NO783997L - Faste, hydrolysebestandige fosforsyrlingestertilberedninger med forbedret stabilisatorvirkning i kunststoffer - Google Patents
Faste, hydrolysebestandige fosforsyrlingestertilberedninger med forbedret stabilisatorvirkning i kunststofferInfo
- Publication number
- NO783997L NO783997L NO783997A NO783997A NO783997L NO 783997 L NO783997 L NO 783997L NO 783997 A NO783997 A NO 783997A NO 783997 A NO783997 A NO 783997A NO 783997 L NO783997 L NO 783997L
- Authority
- NO
- Norway
- Prior art keywords
- wax
- phosphoric acid
- weight
- acid ester
- stabilizer
- Prior art date
Links
- 229920003023 plastic Polymers 0.000 title claims description 22
- 239000004033 plastic Substances 0.000 title claims description 22
- 239000003381 stabilizer Substances 0.000 title claims description 19
- 239000007787 solid Substances 0.000 title claims description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title claims description 6
- 230000001976 improved effect Effects 0.000 title claims description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 title claims description 3
- 230000000694 effects Effects 0.000 title description 7
- 239000007858 starting material Substances 0.000 title 1
- 239000001993 wax Substances 0.000 claims description 44
- 238000002360 preparation method Methods 0.000 claims description 24
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 17
- 150000003014 phosphoric acid esters Chemical class 0.000 claims description 16
- 230000007062 hydrolysis Effects 0.000 claims description 10
- 238000006460 hydrolysis reaction Methods 0.000 claims description 10
- 229920000098 polyolefin Polymers 0.000 claims description 9
- 239000000155 melt Substances 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000012188 paraffin wax Substances 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 230000000087 stabilizing effect Effects 0.000 claims description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 230000009931 harmful effect Effects 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 230000006641 stabilisation Effects 0.000 claims description 4
- 238000011105 stabilization Methods 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000012965 benzophenone Substances 0.000 claims description 2
- 235000009508 confectionery Nutrition 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims description 2
- 239000004611 light stabiliser Chemical class 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 239000002530 phenolic antioxidant Substances 0.000 claims description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 1
- 150000008366 benzophenones Chemical class 0.000 claims 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical class C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims 1
- 239000008187 granular material Substances 0.000 claims 1
- -1 polyethylene Polymers 0.000 description 17
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- 239000004698 Polyethylene Substances 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 229920000573 polyethylene Polymers 0.000 description 8
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- OCSIKZYSDOXRPA-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)-3-octadecylhenicosane-1,3-diol dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.C(CCCCCCCCCCCCCCCCC)C(O)(C(CO)(CO)CO)CCCCCCCCCCCCCCCCCC OCSIKZYSDOXRPA-UHFFFAOYSA-N 0.000 description 2
- 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 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- QCEPBLYEWUSQMX-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] dihydrogen phosphite;3-oxobutanoic acid Chemical compound CC(=O)CC(O)=O.OCC(CO)(CO)COP(O)O QCEPBLYEWUSQMX-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 238000000889 atomisation Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- ANINPCIIERUOQH-AYNSAMJBSA-N (2S,3R)-butane-1,2,3,4-tetrol phosphorous acid Chemical compound P(O)(O)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O ANINPCIIERUOQH-AYNSAMJBSA-N 0.000 description 1
