TW438856B - Polyvinyl alcohol compositions - Google Patents
Polyvinyl alcohol compositions Download PDFInfo
- Publication number
- TW438856B TW438856B TW086112834A TW86112834A TW438856B TW 438856 B TW438856 B TW 438856B TW 086112834 A TW086112834 A TW 086112834A TW 86112834 A TW86112834 A TW 86112834A TW 438856 B TW438856 B TW 438856B
- Authority
- TW
- Taiwan
- Prior art keywords
- polyvinyl alcohol
- water
- scope
- soluble
- patent application
- Prior art date
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- 229920002451 polyvinyl alcohol Polymers 0.000 title claims abstract description 79
- 239000004372 Polyvinyl alcohol Substances 0.000 title claims abstract description 78
- 239000000203 mixture Substances 0.000 title claims abstract description 43
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 45
- 239000007864 aqueous solution Substances 0.000 claims abstract description 30
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims abstract description 17
- 239000000853 adhesive Substances 0.000 claims abstract description 12
- 230000001070 adhesive effect Effects 0.000 claims abstract description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 12
- 150000001875 compounds Chemical class 0.000 claims abstract description 12
- 229920001744 Polyaldehyde Polymers 0.000 claims abstract description 10
- 230000002378 acidificating effect Effects 0.000 claims abstract description 9
- 229940079826 hydrogen sulfite Drugs 0.000 claims abstract description 7
- 150000001299 aldehydes Chemical class 0.000 claims description 18
- 239000002245 particle Substances 0.000 claims description 16
- 150000007513 acids Chemical class 0.000 claims description 15
- 238000011049 filling Methods 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 10
- -1 gold sulfonium pyrosulfite Chemical compound 0.000 claims description 9
- 230000007062 hydrolysis Effects 0.000 claims description 7
- 238000006460 hydrolysis reaction Methods 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 7
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical group O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 5
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical group OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 3
- 230000004888 barrier function Effects 0.000 claims description 3
- WBZKQQHYRPRKNJ-UHFFFAOYSA-L disulfite Chemical compound [O-]S(=O)S([O-])(=O)=O WBZKQQHYRPRKNJ-UHFFFAOYSA-L 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 2
- 238000005266 casting Methods 0.000 claims description 2
- 150000001768 cations Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims 2
- WWILHZQYNPQALT-UHFFFAOYSA-N 2-methyl-2-morpholin-4-ylpropanal Chemical compound O=CC(C)(C)N1CCOCC1 WWILHZQYNPQALT-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 claims 1
- 150000007857 hydrazones Chemical class 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 239000008267 milk Substances 0.000 claims 1
- 210000004080 milk Anatomy 0.000 claims 1
- 235000013336 milk Nutrition 0.000 claims 1
- 229920003169 water-soluble polymer Polymers 0.000 claims 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 56
- 239000000243 solution Substances 0.000 description 15
- 238000009835 boiling Methods 0.000 description 12
- 238000003860 storage Methods 0.000 description 10
- 239000000123 paper Substances 0.000 description 9
- 230000001588 bifunctional effect Effects 0.000 description 6
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical class OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- PCSMJKASWLYICJ-UHFFFAOYSA-N Succinic aldehyde Chemical compound O=CCCC=O PCSMJKASWLYICJ-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
