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INNO SPECIALTY CHEMICALS is Photoinitiator 651
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"Open access journals are freely available online throughout the world, for you to read, download, copy, distribute, and use. The articles published in the open access journals are high quality and cover a wide range of fields." Kenji Hashimoto(Chiba University, Japan) Molarity Calculator Calculate the mass, volume, or concentration required for a solution. Mass picograms nanograms micrograms milligrams grams kilograms = Concentration femtomolar picomolar nanomolar micromolar millimolar molar x Volume nanoliter microliter milliliter liter x M. Wt* g/mol *When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and SDS / CoA (available online). Although the photoinitiating action of Irgacure compounds is well documented, the idea of using of these photoinitiators as degrading agents for the purpose of obtaining of the degradable materials is rather new. Our preliminary work, considering this topic, gives the promising information useful for designing the polymeric materials with controlled life-time. If no price is listed, this means the product is not in stock at the moment, which may be available via custom synthesis. For cost-effective reason, minimum order of 1g is requested (typically very expensive). The lead time is usually 2-4 months. Quote of less than 1g will not be provided. INTRODUCTION Irgacure photoinitiators constitute a family of commercial compounds, produced by Ciba Specialty Chemicals, Switzerland. They are well known as efficient intiators of polymerization of various kinds of monomers . Such initiators as benzyl ketals, u03b1,u03b1-dialkoxyacetophenones and u03b1-hydroxyalkylphenones contain chromophoric groups that absorb radiation in ultraviolet or visible range and undergo photolysis with formation of free radicals. The photochemical properties and photoinitiation activity of these organic compounds in polymerization and crosslinking of acrylated monomers were studied by various experimental methods. One of the most efficient photoinitiators in this group is Irgacure 651 (DMPA), C6H5-CO-C(OCH3)2-C6H5 . The compound is characterized by high phosphorescence quatum yield (u03a6=0.62) and relatively long triplet lifetime (u03c41/2= 2.59ms). High polymerization rate and large conversion degree in the presence of DMPA is explained by the significant benzoyl radical concentration, which was confirmed by flash photolysis. The initial concentration of the initiator in photopolymerised formulation has a great influence on the molecular weight and polydispersity of the obtained polymer . Although the photoinitiating action of Irgacure compounds is well documented, the idea of using of these photoinitiators as degrading agents for the purpose of obtaining of the degradable materials is rather new. Our preliminary work, considering this topic, gives the promising information useful for designing the polymeric materials with controlled life-time. The aim of this presentation is to study the photostability of poly(methyl methacrylate) (PMMA) doped with 2,2-dimethoxy-2-phenyl acetophenone initiator (abbreviation - DMPA, trade name - uIRGACURE 651) and to compare the course of photochemical reaction in doped and undoped polymers using UV-Vis spectroscopy. "Open access journals have become a fundamental tool for students, researchers, patients and the general public. Many people from institutions which do not have library or cannot afford to subscribe scientific journals benefit of them on a daily basis. The articles are among the best and cover most scientific areas." M. Bendandi(University Clinic of Navarre, Spain) "Open access journals are a novel concept in the medical literature. They offer accessible information to a wide variety of individuals, including physicians, medical students, clinical investigators, and the general public. They are an outstanding source of medical and scientific information." Jeffrey M. Weinberg(St. Lukes-Roosevelt Hospital Center, USA) RESULTS AND DISCUSSIONS The changes of electronic spectra of Irgacure 651 in ACN solutions caused by the UV-irradiation are shown in Fig. . The main bands with the maxima at 205, 251 and 341 nm are present, which is in a good agreement with the literature data . These bands are attributed to u03c0u2192u03c0* and nu2192u03c0* transitions. Fig. The changes in UV-Vis absorption spectra of Irgacure 651 in ACN solutions during UV-irradiation: (A) Cm= 8.8x10-5mol/dm3; (B) Cm= 4.4x10-3mol/dm3. The Fig. (1A) shows the decrease of the band intensity at 205 and 251 nm with the simultaneous formation of a new absorption peak at 223 nm during the 20 minutes of exposure. The low-intensity band at higher wavelenght (341 nm) also disapears rapidly, which is clearly observed in spectrum recorded for more concentrated solution (Fig. 1B). It indicates that Irgacure 651 undergoes the efficient photolysis in applied conditions. The carbonyl organic compounds of benzoin type, after the photon absorption and excitation undergo the u03b1-dissociation (Norrish type I cleavage) according to Scheme 1. This reaction is very fast and formed benzoyl and u03b1,u03b1-dimethoxybenzyl radicals differ significantly in their reactivity . The fragmentation of the latter one leads to the formation of small methyl radical and methyl benzoate . Both and radicals participate in photoinitiated polymerization but the action of u2022CH3 is much less effective than this of . Moreover, other major products of DMPA photolysis are benzaldehyde, benzil and acetophenone . Benzil, which is diketone (C6H5C=O)2 is also used as a photoinitiator in the polymer curing. Scheme 1Photolysis of Irgacure 651 initiator. The photostability of PMMA and PMMA + Irgacure 651 films of the same thickness were investigated using UV-Vis spectroscopy. The examples of changes in UV-Vis spectra of these samples are presented in Fig. . As can be noticed, the band at 251 nm, atributed to the photoinitiator, is present in the spectrum of the modified PMMA. However, it disapears already in the first hour of UV-irradiation. Fig. Changes of UV-Vis spectra of the pure PMMA (A) and PMMA doped with Irgacure 651 (B) during the exposure to Xenon lamp. The other signals due to initiator are difficult to detect in PMMA spectrum. The maximum at 205 nm overlaps the carbonyl band from PMMA; the band at 341 nm, owing to its low absorption coefficient and because of low DMPA concentration in polymeric sample is hardly seen. The prolongation of exposure time causes an increase of the absorbance in the 200-400nm range. The observed changes in UV-Vis spectra of both polymeric samples are irregular - particularly fast increase of the absorbance was observed at the beginning of the irradiation. The broad absorption band formed during the sample exposure indicates that the complex mixture of photoproducts arises. The increase of the absorbance in both UV-irradiated samples can be explained by the formation of the new functional groups such as carbonyls in main chain and separated or conjugated double bonds. It is known that PMMA undergoes mainly depolymerisation but furthermore a random chain scission takes place . The created monomer and oligomers containing unsaturated bonds accumulated in the matrix additionally increase the absorption of the degraded polymer. The solvent impurities which are present in both unexposed samples have no significant effect on the photodegradation rate, what was proved in the previous experiment. However, to investigate the kinetics of chromphore formation more thoroughly and to avoid the possible errors, the absorbance at 300 nm (which is outside of initiator absorption) was chosen for comparison the behavior of the PMMA and PMMA + DMPA samples. Fig. shows the differences in the kinetics of the photochemical reaction leading to the generation of the products absorbing at 300 nm. The rapid absorbance increase after 1h irradiation is an evidence of the fast reaction in the first period of the experiment. The next stage of photooxidative degradation is significantly restrained. The yield of the chromophoric group formation in the modified PMMA is a few times higher that in pure polymer. It is obviously caused by high concentration of the free radicals formed as a result of the DMPA decay. Fig. The kinetics of chromophore formation in the pure PMMA and the PMMA containing 5% Irgacure 65 during the exposure to Xenon lamp. The enhancement of the photoreaction in the modified PMMA can be explained by the reaction of the initiating species from DMPA with macromolecules. Most probable is the hydrogen abstraction from PMMA (Scheme 2). Scheme 2Initiation of PMMA decomposition by benzoyl radical. The macroradical (Pu2022) undergoes the secondary reactions, for example the addition of the oxygen molecules with the formation of peroxyradicals (POOu2022), which is a typical process for many polymers .

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