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Binary mixtures, preparation

Also obtained from mesityl o-methoxyphenyl ketone (2 -methoxy-2,4,6-trim-ethylbenzophenone) by cleavage of methoxy group with hydriodic acid or with a binary mixture prepared from magnesium and iodine in refluxing toluene/butyl ether solution (poor yield) [1026]. [Pg.182]

Jso-propyl alcohol is very difficult to dry satisfactorily. The water binary mixture, boiling at 80.35°, contains 12.1 per cent of water by weight. The ternary mixture with benzene, boiling at 66.5°, contains 73.8 per cent benzene, 18.7 per cent iso-propyl alcohol and 7.5 per cent water. Hence by adding 120 g. of dry benzene to 100 g. of the iso-propyl-water binary, and distilling off until the temperature reaches 82°, there will remain 55 to 60 g. of nearly dry iso-propyl alcohol. The commercial anhydrous alcohol was used in this preparation. [Pg.108]

Examples considered in this paper deal with binary heteropolymers prepared by the method of chemical modification of homopolymers and by the free-radical copolymerization of a mixture of two monomers, Mi and M2. The products of each of these processes is a mixture of an enormous... [Pg.143]

It has been shown for many metal halides and monomers that binary mixtures of these can be prepared (usually in a solvent) without any polymerization taking place. Such a quiescent mixture can be made to react by the addition of a suitable third compound, which is called the co-catalyst. This term is preferable to the word promoter , because in certain contexts a substance is called promoter which enhances the rate or yield of a reaction that will also go in the absence of the promoter herein lies the true distinction between promoter and co-catalyst [28]. (For example, small quantities of epoxides or epichlorohydrin act as promoters in the cationic polymerization of tetrahydrofuran.) I will take it that in the above quotation the word promoter was inadvertently used in place of co-catalyst , for only thus does it become really meaningful. [Pg.116]

For the titration of LDAO, solutions were made with their pH adjusted to 12 with NaOH and titrated with HCl. Binary mixtures of LDAO and SDS solutions were prepared by mixing different volumes of the surfactant solutions at equal molar concentration. [Pg.130]

Extraction of 25 different binary mixtures of racemic acids (2-(4-isobutylphenyl)-propionic acid (1), and cis- and trans-chrysanthemic (2)), and various chiral bases with supercritical carbon dioxide permitted the conclusion that molecular chiral differentiation in a supercritical fluid is more efficient than in conventional solvents. In the majority of cases, however, complete separation could not be achieved. In five cases, remarkable partial resolutions were realized (30-75% ee) and resolution was possible on a preparative scale. The pair ds-chrysanthemic acid and (S)-(-i-)-2-(benzylamino)-1-butanol (3) was studied in detail. Pressure, temperature, and time, as well as the molar ratio of base and acid, had a marked influence on the quantity and quality of the products. Increasing pressure or decreasing temperature resulted in higher ee values. (-)-cw-Chrysanthemic acid in 99% ee was obtained from the raffinate in a single extraction step. Multiple extractions produced the (-i-)-cA-acid in 90% ee (see fig. 6.3) (Simandi et al., 1997). [Pg.147]

Domain formation in binary mixtures of a polymerizable lipid and non-polymerizable lipid is well established for diacetylenic lipids. The rigid diacetylenic unit facilitates the formation of enriched domains in the condensed phase of monolayers or the solid-analogous phase of bilayers. Since diacetylenes polymerize most readily in solid-like states, most studies have focused on conditions that favor domain formation. Only in the case of a mixture of a charged diacetylenic lipid and a zwitterionic PC was phase separation not observed. Ringsdorf and coworkers first reported the polymerization of a phase-separated two-dimensional assembly in 1981 [33], Monolayer films were prepared from mixtures consisting of a diacetylenicPC (6) (Fig. 5) and a nonpolymerizable distearoyl PE (DSPE). [Pg.61]

