O3/H2O2法去除浮选药剂丁基黄药

采用O3/H2O2法去除水中丁基黄药,考察了H2O2/O3摩尔比、pH值、丁基黄药初始浓度、温度和自由基抑制剂对丁基黄药的去除效果的影响。结果表明,在相同O3投加量下,H2O2量越大,丁基黄药去除率越高。pH值为7～9,温度在293～303 K的范围内,O3/H2O2对丁基黄药都有很高的去除率。碳酸氢根和叔丁醇能在一定程度上降低丁基黄药的降解效率。研究还发现,在O3和H2O2投加量相同的条件下,H2O2多次投加对水中丁基黄药的处理效果明显优于一次性投加。GC/MS分析表明,O3/H2O2氧化丁基黄药氧化产物为羧酸类物质。     

3种污泥对磺胺二甲基嘧啶的吸附性能

研究了厌氧颗粒污泥、厌氧污泥及好氧污泥对磺胺二甲基嘧啶(SM2)的吸附性能。当SM2初始浓度为50μg/L时,采用活性污泥灭活吸附,考察了吸附平衡时间、吸附等温线及温度对污泥吸附的影响,并比较了失活污泥与活性污泥的吸附性能。结果表明,3种污泥对SM2的吸附均在1 h内达到吸附平衡;3种失活污泥对SM2的吸附都可用Freundl-ich和Langmuir吸附模型来描述,并且Freundlich吸附模型的拟合效果要好于Langmuir模型(R2F>R2L);温度对3种污泥吸附影响规律一致,并且吸附常数KF(15℃)>KF(25℃)>KF(35℃),这说明吸附为放热反应,低温有利于吸附反应的进行。活性污泥对SM2的吸附与失活污泥吸附规律一致,都符合Freundlich模型。3种活性污泥对SM2的去除是吸附和降解的共同作用,并且都是降解占主导地位,降解效率为厌氧污泥>好氧污泥>厌氧颗粒污泥。     

烟草工业废弃物中提取氨基酸

以生产烟碱及茄尼醇后的烟叶废渣为原料,采用酸水解及活性炭脱色处理提取氨基酸,研究了酸水解中HCl用量、水解时间以及活性炭脱色处理中活性炭处理方式、pH、活性炭用量、脱色温度和脱色时间等因素对氨基酸收率和脱色率的影响。结果表明,最佳水解条件:以6 mol/L HCl溶液为水解液,在120℃、料液比1∶18条件下,水解12 h,所得水解液经以下工艺脱色处理:0.25%KOH处理活性炭、pH=10、活性炭用量为2.5%、脱色温度80℃、脱色40 min,所得产物氨基酸收率86.65%,脱色率达84.31%。     

填埋垃圾中TOC含量的测定方法优化

垃圾的TOC含量是评价垃圾矿质腐殖化机理研究的重要指标,以本课题组模拟垃圾填埋系统中的垃圾样品为研究对象,以土壤TOC测定方法为基础,通过单因素实验和正交实验(L25(56))对垃圾样品的TOC的测定方法进行优化。结果表明,TOC测定优化条件为:风干样品(0.1±0.0005)g,Ag2SO40.075 g,0.4 mol/L(1/6K2Cr2O7)-H2SO4溶液(含1/2H2SO412.6 mol/L)10 mL,180℃的砂浴加热45 min。此条件下,RSD小于3.23%,表明该方法精密度高,可行性强。     

高温载硫活性炭的制备及脱汞能力研究

研究了载硫温度、硫炭比(简称S/C),吸附温度等因素对载硫活性炭的硫含量、脱汞能力以及硫损失的影响,探讨载硫活性炭制备的工艺条件优化。结果表明,不同载硫温度下制备的载硫活性炭的气态Hg0吸附能力远强于原料活性炭;载硫温度不同时,负载到活性炭孔隙或表面上的硫的形态不同,导致了脱汞能力的差异,较合适的载硫温度为350℃;S/C为5%(质量分数,下同)时,随着吸附温度的升高,载硫活性炭的气态Hg0吸附量降低;在一定的载硫温度下,原料中S/C越高时,制备的载硫活性炭的硫含量越高、气态Hg0吸附能力越强,但其硫损失率也越高,从实际的使用效果来看,较合适的S/C为10%。     

