effective sanitation over the past three decades, the number of those without these privileges has increased even greater. This is a result of mass population influx from rural to urban areas, coupled with the tremendous population growth that has accompanied much of the last 30 years (Daniels, 1990; Okun, 1991). The recent evolution of drug-resistant malaria, inaccessibility to effective health care facilities, and the introduction of industrial by-products to the environment has caused morbidity to raise (Okun, 1991). Those who escape fatal exposure suffer for much of their lives. Life expectancy at birth for coastal African nations in the tropics is 51.63 years, compared to 77.56 years for seven major industrialized nations – Canada, France, Germany, Great Britain, Italy, Japan and the United States (CIA, 1997).

Like many industrialized nations, developing nations have done little to curb practices that cause ecological disturbances. Unlike industrialized nations, developing nations have little capital resource to expend on projects that promote long-term ecological stability. In fact, developing nations spend nearly all development funds on industrialization (Gore, 1992). Most efforts toward ecological accountability have been through nonprofit organizations from the industrialized West and Japan, although local grassroots efforts are beginning to appear (Carr, 1984). Unfortunately, the cost these nations will eventually pay for their efforts to industrialize will create an even greater economic burden for future generations.

 

III.             Identification of Problems

 

A.     Integrated Design

 

The reason this project has been written is to help improve the quality of life for people living in coastal zones within the tropics where coconut shells are currently being underutilized. This objective will be accomplished by reducing the amount of coconut waste being discarded to local dumps through the production of activated carbon for water treatment. At the same time public health will be improved and mechanisms for environmental protection and remediation will be provided. The approach presented in the following sections promotes complete resource recycling to achieve a higher level of local sustainability and self-reliance. Mombasa, Kenya, a city of over one million, was chosen for this study because of the author’s familiarity with its problems, gained through nearly fifty visits over a three year period.

Figure 3-1: Map of Mombasa, Kenya (not included)

 


B.     Solid Waste

 

In rural parts of developing regions, where incomes are low and animal populations are substantial, most refuse consists of food and other organic wastes, which are left to be consumed by chicken, goats and cattle. However, in urban areas, where animals and land are scarce, and incomes and proximity to goods allow for greater consumption, these practices are not possible. Large amounts of material are thus discarded, creating a need for interactive waste management. Landfills require proper engineering, from siting and design to operation and maintenance, to be effective and safe. Unfortunately, concerted efforts to control waste rarely occur in developing nations.

            For example, the present situation of solid waste disposal in Mombasa is abysmal. There are no sanitary landfill facilities for the city. The city uses an area adjacent to the Nairobi-Mombasa Road for dumping. The dump is not managed and all are allowed to discard with no permitting, monitoring or regulation.

The severity of the situation is obvious from the anaerobic conditions that exist and the absence of any waterfowl in the adjacent section of the waterway that surrounds Mombasa, as noted by the author during multiple visits to the site in 1992 and 1993. The rest of the island is rife with avian species. Also, the site bordering the channel appeared badly contaminated with leachate, a hazardous liquid formed as rainwater mixes with decomposing matter. Flow in the channel, bifurcated by the vehicular causeway, is very limited since lack of tidal effect allows for only minimal mixing.

The smell from the dump is putrid, noticeable from as far away as three miles. It is possible that air carrying odor can carry disease vectors that cause harm to humans and animals. Although no figures were uncovered to verify statistically the health threat, members of nearby communities claim they suffer from chronic intestinal ailments. Members of smaller communities farther downwind of the dump support this claim. The author recorded all statements.

 

C.     Water Quantity and Quality

 

As a result of shifting political and economic objectives after World War II, international development agencies and missionaries implemented vast modern health care programs (Hancock, 1989). Immunization campaigns proliferated throughout the developing world, and reduced infant mortality substantially. In Kenya, morbidity declined from 330 per 1000 in 1960 (Ominde, 1968) to under 100 in the late 1980's (UNICEF, 1991). The result was a rapid rise in population throughout the region.

The need for increased agricultural production to feed the rising population, coupled with inappropriate farming practices and overgrazing, has caused a tremendous amount of erosion in East Africa, resulting in loss of huge tracts of arable land (Tiffen, 1994). Furthermore, due to inconsistencies in annual precipitation and increased occurrences of drought, the quality of topsoils has dwindled. When rains do arrive, the force of torrential downpours easily dislodges vulnerable particles, removing nutrients and leaving unproductive soil. As a result of this accelerated erosion, the amount of land classified as arid or semi-arid is increasing (Tiffen, 1994). Simply stated, desertification is spreading throughout Africa as a result of human activity.

Precipitation is a factor of the amount of vegetation in a region and, since vegetation has decreased, there persists a downward cycle of less precipitation, which diminishes opportunity for natural regrowth. According to Finkel (1986), there is a great need to employ soil conservation methods for the preservation of water.

Water levels throughout much of the developing world are dropping to near crisis levels. Since there is less availability of water, people are more willing to compromise quality for quantity. For example, in drier regions, people will take water from unsafe sources (i.e., puddles where livestock have defecated or polluted wells) to placate demand. Without sufficient energy to boil water for disinfection, pathogens are easily passes from animals to humans, resulting in diarrhea, which in turns leads to dehydration. Dehydration is the second leading cause of infant death in Africa, behind malaria (UNICEF, 1991).

Additionally, industrialization in this region has led to contamination of local water supplies. Recent oil and chemical spills in Mombasa, Kenya have resulted in thousands of gallons of toxins introduced to the ecosystem (Reuters, 1996). Refineries, processing facilities and factories line the harbor channel in Mombasa, indicating a potential for the discharge of industrial wastes to the environment. Personal observances by the author of overdrawn aquifers lead to the assumption of salt-water intrusion and, subsequently, the intrusion of toxins released in factory effluent. The assumption of salt-water intrusion is supported by the brackishness of water drawn from wells in the Mombasa region.

 

D.    The Coconut

 

The coconut can play a role in helping to alleviate both solid waste and water quality problems in tropical developing countries. First, according to studies conducted by the author in 1992, coconut waste comprises 7% of material dumped in Mombasa (see Section IV). Due to its slow rate of decay, coconut percentage in the dump continues to grow in comparison to other biodegradable materials, causing concern in terms of sustainable waste management. Recognizing the need for understanding qualities of the material to be removed from the waste stream, analysis of the physical properties of coconut are included in Appendix A. Coconuts can be used to produce activated carbon, which can be used to purify water. Appendix B discusses the production of activated carbon.

 

 

IV.              Waste Analysis – Mombasa, Kenya

 

A.  Waste Study

 

According to Jeanes (1997), “in order to gain a proper understanding of the size and characteristics of the local waste stream, a waste composition and generation study must be performed.” Using professionally accepted techniques and information, remote sensing, and the personal experiences of the project designer, a preliminary waste study has been formulated for Mombasa, Kenya.

An examination of the Mombasa dump was conducted in November 1992. A small section of the area was scrutinized for types and quantities of waste and estimates recorded. The quality of the area examined was approximately 100 square feet of the most recently deposited material, chosen because older areas would represent a degree of decomposition and lessen the accuracy of the study. Once tallied for the sample area, an aerial photograph was used to estimate the area of the dump and figures for the entire site were extrapolated. Using data obtained from Tchobanoglous (1993) and adjusted for Kenyan consumption patterns, the portion of the waste stream that terminates at the Mombasa dump was characterized.

Sources of waste are not dissimilar to those in the United States, although domestic generation is drastically reduced, partly because of purchasing power and partly a result of the ‘newness’ of industrial-age consumption. Activities associated with shipping generate cardboard boxes, wooden crates and plastic as refuse. Food processing yields meat scraps, fats, oils, bone, and other offal. The refining of petroleum products creates numerous hazardous wastes including asphalt, tars, felts and asbestos. Other manufacturing activities produce such wastes as scrap metals, rubber, paper, wood, cloth and chemical residue. Large tourist hotels provide visitors all the amenities of western society, producing many of the same wastes that one would find in a typical American city, namely large amounts of food wastes, paper, cardboard, plastics and glass. Table 4-1 shows a summary of the characterization sheet for the Mombasa waste stream.

 

Table 4-1: Summary of Waste Characterization (conducted November 1992)

Type of Waste

Volume

(% total)

Total Volume

(m3)

Food Waste

 

 

69

 

  5,202,821

 

Meat

2

 

150,806

 

 

Vegetables

28

 

2,111,290

 

 

Agricultural

Waste

32

 

2,412,902

 

 

Coconut

Waste

7

 

   527,822

 

Paper

 

 

7

 

     527,822

Cardboard

 

 

2

 

     150,806

Wood

 

 

1

 

     150,806

Plastics

 

 

6

 

       75,403

Textiles

 

 

2

 

     452,419

Glass

 

 

1

 

       75,403

Tin Cans

 

 

2

 

     150,806

Appliances

 

 

4

 

     301,613

Batteries

 

 

2

 

     150,806

Tires

 

 

4

 

     301,613

Total

 

 

100

 

   7,540,320

 

 

The only recycling conducted in Mombasa in 1992 was the return of beverage bottles, which is mandated by a substantial deposit placed on containers of this type. Reuse of materials is widespread, which helps keep the quantities of solid waste below that of Western countries. This reuse is dictated by the economic situation of many residents, requiring exhaustive use of materials for which alternative functions can be found. This includes plastic bottles utilized as water storage containers, or for food storage. As convenience begins to drive the economy of the more affluent, larger amounts of materials that were once reused will be discarded.

A mathematical model for the volumetric growth of the Mombasa dump was developed for this project:

 

VT(t) =  [ VI + VB + VC] * ert  – [ VBed(b)t + VBed(c)t ],                 (Equation 4-1)

 

where,  VT(t)     =  Total volume of waste at time t,

VI         =  Volume of inorganic waste at t = 1,

VB          =  Volume of biodegradable, non-coconut waste at t = 1,

VC        =  Volume of coconut waste at t = 1,

r           =  Rate of waste disposal growth,

t           =  Time (years),

d(b)      =  Rate of decomposition for biodegradable, non-coconut waste,

d(c)      =  Rate of decomposition for coconut wastes (annual).

