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Solutions cont solutes

The p-acetamidobenzenesulphonyl chloride (Section IX,9) must be pure under no circumstances should it contain more than 1-2 per cont. of the corresponding sulphonic acid. This may be ensured by lixiviating the sulphonyl chloride with pure anhydrous acetone and filtering the solution from the acid. [Pg.1008]

Summary Problem—cont d An electrolytic cell contains an aqueous solution of chromium(III) nitrate at 25°G Assume that chromium... [Pg.506]

Potential of zero charge cont.) contribution of the solvent, 158 Conway and Colledan, and the determination of, 34 on copper, and aqueous solution, 89 crystal phase and, 44 crystal face specificity of, 21 and the crystal surface specificity, 152 DeLevie, on the effect of the density of broken bonds on, 75 dependence upon crystal phase, 154 dependence upon time of measurement, 150,151... [Pg.639]

Kharkar DP, Thomson J, Turekian KK, Forster WO (1976) Uranium and thorium series nuclides in plankton from the Caribbean. Limnol Oceanogr 21 294-299 Krishnaswami S, Lai D, Somayajulu BLK, Weiss R, Craig H (1976) Large-volume in situ filtration of deep Pacific waters mineralogical and radioisotope studies. Earth Planet Sci Lett 32 420-429 Livingston HD, Cochran JK (1987) Determination of transuranic and thorium isotopes in ocean water in solution and in filterable particles. J Radioanal Nucl Chem 115 299-308 Masque P, Sanchez-Cabeza JA, Braach JM, Palacios E, Canals M (2002) Balance and residence times of °Pb and 4 o in surface waters of the northwestern Mediterranean Sea. Cont Shelf Res 22 2127-2146 Matsumoto E (1975) Th-234-U-238 radioactive disequilibrium in the surface layer of the oceans. Geochim Cosmochim Acta 39 205-212... [Pg.490]

Guillemin, C. L., Problems and proposed solutions for on-line process liquid chromatography the software-driven chromatograph, Proc. Cont. Qua ., 1, 23, 1990. [Pg.95]

A. Ethyl Nitrite.—Two solutions are prepared. Solution I contains 620 g. (9 moles) of sodium nitrite (650 g. of technical 95 per cent), 210 g. (4.57 moles) of alcohol (285 cc. of 90 per cent denatured, or its equivalent) and water to make a total volume of 2500 cc. Solution II contains 440 g. of sulfuric acid (255 cc. of sp. gr. 1.84) and 210 g. of alcohol, diluted with water to 2500 cc. Ethyl nitrite may he generated cont inuously in gaseous form by allowing solution II to (low into solution I. [Pg.12]

Solution, steps of purification of (cont.) by scavenging, 1093 by UV radiation, 1093 Solvation, 964... [Pg.50]

Correct answer D. in proteins found in aqueous solutions, the side chains ot the nonpolar amino acids,. tfi. otoucme tend to duster together in the interior of the protein. G -nmeiecontans an amide in its side chains. Seme and threonine contains a hydroxyl group in their side chain. Cysteine can form (teUfide bonds. Gtyune conte s the smalest side chain. [Pg.12]

Having accomplished the homogenization of the sample, extraction of free amino acids is usually a simple process of stirring the sample in an appropriate solvent. This is typically a dilute solution (0. IN) of hydrochloric acid (2,7). Elevated temperatures may be used to assist dissolution, but care must be taken not to damage the more acid-labile amino acids. More recently, Moret and Conte (8) report that 0.1N HC1 was not a suitable solvent for all types of food samples. For some types of meat samples, 5% trichloroacetic acid is reported to afford superior performance (for biogenic amines, also amino acids ). It is not unusual to see perchloric acid employed for extraction from meat tissues (also more commonly for biogenic amines). [Pg.60]

