PRODUCTION OF SYNTHETIC ADHESIVE FROM CASSAVA STARCH
THE DEPARTMENT OF CHEMICAL ENGINEERING
DEDICATION
This work is dedicated to God Almighty, the giver of
life, wisdom and good health for his infinite mercy, guidance and providence
throughout the project.
ABSTRACT
Wet extraction method was used to extract starch from cassava tubers. As a result of the development of several formulas, the highest quality was achieved. The formulations were made using a gelatinization technique, and the grade of the ingredients utilized was varied. The following tests were performed on the formulations: - PH determination; the PH of the formulated adhesive is 6.8, which is quite equivalent. The formulations' solid/moisture content is 19.4 percent and 82.2 percent, respectively, while the standard is 15-30 percent and 65-85 percent. The developed adhesive has a tack duration of 16 minutes, which is equivalent to the industry standard of 15 minutes. The shelf life of the prepared adhesives has exceeded two months and is still appropriate, indicating that it may be comparable to market shelf life. Finally, the compositions' wettability was comparable to that of commercial adhesives.
CHAPTER
ONE
INTRODUCTION
1.1
BACKGROUND OF STUDY
Cassava, a relatively obscure crop in the old world before to the discovery of America, is quickly assuming the role of world savior, as it is now growing throughout the tropical world. It is now only second to potato as the most significant starchy root crop for food and industry in the tropics. It's eaten raw or cooked in Nigeria, and it's used to make garri, starch flour and a variety of other items (Tonukari, 2004; Grace, 1977). The current drive towards earning foreign exchange from cassava products in Nigeria had raised more awareness on the importance of the crop.
However, most processing enterprises do not efficiently utilize the secondary product (cassava starch and milk) from the product of garri (the most important food item made from cassava in Nigeria). These items are simply drained without any consideration for their use, particularly in rural areas. It is in the light of this and the fact that this cassava is readily available that these studies were conducted to investigate the possible utilization of cassava starch as a binding material (adhesive).
An adhesive is a substance capable of binding materials together via surface adhesion and sustaining the designed load requirement without deformation or failure (Anonymous, 1982). Adhesives exist in a variety of forms, liquid paste, film, powder, granules and in solid forms, materials being fastened together by adhesives are called substrates. Adhesive materials have been used successfully in a variety of applications for centuries, not until the demands were made for major advancement in adhesive technology, as a result in availability of metals in large volumes and the introduction of plastics, rising needs to join this diversity of materials became a problem. Adhesives are now more vital than ever in our daily lives, and their utility is continually expanding. People now routinely entrust their fortunes and lives to adhesively bonded structures and barely think about it, but researchers are interested in learning more about adhesives and adhesive bonding.
There are two essential characteristics that anadhesive must have in order to be effective. Theadhesive must be capable of impacting adequate bondbetween the two materials by principle of resistance to load shear, which implies creep static or time independent deformation under sustained load(Foschi, 1977). Other desired requirements are ease of application, reasonable setting time, resistance to moisture, aging, heat and fungal attack, non-staining and gap filling(Knight, 1984). Although the primary effect of solidified adhesives in pore spaces may be minor, cassava-based adhesives might be easily manufactured from by-products that would otherwise be discarded, providing a distinct economic benefit. Adhesives work by forming a bond between the adhesive and the product to be adhered. Cassava starch has a fine, silky texture and is non-staining and non-poisonous which makes cassava adhesives a desirable choice particularly for domestic uses and most non-structural utilization of adhesives(FOA, 1983).The use of starch as an adhesive, on the other hand, has a number of drawbacks. It is important to note that starch-based adhesives are made possible by starch's capacity to gelatinize at a specific temperature. The starch is hydrolyzed to form a gel, paste, or solution during the gelatinization process. Degraded or transformed starch, such as dextrose, is also used in starch-based adhesives. The most important of these is the stability of the product over time, hence very short pot-life. Adhesives generally found its applications in industries and starch-based applied in packaging labeling, leatherworks, binding of books etc. essentially adhesives especially the synthetic types found their application in components needed to make many products such as aircraft, corrugated cartons, plywood, automobiles, envelopes, stamps, etc. The main objective of this study, therefore, is the development of conditions that could ensure the stability of adhesives produced from cassava starch
1.2
PROBLEM STATEMENT
The research project is
“Production
of synthetic adhesive from cassava starch”
Adhesive sold in the market are made of conventional
organic materials operating with forces to bind or bond two surfaces together.
In this project, it is wished to produce adhesive from local raw materials such
as cassava starch to compare its bond strength with adhesives or glues sold in
the market.
1.3AIM
OF STUDY
1.
The goal of this research is to look at
the qualities of Cassava starch for the production of adhesives as a potential
career path in chemical engineering.This is a good notion since the time has
come when we should not rely only on foreign technology for all of our needs;
instead, we should aim for self-sufficiency in terms of economics by employing
abundant raw materials, such as cassava which is surplus in the south eastern
part of the nation.
