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991.
Determination of triclosan in foodstuffs   总被引:1,自引:0,他引:1  
A reverse-phase high-performance liquid chromatographic (RP-HPLC) method coupled with an ultraviolet detector was developed to determine triclosan which had migrated into foodstuffs from packaging materials. The method includes extraction with hexane, followed by evaporation to dryness and residue re-dissolution in ACN 90%. Chromatographic separation was performed with a Kromasil 100 C18 column (15 cm x 0.4 cm ID, 5 microm particle size) at 30 degrees C and using ACN and water as mobile phases. Regarding recoveries, good results (higher than 83% and lower than 112%) were obtained for the three representative food matrixes selected (orange juice, chicken breast meat, and Gouda cheese).  相似文献   
992.
This perspective article describes the combination of experimental data and quantum chemical methods for the determination of structure and reaction mechanisms of uranyl(vi) complexes in aqueous solution. The first part assesses the accuracy of the chemical and thermodynamic properties of solvated uranyl(vi) complexes as obtained by various quantum chemical methods. The second part discusses structure determination, mechanisms for ligand exchange and the lability of coordinated water molecules for various uranyl(vi) complexes using a combination of NMR and quantum chemical data.  相似文献   
993.
The role of electrochemistry in the discovery and interpretation of the alleged cold nuclear fusion is discussed.  相似文献   
994.
The preparation of indigo from Indigofera suffruticosa following the procedures attributed to ancient Mayas was electrochemically monitored using the voltammetry-of-microparticles approach. The mechanism formation of indigotin and indirubin from its precursors, indican and isatan, is discussed. Comparison of voltammetric profiles for differently prepared and commercial indigos and genuine Maya Blue samples suggests that the preparation procedure of indigo changed during the Late Classical Maya period. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   
995.
996.
A procedure has been developed for the direct fourth-derivative spectrophotometric determination of iron(III) dimethyldithiocarbamate by converting it into an iron(II) 2,2'-bipyridyl complex, which is then dissolved in Triton X-100. Beer's law is obeyed over the concentration range 0.5-20 microg mL(-1 )in the final solution. Various parameters such as the effect of pH and interference of large number of ions on the determination of ferbam have been studied in detail. The method is sensitive, highly selective and can be used for the determination of ferbam in a commercial sample and in mixtures with various dithiocarbamates (ziram, zineb, maneb, etc.) and from wheat grains.  相似文献   
997.
A simple and accurate method is described for the determination of acctyl groups in various organic compounds. The compound is dissolved or suspended in absolute methanol and saponified with a known quantity of potassium methylate solution. The excess potassium methylate is then hydrolysed and determined as potassium hydroxide by titration, an appropriate indicator being used.  相似文献   
998.
The prevulcanisation of skim latex, a by-product of field natural rubber (NR) latex concentrated by centrifugation, using sulphur and peroxide systems was investigated. Compared to the peroxide prevulcanisation, the lower swelling ratio of film casted from sulphur-prevulcanised skim (SPVS) latex was observed. The latter was then employed for preparation of NR/SPVS core–shell particles by using heterocoagulation technique whose driving force was an interpolymer complex between poly(ethylene oxide) (PEO) moieties of a non-ionic surfactant (Nonidet) adsorbed on small SPVS particles and the indigenous surfactant (protein–lipid) on a large NR particle. The value of zeta potential of heterocoagulated particle and the better oil resistance of films casted from the composite latex when compared to that of the NR film revealed the NR/SPVS core–shell structure.  相似文献   
999.
1000.
Two methods are developed, when solving the related time-independent Schrodinger equation (TISE), to cope with the singular terms of the vibrational kinetic energy operator of a triatomic molecule given in orthogonal internal coordinates. The first method provides a mathematically correct treatment of all singular terms. The vibrational eigenfunctions are approximated by linear combinations of functions of a three-dimensional nondirect-product basis, where basis functions are formed by coupling Bessel-DVR functions, where DVR stands for discrete variable representation, depending on distance-type coordinates and Legendre polynomials depending on angle bending. In the second method one of the singular terms related to a distance-type coordinate, deemed to be unimportant for spectroscopic applications, is given no special treatment. Here the basis set is obtained by taking the direct product of a one-dimensional DVR basis with a two-dimensional nondirect-product basis, the latter formed by coupling Bessel-DVR functions and Legendre polynomials. With the basis functions defined, matrix representations of the TISE are set up and solved numerically to obtain the vibrational energy levels of H3+. The numerical calculations show that the first method treating all singularities is computationally inefficient, while the second method treating properly only the singularities having physical importance is quite efficient.  相似文献   
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