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Bases chemical properties

In view of the indefinite melting-points of many sugars and of their readily obtainable derivatives e.g., osazones, cf. p. 139), their identification should be based primarily on their chemical properties. Their rotatory power can often be used for identification purposes, but is not considered in this book. [Pg.547]

Separations based upon differences in the chemical properties of the components. Thus a mixture of toluene and anihne may be separated by extraction with dilute hydrochloric acid the aniline passes into the aqueous layer in the form of the salt, anihne hydrochloride, and may be recovered by neutralisation. Similarly, a mixture of phenol and toluene may be separated by treatment with dilute sodium hydroxide. The above examples are, of comse, simple apphcations of the fact that the various components fah into different solubihty groups (compare Section XI,5). Another example is the separation of a mixture of di-n-butyl ether and chlorobenzene concentrated sulphuric acid dissolves only the w-butyl other and it may be recovered from solution by dilution with water. With some classes of compounds, e.g., unsaturated compounds, concentrated sulphuric acid leads to polymerisation, sulphona-tion, etc., so that the original component cannot be recovered unchanged this solvent, therefore, possesses hmited apphcation. Phenols may be separated from acids (for example, o-cresol from benzoic acid) by a dilute solution of sodium bicarbonate the weakly acidic phenols (and also enols) are not converted into salts by this reagent and may be removed by ether extraction or by other means the acids pass into solution as the sodium salts and may be recovered after acidification. Aldehydes, e.g., benzaldehyde, may be separated from liquid hydrocarbons and other neutral, water-insoluble hquid compounds by shaking with a solution of sodium bisulphite the aldehyde forms a sohd bisulphite compound, which may be filtered off and decomposed with dilute acid or with sodium bicarbonate solution in order to recover the aldehyde. [Pg.1091]

PW91 (Perdew, Wang 1991) a gradient corrected DFT method QCI (quadratic conhguration interaction) a correlated ah initio method QMC (quantum Monte Carlo) an explicitly correlated ah initio method QM/MM a technique in which orbital-based calculations and molecular mechanics calculations are combined into one calculation QSAR (quantitative structure-activity relationship) a technique for computing chemical properties, particularly as applied to biological activity QSPR (quantitative structure-property relationship) a technique for computing chemical properties... [Pg.367]

Now that we know something about EDTA s chemical properties, we are ready to evaluate its utility as a titrant for the analysis of metal ions. To do so we need to know the shape of a complexometric EDTA titration curve. In Section 9B we saw that an acid-base titration curve shows the change in pH following the addition of titrant. The analogous result for a titration with EDTA shows the change in pM, where M is the metal ion, as a function of the volume of EDTA. In this section we learn how to calculate the titration curve. We then show how to quickly sketch the titration curve using a minimum number of calculations. [Pg.317]

Traditionally, chiral separations have been considered among the most difficult of all separations. Conventional separation techniques, such as distillation, Hquid—Hquid extraction, or even some forms of chromatography, are usually based on differences in analyte solubiUties or vapor pressures. However, in an achiral environment, enantiomers or optical isomers have identical physical and chemical properties. The general approach, then, is to create a "chiral environment" to achieve the desired chiral separation and requires chiral analyte—chiral selector interactions with more specificity than is obtainable with conventional techniques. [Pg.60]

Thus it can be seen that elements in and near the island of stabiHty based on element 114 can be predicted to have chemical properties as foUows. Element 114 should be a homologue of lead, that is, should be eka-lead, and element 112 should be eka-mercury, element 110 should be eka-platinum, etc (26,27). If there is an island of stabiHty at element 126, this element and its neighbors should have chemical properties like those of the actinide and lanthanide elements (26). [Pg.227]

Chemical Properties. The hydrolysis of PET is acid- or base-catalyzed and is highly temperature dependent and relatively rapid at polymer melt temperatures. Treatment for several weeks in 70°C water results in no significant fiber strength loss. However, at 100°C, approximately 20% of the PET tenacity is lost in one week and about 60% is lost in three weeks (47). In general, the hydrolysis and chemical resistance of copolyester materials is less than that for PET and depends on both the type and amount of comonomer. [Pg.326]

Chemical Properties. A combination of excellent chemical and mechanical properties at elevated temperatures result in high performance service in the chemical processing industry. Teflon PEA resins have been exposed to a variety of organic and inorganic compounds commonly encountered in chemical service (26). They are not attacked by inorganic acids, bases, halogens, metal salt solutions, organic acids, and anhydrides. Aromatic and ahphatic hydrocarbons, alcohols, aldehydes, ketones, ethers, amines, esters, chlorinated compounds, and other polymer solvents have Httle effect. However, like other perfluorinated polymers,they react with alkah metals and elemental fluorine. [Pg.375]

Chemical Properties. Trimethylpentanediol, with a primary and a secondary hydroxyl group, enters into reactions characteristic of other glycols. It reacts readily with various carboxyUc acids and diacids to form esters, diesters, and polyesters (40). Some organometaUic catalysts have proven satisfactory for these reactions, the most versatile being dibutyltin oxide. Several weak bases such as triethanolamine, potassium acetate, lithium acetate, and borax are effective as stabilizers for the glycol during synthesis (41). [Pg.373]

