WO1991007383A1 - VERFAHREN ZUR HYDROLYSE VON α-NAPHTHALINSULFONSÄURE IN EINEM NAPHTHALIN-SULFONIERGEMISCH - Google Patents
VERFAHREN ZUR HYDROLYSE VON α-NAPHTHALINSULFONSÄURE IN EINEM NAPHTHALIN-SULFONIERGEMISCH Download PDFInfo
- Publication number
- WO1991007383A1 WO1991007383A1 PCT/EP1990/001849 EP9001849W WO9107383A1 WO 1991007383 A1 WO1991007383 A1 WO 1991007383A1 EP 9001849 W EP9001849 W EP 9001849W WO 9107383 A1 WO9107383 A1 WO 9107383A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- column
- naphthalene
- mixture
- hydrolysis
- sulfonation mixture
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/42—Separation; Purification; Stabilisation; Use of additives
- C07C303/44—Separation; Purification
Definitions
- ß-naphthol In the large-scale production of. ß-naphthol is first reacted with naphthalene with sulfuric acid and the resulting ß-aphthalinsulfonic acid is subsequently converted into ß-naphthol by alkali melt (Ullmann, Enzyklopadie der techn. Chemie, 4th edition, vol. 17 (1979), pp. 115-120);
- the mixture formed in the sulfonation of naphthalene contains, in addition to the desired ⁇ -naphthalenesulfonic acid, the most important by-product also ⁇ -aphthalinsulfonic acid.
- ⁇ -aphthaline sulfonic acid the most important by-product also ⁇ -aphthalinsulfonic acid.
- This hydrolysis process can be improved by introducing steam into the sulfonation mixture.
- the naphthalene formed during hydrolysis becomes constantly removed and achieved a corresponding shift in the hydrolysis balance.
- This "steam hydrolysis” can reduce the ⁇ -acid content from approx. 5% by weight to less than 0.3% by weight. Based on the content of naphthalene monosulfonic acids, this means that the ⁇ -acid content is less than 0.5% by weight.
- steam has generally been introduced into the molten sulfonation mixture, which is either still in the sulfonation vessel or in a special hydrolysis vessel. Temperatures between 140 ° C. and 160 ° C. and steam introduction times of up to 8 hours are customary (DE-Auslegeschrift 1,080,566 and 1,167,333 and US Pat. No. 1,922,813).
- trickle column can be used successfully if the sulfonation mixture is circulated from a receiver vessel over the column and treated with steam in countercurrent.
- the invention therefore relates to a process for the hydrolysis of ⁇ -naphthalenesulfonic acid in a naphthalene-sulfonation mixture by treatment with steam, characterized in that the
- the "total amount of sulfonation mixture introduced at the top of the column” is composed of the sulfonation mixture which has not yet been treated with water vapor and which is introduced for the first time at the top of the column and the bottom effluent from the column which has already been treated with water vapor and then again added to the top.
- This total amount added at the top of the column can be easily measured, for example using a flow meter or calibrated accordingly
- the total residence time of the sulfonation mixture in the column is preferably at least 30 minutes, in particular 30 to 180 minutes.
- the total residence time can be increased by lengthening the column or by increasing the total amount of sulfonation mixture charged at the top of the column (i.e. roughly speaking, by the number of passes through the column).
- FIG. 1 The principle of the method is illustrated in FIG. 1.
- the molten sulfonation mixture is poured into the container (1) equipped with a stirrer and heating jacket and fed via line (2) to the top of the heated packed column (4) with the aid of the pump (3).
- the melt trickles down on the packing in a thin film and comes into contact with the rising water vapor, which is fed in via line (5) at the bottom of the column.
- the water vapor containing naphthalene leaves the column via line (6) and is fed to a condenser where it is condensed.
- the naphthalene is separated from the condensate water and thus recovered.
- the steam treatment in the trickle column is continued until the proportion of ⁇ -naphthalenesulfonic acid in the total content of the monosulfonic acids in the sulfonation mixture has reached the desired value, e.g. 0.4% by weight.
