AU541568B2 - ** - Google Patents
**Info
- Publication number
- AU541568B2 AU541568B2 AU63302/80A AU6330280A AU541568B2 AU 541568 B2 AU541568 B2 AU 541568B2 AU 63302/80 A AU63302/80 A AU 63302/80A AU 6330280 A AU6330280 A AU 6330280A AU 541568 B2 AU541568 B2 AU 541568B2
- Authority
- AU
- Australia
- Prior art keywords
- coating
- reactor
- coating solution
- solution
- group
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
Links
- 238000000576 coating method Methods 0.000 claims description 97
- 239000011248 coating agent Substances 0.000 claims description 91
- 239000000243 solution Substances 0.000 claims description 57
- 238000000034 method Methods 0.000 claims description 41
- 238000006116 polymerization reaction Methods 0.000 claims description 37
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 36
- 229920000642 polymer Polymers 0.000 claims description 36
- 239000000463 material Substances 0.000 claims description 34
- 230000008569 process Effects 0.000 claims description 29
- 239000000178 monomer Substances 0.000 claims description 27
- 229920001864 tannin Polymers 0.000 claims description 19
- 235000018553 tannin Nutrition 0.000 claims description 19
- 239000001648 tannin Substances 0.000 claims description 19
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 16
- 150000001412 amines Chemical class 0.000 claims description 13
- 150000002989 phenols Chemical class 0.000 claims description 11
- -1 azines Chemical class 0.000 claims description 10
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical group CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 9
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 9
- 239000007859 condensation product Substances 0.000 claims description 7
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
- 229910006069 SO3H Inorganic materials 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 3
- 229920002253 Tannate Polymers 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 229920002770 condensed tannin Polymers 0.000 claims description 3
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims description 3
- 239000002270 dispersing agent Substances 0.000 claims description 3
- 229920001461 hydrolysable tannin Polymers 0.000 claims description 3
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 108010010803 Gelatin Proteins 0.000 claims description 2
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 claims description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 2
- 229920002472 Starch Polymers 0.000 claims description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
- 239000012736 aqueous medium Substances 0.000 claims description 2
- 150000001555 benzenes Chemical class 0.000 claims description 2
- 244000309466 calf Species 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 229920000159 gelatin Polymers 0.000 claims description 2
- 239000008273 gelatin Substances 0.000 claims description 2
- 235000019322 gelatine Nutrition 0.000 claims description 2
- 235000011852 gelatine desserts Nutrition 0.000 claims description 2
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 2
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 2
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims description 2
- 229910021645 metal ion Inorganic materials 0.000 claims description 2
- 150000004893 oxazines Chemical class 0.000 claims description 2
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 claims description 2
- 229960001553 phloroglucinol Drugs 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 239000008107 starch Substances 0.000 claims description 2
- 235000019698 starch Nutrition 0.000 claims description 2
- 150000004897 thiazines Chemical class 0.000 claims description 2
- 150000001251 acridines Chemical class 0.000 claims 1
- 238000006482 condensation reaction Methods 0.000 claims 1
- 229960004337 hydroquinone Drugs 0.000 claims 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims 1
- 239000000975 dye Substances 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 13
- 239000007787 solid Substances 0.000 description 9
- 238000013019 agitation Methods 0.000 description 6
- 239000008199 coating composition Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000003595 mist Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000002609 medium Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 4
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 3
- 239000001263 FEMA 3042 Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- SNVLJLYUUXKWOJ-UHFFFAOYSA-N methylidenecarbene Chemical group C=[C] SNVLJLYUUXKWOJ-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000010557 suspension polymerization reaction Methods 0.000 description 3
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 3
- 235000015523 tannic acid Nutrition 0.000 description 3
- 229920002258 tannic acid Polymers 0.000 description 3
- 229940033123 tannic acid Drugs 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000000987 azo dye Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 238000007790 scraping Methods 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-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
