Chemical zinc oxide

Physico-chemical Zinc oxide Tyres, all rubber goods <—( 00... 

Gases which are high in FIjS are subject to a de-sulphurisation process in which H2S is converted into elemental sulphur or a metal sulphide. There are a number of processes based on absorption in contactors, adsorption (to a surface) in molecular sieves or chemical reaction (e.g. with zinc oxide). 

Henkel Rearrangement of Benzoic Acid and Phthalic Anhydride. Henkel technology is based on the conversion of benzenecarboxyhc acids to their potassium salts. The salts are rearranged in the presence of carbon dioxide and a catalyst such as cadmium or zinc oxide to form dipotassium terephthalate, which is converted to terephthahc acid (59—61). Henkel technology is obsolete and is no longer practiced, but it was once commercialized by Teijin Hercules Chemical Co. and Kawasaki Kasei Chemicals Ltd. Both processes foUowed a route starting with oxidation of napthalene to phthahc anhydride. In the Teijin process, the phthaHc anhydride was converted sequentially to monopotassium and then dipotassium o-phthalate by aqueous recycle of monopotassium and dipotassium terephthalate (62). The dipotassium o-phthalate was recovered and isomerized in carbon dioxide at a pressure of 1000—5000 kPa ( 10 50 atm) and at 350—450°C. The product dipotassium terephthalate was dissolved in water and recycled as noted above. Production of monopotassium o-phthalate released terephthahc acid, which was filtered, dried, and stored (63,64). 

Activators. Activators are chemicals that increase the rate of vulcanization by reacting first with the accelerators to form mbber soluble complexes. These complexes then react with the sulfur to achieve vulcanization. The most common activators are combinations of zinc oxide and stearic acid. Other metal oxides have been used for specific purposes, ie, lead, cadmium, etc, and other fatty acids used include lauric, oleic, and propionic acids. Soluble zinc salts of fatty acid such as zinc 2-ethyIhexanoate are also used, and these mbber-soluble activators are effective in natural mbber to produce low set, low creep compounds used in load-bearing appHcations. Weak amines and amino alcohols have also been used as activators in combination with the metal oxides. 

In order to obtain a homogenous and stable latex compound, it is necessary that insoluble additives be reduced in particle size to an optimum of ca 5 )Tm and dispersed or emulsified in water. Larger-size chemical particles form a nucleus for agglomeration of smaller particles and cause localized dispersion instabiHty particles <3 fim tend to cluster with similar effect, and over-milled zinc oxide dispersions are particularly prone to this. Water-soluble ingredients, including some accelerators, can be added directly to the latex but should be made at dilute strength and at similar pH value to that of the latex concentrate. 

Dry basis natural mbber compound recipe, in part by wt high ammonia natural latex mbber concentrate, 100.0 potassium hydroxide, 0.5 Nacconal 90F (alkylarenesulfonate (AHied Chemical Co.)), 1.0 zinc oxide, 3.0 sulfur, 1.0 ZMBT, 1.0 zinc diethyldithiocarbamate (ZEDC) (trade names Ethazate (Uniroyal, Inc.), Ethyl Zimate (R. T. Vanderbilt), 0.3 antioxidant, as indicated. Wet-basis natural mbber compound recipe, in parts by wt natural latex (NC 356), 167.9 potassium hydroxide, 2.5 Nacconal 90F, 5.0 zinc oxide, 5.45 sulfur, 1.65 ZMBT, 2.0 ZEDC, 2.0 antioxidant, as indicated. AH films poured from freshly mixed compounds, dried overnight in place, then lifted and dried 1 h in air at 50°C before curing. 

Hydrogenation. Gas-phase catalytic hydrogenation of succinic anhydride yields y-butyrolactone [96-48-0] (GBL), tetrahydrofiiran [109-99-9] (THF), 1,4-butanediol (BDO), or a mixture of these products, depending on the experimental conditions. Catalysts mentioned in the Hterature include copper chromites with various additives (72), copper—zinc oxides with promoters (73—75), and mthenium (76). The same products are obtained by hquid-phase hydrogenation catalysts used include Pd with various modifiers on various carriers (77—80), Ru on C (81) or Ru complexes (82,83), Rh on C (79), Cu—Co—Mn oxides (84), Co—Ni—Re oxides (85), Cu—Ti oxides (86), Ca—Mo—Ni on diatomaceous earth (87), and Mo—Ba—Re oxides (88). Chemical reduction of succinic anhydride to GBL or THF can be performed with 2-propanol in the presence of Zr02 catalyst (89,90). 

In paints, zinc oxide serves as a mildewstat and acid buffer as well as a pigment. The oxide also is a starting material for many zinc chemicals. The oxide supphes zinc in animal feeds and is a fertilizer supplement used in zinc-deficient soils. Its chemical action in cosmetics (qv) and dmgs is varied and complex but, based upon its fungicidal activity, it promotes wound healing. It is also essential in nutrition. Zinc oxide is used to prepare dental cements in combination with eugenol and phosphoric and poly(acrylic acid)s (48) (see Dental materials). 

For example, if a mixture contains a chemical (i.e., 12 percent zinc oxide) that is a member of a reportable chemical category (i.e., zinc compounds), the notification must include that the mixture contains a zinc compound at 12 percent by weight. Supplying only the weight percent of the parent metal (zinc) does not fulfill the requirement. The customer must be told the weight percent of the entire compound within a listed chemical category present in the mixture. 

