Washing
May 25, 2020
How to Pigment wash ll Textile Farm
Pigment wash:
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| How to Pigment wash |
Pigment is usually done in pigment dyeing scales of garments
or pigments in garment scales. This is due to the antique look of fabric.
Garment stiff after pigment dyeing is done to remove it altogether.
First Stage:
1. Batch Weight Holds 80 Kg Twill / Canvas Pants
2. Water ratio or Liquor line is L: R - 1: 8, then according
to the water requirement (80 x 8) = 640 liter
3. When the water is given, the machine wash be run.
4. Camel Docking:Kosic soda 512 grams at 0.8 gplSoda AS is 960 g at 1.50 gplDitergent is 512 grams at 0.8 gpl
5. Temperatures should be run at 50 ° C - 60 ° C degree
temperature
6. Run-time is not specific or it wash depend on our Sed
Achievement. The fabric wash be run on the machine as long as it does not come.
7. After that the sedance wash then drain the bath.
8. 5 minutes of hot air in 50 degree temperature
9. Drain the bath and take 5 minutes of hot water in cold
water.
10. After that you have to give a cold breath
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| How to Pigment wash |
Second Stage:
1. Water Liquor Ratios L: R - 480 Liters at 6: 6
2. Machine running
3. Camel Docking:Flex sifenera 0.6 gm / liter - 252 gmAcetic Acid 0.5 Gram / Liter - 210gm (pH 4.5-5.5)Silicone 0.4 gram / liter for slip hand Fill - 192 gramsRuntime wash be given 15-225 minutes by docking the camera
4. After 15 to 25 minutes the bath wash be drained.
5. After that, the garments wash be taken by the cold winds.
6. Unload and take the trolley.
3rd stepHydroxactor wash have to remove the access water within the
fabric, 2-4 minutes extracting time.
4th StepDrying can be done using a steam dryer / gas dryer and here
are two dryer drying procedures.
Steam dryerLoads of steam drawers - 50kgTemperatures 60-70 DegreeTime 40-50 minutesTime 10-15 minutes cold dry
Gas dryerLoad gas dirair - 50 kgTemperatures 70-85 DegreeTime 30-35 minutesTime 10-15 minutes cold dry

How to Pigment wash
5th Stage
When unloading from the machine, multiply the body by
squeezing it out and check it out in 100% hot water. Deep shed machine wash be
lifted again and again.
Some samples of pigment was found










![Textile processing with enzymes Textile processing with enzymes:- Examples of enzyme cofactors and their roles Cofactor Role Nicotinamide adenine dinucleotide Oxidation/reduction (NAD+, NADP+). reactions [those involving transfer of H- (hydride) ion] Flavin adenine dinucleotide (FAD) . Oxidation/reduction reactions. Flavin mononucleotides (FMN). Oxidation/reduction reactions . Biotin Carboxyl group transfer. Cobalamin Methyl group transfer. Coenzyme A (CoA) Transfer of groups, e.g. acetyl. Thiamine pyrophosphate (TPP) Acetaldehyde transfer. Tetrahydrofolate (THF) One-carbon transfer reactions. Pyridoxal phosphate Transamination and decarboxylation reactions. Textile processing with enzymes Metal ions: Fe, Cu, Mo Oxidation/reduction reactions. Zn Helps bind NAD+ Co Part of cobalamin coenzyme. Mn Aids in catalysis by electron withdrawal. relationship between the primary amino acid sequence and its higher structural conformation can be obtained. Site-directed mutagenesis is also a valuable tool for studying structural and functional relationships of enzymes and for enhancing the attributes for commercially important enzymes.The catalytic capabilities of several enzymes have been improved by changes to the amino acids forming the active sites. Other studies have shown that it is possible to improve temperature and pH stability of enzymes. For example, introduction of cysteine residues into the polypeptide chain tends to enhance protein stability through disulfide bond formation. Replacement of lysine with arginine in a polypeptide chain also tends to enhance enzyme stability through increase in the extent of overall hydrogen bonding. Ultimately, continuing advances in this field could facilitate routine de-novo design of enzymes to suite particular applications; the ‘Holy Grail’ of applied enzymology! The advances made in molecular biology and the associated research equipment have accelerated DNA sequence determination and large portions of the genome of several species have been sequenced. This genomic information will increasingly drive future trends in enzymology – within the emerging fields of proteomics and bioinformatics – leading to greatly improved understanding of structure, function and expression of newly discovered proteins.](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhML10cFUyzOaqBpg2vbcI4l92k3heBwtuqK9puLS-IzDhKbhA4BYPQorMCMyciktYOtagG06b_GCa1MNOAlWJRDOFpJbOQBa4N3eVmrg3X22fo7aYKeYGP8dOTHmGSjXdmjMitEZaCjjBO/s320/solutions-banner.jpg)
