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Particular zinc oxide

The polyelectrolyte cements are modern materials that have adhesive properties and are formed by the cement-forming reaction between a poly(alkenoic acid), typically poly(acrylic acid), PAA, in concentrated aqueous solution, and a cation-releasing base. The base may be a metal oxide, in particular zinc oxide, a silicate mineral or an aluminosilicate glass. The presence of a polyacid in these cements gives them the valuable property of adhesion. The structures of some poly(alkenoic acid)s are shown in Figure 5.1. [Pg.90]

Applied to certain compounding ingredients (particularly zinc oxide and precipitated whiting) which have been surface-treated to improve their reinforcing power or their ease of incorporating into rubber. Also applied to a lining which has... [Pg.67]

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. [Pg.276]

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. [Pg.252]

As in dry compounding, acid acceptors must be incorporated into neoprene latices because of the wide use of these latices in coating fabrics and metals. The hydrochloric acid that forms during service life has a particularly destmetive effect on coated cotton fabrics that are not adequately protected. High zinc oxide concentration (ca 15 parts) and use of 0.4 parts AJ-phenyl-AT(p-toluenesulfonyl)-/)-phenylenediamine (Aranox, Uniroyal) as an antioxidant provides adequate protection. [Pg.256]

Cure Characteristics. Methods of natural rubber production and raw material properties vary from factory to factory and area to area. Consequentiy, the cure characteristics of natural mbber can vary, even within a particular grade. Factors such as maturation, method and pH of coagulation, preservatives, dry mbber content and viscosity-stabilizing agents, eg, hydroxylamine-neutral sulfate, influence the cure characteristics of natural mbber. Therefore the consistency of cure for different grades of mbber is determined from compounds mixed to the ACSl formulation (27). The ACSl formulation is as follows natural mbber, 100 stearic acid, 0.5 zinc oxide, 6.0 sulfur, 3.5 and 2-mercaptobenzothiazole (MBT), 0.5. [Pg.269]

Polyisobutylene and isobutylene—isoprene copolymers are considered to have no chronic hazard associated with exposure under normal industrial use. Some grades can be used in chewing-gum base, and are regulated by the PDA in 21 CPR 172.615. Vulcanized products prepared from butyl mbber or halogenated butyl mbber contain small amounts of toxic materials as a result of the particular vulcanization chemistry. Although many vulcanizates are inert, eg, zinc oxide cured chlorobutyl is used extensively in pharmaceutical stoppers, specific recommendations should be sought from suppHers. [Pg.487]

This chapter reports the results of studies on the physical, dynamic mechanical, and rheological behavior of zinc oxide neutralized m-EPDM, particularly in the presence of stearic acid and zinc stearate, with special reference to the effects of precipitated silica filler. [Pg.441]

Sulphur oxides These (SO2 is the most frequently encountered oxide) are powerful stimulators of atmospheric corrosion, and for steel and particularly zinc the correlation between the level of SO2 pollution and corrosion rates is good However, in severe marine environments, notably in the case of zinc, the chloride contamination may have a higher correlation coefficient than SO2. [Pg.338]

The silicophosphate cement originated with the dental silicate cement, for there is no doubt that early investigators experimented with mixtures of aluminosilicate glass and zinc oxide (Fletcher, 1878,1879 Eberly, 1928). It appears to have no particular advantages. As is often the case with hybrids, it can combine the worst features as well as the best of the parents, and often properties have intermediate values. Nevertheless, it continues to have a small but persistent usage arising from its one advantage over the... [Pg.263]

The importance of water as an initiator and catalyst for the reaction between zinc oxide and plain eugenol has been demonstrated by a number of studies (Smith, 1958 Crisp, Ambersley Wilson, 1980 Batchelor Wilson, 1969 Prosser Wilson, 1982). In particular, the reaction is accelerated by the humidity of the atmosphere during mixing (Batchelor Wilson, 1969 Crisp, Ambersley Wilson, 1980). [Pg.326]

Skinner, Molnar Suarez (1964) studied the cement-forming potential of 28 liquid aromatic carboxylic acids with zinc oxide. Twelve yielded cohesive products of some merit. Of particular interest were cements formed with hydrocinnamic, cyclohexane carboxylic, p-tertiary butyl-benzoic, thiobenzoic and cyclohexane butyric acids. One of these cements is on the market as a non-eugenol cement. It is very weak with a compressive strength of 4 0 MPa, a tensile strength of 11 MPa and a modulus of 177 MPa, and is only suitable as a temporary material (Powers, Farah Craig, 1976). [Pg.347]

