Oxy-steam combustion is a promising next-generation combustion technology.Conversions of fuel-N,volatile-N,and char-N to NO and N2O during combustion of a single coal particle in O2/N2and O2/H2O were studied in a tube...Oxy-steam combustion is a promising next-generation combustion technology.Conversions of fuel-N,volatile-N,and char-N to NO and N2O during combustion of a single coal particle in O2/N2and O2/H2O were studied in a tube reactor at low temperature.In O2/N2,NO reaches the maximum value in the devolatilization stage and N2O reaches the maximum value in the char combustion stage.In O2/H2O,both NO and N2O reach the maximum values in the char combustion stage.The total conversion ratios of fuel-N to NO and N2O in O2/N2are obviously higher than those in O2/H2O,due to the reduction of H2O on NO and N2O.Temperature changes the trade-off between NO and N2O.In O2/N2and O2/H2O,the conversion ratios of fuel-N,volatile-N,and char-N to NO increase with increasing temperature,and those to N2O show the opposite trends.The conversion ratios of fuel-N,volatile-N,and char-N to NO reach the maximum values at 〈O2〉=30 vol%in O2/N2.In O2/H2O,the conversion ratios of fuel-N and char-N to NO reach the maximum values at 〈O2〉=30 vol%,and the conversion ratio of volatile-N to NO shows a slightly increasing trend with increasing oxygen concentration.The conversion ratios of fuel-N,volatile-N,and char-N to N2O decrease with increasing oxygen concentration in both atmospheres.A higher coal rank has higher conversion ratios of fuel-N to NO and N2O.Anthracite coal exhibits the highest conversion ratios of fuel-N,volatile-N,and char-N to NO and N2O in both atmospheres.This work is to develop efficient ways to understand and control NO and N2O emissions for a clean and sustainable atmosphere.展开更多
Niobium oxide as the promoter was doped in the V/WTi catalyst for the selective catalytic reduction（SCR）of NO.The results showed that the addition of Nb2O5could improve the SCR activity at low temperatures and the 6...Niobium oxide as the promoter was doped in the V/WTi catalyst for the selective catalytic reduction（SCR）of NO.The results showed that the addition of Nb2O5could improve the SCR activity at low temperatures and the 6 wt.%additive was an appropriate dosage.The enhanced reaction activity of adsorbed ammonia species and the improved dispersion of vanadium oxide might be the reasons for the elevation of SCR activity at low temperatures.The resistances to SO2of 3V6Nb/WTi catalyst at different temperatures were investigated.FTIR spectrum and TG-FTIR result indicated that the deposition of ammonium sulfate species was the main deactivation reason at low temperatures,which still exhibited the reactivity with NO above 200℃ on the catalyst surface.There was a synergistic effect among NH3,H2O and SO2that NH3and H2O both accelerated the catalyst deactivation in the presence of SO2at 175℃.The thermal treatment at 400℃ could regenerate the deactivated catalyst and get SCR activity recovered.The particle and monolith catalysts both kept stable NOxconversion at 225℃ with high concentration of H2O and SO2during the long time tests.展开更多
We used a ultrasound/Fe2＋/H2O2 process in continuous dosing mode to degrade the alachlor. Experimental results indicated that lower pH levels enhanced the degradation and mineralization of alachlor. The maximum alach...We used a ultrasound/Fe2＋/H2O2 process in continuous dosing mode to degrade the alachlor. Experimental results indicated that lower pH levels enhanced the degradation and mineralization of alachlor. The maximum alachlor degradation （initial alachlor concentration of 50 mg/L） was as high as 100% at pH 3 with ultrasound of 100 Watts, 20 mg/L of Fe2＋, 2 mg/min of H2O2 and 20℃ within 60 min reaction combined with 46.8% total organic carbon removal. Higher reaction temperatures inhibited the degradation of alachlor. Adequate dosages of Fe2＋ and H2O2 in ultrasound/Fe2＋/H2O2 process not only enhance the degradation efficiency of alachlor but also save the operational cost than the sole ultrasound or Fenton process. A continuous dosing mode ultrasound/Fe2＋/H2O2 process was proven as an effective method to degrade the alachlor.展开更多
CuCeZrO_x and KCuCeZrO_x catalysts were synthesized and coated on the blank diesel particulate filter(DPF)substrate and a particulate matter(PM)loading apparatus was used for soot loading.The catalytic performances of...CuCeZrO_x and KCuCeZrO_x catalysts were synthesized and coated on the blank diesel particulate filter(DPF)substrate and a particulate matter(PM)loading apparatus was used for soot loading.The catalytic performances of soot oxidation were evaluated by temperature programmed combustion(TPC)test and characterization tests were conducted to investigate the physicochemical properties of the catalysts.The reaction mechanism in the oxidation process was analyzed with diffuse reflectance infrared Fourier transform spectroscopy.The results demonstrated that CuCeZrO_x catalyst exhibited high activities of soot oxidation at low temperature and the best results have been attained with Cu_(0.9)Ce_(0.05)Zr_(0.05)O_x over which the maximum soot oxidation rate decreased to 410~?C.Characterization tests have shown that catalysts containing 90%Cu have uniformly distributed grains and small particle sizes,which provide excellent oxidation activity by providing more active sites and forming a good bond between the catalyst and the soot.The low-temperature oxidation activity of soot could be further optimized due to the excellent elevated NO’s conversion rate by partially substituting Cu with K.The maximum particle oxidation rate can be easily realized at such a low temperature as 347~?C.展开更多
