Synthesis and Properties of New Cleavable Cationic Surfactants Containing Carbonate Groups

A novel series of cleavable alkyltrimethylammonium surfactants with different hydrocarbon chain lengths (C8–16) were synthesized. A carbonate break site inserted between the polar head and the hydrocarbon chain makes these compounds hydrolyzable. The reagents used are renewable, (bio)degradable, or reusable. The hydrolysis of these cleavable surfactants will lead to the generation of fatty alcohols and choline, which is an essential biological nutrient. The surface activities in aqueous solution of the synthesized carbonates fulfill the requirement of being good surfactants. In addition, the cleavable compounds containing n-decyl and n-dodecyl chains showed similar or higher antimicrobial activities when compared to a non-cleavable analog.     

Manganese oxides treated with organic compounds as catalysts for water oxidation reaction

Manganese oxides of different crystalline structures: α-MnO₂, δ-MnO₂, α,γ-MnO₂ and Mn₂O₃; were treated with the organic compounds picolinic acid, ethylenediamine and pyridine; and were applied as catalysts in the chemical water oxidation reaction using Ce(IV) ammonium nitrate as sacrificial oxidant. The treatment led to modifications in the oxides properties, such as reduction of the particle size, increase of surface area and partial reduction of Mn⁴⁺ to Mn³⁺ for the Mn(IV) oxides, or of Mn³⁺ to Mn²⁺ for Mn₂O₃, because of favored interactions of the organic molecules with the lattice planes with higher d spacing. Oxygen evolution reaction (OER) tests showed the superior catalytic activity of the treated Mn(IV) oxides, for instance α,γ-MnO₂-en presented TOF five times higher than pure α,γ-MnO₂. The increase in surface area as well as the higher Mn³⁺ content caused by the treatment of the Mn(IV) oxides were correlated with the improvement in the OER catalytic activity.     

复合固体推进剂中固体填料的安息角测试与仿真

复合固体推进剂含有固体颗粒较多，离散单元法是一种适合固体推进剂生产过程数值仿真的有效方法，颗粒物料的接触参数是保证离散单元法仿真精度的关键。本文以复合固体推进剂的主要组分铝粉和高氯酸铵固体颗粒为研究对象，通过实验测试获得了相关物料的安息角，利用专业离散元软件EDEM仿真模拟了安息角测试实验过程，建立了物料安息角与接触参数之间的联系。研究表明，滚动摩擦系数和滑动摩擦系数越大，安息角越大，物料流动性越差。对比仿真与实验结果，通过逆向反推法确定了物料的滑动摩擦系数和滚动摩擦系数两个关键接触参数。铝粉与高氯酸铵1∶2混合颗粒的滑动摩擦系数为0.2，滚动摩擦系数为0.05。为固体推进剂加工生产过程离散元数值仿真提供了关键基础数据。     

短程反硝化耦合厌氧氨氧化工艺及其应用前景研究进展

短程反硝化以其碳源消耗量、废污泥产量、温室气体排量极低及无需曝气等优势，被认为是最具研究潜势的厌氧氨氧化底物供给技术，成为近年来研究热点。本文首先介绍了短程反硝化工艺原理；其次从污泥源、反应时间、碳源类型、碳源量及pH等5个方面总结了影响短程反硝化工艺启动因素；随后综述了短程反硝化耦合厌氧氨氧化工艺的重要研究进展，同时指出了耦合工艺实验研究与工程应用的不足，并提出了解决实验与工程应用缺陷的方案；最后展望了耦合工艺处理城市污水和工业硝酸盐废水的可行性及应用前景，认为全面分析工业硝酸盐废水化学组分与基于分子生物学水平的宏基因组学测序、元转录组学技术是未来耦合工艺同步处理城市污水和工业硝酸盐废水的研究重点。     

氯化铵蒸发器结垢成分鉴别及原因分析

多效蒸发器结垢的问题常常发生,影响热效率和装置的正常运行。为明确导致蒸发器结垢的原因和成分,利用X射线衍射（XRD）、等离子发射光谱（ICP）、扫描电镜能谱（SEM-EDS）、偏光显微镜、拉曼光谱和离子色谱等分析测试技术,对浙江大洋生物科技集团股份有限公司的氯化铵多效蒸发器上的不明结垢物做了表征和分析。结果表明,该结垢物的主要成分为磷酸铁、氧化铝和有机物的混合物。探讨了发生上述结垢的原因,并提出相应的解决方案,减少了公司氯化铵蒸发器的结垢。     

河南某硫酸烧渣制备氯化铁铵的试验研究

以河南某硫酸烧渣为原料, 采用盐酸浸出-浓缩净化-氯化铵诱导-冷却结晶工艺制备优级纯氯化铁铵晶体。实验所得最佳工艺条件为: 盐酸溶液浓度40%、液固比8∶1、浸出温度85 ℃、浸出时间40 min、氯化铵过量系数0.9, 此条件下原料中铁浸出率为91.43%, 所制备的氯化铁铵纯度达到99.85%。     

