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The use of acrylic pressure-sensitive adhesives (PSAs) is increasing in a variety of industrial fields. They have been applied in the manufacture of mounting tapes, self-adhesive labels, protective films, masking tapes, splicing tapes, carrier-free tapes, sign and marking films, and in diverse medical products, such as pads or self-adhesive bioelectrodes. In this study, the application of SiO2 nanoparticles in acrylic PSA was investigated. The properties of the newly synthesized and modified PSA were evaluated via the tack, peel adhesion, shear-strength and shrinkage. It has been found that the nanotechnologically-reinforced systems consisting of monodisperse non-agglomerated SiO2 nanoparticles and self-crosslinked acrylic PSAs showed a great enhancement in tack, peel adhesion, shear resistance and shrinkage, without showing the disadvantages known to result from the use of other inorganic additives. In this paper we evaluate the performance of SiO2 nanoparticles with a size of about 30 nm as inorganic filler into the synthesized solvent-borne acrylic PSA.
EN
The performance of 1-(9-ethylcarbazol-3-yl)-4,4,4-trifluorobutane-1,3-dione (1) as a fluorescent probe for the monitoring of cationic photopolymerization processes by Fluorescence Probe Technique (FPT) has been evaluated in comparison with the response of 7-diethylamino-4-methylcoumarin (Coumarin 1) (2). Triethylene glycol divinyl ether and diphenyliodonium hexafluorophosphate were used as an example monomer and a cationic photoinitiator respectively. It has been found that the probe 1 withstands the cationic polymerization conditions and provides correct probe response. 1-(9-ethylcarbazol-3-yl)-4,4,4-trifluorobutane-1,3-dione shifts its fluorescence spectrum with progress of cationic photopolymerization of the monomer, which enables the monitoring of the polymerization progress using the fluorescence intensity ratio measured at two different wavelengths as the progress indicator. By comparing the behavior of 1 and 2, it has been documented that the fluorescence spectrum of probe 1 shows a spectacular hypsochromic shift (Δλ = 33 nm) upon the monomer polymerization, while the shift of 2 is three times smaller (Δλ = 11 nm). Moreover, the sensitivity of probe 1 is more than 2.5-times higher than that of any other probes suitable for monitoring cationic polymerization processes, reported previously. Therefore, application of the carbazole derivative (1) as a new probe for the monitoring of the crosslinking process of coatings cured by cationic photopolymerization has been proposed.
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