2. Comparison of synthetic adhesive from cassava starch to that of potato starch and yam starch
1.4
SCPE OF STUDY
The design project is within the boundaries of
Chemical Engineering processes and does not delve into specific areas like
electrical engineering, mechanical fabrications and management.
Hence, the design project focuses on the following
chemical process engineering principles and assumptions;
·
Extraction of starch from cassava tubers
·
The selection of best process route.
·
The selection of the best separation
technique needed to perform the project.
·
Cost estimation of the production for
economical use.
· Possible plant design for the synthesis of the adhesive
1.5
LIMITATION OF STUDY
The design project is limited to the following area of
consideration:
i.
Non-availability of required materials
within school environment
ii.
Inadequate funding experienced during the
production and information acquiring
iii. Lack of constant power supply due to failure of generation plant
CHAPTER TWO
LITERATURE REVIEW
2.1
CASSAVA STARCH (TAPIOCA)
Starch is one of nature's most plentiful compounds, a
renewable and virtually limitless resource. Grain or root crops are used to
make starch. Starch is mostly utilized as a food, but it can also be easily
transformed chemically, physically, and biologically into a variety of valuable
items. To date, starch has been used to make food, paper, textiles, adhesives,
beverages, confectionary, pharmaceuticals, and building materials. Cassava
starch has many remarkable characteristics, including high paste viscosity,
high paste clarity, and high freeze-thaw stability, which are advantageous to
many industries.
FIGURE 2.1
2.1.1
PRODUCTION OF CASSAVA STARCH
Cassava starch is produced primarily by the wet
milling of fresh cassava roots
but in some countries such as in the South East Asia, it is made up of dried
cassava chips. Cassava is primarily made up of starch. Tubers that are mature
and of good grade contain about 25% starch. Per 100 kg of cassava roots,
roughly 60% starch and 10% dry pulp can be recovered from dry cassava chips.
In certain places, fresh
tubers are processed during the season while dry chips are processed during the
off-season. Preparation (peeling and washing), rasping/pulping/grating,
purification (starch washing), dewatering and drying, and finishing are the
five primary phases of starch extraction from fresh cassava roots (milling and
packaging).
Figure
2.1
Process route showing the production of cassava starch
From the figure above
(fig 2.1), we can see the various process route involved in production of
cassava starch, and they are detailed as follows;
Sorting and Weighing:
The tubers are sorted to
determine which roots are fit for production. After that, the tubers are
weighed.
Peeling: Due to the uneven shape of cassava roots, human
peeling was used to avoid the significant peeling loss associated with
mechanical peelers.
Washing: The peeled root is rinsed with enough drinkable
water to remove sand, dirt, and other contaminants.
Grating: To
make cassava mash, the root is grated.
Detoxification: To remove the poisonous hydrogen cyanide present in
cassava, the mash is mechanically detoxified in a mash agitator for a period of
time.
Dewatering: To
prepare for the drying procedure, the moisture level of the mash is
mechanically decreased to around 50%.
Granulation: A
hammer mill is used to breakdown the dewatered cake into fine granules.
Drying: To produce cassava flour of the necessary quality,
the granulation step is followed by the drying process.
Milling: The flour obtained is milled to the desired particle size.
2.2 STARCH AND MOLECULAR
STRUCTURE
2.2.1 STARCH
This is an important part
of the glue. It's a carbohydrate, specifically a high molecular weight
polysaccharide, with the empirical formula (
)n, where n is a huge but
unknown number. Polysaccharides are
sugar polymers having hydroxyl groups that allow them to form a paste with
water. Starch is made up of two molecular constituents: amylose, which is a
straight chain, and amylopectin, which is a branched structure.
Starch is a carbohydrate that is found in plants' roots, seeds, and stems. It is the second most abundant carbohydrate source after cellulose. Although starch is ubiquitous in plants, only a few sources are numerous enough to make starch extraction commercially viable. Potatoes, corn, tapioca, arrow root, rice, sorghum, sago, wheat, and waxy maize are some of these sources. A variety of processes are used to remove naturally occurring starch from the seed, as in corn, wheat, waxy maize, sorghum, and rice, from the root, as in tapioca, potato, and arrow root, or from the stem, as in sago. Cleaning the plant material is normally followed by grinding, soaking, washing, sieving, and filtering the cake before drying and grinding it. In this form, starch is a white powder, and the naked eye can't tell the difference between plants. In alcohol, most solvents, and cold water, all starches are insoluble. A dilute solution of iodine stain starch blue to bluish red. Under the microscope, the starch appear as cellular or granular material with shapes varying with the botanical origin.
2.2.2 MOLECULAR STRUCTURE
OF STARCH
The primary difference in
molecular structure that the various plants produce for their specific needs is
related to granular differences. Starch and cellulose, the two main
carbohydrates of plant origin, are quite similar in molecular structure. Both
are glucose polymers that occur naturally. The glucose units are joined by - 1,
4 – glycoside linkages to form cellulose straight chain molecule, and 1, 4 –
glycoside linkages bond the straight chain starch molecules know as amylose,
there are branched starch molecules, known as amylopectin. The branches are formed occasionally in tree
like fashion from the 1, 6 -glucoside linkages in a normal 1, 4 – glucoside
straight chain polymer.
