IL22234A - Thermoplastic composition - Google Patents

Thermoplastic composition

Info

Publication number: IL22234A
Authority: IL; Israel
Prior art keywords: mole; polyesteramide; melting point; polyoxymethylene; following
Prior art date: 1963-10-17

Application number

IL22234A

Other languages

English (en)

Original Assignee

Houilleres Bassin Du Nord

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.)

1963-10-17

Filing date

1964-10-12

Publication date

1968-02-26

1964-10-12 Application filed by Houilleres Bassin Du Nord filed Critical Houilleres Bassin Du Nord

1968-02-26 Publication of IL22234A publication Critical patent/IL22234A/en

Links

239000000203 mixture Substances 0.000 title claims description 15
229920001169 thermoplastic Polymers 0.000 title claims description 3
239000004416 thermosoftening plastic Substances 0.000 title claims description 3
229920006149 polyester-amide block copolymer Polymers 0.000 claims description 46
238000002844 melting Methods 0.000 claims description 20
230000008018 melting Effects 0.000 claims description 20
239000004215 Carbon black (E152) Substances 0.000 claims description 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
-1 polyoxymethylenes Polymers 0.000 description 44
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 34
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 24
229920006324 polyoxymethylene Polymers 0.000 description 24
229930040373 Paraformaldehyde Natural products 0.000 description 18
238000000034 method Methods 0.000 description 18
235000011037 adipic acid Nutrition 0.000 description 17
239000001361 adipic acid Substances 0.000 description 17
239000004615 ingredient Substances 0.000 description 15
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
239000000654 additive Substances 0.000 description 11
238000006731 degradation reaction Methods 0.000 description 8
230000015556 catabolic process Effects 0.000 description 7
INSRQEMEVAMETL-UHFFFAOYSA-N decane-1,1-diol Chemical compound CCCCCCCCCC(O)O INSRQEMEVAMETL-UHFFFAOYSA-N 0.000 description 6
ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 6
230000000996 additive effect Effects 0.000 description 5
239000003963 antioxidant agent Substances 0.000 description 5
235000006708 antioxidants Nutrition 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
229920002292 Nylon 6 Polymers 0.000 description 3
229920002302 Nylon 6,6 Polymers 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
229920001897 terpolymer Polymers 0.000 description 3
NSMWYRLQHIXVAP-UHFFFAOYSA-N 2,5-dimethylpiperazine Chemical compound CC1CNC(C)CN1 NSMWYRLQHIXVAP-UHFFFAOYSA-N 0.000 description 2
SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
229920000305 Nylon 6,10 Polymers 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 2
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 2
239000000370 acceptor Substances 0.000 description 2
239000002253 acid Substances 0.000 description 2
229960002684 aminocaproic acid Drugs 0.000 description 2
230000003078 antioxidant effect Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
229940093476 ethylene glycol Drugs 0.000 description 2
OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
230000006641 stabilisation Effects 0.000 description 2
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
238000005809 transesterification reaction Methods 0.000 description 2
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
QIEFMYFGTMMHEN-UHFFFAOYSA-N 2-[[2-hydroxy-5-methyl-3-(2-methylcyclohexyl)phenyl]methyl]-4-methyl-6-(2-methylcyclohexyl)phenol Chemical compound CC1CCCCC1C1=CC(C)=CC(CC=2C(=C(C3C(CCCC3)C)C=C(C)C=2)O)=C1O QIEFMYFGTMMHEN-UHFFFAOYSA-N 0.000 description 1
KRPRVQWGKLEFKN-UHFFFAOYSA-N 3-(3-aminopropoxy)propan-1-amine Chemical compound NCCCOCCCN KRPRVQWGKLEFKN-UHFFFAOYSA-N 0.000 description 1
RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000001273 butane Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
OWEZJUPKTBEISC-UHFFFAOYSA-N decane-1,1-diamine Chemical compound CCCCCCCCCC(N)N OWEZJUPKTBEISC-UHFFFAOYSA-N 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000000265 homogenisation Methods 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
150000003951 lactams Chemical class 0.000 description 1
208000020442 loss of weight Diseases 0.000 description 1
WRIRWRKPLXCTFD-UHFFFAOYSA-N malonamide Chemical compound NC(=O)CC(N)=O WRIRWRKPLXCTFD-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000005259 measurement Methods 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
229960001047 methyl salicylate Drugs 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 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
239000000843 powder Substances 0.000 description 1
239000005297 pyrex Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
239000011342 resin composition Substances 0.000 description 1
230000007017 scission Effects 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
229920005992 thermoplastic resin Polymers 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/12—Polyester-amides
- 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
- C08G69/44—Polyester-amides
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L59/00—Compositions of polyacetals; Compositions of derivatives of polyacetals
- C08L59/02—Polyacetals containing polyoxymethylene sequences only

Landscapes

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

IL22234A 1963-10-17 1964-10-12 Thermoplastic composition IL22234A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR950859A FR1379756A (fr)	1963-10-17	1963-10-17	Procédé perfectionné pour la stabilisation des polyoxyméthylènes
FR978012A FR1406658A (fr)	1963-10-17	1964-06-12	Procédé de stabilisation des polyoxyméthylènes

Publications (1)

Publication Number	Publication Date
IL22234A true IL22234A (en)	1968-02-26

Family

ID=26203927

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL22234A IL22234A (en)	1963-10-17	1964-10-12	Thermoplastic composition

