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ENHANCEMENT OF DEGREE OF DEACETYLATION OF CHITIN IN CHITOSAN PRODUCTION
STEPHENIE AK KALUT
A thesis submitted in fulfillment of the requirements for the award of the degree of
Bachelor of Chemical Engineering
Faculty of Chemical Engineering and Natural Resources Universiti Malaysia Pahang
MAY 2008
ii
I declare that this thesis entitled “Enhancement of Degree of Deacetylation of Chitin in
Chitosan Production” is the result of my own research except as cited in the references.
The thesis has not been accepted for any degree and is not concurrently submitted in
candidature of any other degree.
Signature : …………………….
Name : Stephenie A/K Kalut
Date : May 2008
iii
To my beloved mother, Silia ak Mandung, and father, Kalut ak Legan and also my siblings.
For Rome was not built in a day, you were there to help me make it through.
iv
ACKNOWLEDGEMENT
I wish to express my sincere appreciation to my superisor, Mrs Ruwaida binti
Abdul Rasid, for her guidance, encouragement, patience, and understanding throughout
the course of this research. I am also thankful to her for providing me the research topic
and valuable suggestions. I would like to thank Mr Mohd Anuar bin Hj. Ramli for
helping me during my experiment progress and not only for providing me the research
facilities but also for imparting valuable knowledge that I used in this research.
My sincere gratitude and appreciation goes to my dear collegues and friends, Siti
Nurshuhada binti Mat Yusof, Fauziah binti Hairan, and Nurul Yazlin binti Yussuf who
have assisted and supported me throughout the most rigorous phase of my research with
their expertise, wisdom, and friendship. Last but not least, I thank my mama and papa
who are the sunshine of my life for their encouragement and support throughout every
endeavor of mine. It is to them that this work is dedicated. May God bless all of you.
v
ABSTRACT
Chitosan is made from crustacean shells by a chemical process involving
demineralization, deproteinization, decolorization, and deacetylation. The process of
deacetylation involves the removal of acetyl groups from the molecular chain of chitin,
leaving behind a complete amino group (-NH2) and chitosan versatility depends mainly
on this high degree chemical reactive amino groups. The purpose of this research is to
observe the parameters that can enhance the degree of deacetylation of chitosan
production to the highest percentage. The observed parameters are the temperature of
heating, concentration of sodium hydroxide, and the time of heating. The obtained chitin
was converted into the more useful soluble chitosan by reaction with sodium hydroxide
(NaOH) solution of various concentrations, then the alkaline chitin was heated in an
autoclave with different time and temperature of heating which dramatically reduced the
time of deacetylation. The method used to determine the degree of deacetylation of
chitosan is the linear potentiometric titration. From the result, the highest degree of
deacetylation can be achieved at the temperature of 134oC, and 70% concentration of
sodium hydroxide with DDA% of 98.38% and 98.79% respectively. It took only 10
minutes to also achieve highest degree of deacetylation, 89.05%. In conclusion, the
increasing of temperature and concentration of sodium hydroxide will increase the
degree of deacetylation of chitin. The increasing of time of heating will decrease the
degree of deacetylation.
vi
ABSTRAK
Chitosan terhasil daripada kulit udang melalui proses kimia yang melibatkan
proses “demineralization” iaitu penyingkiran bahan mineral, “deproteinization” iaitu
penyingkiran bahan berprotin, “decolorization” iaitu penyingkiran bahan berwarna, dan
“deacetylation” iaitu penyingkiran kumpulan ikatan polimer N-acetyl. Tujuan utama
kajian ini dijalankan adalah untuk mengkaji factor-faktor yang meningkatkan peratusan
proses penyingkiran ikatan polimer N-acetyl iaitu suhu pemanasan, kepekatan alkali
iaitu natrium hidroksida, dan masa pemanasan. Chitin yang diperoleh akan ditukar
kepada chitosan yang mempunyai lebih banyak kegunaan dan boleh melarut dalam air
dengan baik. Ini dilakukan dengan mencampurkan chitin dengan larutan natrium
hidroksida dengan kepekatan yang berbeza dalam masa dan suhu pemanasan yang
berbeza dan membiarkan ia bertindakbalas. Selepas itu, chitin beralkali itu dipanaskan di
dalam alat pemanas “autoclave” di mana proses pemanasan ini akan mempercepatkan
masa untuk proses penyingkiran ikatan polimer N-acetyl. Kaedah yang digunakan untuk
mengira peratusan penyingkiran ikatan polimer N-acetyl itu adalah pentitratan
potensiometrik. Daripada hasil eksperimen yang dijalankan, didapati peratusan yang
paling tinggi diperoleh pada suhu 134oC, dengan peratusan sebanyak 98.38% dan pada
kepekatan natrium hidroksida sebanyak 70% dengan peratusan sebanyak 98.79%. Masa
pemanasan dalam 10 minit pula menghasilkan peratusan penyingkiran yang paling
tinggi iaitu sebanyak 89.05%. Kesimpulannya, semakin tinggi suhu pemanasan dan
kepekatan alkali, semakin meningkat peratusan proses penyingkiran ikatan polimer N-
acetyl di dalam chitosan. Semakin meningkat masa pemanasan pula, semakin rendah
peratusan proses penyingkiran ikatan polimer N-acetyl tersebut.
vii
TABLE OF CONTENTS
CHAPTER TITLE PAGE
DECLARATION ii
DEDICATION iii
ACKNOWLEDGEMENT iv
ABSTRACT v
ABSTRAK vi
TABLE OF CONTENTS vii
LIST OF SYMBOLS x
LIST OF FIGURES xi
LIST OF TABLES xii
LIST OF APPENDICES xiii
1 INTRODUCTION
1.1 Background Study 1
1.2 Problem Statement 3
1.3 Objectives 3
1.4 Scope of Study 4
2 LITERATURE REVIEW
2.1 Definition and Composition of Chitosan 5
2.2 Characteristics of Chitosan 7
2.2.1 Degree of Deacetylation in Chitosan 8
viii
2.2.2 Molecular Weight 10
2.2.3 Viscosity 10
2.2.4 Solubility 12
2.2.5 Bulk Density 13
2.2.6 Color 13
2.2.7 Water Binding Capacity and Fat
Binding Capacity 14
2.2.8 Emulsification 15
2.2.9 Antimicrobial Properties 15
2.2.10 Formation of Film 17
2.3 Production of Chitin and Chitosan 18
2.3.1 Isolation of Chitin 19
2.3.2 Deproteinization 22
2.3.3 Demineralization 22
2.3.4 Decolorization 23
2.3.5 Deacetylation 24
2.4 Factors Affecting Production of Chitosan 25
2.4.1 Temperature of Deacetylation 25
2.4.2 Time of Deacetylation and Alkali
Concentration 26
2.4.3 Effect of Treatment Conditions Applied
in Chitin Isolation 26
2.4.4 Atmosphere, Ratio of Chitin to Alkali
Solution, and Particle Size 27
2.5 Determination of Deacetylation Degree 27
2.6 Applications of Chitosan 29
2.6.1 Dietary Suppliments 29
2.6.2 Industrial Wastewater Treatment 30
2.6.3 Medical Applications 31
3 MATERIALS AND METHODS
ix
3.1 Isolation of Chitin 33
3.2 Purification Process 33
3.2.1 Deproteinization 34
3.2.2 Demineralization 35
3.2.3 Decoloriztion 35
3.2.4 Deacetylation 35
3.2.4.1 Time of Heating 36
3.2.4.2 Temperature of Heating 36
3.2.4.3 Alkaline (NaOH) Concentration 36
3.3 Determination of Deacetylation Degree 37
3.3.1 Linear Potentiometric Titration 37
4 RESULTS AND DISCUSSIONS
4.1 Results 38
4.1.1 Time of Heating in Autoclave 38
4.1.2 Temperature of Heating in Autoclave 40
4.1.3 Concentration of Sodium Hydroxide
(NaOH) 41
4.2 Discussions 42
4.2.1 Time of Heating in Autoclave 42
4.2.2 Temperature of Heating in Autoclave 43
4.2.3 Concentration of Sodium Hydroxide
(NaOH) 43
4.2.4 Limitation of Research 44
5 CONCLUSION
5.1 Conclusion 45
5.2 Recommendation 46
REREFENCES 47
APPENDICES 52
x
LIST OF SYMBOLS
> - Bigger than
≈ - Nearly equal to
DDA - Degree of Deacetylation
w/w - weight per weight
w/v - weight per volume
v/v - volume per weight
WBC - Water Binding Capacity
FBC - Fat Binding Capacity
KOH - Potassium hydroxide
HCl - Hydrochloric acid
NaOCl - Sodium hypochloride
NaOH - Sodium hydroxide
xi
LIST OF FIGURES
FIGURE NO. TITLE PAGE
2.1 The structural formula of chitin and chitosan 6
2.2 The structural formula of chitin and glucose. 6
2.3 Structure of cellulose, chitin, and chitosan 7
2.4 Isolation of chitin 20
2.5 Traditional Crawfish Chitosan Production Flow
Scheme (Modified from No and Meyers, 1995) 21
3.1 Steps of purification process 34
4.1 Effect of time of heating on DDA% 39
4.2 Effect of temperature of heating on DDA% 40
4.3 Effect of NaOH concentration on DDA% 41
xii
LIST OF TABLES
TABLE NO. TITLE PAGE
2.1 Applications of Chitosan 31
4.1 DDA% of different time of heating 38
4.2 DDA% of different temperature of heating 40
4.3 DDA% of different NaOH concentration 41
xiii
LIST OF APPENDICES
APPENDIX TITLE PAGE
A Calculation of Degree of Deacetylation of Chitosan on various times of autoclave. 52
B Calculation of Degree of Deacetylation of Chitosan on various temperatures of autoclave. 55
C Calculation of Degree of Deacetylation of Chitosan on various concentration of sodium hydroxide in autoclave. 58
D Isolation of chitin processes. 62
E Deacetylation process. 63 F Type of Autoclave 65
CHAPTER 1
INTRODUCTION
1.1 Background of Study
Chitosan is a natural polysaccharide comprising copolymers of glucosamine and
N-acetylglucosamine, and can be obtained by the partial deacetylation of chitin, from
crustacean shells, the second most abundant natural polymer after cellulose. Chitin can
be converted into chitosan by enzymatic means or alkali deacetylation, this being the
most utilized method. During the course of deacetylation, part of polymer N-acetyl links
are broken with the formation of D-glucosamine units, which contain a free amine
group, increasing the polymer’s solubility in aqueous means (Chen & Tsaih, 1998).
