GB1049828A - Sulphating alpha-olefins - Google Patents
Sulphating alpha-olefinsInfo
- Publication number
- GB1049828A GB1049828A GB2879265A GB2879265A GB1049828A GB 1049828 A GB1049828 A GB 1049828A GB 2879265 A GB2879265 A GB 2879265A GB 2879265 A GB2879265 A GB 2879265A GB 1049828 A GB1049828 A GB 1049828A
- Authority
- GB
- United Kingdom
- Prior art keywords
- olefine
- medium
- crystallization
- weight
- secondary alkyl
- 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
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
- C07C303/24—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfuric acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
Abstract
A laundering composition comprises 2-tetradecyl sodium sulphate, mixed with three times its weight of sodium tripolyphosphate (see Example I).ALSO:<PICT:1049828/C2/1> A process for manufacturing sulphated olefines comprises (A) reacting with agitation from 1.5 to 4 moles of H2SO4 of 94.5-100% by weight concentration and 1 mole of an a -olefine containing 9-24 C atoms in the presence of a nonionic organic crystallization medium which is inert to H2SO4 and the a -olefine, said medium being in liquid form and present in amount from 0.5-4 times the weight of the a -olefine and which amount is sufficient to maintain a fluid reaction mixture, said medium also being in a physical state of boiling under reflux to control the reaction temperature, the temperature of boiling being within the shaded area of Fig. 2 of the accompanying drawing, the proportions of reactants to medium being such that prompt crystallization is effected of 2-carbon secondary alkyl sulphuric acid as it is formed; (B) continuing the agitation under the conditions specified in (A) until reaction and crystallization are substantially complete, and (C) neutralizing the secondary alkyl sulphuric acid crystals so formed directly from their crystalline state to a pH above 8 by addition of a base to produce a 2-carbon secondary alkyl sulphate. The process may be batch or continuous; Fig. 1 (not shown), shows suitable apparatus for the latter procedure. Fig. 2 shows how the M.W. of the starting a -olefine affects the range of crystallization temperature of the secondary alkyl sulphuric acid products. Preferred conditions in order to keep on line A of Fig. 2 are an H2SO4 concentration of 97.4\sB0.3% by weight, an H2SO4 : a -olefine mole ratio of 2.1-2.2:1, and a weight of ratio of crystallization medium to a -olefine of 1:1. Preferred embodiments are the use of a -olefines with 12-18 C atoms having straight chains, and a recrystallization medium that is a C3-C5 alkane, or a halogenated ethane or methane, or mixtures of these. Detail is given of how pressure, temperature, and concentration all affect the reaction to assist or prevent crystallization. This latter may be invoked by a seeding process, wherein crystals of secondary alkyl sulphuric acid are added to the reacting ingredients. The products have application as detergents (see Division C5).
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2879265A GB1049828A (en) | 1965-07-07 | 1965-07-07 | Sulphating alpha-olefins |
DE19651468825 DE1468825A1 (en) | 1965-07-07 | 1965-07-28 | Process for sulfating alpha-olefins |
CH1103765A CH463484A (en) | 1965-07-07 | 1965-08-05 | Process for the preparation of sulfation products of α-olefins |
NL6510444A NL6510444A (en) | 1965-07-07 | 1965-08-11 |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2879265A GB1049828A (en) | 1965-07-07 | 1965-07-07 | Sulphating alpha-olefins |
DEP0037341 | 1965-07-28 | ||
CH1103765A CH463484A (en) | 1965-07-07 | 1965-08-05 | Process for the preparation of sulfation products of α-olefins |
NL6510444A NL6510444A (en) | 1965-07-07 | 1965-08-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1049828A true GB1049828A (en) | 1966-11-30 |
Family
ID=27429331
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2879265A Expired GB1049828A (en) | 1965-07-07 | 1965-07-07 | Sulphating alpha-olefins |
Country Status (4)
Country | Link |
---|---|
CH (1) | CH463484A (en) |
DE (1) | DE1468825A1 (en) |
GB (1) | GB1049828A (en) |
NL (1) | NL6510444A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU528816B2 (en) * | 1978-02-14 | 1983-05-12 | Unilever Ltd. | Detergent composotions |
US5075041A (en) * | 1990-06-28 | 1991-12-24 | Shell Oil Company | Process for the preparation of secondary alcohol sulfate-containing surfactant compositions |
US5349101A (en) * | 1992-05-28 | 1994-09-20 | Shell Oil Company | Process for the preparation of secondary alkyl sulfate-containing surfactant compositions |
-
1965
- 1965-07-07 GB GB2879265A patent/GB1049828A/en not_active Expired
- 1965-07-28 DE DE19651468825 patent/DE1468825A1/en active Pending
- 1965-08-05 CH CH1103765A patent/CH463484A/en unknown
- 1965-08-11 NL NL6510444A patent/NL6510444A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
NL6510444A (en) | 1967-02-13 |
DE1468825A1 (en) | 1969-01-02 |
CH463484A (en) | 1968-10-15 |
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