Historically, the discovery of one effective herbicide has led quickly to the preparation and screening of a family of imitative chemicals (3). Herbicide developers have traditionally used combinations of experience, art-based approaches, and intuitive appHcations of classical stmcture—activity relationships to imitate, increase, or make more selective the activity of the parent compound. This trial-and-error process depends on the costs and availabiUties of appropriate starting materials, ease of synthesis of usually inactive intermediates, and alterations of parent compound chemical properties by stepwise addition of substituents that have been effective in the development of other pesticides, eg, halogens or substituted amino groups. The reason a particular imitative compound works is seldom understood, and other pesticidal appHcations are not readily predictable. Novices in this traditional, quite random, process requite several years of training and experience in order to function productively. [Pg.39]

M. L. Davis, V. V. Vesselovsky, and H. L. Johnston, Kinetics, Thermodynamics, Physico-Chemical Properties and Manufacture ofHydra ne, Ohio State University, Wright-Patterson Air Eorce Base, Dayton, Ohio, Mar. 15, 1952. [Pg.292]

Chemical Properties. Although the chemical properties of the trivalent lanthanides are quite similar, some differences occur as a consequence of the lanthanide contraction (see Table 3). The chemical properties of yttrium are very similar too, on account of its external electronic stmcture and ionic radius. Yttrium and the lanthanides are typical hard acids, and bind preferably with hard bases such as oxygen-based ligands. Nevertheless they also bind with soft bases, typicaUy sulfur and nitrogen-based ligands in the absence of hard base ligands. [Pg.540]

Although the size separation/classification methods are adequate in some cases to produce a final saleable mineral product, in a vast majority of cases these produce Httle separation of valuable minerals from gangue. Minerals can be separated from one another based on both physical and chemical properties (Fig. 8). Physical properties utilized in concentration include specific gravity, magnetic susceptibility, electrical conductivity, color, surface reflectance, and radioactivity level. Among the chemical properties, those of particle surfaces have been exploited in physico-chemical concentration methods such as flotation and flocculation. The main objective of concentration is to separate the valuable minerals into a small, concentrated mass which can be treated further to produce final mineral products. In some cases, these methods also produce a saleable product, especially in the case of industrial minerals. [Pg.401]

The same chemical separation research was done on thorium ores, leading to the discovery of a completely different set of radioactivities. Although the chemists made fundamental distinctions among the radioactivities based on chemical properties, it was often simpler to distinguish the radiation by the rate at which the radioactivity decayed. For uranium and thorium the level of radioactivity was independent of time. For most of the radioactivities separated from these elements, however, the activity showed an observable decrease with time and it was found that the rate of decrease was characteristic of each radioactive species. Each species had a unique half-life, ie, the time during which the activity was reduced to half of its initial value. [Pg.443]

The popularity of MSA as an electrolyte in electrochemical appHcations has developed as a result of the following unique physical and chemical properties (/) exhibits low corrosivity and is easy to handle, (2) nonoxidizing, (7) manufacturing process yields a high purity acid, (4) exceptional electrical conductivity, (3) high solubiHty of metal salts permits broad appHcations, (6) MSA-based formulations are simpler, (7) biodegradable, and (8) highly stable to heat and electrical current. [Pg.154]

Because of their diverse stmctures, there are few common threads to vitamin chemical properties aside from their fat or water solubiUty. Of general concern ia all appHcations, however, is vitamin stabiUty. Table 5 provides generic iaformation regarding stabiUty under several conditions. Levels of stabiUty vary greatly and are impacted by acid or base strength, light iatensity, etc. [Pg.6]

Step 4 deals with physical and chemical properties of compounds and mixtures. Accurate physical and chemical properties ate essential to achieve accurate simulation results. Most simulators have a method of maintaining tables of these properties as well as computet routines for calculations for the properties by different methods. At times these features of simulators make them suitable or not suitable for a particular problem. The various simulators differ ia the number of compounds ia the data base number of methods for estimating unknown properties petroleum fractions characterized electrolyte properties handled biochemical materials present abiUty to handle polymers and other complex materials and the soflds, metals, and alloys handled. [Pg.73]

Alloys having varying degrees of corrosion resistance have been developed in response to various environmental needs. At the lower end of the alloying scale are the low alloy steels. These are kon-base alloys containing from 0.5—3.0 wt % Ni, Cr, Mo, or Cu and controlled amounts of P, N, and S. The exact composition varies with the manufacturer. The corrosion resistance of the alloy is based on the protective nature of the surface film, which in turn is based on the physical and chemical properties of the oxide film. As a rule, this alloying reduces the rate of corrosion by 50% over the fkst few years of atmosphere exposure. Low alloy steels have been used outdoors with protection. [Pg.282]


See other pages where Bases chemical properties is mentioned: [Pg.2422]    [Pg.2777]    [Pg.79]    [Pg.202]    [Pg.209]    [Pg.209]    [Pg.227]    [Pg.522]    [Pg.271]    [Pg.314]    [Pg.33]    [Pg.320]    [Pg.131]    [Pg.437]    [Pg.473]    [Pg.394]    [Pg.390]    [Pg.426]    [Pg.75]    [Pg.163]    [Pg.321]    [Pg.309]    [Pg.278]    [Pg.444]    [Pg.470]    [Pg.220]    [Pg.67]    [Pg.463]    [Pg.225]    [Pg.193]    [Pg.458]    [Pg.492]   


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