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91.
Ayman Ben Mabrouk Hamid Kaddami Sami Boufi Fouad Erchiqui Alain Dufresne 《Cellulose (London, England)》2012,19(3):843-853
The microstructure and chemical composition of alfa (Stipa tenacissima) were investigated. The polysaccharide and lignin contents were around 70 and 20 wt%, respectively. From the bleached and delignified fibers, two types of nanosized cellulosic particles were extracted, namely cellulose nanocrystals and microfibrillated cellulose (MFC). The former correspond typically to the elementary crystallite units of the cellulose fibers, with a rod-like morphology and an aspect ratio of about 20. The latter, mechanically disintegrated from oxidized bleached fibres, presents an entangled fibrillar structure with widths in the range 5-20 nm. The reinforcing potential of the ensuing nanoparticles was investigated by casting a mixture of acrylic latex and aqueous dispersion of cellulose nanoparticles. Thermo-mechanical analysis revealed a huge enhancement of the stiffness above the glass transition of the matrix. Significant differences in the mechanical reinforcing capability of the nanoparticles were reported. 相似文献
92.
Abstract The chemical dehydrochlorination of polyvinyl chloride was studied in solution in tetrahydrofuran. The dehydrochlorinated products were characterized by their chlorine contents and by UV/visible spectroscopy. The absorption spectra of dehydrochlorinated PVC consist of a series of absorption maxima between 200 and 600 nm due to the formation of conjugated polyenic sequences. In this article we describe a new method for polyenic sequences evaluation based on deconvolution of the experimental spectrum. A comparison with the former technique usually employed is presented. 相似文献
93.
Three new porphyrins bearing in the meso positions 4-(pyrazol-1-yl)-2,3,5,6-tetrafluorophenyl substituents have been prepared and characterized by nmr spectroscopy. 相似文献
94.
95.
Karine Vuignier Szabolcs Fekete Pierre‐Alain Carrupt Jean‐Luc Veuthey Davy Guillarme 《Journal of separation science》2013,36(14):2231-2243
In the present study, three types of silica‐based monoliths, i.e. the first and second generations of commercial silica monolithic columns and a wide‐pore prototype monolith were compared for the analysis of large biomolecules. These molecules possess molecular weights between 1 and 66 kDa. The gradient kinetic performance of the first‐generation monolith was lower than that of the second generation, for large biomolecules (>14 kDa) but very close with smaller ones (1.3–5.8 kDa). In contrast, the wide‐pore prototype column was particularly attractive with proteins larger than 19 kDa (higher peak capacity). Among these three columns, the selectivity and retention remained quite similar but a possible larger number of accessible and charged residual silanols was noticed on the wide‐pore prototype material, which led to unpredicted small changes in selectivity and slightly broader peaks than expected. The peak shapes attained with the addition of 0.1% formic acid in the mobile phase remained acceptable for MS coupling, particularly for biomolecules of less than 6 kDa. It was found that one of the major issues with all of these silica‐based monoliths is the possible poor recovery of large biomolecules (principally with monoclonal antibody fragments of more than 25 kDa). 相似文献
96.
Alain Valla Nathalie Méheux Dominique Cartier Benoist Valla Laurent Dufossé 《合成通讯》2013,43(2):184-190
A synthesis of a new C-15 phosphorus ylide from a C-14 enaminone is reported. This reagent, which undergoes selective 1,2- or 1,4-additions with saturated and unsaturated aldehydes, may find some synthetic use for the preparation of β-end-group retinoid derivatives. 相似文献
97.
José Elguero Alain Fruchier El Mostafa Tjiou Sviatoslav Trofimenko 《Chemistry of Heterocyclic Compounds》1995,31(9):1006-1026
The carbon-13 chemical shifts and some selected coupling constants of 183 indazoles are reported. The main conclusions of the original references are briefly summarized.Published in Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1159–1179, September, 1995. 相似文献
98.
Pei X Fernandes A Mathy B Laloyaux X Nysten B Riant O Jonas AM 《Langmuir : the ACS journal of surfaces and colloids》2011,27(15):9403-9412
Photoresponsive monolayers of hydrophilically substituted azobenzenes have been prepared by reaction on aminosilane monolayers on silicon surfaces. Grafting densities in the 0.2-1.0 molecule/nm(2) range were determined by X-ray reflectometry. The monolayers exhibit reversible photoisomerization, switching from a more hydrophilic trans state to a less hydrophilic cis state upon UV irradiation, in contrast with the usual behavior of most azobenzene monolayers that switch from a less to a more hydrophilic state. This indicates that the wettability is not dominated by the change in the dipole moment of the azobenzene moiety but originates from variations in the composition of the outer surface of the monolayers resulting from the reorientation of the substituent groups. The light-driven change in the water contact angle correlates linearly with the grafting density but remains small. However, the wettability contrast can be increased by forcing the molecules to stand in an improved vertical orientation, either by densifying the underlying aminosilane monolayer or by filling the voids left at the bottom of the layer of grafted azobenzene molecules. 相似文献
99.
Dr. Véronique Jubera Dr. Marie Chavoutier Dr. Alla Artemenko Dr. Philippe Veber Dr. Matias Velazquez Dr. Alain Garcia 《Chemphyschem》2011,12(7):1288-1293
Synthesized powders and grown single crystals of nominal compositions Li6Ln(BO3)3:Yb3+ (Ln=Y, Gd) were investigated by means of powder and single‐crystal X‐ray diffraction (XRD), as well as optical near‐IR spectroscopy in conjunction with electron paramagnetic resonance (EPR) spectroscopy. The appearance of two distinct zero‐phonon lines suggests the existence of two kinds of Yb3+ ions in the single crystals. The XRD results exclude the possibility of a phase transition occurring between room and low temperatures. EPR spectra of single crystals show the presence of both isolated ions and pairs of ytterbium ions substituted for Y3+. A strong temperature dependence of the intensity of Yb–Yb pairs resonance lines coincides with temperature dependence of emission peak at 978 nm, confirming a common origin of the defect giving rise to these spectra. Calculated from EPR spectra, the distance between pairs of Yb3+ is in good agreement with crystallographic ones: R=3.856 Å, Rcryst=3.849 Å. 相似文献
100.