Chitosan has been widely used in vastly diverse fields, ranging from waste
management to food processing, medicine and biotechnology. It becomes an interesting
material in pharmaceutical applications due to its biodegradability and biocompatibility,
and low toxicity. Chitosan has found wide applicability in conventional pharmaceutical
devices as a potential formulation excipient. The use of chitosan in novel drug delivery
as mucoadhesive, peptide and gene delivery, as well as oral enhancer have been reported
2
in the literature. Chitosan exhibits myriad biological actions such as
hypocholesterolemic, antimicrobial, and wound healing properties. Since chitosan is a
new substance, it is important to carry out precise standardization for its pharmaceutical
and biomedical applications like other auxiliary substances.
Chitosan can be characterized in terms of its quality, intrinsic properties (purity,
molecular weight, viscosity, and degree of deacetylation) and physical forms.
Furthermore, the quality and properties of chitosan product may vary widely because
many factors in the manufacturing process can influence the characteristics of the final
product. Chitosan is commercially available from a number of suppliers in various
grades of purity, molecular weight, and degree of deacetylation. The variations in
preparation methods of chitosan result in differences in its deacetylation degree, the
distribution of acetyl groups, the viscosity and its molecular weight (Berger et al., 2005).
These variations influence the solubility, antimicrobial activity among other properties,
being that commercial chitosan usually has a deacetylation degree varying from 70% to
95%, and a molecular weight ranging from 50 to 2000 kDa (Rege et al., 2003).
The deacetylation degree is the proportion of glucosamine monomer residues in
chitin. It has a striking effect on the solubility and solution properties of chitin. By
convention, chitin and chitosan are distinguished by their solubility in dilute aqueous
acids such as acetic acid (Muzzarelli, 1977). Chitin does not dissolve in dilute acetic
acid. When chitin is deacetylated to a certain degree (~ 60% deacetylation) where it
becomes soluble in the acid, it is referred to as chitosan. A typical deacetylation process
of chitin involves the reaction of chitin powder or flake in an aqueous 40-50% sodium
hydroxide solution at 100-120°C for several hours to hydrolyze N-acetyl linkages
(Roberts, 1992). Repetition of the process can give deacetylation values up to 98% but
the complete deacetylation can never be achieved by this heterogeneous deacetylation
process without modification. Fully deacetylated (nearly 100%) chitosan can be
3
prepared by the alkaline treatment of a gel form instead of the powder form of chitosan
(Mima et al., 1983).
1.2 Problem statement
The degree of deacetylation could influence the performance of chitosan in many
of its applications. It determines the content of free amino groups in the polysaccharides
and can be employed to differentiate between chitin and chitosan. The process of
deacetylation involves the removal of acetyl groups from the molecular chain of chitin,
leaving behind a complete amino group (-NH2) and chitosan versatility depends mainly
on this high degree chemical reactive amino groups. There are methods available to
increase or decrease the degree of deacetylation. For example, increase either in
temperature or strength of sodium hydroxide solution could enhance the removal of
acetyl groups from chitin, resulting in a range of chitosan molecules with different
properties and hence its applications. Preliminary experiments were carried out by
refluxing chitin in strong NaOH solution at normal atmosphere. The experiments took
more than 20 hours producing low deacetylation content and the reaction was
accompanied by drastic degradation of the final chitosan.
1.3 Objective
The objective of this research is to enhance the degree of deacetylation of chitin in
chitosan production.
4
1.4 Scope of study
The scope of this study covers the effect of temperature, concentration of NaOH
solution, and time of heating in autoclave on the degree of deacetylation.
CHAPTER 2
LITERATURE REVIEW
2.1 Definition and Composition of Chitosan
Chitosan is a fiber-like substance derived from chitin. Chitin is the fiber in
shellfish shell such as crab, lobster and shrimp. It is also found in common foods we eat
such as grain, yeast, bananas, and mushrooms. Chitin, a naturally abundant polymer
consists of 2-acetamido 2-deoxy-β-D-glucose through a β(1 → 4) linkage. In spite of the
presence of nitrogen, it may be regarded as cellulose with hydroxyl at position C-2
replaced by an acetamido group. Like cellulose, it functions as structural
polysaccharides. Its natural production is inexhaustible; arthropods, by themselves,
count more than 106 species from the 1.2 X 106 of total species compiled for animal
kingdom, constitute permanent and large biomass source. The chitin is deproteinized,
demineralized and de-acetylated. It is a dietary fiber, meaning that it cannot be digested
by the digestive enzymes of a person (Razdan A., and Petterson D., 1994). Chitin is a
white, hard, inelastic, nitrogenous polysaccharide and the major source of surface
pollution in coastal areas.
6
Chitin is made up of a linear chain of acetylglucosamine groups while chitosan is
obtained by removing enough acetyl groups (CH3-CO) for the molecule to be soluble in
most diluted acids. This process is called deacetylation. The actual difference between
chitin and chitosan is the acetyl content of the polymer. Chitosan having a free amino
group is the most useful derivative of chitin (No and Meyers, 1992).
Chitin Chitosan
Figure 2.1 The structural formula of chitin and chitosan
Figure 2.2 The structural formula of chitin and glucose.
7
2.2 Characteristics of Chitosan
Chitosan is a non toxic, biodegradable polymer of high molecular weight, and is
very much similar to cellulose, a plant fiber.
(a) (b)
(c)
Figure 2.3 Structure of a) chitin, b) chitosan, and c) cellulose.
As seen in Figure 2.3, the only difference between chitosan and cellulose is the
amine (-NH2) group in the position C-2 of chitosan instead of the hydroxyl (-OH) group
found in cellulose. However, unlike plant fiber, chitosan possesses positive ionic
charges, which give it the ability to chemically bind with negatively charged fats, lipids,
cholesterol, metal ions, proteins, and macromolecules (Li et al., 1992). In this respect,
chitin and chitosan have attained increasing commercial interest as suitable resource
8
materials due to their excellent properties including biocompatibility, biodegradability,
adsorption, and ability to form films, and to chelate metal ions (Rout, 2001).
2.2.1 Degree of Deacetylation in Chitosan
The process of deacetylation involves the removal of acetyl groups from the
molecular chain of chitin, leaving behind a compound (chitosan) with a high degree
chemical reactive amino group (-NH2). This makes the degree of deacetylation an
important property in chitosan production as it affects the physicochemical properties,
hence determines its appropriate applications (Rout, 2001). Deacetylation also affects
the biodegradability and immunological activity (Tolaimate et al., 2000).
