NO863160L - Kjernedannelse av propylenpolymerer. - Google Patents

Kjernedannelse av propylenpolymerer.

Info

Publication number: NO863160L
Authority: NO; Norway
Prior art keywords: approx; polymer; weight; propylene; propylene polymer
Prior art date: 1985-08-06

Application number

NO863160A

Other languages

English (en)

Norwegian (no)

Other versions

NO863160D0 (no

Inventor

Frederick Michael Teskin

Original Assignee

El Paso Products 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.)

1985-08-06

Filing date

1986-08-05

Publication date

1987-02-09

1986-08-05 Application filed by El Paso Products Co filed Critical El Paso Products Co

1986-08-05 Publication of NO863160D0 publication Critical patent/NO863160D0/no

1987-02-09 Publication of NO863160L publication Critical patent/NO863160L/no

Links

229920001155 polypropylene Polymers 0.000 title claims description 20
239000000203 mixture Substances 0.000 claims description 30
239000003054 catalyst Substances 0.000 claims description 26
229920000642 polymer Polymers 0.000 claims description 26
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 24
-1 aluminum alkoxide Chemical class 0.000 claims description 17
239000003795 chemical substances by application Substances 0.000 claims description 15
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 14
235000010233 benzoic acid Nutrition 0.000 claims description 14
230000003472 neutralizing effect Effects 0.000 claims description 14
239000005711 Benzoic acid Substances 0.000 claims description 12
238000000034 method Methods 0.000 claims description 12
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 10
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 10
235000011037 adipic acid Nutrition 0.000 claims description 9
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 8
239000005977 Ethylene Substances 0.000 claims description 8
239000001361 adipic acid Substances 0.000 claims description 7
229910052782 aluminium Inorganic materials 0.000 claims description 7
229920001577 copolymer Polymers 0.000 claims description 6
239000011777 magnesium Substances 0.000 claims description 6
229910052749 magnesium Inorganic materials 0.000 claims description 6
238000006116 polymerization reaction Methods 0.000 claims description 6
SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 claims description 5
230000008018 melting Effects 0.000 claims description 4
238000002844 melting Methods 0.000 claims description 4
238000002156 mixing Methods 0.000 claims description 4
WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 3
239000010936 titanium Substances 0.000 claims description 3
229910052719 titanium Inorganic materials 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 2
239000002667 nucleating agent Substances 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
238000002425 crystallisation Methods 0.000 description 5
230000008025 crystallization Effects 0.000 description 5
238000009472 formulation Methods 0.000 description 5
230000006911 nucleation Effects 0.000 description 5
238000010899 nucleation Methods 0.000 description 5
229920005604 random copolymer Polymers 0.000 description 5
239000002253 acid Substances 0.000 description 4
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
239000002952 polymeric resin Substances 0.000 description 4
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
239000003963 antioxidant agent Substances 0.000 description 3
150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
238000005266 casting Methods 0.000 description 3
230000008014 freezing Effects 0.000 description 3
238000007710 freezing Methods 0.000 description 3
229920005989 resin Polymers 0.000 description 3
239000011347 resin Substances 0.000 description 3
230000000007 visual effect Effects 0.000 description 3
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
239000007983 Tris buffer Substances 0.000 description 2
150000001279 adipic acids Chemical class 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
150000001559 benzoic acids Chemical class 0.000 description 2
238000009529 body temperature measurement Methods 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
238000001816 cooling Methods 0.000 description 2
239000012967 coordination catalyst Substances 0.000 description 2
PWZFXELTLAQOKC-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide;tetrahydrate Chemical compound O.O.O.O.[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O PWZFXELTLAQOKC-UHFFFAOYSA-A 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
229920000092 linear low density polyethylene Polymers 0.000 description 2
239000004707 linear low-density polyethylene Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000000155 melt Substances 0.000 description 2
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
230000009467 reduction Effects 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 2
235000010234 sodium benzoate Nutrition 0.000 description 2
239000004299 sodium benzoate Substances 0.000 description 2
238000007711 solidification Methods 0.000 description 2
230000008023 solidification Effects 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000725 suspension Substances 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
MQRCHVBRBGNZGJ-UHFFFAOYSA-N 2-[3,5-bis[2-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]ethyl]-2,4,6-trioxo-1,3,5-triazinan-1-yl]ethyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCCN2C(N(CCOC(=O)CCC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C(=O)N(CCOC(=O)CCC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C2=O)=O)=C1 MQRCHVBRBGNZGJ-UHFFFAOYSA-N 0.000 description 1
WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 description 1
VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 1
239000004322 Butylated hydroxytoluene Substances 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 1
239000006057 Non-nutritive feed additive Substances 0.000 description 1
BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
CSJKPFQJIDMSGF-UHFFFAOYSA-K aluminum;tribenzoate Chemical compound [Al+3].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 CSJKPFQJIDMSGF-UHFFFAOYSA-K 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
150000004982 aromatic amines Chemical group 0.000 description 1
125000003118 aryl group Chemical class 0.000 description 1
150000007514 bases Chemical class 0.000 description 1
238000007664 blowing Methods 0.000 description 1
235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
229940095259 butylated hydroxytoluene Drugs 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000008395 clarifying agent Substances 0.000 description 1
238000007906 compression Methods 0.000 description 1
230000006835 compression Effects 0.000 description 1
239000013078 crystal Substances 0.000 description 1
235000013766 direct food additive Nutrition 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000013538 functional additive Substances 0.000 description 1
YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
229960001545 hydrotalcite Drugs 0.000 description 1
229910001701 hydrotalcite Inorganic materials 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
238000001746 injection moulding Methods 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
229910001629 magnesium chloride Inorganic materials 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
239000000178 monomer Substances 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
125000002370 organoaluminium group Chemical group 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
239000008188 pellet Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
150000004986 phenylenediamines Chemical class 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
229920005672 polyolefin resin Polymers 0.000 description 1
229920005606 polypropylene copolymer Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
229920001384 propylene homopolymer Polymers 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
230000000707 stereoselective effect Effects 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
150000003609 titanium compounds Chemical class 0.000 description 1
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
238000005406 washing 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
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
- 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
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/092—Polycarboxylic acids

