氨基化有机-无机杂化整体柱分离富集环境水中五价砷

将四乙氧基硅烷(TEOS)和N-(β-氨乙基)-γ-氨丙基三乙氧基硅烷(AEAPTES)作为共聚前体,采用在毛细管内原位聚合的方式制备得到氨基功能化的有机-无机杂化整体柱,将其作为针式固相微萃取(SPME)介质,建立了现场分离富集环境水中As(V)的SPME方法,优化了有机-无机杂化整体柱富集As(V)的实验条件,并研究了整体柱对As(V)的吸附/洗脱性能和富集能力,实现了环境水样中As(V)的高效、快速、高选择性检测。     

Leaching,mobility and persistence of tebufenozide in columns packed with forest litter and soil

Abstract

Leaching, downward mobility and persistence of tebufenozide was investigated under laboratory conditions in columns packed with forest litter and soil, after fortification with the analytical grade material (purity > 99.6%) and with two commercial formulations, RH‐5992 2F (aqueous flowable) and RH‐5992 ES (emulsion suspension). Two types of litter and soil were used: one type with relatively high amounts of sand and the other with high amounts of clay.

The concentrations eluted in the leachates were lower when the analytical material (dissolved in acetone) was used for fortification, than when the two formulations (diluted with water) were used. The amount leached was higher for RH‐5992 2F than for RH‐5992 ES. The type of substrate, i.e., sandy or clay type, had only marginal influence on the amounts eluted in the leachates. Downward movement of tebufenozide from the top 2‐cm layer to the untreated middle and bottom layers (3‐cm segments) was consistently lower when the analytical material was used for fortification, than when the two formulations were used. Downward movement was higher for RH‐5992 2F than for RH‐5992 ES. Persistence of tebufenozide in substrates, maintained under submerged conditions for 70 days after leaching, indicated an initial 2‐week lag period prior to the onset of degradation. Formulation‐related differences were observed in the half‐life (DT₅₀) values. When the analytical material was used for fortification, the DT₅₀ ranged from ca 54 to 59 d. However, when the formulations were used for fortification, the DT₅₀ showed a higher range, i.e., from ca 62 to 67 d for RH‐5992 2F and ca 70 to 80 d for RH‐5992 ES. Formulation ingredients appear to have caused enhanced adsorption of tebufenozide onto the substrates, thus delaying degradation.     

移动式颗粒床除尘器最佳入口风速下的阻力计算

分析论述了ＹＸＫＣ型除尘器在最佳入口风速下的阻力计算方法及其影响，指出了进一步研究和改进设计的方向与途径。     

气相色谱仪检测溶解气H_2、He最佳观测条件的选择

通过色谱柱、固定相以及载气流速的选择性实验 ,提高了气相色谱仪在观测地下水中H2 、He分离效能和检测效能。本文对此作介绍 ,以期对使用气相色谱仪进行地下水H2 、He观测的台站能有所启发和借鉴     

Catalytic decomposition of hydrocarbon into hydrogen and carbon in a spouted-bed reactor as the second-stage reactor of a plastic recycling process

A two-stage process for the chemical recycling of plastics is proposed. In this process, which consists of two reactors, plastics are converted into hydrogen and carbon. In the first reactor, plastic chips are thermally decomposed into hydrocarbons. In the second reactor, the hydrocarbons formed in the first reactor are catalytically decomposed into carbon and hydrogen. In this study, in order to obtain basic data for the second reactor, propene was catalytically decomposed in a laboratory-scale spouted-bed reactor (600mm high, 21.6mm internal diameter, made of SUS304). The effect of the type of spouting medium used on the decomposition behavior of propene was investigated using four types of spouting medium (nickel-plated -alumina, palladium-plated -alumina, nickel-impregnated -alumina, and -alumina). The nickel-impregnated -alumina gave the best propene conversion and hydrogen yield.     

