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Acidic polymer component

Nucleic Acids. Phosphoms is an essential component of nucleic acids, polymers consisting of chains of nucleosides, a sugar plus a nitrogenous base, and joined by phosphate groups (43,44). In ribonucleic acid (RNA), the sugar is D-ribose in deoxyribonucleic acids (DNA), the sugar is 2-deoxy-D-ribose. [Pg.378]

Pyrotechnic mixtures may also contain additional components that are added to modify the bum rate, enhance the pyrotechnic effect, or serve as a binder to maintain the homogeneity of the blended mixture and provide mechanical strength when the composition is pressed or consoHdated into a tube or other container. These additional components may also function as oxidizers or fuels in the composition, and it can be anticipated that the heat output, bum rate, and ignition sensitivity may all be affected by the addition of another component to a pyrotechnic composition. An example of an additional component is the use of a catalyst, such as iron oxide, to enhance the decomposition rate of ammonium perchlorate. Diatomaceous earth or coarse sawdust may be used to slow up the bum rate of a composition, or magnesium carbonate (an acid neutralizer) may be added to help stabilize mixtures that contain an acid-sensitive component such as potassium chlorate. Binders include such materials as dextrin (partially hydrolyzed starch), various gums, and assorted polymers such as poly(vinyl alcohol), epoxies, and polyesters. Polybutadiene mbber binders are widely used as fuels and binders in the soHd propellant industry. The production of colored flames is enhanced by the presence of chlorine atoms in the pyrotechnic flame, so chlorine donors such as poly(vinyl chloride) or chlorinated mbber are often added to color-producing compositions, where they also serve as fuels. [Pg.347]

In an industrial application dissolution/reprecipitation technology is used to separate and recover nylon from carpet waste [636]. Carpets are generally composed of three primary polymer components, namely polypropylene (backing), SBR latex (binding) and nylon (face fibres), and calcium carbonate filler. The process involves selective dissolution of nylon (typically constituting more than 50wt% of carpet polymer mass) with an 88 wt % liquid formic acid solution and recovery of nylon powder with scCC>2 antisolvent precipitation at high pressure. Papaspyrides and Kartalis [637] used dimethylsulfoxide as a solvent for PA6 and formic acid for PA6.6, and methylethylketone as the nonsolvent for both polymers. [Pg.152]

However, on a lightly cross-linked hydroxyethylmethacrylate/styrene polymer that swells in polar solvents (22, 365), or on a silica-gel support (366), catalyst performance matches that of the soluble one for the precursor amino acid substrates. A rhodium-DIOP analog has also been supported on a polymer containing pendent optically active alcohol sites [incidentally, formed via hydrosilylation and hydrolysis of a ketonic polymer component using an in situ rhodium(I)-DIOP catalyst]. The supported catalyst in alcohol again matched that of the soluble catalyst for... [Pg.366]

Amphoteric a substance that exhibits both acidic and basic properties Amylopectin branched glucose polymer component of starch... [Pg.336]

As with proteins, the nucleic acid polymers can denature, and they have secondary structure. In DNA, two nucleic acid polymer chains are twisted together with their bases facing inward to form a double helix. In doing so, the bases shield their hydrophobic components from the solvent, and they form hydrogen bonds in one of only two specific patterns, called base pairs. Adenine hydrogen bonds only with thymine (or uracil in RNA), and guanine pairs only with cytosine. Essentially every base is part of a base pair in DNA, but only some of the bases in RNA are paired. The double-helix structure... [Pg.118]

Figure 3 Chemical structure of poly(lactic-co-glycolic) acid polymer. The x component represents lactic acid and y component represents glycolic acid. For other poly(hydroxy acids), the side-chain methyl group is replaced by other alkyl groups. Figure 3 Chemical structure of poly(lactic-co-glycolic) acid polymer. The x component represents lactic acid and y component represents glycolic acid. For other poly(hydroxy acids), the side-chain methyl group is replaced by other alkyl groups.
Formation of L-guluronic acid, a component of the alginic acid-like polysaccharide produced by P. aeruginosa and Azotobacter vinelandii, requires special comment. In this case, a polymer built from /3-(l- 4)-linked D-mannosyluronic acid residues serves as an intermediate in the biosynthesis.204,205 Part of the D-mannosyluronic acid residues in the polymer is subjected to an epimerization at C-5 catalyzed by an exocellular enzyme of the micro-organism,205-207 producing a polysaccharide composed of structural blocks that contain only D-mannosyluronic acid or only l-gulosyluronic acid residues, as well %s some having both. The mechanism of the epimerization remains unclear. [Pg.297]

As a final example it should be mentioned that precondensed enones, prepared by standard Knoevenagel condensation of the aldehyde with the CH-acidic carbonyl component, when reacted with thioureas provided 1,3-thiazines 37, which are isomeric to thio-Biginelli compounds of the general formula 14 (see Figure 4.5). A published report describes the combinatorial synthesis of a library of 29 derivatives of thiazines 37 utilizing polymer-supported reagents and catalysts [168]. [Pg.109]

The variety of suitable nucleophiles is far greater water, alcohols, phenols, amines and carboxylic acids are commonly used, but others including silanes or compounds with acidic C-H bonds such as malonates have been reported as well. The resulting products can, in some cases after further conversion, be used in many different applications, such as nonionic surfactants, emulsifiers, fragrances, flavouring agents, cosmetics and polymer components. [Pg.48]

Seals, o-rings, and valve membranes must be manufactured out of polymers that are resistant to thermal sterilization and to the bases and acids used in the biopharmaceutical industry. When in contact with the product, the elastomers employed must additionally present the following safety characteristics the rates of release of polymer components must be low and remain below well-established threshold levels the components released must be innocuous to human health, according to rules previously established. [Pg.225]

Amino acid A component of every protein, in which up to 20 different amino acids are strung together into polymer chains. [Pg.377]

The effect of conformation of the polymer components on complexation has been discussed by using poly(amino acid)s, e.g. in the systems of poly(L-... [Pg.55]

Fig. 46a, b. Time dependence of the complexation. (a) conformational changes of the polymer components in the complexes Poly(L-glutamic acid) (PGA)-tetraethylenepentamine, O PGA-pentaethylenehexamine (b) pH change of the complex solutions Poly(acrylic acid) (PAA)-integral-type polycation (10,10-ionene) O PAA-poly(N-vinyl-2-pyrrolidone) (PVPo)... [Pg.95]

Procter Gamble is the other leading pioneer on the field of PHA biodegradable polymers. The Nodax biopolymers are based on the copolymer PHBH, a copolymer polyester of 3-hydroxybutyric and 3-hydroxyhexanoic acid. The higher the 3-hydroxyhexanoic acid comonomer component, the more flexible... [Pg.80]

Boc-deprotected branched polypeptide with the Cys(Npys) moiety, poly [Lys(Cyso 2 -DL-Ala3 i)] trifluoroacetate salt (10 mg, 16.5 pmol), was dissolved in 10 mL 0.06 M phosphate buffer (pH 5.5) (see Note 6) 1.35 amount of H-LKNleADPNRFRGKDL-Acp-CSALLEDPVG-NHj (14.8 mg, 5.4 pmol), calculated from the Npys-content of polymer, was added to the reaction mixture. The final concentration was 1 mg/mL for the polymer component. The solution was stirred for 4 h at RT, transferred to a Visking tube (cutoff 8000-12,000), and dialyzed for 2 d against 0.1% acetic acid. No Npys content was detected by UV spectroscopy at A, = 350 nm in the conjugate after freeze drying (see Note 7). [Pg.220]


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