Sodium poly surface

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). 

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). 

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... 

The first ellipsometric measurement of the thickness of the adsorbed layer and the adsorbance of a polyelectrolyte and a negative adsorbance of salt onto a solid surface was reported by Takahashi et al.U4) They measured the adsorption of sodium poly(acrylate) (M = 950 x 103) onto a platinum plate as a function of the concentration of added sodium bromide. In an aqueous polyelectrolyte solution with an added simple salt, the bulk phase is a three-component system which consists of a polyelectrolyte, a simple salt, and water. The adsorbed layer on the solid surface is a three-component phase as well. The adsorbance of polyelectrolytes thus cannot easily be determined from measurements of the refractive index nf of the adsorbed phase. Hence, it was assumed that the adsorbed layer is a homogeneous layer of thickness t and further that nf is represented by the Lorenz-Lorentz equation as follows ... 

Adsorption of block copolymers onto a surface is another pathway for surface functionalization. Block copolymers in solution of selective solvent afford the possibility to both self-assemble and adsorb onto a surface. The adsorption behavior is governed mostly by the interaction between the polymers and the solvent, but also by the size and the conformation of the polymer chains and by the interfacial contact energy of the polymer chains with the substrate [115-119], Indeed, in a selective solvent, one of the blocks is in a good solvent it swells and does not adsorb to the surface while the other block, which is in a poor solvent, will adsorb strongly to the surface to minimize its contact with the solvent. There have been a considerable number of studies dedicated to the adsorption of block copolymers to flat or curved surfaces, including adsorption of poly(/cr/-butylstyrcnc)-ft/od -sodium poly(styrenesulfonate) onto silica surfaces [120], polystyrene-Woc -poly(acrylic acid) onto weak polyelectrolyte multilayer surfaces [121], polyethylene-Wocfc-poly(ethylene oxide) on alkanethiol-patterned gold surfaces [122], or poly(ethylene oxide)-Woc -poly(lactide) onto colloidal polystyrene particles [123],... 

Boisvert, J.P. et al., Effect of surface charge on the adsorption mode of sodium poly(acrylate) on alumina-coated TiO, used as coating pigment. Colloids Sutf. A, 168, 287, 2000. 

Figure 13 demonstrates the segment density profile of sodium poly(styrene sulfonate) adsorbed on polystyrene latex in NaCl solution [48]. The segment density profiles of Na poly(styrene sulfonate) do not practically depend on the surface charge. The shape of curve depends on the NaCl concentration. An increase of salt concenliation leads to an increase of the thickness of the adsorption layer, as predicted by theory. 

Biggs S, Burns JL, Yan YD, Jameson GJ, Jenkins P (2000) Molecular weight dependence of the depletion interaction between silica surfaces in solutions of sodium poly(styrene sulfonate). Langmuir 16(24) 9242-9248... 

The typical shifts in A/ and AD for the LbL deposition of sodium poly(styrene sulfonate)/poly[2-(dimethylamino)ethyl methacrylate] (PSS/PDEM) are shown in Fig. 4.1, where pH is fixed at 4, ionic strength is fixed at 0.2 M, and T is of 20 °C. A measurement of LbL deposition is initiated by switching the liquid exposed to the resonator from water to a poly(ethylene imine) (PEI) solution with a polymer concentration of 1.0 mg/mL. PEI is allowed to adsorb onto the resonator surface for 20 min before the surface is rinsed with water to ensure a uniform coating with positive charges, so that the effects of substrate on the growth of multilayer are minimized [21]. After water is replaced with phosphate buffer, 0.1 mg/mL PSS and PDEM are alternately introduced for 20 min with buffer rinsing in between in case the poly electrolytes form complexes in the solution. The decrease in Af and the increase in AD clearly indicate that the polyelectrolyte chains gradually deposit onto the resonator surface driven by the electrostatic interaction. 

The anodized surface is often subjected to additional treatment before the radiation-sensitive coating is appHed. The use of aqueous sodium siUcate is well known and is claimed to improve the adhesion of diazo-based compositions ia particular (62), to reduce aluminum metal-catalyzed degradation of the coating, and to assist ia release after exposure and on development. Poly(viQyl phosphonic acid) (63) and copolymers (64) are also used. SiUcate is normally employed for negative-workiag coatings but rarely for positive ones. The latter are reported (65) to benefit from the use of potassium flu o r o zirc onate. 

With Phenols. The 2-hydroxylethyl aryl ethers are prepared from the reaction of ethylene oxide with phenols at elevated temperatures and pressures (78,79). 2-Phenoxyethyl alcohol is a perfume fixative. The water-soluble alkylphenol ethers of the higher poly(ethylene glycol)s are important surface-active agents. They are made by adding ethylene oxide to the alkylphenol at ca 200°C and 200—250 kPa (>2 atm), using sodium acetate or... 

When undiluted 2-vinylfuran was added to metallic sodium (mirror or particles) an orange colour developed and some resinous material was deposited on the metal surface. On prolonged contact much of the monomer was converted into a partly-insoluble reddish resin with spectra unrelated to those of standard poly(2-vinyl-furan). Reaction of diluted monomer with sodium gave a milder interaction, but no evidence of living anionic polymerization. 

Whereas nonionic ethylene oxide adducts discolor badly on contact with sodium hydroxide, phosphate derivatives of these nonionics exhibit good color stability even under these conditions. But in the presence of strong acids poly-oxyethylated phosphate esters undergo hydrolysis to the base nonionic and phosphoric acid. However, the free surface-active acids by themselves show little tendency to hydrolyze. They have a pH value of 2 in aqueous solution. 

Vaterite is thermodynamically most unstable in the three crystal structures. Vaterite, however, is expected to be used in various purposes, because it has some features such as high specific surface area, high solubility, high dispersion, and small specific gravity compared with the other two crystal systems. Spherical vaterite crystals have already been reported in the presence of divalent cations [33], a surfactant [bis(2-ethylhexyl)sodium sulfate (AOT)] [32], poly(styrene-sulfonate) [34], poly(vinylalcohol) [13], and double-hydrophilic block copolymers [31]. The control of the particle size of spherical vaterite should be important for application as pigments, fillers and dentifrice. 

Flocculants cause colloidal clay particles to coagulate thus promoting separation from the drilling fluid which has been circulated down the wellbore and returned to the surface. The treated fluid may then be pumped back down the well bore. Sodium chloride, hydrated lime, gypsum, sodium tetraphosphate, polyacrylamide, poly(acrylamide-co-acrylic acid), cationic polyacrylamides, and poly(ethylene oxide) have been used commercially. 

Polyamide and polyester fibres are generally scoured using an alkyl poly(oxyethylene) sulphate and sodium carbonate. Some polyester qualities are subjected to a causticisation treatment with sodium hydroxide in the presence of a cationic surfactant to give a lighter fabric with a silkier handle [154,156]. This treatment involves etching (localised saponification) of the polyester surface and is broadly analogous to the S-finish used on triacetate fibres. The process has attracted considerable interest in recent years but its... 

Recently, Kong et al. [159] functionalized MWNT with polyacrylic acid (PAA) and poly(sodium 4-styrenesulfonate) (PSS) by surface-initiating ATRP (atom transfer radical polymerization) following the Schemes 1 and 2 ... 

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