LU83317A1 - Compositions de matieres plastiques ameliorees a base de polyolefines - Google Patents
Compositions de matieres plastiques ameliorees a base de polyolefines Download PDFInfo
- Publication number
- LU83317A1 LU83317A1 LU83317A LU83317A LU83317A1 LU 83317 A1 LU83317 A1 LU 83317A1 LU 83317 A LU83317 A LU 83317A LU 83317 A LU83317 A LU 83317A LU 83317 A1 LU83317 A1 LU 83317A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- sorbitol
- group
- olefin
- aliphatic
- chlorobenzylidene
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 39
- 229920000098 polyolefin Polymers 0.000 title claims description 24
- 229920003023 plastic Polymers 0.000 title claims description 9
- 239000004033 plastic Substances 0.000 title claims description 8
- 229960002920 sorbitol Drugs 0.000 claims description 37
- 239000000600 sorbitol Substances 0.000 claims description 36
- -1 aliphatic olefin Chemical group 0.000 claims description 30
- 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 claims description 15
- 235000010356 sorbitol Nutrition 0.000 claims description 15
- FMZUHGYZWYNSOA-VVBFYGJXSA-N (1r)-1-[(4r,4ar,8as)-2,6-diphenyl-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol Chemical compound C([C@@H]1OC(O[C@@H]([C@@H]1O1)[C@H](O)CO)C=2C=CC=CC=2)OC1C1=CC=CC=C1 FMZUHGYZWYNSOA-VVBFYGJXSA-N 0.000 claims description 13
- 229940087101 dibenzylidene sorbitol Drugs 0.000 claims description 13
- 229920000642 polymer Polymers 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 9
- ZETHHMPKDUSZQQ-UHFFFAOYSA-N Betulafolienepentol Natural products C1C=C(C)CCC(C(C)CCC=C(C)C)C2C(OC)OC(OC)C2=C1 ZETHHMPKDUSZQQ-UHFFFAOYSA-N 0.000 claims description 6
- PCSMJKASWLYICJ-UHFFFAOYSA-N Succinic aldehyde Chemical compound O=CCCC=O PCSMJKASWLYICJ-UHFFFAOYSA-N 0.000 claims description 6
- HEOKFDGOFROELJ-UHFFFAOYSA-N diacetal Natural products COc1ccc(C=C/c2cc(O)cc(OC3OC(COC(=O)c4cc(O)c(O)c(O)c4)C(O)C(O)C3O)c2)cc1O HEOKFDGOFROELJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims description 4
- 239000004014 plasticizer Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 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 claims description 2
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- MIMDHDXOBDPUQW-UHFFFAOYSA-N dioctyl decanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCC MIMDHDXOBDPUQW-UHFFFAOYSA-N 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims 2
- 150000005673 monoalkenes Chemical class 0.000 claims 2
- SONZVMBIAGVDAT-IYWMVGAKSA-N (3s,4s,5s,6r)-1,8-bis(3,4-dichlorophenyl)octa-1,7-diene-2,3,4,5,6,7-hexol Chemical compound OC([C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=CC=1C=C(Cl)C(Cl)=CC=1)=CC1=CC=C(Cl)C(Cl)=C1 SONZVMBIAGVDAT-IYWMVGAKSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 229920001519 homopolymer Polymers 0.000 claims 1
- 230000000379 polymerizing effect Effects 0.000 claims 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 239000000654 additive Substances 0.000 description 14
- 238000000034 method Methods 0.000 description 13
- 239000000047 product Substances 0.000 description 13
- 239000004743 Polypropylene Substances 0.000 description 11
- 229920001155 polypropylene Polymers 0.000 description 11
- 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 9
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- 150000001299 aldehydes Chemical class 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000126 substance Substances 0.000 description 5
- HDUNAIVOFOKALD-RLCYQCIGSA-N (1s,2s)-1-[(4r)-2-(4-methylphenyl)-1,3-dioxolan-4-yl]-2-[(4s)-2-(4-methylphenyl)-1,3-dioxolan-4-yl]ethane-1,2-diol Chemical compound C1=CC(C)=CC=C1C1O[C@@H]([C@@H](O)[C@H](O)[C@H]2OC(OC2)C=2C=CC(C)=CC=2)CO1 HDUNAIVOFOKALD-RLCYQCIGSA-N 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000005022 packaging material Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- HZVFRKSYUGFFEJ-YVECIDJPSA-N (2r,3r,4s,5r)-7-phenylhept-6-ene-1,2,3,4,5,6-hexol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=CC1=CC=CC=C1 HZVFRKSYUGFFEJ-YVECIDJPSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- AVPYQKSLYISFPO-UHFFFAOYSA-N 4-chlorobenzaldehyde Chemical compound ClC1=CC=C(C=O)C=C1 AVPYQKSLYISFPO-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
