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Zinc sulfide

Chemical resistance not resistant to strong acids and alkalis [Pg.176]

Sachtolith L (standard paints), HD (high quality paints), HD-S (plastics) [Pg.176]

MAJOR PRODUCT APPLICATIONS paints, coatings, inks, UV-curable systems, powder coatings, adhesives, insulating and sealing compounds, fibers, paper, sealants, mastics, lubricants [Pg.176]

MAJOR POLYMER APPLICATIONS alkyd, epoxy, acrylics, PVC, PE, PP, PS, PET, PA [Pg.176]

Zinc sulfide has the next highest refractive index to titanium dioxide and zirconium oxide making it a very efficient pigment. The spectrum of absorption of zinc sulfide resembles more closely anatase than rutile. Because it does not absorb certain UV wavelength, zinc sulfide is useful as a pigment for UV curable materials. [Pg.176]


Zinc is also used extensively to galvanize other metals such as iron to prevent corrosion. Zinc oxide is a unique and very useful material for modern civilization. It is widely used in the manufacture of paints, rubber products, cosmetics, pharmaceuticals, floor coverings, plastics, printing inks, soap, storage batteries, textiles, electrical equipment, and other products. Lithopone, a mixture of zinc sulfide and barium sulfate, is an important pigment. [Pg.54]

Zinc sulfide is used in making luminous dials. X-ray and TV screens, and fluorescent lights. [Pg.54]

Zinc sulfide as pigment [PIGMENTS - INORGANIC] poll9)... [Pg.400]

Depressants are reagents that selectively prevent the reaction between a coUector and a mineral, thus preventing its flotation. For example, sodium cyanide [143-33-9] depresses sphalerite [12169-28-7] (zinc sulfide) and pyrite [1309-36-0] (iron sulfide) but not galena. It thus enhances selective flotation of the galena. [Pg.34]

Zinc Sulfide. Whereas 2inc sulfide is mainly important as a component of the composite white pigment Hthopone, it also has a limited use as a single pigment. Under the commercial name SachtoHth, pure ZnS is produced by Sachtieben Chemie in Germany. [Pg.10]

Production. Zinc sulfide production started in the United States and in Europe in the 1920s. Starting in the early 1950s, 2inc sulfide, like most white pigments, was slowly replaced by the more superior titanium white. Zinc sulfide can be prepared by a process similar to the one used to manufacture Hthopone. In the first step, barium sulfide reacts with sodium sulfate to produce sodium sulfide solution ... [Pg.10]

Zinc sulfide can also be prepared by the direct reaction of barium sulfide and 2inc chloride solution ... [Pg.10]

Phosphorescent pigments are used in military appHcations, plastics, and paints. Zinc sulfide doped with Ag" (blue) cations, or with Cu" (green) cations are important pigments for the production of color television screens. Phosphorescent sulfide pigments are produced in the United States by Radium Corp. and by Conrad Precision Ind., Inc. [Pg.16]

Manufacture. Small cylinders of hydrogen sulfide are readily available for laboratory purposes, but the gas can also be easily synthesized by action of dilute sulfuric or hydrochloric acid on iron sulfide, calcium sulfide [20548-54-3], zinc sulfide [1314-98-3], or sodium hydrosulfide [16721 -80-5]. The reaction usually is mn in a Kipp generator, which regulates the addition of the acid to maintain a steady hydrogen sulfide pressure. Small laboratory quantities of hydrogen sulfide can be easily formed by heating at 280—320°C a mixture of sulfur and a hydrogen-rich, nonvolatile aUphatic substance, eg, paraffin. Gas evolution proceeds more smoothly if asbestos or diatomaceous earth is also present. [Pg.135]

The zinc oxide [1314-13-2] process is similar to the iron oxide process. There is, however, one key distinction. The zinc sulfide [1314-98-3] ZnS,... [Pg.209]

Zinc does not react with nitrogen, even at elevated temperatures but zinc nitride, Zn N2, forms with ammonia at red heat. Zinc sulfide, the most common form of zinc in nature, is not reduced direcdy in commercial practice because of reactions of the zinc vapor during condensation. Rather, the sulfide is burned (roasted) to the oxide plus sulfur dioxide before reduction. However, zinc can be reduced to the metal at ca 1300°C with carbon or iron. [Pg.399]

