Zinc Oxide Systems

Hotchandani S, Kamat P (1992) Charge-transfer processes in coupled semiconductor systems. Photochemistry and photoelectrochemistry of the colloidal cadmium sulfide-zinc oxide system. J Phys Chem 96 6834—6839... 

The reaction is of the acceptor type (28). Consistent with this and the views presented above, the data of Table VI suggest that contact with silver has bent the bands in zinc oxide and thus lowered the activation energy and the start temperature. However, a bifunctional catalytic action of the silver-zinc oxide system canot be excluded with certainty. 

Methanol is synthesized from H2/(C0-1-C02) mixtures over copper-zinc oxide systems appropriately modified with stmctural promoters (AI2O3, Cr203). Working with these catalysts, KUer [21] has proposed that methanol would be produced from the CO component of the reactant mixture, carbon dioxide being present to maintain the catalyst surface partially oxidized. The site responsible for the reaction was suggested to be a Cu+ion, located in substitution positions in the ZnO lattice. 

The concept of acceleration was discovered in 1906 when it was found that addition of aniline to a suUur/zinc oxide system significantly decreased vulcanization times. Dialkyl amines were also found to provide acceleration, and so aniline and the dialkyl amines were derivatized to the range of... 

Natural gas contains both organic and inorganic sulfur compounds that must be removed to protect both the reforming and downstream methanol synthesis catalysts. Hydrodesulfurization across a cobalt or nickel molybdenum—zinc oxide fixed-bed sequence is the basis for an effective purification system. For high levels of sulfur, bulk removal in a Hquid absorption—stripping system followed by fixed-bed residual clean-up is more practical (see Sulfur REMOVAL AND RECOVERY). Chlorides and mercury may also be found in natural gas, particularly from offshore reservoirs. These poisons can be removed by activated alumina or carbon beds. 

Smoke-Generating Devices. Smoke generators are used by the military for daytime obscuration and signaling. For field use where portable stable systems ate requited, pyrotechnic devices are often employed. The primary composition since the 1940s has been HC smoke, which generates a cloud of zinc chloride, ZnCl, smoke by a series of reactions between hexachloroethane, C2Clg(HC), zinc oxide, and aluminum (3) (eq. 4—6). The zinc regenerated in... 

Zinc oxide and stearic acid are used to activate the curing system as well as to preserve cured properties when overcuring, which is curing beyond the point of time and temperature at which maximum properties are obtained. 

Nickel—2iiic batteries containing a vibrating zinc anode lias been reported (83). In this system zinc oxide active material is added to the electrol 1 e as a slurry. During charge the anode substrates are vibrated and the zinc is electroplated onto the surface in a unifomi mamier. Tlie stationary positive electrodes (nickel) are encased in a thin, open plastic netting which constitutes the entire separator system. 

The compositions of zinc oxide—eugenol impression pastes are similar to those of the zinc oxide—eugenol cements (86). Variations in specific characteristics are achieved by the proportions of the ingredients (87). Properties vary in commercial products (88). The modifications of the zinc oxide—eugenol system intended for bite-registration pastes may include agents to increase the body or thixotropic character of the unset mix to improve... 

Calcium Chelates (Salicylates). Several successhil dental cements which use the formation of a calcium chelate system (96) were developed based on the reaction of calcium hydroxide [1305-62-0] and various phenohc esters of sahcyhc acid [69-72-7]. The calcium sahcylate [824-35-1] system offers certain advantages over the more widely used zinc oxide—eugenol system. These products are completely bland, antibacterial (97), facihtate the formation of reparative dentin, and do not retard the free-radical polymerization reaction of acryhc monomer systems. The principal deficiencies of this type of cement are its relatively high solubihty, relatively low strength, and low modulus. Less soluble and higher strength calcium-based cements based on dimer and trimer acid have been reported (82). 

A useful classification of sensitizing dyes is the one adopted to describe patents in image technology. In Table 1, the Image Technology Patent Information System (ITPAIS), dye classes and representative patent citations from the ITPAIS file are Hsted as a function of significant dye class. From these citations it is clear that preferred sensitizers for silver haUdes are polymethine dyes (cyanine, merocyanine, etc), whereas other semiconductors have more evenly distributed citations. Zinc oxide, for example, is frequendy sensitized by xanthene dyes (qv) or triarylmethane dyes (see Triphenylmethane and related dyes) as well as cyanines and merocyanines (see Cyanine dyes). 

Halobutyl Cures. Halogenated butyls cure faster in sulfur-accelerator systems than butyl bromobutyl is generally faster than chlorobutyl. Zinc oxide-based cure systems result in C—C bonds formed by alkylation through dehydrohalogenation of the halobutyl to form a zinc chloride catalyst (94,95). Cure rate is increased by stearic acid, but there is a competitive reaction of substitution at the halogen site. Because of this, stearic acid can reduce the overall state of cure (number of cross-links). Water is a strong retarder because it forms complexes with the reactive intermediates. Amine cure may be represented as follows ... 