- 239000007848 Bronsted acid Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000003172 aldehyde group Chemical group 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000002841 Lewis acid Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 150000001241 acetals Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002313 adhesive film Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 239000011111 cardboard Substances 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- PHFQLYPOURZARY-UHFFFAOYSA-N chromium trinitrate Chemical compound [Cr+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O PHFQLYPOURZARY-UHFFFAOYSA-N 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000002079 cooperative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 238000010191 image analysis Methods 0.000 description 2
- 150000007517 lewis acids Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
- 239000005022 packaging material Substances 0.000 description 2
- 239000011101 paper laminate Substances 0.000 description 2
- 239000011087 paperboard Substances 0.000 description 2
- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- 235000015170 shellfish Nutrition 0.000 description 2
- 229940124024 weight reducing agent Drugs 0.000 description 2
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- XHTYQFMRBQUCPX-UHFFFAOYSA-N 1,1,3,3-tetramethoxypropane Chemical compound COC(OC)CC(OC)OC XHTYQFMRBQUCPX-UHFFFAOYSA-N 0.000 description 1
- ZLKHNURELCONBB-UHFFFAOYSA-N 2,5-diethoxyoxolane Chemical compound CCOC1CCC(OCC)O1 ZLKHNURELCONBB-UHFFFAOYSA-N 0.000 description 1
- GFISDBXSWQMOND-UHFFFAOYSA-N 2,5-dimethoxyoxolane Chemical compound COC1CCC(OC)O1 GFISDBXSWQMOND-UHFFFAOYSA-N 0.000 description 1
- BIQXDHHBTSGBPW-UHFFFAOYSA-N 2,6-diethoxyoxane Chemical compound CCOC1CCCC(OCC)O1 BIQXDHHBTSGBPW-UHFFFAOYSA-N 0.000 description 1
- VTERBIYJBWDXDT-UHFFFAOYSA-N 2-hydroxybutanedial Chemical compound O=CC(O)CC=O VTERBIYJBWDXDT-UHFFFAOYSA-N 0.000 description 1
- WWMIMRADNBGDHP-UHFFFAOYSA-N 2-hydroxyhexanedial Chemical compound O=CC(O)CCCC=O WWMIMRADNBGDHP-UHFFFAOYSA-N 0.000 description 1
- UIVALZXFWDRKKE-UHFFFAOYSA-N 3-hydroxypentanedial Chemical compound O=CCC(O)CC=O UIVALZXFWDRKKE-UHFFFAOYSA-N 0.000 description 1
- JDQDSEVNMTYMOC-UHFFFAOYSA-N 3-methylbenzenesulfonic acid Chemical compound CC1=CC=CC(S(O)(=O)=O)=C1 JDQDSEVNMTYMOC-UHFFFAOYSA-N 0.000 description 1
- LUNMJPAJHJAGIS-UHFFFAOYSA-N 3-methylpentanedial Chemical compound O=CCC(C)CC=O LUNMJPAJHJAGIS-UHFFFAOYSA-N 0.000 description 1
- UMHJEEQLYBKSAN-UHFFFAOYSA-N Adipaldehyde Chemical compound O=CCCCCC=O UMHJEEQLYBKSAN-UHFFFAOYSA-N 0.000 description 1
- 229920002085 Dialdehyde starch Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229940123457 Free radical scavenger Drugs 0.000 description 1
- WSMYVTOQOOLQHP-UHFFFAOYSA-N Malondialdehyde Chemical compound O=CCC=O WSMYVTOQOOLQHP-UHFFFAOYSA-N 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical class OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 description 1
- 101100460844 Mus musculus Nr2f6 gene Proteins 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- ZNWNWEHQFXOPGK-UHFFFAOYSA-N decanedial Chemical compound O=CCCCCCCCCC=O ZNWNWEHQFXOPGK-UHFFFAOYSA-N 0.000 description 1
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 1
- YGZZDQOCTFVBFC-UHFFFAOYSA-L disodium;1,5-dihydroxypentane-1,5-disulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C(O)CCCC(O)S([O-])(=O)=O YGZZDQOCTFVBFC-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000005021 flexible packaging material Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229960003505 mequinol Drugs 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- OADYBSJSJUFUBR-UHFFFAOYSA-N octanedial Chemical compound O=CCCCCCCC=O OADYBSJSJUFUBR-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical group [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- DJEHXEMURTVAOE-UHFFFAOYSA-M potassium bisulfite Chemical compound [K+].OS([O-])=O DJEHXEMURTVAOE-UHFFFAOYSA-M 0.000 description 1
- 229940099427 potassium bisulfite Drugs 0.000 description 1