A sharp nomenclature border has not been defined between chitin and chitosan
based on the degree of N-deacetylation (Rout, 2001). In an earlier study by Rudall
(1963), he reviewed evidences suggesting that approximately one in every six to seven
residues in the chain has a proportion of free amino groups that manifests some
histochemical properties. In any case, the degree of deacetylation can be employed to
differentiate between chitin and chitosan because it determines the content of free amino
groups in the polysaccharides. There are two advantages of chitosan over chitin. The
first one is, in order to dissolve chitin, highly toxic solvents such as lithium chloride and
dimethylacetamide are used whereas chitosan is readily dissolved in diluted acetic acid.
The second advantage is that chitosan possesses free amine groups which are an active
site in many chemical reactions (Knaul et al., 1999).
9
The degree of deacetylation of chitosan ranges from 56% to 99% with an average
of 80%, depending on the crustacean species and the preparation methods (No and
Meyers, 1995). Chitin with a degree of deacetylation of 75% or above is known as
chitosan (Knaul et al., 1999). Various methods have been reported for the determination
of the degree of deacetylation of chitosan. These included ninhydrin test, linear
potentiometric titration, near-infrared spectroscopy, nuclear magnetic resonance
spectroscopy, hydrogen bromide titrimetry, infrared spectroscopy, and first derivative
UV-spectrophotometry (Khan et al., 2002).
The infrared spectroscopy method, which was first proposed by Moore and
Roberts (1980), is commonly used for the estimation of chitosan degree of deacetylation
values. This method has a number of advantages and disadvantages. First, it is relatively
fast and unlike other spectroscopic methods, does not require purity of the sample to be
tested nor require dissolution of the chitosan sample in an aqueous solvent (Baxter et al.,
1992). However, the infrared method utilizing baseline for degree of deacetylation
calculation, and as such there may be possible argument for employment of different
baseline which would inevitably contribute to variation in the degree of deacetylation
values. Secondly, sample preparation, type of instrument used and conditions may
influence the sample analysis. Since chitosan is hygroscopic in nature and samples with
lower degree of deacetylation may absorb more moisture than those with higher degree
of deacetylation, it is essential that the samples under analysis be completely dry (Khan
et al., 2001; Blair et al., 1987).
10
2.2.2 Molecular Weight
Chitosan is a biopolymer of high molecular weight. Like its composition, the
molecular weight of chitosan varies with the raw material sources and the method of
preparation. Molecular weight of native chitin is usually larger than one million Daltons
while commercial chitosan products have the molecular weight range of 100,000 –
1,200,000 Daltons, depending on the process and grades of the product (Li et al., 1992).
In general, high temperature, dissolved oxygen, and shear stress can cause degradation
of chitosan. For instance at a temperature over 280˚C, thermal degradation of chitosan
occurs and polymer chains rapidly break down, thereby lowering molecular weight
(Rout, 2001). Also, maximal depolymerization caused by utilization of high temperature
or concentrated acids, such as hydrochloric acid followed by acetic acid and sulfurous
acid, results in molecular weight changes with minimal degradation with the use of
EDTA (Rout, 2001). The molecular weight of chitosan can be determined by methods
such as chromatography (Bough et al., 1978), light scattering (Muzzarelli, 1977), and
viscometry (Maghami and Roberts, 1988)
2.2.3 Viscosity
Just as with other food matrices, viscosity is an important factor in the
conventional determination of molecular weight of chitosan and in determining its
commercial applications in complex biological environments such as in the food system.
Higher molecular weight chitosans often render highly viscous solutions, which may not
be desirable for industrial handling. But, a lower viscosity chitosan obtained from
crawfish waste as shown in this thesis research may facilitate easy handling.
11
Some factors during processing such as the degree of deacetylation, molecular
weight, concentration of solution, ionic strength, pH, and temperature affect the
production of chitosan and its properties. For instance, chitosan viscosity decreases with
an increased time of demineralization (Moorjani et al., 1975). Viscosity of chitosan in
acetic acid tends to increase with decreasing pH but decrease with decreasing pH in HCl,
giving rise to the definition of ‘Intrinsic Viscosity’ of chitosan which is a function of the
degree of ionization as well as ion strength. Bough et al. (1978) found that
deproteinization with 3% NaOH and elimination of the demineralization step in the
chitin preparation decrease the viscosity of the final chitosan products. Moorjani et al.
(1975) also stated that it is not desirable to bleach the material (i.e., bleaching with
acetone or sodium hypochlorite) at any stage since bleaching considerably reduces the
viscosity of the final chitosan product.
Similarly, No et al. (1999) demonstrated that chitosan viscosity is considerably
affected by physical (grinding, heating, autoclaving, ultrasonication) and chemical
(ozone) treatments, except for freezing, and decreases with an increase in treatment time
and temperature. Chitosan solution stored at 4˚C is found to be relatively stable from a
viscosity point of view (No et al., 1999). The effect of particle size on the quality of
chitosan products was investigated by Bough et al. (1978), who reported that smaller
particle size (1mm) results in chitosan products of both higher viscosity and molecular
weight than those of either 2 or 6.4 mm particle size. They further enumerated that a
larger particle size requires longer swelling time, resulting in a slower deacetylation rate.
But, in contrast, Lusena and Rose (1953) reported that the size of chitin particle within
the 20-80 mesh (0.841-0.177 mm) range had no effect on the viscosity of the chitosan
solutions.
12
2.2.4 Solubility
While chitin is insoluble in most organic solvents, chitosan is readily soluble in
dilute acidic solutions below pH 6.0. Organic acids such as acetic, formic, and lactic
acids are used for dissolving chitosan. The most commonly used is 1% acetic acid
solution at about pH 4.0 as a reference. Chitosan is also soluble in 1% hydrochloric acid
but insoluble in sulfuric and phosphoric acids. Solubility of chitosan in inorganic acids is
quite limited. Concentrated acetic acid solutions at high temperature can cause
depolymerization of chitosan (Roberts and Domszy, 1982). Above pH 7.0 chitosan
solubility’s stability is poor. At higher pH, precipitation or gelation tends to occur and
the chitosan solution forms poly-ion complex with anionic hydrocolloid resulting in the
gel formation (Kurita, 1998).
The concentration ratio between chitosan and acid is of great importance to
impart desired functionality (Mima, 1983). At concentrations as high as 50 percent
organic solvent, chitosan still works as a viscosifier causing the solution to remain
smooth. There are several critical factors affecting chitosan solubility including
temperature and time of deacetylation, alkali concentration, and prior treatments applied
to chitin isolation, ratio of chitin to alkali solution, and particle size.
The solubility, however, is controlled by the degree of deacetylation and it is
estimated that deacetylation must be at least 85% complete in order to achieve the
desired solubility (No et al., 1995). The acid-soluble chitosans with >95% solubility in
1% acetic acid at a 0.5% concentration could be obtained by treatment of the original
chitin with 45-50% NaOH for 10-30 min. Chitosans treated with 45% NaOH for only 5
min, and/or with 40% NaOH for 30 min, were not deacetylated sufficiently to be soluble
in 1% acetic acid. Insoluble particles were found in both solutions. According to Bough
et al. (1978), a reaction time of 5 min with 45% NaOH may not be enough for chitin
13
particles to be sufficiently swollen. A decrease of the NaOH concentration to 40%
required increased time of >30 min to obtain a soluble chitosan (No et al., 2000).
2.2.5 Bulk Density
The bulk density of chitin from shrimp and crab is normally between 0.06 and
0.17 g/ml, respectively (Shahidi and Synowiecki, 1991), indicating that shrimp chitin is
more porous than crab chitin. Krill chitin was found to be 2.6 times more porous than
crab chitin (Anderson et al., 1978). In a study conducted by Rout (2001), the bulk
density of chitin and chitosan from crawfish shell, is very high (0.39 g/cm3). This
perhaps could be due to the porosity of the material before treatment. But once crawfish
shell had been demineralized or deproteinized or both there seem to be very minor
variations unpacked in bulk density between chitin and chitosan produced. A
comparison of the bulk densities of crawfish and commercial chitin and chitosan
indicated some variations, which can be attributed to crustacean species or sources of
chitosan and the methods of preparation (Rout, 2001), as also stated earlier by Brine and
Austin (1981). Rout (2001) reported that increased degree of deacetylation decreased
bulk density.
