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There is a group of chemicals used in polyurethanes that have an influence on the physical properties of the final product but do not take part in any chemical reaction. [Pg.23]

Fillers are not normally used in polyurethanes to bulk out the product, because they reduce the properties too drastically. This is in contrast to conventional elastomers, where they can be used to reinforce the product. Ultra fine silica is used as a thixotrophic filler in trowelable polyurethanes. [Pg.23]

Nanoparticles are now being investigated and used to provide some extra stiffness to polyurethanes. These are very small, flat, claylike platelets of micron size. Montmorillonites of size 2 to 13 microns have been used. They can have functional groups such as amine attached to them. The particles have to be fully defoliated and wetted by the polyurethane. The functional groups will bond to the hard segments. [Pg.23]

Plasticizers can be either reactive or nonreactive. The nonreactive plasticizers are from the phthalate and ester groups. Typical plasticizers are DIOP, TCP, and Benzoflex 9-88. The level of plasticizer must be controlled because the physical properties decrease as the levels increase. [Pg.24]

Molecular sieves are synthetic crystalline metal alumino-silicates that have very fine holes in their structure. The size of the holes is in the order of 4 to 5 angstroms (10 10 m) in diameter. The water molecules enter the holes and are trapped in them. Commercially, they are supplied in the form of a castor oil paste. [Pg.24]

MAO and boron compounds are expensive chemicals that increase the cost of the SPS production. However, the cocatalyst is an indispensable compound for the titanium complexes used as styrene polymerization catalysts. The roles of the cocatalyst are supposed to reduce the valence of the titanium compounds by forming the precursor of the active site, to activate the precursor, and subsequently to stabilize the active site by weak coordination. TIBA reacts with the transition metal and reduces Tl(IV) to 11(111), and this may be the precursor of the active site. Yabunouchi found that the catalytic activity in the styrene polymerization increased by the addition of a small amount of ((R )3CO)n-Al-(R )3 n to the styrene monomer, even if the amount of MAO is decreased [17]. One of these compounds is [(C6Hs)3CO](i-C4H9)2Al (Fig. 3.8). The catalytic activitiy was increased more than two times by the addition of a small amount of [(C6H5)3CO](i-C4H9)2Al to a mixture consisting of Tl MAO TIBA = 1 50 25 in molar ratio. [Pg.39]

These compounds can be used for every titanium compound with MAO as a cocatalyst. This is a kind of alkylaluminum, but the effect on the catalytic activity is different from usual alkylaluminums like TMA, TIBA, or trioctylaluminum. [Pg.39]

Such a chemical is also applicable for borane compounds as cocatalyst. In the catalyst system with borate compounds, the catalytic activity is also increased by the addition of [(C6H5)3CO](i-C4H9)2Al. [Pg.39]

This aluminum compound does not change the syndiotacticity of the polymer produced. The detailed mechanism of increasing the efficiency of MAO and borate cocatalysts has not been clarified yet. [Pg.40]

The cocatalysts for the syndiospecific polymerization of styrene were summarized. MAO and borate or borane compounds are useful cocatalysts for the syndiotactic styrene polymerization. There is an optimum molecular weight of MAO with regard to the polymerization activity of the transition metal complex, whereas TMA as an impurity in MAO reduces the activity of the catalyst complex [18]. The performance of MAO and borane compounds as cocatalysts can successfully be enhanced by the addition of selected new chemicals. [Pg.40]

5 Toxicity of Ethanol Mixtures with Other Chemicals [Pg.231]

Combined exposure to ethanol and numerous other chemicals produces enhanced toxic effects. The following studies are examples of such interactive effects. [Pg.231]

Benzene s toxicity is attributed to its metabolites. These can be accurately measured in urinary output. In a study to measure the effect of alcohol on benzene metabolic output, laboratory animals were treated with ethanol and exposed to benzene vapors. The urinary output of benzene metabolites was significantly lower in the animals treated with both ethanol and benzene [Pg.231]

The human CNS toxicity of inhaled m-xylene is enhanced by ethanol ingestion. This effect markedly and nonlinearly increases with ethanol dose and is attributed to the fact that both m-xylene and ethanol are metabolized by the CYP2E1 enzyme and that ethanol is preferentially metabolized, resulting in higher residual levels of m-xylene.I12 The action of ethanol on m-xylene CNS toxicity points out the need to consider ethanol consumption when establishing safe exposure levels for volatile organic compounds. [Pg.232]

Ethanol potentiates the toxicity of carbon tetrachloride. This phenomenon is exemplified by a report in the literature of human exposure to carbon tetrachloride. In two separate instances, acute liver and kidney poisoning ensued following exposure to carbon tetrachloride vapors from a discharged fire extinguisher. In both cases, other workers exposed to the same vapors for the same period of time showed no toxic signs or symptoms. Upon investigation, it was determined that the two injured individuals were chronic ethanol users, with daily consumptions of 120 and 250 g/day, respectively. Each of their nonaffected coworkers consumed less than 50 g of ethanol per dayJ13l [Pg.232]

