For surface modification

Patterns of ordered molecular islands surrounded by disordered molecules are common in Langmuir layers, where even in zero surface pressure molecules self-organize at the air—water interface. The difference between the two systems is that in SAMs of trichlorosilanes the island is comprised of polymerized surfactants, and therefore the mobihty of individual molecules is restricted. This lack of mobihty is probably the principal reason why SAMs of alkyltrichlorosilanes are less ordered than, for example, fatty acids on AgO, or thiols on gold. The coupling of polymerization and surface anchoring is a primary source of the reproducibihty problems. Small differences in water content and in surface Si—OH group concentration may result in a significant difference in monolayer quahty. Alkyl silanes remain, however, ideal materials for surface modification and functionalization apphcations, eg, as adhesion promoters (166—168) and boundary lubricants (169—171). 

UV irradiation on a polymer surface produces chemical modification as well as wettability and bondability improvement. It causes chain scission and oxidation on polymer surfaces. -iven in the presence of an inert gas [45]. Carbonyls are found to be introduced onto polyethylenes on UV irradiation. Sivram et al. [46] have used photochemical treatments for surface modification of polymers. They have generated surfaces of vaying surface energies by simple organic reactions. 

Radiation-induced grafting and curing processes have been discussed in a number of reviews.203 28 291 The process is widely used for surface modification. Recent applications are the modification of fuel cell membranes and improving... 

When the films were treated in either an oxygen plasma environment or under UV/ozone irradiation, the rates of oxidation were faster for the plasma process. Irradiation of chitosan solution showed that UV/ozone induces depolymerization. In both plasma and UV/ozone reactions, the main active component for surface modification was UV irradiation at a wavelength below 360 nm [231]. 

Ti02 thin films for surface modification were prepared by sol-gel method and dip-coating... 

The reason for surface modification of a polymer is in most cases a wish to improve wettability and adhesion towards more hydrophilic materials. Both adhesion and wettability are interfacial phenomena. 

Fig. 20 Reaction mechanism for surface modification of luminomagnets with folic acid. (Adapted from [76])...

Figure 2.2 A number of small thiol-containing molecules have proven useful for modification of gold or metallic surfaces. The dithiol derivatives provide better dative bond stability and can t be displaced easily by competing thiols or oxidation. Most thiol-containing compounds used for surface modification also contain terminal functional groups or reactive groups for coupling affinity ligands.

Hong et al. (2004) also found that modification of PAMAM dendrimers with a short PEG linker arm could act to reduce nonspecificity caused by the amines on the dendrimer-modified surface. An azido-PEGj-aininc spacer was activated with nitrophenyl carbamate to yield an activated intermediate that could be used to modify the amines on the dendrimer (Figure 7.24). Reaction at high molar ratio resulted in about 61 PEG-azido spacers on the dendrimer. Reduction of the azido group to an amine using triphenylphosphine in THF provided the dendrimer-PEG-amine derivative for surface modification. The added presence of the PEG spacer arm reduced... 

Figure 7.26 Dendrimers made with a disulfide-containing core can be reduced to produce dendrons having free thiol groups for surface modification. Dative binding of these thiol-dendrons to gold or metallic surfaces can provide a high density of amine groups for coupling proteins or other molecules.

A. N. Khramov, V. N. Balbyshev, L. S. Kasten and R. A. Mantz, Sol-gel coatings with phosphonate functionalities for surface modification of magnesium alloys, Thin Solid Films, 2006, 514, 174. 

In the category of silicone coatings used for surface modification of the specific substrates, functional silicone fluids are often used, which can selectively interact with the chemical groups of the substrate, thus modifying its surface properties. The use of functional silicones in the textile industry has been discussed in a number of recent publications.5 421 422 The use of different types of high-performace silicone-coated textiles, which include elastomers and resins, has recently been reviewed.423 The use of functional silicones in personal-care products, for example, in shampoos and hair conditioners, mentioned before,381 provides another well-known example. 

TRIDENDRON DENDRIMER AND GENERAL PROCEDURE FOR SURFACE MODIFICATION OF THE HYDROXYL TERMINATED DENDRIMERS... 

All plasma experiments were performed with an LMP reactor which has been described elsewhere in detail (5). The reactor is equipped with a heatable, rotating platen, 15 cm. in diameter, to which are fastened specimens for surface modification. The reactor operates at 2.45 GHz frequency and at power in the range 0.1 - 2.5 kW. 

In general, in the field of materials or condensed matter, the preparation of polymer brushes on solid surfaces is of great interest for surface modification and composite material preparation [4-6]. A number of model surface grafting techniques have been used on planar surfaces and particles and have been the subject of previous reviews. While a munber of polymer brush preparation methods have been reported using physisorption or chemisorption or so-called grafting onto methods, the emphasis of this review is on surface-initiated polymerization (SIP) methods or grafting from methods. 

Miscellaneous methods for surface modifications that were not taken up in the previous sections are presented in this section. 

This chapter focuses its attention on the discussion of the most relevant questions of interfacial adhesion and its modification in particulate filled polymers. However, because of the reasons mentioned in the previous paragraph, the four factors determining the properties of particulate filled polymers will be discussed in the first section. Interactions can be divided into two groups, parti-cle/particle and matrix/filler interactions. The first is often neglected although it may determine the properties of the composite and often the only reason for surface modification is to hinder its occurrence. Similarly important, but a very contradictory question is the formation and properties of the interphase a separate section will address this question. The importance of interfacial adhesion... 

Kang YC, van Ooij WJ (2006) RF plasma polymerization for surface modification of carbon black rubber filler. ACS Rubber Division Meeting, Cincinnati, 2006. ACS, Akron, Ohio,... 

Fig. 1 shows the increase of nitrite band near 780 cm- for various alcohol contents in ethylene-vinyl alcohol copolymers. The analysis of the hydroxyl region of the IR spectra (not shown) indicated that the reaction was not quantitative (residual OH band). The precise analysis of this band ( 34(X) 70 I / mol. cm) as w ell as the nitrite band (e780 639 I / mol. cm) allows to evaluate the reaction yield considering the total film thickness (Transmission 1R). The values decrease when the OH content increases (0.75 0.62 0.59 ans 0.59 for vinyl alcohol contents 2.6,4.9, 7.7 and 10.1% respectively). Complementary analysis by reflexion IR (HATR) showed that the first 5-8 pm (Germanium crystal) were fully transformed while the analysis of the first 20-25 pm (Zinc Selenide crystal) revealed a decrease of the yield from 1 to 0.5 when the alcohol content was increasing. Then, this treatment can be helpfull for surface modification of membranes. 

Silylating agents and SiR3/Si02 molar ratios employed for surface modification of Ti-MCM-41 catalyst. 

Fig. 9 Synthesis scheme for surface modification of silica. Formation of (A) a monomeric phase and (B) a polymeric phase. (From Ref. 112.)...

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