粉煤灰储能复合材料的实验研究

通过吸附、熔融浸滞将粉煤灰、月桂酸复合制备得到复合相变储能材料。通过DTA/TG、SEM测试分析,相变储能材料的相变峰值温度为46.01℃,且在44.0℃～55.0℃范围内有一个较大的吸热峰,可实现相变吸放热,且热稳定性好,粉煤灰基本不影响其热性能。微相结构显示粉煤灰能有效吸入大量的月桂酸,具有较好的吸附结合能力。     

烧结烟气脱硫灰-矿渣复合粉反应性能的研究

烧结烟气脱硫灰中由于含有大量的亚硫酸钙和游离氧化钙,在将其直接用于胶凝材料时,不但延长凝结时间,降低早期强度,而且还容易导致水泥硬化体体积膨胀,恶化硬化体性能。实验研究了脱硫灰不同掺入方式和掺入量,以及氧化温度对复合粉反应性能的影响。结果表明,在将脱硫灰经过550℃氧化处理后,再采用加水预拌的方式,在脱硫灰掺入量为5%时可获得具有较好反应性能的复合粉。     

氧化时间对总氮测定结果的影响研究

根据总氮前期氧化的特点,对氧化时间进行了分段试验研究,得到氧化时间对总氮分析结果的影响结论,提出了总氮分析时对氧化时间的控制建议。     

Combined fluorescence and electrochemical investigation on the binding interaction between organic acid and human serum albumin

Human serum albumin (HSA) is a plasma protein responsible for the binding and transport of fatty acids and a variety of exogenous chemicals such as drugs and environmental pollutants. Such binding plays a crucial role in determining the ADME (absorption, distribution, metabolism, and excretion) and bioavailability of the pollutants. We report investigation on the binding interaction between HSA and acetic acid (C2), octanoic acid (C8) and dodecanoic acid (C12) by the combination of site-specific fluorescent probe, tryptophan intrinsic fluorescence and tyrosine electrochemistry. Two fluorescent probes, dansylamide and dansyl-L-proline, were employed in the displacement measurement to study fatty acid interaction with the two drug-binding sites on HSA. Intrinsic fluorescence of tryptophan in HSA was monitored upon addition of the fatty acids into HSA. Electrocatalyzed response of the tyrosine residues in HSA by a redox mediator was used to investigate the binding interaction. Qualitatively, observations made by the three approaches are very similar. HSA did not show any change in either fluorescence or electrochemistry after mixing with C2, suggesting there is no significant interaction with the short-chain fatty acid. For C8, the measured signal dropped in a single-exponential fashion, indicative of independent and non-cooperative binding. The calculated association constant and binding ratio is 3.1×106 L/mol and 1 with drug binding Site I, 1.1×107 L/mol and 1 with Site II, and 7.0×104 L/mol and 4 with the tryptophan site. The measurement with C12 displayed multiple phases of fluorescence change, suggesting cooperativity and allosteric effect of C12 binding. These results correlate well with those obtained by the established methods, and validate the new approach as a viable tool to study the interactions of environmental pollutants with biological molecules.     

硝酸-高氯酸消解——原子荧光法测定茶叶中的硒

建立硝酸-高氯酸消解-原子荧光法测定茶叶中的硒的方法,硒浓度在0．00～40．00μg／L范围内与荧光强度呈线性关系,线性方程为y=31．2647,线性相关系数r=0．9996。样品6次定结果的相对标准偏差为3．9％,加标回收率为90．8％-95．2％。环境标准物质测定结果与标准值相吻合。     

富营养化水体中微囊藻毒素（MCs）去除技术研究进展

当前,随着工业的发展水体富营养化程度日益严重。引起富营养化的主要藻类一蓝藻,能够释放对人体及鱼类具有多器官毒性、遗传性和致癌性的毒素——微囊藻毒素（MCs）。MCs治理技术种类繁多,传统的物理法如：混凝沉淀、膜过滤、活性炭吸附、气浮以及直接过滤只能对简单的处理细胞内的MCs;化学氧化法、光催化氧化法以及高级氧化法虽然能有效处理水体中的MCs．但有成本高、易二次污染和操作复杂等缺点,难以满足日益严格的环保要求;生物酶法除了具有生物降解法所具有的廉价、无二次污染、降解彻底和易操作等特点外,还被刺用来监控水体中MCs,它将成为今后重点研究的技术领域．     

