GB1283065A - Aromatic polyamide fibers - Google Patents

Aromatic polyamide fibers

Info

Publication number
GB1283065A
GB1283065A GB4939571A GB4939571A GB1283065A GB 1283065 A GB1283065 A GB 1283065A GB 4939571 A GB4939571 A GB 4939571A GB 4939571 A GB4939571 A GB 4939571A GB 1283065 A GB1283065 A GB 1283065A
Authority
GB
United Kingdom
Prior art keywords
fibres
gpd
water
sec
fibre
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.)
Expired
Application number
GB4939571A
Inventor
Stephanie Louise Kwolek
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority claimed from GB2977269A external-priority patent/GB1283064A/en
Publication of GB1283065A publication Critical patent/GB1283065A/en
Expired 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
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/58Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/60Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
    • D01F6/605Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides from aromatic polyamides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/10Polyamides derived from aromatically bound amino and carboxyl groups of amino-carboxylic acids or of polyamines and polycarboxylic acids

Abstract

1283065 Aromatic polyamide fibres E I DU PONT DE NEMOURS & CO 12 June 1969 [12 June 1968] 49395/71 Divided out of 1283064 Heading B5B] A fibre comprises polymer consisting essentially of at least one type of carbocyclic wholly aromatic homo- or copolyamide whose bonds linking each aromatic nucleus are coaxial or parallel and oppositely directed, said fibre being characterized by an orientation angle of less than 45 degrees, preferably less than 35 degrees and desirably less than 25 degrees, and an initial modulus of at least 192 gpd., preferably at least 200 gpd. and especially at least 300 gpd. Such fibres may also be characterized by a sonic velocity of at least 4À0 km./sec., preferably at least 6À0 km./sec. and especially at least 7À0 km./sec., a tenacity of at least 5 gpd., an initial modulus of at least 400 gpd, an elongation, in the as-extruded state, of at least 5%. In such fibres about 77% of the crystallites may be aligned within one half of the orientation angle. Such fibres may be made by spinning an anisotropic dope as disclosed in Specifications 1,283,064 and 1,283,066 and optionally heatsetting the fibres so made. A preferred heattreated fibre so made has a sonic velocity of at least 4.0 km./sec., especially at least 7À0 km/sec., an orientation angle of less than 25 degrees and an initial modulus of at least 400 gpd. The optically anisotropic dope of Specification 1,283,064 comprises (I) a carbocyclic wholly aromatic homo- or co-polyamide wherein at least 90% of the bonds linking each aromatic undens are coaxial or parallel and oppositely extended and (II) a liquid medium comprising at least one of concentrated sulphuric acid, oleum, HF, chloro- or fluoro-sulphonic acid or methane sulphonic acid, the concentration of (I) being above the "critical concentration point" (C.C.P.) at which there is a sharp discontinuity, in the viscosity v. concentration curve. The dope may also include solvation additives, e.g. Na 2 HPO 4 , Na 2 SO 4 or CH 3 COOK with sulphuric acid or oleum, NaF, KF or CH 2 Cl 2 with HF, or LiCl with sulphonic acids, dyes, fillers, delusterants, U-V. stabilizers or antioxidants. The optically anisotropic dope of Specification 1,283,066 comprises a polyamide as in (I), having an inherent viscosity of at least 0À7 as determined in sulphuric acid at 30‹ C., (II) a liquid medium comprising at least one of N,N- dimethylacet-, propion- or butyr-amide; N,N - dimethylmethoxyacetamide; N,N- diethylacetamide; N - methyl pyrrolidone, -piperidone or -caprolactam; N - ethyl pyrrolidone; N - acetyl - pyrrolidine or - piperidine; N,N<SP>1</SP> - dimethyl - ethylene or -propylene urea; N,N,N<SP>1</SP>,N<SP>1</SP>-tetramethyl urea; and hexamethyl phosphoramide and (III) LiCl, CaCl 2 or HCl, the concentration of (I) being above the C.C.P. Component (III) may be formed in situ, e.g. by using Li 2 CO 3 to neutralize HCl formed during polymer preparation. The dope may also contain dyes, fillers, delusterants, U-V-stabilizers and antioxidants. Alternative techniques to "C.C.P." for determining anisotropy are described in both Specifications 1,283,064 and 1,283,066. Other polyamides useful in the making of the fibres of the invention may be made by the reaction of pphenylene diamine or 2-chloro-p-phenylene diamine with polyamide-forming derivatives of terephthalic acid by a low temperature polymerization procedure. Conventional wet- or dry-spinning techniques are used. In wet-spinning, specified coagulants include water, ethylene glycol, glycerol, mixtures of water, methanol and an amide or urea solvent, mixtures of water and alcohols and aqueous salt baths, suitably at from -20‹ to +90‹ C. After wind-up, the fibres may be soaked, on the bobbins, in water or mixtures of water and water-miscible inert organic liquids, e.g. acetone, ethyl alcohol, glycerol, N,N,N<SP>1</SP>,N<SP>1</SP> - tetramethyl urea, or N,N- dimethylacetamide, to remove residual amide liquid and salt or acidic solvents followed by drying. Alternatively, removal of such residues may be effected by continuous treatment of the running fibre, or by washing and soaking skeins, rather than bobbins. Dry-spun yarn may be strengthened by washing with a small amount of water. As indicated above, fibres may possess the specified high tensile properties in the asextruded state, and require only washing and drying, or may require heat-treatment, which is suitably effected by heating the fibre, maintained in a taut state, or drawn in a nitrogen atmosphere at 300-1000‹ C., preferably 500- 600‹ C., for 0À1 sees. to 5 mins., preferably 0À1- 10 sees., or by using hot air ovens, hot liquid baths, or heated pins, plates or slots, using draw ratios up to 1À75, but generally of 1À04 to 1À16.
GB4939571A 1968-06-12 1969-06-12 Aromatic polyamide fibers Expired GB1283065A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US73641068A 1968-06-12 1968-06-12
GB2977269A GB1283064A (en) 1968-06-12 1969-06-12 Optically anisotropic dopes comprising wholly aromatic polyamides

