EP1224343A1 - Procede de production de corps faconnes en cellulose - Google Patents

Procede de production de corps faconnes en cellulose

Info

Publication number
EP1224343A1
EP1224343A1 EP00978960A EP00978960A EP1224343A1 EP 1224343 A1 EP1224343 A1 EP 1224343A1 EP 00978960 A EP00978960 A EP 00978960A EP 00978960 A EP00978960 A EP 00978960A EP 1224343 A1 EP1224343 A1 EP 1224343A1
Authority
EP
European Patent Office
Prior art keywords
cellulose
bleached
carboxyl group
group content
range
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP00978960A
Other languages
German (de)
English (en)
Other versions
EP1224343B1 (fr
Inventor
Ralf-Uwe Bauer
Uwe Kind
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
LL Plant Engineering AG
Original Assignee
Alceru Schwarza GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Alceru Schwarza GmbH filed Critical Alceru Schwarza GmbH
Publication of EP1224343A1 publication Critical patent/EP1224343A1/fr
Application granted granted Critical
Publication of EP1224343B1 publication Critical patent/EP1224343B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F2/00Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof

Definitions

  • the invention relates to a process for the production of cellulose moldings, such as fibers, filaments or foils, from TCF or ECF bleached cellulose, in which the bleached cellulose is dissolved in an aqueous tertiary amine oxide to form a formable cellulose solution, the cellulose solution is deformed and by Coagulation of the deformed solution forms the shaped body.
  • the invention further relates to the use of a TCF or ECF bleached cellulose for the production of cellulose moldings.
  • the object of the present invention is to create a process for the production of cellulose moldings with reduced cellulose degradation starting from TCF or ECF bleached cellulose.
  • the reduction in cellulose breakdown should be achieved essentially without special measures in the Lyocell process. Further advantages of the invention result from the following description.
  • Pulp and fiber whiteness levels of different pulp provenances were determined, which were either ECF or TCF bleached.
  • the whiteness of the pulp was determined in accordance with DIN 53145, part 2.
  • the whiteness of the fiber was determined by the method described in WO 97/23666, page 6.
  • the average degree of polymerization of the pulps by the Cuoxam method was about 550.
  • the degrees of whiteness measured on the pulp and fiber are summarized in Table 1. Table 1
  • the above-mentioned object is therefore achieved according to the invention in the method mentioned at the outset by reducing of cellulose degradation in the process, a TCF-bleached pulp with a carboxyl group content in the range of 1 to 35 ⁇ mol / g or an ECF-bleached pulp with a carboxyl group content in the range of 1 to 50 ⁇ mol / g is used. It has been shown that the lower the carboxyl group content of the pulp used, the more the cellulose degradation is kept behind in the course of the production and processing of the extrusion solution.
  • TCF and ECF bleached pulps are used in the spinning solution production, the carboxyl group content of which lies in the ranges mentioned. Pulp with the carboxyl group contents mentioned can be produced by various pulp manufacturers.
  • the reduced degradation of the spinning solution components also results in fewer coloring constituents, so that the whiteness of the shaped bodies formed is also improved secondarily.
  • a TCF-bleached cellulose with a carboxyl group content in the range from 15 to 30 ⁇ mol / g or an ECF-bleached cellulose with an arboxyl group content in the range from 25 to 35 ⁇ mol / g is preferably used in the dissolving stage.
  • the carboxyl group content of the cellulose to be used can be determined according to Döring, see K. Goetze, man-made fibers according to the viscose method, 2nd vol. 3rd edition, 1997, p. 1079.
  • NMMO-MH N-methyl 'lmorpholin-N-oxide monohydrate
