尖孢镰刀菌致病相关因子及其分子生物学研究进展

由致病性尖孢镰刀菌(Fusarium oxysporum)侵染引起的植物枯萎病是一种世界性的土传真菌病害,对农业生产造成了巨大经济损失.研究表明,尖孢镰刀菌的致病与多种致病因子相关,包括信号传导系统(环腺苷酸单磷酸-蛋白激酶A和促分裂素原活化蛋白激酶信号途径)、细胞壁降解酶(木聚糖酶、果胶酶、果胶裂解酶、细胞毒素、纤维素酶、半纤维素酶和木质素降解酶等)、克服植物防御响应系统(降解抗真菌化合物和破坏植物细胞壁的化学修饰)以及其它(细胞毒素和过氧化物酶)等.此外对今后的研究工作提出展望.参26     

紫色光合细菌捕获太阳能的分子机理

光合作用是地球上最重要的化学反应,生物体通过它捕获太阳能,转为化学能供生长繁殖需要.光合细菌是地球上最早出现的具有原始光能合成体系的微生物,其光合反应中心是一个由多种色素分子与蛋白质以非共价键方式结合的、具有特定构象的色素-蛋白复合体-光反应中心RC(Reaction center)和LH(Light Harvesting),光能通过电荷分离及电子转移反应转化为化学能,其效率是当前人工模拟远远不能及的.本文综述了紫色光合细菌捕获太阳能的分子结构、作用机理的研究进展,并结合作者在R.sphaeroides LHII蛋白组份同源及异源基因表达方面的研究结果进行相应的分析,明确了Rhodobacter sphaeroides基因组中同源基因puc2BA的表达特点和功能,Rhodovulum sulfidophilum pucsBA与R.sphaeroides pufBA能够同时在R.sphaeroides中表达,能同时形成LHII和LHI,并具有能量传递功能.     

分子键合TM技术在垃圾焚烧飞灰治理中的应用

结合国内垃圾焚烧飞灰的治理现状,对分子键合TM技术治理垃圾焚烧飞灰的原理、工艺进行了介绍分析,并通过实验研究对分子键合TM技术在垃圾焚烧飞灰治理中的应用进行了探讨。     

中国民航业中长期碳排放预测与技术减排潜力分析

基于LEAP构建自下而上的中国民航业能源系统模型,设置冻结、现有政策、力度、替代和革命五组情景,深入分析民航业的驱动因子和发展趋势,探讨中国民航业中长期低碳发展的技术路径.结果显示,预计2060年左右人均乘机次数翻两番,突破2人次,冻结情景下2060年会带来高达6.9亿t的碳排放.力度情景下,民航业碳排放有望在2044年左右达峰,峰值水平控制在3亿t左右,40年累积减排近50%,仅需增加约1万亿人民币的成本.稳步推进机队更新换代,加快基础设施提升和运营操作改进,发展可持续航空燃料是民航业必须依赖的减排手段,分别能带来44.1%、29.5%和26.4%的减排量.因此,民航业要尽早制定行业"双碳"目标和实施路径计划,中短期统筹推进空域改革、空中交通管理和航司精细化管理,大力支持国产大飞机的发展,长期推动可持续航空燃料全产业链商业化和市场化.     

Fe(II)、Fe(III)对砷与不同分子量腐植酸络合性能的影响

以腐植酸（HA）代表天然有机质,采用平衡透析和超滤的方法研究铁离子（Fe （II）、Fe （III））对不同分子量HA与砷离子（As （V）、As （III））络合作用的影响,并利用红外光谱（FT-IR）表征其络合特征.结果发现,Fe （II）和Fe （III）均能增强HA络合As能力,且对As （V）络合能力的增强作用大于As （III）;pH值显著影响HA络合As能力;溶解性有机碳（DOC）浓度由5mg/L增大到200mg/L,As络合百分比随之增加,此时HA-Fe （III）络合As （III）百分比最大,为24.55%;初始As浓度由10μg/L增加1000μg/L,As络合百分比随之降低,其中HA-Fe （III）络合As （III）百分比最低,为3.11%.相同环境条件下,分子量>100kDa络合As百分比最大,其中HA-Fe （II）络合As （III）的百分比最高为26.43%;分子量小于10kDa的HA络合As百分比明显高于其他分子量的HA.Fe的增强作用主要源于Fe与羧基形成桥梁再与As络合形成三元络合物.     

Seasonal variation of transport pathways and potential source areas at high inorganic nitrogen wet deposition sites in southern China

This study attempts to identify the dominant transport pathways, potential source areas, and their seasonal variation at sites with high inorganic nitrogen (IN) wet deposition flux in southern China. This is a long-term study (2010–2017) based on continuous deposition measurements at the Guangzhou urban site (GZ) and the Dinghushan Natural Reserve site (DHS) located in the Pearl River Delta (PRD) region. A dataset on monthly IN concentration in precipitation and wet deposition flux were provided. The average annual fluxes measured at both sites (GZ: 33.04±9.52, DHS: 20.52±10.22 kg N/(ha∙year)) were higher, while the ratios of reduced to oxidized N (GZ: 1.19±0.77, DHS: 1.25±0.84) were lower compared with the national mean level and the previous reported level throughout the PRD region. The dominant pathways were not always consistent with the highest proportional trajectory clusters. The transport pathways contributing most of deposition were identified in the north and north-northeast in the dry season and in the east-southeast, east, and south-southwest in the wet season. A weighted potential source contribution function (WPSCF) value >0.3 was determined reasonably to define the potential source area. Emission within the PRD region contributed the majority (≥95% at both sites) of the IN deposition in the wet season, while the contribution outside the region increased significantly in the dry season (GZ: 27.86%, DHS: 95.26%). Our results could help create more effective policy to control precursor emissions for IN fluxes, enabling reduction of the ecological risks due to excessive nitrogen.     

