负载型Mn-Ce/TiO2催化剂的制备及其低温脱硝活性简

以成型TiO₂作为载体,通过浸渍法制备了Mn-Ce/TiO₂低温SCR催化剂,并系统研究了制备方法、煅烧条件、活性组分担载量、Mn含量等参数对催化剂催化还原NO性能的影响。结果表明,煅烧温度的升高会促使活性组分结晶度的提高,从而引起催化活性的降低,在500℃和600℃下所得Mn-Ce/TiO₂催化剂活性组分为无定型态,表现出较高的脱硝活性。活性组分担载量的增加有利于催化活性的提高。Mn含量对Mn-Ce/TiO₂催化剂的活性有较大影响,当Mn/（Mn+Ce）摩尔比为40%和85%时,催化剂活性最高。     

5种植物材料的水解释碳性能及反硝化效率

碳源在硝酸盐去除过程中起电子供体的作用,是生物反硝化反应的关键物质之一。为解决污水处理脱氮时碳源不足抑制反硝化反应造成脱氮效率低的问题,本研究选取风车草、甘蔗渣、芦竹、美人蕉和稻草秆5种植物材料作为反硝化碳源,探讨不同植物材料的水解释碳能力和释放规律;并进一步以其水解液作为外加碳源,探讨其对反硝化脱氮效率的影响。研究结果表明,植物材料水解释碳过程符合二级动力学反应规律,不同植物材料的释碳能力具有显著性差异,以甘蔗渣在固液比1∶80时COD释放当量最大,为45.45 mg/L;添加植物水解液可显著提高反硝化脱氮效率,以芦竹水解液脱氮效果最好,达到71.9%。此外,碳氮比是影响脱氮效率的重要因素之一,以碳氮比为9时反硝化脱氮效果最佳。     

废旧冰箱拆解聚氨酯泡沫塑料制备PU/PP复合材料

利用废旧冰箱拆解的聚氨酯泡沫塑料(PU)和聚丙烯(PP)、聚丙烯接枝马来酸酐(PP-g-MAH)为原料,采用物理化学回收技术制备PU/PP复合材料。用正交实验法分析PU填充量、PU粒径和PP-g-MAH 3个因素对PU/PP复合材料力学性能影响的显著性。结果表明,PU填充量对PU/PP复合材料拉伸性能有显著影响,对冲击性能和弯曲性能没有显著影响;在本文的实验范围内,PU粒径对PU/PP复合材料的力学性能影响不大;而PP-g-MAH投加量对PU/PP复合材料具有一定的影响。确定的优化工艺配方为:PU 40%;PU粒径选择2.00 mm;PP-g-MAH投加量10%。采用优化工艺制备的PU/PP复合材料的密度为1 042.88 kg/m3;冲击强度为2.9 kJ/m2;拉伸强度为10.30 MPa;拉伸模量为1 100 MPa;弯曲强度为18.5 MPa;弯曲模量为733 MPa。     

石墨气体扩散电极的制备与性能优化

电极的制备工艺及参数直接影响电极材料的活性。主要考察了C/PTFE质量比、碾压压力、煅烧温度、造孔剂NH4HCO3及稀土掺杂等因素对电极产出H2O2的影响规律。研究结果表明,电极最佳制备条件为:石墨和PTFE质量比为2∶1、石墨、造孔剂和稀土元素质量比为6∶1∶1、碾压压力10 MPa、煅烧温度330℃。在pH=3、电解质Na2SO4浓度为0.05mol/L条件下,电解2 h后,改性电极产生的H2O2从95 mg/L提高到350 mg/L,提高了268.4%。     

A/O工艺N_2O的产生与释放的影响因素

采用A/O工艺,在连续运行条件下,以DO、SRT和硝化液回流比(R)为影响因素,对A/O生物脱氮工艺处理模拟城市生活污水过程中N2O的释放进行了研究。实验结果表明,SRT对A/O工艺N2O释放的影响最大,其次是DO,R的影响最小。N2O转化率随着SRT的升高而降低,当SRT从10 d升高到20 d时,总N2O平均转化率从0.319%下降到0.002%。总N2O转化率随着好氧池DO的升高先降低后有所升高,当DO分别为0.6 mg O2/L、1.2 mg O2/L、2.5 mg O2/L时,反应器的总N2O平均转化率分别为0.306%、0.007%和0.013%。R对N2O释放的影响差异不明显,总N2O平均转化率在300%时最低,为0.007%。N2O释放量最低的工艺运行条件组合是SRT为20 d、DO为1.2 mg O2/L、R为300%。     

