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Monday, 26 November 2018

Importance of Quality Control in Textile and Apparel Industry

The garment industry has high standards of quality control. You could blame it on sub-standard manufacturing and complaining customers and you would not be far off the mark. The results of these factors have played a role in the textiles industry is setting quality control standards that can be measured and monitored.

There are five main factors measured in the garment industry that point to the quality of a particular clothing item. They include the following: reliability, performance, visual quality, perceived quality and durability.

Things you need to know in quality control process for textile and apparel:
As customers demand quality for what they spend on any kind of item, the clothing industry is also viewed under the same microscope. As a result the following tests are conducted on textiles in the factory:

1 – Quality Control:
Textile testing equipment such as the Martindale Abrasion Tester and Crockmeter are used to perform inspection of products used in the clothing industry. Using standards set at the international level measurements and durability tests are conducted.

2 – Conformity:
Using pre-production samples, the product is examined for such things as type of raw materials used, design, colors and all associated factors that are used to produce a finished item.

3 – Quality:
Such textile testing equipment as the launderometer examines products for defects in the fabric, colors, accessories, defects to the labeling and manufacturing. Products that do not pass this stage are eliminated and do not end up in the marketplace.

4 – Measurement:
Each product undergoes strict measurements as prescribed by a standard chart. The measurements are specific to the item but can reveal errors created somewhere through the production line.

5 – Packaging:
Even after the finished product meets the strict textile testing equipment standards, the shipping containers and packaging also require standardization. The checks include carton sizes, weights, labeling and assorted other details related to shipping and receiving.

How to control quality:
The key step to controlling quality in the textile industry should start at the garments factory and that requires specialized equipment. Textile testing equipment is the most efficient and cost effective way of keeping standards in place through various product line productions. There are additional ways to ensure quality control in the factory and they include:
  1. Ensure operators have proper training and use quality sewing materials
  2. Understand and follow quality specifications
  3. Provide good and bad feedback on products being manufactured
  4. Check on work being produced on a daily basis
  5. Reference a quality control checklist
  6. Use textile testing equipment to maintain quality standards
  7. Do not compromise quality under any circumstance
Offer training programs:
Another way to keep high quality standards in place is to have qualified staff monitoring production. By training staff to understand the purpose behind maintaining quality control systems, many issues can be resolved as soon as they become apparent. By working together as a team to achieve the same goals, quality control in the garments industry is easy to meet and maintain.

Sunday, 25 November 2018

Degumming of Silk

Objective :
       De gumming or boiling-off is the process employed to remove the silk gum (sericin) enveloping the two raw silk threads (fibrion) . During the spinning process of silk by silkworms the two filaments are made into one by means of pretentious gummy substance called sericin.
The gum content of silk varies according to quality and origin. Bombyx mori or Mulbery silks have about 20-30% gum and Tussah 5-15%. The gum is not completely removed in every case. The extent of de gumming gives rise to different varieties of silk . ‘Ecru silk’ (crude, bast silk) is rarely degummed, quite hard and without lustre. The degumming loss is maximum 4%, since mostly only grease, wax and resin substances are removed. This type of silk is mainly used as warp threads. ‘Half-boiled silk (souple, soft, matt silk) is partially degummed. The degumming loss is approximately 6-12%. ‘Cuite silk’ (lustre silk) with nearly 18-30% gum loss can be classified as a completely degummed variety with a soft handle and high lustre.



