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Polyacrylics and polymethacrylics

In the case of boilers operating at low pressure, organic materials such as natural and modified tannins, starches, or alginates are added to aid blowdown. For boilers operating at high pressure, synthetic materials such as polyacrylates and polymethacrylates have been developed. The most commonly used chemicals for boiler feedwater treatment are phosphates and hydrazine. [Pg.155]

Complex formation of Hg +, Zn +, and Pb + with polyacrylic and polymethacrylic acids has been studied [63] voltammet-rically, using mercury drop and glassy carbon rotating disk electrodes. The formation constants of these complexes were calculated. [Pg.970]

Figure 1. Brittle point of n-alkyl esters of polyacrylic and polymethacrylic acid (27)... Figure 1. Brittle point of n-alkyl esters of polyacrylic and polymethacrylic acid (27)...
As the formation of LC phase in comb-like polymers is predetermined by the interaction of mesogenic groups, it would have seemed, that the temperature range of LC state for such systems should not depend on the length of the main chain, i.e. on the degree of polymerization (DP). However, studies 44,49) on the dependence of Tc] on DP carried out for some polyacrylic and polymethacrylic derivatives of cyanobiphenyl, as well as for polyparabiphenylacrylate 51 (Fig. 5), have shown that... [Pg.183]

Further growth of the polymeric chain proceeds in the usual manner. Compared to the polymeric materials obtained via conventional methods, the mechanochemically synthesized polyacryl and polymethacryl amides have lower molecular weights (Simonescu et al. 1983). Acrylonitrile, styrene, e-caprolactam, isoprene as well as aryl- and methacryl amides have a special optimal duration of the polymerization upon grinding (Oprea Popa 1980). In the case of the aryl- and metacrylamides, the polymerization proceeds slowly, usually between 24 and 72 hr. After that, some acceleration takes place and the process is completed within 96 hr (total). [Pg.321]

Oxalate viologen ion pair complexes have been examined in detail under pulsed laser flash and continuous photolysis [205], As the photolysis leads to the oxidation of oxalate dianion, the strongly reducing CO 2"is formed after decarboxylation and a second MV2 + is reduced, generating another equivalent of MV +. Malonate, succinate, glutarate, polyacrylate and polymethacrylate were also tested and found to be effective as CTC donors for MV + formation. In the case of malonate, decomposition of the carboxylate was not accompanied by MV2 + consumption. This was attributed to the efficiency of a back electron transfer step following immediately the decarboxylation [206]. [Pg.131]

A large number of azobenzene-based amorphous and liquid crystalline polymers, particularly polyacrylates and polymethacrylates with chiral azobenzene pendants, have been prepared for the development of data storage and photonic devices [1-3,11-14]. For instance, the introduction of optically active mesogenic azobenzene residues into the side groups of the polymers produces chiral nematic and cholesteric phases, which are regulated by photoisomerization of the azobenzene units [10,14]. In most cases, however, the optical activity and chiroptical... [Pg.650]

Polyacrylates and Polymethacrylates Containing Nucleic Add Bases 3.1 Polymer Synthesis... [Pg.10]

Walsh, D. J. McKeown, J. G., "Compatibility of Polyacrylates and Polymethacrylates with Poly(vinyl chloride) 2. Measurement of Interaction Parameters," Polymer, 21, 1335 (1980). [Pg.183]

We have already described how the heats of mixing dominate the miscibility of polymers and so it was obvious to examine the heats of mixing of the above acrylates with PVC in order to understand the reasons for their miscibility or immisdbility. Fig. 19 shows the heats of mixing of various oligomeric polyacrylates and polymethacrylates with a chlorinated hydrocarbon which was used as an analogue for PVC. One can see... [Pg.154]

Polyacrylates and polymethacrylates can be end-capped by a functional group at one chain-end according to two strategies, by which either the initiator bears the envisioned functional group (protected or not), or living polymer chains are reacted with a duly substituted electrophile. [Pg.857]