The linear starch polymer and the branchud starch polymer are the two primary forms of starch molecules. The size of amylose molecules ranges from roughly 100 to over 1000 glucose units. The molecule of amylopectin is three or more times bigger. The specific features of each starch granule are determined by the size of the molecules and the amount of each kind contained in the granule. Both types are generally produced by plants and are found in them. The majority of starch granules comprise roughly 20-30% amylose type molecules and the rest amylopectin. Only amylopectin molecules are found in the waxy grain's starches. Some unique hybrids resulted in amylose-rich granules.
Figure : Amylose starch
molecule
Figure ; linear molecular structure of starch
2.3
ADHESIVES
Adhesive is a material
capable of fastening two materials together by surface attachment. Adhesive is
synonymous to glue, mastic, cement and mucilage.
Adhesive practically
implies the broad set of materials composed of organic compounds (mainly
polymeric) which can be used to fasten two materials together.
Generically, adhesives
implies any material capable of being fastened by surface attachment, which
would include inorganic materials such as Portland cement and solders such as
wood’s metal. The materials being fastened together by the adhesive are the
adherends and the resulting assembly is the adhesive bonds (McGraw Hill, 1971).

Figure ; starch based adhesive
2.3.1
CLASSIFICATIONS OF ADHESIVES
Adhesives can be generally classified into inorganic and organic adhesives.
ORGANIC
ADHESIVES
The organic adhesives are sub classified into natural and synthetic adhesives. Synthetic adhesives tend to cover most of the adhesives used today in modern world.
Natural
Adhesives;
These
includes dextrin, animal glue, starch, casein glue, natural rubber resin, etc.
Starch and dextrin and derived from low cost readily corn, cassava, potatoes
and are used in paper and paper board. Protein glues are made from hide, bone,
blood albumin of animals, soy proteins and casein, they are used on woods,
sometimes in combination with synthetic resins.
Natural
rubber is useful in pressure cases as it has the ability to stick fast to any
surface it comes in contact with.
Synthetic
Adhesives;
Synthetic
adhesives have recently gained popularity in various applications due to their
increased strength. Thermoplastic resin, vinyl and polyvinyl, cellulose,
thermosetting resin, Epoxy, polyester, and other synthetic adhesives are
divided into subcategories.
When
heated, thermoplastic adhesive softens and hardens as it cools. They can be
dissolved in a variety of liquids, including water and organic solvents.
When
heated, thermosetting adhesives become permanently stiffened and insoluble.
Waxes and asphalts, as well as different cellulose compound vinyls and
unvulcanized rubber, are among the thermoplastic synthetic adhesives. Multi-wall
bags, whose contents must be kept dry, are laminated with asphdt adhesives.
Paraffin wax is the primary coating material on paper for bread wraps, and
micro crystalline wax, a wax with an exceptionally fine grain structure, is used
for laminating food wraps.
Among
the cellulose compounds, cellulose nitrate, commonly known as celluloid or
pyroxylin, is the oldest synthetic adhesive. It is used in the bonding of wood,
as cellulose plastics, as home cement, and in various shoe-making activities.
The
most commonly used synthetic rubbers for structural bonding are neoprene and
nitrite rubber, which attach particularly effectively to metal and wood, and
polyisobutylene and butyl rubber, which are resistant to oxidation.
Many
high-speed packaging operations use vinyl adhesives made of polyvinyl acetate
or vinyl acetate to replace starch and dextrin. Polyvinyl alcohol, a water
soluble and remoistenable material, is used to make flat envelopes, polyvinyl
butyral is used to make safety glass adhesive, and polyvinyl other materials
are used to make pressure-sensitive labels.
When
rubber-based adhesives are applied to a surface, they are flexible, durable,
and normally thermoplastic; however, they can be vulcanized to render them insoluble
and heat resistant. They're employed in places like leather, vinyl upholstery,
and cloth where a flexible bond is desired. They form a strong and robust
metallic bond when mixed with phenolic resin.
The
cyanoacrylates when are costly, bond many types of surfaces almost
instantaneously. Polyamides are used in adhesive hot melt for paper, plastic
film and metal foil.
The
most common thermosetting adhesives are phenol-formaldehydes, which are
particularly helpful in plywood for outdoor use, amino resins such as
urea-formaldehyde for interior grades of plywood, and melamine-formaldehyde for
wet-strength sheets. Epoxy resin that contain no volatile solvent and have
outstanding adhesion to metals glass, ceramics and thermosetting plastics(Edward
H et al, 1978)
2.3.2 PHYSICAL FORMS OF ADHESIVES
Physically,
adhesives exist in many forms, these include:
(i) Liquid of high or low viscosity: Most
adhesive formulations are available in this form, either as a solvent
dispersion or as an aqueous emulsion with lattices. They are simple to use and
allow the user to alter the viscosity.
(ii) Powders: To
attain the liquid state, these adhesives must be mixed with a liquid or heated.
Some types contain latent catalysts that are activated during cure at a
specific temperature. Powder adhesives, in general, are a cost-effective option
with a lengthy shelf life.
