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Frequency polymer synthesis

Polymer-immobilized nanogold catalysts promote very efficiently the synthesis of symmetric disubstituted ureas (RNH)2CO (R = alkyl), with a turnover frequency (TOF) of up to 3000 IT1 [132], After 20h at 453 K, the reactions of C02 (5 MPa) with cyclohexyl- or benzylamine gave the corresponding disubstituted ureas in 85% and 83% yields, respectively. [Pg.159]

These results illustrate the diversity of synthetic and processing approaches that can be taken in the synthesis of thin-film frequency doubling materials. Specifically, we have demonstrated that it is possible to assemble chromophore-functionalized polymers with greater than one chromophore substitutent per monomer subunit, with d33 values as high as 65 x 10 esu, with Tg values as high as 173°C, with improved temporal stability, and with good transparency characteristics at A 0.633 fim. We have also shown that known chromophore-functionalized polymers can be simultaneously poled and cross-linked... [Pg.249]

Not many high molecular weight polymers have been obtained from this reaction, however. In most cases, failure can be attributed to the reversal of the diene synthesis (23) (Reaction 1), a high frequency of side reactions, such as chain-growth polymerization of the diene (23, 25), or the insolubility of the rigid, ring-containing polymer which removes it from the reaction medium (3). [Pg.646]

Interactions between soluble polymer and colloidal particles control the behavior of a large number of chemical products and processes and, hence, their technological viability. These dispersions have also attracted considerable scientific interest because of their complex thermodynamic and dynamical behavior—stimulated by the synthesis of novel polymers, improved optical and scattering techniques for characterization, and a predictive capability emerging from sophisticated statistical mechanical theories. Thus, the area is active both industrially and academically as evidenced by the patent literature and the frequency of technical conferences. [Pg.137]

Especially for the synthesis of nanogels (e.g. by intramolecular cross-linking of polymer molecules with high molecular weights), the method of pulse irradiation is useful, see Fig. 10. The polymer is dissolved and the solution, flowing through a quartz irradiation cell (effective volume about 1 ml), is pulse-irradiated with electrons of several MeV (in our experiments 6 MeV) generated by a linear accelerator (ELU-6, Eksma, Russia). Pulse frequency of 5.0 Hz and pulse duration of 3 ps were applied at a flow rate of 5.0 ml/s. [Pg.35]

Figure 9 shows the temperature dependence of the elastic part of the complex Young s modulus E a>) for various poly(vinyl methyl ether) hydrogel samples in water at a selected frequency of 20.1 rad/s. The polymer was cross-linked by electron beam irradiation (see Sect. 2.4, chapter Synthesis of hydrogels ). These data were compared with the temperature shrinking behaviour of sample PVME 20/80... [Pg.98]

Synthesis of highly crowded graft copolymers with graft frequencies of up to 50% of the total monomeric units in approximately alternate positions on the polymer backbone (structure 24). [Pg.30]

In last years one observes a fast progress in synthesis and elaboration of non-centrosymmetric functionalized polymers for applications primarily in electrooptic modulation and frequency conversion. These materials possess large second order nonlinear optical susceptibility x and can be easily processed into good optical quality thin films for travelling wave applications. Essentially four types of polymeric structures have been developed, as shown in Fig. 1 ... [Pg.141]

Only cation exchange, which can be enforced by incorporation of immobile anions in the polymer during the synthesis, e.g., polystyrene sulfonate. In this case a strong change of Aw accompanies the frequency change A/and the simple Sauerbrey equation cannot be applied. Moreover, values of A/ and Aw do not return to the initial values. Such behavior can be explained by a break-in effect. ... [Pg.334]


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See also in sourсe #XX -- [ Pg.202 ]




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Frequency polymers

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