Poly sodium

Sodium poly(acrylamido-2-methyl-2-propane sulfonic acid)... 

Sodium Poly(4-styrene sulfonate). The sol—gel processing of TMOS in the presence of sodium poly-4-styrene sulfonate (NaPSS) has been used to synthesize inorganic—organic amorphous complexes (61). These sodium siUcate materials were then isotherm ally crystallized. The processing pH, with respect to the isoelectric point of amorphous siUca, was shown to influence the morphology of the initial gel stmctures. Using x-ray diffraction, the crystallization temperatures were monitored and were found to depend on these initial microstmctures. This was explained in terms of the electrostatic interaction between the evolving siUcate stmctures and the NaPSS prior to heat treatment at elevated temperatures. 

Sodium poly(a-L-glutamate). It was washed with acetone, dried, dissolved in water and ppted with isopropanol at 5°. Impurities and low molecular weight fractions were removed by dialysis of the aqueous solution for 50h, followed by ultrafiltration through a filter impermeable to polymers of molecular weights greater the 10. The polymer was recovered by freeze-drying. [Mori et al. J Chem Soc, Faraday Trans I 2583 1978.]... 

Webber et al. [60, 78] also studied the fluorescence quenching of diphenylan-thracene (DPA) covalently bound to poly(methacrylic acid), PMAvDPA (23) [60], and to sodium poly(styrenesulfonate), PSSvDPA (24 )[78]. The fluorescence quenching of the excited DPA moiety by MV2+ and Cu2+ was also highly efficient. For example, with PMAvDPA of 0.073 mol% DPA content, the kq values at pH... 

Li Jiang, Dahong Yang, and Shing Bor Chen. Electroviscous Effects of Dilute Sodium Poly(styrenesulfonate) Solutions in Simple Shear Flow. Macromolecules 2001, 34, 3730-3735. 

Chelation of the divalent cation Ca to alginate chains has been studied extensively. The negative c.d. band at 205 nm for aqueous solutions of sodium poly-(L-gulopyranuronate) (called the tttt band rather than the WTT band in this early paper) loses negative intensity as Ca " is added (see Fig. 24). This change is equivalent to gaining positive c.d. intensity for a... 

It is convenient to include under Aromatic Amines the preparation of m-nitroaniline as an example of the selective reduction of one group in a polynitro compound. When m-diuitrobenzene is allowed to react with sodium poly-sulpliide (or ammonium sulphide) solution, only one of the nitro groups is reduced and m-nitroaniline results. Some sulphur separates, but the main reaction is represented by ... 

Hydrophobic side chain polyamides from N,N-didodecylamine and sodium poly aery late or polyacrylic acid [1240]... 

Many synthetic water-soluble polymers are easily analyzed by GPC. These include polyacrylamide,130 sodium poly(styrenesulfonate),131 and poly (2-vinyl pyridine).132 An important issue in aqueous GPC of synthetic polymers is the effect of solvent conditions on hydrodynamic volume and therefore retention. Ion inclusion and ion exclusion effects may also be important. In one interesting case, samples of polyacrylamide in which the amide side chain was partially hydrolyzed to generate a random copolymer of acrylic acid and acrylamide exhibited pH-dependent GPC fractionation.130 At a pH so low that the side chain would be expected to be protonated, hydrolyzed samples eluted later than untreated samples, perhaps suggesting intramolecular hydrogen bonding. At neutral pH, the hydrolyzed samples eluted earlier than untreated samples, an effect that was ascribed to enlargement... 

Mori, S., Secondary effects in aqueous size exclusion chromatography of sodium poly(styrene sulfonate) compounds, Anal. Chem., 61, 530, 1989. 

The only example to date of direct addition of a carbohydrate residue to a peptide chain was the coupling72 of 2-acetamido-4-0-(2-acetamido-2-deoxy-/ -D-glucopyranosyl)-2-deoxy-/ -D-glucopyranosylamine (37) with sodium poly(L-aspartate) in the presence of 3-(3-dimethylamino-propyl)-l-ethylcarbodiimide hydrochloride.73 The proportion of sugar residues introduced into the peptide chain was limited. 

Controlling fluid loss loss is particularly important in the case of the expensive high density brine completion fluids. While copolymers and terpolymers of vinyl monomers such as sodium poly(2-acrylamido-2-methylpropanesulfonate-co-N,N-dimethylacrylamide-coacrylic acid) has been used (H)), hydroxyethyl cellulose is the most commonly used fluid loss additive (11). It is difficult to get most polymers to hydrate in these brines (which may contain less than 50% wt. water). The treatment of HEC particle surfaces with aldehydes such as glyoxal can delay hydration until the HEC particles are well dispersed (12). Slurries in low viscosity oils (13) and alcohols have been used to disperse HEC particles prior to their addition to high density brines. This and the use of hot brines has been found to aid HEC dissolution. Wetting agents such as sulfosuccinate diesters have been found to result in increased permeability in cores invaded by high density brines (14). 

Thinners and dispersants are used to prevent excessive flocculation of clay particles and maintain pumpability of the fluid. Tannins, various lignosulfonate salts, sodium tetraphosphate and other phosphates, and synthetic polymers such as sodium poly(styrene sulfonate-co-maleic anhydride) have been used. 