2.2.6 Color
The pigment in the crustacean shells forms complexes with chitin (4-keto and
three 4, 4'-diketo-ß-carotene derivatives) (Rout, 2001). Chitosan powder is quite flabby
14
in nature and its color varies from pale yellow to white whereas starch and cellulose
powder have smooth texture and white color.
2.2.7 Water Binding Capacity (WBC) and Fat Binding Capacity (FBC)
Water uptake of chitosan was significantly greater than that of cellulose and even
chitin (Knorr, 1982). Basically, WBC for chitosan ranges between 581 to 1150% with an
average of 702%, according to Rout (2001). In his report, Rout (2001) also noted that
reversing the sequence of steps such as demineralization and deproteinization had a
pronounced effect on WBC and FBC. Deproteinization of demineralized shell also gives
higher WBC compared to the process when demineralization of the deproteinized shell
is conducted. Besides, the process of decoloration also causes a decrease in WBC of
chitosan than those of unbleached crawfish chitosan.
The fat uptake of chitin and chitosan ranges from 315 to 170% with chitosan
having the lowest and chitin the highest fat uptake (Knorr, 1982). In a study by Rout
(2001) on this aspect, he reported that the average FBC of crawfish chitosans and
commercial crab chitosans for soybean oil was 706% and 587%, respectively. The
inclusion of decoloration step during the production of chitosan was found to decrease
the fat binding capacity of crawfish chitosans, affect the viscosity of chitosan (Moorjani,
1975). The decreased viscosity as evidenced may be a cause for decrease in fat binding
capacity among unbleached and bleached crawfish chitosan samples.
Rout (2001) also reported that changing the sequence of steps, i.e., when
demineralization is conducted prior to deproteinization, followed by deacetylation,
15
caused an increase in FBC compared with when deproteinization is performed prior to
demineralization, followed by deacetylation.
2.2.8 Emulsification
Even though chitosan alone does not produce emulsions, Cho et al. (1998)
reported that emulsifying capacity of egg yolk (protein) increased with the addition of
chitosan compared with the control. At 0.5% chitosan concentration, better emulsifying
capacity was observed compared with at 0.1 or 0.3% chitosan. In general, chitosan
emulsions tend to be very stable under temperature changes and aging. With viscosity,
the degree of deacetylation is reported to be a determining factor in the emulsification
properties of chitosan. The protein solution containing chitosan with intermediate degree
of deacetylation produces less effective emulsion compared with that containing
chitosan with higher DDA.
2.2.9 Antimicrobial Properties
Recent studies in antibacterial activity of chitosan have revealed that chitosan is
effective in inhibiting growth of bacteria. The antimicrobial properties of chitosan
depend on its molecular weight and the type of bacterium. Gram-positive bacteria retain
crystal violet dye after iodine fixation and alcohol decolorization, whereas gram-
negative bacteria do not. Gram-negative bacteria have an additional outer membrane
containing lipopolysaccharide (endotoxin). For gram-positive bacteria, chitosan with
16
470 KDa was the most effective, except for Lactbacillus sp., whereas for gram-negative
bacteria, chitosan with 1,106 KDa was effective. Chitosan generally showed stronger
bactericidal effects for grampositive bacteria (Listeria monocytogenes, Bacillus
megaterium, B. cereus, Staphylococcus aureus, Lactobacillus plantarum, L. brevis, and
L. bulgaris) than for gram-negative bacteria (E.coli, Pseudomonas fluorescens,
Salmonella typhymurium, and Vibrio parahaemolyticus) in the presence of 0.1%
chitosan (No et al., 2002).
Koide (1998) reported that chitin and chitosan in vitro show antibacterial and
anti-yeast activities. One of chitosan derivatives, N-carboxybutyl chitosan, was tested
against 298 cultures of different pathogenic microorganisms that showed bacteriostatic
and bactericidal activities, and there were marked morphological alterations in treated
microorganisms when examined by electron microscopy (Muzzarelli, 1990).
Conversely, growth inhibition and inactivation of mould and yeasts seem to depend on
chitosan concentration, pH, and temperature (Rout, 2001). According to Cuero (1999),
the antimicrobial action of chitosan is influenced by intrinsic and extrinsic factors such
as the type of chitosan (e.g., plain or derivative), degree of chitosan polymerization, host
nutrient constituency, substrate chemical and/ or nutrient composition, and
environmental conditions such as substrate water activity.
In an extensive research by Tsai and Su (1999) on the antimicrobial activity of
chitosan prepared from shrimp against Ecoli, they found that higher temperature and
acidic pH of foods increased the bactericidal effect of chitosan. They also explained the
mechanism of chitosan antibacterial action involving a cross-linkage between
polycations of chitosan and the anions on the bacterial surface that changes membrane
permeability. Chitosan has been approved as a food additive in Korea and Japan since
1995 and 1983, respectively (KFDA, 1995). Higher antibacterial activity of chitosan at
lower pH suggests that addition of chitosan to acidic foods will enhance its effectiveness
as a natural preservative (No et al., 2002).
17
2.2.10 Formation of Film
Chitosan coating have been shown to significantly delay fruit spoilage or
decaying of fruits and vegetables such as tomatoes, strawberries, etc., at different
temperatures. Chitosan coated fruits were not only firmer and higher in titratable acidity,
but were slow to decay and exhibited less pigmentation than control samples at the end
of storage (El Ghaouth et al., 1992). The low molecular weight chitosan has a greater
inhibitory effect against phytopathogens than the high molecular weight chitosan
(Hirano et al., 1989).
Chitosan has an ability to form film which makes it suitable for use as food
preservation for control of psychotropic pathogen in fresh or processed meat and fish
products packaged under modified atmosphere (Smith et al., 1994). According to
Charles et al. (1994), the most potential application of chitosan is as a coating agent in
the area of fruit preservation. The biodegradability of chitosan is one of the most
advantageous features for concern of the environmental damage occurring by improper
disposal of petrochemical based plastics (Knorr, 1991).
N, O-carboxymethyl chitosan can form a strong film that is selectively
permeable to such gases as oxygen and carbon dioxide. Apples coated with this material
remain fresh for up to six months. The chitosan coating has been shown to delay
ripening of banana for up to 30 days where as chitosan film manifests a slightly yellow
appearance, with the color darkening as thickness increased (Setha et al., 2000).
18
2.3 Production of Chitin and Chitosan
Chitosan is easily obtained from crab especially Dungeness crab (Cancer
magister), shrimp particularly the Pacific shrimp (Pandalus borealis), lobster, or
crawfish shells. These are the richest source of chitin and the major sources of
crustaceans that are processed into chitin and chitosan (Knorr, 1991). While much
research has been done with chitosan extraction from crab shell, limited information is
available on the extraction possibilities with crawfish shell waste.
Previous studies demonstrated that crawfish and crustacean wastes, as well as
organically-rich shellfish processing streams in general, can no longer be considered as
disposable “waste” products with minimal economic value, but should be considered as
profitable alternatives leading to valuable products of commerce (No et al., 1992).
Similar research studies by Lee (1989) demonstrated that the astaxanthin-rich shell from
crawfish waste is a valuable natural resource for commercially feasible pigment which is
marketed as a fish food additive in aquaculture, especially for Salmon.
Apart from the recoverable pigment, it has been shown that crawfish shell waste
possesses a significant and renewable major resource for the biopolymer chitin (23.5%
on a dry basis compared to 14-27% and 13-15% of the dry weight of shrimp and crab
processing waste, respectively) and chitosan (No and Meyers, 1989,1992). Therefore,
the applications of crawfish shell wastes as a source of astaxanthin, chitin and chitosan
represent a total byproduct utilization concept with realistic implications in other
crustacean waste recovery industries (No and Meyers, 1989). Further significance can be
seen in the utilization of astaxanthin pigment, chitin, and protein from crawfish shell as
mentioned earlier in a variety of fields with different applications.
19
Chitin was obtained in pilot scale, according to the procedure of Soares, Moura,
Vasconcelos, Rizzi, and Pinto (2003), through the stages of demineralization, that
consists of the reduction of raw material’s ashes; deproteinization, where there is a
reduction of shrimp wastes’ protein nitrogen; and deodorization, for the reduction of
shrimp’s characteristic odor. Chitin was dried in a tray drier until reaching commercial
moisture content (5.0–6.0%, wet basis).