UV/Fenton技术处理某工厂高浓度乳化油废水

研究了UV/Fenton技术对高浓度金属清洗乳化油废水的处理效果,考察了亚铁与双氧水浓度、pH、反应时间和搅拌对COD去除效果的影响。实验结果表明,UV/Fenton技术对高浓度乳化油废水(COD平均浓度为35 000 mg/L)具有较高的去除效果,最佳工艺条件为:亚铁与双氧水浓度分别为2 400 mg/L和6 000 mg/L,pH为3,经过2 h反应,COD可降低至1 050 mg/L,去除率为97%。搅拌会降低COD的去除率。研究表明,UV/Fenton技术对高浓度乳化油废水具有很好的降解效果,且药品消耗较低,为目前此类高浓度有机废水的处理提供了技术参考。     

介质阻挡放电协同Ag/Al_2O_3对NO_x脱除的影响

为有效去除发电厂烟气中产生的NOx,利用介质阻挡放电(DBD)产生低温等离子体并结合催化剂Ag/Al2O3进行烟气脱硝实验,研究了在加入乙烯的条件下,平均负载量、催化温度和装置的布置方式对NOx脱除的影响。结果表明,随着负载的增多,NO脱除率呈现先增大后减小的趋势,5种负载量中最佳为1.76%;随着催化温度的升高,NO脱除率同样呈现先增大后减小的趋势,最佳的催化温度为150℃左右;3种不同布置方式对NO和NOx脱除有明显差别,单独催化剂在NO和NOx的脱除率都比较低;单独介质阻挡放电NO脱除率很高,但是NOx很却很低;而两者结合在NO和NOx都达到了很好的效果。     

Fate of azadirachtin A and related azadirachtoids on tomatoes after greenhouse treatment

The degradation of the main azadirachtoids on tomatoes was studied after greenhouse treatment. These experiments were carried out at 1 and 5× the concentration recommended by the manufacturer. In all experiments the deposition of azadirachtin A (AZA-A) was below the maximum residue level (MRL). Even if at the highest dose, AZA-A half-life time calculated as pseudo first order kinetic was 1.2 days in agreement with the recommended preharvest interval (PHI) of 3 days. Experiments with a model system showed that sunlight photodegradation is the main factor influencing the rate of disappearance of AZA-A after greenhouse treatment while tomato epicuticular waxes doubled the photodegradation rate of AZA-A in a commercial formulation.     

Multiresidue determination of carbamate,organochlorine, organophosphorus,and dicarboximide pesticides in lettuce by GC/MS

An extraction method based on matrix solid-phase dispersion was developed to determine pirimicarb, methyl parathion, malathion, procymidone, α -endosulfan and β -endosulfan in lettuce using gas chromatography-mass spectrometry. The best results were obtained using 4.0 g of lettuce, 2.0 g of silica as dispersant sorbent, 0.1 g of activated carbon as clean up sorbent and acetonitrile as eluting solvent. The method was validated using lettuce samples fortified with pesticides at six different concentration levels (0.1 to 2.0 mg/kg). Average recoveries (7 replicates) ranged from 50 to 120 %, with relative standard deviations between 0.6 and 8.0 %. Detection and quantification limits for lettuce ranged from 0.01 to 0.02 mg/kg and 0.04 to 0.10 mg/kg, respectively.     

Evaluation and validation of two different chromatographic methods (HPLC and LC-MS/MS) for the determination and confirmation of ochratoxin A in pig tissues

This study was undertaken to compare two different analytical methods for the determination and confirmation of ochratoxin A (OTA) in blood serum, kidney and liver of pigs. Sample clean-up was based on liquid-liquid phase extraction. The detection of OTA was accomplished with high-performance liquid chromatography (HPLC) combined either with fluorescence detection (FL) or electro spray ionization (ESI+) tandem mass spectrometry (MS–MS). Comparative method evaluation was based on the investigation of 90 samples of blood serum, kidney and liver per animal originating from different regions of Serbia. The analytical results are discussed in view of the respective method validation data and the corresponding experimental protocols. In general, analytical data obtained with (LC–MS–MS) liquid chromatography electro spray tandem mass spectro metry detection offered comparable good results at the sub-ppb concentration level. The results indicate that the liquid chromatography electro spray tandem mass spectrometric (LC-MS/MS) method was more specific and sensitive for the analysis and confirmation of ochratoxin A in pig tissues then high pressure liquid chromatography (HPLC) method after methylation of OTA.