Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Initiators / modifiers

Free Radical Initiator Modifiers a. Piperidine N-oxide derivatives... [Pg.322]

The total costs can be divided into fixed-capital- and variable costs. Fixed-capital costs have to be taken into account also when a plant is out of operation, whereas variable costs depend on the production rate. Fixed-capital costs are depreciation, maintenance, manpower, overheads, etc. Variable costs are utilities, monomers, and other chemicals such as initiators, modifiers, or stabilizers. The costs are presented in Table 8.2-3. The total costs are 1,491 DM/t LDPE for the lower-, and 1,431 DM/t LDPE for the higher-plant capacity. [Pg.455]

Since the cross-linker is cleavable, SAED provides a means of fluorescent transfer of the coumarin tag to a second molecule, which interacts with the initially modified protein (Fig. 181). For example, soybean trypsin inhibitor (STI) was labeled with SAED and then allowed to interact with trypsin. After photoreactive cross-linking of the two interacting molecules, the complex was reduced with DTT, breaking the conjugate and transferring the fluorescent tag to trypsin near the STI binding site (Thevenin et al., 1991). [Pg.290]

Variables in Table III from which combinations were made P = initial pressure, T = initial temperature, X = initial modifier, AP = pressure gradient, AT= temperature gradient, and AX = modifier gradient. [Pg.320]

This chapter documents enhancements of the efficiency of SFE extraction of alkaloids from plant matrices using basified modifiers. Hence (1) The pure compound solubility of some free bases in pure supercritical C02 has been measured by investigating the effects of temperature, pressure or density of C02 (2) The solubilities of the alkaloidal salts were compared with those of their free bases in order to evaluate the difference of their solubilities influenced by a changing from free bases to salts (3) Polar solvents such as methanol and water, as initial modifiers, were used for the enhancement of the solubilities (4) The solubilities of the salts by non-basified modifiers such as neat methanol or water were compared with those of methanol or water basified with diethylamine (5) The effect of modifiers employed on the desorption of the compounds from a matrix were measured and compared with each other (5) On the basis of the results of pure compound extractability, SFE was performed on alkaloids from the plant... [Pg.420]

Loschonsky, S., Couet, J., and Biesalki, M. "Synthesis of peptide/polymer conjugates by solution ATRP of butylacrylate using an initiator-modified cyclic D-alt-L-peptide". Macromol. [Pg.222]

Polyimide surface modification by a wet chemical process is described. Poly(pyromellitic dianhydride-oxydianiline) (PMDA-ODA) and poly(bisphenyl dianhydride-para-phenylenediamine) (BPDA-PDA) polyimide film surfaces are initially modified with KOH aqueous solution. These modified surfaces are further treated with aqueous HC1 solution to protonate the ionic molecules. Modified surfaces are identified with X-ray photoelectron spectroscopy (XPS), external reflectance infrared (ER IR) spectroscopy, gravimetric analysis, contact angle and thickness measurement. Initial reaction with KOH transforms the polyimide surface to a potassium polyamate surface. The reaction of the polyamate surface with HC1 yields a polyamic acid surface. Upon curing the modified surface, the starting polyimide surface is produced. The depth of modification, which is measured by a method using an absorbance-thickness relationship established with ellipsometry and ER IR, is controlled by the KOH reaction temperature and the reaction time. Surface topography and film thickness can be maintained while a strong polyimide-polyimide adhesion is achieved. Relationship between surface structure and adhesion is discussed. [Pg.179]

Musyanovych A, Adler H-JP (2005) Grafting of amino functional monomer onto initiator-modified polystyrene particles. Langmuir 21(6) 2209-2217... [Pg.61]

Polyvinyl chloride-montmorillonite nanocomposites were prepared either by in-situ suspension polymerisation using initiator- and comonomer-modified montmorillonite in the presence of free-radical initiators, such as AIBN, and compared. It was found that monomer conversion was low when the nanocomposites were prepared using initiator-modified montmorillonite. Exfoliated nanocomposites... [Pg.51]

The contrary synthesis of the initial modifier for subsequent immobilization on silica has shown that reaction can proceed in two directions with formation of mono-(a) and two-substituted (b) product, where R is Ph or NEt2 ... [Pg.322]