Bioaccumulation of cadmium bound to humic acid by the bivalve Meretrix meretirx Linnaeus from solute and particulate pathways

Humic acid is an important pool of heavy metals in sediments.Generally,the presence of refractory humic matter in aquatic systems would decrease the bioavailability of Cd and hence control the bioaccumulation of Cd in benthic animals.In the present work,we applied a suspending system to determine the relative importance of particulate and dissolved fractions of humic acid as Cd sources for the bivalve Meretrix meretrix and to investigate the difference of bioaccumulation characteristics of Cd adsorbed on di...     

Selective removal of 2,4-dichlorophenoxyacetic acid from water by molecularly-imprinted amino-functionalized silica gel sorbent

A molecularly-imprinted amino-functionalized sorbent for selective removal of 2,4-dichlorophenoxyacetic acid(2,4-D) was prepared by a surface imprinting technique in combination with a sol-gel process.The 2,4-D-imprinted amino-functionalized silica sorbent was characterized by FT-IR,nitrogen adsorption and static adsorption experiments.The selectivity of the sorbent was investigated by a batch competitive binding experiment using an aqueous 2,4-D and 2,4-dichlorophenol(2,4-DCP) mixture or using an aqueous 2...     

纳米催化剂Pd/SnO_2的制备及催化还原硝酸盐反应的调控

采用热分解法制备了SnO2载体,并用浸渍法制备了Pd/SnO2催化剂.同时,采用X射线衍射仪(XRD)、透射电镜(TEM)、扫描电镜(SEM)及BET比表面积仪等对所制载体和催化剂材料进行了分析表征.结果表明,热分解法和浸渍法都能够获得纳米材料,SnO2及Pd/SnO2的粒径均在9～10nm左右,比表面积分别达到144.99m·2g-1和147.36m·2g-1.在以甲酸为还原剂的Pd/SnO2催化还原硝酸盐体系中,在Pd与SnO2负载比为2%～7%,反应温度为20～50℃和甲酸投加量4.0～24.0mmol·L-1的条件下,催化活性为0.70～9.48mg·min-·1g-1,且催化活性随着负载比、温度和甲酸投加量的增大而增大,随着pH的升高先升后降,最佳pH为3.反应温度升高及pH降低都能够提高Pd/SnO2的选择性.甲酸-Pd/SnO2催化还原硝酸盐体系中还原反应的调控策略为:反应温度宜控制在40～50℃内,这样可同时获得较高的催化活性和选择性,温度过高对催化活性和选择性影响很小,温度过低则会同时降低催化活性和选择性;控制pH为3时,可以获得最大的催化活性及较好的选择性,pH升高会降低Pd/SnO2的催化活性和选择性,pH降低会导致催化活性迅速降低,但对选择性影响不大;甲酸与硝酸盐的物质的量比宜大于4:1,此时可以有效地抑制pH的上升,同时获得较高的催化活性和选择性,甲酸与硝酸盐的物质的量比小于4:1时,会同时降低Pd/SnO2的催化活性和选择性.     

Degradation of acid fuchsine by a modified electro-Fenton system with magnetic stirring as oxygen supplying

The current modified electro-Fenton system was designed to develop a more convenient and e cient undivided system for practical wastewater treatment. The system adopted a cathode portion that employed magnetic stirring instead of common oxygen gas di usion or gas sparging to supply oxygen gas for the electrolyte solution. Key factors influencing the cathode fabrication and activity were investigated. The degradation of acid fuchsine with a self-made graphite-polytetrafluorethylene cathode was studied using a spectrophotometer. It was found that the cathode generated hydrogen peroxide with high current e ciency and the hydrogen peroxide yield of the cathode did not decay after 10 times reuse. With the Pt anode at a ferrous ion concentration of 0.5 mmol/L, a pH of 3, and using magnetic stirring, dye decolorization could be rapidly accomplished but the destruction of benzene rings and intermediates was fairly di cult. With a Fe anode, dye degradation was more complete.