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Abstract

Hydrogen (H2) and liquid petroleum gas (LPG) sensing properties of SnO2 thin films obtained by direct oxidation of chemically deposited SnS films has been studied. The SnS film was prepared by a chemical technique called SILAR (Successive Ionic Layer Adsorption and Reaction). The sensor element comprises of a layer of chemically deposited SnO2 film with an overlayer of palladium (Pd) sensitiser. The Pd sensitiser layer was also formed following a chemical technique. The double layer element so formed shows significantly high sensitivity to H2 and LPG. The temperature variation of sensitivity was studied and the maximum sensitivity of 99.7% was observed at around 200°C for 1 vol% H2 in air. The response time to target gas was about 10 seconds and the sensor element was found to recover to its original resistance reasonably fast. The maximum sensitivity of 98% for 1.6 vol% LPG was observed at around 325°C. The sensor response and recovery was reasonably fast (less than one minute) at this temperature.
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Abstract

Catalytic converters contain the catalytic substance in their structure, which is a mixture of Platinum Group Metals (PGMs). The prices of these metals and a growing demand for them in the market, make it necessary to recycle spent catalytic converters and recovery of PGMs. In the study, the effect of ozone and hydrogen peroxide application on the possibility of extracting PGM from used car catalysts was investigated. The catalytic carrier was milled, sieved and then the fractions with the desired grain size were treated with the appropriate HCl mixture and 3%, 5%, 10%, 15% and 30% H2O2, respectively, and the tests were also carried out at temperature 333 K. Ozone tests were conducted with the O3 flow in the range of 1,3,5 g/h. Samples for analysis were collected after 30 min, 1 h, 2 h, 3 h and after 4 h, respectively. The residue after the experiments and filtration process was also analysed. The obtained results confirmed the assumption that PGMs can be extracted using hydrochloric acid with the addition of H2O2 or ozone as oxidants. It allows to significantly intensify the carried out reactions and to improve the rate of PGMs transfer to the solution.
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Abstract

Surfactants after their use are discharged into aquatic ecosystems. These compounds may be harmful to fauna and flora in surface waters or can be toxic for microorganisms of the activated sludge or biofilm in WWTP. In order to determine effectiveness of different advanced oxidation processes on the degradation of surfactants, in this study the degradation of anionic surfactants in aqueous solution using photolysis by 254 nm irradiation and by advanced oxidation process in a H2O2/UVC system was investigated. Two representatives of anionic surfactants, linear alkyl benzene sulphonate (LAS-R11–14) and ether carboxylic derivate (EC-R12–14E10) were tested. The influence of pH, initial surfactant concentration and dose of hydrogen peroxide on the degradation was also studied. Results show outstanding effectiveness of the H2O2/UVC system in the removal of surfactant from aqueous solutions.
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