2.3.1 Isolation of Chitin
Isolation of chitin from crawfish shell wastes involves four traditional steps:
demineralization, deproteinization, decolorization, and deacetylation. However, the
isolation of chitin specifically consists of only two steps: demineralization and
deproteinization, which involves the dissolution of calcium carbonate with 1.0 N HCl
and the removal of proteins with 3% NaOH, respectively.
20
Figure 2.4 Isolation of chitin.
From Shrimp Shells Waste
Step 1 : Demineralization (removing calcium carbonate,phosphate) Step 2 : Deproteinization
Step 3 : Decolorization (removing mainly astaxanthin,pigment)
From Chitin :
Step 1 : Deacetylation (removing acetyl groups from polymer)
We get Chitosan
21
Figure 2.5 Traditional Crawfish Chitosan Production Flow Scheme (Modified from No
and Meyers, 1995)
Wet crawfish shell
Washing and drying
Grinding and sieving
Deproteinization
Washing
Dimineralization
Washing
Decolorization
Washing and drying
Deacetylation
Washing and drying
Chitosan
22
2.3.2 Deproteinization
Chitin occurs naturally in association with protein (chitinoprotein). Some of this
protein can be extracted by mild methods, but other portion is not readily extracted,
suggesting strong covalent bonding to chitin (Attwood and Zola, 1967). With regards to
chemical structure, protein is bound by covalent bonds to the chitin through aspartyl or
histidyl residues, or both, thus forming stable complexes such as glycoproteins.
Crustacean shell waste is usually grounded and treated with dilute sodium hydroxide
solution (1-10%) at elevated temperature (65-100ºC) to dissolve the proteins present.
Reaction time usually ranges from 0.5 to 12 hr depending on preparation methods.
Prolonged alkaline treatment under severe conditions causes depolymerization and
deacetylation. To obtain uniformity in reaction, it is recommended to use relatively high
ratios of solid to alkali solution of 1:10 or 1:15-20 with proper agitation because a
minimum ratio of 1:4 (w/v) of shell weight to potassium hydroxide (KOH) solution, had
only a minor effect on the deproteinization efficiency of shells (No and Meyers, 1995).
2.3.3 Demineralization
The conventional demineralization process of crustacean waste is costly and
causes environmental problems. Hydrochloric acid is the most commonly used chemical
in the demineralization of crustacean waste. The use of this strong acid are to harm the
physiochemical properties of chitin, results in a harmful effluent wastewater, and
increases the cost of chitin purification process. Percot et al. reported that using
hydrochloric acid (HCl) for the demineralization of chitin results in detrimental effects
on the molecular weight and the degree of acetylation that negatively affects the intrinsic
properties of the purified chitin. The authors elaborated on the importance of the
23
optimization of the extraction process parameters (pH, time, temperature and solids to
acid ratio) in order to minimize chitin degradation and bring the impurity levels down to
the satisfactory level for specific applications. Therefore, a less harmful cheaper
demineralization process is needed.
The current study proposes the use of a novel demineralization process in which
organic acids (lactic and acetic) are used. Using organic acids such as lactic and/or acetic
acids for the demineralization process is a Am. J. (2007) promising idea, since organic
acids can be produced from low cost biomass such as cheese whey, are less harmful to
the environment, can preserve the characteristics of the purified chitin, and the resulting
organic salts from the demineralization process can be used as an environmentally
friendly deicing/ anti-icing agents and/or as preservatives.
2.3.4 Decolorization
Acid and alkali treatments alone produce a colored chitin product. For
commercial acceptability, the chitin produced from crustacean sources, needs to be
decolorized which is a process to remove astaxanthins and pigments or bleached to yield
cream white chitin powder (No et al., 1989). The pigment in the crustacean shells forms
complexes with chitin. In earlier research studies, one 4-keto-and three 4, 4’-diketo-
ßcarotene derivatives was firmly bound to the exoskeletal chitin of red kelp crab. The
level of association of chitin and pigments varies from species to species among
crustacean. Several workers have used reagents to eliminate pigments from crustacean
exoskeleton, usually crab.
24
However, with crawfish shell the reagents alone do not seem as effective as the
procedure developed currently. This suggests that carotenoids, are more strongly bound
to the crawfish shell matrix than are those reported from other crustacea (No et al.,
1989). Hence, the stronger the bond the more harsh treatment is required to prepare a
white colored chitin. During the process of decoloration, it should be noted that the
chemical used should not affect the physicochemical or functional properties of chitin
and chitosan. No et al. (1989) was able to prepare a near white colored crawfish chitin
by extraction with acetone and dried for 2 hr at ambient temperature, followed by
bleaching with 0.315 % (v/v) sodium hypochloride solution (containing 5.25% available
chlorine) for 5 min with a solid to solvent ratio of 1:10 (w/v), based on dry shell. But,
the color of chitin products varied from cream white to intermediate pink color (No et
al., 1989). Without prior acetone extraction, bleaching for more than 1 hr was needed to
obtain a commercially acceptable white product.
2.3.5 Deacetylation
The major procedure for obtaining chitosan is based on the alkaline deacetylation
of chitin with strong alkaline solution. Deacetylation is the process to convert chitin to
chitosan by removal of acetyl group. It is generally achieved by treatment with
concentrated sodium or potassium hydroxide solution (40-50%) usually at 100ºC or
higher for 30 min or longer to remove some or all of the acetyl groups from the polymer
(No and Meyers, 1989). The N-acetyl groups cannot be removed by acidic reagents
without hydrolysis of the polysaccharide, thus, alkaline methods must be employed for
N-deacetylation (Muzzarelli, 1977).
25
Kurita (2001) has indicated that deacetylation of chitin can be highly facilitated
by steeping in strong sodium hydroxide solution at room temperature before heating.
This approach was then adapted and the effect of steeping time on the feasibility of
deacetylation was investigated. There are several critical factors that affect the extent of
deacetylation including temperature and time of deacetylation, alkali concentration, prior
treatments applied to chitin isolation, atmosphere (air or nitrogen), ratio of chitin to
alkali solution, density of the chitin, and particle size (Rigby, 1936). Considering all
these as necessary conditions, the ideal purpose of deacetylation is to prepare a chitosan
that is not degraded and is soluble in dilute acetic acid in minimal time.
2.4 Factors Affecting Production of Chitosan
A number of processing factors affect chitosan's physicochemical characteristics
such as temperature of deacetylation, time of deacetylation and alkali concentration,
effect of treatment conditions applied in chitin isolation, atmosphere, ratio of chitin to
alkali solution, and particle size.
2.4.1 Temperature of Deacetylation
Higher temperature tends to increase the degree of deacetylation but reduces
molecular size (Lusena and Rose, 1953). There is a substantially linear relationship
between temperature (plotted along the abscissa as 1/T in K) and the rate of
deacetylation (plotted logarithmically along the ordinate) (Peniston and Johnson, 1980).
26
2.4.2 Time of Deacetylation and Alkali Concentration
Wu and Bough (1978) suggested that deacetylation proceeds rapidly to about
68% during the first 1hr in 50% NaOH solution at 100oC. However, the reaction
progresses gradually thereafter reaching about 78% in 5 hr. Thus, alkali treatment
beyond 2 hr does not deacetylate chitin significantly; rather it degrades the molecular
chain. In a concentration study with 35, 40, and 50% NaOH (Bough et al., 1978), as
alkali concentration decreased, rates of decrease in both viscosity and molecular weight
distribution also slowed. Bough et al. (1978) alluded that chitosan deacetylated for 5 min
with 50% NaOH at 145-150oC had higher viscosities (1.7-16.4 fold) and molecular
weight (1.1-1.8 fold) than did chitosans deacetylated for 15 min. Similarly, decrease in
viscosity with increased reaction time was shown and confirmed.
2.4.3 Effect of Treatment Conditions Applied in Chitin Isolation
Treatment conditions applied to chitosan isolation primarily affect viscosity of
the product than any other property. The use of HCl at concentrations above 1.25 N
adversely affected the viscosity of the final chitosan product. In addition, chitosan
viscosity tends to decrease with increased time of demineralization (Moorjani et al.,
1975). On the other hand, Bough et al. (1978) found that deproteinization with 3%
NaOH, and elimination of the demineralization step in chitin preparation, decreased the
viscosities of chitosan samples, where as Moorjani et al. (1975) indicated that it is not
desirable to bleach the material at any stage since bleaching considerably reduces the
viscosity of the final chitosan product.
