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1.
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) was used for the simultaneous detection of sugars, ascorbic acid, citric acid, sodium and/or potassium benzoate in non-alcoholic beverages, with meso-tetrakis(pentafluorophenyl)porphyrin (MW 974) as a matrix. Using potassium hydroxide as dopant, fructose/glucose was detected as the potassiated molecule at m/z 219, whereas potassiated sucrose, [Sucrose. K](+), was detected at m/z 381. Using sodium hydroxide as dopant, the fructose and sucrose ions were detected at m/z 203 and 365, respectively. Citric acid generated multiple ions at m/z 269, 307, and 345, which were assigned to [Citricbond;H+2K](+), [Citricbond;2H+3K](+), and [Citricbond;3H+4K](+), respectively. However, a stored methanolic solution of citric acid produced additional ions at m/z 283, 297, and 321, which were attributed to [Citricbond;2H+CH(3)+2K](+), [Citricbond;3H+2CH(3)+2K](+), and [Citricbond;3H+CH(3)+3K](+), respectively, due to esterification that took place during storage. The limits of detection in water were: ascorbic acid, 0.30 wt%; citric acid, 0.5 wt%; and sodium benzoate, 0.001 wt%. In the beverage formulations, the limits of detection were: ascorbic acid 0.3 wt%, citric acid 0.3 wt%, and sodium benzoate 0.02 wt%. Spiking a water or beverage solution that contained ascorbic and/or citric acid with less than 0.6 wt% of tartaric acid lowered the detection limits of ascorbic and citric acids to 0.2 wt%. This study demonstrates the potential for using MALDI-TOFMS in the quality control analyses of non-alcoholic beverages, particularly with regard to the detection of low molecular weight organic acids in commercial beverage formulations.  相似文献   
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Summary.  Three bisdesmosidic saponins, 20-hydroxyecdysone, and quercetin-3-O-β-D-galactoside were isolated from the methanol extract of the aerial parts of Achyranthes aspera L. (Amaranthaceae). Their structures were established on the basis of NMR spectroscopic analysis; the complete 1H and 13C assignments of the compounds were achieved by means of 2D NMR studies. Received July 21, 1999. Accepted August 26, 1999  相似文献   
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Summary.  The MeOH extract of the stem bark of Entada abyssinica and of the leaves and stem bark of Securidaca longipedunculata yielded a diterpene, a flavonol glycoside, and a phytosterol glycoside. Their structures were established on basis of NMR spectroscopic analysis; the complete 13C and 1H assignment of the compounds was achieved by means of 2D NMR studies. Received October 13, 1999. Accepted November 3, 1999  相似文献   
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Laser surface texturing (LST) is a well-known surface engineering process used to create arranged dimples on surface using a material ablation process. In this process, a well arranged micro-dimple can produce significant improvements of engineering components in aspects such as load carrying capacity, wear resistance, wetting characteristics and reduction of friction coefficient. In the present work, we investigated the effect of multi-dimple LST steel surfaces on tribological properties under non-conforming contact. The multi-dimple textured surfaces with some specific formula arrays were fabricated by laser ablation process on steel disc by combining patterns of circles and triangles, and circles and squares, having different dimple densities to optimize the surface texturing effect on tribological performance. The tribological test of multi-dimple textured surface was performed by a ball-on-flat unidirectional tribometer in lubricated condition, and the results compared with that of a single-dimple and untextured (polished and ground) surfaces. The results indicate that the surface with multi-dimple textured patterns had better friction performance than the untextured and single-dimple textured surfaces. The beneficial effect of multi-dimple textured patterns was associated with transition of lubrication from boundary to mixed lubrication regime.  相似文献   
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Two new bisdesmosidic triterpenoid saponins, i.e. 1 and 2 , were isolated, besides the three known saponins 3 – 5 , from the MeOH extract of the aerial parts of Achyranthes aspera Linn. (Amaranthaceae). Their structures were elucidated as β‐D ‐glucopyranosyl 3β‐[Oα‐L ‐rhamnopyranosyl‐(1→3)‐Oβ‐D ‐glucopyranuronosyloxy]machaerinate ( 1 ) and β‐D ‐glucopyranosyl 3β‐[Oβ‐D ‐galactopyranosyl‐(1→2)‐Oα‐D ‐glucopyranuronosyloxy]machaerinate ( 2 ) by NMR spectroscopy, including 2D‐NMR experiments (machaerinic acid=3β,21β‐dihydroxyolean‐12‐en‐28‐oic acid). The other saponins were identified as β‐D ‐glucopyranosyl 3β[Oα‐L ‐rhamnopyranosyl‐(1→3)‐Oβ‐D ‐glucopyranuronosyloxy]oleanolate ( 3 ), β‐D ‐glucopyranosyl 3‐β‐[Oβ‐D ‐galactopyranosyl‐(1→2)‐Oβ‐D ‐glucopyranuronosyloxy]oleanolate ( 4 ), and β‐D ‐glucopyranosyl 3β‐[Oβ‐D ‐glucopyranuronosyloxy]oleanolate ( 5 ) (oleanolic acid=3β‐hydroxyolean‐12‐en‐28‐oic acid).  相似文献   
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Nitrated polycyclic aromatic hydrocarbons (nitro-PAHs) are widespread environmental pollutants that are generated by incomplete combustion and by atmospheric transformation of polycyclic aromatic hydrocarbons (PAHs). Many nitro-PAH compounds are potent genotoxins and some are direct acting mutagens. Detection of nitro-PAHs in aerosols is complicated by small sample sizes and nitro-PAH abundances that are 1–2 orders of magnitude less than analogous unsubstituted PAHs. Selective detection of several nitro-PAHs by using laser desorption ionization time-of-flight mass spectrometry in negative ion mode has been achieved. Desorption and ionization of nitro-PAHs were effected by using pulsed UV radiation at 266 and 213 ran. Intense molecular anions were observed in addition to fragments identified as CN? and NO 2 ? , which were characteristic indicators of the presence of nitro-PAHs. Selective detection of nitro-PAHs in negative ion mode was demonstrated in the analysis of a diesel particulate sample.  相似文献   
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The utility of intramolecular anodic olefin coupling reactions involving electron-rich aromatic rings for constructing fused, bicyclic ring skeletons has been examined. Reactions involving alkoxy-substituted phenyl rings were found to benefit strongly from a 3-methoxy substituent on the phenyl ring. Although overoxidation of the bicyclic product was observed in these reactions, this problem could be minimized with the use of controlled potential electrolysis conditions when a monomethoxy phenyl ring was used and avoided entirely with the use of a vinyl sulfide moiety as the initiator when a more electron-rich phenyl ring was used. Reactions involving 4-alkoxy-substituted phenyl rings as substrates did not lead to good yields of fused products. Furan rings were found to be excellent coupling partners for the reactions and afforded products having fused, bicyclic furan ring skeletons. Cyclizations involving furans were shown to be compatible with the formation of both six- and seven-membered rings, the generation of a quaternary carbon, and the use of a variety of electron-rich olefins as the other coupling partner. It appears that the furan can serve as either the initiating group or the terminating group for the cyclizations. Finally, the reactions were shown to be compatible with the use of a pyrrole ring as one of the participants.  相似文献   
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