臭氧氧化-循环喷淋法处理钨钼选矿废水

采用臭氧氧化-循环喷淋法去除钨钼选矿废水中COD,研究了pH值、臭氧流量、循环频率对COD去除效果的影响。结果表明: 废水COD去除率随pH值、臭氧流量、循环频率增大而增加,在pH值为10、臭氧流量3.0 L/min、循环频率4.0次/min条件下,氧化120 min后废水COD含量由131 mg/L降至11.5 mg/L,COD去除率达91.2%,满足《污水综合排放标准》(GB 8978-1996)一级标准。与O₂、NaClO处理废水COD的对比试验结果表明,循环喷淋法结合O₃表现出较好的COD去除效果。     

Improving room-temperature electrochemical performance of solid-state lithium battery by using electrospun La2Zr2O7 fibers-filled composite solid electrolyte

Low ionic conductivity at room temperature and poor interfacial compatibility are the main obstacles to restrain the practical application of polymer solid electrolytes. In this work, lanthanum zirconate (LZO) fibers were prepared by electrospinning method and used for the first time as fillers in sandwich polypropylene carbonate (PPC)-based solid electrolyte. Meanwhile, a graphite coating was applied on one surface of the composite solid electrolyte (CSE) membrane. The results show that the LZO fibers significantly increases the room-temperature electrochemical performance of the CSE, and the graphite coating enhances the interfacial compatibility between electrolyte and lithium anode. Furthermore, an ultra-thin PPC-LZO CSE with a total thickness of 22 μm was prepared and used in NCM622/CSE/Li solid-state cell, which shows an initial discharge capacity of 165.6 mAh/g at the current density of 0.5C and a remaining capacity of 113.0 mAh/g after 250 cycles at room temperature. Rise to 1C, the cell shows an initial discharge capacity of 154.2 mAh/g with a remaining capacity of 95.6 mAh/g after 250 cycles. This ultra-thin CSE is expected to be widely applied in high energy-density solid-state battery with excellent room-temperature electrochemical performances.     

印度洋海盆沉积物中稀土的赋存状态及其浸出研究

印度洋海盆沉积物作为重要的稀土资源，已成为保障我国稀土供应的重要途径。为探究利用印度洋海盆沉积物提取稀土的可行性，通过激光粒度分析、化学物相分析、SEM分析等考察了某印度洋海盆沉积 物中稀土元素赋存状态，并采用硫酸为浸出剂，研究硫酸浓度、液固比、浸出温度及时间对稀土浸出率的影响，对最佳条件下获得的浸出液通过氨水中和沉淀净化。结果表明：①沉积物颗粒极细，体积平均粒径仅 4.47 μm，其主要矿物组成为黏土、锰氧化物、石英、长石、云母、绿泥石和石盐，其中稀土主要赋存于磷灰石中，占总稀土比例达73.10%；②在硫酸浓度2 mol/L，液固比7∶1，浸出温度55 ℃，浸出时间120 min的 最佳条件下，主要稀土元素La、Ce、Nd和Y的浸出率分别为80.57%，66.33%，88.42%和93.25%，高价值的重稀土Gd、Dy和Er浸出率分别为92.63%、55.30%和93.17%。③稀土浸出液成分复杂，且稀土含量偏低，仅有100 mg/L左右，采用氨水调节pH值至5.14，可有效去除Al和Fe，但稀土损失率也达到了30.85%。该研究结果对进一步开发利用深海稀土资源具有重要意义。     

潮流能水平轴水轮机在剪切来流下的水动力分析

采用基于计算流体力学方法的全尺度数值模拟计算,建立了适用于潮流能水轮机模拟的剪切来流环境,通过数值计算结果,对潮流能水轮机随时间变化的宏观力和流场特征进行了系统分析,探索水轮机在复杂工况下的水动力特性规律。结果表明,水轮机整个叶轮的总体平均受力在剪切流工况中未受到明显影响; 单个叶片的瞬态轴向力系数和瞬态轴向扭矩系数在旋转周期内出现了明显的周期性变化,且周期性变化幅值随转速增大而增大; 非定常的瞬时轴向扭矩和力的周期性振荡容易引起单个叶片的结构性振动,可能对水轮机的机械结构造成影响。     

Super-tough poly(butylene terephthalate) based blends by modification with core-shell structured polyacrylic nanoparticles

Core-shell structured polyacrylic nanoparticles (named CSPN) impact modifiers consisting of a rubbery poly(n-butyl acrylate) core and a rigid poly(methyl methacrylate) shell with a size of about 352 nm were synthesized by seed emulsion polymerization. The CSPN modifier with core-shell weight ratio 80/20 was used to toughen poly(butylene terephthalate) (PBT) by melt blending. With an increase in CSPN content, the impact strength and the elongation at break of PBT/CSPN blends increased significantly compared with those of PBT; however, the tensile strength decreased. It was found that the polymerization had a very high instantaneous conversion (> 93%) and overall conversion (99%). The core-shell structure of CSPN was examined by means of transmission electron microscope. Scanning electron microscope was used to observe the morphology of CSPN particle and fractured surfaces of the blends. The dynamic mechanical analyses of PBT/CSPN blends showed two merged transition peaks of PBT matrix, with the presence of CSPN modifier, which was responsible for the improvement of PBT toughness. The results indicated that the notched impact strength of PBT/CSPN blend with a weight ratio of 80/20 was 8.61 times greater than that of pure PBT where the brittle-ductile transition point appeared.     

