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Solvent propertie

The powerful solvent properties of dimethylsulfoxide (DMSO), for example, are used to dissolve selectively the polynuclear aromatics found in oils and paraffins. The procedure is shown in Figure 2.5. [Pg.25]

Dearomatized or not, lamp oils correspond to petroleum cuts between Cio and C14. Their distillation curves (less than 90% at 210°C, 65% or more at 250°C, 80% or more at 285°C) give them relatively heavy solvent properties. They are used particularly for lighting or for emergency signal lamps. These materials are similar to kerosene solvents , whose distillation curves are between 160 and 300°C and which include solvents for printing inks. [Pg.272]

F. M. Fowkes, in Solvent Properties of Surfactant Solutions, K. Shinoda, ed., Marcel Dekker, New York, 1967. [Pg.497]

Homologous mono-alkyl ethers of ethylene glycol, such as monoethyl glycol (or 2-ethoxyethanol), HOC2H4OC2H5, form excellent solvents as they combine to a large extent the solvent properties of alcohols and ethers. The monoethyl and the monomethyl members have the technical names of ethyl cellosolve and methyl cellosolve respectively. Dioxan... [Pg.15]

HC0N(CH3)2, also possess exceptional solvent properties. The alkyl-glycols, dioxan and dimethyl-formamide should be used with caution, however, as their hot vapours are poisonous. [Pg.15]

The most widely used cleansing agent is the chromic acid cleaning mixture. It is essentially a mixture of chromic acid (CrOj) and concentrated sulphuric acid, and possesses powerful oxidising and solvent properties. Two methods of preparation are available —... [Pg.53]

Solvents exert their influence on organic reactions through a complicated mixture of all possible types of noncovalent interactions. Chemists have tried to unravel this entanglement and, ideally, want to assess the relative importance of all interactions separately. In a typical approach, a property of a reaction (e.g. its rate or selectivity) is measured in a laige number of different solvents. All these solvents have unique characteristics, quantified by their physical properties (i.e. refractive index, dielectric constant) or empirical parameters (e.g. ET(30)-value, AN). Linear correlations between a reaction property and one or more of these solvent properties (Linear Free Energy Relationships - LFER) reveal which noncovalent interactions are of major importance. The major drawback of this approach lies in the fact that the solvent parameters are often not independent. Alternatively, theoretical models and computer simulations can provide valuable information. Both methods have been applied successfully in studies of the solvent effects on Diels-Alder reactions. [Pg.8]

The solvents listed in Table 2.1 were chosen to cover a broad range in solvent properties. In fact hexane was initially also among them, but unfortunately the rate of the reaction in this solvent is extremely low. It turned out that in this solvent spontaneous decomposition of 2.4a competes with the Diels-Alder reaction. [Pg.52]

At one time benzene was widely used as a solvent This use virtually disappeared when statistical studies revealed an increased incidence of leukemia among workers exposed to atmospheric levels of benzene as low as 1 ppm Toluene has replaced benzene as an inexpensive organic solvent because it has similar solvent properties but has not been determined to be carcinogenic m the cell systems and at the dose levels that benzene is... [Pg.438]

Solvent molecules Solvent Orange 60 Solvent Orange 63 Solvent preparation Solvent process Solvent properties... [Pg.915]

The extremely nonpolar character of PFCs and very low forces of attraction between PFC molecules account for their special properties. Perfluorocarbons bod only slightly higher than noble gases of similar molecular weight, and their solvent properties are much more like those of argon and krypton than hydrocarbons (2). The physical properties of some PFCs are Hsted in Table 1. [Pg.282]

The combined pharmaceutical appHcations account for an estimated 25% of DMF consumption. In the pharmaceutical industry, DMF is used in many processes as a reaction and crystallizing solvent because of its remarkable solvent properties. For example, hydrocortisone acetate [50-03-3] dihydrostreptomycin sulfate [5490-27-7] and amphotericin A [1405-32-9] are pharmaceutical products whose crystallization is faciHtated by the use of DMF. Itis also a good solvent for the fungicide griseofulvin/72%(97-< 7 and is used in its production. [Pg.514]

