EP0902852A1

EP0902852A1 - Method of producing a cellulosic yarn

Info

Publication number: EP0902852A1
Application number: EP97927053A
Authority: EP
Inventors: Abdulmajid Hashemzadeh; Peter Raidt
Original assignee: Akzo Nobel NV
Current assignee: Akzo Nobel NV
Priority date: 1996-05-30
Filing date: 1997-05-27
Publication date: 1999-03-24
Anticipated expiration: 2017-05-27
Also published as: JP2000511598A; EP0902852B1; ID18177A; WO1997046745A1; DE59701182D1; AU3168297A; TW382030B; ES2145609T3; ATE190098T1; US6042767A

Abstract

PCT No. PCT/EP97/02742 Sec. 371 Date Nov. 24, 1998 Sec. 102(e) Date Nov. 24, 1998 PCT Filed May 27, 1997 PCT Pub. No. WO97/46745 PCT Pub. Date Dec. 11, 1997In a process for manufacturing a cellulosic yarn by spinning of a solution of cellulose in a tertiary amine oxide, the solution possibly containing water and/or a stabilizer, to form fibers or filaments, coagulating, washing, and drying, the yarns are treated prior to drying with an aqueous alkaline solution for a period less than 20 seconds.

Description

Process for the production of a cellulosic yarn

* *

Description:

The invention relates to a process for the production of a cellulosic yarn by spinning a solution of cellulose in a tertiary amine oxide, possibly also containing water and possibly a stabilizer, to give fibers or filaments, precipitation, washing and drying.

WO95 / 24524 discloses a method for improving the color properties of fabrics made of so-called lyocell yarns. Lyocell yarns are solvent-spun cellulose yarns that are made by spinning a solution of cellulose in an organic solvent. The solvent is essentially an aqueous tertiary amine oxide, for example N-methylmorpholine-N-oxide (NMMO). According to W095 / 24524, fabrics made from the cellulose yarns mentioned are subjected to a mercerization, ie treated with an alkaline solution. This mercerization corresponds in principle to that which is customary for cotton fabrics, and an aqueous NaOH solution with a concentration of 10 to 30% by weight at room temperature or slightly elevated temperature (for example up to 35 ° C.) is preferably used for this purpose. The fabrics may then be washed with water. To neutralize the lye, the tissue is treated with a dilute aqueous acid and several times washed to remove the acid, and then dried. According to the examples of WO95 / 24524, in which aqueous NaOH solutions with a concentration of 14% by weight or 25% by weight were used, the fabrics from Lyocell yarns were treated at room temperature over a period of 45 seconds. This gave tissues which, after dyeing, had a deeper shade than non-mercerized tissues. Although the appearance of the mercerized fabrics after washing five times was better than that of non-mercerized fabrics and the yarns of the mercerized fabrics had shorter fibrils than non-mercerized fabrics, it has been shown that they were made on the fabric, ie on previously dried yarns Mercerization, among other things, leads to a deterioration of the textile data, especially the strength.

The invention was therefore based on the object of providing a process for the production of cellulosic yarns by spinning a solution of cellulose in a tertiary amine oxide, possibly also containing water and possibly a stabilizer, to give fibers or filaments, precipitation, washing and drying, with which the disadvantages described above are at least reduced.

This object is achieved in the process mentioned in that the yarns are treated with an aqueous alkaline solution for a period of less than 20 seconds before drying.

As further explained below, on the one hand, the method according to the invention can effectively reduce the fibrillization of Lyocell yarns. In addition, the process is time-saving and inexpensive because it can be integrated directly into the yarn manufacturing process itself can, and thus no separate treatment step is required for the textile fabrics made therefrom.

Treatment of the yarn with the aqueous alkaline solution increases the degree of whiteness of the yarn. This has the advantage that subsequent bleaching of the yarns is no longer necessary if they are to be used, for example, for the production of so-called "white goods" or if they are to be dyed in very light colors.

The treatment with the aqueous alkaline solution is preferably carried out over a period of 1 to 15 seconds, particularly preferably 1 to 10 seconds, in particular 2 to 6 seconds. An aqueous NaOH or KOH solution is preferably used. The concentration of alkali in the aqueous alkaline solution should be between 0.5 and 20% by weight, preferably between 10 and 14% by weight. The aqueous alkaline solution can contain further inorganic or organic auxiliaries, such as in particular emulsifiers, salts, glycerol or the like. The addition of such surface-active substances advantageously accelerates the wetting of the yarn and thus also of the filaments or fibers with the aqueous alkaline solution. In addition, the addition of salts, such as, for example, table salt, or glycerol reduces damage to the yarn surface by treatment with the aqueous alkaline solution.