  • a cellulose solution containing alkali or organic compounds can be formed, the latter containing at least four carbon atoms, at least two conjugated double bonds and at least two substituents -XH, where X is 0 or NR and R can be hydrogen or an alkyl group of 1 to 4 carbon atoms.
  • the low degradation achieved according to the invention can be reduced even further by these solution additives.
  • the amount of the organic compound may be in the range of 0.01 to 0.5% by mass based on the amount of the solvent. Suitable organic compounds are known from EP-A-0047 929. A commonly used compound is isopropyl gallate.
  • the process according to the invention limits cellulose degradation to a proportion in the range from 3 to 20% by mass, based on the pulp used.
  • the cellulose fraction degraded is preferably in the range from 8 to 15% by mass.
  • the invention further relates to the use of a TCF-bleached cellulose or an ECF-bleached cellulose with a carboxyl group content in the range of 1 to 35 ⁇ mol / g or 1 to 50 ⁇ mol / g for the formation of a cellulose solution in a solvent containing tertiary amine oxide for the Production of moldings using the Lyocell process.
  • the use of these pulps not only reduces the degradation in the course of the lyocell process, but also increases the whiteness of the shaped bodies formed.
  • Long fiber sulfite pulp was bleached in a known manner by alkaline, peroxide-enhanced oxygen extraction, then with ozone and with peroxide.
  • the bleaching methods are described, for example, in RP Singh, The Bleaching of Pulp, TAPPI Press, Atlanta, USA. Three different carboxyl group contents were set (Examples 1 to 3). Three more samples of the pulp were bleached with hypochlorite. The degree of polymerization and the initial degree of whiteness of the pulps were determined according to the above-mentioned methods, and the carboxyl and carbonyl group content of the pulp. Spinning solutions with 13% cellulose, 10.5% water and 76.5% NMMO were produced in a known manner from the bleached cellulose.
  • the solutions were spun using the dry-wet process at 95 ° C. with a nozzle with a hole diameter of 65 ⁇ m.
  • the degree of polymerization and the degree of whiteness were determined on the fibers obtained.
  • the degree of polymerization was determined by the Cuoxam method, the degree of fiber whiteness by the method given above. The numerical values determined are given in Table 2.
  • the degree of polymerization, the carboxal group content and the carbonyl group content and the starting whiteness were determined on four bleached dissolving pulps.
  • Four spinning solutions with 13% cellulose, 10.5% water and 76.5% NMMO were produced from the cellulose.
  • the zero shear viscosity was measured at 85 ° C on the spinning masses (Haake RS 75, year of construction 1998).
  • the spinning solutions were spun at 95 ° C. with a nozzle with a hole diameter of 65 ⁇ m by the usual dry-wet method.
  • the degree of polymerization of the cellulose was determined on the spinning solution and the degree of whiteness on the fibers. The results are summarized in Table 3.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Artificial Filaments (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Paper (AREA)
EP00978960A 1999-10-07 2000-09-29 Procede de production de corps faconnes en cellulose Expired - Lifetime EP1224343B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19948401 1999-10-07
DE19948401A DE19948401C1 (de) 1999-10-07 1999-10-07 Verfahren zur Herstellung von Cellulose-Formkörpern
PCT/DE2000/003408 WO2001025515A1 (fr) 1999-10-07 2000-09-29 Procede de production de corps façonnes en cellulose

Publications (2)

Publication Number Publication Date
EP1224343A1 true EP1224343A1 (fr) 2002-07-24
EP1224343B1 EP1224343B1 (fr) 2006-02-01

Family

ID=7924866

Family Applications (1)

Application Number Title Priority Date Filing Date
EP00978960A Expired - Lifetime EP1224343B1 (fr) 1999-10-07 2000-09-29 Procede de production de corps faconnes en cellulose

Country Status (15)

