NO325683B1 - Fremgangsmate for fremstilling av et adhesive med lavt niva av restmonomerer - Google Patents

Fremgangsmate for fremstilling av et adhesive med lavt niva av restmonomerer Download PDF

Info

Publication number: NO325683B1
Authority: NO; Norway
Prior art keywords: catalyst; hydrogenation; bar; residual; palladium
Prior art date: 1996-10-31

Application number

NO19992081A

Other languages

English (en)

Norwegian (no)

Other versions

NO992081D0 (no

NO992081L (no

Inventor

Thomas Hille

James Burkert

Paul M Petersen

Paul B Foreman

Original Assignee

Lohmann Therapie Syst Lts

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.)

1996-10-31

Filing date

1999-04-29

Publication date

2008-07-07

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26030668&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO325683(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1996-10-31 Priority claimed from DE19643959A external-priority patent/DE19643959A1/de

1999-04-29 Application filed by Lohmann Therapie Syst Lts filed Critical Lohmann Therapie Syst Lts

1999-04-29 Publication of NO992081D0 publication Critical patent/NO992081D0/no

1999-06-25 Publication of NO992081L publication Critical patent/NO992081L/no

2008-07-07 Publication of NO325683B1 publication Critical patent/NO325683B1/no

Links

239000000178 monomer Substances 0.000 title claims abstract description 35
239000000853 adhesive Substances 0.000 title claims abstract description 26
230000001070 adhesive effect Effects 0.000 title claims abstract description 26
238000004519 manufacturing process Methods 0.000 title claims description 6
229920000642 polymer Polymers 0.000 claims abstract description 47
238000005984 hydrogenation reaction Methods 0.000 claims description 54
239000003054 catalyst Substances 0.000 claims description 47
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical group CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 45
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 45
238000000034 method Methods 0.000 claims description 35
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 24
239000001257 hydrogen Substances 0.000 claims description 20
229910052739 hydrogen Inorganic materials 0.000 claims description 20
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 17
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 16
229910052763 palladium Inorganic materials 0.000 claims description 14
239000003960 organic solvent Substances 0.000 claims description 11
239000002815 homogeneous catalyst Substances 0.000 claims description 9
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 8
229910052799 carbon Inorganic materials 0.000 claims description 7
239000002638 heterogeneous catalyst Substances 0.000 claims description 7
238000006116 polymerization reaction Methods 0.000 claims description 7
QBERHIJABFXGRZ-UHFFFAOYSA-M rhodium;triphenylphosphane;chloride Chemical compound [Cl-].[Rh].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 QBERHIJABFXGRZ-UHFFFAOYSA-M 0.000 claims description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
229910052697 platinum Inorganic materials 0.000 claims description 4
238000007334 copolymerization reaction Methods 0.000 claims description 3
239000002537 cosmetic Substances 0.000 abstract description 4
238000009903 catalytic hydrogenation reaction Methods 0.000 abstract description 3
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 25
239000000243 solution Substances 0.000 description 25
238000001914 filtration Methods 0.000 description 16
229920001577 copolymer Polymers 0.000 description 15
239000000203 mixture Substances 0.000 description 11
239000002904 solvent Substances 0.000 description 10
239000007787 solid Substances 0.000 description 9
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
239000004820 Pressure-sensitive adhesive Substances 0.000 description 6
230000001225 therapeutic effect Effects 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
229940048053 acrylate Drugs 0.000 description 5
238000002474 experimental method Methods 0.000 description 5
239000003999 initiator Substances 0.000 description 5
239000010410 layer Substances 0.000 description 5
239000011159 matrix material Substances 0.000 description 5
229910052759 nickel Inorganic materials 0.000 description 5
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
239000011248 coating agent Substances 0.000 description 4
238000000576 coating method Methods 0.000 description 4
229910001873 dinitrogen Inorganic materials 0.000 description 4
238000009472 formulation Methods 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
239000002245 particle Substances 0.000 description 4
238000006722 reduction reaction Methods 0.000 description 4
238000012360 testing method Methods 0.000 description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 3
150000001252 acrylic acid derivatives Chemical class 0.000 description 3
238000001514 detection method Methods 0.000 description 3
239000003814 drug Substances 0.000 description 3
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 3
229920001519 homopolymer Polymers 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
239000011995 wilkinson's catalyst Substances 0.000 description 3
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
239000004342 Benzoyl peroxide Substances 0.000 description 2
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
239000013543 active substance Substances 0.000 description 2
239000002390 adhesive tape Substances 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
235000019400 benzoyl peroxide Nutrition 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
238000001816 cooling Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
-1 ethyl hexyl ester Chemical class 0.000 description 2
239000000463 material Substances 0.000 description 2
150000002734 metacrylic acid derivatives Chemical class 0.000 description 2
150000002739 metals Chemical class 0.000 description 2
238000004806 packaging method and process Methods 0.000 description 2
239000008188 pellet Substances 0.000 description 2
230000000737 periodic effect Effects 0.000 description 2
229920000058 polyacrylate Polymers 0.000 description 2
239000000843 powder Substances 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
229910052703 rhodium Inorganic materials 0.000 description 2
239000010948 rhodium Substances 0.000 description 2
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 1
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
239000012159 carrier gas Substances 0.000 description 1
238000010531 catalytic reduction reaction Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000001035 drying Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
238000000769 gas chromatography-flame ionisation detection Methods 0.000 description 1
239000003292 glue Substances 0.000 description 1
239000001307 helium Substances 0.000 description 1
229910052734 helium Inorganic materials 0.000 description 1
SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 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
150000001451 organic peroxides Chemical class 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000003495 polar organic solvent Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
239000003505 polymerization initiator Substances 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
238000011085 pressure filtration Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
239000002356 single layer Substances 0.000 description 1
229940047670 sodium acrylate Drugs 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
239000011550 stock solution Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000013589 supplement Substances 0.000 description 1
230000001502 supplementing effect Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
229940100640 transdermal system Drugs 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000002569 water oil cream Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0208—Tissues; Wipes; Patches
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/58—Adhesives
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/58—Adhesives
- A61L15/585—Mixtures of macromolecular compounds
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/04—Reduction, e.g. hydrogenation