A treatment temperature range of 0 to 60 ° C has proven to be favorable, with 20 to 60 ° C, in particular 40 to 60 ° C being preferred.

In addition to adhering to the short duration of treatment according to the invention, it is essential that the treatment with the aqueous alkaline solution takes place on yarns which have not previously been dried. The treatment is therefore preferably carried out after washing the yarn. It is also possible to carry out the treatment with the aqueous alkaline solution before washing, ie after precipitation, but it makes it more difficult to recover the tertiary amine oxide from the wash water, since the tertiary amine oxide and the alkaline solution get into the wash water during subsequent washing.

After treatment with the aqueous alkaline solution, the yarn should be neutralized in an aqueous acidic solution such as an acetic acid solution, washed again and then dried.

N-methylmorpholine-N-oxide (NMMO) is preferably used as the tertiary amine oxide as the solvent for the cellulose and the cellulose solution optionally contains propyl gallic acid as a stabilizer.

X-ray wide-angle scattering measurements with a diffractometer from STOE & CIE GmbH (45 kV, 40 mA, Cu Kμ) and a position-sensitive detector from the same company, the yarns examined being wound in parallel on frames and measured in transmission, showed that cellulosic Yarns made by spinning a water-containing solution of cellulose in NNMO and not treated with an aqueous alkaline solution, the equatorial reflections of the (1-10) and (020) peaks to a total peak without separately recognizable maxima for the overlay individual crystallographic directions.

Treatment with aqueous alkaline solution of yarns which have not yet dried (ie yarns according to the invention) and yarns which have already dried beforehand causes these peak maxima to be separated. The main reason for this effect is the increase in the crystal size LM_IO) - This crystal dimension in particular is influenced by treatment with an aqueous alkaline solution. For yarns not treated with the aqueous alkaline solution, L (i_i0) has values in the range from 3 to 4 nm. Treatment of the yarns with aqueous alkaline solution results in an increase in LΠ.IQ) by 50%.

It was found that the influence of the treatment with aqueous alkaline solution on the structural parameters accessible by means of wide-angle X-ray scattering is practically the same for yarns according to the invention and for previously dried yarns which were subsequently treated with the aqueous alkaline solution. It is therefore all the more surprising that the yarns according to the invention have a lower tendency to fibrillation and no decrease in strength compared to dried yarns which were subsequently aftertreated with aqueous alkaline solution.

Wet scrubbing equipment

The wet scrub test apparatus shown schematically in the figure is used to measure the tendency to fibrillation of the cellulosic yarns. The wet abrasion test apparatus essentially consists of the elements identified by the reference numbers 1 to 6, which are described in more detail below. The yarn 2 is fixed in a PVC block 1. The scrubbing load is generated in that the yarn 2 is guided over a rotating glass rod 5 with a diameter of 6 mm, to which a ceramic rod 4 with a diameter of 2.5 mm is attached. The glass rod 5 is arranged at a distance of 80 mm from the PVC block 1. The glass rod 5 and with it the ceramic rod 4 rotate at a speed of 25 revolutions per minute. The yarn 2, tightened by a weight 6 of 3 g, is kept wet by dropping water 3. The distance of the weight 6 to the glass rod 5 is 60 mm. The wet scrub test was carried out for one or two minutes in the examples below. The defined and reproducible filament produced with the apparatus was evaluated on a scale with the marks 1 to 6 by microscopic evaluation of the scrubbed yarn area.

To assess the fibrillation caused by scrubbing, it is useful to introduce the terms primary and secondary fibrillation:

Primary fibrillation means that fibrils are only observed on the fiber surface.

Secondary fibrillation means that the fibrils are also observed in the deeper layers of the filaments. The more secondary fibrillation progresses, the longer and thicker the fibrils become.

A grade scale from 1 to 6 was defined using the terms just described. The means

Grade 1 no fibrils

Grade 2 weak primary fibrillation

Grade 3 strong primary fibrillation

Grade 4 weak secondary fibrillation

Grade 5 strong secondary fibrillation

Grade 6 the damage to the entire fiber surface

Primary and secondary fibrillation, such as those on untreated

Yarn is observed.

