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111.
Abstract

The use of classical urea inclusion techniques for the separation of straight chain hydrocarbons from branched and cyclic compounds is satisfactory when applied to mixtures in the milligram to gram ranges, but leads to low separation efficiencies when quantities in the microgram to milligram range are involved. In this study, a modified inclusion technique using an urea-packed milli-bore column and a catalytic eluent is described. Examples of its use for the separation of mixtures of linear and cyclic hydrocarbons from 30μg up to a few milligrams are given. The versatility of this technique for the analyses of low amounts of environmental samples is described, and an application to the hydrocarbon fraction of surface sediment from lake Leman (Switzerland) is presented.  相似文献   
112.
113.
High‐level incorporation of Ag in Au nanoclusters (NCs) is conveniently achieved by controlling the concentration of Ag+ in the synthesis of bovine serum albumin (BSA)‐protected Au NCs, and the resulting structure is determined to be bimetallic Ag28Au10‐BSA NCs through a series of characterizations including energy‐dispersive X‐ray spectroscopy, mass spectroscopy, and X‐ray photoelectron spectroscopy, together with density functional theory simulations. Interestingly, the Ag28Au10 NCs exhibit a significant fluorescence redshift rather than quenching upon interaction with hydrogen peroxide, providing a new approach to the detection of hydrogen peroxide through direct comparison of their fluorescence peaks. Furthermore, the Ag28Au10 NCs are also used for the sensitive and selective detection of herbicide through fluorescence enhancement. The detection limit for herbicide (0.1 nm ) is far below the health value established by the U.S. Environmental Protection Agency; such sensitive detection was not achieved by using AuAg NCs with low‐level incorporation of Ag or by using the individual metal NCs.  相似文献   
114.
Benzoyl peroxide has been used as a mild and efficient reagent for the preparation of benzoyl ester of oxime in moderate to good yields.  相似文献   
115.
116.
Considering the previous study dealing with thermodynamic and kinetic phenomena (nucleation and crystal growth) during the uranium peroxide precipitation, this work focuses on the agglomeration mechanism. It provides the results obtained from the experiments carried out in a MSMPR reactor operating at steady state. The influence of the operating parameters on the uranium peroxide agglomerates was studied in order to identify the agglomeration kernel. The method is based on the resolution of the population balance equation using the method of moments and the experimental particle size distributions. The results lead to a size-independent kernel directly proportional to the crystal growth rate. Under the stirring conditions studied, the agglomeration appears to be significantly reduced by mixing which results in a kernel inversely proportional to the average shear rate. The agglomeration kinetic law obtained in this study will be used for the process modelling in a further study.  相似文献   
117.

Three urea derivatives of anthraquinone were synthesized and they showed a high selectivity for dihydrogen phosphate ions.  相似文献   
118.
The present article describes a miniaturized potentiometric urea lipid film based biosensor on graphene nanosheets. Structural characterization of graphene nanosheets for miniaturization of potentiometric urea lipid film based biosensors have been studied through atomic force microscopy (AFM) and transmission electron microscopy (TEM) measurements. UV‐Vis and Fourrier transform IR (FTIR) spectroscopy have been utilized to study the pre‐ and postconjugated surfaces of graphene nanosheets. The presented potentiometric urea biosensor exhibits good reproducibility, reusability, selectivity, rapid response times (~4 s), long shelf life and high sensitivity of ca. 70 mV/decade over the urea logarithmic concentration range from 1×10?6 M to 1×10?3 M.  相似文献   
119.
Three novel paramagnetic metal complexes (MH2ID) of Ni2+, Cu2+ and VO2+ ions with 3‐hydroxy‐3,3’‐biindoline‐2,2’‐dione (dihydroindolone, H4ID) were synthesized and characterized by different spectroscopic methods. The ligand (H4ID) was synthesized via homocoupling reaction of isatin in presence of phenylalanine in methanol. Complexation of low valent Ni2+, Cu2+ ions and high valent VO2+ ions with H4ID carried out in 1: 2 molar ratios. A comparison in the catalytic potential of paramagnetic complexes of low and high valent metal ion was explored in the oxidation processes of cis‐cyclooctene, benzyl alcohol and thiophene by an aqueous H2O2, as a green terminal oxidant, in the presence and absence of acetonitrile, as an organic solvent, at 85 °C. NiH2ID, CuH2ID and VOH2ID show good catalytic activity, i.e. good chemo‐ and regioselectivity. VOH2ID has the highest catalytic potential compared to both Ni2+‐ and Cu2+‐species in the same homogenous aerobic atmosphere. Catalytic oxidation of other alkenes and alcohols was also studied using NiH2ID, CuH2ID or VOH2ID as a pre‐catalyst by an aqueous H2O2. A mechanistic pathway for those oxidation processes was proposed.  相似文献   
120.
A heterogeneous catalyst (FeSi/Ag/VO) based on silver and vanadyl as active sites and mesoporous silica‐coated nanospheres of magnetite (Fe3O4@m‐SiO2) as support was successfully prepared by deposition of Ag nanoparticles and the covalent grafting of vanadyl(IV) acetylacetonate on Fe3O4@m‐SiO2. The catalyst exhibited excellent activity for the oxidation of alkanes, benzene and alkylaromatics using green oxidant H2O2 and oxalic acid in acetonitrile at 60 °C.  相似文献   
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