NO772868L - Flammehemmende mykner for pvc. - Google Patents

Flammehemmende mykner for pvc.

Info

Publication number: NO772868L
Authority: NO; Norway
Prior art keywords: approx; preparation; weight; plasticizer; phosphate
Prior art date: 1976-09-17

Application number

NO772868A

Other languages

English (en)

Norwegian (no)

Inventor

John Hutcheson Deatcher

Original Assignee

Stauffer Chemical Co

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.)

1976-09-17

Filing date

1977-08-17

Publication date

1978-03-20

1977-08-17 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1978-03-20 Publication of NO772868L publication Critical patent/NO772868L/no

Links

239000004014 plasticizer Substances 0.000 claims description 61
238000002360 preparation method Methods 0.000 claims description 45
239000004800 polyvinyl chloride Substances 0.000 claims description 29
239000003063 flame retardant Substances 0.000 claims description 28
229920000915 polyvinyl chloride Polymers 0.000 claims description 28
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 22
-1 haloalkyl phosphate Chemical compound 0.000 claims description 15
229910019142 PO4 Inorganic materials 0.000 claims description 14
239000010452 phosphate Substances 0.000 claims description 13
229920000642 polymer Polymers 0.000 claims description 12
VONWDASPFIQPDY-UHFFFAOYSA-N dimethyl methylphosphonate Chemical compound COP(C)(=O)OC VONWDASPFIQPDY-UHFFFAOYSA-N 0.000 claims description 10
150000002148 esters Chemical class 0.000 claims description 7
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 6
YAOMHRRYSRRRKP-UHFFFAOYSA-N 1,2-dichloropropyl 2,3-dichloropropyl 3,3-dichloropropyl phosphate Chemical compound ClC(Cl)CCOP(=O)(OC(Cl)C(Cl)C)OCC(Cl)CCl YAOMHRRYSRRRKP-UHFFFAOYSA-N 0.000 claims description 5
150000005846 sugar alcohols Polymers 0.000 claims description 5
229920012485 Plasticized Polyvinyl chloride Polymers 0.000 claims description 2
WOURXYYHORRGQO-UHFFFAOYSA-N Tri(3-chloropropyl) phosphate Chemical compound ClCCCOP(=O)(OCCCCl)OCCCCl WOURXYYHORRGQO-UHFFFAOYSA-N 0.000 claims description 2
PQYJRMFWJJONBO-UHFFFAOYSA-N Tris(2,3-dibromopropyl) phosphate Chemical group BrCC(Br)COP(=O)(OCC(Br)CBr)OCC(Br)CBr PQYJRMFWJJONBO-UHFFFAOYSA-N 0.000 claims description 2
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 2
HQUQLFOMPYWACS-UHFFFAOYSA-N tris(2-chloroethyl) phosphate Chemical compound ClCCOP(=O)(OCCCl)OCCCl HQUQLFOMPYWACS-UHFFFAOYSA-N 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims 1
150000002367 halogens Chemical class 0.000 claims 1
239000000203 mixture Substances 0.000 description 26
235000021317 phosphate Nutrition 0.000 description 9
239000000047 product Substances 0.000 description 9
239000000523 sample Substances 0.000 description 8
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 7
239000000126 substance Substances 0.000 description 7
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 6
MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 6
239000000654 additive Substances 0.000 description 5
239000000779 smoke Substances 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
239000000178 monomer Substances 0.000 description 4
125000001188 haloalkyl group Chemical group 0.000 description 3
229920001519 homopolymer Polymers 0.000 description 3
239000000463 material Substances 0.000 description 3
230000035515 penetration Effects 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
239000004033 plastic Substances 0.000 description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
230000005540 biological transmission Effects 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000007373 indentation Methods 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000000034 method Methods 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
235000005985 organic acids Nutrition 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
238000009864 tensile test Methods 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
230000004580 weight loss Effects 0.000 description 2
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
DSSAWHFZNWVJEC-UHFFFAOYSA-N 3-(ethenoxymethyl)heptane Chemical compound CCCCC(CC)COC=C DSSAWHFZNWVJEC-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 1
241000156978 Erebia Species 0.000 description 1
229930195725 Mannitol Natural products 0.000 description 1
239000006057 Non-nutritive feed additive Substances 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
229920006266 Vinyl film Polymers 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
150000001279 adipic acids Chemical class 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000005250 alkyl acrylate group Chemical group 0.000 description 1
MGFRKBRDZIMZGO-UHFFFAOYSA-N barium cadmium Chemical compound [Cd].[Ba] MGFRKBRDZIMZGO-UHFFFAOYSA-N 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Chemical group 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000002485 combustion reaction Methods 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
239000013068 control sample Substances 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
JBSLOWBPDRZSMB-BQYQJAHWSA-N dibutyl (e)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C\C(=O)OCCCC JBSLOWBPDRZSMB-BQYQJAHWSA-N 0.000 description 1
239000000539 dimer Substances 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000000975 dye Substances 0.000 description 1
AZDCYKCDXXPQIK-UHFFFAOYSA-N ethenoxymethylbenzene Chemical compound C=COCC1=CC=CC=C1 AZDCYKCDXXPQIK-UHFFFAOYSA-N 0.000 description 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
LQZZUXJYWNFBMV-UHFFFAOYSA-N ethyl butylhexanol Natural products CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000012467 final product Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
150000002398 hexadecan-1-ols Chemical class 0.000 description 1
BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
238000011835 investigation Methods 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
239000002075 main ingredient Substances 0.000 description 1
239000000594 mannitol Substances 0.000 description 1
235000010355 mannitol Nutrition 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
150000003022 phthalic acids Chemical class 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
150000003330 sebacic acids Chemical class 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
239000013638 trimer Substances 0.000 description 1
ASLWPAWFJZFCKF-UHFFFAOYSA-N tris(1,3-dichloropropan-2-yl) phosphate Chemical compound ClCC(CCl)OP(=O)(OC(CCl)CCl)OC(CCl)CCl ASLWPAWFJZFCKF-UHFFFAOYSA-N 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5317—Phosphonic compounds, e.g. R—P(:O)(OR')2
- C08K5/5333—Esters of phosphonic acids
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S260/00—Chemistry of carbon compounds
- Y10S260/24—Flameproof

