Polymers polyacrylic acid

Specialty polymers Polyacrylic acid, polyethylene glycol 0-2 0-0.04... 

Carbopol . [BFGoodrich/Spec. Polymers] Polyacrylic acids emulsifier. 

Good-rite K. [BFGoodrich/Spec. Polymers] Polyacrylic acids or salts cobuilder for laundry, dish, and other cleaners dispersant sequestrant... 

Water-soluble polymers and polyelectrolytes (e.g., polyethylene glycol, polyethylene imine polyacrylic acid) have been used success-hilly in protein precipitations, and there has been some success in affinity precipitations wherein appropriate ligands attached to polymers can couple with the target proteins to enhance their aggregation. Protein precipitation can also be achieved using pH adjustment, since proteins generally exhibit their lowest solubility at their isoelectric point. Temperature variations at constant salt concentration allow for frac tional precipitation of proteins. 

FIGURE 4.17 Effect of ionic strength on the elution of anionic polymers. Column TSK-GEL GMPW, two 17 fjLirt, 7.5 mm X 60 cm columns in series. Sample 0.5 ml of 0.05-0.1% of the sodium salt of polyacrylic acid, an anionic polymer. Elution Water 0.01, 0.025, 0.05, or 0.1 M NaNOs in water. Flow rate 0.5 ml/min. Detection Rl. 

The GBR resin works well for nonionic and certain ionic polymers such as various native and derivatized starches, including sodium carboxymethylcel-lulose, methylcellulose, dextrans, carrageenans, hydroxypropyl methylcellu-lose, cellulose sulfate, and pullulans. GBR columns can be used in virtually any solvent or mixture of solvents from hexane to 1 M NaOH as long as they are miscible. Using sulfonated PDVB gels, mixtures of methanol and 0.1 M Na acetate will run many polar ionic-type polymers such as poly-2-acrylamido-2-methyl-l-propanesulfonic acid, polystyrene sulfonic acids, and poly aniline/ polystyrene sulfonic acid. Sulfonated columns can also be used with water glacial acetic acid mixtures, typically 90/10 (v/v). Polyacrylic acids run well on sulfonated gels in 0.2 M NaAc, pH 7.75. 

Polyacrylic acid (pAA) homopolymers and related copolymers have become a commercially important class of water-soluble polymers. Acrylic acid polymers can range in molecular mass from less than 1000 Da to greater than 1,000,000 Da. A representative set of analysis conditions is... 

In the same year, Fulda and Tieke [75] reported on Langmuir films of monodisperse, 0.5-pm spherical polymer particles with hydrophobic polystyrene cores and hydrophilic shells containing polyacrylic acid or polyacrylamide. Measurement of ir-A curves and scanning electron microscopy (SEM) were used to determine the structure of the monolayers. In subsequent work, Fulda et al. [76] studied a variety of particles with different hydrophilic shells for their ability to form Langmuir films. Fulda and Tieke [77] investigated the influence of subphase conditions (pH, ionic strength) on monolayer formation of cationic and anionic particles as well as the structure of films made from bidisperse mixtures of anionic latex particles. 

Lin, TH Phillies, GDI, Prohe Diffusion in Polyacrylic Acid Water—Effect of Polymer Molecular Weight, Journal of Colloid and Interface Science 100, 82, 1984. 

Wall, F. T. Drenan, J. W. (1951). Gelation of polyacrylic acid by divalent ions. Journal of Polymer Science, 7, 83-8. 

Gregor, H. P. Frederick, M. (1957). Titration studies of polyacrylic acid and polymethacrylic acids with alkali metals and quaternary ammonium bases. Journal of Polymer Science, 23, 451-65. 

Jacobsen, A. (1962). Configurational effects of binding of magnesium to polyacrylic acids. Journal of Polymer Science, 57, 321-36. 

Wilson, A. D. (1974). Alumino-silicate polyacrylic acid and related cements. British Polymer Journal, 6, 165-79. 

Flocculation is indeed dependent on polymer adsorption, and there are hypotheses correlating the two phenomena, but often these have been put forth without detailed measurement of the two phenomena simultaneously (10-13). In this paper, flocculation is investigated as a function of polymer and solution properties and hydrodynamic conditions by measuring different properties of the system, including adsorption, using well characterized kaolinite and polymer samples prepared specifically for this purpose. Also, the role of concentration and charge density of polyacrylamide and polyacrylamide-polyacrylic acid co-polymers in determining kaolinite flocculation is examined under controlled hydrodynamic conditions. 

A comparison of Tables 9-12 indicates that naturally occurring species tend to produce stable membranes more abundantly. We believe this is due to the cyclic nature and rigidity of the backbone, as will be discussed in the following section of the paper. Several trends are immediately obvious. For example, the hydrophobicity of the polymer appears to be a critical parameter. While polyacrylic acid can form a stable membrane with virtually all polycations, poly-methacrylic acid is much less effective. Similarly, propylene glycol modified alginate is less effective than sodium alginate. Furthermore, when the poly-... 

Thus, polymethacrylic acid undergoes net scission on gamma radiolysis with a G-value of approximately 4, while polyacrylic acid, on the other hand, undergoes net crosslinking with a G-value of approximately 1.2 (7). Crosslinking in polyacrylic acid is favourable because of the formation of main chain radicals. These can react to form crosslinks between polymer chains. 

Use anionic polymers such as polyacrylic acids cross-linked with allyl ethers of pentaerythritol or sucrose as thickeners, if a gel structure and pseudoplastic (shear-thinning) properties are desirable. Consider adding colloidal alumina to further increase the viscosity at pH 13 [ 15]. 

The dyes with long-lived luminescence are particularly attractive since background fluorescence can easily be discarded in time domain measurements. Crosssensitivity to oxygen may be problematic but it can be minimized by utilizing gas-blocking polymers. For example, Kuemer et al. [15] used the precipitation technique to prepare polyacrylonitrile-based beads doped with a ruthenium(II) complex which showed virtually no cross-sensitivity to oxygen. Copolymers of polyacrylonitrile and polyacrylic acid were used to provide the beads with... 

The first section, Chemical Reactions on Polymers, deals with aspects of chemical reactions occurring on polymers—aspects relating to polymer size, shape, and composition are described in detail. One of the timely fields of applications comprises the use of modified polymers as catalysts (such as the immobilization of centers for homogeneous catalysis). This topic is considered in detail in Chapters 2, 3, 8, 9, and 11 and dealt with to a lesser extent in other chapters. The use of models and neighboring group effect(s) is described in detail. The modification of polymers for chemical and physical change is also described in detail in Chapters 2 (polystyrene) 4 (polyvinyl chloride) 5 (polyacrylic acid, polyvinyl alcohol, polyethyleneimine, and polyacrylamide) 6 (polyimides) 7 (polyvinyl alcohol) 8 (polystyrene sulfonate and polyvinylphosphonate) 10 (polyacrylamide) and 12 (organotin carboxylates). 

The third approach has been to graft the redox couple by means of a covalent bond to the polyelectrolyte backbond as described early in 1965 in the book of Cassidy and Run [20]. Several of these systems are charged polymers in at least one oxidation state, like poly(viologen), poly(vinylferrocene), and so on. Examples of polyelectrolytes like polyacrylic acid with covalently bound viologen were reported by Fernandez, Katz and coworkers [21], hydroquinone [22] and Anson et al. with bound ferrocene [23]. 

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