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Veterinary Medicine (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Epidemiology (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Hematology (AREA)
Birds (AREA)
Organic Chemistry (AREA)
Medicinal Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Dermatology (AREA)
Polymers & Plastics (AREA)
Biomedical Technology (AREA)
Bioinformatics & Cheminformatics (AREA)
Pharmacology & Pharmacy (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Adhesives Or Adhesive Processes (AREA)
Medicinal Preparation (AREA)
Materials For Medical Uses (AREA)
Chemical And Physical Treatments For Wood And The Like (AREA)
Processing Of Solid Wastes (AREA)

NO19992081A 1996-10-31 1999-04-29 Fremgangsmate for fremstilling av et adhesive med lavt niva av restmonomerer NO325683B1 (no)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
DE19643959A DE19643959A1 (de)	1996-10-31	1996-10-31	Kleber, enthaltend Polymere mit einem sehr geringen Gehalt an Restmonomeren, ein Verfahren zu ihrer Herstellung und ihre Verwendung
US08/928,313 US5990229A (en)	1996-10-31	1997-09-12	Adhesives with low level of residual monomers and process for manufacturing same
PCT/US1997/018622 WO1998018829A1 (en)	1996-10-31	1997-10-14	Adhesives with low level of residual monomers and process for manufacturing same

Publications (3)

Publication Number	Publication Date
NO992081D0 NO992081D0 (no)	1999-04-29
NO992081L NO992081L (no)	1999-06-25
NO325683B1 true NO325683B1 (no)	2008-07-07

Family

ID=26030668

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO19992081A NO325683B1 (no)	1996-10-31	1999-04-29	Fremgangsmate for fremstilling av et adhesive med lavt niva av restmonomerer

Country Status (20)

