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841.
Summary Two -cyclodextrin (-CD)-containing polymers have been prepared either by condensation of -CD molecules with a bifunctional reagent or by grafting a -CD derivative on to a linear polymer (polyvinylimidazole). HPLC stationary phases were obtained by adsorption of the -CD polymers on to silica. The ability of these chromatographic supports to resolve racemic mixtures of organic compounds such as amino acid derivatives, phenylhydantoins, barbiturates, and hydroxycoumarin derivatives has been investigated. Results were found to depend on the chemical structure of the -CD polymers 相似文献
842.
The surface area was determined for various papermaking woodpulps: bleached eucalyptus globulus sulphate pulp; bleached eucalyptus grandis sulphate pulp; bleached betula verrucosa sulphate pulp; bleached pine/spruce sulphate pulp; bleached pine/spruce sulphate pulp fines. The method of negative adsorption was used which gives an effective wet surface area. By looking at negative adsorption data more closely, some inference can be made about the morphology of the substrate.Glossary of symbols
B
(e2/2kT)1/2
-
¯C
concentration of fibre per unit volume of pulp
-
1 - ¯¯c
-
h
angle between pore and the axis of the bed in a permeable material
-
K
permeability coefficient
-
k
Boltzmann constant
-
k
0
shape factor for pores in a permeable material
-
n
i
concentration of co-ion in the bulk solution
-
n
i
experimentally observed increase in concentration of co-ion in the bulk solution
-
S
surface area
-
S
t
wS
-
S
0
surface area per unit volume of permeable material
-
V
t
total volume of solution
-
V
excluded volume
- V
s
excluded volume accessible to water but not to ions
- V
obs
experimentally observed excluded volume
-
w
weight of dry fibre
-
¯
effective volume of fibres in a permeable pad
-
surface potential at outer Helmholtz plane 相似文献
843.
Summary A rapid and efficient procedure is described for extraction and determination of aminocaproic acid in horse urine. Urine was
extracted by passing through a bonded silica column (Bond-Elut). The adsorbed drug was washed free of endogenous materials
before being eluted. The extract was then examined by thin-layer chromatography and HPLC. The purity of the extract was determined
by gas chromatography-mass spectrometry. 相似文献
844.
H. OelschlÄger S. Lumbantoruan J. Volke und G. Kraft 《Fresenius' Journal of Analytical Chemistry》1976,279(4):257-261
Zusammenfassung Auf DC-Plastikfolien getrennte Substanzen lassen sich mit guter Genauigkeit (Wiederfindungsraten > 95 %) in Gegenwart des Folienmaterials gleichspannungspolarographisch durch Reduktion an der Hg-Tropfelektrode bestimmen. Die von den Leuchtpigmenten abgegebenen Zn-Ionen müssen vor der Registrierung der i-E-Kurven durch ÄDTA maskiert werden.Wir danken dem Fonds der Chemischen Industrie, Frankfurt am Main, für finanzielle Unterstützung dieser Arbeit und Herrn O. Schreiber für gewohnte sorgfÄltige Mitarbeit. 相似文献
845.
Fine particle superacidic sulfated zirconia (SO42−/ZrO2, S-ZrO2) was synthesized by ameliorated method, and composite membranes with different S-ZrO2 contents were prepared by a recasting procedure from a suspension of S-ZrO2 powder and Nafion solution. The physico-chemical properties of the membranes were studied by ion exchange capacity (IEC) and liquid water uptake measurements, scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis, thermogravimetry–mass spectrometry (TG–MS) and Fourier transform infrared (FT-IR) spectroscopy. The results showed that the IEC of composite membrane increased with the content of S-ZrO2, S-ZrO2 was compatible with the Nafion matrix, the incorporation of the S-ZrO2 could increase the crystallinity and also improve the initial degradation temperature of the composite membrane. The performance of single cell was the best when the S-ZrO2 content was 15 wt.%, and achieved 1.35 W/cm2 at 80 °C and 0.99 W/cm2 at 120 °C based on H2/O2 and at a pressure of 2 atm, the performance of the single cell with optimized S-ZrO2 was far more than that of the Nafion at the same condition (e.g. 1.28 W/cm2 at 80 °C, 0.75 W/cm2 at 120 °C). The 15 wt.% S-ZrO2/Nafion composite membrane showed lower fuel cell internal resistance than Nafion membranes at high temperature and low relative humidity (RH). 相似文献
846.
