JPH0423642B2 - - Google Patents
Info
- Publication number
- JPH0423642B2 JPH0423642B2 JP61241532A JP24153286A JPH0423642B2 JP H0423642 B2 JPH0423642 B2 JP H0423642B2 JP 61241532 A JP61241532 A JP 61241532A JP 24153286 A JP24153286 A JP 24153286A JP H0423642 B2 JPH0423642 B2 JP H0423642B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- plac
- water
- polymerization
- wet
- 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.)
- Expired - Lifetime
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 34
- 238000006116 polymerization reaction Methods 0.000 claims description 25
- 239000002253 acid Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 16
- 230000000379 polymerizing effect Effects 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 7
- 239000002685 polymerization catalyst Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- FEWFXBUNENSNBQ-UHFFFAOYSA-N 2-hydroxyacrylic acid Chemical compound OC(=C)C(O)=O FEWFXBUNENSNBQ-UHFFFAOYSA-N 0.000 claims description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical compound OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 description 17
- 238000006243 chemical reaction Methods 0.000 description 16
- 239000000243 solution Substances 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 9
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 8
- 235000011121 sodium hydroxide Nutrition 0.000 description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- GKFWNPPZHDYVLI-UHFFFAOYSA-N 2,3-dichloropropanoic acid Chemical compound OC(=O)C(Cl)CCl GKFWNPPZHDYVLI-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- SZTBMYHIYNGYIA-UHFFFAOYSA-M 2-chloroacrylate Chemical compound [O-]C(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-M 0.000 description 4
- 238000007273 lactonization reaction Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-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
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- NDUPDOJHUQKPAG-UHFFFAOYSA-N Dalapon Chemical compound CC(Cl)(Cl)C(O)=O NDUPDOJHUQKPAG-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 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 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- -1 azobisisobutynitrile Chemical compound 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000007033 dehydrochlorination reaction Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000004534 enameling Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000002955 isolation Methods 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
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 238000003918 potentiometric titration Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/22—Esters containing halogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/14—Esterification
- C08F8/16—Lactonisation
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polyesters Or Polycarbonates (AREA)
- Polymerisation Methods In General (AREA)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61241532A JPS6395206A (ja) | 1986-10-13 | 1986-10-13 | 低含水率の湿潤ポリラクトンの製造方法 |
DE3719999A DE3719999C2 (de) | 1986-10-13 | 1987-06-15 | Verfahren zur Herstellung eines feuchten Polylactonkuchens mit vermindertem Wassergehalt |
CH2262/87A CH672131A5 (ko) | 1986-10-13 | 1987-06-16 | |
KR1019870011257A KR910008294B1 (ko) | 1986-10-13 | 1987-10-12 | 저함수율의 습윤 폭리락톤 케이크의 제조방법 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61241532A JPS6395206A (ja) | 1986-10-13 | 1986-10-13 | 低含水率の湿潤ポリラクトンの製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6395206A JPS6395206A (ja) | 1988-04-26 |