- FWLHAQYOFMQTHQ-UHFFFAOYSA-N 2-N-[8-[[8-(4-aminoanilino)-10-phenylphenazin-10-ium-2-yl]amino]-10-phenylphenazin-10-ium-2-yl]-8-N,10-diphenylphenazin-10-ium-2,8-diamine hydroxy-oxido-dioxochromium Chemical compound O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.Nc1ccc(Nc2ccc3nc4ccc(Nc5ccc6nc7ccc(Nc8ccc9nc%10ccc(Nc%11ccccc%11)cc%10[n+](-c%10ccccc%10)c9c8)cc7[n+](-c7ccccc7)c6c5)cc4[n+](-c4ccccc4)c3c2)cc1 FWLHAQYOFMQTHQ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- AEPWOCLBLLCOGZ-UHFFFAOYSA-N 2-cyanoethyl prop-2-enoate Chemical compound C=CC(=O)OCCC#N AEPWOCLBLLCOGZ-UHFFFAOYSA-N 0.000 description 1
- 244000283070 Abies balsamea Species 0.000 description 1
- 235000007173 Abies balsamea Nutrition 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 244000036978 Caesalpinia bonduc Species 0.000 description 1
- 235000014145 Caesalpinia bonduc Nutrition 0.000 description 1
- 235000009133 Caesalpinia coriaria Nutrition 0.000 description 1
- 235000005082 Caesalpinia paraguariensis Nutrition 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- 235000015489 Emblica officinalis Nutrition 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- 235000017343 Quebracho blanco Nutrition 0.000 description 1
- 240000002044 Rhizophora apiculata Species 0.000 description 1
- 240000003152 Rhus chinensis Species 0.000 description 1
- 235000014220 Rhus chinensis Nutrition 0.000 description 1
- 244000264648 Rhus coriaria Species 0.000 description 1
- 241000065615 Schinopsis balansae Species 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- 244000277583 Terminalia catappa Species 0.000 description 1
- 235000011517 Terminalia chebula Nutrition 0.000 description 1
- 241001478802 Valonia Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000000641 acridinyl group Chemical class C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 239000012431 aqueous reaction media Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000004054 benzoquinones Chemical class 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- NSGQRLUGQNBHLD-UHFFFAOYSA-N butan-2-yl butan-2-yloxycarbonyloxy carbonate Chemical compound CCC(C)OC(=O)OOC(=O)OC(C)CC NSGQRLUGQNBHLD-UHFFFAOYSA-N 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
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
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- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000012674 dispersion polymerization Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 239000000983 mordant dye Substances 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000001005 nitro dye Substances 0.000 description 1
- 239000001006 nitroso dye Substances 0.000 description 1
- 229940065472 octyl acrylate Drugs 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 239000006200 vaporizer Substances 0.000 description 1
- 239000000984 vat dye Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 210000000051 wattle Anatomy 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 125000001834 xanthenyl group Chemical class C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 description 1
- 244000089265 zong er cha Species 0.000 description 1
Landscapes
- Polymerisation Methods In General (AREA)
Description
PROCESS FOR COATING REACTORS USING ORGANIC COMPOUND VAPOR APPLICATION
BACKGROUND OF THE INVENTION In polymerization type reactions, deposit or buildup of polymer occurs on the inner surface of the reactor which not only interferes with heat transfer, but decreases productivity and adversely affects polymer quality. This problem is particularly troublesome in the commercial production of polymers and copolymers of vinyl and vinylidene halides when polymerized alone or with other vinylidene monomers having a terminal CH2=C< group, or with polymerizable monoolefinic monomers. For example, in the commercial production of vinyl chloride polymers, the same are usually produced in the form of discrete particles by polymerizing in aqueous suspension systems. When employing such systems the vinyl chloride, and other comonomers when used, are maintained in the form of small discrete droplets by the use of suspending agents and agitation. When the reaction is complete, the resultant polymer is washed and dried. The reaction is usually conducted under pressure in metal reactors or glass-lined reactors equipped with baffles and high speed agitators. However, these polymerization systems are, in many cases, unstable. As a consequence, polymer buildup forms on the interior surfaces of the polymerization reactor, including the surfaces of the baffles and agitators. Obviously this polymeric buildup must be removed due to the deleterious effect it causes. Various methods have heretofore been proposed for removing the polymer buildup on polymerization reactor surfaces, such as solvent cleaning, the use of various hydraulic and mechanical reactor cleaners, and the like. Also, various methods have been proposed to reduce the amount of formation and the nature of polymer buildup on said surfaces, such as the application to
said surfaces of various coatings prior to polymerization. In this regard, see, for example, U.S. Patents No's. 3,669,946; 4,024,301; 4,024,330; and 4,081,248. These various methods and coatings have done a more than acceptable job. However, the art continues to strive to find the ultimate in the prevention of polymer buildup, particularly from an economic and environmental point of view.