Apart from sericin, other impurities present in silk are lubricants and softeners added during throwing or in preparation for weaving or knitting, dirt and oils picked up incidentally during processing and undesirable natural colors. The component of fats and oils is around 0.5-1% and that of natural pigments 1.0-1.4%. During the degumming process soil, stain, oil and fats sticking to the material will also be removed. Thus degumming is synonymous with the scouring process normally used for the purification of cotton and wool. Silk warp is not subjected to sizing before weaving like cotton. However, grey silk fabric and its blended fabrics are subjected to singeing prior to degumming. Degumming can be carried out by physical or chemical means on silk in the form of hank and also on fabrics which are subsequently taken for dyeing. The choice of degumming conditions depends on the type of silk product (yam, twist, fabrics of different densities). Wild silk fabric is more difficult to degum than Mulbery silk. Tussah silk contains higher quantities of calcium salt. Loss in weight of silk by degumming process is also accompanied by a loss in strength of approximately 20%. The loss of weight and volume can be completely or partially compensated by the subsequent weighting process. Degumming is effected by careful treatment of silk with high pressure water, acids, alkalies, soaps and synthetic detergents. Chemical dissolution of sericin is obtained partly by hydrolysis and partly by dispersion, independent of the method used. Soap works mainly by dispersion whilst alkalies have a strong hydrolytic effect .
METHODS OF DEGUMMING :
Degumming of Silk in Water :
Cultivated varieties of silk can be degummed by extraction with water at 120 deg celcius for about 2 h and repeating the process three to four times. In this case degradation of silk is minimum, but use of pressure equipment is essential. However, some modification of the protein molecule does take place.
Degumming of Silk With Alkali and Acid :
         Silk degumming in aqueous solutions of acids and alkalies is greatly influenced by pH and temperature. An alkaline reaction at a pH > 9 and acid reaction at pH < 2.5 ensure a rapid elimination of sericin completely after 30 min of treatment. The temperature should not exceed 95 deg celcius to avoid weakening of the fibre. The degree of hydrolysis of fibrion also depends on pH of the bath.
Degumming of Silk With Soap :
        Degumming is effected by careful boiling-off in soap baths which should be slightly alkaline. The fibre is treated with soap solution to give a pH around 10.0 at 90-95 deg celcius for 1.5-2 h. In order to avoid lien soap deposits and resulting stains, the water should be properly softened. Sequestering agent may be added in the bath to correct the hardness of water. In case of white and delicate varieties a two bath method may be employed. The second degumming bath will consist of 50% quantity of soap taken for the first degumming bath and the duration of treatment may be divided equally between 40-45 min for each bath. Neutral soap like Merseille soap or olive oil soap have no degumming property as the free alkali present in them are very negligible. However, Merseille soap (8 g/l) can be used in presence of non-ionic tenside (fatty alcohol polyglycol ether) (1-3 g/l), polyphosphate (1-3 g/l) (for softening the water) and soda (1 g/l) at 95 deg celcius for 1-2 h with a material to liquor ratio of 1:30. Here also a two bath method can be resorted to. Non-ionic tenside accelerates the degumming process and facilitates rinsing out the soap. Tussah silk is usually prewetted with boiling water before degumming and then degummed in strong alkaline bath.

Drawbacks of Degumming with Soap :
            The main drawbacks are soap is expensive, great quantity of soap is required and longer treatment time.
Degumming of Silk With Synthetic Detergents:
           A large number of synthetic detergents are available in the market and their selection is very important particularly on the requirement of soft feel as that achieved with soap. Non-ionic product like nonyl phenol ethoxylated com- pound in the pH range of 11.2-11.5 for a treatment time of 40 min at 95 deg celcius is found to remove the gum and maintain the strength of the yarn .
Enzymatic Degumming of Silk :
           Enzyme which can hydrolyze the sericin is classified as proteolytic enzymes . The proteolytic enzymes cleave the peptide/amide linkages and convert them into amino acid. Mainly there are three types of proteolytic enzymes such as zinc protease (e.g. carboxy peptidase A), serine protease (Chymotrypsin, Trypsin, Thrombin) and thiol protease (acts as cystine residue in the protein). The function of proteolytic enzymes in their degree of degumming depends on the pH of the bath and the optimum activity is found to be different at different pH for different enzymes. Usually enzymatic desizing of silk is a two stage process. In pre degumming stage, the cloth is treated with a solution containing soda-ash (1 g/l) at 95 deg celcius for 20 min at a liquor ratio of 30. In the second stage, further degumming is carried out by treatment in a solution containing protein enzyme (0.06-0.1 g/l), non-ionic detergent (1 g/l) for 30 min at 55 to 60 deg celcius .It is usually impossible to achieve full degumming of silk by enzymes. A short-time treatment in a third bath containing soda-ash or soap may be given for the removal of the remaining sericin.
Foam Degumming :
            The degumming of silk can also be carried out by foam method. The silk skiens are subjected to the action of foam from a boiling soap bath. Skiens are actually hung above the soap solution and the foam action has a tendency to dissolve and eliminate sericin. This method, however, is not popularly adopted.
Partial Degumming of Silk :
            Before partial degumming the silk is degreased in moderately warm (30-40 deg celcius) and slightly alkaline soap baths. The actual degumming is then taken place in a bath containing acid salts or acids. The sericin is not released as much in an acid medium as it is in a neutral or alkaline bath, thus only partial degumming results. Acid degumming has also a positive effect on the strength and handle. The actual degumming bath can have various compositions :
  1. – Sulphuric acid and magnesium sulphate,
  2. – Sulphuric acid and soap,
  3.  – Sulphuric acid and tartar,
  4.  – 4% strength soap solution,
  5. –  NaHSO 3 solution.
Depending on the nature of silk, it is treated for 1-3 h at boiling temperature. The weight loss with half boiled silk lies in the range of 6-12% on the original raw weight.

