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971.
The reaction between thallium(I) and [CoIIIW12O40]5- in the presence of ruthenium(III) as catalyst proceeds viainitial outer-sphere oxidation of the catalyst to ruthenium(VI). The ruthenium(IV) thus generated will oxidize thallium(I)
to an unstable thallium(II) which by reacting with oxidant gives the final product, thallium(III). The formation of ruthenium(II)
by direct two-electron reduction of the catalyst by thallium(I) is thermodynamically less favorable. The reaction rate is
unaffected by the [ H+ ], whereas it is catalyzed by chloride ion . The formation of reactive chlorocomplex,TlCl, in a prior equilibrium is the
reason for the chloride ion catalysis. Increasing the relative permittivity of the medium increases the rate of the reaction,
which is attributed to the formation of an outer-sphere complex between the catalyst and oxidant.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
972.
We have developed a method for obtaining 2-substituted 3-amino-6,6-dimethyl-5,6-dihydro-8H-pyrano[4′,3′:4,5]-and 5,6,7,8-tetrahydrobenzo[b]thieno[2,3-d]pyrimidin-4(3H)-ones,
converted by deamination to the corresponding dihydropyranothieno-3H-pyrimidinones.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 441–444, March, 2006. 相似文献
973.
C12-s-C12•2Br和C12En混合水溶液的胶团化行为 总被引:3,自引:0,他引:3
季铵盐二聚表面活性剂C12 s C12•2Br(s=2、3、4、6)和非离子表面活性剂C12E10或C12E23在水溶液中生成混合胶团.其临界胶团总浓度cmcT值介于二元复配体系中各组分的临界胶团浓度和之间.当添加少量非离子型表面活性剂(在水溶液中的摩尔分数α2=0.1)时,混合胶团中C12E10或C12E23的摩尔分数均已超过0.35;随着溶液中非离子型表面活性剂含量的增大,混合胶团中逐渐以C12E10或C12E23成分为主. 相似文献
974.
The effect of a weak convective heat transfer on the thermocapillary interaction of two bubbles with an arbitrary orientation relative to an externally imposed temperature gradient is examined. Asymptotic analysis of the case of large separation distances, Z, suggests that the corrections to the bubbles' velocities are of
(Pe/Z2), rather than
(Pe2) previously found for an isolated bubble. Equal-sized bubbles are known to move with the same velocities, as if they were isolated, when heat conduction is the only transport mechanism. However, the convective transport results in a relative motion of the bubbles. The tendency of equal bubbles to line up in a plane perpendicular to the applied thermal gradient is shown analytically in the weakly nonlinear limit of small Pe numbers, and an interesting interaction behavior in the case of unequal bubbles is discussed. 相似文献
975.
The fluorescence decay of the tertiary aliphatic animes trimethylamine (TMA), triethylamine (TEA) and tri-n-propylamine (TPA) in the vapour phase excited between 260 and 215 nm has been shown to consist of a single, wavelength-dependent, component when the first excited state is uniquely excited, but two components when the first and second excited states are simultaneously excited. This dual exponentiality persists at pressures as low as 10 mTorr, and it is argued that the two-component decay does not arise from collisional vibrational relaxation. 相似文献
976.
Purification and reversible immobilization of d-amino acid oxidase from Trigonopsis variabilis could be simultaneously accomplished by hydrophobic interaction on Phenyl Sepharose CL-4B in the presence of 50 mM pyrophosphate buffer (pH 8.5). The presence of a high salt concentration of 2M, which is generally required for the hydrophobic interactions, was not essential for the hydrophobic immobilization. The
enzyme in free as well as immobilized form was optimally active between pH 7.0 and 9.0. The immobilized preparation could
be reused in a batch process for the conversion of d-amino acids to α-keto acids. When the activity of the preparation dropped below practical limits, the gel could be regenerated
by water wash and recharged with fresh crude extract from yeast. 相似文献
977.
Marcin Marczak Lidia Wolska Wojciech Chrzanowski Jacek Namieśnik 《Mikrochimica acta》2006,155(3-4):331-348
Volatile organic compounds (VOCs), due to their toxicity and persistence in the environment, are particularly important pollutants.
