The influence of distribution and deposit of conductive coating on shielding effectiveness of textiles

This study presents the investigation of electrically conductive fabrics with low resistivity, coated with formulation containing the conjugated polymer system – poly(3,4-ethylenedioxythiophene)-polystyrene sulphonate (PEDOT-PSS). The samples of fabrics were coated with PEDOT-PSS, using a screen printing method, by different patterns or coating their surface fully with different coating deposit. Methods for measurement of electrostatic properties, reflection and transmission as well as the assessment of electromagnetic radiation (EMR) shielding effectiveness were used for the characterization of electrical properties of developed samples. EMR shielding properties were investigated within 2–12 GHz frequency bands. The highest attenuation of the electromagnetic energy among tested fabrics was obtained on the fabrics fully coated with paste and it depended on deposit considerably. The influence of distribution and deposit of conductive coating on shielding effectiveness of textiles were determined. Correlation between shielding effectiveness and electrostatic properties of developed coated fabrics was also discussed. Electrical properties of samples coated with formulation containing PEDOT-PSS were compared with these of fabrics with metalized yarns, developed by us earlier. The results of EMR shielding measurements showed that fabrics coated with the paste containing conductive polymer system compared to fabrics with in-weaved conductive metalized yarns have certain advantages as EMR shields.     

Risk assessment of Fusarium mycotoxins in Lithuanian small cereal grains

A total of 125 small grain samples, including 60 of winter crop and 65 of spring crop collected during 2006–2007 at harvesting in Lithuanian fields, were involved in the current study on co-occurrence of three Fusarium mycotoxins. All grain samples tested were found to be contaminated with mycotoxins. In 2006, winter cereal grain samples contaminated with one mycotoxin accounted for 16%, and those contaminated with three mycotoxins for 25%. No spring cereal grain samples containing only one toxin were found, while those contaminated with three toxins accounted for 91% of the total samples tested. In the year 2007 winter cereal grain samples contaminated with one toxin accounted for as little as 4%, and all spring cereal grain samples tested were found to be 100% contaminated with deoxynivalenol, zearalenone, and T-2 toxin. Mycotoxin concentrations in grain samples, in most cases, were within the permissible range. A trend was revealed that spring barley grain samples tested contained higher T-2 concentrations irrespective of the test year.     

The Study of NADPH-Dependent Flavoenzyme-Catalyzed Reduction of Benzo[1,2-c]1,2,5-oxadiazole N-Oxides (Benzofuroxans)

The enzymatic reactivity of a series of benzo[1,2-c]1,2,5-oxadiazole N-oxides (benzofuroxans; BFXs) towards mammalian single-electron transferring NADPH:cytochrome P-450 reductase (P-450R) and two-electron (hydride) transferring NAD(P)H:quinone oxidoreductase (NQO1) was examined in this work. Since the =N⁺ (→O)O⁻ moiety of furoxan fragments of BFXs bears some similarity to the aromatic nitro-group, the reactivity of BFXs was compared to that of nitro-aromatic compounds (NACs) whose reduction mechanisms by these and other related flavoenzymes have been extensively investigated. The reduction of BFXs by both P-450R and NQO1 was accompanied by O₂ uptake, which was much lower than the NADPH oxidation rate; except for annelated BFXs, whose reduction was followed by the production of peroxide. In order to analyze the possible quantitative structure-activity relationships (QSARs) of the enzymatic reactivity of the compounds, their electron-accepting potency and other reactivity indices were assessed by quantum mechanical methods. In P-450R-catalyzed reactions, both BFXs and NACs showed the same reactivity dependence on their electron-accepting potency which might be consistent with an “outer sphere” electron transfer mechanism. In NQO1-catalyzed two-electron (hydride) transferring reactions, BFXs acted as more efficient substrates than NACs, and the reduction efficacy of BFXs by NQO1 was in general higher than by single-electron transferring P-450R. In NQO1-catalyzed reactions, QSARs obtained showed that the reduction efficacy of BFXs, as well as that of NACs, was determined by their electron-accepting potency and could be influenced by their binding mode in the active center of NQO1 and by their global softness as their electronic characteristic. The reductive conversion of benzofuroxan by both flavoenzymes yielded the same reduction product of benzofuroxan, 2,3-diaminophenazine, with the formation of o-benzoquinone dioxime as a putative primary reductive intermediate, which undergoes a further reduction process. Overall, the data obtained show that by contrast to NACs, the flavoenzyme-catalyzed reduction of BFXs is unlikely to initiate their redox-cycling, which may argue for a minor role of the redox-cycling-type action in the cytotoxicity of BFXs.     

Preventing Environmental Contamination by Nonionic Surfactants and Nickel

Protecting the environment from contamination by heavy metals and nonionic surfactants, the sorption of oxyethylated alcohols OS-20, alkylmonoethers ALM-10 and nickel has been investigated, on the hydrogen form of Purolite C 106 cation exchanger. The problem is that nonionic surfactant is not removed by conventional ion exchange. Sorption isotherms were measured, coefficients for intraparticle diffusion were calculated. The sorption of nonionic surfactant from the solution, containing 10 mmol/l, amounts to 400 mg/g for OS-20 and 500 mg/g for ALM-10. The presence of nickel has no appreciable effect on the rate of intraparticle diffusion and the equilibrium sorption of surfactant. The sorption of nickel takes place in the form of both free cations and cations bonded with surfactant.

The sorption of nonionic surfactant and nickel in Purolite C 106 cation exchanger was found to be suitable for the simultaneous removal of both contaminants in order to reuse the water, recovered from nickel plating rinsewater, preventing the contamination of environment.