Dry and heat stress affects H2S production of Salmonella on selective plating media

The pH of Salmonella pre-enrichment media can become acidic (pH 4.0–5.0) when feeds/ingredients are incubated for 24?h. Salmonella in feed that have been stressed by heat and desiccation exhibit different pH tolerances than non-stressed cultures. Acidic conditions can result in cell injury/death and affect biochemical pathways. In this study, eight serotypes of Salmonella were grown in sterile meat and bone meal that was subjected to desiccation and heat stress. Cultures of non-stressed and stressed isolates were subsequently exposed to acidic pH from 4.0 to 7.0 in 0.5?pH increments (3 replicates/pH increment) in citrate buffer. At 6 and 24?h, serial dilutions were plated in duplicate on XLT-4 (xylose lysine tergitol-4) agar. Four serotypes showed an impaired ability to decarboxylate lysine on XLT-4. This inability to decarboxylate lysine was dependent on isolate, stress status, and incubation time. When the isolates’ ability to decarboxylate lysine was examined using biochemical tests, cultures were found to be able to decarboxylate lysine with the exception of S. Infantis. This suggests that XLT-4 contains a biochemical stressor(s) which affects the rate of decarboxylation by these Salmonella. These results suggest that acidic conditions may influence the detection and confirmation of Salmonella in feed.     

TiO2气溶胶快速去除空气中的芥子气模拟剂

在自制反应器内,通过喷射法将纳米TiO_2分散成气溶胶形式,用以降解空气中的芥子气模拟剂二乙基硫醚(DES)。利用自行设计的一套气溶胶沉降行为评价装置,对TiO_2气溶胶的释放条件进行了优化。系统研究了相对湿度、反应温度、光强、催化剂加入量、反应物浓度等因素对DES降解速率和彻底矿化速率的影响。结果表明:TiO_2气溶胶对2.80 mg/L(近似芥子气快速致死浓度)DES降解的半衰期由涂覆型TiO_2的34.5 min缩短至8.5 min;TiO_2气溶胶光催化降解DES的最佳相对湿度为35%,此时CO_2最快生成速率可达34.64μg/(L·min),150 min内彻底矿化比例达66.1%;对于1.5 L反应器,催化剂加入量为30 mg时降解DES的量效比达到最佳状态;TiO_2气溶胶光催化适用于含低浓度DES空气的快速净化。     

CePO4-TiO2固溶体的NH3-SCR活性

采用共沉淀法合成了不同Ce与Ti摩尔比的CePO₄-TiO₂复合材料,利用XRD、TEM、NH₃-TPD和H₂-TPR技术对其物理化学性质进行了表征,并对其NH₃-SCR活性进行了评价。实验结果表明：随着CePO₄含量的增加,催化剂的活性提高;当Ce与Ti的摩尔比为8:2时催化剂的活性最高,230 ℃的NO转化率达到100%,且具有更广的温度窗口,优于纯CePO₄。表征结果显示,CePO₄与TiO₂形成固溶体后,颗粒尺寸较为均匀,强酸位的数量增多,氧化还原性能提升,从而提高了催化剂的SCR反应活性,同时改善了其抗水抗硫性能。     

半干法脱除球团烟气中的SO2及Hg0

采用钙基吸收剂及复合氧化剂半干法脱除模拟球团烟气中的SO_2及Hg~0,考察了多因素条件对吸收效果的影响。实验结果表明,在以NaClO和NaClO_2为复合氧化剂、 NaClO与NaClO_2体积比1∶0.5、复合氧化剂质量分数3%、反应温度110℃、钙基吸收剂质量3.0 g、模拟烟气进气流量1.2 L/min的条件下,SO_2和Hg~0的脱除率分别为98%和93%,证明钙基吸收剂与复合氧化剂对污染物球团烟气中的SO_2和Hg~0有良好的脱除作用。     

基于废陶瓷的多孔陶瓷研制及其对Ni2+的吸附性能

通过SEM、XRD、FT-IR表征及多孔陶瓷对废水中镍的去除能力,确定多孔陶瓷的制备条件:原料中田菁粉掺杂质量分数为4%,焙烧温度为800℃.SEM和孔结构表征说明,焙烧使多孔陶瓷形貌、结构发生变化;随着焙烧温度的升高,多孔陶瓷的比表面积和孔容呈现降低的趋势,而孔径呈现增大的趋势;EDS分析能表明,原废瓷粉和多孔陶瓷的主要元素组成均为Si、Al、O.SEM、XRD和FT-IR分析表明,多孔陶瓷吸附前后结构稳定.吸附Ni2+的系列实验表明,多孔陶瓷用量为10 g·L-1,吸附时间为60 min,进水pH值为6.32,进水Ni2+浓度在100 mg.L-1以内.在此条件下废水的Ni2+去除率可达89.7%,多孔陶瓷对废水中镍有较好的去除效果.以制备的多孔陶瓷处理含镍废水,考察多孔陶瓷对废水中Ni2+的吸附动力学和吸附等温线,结果表明,多孔陶瓷对Ni2+的吸附过程符合准二阶动力学模型(R2=0.999 9),Qe为9.09 mg·g-1;吸附过程可用Freundlich方程和Langmuir方程来描述,温度由20℃升高至40℃,最大吸附量Qm由14.49 mg·g-1上升至15.38 mg·g-1.     