Further, work continues to find more dilute coating solutions not only to reduce costs, considering the size of commercial reactors, but also to reduce the color of the coating solutions, since most all of the known and useful coating solutions are colored. These coating solutions are applied to reactor surfaces in various ways such as, for example by brushing or painting, flooding the reactor, spraying on, and the like. However, efforts continue to find the ultimate means of applying a coating to the reactor surfaces, not only from simplicity of operation and from an economic point of view on a commercial scale, but also a process of application in which the discoloration problem is substantially eliminated or substantially reduced.
SUMMARY OF THE INVENTION It has been found that if a reaction vessel has been previously coated on the interior surfaces with the proper coating, undesirable polymer buildup on said surfaces can be substantially decreased, and in some cases entirely eliminated, when polymerizing olefinic monomers therein. We have found that various coating materials can be applied to the reactor surfaces in the form of a mist of the coating material by making such application by the use of vinyl chloride gas under pressure. As examples of suitable coating materials that may be used in the present invention are straight chain or branched polyaromatic amines, self-condensed polyhydric phenols, tannic acid and tannates, either
natural or synthetic, various alkali-soluble and water- soluble dyes, organic solvent-soluble dyes, and the like. Due to the nature of the coating composition, and the method of application to the reactor surfaces of the present invention, it can be applied to said surfaces without opening the reactor thus providing a closed polymerization system. In polymerizing the olefinic monomers, the same is done in an aqueous polymerization medium which is kept in contact with said coated surfaces throughout the polymerization reaction.
DETAILED DESCRIPTION In accordance with the present invention, a film or coating of the coating material, as hereinafter defined and described, is applied to the internal surfaces of a polymerization reactor or vessel by means of gaseous vinyl chloride under pressure. The vinyl chloride, hereinafter referred to as VCM, gas under pressure picks up the coating solution in an aspirator valve, or any other suitable apparatus, such as a vaporizer, etc., and through appropriate spray nozzles strategically mounted on the reactor, carries the coating to the reactor surfaces in the form of a mist of the coating material. All exposed surfaces in the interior of the reactor, in addition to the walls, such as the baffles, agitator, and the like, are also coated in like manner at the same time since the spray nozzles are so arranged as to cover the entire interior of the reactor. Further, since the coating is in the form of a mist, all hard to get at sections, such as blind or shadowed areas, of the reactor are likwise uniformly coated employing the instant invention. After the coating solution has been applied to said surfaces, the polymerization medium can be introduced to the reactor and the reaction started without the necessity of drying the surfaces prior to said introduction of the polymerization medium.
The VCM gas is run through the aspirator, or like apparatus, where it picks up the coating solution, under a pressure in the range of about 20 psig. to about 1000 psig. The pressure of the VCM will depend upon the nature and viscosity of the coating solution being employed, as well as the spraying system being used. Usually a pressure in the range of about 80 psig. to about 250 psig. is sufficient to give satisfactory results. The temperature of the VCM gas, as employed in the present invention, is usually in the range of about 20°C. to about 100°C. Preferably, the temperature of the VCM gas will be in the range of about 50°C to about 80°C.
The coating solutions used in the present invention are usually aσueous solutions of the coating materials, said solutions being neutral, basic or acidic. For example, when employing a polyaromatic amine or polyhydric phenol as the coating material, an aqueous alkali metal hydroxide solution thereof can be employed. While the aqueous coating solutions are preferred, organic solvents can also be used, such as methanol and dimethyl formamide, for example. The organic solvents are particularly useful with water-insoluble systems, such as certain dyes, for example, nigrosine, and the like. Irrespective of the solvent employed in making the coating solution, a portion of the solvent, and sometimes all of the same, is vaporized as a result of the heat and pressure produced in the coating operaton. In any event, the coating material reaches all the inner surfaces of the reactor in the form of a mist. As a result of the improved efficiency of the present coating process, the quantity of coating material required is considerably reduced. In fact, the amount of coating material required is reduced to the point where flushing the reactor with water, or other liquid solvent or nonsolvent, followed by stripping of the effluent and waste disposal, is no longer always necessary. The VCM
gas employed in coating the reactor can be left in the reactor and become part of the reaction medium and no special apparatus or process steps are necessary for its removal. The amount of VCM gas is so small by comparison to the amount of monomer (s) in the polymer charge that it has little or no effect on the balance of the polymerization recipe. Of course, the VCM gas can be removed, if one so desires, but for cost and environmental reasons, it is best to leave the same in the reactor. After the coating solution is made up, it is fed to the aspirator, or like apparatus, where it is picked up by the VCM gas. As previously pointed out, the coating material is carried to the reactor surfaces in the form of a mist. Depending upon the particular coating material being used, and the solvent, usually a coating solution having a concentration of coating material therein in the range of about 0.001% to about 20.0% by weight is satisfactory. Coating solutions in the range of about 0.05% to about 10.0% by weight are preferred. The concentration and amount of coating solution used will depend to a large extent on the type of coating material used and to some extent on the system employed to apply the coating. For example, when employing a polyaromatic amine as the coating material, eight ounces of a 1% by weight solution is sufficient to coat a 1100 gallon reactor using VCM gas. This is a vast improvement over coating application processes heretofore known in the art.