- 235000010259 potassium hydrogen sulphite Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- AVIMKMSIMDFRKB-UHFFFAOYSA-J tetrasodium pentanedial disulfite Chemical compound S(=O)([O-])[O-].S(=O)([O-])[O-].C(CCCC=O)=O.[Na+].[Na+].[Na+].[Na+] AVIMKMSIMDFRKB-UHFFFAOYSA-J 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000007725 thermal activation Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000002982 water resistant material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L29/00—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 an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
- C08L29/02—Homopolymers or copolymers of unsaturated alcohols
- C08L29/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
-
- 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
- C08J5/18—Manufacture of films or sheets
-
- 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
-
- 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
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
-
- 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
- C08K5/07—Aldehydes; Ketones
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/372—Sulfides, e.g. R-(S)x-R'
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/02—Condensation polymers of aldehydes or ketones only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/16—Applications used for films
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/904—Powder coating compositions
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/934—Powdered coating composition
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Paper (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19636510A DE19636510A1 (de) | 1996-09-09 | 1996-09-09 | Polyvinylalkohol-Kompositionen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW438856B true TW438856B (en) | 2001-06-07 |
Family
ID=7805011
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW086112834A TW438856B (en) | 1996-09-09 | 1997-09-05 | Polyvinyl alcohol compositions |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US6054519A (cg-RX-API-DMAC10.html) |
| EP (1) | EP0829509B1 (cg-RX-API-DMAC10.html) |
| JP (1) | JPH10139971A (cg-RX-API-DMAC10.html) |
| KR (1) | KR19980024413A (cg-RX-API-DMAC10.html) |
| CN (1) | CN1139633C (cg-RX-API-DMAC10.html) |
| AT (1) | ATE198214T1 (cg-RX-API-DMAC10.html) |
| DE (2) | DE19636510A1 (cg-RX-API-DMAC10.html) |
| ES (1) | ES2154437T3 (cg-RX-API-DMAC10.html) |
| PT (1) | PT829509E (cg-RX-API-DMAC10.html) |
| SI (1) | SI0829509T1 (cg-RX-API-DMAC10.html) |
| TR (1) | TR199700914A3 (cg-RX-API-DMAC10.html) |
| TW (1) | TW438856B (cg-RX-API-DMAC10.html) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2320456B (en) * | 1996-12-18 | 2001-09-05 | Fip Holdings Ltd | Polymer processing method |
| DE19827475A1 (de) * | 1998-06-19 | 1999-12-23 | Wacker Chemie Gmbh | Faserbindepulver-Zusammensetzung zur Verwendung für die Verfestigung von Fasermaterialien |
| GB2340835B (en) | 1998-08-26 | 2003-01-15 | Pvax Ploymers Ltd | PVA-containing compositions |
| WO2001023668A1 (en) * | 1999-09-28 | 2001-04-05 | University Of Georgia Research Foundation, Inc. | Polymer-aldehyde additives to improve paper properties |
| DE19949332A1 (de) * | 1999-10-13 | 2001-05-23 | Clariant Gmbh | Verfärbungsarme Dispersionsklebstoffe mit verlängerter Topfzeit |
| US6622428B2 (en) * | 2000-02-14 | 2003-09-23 | II Locke White | Method for containing organic debris |
| GB0005016D0 (en) * | 2000-03-01 | 2000-04-26 | Jumik Technologies Limited | PVA-Containing compositions |
| DE102005011722B4 (de) * | 2005-03-15 | 2010-04-08 | Clariant Produkte (Deutschland) Gmbh | Verfahren zur chemischen Reinigung von Textilmaterial |
| RU2421483C2 (ru) * | 2006-01-12 | 2011-06-20 | Дайнеа Ой | Полимер-альдегидная связующая система для изготовления изделий из дерева |
| DE102006030557A1 (de) * | 2006-07-03 | 2008-01-10 | Celanese Emulsions Gmbh | Verfahren zur Herstellung wässriger Vinylester-Dispersionen |
| US20080176985A1 (en) * | 2006-11-13 | 2008-07-24 | Verrall Andrew P | Water-soluble film |
| US20080110370A1 (en) * | 2006-11-13 | 2008-05-15 | Verrall Andrew P | Water-soluble film |
| DE102007012247A1 (de) | 2007-03-14 | 2008-09-25 | Celanese Emulsions Gmbh | Vernetzbare Polymerdispersionen, Verfahren zu deren Herstellung und Verwendung |
