Showing posts with label quality control. Show all posts
Showing posts with label quality control. Show all posts

Wednesday, 13 May 2026

How to Determine Fibre Composition in Blended Fabrics



How to Determine Fibre Composition in Blended Fabrics

Blended fabrics are very common in textiles. A fabric may contain polyester with cotton, cotton with viscose, acrylic with wool, elastane with cotton, or many other combinations. But when a fabric is made from more than one fibre, one important question arises:

How do we know the percentage of each fibre in the fabric?

This is important for quality control, costing, labelling, performance evaluation, buyer communication, export documentation and compliance.

Why Are Fibres Blended?

No single fibre gives all the desirable properties needed in a fabric. One fibre may give strength, another may give comfort, another may improve appearance, and another may reduce cost.

For example, polyester has very good strength, but it does not absorb much moisture. Because of this, 100% polyester fabric may not feel as comfortable as cotton. When polyester is blended with cotton, the fabric can get the strength of polyester and the comfort of cotton.

Fibre blending is generally done for three major reasons:

  • To obtain different properties
  • To suit changing fashion requirements
  • To control the cost of the fabric

Once fibres are blended, it becomes necessary to determine the actual percentage of each fibre in the fabric. This is usually done by dissolving one fibre selectively and weighing the remaining fibre.

Fibre blending concept showing strength comfort cost and fashion requirements

Visual 1: Why fibres are blended — strength, comfort, fashion and cost.

Basic Principle of Fibre Composition Testing

Most chemical methods for fibre composition work on a simple principle:

One fibre is dissolved in a specific chemical, while the other fibre remains undissolved.

The undissolved fibre is then:

  • filtered,
  • washed,
  • neutralised if required,
  • dried,
  • cooled,
  • weighed.

From the weight of the remaining fibre, the percentage of each fibre in the blend can be calculated.

1. Polyester and Cellulosic Fibre Blends

This method is used for blends such as:

  • Polyester + cotton
  • Polyester + viscose

A small sample of the blended fabric, usually 0.5 to 1.0 gram, is weighed accurately and placed in a flask. Then 75% w/w sulphuric acid is added. The material-to-liquid ratio is kept at about 1:200.

The flask is kept in a water bath at 50 ± 5°C for about one hour.

In this process, the cellulosic fibre dissolves, while the polyester remains undissolved.

The remaining polyester fibre is then:

  • filtered,
  • washed properly with water,
  • neutralised with dilute ammonia solution,
  • dried at 110°C,
  • cooled,
  • weighed.

The weight of the remaining fibre gives the percentage of polyester. The percentage of cotton or viscose can be calculated by subtracting the polyester percentage from 100.

Example:

If polyester remaining after the test is 65%, then:

Cellulosic fibre percentage = 100 − 65 = 35%

So the fabric composition is:

65% polyester and 35% cotton or viscose.

Selective dissolution method for testing fibre composition in blended fabrics
Visual 2: Selective dissolution principle — dissolve one fibre, weigh the remaining fibre.

2. Cotton and Viscose Blends

Cotton and viscose are both cellulosic fibres, so their separation is more delicate. The Bureau of Indian Standards has described four methods for determining cotton and viscose percentages:

  1. 60% w/w sulphuric acid method
  2. Sodium zincate method
  3. Formic acid and zinc chloride method
  4. Cadoxen solution method

Among these, the 60% w/w sulphuric acid method is commonly used.

60% w/w Sulphuric Acid Method

In this method, 0.5 to 1.0 gram of sample is weighed accurately and placed in 60% w/w sulphuric acid. The material-to-liquid ratio is kept at 1:100.

The solution is stirred properly by mechanical action for about 30 minutes.

In this process:

  • Viscose dissolves
  • Cotton remains undissolved

The cotton fibres are then filtered out and washed. After that, they are washed with water and treated with dilute ammonium hydroxide solution for neutralisation. Finally, they are dried and weighed.

However, in this method, the weight of cotton may also reduce by about 5%. Therefore, a correction factor is applied to calculate the actual cotton percentage accurately.

3. Polyester, Cotton and Viscose Blends

In a three-fibre blend containing polyester, cotton and viscose, separation is done step by step.

First, the sample is placed in 60% w/w sulphuric acid.

In this stage:

  • Viscose dissolves first.
  • Cotton and polyester remain.

The remaining fibres are washed, dried and weighed.

Then the remaining fibres are placed in 75% sulphuric acid.

