光电技术在大气氮氧化物检测中的应用

介绍了大气中氮氧化物的组成,综述了激光诱导荧光法、光纤传感法、激光雷达探测法和化学发光法测定大气中氮氧化物的原理和特点,指出光电技术已在大气氮氧化物检测中得到了广泛的应用,并具有良好的发展前景。     

宏量和微量元素在炉内喷钙脱硫过程中的作用

研究添加粉煤灰对脱硫过程的作用,实验在滴管炉上进行,温度为１２００℃,结果表明,一些宏量元素的金属氧化物对脱硫过程具有催化作用,但这种催化作用随Ｆｅ２Ｏ３掺加量的改变而变化,先升高后降低,有一个最佳值;一些微量元素的金属氧化物对脱硫过程更强的催化氧化作用,当ＭｎＯ２的掺加量为３％时,充效率提高近１倍。     

环境空气监测中NO_x、SO_2空白值的研究

本文研究了惠州市市区环境空气监测中氮氧化物、二氧化硫的现场空白值与室内空白值的差异,得出了二氧化硫测定的两种空白值相差无几,氮氧化物测定的两种空白值相差较显著的结论。提出了在计算环境空气氮氧化物浓度时,扣除现场空白值是消除分析误差的一个不可忽视的环节。讨论了现场空白值受环境条件（气温、光照强度等）影响的情况     

NiB2O4 (B = Mn or Co) catalysts for NH3-SCR of NOx at low-temperature in microwave field

● Microwave-assisted catalytic NH₃-SCR reaction over spinel oxides is carried out. ● SCR reaction temperature is tremendously lowered in microwave field. ● NO conversion of NiMn₂O₄ is highly up to 90.6% at 70°C under microwave heating. Microwave-assisted selective catalytic reduction of nitrogen oxides (NO_x) was investigated over Ni-based metal oxides. The NiMn₂O₄ and NiCo₂O₄ catalysts were synthesized by the co-precipitation method and their activities were evaluated as potential candidate catalysts for low-temperature NH₃-SCR in a microwave field. The physicochemical properties and structures of the catalysts were characterized by X-ray diffraction (XRD), Scanning electron microscope (SEM), N₂-physisorption, NO adsorption-desorption in the microwave field, H₂-temperature programmed reduction (H₂-TPR) and NH₃-temperature programmed desorption (NH₃-TPD). The results verified that microwave radiation reduced the reaction temperature required for NH₃-SCR compared to conventional heating, which needed less energy. For the NiMn₂O₄ catalyst, the catalytic efficiency exceeded 90% at 70 °C and reached 96.8% at 110 °C in the microwave field. Meanwhile, the NiMn₂O₄ also exhibited excellent low-temperature NH₃-SCR reaction performance under conventional heating conditions, which is due to the high BET specific surface area, more suitable redox property, good NO adsorption-desorption in the microwave field and rich acidic sites.     

脱硫类水滑石衍生复合氧化物不同方法的制备与表征

采用尿素水解法和共沉淀法制备了MgAl类水滑石,高温焙烧获得衍生复合氧化物.采用X射线衍射(XRD)、热重分析(TG-DTG)、扫描电镜(SEM)、N2-吸附/脱附和CO2程序升温脱附(CO2-TPD)等手段对所制备的复合氧化物结构特征进行表征,并研究其对SO2脱除性能的差异.结果表明,共沉淀法制备的MgAlO复合氧化物比尿素法具有更大的比表面积(148.1m2·g-1)和更多碱性位,这些特点可能促使该方法制备的复合氧化物具有更高的SO2储存容量和反应速率.采用尿素法和共沉淀法制备的MgAl水滑石复合氧化物在700℃温度下SO2吸附容量分别可达0.55g·g-1和0.79 g·g-1.     

铁-镧系合金氧化物污水除磷及再生简

采用共沉淀法制备了系列铁-镧系合金氧化物并研究其除磷能力。结果表明：以铁、镧摩尔比为0.08的吸附剂除磷能力最强，吸附曲线适合Langmuir等温线方程。该吸附剂的吸附量受pH影响显著，pH在4.0~7.0之间时吸附量较大。进行了抗共存阴离子能力测试，结果表明CO₃^2-对磷吸附量影响较大，给出了共存阴离子对吸附量的影响顺序。对该吸附剂进行了真空高温再生，再生率最高可达62.27%。     

Catalytic oxidation of o-chlorophenol over Co2XAl (X= Co,Mg, Ca,Ni) hydrotalcite-derived mixed oxide catalysts