For each of the following examples, the wet abrasion test was carried out five times and an average grade was calculated. Examples

For the examples listed below, 50 fibers or filaments were spun from a solution of cellulose in NMMO and water. After passing through an air gap, the precipitation took place in a water bath. The filaments were combined into a yarn (75 dtex, f 50) and washed. The yarns were treated with aqueous alkaline solution in a bath with NaOH solution. The following tables show the further test conditions, such as the condition of the yarns - dried (dried) or not dried (dried) - concentration C of the alkaline solution in% by weight, temperature T of the bath in ° C and Residence time t in the bath is given in s. The fibrillation behavior of the samples was tested and assessed as described above. For the determination of the fibrillization, wet abrasion tests were carried out over 1 and 2 min. carried out. The tables show the mean fibrillation grades (grade) of five series of measurements.

example 1

In experiment 1, a dried yarn was subjected to the wet scrub test, which was not subjected to any treatment with aqueous NaOH. This yarn showed for 1 min after running the test. the average fibrillation grade 5 and after the test over 2 min. the grade 6. Yarns which had already dried (experiments 2 to 6) and not yet dried, so-called initially moist yarns (experiments 7 to 11) were immersed in a bath with aqueous NaOH and then neutralized in a bath with 60% acetic acid, washed and dried at room temperature. The experimental data are summarized in Table 1. Table 1:

Vers. Condition C / wt.% T / ° C t / s Note

No. 1 min. 2 min

1 dr. unhindered - _ 5 6

2 drops 12.0 60 2 5 6

3 drops 12.0 60 5 5 6

4 dr. 12.0 60 10 4 5

5 dr. 12.0 60 30 3 6

6 dr. 12.0 60 600 2 4

7 n. 12.0 60 2 3 5

8 n. 12.0 60 5 2 3

9 n. 12.0 60 10 2 3

10 n. 12.0 60 30 2 3

11 n. 12.0 60 600 2 3

The data in Table 1 show that the fibrillation behavior of already dried yarns which were immersed in a bath with 12% NaOH solution at a temperature of 60 ° C. at treatment times of 2 or 5 s compared to an untreated yarn (Experiment 1, Table 1) not improved. Initial moist yarns, on the other hand, show a significant reduction in fibrillation after just 2 s in the bath under the same conditions. In the case of previously dried yarns, an improved fibrillation can be achieved with longer dwell times (from about 30 s), but not to the extent that it is achieved with initially moist yarns during a treatment with a short treatment time according to the invention.

Example 2

In order to determine the weight loss of the yarns due to the solubility of the cellulose in the aqueous alkaline solution due to the treatment, dried yarns were treated with NaOH solution and neutralized with acetic acid, washed with water and dried under vacuum at 65 ° C. overnight. The Weight loss of the yarns was determined by weighing before and after the treatment. Since the untreated yarn contained some moisture before the treatment, it was subjected to the same drying conditions as the treated yarns. The weight loss of the untreated yarn due to moisture loss was 4.6% by weight. This moisture loss was taken into account when determining the total weight loss of the yarns treated with NaOH solution. The respective treatment conditions and the weight loss attributable to the treatment with the NaOH solution are summarized in Table 2.

Table 2:

Vers. C / wt.% T / ° C t / s weight loss /

No.%

1 7.0 22 5 -0.5

2 7.0 22 10 -0.9

3 7.0 22 40 -3.9

4 7.0 22 60 -4.2

5 7.0 60 5 -0.4

6 7.0 60 10 -1.0

7 7.0 60 40 -1.9

8 7.0 60 60 -2.4

9 9.0 22 2 -1.1

10 9.0 22 5 -2.5

11 9.0 22 10 -3.6

12 9.0 22 40 -7.6

13 9.0 22 60 -8.6

14 9.0 60 5 -1.4

15 9.0 60 10 -2.4

16 9.0 60 40 -2.7

17 9.0 60 60 -2.9

18 11.0 22 5 -1.8

19 11.0 22 10 -2.8

20 11.0 22 40 -4.4

21 11.0 22 60 -4.5

22 11.0 60 5 -1.2

23 11.0 60 10 -2.3

24 11.0 60 40 -3.4

25 11.0 60 60 -3.5

26 12.0 22 2 -0.6

27 12.0 22 5 -1.0

28 12.0 22 10 -2.0

29 12.0 22 40 -2.8

30 12.0 22 60 -3.2

31 12.0 60 5 -0.4

32 12.0 60 10 -1.6

33 12.0 60 40 -2.6

34 12.0 60 60 -2.6

The experiments according to Table 2 show that the weight loss due to the solubility of the cellulose in the NaOH solution is lower at a higher temperature (60 ° C.) than at a lower temperature (22 ° C.) and increases with the duration of the treatment. The weight loss also depends on the NaOH concentration. In the tests listed in Table 2, the highest weight loss was - 8.6% by weight at a concentration of 9% by weight, a temperature of 22 ° C. and a treatment time of 60 s (test no. 13, table 2).