| DE102007033595A1 (de) | 2007-07-19 | 2009-01-22 | Celanese Emulsions Gmbh | Polyvinylesterdispersionen, Verfahren zu deren Herstellung und deren Verwendung |
| DE102007033596A1 (de) | 2007-07-19 | 2009-01-22 | Celanese Emulsions Gmbh | Beschichtungsmittel mit hoher Bewitterungsbeständigkeit, Verfahren zu deren Herstellung und deren Verwendung |
| EP2250317A4 (en) * | 2008-03-07 | 2012-07-25 | Sca Hygiene Prod Ab | MULTILAYER STRIP OF FLEXIBLE MATERIAL, SUCH AS TISSUE PAPER OR NONWOVEN FABRIC, AND PRODUCT AND METHOD FOR IMPROVING THE BLOOD OF A OPTICAL LIGHTER OF A MULTILAYER RAIL |
| JP5369521B2 (ja) * | 2008-07-15 | 2013-12-18 | 東京電力株式会社 | 油入変圧器コンサベータ用複合膜 |
| CN102786897B (zh) * | 2012-08-03 | 2015-09-30 | 祁高标 | 高标无醛胶水及其制备方法 |
| EP2982509B1 (en) * | 2013-04-06 | 2018-03-28 | Mitsubishi Chemical Corporation | Applied film |
| KR102186080B1 (ko) | 2017-06-27 | 2020-12-03 | 주식회사 엘지화학 | 접착제 조성물, 이를 포함하는 접착제층을 포함하는 보호필름 및 편광판, 및 이를 포함하는 화상표시장치 |
| KR101997524B1 (ko) * | 2017-06-30 | 2019-07-11 | (주)인테크놀로지 | 식품 연포장용 고분자 필름 제조방법 및 접착 조성물 |
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| US3700611A (en) * | 1968-11-12 | 1972-10-24 | Monsanto Co | Polyvinyl alcohol-glyoxal-polyol adhesive composition |
| JPS52117991A (en) | 1976-03-30 | 1977-10-03 | Aicello Chemical Co | Process for producing hot water resis tant polyvinyl alcohol resin article |
| US4424302A (en) * | 1980-04-21 | 1984-01-03 | W. R. Grace & Co. | Method of forming polymer particles |
| US4376183A (en) | 1981-09-14 | 1983-03-08 | E. I. Du Pont De Nemours And Company | Inorganic films with poly(vinyl alcohol) and coating compositions for making them |
| CA1254337A (en) * | 1984-06-25 | 1989-05-16 | Burton B. Sandiford | Gel and process for retarding fluid flow |
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| JP3043163B2 (ja) | 1991-12-18 | 2000-05-22 | 株式会社クラレ | ポリビニルアルコール系合成繊維の製造方法 |
| JP3195817B2 (ja) | 1992-01-17 | 2001-08-06 | 株式会社クラレ | 耐水性組成物 |
| DE4420484C2 (de) * | 1994-06-11 | 1999-02-04 | Clariant Gmbh | Wäßriger Dispersionsklebstoff auf Polyvinylester-Basis, Verfahren zur Herstellung sowie dessen Verwendung |
| DE19545609A1 (de) * | 1995-12-07 | 1997-06-12 | Hoechst Ag | Redoxkatalysatorsystem zur Initiierung von Emulsionspolymerisationen |
| DE19545608A1 (de) * | 1995-12-07 | 1997-06-12 | Hoechst Ag | Dispersionspulver für wasserfeste Klebstoffe |
-
1996
- 1996-09-09 DE DE19636510A patent/DE19636510A1/de not_active Withdrawn
-
1997
- 1997-09-02 SI SI9730101T patent/SI0829509T1/xx unknown
- 1997-09-02 PT PT97115231T patent/PT829509E/pt unknown
- 1997-09-02 EP EP97115231A patent/EP0829509B1/de not_active Expired - Lifetime
- 1997-09-02 DE DE59702781T patent/DE59702781D1/de not_active Expired - Lifetime
- 1997-09-02 AT AT97115231T patent/ATE198214T1/de active
- 1997-09-02 ES ES97115231T patent/ES2154437T3/es not_active Expired - Lifetime
- 1997-09-05 US US08/924,732 patent/US6054519A/en not_active Expired - Lifetime
- 1997-09-05 TW TW086112834A patent/TW438856B/zh not_active IP Right Cessation
- 1997-09-08 KR KR1019970046094A patent/KR19980024413A/ko not_active Ceased
- 1997-09-08 TR TR97/00914A patent/TR199700914A3/tr unknown
- 1997-09-08 CN CNB971182302A patent/CN1139633C/zh not_active Expired - Fee Related
- 1997-09-08 JP JP9242731A patent/JPH10139971A/ja active Pending
-
2000
- 2000-04-13 US US09/549,043 patent/US6608128B1/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| ATE198214T1 (de) | 2001-01-15 |
| TR199700914A2 (xx) | 1998-03-21 |
| PT829509E (pt) | 2001-04-30 |
| US6054519A (en) | 2000-04-25 |
| EP0829509A1 (de) | 1998-03-18 |
| ES2154437T3 (es) | 2001-04-01 |
| DE19636510A1 (de) | 1998-03-12 |
| JPH10139971A (ja) | 1998-05-26 |
| SI0829509T1 (en) | 2001-04-30 |
| TR199700914A3 (tr) | 1998-03-21 |
| CN1139633C (zh) | 2004-02-25 |
| KR19980024413A (ko) | 1998-07-06 |
| US6608128B1 (en) | 2003-08-19 |
| DE59702781D1 (de) | 2001-01-25 |
| EP0829509B1 (de) | 2000-12-20 |
| CN1193028A (zh) | 1998-09-16 |
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