碳酸性侵蚀与AAR作用下纳米混凝土的耐久性

地铁混凝土处于地下空间,容易受到地下水的碳酸性侵蚀；碱集料反应 (AAR)是一种严重的混凝土耐久性问题,既难以发现又难以修补,由两者共同作用引起的混凝土耐久性降低严重影响地铁隧道的正常使用.为研究纳米材料对地铁混凝土在碳酸性侵蚀和AAR共同作用下耐久性的影响,在普通混凝土中掺入适量纳米SiO₂和纳米Fe₂O₃,利用自行研制的碳酸性侵蚀试验箱进行试验,采用碳酸性侵蚀深度、膨胀率和声速作为测试指标来评价纳米混凝土在碳酸性侵蚀和AAR共同作用下的耐久性.试验结果表明:掺入纳米颗粒后,混凝土的膨胀率和侵蚀深度有了明显降低,而声速有了明显提升,说明纳米混凝土的耐久性优于普通混凝土；在182 d龄期时,掺量为2%的纳米SiO₂混凝土耐久性改善最明显,侵蚀深度和膨胀率最小,声速最大且声速下降幅度最小；其次是掺量为1%的纳米Fe₂O₃混凝土.由于纳米颗粒特殊的物理化学性质,改善了混凝土内部的微观结构和孔溶液的化学组成,使碳酸性侵蚀和碱集料反应共同作用下混凝土的耐久性得到了提高.     

碱铝硅酸盐玻璃化学强化关键影响因素概述

化学强化是一种玻璃机械强度增强方法,适用于异型、超薄、高碱、高膨胀玻璃增强,因新型超薄显示产品的屏幕保护玻璃发展需要,化学强化技术重新在碱铝硅酸盐玻璃品种掀起研究热潮。本文对化学强化本质及铝硅酸盐玻璃在屏幕保护玻璃应用进行了回顾,基于玻璃化学强化的高CS、DOL和低CT诉求,归纳总结了关键影响因素,第1,碱铝硅酸盐玻璃的成分及结构是基础,氧化铝有利玻璃网络孔隙增大创造交换通道,氧化钠或氧化锂是离子交换关键物质;第2,对于玻璃组成和结构设计,要求玻璃网络键合度R=O/Si或O/(Si+Al)满足2.15~2.40,碱金属氧化物质量分数大于13%且膨胀系数大于6×10^-6/℃;第3,在化学强化工艺方面,化学强化温度决定离子扩散系数,化学强化时间决定DOL,一步法仅能获得相对较大的CS,而DOL不很理想,只有两种离子参与交换的二步法才有利于CS和DOL同步提高。     

Phosphoric Acid-assisted Pretreatment Strategy for the Rational Synthesis of Lignin-derived Hierarchical Porous Carbon Toward High-performance Supercapacitors

In this article, a facile two-step activation method, coupled with phosphoric acid (H₃PO₄)-assisted pretreatment and followed KOH activation, was reported for constructing hierarchical porous carbon (HPC) materials derived from lignin. The introduction of H₃PO₄, cross-linked with lignin sources generated phosphate (and/or polyphosphate) ester groups throughout the lignin structure, which endowed the pre-activated intermediate char (IC) with a hierarchical porous structure. Such phosphate esters contributed to the multi-scale pore structure within the pre-activated IC, which was beneficial for the uniform distribution and impregnation of subsequent KOH activators, thus leading to the formation of HPC materials. The as-prepared HPC exhibited a large specific surface area (SSA) of 1345.1 m²/g, which ensures the accessibility of the ion diffusion pathways. The supercapacitors integrated with HPC delivered a high specific capacitance of 241 F/g (in a three-electrode system) and outstanding rate capability with an 80.9% capacitance retention from 0.5 A/g to an ultra-high current density of 50 A/g.     

伞帽用高铬铸铁在热强碱腐蚀环境下的磨损分析

针对氧化铝行业中常用的Cr28和Cr20高铬铸铁伞帽在相同工况条件下的磨损机理进行分析,并对比研究了实际生产中两种失效材料的成分、组织及性能。结果表明,伞帽部件在高温强碱腐蚀条件下受到外界冲刷时,磨损量由微切削磨损与变形磨损这两种机制共同决定。含铬量较高的Cr28高铬铸铁,其冲刷和抗腐蚀磨损性能均优于Cr20高铬铸铁。伞帽服役寿命主要受浆料和表层的铸铁材料两大因素影响。两种试验材料经淬火+回火处理后,基体组织中主要为回火马氏体+M₇C₃型碳化物+少量残留奥氏体,其中含铬量较高的Cr28高铬铸铁中共晶碳化物含量更高,且分布更加弥散,其平均硬度值为64.0 HRC,高于Cr20高铬铸铁的60.2 HRC。最终确定Cr28高铬铸铁作为伞帽材质更能满足氧化铝生产及设备检修周期的需要。     