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

NO772868A 1976-09-17 1977-08-17 Flammehemmende mykner for pvc. NO772868L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/724,424 US4111882A (en)	1976-09-17	1976-09-17	Flame retardant plasticizer formulation for polyvinyl chloride containing dimethyl methylphosphonate for haze reduction

Publications (1)

Publication Number	Publication Date
NO772868L true NO772868L (no)	1978-03-20

Family

ID=24910394

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO772868A NO772868L (no)	1976-09-17	1977-08-17	Flammehemmende mykner for pvc.

Country Status (16)

Country	Link
US (1)	US4111882A (de)
JP (1)	JPS5336552A (de)
AR (1)	AR213119A1 (de)
AU (1)	AU512047B2 (de)
BE (1)	BE858763A (de)
BR (1)	BR7704808A (de)
CA (1)	CA1106092A (de)
DD (1)	DD132665A5 (de)
DE (1)	DE2740589A1 (de)
EG (1)	EG12764A (de)
FR (1)	FR2364944A1 (de)
GB (1)	GB1537613A (de)
NL (1)	NL7707638A (de)
NO (1)	NO772868L (de)
PH (1)	PH13043A (de)
SU (1)	SU831081A3 (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2601592B1 (fr) *	1986-07-21	1988-11-10	Reckitt Colman	Liquide desodorisant ininflammable
CN1146926C (zh) *	1997-01-20	2004-04-21	大同特殊钢株式会社	电磁和磁屏蔽用软磁合金粉末,包含该粉末的屏蔽部件
WO2007066765A1 (ja) *	2005-12-09	2007-06-14	Denki Kagaku Kogyo Kabushiki Kaisha	接着性組成物およびこれを用いた接着剤
EP2275499A3 (de) *	2007-11-01	2011-04-27	E.M.A.T. Technologies Ltd.	Flammhemmende Formulierungen auf Polymerbasis
CN101974185A (zh) *	2010-10-19	2011-02-16	北京化工大学	一种输送带用低卤膨胀阻燃树脂糊料及其制备方法
CN101962459B (zh) *	2010-10-22	2013-04-03	青岛国恩科技股份有限公司	一种阻燃高流动复合材料及制备方法
CN111372991B (zh) *	2017-09-15	2023-11-17	吉昂功能材料(东莞)有限公司	阻燃聚(氯乙烯)复合物
CN113004640B (zh) *	2021-04-09	2022-12-06	广州雷诺丽特塑料有限公司	一种pvc膜及其制备方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2934507A (en) *	1954-06-18	1960-04-26	Monsanto Chemicals	Polyvinyl chloride resins stabilized with mixtures of phosphonate esters, epoxy compounds and metallic salts of fatty acids
US3064031A (en) *	1962-02-05	1962-11-13	Procter & Gamble	Process for preparing dialkyl alkyl phosphonates
DE1230801B (de) *	1965-03-20	1966-12-22	Bayer Ag	Verfahren zur Herstellung von Phosphonsaeuremischestern
US3558537A (en) *	1968-01-02	1971-01-26	Argus Chem	Imparting antifogging properties to polyvinyl chloride resins and compositions therefor
US3801526A (en) *	1970-11-30	1974-04-02	Monsanto Co	Plasticized vinyl chloride polymer blends having improved fire retardancy
US3812073A (en) *	1972-03-02	1974-05-21	Sumitomo Chemical Co	Process for producing vinyl chloride resin

