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Assistant Professor, Dept. of Textile Technology, Ahsanullah University of Science and Technology Assistant Professor, Dept. of Textile Technology, Ahsanullah University of Science and Technology
Abstract: The textile is a growing sector which traditionally requires huge amounts of water, energy, harsh chemicals, starting from pesticides for growing cotton to a variety of finishing chemicals, which results in high amounts of wash water in waste streams causing environmental burdens. Thus the desired textile processing procedures are those environmental friendly and economic ones that can save water, time and chemicals, yet preserve product qualities. Enzymes are known for their specificity, high efficiency and ability to work under milder conditions and thus inexorably provide a promising solution to those problems. This research paper focuses on a comparative analysis between the conventional pre-treatment processes with bio-preparations using enzymes. Since use of the gentle enzyme process replaces the need for harsh processing with sodium hydroxide and other harmful chemicals, there is less contribution to the textile effluent and gives a softer textile product.
that the new technology becomes an economically viable alternative. Instead of using hot sodium hydroxide to remove the impurities and damaging parts of the fibre enzymes do the same job leaving the cotton fibre intact. It is believed that the replacement of caustic scouring of cotton substrates by bio-preparation with selected enzymes will result in the following quantifiable improvements: lower BOD, COD, TDS and alkalinity, process time, cotton weight loss and harshness to handle.
2. GENERAL INFORMATION
Composition of cotton: Cotton fibre is a single biological cell. It is built up of four parts lumen, secondary wall, primary wall and cuticle. Lumen is the nutrient transportation tube for the cell containing small amounts of bio-organic materials, which add a yellowish shade to the fibre. The secondary wall is built up of cellulose layers which contribute about 91.5% of fibre and a crystallinity index of 70%. The primary cell wall, which mainly consists of protein, pectic substances and glucans, is about 2.5% of fibre weight. It has a crystallinity index of about 30%. The protective cuticle is made of wax, mineral matters, pectins, fatty acids, high molecular weight alcohols and their esters. Viscose Rayon: The regenerated cellulose fibres are simply regenerated from wood pulp or cotton linters, which are sources of pure natural cellulose, without any change in chemical constitution in polymer. But there is only a certain variation in degree of polymerization and as well as modified physical properties. Since viscose is a regenerated fibre the raw material undergoes purification before it is spun into yarns and thus contains very little (acquired during spinning like spin finish etc.) or no impurities.
1. INTRODUCTION
For perfect coloration of a substrate, it is necessary that all the impurities, either natural or acquired, be removed so that the colorants can perfectly sit on the surface or penetrate inside the substrate as required by the particular system. The colorant should also be clearly visible without interference by the color of impurities. Before cotton fabric or yarn can be dyed, it goes through a number of preparatory processes. One of the most negative environmental impacts from textile production is the traditional processes used to prepare cotton fibre, yarn or fabric. The conventional highly alkaline preparation of cotton can be an example. About 75% of the organic pollutants arising from textile finishing are derived from preparation of cotton goods. In the conventional preparatory process concentrated sodium hydroxide solution and hydrogen peroxide or sodium hypochlorite solutions are applied for removing the impurities from raw cotton. By doing so the preparatory processes yields an adequately absorbent and appropriately white material with cellulose content of 99%, but the processes generates huge amounts of effluent. On the fibre level oxidative damage may occur and be reflected in a lower degree of polymerization and decreased tensile strength. Bio-preparation may be a valuable and environmentally friendly alternative to harsh alkaline chemicals for preparing cotton. Enzymes can be used to prepare cotton under very mild conditions. The environmental impact is reduced since there is less chemicals in the waste and a lower volume of water. The bio-preparation process decreases both effluent load and water usage to the extent
2.1 Pretreatment:
Textile materials possess a variety of impurities. Some are natural or inheriting, or may be added purposely for better spinnability or weavability. Materials are also occasionally contaminated by accidental impurities acquired while handling of materials. All such impurities are to be removed before actual dyeing or printing. Such processes which are used for the removal of these impurities are called preparatory processes and may be broadly classified into two categories: 1. Cleaning processes, where bulk of the foreign matters or impurities are removed by physical or chemical means.
