Electrochemical activation of freons using electron transfer mediators

This overview discusses the electrochemical activation of freons CF₂ClCFCl₂ (CFC113), CF₃Br (FC13B1), and CF₂Cl₂ (CFC12) using various electron transfer mediators: complex nickel(ii) compounds with nitrogen-containing tetradentate ligands and bipyridyl, aromatic derivatives (perylene, p-dicyanobenzene, Å-azobenzene, and others), and sulfur dioxide. A possibility was shown of the homogeneous catalytic activation of freons by two mutually supplementing electron transfer mediators: methylviologen—SO₂ and I₂—SO₂. The involvement of freons by the electron transfer mediators into the syntheses of valuable organic products under mild conditions was demonstrated for several examples.     

Application and measurement of underwater acoustic reciprocity transfer functions in reverberant sound field

The reciprocity measurement theory in anomalous reverberant sound fields was investigated.An improved method Was proposed due to the interrelated errors.The source volume velocity Was corrected by spatial average of measurement results and evaluation of the reverberant sound field influence on acoustic energy density.The result was validated in underwater experiment,corrected reciprocity measurement results were almost the same as direct measurement results.It indicates that reverberant sound field does not affect the validitv of the principle,but influences the obtainment of source volume velocity,then influences the measurement of transfer functions with the principle.The proposed method is simple and effective in anomalous reverberant sound fields.The study mav be valuable for the applications which are based on the principle.     

The deferred standard method–a technique for quantitative analysis in laboratory and process HPLC

Among the methods of quantitation commonly used in chromatography, the internal standard may be considered as the most useful and accurate; however, use of internal standards in liquid chromatography with UV and fluorometric detectors runs into considerable difficulties because the response factors may differ from each other by several orders of magnitude. Under these conditions, the search for an IS with a response factor similar to that of the analyte and adequately resolved from other peaks may prove very tedious. The deferred standard concept, already used in process and laboratory gas chromatography, is proposed as a solution; its definition, details of instrumentation, operation, and results are described in this paper. The material presented demonstrates its ability to solve this specific problem. In addition, use of the deferred standard approach is seen to save time and money.     

An advanced partitioning process for key elements separation from high level liquid waste

To separate MA(Am,Cm) and some fission product elements(FPs) such as Tc,Pd,Cs and Sr from high level liquid waste(HLLW) systematically,we have been studying an advanced aqueous partitioning process,which uses selective adsorption as the separation method.For this process,we prepared several novel adsorbents which were immobilized in a porous silica/polymer composite support(SiO 2-P).Adsorption and separation behavior of various elements was studied experimentally in detail.Small scale separation tests using simulated HLLW solutions were carried out.Pd(II) was strongly adsorbed by the AR-01 anion exchanger and effectively eluted off by using thiourea.Successful separation of Pd(II) from simulated HLLW was achieved.Tc(VII) also exhibited strong adsorption on AR-01 and could be eluted off by using U(IV) as a reductive eluent.Am(III) presented significantly high adsorbability and selectivity onto R-BTP/SiO 2-P adsorbents over various FPs including Ln(III).The R-BTP adsorbents were fairly stable in 3 M HNO 3,but instable against-irradiation-3M HNO 3.An advanced partitioning process consisting of three separation columns for the target elements separation from HLLW was proposed and the obtained experiment results indicated that the proposed process is essentially feasible.     

Fractionation and Extraction Optimization of Potentially Valuable Compounds and Their Profiling in Six Varieties of Two Nicotiana Species

There is an increasingly urgent call to shift industrial processes from fossil fuel feedstock to sustainable bio-based resources. This change becomes of high importance considering new budget requirements for a carbon-neutral economy. Such a transformation can be driven by traditionally used plants that are able to produce large amounts of valuable biologically relevant secondary metabolites. Tobacco plants can play a leading role in providing value-added products in remote areas of the world. In this study, we propose a non-exhaustive list of compounds with potential economic interest that can be sourced from the tobacco plant. In order to optimize extraction methodologies, we first analyzed their physico-chemical properties using rapid solubility tests and high-resolution microfractionation techniques. Next, to identify an optimal extraction for a selected list of compounds, we compared 13 different extraction method–solvent combinations. We proceeded with profiling some of these compounds in a total of six varieties from Nicotiana tabacum and Nicotiana rustica species, identifying the optimal variety for each. The estimated expected yields for each of these compounds demonstrate that tobacco plants can be a superior source of valuable compounds with diverse applications beyond nicotine. Among the most interesting results, we found high variability of anatabine content between species and varieties, ranging from 287 to 1699 µg/g. In addition, we found that CGA (1305 µg/g) and rutin (7910 µg/g) content are orders of magnitude lower in the Burley variety as compared to all others.