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Structure in an Aqueous Solution

13C NMR spectra of the inulooligosaccharides 1-kestose (GF2) and nystose (GF3) have also been assessed (Jarrell et al., 1979), as have the II and 13C chemical shifts of 1-kestose (Calub et al., 1990), nystose (Liu et al., 1993 Timmermans et al., 1993a), and 1,1,1-kestopentaose (GF4) [Pg.61]

Biology and Chemistry of Jerusalem Artichoke Helianthus tuberosus L. [Pg.62]

Physical and Chemical Characteristics of Inulin (Chicory) A High-DP Fraction and Oligofructose [Pg.62]

Appearance White powder White powder White powder [Pg.62]

Source. Adapted from Franck, A., Br. J. Nutr.y 87, S287-S291, 2002. [Pg.62]


A simplified micelle structure in an aqueous solution is shown in Figure 3. [Pg.133]

It has been reported that protein-free, lipid-pigment extracts from chlorosomes can spontaneously reform chlorosome-like structures in an aqueous solution. ... [Pg.150]

An amphiphilic block copolymer with a precisely hydrophilic/hydrophobic balance can form a core-shell micelle structure in an aqueous solution. The hydrophobic inner core can encapsulate the hydrophobic drugs and the high drug-loading capacity has been applied to an excellent drug carrier (Fig. 2.1.2) [36-38]. Kataoka et al. have reported various... [Pg.9]

One anomaly inmrediately obvious from table A2.4.2 is the much higher mobilities of the proton and hydroxide ions than expected from even the most approximate estimates of their ionic radii. The origin of this behaviour lies in the way hr which these ions can be acconmrodated into the water structure described above. Free protons cannot exist as such in aqueous solution the very small radius of the proton would lead to an enomrous electric field that would polarize any molecule, and in an aqueous solution the proton inmrediately... [Pg.574]

But when the reaction is carried out in an aqueous solution of sodium hydrogen carbonate, extension of the ring occurs with formation of dihydro-l,4-thiazine derivative (Scheme 19). the structure of which has been established by mean of NMR and infrared spectra (41). [Pg.36]

In principle, cathodic protection can be used for a variety of applications where a metal is immersed in an aqueous solution of an electrolyte, which can range from relatively pure water to soils and to dilute solutions of acids. Whether the method is applicable will depend on many factors and, in particular, economics — protection of steel immersed in a highly acid solution is theoretically feasible but too costly to be practicable. It should be emphasised that as the method is electrochemical both the structure to be protected and the anode used for protection must be in both metallic and electrolytic contact. Cathodic protection cannot therefore be applied for controlling atmospheric corrosion, since it is not feasible to immerse an anode in a thin condensed film of moisture or in droplets of rain water. [Pg.199]

Recently, Farrel and Oliveria200 have studied the behaviour of cis-[RuCl2(Me2SO)4] and [Ru(Me2SO)6](BF4)2 in an aqueous solution. The crystal structure of the former shows that three Me2SO ligands are S-bound and one is O-bound. [Pg.568]

As a result of the micellar environment, enzymes and proteins acquire novel conformational and/or dynamic properties, which has led to an interesting research perspective from both the biophysical and the biotechnological points of view [173-175], From the comparison of some properties of catalase and horseradish peroxidase solubilized in wa-ter/AOT/n-heptane microemulsions with those in an aqueous solution of AOT it was ascertained that the secondary structure of catalase significantly changes in the presence of an aqueous micellar solution of AOT, whereas in AOT/n-heptane reverse micelles it does not change. On the other hand, AOT has no effect on horseradish peroxidase in aqueous solution, whereas slight changes in the secondary structure of horseradish peroxidase in AOT/n-heptane reverse micelles occur [176],... [Pg.489]