(iii) Mastic or Paste: When
void fillers and non-slump properties are required, this shape is ideal. It is
possible to achieve a wide range of consistency.
(iv) Film Tapes: There
are supported and unsupported types. These forms are limited to smooth surfaces
and are distinguished by quick application, minimal waste, and a homogeneous
glue-like thickness.
(v) Granule, Rods, Cubes and other solid forms: These are convenient forms for ease of application and are for particular application. “solid” types are basis for adhesive solder sticks and hot-metal materials for long shelf life. (Shields J. 1974)
2.3.3 COMPOSITION OF ADHESIVES
The basic components of adhesives irrespective of the type are:
(i) BINDERS: The binders serve as a foundation for the adhesives. The binders are in charge of creating adhesive forces that hold two adherents together. A binder is something like starch.
(ii) SOLVENTS: These are the media used to disperse the binders into a spreadable liquid. Water is the most common solvent. To achieve the needed solubility in many adhesives based on synthetic resins, rubbers, and even natural gum, a range of organic solvents are required.
(iii) FILLERS: These are generally non-adhesive substances that are added to adhesives to increase their working qualities, persistence, and production costs. Calcium carbonate silicate oxide, alumna, or aluminum silicate are examples of common additives to epoxyresin adhesives.
(iv) PRESERVATIVES: These are compounds that are added to certain
adhesives to slow or stop the growth of microorganisms, either while the glue
is being stored, applied, or while the completed bond is being serviced. These
agents are typically used in formulations that contain carbohydrates or
proteins that are susceptible to mold, fungi, or bacteria, such as flour,
starch, casein, or animal protein. The preventatives used are either, sodium
benzoate or formaldehyde.
(v) CATALYSTS: These are substances that, when added in little amounts relative to the amounts of the major resistance, significantly speed up the core of an adhesive. Catalysts are used to speed up the rate of a specific chemical reaction in the adhesive base when it solidifies in the joint. Ammonium chloride, which is widely used to speed up the coming or cross-linking of proteins, is a good example of a catalyst.
(vi) THINNERS OR DILVENTS: These are volatile liquids that are mixed into an adhesive to change its consistency and other characteristics. When utilized properly, such liquids are not genuine solvents for the other components, but they are efficient in diluting or thinning the mixture as needed for spray application.
(vii) HARDENERS: These are compounds or mixes of substances that are added to an adhesive in order to promote or control the curing reaction by participating in it. Para-formaldehyde, which is widely used with resorcinol-formaldehyde wood adhesives, is an example of a hardener.
(viii) EXTENDERS: It has some adhesion properties. They're included to cut down on the amount of primary binder needed per unit area, lowering the cost of the actual joints. Wheat flour, for example, can be used to urea-formaldehyde wood adhesive to lower glue line expenses.
(ix) FORTIFIERS: They are ingredients that are added to an adhesive binder primarily to strengthen the persistence of the ensuing bond, which is not yet widely accepted. They could be binders or at the very least have a high sticky value. The addition of resorcinol and para-formaldehyde to a urea-formaldehyde wood glue, for example, can improve the weathering resistance of the resulting joints.
2.3.4 PROPERTIES
OF ADHESIVES
There
are a number of aspects to consider when evaluating an adhesive; these factors
refer to the behavior of an adhesive from the time it is made until the time it
achieves its ultimate bond.
These
factors include:
(i) VISCOSITY: The adhesive materials aren't just ordinary
liquids. In general, they are made up of a polymer that is usually dissolved in
a solvent and often mixed with particles that have different physical or
chemical properties. As a result, it's not unexpected that adhesive materials
don't show. More than one measurement is required for Newtonian flow and the
characterization of ryhlogical features. Many apparatus are used for
determining the viscosity of free flow adhesives. These include the Brookfield viscometer and
the stormer viscometer.
(ii) TACK: This is the property of an adhesive that causes one adhesive-coated surface to stick to another when they come into contact. It's basically the adhesive's stickiness. It is one of the most essential characteristics in establishing an adhesive's viability for specific applications. Tack can change depending on time, temperature, and film thickness. The instrument used in measuring tack is called tackmeter.
(iii) BLOCKING: Is an unfavorable adhesive that forms between layers of similar or dissimilar materials when they come into contact, such as when stored under moderate pressure. Adhesives are applied to one or both of the surfaces to be bonded and kept until ready for use or assembly in some applications. It is essential that the coated surface do not bond or block during storage even if subjected to slight contact pressure or minor variations in humidity or temperature.
(iv) CURING RATE: Many adhesives require curing be either
the application of heat or the addition of catalyst or both, with or without
pressure for specified periods of time.
(v) PENETRATION: An adhesive that penetrates far beyond the surface of the coating material adds nothing to the bonding of the two layers and is therefore wasted. Adhesive costs rise when extensive substrate penetration occurs. Additionally, a starved ‘glue line' or adhesive layer may result, resulting in a wet or soggy product, which could result in warpage, lower production speed, and process delays.
(vi) COVERAGE: Is the quality of an adhesive that governs the extent to which a unit weight or volume of glue can be uniformly dispersed over an area to be bonded.