![Textile processing with enzymes Textile processing with enzymes:- Examples of enzyme cofactors and their roles Cofactor Role Nicotinamide adenine dinucleotide Oxidation/reduction (NAD+, NADP+). reactions [those involving transfer of H- (hydride) ion] Flavin adenine dinucleotide (FAD) . Oxidation/reduction reactions. Flavin mononucleotides (FMN). Oxidation/reduction reactions . Biotin Carboxyl group transfer. Cobalamin Methyl group transfer. Coenzyme A (CoA) Transfer of groups, e.g. acetyl. Thiamine pyrophosphate (TPP) Acetaldehyde transfer. Tetrahydrofolate (THF) One-carbon transfer reactions. Pyridoxal phosphate Transamination and decarboxylation reactions. Textile processing with enzymes:- Examples of enzyme cofactors and their roles Cofactor Role Nicotinamide adenine dinucleotide Oxidation/reduction (NAD+, NADP+). reactions [those involving transfer of H- (hydride) ion] Flavin adenine dinucleotide (FAD) . Oxidation/reduction reactions. Flavin mononucleotides (FMN). Oxidation/reduction reactions . Biotin Carboxyl group transfer. Cobalamin Methyl group transfer. Coenzyme A (CoA) Transfer of groups, e.g. acetyl. Thiamine pyrophosphate (TPP) Acetaldehyde transfer. Tetrahydrofolate (THF) One-carbon transfer reactions. Pyridoxal phosphate Transamination and decarboxylation reactions. Textile processing with enzymes Metal ions: Fe, Cu, Mo Oxidation/reduction reactions. Zn Helps bind NAD+ Co Part of cobalamin coenzyme. Mn Aids in catalysis by electron withdrawal. relationship between the primary amino acid sequence and its higher structural conformation can be obtained. Site-directed mutagenesis is also a valuable tool for studying structural and functional relationships of enzymes and for enhancing the attributes for commercially important enzymes.The catalytic capabilities of several enzymes have been improved by changes to the amino acids forming the active sites. Other studies have shown that it is possible to improve temperature and pH stability of enzymes. For example, introduction of cysteine residues into the polypeptide chain tends to enhance protein stability through disulfide bond formation. Replacement of lysine with arginine in a polypeptide chain also tends to enhance enzyme stability through increase in the extent of overall hydrogen bonding. Ultimately, continuing advances in this field could facilitate routine de-novo design of enzymes to suite particular applications; the ‘Holy Grail’ of applied enzymology! The advances made in molecular biology and the associated research equipment have accelerated DNA sequence determination and large portions of the genome of several species have been sequenced. This genomic information will increasingly drive future trends in enzymology – within the emerging fields of proteomics and bioinformatics – leading to greatly improved understanding of structure, function and expression of newly discovered proteins. Textile processing with enzymes Metal ions: Fe, Cu, Mo Oxidation/reduction reactions. Zn Helps bind NAD+ Co Part of cobalamin coenzyme. Mn Aids in catalysis by electron withdrawal. Textile processing with enzymes relationship between the primary amino acid sequence and its higher structural conformation can be obtained. Site-directed mutagenesis is also a valuable tool for studying structural and functional relationships of enzymes and for enhancing the attributes for commercially important enzymes.The catalytic capabilities of several enzymes have been improved by changes to the amino acids forming the active sites. Other studies have shown that it is possible to improve temperature and pH stability of enzymes. For example, introduction of cysteine residues into the polypeptide chain tends to enhance protein stability through disulfide bond formation. Replacement of lysine with arginine in a polypeptide chain also tends to enhance enzyme stability through increase in the extent of overall hydrogen bonding. Ultimately, continuing advances in this field could facilitate routine de-novo design of enzymes to suite particular applications; the ‘Holy Grail’ of applied enzymology! The advances made in molecular biology and the associated research equipment have accelerated DNA sequence determination and large portions of the genome of several species have been sequenced. This genomic information will increasingly drive future trends in enzymology – within the emerging fields of proteomics and bioinformatics – leading to greatly improved understanding of structure, function and expression of newly discovered proteins.](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEgmwliL-yds_JqUk64efFIqTS8jGfBhBnnES6ObaE5u26eVICu6IZcvCDlf0BeX7qN1dwUeubbhZgajUB00ffEpw4CnIfE2PTtyi-nOQ07pAhEBLlxlm_GkfUPyHP3Cp1og8j1IeVKmKM1w/s400/applications-of-enzymes-in-textile-wet-processing.jpg)
