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Admixtures

Admixtures of oxygen or oxidizing agents such as N2O to the silane plasma enable the deposition of Si02 films. Other Si-containing compounds such as SiCl or tetraethoxysilane (Si(OCH2CH2)4) are used for plasma-enlranced Si02 deposition at lower temperatures [33],... [Pg.2807]

Projecting the nuclear solutions Xt( ) oti the Hilbert space of the electronic states (r, R) and working in the projected Hilbert space of the nuclear coordinates R. The equation of motion (the nuclear Schrddinger equation) is shown in Eq. (91) and the Lagrangean in Eq. (96). In either expression, the terms with represent couplings between the nuclear wave functions X (K) and X (R). that is, (virtual) transitions (or admixtures) between the nuclear states. (These may represent transitions also for the electronic states, which would get expressed in finite electionic lifetimes.) The expression for the transition matrix is not elementaiy, since the coupling terms are of a derivative type. [Pg.151]

The tribromobenzene obtained in this way should be entirely free from unchanged tribromoaniline. To test its purity, dissolve a small quantity in hot dry benzene and pass in hydrogen chloride gas from a Kipp s apparatus no trace of crystals of tribromoaniline hydrochloride should appear. Note also that although the m.p.s of the two compounds are almost identical, that of the recrystallised product from the above preparation is considerably depressed by admixture with tribromoaniline. [Pg.203]

If the methyl alcohol is distilled off before thorough cooling in a freezing mixture, the yield of hydrazobenzene is appreciably increased, but the product is considerably more coloured due to admixture with a trace of azobenzene. About 12 g. of impure hydrazobenzene may be recovered by distilling off the methyl alcohol from the hltrato after the colourless hydrazobenzene has been collected. [Pg.633]

Determination of purity. The ultraviolet and visible absorption is often a fairly intensive property thus e values of high intensity bands may be of the order of 10 -10 . In infrared spectra e values rarely exceed 10 . It is therefore often easy to pick out a characteristic band of a substance present in small concentration in admixture with other materials. Thus small amounts of aromatic compounds can be detected in hexane or in cyclohexane. [Pg.1149]

Synthesis by high-dilution techniques requires slow admixture of reagents ( 8-24 hrs) or very large volumes of solvents 100 1/mmol). Fast reactions can also be carried out in suitable flow cells (J.L. Dye, 1973). High dilution conditions have been used in the dilactam formation from l,8-diamino-3,6-dioxaoctane and 3,6-dioxaoctanedioyl dichloride in benzene. The amide groups were reduced with lithium aluminum hydride, and a second cyclization with the same dichloride was then carried out. The new bicyclic compound was reduced with diborane. This ligand envelops metal ions completely and is therefore called a cryptand (B. Dietrich, 1969). [Pg.247]

A schematic diagram showing the general construction of an arc or spark source. Actual construction details depend partly on whether samples need to be analyzed automatically. The sample material can be placed on the cathode or can even compose the whole of the cathode. If graphite is used, the sample needs to be pressed into the shape of a cathode after admixture with the carbon. [Pg.113]

Figure 6.35 illustrates how anharmonicity mixes the two vibrations Vj and V3 of CO2. If the molecule starts from the point X and proceeds to B it will tend to follow the line of maximum slope shown. In doing so it deviates considerably from the dashed line representing and so involves an admixture of Qi and Qj. [Pg.186]

Positive-Tone Photoresists based on Dissolution Inhibition by Diazonaphthoquinones. The intrinsic limitations of bis-azide—cycHzed mbber resist systems led the semiconductor industry to shift to a class of imaging materials based on diazonaphthoquinone (DNQ) photosensitizers. Both the chemistry and the imaging mechanism of these resists (Fig. 10) differ in fundamental ways from those described thus far (23). The DNQ acts as a dissolution inhibitor for the matrix resin, a low molecular weight condensation product of formaldehyde and cresol isomers known as novolac (24). The phenoHc stmcture renders the novolac polymer weakly acidic, and readily soluble in aqueous alkaline solutions. In admixture with an appropriate DNQ the polymer s dissolution rate is sharply decreased. Photolysis causes the DNQ to undergo a multistep reaction sequence, ultimately forming a base-soluble carboxyHc acid which does not inhibit film dissolution. Immersion of a pattemwise-exposed film of the resist in an aqueous solution of hydroxide ion leads to rapid dissolution of the exposed areas and only very slow dissolution of unexposed regions. In contrast with crosslinking resists, the film solubiHty is controUed by chemical and polarity differences rather than molecular size. [Pg.118]

Adipic acid is an irritant to the mucous membranes. In case of contact with the eyes, they should be flushed with water. It emits acrid smoke and fumes on heating to decomposition. It can react with oxidizing materials, and the dust can explode ia admixture with air (see Table 3). Fires may be extinguished with water, CO2, foam, or dry chemicals. [Pg.246]

Almost all of the cyclohexane that is produced in concentrated form is used as a raw material in the first step of nylon-6 and nylon-6,6 manufacture. Cyclohexane also is an excellent solvent for cellulose ethers, resins, waxes (qv), fats, oils, bitumen, and mbber (see Cellulose ethers Resins, natural Fats AND FATTY OILS Rubber, NATURAL). When used as a solvent, it usually is in admixture with other hydrocarbons. However, a small amount is used as a reaction diluent in polymer processes. [Pg.409]