(vii) STORAGE LIFE: When an adhesive is kept at high temperatures for an extended period of time, physical and chemical changes can occur. The storage life of an adhesive refers to the amount of time it may be kept, preferably under controlled circumstances, and still be used. The storage life of an adhesive can be measured by taking measurements of the adhesive's consistency, binding strength, or both, before and after storage at a specific temperature for a defined amount of time. It is recommended that the adhesive be stored at a temperature that is close to that of real service, so that changes in the adhesive can be seen. To determine these changes both consistency and bond strength test should be periodically conducted.
(viii) SHELF LIFE: The duration between when an adhesive is ready to use and when it is no longer usable is referred to as the shelf life of an adhesive.
2.3.5 CHEMISTRY OF
ADHESIVES
The science of adhesion has only been studied extensively in the last ten years. Researchers have released a number of publications that have begun to provide the groundwork for why and how things stick together. Although much progress has been made in understanding how an adhesive adheres to a surface, the following theory is commonly accepted.
ADHESION:
This is a phenomena in which interfacial forces, such as valence forces,
interlocking action, or both, hold two surfaces together. The glue must be
liquid and in close contact with the substrates for adhesion to occur. The bond has more tenacions as the
interfacial contact between atoms and molecules becomes closer to electrostatic
interaction. The adhesive must displace air and other impurities from the
surface in order to produce a strong bind. When the contact angle approaches
zero and the following conditions are present, a phenomenon known as
"wetting" occurs, the conditions include; the substrate posses a
relatively high surface attraction energy; the adhesive has a real affurity for
the substrate and the surface tension of the adhesive is low. For an adhesive to wet a solid surface, it
requires a lower surface tension than the solid. For example polytetraflooethone (PTF) is a
‘non stick’ material because its surface tension is so low that no liquid
adhesive has a surface tension low enough to wet it and hence bond to it. Metal
adherends are readily wetted by most organic adhesives. When tight contact is
created through wetting, the forces of molecular attraction maintain it, and it
can be regarded permanent once the adhesive has set or cured. When the adhesive
and substrate molecules come together, a multitude of forces are at work, the
most important of which are the van Der Waals forces. There are some times
reinforced by the attraction forces of primary chemical bonds. The van De Walls forces can be likened to a
magnetic attraction, except in this case, it is the electrical changes that are
involved. Calculations have indicated
that the van Der Waal forces alone can produce theoretical bond strengths
substantially greater than those observed in practice, with the difference owing
to the challenges in creating a perfect joint and stressing it suitably.
The shift from a liquid to a solid
film largely completes the adhesion process. This transition can take the form
of a physical change, such as in thermoplastic glue, or a chemical change, such
as in thermosetting adhesive. The physical shift to a solid film in
thermoplastic adhesive occurs when a molten liquid cools on a cool surface or
when the solvent is lost by evaporation and diffusion. Polymerization creates
the solid state in thermosetting glue. When heated to form a strongly connected
structure, risin intermediates in a partially reacted state may react with
other intermediates or complete their reaction.
THE
BONDING PROCESS
The adhesive bonding method is applying the adhesive to the adherend and holding it together (typically under pressure) until the glue has hardened to a given degree of strength. Surface treatment of the adherend may be required as a preliminary step, and heat may be required for hardening. Pure liquid, solution, dispersion (including avulsion), paste, fusible solid (particle, rod, etc.) and fusible film are all examples of adhesives (dropping, or no draping). Spray, brush, roller, knife, curtain coated (called cascade gluing) are all options for applying liquids, depending on the rheology of the liquid, Netonian or thixotropic, for example; the application of solid particles is sometimes affected by gravitational flow on to the adherend moving below. With the adhesive reduse, a unique procedure is used, which in one form needs the application of liquid and solid particles separately; first, a phenolic resin is applied to the adherend, followed by the solid surface. There are four different types of adhesive hardening processes. Although the terms curing, setting, and even drying are all used interchangeably to describe the process of hardening. Curing refers to a chemical process including polymerization and setting that is used to harden emulsion and gelation glues, although drying is more typically utilized with starch adhesives.
The
four bonding processes are:
(1) Evaporation and
absorption are used to dry a solvent or dispersion media (a process that
usually necessitates are or both adherends being porous).
(2) Melting a solid involves
raising its temperature to the point where it becomes liquid and wets the
adherend, then cooling and resolidification.
(3) Increasing the rate at
which a liquid or molten adhesive polymerizes into a solid to build a big
structure, usually with the help of a chemical catalyst and commonly aided by
heat.
(4) Reacting two chemicals
together to create a bigger molecular structure with repeating chemical units.
This entails the addition of a liquid or solid that, while referred to as a
hardener or curing agent, is not principally catalytic in nature. In some
situations, the use of heat is required.
Curing is a gradual process with
various degrees of cure, but the end state of cure is somewhat arbitrary. Bone
and skin glues, starch case in, poty vinyl acetate dispersions, and sodium
silicate are some of the adhesives used in the first curing step. The second method, known as hot melt gluing,
is primarily used in packaging.