硫酸铵法利用中低品位锂瓷土矿制备碳酸锂技术研究

针对江西宜丰地区氧化锂质量分数<2.0%以下中低品位锂瓷土矿,研究了硫酸铵法提取碳酸锂技术路线。首先,利用二步焙烧工艺,有利于脱氟、提高锂浸出率,并且能够有效防止结窑现象发生。在浸出液除杂过程中,采用成矾除铝的方法将大量溶出的铝离子转变为KAl（SO₄）₂·12H₂O、NH₄Al（SO₄）₂·12H₂O等有价值复盐,规避了传统石膏法产生的大量固废,有70%的铝离子被转变为矾盐晶体,同时带出大量的结晶水,减轻后续浓缩压力,对比传统的石膏法产生大量固废而言,其优点是显而易见的。碳化反应产品的XRD以及氧化锂含量分析表明,碳酸锂的纯度达到99%以上,全程锂收率为50%~60%。作为提锂实验对比,采用宜春414矿锂质量分数为4.0%的锂云母,由于414矿样中铝的相对含量更低,导致相同的除杂难度下得到的414矿样中浸出液锂离子浓度更高,浓缩倍数更小,414矿样的锂回收率更高。实验结果表明,中低品位锂瓷土提锂的工艺规律,通过适当改变参数,能够应用于难度更低的高品位的锂云母提锂过程。     

植酸的铵化及其对Lyocell织物的阻燃整理

为提高Lyocell织物的阻燃效果,对天然磷化物植酸进行铵化改性,并以双氰胺为催化剂应用于Lyocell织物的阻燃整理。利用傅里叶红外光谱仪、扫描电子显微镜、热重分析仪,测定了阻燃整理Lyocell织物的特征红外吸收、表面形貌以及热稳定性能。对阻燃织物进行了垂直燃烧实验,测定了织物的燃烧性能,并对整理织物的耐洗性进行了测试。结果表明:与未整理Lyocell织物相比,阻燃整理后织物的吸热降解质量损失率下降了20.11%,800 ℃ 时热解残炭量提高了27.98%,垂直燃烧的损毁长度下降至3.4 cm;极限氧指数高达36.6%,达到难燃的级别;且阻燃织物经20次标准洗涤后,仍能达到国家B2标准。     

Drag Reduction by Wormlike Micelles of a Biodegradable and Non-Biodegradable Surfactants

This study describes the effects of wormlike micelles formed by the commercial surfactants tallowalkylamidopropyl dimethylamine oxide (Aromox APA-TW) and oleyl methyl bis(2-hydroxyethyl) ammonium chloride (Ethoquad O/12) as drag reducers. Ethoquad O/12 is immune to degradation by heat and microorganisms. Conversely, Aromox APA-TW is biodegradable in the environment, and its susceptibility to heat-induced degradation was previously assessed. This work considers the effects of temperature, salt, and time on the drag-reduction capacity (in different Reynolds number) of wormlike micelles of these two surfactants. Wormlike micelles formed by Aromox APA-TW are able to reduce drag at higher temperatures compared to wormlike micelles formed by Ethoquad O/12. However, Aromox APA-TW can degrade after being heated to 80 °C and also after storage of the wormlike micelle solutions. Ethoquad O/12 does not undergo degradation after being heated or stored. These surfactants have the potential to be used as additives in industrial operations, as the wormlike micelles formed are able to reduce drag in systems with long pumping distances or recirculation, even in solutions with high salt concentrations (brine) and high temperatures.     

高铁酸盐-亚硫酸盐体系氧化降解水中污染物阿特拉津

针对目前日益严峻的农药污染问题，本文以阿特拉津（ATZ）为目标污染物，利用高铁酸盐活化亚硫酸盐的方式对其进行降解。探究了亚硫酸盐浓度、高铁酸盐浓度、ATZ浓度、pH以及亚硫酸盐投加方式对ATZ去除率的影响。研究结果表明，在pH为7、高铁酸盐浓度为100μmol/L、亚硫酸盐浓度为400μmol/L、ATZ的浓度为5μmol/L的条件下，10s时间内可以去除95%的ATZ。利用自由基淬灭实验对体系中的活性物质进行鉴定，结果表明，高铁酸盐-亚硫酸盐体系中起主要作用的是硫酸根自由基（SO{}_{\mathrm{4}}^{·-}），其对ATZ降解的贡献约占53%；其次是羟基自由基（·OH），约占36%。通过改变亚硫酸盐投加方式，减少了SO{}_{\mathrm{4}}^{·-}的自我消耗，提高了高铁酸盐-亚硫酸盐降解ATZ的效率。这些实验结果有助于高铁酸盐-亚硫酸盐体系的实际水处理应用。