镍基惰性阳极的耐腐蚀性研究(下)

探讨Ni0—NiFe204基金属陶瓷惰性阳极在冰晶石——氧化铝熔体中的腐蚀行为，通过实验作出电解质分子比、电流密度及氧化铝浓度与腐蚀速率的关系曲线。针对该镍基惰性阳极，找出了该惰性阳极材料腐蚀速率较小时对应分子比，电流密度及氧化铝浓度等电解过程控制的较佳条件。     

300kA预焙铝电解槽中修的可行性探讨

通过对300kA电解槽停槽后的炉底状况分析,表明大型预焙槽具备中修和二次启动的可行性。同时提出大型预焙电解槽具备中修的要求,为大型电解槽进一步延长槽寿命提供了新思路。     

Materials for global carbon dioxide recycling

CO₂ emissions, which induce global warming, increase with the development of economic activity. It is impossible to decrease the CO₂ emissions by suppression of the economic activity. Global CO₂ recycling can solve this problem. The global CO₂ recycling consists of three district: The electricity is generated by solar cells on deserts. At desert coasts, the electricity is used for H₂ production by seawater electrolysis and H₂ is used for CH₄ production by the reaction with CO₂. CH₄ which is the main component of liquefied natural gas is liquefied and transported to energy consuming districts where CO₂ is recovered, liquefied and transported to the desert coasts. A CO₂ recycling plant for substantiation of our idea has been built on the roof of the Institute for Materials Research in 1996. Key materials necessary for the global CO₂ recycling are the anode and cathode for seawater electrolysis and the catalyst for CO₂ conversion. All of them have been tailored by us. They have very high activity and selectivity for necessary reactions in addition to excellent durability. A pilot plant consisting of minimum units in an industrial scale is going to be built in three years.     

Zn─Fe合金镀层耐蚀性能研究

利用X-射线衍射和扫描电镜技术研究了纯Zn和Zn-Fe合金(含Fe0.2～0.7wt%)镀层的结构,发现Zn-Fe合金镀层的晶粒较纯Zn镀层细小,晶体排布更为致密;利用电化学综合测试仪研究了纯Zn和Zn-Fe合金镀层的极化电阻和腐蚀电流,结果表明Zn-Fe合金镀层的极化电阻更高而腐蚀电流较纯Zn镀层显著减小。     

网状阳极在大型储罐底板阴极保护工程中的应用

文章介绍了网状阳极在茂名、湛江、岚山和上海地区的大型储罐阴极保护系统的应用情况。从实际运行的结果看,罐底板的保护电位都达到了设计要求和标准规定,保护电位分布相当均匀。保护电流密度也满足了设计要求。保护效果较好,表明网状阳极对于大型储罐的外底板的阴极保护是一种较好的解决方案。对于发现的几个问题也作了讨论。     

钢筋混凝土阴极保护用高性能涂层钛阳极

通过对传统钛阳极涂液的改性以及烧结工艺的改进,制备出Ru-Ti-Ir新涂层阳极。X射线衍射及扫描电镜分析表明,涂层氧化物晶粒细小、均匀、达到纳米级,涂层表面无龟裂纹。电化学测试分析表明,电极的电催化活性及强化寿命明显优于传统阳极,此电极在钢筋混凝土外加电流阴极保护中具有很好的使用效果。     

巴基斯坦成品油管线工程储罐罐底外壁阴极保护

网状阳极已在储罐罐底的阴极保护系统中大量使用，保护效果明显，并得到很多应用单位的认可。本文主要结合巴基斯坦国家重点工程——成品油管线工程（White Oil Pipeline Project）具体情况，对该项目储罐罐底外壁阴极保护的设计、计算、实施情况等进行了详细介绍，并对实际保护效果和存在问题进行了分析讨论。     