Figure. 44 shows the C Is (a-d), O Is (e-h), and Fe 2p 2 (i-j) XPS peaks of CWZ (NM and Ox) samples with adsorbed iron ions. There were marked differences between the experimental (dotted) and synthesized (continuous) lines in all the spectra. The position of deconvoluted peaks (dashed lines) were determined according to both literature data [188,191,240-247] and empirically derived values. The relative areas (%) of the fitted peaks were also calculated. Several peaks attributable to carbon, oxygen, nitrogen, and iron were present. The XP survey spectra of the initial modified carbons (before adsorption) were discussed... [Pg.186]

The recorded differences in adsorption capability indicate a different mechanism of interaction between the carbon surface and the ionic metal species pre.sent in the aqueous solution (aqua and hydroxy complexes, hydroxide ions, and electronegative complexes). To discover the state of the adsorbed. species, some independent measurements of the surface layer of adsorbent were carried out. The selected carbon samples were studied by the XPS method in powdered form following copper uptake (Figs. 42 and 43). Several peaks attributable to carbon, oxygen, nitrogen, and copper were present. The XPS survey spectra of the initial modified carbons (before adsorption) were discussed in the previous section. The surface elemental composition estimated from XPS data for modified D43/1 car-... [Pg.197]

By adjusting the reactivity of the initiator/modifier system toward metallation of the polymer backbone, Kerns and Henning have developed synthetic strategies... [Pg.2875]

It is seen that all three known types of distribution are observed experimentally. One can see that the nature of surface bonded groups of initial modified silica plays an important role. Namely, reactions between the amines studied and the bromopropyl-modified silica run according to the island-like mechanism. Whereas, both random and uniform coverages are more frequent for the tosyl- and the epoxy-modified silicas. [Pg.202]

For the incorporation of AM antibody into the liposomal membrane, AM-Fab is initially modified with a hydrophobic anchor, NGPE, as described in ref. 44. [Pg.181]

Originally only low reactivity quicklime was used and many producers specify that quality. In the UK, however, suitable quicklimes were not generally available and many of the processes were initially modified to use cement as the sole binder. Subsequently, part of the cement has been replaced, with advantage, by moderate and high reactivity high-calcium quicklimes. [Pg.288]

Surface coupling reactions on porous materials with an inner svurface will be investigated first. Silica gel was chosen as a model substrate with surface silanol groups which react under condensation with triethoxysilylsubstituted initiators. The resulting initiator modified silicas are used to stxxiy the polymerization of monofunctional monomers which should occur on the surface of the solid material. [Pg.107]

Thermal gravimetric analysis (t.g.a) The weight loss of photo-initiator modified silicas II eis a function of the temperature was measured with a Du Pont Instruments 9900 Computer / Thermal Analysis. System. The measurement was carried out at a heating rate of 2 min and an air flow rate of 0.15 1 min. ... [Pg.108]

Benzophenone (BP) is a photoinitiator that can be employed in a number of ways for the preparation of patterned graft polymers. BP can be directly used as an initiator for radical polymerization, either via immobilization of BP on the surface or by adding BP to the monomer solution (Figures 3.9A and 3.9B). Another possibility is to synthesize initiators modified with BP, which can then be immobilized on surfaces using UV light (Figure 3.9C). Yet another alternative is to add BP to the initiator solution for BP-mediated attachment of the initiator to the surface (Figure 3.9D). [Pg.51]


See other pages where Initiators / modifiers is mentioned: [Pg.463]    [Pg.139]    [Pg.405]    [Pg.416]    [Pg.494]    [Pg.319]    [Pg.326]    [Pg.363]    [Pg.387]    [Pg.391]    [Pg.317]    [Pg.664]    [Pg.118]    [Pg.297]    [Pg.313]    [Pg.294]    [Pg.61]    [Pg.464]    [Pg.191]    [Pg.200]    [Pg.701]    [Pg.2875]    [Pg.555]    [Pg.181]    [Pg.70]    [Pg.277]    [Pg.293]    [Pg.186]   


SEARCH



Free Radical Initiator Modifiers

Initiators / modifiers Photoinitiators

Modifiers Initially Miscible in Thermoset Precursors

© 2024 chempedia.info