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991.
Stefanie K. Nguyen Supaporn Sophonputtanaphoca Eugene Kim Michael H. Penner 《Applied biochemistry and biotechnology》2009,158(2):352-361
A low, but significant, fraction of the carbohydrate portion of herbaceous biomass may be composed of fructose/fructosyl-containing
components (“fructose equivalents”); such carbohydrates include sucrose, fructooligosaccharides, and fructans. Standard methods
used for the quantification of structural-carbohydrate-derived neutral monosaccharide equivalents in biomass are not particularly
well suited for the quantification of fructose equivalents due to the inherent instability of fructose in conditions commonly
used for hemicellulose/cellulose hydrolysis (>80% degradation of fructose standards treated at 4% sulfuric acid, 121°C, 1 h).
Alternative time, temperature, and acid concentration combinations for fructan hydrolysis were considered using model fructans
(inulin, β-2,1, and levan, β-2,6) and a grass seed straw (tall fescue, Festuca arundinacea) as representative feedstocks. The instability of fructose, relative to glucose and xylose, at higher acid/temperature combinations
is demonstrated, all rates of fructose degradation being acid and temperature dependent. Fructans are shown to be completely
hydrolyzed at acid concentrations well below that used for the structural carbohydrates, as low as 0.2%, at 121°C for 1 h.
Lower temperatures are also shown to be effective, with corresponding adjustments in acid concentration and time. Thus, fructans
can be effectively hydrolyzed under conditions where fructose degradation is maintained below 10%. Hydrolysis of the β-2,1
fructans at temperatures ≥50°C, at all conditions consistent with complete hydrolysis, appears to generate difructose dianhydrides.
These same compounds were not detected upon hydrolysis of levan, sucrose, or straw components. It is suggested that fructan
hydrolysis conditions be chosen such that hydrolysis goes to completion; fructose degradation is minimized, and difructose
dianhydride production is accounted for. 相似文献
992.
Jinzhu Tan Y.J. Chao Haifeng Wang Jianming Gong J.W. Van Zee 《Polymer Degradation and Stability》2009,94(11):2072-2078
Proton exchange membrane (PEM) fuel cell stack requires elastomeric gaskets in each cell to keep the reactant gases within their respective regions. Long-term durability of the fuel cell stacks depends heavily on the functionality of the elastomeric gasket material. Chemical and mechanical stability of the elastomeric material is of great concern to the overall performance of the fuel cell stacks. The degradation of a commercially available gasket material, ethylene-propylene-diene monomer (EPDM), was investigated in a simulated PEM fuel cell environment in this work. One solution and two temperatures, based on actual fuel cell operation, were used in this study. Optical microscopy was used to show the topographical changes on the sample surface. Attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy was employed to study the surface chemistry of the gasket material before and after exposure to the simulated PEM fuel cell environment over time. Atomic absorption spectrometry was used to identify the leachants in the soaking solution from the elastomeric material. Microindentation test and dynamic mechanical analysis (DMA) were conducted to assess the change of mechanical properties of the samples exposed to the environment. The atomic absorption spectrometer analysis shows that silicon and calcium were leached from the material into the soaking solution. The ATR-FTIR results indicate that the chemical changes were not apparent. The microindentation test and DMA results reveal that mechanical properties were not changed significantly. 相似文献
993.
Binh Thi Thanh Nguyen Jin Qiang Ang Chee-Seng Toh 《Electrochemistry communications》2009,11(10):1861-1864
A model K+ sensor using Prussian blue nanotubes is fabricated by electrochemical deposition of Prussian blue (PB) within the nanochannels of a porous metal-coated membrane with partially covered pore openings. The PB nanotube sensor exhibits excellent stability giving reproducible peak potentials up to 500 measurement cycles, a very low detection limit of 2.0 × 10−8 M and extremely wide logarithmic linear ranges between 5.0 × 10−8–7.0 × 10−4 M and 7.0 × 10−4–1.0 M. Negligible interferences by Na+, Mg2+ and Ca2+ are observed and a rapid analysis time of 30 s is readily achieved. The ease of electrodeposition, high stability of PB nanotubes and outstanding analytical performance which surpasses conventional PB voltammetric and potentiometric sensors demonstrates potential sensing applications including ion sensors and biosensors using PB and other metal hexacyanoferrate nanotubes. 相似文献
994.
Tan Tai Nguyen Floris Chevallier Viatcheslav Jouikov Florence Mongin 《Tetrahedron letters》2009,50(49):6787-6790
Deprotonative cupration of aromatics including heterocycles (anisole, 1,4-dimethoxybenzene, thiophene, furan, 2-fluoropyridine, 2-chloropyridine, 2-bromopyridine, and 2,4-dimethoxypyrimidine) was realized in tetrahydrofuran at room temperature using the Gilman-type amido-cuprate (TMP)2CuLi in situ prepared from CuCl2·TMEDA through successive addition of 1 equiv of butyllithium and 2 equiv of LiTMP. The intermediate lithium (hetero)arylcuprates were evidenced by trapping with iodine, allyl bromide, methyl iodide, and benzoyl chlorides, the latter giving the best results. Symmetrical dimers were also prepared from lithium azine and diazine cuprates using nitrobenzene as an oxidative agent. 相似文献
995.