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Compositions Of Macromolecular Compounds (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

NO863160A 1985-08-06 1986-08-05 Kjernedannelse av propylenpolymerer. NO863160L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/762,903 US4704421A (en)	1985-08-06	1985-08-06	Nucleation of propylene polymers

Publications (2)

Publication Number	Publication Date
NO863160D0 NO863160D0 (no)	1986-08-05
NO863160L true NO863160L (no)	1987-02-09

Family

ID=25066347

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO863160A NO863160L (no)	1985-08-06	1986-08-05	Kjernedannelse av propylenpolymerer.

Country Status (5)

Country	Link
US (1)	US4704421A (fr)
EP (1)	EP0211650A3 (fr)
JP (1)	JPS6257405A (fr)
CA (1)	CA1269490A (fr)
NO (1)	NO863160L (fr)

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US5231126A (en) *	1985-04-01	1993-07-27	Shi Guan Yi	Beta-crystalline form of isotactic polypropylene and method for forming the same
US4801637A (en) *	1986-06-18	1989-01-31	Shell Oil Company	Nucleation process for inducing crystallization in poly(alpha olefins)
ES2028101T3 (es) *	1986-11-11	1992-07-01	Imperial Chemical Industries Plc	Una composicion que comprende un acido carboxilico y una amina.
KR100227663B1 (ko) *	1991-04-02	1999-11-01	가지와라 야스시	폴리프로필렌-계 수지조성물
AT404252B (de) *	1994-05-13	1998-10-27	Danubia Petrochem Polymere	Verfahren zur erhöhung des anteiles der beta-modifikation in polypropylen
US5674630A (en) *	1995-05-08	1997-10-07	Union Carbide Chemicals & Plastics Technology Corporation	Polymer compositions and cast films
US5929146A (en) *	1996-12-27	1999-07-27	Minnesota Mining And Manufacturing Company	Modifying agents for polyolefins
US6169133B1 (en) *	1997-06-25	2001-01-02	Lonza Inc.	Glycerol monostearate blends as antistats in polyolefins
US6303233B1 (en)	1998-04-06	2001-10-16	Mobil Oil Corporation	Uniaxially shrinkable biaxially oriented polypropylene film
US6387317B1 (en)	2000-01-20	2002-05-14	Aristech Chemical Corporation	Process for manufacturing clear shaped articles from polyolefin compositions
WO2002020528A2 (fr)	2000-09-01	2002-03-14	Milliken & Company	Nouveaux derives et nouvelles compositions d'alditol alkyles et fluores et articles en polyolefine les contenant
US6555696B2 (en) *	2001-03-23	2003-04-29	Milliken & Company	Asymmetric dipolar multi-substituted alditol derivatives, methods of making thereof, and compositions and articles containing same
US6599971B2 (en) *	2001-03-29	2003-07-29	Milliken & Company	Metals salts of hexahydrophthalic acid as nucleating additives for crystalline thermoplastics
US6559211B2 (en) *	2001-05-23	2003-05-06	Milliken & Company	Highly versatile thermoplastic nucleators
CA2449829A1 (fr)	2001-07-31	2003-02-13	Avery Dennison Corporation	Etiquettes holographiques adaptables
US6559216B1 (en) *	2001-08-21	2003-05-06	Milliken & Company	Low-color ultraviolet absorber compounds and compositions thereof
US6602447B2 (en) *	2001-08-21	2003-08-05	Milliken & Company	Low-color ultraviolet absorbers for high UV wavelength protection applications
US6703434B2 (en) *	2002-04-12	2004-03-09	Milliken & Company	Methods of producing highly nucleated syndiotactic polypropylene
AU2003226284A1 (en) *	2002-04-12	2003-10-27	Milliken And Company	Highly nucleated syndiotactic polypropylene
AU2003247735B2 (en)	2002-06-26	2010-03-11	Avery Dennison Corporation	Oriented films comprising polypropylene / olefin elastomer blends
US7094918B2 (en) *	2003-04-28	2006-08-22	Milliken & Company	Low-color ultraviolet absorbers for thermoplastic and thermoset high UV wavelength protection applications
US8870814B2 (en) *	2003-07-31	2014-10-28	Boston Scientific Scimed, Inc.	Implantable or insertable medical devices containing silicone copolymer for controlled delivery of therapeutic agent
US20050038151A1 (en) *	2003-08-12	2005-02-17	Christopher Kochanowicz	Low density polyethylene articles exhibiting significantly decreased warpage at reduced cooling times
US20050038157A1 (en) *	2003-08-12	2005-02-17	Christopher Kochanowicz	Low density polyethylene articles exhibiting significantly decreased warpage at reduced cooling times
US20050038156A1 (en) *	2003-08-12	2005-02-17	Stephane Berghmans	Polypropylenes exhibiting excellent long-term hydrostatic strength for high-pressure applications
US20050038155A1 (en) *	2003-08-12	2005-02-17	Stephane Berghmans	Thermoplastics exhibiting excellent long-term hydrostatic strength for high-pressure applications
US20050046065A1 (en) *	2003-08-30	2005-03-03	Cowan Martin E.	Thermoplastic fibers exhibiting durable high color strength characteristics
US6946507B2 (en) *	2003-10-03	2005-09-20	Milliken & Company	Nucleating additive formulations of bicyclo[2.2.1]heptane dicarboxylate salts
US6936650B2 (en) *	2003-10-03	2005-08-30	Milliken & Company	Nucleating additive formulations of bicyclo[2.2.1]heptane dicarboxylate salts
TW200631965A (en) *	2004-12-07	2006-09-16	Fina Technology	Random copolymers and formulations useful for thermoforming and blow molding applications
ES2398725T3 (es)	2006-06-14	2013-03-21	Avery Dennison Corporation	Material para etiquetas orientado en la dirección longitudinal que se puede conformar y cortar con troquel y etiquetas y proceso para su preparación
BRPI0713492A2 (pt)	2006-06-20	2012-01-24	Avery Dennison Corp	filme polimérico de multi-camadas para rotulagem de adesivos de derretimento a quente e etiqueta e rótulo dos mesmos
JP5579436B2 (ja)	2006-07-17	2014-08-27	エーブリーデニソンコーポレイション	非対称の多層高分子フィルム、並びにラベルストック及びそのラベル
US9676532B2 (en)	2012-08-15	2017-06-13	Avery Dennison Corporation	Packaging reclosure label for high alcohol content products
JP2017520642A (ja)	2014-06-02	2017-07-27	アベリー・デニソン・コーポレイションＡｖｅｒｙＤｅｎｎｉｓｏｎＣｏｒｐｏｒａｔｉｏｎ	耐スカッフ性、透明性、及び順応性が改善されたフィルム