In this stage:

  • Cotton dissolves.
  • Polyester remains.

The final remaining fibre is polyester. It is washed, dried and weighed.

In this way, the percentage of viscose, cotton and polyester can be determined separately.

4. Acrylic Blends with Wool, Silk, Cotton, Viscose, Polyester or Nylon

Acrylic fibre may be blended with many other fibres such as wool, silk, cotton, viscose, polyester or nylon.

In such blends, acrylic is first dissolved in dry dimethyl formamide, commonly known as DMF.

In this method:

  • Acrylic dissolves in DMF.
  • Other fibres remain undissolved.

The undissolved fibres are filtered, washed, dried and weighed. From this, the percentage of acrylic fibre in the blend can be calculated.

5. Protein Fibres with Cotton, Polyester, Nylon or Acrylic

Protein fibres include fibres such as wool and silk.

When protein fibres are blended with cotton, polyester, nylon or acrylic, they can be separated using alkali.

The accurately weighed sample is placed in a conical flask. Then 5% w/w sodium hydroxide or potassium hydroxide solution is added. The mixture is boiled for about 10 minutes.

In this process:

  • Protein fibres dissolve.
  • Other fibres remain undissolved.

The remaining fibres are filtered and washed thoroughly with water. Then they are washed with dilute acetic acid to neutralise the alkali.

Finally, the sample is dried, cooled and weighed. From this, the percentage of protein fibre and the other fibre can be calculated.

6. Polyester with Cotton or Viscose

Polyester can also be determined by using meta-cresol.

In this method, the blended fibres are weighed accurately and heated with meta-cresol.

In this process:

  • Polyester dissolves.
  • Cotton or viscose remains undissolved.

The remaining insoluble fibres are washed, dried and weighed. From this, the percentage of polyester is calculated.

7. Elastane, Spandex or Lycra with Cotton or Viscose

Elastane is also known by names such as spandex and Lycra.

When elastane is blended with cotton or viscose, it can be separated using DMF.

In this method, the mixed fibres are treated with DMF.

In this process:

  • Elastane dissolves in DMF.
  • Cotton or viscose remains undissolved.

The remaining fibres are filtered, washed, dried and weighed. From this, the percentage of elastane is calculated.

Summary chart of chemicals used for testing fibre blends
Visual 3: Fibre blend testing summary — fibre blend, chemical used and fibre dissolved.

Summary Table: Fibre Blend Testing Methods

Fibre Blend Chemical Used Fibre Dissolved Fibre Remaining
Polyester + cotton/viscose 75% sulphuric acid Cotton/viscose Polyester
Cotton + viscose 60% sulphuric acid Viscose Cotton
Polyester + cotton + viscose 60% and 75% sulphuric acid Viscose first, then cotton Polyester
Acrylic + other fibres DMF Acrylic Other fibres
Wool/silk + cotton/polyester/nylon/acrylic Sodium hydroxide or potassium hydroxide Wool/silk Other fibres
Polyester + cotton/viscose Meta-cresol Polyester Cotton/viscose
Elastane/spandex/Lycra + cotton/viscose DMF Elastane Cotton/viscose

Why Fibre Composition Testing Matters

Fibre composition testing is very important in the textile industry because it helps in:

  • correct fabric labelling,
  • buyer compliance,
  • export documentation,
  • quality control,
  • cost verification,
  • performance evaluation,
  • identifying wrong claims in fabric composition.

For example, if a fabric is sold as 80% cotton and 20% polyester, a laboratory can verify whether the actual fibre content matches the claim.

Similarly, in stretch fabrics, the elastane percentage may be small but very important. Even 2% to 5% elastane can change the stretch, recovery and comfort of the fabric.

Important Precautions

While carrying out fibre composition testing, the following precautions are important:

  1. The sample should be weighed accurately.
  2. The correct chemical concentration should be used.
  3. The material-to-liquid ratio should be maintained.
  4. Temperature and time should be controlled.
  5. The residue should be washed completely.
  6. Neutralisation should be done properly.
  7. The sample should be dried and cooled before final weighing.
  8. Correction factors should be applied wherever required.

Small errors in weighing, washing or drying can affect the final fibre percentage.

Conclusion

Fibre blending is done to improve fabric properties, reduce cost and meet fashion requirements. But once fibres are blended, it becomes necessary to know their exact proportion.

