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Water-rich acids

A clean-up process-scale RP-HPLC step has been introduced into production of human insulin prb. The C8 or C18 RP-HPLC column used displays an internal volume of 80 1 or more, and up to 1200 g of insulin may be loaded during a single purification run (Figure 11.4). Separation is achieved using an acidic (often acetic-acid-based) mobile phase (i.e. set at a pH value sufficiently below the insulin pi value of 5.3 in order to keep it fully in solution). The insulin is usually loaded in the water-rich acidic mobile phase, followed by gradient elution using acetonitrile (insulin typically elutes at 15-30 per cent acetonitrile). [Pg.297]

Water rich acids (e.g. methyl methacrylate spent acid) often have part of their water evaporated before they are sent to the H2S04 decomposition furnace (Rohm and Haas, 2003). This decreases ... [Pg.49]

The structure of cholic acid helps us understand how bile salts such as sodium tauro cholate promote the transport of lipids through a water rich environment The bot tom face of the molecule bears all of the polar groups and the top face is exclusively hydrocarbon like Bile salts emulsify fats by forming micelles m which the fats are on the inside and the bile salts are on the outside The hydrophobic face of the bile salt associates with the fat that is inside the micelle the hydrophilic face is m contact with water on the outside... [Pg.1098]

On the Brpnsted theory (p. 51), solutions with concentrations of H3O+ greater than that in pure water are acids (proton donors), and solutions rich in OH are bases (proton acceptors). The same classifications follow from the solvent-system theory of acids and bases... [Pg.628]

Richardson SD, AD Thurston, C Rav-Acha, L Groisman, 1 Popilevsky, O Juraev, V Glezer, AB McKague, Ml Plewa, ED Wagner (2003) Tribromopyrrole, brominated acids, and other disinfection byproducts produced by disinfection of drinking water rich in bromide. Environ Sci Technol 37 3782-3793. [Pg.46]

Brown and Bellinger [123] have proposed an ultraviolet technique that is applicable to both polluted and unpolluted fresh and some estuarine waters. Humic acid and other organics are removed on an ion exchange resin. Bromide interference in seawater samples can be minimised by suitable dilution of the sample but this raises the lower limit of detection such that only on relatively rich (0.5 mg/1 NO3N) estuarine and inshore waters could the method be used. Chloride at concentrations in excess of 10 000 mg/1 do not interfere. [Pg.85]

Fig. 5 Schematic representation of locations of a weakly acidic indicator, , adjacent to the cationic head groups, , and of a functional hydroxyl group in the water-rich region... Fig. 5 Schematic representation of locations of a weakly acidic indicator, , adjacent to the cationic head groups, , and of a functional hydroxyl group in the water-rich region...
The results are straight forward and the interpretation immediately evident. The liquid crystalline phase formed in these extremely water rich systems was destabilized by the dicarboxylic acid and transformed to an isotropic solution. The conclusion that the hydrotropic action of the dicarboxylic acid is intimately related to its capacity to destabilize a liquid crystalline phase also under the water-rich conditions during actual laundering conditions appears well justified. [Pg.111]

Sridharan and Mathai noticed that the transesterification of small esters under acid-catalyzed conditions was retarded by the presence of spectator polar compounds. " Thus, given that water can form water-rich clusters around protons (solvent-proton complexes) with less acid strength than methanol-only proton complexes, some catalyst deactivation may be expected with increased water concentrations. Also, water-rich methanol proton complexes should be less hydrophobic than methanol-only clusters, thus making it more difficult for the catalytic species (H" ) to approach the hydrophobic TG (and possibly DG) molecules and contributing to catalyst deactivation. Therefore, with water present in the feedstock or produced during the reaction in significant quantities, some catalyst deactivation can take place by hydration. [Pg.69]

The titration of very weak acids and bases requires the use of strongly acidic or basic solutions. The determination of thermodynamic pKs is considerably more difficult in these media than in water-rich solutions. Thus, problems are always met when attempting to evaluate activity terms. Also, spectrophoto-metric and NMR titrations are frequently subject to perturbations induced by large changes in solvent composition. [Pg.207]


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See also in sourсe #XX -- [ Pg.47 ]




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Spent water-rich acids

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