JPH0257574B2 - - Google Patents

Info

Publication number: JPH0257574B2
Authority: JP; Japan
Prior art keywords: dope; formula; group; weight; polyamide
Prior art date: 1982-03-16
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

JP4027282A

Other languages

English (en)

Japanese (ja)

Other versions

JPS58163722A (ja

Inventor

Juji Yabuki

Takashi Fujiwara

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.)

Asahi Chemical Industry Co Ltd

Original Assignee

Asahi Chemical Industry Co Ltd

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.)

1982-03-16

Filing date

1982-03-16

Publication date

1990-12-05

1982-03-16 Application filed by Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd

1982-03-16 Priority to JP4027282A priority Critical patent/JPS58163722A/ja

1983-09-28 Publication of JPS58163722A publication Critical patent/JPS58163722A/ja

1990-12-05 Publication of JPH0257574B2 publication Critical patent/JPH0257574B2/ja

Status Granted legal-status Critical Current

Links

239000000835 fiber Substances 0.000 claims description 47
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 45
239000004952 Polyamide Substances 0.000 claims description 34
229920002647 polyamide Polymers 0.000 claims description 34
229920000642 polymer Polymers 0.000 claims description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
239000003063 flame retardant Substances 0.000 claims description 9
238000000465 moulding Methods 0.000 claims description 9
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 8
125000000751 azo group Chemical group [*]N=N[*] 0.000 claims description 4
125000005337 azoxy group Chemical group [N+]([O-])(=N*)* 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims description 4
238000000034 method Methods 0.000 description 24
-1 halogen halogenated aromatic sulfonic acids Chemical class 0.000 description 13
125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 10
239000002904 solvent Substances 0.000 description 10
230000001112 coagulating effect Effects 0.000 description 9
239000000203 mixture Substances 0.000 description 9
229920003366 poly(p-phenylene terephthalamide) Polymers 0.000 description 9
238000009987 spinning Methods 0.000 description 8
230000003287 optical effect Effects 0.000 description 7
230000000052 comparative effect Effects 0.000 description 6
XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 5
125000005407 trans-1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])[C@]([H])([*:2])C([H])([H])C([H])([H])[C@@]1([H])[*:1] 0.000 description 5
230000015271 coagulation Effects 0.000 description 4
238000005345 coagulation Methods 0.000 description 4
230000000704 physical effect Effects 0.000 description 4
125000004959 2,6-naphthylene group Chemical group [H]C1=C([H])C2=C([H])C([*:1])=C([H])C([H])=C2C([H])=C1[*:2] 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
239000000654 additive Substances 0.000 description 3
239000004760 aramid Substances 0.000 description 3
229920003235 aromatic polyamide Polymers 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
125000005677 ethinylene group Chemical group [*:2]C#C[*:1] 0.000 description 3
UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 3
239000007788 liquid Substances 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
238000007872 degassing Methods 0.000 description 2
238000004090 dissolution Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000012779 reinforcing material Substances 0.000 description 2
239000005060 rubber Substances 0.000 description 2
MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 2
238000005406 washing Methods 0.000 description 2
238000002166 wet spinning Methods 0.000 description 2
125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 1
ODNBVEIAQAZNNM-UHFFFAOYSA-N 1-(6-chloroimidazo[1,2-b]pyridazin-3-yl)ethanone Chemical compound C1=CC(Cl)=NN2C(C(=O)C)=CN=C21 ODNBVEIAQAZNNM-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
229910021630 Antimony pentafluoride Inorganic materials 0.000 description 1
GUNJVIDCYZYFGV-UHFFFAOYSA-K Antimony trifluoride Inorganic materials F[Sb](F)F GUNJVIDCYZYFGV-UHFFFAOYSA-K 0.000 description 1
229910015900 BF3 Inorganic materials 0.000 description 1
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
229920002430 Fibre-reinforced plastic Polymers 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
230000006750 UV protection Effects 0.000 description 1
239000012963 UV stabilizer Substances 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
150000001243 acetic acids Chemical class 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000005233 alkylalcohol group Chemical group 0.000 description 1
150000001408 amides Chemical group 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
VBVBHWZYQGJZLR-UHFFFAOYSA-I antimony pentafluoride Chemical compound F[Sb](F)(F)(F)F VBVBHWZYQGJZLR-UHFFFAOYSA-I 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
239000001110 calcium chloride Substances 0.000 description 1
229910001628 calcium chloride Inorganic materials 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000013329 compounding Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
239000000975 dye Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000011151 fibre-reinforced plastic Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
239000012760 heat stabilizer Substances 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
229920006017 homo-polyamide Polymers 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004973 liquid crystal related substance Substances 0.000 description 1
239000006224 matting agent Substances 0.000 description 1
239000012528 membrane Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000000178 monomer Substances 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
150000003018 phosphorus compounds Chemical class 0.000 description 1
OBCUTHMOOONNBS-UHFFFAOYSA-N phosphorus pentafluoride Chemical compound FP(F)(F)(F)F OBCUTHMOOONNBS-UHFFFAOYSA-N 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920005604 random copolymer Polymers 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000009958 sewing Methods 0.000 description 1
239000000779 smoke Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
230000008961 swelling Effects 0.000 description 1
ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1