- 239000008395 clarifying agent Substances 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 230000001965 increasing effect Effects 0.000 description 2
- 239000013081 microcrystal Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- ZDFKSZDMHJHQHS-UHFFFAOYSA-N 2-tert-butylbenzoic acid Chemical compound CC(C)(C)C1=CC=CC=C1C(O)=O ZDFKSZDMHJHQHS-UHFFFAOYSA-N 0.000 description 1
- SUISZCALMBHJQX-UHFFFAOYSA-N 3-bromobenzaldehyde Chemical compound BrC1=CC=CC(C=O)=C1 SUISZCALMBHJQX-UHFFFAOYSA-N 0.000 description 1
- 229910014033 C-OH Inorganic materials 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 229910014570 C—OH Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- OVWYEQOVUDKZNU-UHFFFAOYSA-N m-tolualdehyde Chemical compound CC1=CC=CC(C=O)=C1 OVWYEQOVUDKZNU-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- FXLOVSHXALFLKQ-UHFFFAOYSA-N p-tolualdehyde Chemical compound CC1=CC=C(C=O)C=C1 FXLOVSHXALFLKQ-UHFFFAOYSA-N 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000010998 test method Methods 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
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/156—Heterocyclic compounds having oxygen in the ring having two oxygen atoms in the ring
- C08K5/1575—Six-membered rings
-
- 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
- C08K5/04—Oxygen-containing compounds
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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14325880A | 1980-04-24 | 1980-04-24 | |
| US14325880 | 1980-04-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU83317A1 true LU83317A1 (fr) | 1981-07-24 |
Family
ID=22503279
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU83317A LU83317A1 (fr) | 1980-04-24 | 1981-04-24 | Compositions de matieres plastiques ameliorees a base de polyolefines |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS56161444A (de) |
| BE (1) | BE888550A (de) |
| CA (1) | CA1161975A (de) |
| DE (1) | DE3116408C2 (de) |
| FR (1) | FR2481296B1 (de) |
| GB (1) | GB2077255B (de) |
| IT (1) | IT1143201B (de) |
| LU (1) | LU83317A1 (de) |
| MX (1) | MX158562A (de) |
| NL (1) | NL180842C (de) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58180543A (ja) * | 1982-04-19 | 1983-10-22 | Mitsubishi Petrochem Co Ltd | プロピレン重合体組成物 |
| JPS58180546A (ja) * | 1982-04-19 | 1983-10-22 | Iic Kagaku Kogyo Kk | アクリル樹脂成形品 |
| JPS58185632A (ja) * | 1982-04-23 | 1983-10-29 | Iic Kagaku Kogyo Kk | ポリオレフイン樹脂組成物 |
| JPS59174382A (ja) * | 1983-03-24 | 1984-10-02 | Canon Inc | 被記録材 |
| JPS60127335A (ja) * | 1983-12-13 | 1985-07-08 | Mitsui Toatsu Chem Inc | ポリプロピレン樹脂製容器 |
| JPS60127336A (ja) * | 1983-12-13 | 1985-07-08 | Mitsui Toatsu Chem Inc | 透明なポリプロピレン製ブロ−成形容器 |
| JPH0639554B2 (ja) * | 1983-12-13 | 1994-05-25 | 三井東圧化学株式会社 | 透明なポリプロピレン樹脂製容器 |
| JPS60127338A (ja) * | 1983-12-13 | 1985-07-08 | Mitsui Toatsu Chem Inc | 良好な透明性を有するポリプロピレン樹脂製容器 |
| US6300525B1 (en) | 2000-09-01 | 2001-10-09 | Milliken & Company | Method of producing fluorinated and chlorinated benzaldehydes and compositions thereof |
| US6297405B1 (en) | 2000-09-01 | 2001-10-02 | Milliken & Company | Fluorinated and chlorinated benzaldehydes |
| WO2024171881A1 (ja) * | 2023-02-17 | 2024-08-22 | 三菱瓦斯化学株式会社 | 化合物、組成物、成形体、及び製造方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5122740A (de) * | 1974-08-16 | 1976-02-23 | Kenzo Hamada | |
| JPS5428348A (en) * | 1977-08-06 | 1979-03-02 | New Japan Chem Co Ltd | Modification of polyethylene |
| JPS54149752A (en) * | 1978-05-17 | 1979-11-24 | Mitsui Toatsu Chem Inc | Polyolefin resin composition for injection molding |
