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Formose sugar and formaldehyde (HCHO) were analyzed using high-performance liquid chromatography (HPLC) utilizing a CarboPac PA1 column (Dionex) and pulsed amperometric detection. This HPLC system was unsuitable for the analysis of formose sugar and HCHO and thus reducing sugars and unconverted HCHO were determined by endowing them with charges through a derivatization method using 2,4-dinitrophenylhydrazine. The separation and detection of compounds were performed by three Chromolith RP-C18 columns (Merck) and diode array detection, at a wavelength of 360 nm ultraviolet light, respectively. Lower sugars (except HCHO) showed some instabilities when the derivatized samples were kept for the extended periods of time. For C5 and consecutive higher sugars, a certain derivatization time was necessary. In the present case (formose reaction with partial HCHO conversion), approximately 18 h may be a reasonable compromise for the derivatization reaction. A derivatization agent to compound mole ratio of up to 100:1 was required to complete the derivatization of C4 and higher sugars. However, the analysis of C4 and consecutive higher sugars is problematic for example due to overlapping of peaks or branched-chain sugars.  相似文献   
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Applied Biochemistry and Biotechnology - The production of sorbitol and gluconic acid by isolated glucose-fructose oxidoreductase (GFOR) fromZymomonas mobilis has been studied in a convective,...  相似文献   
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Strong-field ionization of nonlinear planar triatomic molecules by a bicircular laser field is analyzed within the improved molecular strong-field approximation. Our calculations include additional interaction between the liberated electrons and atomic or ionic centers of the parent molecular ion. The used bicircular field consists of two counterrotating circularly polarized fields having angular frequencies \(r \omega\) and \(s \omega\), with integer r and s. In the case when the laser-field-polarization plane is parallel to the plane of the considered molecule (example of ozone molecule is analyzed), the corresponding photoelectron spectra are not rotationally symmetric. On the other hand, when these planes are mutually perpendicular, for the \((r\omega ,s\omega )=(\omega ,3\omega )\) bicircular field, the electron spectra satisfy the corresponding rotational symmetries. Analyzing the obtained spectra and the corresponding symmetries, one can extract information about molecular orientation and structure. This technique may also be useful for more complex polyatomic molecules.  相似文献   
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