Zinc ores are generally floated at the mine (18). In the case of simple zinc sulfide ores, flotation is carried out by treatment with copper sulfate to activate the sphalerite causing it to be wet by the organic collector (eg, xanthate). The now-hydrophobic zinc ore particles attach themselves to the rising bubbles. Oxidized ore particles present must be sulftdized with sodium sulfide to be floated (19). Flotation produces concentrates which are ca 50—60% zinc. In mixed ore, the lead and copper are usually floated after depressing the sphalerite with cyanide or zinc sulfate. The sphalerite is then activated and floated. [Pg.399]

Roasting. Copper and lead sulfides are direcdy smelted but not zinc sulfide. However, theoretical calculations are encouraging (20) and, if an efficient means of condensing zinc rapidly from 1600 K in the presence of carbon dioxide, sulfur dioxide, and steam can be devised, the process may be feasible. The reaction of zinc vapor to yield zinc oxide or zinc sulfide presents the main difficulty. [Pg.399]

The zinc sulfide in the concentrate is always converted to oxide by roasting. An exception is the direct leach process described below. The principal overall roasting reaction is strongly exothermic and provides excess heat which is recovered. [Pg.399]

For environmental and economic reasons, the eady practice of roasting zinc sulfide and discharging the sulfur dioxide to the atmosphere gave way to plants where the sulfur dioxide is converted to sulfuric acid. Desulfurization takes place while the ore particles are suspended in hot gases. Called flash-and fluid-bed roasters, these processes are described below. Some plants use combinations of roasters and sintering for desulfurization. [Pg.399]

Direct l eaching of Concentrates. Sherri tt Gordon Mines, Ltd., has adapted the process first used on nickel sulfide ores to zinc sulfide oxidation with air in aqueous slurry under pressure (42,43). The concentrates are leached direcdy with return acid from the cells and the sulfide is converted to free sulfur ... [Pg.402]

SoHd lubricants ate added to help control high friction characteristics in high speed or heavy-duty appHcations where high temperatures are generated. Molybdenum disulfide [1317-33-5] M0S2, may be used alone or in a complex compound formed by grinding with fine natural graphite, and zinc sulfide [1314-98-3] ZnS. Other compounds include calcium fluoride, cryoHte [15096-52-3] Na AlF, rare-earth oxides, and metal sulfides, eg, iron, antimony, or zinc (see LUBRICATION AND LUBRICANTS). [Pg.274]

Donor and acceptor levels are the active centers in most phosphors, as in zinc sulfide [1314-98-3] ZnS, containing an activator such as Cu and various co-activators. Phosphors are coated onto the inside of fluorescent lamps to convert the intense ultraviolet and blue from the mercury emissions into lower energy light to provide a color balance closer to daylight as in Figure 11. Phosphors can also be stimulated directly by electricity as in the Destriau effect in electroluminescent panels and by an electron beam as in the cathodoluminescence used in television and cathode ray display tubes and in (usually blue) vacuum-fluorescence alphanumeric displays. [Pg.421]

Finally, selective separation and dewatering of one suspended substance in a slurry containing different minerals or precipitates is possible by selectively adsorbing a magnetic material (usually hydrophobic) onto a soHd that is also naturally or chemically conditioned to a hydrophobic state. This process (Murex) was used on both sulfide ores and some oxides (145). More recently, hydrocarbon-based ferrofluids were tested and shown to selectively adsorb on coal from slurries of coal and mineral matter, allowing magnetic recovery (147). Copper and zinc sulfides were similarly recoverable as a dewatered product from waste-rock slurries (148). [Pg.27]

