The electrochemical properties of membranes based on dibenzo-crown ethers bearing hydroxyl and chloromethyl groups in polyether rings were studied. These substances were tested as membrane ionophores for ion-selective electrodes (ISEs) reversible to potassium ion. The developed ISEs were used for determining potassium in blood plasma samples. The generalized results of determining potassium in the blood of different patients with cardiovascular diseases revealed quantitative regularities that allowed the diseases to be diagnosed early. 相似文献
The kinetics of the system O2/HO2?, OH? were studied at pyrolytic carbon in alkaline electrolytes. The rest potentials are close to the reversible values. They decrease by 30 mV when the HO2?-concentration is increased by a factor 10. CathodicTafel lines displayb-values between 70 and 95 mV. The exchange current densities are evaluated by extrapolation ofTafel lines to zero overvoltage and from the charge transfer resistance. Two different succeeding charge transfer reactions occur in course of the overall process, the first of which is the rate-determining step. A cathodic reaction order of zero is obtained with respect to HO2?. Theb values of anodicTafel lines are between 60 and 80 mV, the corresponding reaction order concerning the HO2? concentration is found to be +0.5. The kinetic studies prove the reversibility of the system O2/HO2?, OH? at carbon electrodes. The reaction mechanism is: $$\begin{array}{*{20}c} {O_2 + e^ - \rightleftarrows O_2 } \\ {O_{2^ - } + H_2 O \rightleftarrows HO_2 + OH - } \\ {HO_2 + e^ - \rightleftarrows HO_{2^ - } } \\ \end{array} $$ . 相似文献
The gas–liquid gliding arc discharge plasma is used directly to study degradation and dechlorination of 4-Chlorophenol (4-CP)
in solution. The typical AC waveforms of discharge voltage and current revealed that the discharge behavior was not definitely
periodic. The chemical oxygen demand (COD) abatement of 4-CP solution with stainless steel electrode is higher than that with
aluminum or brass electrode; When air was used as carrier gas the COD abated from 1,679.2 to 190 mg/L (i.e., 88.68% abatement)
after 76 min plasma treatment; Increasing gas–liquid mixing rate could also increase the degradation of 4-CP; adding appropriate
amounts of Fe2+ or iron chips to the solution were found to be favorable for 4-CP degradation. The main intermediates of 4-CP degradation
are p-benzoquinone, hydroquinone, 4-chlorocatechol, p-chloronitrobenzene, and ring cleavage products (acetic acid, glycol,
propanone, and others). Furthermore, possible pathways of 4-CP degradation in solution are proposed. 相似文献
Enzymatic kinetic resolution of (±)-hydroxytetrahydropyrans has been achieved for the first time by means of lipase-mediated transesterification to afford optically active (2S,4R)-tetrahydropyranyl acetates and (2R,4S)-tetrahydropyranols in excellent yields with high enantioselectivity. Absolute configurations of the tetrahydropyranyl acetates were assigned as (S) by chemical correlation. 相似文献
On the Crystal Chemistry of a New Barium Rare-Earth Oxozincate: Ba2Er2Zn8O13 High temperature reactions led to single crystals of Ba2Er2Zn8O13. It crystallizes with orthorhombic symmetry, space group C122v? Cmc21, a = 6.276, b = 10.871, c = 10.195 Å, Z = 2. The hitherto unknown crystal structure shows Zn2+ with tetrahedral, Er3+ octahedral and Ba2+ cuboctahedral coordination by O2?. It will be shown that parts of the [Zn8O13] network are fragments of the ZnO structure showing O2? within a tetrahedral zinc coordination. A deficit of two O2? ions per unit cell is focused on two point positions. 相似文献
Collision-induced rotational transitions in the electronically excited NaLi molecule have been studied using laser excited fluorescence. Due to the greater number of allowed transitions as compared with Na2 and Li2, more cases were found of transitions +ΔJ and ?ΔJ having greatly different cross sections (“+/ - asymmetry”). This observation is in agreement with recent predictions on the basis of Born's approximation. All observed transitions are classified according to the symmetry of the contributing potential terms. Data are presented which indicate the necessity for refinements of the theory. 相似文献
It is shown by i.r. spectroscopy that the anionic polymerization of methacrylonitrile using organomagnesium compounds as initiators leads to two types of “living” ends i.e. and The active centres form complexes with the monomer, as well as with the nitrile groups of the monomer units in the polymer chain, in a hydrocarbon medium. The complexes are characterized by bands in the 2250–2280 cm?1 region. Addition of donors destroys the complexes and in some cases (hexamethylphosphorous triamide) converts the complex of organomagnesium compound with monomer into a “living” end. In ethers as solvent, the dominant side-reaction is addition of the initiator to the nitrile group of the monomer. 相似文献
Zusammenfassung Monomere Phosphinimine der allgemeinen Formel C6H5N= =PCln(NEt2)3-n (n=0,1,2) lassen sich (I) aus dimerem Phenylimino-phosphorsäure-trichlorid und Diäthylamin in Gegenwart eines Chlorwasserstoffakzeptors und (II) durch Reaktion der Phosphine PCln(NEt2)3-n mit Phenylazid darstellen. Die Phosphorane Et2NPCl4, (Et2N)2PCl3 und (Et2N)3PBr2 reagieren mit Anilin nicht zu Phenylimino-Verbindungen. Durch alkalische Hydrolyse von C6H5N=PCl(NEt2)2 entsteht das Phosphorsäure-bis[diäthylamino]-anilid. Die IR- und1H- und31P-NMR-Spektren der Verbindungen werden mitgeteilt.
Monomeric phosphinimines of the general formula C6H5N= =PCln(NEt2)3-n (n=0,1,2) are formed (I) from dimeric phenyliminophosphoricacid-trichloride and diethylamine in the presence of a HCl-acceptor and (II) by reacting the phosphines PCln(NEt2)3-n with phenylazide. The phosphoranes Et2NPCl4, (Et2N)2PCl3 and (Et2N)3PBr2 do not give the corresponding phenylimines with aniline. Alkaline hydrolysis of C6H5N= =PCl(NEt2)2 gives bis[diethylamino]-anilido-phosphinoxid. IR-,1H- and31P-NMR-spectra are given.