Textile Notes related to fiber, yarn, fabric knowledge, spinning, weaving, processing, projects, knitting, Indian Traditional Textiles and denim manufacturing
Sunday, 31 May 2009
Determination of Abrasion Resistance of Fabric
Determination of Abrasion Resistance of Fabrics
Plain Abrasion Resistance
Apparatus - Universal Wear Tester
Prior to test, the fabric should be Conditioned to moisture equilibrium from the dry side, in the standard atmosphere of 65+-2% relative humidity and 27+-2 deg C temperature. The test should be carried under standard atmospheric conditions.
Method for determination of plane Abrasion Resistance
1. Cut five circular test specimens of 112 mm in diameter, taking care to take specimens from areas containin the same wales or courses in knitted fabric or the same warp or weft yarn in woven fabric.
2. Set the instrument for inflated diaphram test.
3. Place the specimen over the rubber diaphram in smooth condition and clamp the specimen in place without disturbing it.
4. Place the abrasive paper on the abradent plate under sufficient tension to be held smooth and in such a position that the contact pin, reaching through a hole in the abradent is even with the surface of the abradent. In the absence of any specific material specification , zero emery polishing paper should be used as the abradent.
5. Set the air pressure under the diaphram and load on the abradent plate. In the absence of any specific material specifications, the air pressure should be 0.3kg/sq.cm (4 p.s.i.) and the load on the abradent should be 454 gm. Ensure that the air pressure control and contact between the inflated specimen and loaded abradent is in a state of equilibrium before abrasion is started. To ensure consistent inflation of the diaphragm, inflate to a higher air pressure ( 25 per cent) and then reduce the testing pressure.
6. If the unidirectional abrasion is desired, disengage the rotation mechanism of the specimen clamp and bring the specimen into the direction by turning and setting the clamp after the diaphragm has been inflated.
7. In the event that multi-directional abrasion is required, or if no specific indication as to the abrasion direction is given in the fabric specification, engage rotation mechanism of the specimen clamp.
8. Remove pills of matted fibres interfering with proper contact between specimen and abradent during the test if they cause a marked vibration of the abradent plate.
9. If the specimen slips in the clamp or the air pressure does not remain constant during the test or anomalous wear pattern is obtained, discard such individual measurements and test an additional specimen..
10. One of the following methods is selected for determination of end point as per test specifications:
a. Breakage of Thread: Abrade the specimen until all fibres in the centre of the abraded area are worn off so that the diaphragm and abradent head come into contact and the instrument automatically stops.
b. Removing a predetermined thickness of the material. Abrade the specimen using the electrical depth micrometer to determine the automatic end-point for removing a predetermined thickness of the material from the specimen.
11. Unless the continuous changing abrasion head is used, abradent paper is changed after every 300 cycles.
12. Report shall include the following information :
a. Type of abradent
b. Type of abrasion ( unidirectional or multi directional)
c. No. of cycles to reach the end point as determined by electrical contact.
Related Links
Testing Abrasion Resistance For Socks
Properties of Polyester
| Tenacity (gpd) | High Tenacity | Normal Tenacity | Staple |
| Dry | 6-7 | 4.5-5.5 | 3.5-4 |
| Wet | 6-7 | 4.5-5.5 | 3.5-4 |
| Elongation (%) | |||
| Dry | 12.5-7.5 | 25-15 | 40-25 |
| Wet | 12.5-7.5 | 25-15 | 40-25 |
| Density | 1.38 | 1.38 | 1.38 |
Moisture Regain
At 65% RH and 70 deg F--> 0.4%
Because of low moisture regain, it develops static charge. Garments of polyester fibres get soiled easily during wear.
Thermal Properties
Polyester fibres are most thermally stable of all synthetic fibres. As with all thermoplastic fibres, its tenacity decreases and elongation increases with rise in temperature. When ignited, polyester fibre burns with difficulty.
Shrinkage
Polyester shrinks approx 7% when immersed in an unrestrained state in boiling water. Like other textile fibres, polyester fibres undergo degradation when exposed to sunlight.
Its biological resistance is good as it is not a nutrient for microorganisms.
Swelling and Dissolving
The fibre swells in 2% solution of benzoic acid, salycylic acid and phenol.
Alcohols, Ketones, soaps, detergents and drycleaning solvents have no chemical action on polyester fibres.
Chemical Resistance
Polyester fibres have a high resistance to organic and mineral acids. Weak acids do not harm even at boil. Similarly strong acids including hydrofluoric acids do not attack the fibres appreciably in the cold.