27
2.4.4 Atmosphere, Ratio of Chitin to Alkali Solution, and Particle Size.
Many scientists have agreed that free access of oxygen to chitin during
deacetylation has a substantial degrading effect on chitosan. Deacetylation in the
presence of nitrogen yielded chitosan of higher viscosity and molecular weight
distributions than did in air. However, little differences in nitrogen and ash compositions
were observed (Bough et al., 1978). Moorjani et al. (1978) emphasized that the ratio of
chitin solids to alkali solution plays a significant role in determining the quality of
chitosan, based on viscosity determination.
Particle size in chitosan productions has sparked controversial reports on its
effect on chitosan quality. Some agree that small particle size is better than large particle
size. According to Bough et al. (1978), smaller particle size (1mm) results in a chitosan
product of both higher viscosity and molecular weight than that of larger particle size
(above 2 to 6.4 mm). The larger particle sizes require longer swelling time resulting in a
slower deacetylation rate. However, Lusena and Rose (1953) indicated that the size of
chitin particle within the 20-80 mesh range (0.841-0.177 mm) had no effect on the
extent of deacetylation and viscosity of the chitosan solutions.
2.5 Determination of Deacetylation Degree
Dodane and Vilivalam (1998) reported that the degree of deacetylation is one of
the more important chemical characteristics, which could influence the performance of
chitosan in many of its applications (Kofuji et al. 2004). In addition, the degree of
deacetylation, which determines the content of free amino groups in the polysaccharides,
28
can be employed to differentiate between chitin and chitosan. For instance, chitin with a
degree of deacetylation of 75% or above is generally known as chitosan (Brine and
Austin, 1981). The process of deacetylation involves the removal of acetyl groups from
the molecular chain of chitin, leaving behind a complete amino group (-NH2) and
chitosan versatility depends mainly on this high degree chemical reactive amino groups.
There are methods available to increase or decrease the degree of deacetylation. For
example, increase either in temperature or strength of sodium hydroxide solution could
enhance the removal of acetyl groups from chitin, resulting in a range of chitosan
molecules with different properties and hence its applications (Kofuji and Shibata,
1999). Since the degree of deacetylation depended mainly on the method of purification
and reaction conditions (Khor and Lim, 2003; Brine and Austin, 1981), it is therefore
essential to characterize chitosan by determining its degree of deacetylation prior to its
utilization at the developmental stage of drug delivery systems.
Various methods have been reported for the determination of the degree of
deacetylation of chitosan. The methods that have been reported by Kofuji (1999)
included ninhydrin test, linear potentiometric titration, near-infrared spectroscopy,
nuclear magnetic resonance spectroscopy, hydrogen bromide titrimetry, infrared
spectroscopy, and Hirano et al. (1989) reported on first derivative UV-
spectrophotometry. Some of the methods are either too tedious, costly for routine
analysis (nuclear magnetic resonance spectroscopy), or destructive to the sample
(ninhydrin test). Furthermore, many limit the range of degree of deacetylation to which
they are applicable. Lately, the first derivative UV-spectrophotometry was advocated for
the degree of deacetylation determination. The degree of deacetylation values of
chitosan appeared to be highly associated with the analytical methods employed.
29
2.6 Application of Chitosan
Chitin has long been viewed as the nature’s second most abundant polymer. This
is for the fact that it is found not only in shellfish, but also found in insect shells and
fungi cell walls. Chitosan, a refined form of chitin, is prepared by removing the shells
from shellfish. The shells are then ground into a pulverous powder, which is
deacetylated or stripped of specific chemical groups allowing the compound to actively
soak up fats. This aspect of it being able to absorb fat is the main feature which makes it
effective in helping weight loss.
2.6.1 Dietary Supplements
It is effectively a fantastic fat inhibitor which work wonders for those in search
of a safe way to lose body fat. It was universally accepted not as a nutritional
supplement in many past cultures, but rather as a potent water detoxifier and was used in
the depletion and eradication of certain waterborne illnesses and toxic substances often
found in municipal sources. Scientific advances in clinical research have proved that
upon ingestion, chitosan is well tolerated and acts as a cellulose-like fiber within the
human body. This finding proved influential for a myriad of health concerns including;
a potent aid in the weight loss of adults, wound healing, and disease prevention. It
provides much of the fiber that is one of the keys to a healthy, cancer-free diet.
There are a number of functions or uses linked to chitosan. Because of these
applications, chitosan is now marketed as a dietary supplement and is used to thicken
foods, paints and makeup (Rout, 2001). Studies in Japan, the U.S. and Europe have
30
shown that chitin and its derivatives help the digestive process and promote the growth
of beneficial intestinal bacteria necessary for proper digestion and excretion of wastes.
These studies have shown chitin to be helpful in better bowel health and the prevention
of tumors or intestinal polyps that are often the precursor to cancers of the bowel and
colon. Chitin has also been shown to have anti-gastritis, anti-toxin, anti-diarrheal, and
anti-constipation properties.
2.6.2 Industrial Wastewater Treatment
In industrial wastewater treatment, chitosan carries a partial positive charge and
binds to metal ions, thus makes the metal ions removal from waste streams or
contamination sites easier (Asano, 1978). In terms of utilization, crawfish chitosan as a
coagulant for recovery of organic compounds in wastewater was demonstrated to be
equivalent or superior to, the commercial chitosans from shrimp and crab waste shell
and synthetic polyelectrolytes in turbidity reduction (No and Meyers, 1992). The
wastewater released from food processing plants typically seafood, dairy or meat
processing industries contains appreciable amount of protein which can be recovered
with the use of chitosan; this protein, after drying and sterilization, makes a great source
of feed additives for farm animals (Rout, 2001).
31
2.6.3 Medical Applications
Chitin has strong anti-bacterial, anti-fungal and anti-viral properties that make it
extremely useful in medical applications such as bandages, wound dressings, surgical
sutures, periodontal treatments, and cataract surgery (Kratz and Arnander, 1997).
Extensive research has shown chitin and its derivative chitosan to be non-toxic and non-
allergenic. Asano et al. (1978) found that chitin is fully biodegradable and therefore
environmentally friendly.
Chitin and chitosan have been extensively examined and tested by researchers
world-wide in a wide range of medical applications, food and nutrition uses, cosmetics,
beauty aids and other new discoveries. Today, mainly in the U.S. and Japan, more than
two million people take chitin and chitosan as dietary supplements.
Table 2.1 Applications of Chitosan
Industry Application
Wastewater Treatment Removal of metal ions, flocculant/coagulant, protein,
dye, amino acids
Food Industry Removal of dye, suspended solids, preservative, color
stabilization, food stabilizer, thickener and gelling agent,
animal feed additive, etc.
Medical Wound and bone healing, blood cholesterol control, skin
burn, contact lens, surgical sutures, dental plaque
inhibition, clotting agent, etc.
32
Agriculture Seed coating, fertilizer, controlled agrochemical release
Cosmetics Moisturizer, face, hand, and body creams, bath lotion, etc.
Biotechnology Enzyme immobilization, protein separation, cell recovery,
chromatography
Chitin has become known as the miracle fiber. Extensive research has
demonstrated it has no known adverse side effects. Japanese medical doctors have been
recommending for at least 20 years that their patients consume large quantities of chitin.
Much of this enthusiasm is unrelated to weight loss. In Japan medical doctors
recommend chitin as a means of helping cure such conditions as allergies, high blood
pressure, elevated blood fats, arthritis and other problems. In Japan chitin is a food
supplement used in place of dangerous prescription drugs.
CHAPTER 3
MATERIALS AND METHODS
3.1 Isolation of Chitin
Chitin was isolated from shrimp shells that were obtained from local wet market
in Kuantan, Pahang. The raw materials were obtained in solid form from the shrimp
shells, washed with water, dried in oven at 60oC for 24 hours, and was blended into
small pieces (nearly powdered).
3.2 Purification Process
The purpose of purification process is to get rid of the impurities in chitin. It
consists of four steps; deproteinization, demineralization, decolorization, and
deacetylation. Of all these process, the deacetylation process is the important part in this
research for it will determine the effectiveness of chitosan in many of its application by
its degree. The steps of these processes are shown in Figure 3.1 below:
34
Figure 3.1 Steps of purification process
3.2.1 Deproteinization
Dried shrimp shells was deproteinized with 3.5% (w/w) NaOH solution for 2
hours at 65oC with constant stirring inside the incubator shaker at a solid to solvent ratio
of 1:10 (w/v). Samples were then filtered, and filtrate was washed with tap water for 30
minutes and oven-dried.