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International Journal of Engineering & Technology IJET-IJENS Vol: 11 No: 03 2. Whitening processes, in which trace coloring matters are destroyed chemically or the whiteness of the material is improved optically.
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for pretreatment processes of textile materials. Such processes include scouring and bleaching of cellulosic materials, degumming of silk, carbonizing, bleaching and shrink-resisting treatments of wool. In stone washing of denim fabrics, the color of indigo or sulphur dyed materials is faded at certain places with oxidizing agents. Enzymes are nowadays used for such coloration. Biostoning has achieved considerable importance for treating casual-wear garments to give them a washed-down or worn appearance. This is more environmentally acceptable and it replaces or decreases the amount of pumice stones that may damage machinery and causes harshness of the fabric. Because bioprocesses use living material, they offer several advantages over conventional chemical methods of production: they usually require lower temperature, pressure, and pH (the measure of acidity); they can use renewable resources as raw materials; and greater quantities can be produced with less energy consumption.
2.4 Enzymes:
Enzymes are proteins that catalyze (i.e., increase the rates of) chemical reactions. In enzymatic reactions, the molecules at the beginning of the process are called substrates, and the enzyme converts them into different molecules, called the products. Almost all processes in a biological cell need enzymes to occur at significant rates. Since enzymes are selective for their substrates and speed up only a few reactions from among many possibilities, the set of enzymes made in a cell determines which metabolic pathways occur in that cell. Like all catalysts, enzymes work by lowering the activation energy (Ea) for a reaction, thus dramatically increasing the rate of the reaction. Most enzyme reaction rates are millions of times faster than those of comparable un-catalyzed reactions. As with all catalysts, enzymes are not consumed by the reactions they catalyze, nor do they alter the equilibrium of these reactions. However, enzymes do differ from most other catalysts by being much more specific. Enzymes are known to catalyze about 4,000 biochemical reactions. Synthetic molecules called artificial enzymes also display enzyme-like catalysis.
2.5 Structure:
Enzymes are proteins, i.e. sequences of amino acids linked by peptide bonds. The sequence of amino acids within the polypeptide chain is characteristic of each enzyme. This leads to a specific three-dimensional conformation for each enzyme in which the molecular chains are folded in such a way that certain key amino acids are situated in specific strategic locations. This folded arrangement, together with the positioning of key amino acids, gives rise to the remarkable catalytic activity associated with enzymes. Enzymes are usually very specific as to which reactions they catalyze and the substrates that are involved in these reactions. Complementary shape, charge and hydrophilic/hydrophobic characteristics of enzymes and substrates are responsible for this specificity.
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F Figure 1: Diag grams to show the induced fit t hypothesis of f e action enzyme In I 1958, Dani iel Koshland suggested s a modification m to o th he lock and ke ey model: since e enzymes are rather flexible e structures, s the active site is i continually reshaped by y in nteractions wi ith the substra ate as the subs strate interacts s with w the enzym me. As a res sult, the subst trate does not t simply s bind to o a rigid activ ve site; the am mino acid side e chains c which make m up the ac ctive site are molded m into the e precise p position ns that enable e the enzyme to perform its s catalytic c functi ion. In some cases, c such as s glycosidases, , th he substrate molecule m also changes shape e slightly as it t enters e the activ ve site. The act tive site contin nues to change e until u the substra ate is complete ely bound, at which w point the e final f shape and d charge is dete ermined.
