NO783997L - Faste, hydrolysebestandige fosforsyrlingestertilberedninger med forbedret stabilisatorvirkning i kunststoffer - Google Patents

Faste, hydrolysebestandige fosforsyrlingestertilberedninger med forbedret stabilisatorvirkning i kunststoffer

Info

Publication number: NO783997L
Authority: NO; Norway
Prior art keywords: wax; phosphoric acid; weight; acid ester; stabilizer
Prior art date: 1977-11-29

Application number

NO783997A

Other languages

English (en)

Norwegian (no)

Inventor

Walter Brotz

Norbert Mayer

Gerhard Pfahler

Eberhard Prinz

Hartmut Wiezer

Original Assignee

Hoechst Ag

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.)

1977-11-29

Filing date

1978-11-28

Publication date

1979-05-30

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=6024859&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO783997(L) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1978-11-28 Application filed by Hoechst Ag filed Critical Hoechst Ag

1979-05-30 Publication of NO783997L publication Critical patent/NO783997L/no

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)

NO783997A 1977-11-29 1978-11-28 Faste, hydrolysebestandige fosforsyrlingestertilberedninger med forbedret stabilisatorvirkning i kunststoffer NO783997L (no)

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 (fr)
JP (1)	JPS5483951A (fr)
AT (1)	AT368769B (fr)
AU (1)	AU522136B2 (fr)
BR (1)	BR7807807A (fr)
CA (1)	CA1113706A (fr)
DE (2)	DE2753136B2 (fr)
ES (1)	ES475321A1 (fr)
IT (1)	IT1101440B (fr)
NO (1)	NO783997L (fr)
ZA (1)	ZA786674B (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1120793A (fr) *	1977-12-23	1982-03-30	Ved K. Sahajpal	Phosphites encapsules
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)

* Cited by examiner, † Cited by third party
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/fr 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 JP JP14612978A patent/JPS5483951A/ja active Pending
- 1978-11-28 ZA ZA00786674A patent/ZA786674B/xx unknown
- 1978-11-28 BR BR7807807A patent/BR7807807A/pt unknown
- 1978-11-28 AU AU41981/78A patent/AU522136B2/en not_active Expired
- 1978-11-28 NO NO783997A patent/NO783997L/no unknown
- 1978-11-28 CA CA316,970A patent/CA1113706A/fr not_active Expired

Also Published As

Publication number	Publication date
EP0002243B1 (fr)	1982-06-02
BR7807807A (pt)	1979-07-31
ATA850078A (de)	1982-03-15
EP0002243A1 (fr)	1979-06-13
DE2861885D1 (en)	1982-07-22
DE2753136A1 (de)	1979-06-07
JPS5483951A (en)	1979-07-04
ES475321A1 (es)	1979-04-01
IT7830238A0 (it)	1978-11-27
AU522136B2 (en)	1982-05-20
ZA786674B (en)	1979-11-28
AT368769B (de)	1982-11-10
DE2753136B2 (de)	1981-04-02
IT1101440B (it)	1985-09-28
CA1113706A (fr)	1981-12-08
AU4198178A (en)	1979-06-07

Publication	Publication Date	Title
DE3876110T2 (de)	1993-05-27	Feste stabilisatormischung fuer organische polymere und verfahren zu ihrer herstellung.
CZ277731B6 (en)	1993-04-14	Polypropylene and process for preparing thereof
Cebula et al.	1993	Studies of bloom formation using X‐ray diffraction from chocolates after long‐term storage
NO783997L (no)	1979-05-30	Faste, hydrolysebestandige fosforsyrlingestertilberedninger med forbedret stabilisatorvirkning i kunststoffer
CA1126047A (fr)	1982-06-22	Compositions solides d'un sel de pyrazolium, d'uree et d'un surfactant liquide
US4973491A (en)	1990-11-27	Honey product
US2929723A (en)	1960-03-22	Compositions containing flavoring agent and lecithin in a sugar base and process of making the same
NO803095L (no)	1982-04-19	Tilsetningsmiddel i enkeltforpakning for thermoplastiske materialer
US2911303A (en)	1959-11-03	Peanut butter product
YUKI et al.	1990	Effect of sucrose polyesters on crystallization behavior of vegetable shortening and margarine fat
DE3636023C2 (fr)	1989-03-23
JPH0339655B2 (fr)	1991-06-14
US3947367A (en)	1976-03-30	Hydroxy acid heat stabilizers for ABS resins lubricated with ethylenediamine bis-stearamide
US3687691A (en)	1972-08-29	Method of incorporating volatile aromatics into hard candy
JPH0339654B2 (fr)	1991-06-14
DE69711379T2 (de)	2002-10-10	Verfahren für einkapselung von flüssigkeiten
US5300539A (en)	1994-04-05	Post-polymerization additive incorporation process
FI94825B (fi)	1995-07-31	Kiinteä koostumus ruoan jäähdytysapuainetta varten, jäähdytysapuaine sekä menetelmät tämän koostumuksen sekä jauhelihaan perustuvan ruoka-aineen valmistamiseksi
US4012534A (en)	1977-03-15	Preparation of process cheese
US2906727A (en)	1959-09-29	Cloroethylene polymer and di-9-fluorenyl ethers or dibenzhydryl ethers
SU1542519A1 (ru)	1990-02-15	Способ получени концентрата молочной сыворотки
US2812264A (en)	1957-11-05	Coatings for simplifying frost removal from refrigerated surfaces
RU2045545C1 (ru)	1995-10-10	Способ получения полимерной композиции
JP3556070B2 (ja)	2004-08-18	食品包装フィルム用塩化ビニル系樹脂組成物
JPH03503290A (ja)	1991-07-25	塩化ビニリデンインターポリマー