 

Volumes of inorganic, biodegradable, non-coconut waste and coconuts are based on the preliminary waste study for the landfill and are 301,613, 1,102,345 and 104,106 cubic meters respectively. The growth rate of waste disposal, assuming no variation in the consumptive pattern, is equal to the population growth rate for Kenya, or 2.2% annually (CIA, 1997). Rates of decomposition for biodegradable, non-coconut waste and coconut waste are stated figures (Tchobanoglous, 1993; Duke, 1989; Copeland, 1931) and from personal experiences with composting. They are 67% and 5% respectively.

With an estimated 7.5 million cubic meters of garbage added annually, decomposition of organic material becomes a very important factor in the overall volume of the dump. Figure 4-1 shows the projection of the waste volumes. Although there is 10 times as much biodegradable, non-coconut waste as coconut waste deposited each year, the rate of decomposition for coconut waste is such that after only 7 years, there is more volume occupied by coconut waste than by biodegradable, non-coconut waste (Figure 4-2). After 50 years, there are 2 ½ times as much coconut waste as biodegradable, non-coconut waste.


Figure 4-1: Mombasa Dump – Waste Projections

 

 

Figure 4-2: Decomposition Study for Bio-Degradable, Non-Coconut Waste vs. Coconut Waste at Mombasa Dump


B.        Coconut Consumption and Waste Disposal

 

As temperatures rise throughout the day in Mombasa, merchants, civil servants and tourist will purchase coconut water to quench their thirst. In 1992, the cost of a nut was 4 shillings ($0.14 USD), affordable by most of the employed population and certainly all of the tourists. The top of the coconut is removed by the vendor with a single swat of a long knife, called a panga, and the water is consumed, using the nut itself as a cup. The remainder, husk and empty shell, is discarded into a pile on the street or in the market with other agricultural wastes to be removed at the end of each day by municipally-employed city sweepers. 

The entire quantity of the agricultural waste is loaded onto a flatbed truck, or lorry, transported over the causeway, and disposed with the rest of the city's waste at the dump. Discarded coconuts cause unique solid waste problems, as they are a slowly degrading cellulose body that is hollow in the center. This results in a large amount of empty space due to the large quantity of coconut husks discarded, the lack of degradability and, subsequently, the rapid spread of the footprint of the dump. It is estimated that the volume of 43 Olympic-size swimming pools, over 100,000 cubic meters, are added to the Mombasa dump each year due to discarded coconuts. The coconut is very slow to break down, which introduces a problem for a system that has been self-monitoring for decades.

Figure 4-2 depicts the composition of the Mombasa dump projected over a fifty-year period. Note that the majority of the waste is non-coconut, organic waste, which will be biologically reduced considerably over extended periods of time. Contrarily, at the end of a 50-year period, only 57.7 percent of the coconuts mass will have been reduced and will occupy approximately 15.5 percent of the landfill volume. There is no other organic component of the dump which has this much of an impact on the volume of the dump.

 

C.  Problems

 

During the rainy seasons, precipitation can accumulate in the hollow center of the shell, acting as a suitable and nutritious breeding habitat for malaria-carrying mosquitoes. This poses a great public health risk to the residents and travelers, as malaria is the cause of more deaths than any other disease in the coastal region. Malaria is the number one cause of death for infants in tropical regions worldwide (WHO, 1990; UNICEF, 1991) and any opportunity to reduce mosquito breeding habitats should be seriously examined. Other public health effects have been discussed in the previous section.

The amount of energy and person-power consumed in the civic activity of waste collection is tremendous. Over 20 individuals were observed in a medium sized market cleaning up agricultural wastes. There are 22 major market places on the island, and it assumed that many more exist in the mainland portion of the city. Extrapolated, there are at least 440 market sweepers employed by the city. Additionally, vehicles and petrol must be purchased to transport the waste to the dump. Reducing the need to discard coconut waste will relieve the municipality of a major resource drain.

 

D.  Coconut Survey

 

The coconut is the largest indigenous crop in the coastal strip of Kenya.  There are estimated to be over 10 million coconut trees in the ten mile wide coastal strip, producing as many as 150 nuts annually (Duke, 1989). Yet, because very little of the official Kenyan economy is derived from coconuts, there have been no comprehensive studies executed to determine the availability of coconuts since independence. It is therefore proposed that a detailed survey of coconuts and coconut trees be conducted for ecological and economic purposes.

The basic purpose of the survey for this project is to estimate the amount of coconuts available for use in the 5,000 square kilometers of Kenya’s coastal zone. The survey results will be used to estimate the possibility for economic growth based on an agricultural product that has not reached its potential. Aspects for which data will be collected include number of trees, number of coconuts per tree, size of tree, variety of species, number of trees being actively harvested by humans, whether trees are government or privately owned, size of nuts, and a record of local uses.

 

E.   Coconut Quantities Available in Mombasa

 

Based on personal experience, it is estimated that there are an average of 10 vendors in each of the 20 major market places. Additionally it is estimated that there are 30 mobile carts vending coconut water on the streets, bring the total to 230 vendors. Examining various juice stands, restaurants and hotels which may utilize coconut water, a figure of 20 additional major sources of coconut waste is reached, for a total of 250 potential coconut-producing locations.

Assuming that vendors sell and discard 15 coconuts per hour during the hottest hours of the day, from 11 a.m. to 4 p.m., plus another 20 for all non-peak hours brings the total coconuts available to 80 per day per vendor. For 230 vendors, the total for the vendors is 18,400. The production of waste by the other sources, juice stand, restaurants and hotels, is estimated to be 100 per day, or a total of 2,100 coconuts. The amount of coconuts available for reprocessing in the city of Mombasa is 20,500 coconuts per day.

 

 

V.                 Adsorptive Capacity of Coconut Waste-Derived Carbon

 

There are two media from which carbon is able to adsorb: from gas-phase and from solution. This report examines adsorption from solution.

 

A.     Adsorptive Uses of Carbon

 

Carbon has been used as an adsorbant for impurities in water since the Roman Empire. The first known industrial use of carbon was for purification of sugar solutions, dating back to the Middle Ages. In the 19th Century, carbon was used to remove taste and odor in municipal water systems in England (Cheremisinoff et al, 1978). The first use of carbon for water purification in the United States was in 1930 (Huang, 1978).

As technology improved throughout the 20th Century, the ability to study and activate, or prepare carbon for highly specialized use, increased. There are many modern applications for activated carbon including tertiary treatment for municipal wastewater (Gearheart et al, 1996), industrial wastewater treatment, removing gold from rivers, heavy metals recovery, and environmental remediation of hydrocarbon contamination (Cheremisinoff et al, 1978; Huang, 1978). Carbon is regarded as the foremost removal substance for odors caused by phenols, surfactants, pesticides and herbicides (Tchobanoglous, 1987). Additionally, activated carbon is highly effective in removing radon-222, organic mercury, and trihalomethane precursors. Unfortunately, production of activated carbon is comparatively expensive, primarily due to the cost of equipment used to activate it, and its use remains limited (Gearheart et al, 1996).

 

B.     Parent Material

 

As an elemental substance, carbon can be derived from any material that has volatile carbon compounds. Because carbon for adsorption is most commonly produced through thermal distillation, which effectively destroys bonds without volatizing the carbon, naturally dense materials are preferable.

Some of the first materials used for carbon production were coal, peat and nut shells. During the research of the processes of carbon production, it was discovered that char remains of wood from the Pacific Lumber, Scotia (CA) Cogeneration Plant were also use as a source of carbon at the Calgon Carbon Regeneration Plant in Blue Lake, California.

Widely accepted as one of the best sources of adsorptive carbon is coconut shell. Coconut shell is a very dense, highly cellulosic material found in abundance throughout the tropical regions of the world. In fact, most of the experimentation on carbon adsorption examined for this report has used at least one sample derived from coconut shells (Arulananatham et al, 1989; Cheremisinoff et al, 1978; Cookson, 1978; Gergova et al, 1993; Huang, 1978; Laine et al, 1989; Mattson et al, 1971; Namasinayan et al, 1994, Rao et al, 1992). One reasons that coconut shells have not assumed a greater role in carbon production is that production facilities are primarily in industrialized countries in Europe and America, resulting in high transportation costs from less developed coastal zones in the tropics.

 

C.     Production of Carbon for Adsorption

 

Carbon is most commonly formed through a three-step process of dehydration, carbonization and activation (Cheremisinoff et al, 1978; Cookson, 1978). Dehydration is the removal of moisture from the material. By causing excess water to vaporize, temperatures in latter steps of conversion are more easily controlled. Dehydration can either be done mechanically, in a controlled heating environment, or naturally, using favorable climatic conditions. Carbonization is the reduction of organic matter to elemental carbon. This is achieved through breaking carbon bonds and volatilizing the non-carbonaceous portion. Because the process includes additional energy and efficiency translates to a financial consideration, this step is typically executed in a specifically designed furnace.

The final step, activation, is achieved by thermally cracking, or pyrolizing, carbon in the absence of atmospheric oxygen. Cracking of carbon particles increases surface area by increasing the number of small diameter fissures in the material. Heated anaerobically, carbon is exposed to oxygen during a gradual cooling phase, forming oxide groups on the surface of the carbon. Another activation process that is currently being used is the addition of chemical solutions that replaces the final thermal process. Common oxidizing agents are potassium permanganate, nitric acid, sodium hypochlorite, ammonium persulfate, and zinc chloride (Rao et al, 1992).

Reactants effect the portions of char with high oxidization potential, developing an extensive pore structure and a complex internal surface. The fissures, or pores, and the oxide groups are critical in the adsorptive characteristic of activated carbon. Several factors influence the quality of activation, including type and amount of oxidant introduced during the process, heating and cooling temperatures and rates, contact time between carbon and oxidant, and parent material (Rao et al, 1992).

 

D.    Adsorption Processes

 

Carbon adsorption is a function of two primary processes: particle attachment and chemical reactivity. Pore-size distribution and surface area of the material dictate attachment of particles, while surface oxide groups determine chemical reactivity.