The measures of solid state reactivity to be described include experiments on solid-gas, solid-liquid, and solid-solid chemical reaction, solid-solid structural transitions, and hot pressing-sintering in the solid state. These conditions are achieved in catalytic activity measurements of rutile and zinc oxide, in studies of the dissolution of silicon nitride and rutile, the reaction of lead oxide and zirconia to form lead zirconate, the monoclinic to tetragonal transformation in zirconia, the theta-to-alpha transformation in alumina, and the hot pressing of aluminum nitride and aluminum oxide. 

PRENTOX , pyrethrum pesticides, 111 PRESPERSION PAB , zinc oxide, 111 Pressure Chemical Company, 245 PREVAIL , cypemietlu-in, 111 Priborlabs, 197... 

The pneumatic tire has the geometry of a thin-wallcd toroidal shell. It consists of as many as fifty different materials, including natural rubber and a variety ot synthetic elastomers, plus carbon black of various types, tire cord, bead wire, and many chemical compounding ingredients, such as sulfur and zinc oxide. These constituent materials are combined in different proportions to form the key components of the composite tire structure. The compliant tread of a passenger car tire, for example, provides road grip the sidewall protects the internal cords from curb abrasion in turn, the cords, prestressed by inflation pressure, reinforce the rubber matrix and carry the majority of applied loads finally, the two circumferential bundles of bead wire anchor the pressnrized torus securely to the rim of the wheel. 

In dry air, a film of zinc oxide is initially formed by the influence of the atmospheric oxygen, but this is soon converted to zinc hydroxide, basic zinc carbonate and other basic salts by water, carbon dioxide and chemical impurities present in the atmosphere. 

Protection of niobium and its alloys from oxidation in air is accomplished by coating, e.g. with zinc deposited by holding in zinc vapour at 865°C or coating with a layer of chemically stable oxide, nitride or silicide. Silicide coatings applied by pack cementation, fused slurry or by electrolytic methods have been found to be one of the most effective means of preventing oxidation of the metal. 

There are two ways in which chemicals can protect the skin from ultraviolet light they can either absorb the light or reflect the light. Zinc oxide and titanium dioxide reflect or scatter light of many frequencies, from infrared through ultraviolet. That is why these chemicals appear opaque white. 

The precise structural role played by the water molecules in these cements is not clear. In the zinc oxychloride cement, water is known to be thermally labile. The 1 1 2 phase will lose half of its constituent water at about 230 °C, and the 4 1 5 phase will lose water at approximately 160 C to yield a mixture of zinc oxide and the 1 1 2 phase. Water clearly occurs in these cements as discrete molecules, which presumably coordinate to the metal ions in the cements in the way described previously. However, the possible complexities of structure for these systems, which may include chlorine atoms in bridging positions between pairs of metal atoms, make it impossible to suggest with any degree of confidence which chemical species or what structural units are likely to be present in such cements. One is left with the rather inadequate chemical descriptions of the phases used in even the relatively recent original literature on these materials, from which no clear information on the role of water can be deduced. 

In their original form these cements came as a zinc oxide powder and a concentrated solution of poly(acrylic acid) (Wilson, 1975b). Since then they have been subject to a number of chemical modifications. 

Zinc phosphate cement, as its name implies, is composed principally of zinc and phosphate. It is formed by mixing a powder, which is mainly zinc oxide, with a solution based on phosphoric acid. However, it is not as simple chemically as it appears because satisfactory cements caimot be formed by simply mixing zinc oxide with phosphoric acid solution. 

Crisp and coworkers found that the development of surface crystallinity was related to the speed of set. The faster the reaction, the shorter was the inhibition period before surface crystallization took place. When the setting time of a cement was between two and three minutes, surface crystallinity developed in a few minutes. When it was seven minutes, surface crystallinity was delayed by three hours. The reaction rate was affected by the chemical composition and physical state of the cement components. Well-ignited zinc oxide, the presence of magnesium in the... 

Salmon, J. E. Terrey, J. H. (1950). The system zinc oxide-phosphoric acid-water at temperatures between 25° and 100°. Journal of the Chemical Society, 2813-24. 

Holland, H. C. (1930). The ternary system zinc oxide-zinc chloride-water. Journal of the Chemical Society, 643-8. 

The physical and chemical characteristics of zinc oxide powders are known to affect cement formation (Smith, 1958 Norman et al., 1964 Crisp, Ambersley Wilson, 1980 Prosser Wilson, 1982). The rate of reaction depends on the source, preparation, particle size and surface moisture of the powder. Crystallinity and lattice strain have also been suggested as factors that may change the reactivity of zinc oxide powders towards eugenol (Smith, 1958). 

All cements that contain eugenol inhibit the polymerization of acrylates, and those of EBA-eugenol are no exception. In order to remedy this and other defects, Brauer and his coworkers examined alternatives to eugenol (Figure 9.7). These included the esters of vanillic acid (3-methoxy-4-hydroxybenzoic acid, HV) and syringic acid (3,5-dimethoxy-4-hydroxy-benzoic acid). Both are 3-methoxy-4-hydroxy compounds and are thus chemically related to eugenol and guaiacol. Both are solids and have to be dissolved in EBA where they form satisfactory cements with EBA zinc oxide powder. The vanillate (EBA-HV) cements are the more important. 

Wilson, A. D. Mesley, R. J. (1974). Chemical nature of cementing matrices of cements formed from zinc oxide and 2-ethoxybenzoic add-eugenol liquids. Journal of Dental Research, 53, 146. 

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