The basic method of fibre composition analysis is selective dissolution. One fibre is dissolved in a suitable chemical, while the other fibre remains. The remaining fibre is then washed, dried and weighed.

Different fibres require different chemicals. Polyester, cotton, viscose, acrylic, wool, silk and elastane all behave differently in different solvents. Therefore, correct identification of the fibre blend is necessary before selecting the test method.

For merchandisers, textile students, quality professionals and buyers, understanding these methods is very useful. It helps them read laboratory reports better and understand how fibre composition claims are verified scientifically.

Understanding 75% (w/w) Sulphuric Acid and M:L Ratio

In textile testing instructions, we often come across statements such as:

Add 75% (w/w) sulphuric acid (M:L :: 1:200).

At first glance, this looks like a short laboratory instruction, but it contains two important pieces of information. The first is the concentration of sulphuric acid, and the second is the amount of acid solution to be used in relation to the weight of the textile material.

What is meant by 75% (w/w)?

The term w/w means weight by weight. Therefore, 75% (w/w) sulphuric acid means that 75 parts by weight of pure sulphuric acid are present in 100 parts by weight of the final solution.

In simple terms:

\[ 75\% \; (w/w) = \frac{75 \text{ g pure } H_2SO_4}{100 \text{ g final solution}} \]

So, if we prepare 100 g of 75% (w/w) sulphuric acid solution, it should contain 75 g of pure sulphuric acid and 25 g of water.

What is meant by M:L :: 1:200?

The term M:L means Material to Liquor ratio. In textile processing and testing, “material” usually refers to the fabric, fibre, yarn, or textile sample. “Liquor” refers to the solution in which the textile material is treated.

Therefore:

\[ M:L = 1:200 \]

means that for every 1 g of textile material, 200 mL of acid solution should be used.

Fabric Weight M:L Ratio Required Acid Liquor
1 g 1:200 200 mL
2 g 1:200 400 mL
5 g 1:200 1000 mL
10 g 1:200 2000 mL

The general formula is:

\[ \text{Liquor required in mL} = \text{Weight of material in g} \times 200 \]

Example: If the fabric sample is 5 g

If the fabric sample weighs 5 g and the required M:L ratio is 1:200, then:

\[ 5 \times 200 = 1000 \text{ mL} \]

So, 5 g of textile material will require 1000 mL of 75% (w/w) sulphuric acid solution.

How to Prepare 75% (w/w) Sulphuric Acid Solution

Since the concentration is given as w/w, the correct method is to prepare the solution by weight, not simply by volume. Laboratory concentrated sulphuric acid is commonly about 98% (w/w), not 100% pure. Therefore, we must account for this while calculating the amount of concentrated acid required.

Suppose we want to prepare 100 g of 75% (w/w) sulphuric acid solution.

Required pure sulphuric acid:

\[ 75 \text{ g} \]

If concentrated sulphuric acid is 98% (w/w), then the amount of concentrated acid required is:

\[ \frac{75}{0.98} = 76.53 \text{ g} \]

Therefore, water required will be:

\[ 100 - 76.53 = 23.47 \text{ g} \]

For 100 g of 75% (w/w) sulphuric acid solution:
Take approximately 23.5 g water and slowly add 76.5 g concentrated sulphuric acid.

Preparation for 1000 g of Final Solution

If a larger amount is required, the same calculation can be scaled up. For example, to prepare 1000 g of 75% (w/w) sulphuric acid solution:

Required pure sulphuric acid:

\[ 75\% \text{ of } 1000 = 750 \text{ g} \]

Amount of 98% concentrated sulphuric acid required:

\[ \frac{750}{0.98} = 765.3 \text{ g} \]

Amount of water required:

\[ 1000 - 765.3 = 234.7 \text{ g} \]

For 1000 g of 75% (w/w) sulphuric acid solution:
Take 234.7 g water first, then slowly add 765.3 g concentrated sulphuric acid with stirring and cooling.

Important Safety Precaution

Always add acid to water, never water to acid.

Dilution of sulphuric acid releases a large amount of heat. If water is added directly to concentrated acid, the mixture can heat suddenly, splash, or even boil violently. Therefore, the safe method is to take the required quantity of water first and then add concentrated sulphuric acid slowly, with continuous stirring.

The preparation should be done using proper laboratory safety equipment such as chemical-resistant gloves, safety goggles, apron or lab coat, and acid-resistant glassware. Cooling should be provided if necessary, especially when preparing larger quantities.