This is a fine red powder with a molecular weight of 159.69 it has a specific gravity of 5.24, and melts at 1550°C. Insoluble in water, soluble in hydrochloric acid reacting with it, but it is hardly soluble in other acids. [Pg.143]

A mixture of red iron oxide and aluminium burns generating sparks at a high temperature (about 2400°C), leaving melted iron and melted aluminium oxide, as described in Chapter 5 on page 26. [Pg.143]

Manufacture. Obtained by heating iron(II)sulphate, FeS04.7H20, at 650 700°C. There are other several processes(from ores or some bi-products, which contain iron sulphate, iron hydroxide or iron(III)oxide). [Pg.143]

Quality. There are various kinds of quality. JIS provides for following kinds of purity. Made from iron sulphide, the special No.l is [Pg.143]

Molecular weight 685.57. Clear yellowish red powder or crystals, which have a specific gravity of 9.07 it decomposes generating oxygen over 500°C. Insoluble in water, but soluble in acetic acid, nitric acid and hot hydrochloric acid, reacting with them. [Pg.143]


Benzene was first isolated by Faraday in 1825 from the liquid condensed by compressing oil gas. It is the lightest fraction obtained from the distillation of the coal-tar hydrocarbons, but most benzene is now manufactured from suitable petroleum fractions by dehydrogenation (54%) and dealkylation processes. Its principal industrial use is as a starting point for other chemicals, particularly ethylbenzene, cumene, cyclohexane, styrene (45%), phenol (20%), and Nylon (17%) precursors. U.S. production 1979 2-6 B gals. [Pg.55]

Dimeihylamine, C2H7N, (CH3)2NH. Colourless, inflammable liquid with an ammoniacal odour, mp -96" C, b.p. 7°C. Occurs naturally in herring brine. Prepared in the laboratory by treating nitrosodimetbyl-aniline with a hot solution of sodium hydroxide. Dimethylamine is largely used in the manufacture of other chemicals. These include the solvents dimethylacetamide and dimethyl-formamide, the rocket propellant unsym-metrical dimethylhydrazine, surface-active agents, herbicides, fungicides and rubber accelerators. [Pg.260]

Studies of surfaces and surface properties can be traced to the early 1800s [1]. Processes that involved surfaces and surface chemistry, such as heterogeneous catalysis and Daguerre photography, were first discovered at that time. Since then, there has been a continual interest in catalysis, corrosion and other chemical reactions that involve surfaces. The modem era of surface science began in the late 1950s, when instmmentation that could be used to investigate surface processes on the molecular level started to become available. [Pg.283]

The entire Hving and material world consists of compounds and mixtures of compounds. Basic chemicals, such as ethylene, are produced in many millions of tons each year and are converted into a wide variety of other chemicals. Complicated molecular structures are synthesized by Mother Nature, or by chemists having taken up the challenge posed by Nature. However, we also have materials such as glues which are composed of mixtures of rather ill-defined polymers. [Pg.1]

The most important feature of editing software is the option to save the structure in standard file formats which contain information about the structure (e,g., Mol-filc. PDB-filc). Most of these file formats arc ASCII text files (which can be viewed in simple text editors) and cover international standardized and normalized specifications of the molecule, such as atom and bond types or connectivities (CT) (see Section 2,4). Thus, with these files, the structure can be exchanged between different programs. Furthermore, they can seiwe as input files to other chemical software, e.g, to calculate 3D structures or molecular properties. [Pg.138]

These numbers carry other chemical information. For example, z - h = x gives the oxidation state of a carbon atom. In effect, each carbon atom is classified according to its oxidation state, x, and its attachment to other carbon atoms. [Pg.184]

TOXCENTER TOXCENTER on STN is a bibliographic database that covers the pharmacological, biochemical, physiological, and toxicologicitl effects of drugs and other chemicals. The data m TOXCENTER are from 1907 to the preseni, Tliere are more Ihan 5,7 million records (December, 2002). It is updaled weekly... [Pg.243]

Clearly there was no lack of devoted adversaries (perhaps a more proper term than enemies) on both sides of the norbornyl ion controversy. It is to their credit that we today probably know more about the structure of carbocations, such as the norbornyl cation, than about most other chemical species. Their efforts also resulted not only in rigorous studies but also in the development or improvement of many techniques. Although many believe that too much effort was expended... [Pg.146]

Among the other chemicals prepared from ethylene are ethanol and acetaldehyde... [Pg.269]

Life forms are based on coded chemicals that, in the right environment, can reproduce themselves and make other chemicals needed to break down and utilize food. Within an organism, these biochemical reactions constitute nonnal metabolism. Biotechnology is the manipulation of these biochemical reactions at either the cellular or the molecular level. [Pg.422]