Reducing the e reaction entropy e chang ge by bringing sub bstrates togeth her in the c correct orientation to o react. Cons sidering H alone overlooks this s effect. Increases in temperatures speed up rea actions. rature increase e help the enzyme Thus, temper function and develop the end product t even ever, if heate ed too much h, the faster. Howe enzymes shap pe deteriorates s and only wh hen the temperature c comes back to t normal does the enzyme regai in its shape. Some enzyme es like thermo labile e enzymes work w best at a low temperatures. Based on n the medium m of their prep paration enzym mes are classified d as bacterial, pancreatic (bl lood, lever etc c) malt (germina ated barely) etc. Accordin ng to their major functions s enzymes ar re grouped under u the foll lowing groups Oxidored ductases: Cata alyze oxidation n reduction reac ctions. Such as dehydrogenase d es, reductases Transfer rases: Catalyze e functional gro oup transfer. Such as kinases, aminotransfera ases, thiolases. Hydrolas ses: Catalyze hydrolysis h reac ctions. Such as peptidase es, glycosidase es, lipases, pho osphatases Lyases: Catalyze C elimin nation/addition n of groups to form/bre eak double bonds. Suchassy ynthases, decarbox xylases, dehydr ratases. Isomeras ses: Catalyze reactions r that alter a structure, not n composit tion (optical, geometric, g or st tructural isome ers). Suchasisomerases, mu utases Ligases: Catalyze coup pling of two co ompounds along with sis of a phospho oanhydride bon nd. Suchas hydrolys synthetas ses, carboxylas ses, polymerases HYDRO OLASES type of enzyme is mostly us sed in textileprocessing. p TYPE Amy ylase Cata alase Protease e, lipase and pec ctinase Lacc case Cellu ulase AC CTION To decompose sta arches applied in sizi ing ecompose it in nto Act on H2O2 to de ater & oxygen wa Wh hen combined, act on proteins, pec ctins and natural waxes to eff fect sco ouring igo molecules for f Decomposes indi wa ash-down effect t on denim Bre eak down cellu ulosic chains to o rem move protrudin ng fibres by deg grading & crea ate wash-down effect by surface etching g on denims et tc. atural triglyceri ides Elimination of na p in desiz zing (in scouring) or present llow compound ds) (tal Bre eaks down pectins in scouring g
Enzymes E can ac ct in several ways, w all of which lower G: Lower ring the activa ation energy by b creating an n enviro onment in wh hich the trans sition state is s stabilized (e.g. st training the shape of a substra ateby binding the transition-state t e confor rmation of the substrate/prod duct molecules, , the en nzyme distorts the bound su ubstrate(s) into o their transition t state e form, thereby y reducing the e amoun nt of energy required to complete the e transit tion). Lower ring the energy y of the transi ition state, but t withou ut distorting th he substrate, by b creating an n enviro onment with h the oppo osite charge e distrib bution to that of the transition n state. Provid ding an alterna ative pathway. For example, , tempo orarily reacting g with the sub bstrate to form m an int termediate ES complex wh hich would be e impossible in the abs sence of the en nzyme.
Lipase
Pecti inase
ymatic scourin ng and bleachi ing: 2.7 Enzy Compare ed to conven ntional alkalin ne boiling of ff, the advantag ges of bioscou uring are obvio ous that it can n save water an nd time by r reducing one rinsing cycle: save
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International Journal of Engineering & Technology IJET-IJENS Vol: 11 No: 03 energy by lowering the treatment temperature from boiling to around 50-600C; and permit less fibre weight loss and less COD and BOD in the effluent. In addition the super soft handle, probably due to the retention of the beneficial wax, is unattainable by alkaline pre-treatment. Major companies involved in the preparation and marketing of enzymes useful for textile industries are Dystar, Clariant, Genencor and Novoenzymes (formerly Novo Nordisk), etc. In our research we worked with the Gentle Power BleachTM, a joint-venture product from Huntsman and Genencor. The novel enzyme allows for the system to perform at much lower temperatures for bleaching and at neutral pH levels. Historically, the textile bleaching process requires temperatures of 95C. Genencors unique enzyme allows this to be lowered to 65C. By lowering the treatment and rinsing temperature considerably, savings in water and energy consumption of up to 40% are possible.
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Product Overview: Invatex LTA: Agent to assist and boost the peroxide reaction in the Gentle Power Bleach. Invazyme LTE: Enzyme for the Gentle Power Bleach to catalyze the peroxide bleach in combination with Invatex LTA.