Aerosols. Pressurized containers to deHver aerosolized dmg products through appropriate systems of valves and actuators have been available since the 1950s (see Aerosols). Such dosage forms are used as external appHcations of lotions and creams, for oral inhalation, or for treatment of the vaginal cavity, eg, contraceptive foams. Aerosols contain two- or three-phase systems, wherein a volatile Hquid or admixture of Hquids is sealed in a... [Pg.234]

In concrete, triethanolamine accelerates set time and increases early set strength (41—43). These ate often formulated as admixtures (44), for later addition to the concrete mixtures. Compared to calcium chloride, another common set accelerator, triethanolamine is less corrosive to steel-reinforcing materials, and gives a concrete that is more resistant to creep under stress (45). Triethanolamine can also neutralize any acid in the concrete and forms a salt with chlorides. Improvement of mechanical properties, whiteness, and more even distribution of iron impurities in the mixture of portland cements, can be effected by addition of 2% triethanolamine (46). Triethanolamine bottoms and alkanolamine soaps can also be used in these type appUcations. Waterproofing or sealing concrete can be accompUshed by using formulations containing triethanolamine (47,48). [Pg.10]

The Co nucleus decays with a half-life of 5.27 years by /5 emission to the levels in Ni. These levels then deexcite to the ground state of Ni by the emission of one or more y-rays. The spins and parities of these levels are known from a variety of measurements and require that the two strong y-rays of 1173 and 1332 keV both have E2 character, although the 1173 y could contain some admixture of M3. However, from the theoretical lifetime shown ia Table 7, the E2 contribution is expected to have a much shorter half-life and therefore also to dominate ia this decay. Although the emission probabilities of the strong 1173- and 1332-keV y-rays are so nearly equal that the difference cannot be determined by a direct measurement, from measurements of other parameters of the decay it can be determined that the 1332 is the stronger. Specifically, measurements of the continuous electron spectmm from the j3 -decay have shown that there is a branch of 0.12% to the 1332-keV level. When this, the weak y-rays, the internal conversion, and the internal-pair formation are all taken iato account, the relative emission probabilities of the two strong y-rays can be determined very accurately, as shown ia Table 8. [Pg.450]

If the viscous bitumen in a tar sand formation can be made mobile by an admixture of either a hydrocarbon diluent or an emulsifying fluid, a relatively low temperature secondary recovery process is possible (emulsion steam drive). If the formation is impermeable, communication problems exist between injection and production weUs. However, it is possible to apply a solution or dilution process along a narrow fracture plane between injection and production weUs. [Pg.356]

TYZOR TPT and the tetraethyl titanate, TYZOR ET [3087-36-3], have also been prepared by direct electrochemical synthesis. The reaction involves anode dissolution of titanium in the presence of the appropriate alcohol and a conductive admixture (3). [Pg.138]

P-Ghloroalkoxy Titanates. The reaction of TiCl with epoxides, such as ethylene or propylene oxide (qv), gives P-chloroalkyl titanates (8,9). One example is Ti(OCH2CH2Cl)4 [19600-95-5]. The P-chloroalkoxy titanates can be used to biad refractory powders and ia admixture with diethanolamine to impart thixotropy to emulsion paints (10). [Pg.139]

Admixtures are sometimes used to reduce permeabiUty of concrete (80—82). These iaclude pore-filling materials such as chalk. Fuller s earth, or talc water repellents such as mineral oil, asphalt, or wax emulsions organic polymers (acryflc latexes, epoxies) and salts of fatty acids, especially stearates. [Pg.311]

Fast Color Salts. In order to simplify the work of the dyer, diazonium salts, in the form of stable dry powders, were introduced under the name of fast color salts. When dissolved in water they react like ordinary diazo compounds. These diazonium salts, derived from amines, free from solubilizing groups, are prepared by the usual method and are salted out from the solutions as the sulfates, the metallic double salts, or the aromatic sulfonates. The isolated diazonium salt is sold in admixture with anhydrous salts such as sodium sulfate or magnesium sulfate. [Pg.445]

For special high strength appHcations, ie, up to 69 MPa (10,000 psi), special formulations of Pordand cement concretes have been developed. These ate based on the use of chemical and mineral admixtures. The typical mineral admixtures ate fumed siUca and other po22olanics. The chemical admixtures ate generally chemicals termed supetplastici2ets that allow very low water to cement ratios, ie, between 0.4 and 0.25, and reduce the amount of water needed to provide plasticity or dow to the concrete. PubHc works appHcations take just under 32% of the total Pordand cement market streets and highways represent 68% of this usage, and water and waste account for 23%. [Pg.324]

Accelerator in Ready-Mix Concrete. Calcium chloride accelerates the set time of concrete giving it a high early strength development. It is not an antifreeze, but by using it duriag cold weather protection can proceed in a timely manner (31—34). In Russia, calcium chloride forms a component of several antifreeze admixtures (33). Reviews of the concerns and possible remedies of calcium chloride corrosion problems in concrete are available (21,35). There is no consensus on what the safe levels of calcium chloride in concrete are. [Pg.416]

