The biodegradability of two primary alcohol ethoxylate nonionic surfactants under practical conditions,and the toxicity of the biodegradation products to rainbow trout

A field trial has been performed to measure the biodegradability of two typical alcohol ethoxylate nonionic surfactants, “Dobanol” 45-7 and “Dobanol” 45-11, by dosing them to biological filters in a mixture with domestic sewage. Influent levels were 10 and 25 mg l^?1 of each surfactant and 96–98% degradation was achieved within a temperature range of 5–10°C. The surfactants had no adverse effects on the filters in terms of the usual sanitary parameters (BOD, COD, TOC and ammoniacal nitrogen). Tests on the effluents indicated no residual acute lethal toxicity to rainbow trout Salmo gairdneri).     

抽余C_4烃中异丁烯催化逆流水合制叔丁醇

采用大颗粒离子交换树脂催化剂,在φ100mm×10m的反应器中进行了异丁烯催化逆流水合制叔丁醇的中间试验。考察了反应温度、水油体积比和抽余C4烃的流速等对异丁烯转化率的影响。试验结果表明,异丁烯催化逆流水合制叔丁醇的适宜操作条件为:反应温度80~90℃,水油体积比为4~5,抽余C4烃的流速为0.45~0.55mm/s。在此条件下,异丁烯的转化率可达88.8%。工业装置运转结果表明,异丁烯转化率大于75%。     

碘与淀粉的相互作用及在Vc分析中的应用

本文探讨了碘与淀粉的相互作用以及碘－淀粉显色体系的稳定性。结果表明：在碘量一定时，体系的吸光度随淀粉用量的增大而增大，最后趋向稳定；在淀粉量一定时，体系的吸光度随碘用量的增大而增大，最后亦趋向稳定。碘－淀粉显色体系很不稳定，吸光度随时间呈比较明显的下降趋势，但加入复合表面活性剂可以使显色体系的稳定性大大提高。在上述结果的基础上，我们建立了测定Ｖｃ的新方法，此法具有简单、快捷、试剂易得、灵敏度高以及对浑浊试液不必分离即可直接测定等优点。该法的灵敏度为０．２５μｇ／ｍｌ，对１μｇ／ｍｌ的Ｖｃ试液进行平行测定，１０次平行测定结果的相对标准偏差为８．８６％，加标回收率为９０．５％－９３．６％，用于番石榴汁饮料中Ｖｃ的测定，结果满意。     

岩石样品中铷的中子活化分析

研究了苦味酸溶液的ｐＨ变化对用１８－Ｃ－６（１８Ｃ６）的硝基苯溶液定量萃取Ｒｂ的影响及１８Ｃ６浓度变化对定量萃取Ｒｂ的影响，确定了定量反萃Ｒｂ的实验条件。作出了磷酸锆无机离子交换柱上的Ｒｂ－Ｃｓ分离曲线。测定了岩石样品的微量Ｒｂ和痕量＾８４Ｒｂ。     

H-PSMA/PVA/PP复合膜的制备及油-水乳液分离性能

通过两步法对聚丙烯（PP）膜进行了亲水改性:首先,通过在碱性条件下水解苯乙烯-马来酸酐共聚物（PSMA）制备了水解的苯乙烯-马来酸酐共聚物（H-PSMA）;然后,以聚乙烯醇（PVA）为亲水性改性剂,戊二醛（GA）为交联剂,将H-PSMA/PVA/GA复合材料浸涂在PP基底膜上,制备了亲水性水解苯乙烯-马来酸酐共聚物/聚乙烯醇/聚丙烯（H-PSMA/PVA/PP）复合膜。利用傅里叶变换红外光谱（FT-IR）分析表征了H-PSMA和H-PSMA/PVA/GA的结构;通过测试复合膜表面的静态接触角,探究了PVA和GA含量及成膜溶液的质量浓度等对膜表面润湿性能的影响;最后,测试了复合膜的油水分离效率和重复利用率。结果表明:当GA、PVA和H-PSMA的质量比为0.225∶1∶1,成膜溶液的质量浓度为0.03 g/mL时,所制备的H-PSMA/PVA/PP复合物膜对水包油乳液（O/W）表现出优异的分离性能,初次油水分离效率为99.40%,当重复分离10次后,油水乳液的分离效率仍达到98.83%以上。该复合膜的制备工艺具有安全性好、成本低和环境友好的特点。     

