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Salt transfer

Glowing embers, brands Drying equipment Molten metal or glass Heat transfer salt Hot oil/salt transfer lines... [Pg.182]

If we are concerned only with the case in which the total mass of salt transferred is small relativetothevolumeofsolventandthesaturationlimit,thentheequationbecomes ... [Pg.212]

X An alternative technique is as follows. Plunge the hot tube into about 10 ml. of water contained in a small, clean mortar and cover the latter immediately with a dean wire gauze. When the reaction is over, grind the mixture of solution and broken glass to ensure thorough extraction of the sodium salts. Transfer with the aid of a little water to a porcelt basin, heat to boiling, and filter. [Pg.1040]

LB films prepared from TCNQ octadecyl-dimethylsulfonium, octadecyl-methyl-ethyl-sulfonium, and octadecyl-trimethyl-phosphonium salts, transferred to substrates, and exposed to iodine vapor Absorption, infrared spectra, and ESR spectra Lateral d.c. conductivity was estimated (from energy of the maximum of the charge transfer absorption band) to be about 20-50 Scm-1 731, 732, 733... [Pg.163]

It is assumed that the rate of salt transfer is proportional to the difference in the average salt concentration of the two passing streams at any level in the column the equations for describing this system may be set up and solved directly with no recourse to graphical analysis. [Pg.102]

In an adiabatic column in which there is 7% salt in the brine at the bottom and essentially no salt at the top, some ice will form as the bed moves upward through the vertical concentration gradient, and this will affect the rate, B, but this effect is small and is ignored below. Following the nomenclature in Figure 7, in the differential height, dLy the rate of salt transfer is... [Pg.102]

L = height of column above screens, feet H = height of a salt transfer unit, feet... [Pg.103]

Maetz, J. (1971). Fish gills mechanisms of salt transfer in fresh water and sea water. Philosophical Transactions of the Royal Society of London B 262,209-249. [Pg.292]

Apart from the above two major general reaction pathways, there are some further possibilities for instance, [bis(trifluoroacetoxy)iodo]benzene reacts as an ambident electrophile and is attacked by hard nucleophiles at its carbonyl carbon, whereas iodylarenes may react similarly from carbon rather than iodine. Alkynyl iodonium salts are actually tetraphilic electrophiles, whereas iodosylbenzene reacts also as a nucleophile from oxygen. Diaryl iodonium salts serve as arylating reagents, mostly homolytically other iodonium salts transfer groups such as perfluoroalkyl, vinyl, alkynyl or cyano to several nucleophiles in various ways. [Pg.6]

Oxoalkyl- and 3-oxoalkyl-triphenylbismuthonium salts transfer the alkyl groups to various hetero nucleophiles such as piperidine, triphenylphosphane, arylsulfinates, alcohols, arylthiolates, dimethyl sulfide, and metal halides under mild conditions (Equation (132)).214 215 Methyl- and allyl-triphenylbismuthonium salts also alkylate some heteronucleophiles.216 The leaving ability of the triphenylbismuthonio group has been found to be higher than that of the triflate anion. [Pg.449]

First we review processes that ordinarily accompany the redox switching of an electroactive polymer. The key step is coupled electron/ion transfer, which converts one or more reduced forms of the polymer to one or more oxidized forms of the polymer. Solvent and neutral species transfers and polymer structural changes (reconfigurations or coordination state changes) accompany the switching process under permselective conditions. Under nonpermselective conditions, salt transfer also occurs [12]. [Pg.494]

Amino Acids Add 1 mL of ninhydrin TS to 5 mL of a 1 1000 aqueous solution, and heat for 3 min. No color appears. Ammonium Salts Transfer about 100 mg of sample into a small test tube, and add 50 mg of magnesium oxide and 1 mL of water. Moisten a piece of red litmus paper with water, suspend it in the tube, cover the mouth of the tube, and heat in a water bath for 5 min. The litmus paper does not change to blue. [Pg.144]

Sample Preparation for Rock and Solar Salts Transfer 50.0 g of sample into a 500-mL volumetric flask, dissolve in 400 mL of water containing 2 mL of hydrochloric acid, dilute to volume with water, and mix. Filter a 50-mL aliquot, then pipet 10.0 mL of the filtrate into a 400-mL beaker, and add 190 mL of water. [Pg.408]

Sample Preparation for Evaporated Salt Transfer 10.0 g of sample into a 400-mL beaker, and dissolve in 100 mL of water. If free-flowing agents are present, filter and rinse quantitatively. Dilute the solution or filtrate to 200 mL with water. [Pg.408]

Test for nitrate (andI or nitrite) If ammonium is found, transfer the solution from test 5 with the aid of 0-5 ml water to a semimicro boiling tube (or crucible), add 0 5 ml sodium hydroxide solution and evaporate down to a volume of about 0-2 ml - this treatment completely decomposes the ammonium salt. Transfer the residue to a semimicro test-tube, rinse the vessel with 0-5 ml sodium hydroxide solution and add this to the contents of the test-tube. Then add 10 mg of Devarda s alloy (or of aluminium powder or thin foil), introduce a Pyrex filter tube provided with a loose plug of cotton wool at the lower end and containing a strip of red litmus paper or mercury(I) nitrate paper (Fig. II.29a), and place the assembly in the hot water rack. If frothing occurs, remove the apparatus from the water bath until the vigorous reaction has subsided. [Pg.467]