ROOC—COOH, are not. The dialkyl esters are characterized by good solvent properties and serve as starting materials in the synthesis of many organic compounds, such as pharmaceuticals, agrochemicals, and fine chemicals (qv). Among the diesters, dimethyl, diethyl, and di- -butyl oxalates are industrially important. Their physical properties are given in Table 7. [Pg.463]

Solvent. The solvent properties of water and steam are a consequence of the dielectric constant. At 25°C, the dielectric constant of water is 78.4, which enables ready dissolution of salts. As the temperature increases, the dielectric constant decreases. At the critical point, the dielectric constant is only 2, which is similar to the dielectric constants of many organic compounds at 25°C. The solubiUty of many salts declines at high temperatures. As a consequence, steam is a poor solvent for salts. However, at the critical point and above, water is a good solvent for organic molecules. [Pg.354]

Sulfolane was first described ia the chemical Hterature ia 1916. It has been noted for its exceptional chemical and thermal stabiUty and unusual solvent properties. The search for a commercial process to produce sulfolane began about 1940. Market development quantities became available ia 1959. Siace then, both the use of and the appHcations for sulfolane have iacreased dramatically. [Pg.67]

Reactions. Supercritical fluids are attractive as media for chemical reactions. Solvent properties such as solvent strength, viscosity, diffusivity, and dielectric constant may be adjusted over the continuum of gas-like to Hquid-like densities by varying pressure and temperature. Subsequently, these changes can be used to affect reaction conditions. A review encompassing the majority of studies and apphcations of reactions in supercritical fluids is available (96). [Pg.227]

Distillation By-Products. Of the CTO distiHation by-products, ie, pitch, heads, and DistiHed TaH Oil (DTO), only the last, a unique mixture of rosin and fatty acids, has significant commercial value. Pitch and heads are used as fuel the former has a fuel value of 41,800 kj/kg. TaH oil heads have outstanding solvent properties, but also have a bad odor, which is hard to remove. They contain a relatively high fraction of palmitic acid which can be recovered by crystallization. [Pg.306]

Salts and Derivatives. Generally the vitamers are high melting crystalline soHds that are very soluble in water and insoluble in most other solvents. Properties of the common forms are Hsted in Table 1. The only commercially important form of vitamin B is pytidoxine hydrochloride (7). This odorless crystalline soHd is composed of colorless platelets melting at 204—206°C (with decomposition). In bulk, it appears white and has a density of - 0.4 kg/L. It is very soluble in water (ca 0.22 kg/L at 20°C), soluble in propylene glycol, slightly soluble in acetone and alcohol (ca 0.014 kg/L), and insoluble in most lipophilic solvents. A 10% water solution shows a pH of 3.2. Both the hydrochloride and corresponding free base sublime without decomposition (16). [Pg.68]

The NF and reagent grades are employed in the pharmaceutical industry which makes use of benzyl alcohol s local anesthetic, antiseptic, and solvent properties (17—20). It also finds use in cough symps and drops ophthalmic solutions bum, dental (21), and insect repeUant solutions and ointments and dermatological aerosol sprays. It is used in nail lacquers and as a color developer in hair dyes by the cosmetics industry (22), and in acne treatment preparations (23). [Pg.61]

Tetrachloroethylene [127-18-4] perchloroethylene, CCl2=CCl2, is commonly referred to as "perc" and sold under a variety of trade names. It is the most stable of the chloriaated ethylenes and ethanes, having no flash poiat and requiring only minor amounts of stabilizers. These two properties combiaed with its excellent solvent properties account for its dominant use ia the dry-cleaning iadustry as well as its appHcation ia metal cleaning and vapor degreasiag. [Pg.27]

