NO832545L - Polymerkomposisjon - Google Patents

Polymerkomposisjon

Info

Publication number: NO832545L
Authority: NO; Norway
Prior art keywords: polymer; dispersion; polyurethane; impregnated; fibrous web
Prior art date: 1982-07-14

Application number

NO832545A

Other languages

English (en)

Norwegian (no)

Inventor

John Richard Mccartney

Original Assignee

Norwood Ind Inc

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.)

1982-07-14

Filing date

1983-07-13

Publication date

1984-01-16

1983-07-13 Application filed by Norwood Ind Inc filed Critical Norwood Ind Inc

1984-01-16 Publication of NO832545L publication Critical patent/NO832545L/no

Links

229920000642 polymer Polymers 0.000 title claims description 73
239000000203 mixture Substances 0.000 title description 35
239000000463 material Substances 0.000 claims description 47
229920002635 polyurethane Polymers 0.000 claims description 33
239000004814 polyurethane Substances 0.000 claims description 33
239000006185 dispersion Substances 0.000 claims description 30
229920003009 polyurethane dispersion Polymers 0.000 claims description 29
125000000129 anionic group Chemical group 0.000 claims description 25
238000000034 method Methods 0.000 claims description 21
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
239000000839 emulsion Substances 0.000 claims description 16
229920001084 poly(chloroprene) Polymers 0.000 claims description 16
230000015271 coagulation Effects 0.000 claims description 15
238000005345 coagulation Methods 0.000 claims description 15
229920003002 synthetic resin Polymers 0.000 claims description 12
239000002952 polymeric resin Substances 0.000 claims description 11
239000004815 dispersion polymer Substances 0.000 claims description 7
239000003795 chemical substances by application Substances 0.000 claims description 6
125000002091 cationic group Chemical group 0.000 claims description 5
239000004800 polyvinyl chloride Substances 0.000 claims description 5
229920000915 polyvinyl chloride Polymers 0.000 claims description 5
239000008240 homogeneous mixture Substances 0.000 claims description 4
239000002131 composite material Substances 0.000 claims description 3
229920000058 polyacrylate Polymers 0.000 claims description 3
150000002500 ions Chemical class 0.000 claims description 2
229920000098 polyolefin Polymers 0.000 claims description 2
229940070721 polyacrylate Drugs 0.000 claims 1
239000002253 acid Substances 0.000 description 21
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 17
-1 ether polyol Chemical class 0.000 description 17
239000002904 solvent Substances 0.000 description 16
239000010410 layer Substances 0.000 description 13
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
238000005470 impregnation Methods 0.000 description 12
229920002959 polymer blend Polymers 0.000 description 12
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 10
239000000047 product Substances 0.000 description 9
229920005989 resin Polymers 0.000 description 9
239000011347 resin Substances 0.000 description 9
239000000758 substrate Substances 0.000 description 9
229920005862 polyol Polymers 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
150000007513 acids Chemical class 0.000 description 6
150000001412 amines Chemical class 0.000 description 6
125000005442 diisocyanate group Chemical group 0.000 description 6
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 6
239000012948 isocyanate Substances 0.000 description 6
150000002513 isocyanates Chemical class 0.000 description 6
239000004816 latex Substances 0.000 description 6
229920000126 latex Polymers 0.000 description 6
229920000728 polyester Polymers 0.000 description 6
150000003077 polyols Chemical class 0.000 description 6
239000007787 solid Substances 0.000 description 6
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
239000012467 final product Substances 0.000 description 5
239000002649 leather substitute Substances 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
229920006395 saturated elastomer Polymers 0.000 description 5
239000011734 sodium Substances 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
150000001875 compounds Chemical class 0.000 description 4
238000007654 immersion Methods 0.000 description 4
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 4
239000003960 organic solvent Substances 0.000 description 4
229920001281 polyalkylene Polymers 0.000 description 4
230000008569 process Effects 0.000 description 4
239000000243 solution Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
150000001735 carboxylic acids Chemical class 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
150000002334 glycols Chemical class 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
239000010985 leather Substances 0.000 description 3
229920001343 polytetrafluoroethylene Polymers 0.000 description 3
239000004810 polytetrafluoroethylene Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
229920002554 vinyl polymer Polymers 0.000 description 3
239000005058 Isophorone diisocyanate Substances 0.000 description 2
239000004721 Polyphenylene oxide Substances 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
150000001299 aldehydes Chemical class 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910021538 borax Inorganic materials 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
