Catalytic ozonation of NH4+-N in wastewater over composite metal oxide catalyst

Large amounts of water containing-ammonium nitrogen(NH₄⁺-N)have attracted increasing attention.Catalytic ozonation technology,involving the generation of hydroxyl radical(OH)with strong oxidation ability,was originally utilized to degrade organic-containing wastewater.In this paper,Ce/MnOx composite metal oxide catalysts prepared with different preparation conditions were used to degrade wastewater containing inorganic pollutant(NH₄⁺-N).The as-prepared catalyst features were characterized using X-ray diffraction(XRD),Brunauer-Emmett-Teller method(BET),scanning electron microscopy(SEM),energy dispersive X-ray spectroscopy(EDS),Fourier transform infrared spectroscopy(FTIR),X-ray photoelectron spectroscopy(XPS)and H₂-temperature programmed reduction(H₂-TPR)techniques.The results show that the catalyst,prepared by conditions with precipitant Na₂CO₃ and Ce/Mn molar ratio 1:2 calcined at 400℃for 3 h in pH 11.0,displays the optimal performance,with the removal rate of NH₄⁺-N and selectivity to gaseous nitrogen,88.14 wt%and 53.67 wt%,respectively.The effects of several operating factors including solution pH,initial NH₄⁺-N concentrations and scavengers were evaluated.In addition,XRD patterns of catalyst with the best performance and the comparative study on decontamination of NH₄⁺-N by various processes(O₃,catalyst and catalyst/O₃)show that the primary metal oxides are CeO₂ and MnO₂ in Ce/MnOx composite metal oxide catalysts,which have a synergistic effect on the catalytic ozonation of NH₄⁺-N,and the new phase MnO₂ plays a great role.After 5 consecutive use cycles,the degradation efficiency is declined slightly,and can still achieve better than 70 wt%over 1 h reaction.Additionally,the application of catalytic ozonation for actual wastewater on the removal rate of NH₄⁺-N was investigated.Possible mechanism and degradation pathway of NH₄⁺-N were also proposed.In a word,the application of CeO₂-MnO₂ composite metal oxide catalysts in catalytic ozonation can be regarded as an effective,feasible and promising method for the treatment of NH₄⁺-N.     

硫酸铀酰印迹离子交换树脂的合成及识别特性研究

为进行稀溶液中铀的浓缩,以硫酸铀酰为模板、二乙基烯丙基胺为功能单体,在水中采用自组装分子印迹技术制备了硫酸铀酰印迹离子交换树脂.对树脂合成条件进行了优化,研究了pH值对吸附量的影响、分子印迹聚合物MIPs-4的等温吸附与吸附动力学、柱内吸附与淋洗曲线等树脂识别性能.结果表明:印迹树脂对硫酸铀酰的吸附性能比非印迹树脂好,可以在pH=1～6范围内应用,并在pH为2左右时吸附能力最强.MIPs-4树脂的吸附等温线为"优吸"型,吸附在约3h达到平衡.当C0=0.125mg·mL-1时,Kd=0.249L·g-1.吸附液ρ(U)=1.0 mg·mL-1、接触时间4min进行的柱内试验得出MIPs-4的穿透体积、穿透容量和饱和容量分别为柱内树脂的床体积(BV)的22倍、21.6 mg·mL-1和36.2 mg·mL-1.以0.05 mol·L-1 H2SO4 1.0 mol·L-1 NaCl为淋洗液时,淋洗体积仅4BV,流出液中最大铀浓度达到17.6 mg·mL-1.印迹树脂的吸附和解吸性能好,可应用于低浓度铀的浓缩及含铀废水的处理.     

氧化铁生产废液的治理和利用

氧化铁生产产生的含铁硫酸铵废液和洗涤废水中含有铁、硫酸根、铵等离子。采用化学沉淀、过滤、蒸发等方法处理该废水可回收废水中的硫酸铵、氧化铁、处理后的废水可回用于生产。     

硫酸法钛白粉生产中钛液的分析和铁分离

以硫酸法钛白粉生产工艺中间体浓钛液(硫酸氧钛)和偏钛酸为原料,分析了浓钛液中二氧化钛和铁的含量。总Ti的测试采用Al片还原法和高铁盐氧化还原滴定法,浓钛液中Ti3 直接用高铁盐氧化还原滴定法测定,铁含量用KMnO4氧化还原滴定法进行分析。采用无机陶瓷膜洗涤分离方法考查了水解后偏钛酸中的除铁效率,利用分光光度法和火焰原子吸收法分别测定洗涤液和二氧化钛粉体中的铁含量。试验表明,无机陶瓷膜洗涤分离方法可以将二氧化钛粉体中铁含量降到30×10-3‰以下,煅烧后产品白度大于94。陶瓷膜洗涤工艺可以实现连续操作,是一种值得推广的新工艺。     

Physicochemical investigation of the decomposition products of ammonium metal carboxylates: ammonium ferric citrate hydrate

The thermal decomposition up to 400 °C of ammonium ferric citrate hydrate, of unknown structure and formula weight, was studied by thermogravimetry, differential thermal analysis, infrared (IR) spectroscopy and X-ray diffractometry. The possible identities of the formula weight and the intermediate products of calcination are discussed. The results revealed that the parent material is amorphous and contains two moles of water and two moles of ammonia. Decomposition takes place via six weight-loss processes, three endothermic (90–230 °C) and three exothermic (240–298 °C), leading eventually to the formation of Fe₂O₃. The intermediate solid products are mainly unstable amorphous oxycarbonates, as indicated by X-ray and IR spectroscopies. The gas-phase decomposition products identified by IR spectroscopy are NH₃, CO₂, CO, CH₃COCH₃, CH₄ and NH₄OH. Surface area measurement and scanning electron microscopy showed that Fe₂O₃, the final product at 400 °C, hada surface area of 40 m²/g and good crystalline and porous character.     

碳铵化肥发青问题解决小结

探讨了该厂化肥生产中碳铵发青的原因,通过硫化氢含量的测定,分析了系统内外影响因素,提出了解决措施,达到了不停车稳定产品质量的目的。     

改性硝酸铵的工业制备方法及其性能

硝酸铵饱和溶液中加入表面活性剂辛基三甲基溴化铵，采用真空膨胀结晶技术工业制备一种新型改性硝酸铵，并介绍其性能特点。     

Foliar fertilization of high-yielding peanuts during the pod-filling period

A 2-year field experiment was carried out in a sandy soil (Xeropsament-Torripsament) at Nir Yizhaq, Israel, where commercially grown peanut plants were sprayed with different NPKS solutions during the pod-filling period. All foliar sprays were applied in addition to the fertilizer which had been added to the soil before planting. The differences in yield between the treatments were not significant in either year. In the first year, there was a tendency toward increased yields of pods (up to 13%) and of hay (up to 16%) when four foliar fertilizer applications (10 kg N, 1 kg P, 3 kg K and 0.5 kg S/ha/application) were given, at one-week intervals. N was added mainly as urea, P and K as potassium polyphosphate, and S as ammonium sulphate. In the second year, the highest yield was obtained in the control plots and the differences between the treatments were not significant. Utilization of foliar nutrient application seems to be dependent upon availability of these nutrients in the soil.Contribution from the Agricultural Research Organization, The Volcani Center, Bet Dagan, Israel. No. 1976-E. 1087 series.