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The influence factors on CeSn0.8W0.6Ox/TiO2 for catalytic removals of NO, CO and C3H8
Guorong Sui,Zhiwei Xue,Dan Zhou,Yan Wang,Yuesong Shen,Yuhao Zong,Youlin Liu,Tai Qiu,Shemin Zhu 한국공업화학회 2017 Journal of Industrial and Engineering Chemistry Vol.51 No.-
Series of CeSn0.8W0.6Ox/TiO2 catalysts were tested for selective catalytic reduction of NO and forsynergistic catalytic removals of CO and C3H8 from diesel engine exhaust. Results revealed that catalyst12%-CeSn0.8W0.6Ox/TiO2 calcined at 500 C exhibited the optimal catalytic performance for NH3-SCR ofNO. The catalyst obtained more than 90% NO conversion at a wide temperature range of 252–456 C. BothCO and C3H8 could be oxidized into CO2 by the optimized catalyst. Moreover, excellent redox property,rich surface acidity and big specific surface area were the promotional factors for good catalyticperformance in catalytic removals of NO, CO and C3H8.
Ze-Jian Wang,Xingzi Zhang,Ping Wang,Zhiwei Sui,Meijin Guo,Siliang Zhang,Yingping Zhuang 한국생물공학회 2020 Biotechnology and Bioprocess Engineering Vol.25 No.3
The effects of different oxygen uptake rates (OUR) on the physiological metabolism of Rhodobacter sphaeroides were investigated systematically in 50 L fermenters due to the significant influence on industrial coenzyme Q10 production under oxygen supply limitation. Meanwhile, the seriously decreased oxygen transfer rate caused by the increased broth viscosity was successfully prevented with OUR-directed continuous ammonium sulfate feeding in the late fermentation phase. The statistical analysis results showed that controlling OUR constantly at 45 ± 2.2 mmol/L/h by the oxygen supply level adjustment and the continuous ammonium sulfate feeding could greatly enhance Q10 production. This OUR-Stat controlling strategy successfully achieved the maximal coenzyme Q10 production (2584 ± 82 mg/L), which was 15.4% higher than that of the control. The highest specific CoQ10 content was 25.9 mg/(g DCW)), and the yield of CoQ10 to glucose consumption was up to 19.37 mg/g. These results demonstrated that the optimal OUR-Stat controlling strategy would be effective and economical for improving the industrial CoQ10 production.
Yoo, Hee-Bong,Park, Sang-Ryoul,Dong, Lianhua,Wang, Jing,Sui, Zhiwei,Pavš,ič,, Jernej,Milavec, Mojca,Akgoz, Muslum,Mozioğ,lu, Erkan,Corbisier, Philippe,Janka, Má,trai,Cosme, Bru American Chemical Society 2016 ANALYTICAL CHEMISTRY - Vol.88 No.24
<P>Enumeration-based determination of DNA copy-concentration was assessed through an international comparison among national metrology institutes (NMIs) and designated institutes (DIs). Enumeration-based quantification does not require a calibration standard thereby providing a route to 'absolute quantification', which offers the potential for reliable value assignments of DNA reference materials, and International System of Units (SI) traceability to copy number 1 through accurate counting. In this study, 2 enumeration based methods, flow cytometric (FCM) counting and the digital polymerase chain reaction (dPCR), were compared to quantify a solution of the pBR322 plasmid at a concentration of several thousand copies per microliter. In addition, 2 orthogonal chemical-analysis methods based on nucleotide quantification, isotope-dilution mass spectrometry (IDMS) and capillary electrophoresis (CE) were applied to quantify a more concentrated solution of the plasmid. Although 9 dPCR results from 8 laboratories showed some dispersion (relative standard deviation [RSD] = 11.8%), their means were closely aligned with those of the FCM-based counting method and the orthogonal chemical-analysis methods, corrected for gravimetric dilution factors. Using the means of dPCR results, the RSD of all 4 methods was 1.8%, which strongly supported the validity of the recent enumeration approaches. Despite a good overall agreement, the individual dPCR results were not sufficiently covered by the reported measurement uncertainties. These findings suggest that some laboratories may not have considered all factors contributing to the measurement uncertainty of dPCR, and further investigation of this possibility is warranted.</P>