Publications (1)

Publication Number Publication Date
GB1283065A true GB1283065A (en) 1972-07-26

Family

ID=26260073

Family Applications (2)

Application Number Title Priority Date Filing Date
GB581572A Expired GB1283066A (en) 1968-06-12 1969-06-12 Optically anisotropic dopes comprising wholly aromatic polyamides
GB4939571A Expired GB1283065A (en) 1968-06-12 1969-06-12 Aromatic polyamide fibers

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB581572A Expired GB1283066A (en) 1968-06-12 1969-06-12 Optically anisotropic dopes comprising wholly aromatic polyamides

Country Status (1)

Country Link
GB (2) GB1283066A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0246732A2 (en) * 1986-05-15 1987-11-25 Kolon Industries Inc. Process for preparing aromatic polyamide fibre and film
EP0260922A2 (en) * 1986-09-16 1988-03-23 E.I. Du Pont De Nemours And Company Aramid copolymer yarn
EP0316486A1 (en) * 1987-11-16 1989-05-24 Kolon Industries Inc. Process for preparing aromatic polyamide fibre and film
US5442003A (en) * 1992-05-28 1995-08-15 Sumitomo Chemical Company, Ltd. Para-aramid dope of low degree of polymerization, para-aramid fiber and para-aramid pulp produced therefrom and processes for producing the same

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL157327C (en) 1975-02-21 1984-05-16 Akzo Nv PROCESS FOR PREPARING POLY-P-PHENYLENE DEPHALAMIDE.
JPS5569649A (en) * 1978-11-21 1980-05-26 Teijin Ltd Aromatic polyamide composition

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0246732A2 (en) * 1986-05-15 1987-11-25 Kolon Industries Inc. Process for preparing aromatic polyamide fibre and film
EP0246732A3 (en) * 1986-05-15 1988-10-05 Kolon Industries Inc. Process for preparing aromatic polyamide fibre and film
EP0260922A2 (en) * 1986-09-16 1988-03-23 E.I. Du Pont De Nemours And Company Aramid copolymer yarn
EP0260922A3 (en) * 1986-09-16 1990-02-28 E.I. Du Pont De Nemours And Company Aramid copolymer yarn
EP0316486A1 (en) * 1987-11-16 1989-05-24 Kolon Industries Inc. Process for preparing aromatic polyamide fibre and film
US5442003A (en) * 1992-05-28 1995-08-15 Sumitomo Chemical Company, Ltd. Para-aramid dope of low degree of polymerization, para-aramid fiber and para-aramid pulp produced therefrom and processes for producing the same

Also Published As

Publication number Publication date
GB1283066A (en) 1972-07-26

Similar Documents

Publication Publication Date Title
EP0951590B1 (en) Wet spinning process for aramid polymer containing salts
US4162346A (en) High performance wholly aromatic polyamide fibers
GB1106190A (en) Novel process for spinning heat resistant polyamide fibers
US4698414A (en) Copoly(p-phenylene terephthalamide/2,6-naphthalamide)aramid yarn
CA2142279A1 (en) Improved process for post-spin finishing of polybenzoxazole fibers
US4758472A (en) High tenacity polyhexamethylene adipamide fiber
GB1283065A (en) Aromatic polyamide fibers
US5411638A (en) Treatment by plasma of an aramid monofilament and monofilament thus obtained
KR101561545B1 (en) Method of manufacturing copolymerized aramid fiber and copolymerized aramid fiber manufactured thereby
US5643518A (en) Process for preparing fibers of soluble wholly aromatic polyamides
US2965437A (en) Process for wet spinning plasticized elastomeric polymers and subsequently removing the plasticizer
US4658004A (en) Polyacrylonitrile fiber with high strength and high modulus of elasticity
US3216965A (en) Blend of a polyterephthalamide and a lower melting polyamide for improved dye receptivity
US4902774A (en) Poly(p-phenyleneterephthalamide) yarn of improved fatigue resistance
US20050093198A1 (en) Wet spinning process for aramid polymer containing salts
US3558763A (en) Process for treating wet spun filaments with shrinking agents
KR101587048B1 (en) Method of manufacturing copolymerized aramid fiber and copolymerized aramid fiber thereby
US3575941A (en) Ultrastable polymers of bbb type,articles such as fibers made therefrom,and high temperature process for forming such polymers and articles
KR100204317B1 (en) High strength, low shrinking polyester section fiber and that manufacture method
Preston et al. Fibers from aromatic copolyamides of limited order
KR910004708B1 (en) Aromatic polyamide fibers and production thereof
KR100469103B1 (en) Polyester industrial engineer with excellent form stability and its manufacturing method
KR800000068B1 (en) Method of preparing a polyester filament reinforced with rubber
KR960702019A (en) High Elongation PPD-T Fibers
JP2851017B2 (en) Method for producing high strength polyvinyl alcohol fiber with good dry heat aging property

Legal Events

Date Code Title Description
PS Patent sealed
PE20 Patent expired after termination of 20 years