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851.
852.
The paper provides an analytical review of some fundamental problems of solid mechanics in high technologies. The review relies partly on the invited report presented by the authors at the 10th All-Russian Congress on Theoretical and Applied Mechanics held in Nizhny Novgorod in 2011. Attention is focused on the problems involved in technologies of materials with a bulk fine-grained (nano) structure and in technologies used to control mechanical properties of surfaces and interfaces. 相似文献
853.
Shinji Suzuki Furitsu Suzuki Yasumasa Kanie Koji Tsujitani Asako Hirai Hironori Kaji Fumitaka Horii 《Cellulose (London, England)》2012,19(3):713-727
The structure and crystallization of carefully isolated sub-elementary fibrils (SEFs) of bacterial cellulose have been investigated
using TEM, WAXD, and high-resolution solid-state 13C NMR. The addition of a suitable amount of fluorescent brightener (FB) to the incubation medium of Acetobacter xylinum effectively suppressed the aggregation of the SEFs into the microfibrils, as previously reported. However, this study confirmed
for the first time that serious structural change in the SEFs occurs during the removal of excess FB by washing with buffer
solutions having pH values higher than 6 or with the alkaline aqueous solution that was frequently used in previous studies.
In contrast, the isolation of unmodified SEFs was successfully performed by utilizing a washing protocol employing pH 7 citrate–phosphate
buffer solution containing 1% sodium dodecyl sulfate. High-resolution solid-state 13C NMR and WAXD measurements revealed that the SEFs thus isolated are in the noncrystalline state in which the pyranose rings
of the almost parallel cellulose chains appear to be stacked on each other. The respective CH2OH groups of the SEFs adopt the gt conformation instead of the tg conformation found in cellulose I
α
and I
β
crystals, and undergo significantly enhanced molecular motion in the absence of intermolecular hydrogen bonding associated
with these groups. The main chains are also subject to rapid motional fluctuations while maintaining the parallel orientation
of the respective chains, indicating that the SEFs have a liquid crystal-like structure with high molecular mobility. Moreover,
the SEFs crystallize into cellulose I
β
when the FB molecules that may adhere to the surface of the SEFs are removed by extraction with boiling 70 v/v% ethanol and
0.1N NaOH aqueous solution. On the basis of these results, the crystallization of the SEFs into the I
α
and I
β
forms is discussed, including the possible formation of the crystalline-noncrystalline periodic structure in native cellulose. 相似文献
854.
Kristin Voiges Roland Adden Marian Rinken Petra Mischnick 《Cellulose (London, England)》2012,19(3):993-1004
The alditol acetate method is a common procedure for sugar analysis, also applied to determine the substituent distribution
in monomer units of polysaccharide ethers like methyl cellulose by gas liquid chromatography. Consisting of several preparation
and work-up steps this procedure is both time consuming and prone to side reactions that promote discrimination of single
constituents, especially when no peralkylation step is performed prior to hydrolysis. As a consequence results scatter in
dependence on individual treatment and conditions. In the context of this work these critical points were overcome by strict
but simplified work-up procedures and using acid instead of alkaline catalyzed acetylation. Under the acidic conditions the
tedious removal of borate is no longer necessary and a reduced time requirement was achieved as well as good reproducibility.
Comparison with independent reference methods excluded a systematic error of the method and confirmed the results obtained.
Without peralkylation, i.e. in the presence of free hydroxyl groups, another fast modification of the method using DMSO as
solvent, no removal of borate, and 1-methylimidazole as catalyst for acetylation was found to produce a systematic error. 相似文献
855.
Pirita Rämänen Paavo A. Penttilä Kirsi Svedström Sirkka Liisa Maunu Ritva Serimaa 《Cellulose (London, England)》2012,19(3):901-912
Cellulose whiskers were prepared from wood- and cotton-based microcrystalline cellulose and dried by two methods: freeze-drying
or air-drying. The effect of drying method on the properties and structure of the whiskers were studied. Furthermore, the
influence of the source of cellulose on the nanoscale structure was investigated. Drying method was observed to slightly influence
the thermal stability of cellulose whiskers, whereas the char residue varied significantly depending on the drying process
performed. Small- and wide-angle X-ray scattering and solid state nuclear magnetic resonance spectroscopy were used to examine
the crystallinity and nanoscale structure of the dried whiskers. It was observed that the crystal structure and crystallinity
of cellulose whiskers remained during all treatments, whereas their nanoscale structure was significantly influenced by drying
method, neutralization, and source of cellulose. Relationships between thermal behavior and nanoscale structure were reported
and discussed. 相似文献
856.
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
857.
Nishesh Kumar Gupta Arijit Sengupta 《Journal of Radioanalytical and Nuclear Chemistry》2017,311(3):1729-1739
Sulphoxide ligands in piperidinium based ionic liquid were demonstrated as highly efficient, selective and environmentally benign systems for the extraction of plutonium from acidic aqueous solution. The extraction followed ‘cation-exchange mechanism’ via [Pu(NO3)·L]3+ and [PuO2(NO3)·L]+ species. The extraction efficiency followed the trend: APSO > BPSO > BMSO. The phenyl substituted sulphoxides showed higher affinity for plutonium due to a combination of steric as well as electronic factors. Extraction process was thermodynamically spontaneous for all three solvent systems. Oxalic acid and sodium carbonate were suitable for quantitative stripping of Pu4+ and PuO2 2+, respectively. APSO in ionic liquid showed good radiolytic stability. 相似文献
858.
Nafise Modanlou Juibari Abbas Eslami 《Journal of Thermal Analysis and Calorimetry》2017,128(3):1327-1334
This work aimed the evaluation of pH influence in the obtainment of composites from palygorskite (PAL) and chitosan (CS). The materials PAL/CS-1 and PAL/CS-2 were obtained by similar methodology with modified pHs: 5.0 ± 0.5 and 11.0 ± 0.5, respectively. Both materials were evaluated for specific surface area analysis, elemental analysis, XRD, FTIR, thermal analysis, MEV and interaction drug composite, using 5-aminosalicylic acid (5-ASA) as model. The surface area analysis data showed the reduction in PAL/CS-2 related to CS presence on surface in contrast with PAL/CS-1, which corroborate with elemental analysis present nine times more of CS in PAL/CS-2 composition. Regarding to XRD data, the interaction of CS with PAL did not cause modification in clay structure in PAL/CS-2. These results were confirmed by FTIR data with the N–H deformation vibration in PAL/CS-2 while PAL/CS-1 was invariable to PAL. In thermal analysis, results were observed 60.2% residual mass to PAL/CS-2, which it was lower than PAL (87.2%) and PAL/CS-1 (86.7%), due to CS decomposition which had enthalpy energy of 62.1 J g?1 K?1, confirming the data previously cited. PAL/CS-2 presented 5-ASA adsorption of 7.9 mg g?1, which was inferior to others probably caused by scarcity of active sites of PAL already occupied by CS. These results showed that pH control was fundamental to enhance efficiency of obtainment of composite in basic pH because the decrease in CS protonation degree increasing interaction between this one and PAL, although it contributed to decrease in 5-ASA adsorption due to low availability of interaction sites. 相似文献
859.
860.