Washing of Degummed Silk :
           After boiling-off, the silk is thoroughly washed with lot of water at 50-60 deg celcius containing 1ml / 1 ammonia for 15-20 min. This is then followed by 1 to 2 cold rinsing baths. Half-boiled silk should not be subjected to hot soap baths and alkaline liquors over 30 deg celcius because this would act on the silk gum still present. Following washing and drying silk is given further mechanical treatment in the form of stretching, beating or glossing. Scroop is imparted to the silk fabric by treatment with 2-5 g/1 of 30% acetic acid at room temperature for 15-30 min. When silk is delivered in dyed condition, scrooping is done after dyeing. Both degumming and partial degumming are only suitable for reeled silk .
Comparative Assessment of Different Degumming Methods:
         Given below is a table which shows comparative assessment of different degumming methods. Different methods have been evaluated on the basis of weight and strength loss after degumming. The values with soap have been taken as the basis. It can be seen that soap, alkali and acidic degumming give the highest gum removal. However, alkali and acid both cause significant strength loss which points to silk damage. On the other hand amines seem to be good at degumming as well as retaining strength. Enzymes while good at retaining strength are not able to remove the sericin very effectively. This is a limitation especially with fabrics where due to their large molecular size enzymes molecules are unable to enter the interstices of the fabric. Hence enzymatic degumming may be preferred for yarns rather than fabrics.
Degumming of Silk | Methods od Degumming of Silk | Textile Study Center | textilestudycenter.com
ASSESSMENT OF DEGUMMING:
            The simplest method to assess degumming is based on weight loss. However, in this case initial rapid weight loss may be followed by attack on fibroin. UV absorption at 280 nm has also been used to assess extent of degumming. Absorption is due to tyrosine and tryptophan.

Friday, 23 November 2018

KIDS BATHROBE ll YARN DYED BATHROBE ll TERRY TOWEL BATHROBE ll









Textile Technologies

Textile technology is a program of study that can cover a broad range of topics, from chemistry and physics in textile production to textiles used in apparel and interior design. Keep reading to discover education and career options in this field.

Inside Textile Technologies

Textile technology programs teach the science of creating and enhancing fibers, fabrics and other textiles used in manufacturing, apparel, healthcare and consumer products. Training in textile technology prepares students for a number of different career paths, such as textile engineer, interior designer, materials scientist and researcher. If any of these occupations interest you, check out the article links from Study.com listed below.

Education Information

Courses in textile technology programs can include textile chemistry, physics, molecular studies, biomedical materials and material composition. Students learn how to create and test fibers from both natural and synthetic sources. Technology programs in textiles and materials can be found in engineering or textile colleges at the undergraduate and graduate degree and certificate level. Online and hybrid programs are also available, often at the master's degree level.