Uses of Polyester
1. Woven and Knitted Fabrics, especially blends.
2. Conveyor belts, tyre cords, tarpaulines etc.
3. For filling pillows
4. For paper making machine
5. Insulating tapes
6. Hose pipe with rubber or PVC
7. Ropes, fish netting and sail cloth.
Saturday, 30 May 2009
Manufacturing Process of Polyester
Manufacture of Polyester
These fibres are also known as Terylene, Terene, Dacron etc.
These fibres are synthetic textile fibres of high polymers which are obtained by esterification of dicarboxylic acids, with glycols or by ester exchange reactions between dicarboxylic acid esters and glycols.
Thus Terylene is made by polymerising using ester exchange reation between dimethyl teraphthlate and ethylene glycol.
Raw Materials
The main raw materials required for the manufacture of Terylene polyester fibres are p-xylene ethylene glycol and methanol.
or Dacron ( Du Pont ) is produced by polycondensation reaction using Teraphthaleic Acid (TPA) and Ethylene Glocol
Manufacture of TPA
P-xylene-- Air, nitric Acid-->P-Toluic Acid--> Teraphthaleic Acid
Manufacture of DMT
p-xylene--Air 200 degC, co-toluate--> Toluic Acid--Ch3OH--> Monomethyl toluate--oxidation--> Monomethyl teraphthalate--CH3OH--> DMT
The use of Dimethyl Teraphthalate is preferred instead of Teraphthalic acid as the purity of the reacting chemicals is essential and it is easier to purify DMT than teraphthalic acid.
Manufacture of Ethylene Glycol
Ethylene--Oxidation with air-->Ethylene Oxide--Hydrolysis-->Ethylene Glycol
or
Ethylene--Hypochlorous Acid HOCl--> Ethylene Chlorohydrin--Alkaline Hydrolysis--> Ethylene Glycol
Production
The polymer is made by heating teraphthalic acid with excess of ethylene glycol ( Both of high priority) in an atmosphere of nitrogen initially at atmospheric pressure. A catalyst like hydrochloric acid speeds up the reaction.
The resulting low molecular weight ethylene glycol teraphthalate is then heated at 280 deg C for 30 minutes at atmospheric pressure and then for 10 hours under vacuum. The excess of ethylene glycol is distilled off. the ester can polymerise now to form a product of high molecular weight. The resulting polymer is hard and almost white substance, melting at 256 deg C and has a molecular weight of 8000-10000. Filaments are prepared from this.
Spinning of Polyester Fibres
The polymer is extruded in the form of a ribbon. This ribbon is then converted into chips.
The wet chips are dried and fed through a hopper, ready for melting. This molten polymer is then extruded under high pressure through spinnerettes down to cylinder.
Each spinnerette contains 24 or so holes. A spinning finish is applied at this stage as a lubricant and an antistatic agent. The undrawn yarn is then wound onto cylinders.
This yarn goes to the drawing zone, where draw twist machines draw it to about four times their original length. This is hot drawn in contrast to cold drawing of nylon filaments.
For the production of staple fibres, the filaments are first brought together to from a thick tow. These are distributed in large cans. The tow is drawn to get correct strength. Then it is passed through a crimping machines, the crimps being stabilized by heating in ovens. It is then cut into specified lengths and baled ready for despatch.
Friday, 29 May 2009
Properties of Nylon 6
Properties of Nylon 6
Nylon 6 has certain advantages over Nylon 6,6,. Firstly the systheisi fo caprolectum is easier than that of Hexamethylene Diamine and Adipic Acid. Therefore it is cheaper to make Nylon 6 than Nylon6,6. Secondly Nylon 6 has greater affinity for acid dyes than Nylon6,6,
Mechanical Properties
Density: 1.14 g/cc
Tenacity: Dry= 4.2-5.8 gpd, Wet=4.0-5.3 gpd
Elongation at Break--> Dry = 24-40, Wet=28-43
Elastic Recovery at 4% extension= 100%
Moisture Regain= 4%
Because of low MR, wet nylon dries quickly.
Melting Point= 215 deg C ( Nylon 66-250 deg C)
It is weakened by prolonged exposure to sunlight.
Chemical Properties
1. It is resistant to most organic acids such as benzene, chloroform, acetone, esters ethers etc.
2. It dissolves in phenol, cresol and strong mineral acids.
3. good resistant towards alkalies.
4. Resistant to inorganic acids
These fibres are cylinderical in shape, with smooth surfaces and without having any markings. The fibres are unifrom in diameter and appear round in cross section.
Uses
a. Tyre Cord Manufacturing
b. Fishing Lines
c. Luxury Yachts
d. Stockings with good fit, sheerness, quick washing and drying properties.