Simply constructed highly dispersed cobalt nanoparticles in diverse N-doped graphitic carbon with remarkable performances for water electrolysis

Metal/carbon composite materials are highly promising electrocatalysts for water electrolysis. In this work, three composites of metal cobalt nanoparticles highly dispersed in N-doped carbon materials were facilely constructed by pyrolysis of different phenylenediamine based Schiff base-Co complexes (PDBs). Interestingly, the composites derived from PDBs based on different phenylenediamine exhibited different morphologies. The superior case is that rodlike composite catalyst was derived from o-phenylenediamine based PDBs. The obtained catalyst exhibited remarkable performances for both cathodic hydrogen evolution reaction (HER) and anodic oxygen evolution reaction (OER), as well as overall water electrolysis. Only 172 and 289 mV of overpotentials and 1.57 V of cell voltage were exhibited at 10 mA cm^?2 for HER, OER and water splitting in 1.0 M KOH, respectively. The catalyst also displayed robust stability and high Faraday efficiency, and thus are potential high-performance catalyst for commercial water electrolysis.     

Elastic modulus of nanocrystalline cemented carbide

The purposes of this work were to obtain the accurate elastic modulus of the nanocrystalline WC–Co cemented carbides, and to propose the mechanism for the difference of elastic modulus between the nanocrystalline and conventional polycrystalline cemented carbides. The nanocrystalline cemented carbide was prepared by spark plasma sintering (SPS) technique. The conventional polycrystalline cemented carbides were prepared by SPS and sinter-HIP techniques as references, respectively. The sintered cemented carbides were characterized by X-ray diffractometry, scanning electron microscopy and the transmission electron microscopy with precession electron diffraction technology. The elastic modulus was obtained by averaging the values measured with the continuous stiffness measurement method of the nanoindentation technology. The results show that the nanocrystalline cemented carbide has a relatively low modulus, which could be attributed to the more interface area and higher fraction ratio of the hcp cobalt phase caused by the rapid heating and cooling process during SPS.     

基于钴改性的钙基吸附剂污泥富氢气化

基于钙基吸附剂的污泥蒸汽气化制取富氢合成气是一种高效环保的污泥处理方式。本文采用溶胶-凝胶法制备了Co改性、Al₂O₃为载体的钙基吸附剂。借助热重分析仪测定不同钙基吸附剂在多个碳酸化和煅烧循环中的CO₂吸附能力和循环稳定性，并在固定床上进行污泥蒸汽气化实验。结果显示：煅烧过程中，以Al₂O₃为载体的钙基吸附剂中的Al₂O₃与CaO生成七铝酸十二钙(Ca₁₂Al₁₄O₃₃)，并表现出优异的孔隙结构的和CO₂吸附能力，其中，Co质量分数为10%的吸附剂在30次循环（700℃碳酸化35min，850℃煅烧5min）中碳酸化率稳定在70%左右；提高气化温度及Co的添加量可促进焦油裂解和甲烷重整反应，显著提高了合成气中H₂的浓度和产量及污泥气化的冷煤气效率，有利于富氢气体的制取；在650℃下，相比于纯CaO，添加Co质量分数为15%的吸附剂时，H₂产量提高了102%，H₂体积分数提高到85%。     

Review on recent advances of zinc substituted cobalt ferrite nanoparticles: Synthesis characterization and diverse applications

Researchers have taken a prodigious consideration in characterizing and synthesizing zinc substituted cobalt ferrite nanoparticles because of their substantial applications across diverse technological and industrial fields. Zinc substituted cobalt ferrite nanoparticles are a class of lenient magnetic nanomaterials, which have potentially high magnetic, optical, electrical, and dielectric properties. These properties include a high value of permeability, low power losses, permittivity, saturation magnetization, coercivity, resistivity, and other beneficial properties that make them promise candidates for applications in various fields. These ferrites are also used in biomedical areas such as MRI and cancer treatments. In electronic fields, zinc substituted cobalt ferrite nanoparticles are used to make transducers, transformers, biosensors, and sensors. Apart from these advantages, they are found in our everyday electronic and electrical appliances like LED bulb, refrigerator, mobile charger, TV, microwave oven, juicer, washing machine, mixer, iron, printer, laptop, mobile, desktop, etc. Hence, the current review reports some properties of these spinel ferrites and emphasizes the different synthesis techniques that can be used to prepare them. Afterward, the impact of dopant on the materials' properties, the characterization techniques, and the momentous application in the present era have been well discussed.     

分光光度法和光度滴定法联合测定湿法炼锌流程中钴渣浸出液中锌钴镍

湿法炼锌流程中钴渣浸出液中含有高浓度的Fe²⁺和Mn²⁺,用分光光度法测定Co²⁺和Ni²⁺时,Fe²⁺-EDTA会严重干扰Co²⁺和Ni²⁺的测定;在用光度滴定法测定Zn²⁺和Co²⁺合量时,Ni²⁺对二甲酚橙指示剂具有封闭作用,Mn²⁺亦与EDTA螯合,导致滴定结果偏高。为消除Fe²⁺和Mn²⁺对Zn²⁺、Co²⁺和Ni²⁺测定的干扰,实验进行氧化分离Fe²⁺和Mn²⁺预处理,在NaAc/Hac缓冲体系下,以EDTA作显色剂用分光光度法测定Co²⁺、Ni²⁺。在波长466nm处,Co²⁺的线性范围为50~500mg/L时与吸光度呈线性,相关系数R²为0.9992;在384nm处,Ni²⁺的线性范围为50~500mg/L时与吸光度呈线性,相关系数R²为0.9998。根据分光光度法测出Ni²⁺物质的量,加入1.1倍的丁二酮肟以除去Ni²⁺,用二甲酚橙为指示剂,EDTA鳌合-光度滴定法测定Zn²⁺、Co²⁺合量,扣减Co²⁺含量得出Zn²⁺含量。选取4个锌湿法炼锌流程中钴渣浸出液实际样品,按照实验方法中的分光光度法测定Co²⁺和Ni²⁺,光度滴定法测定Zn²⁺、Co²⁺合量,Zn²⁺、Co²⁺和Ni²⁺测定结果的相对标准偏差(RSD,n=6)均不大于0.70%,加标回收率分别为99.59%~100.41%、99.69%~100.64%、99.92%~100.08%。     