添加SnO_2组元对RuO_2 SnO_2 TiO_2/Ti钛阳极组织形貌的影响

通过溶胶凝胶 (Sol gel)法经涂刷、烧结、退火等工艺制备了添加不同含量SnO2 的RuO2 SnO2 TiO2 /Ti三元涂层钛阳极。并通过X射线衍射 (XRD)、差热分析 (DTA)、透射电子显微 (TEM )分析了SnO2 组元对RuO2 TiO2 SnO2 /Ti阳极涂层组织、晶粒尺寸和外观形貌的影响。结果表明 ,所获三元涂层颗粒尺寸细小 ,均为纳米结构 ,且添加SnO2 组元后有显著细化涂层晶粒的效果。在不同退火温度下 ,随SnO2 含量的增加 ,涂层晶粒均能发生一定程度的细化。所获三元阳极涂层主要组成物相为金红石 (Ru ,Sn ,Ti)O2 固溶体 ,SnO2 组元含量较高的涂层出现不同成分金红石相共存的现象 ;当涂层退火温度由 45 0℃升高至 6 0 0℃后 ,SnO2 组元不能阻止 (Ru ,Sn ,Ti)O2 固溶体脱溶分解 ,并析出六方晶系Ru单质 ;添加SnO2 组元的RuO2 SnO2 TiO2 涂层晶粒外观呈较理想等轴状特征     

Molecular Adsorption-Induced Interfacial Solvation Regulation to Stabilize Graphite Anode in Ethylene Carbonate-Free Electrolytes

Many organic solvents have excellent solution properties, but fail to serve as lithium-ion batteries (LIBs) electrolyte solvents, due to their electrochemical incompatibility with graphite anodes. Herein, a new strategy is proposed to address this issue by introducing a surface-adsorbed molecular layer to regulate the interfacial solvation structure without the alteration of electrolyte composition and properties. As a proof-of-concept study, it is demonstrated for the first time that the intrinsically incompatible propylene carbonate (PC)-based electrolyte becomes completely compatible with graphite anodes by introducing a layer of adsorbed hexafluorobenzene (HFB) molecules to weaken the Li⁺-PC coordination strength and facilitate the interfacial desolvation process. As a consequence, the graphite/ NCM811 pouch cells using the PC-based electrolyte containing only 1 vol.% HFB demonstrate excellent long-term cycling stabilities over 1150 cycles. This strategy is also proved to be applicable to other ethylene carbonate (EC)–free electrolytes, thus providing a new avenue for developing advanced LIB electrolytes.     

Hydrated Bi-Ti-Bimetal Ethylene Glycol: A New High-Capacity and Stable Anode Material for Potassium-Ion Batteries

Potassium-ion batteries have emerged not only as low-cost alternatives to lithium-ion batteries, but also as high-voltage energy storage systems. However, their development is still encumbered by the scarcity of high-performance electrode materials that can endure successive potassium-ion uptake. Herein, a hydrated Bi-Ti bimetallic ethylene glycol (H-Bi-Ti-EG) compound is reported as a new high-capacity and stable anode material for potassium storage. H-Bi-Ti-EG possesses a long-range disordered layered framework, which helps to facilitate electrolyte ingress into the entire Bi nanoparticles. A suite of spectroscopic analyses reveals the in situ formation Bi nanoparticles within the organic polymer matrix, which can alleviate stresses caused by the huge volume expansion/contraction during deep cycles, thereby maintaining the superior structural integrity of H-Bi-Ti-EG organic anode. As expected, H-Bi-Ti-EG anode exhibits a high capacity and superior long-term cycling stability. Importantly for potassium storage, it can be cycled at current densities of 0.1, 0.5, 1, and 2 Ag⁻¹ for 800, 700, 1000, and even 6000 cycles, retaining charging capacities of 361, 206, 185, and 85.8 mAh g⁻¹, respectively. The scalable synthetic method along with the outstanding electrochemical performance of hydrated Bi-Ti-EG, which is superior to other reported Bi-based anode materials, places it as a promising anode material for high-performance potassium storage.