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Tris acid properties

Air pollution, mainly contributed by the emission from automobiles, has become the most serious urban environmental problems in many eountries. In this study, so as to meet the SULEV regulation, the main idea has been focused on the utilization of HCA(Hydro-Carbon Adsorber) in order to adsorb the excess hydrocarbons emitted during the period of engine cold-start. As a main recipe of HCA materials, many types of zeolite as well as the combination of alumina, precious metals were used. In this study, physico-chemical factors of zeolite such as acidic properties and hydrophobic properties etc. has been characterized, and tried to find the optimum recipe of HCA materials. As results, among the acid properties of zeolites, the Si/Al ratio is found to be the most important factor to get higher hydro-carbon adsorption capacity. [Pg.328]

The first attempt to isolate organic substance from soil appears to have been made by F.K. Achard in 1786, and T. de Saussure is usually credited for introducing the term humus (Latin equivalent of soil) to describe the dark-colored organic material in soil. Several researchers tried to find out the chemical nature of humus. By the end of the nineteenth century, it had been firmly established that humus was a complex mixture of organic substances that were mostly colloidal in nature and which had weakly acidic properties. [Pg.2019]

Strong acidic metal hydrido complexes such as HCofCO) or complexes with Lewis acid properties, such as Rh2Cl2(CO)4, [Ru(MeCN)3(triphos)](CF3S03)2, [Pt(H20)2(dppe)](CF3S03)2, [Pd(H20)2(dppe)](CF3S03)2, or [Ir(MeCN)3(tri-phos)] (CF3S03)3, are able to act in alcohols as acetahzation catalysts, which means they can mediate the transformation of the newly formed aldehydes into acetals (see Section 5.3). [Pg.6]

Physical properties for naphthalene mono-, di-, tri-, and tetracarboxyhc acids are summari2ed in Table 9. Most of the naphthalene di- or polycarboxyLic acids have been made by simple routes such as the oxidation of the appropriate dior polymethylnaphthalenes, or by complex routes, eg, the Sandmeyer reaction of the selected antinonaphthalenesulfonic acid, to give a cyanonaphthalenesulfonic acid followed by fusion of the latter with an alkah cyanide, with simultaneous or subsequent hydrolysis of the nitrile groups. [Pg.500]

These oxazolines have cationic surface-active properties and are emulsifying agents of the water-in-oil type. They ate acid acceptors and, in some cases, corrosion inhibitors (see Corrosion). Reaction to oxazoline also is useful as a tool for determination of double-bond location in fatty acids (2), or for use as a protective group in synthesis (3). The oxazolines from AEPD and TRIS AMINO contain hydroxyl groups that can be esterified easily, giving waxes (qv) with saturated acids and drying oils (qv) with unsaturated acids. [Pg.17]

Trichloroethylene [79-01-6J, trichloroethene, CHCL=CCL2, commonly called "tri," is a colorless, sweet smelling (chloroformlike odor), volatile Hquid and a powerhil solvent for a large number of natural and synthetic substances. It is nonflammable under conditions of recommended use. In the absence of stabilizers, it is slowly decomposed (autoxidized) by air. The oxidation products are acidic and corrosive. Stabilizers are added to all commercial grades. Trichloroethylene is moderately toxic and has narcotic properties. [Pg.22]

There is some confusion in using Bayes rule on what are sometimes called explanatory variables. As an example, we can try to use Bayesian statistics to derive the probabilities of each secondary structure type for each amino acid type, that is p( x r), where J. is a, P, or Y (for coil) secondary strucmres and r is one of the 20 amino acids. It is tempting to writep( x r) = p(r x)p( x)lp(r) using Bayes rule. This expression is, of course, correct and can be used on PDB data to relate these probabilities. But this is not Bayesian statistics, which relate parameters that represent underlying properties with (limited) data that are manifestations of those parameters in some way. In this case, the parameters we are after are 0 i(r) = p( x r). The data from the PDB are in the form of counts for y i(r), the number of amino acids of type r in the PDB that have secondary structure J.. There are 60 such numbers (20 amino acid types X 3 secondary structure types). We then have for each amino acid type a Bayesian expression for the posterior distribution for the values of xiiry. [Pg.329]

Another class of hydrocarbon binders used in propints are the carboxy-terminated polybutadiene polymers which are cross-linked with either tris[l-(2-methyl)aziridinyl] phosphine oxide (MAPO) or combinations with phenyl bis [l -(2-methyl)aziridinyl] phosphine oxide (Phenyl MAPO). Phenyl MAPO is a difunctional counterpart of MAPO which makes possible chain extension of polymers with two carboxylic acid groups. A typical propint formulation with ballistic properties is in Table 11 (Ref 83) Another class of composites includes those using hydroxy-terminated polybutadienes cross-linked with toluene diisocyanate as binders. The following simplified equations illustrate typical reactions involved in binder formation... [Pg.889]

These early observations have evolved into the branch of chemistry called electrochemistry. This subject deals not only with the use of spontaneous chemical reactions to produce electricity but also with the use of electricity to drive non-spontaneous reactions forward. Electrochemistry also provides techniques for monitoring chemical reactions and measuring properties of solutions such as the pK, of an acid. Electrochemistry even allows us to monitor the activity of our brain and heart (perhaps while we are trying to master chemistry), the pH of our blood, and the presence of pollutants in our water supply. [Pg.603]


See other pages where Tris acid properties is mentioned: [Pg.517]    [Pg.1060]    [Pg.299]    [Pg.103]    [Pg.509]    [Pg.517]    [Pg.328]    [Pg.117]    [Pg.207]    [Pg.85]    [Pg.1045]    [Pg.293]    [Pg.508]    [Pg.313]    [Pg.259]    [Pg.494]    [Pg.144]    [Pg.95]    [Pg.500]    [Pg.85]    [Pg.18]    [Pg.2577]    [Pg.328]    [Pg.72]    [Pg.440]    [Pg.281]    [Pg.6]    [Pg.50]    [Pg.74]    [Pg.266]    [Pg.323]    [Pg.243]    [Pg.2148]    [Pg.186]    [Pg.873]    [Pg.581]    [Pg.136]    [Pg.51]    [Pg.149]    [Pg.222]    [Pg.245]    [Pg.340]   
See also in sourсe #XX -- [ Pg.511 ]




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Tris acid

Tris properties

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