Mn/Ti-Zr复合氧化物催化苯甲酸甲酯选择性加氢

以硝酸锆和钛酸四丁酯为原料,采用共沉淀法制备Ti-Zr-O氧化物载体,采用浸渍法制备了Mn/Ti-Zr催化剂;采用XRD、N2物理吸附、H2-TPR、NH3-TPD和TG-DTA对Mn/Ti-Zr催化剂进行了表征,并考察了催化剂组成、结构和反应条件对苯甲酸甲酯（MB）加氢性能的影响,以及催化剂的长周期稳定性、失活和再生行为。结果表明：TiO2含量和Mn负载量分别为12% 和8% （二者均以Ti-Zr-O氧化物的质量为基准,下同）时制备的Mn/Ti-Zr催化剂性能最优,该催化剂在θ = 390 ℃, p = 1.0 MPa,n(H2)∶n(MB) = 9∶1和重时空速（WHSV）= 0.5 h-1的优化条件能够实现98.0% 的苯甲酸甲酯转化率和89.7%的苯甲醛和苯甲醇选择性;苯甲酸甲酯加氢反应的活性和选择性分别与Mn/Ti-Zr表面MnOx物种的氧化还原性和催化剂的酸性密切相关。此外,Mn/Ti-Zr催化剂具有良好的结构稳定性,在反应1000 h后仅因积碳而丧失11% 的活性,且轻微失活的催化剂可以通过焙烧恢复其初始活性和选择性。     

Facile Fabrication of Poly(vinyl alcohol)/Polyquaternium-10 (PVA/PQ-10) Anion Exchange Membrane with Semi-Interpenetrating Network

Anion exchange membranes (AEMs) are one of the core components of AEM fuel cells. A series of poly(vinyl alcohol)/polyquaternium-10 (PVA/PQ-10) AEMs with semi-interpenetrating networks (s-IPNs) are prepared by a simple solution-casting method using glutaraldehyde (GA) as a cross-linking agent. Subsequently, the prepared PVA/PQ-10 cross-linked membranes are characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, mechanical analysis, water uptake and swelling ratio tests, ion exchange capacity (IEC) tests, ionic conductivity measurements, and oxidative/alkaline stability tests. The effects of the mass ratio of PVA and PQ-10 and the amount of cross-linking agent GA on the performance of the PVA/PQ-10 cross-linked membranes are systematically explored. The results show that the cross-linked PVA/PQ-10 AEMs have high IEC and low water uptake and swelling ratio, and its maximum ionic conductivity can reach 79.37 mS cm^–1 at 80 °C. In addition, the PVA/PQ-10 cross-linked membrane has good oxidative and alkaline stability under optimal preparation conditions. These results may provide valuable insights toward more effective scheme designs and new, simple preparation methods for AEMs with s-IPN structures.     

Preparation of High Strength and Toughness Aramid Fiber by Introducing Flexible Asymmetric Monomer to Construct Misplaced-Nunchaku Structure

High performance fibers with high strength and toughness have great potential in composites, but contradiction between tensile strength and elongation at break makes the preparation to become a current challenge. Herein, an asymmetric structure of more flexible diamine, 3,4′-diaminodiphenyl ether (3,4′-ODA), is introduced into heterocyclic aramid (PBIA) fibers to replace rigid symmetric p-phenylenediamine (PDA). By studying the properties of copolymer (mPEBA) fibers with different ratios of diamine, it is found that the mPEBA fiber reached the optimal mechanical properties with the 30% content of 3,4′-ODA. Compared with homopolymerized heterocyclic aramid fibers, the tensile strength and elongation at break of mPEBA fiber are improved by 26.2% and 38.7%, respectively. Results of X-ray diffraction show that the introduction of 3,4′-ODA structure can increase stretchability of mPEBA fibers, improving the orientation degree during hot-drawing. Molecular dynamics simulations confirm that 3,4′-ODA structure undergoes a conformation transformation to form a straightened chain during hot-drawing, while symmetrical 4,4′-diaminodiphenyl ether (4,4′-ODA) cannot form the same conformation. The misplaced-nunchaku structure is formed based on the special meta-para position of 3,4′-ODA, achieving the synergy of high strength and high toughness.