- SBPOXRJRVKTDMN-UHFFFAOYSA-N 1-dimethoxyphosphoryltriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCP(=O)(OC)OC SBPOXRJRVKTDMN-UHFFFAOYSA-N 0.000 description 1
- IHWDIGHWDQPQMQ-UHFFFAOYSA-N 1-octadecylsulfanyloctadecane Chemical class CCCCCCCCCCCCCCCCCCSCCCCCCCCCCCCCCCCCC IHWDIGHWDQPQMQ-UHFFFAOYSA-N 0.000 description 1
- 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
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- CWERGRDVMFNCDR-UHFFFAOYSA-N alpha-mercaptoacetic acid Natural products OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- RBJMENQYBKFGEN-UHFFFAOYSA-N benzene-1,3-dicarboxylic acid 2,2-bis(hydroxymethyl)propane-1,3-diol Chemical compound C(C1=CC(C(=O)O)=CC=C1)(=O)O.OCC(CO)(CO)CO RBJMENQYBKFGEN-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- UDSAIICHUKSCKT-UHFFFAOYSA-N bromophenol blue Chemical compound C1=C(Br)C(O)=C(Br)C=C1C1(C=2C=C(Br)C(O)=C(Br)C=2)C2=CC=CC=C2S(=O)(=O)O1 UDSAIICHUKSCKT-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000004320 controlled atmosphere Methods 0.000 description 1
- NOCMYCSJUZYBNE-UHFFFAOYSA-N dioctadecyl hydrogen phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(O)OCCCCCCCCCCCCCCCCCC NOCMYCSJUZYBNE-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
- HHFDXDXLAINLOT-UHFFFAOYSA-N n,n'-dioctadecylethane-1,2-diamine Chemical compound CCCCCCCCCCCCCCCCCCNCCNCCCCCCCCCCCCCCCCCC HHFDXDXLAINLOT-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000004711 α-olefin Substances 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
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
-
- 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
- C08K5/52—Phosphorus bound to oxygen only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
- C08L91/06—Waxes
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)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2753136A DE2753136B2 (de) | 1977-11-29 | 1977-11-29 | Feste Phosphorigsäureester-Zubereitungen mit verbesserter Stabilisatorwirkung in Kunststoffen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO783997L true NO783997L (no) | 1979-05-30 |
Family
ID=6024859
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO783997A NO783997L (no) | 1977-11-29 | 1978-11-28 | Faste, hydrolysebestandige fosforsyrlingestertilberedninger med forbedret stabilisatorvirkning i kunststoffer |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP0002243B1 (pt) |
| JP (1) | JPS5483951A (pt) |
| AT (1) | AT368769B (pt) |
| AU (1) | AU522136B2 (pt) |
| BR (1) | BR7807807A (pt) |
| CA (1) | CA1113706A (pt) |
| DE (2) | DE2753136B2 (pt) |
| ES (1) | ES475321A1 (pt) |
| IT (1) | IT1101440B (pt) |
| NO (1) | NO783997L (pt) |
| ZA (1) | ZA786674B (pt) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1120793A (en) * | 1977-12-23 | 1982-03-30 | Ved K. Sahajpal | Encapsulated phosphites |
| US4402858A (en) * | 1982-04-14 | 1983-09-06 | Uniroyal, Inc. | Hydrolytically stable antioxidant composition |
| FR2647800A1 (fr) * | 1989-05-31 | 1990-12-07 | Organo Synthese Ste Fse | Phosphite de tris(ditertiobutyl-2,4 phenyle) presentant des proprietes physiques ameliorees |
| DE102008020442A1 (de) | 2008-04-23 | 2009-10-29 | Merck Patent Gmbh | Pigmentpräparationen |
| DE102008064202A1 (de) | 2008-12-22 | 2010-06-24 | Merck Patent Gmbh | Pigmentgranulate |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1131943B (de) * | 1960-11-21 | 1962-06-20 | Deutsche Ges Schaedlingsbek | Feuchtigkeitsgeschuetztes Metallphosphid |