A number of various coating materials, which are capable of resisting polymer buildup, may be employed in making the coating solutions which are useful in practicing the process of the instant invention. Among these materials are the straight chain or branched polyaromatic amines or the condensed polyhydric phenols. The polyaromatic amines are made by the reaction of any one by itself, except the polyhydric phenols, or more
than one, of the compounds selected from polyamino benzenes, polyhydric phenols, aminophenols, alkylsubstituted diphenylamines. As examples of such polyaromatic amines, there may be named a few, by way of example, such as the reaction product of m-phenylenediamine (m- PDA) and resorcinol; m-PDA and p-aminophenol; p-PDA and hydroquinone; toluene-2,4-diamine and resorcinol; self- condensed m-PDA; m-PDA, resorcinol and p-aminophenol; etc. These polyaromatic amines are clearly shown and described in U.S. Patent No. 4,024,330, issued May 17, 1977 to Morningstar and Kehe and is incorporated herein. This patent also shows the method of making the polyaromatic amines and the method of applying the same to reactor walls by means of an organic solvent solution thereof.
In U.S. Patent No. 4,024,301, issued May 17,
1977 to Witenhafer, Haehn, and Cohen, there is described a process of applying the straight chain or branched polyaromatic amines, described above, to the reactor surfaces using an aqueous alkali metal hydroxide solution thereof. This patent is also incorporated herein. In U.S. Patent No. 4,081,248, issued March 28,
1978 to Cohen there is described a process for applying to the reactor surfaces an aqueous alkali metal hydrox- ide coating solution containing a straight chain or branched polyaromatic amine, as herein described, and a dispersant operable in aqueous media. The useful dis- persants, which may be so employed, are polyvinyl alcohol, polyvinyl pyrolidone, gelatin (calf skin), starch and hydroxypropyl methyl cellulose. This patent is also incorporated herein.
Another class of coating materials very useful in substantially eliminating polymer buildup in polymerization reactors is the self-condensed polyhydric phenols which are also operable in the practice of the present process using VCM as the carrier. These coating
materials are shown and described in U.S. Patent No. 4,080,173, issued March 21, 1978, to Cohen, which is incorporated herein. This patent also shows the method of making the self-condensed polyhydric phenols. In the patent, there is applied to the reactor surfaces a coating composition containing, as a primary ingredient, (1) the self-condensation product of a polyhydric phenol, or (2) the condensation product of two or more polyhydric phenols, or (3) the self-condensation product of a polyhydric naphthol, dissolved in an aqueous alkali metal hydroxide solution. The polyhydric phenols used in making the condensation products are resorcinol, hydroquinone, catechol and phloroglucinol.
Another class of materials which are suitable for making aqueous coating solutions for application to reactor surfaces to substantially eliminate polymer buildup thereon, and which can be employed in the present process, are the tannins, such as, for example, tannic acid. The tannins are divided into two main groups, namely hydrolyzable tannins and condensed tannins. The tannins are usually identified from the source of extraction, that is, the tree or plant. As examples of the hydrolyzable tannins and their source, there may be named Chinese gall or tannic acid, myrobalans tannins (nuts), valonia tannins (cups and beards), chestnut tannins (wood), divi-divi tannins (pods), and the like. As examples of the condensed tannins and their source, there may be named oak tannins (bark), hemlock tannins (bark), wattle tannins (Bark), sumach tannins (leaves), quebracho tannins (wood), mangrove tannins (bark), gambier tannins (leaves), and the like. Also useful are the ammonium tannates and tannins complexed with metal ions. The tannins are shown and described in U.S. Patent No. 4,105,840, issued August 8, 1978 to Cohen and incorporated herein.