Ni-P/HZSM-5催化木质素降解制备酚类化学品

采用Ni-P复合改性HZSM-5催化剂催化木质素降解制备高附加值的单酚类化学品，探讨了催化剂种类、金属负载量、反应温度、反应时间以及溶剂种类对木质素催化降解制备酚类化合物的影响。同时采用X射线衍射仪（XRD）、比表面积和孔径分析仪（BET）、化学吸附仪（NH₃-TPD）、热重分析仪（TG）以及气相色谱质谱联用仪（GC/MS）对催化剂以及液相产物进行分析表征，同时探讨其催化失活以及再生机制。结果表明：Ni、P高度分散在HZSM-5催化剂的表面，Ni的添加有效地弱化了C－C键，致使β-O-4和α-O-4发生断裂，有效地提高了木质素加氢解聚的活性，减少了焦炭的生成，但催化剂的再生水热稳定性较差，重复使用性较低。当采用甲醇为供氢试剂，在反应温度为220℃，氢气压力为2MPa，反应时间为8h，催化剂负载量为10%，NaOH为共催化剂时，其木质素的转化率为98.6%，酚类化合物的含量达到74.97%。产物以苯酚、愈创木酚和紫丁香酚为主，低温促进了紫丁香酚的产生。     

Roles of calcium-containing alkali materials on dark fermentation and anaerobic digestion: A systematic review

The accelerated chemical-industry has caused a rapid increase of calcium-containing alkali wastes, containing a large amount of calcium, magnesium, aluminum, and iron ions and caused a great risk to environment. Anaerobic digestion or dark fermentation is one of the most promising technologies to recover biogas, such as methane and hydrogen. Nevertheless, the hydrolysis processes of lignocellulosic biomass and waste activated sludge were the rate-limiting step of the biochemical reactions, which focused on pretreatment to improve the biodegradability of substrate. In addition, when some easily acidified wastes, such as kitchen residue, fruit and vegetable waste, and high concentration organic wastewater, are used as substrate to produce hydrogen and methane, volatile fatty acid accumulation often occurs, causing the process instability. Thus, this paper reviewed the main roles of calcium-based alkali materials such as calcium oxide, calcium peroxide and calcium hydroxide on the substrate pretreatment for obtaining high biodegradability, while others (e.g. calcium carbonate, lime and red muds) used as additives for maintaining process stability, thereby increasing biogas yield from anaerobic digestion and dark fermentation.     

Conversion of aqueous extracts from thermochemical treatment of bagasse into functional emulsifiers

Synthetic emulsifiers in food industries are being replaced with a customer-friendly food ingredient that is derived from biomass using sustainable green technologies. After hydrothermal liquefaction treatment, raw bagasse (21%), pith (26%), and rind portions (25%) were obtained with reduced ash contents. As aqueous extracts, with oligosaccharides and lignin residues, it was used in the preparation of oil-in-water emulsions with 5% soybean oil. Results showed that the emulsions stabilised the oil droplets with particle size between 11 and 17 µm by steric repulsion with raw bagasse-stabilised emulsion showing a better stability at 25 °C (31 days). It was demonstrated that raw bagasse extracts, without alteration, maybe a potential unconventional source for food-grade emulsifiers by integrating a versatile thermochemical conversion of waste without the use of chemicals.     

偏高岭石碱溶合成方钠石相变过程及吸附特性

方钠石具有笼型结构和比表面积大的特性,使其吸附能力较强。以偏高岭石和NaOH为原料,通过碱溶法合成了羟基方钠石,探讨了NaOH浓度、反应温度、反应时间和液固比对合成方钠石的影响。采用XRD、SEM、IR和NMR对碱溶过程的产物进行了表征；探讨了方钠石对Al³⁺的吸附特性。结果表明,反应温度对方钠石合成影响最大,NaOH浓度次之,液固比影响较小,升高反应温度和增大NaOH浓度可缩短反应时间。碱溶过程中,偏高岭石中的活性铝、硅优先溶解于NaOH溶液,随着反应的推进,溶液中的铝、硅达到一定浓度后会发生缩聚反应形成前驱体胶凝相。NaOH浓度对前驱体胶凝相的转变影响显著,低浓度时,胶凝相主要转变成沸石相；高浓度时则转变为方钠石相,反应的本质是处于亚稳定状态的沸石相与NaOH反应形成方钠石相。吸附特性试验表明,方钠石对Al³⁺的吸附符合Langmuir模型,其吸附率高达99.9%,最大吸附量达89.77 mg/g。     

木质素化学降解及其在聚合物材料中应用的研究进展

木质素是自然界储量丰富的可再生天然酚类高分子，可替代传统化石资源应用于聚合物材料合成。木质素分子结构中的大分子刚性骨架可赋予材料独特的力学性能和热稳定性。但木质素化学组成和分子结构复杂、反应活性低，限制了在聚合物材料领域的应用。化学降解是一种高效、高选择性且应用广泛的降解方法，经化学降解处理得到的木质素低聚物具有活性官能团多、反应活性高、溶解性好等优点，有利于拓展木质素在聚合物材料领域的高附加值应用。重点综述了近年来国内外有关木质素化学降解及其降解产物应用于聚合物材料的研究进展。