     

1.      Particle Attachment

 

As mentioned in the previous section, activation increases pore structure of carbon. Typical carbons will have a surface area of 500 - 1400 m2/g after activation. Surface areas for adsorptive material are commonly achieved through measuring uptake of a readily adsorbed liquid, usually iodine. Some studies have shown carbon to achieve surface areas of 2500 m2/g. Commercially available activated carbon produced from coconut shell has a range from 1100 - 1400 m2/g. This tremendously large surface area lends to the ability to adsorb large quantities of materials from solution. Pores in the surface of carbon can be as small as 10 microns in diameter, making removal of very small organic matter and metals possible (Huang, 1978).

As a solution travels over carbon, either by gravity or localized movement depending on the process for which the carbon is being used, particles become lodged in the pores of carbon of the solution. These dissolved ‘adsorbates’ must be smaller in diameter than that of the pore in the carbon surface, allowing it to enter and amass. This is usually the case for smaller particles, which will continue to penetrate a pore until its diameter is equal to that of the pore, becoming fixed (Deithorn, 1986).

Often, reactive forces between the particle and the carbon surface aid attachment. Activated carbon consists of layers of crystalline carbon supported by weak van der Wall’s forces. The amount of impurities in the parent material will determine the structural formation of activated carbon, with the most pure carbon sources producing the most authentic crystalline configurations and the strongest localized forces (Cheremisinoff et al, 1978).

 

2.      Chemical Reactivity

 

Impurities in the parent material, often other organic compounds, result in the chemical bonding of oxygen and hydrogen to the surface of carbon, or the ‘surface oxide’ group mentioned above. It can be assumed that the parent material must be ‘impure’ to form surface oxides, which are a primary factor in chemical reactivity. These oxides groups are most typically CO, CO2, OH and H2O entangled among carbon bonds on the surface (Cookson, 1978; Mattson et al, 1971).

Commonly referred to as ‘double layer’ chemical reactivity, closer scrutiny reveals multiple layers of ions. The surface of the carbon can either be charged ‘positively’ or ‘negatively’, depending on rate of heating, temperatures achieved, length of heating, cooling rates and method of oxidation. If the surface is charged, say positively, the inside layer of attracted matter will consist of negatively charged particles. The next few layers will also be negatively charged as the mass of surface oxide groups on the surface of the carbon will still be attractive. Outside the range of surface forces, designated by the ‘Helmholtz plane’, there will be diffuse forces, attracting both negatively and positively charged particles. In our positively charge carbon example, negative particles will still be under the forces of the carbon surface oxide groups and positive forces will be attracted by negatively charged particles, which are electronically reacting with the surface of the carbon (Mattson et al, 1971).

However, there are additional forces that work against the adsorption process. Since solutions are seldom homogenous in composition, oppositely charged particles will interfere with one another and sometimes inhibit adsorption. Often present in waters are solvents, like surfactants and other chemical compounds, which can alter the charge of the adsorbate, lessening the likelihood of the particle to be adsorbed. As long as the attractive force between the surface of the carbon and the adsorbate exceeds the cumulative effect of distractive forces, the particle will be chemically attracted.

 

3.      Species Removal from Solution

 

Matter will continue to accumulate until there is no more surface with which to react. Rates of degradation vary widely, depending on the nature of the adsorbate and quality of the carbon surface. Organic matter, which carbon is highly effective in removing, is further reduced and rendered harmless through reduction, where a biologically active layer on the surface of the carbon metabolizes more harmful microbes. Biological reduction attenuates the amount of organic matter present within pores of carbon, restoring surface area and lengthening the effective removal period. This is important for water and wastewater treatment processes.

Due to its irregular external surface and porous structure, carbon makes a suitable habitat for microorganisms, which consume degradable particles seeking to attach as well as unconverted impurities in the carbon surface. The biological removal of bacteria through this attached growth treatment system will likely improve the quality of the water. Bacterial colonies build up on the carbon surface and within pores, increasing the removal of organisms over time (Tables 5-1 and 5-2). In their research, Rice et al (1978) show that using granulated activated carbon filtration improved total coliform removal from 58% to 75%.

 

Table 5-1: Biological Loading for Activated Carbon Filters

Maturation (time)

 g organisms adsorbed/

kg of carbon

fresh

 4

2 months

 37

3 months

 63.5

7 months

 68.5

(Adapted from Rice et al, 1978)

Table 5-2: Total Coliform Removal Rates for Activated Carbon

Processes

 Removal Efficiency

Flocculation, sedimentation, filtration

58%

Flocculation, sedimentation, filtration and granular activated carbon filtration

 75%

(Adapted from Rice et al, 1978)

However, effluent from biologically active carbon can begin to increase bacterial counts if hydraulic loading is too great, pushing out bacteria without chance for bioreduction. Additionally, if there are soluble carbon residues in waters with low dissolved oxygen, bacterial growth can become anaerobic, creating sulfur dioxides and associated odor problems. A common preventative measure used in Europe is to preozonate activated carbon, to assure sufficient oxygen availability between regeneration cycles of the carbon and preventing anoxic conditions. For effective operation, carbon must be rinsed thoroughly with distilled water to make certain that residues are not present and that oxygen levels are sufficient to prevent anaerobic conditions (Rice et al, 1978).

Gearheart et al (1996) note that using granular activated carbon for filtration equals sand in removal of residual coagulants and turbidity, and exceeds sand filtration in lowering total organic carbon. Table 5-3 depicts removal efficiency ranges for total suspended solids and oxygen demand, determined by testing a variety of activated carbon samples.

Another advantage of carbon over sand as a filter medium is that empty bed contact times for a carbon filters is around 10 - 20 minutes, far shorter than slow sand filters, allowing for equal treatment in less time (Gearheart et al, 1996).

Table 5-3: Removal Efficiencies for Activated Carbon Filters

Constituent

Low %

High %

Total Suspended Solids

49.3

55.7

Chemical Oxygen Demand

20.1

35.7

Biochemical Oxygen Demand

1.7

75.8

     (Adapted from Cheremisinoff et al, 1978)

A limitation for more focused application is that effectiveness of carbon as an adsorbant depends on the pH of the adsorbate (Gearheart et al, 1996;  Mattson et al, 1971). Adsorption increases as pH decreases in neutrality and, according to Rao et al (1992), effectiveness is maximum at pH 1, indicating that the effectiveness of carbon adsorption is greatest when surface oxides are alkaline in nature.

 

 

VI.       Experiment to Determine Adsorptive Capacity of Coconut Waste-Derived Carbon

 

To justify use as a filtration medium in developing regions, coconut waste-derived carbon (CWD-C) must be shown to improve water quality. An experiment was designed to examine the performance of CWD-C as a filtration medium. Described below, the experiment was conducted in conjunction with the Department of Environmental Resources Engineering at Humboldt State University and the City of Arcata, California. This section presents some results of the CWD-C testing. A power analysis, based on previous experimentation with carbon (Arulananatham et al, 1989; Cheremisinoff et al, 1978; Collins et al, 1990; Mattson et al, 1971; Rice et al, 1978), was used to determine sampling sizes for the design. The performance of the CWD-C was examined from a case-control approach, in comparison to other filtration media, and over time.

 

A.       Experiment Objectives

 

The objectives of the project are:

·        to determine the applicability of using coconut waste-derived carbon, produced using intermediate technologies, for water purification;

·        to examine removal efficiencies for turbidity and coliform for filters containing coconut waste-derived carbon; and,

·        to compare the removal efficiencies of coconut waste-derived carbon with other filtration media.

 

B.       Methods

 

The process design for the examination of the performance of the CWD-C entailed passing water through filters. Filter materials were standardized to decrease design error. To scrutinize the progressive performance of filter media and to make comparisons between media, tests were conducted over a period of one month. The data has been analyzed using a variety of statistical methods and the results are outlined at the end of this section.

 

1.       Indicators

 

Typically in water quality testing, indicator species are chosen and monitored. Coliform and turbidity are two of the primary constituents used for water quality standards in the United States, and often accurately reflect suitability of a water source for consumption. These constituents were chosen as indicators. The source of water was Hauser Marsh, the final constructed wetland at the Arcata (CA) Wastewater Treatment Facility, which is essentially deficient of turbidity. Thus, the role of turbidity in filter performance analysis was de-emphasized for this experiment. Both total and fecal coliform were studied to determine performance of the carbon.

 

2.      Filter Design

 

Experimental filters were constructed to be similar in composition to filter technology propagated throughout the developing world. This filter design was chosen because it most closely represents the intended use of the material, which is as an enhancement to domestic sand filters in developing countries.

Sand filters propagated by United States Peace Corps Volunteers in coastal region of Kenya consist of a 20-liter, high-density polyethylene (HDPE) bucket with a perforated bottom placed upon another 20-liter bucket used for storing of filtered water (Wright, 1991). In the top bucket is placed 5 to 8 cm of small stones, less than 5 cm in diameter, topped with 5 to 8 cm of smaller aggregate, roughly 1 cm in diameter, upon which 15 cm of sand is placed. This layering is used to prevent the filtration media from passing through the perforated bottom, contaminating the stored drinking water, possibly clogging up the holes in the bucket, and causing the filter to fail prematurely. This design maximizes purification of water at a minimum of cost and maintenance.

These filters are slow sand filters, meaning they utilize biological activity within the top layer of sand, or ‘schmutzedecke’, for further reduction of organic matter. Slow sand filters have been shown to produce an effluent with a turbidity below 1.0 NTU, an ideal level for consumption (Roecklein, 1993). By adding carbon to the top of the filter, the performance of the filter is enhanced through the adsorption of species, and by providing a more suitable habitat for the growth of contaminant-reducing microorganisms.

In theory, since performance of a filter is dependent mainly on the vertical cross-section of filter media, it is not necessary to use a bucket of equal diameter to the 20-liter buckets employed in the Peace Corps sand filter. It was expected that a minimum diameter of 20 cm could be used without biasing the outcome as a result of ‘side-channeling’. A 20-cm low-pressure polyvinylchloride (PVC) drainage pipe was chosen as the housing for the filter media. To achieve the depth required for the modified filters while leaving enough freeboard for infiltration of water, the 20-cm PVC pipe was cut to a minimum of 50 cm in length. A section of wire mesh was secured to the bottom of each pipe, serving as the platform upon which media was placed.