Country	Link
EP (1)	EP0935616B2 (cs)
JP (1)	JP2001503796A (cs)
KR (1)	KR100623165B1 (cs)
AT (1)	ATE221088T1 (cs)
AU (1)	AU745244B2 (cs)
BR (1)	BR9712383A (cs)
CA (1)	CA2270220C (cs)
CZ (1)	CZ301008B6 (cs)
DE (1)	DE69714280T3 (cs)
DK (1)	DK0935616T4 (cs)
ES (1)	ES2180953T5 (cs)
HU (1)	HUP0000149A3 (cs)
IL (1)	IL129649A0 (cs)
NO (1)	NO325683B1 (cs)
NZ (1)	NZ335907A (cs)
PL (1)	PL195326B1 (cs)
PT (1)	PT935616E (cs)
RU (1)	RU2215014C2 (cs)
TR (1)	TR199900930T2 (cs)
WO (1)	WO1998018829A1 (cs)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US8148450B2 (en) *	2006-06-23	2012-04-03	Exxonmobil Chemical Patents Inc.	Process to produce a hydrocarbon rubber cement utilizing a hydrofluorocarbon diluent
US8946365B2 (en)	2012-01-18	2015-02-03	Eastman Chemical Company	Low molecular weight polystyrene resin and methods of making and using the same
MX2020001702A (es)	2017-08-16	2020-09-09	Dow Global Technologies Llc	Composiciones adhesivas sensibles a la presion y metodos para realizar las mismas.

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3734819A (en) *	1972-02-14	1973-05-22	Union Oil Co	Ethylene-vinyl acetate emulsion adhesive
US3920592A (en) *	1973-08-01	1975-11-18	Central Soya Co	Method for producing paper coating binder involving grafting unsaturated acrylate monomers onto proteinaceous substrate in water
US4375529A (en) *	1981-08-03	1983-03-01	Nalco Chemical Company	Hydrogenation of residual monomers in partially polymerized acrylamide copolymers in latex form
DD210696B1 (de) †	1982-10-20	1986-11-12	Buna Chem Werke Veb	Verfahren zur herstellung eines verbundlatex
US4725639A (en) *	1983-11-09	1988-02-16	Air Products And Chemicals, Inc.	Process for preparing pressure sensitive adhesives
NL8502134A (nl) *	1985-07-26	1987-02-16	Dsm Resins Bv	Gehydrogeneerde koolwaterstofhars en toepassing daarvan in lijmen.
DD249484A1 (de) †	1986-06-02	1987-09-09	Buna Chem Werke Veb	Verfahren zur herstellung eines latex zur haftvermittlung
US4737577A (en) *	1986-12-31	1988-04-12	Minnesota Mining And Manufacturing Company	Method for removing monomer from an acrylate adhesive by reaction with a scavenger monomer
JPH0753849B2 (ja) †	1988-08-29	1995-06-07	積水化学工業株式会社	アクリル系粘着テープもしくはシートの製造方法
DE3834734A1 (de) *	1988-10-12	1990-04-19	Basf Ag	Verfahren zur herstellung von polymerisaten aus olefinisch ungesaettigten monomeren
DE4118526A1 (de) †	1990-06-15	1991-12-19	Basf Ag	Verfahren zur entfernung von restmonomeren und niedermolekularen verunreinigungen aus waessrigen polymerdispersionen
DE4021961A1 (de) †	1990-07-10	1992-01-16	Basf Ag	Verfahren zur entfernung von fluechtigen bestandteilen aus emulsionspolymerisaten
GB9113912D0 (en) *	1991-06-27	1991-08-14	Ici Resins Bv	Removal of residual monomers from polymers
JPH0768297B2 (ja) *	1991-11-28	1995-07-26	丸善石油化学株式会社	フォトレジスト用ビニルフェノール系重合体の精製方法
JP2539720B2 (ja) †	1992-01-22	1996-10-02	日本製紙株式会社	バインダ―樹脂組成物及びその製法
JP3722858B2 (ja) †	1993-11-25	2005-11-30	ビーエーエスエフアクチェンゲゼルシャフト	ポリアクリレート溶融体から残留揮発分を除去する方法
CN1120180C (zh) †	1994-06-03	2003-09-03	巴斯福股份公司	聚合物水分散液的制备
US6274666B1 (en) *	1994-08-11	2001-08-14	Bridgestone/Firestone, Inc.	Adhesive and polymer for adhesives
DE4435422A1 (de) †	1994-10-04	1996-04-18	Basf Ag	Verfahren zur Herstellung einer wäßrigen Polymerisatdispersion
DE69513943T2 (de) *	1995-02-03	2000-05-18	Hercules Inc., Wilmington	Verfahren zur Hydrobehandlung von Harzen zur Farbverbesserung