A high weight loss is disadvantageous from an economic point of view and moreover makes it very difficult to recover the alkaline solution if it is to be used again in the process after cleaning. The dissolved cellulose concentrates in the aqueous alkaline solution over time. As such, the separation of dissolved cellulose from the aqueous alkaline solution is difficult. Removing the dissolved cellulose, for example by centrifuging or filtration, is in any case associated with higher costs and with losses of alkaline solution, so that as little weight loss as possible should be aimed for, so that as little cellulose as possible is dissolved in the aqueous alkaline solution.

In addition, the weight loss also affects the yarn properties and leads to filament or fiber breaks and lint formation, which in turn negatively affects the processability of the yarns and leads to a reduction in quality.

Even initially moist yarns should experience weight loss when treated with NaOH solution. It is clear, however, that with the method according to the invention with short treatment times, the weight loss of the yarns is considerably less than with treatments over periods of 40 or 60 s, and at the same time significantly better fibrillation notes are achieved than with the treatment of dry fibers. Example 3

A number of non-dried yarn was immersed for 10 s in NaOH solution and then acidified with 60% acetic acid neutra _¬ lisiert, washed with water and dried at room temperature ge. The NaOH concentrations, the treatment temperature and the fibrillation behavior of the treated samples are summarized in Table 3.

Table 3:

Vers. Condition C / wt.% / ° C t / s Nc »te

No. 1 min. 2 min

1 n. 0.5 22 10 3 6

2 n. 0.5 60 10 4 6

3 n. 1.0 22 10 3 6

4 n. 1.0 60 10 4 6

5 n. 3.0 22 10 3 6

6 n. 3.0 60 10 2 5

7 n. 5.0 22 10 2 6

8 n. 5.0 60 10 2 5

9 n. 7.0 22 10 2 5

10 n. 7.0 60 10 2 4

11 n. 10.0 22 10 2 4

12 n. 10.0 60 10 2 3

13 n. 12.0 22 10 2 3

14 n. 12.0 60 10 2 3

15 n. 15.0 22 10 2 4

16 n. 15.0 60 10 2 4

17 n. 20.0 22 10 3 5

18 n. 20.0 60 10 2 5

The experiments according to Table 3 show that even at a low NaOH concentration in initially moist yarns an improvement in. _~ Fibril _. lization is achieved. With a treatment duration of 10 s, however, the best fibrillation scores result at concentrations in the range from 10 to about 15% by weight. At a concentration of 20% by weight Fibrillation grade, in particular that resulting from the wet scrub test over 2 min. resulted, again worse, so that within the scope of the present invention, concentrations in the range from 10 to 14% by weight are preferred.

Example 4

While in Examples 1 to 3, the yarns were immersed in a bath with aqueous NaOH for a certain time and thus subjected to the treatment with the aqueous alkaline solution without tension, in Example 4, dried yarns (Trial Nos. 1 to 4) and before yarns which have not yet dried (Trial Nos. 5 to 13) are continuously drawn through a bath with aqueous NaOH. In contrast to Examples 1 to 3, the treatment according to Example 4 was therefore not stress-free, but in such a way that the yarn was under a tensile stress of the order of 2 to 10 cN. However, the tensile stress should not exceed 10 cN if possible, since otherwise the yarn could be stretched, which in turn would reduce the desired effect of reducing fibrillation.

This treatment method is particularly favorable since it allows the yarn treatment according to the invention to be integrated directly into the production process, ie the yarns are passed continuously in the process through the NaOH bath with subsequent baths for neutralization and washing, and ultimately dried and wound up. In order to carry out comparative experiments 1 to 4, yarns were produced by the customary process, ie precipitation, washing, drying and winding, and then pulled through the NaOH bath from the spool. Both for the initial damp ten and for the dried yarns, the residence time in the bath was 4 s. The neutralization took place in a bath with 60% acetic acid. The yarns were then washed and dried at 180 ° C. The results of these tests are summarized in Table 4.

