Functionalization solubilization

Therapeutic Function Solubilizer for cholesterol gallstones Chemical Name 3,7-Dihydroxycholan-24-oic acid Common Name Chenodeoxycholic acid chenic acid Structural Formula ... 

A. Ghosh, K.V. Rao, R. Voggu, S. J. George, Non-covalent functionalization, solubilization of graphene and single-walled carbon nanotubes with aromatic donor and acceptor molecules, Chemical Physics Letters, vol. 488, pp. 198-201, 2010. 

In a typical functionalization/solubilization experiment, 2 ml of trialkylamine or trialkylphosphine were added to 5 mg of purified BN nanotubes. The mixture was warmed at 70 °C for 12 h and subsequently sonicated for a few minutes. The functionalized BN... 

Function Solubilizing and stabilizing agent in flavor concentrates. 

Miller GW, Nussenzweig V (1975) A new complement function Solubilization of antigen-antibody aggregates. Proc Natl Acad Sci USA 72 418 22. 

For deliming, ammonium salts and acids are used. The proportion of ammonium salts to acids and the type of acids employed is a matter of the tanner s choice. The acid neutralizes the lime, Ca(OH)2, thereby adjusting the pH. The ammonium salts have two functions to buffer the solution to a pH required for bating, and to form calcium ammonium complexes. The acidity and the complex formation solubilize the calcium and serve to bring the hide to the desired pH. 

The process implications of equation 3 go beyond the weU-known properties (27—29) of NMP to faciUtate S Ar processes. The function of the aminocarboxylate is also to help solubilize the sulfur source anhydrous sodium sulfide and anhydrous sodium hydrogen sulfide are virtually insoluble in NMP (26). It also provides a necessary proton acceptor to convert thiophenol intermediates into more nucleophilic thiophenoxides. A block diagram for the Phillips low molecular weight linear PPS process is shown in Eigure 1. 

At room temperature, ca 60 wt % ethylene oxide is needed to solubilize the fatty acids. Surface activity of the ethoxylates is moderate and less than that of alcohol or alkylphenol ethoxylates (84). The ethoxylates are low foamers, a useful property in certain appHcations. Emulsification is the most important function. Its importance is reflected in the wide range of lipophilic solubiHties available in the commercial products. Like all organic esters, fatty acid ethoxylates are susceptible to acid and alkaline hydrolysis. 

The kinetic mechanism of emulsion polymerization was developed by Smith and Ewart [10]. The quantitative treatment of this mechanism was made by using Har-kin s Micellar Theory [18,19]. By means of quantitative treatment, the researchers obtained an expression in which the particle number was expressed as a function of emulsifier concentration, initiation, and polymerization rates. This expression was derived for the systems including the monomers with low water solubility and partly solubilized within the micelles formed by emulsifiers having low critical micelle concentration (CMC) values [10]. 

The function of emulsifier in the emulsion polymerization process may be summarized as follows [45] (1) the insolubilized part of the monomer is dispersed and stabilized within the water phase in the form of fine droplets, (2) a part of monomer is taken into the micel structure by solubilization, (3) the forming latex particles are protected from the coagulation by the adsorption of monomer onto the surface of the particles, (4) the emulsifier makes it easier the solubilize the oligomeric chains within the micelles, (5) the emulsifier catalyzes the initiation reaction, and (6) it may act as a transfer agent or retarder leading to chemical binding of emulsifier molecules to the polymer. 

The formation of a microphase structure can be sensitively detected by using hydrophobic fluorescent probes. Hydrophobic microdomains tend to solubilize hydrophobic small molecules present together in aqueous solution. For example, diphenylhexatriene (DHT) is hydrophobically bound to the St aggregates in ASt-x in aqueous solution and, as a result, the fluorescence intensity is greatly enhanced. Figure 9 shows the fluorescence intensity of DHT in the presence of ASt-x relative to the intensity in its absence (I/I0) as a function of the ASt-x concentration [29],... 

Bacillus thuringiensis produces a variety of organic compounds which are toxic to the larvae of certain susceptible insect hosts. Among the toxic entities are proteinaceous crystals, probably three soluble toxins, and certain enzymes. The protein material is the major toxin active in killing lepidopterous larvae. The protein is formed by the cells apparently in close synchrony with sporulation, and its nature is a constant function of bacterial strain. The mode of action of the protein is under study. The sequence of events in the pathology observed is probably solubilization of the crystal (enzymatic or physical)—>liberation of toxic unit—>alteration of permeability of larval gut wall— change in hemolymph pH—>invasion of hemolymph by spores or vegetative cells of the bacterium. 

---