Chlorotoluene [106-43-4] (l-chloto-4-methylbenzene, PCT) and y -chlorotoluene [108-41-8] (l-chloto-3-methylbenzene, MCT) ate mobile, colorless Hquids with solvent properties similar to those of the ortho isomer. [Pg.52]

K. Shiaoda, ed.. Solvent Properties of Suf actant Solutions, Suf actant Science Series, Vol. 2, Marcel Dekker, Inc., New York, 1967. [Pg.543]

In addition to its ability to make the separation feasible or easier, the ideal solvent is inexpensive, readily available, nontoxic, noncorrosive, thermally stable, and nonreactive with and easily separated from the other components in the mixture. In reaUty some compromise in solvent properties is almost always required. [Pg.190]


See other pages where Solvent propertie is mentioned: [Pg.273]    [Pg.858]    [Pg.270]    [Pg.273]    [Pg.53]    [Pg.149]    [Pg.80]    [Pg.82]    [Pg.30]    [Pg.297]    [Pg.510]    [Pg.512]    [Pg.195]    [Pg.354]    [Pg.362]    [Pg.484]    [Pg.162]    [Pg.104]    [Pg.107]    [Pg.332]    [Pg.13]    [Pg.208]    [Pg.209]    [Pg.311]    [Pg.33]    [Pg.518]    [Pg.28]   
See also in sourсe #XX -- [ Pg.113 , Pg.114 ]




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2-methyltetrahydrofuran solvent properties

Acceptor properties, solvents

Acetic acid solvent properties

Acetone solvent properties

Acetonitrile solvent properties

Acid properties, Lewis, solvents

Amides, from acid derivatives solvent properties

Ammonia, liquid solvent properties

Amphoteric solvents, properties

Aqueous solutions Solvent properties

Base properties, Lewis, solvents

Basic physical and chemical properties of solvents

Biomass properties solvent extraction

Boiling points solvent properties

Carbon dioxide solvent properties

Chemical Properties of Solvents

Chemical process influence solvent properties

Chemical properties of mixed solvents

Chlorinated solvents properties/recovery

Chloroform solvent properties

Chromatographic solvents, properties

Correlations between Empirical Parameters and Other Measurable Solvent Properties

Deep eutectic solvents properties

Desired Properties of Petroleum Solvents

Deuterated solvents properties

Dichloromethane solvent properties

Dielectric properties of solvents

Diethyl ether solvent properties

Dimethyl sulfoxide solvent properties

Dimethylformamide, solvent properties

Donor properties of solvents

Donor properties, solvents

Dynamic properties, solvents

Dynamics and Simulations of Average Solvent Properties

Electrochemical Properties of Water and Selected Organic Solvents

Electroosmotic solvent properties

Enzyme Properties in Organic Solvents

Ethanol solvent properties

Ethanol—continued solvent properties

GEORGE WYPYCH 3 Solvent properties

General properties solvent dynamics

Glycerol solvent properties

HMPA, solvent properties

Hexamethylphosphoramide solvent properties

Hydrocarbons, solvent properties

Hydrogen bonding solvent property scales

Hydrogen halides nonaqueous solvent properties

Inhalant properties volatile solvents

Iodine, as solvent physical properties

Ionic liquids solvent properties

Ionic solvent property

Kamlet-Taft solvent property

Lewis properties, solvents

Methanol solvent properties

Microscopic solvent properties

Microscopic solvent properties protic ionic liquids

Monte Carlo simulation solvent properties

Neoprene rubber solvent properties

Organic ionic liquids solvent properties

Organic solvents electrochemical properties

Organic solvents physical properties

Organic solvents, properties

Other properties affected by solvents

Other typical solvent properties and indicators

Physical Properties of Hydrocarbon Solvents

Physical properties of mixed solvents

Physical properties of solvents

Physical properties of some organic solvents

Physicochemical properties of solvents

Physicochemical properties of the solvents

Polymer HPLC solvents properties

Polymer, chemical property solvent compatibility

Principal properties solvents

Properties of Perfluorinated Solvents

Properties of enzymes affected by organic solvents

Properties of individual solvents

Properties of solvent pairs

Properties of solvents

Properties of supercritical fluids and their uses as solvents

Properties of the Solvent (Matrix Material)

