Classifications

• • D—TEXTILES; PAPER
  • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
  • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
  • D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
  • D01F11/02—Chemical after-treatment of artificial filaments or the like during manufacture of cellulose, cellulose derivatives, or proteins
• • D—TEXTILES; PAPER
  • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
  • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
  • D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof

Definitions

• the invention relates to a method for producing cellulose fibers with a reduced tendency to fibrillation.
• a tertiary amine oxide in particular N-methylmorpholine-N-oxide (NMMO)
• NMMO N-methylmorpholine-N-oxide
• Fibrillation is understood to mean breaking open the wet fiber in the longitudinal direction under mechanical stress in the wet state, as a result of which the fiber is given a hairy, furry appearance.
• One made from these fibers and dyed fabric loses color intensity over the course of a few washes.
• the reason for the fibrillation is assumed to be that the fiber consists of fibrils arranged in the direction of the fibers, between which there is only a small amount of crosslinking.
• WO 92/14871 describes a method for producing a fiber with a reduced tendency to fibrillation. This is achieved in that all baths with which the freshly spun fiber comes into contact before the first drying have a pH of a maximum of 8.5.
• WO 92/07124 also describes a method for producing a fiber with a reduced tendency to fibrillation, according to which the freshly spun, that is to say not yet dried, fiber is treated with a cationic polymer.
• a polymer with imidazole and azetidine groups is mentioned as such a polymer.
• treatment with an emulsifiable polymer e.g. Polyethylene or polyvinyl acetate, or crosslinking with glyoxal.
• the object of the invention is to provide a method which can be carried out in a simple manner and which allows cellulose fibers of the Lyocell genus to be produced with a reduced tendency to fibrillation.
• the process according to the invention for the production of cellulose fibers with reduced tendency to fibrillation consists in that the freshly spun, not yet dried fibers are brought into contact with a textile auxiliary which carries at least two reactive groups and are washed with an aqueous buffer, with the proviso that as Auxiliary textile Glyoxal is not used.
• Dyes which have two reactive groups have proven particularly useful as textile auxiliaries.
• textile auxiliaries which are colorless, i.e. do not absorb visible light.
• Textile auxiliaries which carry one or two vinylsulfone groups as reactive groups are preferably used according to the invention.
• An expedient embodiment of the method according to the invention is characterized in that the freshly spun fibers are brought into contact with the textile auxiliary in an alkaline environment.
• Another preferred variant of the method according to the invention is that the fibers brought into contact with the textile auxiliary are heat-treated.
• the heat treatment drastically shortens the impregnation time.
• EP-A-0 538 977 published on April 28, 1993, describes a heat treatment of cellulose fibers impregnated with a dye.
• heating the fibers impregnated with the textile auxiliary with hot air can shorten the impregnation time, but there is a risk that the fibers will be heated irregularly.
• the outer fibers of a fiber bundle to be dried may already have partially dried, while the fibers inside have not yet reached the required temperature. This has an adverse effect on the quality of the fibers produced. It has been found that this disadvantage, which occurs in simple heat treatment, can be overcome if the fibers are irradiated with electromagnetic waves, in particular with microwaves.
• the fibers When irradiated with microwaves, the fibers are heated uniformly on the one hand, and on the other hand premature drying of the fibers can be prevented, since irradiation with electromagnetic waves offers the possibility of, for example, welding the fiber bundle into a plastic covering and exposing it to the electromagnetic field in the welded state .
• the invention further relates to a process for the production of cellulose fibers with reduced tendency to fibrillation, in which process a solution of cellulose in a tertiary amine oxide is spun into fibers and the freshly spun fibers are brought into contact with a textile auxiliary which carries at least two reactive groups and are heat-treated, which method is characterized in that the heat treatment is carried out by irradiation with electromagnetic waves.
• a textile auxiliary is preferably used which carries vinyl sulfone groups as reactive groups and is preferably a dye.
• textile auxiliaries can also be used are used that are colorless, i.e. do not absorb visible light.
• Another preferred embodiment of the method according to the invention is that the heat treatment is carried out by means of microwaves.
• the friction of the fibers against one another during washing processes or during finishing processes when wet was simulated by the following test: 8 fibers with a length of 20 mm were placed in a 20 ml sample vial with 4 ml of water and were held in a laboratory shaker of the type RO for 9 hours. 10 from Gerhardt, Bonn (FRG) shaken at level 12. The fibrillation behavior of the fibers was then assessed under the microscope by counting the number of fibrils per 0.276 mm fiber length.
• Fiber strength and fiber elongation were tested according to the BISFA regulation "Internationally agreed methods for testing viscose, modal, cupro, lyocell, acetate and triacetate staple fibers and tows", edition 1993.
• Fibers were treated with the dye Remazol Black B and Remazol Red RB as textile auxiliaries (manufacturer: Hoechst AG) in accordance with the process described above.
• the dye Remazol Black B carries two vinyl sulfone groups and the dye Remazol Red B carries a vinyl sulfone group and a monochlorotriazine group.
• the fleet contained 3% Remazol Black B and 0.5% Remazol Red RB.
• the pH of the liquor was 4.6 in each example.
• the aqueous buffer used was an aqueous solution containing 3% acetic acid and 7% sodium acetate. The pH of this solution was 4.6. After the treatment with the buffer, the fibers were washed with water for 15 minutes and then examined.
• Table la shows the fixing agent used in each case, the fibrillation (number of fibrils), the titer (dtex), the fiber strength (cN / tex) and the fiber elongation (%).
• Examples 1, 2 and 3 were carried out with the dye Remazol Black B and Example 4 with the dye Remazol Red RB.
• Table 1b shows the results of comparative tests which were carried out without dye.
• Remazol Black B and Remazol Red RB are therefore representative of other textile auxiliaries that also carry at least two reactive groups.
• Table 2 shows that heat treatment of the fibers impregnated with the textile auxiliary agent drastically reduces the impregnation time and that the tendency to fibrillation is nevertheless reduced.