Table 4:

Vers. Condition C / wt.% T / ° C t / s Note

No. 1 min. 2 min

1 dr. 10.0 22 4 6 _

2 drops 10.0 60 4 6 -

3 drops 12.0 22 4 6 -

4 dr. 12.0 60 4 6 -

5 n. 10.0 22 4 2 4

6 n. 10.0 40 4 1 3

7 n. 10.0 60 4 2 3

8 n. 11.0 22 4 2 3

9 n. 11.0 40 4 3 4

10 n. 11.0 60 4 3 4

11 n. 12.0 22 4 3 4

12 n. 12.0 40 4 3 4

13 n. 12.0 60 4 3 4

The experiments shown in Table 4 show that even in this continuous process, the treatment of undried yarns according to the invention leads to a reduction in fibrillization. No improvement could be achieved with a treatment of previously dried yarns, and regardless of the concentration and the treatment temperature, the fibrillation grade 6 always resulted.

Tables 5 and 6 show textile data of yarns produced according to the invention (Table 5) and of comparison yarns (Table 6). Treatment with the aqueous alkaline solution was carried out continuously, as described in Example 4.

Table 5:

Vers. C / wt.% T / ° C t / s elongation strength modulus 5% No.% cN / tex cN / tex

1 22 4 8.0 35 27 2 7.0 22 4 9.0 37 26 3 7.0 60 4 7.5 33 26

4 10.0 22 4 7.3 34 28 5 10.0 60 4 6.7 33 28

12.0 22 4 7.7 35 27 12.0 60 4 7.8 36 28

As a comparative example, a yarn is listed in Experiment No. 1 in Table 5, which was passed through a water bath at 22 ° C. instead of through a bath with aqueous NaOH. From experiments 2 to 7 it is clear that the textile data of the yarns produced according to the invention show no noteworthy changes. In particular, the strength is not reduced by the method according to the invention.

Table: 6:

Vers. C / wt.% T / ° C t / s elongation strength modulus 5%

% CN / tex cN / tex

1 - 22 4 5.8 34 31

2 10.0 22 4 5.6 30 28

3 10.0 60 4 6.3 31 27

4 12.0 22 4 5.8 31 28

5 12.0 60 4 5.9 29 26

In Comparative Example 1 of Table 6, dried yarns were passed through a water bath at 22 ° C. beforehand. Based on experiments 2 to 5 of table 6 clearly that the treatment with aqueous NaOH of dried yarns leads to lower strength and a lower modulus at 5% elongation. The yarns produced according to the invention (Table 5) are thus not only distinguished by a lower fibrillation, but also by almost unchanged textile data.

Claims

Process for the production of a cellulose yarnAkzo Nobel nv, Arnhem * * Claims:

1. A process for the production of a cellulosic yarn by spinning a solution of cellulose in a tertiary amine oxide, optionally containing water and possibly a stabilizer, into fibers or filaments, precipitation, washing and drying, characterized in that the yarns are dried with a aqueous alkaline solution for less than 20 seconds.

2. The method according to claim 1, characterized in that the treatment with the aqueous alkaline solution over a period of 1 to 10, preferably 2 to 6 seconds.

3. The method according to claim 1 or 2, characterized in that a NaOH or KOH solution is used as the aqueous alkaline solution.

4. The method according to claim 1, 2 or 3, characterized

... shows that the concentration of alkali in the aqueous alkaline solution is between 0.5 and 20% by weight, preferably between 10 and 14% by weight.

5. The method according to one or more of claims 1 to 4, characterized in that the aqueous alkaline solution contains further inorganic or organic auxiliaries.

6. The method according to claim 5, characterized in that emulsifiers, salts or glycerol are used as auxiliaries.

7. The method according to one or more of claims 1 to 6, characterized in that the treatment is carried out at a temperature of 0 to 60 ° C, preferably 20 to 60 ° C.

8. The method according to one or more of claims 1 to 7, characterized in that the treatment with the aqueous alkaline solution is carried out after washing the yarns.

9. The method according to one or more of claims 1 to 8, characterized in that the yarns are neutralized after the treatment with the aqueous alkaline solution in an aqueous acidic solution, washed and then dried.

10. The method according to one or more of claims 1 to 9, characterized in that N-methylmorpholine-N-oxide is used as the tertiary amine oxide.