JPH0340020B2 - - Google Patents
Info
- Publication number
- JPH0340020B2 JPH0340020B2 JP10207882A JP10207882A JPH0340020B2 JP H0340020 B2 JPH0340020 B2 JP H0340020B2 JP 10207882 A JP10207882 A JP 10207882A JP 10207882 A JP10207882 A JP 10207882A JP H0340020 B2 JPH0340020 B2 JP H0340020B2
- Authority
- JP
- Japan
- Prior art keywords
- reaction
- salts
- salt
- water
- acid
- 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
Links
- 150000003839 salts Chemical class 0.000 claims description 21
- 239000002253 acid Substances 0.000 claims description 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
- 239000001301 oxygen Substances 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 11
- 229940079826 hydrogen sulfite Drugs 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 7
- 239000012736 aqueous medium Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- GBXSEMLWYDCLTG-UHFFFAOYSA-N 2-hydroxy-2-phenylpropane-1-sulfonic acid Chemical compound OS(=O)(=O)CC(O)(C)C1=CC=CC=C1 GBXSEMLWYDCLTG-UHFFFAOYSA-N 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 3
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical group CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 description 35
- 239000000243 solution Substances 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 12
- -1 alkali metal salts Chemical class 0.000 description 8
- 239000000126 substance Substances 0.000 description 7
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 150000003863 ammonium salts Chemical class 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 5
- 239000003729 cation exchange resin Substances 0.000 description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 239000011575 calcium Substances 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 229910001882 dioxygen Inorganic materials 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 2
- HTZCNXWZYVXIMZ-UHFFFAOYSA-M benzyl(triethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC1=CC=CC=C1 HTZCNXWZYVXIMZ-UHFFFAOYSA-M 0.000 description 2
- 150000003939 benzylamines Chemical class 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 239000003444 phase transfer catalyst Substances 0.000 description 2
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- WXUZTSKSKUZINC-UHFFFAOYSA-M sodium;2-hydroxy-2-phenylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)(C)C1=CC=CC=C1 WXUZTSKSKUZINC-UHFFFAOYSA-M 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- QDGFXAPUDKVRIY-UHFFFAOYSA-N 2-hydroxy-2-phenylbutane-1-sulfonic acid Chemical compound OS(=O)(=O)CC(O)(CC)C1=CC=CC=C1 QDGFXAPUDKVRIY-UHFFFAOYSA-N 0.000 description 1
- JOANXVZFLFDJFZ-UHFFFAOYSA-N 2-hydroxy-2-phenylpentane-1-sulfonic acid Chemical compound CCCC(O)(CS(O)(=O)=O)C1=CC=CC=C1 JOANXVZFLFDJFZ-UHFFFAOYSA-N 0.000 description 1
- VJZWKKYFRNLTRB-UHFFFAOYSA-N 2-hydroxy-3-methyl-2-phenylbutane-1-sulfonic acid Chemical compound OS(=O)(=O)CC(O)(C(C)C)C1=CC=CC=C1 VJZWKKYFRNLTRB-UHFFFAOYSA-N 0.000 description 1
- POZGETMIPGBFGQ-UHFFFAOYSA-N 3-methylbut-1-en-2-ylbenzene Chemical compound CC(C)C(=C)C1=CC=CC=C1 POZGETMIPGBFGQ-UHFFFAOYSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- ZETCGWYACBNPIH-UHFFFAOYSA-N azane;sulfurous acid Chemical compound N.OS(O)=O ZETCGWYACBNPIH-UHFFFAOYSA-N 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- ZNMZHHBHUPIREW-UHFFFAOYSA-L barium(2+);hydrogen sulfite Chemical compound [Ba+2].OS([O-])=O.OS([O-])=O ZNMZHHBHUPIREW-UHFFFAOYSA-L 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- SQHOHKQMTHROSF-UHFFFAOYSA-N but-1-en-2-ylbenzene Chemical compound CCC(=C)C1=CC=CC=C1 SQHOHKQMTHROSF-UHFFFAOYSA-N 0.000 description 1
- LVGQIQHJMRUCRM-UHFFFAOYSA-L calcium bisulfite Chemical compound [Ca+2].OS([O-])=O.OS([O-])=O LVGQIQHJMRUCRM-UHFFFAOYSA-L 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000010260 calcium hydrogen sulphite Nutrition 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- GYTFTYUIWVUBJC-UHFFFAOYSA-L calcium;2-hydroxy-2-phenylpropane-1-sulfonate Chemical compound [Ca+2].[O-]S(=O)(=O)CC(O)(C)C1=CC=CC=C1.[O-]S(=O)(=O)CC(O)(C)C1=CC=CC=C1 GYTFTYUIWVUBJC-UHFFFAOYSA-L 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000008235 industrial water Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- SUPUVLWGKPVHBQ-UHFFFAOYSA-M lithium sulfite Chemical compound [Li+].OS([O-])=O SUPUVLWGKPVHBQ-UHFFFAOYSA-M 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- LPHFLPKXBKBHRW-UHFFFAOYSA-L magnesium;hydrogen sulfite Chemical compound [Mg+2].OS([O-])=O.OS([O-])=O LPHFLPKXBKBHRW-UHFFFAOYSA-L 0.000 description 1
- XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- KHMYONNPZWOTKW-UHFFFAOYSA-N pent-1-enylbenzene Chemical compound CCCC=CC1=CC=CC=C1 KHMYONNPZWOTKW-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- DJEHXEMURTVAOE-UHFFFAOYSA-M potassium bisulfite Chemical compound [K+].OS([O-])=O DJEHXEMURTVAOE-UHFFFAOYSA-M 0.000 description 1
- 235000010259 potassium hydrogen sulphite Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003440 styrenes Chemical group 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003458 sulfonic acid derivatives Chemical class 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229910001428 transition metal ion Inorganic materials 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000002349 well water Substances 0.000 description 1
- 235000020681 well water Nutrition 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10207882A JPS58219158A (ja) | 1982-06-16 | 1982-06-16 | ヒドロキシアルカンスルホン酸及びその誘導体並びにその製造方法 |
PCT/JP1983/000193 WO1984000031A1 (en) | 1982-06-16 | 1983-06-16 | Hydroxyalkanesulfonic acids and their derivatives, and process for their preparation |
EP83901937A EP0111569B1 (en) | 1982-06-16 | 1983-06-16 | Hydroxyalkanesulfonic acids and their derivatives, and process for their preparation |
DE19833390045 DE3390045C2 (de) | 1982-06-16 | 1983-06-16 | Hydroxyalkansulfons{uren und deren Ammonium-, Alkalimetall- oder Erdalkalimetallsalze sowie Verfahren zu ihrer Herstellung |
GB08403529A GB2133016B (en) | 1982-06-16 | 1983-06-16 | Hydroxyalkanesulfonic acids and their derivatives and process for their preparation |
US06/776,797 US4654177A (en) | 1982-06-12 | 1985-09-17 | Hydroxyalkanesulfonic acids and their derivatives and process for preparing same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10207882A JPS58219158A (ja) | 1982-06-16 | 1982-06-16 | ヒドロキシアルカンスルホン酸及びその誘導体並びにその製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58219158A JPS58219158A (ja) | 1983-12-20 |
JPH0340020B2 true JPH0340020B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1991-06-17 |
Family
ID=14317734
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10207882A Granted JPS58219158A (ja) | 1982-06-12 | 1982-06-16 | ヒドロキシアルカンスルホン酸及びその誘導体並びにその製造方法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58219158A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
-
1982
- 1982-06-16 JP JP10207882A patent/JPS58219158A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS58219158A (ja) | 1983-12-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3117369B2 (ja) | スルホンイミドの製造方法 | |
CN108314633A (zh) | 由羟乙基磺酸碱金属盐和乙烯基磺酸碱金属盐循环制备牛磺酸的方法 | |
US3919295A (en) | Preparation of inorganic fluoride-free perfluoroalkane sulphonates | |
JPH0532610A (ja) | 1,2−ナフトキノンジアジド−5−スルホニルクロリドの製造方法 | |
JPH11209338A (ja) | スルホンイミドの製造方法 | |
JPH0340019B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
JP2000302748A (ja) | スルホンイミドの精製方法 | |
JPH0340020B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
US5159112A (en) | Process of the production of alkanesulfonamides | |
EP0111569B1 (en) | Hydroxyalkanesulfonic acids and their derivatives, and process for their preparation | |
US5312974A (en) | Process for the production of light-colored lower alkane-sulfonic acids, more particularly methanesulfonic acid | |
JPH0244303B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
US5097074A (en) | Process for purifying 4,4'-dihydroxydiphenylsulfone | |
JPH0656758A (ja) | 2−ナフトール−6−スルホン酸塩の製造方法 | |
JP2006213656A (ja) | 安息香酸フェニルエステル誘導体スルホン化物又はその塩の製造方法 | |
JPS6140661B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
JPH0341461B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
JP3486634B2 (ja) | ジヒドロキシジフェニルスルホンのアルカリ金属塩 | |
JPH02204476A (ja) | ベンゼンスルホニルクロリド誘導体の製造方法 | |
JPS6141358B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
JPH021456A (ja) | ビフエニル―4,4′―ジスルホン酸のアルカリ金属塩の製法 | |
JP2003508508A (ja) | アルカノイルオキシベンゼンスルホン酸及びその塩の製造方法 | |
JP3291841B2 (ja) | β−クロロエタンスルホン酸ソーダの精製方法 | |
KR20010078204A (ko) | 설포닐이미드 화합물의 제조방법 | |
JP2000007628A (ja) | 不飽和アミドカルボン酸類の製造法 |