![Textile processing with enzymes Textile processing with enzymes:- Examples of enzyme cofactors and their roles Cofactor Role Nicotinamide adenine dinucleotide Oxidation/reduction (NAD+, NADP+). reactions [those involving transfer of H- (hydride) ion] Flavin adenine dinucleotide (FAD) . Oxidation/reduction reactions. Flavin mononucleotides (FMN). Oxidation/reduction reactions . Biotin Carboxyl group transfer. Cobalamin Methyl group transfer. Coenzyme A (CoA) Transfer of groups, e.g. acetyl. Thiamine pyrophosphate (TPP) Acetaldehyde transfer. Tetrahydrofolate (THF) One-carbon transfer reactions. Pyridoxal phosphate Transamination and decarboxylation reactions. Textile processing with enzymes:- Examples of enzyme cofactors and their roles Cofactor Role Nicotinamide adenine dinucleotide Oxidation/reduction (NAD+, NADP+). reactions [those involving transfer of H- (hydride) ion] Flavin adenine dinucleotide (FAD) . Oxidation/reduction reactions. Flavin mononucleotides (FMN). Oxidation/reduction reactions . Biotin Carboxyl group transfer. Cobalamin Methyl group transfer. Coenzyme A (CoA) Transfer of groups, e.g. acetyl. Thiamine pyrophosphate (TPP) Acetaldehyde transfer. Tetrahydrofolate (THF) One-carbon transfer reactions. Pyridoxal phosphate Transamination and decarboxylation reactions. Textile processing with enzymes Metal ions: Fe, Cu, Mo Oxidation/reduction reactions. Zn Helps bind NAD+ Co Part of cobalamin coenzyme. Mn Aids in catalysis by electron withdrawal. relationship between the primary amino acid sequence and its higher structural conformation can be obtained. Site-directed mutagenesis is also a valuable tool for studying structural and functional relationships of enzymes and for enhancing the attributes for commercially important enzymes.The catalytic capabilities of several enzymes have been improved by changes to the amino acids forming the active sites. Other studies have shown that it is possible to improve temperature and pH stability of enzymes. For example, introduction of cysteine residues into the polypeptide chain tends to enhance protein stability through disulfide bond formation. Replacement of lysine with arginine in a polypeptide chain also tends to enhance enzyme stability through increase in the extent of overall hydrogen bonding. Ultimately, continuing advances in this field could facilitate routine de-novo design of enzymes to suite particular applications; the ‘Holy Grail’ of applied enzymology! The advances made in molecular biology and the associated research equipment have accelerated DNA sequence determination and large portions of the genome of several species have been sequenced. This genomic information will increasingly drive future trends in enzymology – within the emerging fields of proteomics and bioinformatics – leading to greatly improved understanding of structure, function and expression of newly discovered proteins. Textile processing with enzymes Metal ions: Fe, Cu, Mo Oxidation/reduction reactions. Zn Helps bind NAD+ Co Part of cobalamin coenzyme. Mn Aids in catalysis by electron withdrawal. Textile processing with enzymes:- Examples of enzyme cofactors and their roles Cofactor Role Nicotinamide adenine dinucleotide Oxidation/reduction (NAD+, NADP+). reactions [those involving transfer of H- (hydride) ion] Flavin adenine dinucleotide (FAD) . Oxidation/reduction reactions. Flavin mononucleotides (FMN). Oxidation/reduction reactions . Biotin Carboxyl group transfer. Cobalamin Methyl group transfer. Coenzyme A (CoA) Transfer of groups, e.g. acetyl. Thiamine pyrophosphate (TPP) Acetaldehyde transfer. Tetrahydrofolate (THF) One-carbon transfer reactions. Pyridoxal phosphate Transamination and decarboxylation reactions. Textile processing with enzymes:- Examples of enzyme cofactors and their roles Cofactor Role Nicotinamide adenine dinucleotide Oxidation/reduction (NAD+, NADP+). reactions [those involving transfer of H- (hydride) ion] Flavin adenine dinucleotide (FAD) . Oxidation/reduction reactions. Flavin mononucleotides (FMN). Oxidation/reduction reactions . Biotin Carboxyl group transfer. Cobalamin Methyl group transfer. Coenzyme A (CoA) Transfer of groups, e.g. acetyl. Thiamine pyrophosphate (TPP) Acetaldehyde transfer. Tetrahydrofolate (THF) One-carbon transfer reactions. Pyridoxal phosphate Transamination and decarboxylation reactions. Textile processing with enzymes Metal ions: Fe, Cu, Mo Oxidation/reduction reactions. Zn Helps bind NAD+ Co Part of cobalamin coenzyme. Mn Aids in catalysis by electron withdrawal. relationship between the primary amino acid sequence