                                1            2            3            4            5           6

 

                            ß                    ß                    ß                  ß                   ß                     ß

 

 


               

             

                  7 cm

 


 50cm

              

             15 cm

 

 

                         

   ß                     ß                    ß                    ß                  ß                      ß

 


1 - 15 cm sand and 7 cm commercially-activated carbon                                                                                                                           - commercially-               

2 - 15 cm sand and 7 cm commercially-activated carbon                                                 activated carbon

3 - 22 cm of sand

4 - 22 cm of sand                                                                                                             - sand

5 - 15 cm sand and 7 cm coconut waste-derived carbon              

6 - 15 cm sand and 7 cm coconut waste-derived carbon                                       - coconut waste-

                                                                                                                                                   derived carbon

 

Figure 6-1: Filter Types Used in Testing.

 

As described above, 1-cm aggregate was loaded on top of 5-cm aggregate lining the bottom of the filter (not shown in the above schematic drawing). On top of the aggregate was placed 15 cm of sand and 7 cm of either CWD-C and commercially-available activated carbon (CAC), or another 7 cm of sand so that all filters had 22 cm of media. Before filter construction, all of the aggregate was rinsed three times with boiled water to remove contaminants and minimize interference with filter performance criteria. Since the water being filtered was not used for consumption, there was no need to replicate the bottom storage bucket of the Peace Corps filter, although a collection system was used to facilitate sample collection and prevent puddling at the test location.

 

C.        Sample Preparation

 

1.      Coconut Waste-Derived Carbon (CWD-C)

 

Shells of coconuts, imported from Peru and purchased at markets in McKinleyville, California, were converted to activated carbon through a two step process. First, the shells were partially burned, or gasified, in a manually-controlled, continuously-loaded Sweet-HomeŌ wood-stove measuring 40 cm x 40 cm x 60 cm. After the shells turned to char, in 30 minutes, they were removed from the wood-stove and cooled. Cooled pieces of coconut char were carefully crushed and placed inside a 20-cm diameter metal cookie tin.  The tin was placed in the wood-stove for 6 hours. Energy for activating coconuts ‘on-site’ will be derived from charring other coconut shells. However, due to the prohibitive cost of coconut material at the testing site, the subsequent fuel source for this experiment was partially-seasoned alder.

Once removed from the wood-stove, the cookie tin was opened slightly, allowing for oxidation of the carbon surface during cooling. This is the most important step in activating carbon for chemical reactivity adsorption, according to Mattson et al (1971). Because of the relatively low temperature of pyrolization and the method chosen to expose carbon to oxygen, this carbon is considered ‘slow-cooled’, meaning it is designed for removal of acidic substances.

This imperfect method of producing carbon is used to produce a material for testing which will closely resemble the carbon resulting from a project implemented in developing regions. This has been done to avoid biasing results of the experiment should carbon produced through a more controlled thermal environment be used for examination.

The resulting char was rinsed three times with water boiled for 20 minutes to remove surface ash content and char dust, which would otherwise be dislodged during filter usage. For more stringent laboratory experiments, de-ionized or distilled water would be used as a scouring agent. However, using boiled water is consistent with what is expected in villages in developing regions. The 20-minute boiling standard was set by the World Health Organization during the 1980’s Water and Sanitation Decade for the household purification of domestic potable water (WHO, 1987).

Seven coconuts (1.75 kg of coconut shell) were used to produce 0.33 kg, or 1,325 cubic centimeters, of sample carbon used in filter number 5, a CWD-C filter, for testing. The density of the carbon was 248.9 kg/m3. This procedure was replicated, using the same heating times, to produce an equal amount of material for testing of a parallel filter, number 6, replicating natural variation.

As a justification for this informal production of carbon for experimental purposes, Mattson et al (1971) conducted analyses of sugar carbons activated by placing coconut material in a porcelain crucible, with the top left ajar for oxidation, in a muffle furnace at 600°C for 6 hours. Although the temperature obtained for the creation of the experimental batch of coconut waste-derived carbon in this current experiment was not maintained at a constant 600°C for the duration of the heating, the temperature was in the range of 550°C and 700°C for the same amount of time. Further, Rao et al (1992) thermally activated carbon by placing coconut shells inside a small metal box, and immersing the box in sand, which was within a larger metal box. The unit was then heated to 800-850°C in a muffle furnace and allowed to cool over a 10 hour period, yielding activated carbon samples for laboratory experimentation. 

 

2.      Commercially-Activated Carbon (CAC)

 

The original samples of CAC were obtained from the Calgon Carbon, Corporation located in Pittsburgh, PA. These samples were destroyed by vandals during the first attempt at data collection. Carbon samples for subsequent filter tests were purchased through a local retailer, using carbon designed for purification of water tanks to maintain aquatic populations. No data has been made available by the manufacture as to the properties of this material. Sieve analysis showed astonishing homogeneity in the carbon, with 99% of the material retained by the 1.168 mm mesh.

 

3.       Sand

 

When designing a sand filter, it is important to know the size of the sand that is being used. Knowing average particle size allows calculation of hydraulic loading, which controls design and operation of sand filters. For water treatment, it is ideal to have a well graded sand, with a uniformity coefficient in the vicinity of 1.4 to 1.8, and an effective size between 0.7 mm and 1.4 mm (Tchobanoglous, 1987). Sand for this experiment was obtained at the closest possible source, the local hardware store. In developing countries sand would be obtained also at the closest possible site, which might not be a commercial and standardized source.

Results of the sieve analyses for two 500-kg samples of sand used are shown in Figure 6-2. The uniformity coefficient for the means of the two samples is 2.8 with an effective size of  0.65 mm. Engineers designing sand filters for larger projects in more industrialized and regulated countries will utilize this information to calculate head loss, run length, and backwash velocities required to maximize operation. Since these filters are being used where this design is a ‘best alternative’, concern for precision of sand quality is diminished. 

Sieve analysis indicates this is a well-graded sand and has an effective size that is slightly smaller than the 0.70 mm threshold suggested by Tchobanoglous. Since each of the six filters is using sand from the same source, expected performances of the filters, amendments notwithstanding, should be nearly identical. This will enable isolation of filter amendments for study.

Figure 6-2:  Sand Sieve Analysis. For filter media in the six filters used in experiment.  Figures are averages for the sieve analyses performed.

 

D.      Experimentation

 

To determine the effectiveness of CWD-C enhanced filters compared to that of CAC enhanced filters and the Peace Corps sand filter, water samples were taken from each after passing through the filter. To facilitate determining statistical significance by replicating ‘within treatment’ variance, two experimental filters of each type were constructed, resulting in a total of six filters (Figure 6-1).

Since it is known that activated carbon loses ability to adsorb matter once the pores have reached maximum capacity (Rice et al, 1978), the performance of the filters over time was analyzed in an attempt to determine exhaustion. However, due to resource constraints, a limit was placed on the amount of water passed through the filter for the test. The CWD-C was scheduled to be tested over a period equivalent to two month’s use by a typical family in a developing region. Some non-arbitrary factors leading to establishing this limit is that this would require users to replace the media every two months, or six times a year, calling for carbon from 168 coconuts annually per filter, a very attainable amount. Furthermore, when working with families, Peace Corps Volunteers recommend that the media in the sand filters be washed or replaced every two months. Additionally, depending on quality of water being filtered, it has been noticed that the flow rate of a typical Peace Corps sand filter diminished markedly after this amount of time, primarily due to poor quality of raw water (Wright, 1991).

However, the determining factor is not actually time, but quantity of material accumulated in the pores of the activated carbon, which, using this filtration method, is a function of the quality and the volume of water filtered. The quality of drinking water sources varies widely and is essentially uncontrollable. Yet, to emulate the poor quality of water consumed in many situations around the world, it was decided to use water from Widow White Creek in McKinleyville, California, which is a watercourse running through residential, light industrial, commercial and agricultural sections of the town. After this site proved infeasible, an alternative source was located, extracting effluent from Hauser Marsh, the last of the three finishing marshes in the Arcata Wastewater Treatment Facility. Since the limit now focused upon quantity, the time constraint was removed, allowing for accelerated testing. 

To reach the limit of two month’s use for a family of eight people, meeting the 7 liter-per-day-per-person standard set by the World Health Organization (1987), 3,360 liters would need to be filtered per unit. However, since the filters being used have one-fourth the surface area of the Peace Corps filter, the actual amount of water to be filtered per unit is reduced to 25%, or 820 liters. This figure was later reduced to 360 liters to expedite completion of the research. Subsequently seven samples, systematically chosen, were taken from every 60th liter for each filter, using unfiltered water as control measurements, thus compiling the sample pool for analysis.

 

E.       Data Collection

 

Water was loaded into each filter using a 4-liter jar to transport the Hauser Marsh effluent, accessed through a concrete cistern adjacent to a fish bioassay at the Arcata Wastewater Treatment Facility. Once filtered, flow rates were recorded and the desired samples were taken to the Water Quality Laboratory at Humboldt State University for testing. 

As mentioned above, the primary focus of testing was to measure levels of total and fecal coliform. The ‘filter membrane method’ of detection, as described by Clesceri et al (1989), was used to measure levels of coliform in all seven water samples - one from each of the six filters and one of unfiltered water. The amount of water to be filtered for each test was 0.5 mL for total coliform and 100 mL for fecal coliform, quantities determined through a preliminary testing period of three days. 

To improve probability of determining, with statistical significance, whether the sand filters enhanced with coconut-waste derived carbon outperform filters with only sand, a power analysis was implemented to determine number of data points needed. With four samples from each filter type and the unfiltered water, a power of 85% was obtained. Increasing the samples to five resulted in an increase in power of only 3%. It would have required six data points per filter type to obtain 90% power and ten to obtain 95% power. These additional points were determined to be infeasible from a ‘return-on-investment’ perspective, as the cost of laboratory material is prohibitive and funding for the project was provided solely by the author. Therefore, four filter-membrane tests were run for the unfiltered water and for each filter type, with two tests per filter for both total and fecal coliform.

In addition to collecting coliform data, measurements recorded for each filter run included dissolved oxygen (DO), turbidity, conductivity and pH. The purpose of these measurements, besides the relative simplicity of the tests, is to determine if these constituents are affected by interaction with the carbon.