Experimental and theoretical research on the inhibition performance of ethanol gasoline/air explosion by C6F12O

The safety issue of ethanol gasoline and the methods to control or weaken its explosion have attracted attention. To clarify the effect of C₆F₁₂O (perfluoro(2-methyl-3-pentanone)) on the explosion of ethanol gasoline-air mixtures and intrinsic mechanism, the explosion overpressure and flame propagation behavior under different equivalence ratios (φ = 0.6–0.8) and C₆F₁₂O concentrations (χ_inh = 0–4.0%) were experimentally obtained. The detailed inhibitor reaction process was also obtained by CHEMKIN based on a new assembly kinetic mechanism. The results show that the effects of C₆F₁₂O on the explosion characteristics of ethanol gasoline varied with χ_inh and φ. For rich flames, C₆F₁₂O is more effective than and heptafluoropropane (C₃HF₇) and nitrogen (N₂) in suppressing explosions; for lean and equivalence ratio flames, the addition of C₆F₁₂O may result in more severe explosions. The decrease in chemical reactivity is mainly because the mole fractions of OH and H radicals and the proportion of paths H radicals involved decrease after adding C₆F₁₂O, and R1500: CF₃COF + H = CF₃CO + HF, R965: CF₂:O + H = CF:O + HF, R863: CF₃ + H = CF₂ + HF are main suppressing reactions.     

大气14CO2的时空分异特征及其在化石源CO2示踪中的应用

大气CO₂中放射性碳同位素(¹⁴C)的水平可以反映化石源CO₂的影响程度,这对于评估我国目前化石源CO₂的排放状况和制定节能减排政策具有重要的指导意义。本文在概述大气¹⁴CO₂采样和分析方法的基础上,简要介绍了大气¹⁴CO₂观测的起源和主要的源汇过程,重点论述了大气¹⁴CO₂的时空分异特征及其驱动因素;阐述了化石源CO₂浓度的估算方法及¹⁴CO₂在国内外化石源CO₂示踪中的应用现状,并对大气¹⁴CO₂观测在我国化石源CO₂示踪中的应用前景进行了展望;旨在为我国正确地开展大气¹⁴CO₂的观测研究,深刻地理解特定区域大气¹⁴CO₂的时空分异特征和化石源CO₂的分布状况提供参考。     

四环素光催化降解特性与选择性研究

研究了盐酸四环素的光催化降解行为,结果表明四环素光催化降解反应符合一级反应动力学方程,吸附过程为整个光催化降解的控制步骤,推断四环素的主要降解途径是吸附在二氧化钛(TiO2)表面发生光催化氧化反应.同时,通过对四环素与磺胺甲唑或阿莫西林混合样品的降解实验表明,改变pH、TiO2投加量等因素,两种抗生素的降解表现出了明显的选择性.     

2-萘酚生产废水综合治理与资源化利用工程实例

针对2-萘酚生产废水p H值低、色泽深,亚硫酸盐和萘磺酸盐高、COD浓度高的特点,采用酸化脱硫-两级络合萃取-氧化絮凝工艺处理,介绍了专利工艺的流程设计,给出了主要工艺设计参数及投资运行成本。工程运行结果表明,该工艺设计合理、技术成熟、处理效果稳定,2-萘酚生产废水经处理后达到GB 8978—1996《污水综合排放标准》一级排放标准要求;回收的萘磺酸钠固体可返回2-萘酚生产系统套用;反萃取黑液经蒸发浓缩,合成的减水剂产品各项指标达到或超过GB 8076—2008《混凝土外加剂》高效减水剂指标要求。     

V2O5/TiO2催化剂脱除NO的研究

采用了等体积浸渍法制备二氧化钛负载钒氧化物催化剂（V2O5/TiO2）,研究了V2O5负载量、反应温度、烟气流量、氨氮比以及运行时间各因素对NH3选择性催化还原NO反应（SCR）效率的影响.研究结果表明：经过500℃温度下煅烧,烟气流量为200ml/min,负载量为7wt％的V2O5/TiO2催化剂,在400℃温度下反应,NO脱除率可达70.5％.