and its higher structural conformation can be obtained. Site-directed mutagenesis is also a valuable tool for studying structural and functional relationships of enzymes and for enhancing the attributes for commercially important enzymes.The catalytic capabilities of several enzymes have been improved by changes to the amino acids forming the active sites. Other studies have shown that it is possible to improve temperature and pH stability of enzymes. For example, introduction of cysteine residues into the polypeptide chain tends to enhance protein stability through disulfide bond formation. Replacement of lysine with arginine in a polypeptide chain also tends to enhance enzyme stability through increase in the extent of overall hydrogen bonding. Ultimately, continuing advances in this field could facilitate routine de-novo design of enzymes to suite particular applications; the ‘Holy Grail’ of applied enzymology! The advances made in molecular biology and the associated research equipment have accelerated DNA sequence determination and large portions of the genome of several species have been sequenced. This genomic information will increasingly drive future trends in enzymology – within the emerging fields of proteomics and bioinformatics – leading to greatly improved understanding of structure, function and expression of newly discovered proteins. Textile processing with enzymes Metal ions: Fe, Cu, Mo Oxidation/reduction reactions. Zn Helps bind NAD+ Co Part of cobalamin coenzyme. Mn Aids in catalysis by electron withdrawal. Textile processing with enzymes relationship between the primary amino acid sequence and its higher structural conformation can be obtained. Site-directed mutagenesis is also a valuable tool for studying structural and functional relationships of enzymes and for enhancing the attributes for commercially important enzymes.The catalytic capabilities of several enzymes have been improved by changes to the amino acids forming the active sites. Other studies have shown that it is possible to improve temperature and pH stability of enzymes. For example, introduction of cysteine residues into the polypeptide chain tends to enhance protein stability through disulfide bond formation. Replacement of lysine with arginine in a polypeptide chain also tends to enhance enzyme stability through increase in the extent of overall hydrogen bonding. Ultimately, continuing advances in this field could facilitate routine de-novo design of enzymes to suite particular applications; the ‘Holy Grail’ of applied enzymology! The advances made in molecular biology and the associated research equipment have accelerated DNA sequence determination and large portions of the genome of several species have been sequenced. This genomic information will increasingly drive future trends in enzymology – within the emerging fields of proteomics and bioinformatics – leading to greatly improved understanding of structure, function and expression of newly discovered proteins. Textile processing with enzymes relationship between the primary amino acid sequence and its higher structural conformation can be obtained. Site-directed mutagenesis is also a valuable tool for studying structural and functional relationships of enzymes and for enhancing the attributes for commercially important enzymes.The catalytic capabilities of several enzymes have been improved by changes to the amino acids forming the active sites. Other studies have shown that it is possible to improve temperature and pH stability of enzymes. For example, introduction of cysteine residues into the polypeptide chain tends to enhance protein stability through disulfide bond formation. Replacement of lysine with arginine in a polypeptide chain also tends to enhance enzyme stability through increase in the extent of overall hydrogen bonding. Ultimately, continuing advances in this field could facilitate routine de-novo design of enzymes to suite particular applications; the ‘Holy Grail’ of applied enzymology! The advances made in molecular biology and the associated research equipment have accelerated DNA sequence determination and large portions of the genome of several species have been sequenced. This genomic information will increasingly drive future trends in enzymology – within the emerging fields of proteomics and bioinformatics – leading to greatly improved understanding of structure, function and expression of newly discovered proteins.](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEinUpAL4J3IBRrzrkImvTKtTmiOBYZh5OjhHLT6xyDcLpl8mcp0fPqTBAi7r0igjrJ-60xSi2_q06GWKfupQw3kfVjCb1kfY9l-wisbb2vP3Z4TjoVzNBSVvogB4ljJlk4t12MAYMH5t_xu/s400/use-of-enzymes-in-textile-wet-processing_big.jpg)