- the steam hydrolysis should not be continued for an unnecessarily long time, since there is always a small but undesirable hydrolysis of ⁇ -aphthaline sulfonic acid.
- An apparatus made of glass components corresponding to FIG. 1 was used for the experiment.
- a 20 liter round bottom flask served as the storage container.
- a glass tube of 80 mm diameter with packed bed was used as the trickle column; the filling height of the packing was 1 m.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pinball Game Machines (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19893937748 DE3937748A1 (de) | 1989-11-14 | 1989-11-14 | Verfahren zur hydrolyse von (alpha)-naphtalinsulfonsaeure in einem nahptalin-sulfoniergemisch |
DEP3937748.2 | 1989-11-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1991007383A1 true WO1991007383A1 (de) | 1991-05-30 |
Family
ID=6393442
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1990/001849 WO1991007383A1 (de) | 1989-11-14 | 1990-11-06 | VERFAHREN ZUR HYDROLYSE VON α-NAPHTHALINSULFONSÄURE IN EINEM NAPHTHALIN-SULFONIERGEMISCH |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0500660A1 (ja) |
JP (1) | JPH05501412A (ja) |
CN (1) | CN1052476A (ja) |
CS (1) | CS560390A2 (ja) |
DE (1) | DE3937748A1 (ja) |
WO (1) | WO1991007383A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104628607A (zh) * | 2015-02-16 | 2015-05-20 | 曲靖众一合成化工有限公司 | 一种α-萘磺酸连续加压水解方法及其装置 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102746195A (zh) * | 2011-04-27 | 2012-10-24 | 江苏尼高科技有限公司 | 一种改进萘系减水剂磺化工艺的方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1332203A (en) * | 1917-07-06 | 1920-03-02 | Louis M Dennis | Method of sulfonation of hydrocarbons of the aromatic series |
US1922813A (en) * | 1932-09-15 | 1933-08-15 | Nat Aniline & Chem Co Inc | 2-naphthalenemonosulphonic acid |
US3655639A (en) * | 1968-05-17 | 1972-04-11 | Ciba Geigy Ag | Monoazo dyestuffs containing an alkoxy triazine |
-
1989
- 1989-11-14 DE DE19893937748 patent/DE3937748A1/de not_active Withdrawn
-
1990
- 1990-11-06 JP JP2515328A patent/JPH05501412A/ja active Pending
- 1990-11-06 EP EP19900916743 patent/EP0500660A1/de not_active Withdrawn
- 1990-11-06 WO PCT/EP1990/001849 patent/WO1991007383A1/de not_active Application Discontinuation
- 1990-11-13 CS CS905603A patent/CS560390A2/cs unknown
- 1990-11-13 CN CN 90109857 patent/CN1052476A/zh active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1332203A (en) * | 1917-07-06 | 1920-03-02 | Louis M Dennis | Method of sulfonation of hydrocarbons of the aromatic series |
US1922813A (en) * | 1932-09-15 | 1933-08-15 | Nat Aniline & Chem Co Inc | 2-naphthalenemonosulphonic acid |
US3655639A (en) * | 1968-05-17 | 1972-04-11 | Ciba Geigy Ag | Monoazo dyestuffs containing an alkoxy triazine |
Non-Patent Citations (1)
Title |
---|
Ullmans Encyclop{die der Technischen Chemie, 4 Auflage, band 17, 1979, Weinheim, DE, Seiten 115-120 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104628607A (zh) * | 2015-02-16 | 2015-05-20 | 曲靖众一合成化工有限公司 | 一种α-萘磺酸连续加压水解方法及其装置 |
Also Published As
Publication number | Publication date |
---|---|
JPH05501412A (ja) | 1993-03-18 |
CN1052476A (zh) | 1991-06-26 |
CS560390A2 (en) | 1991-09-15 |
EP0500660A1 (de) | 1992-09-02 |
DE3937748A1 (de) | 1991-05-16 |
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