Zinc oxide water

Aluminium Al zinc hydroxide —> zinc oxide + water... 

Healy, T.W. and lellet. V.R., Adsorption-coagulation reactions of Znfll) hydrolyzed species at the zinc oxide-water interface, J. Colloid Interf. Sci., 24, 41,1967. 

Raymand, D., A.C.T. van Duin, W.A. Goddard, K. Hermansson, and D. Spangberg, Hydroxyla-tion structure and proton transfer reactivity at the zinc oxide-water interface. Journal of Physical Chemistry C, 2011. 115(17) p. 8573-8579. 

Figure 9.24(a) Apparent viscosity, zeta potential, amount of adsorption, and pH in zinc oxide-water (50/50) suspensions versus initial concentration, c, curves for Na salt of polyacrylic acid (PA) (O), Na salt of formalin condensate of -naphthalene sulphonate acid (NSF) (C), and sodium tripolyphosphate ( ). The initial concentrations of PA and NSF refer to the mole concentrations expressed/monomer unit of them. A dotted line refers to the apparent viscosity versus c curve for PA at a controlled pH of 10.1. C = initial mole concentration of surfactant and polyphosphate, (b) Apparent viscosity, zeta potential, amount of adsorption, and pH in zinc oxide-water (50/50) suspensions versus initial concentration, c, curves for Na salt of formalin condensate of alkyl (C4) naphthalene sulphonic acid (Al-NSF) (Ci), sodium alkyl (C4) naphthalene sulphonate ( >), and sodium dodecyl benzene sulphonate (O). The initial concentrations of Al-NSF refer to the mole concentrations expressed/monomer unit. C = initial mole concentration of surfactant. From [61] with permission. 

T. Morimoto, M. Nagao, Adsorption anomaly in the system zinc oxide-water, J. Phys. Chem. 78 (1974) 1116-1120. 

In a 2 litre bolt-head flask, equipped with an efficient mechanical stirrer, place 60-5 g. (50 ml.) of pure nitrobenzene and a solution of 30 g. of ammonium chloride in 1 litre of water. Stir vigorously and add 75 g. of a good quality zinc powder (about 90 per cent, purity) in small portions over a period of 5 minutes. The main reaction occurs about 5 minutes after the addition and the temperature rises. When the temperature reaches about 65°, add enough ice to the weU-stirred mixture to reduce the temperature to 50-55°. Filter the solution through a Buchner funnel twenty minutes after the first portion of zinc powder was introduced wash the zinc oxide residues with 600-700 ml. of boiling water. 

This reaction is first conducted on a chromium-promoted iron oxide catalyst in the high temperature shift (HTS) reactor at about 370°C at the inlet. This catalyst is usually in the form of 6 x 6-mm or 9.5 x 9.5-mm tablets, SV about 4000 h . Converted gases are cooled outside of the HTS by producing steam or heating boiler feed water and are sent to the low temperature shift (LTS) converter at about 200—215°C to complete the water gas shift reaction. The LTS catalyst is a copper—zinc oxide catalyst supported on alumina. CO content of the effluent gas is usually 0.1—0.25% on a dry gas basis and has a 14°C approach to equihbrium, ie, an equihbrium temperature 14°C higher than actual, and SV about 4000 h . Operating at as low a temperature as possible is advantageous because of the more favorable equihbrium constants. The product gas from this section contains about 77% H2, 18% CO2, 0.30% CO, and 4.7% CH. ... 

The dehydrogenation of 2-butanol is conducted in a multitube vapor-phase reactor over a zinc oxide (20—23), copper (24—27), or brass (28) catalyst, at temperatures of 250—400°C, and pressures slightly above atmospheric. The reaction is endothermic and heat is suppHed from a heat-transfer fluid on the shell side of the reactor. A typical process flow sheet is shown in Figure 1 (29). Catalyst life is three to five years operating in three to six month cycles between oxidative reactivations (30). Catalyst life is impaired by exposure to water, butene oligomers, and di-j -butyl ether (27). 

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). 

Zinc oxide is a common activator in mbber formulations. It reacts during vulcanization with most accelerators to form the highly active zinc salt. A preceding reaction with stearic acid forms the hydrocarbon-soluble zinc stearate and Hberates water before the onset of cross-linking (6). In cures at atmospheric pressure, such as continuous extmsions, the prereacted zinc stearate can be used to avoid the evolution of water that would otherwise lead to undesirable porosity. In these appHcations, calcium oxide is also added as a desiccant to remove water from all sources. 