3. CHEMICAL BACKGROUND
Mechanism of hydrogen peroxide bleaching: Hydrogen peroxide is a very weak acid. It could be ionized to form perhydroxyl ions(HOO-) H2O2 HOO- + H+
4. TECHNICAL PART
Materials used: Grey woven fabric cotton (plain weave) and grey knit fabric viscose. The different pretreatment chemicals and desizing enzyme was collected from BASF while the gentle power bleach was taken from Huntsman. At first the woven grey cotton fabric was desized using amylase enzymes at 700C for 20 minutes in an automatic laboratory dyeing m/c. Then this fabric along with the viscose was subjected to single bath scouring-bleaching processes using, strong alkali and H2O2 at boiling temperature as in conventional method, and gentle power bleach in a neutral pH and at a temperature of 650C as in the Bio-process. The amount of H2O2 used in both cases was 6g/l and 9g/l. To assess the amount of dye absorbed by the fabrics processed by conventional and bio-process, they were dyed at depths of 0.5%, 2.5% and 6% shade with Drimarine Dark Red HF-CD, reactive dye from Clariant. Dyeing was also performed in the automatic laboratory dyeing m/c according to the manufacturers recommended process.
The formation of the active perhydroxyl ions is favoured by alkaline conditions and these anions are the source of the active oxygen that has the bleaching effect. H2O2 + OHHOOH2O + HOOOH- + [O]
The mechanism of bleaching is very complicated and not completely understood. One opinion is that the color producing agents in natural fibers are often organic compounds containing conjugated double bonds. It is known in dye chemistry that conjugation is necessary for an organic molecule to perform as a dyestuff. Discoloration can occur by breaking up the chromophore, most likely destroying one or more of the double bonds within the conjugated system. Oxidative bleaches oxidize color bodies into colorless compounds. For example, double bonds are known to be oxidizing into epoxides which easily hydrolyze into diols. -C=C-C=C-C=C- + [O] OH -C=C-C-C-C=COH In enzymatic bleaching the following reactions takes place: -C=C-C - C-C=C-
2.
3.
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Internat tional Journal of o Engineering g & Technology y IJET-IJENS Vol: 11 No: 03 3 4. 5. White eness index it was evalu uated using a Dual-b beam spectroph hotometer from m Data color. Assess sment of the amount of dy ye absorbed Color was evaluated d in terms of k/s k values, E C Lab coord dinates (Illumi inant D65/100 and CIE observ ver) with a Data color 650 0 spectro ophotometer. Table 3: Result R for streng gth loss
Proces s Strength before e bleaching Cotto Viscos s n (N) e (KPa) 388 3.84 388 388 388 3.84 3.84 3.84 Strength afte er bleaching Cotton Vis scos e (N) (KPa) 373.1 3.6 667 386.2 360.1 384.8 3.7 73 3.5 51 3.5 567 Strength loss % CotViston cose 3.84 0.46 7.19 0.82 4.50 2.86 8.70 7.10
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10 0
Strengthloss%
Process
Dye upta ake %: It was s found that co otton treated by b bioprocess absorbed m more dyes than t those treated t conventionally, irrespe ective of the shade s %. In case c of viscose the reversed occurred, tha at is conventi ionally treated fa abric absorbed more dyes. A probable answ wer can be while e treating cott ton enzymes might m have re educed crystallin nity and incre eased the amo orphous region n; as a result the e fabric absorb bed more dyes. . But the struct ture of viscose is i already mor re amorphous than t cotton an nd thus the enzym mes had no eff fect in changing the structure. Graphica al representatio on of dye uptak ke: 50 5
k/svalues
Weightloss%
3 2 1 0 Cotton
40 4 30 3 20 2 10 1 0
Con 9 Bio 9 Con 6 Bi 6 Bio Con 9 Bio 9 Con 6 Bio 6
Strength S loss: Compared C to th he conventiona al process, loss of strength h in both the fib bres is found to o be very low in n the respectiv ve bio-processe es. This means that very little damage d occurs when the fibre e are treated wi ith bioprocess. p
Cotton
Viscose
ss index: It ca an be seen fro om the graph that, t in Whitenes case of cotton, the w whiteness index x is highest for f the fabric pr rocessed with 9 9g/l H2O2 in th he conventiona al way