Ethers, esters, amides and imidazolidines containing an epithio group are said to be effective in enhancing the antiwear and extreme pressure peiformance of lubricants. Other uses of thiiranes are as follows fuel gas odorant (2-methylthiirane), improvement of antistatic and wetting properties of fibers and films [poly(ethyleneglycol) ethers of 2-hydroxymethyl thiirane], inhibition of alkene metathesis (2-methylthiirane), stabilizers for poly(thiirane) (halogen adducts of thiiranes), enhancement of respiration of tobacco leaves (thiirane), tobacco additives to reduce nicotine and to reduce phenol levels in smoke [2-(methoxymethyl)thiirane], stabilizers for trichloroethylene and 1,1,1-trichloroethane (2-methylthiirane, 2-hydroxymethylthiirane) and stabilizers for organic compounds (0,0-dialkyldithiophosphate esters of 2-mercaptomethylthiirane). The product of the reaction of aniline with thiirane is reported to be useful in the flotation of zinc sulfide. [Pg.184]

Chemsweet from C. E. Natco is another, H7S-only process. It uses a water dispersion of zinc oxide and zinc acetate to oxidize H7S and form zinc sulfide. The process... [Pg.192]

However, when the vulcanization temperature was increased to 190°C, it was observed that the peaks in the copper and sulfur profiles no longer coincided. Instead, the peak in the sulfur profile coincided with the peaks in the zinc and oxygen profiles. These results indicated that at higher vulcanizing temperatures, zinc sulfide formed in abundance while formation of copper sulfide decreased. [Pg.295]

Geon and Seo [47] also determined the effect of vulcanization time on the adhesion of natural rubber to brass-plated steel. For relatively short times, there was a peak at the end of the copper profile that corresponded well with a peak in the sulfur profile. Similarly, peaks in the zinc and oxygen profiles corresponded well. These results showed that copper sulfide and zinc oxide mostly formed at short times but some evidence for formation of zinc sulfide was also obtained. For long times, the peak in the sulfur profile no longer corresponded with that in the copper profile. Instead, the peak in the sulfur profile corresponded to the peak in the zinc profile. It was concluded that the formation of zinc sulfide increased substantially at long times. An increase in vulcanization time correlated well with a decrease in the force required to pull brass-plated steel wires out of rubber blocks. [Pg.295]

Use suspension or fluidized bed roasters, where appropriate, to achieve high SO2 concentrations when roasting zinc sulfides. [Pg.133]

The zinc oxide process is similar to the iron sponge process. It uses a solid bed of granular zinc oxide to react with the H2S to form water and zinc sulfide ... [Pg.160]


See other pages where Zinc sulfide is mentioned: [Pg.126]    [Pg.756]    [Pg.90]    [Pg.454]    [Pg.579]    [Pg.770]    [Pg.874]    [Pg.1088]    [Pg.1088]    [Pg.1088]    [Pg.68]    [Pg.70]    [Pg.174]    [Pg.4]    [Pg.10]    [Pg.10]    [Pg.337]    [Pg.396]    [Pg.400]    [Pg.402]    [Pg.457]    [Pg.458]    [Pg.1573]    [Pg.293]    [Pg.283]    [Pg.284]   
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A-Zinc sulfide ZnS

Aluminum zinc sulfide

Cadmium zinc sulfide

Colorants zinc sulfide

Hydrochloric acid reaction with zinc sulfide

Lithopone and Zinc Sulfide Pigments

Mineral zinc sulfide

Oxidation of zinc sulfide

Oxygen reaction with zinc sulfide

Polymorphism zinc sulfide

Production of Zinc From Sulfide Ore

Semiconductor photocatalysis zinc sulfide

Solubility zinc sulfide

Structure of cubic zinc sulfide

Structure of hexagonal zinc sulfide

Zinc Sulfide (Cubic)

Zinc hydride sulfide

Zinc sulfide blende

Zinc sulfide coordination number

Zinc sulfide films

Zinc sulfide films precursors

Zinc sulfide particles

Zinc sulfide photocorrosion

Zinc sulfide pigments

Zinc sulfide precipitation

Zinc sulfide properties

Zinc sulfide thermal properties

Zinc sulfide window

Zinc sulfide, crystal

Zinc sulfide, crystal structure

Zinc sulfide, hexagonal form, wurtzite

Zinc-cadmium sulfide, atmospheric

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