DECOLORIZATION
DEACETYLATION
DEMINERALIZATION
DEPROTIENIZATION
35
3.2.2 Demineralization
Deproteinized shrimp shells were then demineralized by addition of 1N HCl for
30 minutes at ambient temperature with a solid to solvent ratio of 1:15 (w/v), and then
filtered. The filtrate was washed for 30 minutes with tap water and oven-dried.
3.2.3 Decolorization
After deproteinization process, the shrimp shells were decolorized by addition of
acetone for 10 minutes and dried for 2 hours at ambient temperature, followed by
bleaching with 0.315% (v/v) sodium hypochloride (NaOCl) solution (containing ≈10%
available chlorine) for 5 minutes at ambient temperature with a solid to solvent ratio of
1:10 (w/v) based on dry shell. Samples were then washed with tap water and oven-dried
at 70oC for 24 hours until the powder was crispy.
3.2.4 Deacetylation
Removal of acetyl groups from chitin was achieved by autoclaving where the
parameters such as concentration of sodium hydroxide solution, time of heating, and
temperature of heating were varied. The pressure in autoclave was 30 psia and is fixed.
There are three experiments in deacetylation process where each experiment studied the
parameter that affect the deacetylation degree of chitosan.
36
3.2.4.1 Time of Heating
For the first experiment, removal of acetyl groups from chitin was achieved by
autoclaving for 10, 20 and 30 minutes at 121oC using 50% concentrated sodium
hydroxide solution (NaOH) with a solid to solvent ratio of 1:10 (w/v) according to No et
al. (1989). The resulting chitosans were washed to neutrality in running tap water, rinsed
with distilled water, filtered, and dried at 70oC for 24 hours in the oven and were kept
for analysis.
3.2.4.2 Temperature of Heating
For the second experiment, the pressure for autoclaving is fixed at 30 psia with
temperatures of 98oC, 121oC, and 134oC. The time for heating is chosen from first
experiment with the highest degree of deacetylation. 50% concentrated sodium
hydroxide (NaOH) solution is used with a solid to solvent ratio of 1:10 (w/v). The
resulting chitosans were washed to neutrality in running tap water, rinsed with distilled
water, filtered, and dried at 70oC for 24 hours in the oven.
3.2.4.3 Alkaline (NaOH) Concentration
For the third experiment, the concentration of NaOH is varied; 10%, 30%, 50%,
and 70%. Here, the time for heating is chosen from the first experiment and the
temperature is chosen from the second experiment, both with the highest degree of
deacetylation. The resulting chitosans were washed to neutrality in running tap water,
rinsed with distilled water, filtered, and dried at 70oC for 24 hours in the oven.
37
3.3 Determination of Deacetylation Degree
After each experiment in deacetylation process via autoclaving, each sample was
analyzed for its degree of deacetylation. This was done after drying the resulting
chitosan in oven.
3.3.1 Linear Potentiometric Titration
The determination of deacetylation degree of resulting chitosan is conducted
using linear potentiometric titration. This method was a modification method of Ke and
Chen (1990). Chitosan 0.25g was dissolved in 20 ml of standardised 0.10N HCl (to give
a non-viscous solution) and diluted with 10 ml of distilled water. The pH of the solution
was adjusted to ≈2 with standard 0.01M NaOH and taken as the start point. Under
continuous stirring, 1 ml of standard NaOH (0.5 ml for purified chitosan) was added,
allowed to equilibrate and the pH recorded. This sequence was repeated until the pH
reached a value of 3. The DDA% was calculated from the relation (Broussignac, 1968):
���% �������
��� Equation 3.1
where Q = NDV/m, DV is the volume of NaOH solution between the two inflection
points (in l), N is the concentration of NaOH and m is the dry weight of chitosan (in g).
CHAPTER 4
RESULTS AND DISCUSSIONS
4.1 Results
In this part, all the results of the DDA% analysis are presented in Table 4.1-4.3.
These data were then illustrated in figures, Figure 4.1-4.3. From this figure, it is shown
clearly the effect of each parameter to the DDA% of chitosan.
4.1.1 Time of Heating in Autoclave
Table 4.1 DDA% of different time of heating
Time (min) DDA%
10 89.05
20 85.82
30 82.40
39
Figure 4.1 Effect of time of heating on DDA%
In this experiment, the fixed parameter is the concentration of NaOH, 50%, and
the temperature, 121oC. From Figure 4.1, the highest DDA%, 89.05%, was achieved
within time 10 mins heating in the autoclave. In the other hand, the increasing of time
heating in autoclave decreased the DDA% of chitosan.
78
80
82
84
86
88
90
10 20 30
DD
A (
%)
Time (min)
40
4.1.2 Temperature of Heating in Autoclave
Table 4.2 DDA% of different temperature of heating
Temperature (oC) DDA%
10 80.52
20 89.00
30 98.38
Figure 4.2 Effect of temperature of heating on DDA%
In this experiment, the concentration of NaOH was fixed at 50%, and time
heating at 10 mins. From Figure 4.2, the highest deacetylation degree, 98.38% was
achieved when temperature was 134oC. Higher temperature tends to increase the
deacetylation degree of chitosan.
0
20
40
60
80
100
98 121 134
DD
A (
%)
Temperature (°C)
41
4.1.3 Concentration of Sodium Hydroxide (NaOH)
Table 4.3 DDA% of different NaOH concentration
NaOH Concentration (%) DDA%
10 66.03
30 75.71
50 87.35
70 98.79
Figure 4.3 Effect of NaOH concentration on DDA%
In this experiment, the time of heating and temperature was fixed at 10 mins and
134oC respectively. It was found that the DDA% increase as the concentration of NaOH
0
20
40
60
80
100
10 30 50 70
DD
A (
%)
NaOH concentration (%)
42
increase. From Figure 4.3, the highest deacetylation degree, 98.79% was achieved when
the concentration of NaOH was 70%.
4.2 Discussions
The objective of this research is to enhance the degree of deacetylation of chitin
in chitosan production. Deacetylation was effectively achieved by treatment of chitin
under autoclaving conditions and elevated NaOH concentrations, heating times and
temperature and was evaluated for the preparation of chitosan. Further explanations on
results are discussed in this part.
4.2.1 Time of Heating in Autoclave
According to Wu and Bough (1978), deacetylation proceeds rapidly about 68%
during first 1 hr in 50% NaOH solution at 100oC, and reaching about 78% in 5 hrs when
no pressure applied to the system. In autoclave, the pressure 30 psia was applied during
heating the solution of chitosan. Therefore, the use of the autoclave leads to dramatic
reduction in the time of deacetylation and conservation of energy. The deacetylation
degree of chitosan increased fast at the beginning of reaction process then slowed over
time. It means that after an extent time of reaction, it will decrease the NaOH
concentration in the liquid phase and stopped the deacetylation reaction.
43
4.2.2 Temperature of Heating in Autoclave
Higher temperature tends to increase the degree of deacetylation but reduces
molecular size (Lusena and Rose, 1953). The higher temperature helps to deacetylate
chitosan faster. It was observed that the DDA% of chitosan increased significantly with
the increase of temperature to 134°C. Chitosan production showed significant
differences even with small increments of temperature. A decrease in the temperature to
95°C at standard period (10 minutes) showed a reduction of 9.52% of the deacetylation
of chitosan produced. Higher temperatures were necessary to enable effective
interactions between NaOH and the constituents of the polysaccharides in shrimp shells
thus making it possible to extract higher levels of chitosan.
4.2.3 Concentration of Sodium Hydroxide (NaOH)
In general, alkaline treatment of the deacetylation of chitin proceeds rapidly until
the deacetylation reaches around 75-98%, after which further treatment has only a very
limited effect on the extent of deacetylation unless drastic conditions are used. The most
probable explanation for this condition is that the morphology of chitin chains is such
that the remaining amide groups are inaccessible to the NaOH molecule for alkali
treatment. As it is reported in the literature review, when the alkali concentration is
below 40% there is no deacetylation reaction. In other words, there is not enough driving
force in order to conduct the reaction. It seems that the ability of NaOH diffusion into
chitin was highly diminished and it depends on whether or not it is easy for NaOH to
contact the C (2)-acetamido group in chitosan, which is mainly determined by the crystal
structure and the aggregated state of chitosan. Chitosan with different physical forms
possess different aggregated states and crystal structures. The physical form of chitosan
relies on the specific route for preparing chitosan sample.