 

F.        Data Analysis

 

Three methods of analysis were used to examine collected data. The first was to inspect manually the data for each constituent, noting any irregularities and searching processes for sampling or data entry error. Second, data was entered into Microsoft Excel 7.0Ó. Averages and removal efficiencies were calculated, data cross-referenced and ordered to facilitate further analysis. This data was plotted to compare visually the performance of each filter and filter type. Finally, the statistical software package, Minitab 9.1Ó, was used to determine means, confidence intervals, and analyses of variance (ANOVAs).

 

G.      Results

 

1.       Raw Water Quality

 

Raw, unfiltered water, had an average dissolved oxygen content (DO) of 4.7 mg/L, an average turbidity of 2.73 NTU, an average conductivity of 376 microMHOS, and an average pH of 6.0 over the test period. Without the spike that occurs in turbidity on the final day of testing, average turbidity is under 1.5 NTU. Results from filter membrane tests showed an average of 150,800 total coliform and 12 fecal coliform colony forming units (CFU) per 100 mL.

As a drinking water supply, this water is considered unsafe by many drinking water standards established in industrialized countries (Tchobanoglous, 1987; World Health Organization, 1987). This is due to relatively low level of dissolved oxygen, a result of biological uptake, and high coliform counts, which should ideally be below 1 CFU per 100 mL, as indicated by the California Department of Public Health (Tchobanoglous, 1987). The high level of coliform in this water proved beneficial to the experiment, as there is high potential for significant reduction in bacteria, especially in terms of total coliform.

 

2.       Filtration

 

DO, turbidity, conductivity and pH measurements for each filter type over the testing period and in relationship to raw water are shown in Figures 6-3, 6-4, 6-5 and 6-7.

 

a.      Dissolved Oxygen

 

The rise in dissolved oxygen concentration was not trivial. Filtration through each filter type caused a 60% increase in DO on average, although there was little difference between filter types themselves. This is believed to be caused by aeration when the water passed through the filter but, more importantly, from the mixing that occurred when the droplets of filtered water were collected in the sample bottles for testing. While a substantial improvement in water quality ensued, and certainly worthy of further study, it is likely that it is unrelated to the media used in the filtration process.

Figure 6-3:  Comparison of Dissolved Oxygen.  Measurements for the filter types are averages.

 

b.      Turbidity

 

As mentioned above, there is little turbidity in the Hauser Marsh effluent and this is a consequence of extensive tertiary treatment of natural wetland systems. Turbidity measurements for filtered water from the first day, after one liter had been filtered, were quite high, doubtless the result of fine particles of sand and carbon dust still present on the media. After 60 liters had been filtered, and probably much before, turbidity levels were satisfactorily low and, before 200 liters had been filtered, the readings were nearly identical for raw water and filtered samples.

Figure 6-4:  Comparison of Turbidity.  Measurements for the filter types are averages.

On the final day of testing, a fortunate event occurred. The water in the cistern was discernibly more turbid, as a result of rainfall, allowing the filters an opportunity to remove some visible material. All filters lowered the turbidity in this water, with the CWD-C outperforming the other two filters by 80%. Note there was only one observation where considerable turbidity was present and no significant conclusions should be inferred from a single observation. However, the CWD-C filters, on average, performed comparably to the sand and CAC filters. Future research in this area may choose to use more turbid water to focus on the turbidity removal capacity of CWD-C.

 

c.       Conductivity

 

Throughout the literature reviewed for this project, many scientists praised the capacity for carbon to adsorb ionic species from concentration (Arulananatham et al, 1989; Collins et al, 1990; Mattson et al, 1971; Rao et al, 1992; Rice, et al, 1978). It was believed that monitoring conductivity levels of the water before and after filtration would indicate whether there was a reduction in ion concentrations, provided substantial ions were present in the raw water.

Average conductivity levels throughout the experiment are such that it is improbable that there were an unusually high level of ions in solution. The treatment the water receives in the marsh system generally leads to high ion removal rates (Gearheart et al, 1996). Average conductivity in the raw water, 376 microMHOs, is not greatly different than the 389 to 394 microMHOs range of the filtered water.

Since levels were higher in the filtered water, not lower as expected, re-evaluation of the processes of adsorption from solution should be conducted. One possible explanation is that some oxide groups on the carbon surface may have been unstable and became soluble, adding to the net ion concentration and an increase in electrical conductivity. Another possibility is that salts contained in the sand material have dissolved in solution and have affected the measurements.

Figure 6-5:  Comparison of Conductivity.  Measurements for the filter types are averages.

 

d.       pH

 

Average pH, or hydrogen ion concentration, of the filtered water was generally higher than the raw water (6.2, 6.3 and 6.2 for CAC, sand and CWD-C, respectively, to 6.0 for the raw water). There was virtually no difference in pH between filter types. In no case was the change in pH greater than 0.6, which occurred between one sand filter and one CWD-C filter on the first day of data collection. Since the first day of testing, the greatest deviation was 0.4, an improvement made by CDW-C filters over the raw water.

Figure 6-6:  Comparison of pH.  Measurements for the filter types are averages.

 

e.      Flow Rate

 

As represented in Figure 6-7, flow rates for each filter gradually decreased in an asymptotic fashion, as is to be expected for the run length of a filter (Gearheart et al, 1996). Clogging actually works in favor of removal efficiencies for two reasons. First, since the pores are decreased in size and number, particulate matter has less opportunity to pass through a larger opening, becoming ‘captured’ in the media. Second, the increased time water takes to pass through the filter allows for increase contact time with the biological layer and a higher level of bio-reduction of pathogens and adsorption of contaminants. A filter that follows this pattern of flow rate can be assumed to be acting properly, increasing treatment until all pores are ‘clogged’ and must be cleaned.

 

Figure 6-7: Comparison of Flow Rate.  Measurements for the filter types are averages.

Flow rates are generally consistent with what is expected of slow sand filters, in the range of 80 to 400 L/m2 * min (Tchobanoglous, 1987), although, toward the end of the experiment, flow rates decreased below the suggested lower limit, indicating that the filters may be close to failure.

 

f.        Coliform

 

Total average removal efficiencies for the three filter types are shown in Table 6-1. The CWD-C filters were able to remove more of the bacteria than the other two filter types, and considerably more in the case of the total coliform. Figures 6-8 and 6-9 depict average levels of total and fecal coliform for each filter type and raw water.

To determine significance using statistical methods, data was first tested for normality. Data sets proved to be highly normal, passing both Bartlett’s and Levene’s test, with p-values less than 0.1%. A summary of the homogeneity of variance test is included in Table 6-2.

Table 6-1.  Coliform Removal Efficiencies

Filter Type

Fecal Coliform

Total Coliform

CAC

55.7%

34.8%

Sand

60.0%

37.0%

CWD-C

61.4%

49.3%

Table 6-2: Homogeneity of Variance Test

 

Bartlett’s Test

Levene’s Test

 

Test Statistic

p-value

Test Statistic

p-value

Total Coliform

25.023

0.000

4.067

0.009

Fecal Coliform

39.941

0.000

11.145

0.000

 

Figure 6-8: Comparison of Fecal Coliform.  Measurements for the filter types are averages.

 

Figure 6-9: Comparison of Total Coliform.  Measurements for the filter types are averages.

A series of ANOVAs was conducted testing difference in the filters, with comparison tests on filter types in relation to one another. Tables 6-3 and 6-4 outline important results from these tests, including p-values for each testing cycle, comparison tests (noting either pass or failure) and the p-value for ANOVAs on the sand and the CWD-C filters. Although the filters themselves noticeably improved the quality of the raw water from the standpoint of coliform removal, variation in the data and the relatively small number of data points obtained for each filter led to an inability to find statistical significance for the hypothesis that CWD-C enhanced filters perform better than filters with just sand.

Table 6-3: Summary of Statistical Analysis for Fecal Coliform

Fecal Coliform

 

 

Comparison Tests for Sand and CDW-C

 

Day

p-value

Dunnett’s

Tukey’s

Fisher’s

p-value**

1

0.106

F

F

F

0.045

2

0.016

F

F

F

0.435

3

0.000

P

P

P

0.025

4

0.000

F

F

F

0.036

5

0.001

P

F

F

0.504

6

0.000

P

F

F

0.693

** Second p-value is for the ANOVA performed directly between sand and CWD-C filters.

P = pass, F = fail.

 

Table 6-4: Summary of Statistical Analysis for Total Coliform

Total Coliform

 

 

Comparison Tests for Sand and CDW-C

 

Day

p-value

Dunnett’s

Tukey’s

Fisher’s

p-value**

1

0.055

P

F

F

0.127

2

0.242

F

F

F

0.382

3

0.070

F

F

F

0.003

4

0.058

F

F

F

0.253

5

0.213

F

F

F

0.473

6

0.000

P

F

F

0.387

** Second p-value is for the ANOVA performed directly between sand and CWD-C filters.

P = pass, F = fail.

 

H.     Confounding Elements

 

Possible areas of bias for the experiment are that the filters may have allowed ‘side-channeling,’ or water moving down the side of the filter, eluding the filter media and avoiding treatment. A 20-cm PVC pipe was chosen to decrease the potential for this but, since total coliform rates are very high and the filters are biologically immature, it is difficult to say whether this became a factor in the results. 

If bacteria were to grow on the PVC pipe, this could be considered a reflection on the material used for the testing, rather than the HDPE buckets which are typically used in the Peace Corps filters. This nuisance, as with the previous one, is consistent from filter to filter and insignificant, unless there is some reactivity between carbon and the filter material. Any reaction between media and HDPE is presently unknown.

Additionally, even though much consideration was given to replicate processes as they would be implemented in the developing world, there are a number of inconsistencies between CWD-C samples used in the experiment and that expected to be made ‘on-site’. First, the sample carbon is derived from a coconut variety from Peru and coconut varieties are known to have slightly different qualities (Copeland, 1931; Duke, 1989). This may cause formation of a different carbon type, and a difference in performance may result. Second, the sample coconut was grown for the purpose of obtaining meat and may have been chemically or genetically altered. Furthermore, the sample coconut was fully matured, with a well defined layer of coconut meat on the inside of the shell, rather than immature, containing 97% water content and a 3% glucose content, which are qualities of the proposed raw material. Next, the sample coconut was air dried for over one-month in McKinleyville, California (roughly 41°N latitude, in the temperate climate of the Pacific Northwest) not the tropical climates in which the project would ideally be implemented. Although both of these climates are very moist, average annual temperature in McKinleyville is nearly 15°C lower than in Mombasa.