Magnesium oxide is a typical acid scavenger for chlorinated mbbers. Compounds containing zinc oxide or magnesium oxide may tend to swell upon immersion in water. These inorganic salts have some water solubiHty and osmotic pressure causes the vulcanizates to imbibe water to equalize pressure (8,9). As such, vulcanizates tend to sweU more in fresh (distilled) water than in salt water. To minimize water sweU, insoluble salts such as lead oxides can be substituted. Because of the health concerns associated with lead, there is much mbber industry interest in other acid acceptors, such as synthetic... 

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. 

Economic Aspects. Table 3 shows that mbber production is the largest market for zinc oxide the downturn in 1980 resulted from a drop in tire production because of the production trend to smaller tires, more importation of tires, and a recession. The drop in paint usage reflects the trend to water-base paints, which originally contained no zinc oxide. However, its growing use in such paints is based upon improved formulations based on zinc oxide. The increased use in agriculture is a result of the realization of the importance of zinc as a trace element. The rise in use of zinc-oxide-coated paper for photocopying is followed by a slackening in use because of a shift to plain-paper copiers. 

Zinc oxide [1314-13-2] (mol wt 81.37 Cl Pigment White 4, Cl No. 77947) is a white or yellowish white amorphous, odorless powder with pH 6.95—7.37. It is practically iasoluble in water but soluble in dilute acetic acid, mineral acids, ammonia, ammonium carbonate, and alkaU hydroxides. 

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 ... 

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... 

Pigments or dyes may be added at this stage and where clear water-white sheet is required a small amount of a soluble violet dye is added to offset the faintly yellow colour of the natural mix. Stabilisers such as zinc oxide, zinc acetate or urea may be added to prevent the composition from developing acidity. 

Solvent-borne polychloroprene adhesives are unsuitable for bonding low-energy substrates, such as PVC. However, water-borne polychloroprene adhesives display good peel adhesion to vinyl substrates. Addition of an accelerator such as zinc oxide is essential for improved hot bond strength. 

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 ... 

Both zinc and zinc alloys have excellent resistance to corrosion in the atmosphere and in most natural waters. The property which gives zinc this valuable corrosion resistance is its ability to form a protective layer consisting of zinc oxide and hydroxide, or of various basic salts, depending on the nature of the environment. When the protective layers have formed and completely cover the surface of the metal, the corrosion proceeds at a greatly reduced rate. 

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. 

Vernon claims that in outdoor atmospheres the corrosion product consists largely of zinc oxide, hydroxide and combined water, but also contains zinc sulphide, zinc sulphate and carbonate. The following table gives the composition of typical films formed in an industrial atmosphere. 

In dry air the stability of zinc is remarkable. Once the protective layer of zinc oxide formed initially is complete, the attack ceases. Even under under normal urban conditions, such as those in London, zinc sheet 0 -8 mm thick has been found to have an effective life of 40 years or more when used as a roof covering and no repair has been needed except for mechanical damage. The presence of water does, of course, increase the rate of corrosion when water is present the initial corrosion product is zinc hydroxide, which is then converted by the action of carbon dioxide to a basic zinc carbonate, probably of composition similar to ZnCOj 3Zn(OH)2 . In very damp conditions unprotected zinc sometimes forms a loose and more conspicuous form of corrosion product known as wet storage stain or white rust (see p. 4.171). 

White rust If a fresh zinc surface is allowed to stand with large drops of dew on it, as may easily happen if it is stored in a closed place in which the temperature varies periodically, it is attacked by the oxygen dissolved in the water, owing to differential aeration between the edges and the centres of the drops. A porous form of zinc oxide builds up away from the surface and quickly takes up carbon dioxide from the air to form the basic carbonate known as white rust or wet storage stain. 

Zinc oxide is a white powder that makes a very opaque paste when mixed with water or oils. It is used as a sunblock and as a colorant in toothpastes and cosmetics. Zinc oxide is used in many of the same products as titanium dioxide. 

The Arrhenius definition is not suitable for AB cements for several reasons. It cannot be applied to zinc oxide eugenol cements, for these are non-aqueous, nor to the metal oxychloride and oxysulphate cements, where the acid component is not a protonic acid. Indeed, the theory is, strictly speaking, not applicable at all to AB cements where the base is not a water-soluble hydroxide but either an insoluble oxide or a silicate. 

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. 

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