1976
- 1976-09-17 US US05/724,424 patent/US4111882A/en not_active Expired - Lifetime
1977
- 1977-06-30 AU AU26644/77A patent/AU512047B2/en not_active Expired
- 1977-07-05 CA CA282,031A patent/CA1106092A/en not_active Expired
- 1977-07-06 AR AR268333A patent/AR213119A1/es active
- 1977-07-08 NL NL7707638A patent/NL7707638A/xx not_active Application Discontinuation
- 1977-07-15 PH PH20000A patent/PH13043A/en unknown
- 1977-07-21 BR BR7704808A patent/BR7704808A/pt unknown
- 1977-07-24 EG EG435/77A patent/EG12764A/xx active
- 1977-08-05 JP JP9407877A patent/JPS5336552A/ja active Pending
- 1977-08-11 SU SU772511606A patent/SU831081A3/ru active
- 1977-08-17 NO NO772868A patent/NO772868L/no unknown
- 1977-08-19 FR FR7725472A patent/FR2364944A1/fr not_active Withdrawn
- 1977-09-09 DE DE19772740589 patent/DE2740589A1/de not_active Withdrawn
- 1977-09-15 DD DD7700201043A patent/DD132665A5/de unknown
- 1977-09-16 GB GB38709/77A patent/GB1537613A/en not_active Expired
- 1977-09-16 BE BE2056251A patent/BE858763A/xx unknown

Also Published As

Publication number	Publication date
CA1106092A (en)	1981-07-28
GB1537613A (en)	1979-01-04
JPS5336552A (en)	1978-04-04
PH13043A (en)	1979-11-21
AU2664477A (en)	1979-01-04
AU512047B2 (en)	1980-09-18
EG12764A (en)	1979-12-31
BE858763A (nl)	1978-03-16
US4111882A (en)	1978-09-05
AR213119A1 (es)	1978-12-15
DD132665A5 (de)	1978-10-18
NL7707638A (nl)	1978-03-21
FR2364944A1 (fr)	1978-04-14
BR7704808A (pt)	1978-03-28
SU831081A3 (ru)	1981-05-15
DE2740589A1 (de)	1978-03-23

Publication	Publication Date	Title
US4178281A (en)	1979-12-11	Flame-retardant polycarbonate compositions
US5374377A (en)	1994-12-20	Phosphorescent polyvinyl chloride films
US4083824A (en)	1978-04-11	Non-vinyl surface covering composition
JPS6349700B2 (de)	1988-10-05
US4111882A (en)	1978-09-05	Flame retardant plasticizer formulation for polyvinyl chloride containing dimethyl methylphosphonate for haze reduction
US4246169A (en)	1981-01-20	Flammable plastics containing a flame retardant amount of polyarylphosphates and the polyarylphosphates
JP2008501844A (ja)	2008-01-24	難燃性組成物
WO2013085714A1 (en)	2013-06-13	Stabilized compositions of halogenated polymers
US4146522A (en)	1979-03-27	Smoke suppressant composition
NO166204B (no)	1991-03-04	Vippbar beholder for metallurgisk ovn.
US9963572B2 (en)	2018-05-08	Chlorinated ester polyvinyl-chloride secondary plasticizer and related methods
US4403056A (en)	1983-09-06	Carbonate esters, carbonate ester compositions, and plasticized compositions
US4560618A (en)	1985-12-24	Building/vapor barrier combination
JP7153029B2 (ja)	2022-10-13	難燃性スチレン含有組成物
JPS59206454A (ja)	1984-11-22	透明性の改良された難燃性アクリル樹脂組成物
EP0389640B1 (de)	1995-05-03	Harzzubereitung mit ausgezeichneter wärmestabilität und wetterfestigkeit
CA1264163A (en)	1990-01-02	Citrate esters and methods
US3804792A (en)	1974-04-16	Fire retardant plasticizers
EP0156219B1 (de)	1989-02-15	Flammhemmende Harzzusammensetzung
AU1066395A (en)	1995-06-06	Polyketone polymer composition
US4104233A (en)	1978-08-01	ω-Bromoalkyl plasticizer compositions
CA1155574A (en)	1983-10-18	Fire retardant polymers
EP0011415A1 (de)	1980-05-28	Dampf-Sperrschicht-Filme
US4280945A (en)	1981-07-28	Vinyl chloride compositions plasticized with meta-tertiary-butylphenyl diphenyl phosphate
SU616272A1 (ru)	1978-07-25	Композици на основе поливинолхлорида