Finally, the data was collected for a period only equivalent to one month’s use and the exhaustion point of neither sand nor carbon filters was attained. In fact, due to an unexplained occurrence in the laboratory on the final day of testing, data points for coliform at 360 liters of water filtered were returned as null. It is obvious that additional data points are required to remedy these shortcomings.

The actual effects that may have occurred due to the above mentioned considerations are presently unclear. Additional study may chose to develop strategies that neutralize any effects these factors may cause.

 

I.       Conclusion of Testing

 

Though the experiment was unable to determine, with statistical significance, the difference in the function of the filters, there are indications that the CWD-C filters did outperform the sand filters for removal of total coliform, notably for the third, fourth and fifth testing cycles. This shows there is potential for CWD-C enhanced filters to improve water quality over simple sand filters, and that more extensive data should be collected.

Due to the relative ease and low cost of accumulating and processing coconut shells in developing regions, the importance of diverting agricultural waste from landfills, and the marked increase in water quality of the CWD-C filters over the sand filters, it is recommended that this technology be implemented on a test basis until such a time as more significant data collection can be supported.

 

 

VII.     Alternative – Energy Production

 

As mentioned previously, this report offers only one of various projects for which implementation of waste reutilization can occur. This section takes a look at an alternative of producing energy for communal use from coconut residues.

It is advantageous for any community to thermally convert organic wastes for energy because it reduces the amount of waste needing to be interred by as much as 95% (Tchobanoglous, 1993). This is critical in urban areas where overconsumption and incomplete utilization of exploited resources result in huge quantities of waste. It is even more beneficial to convert wastes in countries that are economically disadvantaged. These countries typically cannot increase their energy production to meet international standards. A large percentage of fossil fuel consumption in these countries is devoted to vehicles and heavy industry, leaving light manufacturing and domestic energy demands unfulfilled (Shuler, 1980).

In many regions, agricultural residues, such as dung, straw and cob, have been used for centuries as fuel sources. Societies in the Nile, Ganges and Yangtse River valleys were forced to resort to the burning of agricultural residues once the supply of wood was exhausted. Today, over 800 million people, almost 15% of the world’s population, rely solely on agricultural residues for their energy needs (Shuler, 1980).

Combusting refuse derived fuels (RDF) in incinerators for large-scale energy production has been practiced in the United States since the “energy crisis” of the early 1970s. Although motivation for technological advance was economically based, indirect, non-market benefits in terms of waste reduction should not be overlooked.

In addition, alternative and more efficient means were developed (Alter, 1980). A common method of maximizing resource efficiency is to operate a cogeneration facility. One possible scenario could be to utilize the entire load of coconut shells for energy production through combustion, while using the energy to manufacture processed goods from the husk of coconuts.

There are 20,500 coconuts available per day in Mombasa (see Section IV for calculations), or 10,250 kg of shell. At 18,011 BTU/kg (from Appendix A), the resulting daily energy potential is 184,612,750 BTU/day. Considering a conservative 30% efficiency for an old steam turbine, the result is 55,383,825 BTU of electricity, or 16.232 MW-hr of electricity per day. Calculated for an entire year, this cogeneration facility can produce 5,925 MW-hr of electricity.

Consideration can be given to provide electricity to a portion of the city. Looking at the population of 1 million, and using the consumption figure of 117 kW-hr/yr per capita in Kenya (CIA, 1997), 117,000 MW-hr/yr are needed to fulfill projected energy consumption for Mombasa. This facility figures to produce as much as 5% of the energy requirement for the city, while reducing the amount of material sent to the dump measurably.

 

 

VIII.        Conclusion

 

Visiting the beautiful island-city of Mombasa, it becomes immediately apparent to an outsider that environmental problems due to development are increasing. The stench from the landfill is perhaps the most immediately recognized. The need to purchase bottled water because local water sources are contaminated and the general poor health of the residents are impossible to overlook.

This project has shown removing 20,500 coconuts from the waste stream in Mombasa, Kenya and producing activated carbon for water purification at a sub-industrial level is possible. The testing conducted within this project indicates the quality of water after filtration with activated carbon from coconut waste as an amendment to a simple sand filter is better than without the CWD-C. Statistically, this research did not provide sufficient data to conclude, with scientifically accepted confidence, that there is an improvement. This may be a deficiency of data, not in filter performance.

            Reducing solid waste dumped in Mombasa and places like it, providing activated carbon for water filtration, and providing a new source for energy generation can improve the health and well-being of communities in less developed countries. It is hoped the implementation of this project is one of many steps that may lead to an improved quality of life for the disadvantaged people on our planet.

 

References

 

1.      Alter, Harvey, J. J. Dunn, Jr., 1908.  Solid Waste Conversion to Energy.  Marcel Dekker, Inc., New York. 

 

2.      Arulananatham, A., N. Balasubramanian and T.V. Ramakrishna, 1989.  “Coconut Shell Carbon for Treatment if Cadmium and Lead Containing Wastewater.” Metal Finishing, November, 1989.  Indian Institute of Technology, Madras, India.

 

3.      Blaak, Gustaf, 1993. “FAO Support for Coconut Research and Development between 1981-1991. The Coconut Economy. V.L. Chopra, ed. International Science Publisher, New York, N.Y.

 

4.      Brown, Lester R., Christopher Flavin and Hilary French, 1998. State of the World. Worldwatch Institute. W.W. Norton & Company, New York, N.Y.

 

5.      Carr, Marilyn, 1984. Blacksmith, Baker, Roofing-sheet Maker. Intermediate Technology Publications, London.

 

6.      Cheremisinoff, Paul and Angelo C. Morresi, 1978.  “Carbon Adsorption Applications.” Carbon Adsorption Handbook.  Ann Arbor Science Publishers, Inc. Ann Arbor, Michigan.

 

7.      Central Intelligence Agency (CIA), 1997. The World Factbook: 1997-1998. Brassey’s, Washington, D.C.

 

8.      Clesceri, Lenore S., Arnold E. Greenberg, and R. Rhodes Trussell, 1989.  Standard Methods for the Examination of Water and Wastewater.  American Public Health Association, Washington, DC.

 

9.      Collins, M. Robin, T. Taylor Eighmy, James P. Malley, Jr., Mike Bauer, and A.J. Rachwal, 1990.  “Slow Sand Filter Modifications to Enhance Operational and Treatment Performance.”  Presented at AWWA Seminar Titled Emerging Technologies and Practices on June 16, 1990.

 

10.  Cookson, John T., Jr., 1978.  “Adsorption Mechanisms: The Chemistry of Organic Adsorption on Activated Carbon.” Carbon Adsorption Handbook.  Ann Arbor Science Publishers, Inc. Ann Arbor, Michigan.

 

11.  Copeland, Edwin Bingham, 1931. The Coconut. MacMillan and Co., Limited, St. Martin's Street, London, England.

 

12.  Daniels, David L., Simons N. Cousens, Lucia N. Makoae, and Richard G. Feachem. 1990. ”A study of the association between improved sanitation facilities and children’s height in Lesotho.” European Journal of Clinical Nutrition, Vol. 45, pp. 23-32.

 

13.  Diethorn, Robert T., and Anthony F. Mazzoni, 1986.  “Activated Carbon: What Is It, How It Works.”  Water Technology, Vol. 9, No. 8., pp. 26-29.

 

14.  Deivanai, K., Bai, R.K., 1995. Batch Biomethanation of Banana Trash and Coir Pith.  Bioresource Technology, volume 52, number 1, p. 93-94, Oxford, U.K. - Elsevier Science Limited.

 

15.  Donohue, William, 1996. Personal conversation with Public Relations Director for Calgon Carbon, Corporation, Pittsburgh, PA. November 14, 1996.

 

16.  Duke, James A., 1989. CRC Handbook of Nuts. CRC Press, Boca Raton, Florida.

 

17.  Edachal, Muhammad, and T.B Nanda Kumar, 1988.  Coconut Economy in India.  Coconut Development Board, Conchin, India.

 

18.  Erhlich, Paul R. and Anne H. Erhlich, 1991. The Population Explosion. Simon and Schuster, New York.

 

19.  Festin, Teodorico F.; Jose, Wilfredo I., 1979.  Utilization of Waste Coconut Coir Dust as a Source of Fuel. Conservation & Recycling, numbers 3-4, pp 383-388

 

20.  Freeman-Grenville, G.S.P., 1962.  The East African Coast.  Oxford University Press, London.

 

21.  Gearheart, Robert A., M. McKee and Brad Finney, 1996.  WAWTTAR: An Algorithm for Water and Sanitation for the Developing World.  Humboldt State University, Arcata, CA.

 

22.  Gergova, K., N. Petrov, L. Butuzova, V. Minkova, and L. Isaeva, 1993.  “Evolution of the Active Surface of Carbons Produced from Various Raw Materials by Steam Pyrolysis/Activation.” Journal of Chemical Technology and Biotechnology

 

23.  Gore, Albert, 1992. Earth in the Balance. Houghton Mifflin Company, New York.

 

24.  Hancock, Graham, 1989. The Lords of Poverty. Penguin Press, London.

 

25.  Huang, C. P., 1978.  “Chemical Interactions Between Organics and Activated Carbon.” Carbon Adsorption Handbook.  Ann Arbor Science Publishers, Inc. Ann Arbor, Michigan.

 

26.  Jeanes, Henry, 1997.  “Proposal: Solid Waste Recycling Initiative – San Cristobal de las Casas, Chiapas.”  Working document for the Agency for Sustainable Systems in Science and Technology, Incorporated, Arcata, CA.

 

27.  Laine, L., A. Carafat, and M. Labady, 1989.  “Preparation and Characterization of Activated Carbons from Coconut Shell Impregnated with Phosphoric Acid.” Carbon, Vol. 27, No. 2, pp. 191-199.  Pergamon Press, Inc., Great Britain.

