壳聚糖三元接枝共聚物的合成及其阻垢性能

以壳聚糖(CTS)、衣康酸(IA)和马来酸酐(MA)为原料,以醋酸为溶剂、(NH_4)_2S_2O_8为引发剂,合成了CTS-IA-MA三元接枝共聚物。聚合反应的最佳条件为:反应温度90℃,n(CTS):n(IA):n(MA)=1:1.5:1.0,引发剂质量分数0.35%,反应时间5 h。通过傅立叶变换红外光谱(FTIR)表征,所得产物为CTS-IA-MA接枝共聚物。三元接枝共聚物质量浓度为50 mg/L、水样pH为中性或弱酸性时三元接枝共聚物对CaCO_3的阻垢效果较好。     

液相色谱-质谱法测定水中氨基甲酸酯类农药及其代谢物

建立了直接测定水中10种氨基甲酸酯类农药及其代谢物的超高效液相色谱-质谱分析方法。该方法对水样无需进行富集处理,水样过滤后就可以直接测定。实验结果表明:测定液中各氨基甲酸酯类农药及其代谢物的质量浓度与离子对峰面积在质量浓度0.5～1 000.0μg/L内具有良好的线性关系;方法检出限为0.1～5.0μg/L;加标回收率91%～103%;相对标准偏差为2%～5%。该方法具有简便快捷、灵敏度高的特点。     

三元乙丙橡胶超细纤维复合膜的制备及其截留性能

以四氢呋喃和N,N-二甲基甲酰胺为溶剂,配制三元乙丙橡胶(EPDM)纺丝液,通过静电纺丝技术制备了EPDM超细纤维,进而以聚偏氟乙烯(PVDF)微滤膜为基膜制备了EPDM超细纤维复合膜。采用红外光谱(FTIR)和扫描电子显微镜(SEM)对EPDM超细纤维的结构和形态进行了表征。考察了复合膜对苯乙烯废水的截留效果和复合膜通量的变化情况。实验结果表明:EPDM超细纤维具有类似无纺布形式的多孔纤维网状结构,其直径在0.2~2.0μm之间;复合膜在操作压力为0.1MPa的条件下,处理质量浓度为100μg/mL的模拟苯乙烯废水,膜通量约为5.90mL/(cm2.h),苯乙烯去除率可达89.7%。     

Fe2O3/膨润土微波诱导氧化处理染料废水

以膨润土为载体,采用直接沉淀法制备了Fe2O3/膨润土负载型催化剂。制备催化剂的最佳工艺条件:硝酸铁质量浓度为8.08g/L,硝酸铁与膨润土质量比为1.0,焙烧温度为350℃,焙烧时间为3h。用Fe2O3/膨润土负载型催化剂微波诱导氧化处理50mL质量浓度为50mg/L的模拟活性嫩黄废水的最佳工艺条件:催化剂加入量为0.5g,微波功率为900W,微波作用时间为5min。在此条件下模拟活性嫩黄废水脱色率达96.40%。微波诱导氧化处理模拟活性嫩黄废水的反应符合一级反应动力学方程。     

活性碳纤维吸附废气中的丙烯酸和甲苯

采用动态吸附法探讨了在活性碳纤维对模拟废气中丙烯酸和甲苯的吸附过程中,各因素对活性碳纤维穿透吸附量和饱和吸附量的影响。实验结果表明,在模拟废气中丙烯酸质量分数为0.2%、双柱塞泵流量为6.1mL/h、载气流量为1.60L/min的条件下,穿透时间为10min,活性碳纤维的穿透吸附量为227.5mg/g,饱和吸附时间为40min,活性碳纤维的饱和吸附量为460.0m g/g。     

钢筋混凝土梁裂缝宽度与裂缝深度的相关性试验研究

裂缝的出现极大地降低梁的使用寿命。裂缝宽度和裂缝深度作为裂缝的两个主要参数,目前对前者的研究相对成熟,而后者的研究甚少。通过对8根钢筋混凝土梁的静力加载试验,研究由荷载引起的结构裂缝宽度与深度的相关性发展形态,并考虑混凝土强度、保护层厚度和钢筋直径对裂缝特征的影响。结果表明:混凝土梁裂缝宽度的发展主要与钢筋配筋率有关;梁的开裂荷载与混凝土的劈裂抗拉强度有一定关系;裂缝宽度与深度的相关性大致呈三段式的发展,并拟合二者的曲线。     

Effects of organic matter on Leymus chinensis germination,growth, and urease activity and available nitrogen in coastal saline soil

ABSTRACT

The present study was carried out to investigate the effect of three organic matters (stalk powder, microbial fertilizer, and manure) on Leymus chinensis germination, growth, and urease activity and available nitrogen (N) in coastal saline soil. The study was conducted in a completely randomized design with eight treatments: J₀V₀Y₀, J₁V₀Y₀, J₀V₁Y₀, J₀V₀Y₁, J₁V₁Y₀, J₁V₀Y₁, J₀V₁Y₁, J₁V₁Y₁. The notations were based on the quantities of each agent added to 1 kg of coastal saline soil: J₀ – no straw powder, J₁ – 0.2 kg straw powder, Y₀ – no manure, Y₁ – 0.3 kg manure, V₀ – no microbial fertilizer, V₁ – 0.2 L microbial fertilizer, each in quantic repeat. L. chinensis was sown as 50 seeds per pot. Results indicated that addition of organic agents exerted a significantly enhanced germination, increase in fresh weight and elevated soil urease activity. Soil available N levels were significantly positively correlated with soil urease activity and fresh weight, but not with germination rate. It is noteworthy that the halophyte L. chinensis showed improved characteristics when grown in coastal saline soil with addition of organic amendments.     

Catalytic activities and mechanism of formaldehyde oxidation over gold supported on MnO<Subscript>2</Subscript> microsphere catalysts at room temperature

MnO₂ microspheres with various surface structures were prepared using the hydrothermal method, and Au/MnO₂ catalysts were synthesized using the sol-gel method. We obtained three MnO₂ microspheres and Au/MnO₂ samples: coherent solid spheres covered with wire-like nanostructures, solid spheres with nanosheets, and hierarchical hollow microspheres with nanoplatelets and nanorods. We investigated the properties and catalytic activities of formaldehyde oxidation at room temperature. Crystalline structures of MnO₂ are the main factor affecting the catalytic activities of these samples, and γ-MnO₂ shows high catalytic performance. The excellent redox properties are responsible for the catalytic ability of γ-MnO₂. The gold-supported interaction can change the redox properties of catalysts and accelerate surface oxygen species transition, which can account for the catalytic activity enhancement of Au/MnO₂. We also studied intermediate species. The dioxymethylene (DOM) and formate species formed on the catalyst surface were considered intermediates, and were ultimately transformed into hydrocarbonate and carbonate and then decomposed into CO₂. A proposed mechanism of formaldehyde oxidation over Au/MnO₂ catalysts was also obtained.