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1.
Fernandes Joo Lucas Ribeiro e de Souza Altair Lcio de Faria Geraldo Lcio 《Journal of Thermal Analysis and Calorimetry》2022,147(12):6593-6603
Journal of Thermal Analysis and Calorimetry - The hot coil slump is a recurrent problem in the manufacturing process of medium and high equivalent carbon steel plates. Even with the success of the... 相似文献
2.
Quantitative determination of omega-6 and omega-3 polyunsaturated fatty acids in human plasma and urine with high accuracy and precision provides significant information to monitor the underlying etiology of several diseases. In this regard, liquid chromatography-mass spectrometry is a good choice owing to its great selectivity and sensitivity. Additionally, the hybrid quadrupole–time of flight–mass spectrometer systems provides easy identification of target compounds with superior mass measurements. In this study, an analytical method has been developed for simple, accurate and simultaneous determination of linoleic acid, arachidonic acid, docosahexaenoic acid and eicosapentaenoic acid in a short chromatographic analysis period. The developed method is suitable for the quantitative detection of these four compounds with detection limits ranging between 1.1–3.0 ng ml−1 and its applicability was assessed in human urine and plasma samples. As a result, acceptable accuracy (between 83 and 111%) and good precision (<6%) were obtained for target compounds using matrix matching calibration strategy. 相似文献
3.
Mariem Ghali Chaima Brahmi Mahmoud Benltifa Cyril Vaulot Aissam Airoudj Philippe Fioux Frédéric Dumur Corine Simonnet-Jégat Fabrice Morlet-Savary Salah Jellali Latifa Bousselmi Jacques Lalevée 《Journal of polymer science. Part A, Polymer chemistry》2021,59(2):153-169
Different inorganic/organic photocomposites based on polyoxometalate (POM) nanoparticles have been developed for photocatalytic applications. Currently, polyoxometalate nanoparticles have been successfully in-situ embedded into an acrylate polymer network by photopolymerization upon mild visible light irradiation at 405 nm. The proposed POM/polymer photocomposites have been characterized using complementary techniques for a better understanding of their photocatalytic activity. Interestingly, the obtained photocomposites exhibit high rigidity, excellent thermal stability, a non-negligible porosity and new functionalities such as light reactivity and redox properties. Moreover, developed composites showed efficient catalytic activity for the color removal of aqueous solutions of erythrosine and rose Bengal under Light Emitting Diodes LED@375 nm irradiation reaching 80 and 90% as a final color removal, respectively. 相似文献
4.
Naphthalic anhydride derivatives: Structural effects on their initiating abilities in radical and/or cationic photopolymerizations under visible light 下载免费PDF全文
Pu Xiao Frédéric Dumur Jing Zhang Bernadette Graff Fabrice Morlet‐Savary Jean Pierre Fouassier Didier Gigmes Jacques Lalevée 《Journal of polymer science. Part A, Polymer chemistry》2015,53(24):2860-2866
Only one naphthalic anhydride derivative has been reported as light sensitive photoinitiator, this prompted us to further explore the possibility to prepare a new family of photoinitiators based on this scaffold. Therefore, eight naphthalic Naphthalic anhydride derivatives (ANH1‐ANH8) have been prepared and combined with an iodonium salt (and optionally N‐vinylcarbazole) or an amine (and optionally 2,4,6‐tris(trichloromethyl)‐1,3,5‐triazine) to initiate the cationic polymerization of epoxides and the free radical polymerization of acrylates under different irradiation sources, that is, very soft halogen lamp (~ 12 mW cm?2), laser diode at 405 nm (~1.5 mW cm?2) or blue LED centered at 455 nm (80 mW cm?2). The ANH6 based photoinitiating systems are particularly efficient for the cationic and the radical photopolymerizations, and even better than that of the well‐known camphorquinone based systems. The photochemical mechanisms associated with the chemical structure/photopolymerization efficiency relationships are studied by steady state photolysis, fluorescence, cyclic voltammetry, laser flash photolysis, and electron spin resonance spin‐trapping techniques. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 2860–2866 相似文献
5.