Summary

Term Meaning
75% (w/w) 75 g pure sulphuric acid in 100 g final solution
M:L Material to Liquor ratio
M:L :: 1:200 1 g textile material requires 200 mL liquor
For 5 g sample Required liquor = \(5 \times 200 = 1000\) mL
For 100 g of 75% solution Use 23.5 g water + 76.5 g of 98% sulphuric acid

General Formula

If concentrated sulphuric acid strength is known, the required weight of concentrated acid can be calculated as:

\[ \text{Weight of concentrated acid} = \frac{\text{Required pure acid}}{\text{Strength of concentrated acid as decimal}} \]

For 98% sulphuric acid:

\[ \text{Weight of concentrated acid} = \frac{\text{Required pure acid}}{0.98} \]

Water required:

\[ \text{Water required} = \text{Final solution weight} - \text{Weight of concentrated acid} \]

Practical Note for Textile Testing

When a test method says 75% (w/w) sulphuric acid at M:L :: 1:200, it is not merely asking for “some strong acid.” It is specifying both the exact concentration of the acid solution and the amount of solution to be used per gram of textile material. Both are important because fibre dissolution, reaction rate, and test reproducibility depend strongly on acid concentration and liquor ratio.

Disclaimer: Sulphuric acid is highly corrosive and dangerous. The above explanation is for educational understanding of laboratory notation and calculation. Actual preparation and handling should be done only in a properly equipped laboratory by trained personnel, following the relevant test standard, institutional safety protocol, and the chemical safety data sheet.

General Disclaimer

This article is intended for educational and general textile knowledge purposes only. Actual fibre composition testing should be carried out only by trained laboratory personnel using recognised test standards, calibrated equipment, proper safety procedures and appropriate chemical handling protocols. Chemicals such as sulphuric acid, sodium hydroxide, potassium hydroxide, DMF and meta-cresol can be hazardous and should not be handled casually. Always refer to the relevant national or international testing standard before conducting any laboratory procedure.

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Tuesday, 2 June 2009

Flex Abrasion Resistance- Determination



Method for determination of Flex abrasion resistance:

1. Cut five test specimens each 200mm. long and of 32 or 38mm width depending upon wheter the number of yarns/dm of the specimen is below or above 200. Ravel the specimen to 25 mm in width by removing from each side approximately the same number of yarns. Do not take two specimens fro the weft test from the same warp ends or any two specimens fro the weft test from the same picks. Take weft specimens at wide intervals.

2 After positioning the bar by means of the yoke holder, place the specimen between the pressure (upper) plate and the reciprocating (lower) plate of the apparatus and locate centrally. with the specified folding bar or folding blade inserted, after being clamped and loaded by removal of yoke holder, distribute the tension exerted by the bar or blade uniformly over the width of the specimen and align the long dimension both above and below the bar parallel to the direction of the reciprocating motion. Position the specimen with the fold at the centre of the upper plate, and the reciprocating plate at the rear of its stroke when the specimen is clamped.

3. Load the pressure plate and the folding bar or blade as required by the material specifications. In the absence of the material specification, the bar load sufficient to produce rupture in excess of at least 100 cycles and preferably in 300 cycles should be used, in combination with the lowest head load (pressure) sufficient to prevent vibration of the upper plate at the start of the test.

The ratio of the bar to head loads shall be 4:1

4. Check the bar alignment after the first 25 cycles. If shifting of bar from its normal position is noticed, discard the specimen and make the proper adjustment.

5. Remove the pills of matted fibres debris interfering with proper contact between the specimen and the folding bar or folding blade during the test if they cause a marked vibration of the pressure plate or otherwise interfere with proper abrasion. The pill should be removed by careful clipping. Do not correct the vibration of the pressure plate due to pilling by applying additional load. Check the position of the specimen after additional cycles to ensure that the removal of the pills has not altered the bar alignment.

6. If the specimen slips in the clamps or tension and pressure upon the folded specimen do not remain constant during the test, or an anomalous wear pattern is obtained, discard such individual measurements and test an additional specimen.

7. Before every test the blade is rinsed with degreasing agent.

8. The end point is determined by abrading the specimen until rupture and number of cycles is recorded.

9. The report should include the following information:

a. Abradent used, bar or blade
b. Average number of cycles required to produce rupture the specimen

Total No of cycles Report to the nearest cycle
Below 200 10
200 to 299 25
1000 to 4999 50
5000 and above 100

c. Tension and pressure used.







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



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