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High cations

The protonated form of poly(vinyl amine) (PVAm—HCl) has two advantages over many cationic polymers high cationic charge densities are possible and the pendent primary amines have high reactivity. It has been appHed in water treatment, paper making, and textiles (qv). The protonated forms modified with low molecular weight aldehydes are usehil as fines and filler retention agents and are in use with recycled fibers. As with all new products, unexpected appHcations, such as in clear antiperspirants, have been found. It is usehil in many metal complexation appHcations (49). [Pg.320]

A second approach to promoting high cationic transport is to choose a molecular solvent which has the ability to interact with anions than cations. A number of electron deficient borates such as... [Pg.518]

Aluminum Chlorhydrate (ACH), A12(0H)5C1 ACH reacts very similarly to PAC and is available only as a solution. It is a very highly basic product (80%). Upon dilution, PAC and ACH solutions tend to act as highly cationic polymers. After dilution and with time, they also begin to degrade and act like alum. This period may be on the order of 1 to 10 minutes, depending on pH level and temperature, The dose rate is similar to that of PAC. Good turbidity and color removal are achieved with ACH. [Pg.316]

A number of articles considered the association of chitosan with polylactic acid or similar compounds [47-49] another group of articles presented new data on highly cationic chitosans [ 50 - 55]. More data have also been made available on the delivery of growth factors [56] and ophthalmic drugs [57,58], on the activation of the complement, macrophages [59-61] and fibroblasts [62], on mucoadhesion [63] and functionalization of chitin [64]. The development of new carriers for the delivery of drugs, and the interactions of chitosans with living tissues seem therefore to be major topics in the current research on chitosan. Therefore, this chapter will place emphasis on these aspects. [Pg.153]

Corrosion inhibitors used in offshore oil production are highly cationic. However, the use of such cationic-based corrosion inhibitors for offshore oil platforms is becoming less acceptable for environmental reasons. Cationic inhibitors are attracted to metal surfaces, thereby controlling the acid-type corrosion. When these cationic corrosion inhibitors enter seawater, they are attracted to a particular type of algae, diatomes. These algae are part of a food-chain for mussels. The cationic inhibitors inhibit the growth of these algae. Betaines and ampholytes [1067] can be used instead of cationic inhibitors or... [Pg.90]

Especially in dicotyledonous plant species such as tomato, chickpea, and white lupin (82,111), with a high cation/anion uptake ratio, PEPC-mediated biosynthesis of carboxylates may also be linked to excessive net uptake of cations due to inhibition of uptake and assimilation of nitrate under P-deficient conditions (Fig. 5) (17,111,115). Excess uptake of cations is balanced by enhanced net re-lea,se of protons (82,111,116), provided by increased bio.synthesis of organic acids via PEPC as a constituent of the intracellular pH-stat mechanism (117). In these plants, P deficiency-mediated proton extrusion leads to rhizosphere acidification, which can contribute to the. solubilization of acid soluble Ca phosphates in calcareous soils (Fig. 5) (34,118,119). In some species (e.g., chickpea, white lupin, oil-seed rape, buckwheat), the enhanced net release of protons is associated with increased exudation of carboxylates, whereas in tomato, carboxylate exudation was negligible despite intense proton extrusion (82,120). [Pg.58]

The saturation of the SHG response at high cation concentrations suggests that the process of complex formation at the membrane surface may be treated by a Langmuir-isotherm type analysis [24,27]. At constant temperature, the Langmuir equation is given by... [Pg.445]

This material was first synthesized in the middle 1960s by E.I. Du Pont de Nemours and Co., and was soon recognized as an outstanding ion conductor for laboratory as well as for industrial electrochemistry. The perfluorinated polymeric backbone is responsible for the good chemical and thermal stability of the polymer. Nation membrane swollen with an electrolyte solution shows high cation conductivity, whereas the transport of anions is almost entirely suppressed. This so-called permselectivity (cf. Section 6.2.1) is a characteristic advantage of Nation in comparison with classical ion-exchange polymers, in which the selective ion transport is usually not so pronounced. [Pg.143]

Allylic substitution reactions using LPDE have also been reported. The reaction of an allyl alcohol with several nucleophiles proceeds smoothly in a 3.0 M LPDE solution (Scheme 2). 3 Moreover, a highly cationic lithium species has been developed, and a catalytic amount of this species promotes allylic substitution reactions efficiently.14... [Pg.400]