44
4.2.4 Limitations of Research
There are some limitations during the experimental progress. These limitations
come from the autoclave that was used for the deacetylation process. The autoclave can
only vary three different time and temperature of heating, and is fixed. This is because
the autoclave is mainly used for sterilization purpose where the time and temperature is
fixed at 121oC and 15mins respectively. This makes it so difficult to vary much more on
time and temperature of heating plus the pressure inside autoclave. The pressure is also
fixed at 30 psia.
CHAPTER 5
CONCLUSION
5.1 Conclusion
The chitin and chitosan have been characterized as to their degree of
deacetylation. The effect of parameters such as temperature of heating, time of heating,
and alkaline concentration to the enhancement of deacetylation degree of chitosan have
been studied and shown. It has been shown that with pressurized condition, the
increasing of temperature of heating in autoclave and the alkaline concentration will
increase the deacetylation degree of chitosan. The highest degree of deacetylation was
achieved at temperature of 134oC and with 70% sodium hydroxide concentration.
Meanwhile, the increasing of time of heating in autoclave turns out to decrease the
deacetylation degree of chitosan production. The first ten minutes of heating shows the
highest degree of deacetylation.
46
5.2 Recommendation
From the literature review, it stated that conventional way of deacetylation is at
atmospheric pressure, and it produces low deacetylation degree of chitosan. So, in this
research, the pressurize condition inside the autoclave helps to enhance the degree of
deacetylation of chitin. Therefore, it is recommended that an equipment that can vary the
pressure is use to run the deacetylation process for it might have affect the degree of
deacetylation of chitosan. In this experiment, the pressure in the autoclave is fixed and
this made it difficult to vary the pressure during the deacetylation process and to see its
effect in the deacetylation degree.
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52
APPENDIX A
Calculation of Deacetylation Degree of Chitosan on various times of autoclave.
���% �1 � 161�
1 42�
� ���
�
Where, N = NaOH concentration
DV = volume of NaOH used for titration
m = mass of dry chitosan
For 10 mins autoclaved:
1st titration: m = 0.25g
N = 0.01M
DV = 0.0146mL
� ��0.01��0.0146�
0.25� 5.84 � 10��
���% � 1 � 161�5.84 � 10���
1 42�5.84 � 10���� 100 � 88.43%
2nd titration: m = 0.25g
N = 0.01M
DV = 0.013Ml
� ��0.01��0.013�
0.25� 5.2 � 10��
���% � 1 � 161�5.2 � 10���
1 42�5.2 � 10���� 100 � 89.67%
Average DDA% = 88.43% + 89.67%
= 89.05%
53
For 20mins autoclaved:
1st titration: m = 0.25g
N = 0.01M
DV = 0.019mL
� ��0.01��0.019�
0.25� 7.6 � 10��
���% � 1 � 161�7.6 � 10���
1 42�7.6 � 10���� 100 � 85.05%
2nd titration: m = 0.25g
N = 0.01M
DV = 0.017mL
� ��0.01��0.017�
0.25� 6.8 � 10��
���% � 1 � 161�6.8 � 10���
1 42�6.8 � 10���� 100 � 86.58%
Average DDA% = 85.05% + 86.58%
= 85.82%
For 30mins autoclaved:
1st titration: m = 0.25g
N = 0.01M
DV = 0.023mL
� ��0.01��0.023�
0.25� 9.2 � 10��
54
���% � 1 � 161�9.2 � 10���
1 42�9.2 � 10���� 100 � 82.02%
2nd titration: m = 0.25g
N = 0.01M
DV = 0.022mL
� ��0.01��0.022�
0.25� 8.8 � 10��
���% � 1 � 161�8.8 � 10���
1 42�8.8 � 10���� 100 � 82.77%
Average DDA% = 82.02% + 82.77%
= 82.40%
55
APPENDIX B
Calculation of Deacetylation Degree of Chitosan on various temperatures of autoclave.
For T = 98oC,
1st titration: m = 0.25g
N = 0.01M
DV = 0.023mL
� ��0.01��0.023�
0.25� 9.2 � 10��
���% � 1 � 161�9.2 � 10���
1 42�9.2 � 10���� 100 � 82.02%
2nd titration: m = 0.25g
N = 0.01M
DV = 0.027mL
� ��0.01��0.027�
0.25� 1.08 � 10��
���% � 1 � 161�1.08 � 10���
1 42�1.08 � 10���� 100 � 79.03%
Average DDA% = 82.02% + 79.03%
= 80.52%
For T = 121oC,
1st titration: m = 0.25g
N = 0.01M
DV = 0.0146mL
56
� ��0.01��0.0146�
0.25� 5.84 � 10��
���% � 1 � 161�5.84 � 10���
1 42�5.84 � 10���� 100 � 88.43%
2nd titration: m = 0.25g
N = 0.01M
DV = 0.013mL
� ��0.01��0.013�
0.25� 5.2 � 10��
���% � 1 � 161�5.2 � 10���
1 42�5.2 � 10���� 100 � 89.67%
Average DDA% = 88.43% + 89.67%
= 89.05%
For 134oC,
1st titration: m = 0.25g
N = 0.01M
DV = 0.002mL
� ��0.01��0.002�
0.25� 8.0 � 10��
���% � 1 � 161�8.0 � 10���
1 42�8.0 � 10���� 100 � 98.38%
57
2nd titration: m = 0.25g
N = 0.01M
DV = 0.002mL
� ��0.01��0.002�
0.25� 8.0 � 10��
���% � 1 � 161�8.0 � 10���
1 42�8.0 � 10���� 100 � 98.38%
Average DDA% = 98.38%
58
APPENDIX C
Calculation of Deacetylation Degree of Chitosan on various concentration of NaOH in
autoclave.
For 10% NaOH,
1st titration: m = 0.25g
N = 0.01M
DV = 0.045mL
� ��0.01��0.042�
0.25� 1.8 � 10��
���% � 1 � 161�1.8 � 10���
1 42�1.8 � 10���� 100 � 66.03%
2nd titration: m = 0.25g
N = 0.01M
DV = 0.045mL
� ��0.01��0.042�
0.25� 1.8 � 10��
���% � 1 � 161�1.8 � 10���
1 42�1.8 � 10���� 100 � 66.03%
Average DDA% = 66.03%
59
For 30% NaOH,
1st titration: m = 0.25g
N = 0.01M
DV = 0.030mL
� ��0.01��0.030�
0.25� 1.2 � 10��
���% � 1 � 161�1.2 � 10���
1 42�1.2 � 10���� 100 � 76.81%
2nd titration: m = 0.25g
N = 0.01M
DV = 0.033mL
� ��0.01��0.033�
0.25� 1.32 � 10��
���% � 1 � 161�1.32 � 10���
1 42�1.32 � 10���� 100 � 74.61%
Average DDA% = 76.81% + 74.61%
= 75.71%
For 50% NaOH,
1st titration: m = 0.25g
N = 0.01M
DV = 0.016mL
60
� ��0.01��0.016�
0.25� 6.4 � 10��
���% � 1 � 161�6.4 � 10���
1 42�6.4 � 10���� 100 � 87.35%
2nd titration: m = 0.25g
N = 0.01M
DV = 0.016mL
� ��0.01��0.016�
0.25� 6.4 � 10��
���% � 1 � 161�6.4 � 10���
1 42�6.4 � 10���� 100 � 87.35%
Average DDA% = 87.35%
For 70% NaOH,
1st titration: m = 0.25g
N = 0.01M
DV = 0.002mL
� ��0.01��0.002�
0.25� 8.0 � 10��
���% � 1 � 161�8.0 � 10���
1 42�8.0 � 10���� 100 � 98.38%
61
2nd titration: m = 0.25g
N = 0.01M
DV = 0.001mL
� ��0.01��0.001�
0.25� 4.0 � 10��
���% � 1 � 161�4.0 � 10���
1 42�4.0 � 10���� 100 � 99.19%
Average DDA% = 98.38% + 99.19%
= 98.79%
62
APPENDIX D
Isolation of chitin processes.
i) Drying of shrimp shells ii) Blended shrimp shells
iii) Blended shrimp shells iv) Deproteinization prosess
v) Demineralization process vi) After Decolorization process
-Final Chitin
63
APPENDIX E
Deacetylation process
i) Before autoclaving process ii) After autoclaving process
iii) Filtration after autoclaving iv) Drying in oven after filtration
64
v) Resulting chitosan after deacetylation
vi) Titration process
65
APPENDIX F
Type of Autoclave.
66