150000004985 diamines Chemical class 0.000 description 2
KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
150000002009 diols Chemical class 0.000 description 2
238000001035 drying Methods 0.000 description 2
239000000835 fiber Substances 0.000 description 2
235000019256 formaldehyde Nutrition 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
150000002483 hydrogen compounds Chemical class 0.000 description 2
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
238000005259 measurement Methods 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000002245 particle Substances 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
229920000570 polyether Polymers 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
239000005056 polyisocyanate Substances 0.000 description 2
229920001228 polyisocyanate Polymers 0.000 description 2
239000002861 polymer material Substances 0.000 description 2
230000005855 radiation Effects 0.000 description 2
230000009257 reactivity Effects 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
239000004328 sodium tetraborate Substances 0.000 description 2
235000010339 sodium tetraborate Nutrition 0.000 description 2
230000003381 solubilizing effect Effects 0.000 description 2
239000004753 textile Substances 0.000 description 2
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
231100000331 toxic Toxicity 0.000 description 2
230000002588 toxic effect Effects 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
SZBXTBGNJLZMHB-UHFFFAOYSA-N 1-chloro-2,4-diisocyanatobenzene Chemical compound ClC1=CC=C(N=C=O)C=C1N=C=O SZBXTBGNJLZMHB-UHFFFAOYSA-N 0.000 description 1
PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-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
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
239000004970 Chain extender Substances 0.000 description 1
229920006385 Geon Polymers 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
HTLZVHNRZJPSMI-UHFFFAOYSA-N N-ethylpiperidine Chemical compound CCN1CCCCC1 HTLZVHNRZJPSMI-UHFFFAOYSA-N 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
239000004809 Teflon Substances 0.000 description 1
229920006362 Teflon® Polymers 0.000 description 1
235000011054 acetic acid Nutrition 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000000732 arylene group Chemical group 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
230000008901 benefit Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000002843 carboxylic acid group Chemical group 0.000 description 1
239000000969 carrier Substances 0.000 description 1
210000003850 cellular structure Anatomy 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
239000000701 coagulant Substances 0.000 description 1
239000011247 coating layer Substances 0.000 description 1
238000004040 coloring Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 1
QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 1
FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
230000006735 deficit Effects 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
239000004744 fabric Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
239000005350 fused silica glass Substances 0.000 description 1
230000009477 glass transition Effects 0.000 description 1
230000005484 gravity Effects 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
230000006872 improvement Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
RLAWWYSOJDYHDC-BZSNNMDCSA-N lisinopril Chemical compound C([C@H](N[C@@H](CCCCN)C(=O)N1[C@@H](CCC1)C(O)=O)C(O)=O)CC1=CC=CC=C1 RLAWWYSOJDYHDC-BZSNNMDCSA-N 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
CKFGINPQOCXMAZ-UHFFFAOYSA-N methanediol Chemical class OCO CKFGINPQOCXMAZ-UHFFFAOYSA-N 0.000 description 1
230000005012 migration Effects 0.000 description 1
238000013508 migration Methods 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
239000012875 nonionic emulsifier Substances 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
230000035515 penetration Effects 0.000 description 1
239000002530 phenolic antioxidant Substances 0.000 description 1
229920001610 polycaprolactone Polymers 0.000 description 1
239000004632 polycaprolactone Substances 0.000 description 1
229920005906 polyester polyol Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000307 polymer substrate Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920006324 polyoxymethylene Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920000909 polytetrahydrofuran Polymers 0.000 description 1
239000011527 polyurethane coating Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000003825 pressing Methods 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
230000036632 reaction speed Effects 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000009738 saturating Methods 0.000 description 1
231100000241 scar Toxicity 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
125000006850 spacer group Chemical group 0.000 description 1
235000020354 squash Nutrition 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
150000004072 triols Chemical class 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
239000000326 ultraviolet stabilizing agent Substances 0.000 description 1
238000010518 undesired secondary reaction Methods 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
230000004584 weight gain Effects 0.000 description 1
235000019786 weight gain Nutrition 0.000 description 1