Another class of materials which are suitable for making coating solutions for application to reactor surfaces in accordance with the present process, for substantially eliminating polymer buildup, are various dyes or dyestuffs. For example, the alkali soluble dyes which can be dissolved in an aqueous alkali metal hydroxide solution or an ammonium hydroxide solution, as shown and described in U.S. Patent No. 4,068,059, issued January 10, 1978, to Witenhafer, and incorporated herein. The alkali soluble dyes are those which contain in their chemical structure one or more of the following radicals : -OH, -COOH, -SO3H, and -SO3Na, which radicals may be the same or different on any one dye structure. The classes of dyes which have one or more of said radicals are the azo dyes, such as monoazo and polyazo dyes; metal- containing azo dyes; mordant dyes; pyrazolones; stilbene dyes, azoic dyes, phenols, naphthols; anthraquinone dyes; diphenylmethane and triphenylmethane dyes; thiazoles, nitro dyes; nitroso dyes; xanthenes; benzoquinones and naphthoquinones; and solubilized vat dyes, such as indigoids and anthraquinoids. Also the ionic dyes are useful, such as acridines, azines, oxazines and the thiazines.
Further dyes are the water-soluble dyes which are shown and described in pending U.S. application
Serial No. 807,958, filed June 20, 1977, in the name of Witenhafer. These dyes contain one or more of the following radicals: -COONa, -COOH, -SO3H, and -SO3Na. The dyes shown in said application are incorporated herein by reference.
In addition to the dyes mentioned above, various organic solvent-soluble dyes may be used, such as nigrosine, aniline black, etc., such as shown in U.S. Patent No. 3,669,946, issued June 13, 1972, to Koyanagi, et al.
In order to prevent polymer buildup in a reactor, it is believed that you need a water-wettable surface. When a metal or solid surface is non-wettable, a liquid, such as water, thereon will form droplets and not flow out into a smooth uniform film. An ordinary solid surface, such as stainless steel for example, is not water-wettable due to the normal contamination of said surface with organic materials through contact with the atmosphere. The surface can be cleaned, such as with chromic acid or an abrasive cleanser for example, and it will become water-wettable. However, this is not the full answer, since the surface will not remain in that condition for a sufficient length of time, that is, for more than the duration of a single polymerization reaction. That is to say, the surface must be recleaned after each polymerization cycle. Therefore, applying a coating to the surface which will be water-wettable and resist polymer buildup thereon and remain on said surface throughout multiple reaction cycles is more desired.
The wettability of a solid surface can be measured. The angle formed between the tangent of the side of the droplet and the metal or glass surface is called the "contact angle" and is referred to as "theta" (θ) . A further measurement of the wettability of a solid surface is the critical surface tension for wetting a solid surface and is expressed as "γc". The "γc" is measured in dynes per centimeter. Using water as the standard, in order for a solid surface to be wettable, θ must equal 0 or be very close to it, "γc" must be 72 dynes/cm. or greater.
More importantly, the coating material being applied to the surface should not only form a wettable surface, but also form a continuous layer or film thereon which is not readily removable. This film or coating adheres to the solid or metal surface by adsorption and
in many cases, the film is a monolayer of the coating material applied which is of the order of a molecule in thickness. These films of such thickness are invisible to the naked eye, thus further solving the color problem heretofore referred to. Of course, films of greater thickness can result when using higher solids content coating solutions which films or coatings are visible to the naked eye. The film or layer formed by the coating composition applied to the surface by VCM gas, in accordance with the present invention, is not removable by washing with water. That is to say, the coating or film is resistant to removal from the reactor surfaces when a turbulent aqueous reaction medium is in contact therewith, caused by the agitation of the polymerization mixture in the reactor.
The coating solutions useful in the present invention are made by conventional methods, using heat and agitation where necessary. Usually a temperature in the range of about 0°C to about 100°C is satisfactory. Agitation during dissolution of the coating material is desirable. When the concentration of the coating material is within the range given above, the coating solution thereof may be easily applied to the reactor surfaces by means of VCM gas through nozzles mounted on the reactor. Further, the molecular weight of the coating material has an effect on the concentration of the same in the coating solution or the total solids of said solution. Still further, these factors may vary the concentrations of coating materials in the coating solutions given above.