A variety of thermoplastic polymers are used in the glue. The third and fourth processes are almost solely used in structural adhesives made of synthetic resins, such as urea, melamine, and phenol formaldehyde, as well as epoxide, polyisocyamate, and polyester. The two polymer adhesive is a type of structural glue that is commonly used in aircraft, hovercraft, and brake and clutch linings. Both of these adhesives are primarily interactive, and process 2 and 3 are regularly used, with process 2 and 4 being used less frequently. Instant stick adhesives, such as pressure sensitive tapes, usually do not require curing and stay tacky liquid. Because a lot of adhesive bonding is used to unite elements of a stress-bearing structure, the most common materials used are wood, metal (especially high alloys), and strong plastics like resin/glass fibre laminate. However, paper is the most commonly glued material, followed by wood, particularly for polywood manufacturing and veneering.
2.3.6 ADVANTAGES
AND LIMITATION OF ADHESIVE BONDING
When
the adherends are relatively thin, it can be joined by adhesive but cannot be
efficiently bolted, riveted, or welded, as opposed to joining by mechanical
methods or welding. The advantages of gluing however becomes less as the
thickness of the metal increases.
The advantages of adhesive bonding can be summarized as follows:-
(1) It is a very sensible method of joining since it does not necessitate the removal of valuable elements from the adherend.
(2) Normally, there isn't much distortion (Distortion is greatest where an adhesive having high shrinkage is needed with thin adherends).
(3) Other methods of connecting, including as riveting, bolting, nailing, and welding, may not be practicable when one or both adherends are thin. Although the specific strength of a glued joint may be lower than that of a mechanical or welded joint when using thick adhesive, adhesive bonding allows for a considerably broader area to be bonded, providing stress continuity, increased stiffness, reduced stress concentration and less risk of fatigue failure.
(4) When attaching dissimilar elements, a properly chosen glue will not cause corrosion and may even remove the risk of galvanic action.
(5) The sealing properties of adhesive may be utilized to provide fluid tightness in fuel tanks.
THE LIMITATION OF ADHESIVE BONDING
(1) The most significant flaw is the comparatively low heat resistance. This is primarily an issue in structural metal applications, such as high-speed aircraft.
(2) In some application the electrical resistance of adhesives, it is a huge disadvantage.
(3) Despite the fact that many synthetic area adhesives have good chemical resistance, some chemicals damage or disintegrate them. However, in many circumstances, there exist substances that are not commonly seen.
(4) Many adhesives have rather low peel and clearage strength.
(5) It is necessary to hold part in position until the adhesive reaches a certain degree of strength, this may necessitates the use of clamps, complicated jigs etc.
(6) Many high-strength adhesives require the use of heat, which, when paired with the necessity for high pressure, may necessitate the use of a heated hydraulic press or autoclave.
(7) It is difficult to access the quality of the bond because in between the joint cannot be seen
2.3.7 USES
OF ADHESIVES
Hot melt adhesives are utilized in corrugated paper production, packaging, book binding, and shoe manufacturing. The most common application of pressure sensitive adhesives is as a tape coating. From electrical tape to surgical tape, these pressure sensitive adhesive pastes offer a wide range of applications. Structural adhesives come in a variety of forms, including liquids, pastes, and 100% sticky films. Epoxy liquids and pastes are widely used adhesive materials, with uses ranging from ordinary industrial to automotive to aerospace and vehicle building. In the construction of aircraft, solid film structural adhesives are commonly employed. Acrylic adhesives are utilized in thread locking procedures as well as minor activities requiring quick cure times, such as electronics manufacturing. The most adhesive is used in the production of plywood and other wood goods. Acrylic adhesives are used in thread locking and other minor tasks that require short cure times, such as electronics fabrication. The majority of glue is utilized in the manufacturing of plywood and other wood products.
CHAPTER THREE
MATERIALS AND METHODS
3.1 MATERIALS
3.1.1 FEEDSTOCK
Cassava starch was used in this work as the raw material.
3.1.2 CHEMICAL AND REAGENTS
The
following chemicals and reagents were used in this work;
i.
Sodium hydroxide pellets
ii.
Borax
iii.
Formaldehyde
iv.
Calcium carbonate
v.
Distilled water
3.1.3 APPARATUSES
The
following laboratory equipments were used in this work:
i.
Hot Water Bath
ii.
Pipette
iii.
Conical Flasks
iv.
Burette
v.
Beakers
vi.
Measuring Cylinder
vii.
Stop Watch
viii.
Laboratory Oven
ix.
Digital Viscometer
x.
Electronic Weighing Balance
3.2
METHODS
3.2.1 PRODUCTION OF THE CASSAVA
STARCH
Cassava tubers were purchased at Eziobodo market in Owerri west local government area of Imo state. The tuber were debarked and cut into small pieces, allowed to dried for a period of three days, the small chops of cassava was taken to market and grinded into powder form. A mixer was used to puree the debarked tubers. This was sieved with water to make a slurry of starch and gluten, which was separated by allowing the starch to settle and decanting the supernatant gluten liquid. The method above was developed by (Bussy, D. 1972) and was owing to the fact that starch granules are tiny in comparison to fibrous materials.