Three different viewpoints on the humic substances structural conformation are actually reported in the literature. One suggests that HS are macromolecular and assume random coil conformations in solution (Swift, 1999) a second proposes that HS are molecular associations of relatively small molecules held together by weak interaction forces, thus forming a supramolecular structure (Piccolo and Conte, 1999) a third considers that HS are in solution as micelles or pseudomicellar structures (Wershaw, 1999). Viewpoints two and three could be broadly considered to be under the same umbrella (Clapp and Hayes, 1999). [Pg.307]

Conte, P., and Piccolo, A. (1999). Conformational arrangement of dissolved humic substances. Influence of solution composition on association of humic molecules. Environ. Sci. Technol. 33(10), 1682-1690. [Pg.829]

NATIONAL (cont.) solution heat treatment contact cooling water 13.10 6.518 ... [Pg.278]

Bortolini, O., M. Carraro, V. Conte, and S. Moro. 1999. Histidine-containing bisper-oxovanadium(V) compounds Insight into the solution structure by an ESI-MS and 51V-NMR comparative study. Eur. J. Inorg. Chem. 1489-1495. [Pg.27]

Conte, V., O. Bortolini, M. Carraro, and S. Moro. 2000. Models for the active site of vanadium-dependent haloperoxidases Insight into the solution structure of peroxo-vanadium compounds. J. Inorg. Biochem. 80 41 -9. [Pg.27]

Conte, V., F. Di Furia, and S. Moro. 1994. 51V NMR investigation on the formation of peroxo vanadium complexes in aqueous solution Some novel observations. J. Mol. Catal. 94 323-333. [Pg.97]

Figure 3.31 As (due to orientational response of aqueous solvent) versus e, calculated for ET in a large binuclear transition metal complex (D (Ru2+/3+) and A (Co2+/3+) sites bridged by a tetraproline moiety) molecular-level results obtained from a nonlocal polarization response theory (NRFT, solid lines) continuum results are given by dashed lines, referring to numerical solution of the Poisson equation with vdW (cont./vdW) and SAS (cont./SAS) cavities, or as the limit of the NRFT results when the full k-dependent structure factor (5(k)) is replaced by 5(0) 5(k) for bulk water was obtained from a fluid model based on polarizable dipolar spheres (s = 1.8 refers to ambient water (square)). For an alternative model based on TIP3 water (where, nominally, 6 = ), ambient water corresponds to the diamond. (Reprinted from A. A. Milishuk and D. V. Matyushov, Chem Phys., 324, 172. Copyright (2006), with permission from Elsevier). Figure 3.31 As (due to orientational response of aqueous solvent) versus e, calculated for ET in a large binuclear transition metal complex (D (Ru2+/3+) and A (Co2+/3+) sites bridged by a tetraproline moiety) molecular-level results obtained from a nonlocal polarization response theory (NRFT, solid lines) continuum results are given by dashed lines, referring to numerical solution of the Poisson equation with vdW (cont./vdW) and SAS (cont./SAS) cavities, or as the limit of the NRFT results when the full k-dependent structure factor (5(k)) is replaced by 5(0) 5(k) for bulk water was obtained from a fluid model based on polarizable dipolar spheres (s = 1.8 refers to ambient water (square)). For an alternative model based on TIP3 water (where, nominally, 6 = ), ambient water corresponds to the diamond. (Reprinted from A. A. Milishuk and D. V. Matyushov, Chem Phys., 324, 172. Copyright (2006), with permission from Elsevier).
Fig. 11 Three-dimensional structures of epothilones determined in different environments (O red, S yellow, N dark blue). Top structures of free EpoA determined by X-ray crystallography from dichloromethane/petroleum ether (top left [9 8] (a)) and from methanol/water (top right [143](b)). Bottom structures of EpoA bound to tubulin determined by solution NMR in aqueous medium (bottom left [96]) and by electron crystallography from zinc-stabilized tubulin sheets (bottom right [26]).(a) The crystal structure data have been available from the author to interested research groups since October 1995.(b) H.-J. Hecht, G. Hofle, unpublished results CCDC 241333 and CCDC 241334 contain the crystallographic data of this structure. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retiieving.html (or from the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB2 1EZ, UK fax (+ 44) 1223-336-033 or deposit cede. cam. ac. uk)... Fig. 11 Three-dimensional structures of epothilones determined in different environments (O red, S yellow, N dark blue). Top structures of free EpoA determined by X-ray crystallography from dichloromethane/petroleum ether (top left [9 8] (a)) and from methanol/water (top right [143](b)). Bottom structures of EpoA bound to tubulin determined by solution NMR in aqueous medium (bottom left [96]) and by electron crystallography from zinc-stabilized tubulin sheets (bottom right [26]).(a) The crystal structure data have been available from the author to interested research groups since October 1995.(b) H.-J. Hecht, G. Hofle, unpublished results CCDC 241333 and CCDC 241334 contain the crystallographic data of this structure. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retiieving.html (or from the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB2 1EZ, UK fax (+ 44) 1223-336-033 or deposit cede. cam. ac. uk)...
Alongi, D.M., Tirendi, F., and Christoffersen, P. (1993) Sedimentary profiles and sediment-water solute exchange of iron and manganese in reef- and river-dominated shelf regions of the Coral Sea. Cont. Shelf Res. 13, 287-305. [Pg.538]