 

28.  Mattson, James S. and Harry B. Mark, Jr., 1971.  Activated Carbon: Surface Chemistry and Adsorption from Solution.  Marcel Dekker, Inc.  New York, New York.

 

29.  Namasivayam , C.; Kadirvelu , K., 1994. Coirpith, an Agricultural Waste By-Product, for the Treatment of Dyeing Wastewater. Bioresource Technology, volume 48. number1, pp79-81, Oxford, U.K. - Elsevier Science Limited.

 

30.  Okun, Daniel A., 1991. “A Water and Sanitation Strategy for the Developing World.” Environment, Volume 33 Number 8, pp. 16-2, 38-43.

 

31.  Ominde, S.M., 1968. Land and Population Movements in Kenya. Northwestern University Press, Evanston, Illinois.

 

32.  Pomeroy, Roger F. C., 1981.  Pyrolytic Methods in Organic Chemistry.  Academic Press, London.

 

33.  Rao, Padaki Srinivas, Shashikant R. Mise, and G.S. Manjunatha, 1992.  “Kinetic Study on Adsorption of Chromium by Coconut Shell Carbons from Synthetic Effluents.”  Journal of Environmental Science and Health.  Volume A(28), 227-2241.  Marcel Dekker, Inc, London.

 

34.  Reuters News Services, 1996. “Tanker Still in Mombasa Harbor.” Reuters, February 16.

 

35.  Rice, Rip G., G. Wade Miller, C. Michael Robson, and Wolfgang Kühn, 1978.  “A Review of the Status of Preozonation of Granular Activated Carbon for Removal of Dissolved Organics and Ammonia from Water and Wastewater.” Carbon Adsorption Handbook.  Ann Arbor Science Publishers, Inc. Ann Arbor, Michigan.

 

36.  Roecklein, Charles, J., 1993.  “Westhaven Water Treatment System Engineering Report.” SHN Consulting Engineers & Geologists, Eureka, CA.

 

37.  Shuler, Michael L., 1980. Utilization and Reuse of Agricultural Wastes and Residues. CRC Press, Boca Raton, Florida.

 

38.  Sofer, Samir S., Oskar R. Zaborsky, 1981.  Biomass Conversion Processes for Energy and Fuels.  Plenum Press, New York.

 

39.  Tchobanoglous, George, Edward D. Schroeder, 1987. Water Quality. Addison-Wesley Publishing Company, Reading, Massachusetts.

 

40.  Tchobanoglous, George, Hilary Theisen and Samuel Vigil, 1993. Integrated Solid Waste Management: Engineering Principles and Management Issues. McGraw-Hill, Inc., Hightstown, New Jersey.

 

41.  Tiffen, Mary, Michael Mortimore and Francis Gichuki, 1994. More People, Less Erosion: Environmental Recovery in Kenya. Overseas Development Institute, Chichester, England.

 

42.  UNICEF Annual Report on the State of Health of Children in Developing Nations. 1991. United Nations Children Fund, New York.

 

43.  World Health Organization, 1987. Guidelines for Drinking Water Quality. World Health Organization, New York.

 

44.  Wright, Charles, 1991. “Domestic Water Filtration.” United State Peace Corps Technical Paper. Nairobi, Kenya.

 

Appendix A: Analysis of Coconut Waste

As evidenced by the waste stream characterization, a considerable amount of dump space is used for coconut waste. To approach the reuse of this waste product, an understanding of the material must be obtained.

 

A.     The Coconut

           

Cocos nucifera, also known as the coconut tree, is of uncertain origin. Some historians believe the tree is native to the Americas, as they were first encountered by European explorers in the West Indies (Copeland, 1932). However, more recent accounts have suggested that coconut trees may have originated in the Indian Ocean region (Duke, 1989). Coconuts are geographically limited to 25.5° north and south latitude, roughly the tropics, and prefer coastal regions with sandy soil and abundant rainfall, although it can survive long periods of drought. Coconuts are found in coastal regions in Africa, Asia and the Americas where the water tables are close to the surface, a necessity due to the shallow root system. Although shallow, the roots are numerous, perhaps as dense as 1,000 major roots per square meter. Slow to germinate, taking twelve years for the seed to root and an additional fifteen years to reach maturity, the coconut tree will then produce fruit for over fifty years. Due to the consistency of its environment, there may be nuts of a dozen different ages on one tree. This makes the coconut one of the most reliable resource in tropical coastal zones (Duke, 1989).

The nut of the tree is encased in a thick cellulose husk, which provides protection from birds and other animals that have the ability to reach treetops. Fruit, consisting of the husk and nut, develops from an oblong shape to nearly spherical, averaging 20 cm in length and equal in width when fully mature. When coconuts are harvested for their water, they are removed from the tree before their fruit is ripened; this way there is the maximum water. If the fruit is ripe, the quantity of water will be diminished, because the fruit uses the water for self-nourishment.

 

B.     Uses of Coconut Materials

 

The coconut is one of the ten most useful plants in the world (Duke, 1989). The roots are known to be used for traditional medicines, and research continues to study additional medicinal applications for all parts of the tree. Coconut oil is believed to be the least harmful of all agricultural oils and discoveries have led to the conclusion that it actually improves physiological well-being (Duke, 1989). The oil is also used locally for cooking, as a salve and a lubricant. Recent findings have indicated that coconut oil can be used for the eradication of mosquito populations, thus reducing the potential for malaria. Additionally, coconut oil has been used for lamp fuel in the Indian Ocean region for thousands of years (Copeland, 1931).

Uses of carbon made from coconut shells include cigarette filters and air filter charcoal. Recent research has focused on the pyrolization of coconut shell to produce carbon for the absorption of organic matter from water, specifically in removing dyes from the effluent of textile manufacturing (Namasivayam et al, 1994). The wood from the tree is less useful removed from the ground than it is as a coconut producer, however, in the occurrence of fallen trees, wood is often used in the construction of canoes and roofing in traditionally built homes. The wood is not used as a domestic fuel sources as the wood is extremely dense and temperature required for combustion is extremely high. A comprehensive list of uses is given in Figure A-1.


·        Activated carbon

·        Alcoholic beverage

·        Baskets

·        Beverage cup

·        Brooms

·        Canes

·        Canoes

·        Carpet

·        Clothing

·        Coconut water

·        Cooking fuel

·        Copra/coconut oil

·        Curtains

·        Decorative souvenir

·        Edible “coconut meat” or copra

·        Erosion control blankets

·        Fence posts           

·        Furniture

·        Fuel

·        Hats

·        Housing timber

·        Mats and rugs

·        Medicinal ointments

·        Mosquito control

·        Musical instrument

·        Rope and twine

·        Saucer

·        Teapots

·        Thatch roofing material

·        Upholstery


Figure A-1: Uses for Coconuts


Table A-1: Chemical Composition of Coconut (Husk and Shell)

 

% by weight

H

6.62

N

0.34

S

0.75

O

39.66

C

52.63

           Source: Gergova et al, 1993

 

C.     Chemical Composition

 

Table A-1 shows the results from a chemical analysis of the coconut. The high carbon and oxygen content are important factors for determining energy content. Low sulfur and nitrogen levels indicate that the potential for emitting harmful gases during thermal conversion is low. With an ash content of 0.52%, the coconut is among the lowest of all agricultural residues in this category, making it an easily volatized substance. The coconut has a moisture content of 23% by weight, most of which is contained in the husk and the coconut water.

 

D.    Coconut Water

 

The coconut water contains 97% pure and filtered water (H2O) with high levels of glucose (Copeland, 1931), which explains the rate at which it is consumed as a beverage in an unrefined state. With the high temperatures and humidity levels of the coast, body fluids and nutrients are easily lost. The consumption of the coconut fluid returns necessary water and energy to the body, generating a market for a large quantity of coconuts to be brought into urban zones, purchased, consumed and subsequently discarded.

 

E.     Energy Content of Shell

 

1.      Experimentation

 

The shell of the nut consists of dense cellulose material and has been traditionally used for fuel in domestic fires and as a carving material. For this project, one option examined includes releasing the energy of the carbon bonds through thermal conversion. To understanding the potential for use as a fuel source, the energy content of the shell must be determined.

 

a.      Method

 

Through laboratory tests conducted through the Department of Chemistry at Humboldt State University in Arcata, California, the calorific value was determined for partially dried coconut shells. The sample was left with a low moisture content because it is perceived that under processing conditions, a shell devoid of moisture is not available. The calorific value of the sample was found to be 4,765 cal/g (8,577 BTU/lb).

This result was obtained using a 1241 Adiabatic Oxygen Bomb Calorimeter and calibrated using a 0.9736 g sample of benzoic acid. The sample was placed in a Parr 1108 oxygen bomb and ignited with the use of a nickel alloy fuse wire. The bomb was placed in a metallic jacket filled with 2,000 ml water. The jacket sits in a larger bucket-stirrer assembly that provides a continually exchanging thermal bath. The purpose of the water is to stabilize the conductance of heat outside the combustion chamber.

Once the sample was combusted, the change in temperature (DT) was calculated and the rate of combustion constant for the bomb calorimeter (Cp(bomb)) was determined using the following equation:

Cp(bomb) = m * DHc / DT,                                                           (Equation A-1)

 

where   Cp(bomb) =          Rate of combustion constant for the bomb calorimeter

m         =          Mass of the sample (g)

DHc      =          Amount of energy required to consume the sample (cal/g)

DT       =          Change in temperature (°C).

 

The temperature change that was observed was 2.62°C. The resulting Cp(bomb) for the calibration was 2,358 cal/g. 

b.      Results

Next the procedure was repeated for the sample of coconut.  Noting a 1.89°C change of temperature, the calorific value was calculated to be 4,765 cal/g.  Converting this into a more familiar unit of energy, the coconut was found to have an energy content of  8,577 BTU/lb.

 

Appendix B: Production of Activated Carbon

 

A.     Introduction

 

As activated carbon is generally unfamiliar to the populations involved in converting waste to a useful product, sections on the processes of carbon adsorption and the testing of the adsorptive capacity of coconut waste-derived carbon are described in this section.