It should be pointed out that the coating compositions, used in the present invention, work equally well on glass, or metal surfaces, such as stainless steel and the like. While the exact mechanism of adhesion of the coating to the surfaces of the reactor is not known for certain, it is believed to involve some
type of electrical force or adsorption between the reactor surfaces and the coating material, particularly with some coating solutions. At any rate, the coating compositions useful in the present invention do substantially eliminate polymer buildup on said surfaces and what little polymer buildup, if any, that may occur is of the "sandy" type which is of such a nature that it is readily removable from the reactor surfaces without the necessity of manual scraping procedures. The polymer buildup to be avoided is what is referred to as "paper" buildup since this type of buildup is very difficult to remove and usually requires hand scraping or the use of a high pressure jet stream of water or other liquid. In either event, the reactor must be opened in order to clean the same, which of course allows the escape of unreacted monomer, such as vinyl chloride, into the atmosphere which is hazardous to health.
Using the VCM gas application of the coating, in accordance with the present invention, multiple polymerizations may be run without opening the reactor between charges. Although multiple charges may be run without recoating the surfaces, it has been found to be expeditious, and preferred, to recoat the reactor after every charge, or every few charges, to insure uniform and efficient production. This is very easily done using the VCM gas application of the coating composition through the spray nozzles, as heretofore described. When it is decided to recoat the reactor, the reactor is drained, and the inner surfaces are flushed with water by means of the spray nozzles to remove all loose polymer particles thereon. Then the coating is applied by means of the VCM gas. Thereafter, the reactor is charged with the polymerization medium and ingredients in the usual manner and the polymerization reaction commenced. It is understood, of course, that one can
recoat the reactor as often as desired without opening the same, even after every charge is polymerized. It should also be noted that no particular modification of polymerization processing techniques are required due to the presence of the coating. Further, utilization of the internally coated reaction vessel of the present invention does not adversely affect the heat stability or other physical and chemical properties of the polymers produced therein.
While the present invention is specifically illustrated with regard to the suspension polymerization of vinyl chloride, it is to be understood that the instant process may likewise be applied in the dispersion, emulsion or suspension polymerization of any polymerizable ethylenically unsaturated monomer or monomers where undesirable polymer buildup occurs. Examples of such monomers are other vinyl halides and vinylidene halides, such as vinyl bromide, vinylidene chloride, etc., vinyl- idene monomers having at least one terminal CH2=C
grouping, such as esters of acrylic acid, for example, methyl methacrylate., ethyl aerylate, butyl aerylate, octyl acrylate, cyanoethyl acrylate, and the like; vinyl acetate; acrylonitrile; esters of methacrylic acid, such as methyl methacrylate, butyl methacrylate, and the like; styrene and styrene derivatives including α-methyl styrene, vinyl toluene, chlorostyrene, etc., vinyl naphthalene; diolefins including butadiene, isoprene, chloroprene, and the like; and mixtures of any types of these monomers and other vinylidene monomers copolymerizable therewith; and other vinylidene monomers of the types known to those skilled in the art.
The present invention, however, is particularly applicable to the suspension polymerization of vinyl chloride, either alone or in a mixture with one or more other vinylidene monomers having at least one terminal CH2= grouping, copolymerizable therewith in
amounts as great as about 80% or more by weight, based on the weight of the monomer mixture, since polymer buildup is a problem in this area.
In the present invention, the polymerization process is usually conducted at a temperature in the range of about 0°C to about 100°C. depending upon the particular monomer or monomers being polymerized. However, it is preferred to employ temperatures in the range of about 40°C. to about 70°C, since, at these temperatures, polymers having the most beneficial properties are produced. The time of the polymerization reaction will vary from about 2 to about 15 hours .
The polymerization process may be carried out at autogeneous pressures, although superatmospheric pressures of up to 10 atmospheres or more may be employed with some advantage with the more volatile monomers. Superatmospheric pressures may also be employed with those monomers having the requisite volatilities at reaction temperatures permitting reflux cooling of the reaction mixture.
Further, the polymerization process may be carried out utilizing a full reactor technique. That is, the reaction vessel is completely filled with the polymerization medium and kept that way throughout the reaction by constant addition thereto of water or additional make-up liquid containing the monomer or monomers. Upon the addition of a certain predetermined amount of liquid, the polymerization reaction is terminated, usually by the addition thereto of a short- stopping agent. The necessity for the addition of liquid is due to the shrinkage in volume of the reaction medium produced by the conversion of the monomer or monomers to the polymeric state.
The various coatings, as particularly set forth in the specific examples, which follow hereinafter, were rated by visual observation.
In order to further illustrate the present invention, the following specific examples are given. It is to be understood, however, that this is merely intended in an illustrative and not limitative sense. In the examples, all parts and percents are by weight unless otherwise indicated.