Similar results were also found for penicillin amidase-catalyzed transesterification of phenoxyacetate methyl ester with 1-propanol in hexane (Scheme 3.5) [46]. The initial rates of various penicillin amidase preparations containing acetate or chloride salts and their 1 1 binary mixtures were measured, which resulted in the identification of formulations with various degrees of activation. For example, the... [Pg.64]

Binary mixtures of charcoal with sulphur or with saltpetre, being insensitive to friction and impact, are prepared in iron ball mills composed of drums (1.2 m dia. and 1.5 m in length) with bronze balls. The drums (Fig. 91) are fitted inside with... [Pg.348]

Separate drums should be used for the preparation of these binary mixtures. Special care must be taken to ensure that the container for the sulphur mixture is properly sealed, otherwise the sulphur which has been finely milled and heated on milling may oxidize and even ignite in contact with air. [Pg.348]

Occasionally, a single solvent does not provide suitable resolution of solutes. Solvent binary mixtures can be prepared with eluent strengths intermediate between the e° values for the individual solvents. [Pg.96]

The binary mixture of A1C13 and NaCl is the alkali metal chloroaluminate most commonly used as an electrochemical solvent. The preparation, purification, and general properties of this and several related inorganic chloroaluminate systems have... [Pg.517]

Colourless liquid spirituous odour miscible with water in all proportions binary mixture with water contains 75-57% alcohol, and boils at 78-1° at 760 mms. B.P. 760 pure alcohol, 78-3° B.P. 2113° D. 0-790. It forms a ternary mixture with benzene and water, and this property is utilised in the manufacture of industrial absolute alcohol. (J. C. S., 81, 707 see Preparation 198 B., 38, 3612.)... [Pg.214]

When copolymers are prepared by the free-radical initiation of reactions of irradiated cellulose (on which the free-radical site is located) with binary mixtures of vinyl monomers, fractionation of cellulose and... [Pg.336]

Recently, scanning electron microscopy has been used in our laboratory to investigate the effects of abrasion on the morphology of fibrous cellulose copolymers (36). For example, cotton cellulose was woven into fabric form (print cloth construction and weight). Cellulose copolymer fabrics were prepared by irradiating a sample of this fabric, followed by copolymerization of the irradiated fabric with a binary mixture of acrylo-... [Pg.338]

The WRMs are binary mixtures of C02 in nitrogen for each one the concentration with its uncertainty are certified by the supplier. The comparison of WRMs with PRMs was carried out in the range 300 500 mol/mol. PRMs used were supplied by a COFRAC accredited laboratory and were gravimetrically prepared mixtures of C02 in nitrogen. Each cylinder is accompanied by a certificate of analysis which reports the concentration and its uncertainty as provided by the analytical verification of the mixture. [Pg.227]

Large negative values d- values for a binary mixtures with cyclohexane indicates the existence of weak interactions due mainly to dispersion forces. Higher, positive d-values for the mixtures prepared with p - xylene and mesitylene seem to be due to enhanced dipole interactions on account of higher polarizability of the methyl substituted benzenes (negative value for Wvisc)-... [Pg.35]


See other pages where Binary mixtures, preparation is mentioned: [Pg.275]    [Pg.275]    [Pg.144]    [Pg.219]    [Pg.93]    [Pg.144]    [Pg.322]    [Pg.752]    [Pg.231]    [Pg.341]    [Pg.301]    [Pg.27]    [Pg.173]    [Pg.892]    [Pg.125]    [Pg.184]    [Pg.514]    [Pg.638]    [Pg.679]    [Pg.257]    [Pg.271]    [Pg.89]    [Pg.34]    [Pg.144]    [Pg.382]    [Pg.475]    [Pg.169]    [Pg.344]    [Pg.485]    [Pg.67]    [Pg.168]    [Pg.496]   
See also in sourсe #XX -- [ Pg.24 ]




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