Classifications

- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/12—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
- D06N3/14—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyurethanes
- D06N3/142—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyurethanes mixture of polyurethanes with other resins in the same layer
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/24—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Materials Engineering (AREA)
Dispersion Chemistry (AREA)
Manufacturing & Machinery (AREA)
Textile Engineering (AREA)
Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Reinforced Plastic Materials (AREA)
Compositions Of Macromolecular Compounds (AREA)
Biological Depolymerization Polymers (AREA)
Polyurethanes Or Polyureas (AREA)

NO832545A 1982-07-14 1983-07-13 Polymerkomposisjon NO832545L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US39826082A	1982-07-14	1982-07-14

Publications (1)

Publication Number	Publication Date
NO832545L true NO832545L (no)	1984-01-16

Family

ID=23574672

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO832545A NO832545L (no)	1982-07-14	1983-07-13	Polymerkomposisjon

Country Status (17)

Country	Link
JP (1)	JPS5941357A (nl)
KR (1)	KR840005474A (nl)
AT (1)	ATA256783A (nl)
AU (1)	AU1678683A (nl)
BE (1)	BE897293A (nl)
DE (1)	DE3325163A1 (nl)
DK (1)	DK323283A (nl)
ES (1)	ES524091A0 (nl)
FI (1)	FI832552A (nl)
FR (1)	FR2530254A1 (nl)
GB (1)	GB2124239B (nl)
IT (1)	IT1163781B (nl)
LU (1)	LU84913A1 (nl)
NL (1)	NL8302508A (nl)
NO (1)	NO832545L (nl)
PL (1)	PL243009A1 (nl)
SE (1)	SE8303950L (nl)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8721536D0 (en) *	1987-09-14	1987-10-21	Polyvinyl Chemical Ind	Aqueous dispersions
US6303189B1 (en) *	1995-03-03	2001-10-16	Rohm And Haas Company	Method for increasing the open time of aqueous coatings
US6541550B1 (en)	2000-04-05	2003-04-01	3M Innovative Properties Company	Low temperature thermally activated water-dispersed adhesive compositions
US6310125B1 (en)	2000-04-05	2001-10-30	3M Innovative Properties Company	Water-dispersed adhesive compositions
US6444737B1 (en)	2000-04-05	2002-09-03	3M Innovative Properties Company	Water-dispersed polymer stabilizer
US6306942B1 (en)	2000-04-05	2001-10-23	3M Innovative Properties Company	Low temperature thermally activated water-dispersed adhesives
JP2007533778A (ja) *	2003-09-18	2007-11-22	バイエル・マテリアルサイエンス・アクチェンゲゼルシャフト	水性接着性分散液
DE10360368A1 (de)	2003-12-22	2005-07-21	Bayer Materialscience Ag	Dispersionen
WO2020089163A1 (de) *	2018-10-31	2020-05-07	Covestro Deutschland Ag	Kompositbauteil enthaltend ein polychloropren- und/oder polyurethan-bindemittel
CN113549236B (zh) *	2021-09-22	2021-12-31	汇泰渤海水产有限责任公司	可降解海藻膜及其制备方法和包装制品

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1694148C3 (de) *	1967-04-28	1975-05-22	Bayer Ag, 5090 Leverkusen	Verfahren zur Herstellung mikroporöser Flächengebilde oder Formkörper auf Polyurethanbasis
DE1953349C3 (de) *	1969-10-23	1975-07-03	Bayer Ag, 5090 Leverkusen	Verfahren zur Herstellung wäßriger Dispersionen von Polymerisaten aus olefinisch ungesättigten Monomeren
DE2004130A1 (de) *	1970-01-30	1971-08-05	Bayer Ag	Verfahren zur Herstellung von Polyurethan-Kunststoffen
US3756909A (en) *	1972-09-26	1973-09-04	Minnesota Mining & Mfg	Waterlaid leather substitute sheet and method for preparing the sheet
GB1426087A (en) *	1973-04-09	1976-02-25	American Cyanamid Co	Polyurethane lattices
CA1066856A (en) *	1973-07-24	1979-11-27	Guenter Eckert	Leather dressing
US4094847A (en) *	1977-02-11	1978-06-13	Formica Corporation	Elastomer modified melamine resins
US4137209A (en) *	1977-11-14	1979-01-30	Owens-Corning Fiberglas Corporation	Glass fiber size composition
US4197219A (en) *	1979-01-17	1980-04-08	Lord Corporation	Aqueous polyurethane-phenolic-formaldehyde resin emulsions for use as adhesives, primers and surface coatings
DE2930410A1 (de) *	1979-07-26	1981-02-12	Bayer Ag	Verfahren zur herstellung von stabilen waessrigen dispersionen von oligo- oder polyurethanen, sowie ihre verwendung als beschichtungsmittel fuer flexible oder nicht- flexible substrate
CA1178138A (en) *	1980-09-18	1984-11-20	John R. Mccartney	Impregnated non-woven sheet material and products produced therewith