Roel De Mondt Luc Van Vaeck Andreas Heile Heinrich F. Arlinghaus Frank Vangaever Jens Lenaerts 《Analytical and bioanalytical chemistry》2009,393(8):1917-1921
Recent publications on static secondary ion mass spectrometry (S-SIMS) focus on molecular depth profiling by using polyatomic
or ultra-low energy monoatomic projectiles. Since their applicability depends on the relationship between the ion yield and
the depth, which is hard to obtain without extensive studies, a combination of a wear test method with S-SIMS surface analysis
was performed in the current study. Using this non-sputtering procedure, the relation between the signal intensity and the
local concentration remains in principle the same as that at the surface (which is easy to determine). Mechanical erosion
was successfully applied to expose sub-surface material from organic multilayers. Through surface analysis with S-SIMS on
the gradually exposed deeper planes, molecular depth profiles could be obtained. The study was conducted on a model system
relevant to offset printing, consisting of two polymer layers, containing dyes and a surfactant, cast on an Al substrate.
Figure Concept of mechanical erosion followed by S-SIMS surface analysis to obtain molecular depth profiles 相似文献
996.
When observing or describing the damage state in a composite material, often only Young's modulus or residual deformation are considered. Generally, however, the Poisson's ratio is more sensitive to damage than those properties. Rather than observing the Poisson's ratio as a function of crack density, this article studies the evolution of the Poisson's ratio as function of the longitudinal strain, which has a peculiar shape. In Part I, multiple experiments, using strain gauges, optical fibres and an extensometer for transverse strain measurement are discussed to determine whether this behaviour is due to the material or to the sensor used. It can be concluded that the hyperbolic-like shape is entirely caused by material behaviour. A theoretical explanation and validation for this behaviour will be given in part II.The material used for this study is a carbon fabric-reinforced PPS. 相似文献
997.
Peter Nockemann Dr. Ben Thijs Dr. Kyra Lunstroot Dr. Tatjana N. Parac‐Vogt Prof. Dr. Christiane Görller‐Walrand Prof. Dr. Koen Binnemans Prof. Dr. Kristof Van Hecke Dr. Luc Van Meervelt Prof. Dr. Sergey Nikitenko John Daniels Dr. Christoph Hennig Dr. Rik Van Deun Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(6):1449-1461
The dissolution process of metal complexes in ionic liquids was investigated by a multiple‐technique approach to reveal the solvate species of the metal in solution. The task‐specific ionic liquid betainium bis(trifluoromethylsulfonyl)imide ([Hbet][Tf2N]) is able to dissolve stoichiometric amounts of the oxides of the rare‐earth elements. The crystal structures of the compounds [Eu2(bet)8(H2O)4][Tf2N]6, [Eu2(bet)8(H2O)2][Tf2N]6?2H2O, and [Y2(bet)6(H2O)4][Tf2N]6 were found to consist of dimers. These rare‐earth complexes are well soluble in the ionic liquids [Hbet][Tf2N] and [C4mim][Tf2N] (C4mim=1‐butyl‐3‐methylimidazolium). The speciation of the metal complexes after dissolution in these ionic liquids was investigated by luminescence spectroscopy, 1H, 13C, and 89Y NMR spectroscopy, and by the synchrotron techniques EXAFS (extended X‐ray absorption fine structure) and HEXS (high‐energy X‐ray scattering). The combination of these complementary analytical techniques reveals that the cationic dimers decompose into monomers after dissolution of the complexes in the ionic liquids. Deeper insight into the solution processes of metal compounds is desirable for applications of ionic liquids in the field of electrochemistry, catalysis, and materials chemistry. 相似文献
998.
Zhengwei Mao Dr. Jinshan Guo Shuo Bai Tich‐Lam Nguyen Dr. Haibing Xia Dr. Yubin Huang Prof. Paul Mulvaney Prof. Dayang Wang Dr. 《Angewandte Chemie (International ed. in English)》2009,48(27):4953-4956
In the swim : Colloidal nanoparticles coated with polylactide (PLA, red) and poly(ethylene glycol) brushes (PEG, black) can transfer from organic to aqueous phases across liquid/liquid or liquid/gel interfaces during degradation of the PLA coating (see picture: first step), which is driven selectively by the hydrogen bonding of the PEG coating with the aqueous phase (second step).
999.
Vu Quoc Thang Toshiaki Taniike Masaki Umemori Mitsuhiro Ikeya Yuichi Hiraoka Nguyen Duc Nghia Minoru Terano 《大分子反应工程》2009,3(8):467-472
Preservation of initial polymer/catalyst particle morphology under air, was examined using stopped‐flow Ziegler–Natta polymerization with various quenching conditions and post‐chemical treatments. The exposure of the initial particles to air caused the fast formation of cracks on the surface, finally leading to significant reformation of the particle shape, when polymerizing particles were washed with heptane at ?65 °C under N2 or under CO2. On the other hand, when the particles were washed with heptane containing an appropriate amount of tetrahydrofuran under CO2, the particle morphology under air was almost completely maintained even after 1 h exposure. The present results are useful for various ex situ characterizations of unstable initial polymer/catalyst particles.
1000.
Dong‐Je Hong Eunji Lee Haemi Jeong Jeong‐kyu Lee Wang‐Cheol Zin Trung Dac Nguyen Sharon C. Glotzer Myongsoo Lee Prof. 《Angewandte Chemie (International ed. in English)》2009,48(9):1511-1511
Solid scrolls are reversibly formed by self‐assembly of rod‐shaped molecules with laterally attached coil units, in contrast to the layered structures formed from self‐assembly of planar molecules. As described by M. Lee and co‐workers in their Communication on page 1664 ff., the core structure of the scrolls, which are either filled cylinders or hollow tubes, can be controlled by variation of the length of the coil unit. The cover picture shows aligned tubular scrolls displaying well‐defined in‐plane ordering of the rod segments.