 

B.     Incorporating Familiar Technologies

 

Production of activated carbon for use as a filtration media is not an exact duplication of traditional crafts. Activated carbon production incorporates a series of technologies that are familiar to most living in coastal zones, although there are elements in the production processes that have been introduced by foreigners. Many foreign technologies have existed in the developing world since colonial rule and many craftspeople have mastered their operation and maintenance. For those participants who are unfamiliar with these technologies, this report offers opportunity for cognition.

 

C.     Production

 

1.      Summary of Production

 

Production of activated carbon from coconut shells has been the subject of considerable research and development in the past few decades (Deivanai, 1995; Gergova et al, 1993; Laine et al, 1989; Mattson et al, 1971; Rice, 1978; Shuler, 1980). Activated carbon is produced through a three-phase thermal process. When heated, the material, in this case coconut shells, becomes dehydrated, removing moisture which would otherwise continue to absorb heat. The material is then carbonized, to reduce organic matter to elemental carbon. Additional energy is introduced to crack the carbon thermally, increasing pore volume and forming surface oxide groups, which are integral to the adsorptive capacity of carbon.

 

2.      Curing

 

To ensure energy is most efficiently used in production of activated carbon from coconut shells, shells must be cured through a drying process. Shells can be left out to cure passively under the sun during the dry season and covered at other times. Because the coastal zone is extremely humid throughout the year, and especially during the rains, there is not prescribed duration for the curing process; two weeks may be suitable most of the year (Donohue, 1996). Study may be conducted to determine most effective curing times.

 

3.       Thermal Conversion Processes

 

a.      Combustion

 

The most common method for thermally converting waste is combustion, or complete thermal oxidation of matter (Tchobanoglous, 1993). This means there is adequate oxygen available in the system to allow for all carbon bonds to be broken, or oxidized, when temperatures are increased. Combustion occurs in lighting a match, igniting a gas stove, propulsion in most automobiles and operation of many of the world’s power plants.

To begin combustion, an external energy source must be added to the material, initiating oxidation. During reduction of carbonaceous material, excited oxygen molecules react with carbon, breaking bonds and forming other compounds. Breaking these bonds, in turn, releases additional heat, allowing for more bonds to be broken. Thus begins a ‘chain reaction’ that, when in the presence of sufficient oxygen, continues until all available bonds are broken. This continuous reaction is termed ‘exothermic’, or a net energy output for the reaction.

Resultants of this reaction are a gaseous emission, a solid remnant and a liquid vapor. Gases released depend on chemical composition and the amount of oxygen present. Tchobanoglous (1993) gives the following stoichemetric equations for combustion of carbon, hydrogen, nitrogen and sulfur:

C + O2             Ž CO2                                    (Equation B-1),

2H2 + O2          Ž 2H2O                                  (Equation B-2),

N2 + 2O2         Ž 2NO2                                        (Equation B-3); and,

S + O2             Ž SO2                                             (Equation B-4).

The primary emissions of combustion are carbon dioxide (CO2) and carbon monoxide (CO), the latter of which is formed due to incomplete combustion. Other gases produced depend upon the material being combusted and temperatures achieved, however, nitrogen is usually present as nitrous oxides (NOx), as is sulfur in the form of sulfur dioxide (SO2). Solid remnants are typically in the form of ash, although most combustion processes leave an unburned portion. This portion, a char, is the result of insufficient oxygen contact and is discussed more thoroughly in the section on gasification. The water (H2O) content of the fuel source is driven off as vapor. The amount of oxygen in the chamber needs to be regulated, as does addition of fuel. Temperatures typically achieved during combustion are in the range of 760°C to 1425°C for cellulose material, although higher temperatures can be achieved with inert materials (Cheremisinoff et al, 1978).

One deficiency of combustion is the lack of a usable by-products. Neither carbon dioxide nor ash is particularly useful to humans, although plant species can benefit. Because of high temperatures during combustion, NOx is produced and persist as one of the major causes of acid rain in the western United States. On the U.S. East Coast and in many European and Chinese cities, coal is combusted to generate energy, emitting large amounts of sulfur dioxide. Suspended ash or other particulates, which can cause health problems, are often present in the discharged gases.

 

b.      Gasification

 

If the amount of oxygen in the combustion chamber were reduced to below the amount required for complete combustion, the process would be termed ‘gasification’. This thermal system leads to a partial burning by forcing carbon molecules to pair with only one oxygen molecule rather than the desired two. This increases production of combustible carbon monoxide (CO). Intentionally, there is a large char fraction remaining, to be used as stock for manufacturing activated carbon. Often this char is produced and sold in many developing countries as charcoal to be used in domestic food preparation.

Gasification units, or gasifiers, commonly use a mixed source of fuel, but since the system is very sensitive to the quality and characteristics of the feedstock, a homogenous fuel is preferred. Heating temperature should be kept as consistent as possible during processing to ensure uniform conversion. The most accurate manner to control temperature is by regulating oxygen availability. Ideally, pure oxygen is provided, but since the cost of a pure oxygen source is prohibitive in developing countries, oxygen will be incorporated through atmospheric air, which typically contains 18-21% oxygen.

As with combustion, the fuel source determines by-products of gasification. Chemical reactions for gasification are outlined below (Table B-1). Noting net energy for the entire reaction, this system is exothermic and, like combustion, is self-sustaining as long as a fuel source and oxygen are available (Sofer, 1981). Because of endothermic processes, gasification temperatures are typically lower than for combustion, ranging from 540°C to 980°C.

Table B-1:  Chemical Reactions for Gasification

Reaction

Net Energy

C + O2             Ž CO2

Exothermic

C + H2O          Ž CO + H2

Endothermic

C + CO2          Ž 2 CO

Endothermic

C + 2H2           Ž CH4

Exothermic

CO + H2          Ž CO2 + H2

Exothermic

    Source:  Sofer, 1981.

            The solid remnant is mainly carbon char and residual inert matter. The resulting char has approximately 26-30% weight of the original material. If oxygen is allowed to combust completely a portion of the fuel, which is common, then an ash component results. Additionally, there are condensable liquids such as pyrolic oils and tars, yet this portion is very small unless fuel quantities are immense (Shuler, 1980; Sofer, 1981; Tchobanoglous, 1993). The resultant gases from the reactions are typically in the quantities listed in Table B-2.

Incorporating gasification is desired for a number of reasons. Perhaps most outstanding is that it can be a much more efficient energy producer and is more environmentally sensitive than combustion. Energy released as latent heat can be used to drive a more efficient steam engine, while offgases can be harnessed for combustion in a ‘reverse-burn gasification’ process, increasing net energy production. Furthermore, at the low temperatures achieved, there is reduced potential for formation of noxious and sulfurous emissions, as compared to combustion. By-products, therefore, are a usable char portion, a combustible gas, unsaturated hydrocarbon vapors and particulate matter.

Table B-2:  Gaseous Fraction from the Gasification Process

Gas

Quantity (% of total)

CO2

9.9-11

CO

18.0-19.8

H2

16.5-18.2

CH4

0.7-2.0

N2

45.2-49.8

O2

0.18-0.2

Other hydrocarbons

0.28-0.3

H2O

9.1

                                   Source: Sofer, 1981; Tchobanoglous, 1993.

 

c.       Pyrolization (Thermal Distillation)

           

Since most organic substances are thermally unstable, the material, in this case the remaining char from gasification, can be manipulated through a combination of thermal cracking and condensation reactions in the absence of oxygen. This highly endothermic reaction requires extensive external energy. Distillation of char, or ‘pyrolysis’, is desired for there are two usable by-products, combustible gas, mainly saturated hydrocarbons, and an ‘activated’ carbon. Tchobanoglous (1993) provides stoichemetric balance for pyrolysis of cellulose:

3(C6H10O5)  =  8H2O + C6H8O + 2CO + 2CO2 + CH4 + H2 + 7C, (Equation B-5).

            Resulting gases vary depending on temperatures achieved. Pyrolizing units are designed to achieve temperatures of ranging from 315°C to 925°C. The composition of gases released at two moderate temperatures are given in Table B-3.

Table B-3:  Gas Composition for Pyrolic Emissions

Gases

Percent by Volume

(480°C)

Percent by Volume (650°C)

H2

5.56

16.58

CH4

12.43

15.91

CO

33.50

30.49

CO2

44.77

31.78

C2H4

0.45

2.18

C2H6

3.03

3.06

                Source: Tchobanoglous, 1993.

Table B-4:  Product Energy Yields for Pine Bark and Sawdust Residuals (per kg)

 

Case

Feed

(Btu)

 

Char

(Btu)

Gas

(Btu)

Oil

(Btu)

Maximum char

18,011

 

9,030

3,418

1,245

Maximum oil

18,011

 

6,930

3,660

4,395

Maximum gas

18,011

 

5,670

4,305

2,505

                                                                                                                  Source: Pomeroy, 1981.

 

 

            According to Pomeroy (1981), energy potential for the gaseous portion yielded during pyrolization of cellulose is substantial enough for consideration as a harvestable fuel source. Methane (CH4) and carbon monoxide (CO) portions at both temperatures are in the vicinity of  46% of the offgases.  Energy values for residuals derived from a mixture of pine bark and sawdust, cellulosic matter with calorific values similar to coconuts, are given in Table B-4.

            Direct pyrolysis of municipal solid waste has not been successful because of difficulty obtaining pure fuel sources, the technical complexity of the systems, and financial considerations for strict heating controls. However, it has been found that pyrolizing homogeneous char after gasification can provide an adequate quality of activated carbon with substantial economic return (Cheremisinoff et al, 1978).

 

d.      Cooling

           

            Thermally cracking carbon is necessary for adequate adsorption to occur. After heated at the desired temperature and for the prescribed duration, carbon is allowed to return to ambient temperature. Higher temperatures are able to achieve faster cooling rates, as the temperature differential is greater; however, this is not always advantageous. Since the cooling process entails allowing oxygen to come in contact with the surface of the carbon, forming chemically-attractive oxide groups, it is important to know the purposes of the carbon prior to cooling.

Experiments using different temperatures, heating rates and parent material have demonstrated distinct effects on the removal of acidic and basal species. Carbons produced at high temperatures with rapid cooling periods adsorb basic materials more readily, while lower temperatures and slower cooling rates excel in removal efficiency for acidic substances (Cookson, 1978; Mattson et al, 1971; Rao et al, 1992).