Optimal feed profile for a second order reaction in a semi-batch reactor under safety constraints: Experimental study

Maximising the yield of the second order reaction (2-butanol+propionic anhydride) by manipulating the inlet flow rate is considered for an isothermal semi-batch process. First a procedure for the determination of the kinetic parameters using coupled spectroscopic and calorimetric methods is presented. Then an optimisation of the reaction system is performed numerically and verified experimentally. Constraints on the amount of heat produced and on the temperature attainable in the case of cooling failure are imposed for safety consideration.     

水源水细菌SOS反应与模糊综合评判的比较

为探讨细菌学测试和化学测试两类方法在评价水源水有机物污染程度和潜在危害上的关系,用SOS显色法研究了珠江某自来水原水8个水样有机提取物诱导的细菌SOS反应,并用模糊综合评判法分析了水样的BOD、Hg 、Pb 、Cr等化学指标．两个水样诱导了大肠杆菌 PQ37的 SOS反应．比较水样对细菌的 SOS反应诱导系数与化学污染的模糊综合评判结果后显示, SOS显色法这一细菌学短期测试系统与化学测试方法对水质的定性评价具有一致性、互补性和差异性,模糊综合评判法的应用可作为比较和解释这两类不同测试系统的分析结果的一种途径．     

上海市大气中HO2自由基的测定与特征

为研究上海市大气中ＨＯ２自由基的分布特征,建立了化学放大法测定ＨＯ２自由基系统,对上海市大气中ＨＯ２自由基浓度进行了没定邦等结果表明,ＨＯ２自由基的典型日变化基本上为双峰型,峰值出现在阳光辐射较强的中午时分,实验测得ＨＯ２自由基最大浓度达２．２４×１０＾８分子·ｃｍ＾－３,ＨＯ２自然基民ＮＭＨＣ,Ｃ烽Ｏ２等具有一定的相关性,ＨＯ２自由基的研究对于大气光化学烟雾的研究具有重要意义     

紊动对水体中有机物降解影响的实验

利用专门设计的紊动诱发装置,对不同紊动强度水体进行了紊动对有机物生物降解影响的实验研究．通过３种不同紊动强度的实验,发现紊动对有机物的降解有明显的影响紊动强度越大,有机物的降解率和降解速度越大．通过对较高紊动强度水体的降解实验数据分析发现,在水体有紊动时,有机物的降解反应并不遵循一级反应动力学。     

Ozonation of aromatic monomer compounds in water: factors determining reaction outcomes

● p- CNB and IBP were selected, to explore factors determining ozonation outcomes. ● •OH contributed only 50 % to IBP removal, compared to the 90 % for p -CNB removal. ● IBP achieved fewer TOC removal and more by-product types and quantities. ● A longer ring-opening distance existed during the degradation of IBP. ● Multiple positions on both branches of IBP were attacked, consuming more oxidants. For aromatic monomer compounds (AMCs), ozonation outcomes were usually predicted by the substituents of the benzene ring based on the electron inductive effect. However, the predicted results were occasionally unreliable for complex substituents, and other factors caused concern. In this study, p-chloronitrobenzene (p-CNB) and ibuprofen (IBP) were selected for ozonation. According to the electron inductive theory, p-CNB should be less oxidizable, but the opposite was true. The higher rates of p-CNB were due to various sources of assistance. First, the hydroxyl radical (•OH) contributed 90 % to p-CNB removal at pH 7.0, while its contribution to IBP removal was 50 %. Other contributions came from molecular O₃ oxidation. Second, p-CNB achieved 40 % of the total organic carbon (TOC) removal and fewer by-product types and quantities, when compared to the results for IBP. Third, the oxidation of p-CNB started with hydroxyl substitution reactions on the benzene ring; then, the ring opened. However, IBP was initially oxidized mainly on the butane branched chain, with a chain-shortening process occurring before the ring opened. Finally, the degradation pathway of p-CNB was single and consumed fewer oxidants. However, both branches of IBP were attacked simultaneously, and three degradation pathways that relied on more oxidants were proposed. All of these factors were determinants of the rapid removal of p-CNB.     

新型高效三相分离器处理低浓度工业废水的研究

根据三相分离器的工作原理 ,分析了三相分离器在目前实际应用中存在的问题 ,设计出一种结构简单而合理的三相分离器。实验证明 ,采用这种新型的三相分离器 ,固液分离效率高达 93% ;另外 ,实验还表明其在处理低浓度工业废水方面是完全可行的 ,进水COD在 2 10 0mg/L时 ,COD去除率保持在 85 %～ 92 % ,有机负荷可达 8.4 5kgCOD/m3 ·d。     

高锰酸钠去除水中苯胺的动力学

研究了高锰酸钠去除水中苯胺的动力学和机理。结果表明:高锰酸钠能快速去除水中的苯胺,其表观动力学方程为r=0.453C_AC_B~(1/2)。反应的速率常数κ与温度T成正相关,其反应的表观活化能为19.136kJ·mol~(-1),指前因子为1165.34mmol~(-1/2)·L~(1/2)·min~(-1)。水中苯胺是被高锰酸根和新生态的氧氧化而去除的。     

Optimization of biodiesel production from waste cooking oil using ion-exchange resins

Waste cooking oil is a potential substitution of refined vegetable oil for the production of biodiesel due to the low cost of raw material and for solving their disposal problem. In this study, optimization of esterification process of free fatty acids in artificially acidified soybean oil with oleic acid has been carried out using methanol as an agent and ion exchange resin as a heterogeneous catalyst. The esterification reaction has been investigated based on the mass balance of the developed model. The model has been validated against experimental data and effects of temperature and catalyst weight have been analyzed. Thereafter, optimization process has been fulfilled for two different objective functions as conversion of acid oil and benefit. Optimization results indicated that the maximum conversion of acid is 95.95%, which is achievable at 4.48-g catalyst loading and reaction temperature of 120°C. Maximum benefit was obtained as US$0.057 per batch of reaction at a catalyst amount of 1 g and temperature of 120°C.     

臭氧氧化降解苯胺黑药模拟废水

苯胺黑药(学名:二苯胺基二硫代磷酸)是一种良好的有色金属硫化矿浮选捕收剂,属于典型的难降解有机污染物。为研究臭氧氧化苯胺黑药的条件和氧化反应的动力学,选用臭氧作为氧化剂,对苯胺黑药浓度和模拟废水的COD进行测定。结果表明,用5 g/h的臭氧氧化20 min后,初始浓度50、75和150 mg/L的苯胺黑药模拟废水的COD去除率分别为56%、59%和76%,苯胺黑药浓度的去除率分别达到100%、99%和88%,反应后废水p H变为强酸性(4)。对应的氧化反应动力学表观一级速率常数k为-0.372 s-1、-0.331 s-1和-0.259 s-1;R2为0.9926、0.9949和0.9903。探讨了臭氧氧化苯胺黑药前后p H变化的机理。     

异相类Fenton氧化处理T酸废母液的催化剂

为了比较黄铁矿、钛铁矿、磁铁矿、钒钛磁铁矿、零价铁以及亚铁催化双氧水氧化处理T酸废母液的效能,研究了不同体系的催化氧化反应动力学以及pH值变化情况,考察了H2O2投加量、催化剂投加量及循环利用次数的影响.研究结果表明,黄铁矿、钛铁矿催化活性较亚铁离子更好,且受废水pH值变化影响小,T酸废母液TOC去除率高达75％左右,是十分有效的类Fenton反应催化剂.钛铁矿催化活性较黄铁矿好,重复利用5次,TOC去除率依然保持在72％以上,表明钛铁矿有着很好的重复利用性.