Country Link
US (1) US7175792B1 (fr)
EP (1) EP1224343B1 (fr)
KR (1) KR100661454B1 (fr)
CN (1) CN1180141C (fr)
AT (1) ATE317027T1 (fr)
AU (1) AU1645601A (fr)
BR (1) BR0014529B1 (fr)
CA (1) CA2385227A1 (fr)
DE (2) DE19948401C1 (fr)
EA (1) EA200200382A1 (fr)
MY (1) MY129236A (fr)
NO (1) NO20021588D0 (fr)
TW (1) TW522178B (fr)
WO (1) WO2001025515A1 (fr)
ZA (1) ZA200203556B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100359050C (zh) * 2004-11-16 2008-01-02 唐山三友集团化纤有限公司 高白强力细旦粘胶短纤维及其生产工艺
CN101649061B (zh) * 2009-07-13 2012-06-27 潍坊恒联玻璃纸有限公司 一种航空仪表盘专用纤维素膜的制备方法
DE102015103187A1 (de) * 2014-03-11 2015-09-17 Smartpolymer Gmbh Schwer entflammbare Cellulose-Formkörper, hergestellt nach einem Direktlöseverfahren

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3034685C2 (de) * 1980-09-13 1984-07-05 Akzo Gmbh, 5600 Wuppertal Cellulose-Form- und Spinnmasse mit geringen Anteilen an niedermolekularen Abbauprodukten
US4480089A (en) * 1983-06-14 1984-10-30 Purdue Research Foundation Modified cellulose products by bleaching
DD218104B5 (de) * 1983-10-17 1996-06-13 Thueringisches Inst Textil Verfahren zur Herstellung thermisch stabiler Cellulose-Aminoxidloesungen
DE4308524C1 (de) * 1992-06-16 1994-09-22 Thueringisches Inst Textil Verfahren zur Herstellung von Cellulosefasern und -filamenten nach dem Trocken-Naßextrusionsverfahren
DE4219658C3 (de) * 1992-06-16 2001-06-13 Ostthueringische Materialpruef Verfahren zur Herstellung von Cellulosefasern -filamenten und -folien nach dem Trocken-Naßextrusionsverfahren
DE4441468C2 (de) * 1994-11-22 2000-02-10 Ostthueringische Materialpruef Verfahren zur Herstellung einer homogenen Lösung von Cellulose in wasserhaltigem N-Methylmorpholin-N-oxid
AT402827B (de) * 1995-12-22 1997-09-25 Chemiefaser Lenzing Ag Celluloseformkörper und verfahren zu seiner herstellung
WO2000050462A1 (fr) * 1999-02-24 2000-08-31 Sca Hygiene Products Gmbh Materiaux fibreux a base de cellulose oxydes et produits a base de ces materiaux
US6524348B1 (en) * 1999-03-19 2003-02-25 Weyerhaeuser Company Method of making carboxylated cellulose fibers and products of the method
DE19953591A1 (de) * 1999-11-08 2001-05-17 Sca Hygiene Prod Gmbh Metallvernetzbare oxidierte cellulosehaltige Faserstoffe und daraus hergestellte Produkte
US20030051834A1 (en) * 2001-06-06 2003-03-20 Weerawarna S. Ananda Method for preparation of stabilized carboxylated cellulose
US7052540B2 (en) * 2004-03-11 2006-05-30 Eastman Chemical Company Aqueous dispersions of carboxylated cellulose esters, and methods of making them

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0125515A1 *

Also Published As

Publication number Publication date
NO20021588L (no) 2002-04-04
CN1377428A (zh) 2002-10-30
AU1645601A (en) 2001-05-10
NO20021588D0 (no) 2002-04-04
DE19948401C1 (de) 2001-05-03
WO2001025515A1 (fr) 2001-04-12
CN1180141C (zh) 2004-12-15
KR20020037378A (ko) 2002-05-18
US7175792B1 (en) 2007-02-13
KR100661454B1 (ko) 2006-12-27
DE50012169D1 (de) 2006-04-13
ATE317027T1 (de) 2006-02-15
MY129236A (en) 2007-03-30
ZA200203556B (en) 2003-02-26
EP1224343B1 (fr) 2006-02-01
BR0014529A (pt) 2002-08-27
TW522178B (en) 2003-03-01
BR0014529B1 (pt) 2011-08-09
EA200200382A1 (ru) 2002-10-31
CA2385227A1 (fr) 2001-04-12

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