Popov, V. M., "The Solution of a New Stability Problem for Controlled-Subsystems," Automation and Rem. Cont., 1963,... [Pg.115]

The feasibility of Ru as a permanent modi her for the determination of Cd in biological samples treated with TMAH by ET-AAS was investigated [10]. The sample dissolution procedure was very simple a sample aliquot was mixed with a small volume of a 25 percent TMAH solution, the volume was made up to 50 mL and the mixture was kept at 60°C for 1 h. Four biological CRMs (DOLT-2, DORM-1, LUST-1, and TORT-2) were analyzed and the obtained Cd concentrations were within the 95 percent cont>dence interval of the certified values. [Pg.22]

Figure 4.2 (cont.) (b) Dry spinning a stream of hot air impinges on the jets of solution emerging from the spinneret, evaporates the solvent, and leaves the solid filaments. [Pg.62]

Yoshida, N. H. and Roberts, M. S. Solute molecular size and transdermal iontophoresis across excised human skin. J. Cont. Rel. 25 177, 1993. [Pg.341]

AUer, R. C., Mackin, J. E., UUman, W. J., Wang, C., Tsai, S., Jin, J., Sui, Y., and Hong, J. (1985). Early chemical diagenesis, sediment—water solute exchange, and storage of reactive organic matter near the mouth of the Changjiang, East China Sea. Cont. Shelf Res. 4, 227—251. [Pg.292]

The next task is to add to each well, 55 pL of solution A or B (i.e., without or with antibody). Since the accuracy of the assay depends on the accuracy of pipeting, some care is advisable, especially since solutions A and B cont n protein and detergent that cause the solution to wet the pipet tips (see Note 5). [Pg.332]

Carcassi, M., Cerchiara, G., Marangon, A. (2004). Experimental studies of gas vented explosion in real 1) 6 environment. In "Hydrogen Power - Theoretical and Engineering Solutions, Proc. H) othesis V, Porto Conte 2003" (Marini, M., Spazza-fumo, G., eds.), pp. 589-597. Servizi Grafici Editoriali, Padova. [Pg.409]


See other pages where Solutions cont solutes is mentioned: [Pg.213]    [Pg.294]    [Pg.529]    [Pg.295]    [Pg.140]    [Pg.97]    [Pg.409]    [Pg.41]    [Pg.388]    [Pg.311]    [Pg.404]    [Pg.393]    [Pg.317]    [Pg.413]   


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Activity (Cont solute

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Solution (Cont

Solutions (cont concentrated solution

Solutions (cont concentration

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Solutions (cont dilution

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Solutions (cont saturated solution

Solutions (cont solids

Solutions (cont solution formation

Solutions (cont solvent

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