Direct in situ determination of PGE1 in dioxane/water (1:1) at concentrations between 50 μg/ml and 1 mg/ml is described. HPTLC of PGE1 was carried out on HPTLC Kieselgel 60 o.F. plates; application (200 nl) was with a Nano-Appllcator and ethyl acetate/formic acid (400:5, v/v) served as mobile phase. The spots were located by dipping the plates into a 3% cupric acetate solution in 15% aqueous phosphoric acid, followed by heating at 120°C for 15 min. The plates were then evaluated directly at λ = 345 nm by chromatogram spectrometry. The coefficient of variation is 3.6%. 相似文献
847.
用T-jump/FTIR研究MnCP、NiCP和PbCP的快速热分解(英) 总被引:1,自引:0,他引:1
0IntroductionCarbohydrazideisahydrazinederivativewithwhitecrystalofstrongreducingbehaviors.Becauseithasmanycoordinationatoms(fournitrogenatomsandoneoxygenatom),carbohydrazidecan,therefore,beusedasmultidentateligand.Itscoordinationcom鄄poundiswidelyusedint… 相似文献
848.
FAN Jian-Fen② LU Yun-Xiang WANG Qiu-Xia WU Li-Fen SUN Yun-Peng 《结构化学》2005,24(4):413-418
Density functional theory (DFT) has been applied to study the enantioselective reduction of 3-morpholin-4-yl-l-phenyl-l-propanone with borane catalyzed by (S)-4-benzyl-5,5-diphenyl-l,3,2-oxazaborolidine at the B3LYP/6-31G* level. All molecular species involved in the four reaction steps have been fully optimized and the structural parameters are provided, and the micro process of reaction was also investigated. The catalyst-alkoxyborane adduct formed in step Ⅲ exhibits a B-O-B-N tetra-atomic ring. Reaction coordination calculations show that BH3 can react with 3-morpholin-4-yl-l-phenyl-l-propanone spontaneously, resulting in the need of 2 tool BH3 in the reaction. 相似文献
849.
We evaluated a novel strategy for high-sensitivity DNA fragment analysis in a conventional glass double-T microfluidic chip. The microchip allows for a DNA on-channel concentration based on base stacking (BS) with a microchip capillary gel electrophoretic (MCGE) separation step in a poly(vinylpyrrolidone) (PVP) sieving matrix. Depending if low conductivity caused a neutralization reaction between the hydroxide ions and the run buffer component Tris+, the stacking of DNA fragments were processed in the microchip. Compared to a conventional MCGE separation with a normal electrokinetic injection, the peak heights of 50-2650-base pair (bp) DNA fragments on the MCGE-BS separation were increased 3.9-8.0-fold. When we applied the MCGE-BS method to the analysis of a clinical sample of bovine theileria after PCR reaction, the peak height intensity of the amplified 816-bp DNA fragment from the 18S rRNA of T. buffeli was enhanced 7.0-fold compared to that of the normal injection method. 相似文献
850.
This paper reports an improved catalytic molecular beacon. Addition of the target oligonucleotide activates a DNA enzyme (DNAzyme), which, in turn, activates multiple copies of molecular beacons (MB) and gives rise to a strong fluorescence signal. In a previous design, the activated DNAzyme could oligomerize, especially dimerize, and result in inactivation of the DNAzyme. The current design avoids this problem, upon activated by the target DNA, the DNAzyme will stay constantly active. With the improved method, a detection of 10 pM DNA has been demonstrated, which is 1000 times more sensitive than the method previously reported. 相似文献