剪切解络-超滤分离金属关键指标预测与验证

根据剪切解络-超滤过程中金属离子的动态浓度关系和质量守恒定律,采用CodeBlocks17.12软件编写程序,建立了剪切解络-超滤工艺关键指标预测模型,实现了金属离子浓度、回收率、体积稀释倍数等指标的预测,并用实验加以验证。依次在转速800 r/min、1 400 r/min、3 000 r/min下回收模拟废水中43 μg/L的Co²⁺、995 μg/L的Ni²⁺和88 μg/L的La³⁺,3种金属的回收率均达99.8%以上时,超滤过程体积稀释倍数的预测值分别为7.0、7.5、5.75,实验值分别为7.5、7.25、6.25,可见预测值与实验值基本一致。本模型对研究方案制定和调整有实际指导意义。     

Toward high performance solid-state lithium-ion battery with a promising PEO/PPC blend solid polymer electrolyte

A promising solid polymer blend electrolyte is prepared by blending of poly(ethylene oxide) (PEO) with different content of amorphous poly(propylene carbonate) (PPC), in which the amorphous property of PPC is utilized to enhance the amorphous/free phase of solid polymer electrolyte, so as to achieve the purpose of modifying PEO-based solid polymer electrolyte. It indicates that the blending of PEO with PPC can effectively reduce the crystallization and increase the ion conductivity and electrochemical stability window of solid polymer electrolyte. When the content of PPC reaches 50%, the ionic conductivity reaches the maximum, which is 2.04 × 10⁻⁵ S cm⁻¹ and 2.82 × 10⁻⁴ S cm⁻¹ at 25°C and 60°C, respectively. The electrochemical stability window increases from 4.25 to 4.9 V and the interfacial stability of lithium metal anode is also greatly improved. The solid-state LiFePO₄//Li battery with the PEO/50%PPC blend solid polymer electrolyte has good cycling stability, which the maximum discharge specific capacity is up to 125 mAh g⁻¹ at a charge/discharge current density of 0.5 C at 60°C.     

入口弯管对矿用轴流通风机气动性能影响的数值研究

以某大型矿用低压轴流式通风机为研究对象, 采用气体动力学性能试验和数值模拟的方法研究了不同入口弯管对风机性能的影响, 重点分析了入口弯管引起的叶轮内部流动特征和损失分布的变化规律。研究结果表明, 风机入口采用弯管连接缩短了进口管道的轴向长度, 节省了地下空间, 但同时来流的均匀性受到影响。弯管内气流速度梯度较大, 管道内侧易发生流动分离, 产生回流区, 增大了流体流动时的能量损失, 风机的整体性能下降。弯管与叶轮入口之间的连接长度会影响内部流场, 当附加直管段较长时, 来流均匀性得到提高, 风机性能有所改善。     

北洺河铁矿全尾砂胶结充填治理塌陷区的可行性研究

北洺河铁矿为践行“绿水青山就是金山银山”的绿色发展理念,探索利用选厂尾矿治理地表塌陷区方案。通过对北洺河铁矿塌陷区稳定性分析以及对全尾砂膏体制备、输送、胶结充填技术可行性试验研究,并结合经济估算、环境和社会效益等综合分析,认为全尾砂胶结充填治理塌陷区的方案可行。     

Hydrothermal-assisted synthesis of surface aluminum-doped LiCoO2 nanobricks for high-rate lithium-ion batteries

LiCoO₂ nano-particles precursor was synthesized through a mixed-alkalis (LiOH-NaOH) hydrothermal reaction, and finally sintered into LiCoO₂ nanobricks with a sickness of ~300?nm. This LiCoO₂ nanobrick cathode delivered a specific capacity of 131.8 mAh g^?1 at 1?C between 3.0 and 4.2?V and 90% capacity retention after 100 cycles. Those synthesized LiCoO₂ nanobricks were further treated by surface Al³⁺ doping to achieve much enhanced 4.5?V lithium storage capability and cycling stability. EIS results showed the surface Al³⁺ doping operation can signification decrease the charge-transfer resistances of the LiCoO₂ cathodes for both before and after cyclings.