Landscapes

• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Textile Engineering (AREA)
• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
• Artificial Filaments (AREA)
• Polysaccharides And Polysaccharide Derivatives (AREA)
• Chemical Treatment Of Fibers During Manufacturing Processes (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Applications Claiming Priority (3)

Publications (1)

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• 1994
  • 1994-04-06 TW TW083102969A patent/TW257811B/zh active
  • 1994-04-06 TR TR00308/94A patent/TR27503A/xx unknown
  • 1994-04-20 KR KR1019940704628A patent/KR0183419B1/ko not_active IP Right Cessation
  • 1994-04-20 HR HRA-787/93A patent/HRP940261A2/xx not_active Application Discontinuation
  • 1994-04-20 UA UA94129226A patent/UA32560C2/uk unknown
  • 1994-04-20 WO PCT/AT1994/000049 patent/WO1994024343A1/de not_active Application Discontinuation
  • 1994-04-20 BR BR9405150A patent/BR9405150A/pt not_active Application Discontinuation
  • 1994-04-20 NZ NZ263770A patent/NZ263770A/en unknown
  • 1994-04-20 EP EP94912409A patent/EP0647281A1/de not_active Withdrawn
  • 1994-04-20 JP JP6522531A patent/JP2753396B2/ja not_active Expired - Lifetime
  • 1994-04-20 DE DE4492198T patent/DE4492198D2/de not_active Expired - Fee Related
  • 1994-04-20 SK SK1529-94A patent/SK152994A3/sk unknown
  • 1994-04-20 CN CN94190217A patent/CN1041948C/zh not_active Expired - Fee Related
  • 1994-04-20 PL PL94306801A patent/PL176125B1/pl unknown
  • 1994-04-20 RU RU94046330A patent/RU2127775C1/ru active
  • 1994-04-20 CH CH387394A patent/CH685944A5/de not_active IP Right Cessation
  • 1994-04-20 GB GB9424722A patent/GB2284177B/en not_active Expired - Fee Related
  • 1994-04-20 CZ CZ943030A patent/CZ303094A3/cs unknown
  • 1994-04-20 HU HU9403717A patent/HU214882B/hu not_active IP Right Cessation
  • 1994-04-20 AU AU64992/94A patent/AU684274B2/en not_active Ceased
  • 1994-04-20 RO RO94-01951A patent/RO112768B1/ro unknown
  • 1994-04-20 CA CA002137232A patent/CA2137232A1/en not_active Abandoned
  • 1994-04-20 ZA ZA942727A patent/ZA942727B/xx unknown
  • 1994-07-11 MD MD94-0168A patent/MD906C2/ro active IP Right Grant
  • 1994-11-24 LV LVP-94-223A patent/LV11194B/lv unknown
  • 1994-12-02 BG BG99236A patent/BG63049B1/bg unknown
  • 1994-12-02 FI FI945695A patent/FI945695A/fi unknown

Non-Patent Citations (1)

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