It was shown in a number of works [29] that impurity conductivity of thin zinc oxide films are extremely sensitive to adsorption of atoms of various metals (see Chapters 2 and 3). Using this feature of oxide films, we first employed the sensor method to study evaporation of superstechiometric atoms of metals from metal oxide surfaces, zinc oxide in particular [30]. [Pg.237]

In a review of the course and mechanism of the catalytic decomposition of ammonium perchlorate, the considerable effects of metal oxides in reducing the explosion temperature of the salt are described [1], Solymosi s previous work had shown reductions from 440° to about 270° by dichromium trioxide, to 260° by 10 mol% of cadmium oxide and to 200°C by 0.2% of zinc oxide. The effect of various concentrations of copper chromite , copper oxide, iron oxide and potassium permanganate on the catalysed combustion of the propellant salt was studied [2], Similar studies on the effects of compounds of 11 metals and potassium dichromate in particular, have been reported [3], Presence of calcium carbonate or calcium oxide has a stabilising effect on the salt, either alone or in admixture with polystyrene [4],... [Pg.1367]

Figure 23a shows the C—H region of the spectrum about 10 min (solid line) and 60 min (dotted line) after admission of 8 mm of butene-1 to a sample of zinc oxide. These spectra, which are primarily due to physically adsorbed and gas-phase butenes, show sizeable changes as a function of time. The region above 3000 cm-1 is particularly clear cut. Initially, a band is observed only at 3082 cm-1 this corresponds closely to the 3086 cm-1 band for gaseous butene-1 (64). After 1 hr the band at 3082 cm-1 is gone and two new bands (above 3000 cm-1) have appeared at 3035 and 3018 cm-1 which correspond within the experimental uncertainty to the expected bonds for cfs-butene (64) (3030 cm-1) and frans-butene (64) (3021 cm-1). Other bands are consistent with these changes. Thus, it is evident that double-bond isomerization has occurred. [Pg.43]

A dusting agent which is soluble in rubber and thus does not impair the vulcanised bond between rubber components of a composite product. It is also an activator combining the functions of zinc oxide and stearic acid, of particular value in transparent rubbers since it does not produce the same opacity as zinc oxide. [Pg.74]

Zinc borates with different mole ratios of Zn0 B203 H20 can be readily prepared by reacting zinc oxide with boric acid (Fig. 1). Among all these zinc borates, the compound with a molecular formula of 2Zn0-3B203-3.5H20, is the most commonly used fire retardant. This article will review recent research results on the use of this particular form of zinc borate as a multifunctional fire retardant. [Pg.157]

Structural chromosome aberrations, particularly chromatid gaps and increased frequency of fragment exchange, were observed in rat bone marrow cells after 14 days of exposure to 240 mg Zn/L drinking water (Kowalska-Wochna et al. 1988). Chromosomal aberrations were observed in bone marrow cells of mice fed diets equivalent to 650 mg Zn/kg BW daily, in mice exposed to zinc oxide by inhalation, and in mice maintained on a low-calcium diet (USPHS 1989). Aberrations in bone marrow of mice given 5000 mg Zn/kg diet may be associated with calcium deficiency (Leonard and Gerber 1989). Calcium is displaced by zinc in calcium-depleted conditions, leading to chromosomal breaks and interference in the repair process (USPHS 1989). [Pg.647]

Promoter deposition through different mechanisms can account for different catalyst properties. In particular, chromate depositing as chromia does not easily redissolve but, zinc oxide does redissolve once the leach front passes and the pH returns to the bulk level of the lixiviant. Therefore, chromate can provide a more stable catalyst structure against aging, as observed in the skeletal copper system. Of course, promoter involvement in catalyst activity as well as structural promotion must be considered in the selection of promoters. This complexity once again highlights the dependence of the catalytic activity of these materials on the preparation conditions. [Pg.147]


See other pages where Particular zinc oxide is mentioned: [Pg.112]    [Pg.112]    [Pg.189]    [Pg.165]    [Pg.371]    [Pg.67]    [Pg.10]    [Pg.226]    [Pg.256]    [Pg.257]    [Pg.274]    [Pg.349]    [Pg.130]    [Pg.180]    [Pg.203]    [Pg.178]    [Pg.189]    [Pg.26]    [Pg.73]    [Pg.171]    [Pg.202]    [Pg.274]    [Pg.333]    [Pg.335]    [Pg.572]    [Pg.646]    [Pg.221]    [Pg.61]    [Pg.132]    [Pg.311]    [Pg.234]    [Pg.273]    [Pg.227]   
See also in sourсe #XX -- [ Pg.398 ]




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Particular oxides

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