HIGH - PERFORMANCE AND SPECIALTY FIBERS

 HIGH - PERFORMANCE AND SPECIALITY FIBRES
Introduction, Classification and Developments 
This chapter introduces the high-performance fibers and speciality fibres. The classification and developments of these fibres are briefly discussed.
How are High-Performance and Speciality Fibres different from commodity fibres ?
Commodity fibres or general purpose fibres are typically used in a highly competitive price environment which translates into large scale high volume programs in order to compensate for the (often) low margins.
Conversely, high performance and speciality fibres are driven by special technical functions that require specific performance properties unique to these fibres.
High-Performance Fibres are generally characterized by remarkably high :
  • Tensile strength and modulus
  • Resistance to heat and flame
  • Resistance to chemical agents that normally degrade conventional fibres.
Most high-performance fibres have high tensile modulus and strength. Many of them are also known for their thermal resistance; they do not catch fire and provide protection against heat. Therefore, fabrics constructed from these fibres can be used for applications where protection against fire is required.
Similarly, for certain applications, resistance against chemicals is desired.
Speciality Fibres:  These fibres have selected performance properties such as
  • Dyeability
  • Adhesion
  • Absorbency
  • Conductivity
  • Flame retardancy
  • Response to external stimuli ( produced from specialty polymers)
  • Special surface characteristics ( produced by special techniques) etc.
These can be obtained by using different approaches such as :
Using Additives  such as colorants, flame retardants, conducting fillers, antistatic compounds, etc. during the spinning process.
Surface Modification using chemical finishes for specific properties, such as hydrophilicity, high absorbency, low friction, etc. or by plasma modification.
Special Spinning Processes are used to produce different cross-section, bicomponent, micro, nanofibers.
Bicomponent fibres  are "co-extruded" with two different polymers in the cross section.  This allows the fibre to use the properties of both materials, and vastly expands the array of possible fibre performance characteristics. 
A non-circular cross-section can provide added functionality, such as unique lustre or moisture transport. 
The nanofibers have a very high surface to volume ratio and find potential applications in tissue engineering, optoelectronic applications, protective textiles and next generation filters.
Advanced or Special Polymeric Materials   are used for making smart or responsive fibres. These can be shape changing fibres (responsive to pH, temperature or electric field), fibres that can store heat or chemicals and self adaptive fibres( i.e. self tightening sutures, self-fitting shoes and medical devices).
Need?
These are required for meeting the ever increasing applications for fibrous material in non-conventional sectors such as
  • protective clothing
  • medical devices
  • health care products
  • automotive components
  • building material
  • geotextiles
  • agricultural devices
  • sportswear
  • leisurewear
  • filter media
  • environmental protection
Strong demands on good performance properties -such as strength/modulus, durability and dimensional stability and on functions such as flame-retardancy, hydrophilicity, hydrophobicity, biocompatibility, smart and responsive textiles, sensors, etc. Figure 1 shows the applications of high performance and speciality fibres for different end-uses.
Mooring & towing
Gloves
Trilobal fibre: for high lusture