EXAMPLE I In this example, an uncoated reactor was employed to establish a control. The reactor surfaces were cleaned with high pressure water prior to charging the polymerization ingredients. First, 630 gallons of demineraliz'ed water (52°C) were added to the reactor followed by the addition of 72 pounds of a 3% by weight aqueous solution of hydroxylpropyl methyl cellulose with agitation. Then the reactor was closed and evacuated to 25 inches of mercury without agitation. The catalyst was then added, which was 0.54 pound of disecondary butyl peroxydicarbonate as a 20% solution in hexane. The agitator was then started and 3000 pounds of vinyl chloride was added to the reactor. The reaction mixture was then heated to 52°C and the polymerization reaction was carried out at this temperature for 8.5 hours. During the course of the reaction, demineralized water was added at the rate of 0.27 gallons per minute to compensate for the decrease in volume due to the formation of polymer. The polymerization was stopped after a pressure drop of 4 psig. or 8.5 hours. After recovering the polymer produced, the reactor was rinsed with water and and three additional charges were run in the reactor in like manner. After the fourth charge, the reactor was examined for polymer buildup. All of the internal surfaces were heavily coated with knots or lumps of polymer and paper buildup. The control reactor, with no coating on the internal surfaces thereof was classified as "dirty".
EXAMPLE II In this example, the reactor was coated prior to conducting the polymerization reaction therein. The coating solution employed herein comprised 3 grams of nigrosine Z1630 dissolved in 8 ounces of dimethyl formamide. The VCM gas was introduced into the reactor through a spray nozzle mounted on the reactor and under a pressure of 150 psig. After about 5 seconds of good VCM gas flow, the coating solution was slowly added to the VCM gas stream and carried to the inner surfaces of the reactor as a mist. The coating operation took about 20 seconds and upon completion, the reactor surfaces were rinsed with demineralized water. (Note: this step is optional.) After rinsing, the reactor was charged using the recipe and procedure of Example I. Thereafter, the reaction mixture was heated to 52°C and held at this temperature throughout the polymerization reaction which was complete in 8.5 hours. After this charge was completed, the polymer was removed and 3 additional charges were run in the reactor in like manner. Prior to each additional charge, the reactor surfaces were coated in the same manner as described above. Upon examination of the reactor, after completion of the fourth charge, it was found that all the surfaces were clean or substantially free of polymer buildup. What little buildup that was present, was the soft sandy type and readily removable with finger tip pressure. There was no paper buildup present showing the improvement over the uncoated or control reactor of Example I.
EXAMPLE III In this Example, the inner surfaces of the reactor were coated with an aqueous alkali metal hydroxide solution of a self-condensed polyhydric phenol, namely resorcinol. The self-condensed resorcinol was made in accordance with the procedure shown in U.S.
Patent No. 4,080,173. A coating solution concentrate was made up as follows:
15% self-condensed resorcinol 10% NaOH 75% Water (demineralized)
Twenty cc's of the above solution in 8 ounces of demineralized water was then used to coat the internal surfaces of the reactor. The reactor was coated in the same manner as shown in Example II. Again, using the polymerization recipe and procedure of Example I, four charges were made, with rinsing and coating of the inner surfaces after each charge. After the fourth charge was complete and the polymer removed, the reactor was examined and found to be in very good condition with respect to polymer buildup. There was no paper buildup and only a few soft sandy spots which were readily removable. The condition of the reactor was far superior to that of the control of Example I.
Coating the internal surfaces of a polymerization reactor by means of the present process not only substantially eliminates polymer buildup thereon, but also, less coating material is used than heretofore, thus providing a more economic coating process. With the present process, one is enabled to operate a closed polymerization system which, in the case of vinyl chloride polymerization, has the advantage of reducing the parts per million of vinyl chloride in the plant to a point that meets Governmental regulations. Numerous other advantages of the present invention will be apparent to those skilled in the art.
While the present invention has been described in terms of its specific embodiments, certain modifications and equivalents will be apparent to those skilled in the art and are intended to be included within the scope of the present invention, which is to be limited only by the scope of the appended claims.
Claims (17)
1. A process for substantially eliminating the buildup of polymer on the internal surfaces of a polymerization reaction vessel which comprises making a coating solution of a coating material which, in the form of a film, is capable of resisting polymer buildup thereon, applying said coating material to said surfaces by the action of vinyl chloride gas on said coating solution, said vinyl chloride gas acting as a carrier for said coating material, and thereafter conducting the polymerization of the monomer (s) while in constant contact with the coated internal surfaces of said vessel.