3.2.2 PRODUCTION OF ADHESIVE FROM
CASSAVA STARCH
METHOD
185ml
of distilled water was put in a beaker, 12.5g of starch was dissolved in the
water, 0.65g of CaCo3 was also added. To
achieve a uniform dispersion, the mixture was completely stored. The beaker and
its contents were heated in a bursen flame, and 1.24g of Na0H pellets were
added while heating with constant stirring. After a few minutes of continuous
stirring, a temperature of 700C was reached, and gelatinization, or the
swelling of the starch granules, happened. The temperature was maintained at
the same level for two minutes, after which the tick white solution was
completely mixed.
Further stirring increased the
adhesive's strength and viscosity to their maximum levels. After removing the
beaker from the burner, 0.30g of formaldehyde was added as a preservative.
The proportions of the various
chemicals were changed in consecutive batches to achieve the optimal result. In
order to determine the effect of an addition on the adhesive, an additive was
occasionally left out.
3.2.3 pH DETERMINATION
This test was carried out using a digital pH meter. The pH meter was zeroed when the sample was placed in a beaker. The PH electrode was dipped into the sample and the digital display read the value.
3.2.4 DETERMINATION OF TACK TIME
Tack time refers to how long it takes for an adhesive-bonded
joint to reach full strength. It differs between materials and is affected by
temperature and pressure. This was established by separating a sheet of paper
into 2cm by 2cm units and applying a uniform smear of adhesive to the papers
before placing them on a wood surface. To
promote maximal wetting and penetration of the adhesive into the adherend,
pressure was applied to the surface.
The first paper was readily ripped apart for the first two minutes. This tugging action was carried out until a profound fibre failure was achieved, which corresponded to the adhesive's tack time.
3.2.5 SOLID/MOISTURE
CONTENT DETERMINATION
1
gram of adhesive sample was weighed and placed in the oven. The oven was turned
on and the temperature was set to 1000 degrees Celsius. The sample was placed
in the oven for 45 minutes before being retrieved and weighed again. The
formular was used to calculate the solid content of the sample in percentages.
Weight of sample after drying x 100 =
solid content
Weight of sample before drying 1
The
moisture content of the sample expressed in percentage, was determined by the
expression:
Moisture content = 100 x Weight
of sample before drying - weight of dined sample
Weight of sample before drying
3.2.6 WET
ABILITY DETERMINATION
Weighing 1 gram of glue sample and placing it in the oven The oven was turned on with a temperature of 1000 degrees Celsius. Before being recovered and weighed again, the sample was baked in the oven for 45 minutes. The solid content of the sample was calculated in percentages using the formular.
3.2.7 STORAGE
LIFE DETERMINATION
The adhesive was sealed and stored at room temperature for more than a month and a half
CHAPTER FOUR
RESULTS AND CONCLUSION
4.1 RESULTS
|
MATERIAL |
A |
B |
C |
D |
|
Water Starch Na 0H Ca Co3 Borox Formaldehyde |
185ml 12.5g 1.24g 0.65g 0.5g 0.30g |
185ml 12.66g 1.24g 0.65g 0.6g 0.32g |
183.76mls 12.51g 1.23g 0.64g 0.7g 0.35g |
184.34mls 12.36g 1.25g 0.63g 0.8g 0.32g |
Table 4.1;
sample variations in adhesive production
4.1.1 PH VALUES
The PH
value of adhesives is 7.5
The PH
value of standard is 8 – 12
|
FORMULATION |
PH VALUES |
|
A B C D |
7.8 7.0 6.9 5.6 |
Table 4.2 ; pH value of adhesive
4.1.2 TACK TIME DETERMINATION
|
FORMULATION |
TACK TIME (MINUTES) |
|
A B C D |
14 12 18 10 |
Table 4.3; Tack time determination
4.1.3 SOLD AND MOISTURE CONTENT
|
FORMULATION |
MOISTURE CONTENT |
SOLID CONTENT |
|
A B C D |
79% 82% 88% 83% |
20% 17% 11% 18% |
Table 4.4 ; solid and moisture content of standard adhesive.
4.1.3 WET ABILITY
After drying for 24 hours and then wetting
again, all of the formulations were able to adhere correctly.
4.1.4 STORAGE LIFE
There were no visible alterations after 2 months of storage, and the product is still usable.
4.2
DISCUSSION
The goal of stabilizing adhesive made from starch is to help solve
most of the challenges associated with fastening or holding substances together
through surface attachment. The following methods were used in this study:
literature review of starch, its chemical, physical, and adhesive qualities. Also
classification and application of adhesives as well as its formulations and
analysis were investigated.(Eze TC, 1993) and some standard values form
the Standard Organization of Nigeria (SON).
