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71.
72.
研究了油/水界面电解的示差半微分循环伏安行为。在0.01mol/L LiCl(w)-0.01mol/L TBATCIPB(nb)体系“电位窗”比TBATPB(nb)向正方向扩展约50mV,残余电流基本消除,使“电位窗”内的平台向左右拓宽约50mV。算得界面电容约为16μF/cm~2。考察了琥珀酰胆碱离子在w/nb界面的传递伏安特性,结果与一般半微分循环伏安法相似。但峰形改善,检测限降低一个数量级(1×10~(-6)mol/L),相对标准偏差在5%以内,可用于定量测定琥珀酰胆碱。 相似文献
73.
在本文中,我们讨论了带作用群的群系的临界结构,给出了处理允许某些作用群的群的问题的一般方法,作为应用,我们特别给出了关于幂零群及p-幂零群的一些结果。 相似文献
74.
Brian H. Davison Nhuan P. Nghiem Gerald L. Richardson 《Applied biochemistry and biotechnology》2004,114(1-3):653-669
More than 25 sorbents were tested for uptake of succinic acid from aqueous solutions. The best resins were then tested for
successive loading and regeneration using hotwater. The key desired properties for an ideal sorbent are high capacity, complete
stable regenerability, and specificity for the product. The best resins have a stable capacity of about 0.06 g of succinic
acid/g of resin at moderate concentrations (1–5 g/L) of succinic acid. Several sorbents were tested more exhaustively for
uptake of succinic acid and for successive loading and regeneration using hot water. One resin, XUS 40285, has a good stable
isotherm capacity, prefers succinate over glucose, and has good capacities at both acidic and neutral pH. Succinic acid was
removed from simulated media containing salts, succinic acid, acetic acid, and sugar using a packed column of sorbent resin,
XUS 40285. The fermentation byproduct, acetate, was completely separated from succinate. A simple hot water regeneration successfully
concentrated succinate from 10 g/L (inlet) to 40–110 g/L in the effluent. If successful, this would lower separation costs
by reducing the need for chemicals for the initial purification step. Despie promising initial results of good capacity (0.06
g of succinic/g of sorbent), 70% recovery using hot water, and a recovered concentration of >100 g/L, this regeneration was
not stable over 10 cycles in the column. Alternative regeneration schemes using acid and base were examined. Two (XUS 40285
and XFS-40422) showed both good stable capacities for succinic acid over 10 cycles and >95% recovery in a batch operation
using a modified extraction procedure combining acid and hot water washes. These resins showed comparable results with actual
broth. 相似文献
75.
Wolfgang W. Schoeller 《无机化学与普通化学杂志》2003,629(5):816-827
The particular role of the phosphaneiminato ligand as a donor is investigated for a) nitrenes (phosphinidenes) and carbenes and b) cubane formation with transition metals. Accordingly, and as shown for the case a) the ligand is a stronger π‐donor than an amino group and can be considered as a special case of imine‐type substituents. The latter are very effective in π‐donation. In the case b), i.e. the cubane formation with transition metals, one has to consider transition metals with a partially or completely filled d‐shell (with electrons). Hence depending on the transition metal, cubanes are build with weak ferromagnetic coupled or closed shell systems. For the cubanes with closed shell character the matter of insertion of halide anions is discussed. In the last chapter of the review the bond stretching in the dithionitrosyl complexes with rhenium is characterized. 相似文献
76.
CunLiuZHOU YuQingZHOU ZhiYongWANG 《中国化学快报》2003,14(4):355-358
The chemoselective addition of aldehydes in aquoues medium was obtained under mild condition using improved Henry reaction. 相似文献
77.
Ahmed Jalal Uddin Yutaka Ohkoshi Yasuo Gotoh Masanobu Nagura Tetsuya Hara 《Journal of Polymer Science.Polymer Physics》2003,41(22):2878-2891
The effect of moisture on the mechanical relaxation processes of semiaromatic semicrystalline polyamides synthesized by a long‐chain aliphatic diamine and terephthalic acid was investigated by dynamic viscoelastic analysis (DVA) and differential scanning calorimetry (DSC). Moreover, the implication of moisture with the amorphous and crystalline domains was also examined by temperature‐dependent wide‐angle X‐ray diffraction and Fourier transform infrared spectra. The characteristics of the relaxations such as α, β, γ, and the pronounced peak shoulder appeared at 25–100 °C in DVA tan δ curves were found to be strongly susceptible to the presence of moisture. With moisture evaporation, the peak shoulder of 25–100 °C and the β‐relaxation disappeared. The former is anticipated to originate from to the side group motion of hydrogen‐bonded water, whereas the later one is from the motions of the amide–water complex units. With the disappearance of the β‐relaxation, the γ‐relaxation appeared simultaneously in much lower temperatures and ultimately coupled with the δ‐relaxation. The γ‐relaxation is attributed to be associated with the molecular motion of the amide group and δ‐relaxation with for the motion of the methylene units. The existence of two types of water was identified in the polymer, namely, tightly bound and loosely bound. The tightly bound water is believed to be directly connected by hydrogen bonding with the strong polar groups and the loosely bound water weakly links with those connected water making hydrogen bridges. The moisture acts as a plasticizer in the polymer matrix, which causes quite a large depression in its glass transition temperature (Tg). WAXD and FTIR studies corroborated the existence of water solely in amorphous regions, i.e., no rapport of water with the crystalline parts. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 2878–2891, 2003 相似文献
78.
79.
The frequency or dispersion relation for the least‐squares mixed formulation of the shallow‐water equations is analysed. We consider the use of different approximation spaces corresponding to co‐located and staggered meshes, respectively. The study includes the effect of Coriolis, and the dispersion properties are compared analytically and graphically with those of the mixed Galerkin formulation. Numerical solutions of a test problem to simulate slow Rossby modes illustrate the theoretical results. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
80.
V. B. Kobychev N. M. Vitkovskaya I. L. Zaitseva B. A. Trofimov 《Journal of Structural Chemistry》2004,45(6):940-944
The profiles of reactions leading to pyrrole anion N-adducts with CO2 and CS2 have been studied by the ab initio (RHF/6-31+G*, MP2/6-31+G*) and density functional (B3LYP/6-31+G*) methods. Addition of the pyrrole anion to the carbon disulfide molecule is accompanied by the appearance of a minimum corresponding to a pre-reaction complex. The transformation of the complex to the N-pyrrolyldithiocarboxylate anion occurs via a low activation barrier, which is due to repolarization of the C=S bonds. The profile of the reaction leading to the pyrrole anion N-adduct with CO2 does not contain any intermediate stationary points throughout the whole route from reagents to products.Original Russian Text Copyright © 2004 by V. B. Kobychev, N. M. Vitkovskaya, I. L. Zaitseva, and B. A. Trofimov__________Translated from Zhurnal Strukturnoi Khimii, Vol. 45, No. 6, pp. 990–993, November–December, 2004. 相似文献