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Internat tional Journal of o Engineering g & Technology y IJET-IJENS Vol: 11 No: 03 3 and a the others are almost sa ame. While fo or viscose, the e whiteness w achi ieved with all the processe es are almost t same. s So we can conclude e that bio-proc cess can give e excellent e white eness to regener rated fibers. Table e 4: Result for whiteness w inde ex Process Conventional 9 Bio 9 Conventional 6 Bio 6 Conventional 9 Bio 9 Conventional 6 Bio 6 Subst trate Cot tton Cot tton Cot tton Cot tton Visc cose Visc cose Visc cose Visc cose Wh hiteness index 66.00 49.68 48.07 49.05 67.33 66.70 67.24 66.38
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enzymati ic solutions to o pretreatment t has never be een as overwhelming as it is today. The ele evated price of f crude kes petrochem mical based textile auxi iliaries oil mak expensiv ve and once again remin nds people of o the importan nce of sustaina able developm ment. The elec ctricity shortage, , in our coun ntry drove pe eople to use energy e saving technology t and d the water pollution p caus sed by leaves textile ef ffluents, partic cularly from pretreatment, p dye houses no alt ter native but b to choos se an mentally friend dly process. It I is not clea ar why environm bioproce ess has not yet been widely w accepte ed by industrie es. But we can say that, it is only o a matter of o time that the drawbacks will be conquere ed and it will be the f textile processing. It remai ins to be seen n when future of and how this technolog gy becomes a re eality.
ERENCES 8. REFE
1.
Whitenessindex
6. 6 LIMITATI IONS
Scouring S is a process tha at specifically targets noncellulosic c impu urities with pec ctinases. Techn nical feasibility y of o bio-scouring g has been rec cognized. Yet it is not clear r why w bio-scouri ing has not ye et been widely y accepted by y dye d houses. So ome probable limitations ar re discussed Undoubtedly, U t primary li the imitation is th hat bio-process s has h little effec ct on mote rem moval. Althou ugh bioprocess s positions p itself as a pretreatm ment only for th he dark shades, , it t sometimes cannot c preven nt the appeara ance of motes s even e in the dar rk shaded fabr rics. Another factor f limiting g th he wide use of o bio-scouring g is its inabilit ty to give any y whiteness w impr rovement to treated t fabrics. The process s th hus cannot be e used to pre e-treat full wh hite, pale and d medium m shade fabrics. Final lly, inability to o remove wax x im mpurity has greatly g restricted bio-scourin ng from being g accepted. a
7. 7 CONCLUS SION
Enzymatic E proc cess is definitely a break-th hrough and the e path p for a gre eener technolo ogy. Such pret treatment will l sooner s or later r prevail, but in i order for th his to happen, , more m research needs n to be do one to resolve those t technical l problems. p The necessity for the dev velopment of f
Aravin Prince e .P. Bio Proces ssing in Textile es. Available: http://www.fib bre2fashion.com m/industryarticle/textile-industry-articl les/bio-process singin-textiles/bio-processing-in-textiles1.asp 2. Documentary reports of Gen ntle Bleaching, Huntsman. Av vailable: http://www.tex xtileworld.com m/Articles/2009/ 9/Marc h/DPF/Gentle e_Bleaching.htm ml nclature. Avail lable: 3. Enzyme nomen http://www.ch hem.qmul.ac.uk k/iubmb/enzyme s into cotton en nzymatic pre4. H. Lu, Insights treatment, Int. Dyer 2005 vailable: 5. Wikipedia. Av http://en.wikip pedia.org/wiki/ /Enzyme o textilefibres. . 6 J.GordonCook,Handbookof Dyeingandche emicaltechnol logyof 7 ERTrotman,D textilefibre F Scienceand a Technology y 8 HandbookofFibre VolumeI ,Technologyof fBleachingand 9 DrVAShenai, Mercerizing. n(Xi'anInstituteofEngineeri ing 10 ZHAOJiuquan &Technology,Xi'an710048China),Analysisof retreatmentof fCottonFabric c. BioEnzymePr Available: i.com.cn/Article_en/CJFDTOT TAL http://en.cnki GONG200603007.htm DierkKnittel,Eckhard E Schollm meyer, 11. KlausOpwis,D UseofEnzyme esinthePreTr reatmentofCo otton
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