Certain mixtures of polymers have been shown to form complexes which exhibit substantially higher than expected solution viscosity under low shear conditions. Xanthan gum blends with guar gum (38, 39), sodium poly(styrene sulfonate) (40), polyacrylamide (41), sulfonated guar gum (38), sodium poly(vinylsulfonate) (40), hydrolyzed sodium poly(styrene sulfonate-co-maleic anhydride) (38), and poly(ethylene oxide) (41) and blends of xanthan gum and locust bean gum have exhibited substantially higher than expected solution viscosity (42, 43). 

Nitrobenzenediazonium salts [25910-37-6] (ion) N III N+ Sodiiun disulfide, or Sodium poly sulfide See DIAZONIUM SULFIDES AND DERIVATIVES c6h4n3o2z... 

This group of synthetic elastomers is better known under the trade name ThiokoP. Polysulphide rubbers are condensation polymers of sodium poly sulphide and dichloro-compounds they have outstanding resistance to swelling by oils and solvents but tensile strength is... 

Adsorption of sodium poly(styrenesulfonate) from aqueous NaCl solutions onto a platinum plate at 25 °C was studied by ellipsometry as functions of molecular weight and concentration of NaCl. 

For homopolyelectrolyte, we first studied the ellipsometric measurement of the adsorption of sodium poly(acrylate) onto a platinum plate as a function of added sodium bromide concentration (5). We measured the effect of electrolyte on the thickness of the adsorbed layer and the adsorbances of the polyelectrolyte. It was assumed that the Donnan equilibrium existed between the adsorbed layer and the bulk phase. The thickness was larger and the adsorbance of the polyelectrolyte was lower for the lower salt concentration. However, the data on the molecular weight dependence of both the adsorbance and the thickness of the adsorbed polyelectrolyte have been lacking compared with the studies of adsorption of nonionic polymers onto metal surfaces (6-9). 

Materials. Four samples of sodium poly(styrenesulfonate) (NaPSS) prepared by sulfonation of polystyrenes with narrow molecular weight distribution were purchased from Pressure Chemical Co. The characteristics of the samples, according to the manufacturer, are listed in Table I. The intrinsic viscosities of NaPSS in aqueous NaCl solution were measured using an Ubbelhode viscometer at 25 °C. 

The product of the fusion of silica with sodium carbonate, sodium silicate (strictly called sodium poly trioxosilicate but usually metasilicate), dissolves in water to give a clear, viscous solution known as waterglass . It hydrolyses slowly and silica is precipitated. Besides the metasilicate, other silicates of sodium are known, e.g. the poly-tetroxosilicate (orthosilicate), Na4Si04. Only the silicates of the alkali metals are soluble in water. Other silicates, many of which occur naturally, are insoluble, and in these substances the polysilicate anions can have highly complicated structures, all of which are constructed from a unit of one silicon and four oxygen atoms arranged tetrahedrally (cf. the structure of silica). Some of these contain aluminium (the aluminatesilicates) and some have import ant properties and uses. 

As the AO with a direct nonspecific mechanism of action we have chosen Hypoxene - sodium poly(2,5-dihydroxiphenyl)-4-thiosulfonate. Besides a direct AO effect as a scavenger of free radicals it exerts an anti-hypoxic effect shunting I and II complexes of mitochondrial respiratory chain, which are inhibited as a consequence of hypoxia (Eropkin et al., 2007). Hypoxene was introduced into cell incubation media before illumination and left during cells further incubation. Hypoxene in the concentration of 40pg/ml, comparable to doses applied in vivo, completely blocked C60-induced phototoxicity (Table 7.3). Cellular viability has completely recovered to control level, which is a convincing evidence of free radical nature of cellular damage in photodynamic effect of fullerene. 

D. J.F. Taylor, R.K. Thomas, and J. Penfold The Adsorption of Oppositely Charged Polyelectrolyte/Surfactant Mixtures Neutron Reflection from Dodecyl Trimethy-lammonium Bromide and Sodium Poly(Styrene Sulfonate) at the AirAVater Interface. Langmuir 18, 4748 (2002). 

The surface of a carbon electrode was at first coated with a thin film of an anionic polymer such as sodium poly(styrene-sulfonate) 95) or nafion 96) (thickness thousand A) then the cationic Ru(bpy)2+ was adsorbed in the anionic layer electrostatically. The modification was also made by coating water insoluble polymer pendant Ru(bpy)2 + ( ) from its DMF solution 97). These Ru(bpy) +/polymer modified electrode gave a photoresponse in the MV2+ solution with the Pt counter electrode 95-97) The time-current behaviours induced by irradiation and cutoff of the light under argon are shown in Fig. 28. It is interesting to see that the direction of the photocurrent reversed at the electrode potential of ca. 0.4 V (vs. Ag—AgCl) under... 

In a laboratory hood, equip a 500-ml three-necked flask with a sealed stirrer and motor, condenser, thermometer, and an addition funnel. Add 150 ml of a 1% solution of sodium poly (methacrylate) in water and a buffer solution of 0.85 g of disodium phosphate and 0.05 g of monosodium phosphate in 5 ml of water. 

Measure 25 ml of the 5% aqueous solution of sodium poly(methacrylate) into the addition funnel. 

---