Country Status (9)

Country	Link
US (1)	US3355514A (fr)
BE (1)	BE653912A (fr)
CH (1)	CH442743A (fr)
DE (1)	DE1250120B (fr)
FR (2)	FR1379756A (fr)
GB (1)	GB1019786A (fr)
IL (1)	IL22234A (fr)
LU (1)	LU47075A1 (fr)
NL (1)	NL141224B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3459709A (en) *	1965-07-02	1969-08-05	Sir Soc Italiana Resine Spa	Method of stabilizing polyoxymethylenes
IT1006136B (it) *	1973-12-28	1976-09-30	Sir Soc Italiana Resine Spa	Stabilizzazione di polimeri acetalici
US3960984A (en) *	1974-04-16	1976-06-01	E. I. Du Pont De Nemours And Company	Composition of oxymethylene polymer and amide oligomers

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3235624A (en) *	1962-12-04	1966-02-15	Tenneco Chem	Stabilized polyoxymethylene compositions
US3288885A (en) *	1963-04-04	1966-11-29	Tenneco Chem	Composition for stabilizing polyacetals comprising (1) nu-acyl-p-aminophenol, (2) a superpolyamide, and (3) a diester of a thiodialkanoic acid

0
- DE DENDAT1250120D patent/DE1250120B/de active Pending
1963
- 1963-10-17 FR FR950859A patent/FR1379756A/fr not_active Expired
1964
- 1964-06-12 FR FR978012A patent/FR1406658A/fr not_active Expired
- 1964-10-02 BE BE653912D patent/BE653912A/xx unknown
- 1964-10-03 LU LU47075A patent/LU47075A1/xx unknown
- 1964-10-12 IL IL22234A patent/IL22234A/en unknown
- 1964-10-14 GB GB41978/63D patent/GB1019786A/en not_active Expired
- 1964-10-16 US US404499A patent/US3355514A/en not_active Expired - Lifetime
- 1964-10-16 NL NL646412073A patent/NL141224B/xx not_active IP Right Cessation
- 1964-10-16 CH CH1345164A patent/CH442743A/fr unknown

Also Published As

Publication number	Publication date
NL6412073A (fr)	1965-04-20
CH442743A (fr)	1967-08-31
US3355514A (en)	1967-11-28
NL141224B (nl)	1974-02-15
DE1250120B (de)	1967-09-14
GB1019786A (en)	1966-02-09
FR1406658A (fr)	1965-07-23
LU47075A1 (fr)	1964-12-03
FR1379756A (fr)	1964-11-27
BE653912A (fr)	1965-02-01

Publication	Publication Date	Title
US4416668A (en)	1983-11-22	Antistatic agents for organic liquids
US3501442A (en)	1970-03-17	Polymerization of lactams in the presence of an organic oxy-acid of phosphorus
GB548263A (en)	1942-10-02	Manufacture of polymeric materials
US4369305A (en)	1983-01-18	Polyamide molding resin from PACM having specific stereo isomer ratio
KR970006892B1 (ko)	1997-04-30	블록 코폴리아미드의 제조방법
US3448085A (en)	1969-06-03	Anionic polymerization of lactams with symmetrical triazine as cocatalyst
US3437627A (en)	1969-04-08	Polyamide-dibenzenylbenzene compositions
IL22234A (en)	1968-02-26	Thermoplastic composition
US3167554A (en)	1965-01-26	Piperazino alkylamides of polybasic carboxylic acids
US3505246A (en)	1970-04-07	Nitrogen aluminum hydride polymers and method of making the same
US2920059A (en)	1960-01-05	Stabilization of polyoxymethylenes with aromatic amines
US4868280A (en)	1989-09-19	Copolyamide from tetramethylene diamine, adipic acid and terephthalic acid
EP0593577A1 (fr)	1994-04-27	Copolyadipamide contenant des unites d'ethyltetramethyleneadipamide et produits prepares a partir de cet element.
US4794158A (en)	1988-12-27	Transparent copolyamide from bis(3-methyl-4-amino-cyclohexyl)methane
US3776890A (en)	1973-12-04	Polyamides from 2-(4-aminocyclohexyl)-1,1-dimethylethylamine or 2-(4-amino-phenyl)-1,1-dimethylethylamine
US3438948A (en)	1969-04-15	Amino acid copolymers
US3397192A (en)	1968-08-13	Alkoxy-and aryloxy-ethylated polymers of heterocyclic nu-vinyl monomers and process of preparing the same
US3553289A (en)	1971-01-05	Polyoxamides from 3-aminomethyl-3,5,5-trimethyl cyclohexylamine
US3210438A (en)	1965-10-05	Method for increasing polyamide viscosity
US2868769A (en)	1959-01-13	Condensation of p-monoaminomethylbenzoic acid and epsilon-caprolactam
US3412072A (en)	1968-11-19	Polyureas
GB793451A (en)	1958-04-16	Improved polyamides by copolymerising polyethers with certain polyamide-forming ingredients
US3729452A (en)	1973-04-24	Reaction products of an amine and a methyl vinyl ether-maleic anhydride copolymer
US4069277A (en)	1978-01-17	Dyeable polyamides containing an antistatic agent
US3065206A (en)	1962-11-20	Aniline-aldehyde-polyamine polymers and their use as antioxidants in gasolines