Nanofibre: with high surface to volume ratio
Figure 1. Applications of High Performance Fibres
Classification of High Performance Fibres
i) Based on the performance properties: 
These are generally characterized by remarkably high values of:
  1. Tensile strength and modulus
  2. Resistance to heat, flame
  3. Resistance to chemical agents that normally degrade conventional fibres
Figure 2. The step change in strength and stiffness from first generation to second generation manufactured fibres and pointer showing different generations of textile fibres
As shown in Figure 2 , the naturally available fibres, such as cotton, wool and silk have tenacities in the range of 0.1-0.4 N/tex and initial moduli from 2 to 5 N/tex. In earlier days, silk filament was mostly used for the demanding applications such as parachute fabric. However, with the introduction of manufactured fibres, superior strength and modulus are achieved. The reinforcement in automobile tyres moved from cotton cords in 1900, to a sequence of improved rayons from 1935 to 1955, and then to nylon, polyester and steel, which dominate the market now. A similar replacement of natural and regenerated fibres by synthetic fibres occurred in most technical textiles. The maximum strength and moduli of nylon and polyester fibres approaches 10 g/den ( ~1 N/tex) or 1 GPa and 3-10 GPa respectively with breaking extensions exceeding 10%. The moderate strength along with moderate extension in these fibres result in high work of rupture, while the good recovery properties help in withstanding repeated high-energy shocks. These are called First Generation Textile Materials
In 1961, DuPont researchers spun para-aramid fibres from liquid-crystal solutions. High orientation led to tenacities of 2 N/tex and moduli of 80 N/tex. Other polymer fibres have now reached tenacities over 3.5 N/tex and moduli over 150 N/tex. At the Royal Aircraft Establishment (RAE) in UK, Watt and his colleagues produced the first high-strength carbon fibres by high-temperature processing of acrylic fibres under tension. This resulted in tenacities up to over 5 GPa (3 N/tex) and moduli over 800 GPa (400 N/tex). The other group of high-performance fibres are the inorganic fibres e.g. glass fibre. Strengths of glass fibres reach 4 GPa (1.6 N/tex) and moduli 90 GPa (35 N/tex), which, on a weight basis, are less than those of aramids. These fibres are classified as Second Generation Textile Materials. These include - Kevlar, Nomex, Carbon, HPPE fibres. The Second Generation Textile fibres showed a step increase in strength and stiffness. Besides there are sevaral fibre forming materials with high thermal and chemical resistance.
But it must be noted that before the discovery of second generation fibres, some of the natural fibres and manufactured fibres were used for technical textile applications.
Now there is a Third Generation of Fibres called SMART FIBRES with some special physical or chemical properties, which give a new dimension to the use of textiles. A typical example is Softswitch–fibres that become electrically conducting under pressure, or fibres that change shape with external stimuli as shown in Figure 3. Such materials can be used for artificial muscles, sensors and actuators etc.
Figure 3. Animation showing stimuli sensitive fibre
ii)Based on the nature of bonding:
Based upon the nature of bonding, these can be divided into three main categories:
The high performance fibres possess a strong and continuous axial bonding.
Linear polymers :  These polymers belonging to this group are one-dimensional and have a very high aspect ratio. Aramids, gel-spun PE, thermotropic polyesters, PBO etc. are the part of this category. Ultra high molecular weight polyethylene with linear string of covalently linked carbon atoms and hydrogen bonds in the transverse direction is a simplest case of this class. While the other polymers such as Kevlar and rigid rod polymers have a more complicated transverse structure containing aromatic rings and side groups. As shown below, the attempt is to obtain an ideal extended chain conformation of linear polymers with reduced/no defects in the structure. Theoretical moduli of ~100 GPa were calculated in the direction of primary bonds, but only ~0.5 GPa when controlled by Vander Waals bonds.

Figure 4. Ideal extended chain structure
Innovations were required to achieve such fully extended ideal structures. Two extreme of molecular characteristics were employed to achieve the necessary structure. The  two routes used are:
  1. Using rigid and interactive polymer chains
  2. Using flexible and inert polymer chains
During processing, the rigid chains tend to associate as blocks of parallel chains or liquid crystals. The polymer molecules are fully extended because the folding is difficult due to the rigidity of the chain. The deformation of such a system during solidification would result in highly oriented structure. The chemical structure of some rigid polymers suitable for producing high performance fibres are shown in Figure 5.
Figure 5. Chemical structures of rigid polymers
The alternate route of production of HM-HT fibres is based on the ease with which flexible, inert chain-molecules can be pulled out into a fully-extended, oriented state. At molecular level, this has been achieved by spinning of ultrahigh molecular weight polyethylene in the gel form and super drawing of the extruded filament in the gel form to result in an highly extended structure. As shown in Figure 6 these fibres have strong covalent bonds in the axial direction of fibre and weak intermolecular bonding in transverse direction.
Figure 6. Strong axial covalent bonds and weak transverse intermolecular bonding
Two-Dimensional Graphitic Sheets :  Two dimensional molecular sheets or structures can be obtained only by a specific geometry for the bond directions for example: hexagonal planar network of carbon can result in graphite structure. The high temperature controlled oxidation and carbonization of organic fibres under tension can be used to obtain strong and stiff carbon fibres with axial orientation of graphitic sheets (Figure 7).
Figure 7.  2-Dimensional Graphitic Sheets of Carbon Fibre
Three-Dimensional Networks :  Trifunctional or multifunctional precursors/monomers can be used to derive three-dimensional (3D) networks (Figure 8). Such networks in the fibre form are the basis of thermoset, glass and ceramic fibres.
a)
b)
Figure 8. 3D- Network materials: (a) A crystalline network in a ceramic fibre; (b) An amorphous network as in glass.
Generally, these polymeric fibres have strength, stiffness and breaking extensions comparable to conventional textile fibres. Strong intermolecular bonding gives thermal resistance and the inert molecular structure impart chemical resistance in these fibres. The three-dimensional inorganic networks, such as those constituting ceramic and glass fibre also possess high thermal resistance.
High performance fibres can be used for reinforcement of composites to enhance their performance properties. The following example can illustrate how the uniaxially oriented glass fibre in polyester resin can enhance the modulus by nearly 10 times.