Hollow and porous polymer capsules of micrometer size have been fabricated by using emulsion polymerization or through interfacial polymerization strategies [79,83-84, 88-90], Micron-size, hollow cross-linked polymer capsules were prepared by suspension polymerization of emulsion droplets with polystyrene dissolved in an aqueous solution of poly(vinyl alcohol) [88], while latex capsules with a multihollow structure were processed by seeded emulsion polymerization [89], Ceramic hollow capsules have also been prepared by emulsion/phase-separation procedures [14,91-96] For example, hollow silica capsules with diameters of 1-100 micrometers were obtained by interfacial reactions conducted in oil/water emulsions [91],... [Pg.515]

As an example we consider the Au(100) surface of a single crystal Au electrode [3]. This is one of the few surfaces that reconstruct in the vacuum. The perfect surface with its quadratic structure is not thermodynamically stable it rearranges to form a denser lattice with a hexagonal structure (see Fig. 15.3), which has a lower surface energy. In an aqueous solution the surface structure depends on the electrode potential. In sulfuric acid the reconstructed surface is observed at potentials below about 0.36 V vs. SCE, while at higher potentials the reconstruction disappears, and the perfect quadratic structure is ob-... [Pg.199]

UV absorption maxima occur at 236, 274 and 316 nm. The molecular formula of zearalenone is C18H22Os, its molecular weight is 318.4 g/mol and its melting point is 162-163°C (Blackwell et al. 1985 Josephs et al. 2003). The maximum fluorescence in ethanol occurs with irradiation at 314 nm and with emission at 450 nm. Its solubility in water is about 0.002 g/100 ml. In an aqueous solution of inositol, the presence of zearalenone can change the crystal structure of this alcohol, which indicates the possibility of interaction between both substances (our observations). Moreover, zearalenone is slightly soluble in hexane and progressively more so in benzene, acetonitrile, methylene chloride, methanol, ethanol and acetone. However, it is readily soluble in aqueous alkali. [Pg.422]

A wide structural variation is possible within each class of molecules because both the length of the hydrophobic portion and the nature of the hydrophilic head group, as well as its position along the backbone, may be varied. The properties of the aggregates formed from these surfactants and the conditions under which they are formed depends on all these parameters. As the concentration of the surfactant in an aqueous solution is increased, many of the chemical and physical properties of the solution change rather abruptly (but continuously) over a concentration range known as the critical micelle concentration (CMC). [Pg.160]

A tunneling junction device was used to determine the water structure at the mercury electrode in an aqueous solution of 0.25MHg2 (N03)2 + 0.3M HNO3. It was found that the structure of water domains is the same as that of hexagonal ice. Hydrogen bonding is a dominant, structuredetermining factor in liquid water near the mercury electrode surface. ... [Pg.29]

Photolytic. Based on data for phenol, a structurally related compound, an aqueous solution containing 1-naphthoxide ion (3 x 10 M) in room light would be expected to photooxidize to give 2-hydroxy-1,4-naphthoquinone (Tomkiewicz et al., 1971). 1-Naphthol, methyl isocyanate, and other unidentified cholinesterase inhibitors were reported as products formed from the direct photolysis of carbaryl by sunlight (Wolfe et al., 1976). In an aqueous solution at 25 °C, the photolysis half-life of carbaryl by natural sunlight or UV light (X = 313 nm) is 6.6 d (Wolfe et al, 1978a). [Pg.248]

An effort has also been made to determine the structure of products providing coloration in the Maillard reaction prior to melanoidin formation. The reaction between D-xylose and isopropylamine in dilute acetic acid produced 2-(2-furfurylidene)-4-hydroxy-5-methyl-3(2/f)-furanone (116). This highly chromophoric product can be produced by the combination of 2-furaldehyde and 4-hydroxy-5-methyl-3(2//)-furanone (111) in an aqueous solution containing isopropylammonium acetate. The reaction between o-xylose and glycine at pH 6, under reflux conditions, also pro-duces " 116. Other chromophoric analogs may be present, including 117,... [Pg.322]

Structure even in an organic solvent similar to the native DNA in an aqueous solution. [Pg.62]


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Solute structure

Structural solutions

Structure in aqueous solution

Structure in solution

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