Structure/reactivity/photoinitiation ability relationships in novel benzo pyrazolo (or imidazo) isoquinolinone derivatives upon visible light LEDs 下载免费PDF全文
Pu Xiao Frédéric Dumur Jing Zhang Mariem Bouzrati‐Zerelli Bernadette Graff Didier Gigmes Jacques Lalevée 《Journal of polymer science. Part A, Polymer chemistry》2015,53(15):1806-1815
Isoquinolinone derivatives bearing amino‐ or nitro‐ substituent (IQNs) have been synthesized as photoinitiators and combined with various additives (i.e., iodonium salt, N‐vinylcarbazole, amine or 2,4,6‐tris(trichloromethyl)?1,3,5‐triazine) to initiate ring‐opening cationic polymerizations (CP) or free radical polymerizations under exposure to visible LEDs (e.g., LEDs at 405 nm or 455 nm, or cold white LED) or a halogen lamp. Compared to the well‐known camphorquinone‐based systems, the novel IQNs‐based combinations employed here demonstrate higher efficiencies for the CP of epoxides. The photochemically generated reactive species (i.e., cations and radicals) from the IQNs‐based systems have been investigated by steady state photolysis, cyclic voltammetry, fluorescence, laser flash photolysis, and electron spin resonance spin trapping techniques. The structure/reactivity/photoinitiating ability relationships of IQNs‐based combinations are also discussed; the crucial role of the excited state lifetimes of the photoinitiators to ensure efficient quenching by additives is clearly underlined. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 1806–1815 相似文献
6.
7.
Thomas Wittmann Dr. Renée Siegel Nele Reimer Dr. Wolfgang Milius Prof. Dr. Norbert Stock Prof. Dr. Jürgen Senker 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(1):314-323
The resistance of metal–organic frameworks towards water is a very critical issue concerning their practical use. Recently, it was shown for microporous MOFs that the water stability could be increased by introducing hydrophobic pendant groups. Here, we demonstrate a remarkable stabilisation of the mesoporous MOF Al‐MIL‐101‐NH2 by postsynthetic modification with phenyl isocyanate. In this process 86 % of the amino groups were converted into phenylurea units. As a consequence, the long‐term stability of Al‐MIL‐101‐URPh in liquid water could be extended beyond a week. In water saturated atmospheres Al‐MIL‐101‐URPh decomposed at least 12‐times slower than the unfunctionalised analogue. To study the underlying processes both materials were characterised by Ar, N2 and H2O sorption measurements, powder X‐ray diffraction, thermogravimetric and chemical analysis as well as solid‐state NMR and IR spectroscopy. Postsynthetic modification decreased the BET equivalent surface area from 3363 to 1555 m2 g?1 for Al‐MIL‐101‐URPh and reduced the mean diameters of the mesopores by 0.6 nm without degrading the structure significantly and reducing thermal stability. In spite of similar water uptake capacities, the relative humidity‐dependent uptake of Al‐MIL‐101‐URPh is slowed and occurs at higher relative humidity values. In combination with 1H‐27Al D ‐HMQC NMR spectroscopy experiments this favours a shielding mechanism of the Al clusters by the pendant phenyl groups and rules out pore blocking. 相似文献
8.
As the enantiomers of 1-phenylethanol are valuable intermediates in several industries, the lipase catalyzed kinetic resolution of (R,S) -1-phenylethanol is a relevant research topic. In this study, the goal was to determine the optimum reaction parameters to produce enantiomerically pure 1-phenylethanol by lipase (Novozyme 435) catalyzed kinetic resolution using response surface methodology (RSM). Reactions were performed with 40–400 mM (R,S)-1-phenylethanol, 120–1200 mM vinyl acetate and 2–22 mg/mL biocatalyst concentrations (BC L ), at 20–60 °C and with a stirring rate of 50–400 rpm for 5–120 min. The samples were analyzed using high performance liquid chromatography (HPLC) with a Chiralcel OB column. Optimum reaction parameters to reach 100% enantiomeric excess for the substrate ( <em>eeem> <em>sem> ) were determined as follows: substrate concentration (C s ): 240 mM, BC L : 11 mg/mL, at 42 °C with a reaction time of 75 min. Model validation was performed using these conditions and <em>eeem> <em>sem> was calculated as 100%, which indicates the predicted model was efficient and accurate. When compared to the literature, it was observed that the reaction time decreased significantly. This is an important result considering the industrial scale perspective. 相似文献
9.
do Nascimento Marreiro Teixeira Ana Siqueira Siqueira Teixeira Paulo Ronaldo Sousa de Oliveira Farias Emanuel Airton Ferraz e Sousa Brandon Moura Sérvulo Kátia Bonfim de Leite da Silva Durcilene Alves Eiras Carla 《Journal of Solid State Electrochemistry》2020,24(5):1143-1155
Journal of Solid State Electrochemistry - The present work proposes a new electrochemical sulfite biosensor based on babassu mesocarp nanoparticles (BMNPs) immobilized on the surface of a pyrolytic... 相似文献
10.