Degradation of 2,4-D in soils by Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> nanoparticles combined with stimulating indigenous microbes

Purpose  

Degradation of 2,4-dichlorophenoxyacetic acid (2,4-D) in soils by Fe₃O₄ nanoparticles combined with soil indigenous microbes was investigated, and the effects of Fe₃O₄ nanoparticles on soil microbial populations and enzyme activities were also studied.     

反渗透装置处理炼油污水的优化运行

通过对反渗透装置初次化学清洗时进水水质、运行情况、反渗透系统进水端和浓水端情况、保安过滤器滤芯情况分析,确定造成膜污染的主要原因,并针对这些原因采取化学清洗、运行管理等一定措施。措施实施后:反渗透运行周期均有所增加,特别是1#反渗透装置,运行周期增至2 414h,达到健康运行要求。     

耐盐石油降解菌性能及降解条件优化

从冀东油田钻井废液中筛选分离出耐盐石油降解菌Virgibacillus sp.(简称SJ菌),其在高含盐条件下对石油具有较好的降解效果,高达56.12%左右。考察了pH值、盐度、不同N和P形态等因素对SJ菌降解石油效果的影响。结果表明:SJ菌有较宽的pH值适应范围(pH值为6～10)和较好的耐盐能力(0.5%～20%),在pH值为9及NaCl质量浓度为5%时对石油类降解效果最好,其最佳利用N源和P源分别为(NH2)2CO和KH2PO4,该研究为油田高含盐含油废液处理提供了一条新途径。     

Determination of chloramphenicol, enrofloxacin and 29 pesticides residues in bovine milk by liquid chromatography-tandem mass spectrometry

A sensitive method for determination of chloramphenicol, enrofloxacin and 29 pesticides residues in bovine milk by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was developed. Residues of the targets were extracted from milk with acetonitrile, cleaned up by C₁₈-SPE cartridge, and then determined by HPLC-MS/MS. The MS detection was operated in positive or negative ionization mode, depending on the compounds. For confirmation of each target compound, two precursor ion > product ion transitions were selected by multi-reaction monitoring mode (MRM). The method showed good linearity for all the tested compounds over the studied concentration range with correlation coefficient higher than 0.9910. Recoveries for the studied compounds at three spiked levels (0.05, 0.10, 0.19 mg kg⁻¹) in bovine milk were in the range of 71-107% with RSDs not larger than 13.7%, except that recoveries of trifluralin ranged between 62% and 70% at the spiked levels. Limits of quantitation for the analytes were estimated to range between 0.03 × 10⁻³ and 14.5 × 10⁻³ mg kg⁻¹. The proposed method was applied for the determination of the analytes residues in real samples. The found levels of the analytes in milk samples were lower than maximum residues levels (MRL).     

粉煤灰合成NaX型分子筛的表征及其对Fe~（2＋）离子的吸附研究

以高温碱熔融处理粉煤灰合成了NaX型沸石分子筛,考察了不同水热晶化温度对产物结果的影响,用粉末XRD、XRF、SEM和FT-IR等手段对产品进行了表征,结果表明,以粉煤灰为原料用水热合成法合成微孔分子筛时,在晶化温度为90℃时能得到晶形较好的NaX型分子筛。同时考察了NaX分子筛的用量、时间和pH值等因素对Fe2＋离子的吸附影响,在25 mL Fe2＋离子浓度为2×103 mg/L的溶液中,当吸附剂用量为0.2 g,吸附时间为2 h,吸附效率达到最大值（36.41%）,而随着溶液pH值的升高其吸附效率显著增大。