基金Supported by the National Basic Research Program of China(2015CB251501)the Innovative Research Groups of the National Natural Science Foundation of China(51621005)
文摘Oxy-steam combustion is a promising next-generation combustion technology.Conversions of fuel-N,volatile-N,and char-N to NO and N2O during combustion of a single coal particle in O2/N2and O2/H2O were studied in a tube reactor at low temperature.In O2/N2,NO reaches the maximum value in the devolatilization stage and N2O reaches the maximum value in the char combustion stage.In O2/H2O,both NO and N2O reach the maximum values in the char combustion stage.The total conversion ratios of fuel-N to NO and N2O in O2/N2are obviously higher than those in O2/H2O,due to the reduction of H2O on NO and N2O.Temperature changes the trade-off between NO and N2O.In O2/N2and O2/H2O,the conversion ratios of fuel-N,volatile-N,and char-N to NO increase with increasing temperature,and those to N2O show the opposite trends.The conversion ratios of fuel-N,volatile-N,and char-N to NO reach the maximum values at 〈O2〉=30 vol%in O2/N2.In O2/H2O,the conversion ratios of fuel-N and char-N to NO reach the maximum values at 〈O2〉=30 vol%,and the conversion ratio of volatile-N to NO shows a slightly increasing trend with increasing oxygen concentration.The conversion ratios of fuel-N,volatile-N,and char-N to N2O decrease with increasing oxygen concentration in both atmospheres.A higher coal rank has higher conversion ratios of fuel-N to NO and N2O.Anthracite coal exhibits the highest conversion ratios of fuel-N,volatile-N,and char-N to NO and N2O in both atmospheres.This work is to develop efficient ways to understand and control NO and N2O emissions for a clean and sustainable atmosphere.
基金supported by the Policy-induced Project of Jiangsu Province for the Industry-University-Research Cooperation (No. BY2015070-21)the project was also supported by National Science and Technology Ministry (No. 2015BAA05B01)the Natural Science Fund Program of Jiangsu Province (No. BK20150749)
文摘Niobium oxide as the promoter was doped in the V/WTi catalyst for the selective catalytic reduction（SCR）of NO.The results showed that the addition of Nb2O5could improve the SCR activity at low temperatures and the 6 wt.%additive was an appropriate dosage.The enhanced reaction activity of adsorbed ammonia species and the improved dispersion of vanadium oxide might be the reasons for the elevation of SCR activity at low temperatures.The resistances to SO2of 3V6Nb/WTi catalyst at different temperatures were investigated.FTIR spectrum and TG-FTIR result indicated that the deposition of ammonium sulfate species was the main deactivation reason at low temperatures,which still exhibited the reactivity with NO above 200℃ on the catalyst surface.There was a synergistic effect among NH3,H2O and SO2that NH3and H2O both accelerated the catalyst deactivation in the presence of SO2at 175℃.The thermal treatment at 400℃ could regenerate the deactivated catalyst and get SCR activity recovered.The particle and monolith catalysts both kept stable NOxconversion at 225℃ with high concentration of H2O and SO2during the long time tests.
基金supported by the National Science Council, Republic of China (No. 101-2221-E-264-005)
文摘We used a ultrasound/Fe2＋/H2O2 process in continuous dosing mode to degrade the alachlor. Experimental results indicated that lower pH levels enhanced the degradation and mineralization of alachlor. The maximum alachlor degradation （initial alachlor concentration of 50 mg/L） was as high as 100% at pH 3 with ultrasound of 100 Watts, 20 mg/L of Fe2＋, 2 mg/min of H2O2 and 20℃ within 60 min reaction combined with 46.8% total organic carbon removal. Higher reaction temperatures inhibited the degradation of alachlor. Adequate dosages of Fe2＋ and H2O2 in ultrasound/Fe2＋/H2O2 process not only enhance the degradation efficiency of alachlor but also save the operational cost than the sole ultrasound or Fenton process. A continuous dosing mode ultrasound/Fe2＋/H2O2 process was proven as an effective method to degrade the alachlor.
基金the National Key R&D Program of China(Nos.2016YFC0205200 and 2016YFC0208000)the National Natural Science Foundation of China(No.51676127)
文摘CuCeZrO_x and KCuCeZrO_x catalysts were synthesized and coated on the blank diesel particulate filter(DPF)substrate and a particulate matter(PM)loading apparatus was used for soot loading.The catalytic performances of soot oxidation were evaluated by temperature programmed combustion(TPC)test and characterization tests were conducted to investigate the physicochemical properties of the catalysts.The reaction mechanism in the oxidation process was analyzed with diffuse reflectance infrared Fourier transform spectroscopy.The results demonstrated that CuCeZrO_x catalyst exhibited high activities of soot oxidation at low temperature and the best results have been attained with Cu_(0.9)Ce_(0.05)Zr_(0.05)O_x over which the maximum soot oxidation rate decreased to 410~?C.Characterization tests have shown that catalysts containing 90%Cu have uniformly distributed grains and small particle sizes,which provide excellent oxidation activity by providing more active sites and forming a good bond between the catalyst and the soot.The low-temperature oxidation activity of soot could be further optimized due to the excellent elevated NO’s conversion rate by partially substituting Cu with K.The maximum particle oxidation rate can be easily realized at such a low temperature as 347~?C.
