GB122170A - Improvements in or relating to Preparing Pigment Zinc-oxide. - Google Patents

Improvements in or relating to Preparing Pigment Zinc-oxide.

Info

Publication number
GB122170A
GB122170A GB20208/18A GB2020818A GB122170A GB 122170 A GB122170 A GB 122170A GB 20208/18 A GB20208/18 A GB 20208/18A GB 2020818 A GB2020818 A GB 2020818A GB 122170 A GB122170 A GB 122170A
Authority
GB
United Kingdom
Prior art keywords
zinc
lead
sulphur
oxide
crude
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
GB20208/18A
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.)
American Zinc Lead and Smelting Co
Original Assignee
American Zinc Lead and Smelting 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 American Zinc Lead and Smelting Co filed Critical American Zinc Lead and Smelting Co
Publication of GB122170A publication Critical patent/GB122170A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G9/00Compounds of zinc
    • C01G9/02Oxides; Hydroxides

Abstract

122,170. American Zinc, Lead, & Smelting Co., (Assignees of Wemple, L. E.). Jan. 9, 1918, [Convention date]. Pigments.-A process for preparing pigment zinc oxide, free from coloured oxides of lead and cadmium and from soluble zinc salts such as zinc sulphate, consists in first producing: by oxidizing in the presence of sulphur a crude zinc oxide containing a small proportion of zinc sulphate and having any lead and cadmium present as sulphates also, and then treating this crude product with a reducing agent such as carbon under such temperature conditions that the zinc sulphate is eliminated or decomposed whilst the lead and cadmium sulphates remain unchanged. The sulphated crude zinc oxide may be obtained as the immediate product of the usual volatilization process if the raw material contains sufficient sulphur; otherwise, sulphur may be added to the raw material, or the volatilized product may be treated with sulphur. A convenient reducing agent is lampblack, mixed with the crude oxide in the proportion of one to two per cent., the mixture being heated for about half an hour at a temperature between 900 and 1200‹ F., preferably in a muffle to prevent contamination with fuel ash. The material is then stirred with free access to air to burn off any remaining excess of carbon and to facilitate the escape of sulphur dioxide and other excluded gases. The stirring and consequent rapid cooling prevent agglomeration of particles and the formation of crystalline compounds. Some grades of crude oxide produced by volatilization furnaces contain appreciable amounts of carbon or other reducing agents, and the necessity for adding a reducing agent for eliminating the zinc sulphate may be avoided by regulating the volatilization process so that the crude oxide contains either sufficient carbon to permit direct heating, or excess carbon adapted for admixture with other grades deficient in carbon. It is possible to use as the reducing- agent oxide of lead or cadmium or other metal having a white sulphate, but such oxides must be used in carefully regulated quantities as a slight excess would discolour the final product. The pigment zinc oxide prepared by this process contains lead solely as insoluble white sulphur compounds, and sulphur in insoluble form in excess of that required to sulphatize the lead present, probably as zinc sulphide or basic zinc sulphate. Methods of testing the colour, fineness, covering power, and oil-absorbing capacity of the pigment are described.
GB20208/18A 1918-01-09 1918-12-05 Improvements in or relating to Preparing Pigment Zinc-oxide. Expired GB122170A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US122170XA 1918-01-09 1918-01-09

Publications (1)

Publication Number Publication Date
GB122170A true GB122170A (en) 1919-12-05

Family

ID=32391590

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20208/18A Expired GB122170A (en) 1918-01-09 1918-12-05 Improvements in or relating to Preparing Pigment Zinc-oxide.

Country Status (1)

Country Link
GB (1) GB122170A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018026829A1 (en) * 2016-08-01 2018-02-08 Cornell University Polymer compositions for 3-d printing and 3-d printers

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018026829A1 (en) * 2016-08-01 2018-02-08 Cornell University Polymer compositions for 3-d printing and 3-d printers

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