Landscapes

Manufacture Of Macromolecular Shaped Articles (AREA)
Compositions Of Macromolecular Compounds (AREA)
Artificial Filaments (AREA)

JP4027282A 1982-03-16 1982-03-16 難燃性のポリアミド繊維又はフイルムの製造法 Granted JPS58163722A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP4027282A JPS58163722A (ja)	1982-03-16	1982-03-16	難燃性のポリアミド繊維又はフイルムの製造法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP4027282A JPS58163722A (ja)	1982-03-16	1982-03-16	難燃性のポリアミド繊維又はフイルムの製造法

Publications (2)

Publication Number	Publication Date
JPS58163722A JPS58163722A (ja)	1983-09-28
JPH0257574B2 true JPH0257574B2 (mo)	1990-12-05

Family

ID=12575996

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP4027282A Granted JPS58163722A (ja)	1982-03-16	1982-03-16	難燃性のポリアミド繊維又はフイルムの製造法

Country Status (1)

Country	Link
JP (1)	JPS58163722A (mo)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6246070B1 (en)	1998-08-21	2001-06-12	Semiconductor Energy Laboratory Co., Ltd.	Semiconductor device provided with semiconductor circuit made of semiconductor element and method of fabricating the same
JP4493741B2 (ja)	1998-09-04	2010-06-30	株式会社半導体エネルギー研究所	半導体装置の作製方法
JP4624542B2 (ja) *	2000-11-13	2011-02-02	帝人テクノプロダクツ株式会社	全芳香族ポリアミド繊維の染色方法

1982
- 1982-03-16 JP JP4027282A patent/JPS58163722A/ja active Granted

Also Published As

Publication number	Publication date
JPS58163722A (ja)	1983-09-28

Publication	Publication Date	Title
US4018735A (en)	1977-04-19	Anisotropic dopes of aromatic polyamides
US4355151A (en)	1982-10-19	Aromatic copolyamide containing 3,4'-diamino diphenylene moiety
EP0045934B1 (en)	1984-12-05	Wholly aromatic polyamide fiber and film and process for preparation thereof
JP2010163506A (ja)	2010-07-29	芳香族コポリアミドの製造方法
US4539393A (en)	1985-09-03	Dimensionally stable poly-m-phenylene isophthalamide film
US5643518A (en)	1997-07-01	Process for preparing fibers of soluble wholly aromatic polyamides
JPH0257574B2 (mo)	1990-12-05
US5039779A (en)	1991-08-13	Thermoplastically processible aromatic polyetheramide from 2,2-bis(4'-amino phenoxy phenyl) propane and terephthalic acid
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US5334693A (en)	1994-08-02	Aramid composition
JPS58179264A (ja)	1983-10-20	新規なド−プ
US3748298A (en)	1973-07-24	Aromatic-oxalic polyhydrazides and solutions thereof
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JPS58203116A (ja)	1983-11-26	難燃性のポリ（ｐ−フエニレンテレフタルアミド）繊維
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