Some of these compounds are mutagens, teratogens or carcinogens, while others are responsible for the degradation of organoleptic
parameters such as taste and odour of water. This review focuses on a number of key procedural steps in the analysis of volatile
organic compounds (VOCs) in water samples. A wide spectrum of techniques for the isolation and preconcentration of the aforementioned
pollutants for trace organic analysis by gas chromatography are presented and discussed. The advantages and disadvantages
of these techniques are discussed and novel developments are also taken into consideration. 相似文献
978.
Kanchi Suvardhan Kailasa Suresh Kumar Dasari Rekha Pantrangam Subrahmanyam Kapuvedi Kiran Bellum Jayaraj Surasura Ramanaiah Kandhukuri Janardhanam Pattium Chiranjeevi 《Mikrochimica acta》2007,157(3-4):237-244
Cloud point extraction was applied as a method for preconcentration of rhodium after formation of a complex with 2-propylpiperidine-1-carbodithioate
(2-PPC), and later determined by flame atomic absorption spectrometry using TritonX-114 as surfactant. Rhodium was complexed
with 2-PPC in an aqueous phase and kept for 15 min in a thermostatted bath at 40 °C. Separation of the two phases was accomplished
by centrifugation for 15 min at 4000 rpm. The chemical variables affecting the cloud point extraction were optimized and successfully
applied to rhodium determination in various water samples. Under optimized conditions, the preconcentration system (100 mL
sample) permitted an enhancement factor of 50. The detection limits obtained under optimal conditions was 0.052 ng mL−1. The extraction efficiency was investigated at different rhodium concentrations (7.0–42.0 μg mL−1), and good recoveries (96.42–99.14%) were obtained using this method. It has been applied to the determination of rhodium
in water and was compared with reported methods in terms of Student’s ‘t’-test and variance ratio ‘f’-test. 相似文献
979.
N. Bjerre A. O. Mitrushenkov P. Palmieri P. Rosmus 《Theoretical chemistry accounts》1998,100(1-4):51-59
The spin-orbit and the spin-spin coupling constants of the 4Πg state of the He2
− ion, of the parent a3Σu
+, and of the b3Πg states of He2 have been evaluated by a multireference configuration interaction method. The theoretical spin-spin splittings of the a3Σu
+ state and the R-dependent spin-spin function are found to be in excellent agreement with experiment, with deviations in the range of a few
MHz. The theoretical spin-orbit constants and splittings of the b3Πg state are larger than the experimental values by about 370 MHz. The spin-orbit coupling constant of the 4Πg state of He2
− is␣estimated to be three times smaller than in the b3Πg state, but one of the intramultiplet off-diagonal spin-spin interactions is predicted to give a large contribution to the
fine structure of the metastable ion. The theoretical fine structure constants for the He2
− ion are expected to␣aid future spectroscopic investigations of the fine structure splittings of the negative ion.
Received: 14 April 1998 / Accepted: 27 July 1998 / Published online: 19 October 1998 相似文献
980.
The complexity of different quality standards can, in principle, be covered by different approaches and strategies. In-depth
process mapping of quality control (QC) work streams was used by the analytical laboratories of Lonza AG to show up the principle
differences in being compliant to different quality systems. The results identified two main drivers for all necessary actions:
process-related activities and infrastructure-related activities. In addition, a clear indication of the economic impact of
these driving forces was gained, which led the laboratories to decide on a process-oriented approach. This approach has the
advantage of being able to reflect the different demands of different quality assurance (QA) regulations within the same QC
organizational structure. Following the process helps avoid unnecessary efforts in analytical work and represents a very economical
approach, at the same time, providing high flexibility to react to different QA or customer demands.
Received: 5 July 2002 Accepted: 12 November 2002
Acknowledgements The process-oriented approach resulted from many, very challenging discussions for which I would like to thank the staff
of my organization (Analytics & QC), especially, the QA staff and the LIMS team.
Presented at Analytica Conference, 23–26 April 2002, Munich, Germany
Correspondence to B. Ciommer 相似文献