Photoinitiated free-radical systems

All UV curable systems have four basic components which must be included in order to develop a successful coating. They are the photoinitiator(s), oligomer(s), monomer(s), and additive(s). Table II lists the properties of each component which make it essential to the UV curable formulation. In the next few pages, we summarize each of the components and their properties. The photoinitiator section covers both radical and cationic type photoinitiators while the oligomer and monomer sections are restricted to components used in free radical systems. 

The most common restoratives comprise a mineral filler mixed with a vinyl monomer (often called a resin), which undergo photoinitiated free radical Chain polymerization. Typical components inclnde the adduct of bis-phenol A and glycidy methacrylate (bis-GMA) or nrethane dimethacrylate (UDMA), camphorquinone initiator (activated by a visible bine light sonrce of 480 nm) and a filler such as zirconia or borosilicate glass, which can comprise 70% by mass of the system and provides the strength . The whole is referred to as a composite . 

The methods used to prepare NC gels are simple and versatile, i.e., injection of reaction solutions into closed vessels followed by polymerization at ambient temperature. Hence, NC gels can be readily formed in various shapes and sizes, such as films, sheets, rods, spheres, hollow tubes, etc. (Fig. 4a) [21,29]. NC gels can also be prepared by photoinitiated free-radical polymerization using very low concentrations (e.g., 0.1 wt% relative to the monomer) of a hydrophobic photoinitiator in aqueous systems (Fig. 4b) [48], Furthermore, the other type of NC gel, i.e., tetra-PEG-based NC gels, with good biocompatibility can be prepared by incorporating clay nanoparticles into the tetra-PEG network [30],... 

Thus, a mixture of simple carbonyls Me(CO)n and halides should behave as a photoinitiator of free radical polymerization. Many such systems have been found to function in this way. Complexes formed by irradiation of Fe(CO)5 in the presence of a vinyl monomer (M) (such as MMA, styrene, vinyl acetate, propylene, and vinyl ether) have been studied by Koerner Von Grustrof and colleagues [12,13] and shown to have the chemical struc-... 

The initiating radicals are assumed to be SCN, ONO or N3 free radicals. Tris oxalate-ferrate-amine anion salt complexes have been studied as photoinitiators (A = 436 nm) of acrylamide polymer [48]. In this initiating system it is proposed that the CO2 radical anion found in the primary photolytic process reacts with iodonium salt (usually diphenyl iodonium chloride salt) by an electron transfer mechanism to give photoactive initiating phenyl radicals by the following reaction machanism ... 

The block copolymer produced by Bamford s metal carbonyl/halide-terminated polymers photoinitiating systems are, therefore, more versatile than those based on anionic polymerization, since a wide range of monomers may be incorporated into the block. Although the mean block length is controllable through the parameters that normally determine the mean kinetic chain length in a free radical polymerization, the molecular weight distributions are, of course, much broader than with ionic polymerization and the polymers are, therefore, less well defined,... 

The reaction between Cell—O radical and vinyl monomers leads to the formation of grafted cellulose. In the presence of photosensitizers generally used as photoinitiators, such as benzophenone and phenylace-tophenone derivatives, the photoinitiator absorbs the UV radiation and transforms to its singlet (S ) and then triplet (T ) states. After that it may decompose into free radicals or transfer its energy to cellulose or any other molecules in the system. Take benzophenone as an example ... 

The chemistry involved in LfV-curable resin systems has been extensively investigated and thoroughly surveyed [88-94]. LfV-radiation polymerization, is in principle, completely analogous to the conventional addition polymerization. A photoinitiator is used in UV polymerization. Its function is the same as the free-radical initiator. A conventional initiator possesses a thermally labile bond which is cleaved to form free-radical species, but the photoinitiator has a bond which breaks upon absorption of radiant energy. Benzoin ethers, benzyldialkyl ketals, benzophenone, and acetophenone derivatives are the important LfV-photoinitiators [95-99]. 

In this paper, we report efforts to find donor/acceptor systems, comprised of at least one multifunctional monomer, capable of sustaining rapid free-radical polymerization without the need for external photoinitiators. Although we will include in this report comonomer systems which form ground state CT complexes, we stress that the primary mechanism for generating free-radical in each case may not be via excitation of ground state CT complexes. 

Difunctional vinvl ether/difunctional N-maleimide. Up until this point, our results have centered on the reactivity of monofunctional maleimide divinyl ether mixtures. From Kloosterboer s26 work for acrylate polymerization, it is known that the rate of polymerization of a free-radical process is increased dramatically as the functionality of the acrylate is increased. In order to enhance the polymerization rates of maleimide divinyl ether systems, it was decided to synthesize difimctional maleimides for copolymerization with difunctional vinyl ethers. The results in Table V indicate that the photoinitiated TTDBM [bismaleimide made from maleic anhydride and 4,7,10-... 

Free-radical photoinitiators are classified by their chemical nature as type I and type II however, there are a few systems with different chemistry, e.g., borate salt initiators that depend on inter-/intramolecular electron transfer,i that do not fit into either category. 

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