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1001709A (en) *	1962-06-08	1965-08-18	Ici Ltd	Polypropylene compositions
BE633717A (fr) *	1962-06-18
US3367926A (en) *	1964-03-25	1968-02-06	Dow Chemical Co	Modification of crystalline structure of crystallizable high polymers
JPS5580447A (en) *	1978-12-14	1980-06-17	Kyowa Chem Ind Co Ltd	Prevention of rust, deterioration or coloring of polyolefin and composition
DE3133101A1 (de) *	1981-08-21	1983-03-10	Hoechst Ag, 6000 Frankfurt	Verfahren zur entfernung von katalysatorresten aus polyolefinen
IT1151509B (it) *	1982-02-08	1986-12-24	Montefina Sa	Agente di nucleazione per polimeri olefinici cristallini

1985
- 1985-08-06 US US06/762,903 patent/US4704421A/en not_active Expired - Fee Related
1986
- 1986-07-23 CA CA000514454A patent/CA1269490A/fr not_active Expired - Lifetime
- 1986-08-05 JP JP61182838A patent/JPS6257405A/ja active Pending
- 1986-08-05 EP EP86306039A patent/EP0211650A3/fr not_active Withdrawn
- 1986-08-05 NO NO863160A patent/NO863160L/no unknown

Also Published As

Publication number	Publication date
EP0211650A2 (fr)	1987-02-25
EP0211650A3 (fr)	1988-05-04
US4704421A (en)	1987-11-03
JPS6257405A (ja)	1987-03-13
CA1269490A (fr)	1990-05-22
NO863160D0 (no)	1986-08-05

Publication	Publication Date	Title
NO863160L (no)	1987-02-09	Kjernedannelse av propylenpolymerer.
US8173735B2 (en)	2012-05-08	Resin additive master batch
US5681922A (en)	1997-10-28	Process for increasing the proportion of the β-modification in polypropylene
US5120783A (en)	1992-06-09	Stabilized halogen-containing resin compositions
DE4420989B4 (de)	2005-04-14	Verfahren zur Erhöhung des Anteils der ß-Modifikation in Polypropylen
EP2796477B1 (fr)	2016-01-20	Procédé de production d'un polymère stabilisé
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