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Polymer efficiencies

Figure 16 Influence of polymer concentration and weight-average molecular weight (Mw)j)n the polymer efficiency. = Mw - 5.5 X 10 O = Mw = 3.0 x 10. ... Figure 16 Influence of polymer concentration and weight-average molecular weight (Mw)j)n the polymer efficiency. = Mw - 5.5 X 10 O = Mw = 3.0 x 10. ...
Figure 15 Influence of valency of cations on the polymer efficiency. = Eu, O = Co "". Figure 15 Influence of valency of cations on the polymer efficiency. = Eu, O = Co "".
Different samples of aqueous solution containing radionuclides of Co and Eu were prepared at different copper sulphate concentrations and constant polymer concentrations (pAM) of 15 mg/1. The addition of salt to the system was done to reduce both the repulsion forces between the radionuclides and the interaction between the polymeric chains [7]. The polymer efficiency for the prepared samples was determined, results are shown in Fig. 15. It is clear that the polymer efficiency for Eu " is higher than for Co. This can be explained by the difference in the tightly bound structured water associated with different cationic species [14,107]. On this basis, we expect that Co is more hydrated than Eu. This is due to the difference in the ionic size. The hydra-... [Pg.130]

The influence of polymer concentration on the polymer efficiency (F) was studied at constant cop r sulphate concentration of 600 mg/1 at two different of 3.9 x 10 and 5.5 X 10, results are shown in Fig. 16. It is clear that the polymer efficiency (F) increases with increasing the polymer dosage as discussed above. [Pg.130]

The synthesis of luminescent organoboron quinolate polymers (21) (Fig. 15) via a three-step procedure starting from a silylated polystyrene has been communicated. The synthesis was initiated by the highly selective borylation of poly (4-trimethylsilylstyrene) (PS-Si), followed by the replacement of the bromine substituents in poly(4-dibromoborylstyrene) (PS-BBr) with substituted thienyl groups (R = H, 3-hexyl, 5-hexyl). In the final step, the 8-hydroxyquinolato moiety was introduced. The hexyl-substituted polymers efficiently emitted light at 513-514nm upon excitation at 395 nm.40... [Pg.30]

Q. Chu, Y. Pang, L. Ding, and F.E. Karasz, Green-emitting PPE-PPV hybrid polymers efficient energy transfer across the m-phenylene bridge, Macromolecules, 36 3848-3853, 2003. [Pg.269]

J. Jacob, S. Sax, T. Piok, E.J.W. List, A.C. Grimsdale, and K. Mullen, Ladder-type pentapheny-lenes and their polymers efficient blue-light emitters and electron-accepting materials via a common intermediate, J. Am. Chem. Soc., 126 6987-6995, 2004. [Pg.288]

Monomer Irradiation Energy Co-polymer Irradiation Input Co-polymer efficiency... [Pg.480]

Polymer-supported TADDOL-Ti catalyst 79 prepared by chemical modification was poorly active in the Diels-Alder reaction of 3-crotonoyloxazolidinone with cyclo-pentadiene (Eq. 24) whereas polymeric TADDOL-Ti 81 prepared by copolymerization of TADDOL monomer 80 with styrene and divinylbenzene had high activity similar to that of the soluble catalyst. In the presence of 0.2 equiv. 81 (R = H, Aryl = 2-naphthyl) the Diels-Alder adduct was obtained in 92 % yield with an endolexo ratio of 87 13. The enantioseleetivity of the endo product was 56 % ee. The stability and recyclability of the catalyst were tested in a batch system. The degree of conversion, the endolexo selectivity, and the enantioseleetivity hardly changed even after nine runs. Similar polymer-supported Ti-TADDOLate 82 was prepared by the chemical modification method [99]. Although this polymer efficiently catalyzed the same reaction to give the (2R,2S) adduct as a main product, asymmetric induction was less than that obtained by use of a with similar homogeneous species. [Pg.970]

These ferrocene modified polysiloxane polymers were also used to construct glycolate [6,7], lactate [7], acetylcholine [12,81], glutamate [12] and cholesterol [81] sensors. All these electrodes showed that ferrocene containing siloxane polymers efficiently shuttled electrons between redox center(s) of enzyme and the electrode surface. [Pg.350]

The above data indicate that branching dramatically increases polymer efficiency in the treatment of activated sewage sludge. This effect was found to be independent of both polymerization technique (emulsion vs. solution) and polymer composition (homopolymer vs. copolymer). In all cases, filtration time decreases to a minimum and then increases with increasing concentrations of branching agents. [Pg.240]

Therefore, we can state that branching enhances polymer efficiency in dewatering activated sludges. An optimum degree of branching produces the best dewaterability. This effect is specific to waste-activated sludges. [Pg.249]

After the polymerization, the template is removed by 0.1 N aqueous NaOH/acetonitrile (1/1) solution. The obtained polymer efficiently hydrolyzes 3 following the typical Michaelis-Menten kinetics, while the corresponding monomeric amidine solution hydrolyzes 3 about 100 times more slowly. [Pg.137]

The most widely applied preparation method is dipping the supports in a polymeric solution. To remove excess polymer efficiently from the channels, low-viscosity polymer solutions are preferred as carbon precursors. The most straightforward method is the dipcoating method [6] The honeycombs are dipped in a precursor solution and then dried and/or cured. Subsequently, the precursor is carbonized and, if needed, activated. Many different carbon precursors have been nsed, such as saccharides [1,8], polyfurfuryl alcohol (PFA) [5,9], and phenohc... [Pg.403]

The polymer efficiently permeabilises anionic vesicles with compositions which mimic those of bacterial membranes. The polymer binds to anionic phospholipid vesicles but not zwitterionic vesicles, which causes phase separation in anionic phospholipid mixtures, clustering the negative charge. The polymer permeabilises the outer membrane of Escherichia coli ML-35p in a biphasic manner low polymer concentrations permeabilise the inner membrane of Escherichia coli ML-35p, whereas high concentrations of the polymer can block the active transport of or onitrophenyl-P-n-galactoside in wild-type Escherichia coli K12 [17]. [Pg.76]

Polymer solutions lose their potency with age. The more dilute the polymer, the quicker is the deterioration. Making up with hard water also makes deterioration more rapid. Thus, in preference, it is better to make up with soft water as concentrated as possible, and only dilute to the required dilution just before use. Figure 5.3 shows some results of work testing the effect of water hardness. The dewaterability of the sludge was gauged by the amount of supernatant produced after a set spin in a laboratory bottle centrifuge. Note the correlation of the fall in polymer solution viscosity with increased water hardness and resulting decrease in polymer efficiency. [Pg.223]

Y.W. Tang, Z.F. Huang, T. Yang, X.G. Hu and X.O. Jiang, The characteristic and application of molecularly imprinted polymer Efficient sample preconcentration of antibiotic cefa-thiamidine from human plasma and serum by solid phase extraction. Anal. Lett., 38 (2) 219-226, 2005. [Pg.318]

Different options have been considered to tiy and demonstrate polymer efficiency in a shorter time, and move the sanction of the fullfield from 3 to 4 years after phase 1 Camelia start to 1 to 2 years before. [Pg.355]

Dual glass transition behavior is observed in immiscible binary polymer blends or block copolymers which have undergtme microphase separation to create discrete domains of each type of polymer in the rrratrix. The itaconate structures considered here are comb-branch polymers with relatively short side chains which plasticize the polymer efficiently when the chain lengdis are Cj to Cfy but then undergo a subtle change in bdiavior at long chain lengths. While there is no apparent... [Pg.331]


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