| DE1768283B1 (de) * | 1968-04-25 | 1971-02-25 | Hoechst Ag | Verfahren zur Herstellung thermostabiler Carbonsaeureamide und deren Verwendung als Gleitmittel bei der Kunststoffverarbeitung |
| US3666700A (en) * | 1970-12-03 | 1972-05-30 | Exxon Research Engineering Co | Polyvinyl chloride composition |
| US3755200A (en) * | 1972-02-14 | 1973-08-28 | Emery Industries Inc | Liquid stabilizer system for polyvinyl chloride |
| NL7506988A (nl) * | 1975-06-12 | 1976-12-14 | Akzo Nv | Organische trifosfieten met verbeterde hydrolyti- sche stabiliteit. |
-
1977
- 1977-11-29 DE DE2753136A patent/DE2753136B2/de not_active Withdrawn
-
1978
- 1978-11-23 ES ES475321A patent/ES475321A1/es not_active Expired
- 1978-11-25 EP EP78101457A patent/EP0002243B1/de not_active Expired
- 1978-11-25 DE DE7878101457T patent/DE2861885D1/de not_active Expired
- 1978-11-27 IT IT30238/78A patent/IT1101440B/it active
- 1978-11-28 AT AT0850078A patent/AT368769B/de not_active IP Right Cessation
- 1978-11-28 NO NO783997A patent/NO783997L/no unknown
- 1978-11-28 BR BR7807807A patent/BR7807807A/pt unknown
- 1978-11-28 CA CA316,970A patent/CA1113706A/en not_active Expired
- 1978-11-28 AU AU41981/78A patent/AU522136B2/en not_active Expired
- 1978-11-28 JP JP14612978A patent/JPS5483951A/ja active Pending
- 1978-11-28 ZA ZA00786674A patent/ZA786674B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA1113706A (en) | 1981-12-08 |
| AU4198178A (en) | 1979-06-07 |
| IT7830238A0 (it) | 1978-11-27 |
| IT1101440B (it) | 1985-09-28 |
| ZA786674B (en) | 1979-11-28 |
| AU522136B2 (en) | 1982-05-20 |
| EP0002243B1 (de) | 1982-06-02 |
| AT368769B (de) | 1982-11-10 |
| EP0002243A1 (de) | 1979-06-13 |
| DE2753136A1 (de) | 1979-06-07 |
| ATA850078A (de) | 1982-03-15 |
| JPS5483951A (en) | 1979-07-04 |
| DE2861885D1 (en) | 1982-07-22 |
| ES475321A1 (es) | 1979-04-01 |
| DE2753136B2 (de) | 1981-04-02 |
| BR7807807A (pt) | 1979-07-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE3876110T2 (de) | Feste stabilisatormischung fuer organische polymere und verfahren zu ihrer herstellung. | |
| CZ277731B6 (en) | Polypropylene and process for preparing thereof | |
| US4576825A (en) | Method and composition for curing meat | |
| NO783997L (no) | Faste, hydrolysebestandige fosforsyrlingestertilberedninger med forbedret stabilisatorvirkning i kunststoffer | |
| CH634807A5 (de) | Verfahren zur herstellung eines wachs-desensibilisierten sprengstoffs. | |
| US4973491A (en) | Honey product | |
| JPS63227664A (ja) | 固状安定剤組成物 | |
| US3979345A (en) | Friable composition and process | |
| CA1190039A (en) | Anticaking-compositions for treating hygroscopic or water-soluble material in particulate form | |
| YUKI et al. | Effect of sucrose polyesters on crystallization behavior of vegetable shortening and margarine fat | |
| JPH0339655B2 (pt) | ||
| US3687691A (en) | Method of incorporating volatile aromatics into hard candy | |
| US3947367A (en) | Hydroxy acid heat stabilizers for ABS resins lubricated with ethylenediamine bis-stearamide | |
| JPH0339654B2 (pt) | ||
| US4357168A (en) | Cellulosic compositions useful in preparing hot melts | |
| US2225894A (en) | Sugar composition | |
| CA2256622C (en) | Method for the encapsulation of liquids | |
| CA1133155A (en) | Method of preparing dry mixtures in powder form from polyvinylchloride, lubricating agents and stabilisers | |
| US2812264A (en) | Coatings for simplifying frost removal from refrigerated surfaces | |
| US2699996A (en) | Process for preparing a dried egg or citrus juice product | |
| JP2008524419A (ja) | 液体または低融点安定剤配合物 | |
| JPH0513181B2 (pt) | ||
| JP3556070B2 (ja) | 食品包装フィルム用塩化ビニル系樹脂組成物 | |
| RU2045545C1 (ru) | Способ получения полимерной композиции | |
| JPH03503290A (ja) | 塩化ビニリデンインターポリマー |