-
1981
- 1981-04-22 CA CA000375990A patent/CA1161975A/en not_active Expired
- 1981-04-23 GB GB8112611A patent/GB2077255B/en not_active Expired
- 1981-04-23 NL NLAANVRAGE8102012,A patent/NL180842C/xx not_active IP Right Cessation
- 1981-04-23 MX MX186990A patent/MX158562A/es unknown
- 1981-04-23 IT IT48334/81A patent/IT1143201B/it active
- 1981-04-24 FR FR8108241A patent/FR2481296B1/fr not_active Expired
- 1981-04-24 LU LU83317A patent/LU83317A1/fr unknown
- 1981-04-24 DE DE3116408A patent/DE3116408C2/de not_active Expired
- 1981-04-24 BE BE0/204596A patent/BE888550A/fr not_active IP Right Cessation
- 1981-04-24 JP JP6233181A patent/JPS56161444A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DE3116408A1 (de) | 1982-01-28 |
| NL8102012A (nl) | 1981-11-16 |
| FR2481296A1 (fr) | 1981-10-30 |
| MX158562A (es) | 1989-02-15 |
| NL180842B (nl) | 1986-12-01 |
| BE888550A (fr) | 1981-10-26 |
| JPS6140254B2 (de) | 1986-09-08 |
| GB2077255A (en) | 1981-12-16 |
| DE3116408C2 (de) | 1984-09-27 |
| GB2077255B (en) | 1984-03-14 |
| IT8148334A0 (it) | 1981-04-23 |
| NL180842C (nl) | 1987-05-04 |
| IT1143201B (it) | 1986-10-22 |
| FR2481296B1 (fr) | 1985-12-20 |
| CA1161975A (en) | 1984-02-07 |
| JPS56161444A (en) | 1981-12-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4371645A (en) | Polyolefin plastic compositions comprising meta- or papa-derivatives (choro- or bromo-) of di-benzyuidene sorbitol | |
| EP0286522B1 (de) | Alditoldiacetale von grosser Reinheit und frei von organischen Lösungsmittelspuren sowie Verfahren zu ihrer Herstellung | |
| EP1313741B1 (de) | Fluorierte and alkylierte alditolderivate und diese enthaltende gegenstände aus polyolefinen | |
| LU83317A1 (fr) | Compositions de matieres plastiques ameliorees a base de polyolefines | |
| FR2572409A1 (fr) | Absorbant uv polymerisable par voie radicalaire, procede pour sa fabrication et ses polymeres | |
| FR2721036A1 (fr) | Nouveaux produits améliorant la cristallinité des matières polymères. | |
| US20020062034A1 (en) | Novel fluorinated and alkylated alditol derivatives and compositions and polyolefin articles containing same | |
| CA2020133C (fr) | Nouvelles dihydropyridines a groupements amine encombree | |
| CH645910A5 (fr) | Composition polymere thermoplastique apte au faconnage, contenant un acetal cyclique en tant qu'agent de nucleation. | |
| FR2739381A1 (fr) | Stabilisation de matieres polymeres avec des derives du phosphore | |
| BE1012673A3 (fr) | Nouveaux derives de 6-amino-uracile, leur preparation et leur utilisation. | |
| BE879012A (fr) | Procede de preparation de dibenzylidene-sorbitol et composition en contenant | |
| CA1090931A (fr) | Compositions plastifiees et stabilisees a base de poly (chlorure de vinyle) | |
| FR2549074A1 (fr) | Nouvelles compositions ignifugeantes et stabilisantes du polyethylene | |
| WO2023213434A1 (fr) | Procede de preparation d'une composition de diester de 1,4:3,6-dianydrohexitol | |
| US6512030B2 (en) | Asymmetric monofluorinated benzaldehyde alditol derivatives and compositions and articles containing same | |
| JP2023005379A (ja) | 環状オレフィン系共重合体組成物の製造方法、環状オレフィン系共重合体組成物、成形体、成形体の製造方法および光学レンズ | |
| EP0070218A1 (de) | Feuerhemmende halogenierte aromatische Verbindungen | |
| BE581104A (de) | ||
| FR2652584A1 (fr) | Additif pour augmenter l'energie de surface de polyolefines de type a mouler et extruder. | |
| BE665534A (de) | ||
| FR2824067A1 (fr) | Utilisation de b-dicetone diaromatique substituee comme stabilisant de polymeres halogenes et polymere obtenu | |
| CH638544A5 (en) | Chlorinated vinyl resin composition | |
| FR2642066A1 (fr) | Derives triacycles d'amidoximes, leur synthese et leurs applications industrielles notamment comme agents reticulants des polyolefines | |
| BE622997A (de) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| DT | Application date | ||
| TA | Annual fee |