The most successful therapy for cholestasis of pregnancy has been ursodeoxycholic acid (Figure 33-1). Ursodeoxycholic acid is a naturally occurring bile acid, which, when administered, relieves both pruritus and liver function abnormalities. Experimental evidence suggests that it protects hepa-tocytes and cholangiocytes from bile acid-induced cytotoxicity and improves hepatobiliary excretion. Additionally, it decreases bile salt transfer to the fetus and improves the secretory function of placental trophoblast cells. Ursodeoxycholic acid is recycled through the enterohepatic circulation. [Pg.306]

A variety of metal salts, transfer agents, complexes and liquids were examined. Some gave higher yields and rates than others and acceptable yields. However, all of them suffered from either no activity, off-line catalyst preparation, tar formation, product contaminated with catalyst or a requirement for a co-solvent. Emulsion and tar formations were troublesome. This resulted in yield loss and contaminated product after difficult work-up procedures that would be unsatisfactory for large-scale production. The best overall result was obtained using sodium molybdate (5 mole%) and tris[2-(2-methoxyethoxy)ethyl]amine 3 (TDA-1, 5 mole %) at 60°C. The yield was >90% and the catalyst system could readily be removed by water washing. [Pg.50]

In the case of cells with transport we have already seen that the actual amount of salt transferred when one faraday passes is less than one gram-equivalent In the case of such a cell, having electrodes reversible with respect to the cation, the fraction of salt transferred is measured by the amount of amon which passes from the strong to the weak solution The amount of salt transferred per faraday is, m feet, vj u + v) of one equivalent, where /(w + 0) is the transport number of the anion In the case of a similar cell with electrodes reversible with respect to the anion, the corresponding fraction is uj(u + 0) Hence to obtain the transfer of one gram-equivalent of salt it is necessary to allow (u + v)jv faradays in the first case, or (u + v)ju faradays m the second case to flow through the cell... [Pg.160]

Chapter 8 Energetics of ionic salt transfer from water to an organic solvent 215... [Pg.215]

Inserting the concentrations given in Figure 6.6(b), we obtain for the amount of salt transferred... [Pg.88]


See other pages where Salt transfer is mentioned: [Pg.843]    [Pg.1040]    [Pg.843]    [Pg.146]    [Pg.425]    [Pg.30]    [Pg.30]    [Pg.150]    [Pg.93]    [Pg.843]    [Pg.406]    [Pg.1150]    [Pg.143]    [Pg.106]    [Pg.93]    [Pg.1150]    [Pg.43]    [Pg.139]    [Pg.391]    [Pg.189]    [Pg.843]    [Pg.217]    [Pg.86]    [Pg.843]   
See also in sourсe #XX -- [ Pg.83 , Pg.84 , Pg.85 , Pg.86 , Pg.87 , Pg.88 , Pg.89 ]




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Amine Salts as Phase-Transfer Catalysts

Ammonium salts as phase transfer catalysts

Ammonium salts, decompositions, proton transfer

Anions as Electron Donors in Charge-Transfer Salts

Asymmetric epoxidation catalyzed by novel azacrown ether-type chiral quaternary ammonium salts under phase-transfer catalytic conditions

Catalysis, phase-transfer by quaternary ammonium salts

Charge transfer salts, carbonylmetallate

Charge transfer salts, carbonylmetallate anions

Charge-transfer complexes and radical ion salts

Charge-transfer salt, organic

Charge-transfer salts

Chiral Onium Salts (Phase-Transfer Reactions)

Crystals of Molecules with Charge Transfer, Radical-ion Salts

Diaryliodonium salt photolysis electron-transfer

Diaryliodonium salts sensitization, electron transfer

Dienes charge transfer salts

Diphenyliodonium salts, electron transfer

Dithiolenes charge transfer salts

Double salts, transference numbers

Electron transfer reaction, radicals with diphenyliodonium salts

Electron-transfer donor-acceptor salts

Energetics of ionic salt transfer from water to an organic solvent

Heat transfer coefficient salt bath temperature effect

Heat transfer salt

Ionic salts transfer from water to organic solvent

Mass transfer salt dissolution

Molten salts mass transfer

Neutral-Ionic Transition in Organic Charge-transfer Salts

Phase Transfer and Ammonium Salt Catalyzed Reactions

Phase transfer ammonium salts

Phase transfer catalysis quaternary salts

Phase transfer catalysts ammonium salts

Phase transfer catalysts onium salts

Phase transfer phosphonium salts

Phase transfer quaternary ammonium salts

Phase-Transfer-Catalyzed Addition of Anion Supplied as Metal Salt

Phase-transfer catalysis conditions quaternary ammonium salt

Phase-transfer catalysts, phosphonium salts

Phase-transfer reagents quaternary ammonium salts

Phosphonium salts, phase transfer catalysis

Polyethylene glycol phosphonium salts phase-transfer catalysts

Pyridinium salts, charge-transfer

Pyridinium salts, charge-transfer donors

Quaternary ammonium salts as phase transfer catalysts

Quaternary ammonium salts as phase-transfer

Quaternary ammonium salts phase-transfer catalysts

Salts electron transfer

Sulfonium salts phase transfer catalysts

Tetraalkylammonium Salts as Phase-Transfer Catalysts

Transfer Complexes and Radical Cation Salts of 1,2-Dichalcogenoles

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