1997
- 1997-10-14 JP JP52052198A patent/JP2001503796A/ja active Pending
- 1997-10-14 DE DE69714280T patent/DE69714280T3/de not_active Expired - Lifetime
- 1997-10-14 AT AT97911739T patent/ATE221088T1/de not_active IP Right Cessation
- 1997-10-14 PL PL97333125A patent/PL195326B1/pl not_active IP Right Cessation
- 1997-10-14 DK DK97911739.7T patent/DK0935616T4/da active
- 1997-10-14 TR TR1999/00930T patent/TR199900930T2/xx unknown
- 1997-10-14 NZ NZ335907A patent/NZ335907A/en unknown
- 1997-10-14 IL IL12964997A patent/IL129649A0/xx active IP Right Grant
- 1997-10-14 CZ CZ0151799A patent/CZ301008B6/cs not_active IP Right Cessation
- 1997-10-14 PT PT97911739T patent/PT935616E/pt unknown
- 1997-10-14 ES ES97911739T patent/ES2180953T5/es not_active Expired - Lifetime
- 1997-10-14 WO PCT/US1997/018622 patent/WO1998018829A1/en not_active Ceased
- 1997-10-14 KR KR1019997003804A patent/KR100623165B1/ko not_active Expired - Fee Related
- 1997-10-14 BR BR9712383-8A patent/BR9712383A/pt not_active IP Right Cessation
- 1997-10-14 HU HU0000149A patent/HUP0000149A3/hu active IP Right Revival
- 1997-10-14 RU RU99111359/04A patent/RU2215014C2/ru not_active IP Right Cessation
- 1997-10-14 EP EP97911739A patent/EP0935616B2/en not_active Expired - Lifetime
- 1997-10-14 AU AU49042/97A patent/AU745244B2/en not_active Ceased
- 1997-10-14 CA CA002270220A patent/CA2270220C/en not_active Expired - Fee Related
1999
- 1999-04-29 NO NO19992081A patent/NO325683B1/no not_active IP Right Cessation

Also Published As

Publication number	Publication date
DE69714280T3 (de)	2010-10-28
AU4904297A (en)	1998-05-22
NO992081D0 (no)	1999-04-29
ES2180953T3 (es)	2003-02-16
CZ151799A3 (cs)	1999-12-15
EP0935616B2 (en)	2010-04-14
CZ301008B6 (cs)	2009-10-14
BR9712383A (pt)	2001-08-28
NZ335907A (en)	2001-05-25
EP0935616B1 (en)	2002-07-24
TR199900930T2 (xx)	1999-07-21
JP2001503796A (ja)	2001-03-21
CA2270220C (en)	2007-04-10
AU745244B2 (en)	2002-03-14
EP0935616A1 (en)	1999-08-18
RU2215014C2 (ru)	2003-10-27
DK0935616T3 (da)	2002-10-28
DE69714280T2 (de)	2003-03-06
KR100623165B1 (ko)	2006-09-11
DE69714280D1 (de)	2002-08-29
NO992081L (no)	1999-06-25
HUP0000149A3 (en)	2000-11-28
HUP0000149A2 (hu)	2000-06-28
PL195326B1 (pl)	2007-09-28
CA2270220A1 (en)	1998-05-07
PT935616E (pt)	2002-10-31
DK0935616T4 (da)	2010-07-26
ATE221088T1 (de)	2002-08-15
IL129649A0 (en)	2000-02-29
ES2180953T5 (es)	2010-08-24
WO1998018829A1 (en)	1998-05-07
PL333125A1 (en)	1999-11-22
KR20000052933A (ko)	2000-08-25

Legal Events

Date	Code	Title	Description
2011-05-30	MM1K	Lapsed by not paying the annual fees

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