Properties of the Solvent (Matrix)

Properties of the solute and solvent

Properties, Purification, and Use of Organic Solvents

Protic solvents properties

Pyridine, adsorption solvent properties

Redox properties solvent effects

Relation between the complexing power of solvents and their acid-base properties

Relative Solvent Properties of Glycols

Selected solvents, properties

Significance of solvent properties

Solute-solvent interactions property detectors

Solution processing solvents properties

Solutions, formaldehyde Solvent properties

Solvation properties, ionic liquids solvent polarity

Solvatochromic solvent properties scale

Solvatochromic solvent properties scale parameters

Solvent Effect and Aromatic Compounds Magneto-Optic Properties

Solvent Properties Including Polarity

Solvent Properties Related to Their Ion Solvating Ability

Solvent Properties and Structure of Imidazolium ILs

Solvent Properties of CXLs

Solvent Properties of Carbon Dioxide

Solvent Properties of SCFs

Solvent Properties of Supercritical Fluids

Solvent Properties of Water

Solvent Properties that Suit Ion Dissolution

Solvent and Solution Properties

Solvent cation-transport properties

Solvent chemical properties

Solvent continued properties

Solvent coordinating property and electron-donor ability

Solvent dyes, properties

Solvent optical properties

Solvent physicochemical properties

Solvent properties

Solvent properties

Solvent properties and parameters

Solvent properties molecular

Solvent properties of liquid

Solvent properties phosgene

Solvent properties, desirable

Solvent properties, desirable construction materials

Solvent properties, desirable density difference

Solvent properties, desirable environmental requirements

Solvent properties, desirable freezing point

Solvent properties, desirable safety

Solvent properties, desirable solute selectivity

Solvent properties, desirable stability

Solvent properties, desirable viscosity

Solvent properties, pure aqueous solutions

Solvent properties, solution-state nuclear

Solvent property scales

Solvent property scales Drago

Solvent property scales Reichardt

Solvent property scales representative parameters

Solvent spectroscopic properties

Solvent-Related Properties

Solvent-like properties, zeolites

Solvent-property detectors

Solvent-resistant property

Solvents acid-base, properties

Solvents bulk properties

Solvents coordinating properties

Solvents critical properties

Solvents dielectric properties

Solvents electrical properties

Solvents ionizing properties

Solvents physical properties

Solvents properties under microwave

Solvents solution properties

Solvents thermal properties

Solvents thermodynamic properties

Solvents, acceptor properties acidity/basicity

Solvents, acceptor properties conductivity

Solvents, acceptor properties density

Solvents, acceptor properties dipole moment

Solvents, acceptor properties electron pair acceptance

Solvents, acceptor properties hydrogen bond acceptance

Solvents, acceptor properties hydrogen bonded

Solvents, acceptor properties miscibility with water

Solvents, acidic physical properties

Solvents, mixed aqueous acid/base properties

Solvents, organic, fire-hazard properties

Solvents, swelling properties

Some Important Properties of Polar Solvents

Special solvents properties

Subject solvents properties

Supercritical fluid solvents properties

Supercritical solvents, properties

Systematic treatment of solvent properties and mass selectivity

Tetrahydrofuran , solvent properties

The Electronic Properties of Metal Solutions in Liquid Ammonia and Related Solvents

The Physicochemical Properties of Solvents and Their Relevance to Electrochemistry

The Solvent Properties of Adsorbed Water

Thermodynamic Properties of Ions in Mixed Solvents

Thermodynamic properties Polymer-solvent interactions

Thermophysical Properties Required for Selective Solvents

Transport Properties of Ions in Mixed Solvents

Transport properties of supercritical solvents

Water and its Solvent Properties

Water solvent properties

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