Glass fibre reinforced polyester composite:
Example: Uniaxially oriented glass fibre in polyester resin as shown in Figure 9 below.
The reinforced composite prepared using
40% Glass fibres (Vg)
60% Polyester resin (Vr)
Modulus of glass fibre (Eg) = 69 GPa,
Modulus of polyester resin used for the matrix ( Em) = 3.4 GPa
Figure 9. Schematic of unidirectional glass fibre reinforced composite
E = Ef. Vf + Em . Vm
Longitudinal modulus of elasticity = 69 x 0.4+ 3.4 x 0.6 = 30 GPa
Fibre load (Ff) / Matrix load (Fm) = σg .Ag / σr .Ar
= Ef. Vf / Em . Vm =69x 0.4 / 3.4 x 0.6 or Ff / Fm = 13.5

Source: NPTEL

How is polyester fibers made?

Polyester was developed in the years 1939-1941 by British chemists at Calico Printers Association, Ltd., based on the work of W.H. Carothers in 1926 at the United States based E.I.D. Pont de Nemours and Co.  DuPont bought the rights in 1946 to produce polyester fiber in the United States.  By 1951, DuPont had begun to market the fiber under the name Dacron.
Polyester is made up of long-chain polymers. Today there are two primary types of polyester called polyethylene terephthalate (PET) and poly-1, 4-cyclohexylene-dimethylene (PCDT).  PET is the most popular type as it is applicable to a wider variety of uses and is stronger than PCDT.  However, PCDT is more elastic and resilient and is used in heavier consumer applications.
Synthetic polyester is made using a chemical reaction involving coal, petroleum, air and water.  Polyester is made up of purified terephthalic acid (PTS) or its dimethyl ester dimethyl terephthalate (DMT) and monotheluene glycol (MEG). It holds 10% of the market share for all plastic materials, coming third in terms of popularity after polyethylene (33.5%) and polypropylene (19.5%).
The most common type of chemical reaction used to make polyester takes place at high temperatures in a vacuum. A petroleum by-product, alcohol, and carboxyl acid are mixed to form a compound known as monomer or “ester.” This reaction is known as polymerization.  The polymer material created during polymerization is extruded while hot into long fibers that are stretched until they are about five times their original length. The resultant fiber forms an arrangement of molecules that is very strong.
Polyester fibers or threads are made using a spinning process.  There are two types of spinning processes.  One is the filament type, where long fibers are twisted together, and the spun types, in which short pieces of fiber are combined to form something called “staple.” These processes allow for material blends to be made using cotton or wool spun in with the polyester.
Synthetic fabrics like polyester are often criticized for having a less natural feel than fabrics such as cotton, silk, or wool. However, polyester does have some distinct advantages over natural fibers.  Polyester is wrinkle resistant, more durable and has high color retention.  Synthetic fibers also can exhibit superior water, wind and environmental resistance. For this reason, polyester is often used in tents, outdoor clothing such as windbreakers and parkas, and umbrellas. Polyester fabrics have come to replace some of the old school natural fabrics.  For example, “China silk “ is the term used by the textile industry for fabrics made of 100% polyester that closely resemble the sheen, drape, and durability of insect-derived silk.
Polyesters can be thermoplastics or thermo sets. Most polyesters are thermoplastics, meaning they may change their shape with the application of heat. Polyester is combustible at high temperatures but tends to shrink away from flames and is self-extinguishing upon ignition. So just leave your windbreakers off of the ironing board!
Unsaturated polyesters (UPR) are thermoset resins. They are used for non-metallic body fillers, fiberglass laminating resins, and casting materials. Fiberglass-reinforced unsaturated polyesters are used in a wide range of applications including the bodies of yachts and automobiles.
Fabrics and threads made of polyester are used widely in apparel, home furnishings, and in commercial applications. Some examples include blankets and hats, bed sheets, and computer mouse pads.  Industrial polyester fibers are made into ropes, safety belts, tire reinforcements, and conveyor belts.  Polyester is also used to make bottles, films, and holograms. It is used as a wood finish on pianos, guitars, and yacht interiors.