Several other chemical reactions are also widely used for the synthesis of these polymers. This list enumerates some of the possibilities and Table 5.3 illustrates these reactions by schematic chemical equations ... [Pg.299]

They lack resistance to solvents or other chemicals. [Pg.334]

As can be seen, most of the furfural produced in this country is consumed as an intermediate for other chemicals. Hydrogenation to furfuryl alcohol is the largest use. Some of the furfuryl alcohol is further hydrogenated to produce tetrahydrofurfuryl alcohol. The next major product is furan, produced by decarbonylation. Furan is a chemical intermediate, most of it is hydrogenated to tetrahydrofuran, which in turn is polymerized to produce polytetramethylene ether glycol (PTMEG). [Pg.79]


See other pages where Other Chemicals is mentioned: [Pg.93]    [Pg.164]    [Pg.209]    [Pg.259]    [Pg.329]    [Pg.364]    [Pg.401]    [Pg.155]    [Pg.2902]    [Pg.300]    [Pg.495]    [Pg.368]    [Pg.24]    [Pg.118]    [Pg.1]    [Pg.107]    [Pg.108]    [Pg.110]    [Pg.112]    [Pg.114]    [Pg.116]    [Pg.118]    [Pg.120]    [Pg.122]    [Pg.124]    [Pg.189]    [Pg.269]    [Pg.269]    [Pg.382]    [Pg.334]    [Pg.366]    [Pg.422]    [Pg.212]    [Pg.21]    [Pg.80]    [Pg.189]   


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Accidents of Other Self-Reactive Chemicals

Catalytic and Other In Situ Chemical Polymerization

Cement chemical nomenclature and other abbreviations

Chemical Companies and Other World War I Facilities

Chemical Resistance for Other Polyamides

Chemical Shifts of Other Elements

Chemical Shifts with Other Molecular Properties

Chemical Synthesis of Hormones, Pheromones and Other Bioregulators

Chemical evolution in other sorts of galaxies

Chemical industry comparison with other

Chemical ionization other reagent gases

Chemical properties Condensation with other compounds

Chemical properties, inorganic others

Chemical vapor deposition advantages over other techniques

Chemicals (cont others

Chemistry other chemicals

Cocatalysts other chemicals

Compatibility with other textile chemicals

Declarations and other submissions: activities not Schedule 3 chemicals

Ethanol other chemicals

European Union other chemical contaminants

Exposure to other chemicals

Further Chemical Reactions of Noble Metal Porphyrins Notes on Electrochemistry, Catalysis, and Other Applications

Ions and Other Chemicals

Labeling Other Chemical Containers

Mass spectrometry, mechanisms and structure in: a comparison with other chemical

Mass spectrometry, mechanisms and structure in: a comparison with other chemical processes

Moving Boundaries in Other Than Chemical Fields

Other Aqueous Transmethylations Chemical Rate Studies

Other Aspects of Chemical Thermodynamics

Other Chemical Businesses Fast Moves Needed

Other Chemical Ionization Processes

Other Chemical Labeling Methods

Other Chemical Processes

Other Chemical Properties

Other Chemical Reactions

Other Chemical Specific Rules

Other Chemical Systems

Other Chemical Treatments

Other Chemicals or Elements

Other Coupled Chemical Reactions

Other Examples of Reversible Complexation Chemical Shift Reagents

Other Factors Affecting Chemical Reactivity

Other Forms of Chemical Transport Models

Other Hazardous Chemicals

Other Industrial Chemical Reactors

Other Physical Chemical Properties of Miscible Blends

Other Physical-Chemical Properties

Other Sources of Sick Building Syndrome Toxic Chemicals

Other Specialty-Chemical Industries

Other Specific Chemical and Physical Methods

Other Thermal, Chemical and Electrical Structuring Processes

Other Volatile Materials Produced Chemically

Other chemical compounds

Other chemical contaminants

Other chemical industries

Other chemical production facilities

Other chemical production facilities OCPF)

Other chemical products

Other chemical properties of water

Other chemical storage options

Plasma-Chemical Synthesis of NF3 and Other Nitrogen Fluorides

Plasma-Chemical Synthesis of O2F2 and Other Oxygen Fluorides

Plasma-Chemical Synthesis of Xenon Fluorides and Other Fluorine Oxidizers

Production of Other Chemicals from Glutamic Acid

Purchase Costs of Other Chemical Processing Equipment

Reactions and Other Chemical Processes

Regime for other chemical production facilities

Some Other Chemicals from Natural Resources

Some Other Interpretations of Chemical Formulas

Some other Chemical Treatment with Natural Fibers

Structure of Zeolites and Other Chemical Systems

Synthesis of Fine Chemicals and Other Products

The Chemical Potential and Other Partial Molar Quantities

Wood Modification: Chemical. Thermal and Other Processes C. Hill

Wood Modification: Chemical. Thermal and Other Processes C. Hill 2006 John Wiley Sons, Ltd

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