CA1126499A - Stabilisateur de polymeres - Google Patents

Stabilisateur de polymeres

Info

Publication number: CA1126499A
Authority: CA; Canada
Prior art keywords: bis; dialkylphenyl; composition; pentaerythritol diphosphite; triisopropanolamine
Prior art date: 1979-03-28
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

CA324,300A

Other languages

English (en)

Inventor

James F. York

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.)

GE Chemicals Inc

Original Assignee

Borg Warner Chemicals Inc

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.)

1979-03-28

Filing date

1979-03-28

Publication date

1982-06-29

1979-03-28 Application filed by Borg Warner Chemicals Inc filed Critical Borg Warner Chemicals Inc

1979-03-28 Priority to CA324,300A priority Critical patent/CA1126499A/fr

1982-06-29 Application granted granted Critical

1982-06-29 Publication of CA1126499A publication Critical patent/CA1126499A/fr

Status Expired legal-status Critical Current

Links

229920000642 polymer Polymers 0.000 title abstract description 11
239000003381 stabilizer Substances 0.000 title abstract description 10
239000000203 mixture Substances 0.000 claims abstract description 16
SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 claims abstract description 15
GXURZKWLMYOCDX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.OCC(CO)(CO)CO GXURZKWLMYOCDX-UHFFFAOYSA-N 0.000 claims abstract description 7
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims abstract description 7
125000000217 alkyl group Chemical group 0.000 claims description 5
229920002554 vinyl polymer Polymers 0.000 claims description 4
YGPLZBDXFXBLMZ-UHFFFAOYSA-N 1,1-dichloro-2,2-bis(hydroxymethyl)propane-1,3-diol dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.OCC(CO)(CO)C(O)(Cl)Cl YGPLZBDXFXBLMZ-UHFFFAOYSA-N 0.000 claims description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 3
WAOPGHCXGUXHKF-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)-1,1-diphenylpropane-1,3-diol dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.C1(=CC=CC=C1)C(O)(C(CO)(CO)CO)C1=CC=CC=C1 WAOPGHCXGUXHKF-UHFFFAOYSA-N 0.000 claims description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
229940059574 pentaerithrityl Drugs 0.000 claims 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract description 3
229920000098 polyolefin Polymers 0.000 abstract description 3
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 10
ZJIPHXXDPROMEF-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O ZJIPHXXDPROMEF-UHFFFAOYSA-N 0.000 description 8
150000001412 amines Chemical class 0.000 description 4
150000008301 phosphite esters Chemical class 0.000 description 4
238000010521 absorption reaction Methods 0.000 description 3
239000002253 acid Substances 0.000 description 3
230000007062 hydrolysis Effects 0.000 description 3
238000006460 hydrolysis reaction Methods 0.000 description 3
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
150000007530 organic bases Chemical class 0.000 description 2
230000000087 stabilizing effect Effects 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
RGASRBUYZODJTG-UHFFFAOYSA-N 1,1-bis(2,4-ditert-butylphenyl)-2,2-bis(hydroxymethyl)propane-1,3-diol dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C RGASRBUYZODJTG-UHFFFAOYSA-N 0.000 description 1
ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 description 1
DJHGAFSJWGLOIV-UHFFFAOYSA-K Arsenate3- Chemical class [O-][As]([O-])([O-])=O DJHGAFSJWGLOIV-UHFFFAOYSA-K 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000003513 alkali Substances 0.000 description 1
GCPXMJHSNVMWNM-UHFFFAOYSA-N arsenous acid Chemical class O[As](O)O GCPXMJHSNVMWNM-UHFFFAOYSA-N 0.000 description 1
150000001642 boronic acid derivatives Chemical class 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
230000007423 decrease Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
230000003292 diminished effect Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
150000002485 inorganic esters Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000000034 method Methods 0.000 description 1
-1 pentaerythritol diphosphites Chemical class 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
230000004584 weight gain Effects 0.000 description 1
235000019786 weight gain Nutrition 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)

CA324,300A 1979-03-28 1979-03-28 Stabilisateur de polymeres Expired CA1126499A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA324,300A CA1126499A (fr)	1979-03-28	1979-03-28	Stabilisateur de polymeres

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA324,300A CA1126499A (fr)	1979-03-28	1979-03-28	Stabilisateur de polymeres

Publications (1)

Publication Number	Publication Date
CA1126499A true CA1126499A (fr)	1982-06-29

Family

ID=4113846

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA324,300A Expired CA1126499A (fr)	1979-03-28	1979-03-28	Stabilisateur de polymeres

Country Status (1)

Country	Link
CA (1)	CA1126499A (fr)

1979
- 1979-03-28 CA CA324,300A patent/CA1126499A/fr not_active Expired

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Legal Events

Date	Code	Title	Description
1999-06-29	MKEX	Expiry