Aminoethyl-8 has an advantage over ethylenimine modification (see next section), due to the potential polymerization of ethylenimine in aqueous solutions. Such polymers are highly cationic and may nonspecifically block the protein. The specificity of Aminoethyl-8 for sulfhydryls makes it an optimum choice for modification. [Pg.118]

In the radical anions of the norbornane-linked naphthalenes [37] mentioned earlier (Gerson et al, 1990) no counterion effects were detected for [37a], which has a small spatial separation, but the esr/ENDOR spectra of [37b]- and [37c]- indicate that the electron-spin transfer between the naphthalene moieties is determined by the rate of synchronous counterion migration (Gerson et al., 1990). For tight ion pairs the electron is localized, while for loose ion-pair conditions, e.g. by using solvents of high cation-solvating power, the transfer becomes fast on the hyperfine timescale (k > 107 Hz). [Pg.33]

HB-5) unusually high cationic character of central atom B and anionic character of terminal atoms A and C, as reflected in natural atomic charges Qa, Qb, Qc), ionic bond orders (6AB(ion) and Aiic<1011)), and electrovalencies (TA(lon), IV1011 . Vc(l0n)). [Pg.282]

Adsorption at high cationicity is low and relatively independent of molecular weight because the polyelectrolyte is adsorbed in a relatively flat conformation. Adsorption at low to intermediate cationicities is higher and also tends to be dependent upon molecular weight. This is because the polyelectrolyte is adsorbed in a much less compressed conformation. This is represented pictorially in Figure 6.9. [Pg.101]

Rurack K, Rettig W, Resch-Genger U (2000) Unusually high cation-induced fluorescence enhancement of a structurally simple intrinsic lluoroionophore with a donor-acceptor-donor constitution. Chem Commun 407 108... [Pg.101]

CNTs with different characteristics, which will lead to differences in the mechanism of CNT metabolism, degradation or dissolution, clearance and bioaccumulation. On the other hand, most non-viral gene delivery systems today suffer from both limited levels of gene expression and an unfavourable toxicity profile due to their highly cationic surface character. Therefore, opportunities for CNT-based gene transfer systems are still ample. [Pg.39]

To illustrate this point, consider the membrane plated for 60 minutes. The tubules in this membrane average —9.4 nm in inside radius. At low concentrations of salt, the electrical double should be thicker than this tubule radius. Anions are excluded from the tubes, and ideal cation permselectivity is observed. At high salt concentrations, the electrical double layer is thin relative to the tubule radius. Anions can now enter the tubules, and ideal cation permselectivity is lost (Fig. 11). Finally, the membrane plated for 180 minute shows cation permselectivity almost identical to that of the ionomer Nation [92], which is a highly cation-permselective polymer used in industrial electrolytic processes [93],... [Pg.27]


See other pages where High cations is mentioned: [Pg.266]    [Pg.143]    [Pg.34]    [Pg.13]    [Pg.198]    [Pg.77]    [Pg.912]    [Pg.518]    [Pg.92]    [Pg.151]    [Pg.167]    [Pg.167]    [Pg.13]    [Pg.29]    [Pg.796]    [Pg.445]    [Pg.454]    [Pg.454]    [Pg.134]    [Pg.510]    [Pg.736]    [Pg.401]    [Pg.699]    [Pg.101]    [Pg.78]    [Pg.280]    [Pg.140]    [Pg.224]    [Pg.312]    [Pg.45]    [Pg.22]    [Pg.195]    [Pg.39]    [Pg.43]    [Pg.201]   
See also in sourсe #XX -- [ Pg.111 , Pg.209 , Pg.271 , Pg.318 ]




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Cation concentrations, high-alkali

Cation substitution, high temperature

Cation substitution, high temperature transfers

Cationic High-Bulk Material

Cationic Polymerisation from Progress in High Polymers

Cations highly stable

Chitosans highly cationic

High Molecular Weight Polyalkylene Oxide Polyols by Cationic Polymerisation

High performance liquid chromatography cationic surfactants

High performance liquid chromatography, applications cations

High-energy-radiation-induced cationic

High-energy-radiation-induced cationic polymerization

High-mobility cations

High-performance cation-exchange

High-performance cation-exchange chromatography

High-performance liquid chromatography cation-exchange resin columns

Highly cationic starches

Highly soluble cationic organotitanium

Highly soluble cationic organotitanium Lewis acids

Hydrolysis, highly soluble cationic

Phenyl cation, high energy

Reaction chemistry, highly soluble cationic

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