Starch was the main component of this glue and
functioned as the binder; the additional additives utilized improved the
adhesive's working capabilities. The use of starch as an adhesive stems from
its ability to reach a specific temperature. Because of its abundance, cassava
was chosen as a starch source. Although
starch adhesive has weaker working properties than synthetic competitors, such
as a longer tack time and inadequate bonding strength, it nevertheless has a
large market demand due to its low material and production costs. The
adhesive's viscosity was inversely proportional to the volume of water
utilized; the more water used, the less viscous the adhesives were. The
viscosity problem is solved by adding borax, which raises the viscosity to the
required range.
The amount of sodium hydroxide in the formulation
is responsible for the adhesive's gelatinization. Sodium hydroxide offers the
advantage of lowering the gelatinization temperature, increasing the adhesive's
working life, but lowering the adhesive's setting speed. Other ingredients such
as calcium carbonate and formaldehyde were crucial in their own right,
providing strength to the created glue and a preservative with formaldehyde
solution. The thinner, which is an organic volatile liquid, was employed to
thin the glue while simultaneously adding sticky characteristics.
During manufacture, it was discovered that
formulation D took longer to gelatinize than the others, owing to the absence
of sodium hydroxide, which lowers the adhesive's gelling temperature. The
viscosity of Formulation C, which has the highest Borax content, is high. The
results of the test analysis on the formulated adhesive are provided in the
tables above, and the method used to calculate the parameters is shown in
Appendix B. The adhesive on the market had a low solid percentage. This
suggests that low solid content is a characteristic of the starch – based
adhesive. For the tack time, no standard
value is available.
As a result, the tack time must be moderate for
the adhesive to be useful. A long tack time may make the adhesive unsuitable,
yet a short tack time may indicate that the glue has not penetrated the
adherent properly, resulting in an unsatisfactory bond. Despite its
limitations, the starch-based glue has seen a significant growth in demand due
to its inexpensive cost.
CHAPTER FIVE
CONCLUSION AND RECOMMENDATION
5.1 CONLUSION
The goal of this research project, which was to
create a starch-based glue, was accomplished. The most intriguing aspect of it
all was that the adhesive was made with over 70% local raw resources.
The test results demonstrate that the glue created in this project has functioning properties that are within the standard range and that it compares favorably to those on the market. The shelf life of starch-based adhesives is not as lengthy as that of synthetic adhesives, and starch, as an organic component, is susceptible to microbial attack over time.
5.2 RECOMMENDATION
I recommend that the work be done with other raw materials that have starch as its natural extractive.
5.3 CONTRIBUTION TO KNOWLEDGE
From this research work, it has been proven that starch from cassava is a good adhesive but not to all surfaces like metals and addition of inorganic chemicals can improve the adhesive strength of it.
REFRENCES
Alphonsus V.P. (1987): “Adhesives”.
Encyclopedia of
Science and Technology. V. 16th Edition, McGraw
Hill Company New Yrok, Pp. 122 – 123.
De Bussy J.H (1972): Natural
Organic Materials and
Related Synthesis Products, Materials and
Technology.
Volume V. Longman Group Limited.
London P. 63 – 71.
Bikales M.N (1971): Adhesion
and Bonding John Willey
Co. New York P. 20.
Edward H. (1993): New
Age Encyclopedia. Volume 1,
Lexicon Publication, Inc. Pp. 65 – 66.
Eze T.C (1993): Production
of Gum using Cassava
Tubers as the starting raw material. Chemical
Engineering Department, I.M.T, Enugu. (An
Unpublished Paper
French D. (1950): Inker’s
Chemistry and Industry of
Starch. Academic Press Inc. New York. P. 165.
Kinloch A.J (1987): Adhesion
and Adhesives. Chapman
and Hall Limited, London.
Lees W.A (1989): Adhesive
and the Engineer:
Mechanical Engineering Publication Limited,
London Pp. 1, 23 – 25.
Radley, J.A (1968): Starch
and its Derivatives.
Chapman and Hall Limited, London. Pp. 168 – 190
Shelds J. (1974): Adhesive
Bonding Oxford
University Press, London Pp. 3 – 5.
White, T.A (1987): “Starch”.
Encyclopedia of Science
and Technology. Volume 17, 6th Edition. McGraw Hill Company New York pp. 326 – 328
APPENDIX
B
SOLID AND MOISTURE CONTENTDETERMINATION
FORMULATION A
Weight of dish = 33.74g
Weight of sample = 1.00g
Weight of sample + dish = 34.73g
Weight of sample + dish after drying = 33.92g
Weight of sample after drying
33.92 – 33.74 = 0.21g
\ Solid
content = 0.21g
\ Moisture
content = 1 – 0.21g = 0.79g
\ %
Moisture content = 0.79 x 100
1 1
= 19%
APPENDIX C
STANDARD GLUE SAMPLES AND THEIR CHARACTERISTICS
A = PGN Glue
B = Stephen Glue
C = Polar Glue
TYPES OF GLUE
|
CHARACTERISTICS |
A |
B |
C |
|
Moisture Content Solid Content PH Value Tack Time |
55% 15% 15% |
85% 15% 10% |
60% 40% 11% |
The above date was
obtained from laboratory analysis by (Eze T.C, 1993).
Some of the
standard values available are:
a. Solid content 15 -
30
b. PH value 8 - 12
c. Moisture content 65
– 85%
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