SU499815A3 - Способ получени огнестойких полиамидов - Google Patents

Способ получени огнестойких полиамидов

Info

Publication number: SU499815A3
Authority: SU; USSR - Soviet Union
Prior art keywords: polyamides; esters; fire; obtaining fire; resistant
Prior art date: 1973-02-08

Application number

SU1998399A

Other languages

English (en)

Russian (ru)

Inventor

Бернье Сесиль

Жуано Моник

Пуасон Пьер

Original Assignee

Акитэн Тоталь Органико (Фирма)

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.)

1973-02-08

Filing date

1974-02-07

Publication date

1976-01-15

1974-02-07 Application filed by Акитэн Тоталь Органико (Фирма) filed Critical Акитэн Тоталь Органико (Фирма)

1976-01-15 Application granted granted Critical

1976-01-15 Publication of SU499815A3 publication Critical patent/SU499815A3/ru

Links

239000004952 Polyamide Substances 0.000 title description 15
229920002647 polyamide Polymers 0.000 title description 15
238000000034 method Methods 0.000 title description 13
230000009970 fire resistant effect Effects 0.000 title description 5
-1 aliphatic diamines Chemical class 0.000 description 8
125000003118 aryl group Chemical group 0.000 description 8
150000002148 esters Chemical class 0.000 description 6
238000006068 polycondensation reaction Methods 0.000 description 5
125000004429 atom Chemical group 0.000 description 4
235000010290 biphenyl Nutrition 0.000 description 4
239000004305 biphenyl Substances 0.000 description 4
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000000203 mixture Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 2
125000006267 biphenyl group Chemical group 0.000 description 2
229930003836 cresol Natural products 0.000 description 2
150000004985 diamines Chemical group 0.000 description 2
238000004821 distillation Methods 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
239000000178 monomer Substances 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
229940049953 phenylacetate Drugs 0.000 description 2
WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 2
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 description 1
QPBGNSFASPVGTP-UHFFFAOYSA-N 2-bromoterephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(Br)=C1 QPBGNSFASPVGTP-UHFFFAOYSA-N 0.000 description 1
IFNDEOYXGHGERA-UHFFFAOYSA-N 2-methoxy-5-methylphenol Chemical compound COC1=CC=C(C)C=C1O IFNDEOYXGHGERA-UHFFFAOYSA-N 0.000 description 1
BRPLMBGPWZGZJW-UHFFFAOYSA-N 3,4-dibromophthalic acid Chemical compound OC(=O)C1=CC=C(Br)C(Br)=C1C(O)=O BRPLMBGPWZGZJW-UHFFFAOYSA-N 0.000 description 1
OIGFNQRFPUUACU-UHFFFAOYSA-N 3-bromophthalic acid Chemical compound OC(=O)C1=CC=CC(Br)=C1C(O)=O OIGFNQRFPUUACU-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
150000007860 aryl ester derivatives Chemical class 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
LJOSESICVCVVCK-UHFFFAOYSA-N docosane-1,1-diamine Chemical compound CCCCCCCCCCCCCCCCCCCCCC(N)N LJOSESICVCVVCK-UHFFFAOYSA-N 0.000 description 1
JMLPVHXESHXUSV-UHFFFAOYSA-N dodecane-1,1-diamine Chemical compound CCCCCCCCCCCC(N)N JMLPVHXESHXUSV-UHFFFAOYSA-N 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
SYECJBOWSGTPLU-UHFFFAOYSA-N hexane-1,1-diamine Chemical compound CCCCCC(N)N SYECJBOWSGTPLU-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
DDLUSQPEQUJVOY-UHFFFAOYSA-N nonane-1,1-diamine Chemical compound CCCCCCCCC(N)N DDLUSQPEQUJVOY-UHFFFAOYSA-N 0.000 description 1
FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/42—Polyamides containing atoms other than carbon, hydrogen, oxygen, and nitrogen

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Polyamides (AREA)

SU1998399A 1973-02-08 1974-02-07 Способ получени огнестойких полиамидов SU499815A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR7304442A FR2217309A1 (en)	1973-02-08	1973-02-08	Fire-resistant, high molecular weight, polyamides - from aromatic diacids contg bromine in the ring, and diamines, in a one-stage reaction

Publications (1)

Publication Number	Publication Date
SU499815A3 true SU499815A3 (ru)	1976-01-15

Family

ID=9114531

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU1998399A SU499815A3 (ru)	1973-02-08	1974-02-07	Способ получени огнестойких полиамидов

Country Status (3)

Country	Link
BE (1)	BE810737A (fr)
FR (1)	FR2217309A1 (fr)
SU (1)	SU499815A3 (fr)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1400944A (fr) *	1963-08-10	1965-05-28	Chemische Werke Witten Gmbh	Procédé de préparation d'esters aryliques purs d'acides di- et polycarboxyliques

1973
- 1973-02-08 FR FR7304442A patent/FR2217309A1/fr active Granted
1974
- 1974-02-07 SU SU1998399A patent/SU499815A3/ru active
- 1974-02-07 BE BE140661A patent/BE810737A/fr unknown

Also Published As

Publication number	Publication date
FR2217309A1 (en)	1974-09-06
FR2217309B1 (fr)	1976-06-11
BE810737A (fr)	1974-05-29

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