JPH0116948B2 - - Google Patents

Info

Publication number: JPH0116948B2
Authority: JP; Japan
Prior art keywords: aromatic polyamide; thiourea; urea; fibers; group
Prior art date: 1984-03-30
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

JP6112284A

Other languages

English (en)

Japanese (ja)

Other versions

JPS60209068A (ja

Inventor

Isahiro Minemura

Setsuo Yamada

Fumiki Takabayashi

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.)

Teijin Ltd

Original Assignee

Teijin 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.)

1984-03-30

Filing date

1984-03-30

Publication date

1989-03-28

1984-03-30 Application filed by Teijin Ltd filed Critical Teijin Ltd

1984-03-30 Priority to JP6112284A priority Critical patent/JPS60209068A/ja

1984-07-18 Priority to US06/632,205 priority patent/US4631066A/en

1984-07-23 Priority to EP84304994A priority patent/EP0132402B1/fr

1984-07-23 Priority to DE8484304994T priority patent/DE3477816D1/de

1985-10-21 Publication of JPS60209068A publication Critical patent/JPS60209068A/ja

1989-03-28 Publication of JPH0116948B2 publication Critical patent/JPH0116948B2/ja

Status Granted legal-status Critical Current

Links

XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 42
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 28
239000004760 aramid Substances 0.000 claims description 27
229920003235 aromatic polyamide Polymers 0.000 claims description 27
239000000835 fiber Substances 0.000 claims description 27
239000004202 carbamide Substances 0.000 claims description 14
239000006097 ultraviolet radiation absorber Substances 0.000 claims description 12
238000000034 method Methods 0.000 claims description 7
230000000052 comparative effect Effects 0.000 description 11
239000004952 Polyamide Substances 0.000 description 8
230000000694 effects Effects 0.000 description 8
229920002647 polyamide Polymers 0.000 description 8
239000000975 dye Substances 0.000 description 6
239000004744 fabric Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
125000000217 alkyl group Chemical group 0.000 description 5
125000003118 aryl group Chemical group 0.000 description 5
239000000203 mixture Substances 0.000 description 5
239000000243 solution Substances 0.000 description 5
229920000642 polymer Polymers 0.000 description 4
238000010521 absorption reaction Methods 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
OCWYEMOEOGEQAN-UHFFFAOYSA-N bumetrizole Chemical compound CC(C)(C)C1=CC(C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O OCWYEMOEOGEQAN-UHFFFAOYSA-N 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
125000004435 hydrogen atom Chemical class [H]* 0.000 description 3
-1 methoxy, ethoxy Chemical group 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000004753 textile Substances 0.000 description 3
125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 2
239000004953 Aliphatic polyamide Substances 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
229920000297 Rayon Polymers 0.000 description 2
229920003231 aliphatic polyamide Polymers 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
SODJJEXAWOSSON-UHFFFAOYSA-N bis(2-hydroxy-4-methoxyphenyl)methanone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(OC)C=C1O SODJJEXAWOSSON-UHFFFAOYSA-N 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
238000001035 drying Methods 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000005562 fading Methods 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
238000009940 knitting Methods 0.000 description 2
230000014759 maintenance of location Effects 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000002964 rayon Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
229920002994 synthetic fiber Polymers 0.000 description 2
239000012209 synthetic fiber Substances 0.000 description 2
238000009941 weaving 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
MEZZCSHVIGVWFI-UHFFFAOYSA-N 2,2'-Dihydroxy-4-methoxybenzophenone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1O MEZZCSHVIGVWFI-UHFFFAOYSA-N 0.000 description 1
125000005662 2,5-pyridylene group Chemical group [H]C1=NC([*:1])=C([H])C([H])=C1[*:2] 0.000 description 1
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 1
JITACPZFCRQCHZ-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-tert-butyl-6-chlorophenol Chemical compound CC(C)(C)C1=CC(Cl)=C(O)C(N2N=C3C=CC=CC3=N2)=C1 JITACPZFCRQCHZ-UHFFFAOYSA-N 0.000 description 1
MINKQMLOVWFCJM-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-chloro-4-methylphenol Chemical compound CC1=CC(Cl)=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MINKQMLOVWFCJM-UHFFFAOYSA-N 0.000 description 1
BVNWQSXXRMNYKH-UHFFFAOYSA-N 4-phenyl-2h-benzotriazole Chemical compound C1=CC=CC=C1C1=CC=CC2=C1NN=N2 BVNWQSXXRMNYKH-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
229920002292 Nylon 6 Polymers 0.000 description 1
229920002302 Nylon 6,6 Polymers 0.000 description 1
SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
239000000980 acid dye Substances 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
230000004888 barrier function Effects 0.000 description 1
BJFLSHMHTPAZHO-UHFFFAOYSA-N benzotriazole Chemical compound [CH]1C=CC=C2N=NN=C21 BJFLSHMHTPAZHO-UHFFFAOYSA-N 0.000 description 1
239000012964 benzotriazole Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
230000009849 deactivation Effects 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
239000000986 disperse dye Substances 0.000 description 1
MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
238000004043 dyeing Methods 0.000 description 1
BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
239000011810 insulating material Substances 0.000 description 1
QZUPTXGVPYNUIT-UHFFFAOYSA-N isophthalamide Chemical compound NC(=O)C1=CC=CC(C(N)=O)=C1 QZUPTXGVPYNUIT-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000012778 molding material Substances 0.000 description 1
230000000877 morphologic effect Effects 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
239000000843 powder Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000009991 scouring Methods 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
210000004243 sweat Anatomy 0.000 description 1
MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
238000005979 thermal decomposition reaction Methods 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
239000002759 woven fabric Substances 0.000 description 1

Landscapes

Artificial Filaments (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

JP6112284A 1983-07-26 1984-03-30 芳香族ポリアミド繊維の耐光性改良法 Granted JPS60209068A (ja)

Priority Applications (4)

Application Number	Priority Date	Filing Date	Title
JP6112284A JPS60209068A (ja)	1984-03-30	1984-03-30	芳香族ポリアミド繊維の耐光性改良法
US06/632,205 US4631066A (en)	1983-07-26	1984-07-18	Method for improving light-resistance of aromatic polyamide fibers
EP84304994A EP0132402B1 (fr)	1983-07-26	1984-07-23	Méthode pour augmenter la résistance à la lumière de fibres en polyamide aromatique
DE8484304994T DE3477816D1 (en)	1983-07-26	1984-07-23	Method for improving light-resistance of aromatic polyamide fibers

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP6112284A JPS60209068A (ja)	1984-03-30	1984-03-30	芳香族ポリアミド繊維の耐光性改良法

Publications (2)

Publication Number	Publication Date
JPS60209068A JPS60209068A (ja)	1985-10-21
JPH0116948B2 true JPH0116948B2 (fr)	1989-03-28

Family

ID=13161952

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP6112284A Granted JPS60209068A (ja)	1983-07-26	1984-03-30	芳香族ポリアミド繊維の耐光性改良法

Country Status (1)

Country	Link
JP (1)	JPS60209068A (fr)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS6037224B2 (ja) *	1977-06-15	1985-08-24	株式会社クラレ	繊維の加工方法

1984
- 1984-03-30 JP JP6112284A patent/JPS60209068A/ja active Granted

Also Published As

Publication number	Publication date
JPS60209068A (ja)	1985-10-21

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CA1118163A (fr)	1982-02-16	Procede de traitement de fibres synthetiques par des polydiorganosiloxanes contenant des aminoalkyles
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US4631066A (en)	1986-12-23	Method for improving light-resistance of aromatic polyamide fibers
US4014829A (en)	1977-03-29	Flame resistant fiber blends
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JPH0299674A (ja)	1990-04-11	染色されたポリエーテルイミド繊維及びその染色方法
JPS60209068A (ja)	1985-10-21	芳香族ポリアミド繊維の耐光性改良法
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JPS6364544B2 (fr)	1988-12-12
JP3192015B2 (ja)	2001-07-23	パイル布帛
US3484186A (en)	1969-12-16	Composition and method for treating textile products of polyamides
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JPH1072743A (ja)	1998-03-17	難燃性布帛及びその製造方法
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JP2004143605A (ja)	2004-05-20	全芳香族ポリアミド繊維構造物
JPS6037224B2 (ja)	1985-08-24	繊維の加工方法
JPS61138780A (ja)	1986-06-26	芳香族ポリアミド繊維の染色法