GB452661A - Improvements in or relating to the manufacture of products from paraffin wax - Google Patents
Improvements in or relating to the manufacture of products from paraffin waxInfo
- Publication number
- GB452661A GB452661A GB616835A GB616835A GB452661A GB 452661 A GB452661 A GB 452661A GB 616835 A GB616835 A GB 616835A GB 616835 A GB616835 A GB 616835A GB 452661 A GB452661 A GB 452661A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- cent chlorine
- molecular weight
- paraffin wax
- chlorinated
- 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
- 239000012188 paraffin wax Substances 0.000 title abstract 9
- 238000004519 manufacturing process Methods 0.000 title 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical class [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 18
- 229910052801 chlorine Inorganic materials 0.000 abstract 16
- 239000000460 chlorine Substances 0.000 abstract 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 6
- 230000001476 alcoholic effect Effects 0.000 abstract 6
- 239000003513 alkali Substances 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 4
- 238000004821 distillation Methods 0.000 abstract 4
- 238000001035 drying Methods 0.000 abstract 4
- 239000007788 liquid Substances 0.000 abstract 4
- 238000005406 washing Methods 0.000 abstract 4
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical class C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 238000007664 blowing Methods 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000012185 ceresin wax Substances 0.000 abstract 2
- 230000007812 deficiency Effects 0.000 abstract 2
- 238000001704 evaporation Methods 0.000 abstract 2
- 239000010687 lubricating oil Substances 0.000 abstract 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 abstract 2
- 229910052753 mercury Inorganic materials 0.000 abstract 2
- 239000003921 oil Substances 0.000 abstract 2
- 238000000526 short-path distillation Methods 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 abstract 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G73/00—Recovery or refining of mineral waxes, e.g. montan wax
- C10G73/38—Chemical modification of petroleum
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Lubricants (AREA)
Abstract
Unsaturated compounds obtained by the action of alcoholic alkalies on chlorinated paraffin wax are separated by subjecting them to distillation in very high vacuum, for example, 10<-2> p to 10<-4> mm. of mercury, in apparatus having condensing and evaporating surfaces which are substantially co-extensive and separated by a distance of not more than a few inches. The reaction with alkali, which is usually in excess, is effected at elevated temperature and pressure. After washing and drying, the product is subjected to the distillation, essentially unsaturated hydrocarbons being obtained. Unsaturated chlor derivatives are obtained if a deficiency of alkali is used. The paraffin wax used may be crude or partially or completely refined and is chlorinated in any known manner. The unsaturated compounds may be used as components of lubricating oils, or oxidized to alcohols, suitable for making polishes and the like, for example, by blowing air through them at 150--200 DEG C. for 30 hours. According to examples: (1) chlorinated paraffin wax containing 41,2 per cent chlorine is heated under pressure at 140 DEG C. for 18 hours with methyl alcohol and KOH. After washing and drying, the product is subjected to short path distillation at 10<-4> mm. Two fractions are collected at 100--120 DEG and 120--160 DEG C. These are pale yellow oils containing 2,7 and 3,6 per cent chlorine, the molecular weight and number of carbon atoms being 345 and 26, and 385 and 29 respectively; (2) a chlorinated paraffin wax of 20 per cent chlorine content is autoclaved at 180 DEG C. with alcoholic KOH and treated as in (1). At 120--130 DEG C. a pale yellow liquid containing 2,8 per cent chlorine, molecular weight 330, with two double bonds per molecule, distils. The viscous residue contains 5,7 per cent chlorine and has a molecular weight of 510; (3) the product from the reaction of chlorinated ceresin wax (27 per cent chlorine) and alcoholic KOH gives at 10<-4> mm. and 120--140 DEG C. a liquid containing 8 per cent chlorine, molecular weight 352, and a black nearly solid residue, 7,7 per cent chlorine, molecular weight 2000. Specifications 303,078, [Class 32], and 452,662 are referred to.ALSO:Unsaturated compounds obtained by the action of alcoholic alkalies on chlorinated paraffin wax are separated by subjecting them to distillation in very high vacuum, for example 10<-2> to 10<-4> mm. of mercury, in apparatus having condensing and evaporating surfaces which are substantially co-extensive and separated by a distance of not more than a few inches. The reaction with alkali, which is usually in excess, is effected at elevated temperature and pressure. After washing and drying, the product is subjected to the distillation, essentially unsaturated hydrocarbons being obtained. Unsaturated chlor derivatives are obtained if a deficiency of alkali is used. The paraffin wax used may be crude or partially or completely refined and is chlorinated in any known manner. The unsaturated compounds may be used as components of lubricating oils, or oxidized to alcohols, suitable for making polishes and the like, for example by blowing air through them at 150--200 DEG C. for 30 hours. According to examples: (1) chlorinated paraffin wax containing 41,2 per cent chlorine is heated under pressure at 140 DEG C. for 18 hours with methyl alcohol and KOH. After washing and drying, the product is subjected to short path distillation at 10<-4> mm. Two fractions are collected at 100--120 DEG and 120--160 DEG C. These are pale yellow oils containing 2,7 and 3,6 per cent chlorine, the molecular weight and number of carbon atoms being 345 and 26, and 385 and 29 respectively; (2) a chlorinated paraffin wax of 20 per cent chlorine content is autoclaved at 180 DEG C. with alcoholic KOH and treated as in (1). At 120--130 DEG C. a pale yellow liquid containing 2,8 per cent chlorine, molecular weight 330, with two double bonds per molecule, distils. The viscous residue contains 5,7 per cent chlorine and has a molecular weight of 510; (3) the product from the reaction of chlorinated ceresin wax (27 per cent chlorine) and alcoholic KOH gives at 10<-4> mm. and 120--140 DEG C. a liquid containing 8 per cent chlorine, molecular weight 352, and a black nearly solid residue, 7,7 per cent chlorine, molecular weight 2000. Specifications 303,078, [Class 32], and 452,662 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB616835A GB452661A (en) | 1935-02-26 | 1935-02-26 | Improvements in or relating to the manufacture of products from paraffin wax |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB616835A GB452661A (en) | 1935-02-26 | 1935-02-26 | Improvements in or relating to the manufacture of products from paraffin wax |
Publications (1)
Publication Number | Publication Date |
---|---|
GB452661A true GB452661A (en) | 1936-08-26 |
Family
ID=9809644
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB616835A Expired GB452661A (en) | 1935-02-26 | 1935-02-26 | Improvements in or relating to the manufacture of products from paraffin wax |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB452661A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103627437A (en) * | 2013-12-20 | 2014-03-12 | 哈尔滨理工大学 | Method for preparing chlorinated paraffin |
-
1935
- 1935-02-26 GB GB616835A patent/GB452661A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103627437A (en) * | 2013-12-20 | 2014-03-12 | 哈尔滨理工大学 | Method for preparing chlorinated paraffin |
CN103627437B (en) * | 2013-12-20 | 2015-04-15 | 哈尔滨理工大学 | Method for preparing chlorinated paraffin |
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