JPH0423642B2 true JPH0423642B2 (ko) | 1992-04-22 |
Family
ID=17075750
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61241532A Granted JPS6395206A (ja) | 1986-10-13 | 1986-10-13 | 低含水率の湿潤ポリラクトンの製造方法 |
Country Status (4)
Country | Link |
---|---|
JP (1) | JPS6395206A (ko) |
KR (1) | KR910008294B1 (ko) |
CH (1) | CH672131A5 (ko) |
DE (1) | DE3719999C2 (ko) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH669952A5 (en) * | 1984-10-18 | 1989-04-28 | Sandoz Ag | Alpha chloro-acrylic or crotonic acid prodn. - by treating 2,3-di:chloropropionic or butyric acid with aq. base, de-hydro-chlorinating prod. and acidifying |
JP4011156B2 (ja) * | 1997-07-31 | 2007-11-21 | 株式会社日本触媒 | 塗料組成物および塗膜並びに塗装品 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2061584A1 (en) * | 1970-12-15 | 1972-07-06 | Henkel & Cie Gmbh | Water insol alpha-substd-polyacrylates - obtd by basic treatment of alpha, beta-dichloro and/or dibromo propionic acids (est |
LU68037A1 (ko) * | 1973-07-18 | 1975-04-11 | ||
LU68060A1 (ko) * | 1973-07-20 | 1975-04-11 | ||
DE2346500C2 (de) * | 1973-09-15 | 1982-10-14 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von Poly-α-oxyacrylsäure |
JPS545839A (en) * | 1977-06-14 | 1979-01-17 | Foster Wheeler Corp | Pipe butting welding |
JPS5727882A (en) * | 1980-07-21 | 1982-02-15 | Mitsubishi Electric Corp | Small-sized elevator device |
JPS5739249A (en) * | 1980-08-15 | 1982-03-04 | Teijin Ltd | Production of raised fabric having cotton like feeling |
-
1986
- 1986-10-13 JP JP61241532A patent/JPS6395206A/ja active Granted
-
1987
- 1987-06-15 DE DE3719999A patent/DE3719999C2/de not_active Expired - Fee Related
- 1987-06-16 CH CH2262/87A patent/CH672131A5/de not_active IP Right Cessation
- 1987-10-12 KR KR1019870011257A patent/KR910008294B1/ko not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE3719999A1 (de) | 1988-04-21 |
CH672131A5 (ko) | 1989-10-31 |
JPS6395206A (ja) | 1988-04-26 |
DE3719999C2 (de) | 1996-03-07 |
KR880005173A (ko) | 1988-06-28 |
KR910008294B1 (ko) | 1991-10-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4125694A (en) | Process for the polymerization of allyl halides to form polyallyl alcohol | |
JPH0423642B2 (ko) | ||
JP2870183B2 (ja) | 1,3―フェニレンジオキシジ酢酸の製法 | |
JPH0959268A (ja) | アクリル酸またはメタクリル酸のグリシジルエステルの製造方法 | |
JPH0571041B2 (ko) | ||
JPH0427243B2 (ko) | ||
JP2917498B2 (ja) | 1,3―フェニレンジオキシジ酢酸の製法 | |
KR970005475B1 (ko) | 폴리-[α-히드록시-(아크릴,크로톤,또는 아크릴+크로톤)산]의 폴리락톤류 및 상응하는 염류의 제조방법 | |
EP0281266A1 (en) | 3-Amino-2,4,5-trifluorobenzoic acid and its manufacture | |
US5688969A (en) | Process for the preparation of thiophene-2-5-dicarboxylic acid and the dichloride thereof | |
JP2971523B2 (ja) | トリアリルイソシアヌレートの製造法 | |
JPH0632773A (ja) | 4,4’−チオビスベンゼンチオールの製造法 | |
CA1292996C (en) | Process for the preparation of 4-(2'-chloroethyl)- benzoic acid | |
SU499261A1 (ru) | Способ получени ароматических дитиолов | |
US4107411A (en) | Method of preparing salts of poly-alpha-hydroxyacrylic acid | |
KR100418259B1 (ko) | p-TSA를 이용한 5,5-메틸렌 디살리실산의 제조방법 | |
JPH03204833A (ja) | 1,3―フェニレンジオキシジ酢酸の製造方法 | |
JPS6058970A (ja) | 2,2′‐ジベンゾチアゾリルジスルフイドの製法 | |
JPH0651754B2 (ja) | ポリ−α−ヒドロキシアクリル酸あるいはその塩の水溶液の製造方法 | |
SU895976A1 (ru) | Способ получени высших органических иодидов | |
JPS62230774A (ja) | トリクロロメラミンの製造方法 | |
JP3586917B2 (ja) | 2−アクリルアミド−2−メチルプロパンスルホン酸ナトリウム重合体の製造方法 | |
JPS6127979A (ja) | オキシフラバン化合物の製造法 | |
JP3055775B2 (ja) | α−クロロ−アクリル酸および/またはクロトン酸のアルカリ金属および/またはアンモニウム塩の製法 | |
SU988830A1 (ru) | Способ получени сорбента |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |