GB849951A - Improved process for the oxidation of slack waxes - Google Patents

Improved process for the oxidation of slack waxes

Info

Publication number
GB849951A
GB849951A GB1274058A GB1274058A GB849951A GB 849951 A GB849951 A GB 849951A GB 1274058 A GB1274058 A GB 1274058A GB 1274058 A GB1274058 A GB 1274058A GB 849951 A GB849951 A GB 849951A
Authority
GB
United Kingdom
Prior art keywords
acids
wax
parts
slack wax
slack
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
Application number
GB1274058A
Inventor
Rodney Thomas William Hall
Eric Newman White
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Esso Research and Engineering Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Exxon Research and Engineering Co, Esso Research and Engineering Co filed Critical Exxon Research and Engineering Co
Priority to GB1274058A priority Critical patent/GB849951A/en
Publication of GB849951A publication Critical patent/GB849951A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/22Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
    • C07C69/24Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with monohydroxylic compounds
    • C07C69/26Synthetic waxes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Slack waxes are oxidised to slack wax acids by passing a stream of air under a pressure of 25-205 p.s.i.g. through the molten wax in the presence of a minor proportion of carboxylic acids and 0,5-4,4% wt. of a water-soluble permanganate salt at below 150 DEG C. until the product has an acid number of 40-100. A slack wax is defined as the wax containing more than 0,3% wt. of sulphur and more than 3% wt. of lubricating oil obtained from a deasphalted broad or narrow lubricating oil cut. The carboxylic acids may be C12-42 saturated aliphatic acids or mixtures thereof, such as are obtained in the process of the present Specification or of Specification 816,670.ALSO:Aqueous alkaline bitumen emulsion compositions contain slack wax acids obtained by oxidising slack wax by passing a stream of air under a pressure of 25-205 p.s.i.g. through the molten wax in the presence of a minor proportion of carboxylic acids and 0.5-4.4% wt. of a water-soluble permanganate salt at below 150 DEG C. until the product has an acid number of 40-100. The carboxylic acids may be C12-C42 saturated aliphatic acids or mixtures thereof such as are obtained by the above oxidation process or by the process of Specification 816,672 [Group IV(b)]. A specified composition contains bitumen 15-65 parts by weight, slack wax acids 2-6 parts, and water 35-85 parts, NaOH 0.03-0.15 parts. The emulsion may also contain 0.01-1 parts of a bitumen emulsion stabilizer, such as a Tall oil or neutralised Swedish liquid rosin. Preferred emulsions have a particle size range of 1-6 m and a viscosity of 5-7 Engler at 20 DEG C. The emulsions may be made by passing the bitumen and slack wax acid (at 230-270 DEG F.), aqueous NaOH, and stabilizer (at 160-190 DEG F.) through a colloid or Hurrel mill.
GB1274058A 1958-04-22 1958-04-22 Improved process for the oxidation of slack waxes Expired GB849951A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1274058A GB849951A (en) 1958-04-22 1958-04-22 Improved process for the oxidation of slack waxes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1274058A GB849951A (en) 1958-04-22 1958-04-22 Improved process for the oxidation of slack waxes

Publications (1)

Publication Number Publication Date
GB849951A true GB849951A (en) 1960-09-28

Family

ID=10010236

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1274058A Expired GB849951A (en) 1958-04-22 1958-04-22 Improved process for the oxidation of slack waxes

Country Status (1)

Country Link
GB (1) GB849951A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0065704A1 (en) * 1981-05-12 1982-12-01 Ashland Oil, Inc. Redox catalyst plus promoter for oxidation of hydrocarbons
WO2016100180A1 (en) * 2014-12-15 2016-06-23 The Lubrizol Corporation Catalytic oxidation of hydrocarbons

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0065704A1 (en) * 1981-05-12 1982-12-01 Ashland Oil, Inc. Redox catalyst plus promoter for oxidation of hydrocarbons
WO2016100180A1 (en) * 2014-12-15 2016-06-23 The Lubrizol Corporation Catalytic oxidation of hydrocarbons
CN107207977A (en) * 2014-12-15 2017-09-26 路博润公司 The catalysis oxidation of hydrocarbon

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