• Superior catalytic activity observed for o-chlorophenol oxidation on Co₂MgAlO. • The reducibility, oxygen species and basicity influenced catalytic activity. • The organic by-products were generated in o-chlorophenol catalytic oxidation. A cobalt-based hydrotalcite-like compound was prepared using a constant-pH coprecipitation method. Cobalt-transition metal oxides (Co₂XAlO, X= Co, Mg, Ca and Ni) were investigated for the deep catalytic oxidation of o-chlorophenol as a typical heteroatom contaminant containing chlorine atoms. The partial substitution of Co by Mg, Ca or Ni in the mixed oxide can promote the catalytic oxidation of o-chlorophenol. The Co₂MgAlO catalyst presented the best catalytic activity, and could maintain 90% o-chlorophenol conversion at 167.1°C, compared only 27% conversion for the Co₃AlO catalyst. The results demonstrated that the high activity could be attributed to its increased low-temperature reducibility, rich active oxygen species and excellent oxygen mobility. In the existence of acid and base sites, catalysts with strong basicity also showed preferred activity. The organic by-products generated during the o-chlorophenol catalytic oxidation over Co₂MgAlO catalyst included carbon tetrachloride, trichloroethylene, 2,4-dichlorophenol, and 2,6-dichloro-p-benzoquinon, et al. This work provides a facile method for the preparation of Co-based composite oxide catalysts, which represent promising candidates for typical chlorinated and oxygenated volatile organic compounds.     

包膜尿素对水田土壤排放NH3、NOx、CO2影响的研究

为了研究包膜尿素对水田土壤排放NH3、Nox和CO2的影响,采用水稻盆栽的方法,探讨了在水稻不同生育期内不同种类包膜尿素对水田土壤排放NH3、Nq和CO2的影响。结果表明,包膜尿素处理对水田土壤排放NH3、Nq和CO2均具有抑制作用,与普通尿素相比,包膜尿素LP40、LPSS、BB、SC60NH3的挥发总量降低了5．4％-19．3％,Nox的挥发总量降低了8．1％-23．4％,CO2的挥发总量降低了1．6％-13．O％;施用包膜尿素能够抑制水田土壤NH3、NOx和CO2的排放。     

Zn/Cr型阴离子黏土的制备、表征及其对活性艳橙X-GN的去除性能研究

采用共沉淀法制备了Zn/Cr摩尔比为1∶1～5∶1的Zn/Cr型阴离子黏土(Zn/Cr-LDHs),选取2∶1 Zn/Cr-LDHs分别在300、400、500℃条件下放入马弗炉中煅烧2 h,制备了煅烧阴离子黏土(Zn/Cr-LDO).采用X射线衍射光谱(XRD)、傅里叶红外光谱(FTIR)、原子吸收法(ASS)、比表面积测试法(BET)对上述制备的材料结构形态进行表征.研究2∶1 Zn/Cr-LDHs和Zn/Cr-LDO在紫外和避光条件下对活性艳橙X-GN的去除.实验表明,2∶1 Zn/Cr-LDHs的吸附效果不受紫外光照射的影响,煅烧后形成的Zn/Cr-LDO在紫外光的照射下,对活性艳橙X-GN的去除率是避光条件下的2倍,说明煅烧后的Zn/Cr阴离子黏土具有光催化性能,Zn/Cr-LDO对活性艳橙X-GN的去除是吸附和光催化的共同作用.     

岩溶山地土壤氧化铁形态及其与成土环境的关系

土壤氧化铁的数量和形态是成土过程和成土环境的反映.以重庆金佛山为研究对象,采用化学选择溶解法,分析了岩溶山地土壤铁氧化物数量与形态,并探讨了氧化铁数量、形态与成土环境、岩溶环境退化和石漠化发生发展的关系.结果表明,山顶区与坡腰区全铁含量差异大,山顶土壤全铁51.49 g.kg-1,坡腰区全铁含量86.29 g.kg-1,土壤全铁主要受母质影响.山顶区气温低,土壤发育程度弱,黏粒游离铁含量低（29.16 g.kg-1）,黏粒部分铁的游离度小（35.40%）;坡腰区气温高,土壤风化程度较深,黏粒游离铁含量高（43.92 g.kg-1）,黏粒铁的游离度高（60.41%）.山顶区低温潮湿,土壤有机质含量高,铁的活化度和络合度高（73.51%和17.21%）,显著高于坡腰区（13.06%和0.41%）.在坡腰区,灌丛马尾松退化或转化为旱地后,土壤有机质含量下降,黏粒流失,游离铁有伴随黏粒迁移的趋势,使土壤全铁和黏粒游离铁减少;灌丛马尾松土壤全铁98.25g.kg-1,坡耕地84.52 g.kg-1;灌丛马尾松黏粒游离铁50.81 g.kg-1,坡耕地47.86 g.kg-1.土壤铁氧化物数量与形态可以表征岩溶环境退化及石漠化发生发展状况.