2. A process as defined in Claim 1 wherein the monomer is vinyl chloride.
3. A process as defined in Claim 1 wherein the coating material is present in said coating solution in an amount in the range of about 0.001% to about 20.0% by weight.
4. A process as defined in Claim 1 wherein the temperature of the vinyl chloride gas is in the range of about 20°C to about 100°C and under a pressure of about 20 psig to about 1000 psig.
5. A process as defined in Claim 1 wherein the coating material is a polyaromatic amine made by the condensation reaction of any one by itself or more than one by itself or more than one of the compounds selected from the group consisting of polyamino benzenes, polyhydric phenols, aminophenols, alkyl-substituted amino- phenols, diphenylamines, and alkyl-substituted diphenyl- amines.
6. A process as defined in Claim 5 wherein the coating solution is an organic solvent solution of the polyaromatic amine.
7. A process as defined in Claim 5 wherein the coating solution is an aqueous alkali metal hydroxide solution of the polyaromatic amine.
8. A process as defined in Claim 7 wherein the coating solution contains a dispersant operable in aqueous media and selected from the group consisting of polyvinyl alcohol, polyvinyl pyrrolidone, gelatin (calf skin), starch, and hydroxypropyl methyl cellulose.
9. A process as defined in Claim 1 wherein the coating solution is comprised of an aqueous alkali metal hydroxide solution containing a condensation product selected from the group consisting of the self- condensation product of one or more polyhydric phenols, and the self-condensation product of a polyhydric naphthol, and wherein said polyhydric phenol (s) is selected from the group consisting of resorcinol, hydro- quinone, catechol and phloroglucinol.
10. A process as defined in Claim 1 wherein the coating solution is comprised of an aqueous solution of a tannin, said tannin being selected from the group consisting of hydrolyzable tannins, condensed tannins, ammonium tannates, and tannins complexed with metal ions.
11. A process as defined in Claim 10 wherein the monomer is vinyl chloride.
12. A process as defined in Claim 1 wherein the coating solution is comprised of an aqueous alkali metal hydroxide solution of an alkalisoluble dye, said dye having one or more radicals in its chemical structure selected from the group consisting of -OH, -COOH, -SO3H, and -SO3Na.
13. A process as defined in Claim 12 wherein the dye is an ionic dye selected from the group consisting of acridines, azines, oxazines, and thiazines.
14. A process as defined in Claim 1 wherein the coating solution is comprised of an organic solvent solution of an organic solvent-soluble dye.
15. A process as defined in Claim 14 wherein the dye is nigrosine and the solvent is dimethyl formamide.
16. A process as defined in Claim 1 wherein the coating solution is comprised of an aqueous solution of a water-soluble dye, said dye having one or more radicals in its chemical structure selected from the group consisting of -COONa, -COOH, -SO3H and -SO3Na.
17. A process as defined in Claim 1 wherein the monomers are vinyl chloride and vinyl acetate.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/075,552 US4263421A (en) | 1979-09-14 | 1979-09-14 | Process for coating reactors using organic compound vapor application |
US075,552 | 1979-09-14 | ||
PCT/US1980/001063 WO1981000684A1 (en) | 1979-09-14 | 1980-08-18 | Process for coating reactors using organic compound vapor application |
Publications (2)
Publication Number | Publication Date |
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AU6330280A AU6330280A (en) | 1981-03-31 |
AU541568B2 true AU541568B2 (en) | 1985-01-10 |
Family
ID=26757003
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Application Number | Title | Priority Date | Filing Date |
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AU63302/80A Ceased AU541568B2 (en) | 1979-09-14 | 1980-08-18 | ** |
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AU (1) | AU541568B2 (en) |
NO (1) | NO156830C (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU612883B2 (en) * | 1988-08-19 | 1991-07-18 | Shin-Etsu Chemical Co. Ltd. | Method of preventing polymer scale formation |
-
1980
- 1980-08-18 AU AU63302/80A patent/AU541568B2/en not_active Ceased
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1981
- 1981-05-07 NO NO811550A patent/NO156830C/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU612883B2 (en) * | 1988-08-19 | 1991-07-18 | Shin-Etsu Chemical Co. Ltd. | Method of preventing polymer scale formation |
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Publication number | Publication date |
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NO811550L (en) | 1981-05-07 |
NO156830C (en) | 1987-12-02 |
NO156830B (en) | 1987-08-24 |
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