低周荷载下型钢混凝土柱抗剪性能智能分析

为了研究型钢混凝土短柱的抗震性能，通过21根SRC柱在低周反复荷载作用下的剪切黏结破坏试验结果，在利用灰色关联理论进行模型输入变量选择的基础上，建立了其基于改进神经网络模型的受剪承载力分析模型，进而研究了混凝土抗压强度、腹板宽度、轴压比及箍筋间距等因素对SRC柱抗剪能力的影响规律，并对SRC柱的受剪承载力进行了预测。结果表明，所提方法能够反映受剪承载力与影响因素间的非线性变化规律，可供SRC柱在低周往复荷载作用下的受剪承载力分析参考。     

轴心受压钢筋混凝土柱等效火灾荷载的计算

迄今为止，国内外有关计算构件耐火极限的方法，是钢筋混凝土构件与防火研究的主要内容。而在结构设计中，由于直接考虑的是荷载作用，为此提出了一个新概念——等效火灾荷载，将火灾对结构的影响直接考虑成荷载作用。在确定了混凝土柱的截面温度场后，利用一种简化计算方法计算出钢筋混凝土柱的等效火灾荷载，进而计算出钢筋混凝土柱的耐火极限。在火灾中，作为结构最基本的构件柱可能受到单面或多面的火作用，这里仅介绍轴心受压钢筋混凝土柱等效火灾荷载的计算。     

带压开采陷落柱突水影响因素数值模拟

为研究承压水压与煤层陷落柱位置这两种因素对陷落柱突水的影响,在分析固流耦合数学模型的基础上,利用数值模拟软件FLAC3D,以双柳矿地质条件为背景,分别对3 MPa和5 MPa承压水压下开采上、下两组煤4种情况进行模拟,分析陷落柱及其周边围岩的渗流-塑性破坏耦合场、应力场和位移场的变化.结果表明:随着工作面推进至接近陷落柱,工作面前方集中应力场与柱体周边应力场发生耦合,并出现应力集中,当水压为5 MPa开采上组煤时应力集中系数最大,最容易形成突水危险区域;当上组煤工作面距离陷落柱为30 m时,陷落柱渗流场与集中应力场开始连通,在开采下组煤时这一距离比上组煤扩大15 ～ 20 m;煤层底板随工作面推进发生压缩-膨胀周期变化,引起拉伸、剪切破坏.     

三相生物流化床处理低C/N污水的亚硝化过程控制研究

将短程硝化与生物流化床相结合,采用低碳氮比的人工合成污水进行启动,考察进水COD、氨氮、DO、p H对硝化和亚硝化过程的影响。研究表明,较短的水力停留时间(HRT)和较少的接种污泥量有利于生物膜的生长,能够成功实现生物流化床的快速启动。高进水氨氮浓度有助于反应器实现亚硝酸盐的积累,但是这种积累并不稳定。当反应器中p H为7.5~8.1,ρ(DO)为1.5~2.5 mg/L时,最大亚硝化率达到75%左右,氨氮去除率达85%以上。出水NO-2-N和NO-3-N浓度随进水COD浓度的增加而减少;当进水COD浓度为50 mg/L时,出水硝酸盐浓度急剧减少,亚硝酸盐浓度有所降低,反应器发生同步硝化反硝化脱氮现象。     

蒙脱土原位生长MoS2复合材料光催化降解罗丹明B的机理研究

通过在Na⁺-MMT表面生长MoS₂来提高窄带隙半导体光生电子分离速率及稳定性.利用阳离子填充法及水热法成功制备了复合光催化剂Na⁺-MMT/MoS₂,并通过FT-IR、SEM、TEM、Raman、XRD、TG、XPS、UV-DRS和ESR等表征进一步证明了材料的成功负载及光、电化学性能. 同时,以有机染料罗丹明B为待降解染料来评价光催化剂的催化性能,发现其在80 min可有效降解罗丹明B,降解率达96%.经过5次循环使用后,Na⁺-MMT/MoS₂复合光催化剂仍具有较好的光催化性能.因此,利用MMT的表面电负性及稳定的片层结构负载MoS₂,可形成光生电子迁移通道进一步提高电荷迁移速率及光催化剂的稳定性.本研究可为黏土材料调控窄带隙半导体制备环境友好型光催化剂提供新思路.