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Basicity, of monomers

SAHgg (Model C). In this model (Table 2.16) the SB region is considered to consist basically of monomers. Some of these monomers are H bonded to the molecules in the first shell. The SCW and NSCW participate in two and three H bonds with molecules in the SB region. The formation of an SB region of monomers can be treated according to the cycle shown in Fig. 2.39. Therefore, one can write... [Pg.122]

Conclusions for the monovalent ions can be drawn from this fairly detailed analysis. (1) A division of a region around the ion into two parts (Bockris, 1949 Frank and Wen, 1957) is supported. (2) In the first layer around the ion, one can distinguish two kinds of water molecules, referred to as solvated and nonsolvated. (3) The second layer is also one water molecule thick and consists basically of monomers, some of which librate. [Pg.137]

Kinetic parameters in copolymerization of oxetanes and THE," basicities of monomer [158]... [Pg.323]

The pm scale was proposed for solute HBA basicity of monomer amphihydro-gen-bonding compounds acting as non-self-associated solutes. In particular, p , values are taken equal to p values for non-self-associating compounds. [Pg.268]

To a first approximation, the capacity of a given initiator to start the anionic polymerization of a given monomer depends on the basicities of monomer and initiator. Monomers with strong electron acceptor groups need only weak bases as initiators, and vice versa. [Pg.137]

Proton-Transfer Polymerization. Proton-transfer polymerization (PTP) (Fig. 11) has been reported as a versatile route to hyperbranched polymers (56). Conceptnally, PTP is an acid-base controlled reaction where the nucleophilicity and basicity of monomer and intermediates play important roles. [Pg.3866]

A polymer is a macromolecule that is constructed by chemically linking together a sequent of molecular fragments. In simple synthetic polymers such as polyethylene or polystyrer all of the molecular fragments comprise the same basic unit (or monomer). Other poly me contain mixtures of monomers. Proteins, for example, are polypeptide chains in which eac unit is one of the twenty amino acids. Cross-linking between different chains gives rise to j-further variations in the constitution and structure of a polymer. All of these features me affect the overall properties of the molecule, sometimes in a dramatic way. Moreover, or... [Pg.439]

LGP Economics. LCPs are expensive materials. Prices in January 1996 (248) ranged from 15.20/kg for mineral-filled resin, 15.73— 23.43/kg for glass-fiHed resin, and up to 48.40/kg for unfilled extmsion-grade polymer. One of the basic reasons is the fundamental high cost of monomers and intermediates which is a consequence of low volume. [Pg.308]

Nitrile rubbers are produced over a wide range of monomer ratios and molecular weights, so thek physical constants and basic polymer properties also cover a range of values. Some of the more widely used properties are Hsted ki Table 1. [Pg.517]

Considering functional group complementarity, other commodity monomers may also be used. Thus for templates containing acid groups, basic functional monomers are preferably chosen. The 2- or 4-vinylpyridines (VPY) are particularly well-suited for the imprinting of carboxylic acid templates and provide selectivities of the same... [Pg.171]

Currently, graft post-polymerization of monomers in the gaseous phase (2) is the more widely used process because it has at least two basic advantages. First, side processes of homopolymerization are minimized which reduces the consumption of monomers and makes unnecessary additional treatment of the modified materials with solvents. Second, this method is universal and allows the grafting to the surfaces (such as silica) to be carried out with low radiation yields of active sites as compared to the monomers. [Pg.161]

Applications As the basic process of electron transfer at an electrode is a fundamental electrochemical principle, polarography can widely be applied. Polarography can be used to determine electroreductible substances such as monomers, organic peroxides, accelerators and antioxidants in solvent extracts of polymers. Residual amounts of monomers remain in manufactured batches of (co)polymers. For food-packaging applications, it is necessary to ensure that the content of such monomers is below regulated level. Polarography has been used for a variety of monomers (styrene, a-methylstyrene, acrylic acid, acrylamide, acrylonitrile, methylmethacrylate) in... [Pg.671]

The overwhelming majority of synthetic polymers is organic in nature, and it is on these that we will concentrate. The simplest and most common synthetic polymer is polyethylene, which will be our first example. Figure 1.1 shows the basic chemical structure of polyethylene. Pairs of hydrogen atoms are attached to the carbon atoms that make up the backbone. The repeat unit in this structure contains two carbon atoms and is derived from the ethylene monomer. In the case of polyethylene, the number of monomer residues, which is known as the polymerization... [Pg.19]

Perhaps the most common particle type used for bioapplications is the polymeric microsphere or nanosphere, which consists basically of a spherical, nonporous, hard particle made up of long, entwined linear or crosslinked polymers. Creation of these particles typically involves an emulsion polymerization process that uses vinyl monomers, sometimes in the presence of... [Pg.588]

The protection-deprotection reaction sequences constitute an integral part of organic syntheses such as the preparation of monomers, fine chemicals, and reaction intermediates or precursors for pharmaceuticals. These reactions often involve the use of acidic, basic or hazardous reagents and toxic metal salts [30], The solvent-free MW-accelerated protection/deprotection of functional groups, developed during the last decade, provides an attractive alternative to the conventional cleavage reactions. [Pg.183]

The Lewis acidity and reactivity of these alkyl aluminum cocatalysts and activators with Lewis basic polar monomers such as acrylates make them impractical components in the copolymerization of ethylene with acrylates. To address this shortcoming, Brookhart et al. developed well-defined cationic species such as that shown in Fig. 2, in which the counterion (not illustrated) was the now-ubiquitous fluorinated arylborate family [34] such as tetrakis(pentaflurophenyl)borate. At very low methyl acrylate levels the nickel catalysts gave linear copolymers but with near-zero levels of acrylate incorporation. [Pg.164]


See other pages where Basicity, of monomers is mentioned: [Pg.158]    [Pg.323]    [Pg.158]    [Pg.323]    [Pg.1023]    [Pg.195]    [Pg.411]    [Pg.125]    [Pg.461]    [Pg.488]    [Pg.251]    [Pg.521]    [Pg.157]    [Pg.168]    [Pg.197]    [Pg.203]    [Pg.76]    [Pg.398]    [Pg.6]    [Pg.10]    [Pg.13]    [Pg.93]    [Pg.562]    [Pg.892]    [Pg.877]    [Pg.317]    [Pg.169]    [Pg.180]    [Pg.173]    [Pg.288]    [Pg.38]    [Pg.1292]    [Pg.663]    [Pg.137]   
See also in sourсe #XX -- [ Pg.5 ]




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Basicity of Initiators and Monomers

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