Compounding is quite different for the two systems. The solvent base system is dependent on magnesium oxide and a /-butylphenoHc resin in the formulation to provide specific adhesion, tack, and added strength. Neither of these materials have proven useful in latex adhesive formulations due to colloidal incompatibihty. In addition, 2inc oxide slowly reacts with carboxylated latexes and reduces their tack. Zinc oxide is an acceptable additive to anionic latex, however. Other tackifying resins, such as rosin acids and esters, must be used with anionic latexes to provide sufficient tack and open time. 

AH latex compounds should contain at least 5 phr of zinc oxide. This is needed to absorb evolved hydrochloric acid either in the compound or finished part. A larger amount should be considered if the part contains or is in contact with acid-sensitive materials such as cotton cloth. Magnesium oxide may destabilize anionic soap systems, and is avoided for that reason. The compound should also contain two parts of an antioxidant, and consideration should be given to the need for a uv screen in light-colored products. 

Although these curative systems may also be used with the polyepichlorohydrin elastomers containing AGE, the polymers were developed to be cured with conventional mbber curatives, sulfur, and peroxides. These polymers containing the pendent aHyl group are readily cured with a typical sulfur cure system such as zinc oxide, and sulfur along with the activators, tetramethylthiuram mono sulfide [97-74-5] (TMTM) and... 

There are no known practical peroxide cure systems for the PO—AGE polymers. Apparentiy the peroxide attacks the polymer backbone at a rate that is unfavorably competitive with the cross-linking rate. A typical sulfur cure system consists of zinc oxide [1314-13-2] tetramethylthiuram mono sulfide (TMTM), 2-2-mercaptobenzothiazole [149-30-4] (MBT), and sulfur. A sulfur donor cure system is zinc oxide, di-o-tolylguanidine [97-39-2] (DOTG) and tetramethylthiuram hexasulftde. 

Pouring Zinc oxide fume, lead oxide fume cover high-zinc-content brass use of good combustion controls, local exhaust system, and baghouse or... 

Zinc Roasting Sintering Calcining Retorts electric arc Particulates (dust) and SO2 Particulates (dust) and SO2 Zinc oxide fume, particulates, SO2, CO Exhaust system, humidifier, cyclone, scrubber, electrostatic precipitator, and acid plant Exhaust system, humidifier, electrostatic precipitator, and acid plant Exhaust system, baghouse, scrubber or acid plant... 

This continuous process is to be compared with a batch process, such as the Belgian retort process. In this, zinc oxide, free of lead or iron is reduced with carbon to produce zinc vapour, which is condensed in the cold section of the retort. The oxygen potential in this system is very much lower dran in the blast furnace, approximately at the C/CO equilibrium value. A vacuum-operated variant of dris level of reduction is caiTied out to produce zinc vapour which is subsequently converted to zinc oxide before condensation of the metal could take place. 

Accelerated sulphur systems also require the use of an activator comprising a metal oxide, usually zinc oxide, and a fatty acid, commonly stearic acid. For some purposes, for example where a high degree of transparency is required, the activator may be a fatty acid salt such as zinc stearate. Thus a basic curing system has four components sulphur vulcanising agent, accelerator (sometimes combinations of accelerators), metal oxide and fatty acid. In addition, in order to improve the resistance to scorching, a prevulcanisation inhibitor such as A -cyclohexylthiophthalimide may be incorporated without adverse effects on either cure rate or physical properties. 

Other flame retardants and/or smoke suppressants can also be used such as magnesium hydroxide, magnesium carbonate, magnesium-zinc complexes and some tin-zinc compositions. Zinc oxide is a common ingredient in many rubber base formulations used as part of the curing system. At the same time, the action of zinc oxide is similar to that of antimony trioxide, but less effective. 

The Goodyear vulcanization process takes hours or even days to be produced. Accelerators can be added to reduce the vulcanization time. Accelerators are derived from aniline and other amines, and the most efficient are the mercaptoben-zothiazoles, guanidines, dithiocarbamates, and thiurams (Fig. 32). Sulphenamides can also be used as accelerators for rubber vulcanization. A major change in the sulphur vulcanization was the substitution of lead oxide by zinc oxide. Zinc oxide is an activator of the accelerator system, and the amount generally added in rubber formulations is 3 to 5 phr. Fatty acids (mainly stearic acid) are also added to avoid low curing rates. Today, the cross-linking of any unsaturated rubber can be accomplished in minutes by heating rubber with sulphur, zinc oxide, a fatty acid and the appropriate accelerator. 

Curing system. The most common room curing agent is zinc oxide. Isocyanates are also very common. 

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