Graphite lubricants include the dry powder, admixtures with liquid lubricants or greases, volatile liquids compounded with film-forming substances to produce bonded dry films, synthetic resins and powder metal compositions containing graphite for bearings, and finely divided suspensions in liquids (colloidal graphite). [Pg.577]

Electrical Uses. Dry cells (see Batteries, primary cells) use graphite to render the nonconductive pyrolusite (Mn02) conductive through intimate admixture. The degree of graphitization is a factor in that graphites with the same carbon content and from the same locaUty give different results. [Pg.578]


See other pages where Admixtures is mentioned: [Pg.326]    [Pg.191]    [Pg.2031]    [Pg.2808]    [Pg.2809]    [Pg.100]    [Pg.144]    [Pg.470]    [Pg.474]    [Pg.976]    [Pg.44]    [Pg.81]    [Pg.119]    [Pg.142]    [Pg.144]    [Pg.355]    [Pg.103]    [Pg.322]    [Pg.192]    [Pg.322]    [Pg.228]    [Pg.101]    [Pg.144]    [Pg.163]    [Pg.208]    [Pg.336]    [Pg.406]    [Pg.290]   
See also in sourсe #XX -- [ Pg.31 , Pg.32 , Pg.33 , Pg.34 , Pg.35 , Pg.36 , Pg.37 , Pg.232 ]

See also in sourсe #XX -- [ Pg.446 ]

See also in sourсe #XX -- [ Pg.79 , Pg.81 , Pg.249 ]

See also in sourсe #XX -- [ Pg.89 ]

See also in sourсe #XX -- [ Pg.209 ]

See also in sourсe #XX -- [ Pg.23 , Pg.28 ]




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Accelerating admixtures

Admixture Studies

Admixture studies, parenteral

Admixture with diet

Admixtures Modifying Paste and Concrete Properties

Admixtures accelerators

Admixtures air entraining

Admixtures and in-situ soil mixing

Admixtures and special uses of cements

Admixtures chemical

Admixtures classification

Admixtures compatibility

Admixtures definition

Admixtures detection

Admixtures dispersing agents

Admixtures estimating

Admixtures inhibitors

Admixtures on Crystal Growth

Admixtures on Crystal Shape

Admixtures on Nucleation

Admixtures polymeric

Admixtures repair materials

Admixtures selection

Admixtures types)

Admixtures water-reducing agents

Admixtures, desensitizing

Admixtures, dichroic dyes

Air entraining water-reducing admixtures

Air entrainment water-reducing admixtures

Alkali aggregate expansion reducing admixtures

Antifreeze admixtures

Antifreezing admixtures

Antiwashout admixtures

Antiwetting Admixtures to Alumina Silica Refractories

Applications of admixtures

Aqueous phase water-reducing admixtures

Bridges admixtures

Chemical admixture-cement interaction

Chemical admixtures/agents

Compatibility of admixtures

Composite characteristics admixture

Compressive strength effect water-reducing admixtures

Concrete Admixture

Concrete mineral admixtures

Concrete polymer based admixtures

Corrosion inhibiting admixtures

Damp-proofing admixtures

Dampproofing admixtures

Economic aspects of admixture use

Expanding admixtures

Expansion producing admixtures

Flocculating admixtures

High-range water reducing admixtures

High-range water reducing admixtures HRWRA)

Hydration retarding admixtures

Hydrophobic admixtures

Insecticidal admixtures

Introduction to Concrete Admixtures

King Guide to Parenteral Admixtures

Lignosulfonate-based admixtures

Lignosulfonates admixture

Lipid total nutrient admixtures

Mineral and Chemical Admixtures

Minerals admixtures

Miscellaneous admixtures

Non-chloride admixtures

Normal-setting water-reducing admixtures

OTHER ADMIXTURES

Permeability Reducing Admixtures

Permeability water-reducing admixtures

Phosphonate admixtures

Pigment admixtures

Polymer Based Admixtures for Concrete

Polymer-based admixtures

Polymer-modified admixtures

Population admixture

Purification of halide ionic melts from oxide-ion admixtures

Quick setting admixtures

Retarder-based admixture

Retarding admixtures

Retarding and Water Reducing Admixtures

Setting time retarding admixtures

Setting time water-reducing admixtures

Shotcrete admixtures

Shotcrete admixtures aluminates

Shotcreting admixtures

Shrinkage reducing admixtures

Solvent admixture

Special purpose admixtures

Spin admixture

Sulphate admixtures

Superplasticizing admixtures

Total nutrient admixtures

Total nutrient admixtures emulsion stability

Total nutrient admixtures preparation

Types of admixtures

Viscosity Modifying Admixtures

Viscosity-enhancing admixtures

Water Reducing Admixtures (Plasticizers)

Water and admixtures

Water reducing admixtures

Water reducing admixtures concrete

Water reducing admixtures types

Water-repellent admixtures

Waterproofing admixtures

Workability water-reducing admixture dosage

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