1983
- 1983-07-12 SE SE8303950A patent/SE8303950L/xx not_active Application Discontinuation
- 1983-07-12 DE DE3325163A patent/DE3325163A1/de not_active Withdrawn
- 1983-07-13 AU AU16786/83A patent/AU1678683A/en not_active Abandoned
- 1983-07-13 AT AT0256783A patent/ATA256783A/de not_active Application Discontinuation
- 1983-07-13 FR FR8311734A patent/FR2530254A1/fr not_active Withdrawn
- 1983-07-13 ES ES524091A patent/ES524091A0/es active Granted
- 1983-07-13 DK DK323283A patent/DK323283A/da not_active Application Discontinuation
- 1983-07-13 GB GB08318968A patent/GB2124239B/en not_active Expired
- 1983-07-13 FI FI832552A patent/FI832552A/fi not_active Application Discontinuation
- 1983-07-13 NL NL8302508A patent/NL8302508A/nl not_active Application Discontinuation
- 1983-07-13 NO NO832545A patent/NO832545L/no unknown
- 1983-07-14 KR KR1019830003213A patent/KR840005474A/ko not_active Application Discontinuation
- 1983-07-14 PL PL24300983A patent/PL243009A1/xx unknown
- 1983-07-14 IT IT22067/83A patent/IT1163781B/it active
- 1983-07-14 LU LU84913A patent/LU84913A1/fr unknown
- 1983-07-14 JP JP58127018A patent/JPS5941357A/ja active Pending
- 1983-07-14 BE BE0/211176A patent/BE897293A/fr not_active IP Right Cessation

Also Published As

Publication number	Publication date
LU84913A1 (fr)	1983-11-23
IT8322067A0 (it)	1983-07-14
SE8303950L (sv)	1984-01-15
GB2124239A (en)	1984-02-15
PL243009A1 (en)	1984-07-30
GB8318968D0 (en)	1983-08-17
AU1678683A (en)	1984-01-19
DK323283A (da)	1984-01-15
FI832552A0 (fi)	1983-07-13
IT8322067A1 (it)	1985-01-14
NL8302508A (nl)	1984-02-01
DK323283D0 (da)	1983-07-13
IT1163781B (it)	1987-04-08
ATA256783A (de)	1987-04-15
GB2124239B (en)	1986-10-01
BE897293A (fr)	1983-11-03
KR840005474A (ko)	1984-11-12
SE8303950D0 (sv)	1983-07-12
DE3325163A1 (de)	1984-01-19
JPS5941357A (ja)	1984-03-07
ES8501467A1 (es)	1984-11-16
ES524091A0 (es)	1984-11-16
FR2530254A1 (fr)	1984-01-20
FI832552A (fi)	1984-01-15

Publication	Publication Date	Title
EP0184392B1 (en)	1993-01-27	Waterproof, moisture-vapor permeable sheet material and method of making the same
US5238732A (en)	1993-08-24	Waterproof breathable polyurethane membranes and porous substrates protected therewith
US5239036A (en)	1993-08-24	Waterproof breathable polyurethane membranes and porous substrates protected therewith
US3208875A (en)	1965-09-28	Method of making vapor permeable sheet materials
US5283112A (en)	1994-02-01	Waterproof breathable fabric laminates and method for producing same
US3666542A (en)	1972-05-30	Process for the production of microporous structures
US4511605A (en)	1985-04-16	Process for producing polishing pads comprising a fully impregnated non-woven batt
EP0329411A2 (en)	1989-08-23	Waterproof breathable microporous membrane with cellular foam adhesive
US5169906A (en)	1992-12-08	Film-forming copolymers and their use in water vapor permeable coatings
US3496001A (en)	1970-02-17	Method of producing suede-like synthetic leathers
GB2210885A (en)	1989-06-21	Breathable, waterproof sheet materials and methods for making the same
US3595732A (en)	1971-07-27	Process and microporous product
NO832545L (no)	1984-01-16	Polymerkomposisjon
US5173300A (en)	1992-12-22	Hindered phenolic antioxidant containing hydrophilic urethane polymer; dry cleaning solvent resistant, waterproof, moisture-vapor permeable material containing the polymer; and method of making the same
US5239037A (en)	1993-08-24	Waterproof breathable polyurethane membranes and porous substrates protected therewith
US4006052A (en)	1977-02-01	Diffusion method for depositing microporous film
US3895134A (en)	1975-07-15	Process for producing microporous structures
US4496624A (en)	1985-01-29	Fibrous web impregnated with coagulated polyurethane and polyolefin admixture
NO820434L (no)	1982-08-18	Vandig polyuretanpreparat og anvendelse av det
US4746684A (en)	1988-05-24	Polyurethane dispersion and emulsion, sheet-like porous material and production process thereof
JP3850872B2 (ja)	2006-11-29	親水性ポリウレタン
PT96238B (pt)	1998-06-30	Processo para a preparacao de um material ortopedico para moldacao a base de um pre-polimero de poli-isocianato que possui uma reduzida aderencia e um reduzido deslizamento
FI71776B (fi)	1986-10-31	Hartsimpregnerad fiberskiva och foerfarande foer dess framstaellning
US3492154A (en)	1970-01-27	Process for producing microporous polymeric materials
US3579372A (en)	1971-05-18	Deposition of microporous film employing dielectric heating