Reactions of the cyclic compounds with different kinds of organic reagents at room temperature readily give a seri of pyrimidine derivatives without using any cata-lyst One of the typical reactions involves esterification with acetic add in bulk to afford the corresponding acetate. When the reaction is applied to polymeric adds, e.g. poly(acrylic acid) and poly(methacrylic add), polyacrylate and polymethacrylate having pendant uracil and thymine units are obtained in high yield (Schemes 6 and 1) ... [Pg.12]

Other polymeric materials (Figure 3.7) including polystyrene, polyvinylchloride (PVC), polytetrafluoroethylene (PTFE), polyvinylenedifluorate (PVDF), polyacrylonitrile (PAN), polycarbonates, polyacrylates and polymethacrylates, polyetherur-ethane, as well as various inorganic materials have been used as chromatographic supports. [Pg.32]

Use Monomer for polyacrylic and polymethacrylic acids and other acrylic polymers. [Pg.20]

Numerous results (predictions and correlations) are available for snch systems. Many models perform satisfactorily even when pure predictions are considered. In a recent comparison, Pappa et al."° showed that Entropic-FV performs better than the Zwong-Masuoka model (11% vs. 20%). In the review by Lee and Danner, GCLF and Entropic-FV perform similarly for nonpolar systems (15%), but GCLF appears to perform better for the weakly polar systems. This is attributed to problems of the Entropic-FV model for systems containing polyacrylates and polymethacrylates with acetates. UNIFAC-FV has an average error of 23% for these types of systems and GC-Flory of 20%. Typical results are shown in Table 16.4. [Pg.731]

Conformational Behavior of Propagating Chains of Polyacrylate-and Polymethacrylate Guanidines in Water Solutions... [Pg.325]

We have discussed the influence of the flexibility of the polymer backbone on the mesophase formation by examples of polyacrylates and polymethacrylates. More flexible polymers should have a stronger tendency to form more stable mesophases. Nevertheless, smectic liquid crystalline phases are the most common mesophases formed, if they do indeed form, by polymers in which no flexible spacers are used to connect main chain and... [Pg.173]

Preincubation of surfaces with platelet-poor plasma substantially reduced the platelet retention index of polyacrylates and polymethacrylates, but hardly altered the retention index of polystyrene or copolymers with methyl acrylate that are rich in styrene. Even without plasma pretreatment, the surface, when exposed to whole blood, was probably first contacted by molecular elements (including the proteins) before the cellular elements arrived. What then is the mode of action of plasma pretreatment Several hypotheses, none conclusive, can be advanced, such as ... [Pg.46]

Compared to aliphatic hydrocarbons, aromatic hydrocarbons (DIN 51633) have a higher solvency for oils, castor oil, oil-modified alkyd resins, styrene-modfied oils and alkyd resins, saturated polyester resins, polystyrene, poly(vinyl ethers), polyacrylate and polymethacrylate esters. poly(vinyl acetate), vinyl chloride and vinyl acetate copolymers, and many low-polarity resins. [Pg.351]

Polyacrylates and polymethacrylates Chloroform, acetone, ethyl acetate, tetrahydrofuran, toluene Methanol, diethyl ether, petroleum ether... [Pg.29]


See other pages where Polyacrylics and polymethacrylics is mentioned: [Pg.361]    [Pg.75]    [Pg.9]    [Pg.443]    [Pg.100]    [Pg.490]    [Pg.141]    [Pg.12]    [Pg.153]    [Pg.46]    [Pg.47]    [Pg.48]    [Pg.838]    [Pg.857]    [Pg.158]    [Pg.31]    [Pg.546]    [Pg.103]    [Pg.37]    [Pg.655]    [Pg.153]    [Pg.31]    [Pg.58]    [Pg.235]    [Pg.369]    [Pg.18]   


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POLYMETHACRYLIC

Polyacrylate

Polyacrylates

Polyacrylic

Polyacrylics

Polymethacrylate

Polymethacrylates

Polymethacrylates and polyacrylates

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