钴/镍复合中间层真空扩散连接钨与钢

以钴粉/镍箔为复合中间层，采用800，900和1 000 ℃等三种连接温度，加压10 MPa并保温120 min的工艺条件，对钨/钢真空扩散连接. 研究了接头的微观组织、成分分布、力学性能及断口特征. 结果表明，连接温度为800 ℃和900 ℃时，钨/中间层界面金属间化合物生成很少，对应接头抗剪强度分别为186 MPa和172 MPa，断口均位于钨母材中近界面的位置，为典型解理断裂形貌；当连接温度升至1 000 ℃时，钨/中间层界面生成厚度小于2 μm的连续金属间化合物层，接头抗剪强度降至115 MPa，断裂也发生在钨母材中近界面的位置，断口大部分区域为沿晶断裂特征.     

黄豆发芽过程中Zn、Co和Se的富集及交互作用

本研究以黄豆发芽为手段，采用具有交互关联功能的均匀设计U10(103)表设计并实施了Zn、Co、Se三种人体微量元素在黄豆芽菜生长过程的生物富集实验，评价了芽菜样品的Zn、Co和Se富集量以及有机化富集量，研究了不同Zn、Co、Se外源浓度组间样品生物富集量与各元素外源浓度的回归关系，发现了各元素外源浓度对Zn、Co和Se富集的交互作用以及Zn、Co和Se的富集规律。结果表明：交互作用发生在芽菜生长后期（30 h后），[Zn×Co]和[Co×Se]呈现协同作用，外源Se通过双重协同作用促进芽菜吸收Zn，[Zn×Se]和[Zn×Co×Se]呈现拮抗作用，外源Zn通过双重拮抗作用抑制芽菜对Se的吸收；芽菜生长前期（30 h前）元素的有机转化率低，元素的富集是以物理渗析吸收为主，生长后期（30 h后）则通过各元素外源浓度的交互作用产生有机化富集，综合评价结果表明处理方案3、6和9对获得富Zn、Co和Se的芽菜特别有效，特别是处理方案3（Zn2+、Co2+混合液：[Zn2+]=1200 μg/L，[Co2+]=30 μg/L；Se4+溶液：[Se4+]=180 μg/L）45 h的样品达到了最优综合Zn、Co和Se富集：Zn2+ =8.58 mg/kg，Co2+=63.10 μg/kg，Se4+=48.30 μg/kg，有机化率分别为Zn 49.50%，Co 25.94%，Se 56.25%，三个元素的富集总量基本同时达到了Zn、Co和Se在中国膳食指南中推荐摄入量，对于Zn、Co和Se多元富集健康蔬菜的生产实际具有直接的参考作用。     

Highly Stable COF‐Supported Co/Co(OH)2 Nanoparticles Heterogeneous Catalyst for Reduction of Nitrile/Nitro Compounds under Mild Conditions

Ordered nanoporosity in covalent organic framework (COF) offers excellent opportunity for property development. Loading nanoparticles (nPs) onto them is one approach to introducing tailor‐made properties into a COF. Here, a COF–Co/Co(OH)₂ composite containing about 16 wt% of <6 nm sized Co/Co(OH)₂ nPs is prepared on a N‐rich COF support that catalyzes the release of theoretical equivalence of H₂ from readily available, safe, and cheap NaBH₄. Furthermore, the released H₂ is utilized for the hydrogenation of nitrile and nitro compounds to amines under ambient conditions in a facile one‐pot reaction. The COF “by choice” is built from “methoxy” functionalized dialdehydes which is crucial in enabling the complete retention of the COF structure under the conditions of the catalysis, where the regular Schiff bonds would have hydrolyzed. The N‐rich binding pockets in the COF ensure strong nP–COF interactions, which provides stability and enables catalyst recycling. Modeling studies reveal the crucial role played by the COF in exposing the active facets and thereby in controlling the activation of the reducing agent. Additionally, via density functional theory, we provide a rational explanation for how these COFs can stabilize nanoparticles which grow beyond the limiting pore size of the COF and yet result in a truly stable heterogeneous catalyst – a ubiquitous observation. The study underscores the versatility of COF as a heterogeneous support for developing cheap and highly active nonnoble metal catalysts.     

某复杂金多金属矿石选矿试验研究

吉尔吉斯斯坦某金多金属矿石中伴生多种有价元素,有用矿物嵌布状态复杂且嵌布粒度细。针对矿石性质,采用铜优先浮选—金钴混合浮选工艺流程,可初步实现该金多金属矿石中有价金属的有效分选。闭路试验可获得Au品位228.00 g/t、Au回收率12.19%,Ag品位974.00 g/t、Ag回收率37.71%,Cu品位27.590%、Cu回收率80.65%的铜精矿,以及Au品位65.00 g/t、Au回收率57.22%,Ag品位28.00 g/t、Ag回收率17.86%,Co品位0.5500%、Co回收率53.02%的金钴精矿。