Chlorination of para-substituted phenols: Formation of α, β-unsaturated C4-dialdehydes and C4-dicarboxylic acids

Despite the widespread occurrence of phenols in anthropogenic and natural compounds, their fate in reactions with hypochlorous acid (HOCl), one of the most common water treatment disinfectants, remains incompletely understood. To close this knowledge gap, this study investigated the formation of disinfection by-products (DBPs) in the reaction of free chlorine with seven para-substituted phenols. Based on the chemical structures of the DBPs and the reaction mechanisms leading to their formation, the DBPs were categorized into four groups: chlorophenols, coupling products, substituent reaction products, and ring cleavage products. In contrast to previous studies that investigated the formation of early-stage chlorophenols, the primary focus of this study was on the elucidation of novel ring cleavage products, in particular α, β-unsaturated C₄-dialdehydes, and C₄-dicarboxylic acids, which, for the first time, were identified and quantified in this study. The molar yields of 2-butene-1,4-dial (BDA), one of the identified α, β-unsaturated C₄-dialdehydes, varied among the different phenolic compounds, reaching a maximum value of 10.4% for bisphenol S. Molar yields of 2-chloromaleic acid (Cl-MA), one of the identified C₄-dicarboxylic acids, reached a maximum value of 30.5% for 4-hydroxy-phenylacetic acid under given conditions. 2,4,6-trichlorophenol (TCP) was shown to be an important intermediate of the parent phenols and the C₄-ring cleavage products. Based on the temporal trends of α, β-unsaturated C₄-dialdehydes and C₄-dicarboxylic acids, their formation is likely attributable to two separate ring cleavage pathways. Based on the obtained results, an overall transformation pathway for the reaction of para-substituted phenols with free chlorine leading to the formation of novel C₄ ring cleavage products was proposed.     

臭氧-曝气生物滤池组合工艺处理石化二级出水的试验研究

采用臭氧-曝气生物滤池组合工艺对石化废水厂二级出水进行深度处理,系统探讨了pH值对臭氧氧化单元的影响,组合工艺对废水中COD、UV254的去除效果,对废水中有机物相对分子质量分布以及荧光物质含量的影响.结果表明,在臭氧投加量为10 mg·L-1,接触时间为4 min,pH值偏碱性时,臭氧预氧化石化二级出水效果较好.臭氧氧化能将大分子有机物转化为小分子物质,使得相对分子质量小于1 000的有机物比例增加约15%,有效提高了废水的可生化性,有利于后续曝气生物滤池的运行.在曝气生物滤池的停留时间为3 h,气水比为3∶1时,组合工艺对COD、UV254的去除率分别达到40.8%和45.8%.在最佳运行条件下,进水平均COD为86.5 mg·L-1时,组合工艺出水平均COD为49.4 mg·L-1.     

市政污水A/DAT-IAT系统中溶解性有机物表征与生态安全

为了解决市政污水处理出水水质安全与无害化问题,以改良的SBR——A/DAT-IAT工艺为依托,对A/DAT-IAT工艺进水,连续曝气池(DAT)上清液及间歇曝气池(IAT)出水的溶解性有机物(dissolved organic matter,DOM)采用超滤膜法进行了相对分子质量分级,并进行了TOC、UV254、3D-EEM及发光菌毒性测试,探索市政污水毒性的主要物质来源.结果表明,实验室规模的A/DAT-IAT工艺对市政污水各分子量区间的有机物均有较好的去除效果.腐殖质是污水处理厂出水中主要物质,且天然水体中难去除的腐殖质及处理过程中形成的腐殖质成分是二级出水中主要的荧光物质.沿污水处理流程,DOM的组成呈现出由低分子量向高分子量转化的趋势,相对分子质量<1×103区间的物质芳香性显著增加,导致IAT出水与氯的反应活性增高,产生消毒副产物的风险增加.与进水毒性主要来源于原水中相对分子质量<1×103的小分子物质相同,IAT出水的毒性也主要来源于相对分子质量<1×103的小分子物质,但与原水中的小分子物质不同,主要是生物处理过程中产生的类腐殖质.结合对TOC、UV254、3D-EEM及毒性的分析,小分子的类腐殖质是二级出水有机物含量达标、氯化消毒副产物控制及毒性控制应该重点考虑去除的对象.在之后的研究中,应该根据这部分物质进行工艺调节及针对性处理单元的添加.     

FePMo12催化电化学反应降解染料废水的研究

采用IR和XRD等方法对自制磷钼酸铁(FePMo12)杂多酸进行表征,表明杂多阴离子具有Keggin结构.将FePMo12负载于修饰后的4分子筛(4A)上制备FePMo12/APTES-4A催化剂填充于电化学反应器中,考察电化学氧化体系对酸性大红3R染料废水的脱色效果.结果表明,FePMo12/APTES-4A催化剂对酸性大红3R模拟废水具有良好的催化效果,当活性组分负载量为3%时,在pH为4,槽电压为22 V,曝气量为0.08 m3·h-1,极板间距为3.0 cm反应条件下,90 min后脱色率达到75.3%,COD和TOC去除率分别达到65.4%和46.0%.加入支持电解质Na2SO4和NaCl后,NaCl对电催化降解染料废水有促进作用,而Na2SO4的加入使得废水的脱色效率降低.采用可见-紫外光谱对反应过程中间产物进行分析,表明染料分子中的共轭体系已基本被破坏.