Iron-based sulfur and nitrogen dual doped porous carbon as durable electrocatalysts for oxygen reduction reaction

The widespread use of fuel cell technology is hampered by the use of expensive and scarce platinum metal in electrodes which is required to facilitate the sluggish oxygen reduction reaction (ORR). In this work, a viable synthetic approach was developed to prepare iron-based sulfur and nitrogen dual doped porous carbon (Fe@SNDC) for use in ORR. Benzimidazole, a commercially available monomer, was used as a precursor for N doped carbon and calcined with potassium thiocyanate at different temperatures to tune the pore size, nitrogen content and different types of nitrogen functionality such as pyridinic, pyrrolic and graphitic. The Fe@SNDC–950 with high surface area, optimum N content of about 5 at% and high amount of pyridinic and graphitic N displayed an onset potential and half-wave potential of 0.98 and 0.83 V vs RHE, respectively, in 0.1 M KOH solution. The catalyst also exhibits similar oxygen reduction reaction performance compared to Pt/C (20 wt%) in acidic media. Furthermore, when compared to commercially available Pt/C (20 wt%), Fe@SNDC–950 showed enhanced durability over 6 h and poison tolerance in case of methanol crossover with the concentration up to 3.0 M in oxygen saturated alkaline electrolyte. Our study demonstrates that the presence of N and S along with Fe-N moieties synergistically served as ORR active sites while the high surface area with accessible pores allowed for efficient mass transfer and interaction of oxygen molecules to the active sites contributing to the ORR activity of the catalyst.     

Rational Designs for Lithium-Sulfur Batteries with Low Electrolyte/Sulfur Ratio

Lithium-sulfur batteries (LSBs) are considered a promising next-generation energy storage device owing to their high theoretical energy density. However, their overall performance is limited by several critical issues such as lithium polysulfide (PS) shuttles, low sulfur utilization, and unstable Li metal anodes. Despite recent huge progress, the electrolyte/sulfur ratio (E/S) used is usually very high (≥20 µL mg⁻¹), which greatly reduces the practical energy density of devices. To push forward LSBs from the lab to the industry, considerable attention is devoted to reducing E/S while ensuring the electrochemical performance. To date, however, few reviews have comprehensively elucidated the possible strategies to achieve that purpose. In this review, recent advances in low E/S cathodes and anodes based on the issues resulting from low E/S and the corresponding solutions are summarized. These will be beneficial for a systematic understanding of the rational design ideas and research trends of low E/S LSBs. In particular, three strategies are proposed for cathodes: preventing PS formation/aggregation to avoid inadequate dissolution, designing multifunctional macroporous networks to address incomplete infiltration, and utilizing an imprison strategy to relieve the adsorption dependence on specific surface area. Finally, the challenges and future prospects for low E/S LSBs are discussed.     

Approaching Ultrastable High‐Rate Li–S Batteries through Hierarchically Porous Titanium Nitride Synthesized by Multiscale Phase Separation

Porous architectures are important in determining the performance of lithium–sulfur batteries (LSBs). Among them, multiscale porous architecutures are highly desired to tackle the limitations of single‐sized porous architectures, and to combine the advantages of different pore scales. Although a few carbonaceous materials with multiscale porosity are employed in LSBs, their nonpolar surface properties cause the severe dissolution of lithium polysulfides (LiPSs). In this context, multiscale porous structure design of noncarbonaceous materials is highly required, but has not been exploited in LSBs yet because of the absence of a facile method to control the multiscale porous inorganic materials. Here, a hierarchically porous titanium nitride (h‐TiN) is reported as a multifunctional sulfur host, integrating the advantages of multiscale porous architectures with intrinsic surface properties of TiN to achieve high‐rate and long‐life LSBs. The macropores accommodate the high amount of sulfur, facilitate the electrolyte penetration and transportation of Li⁺ ions, while the mesopores effectively prevent the LiPS dissolution. TiN strongly adsorbs LiPS, mitigates the shuttle effect, and promotes the redox kinetics. Therefore, h‐TiN/S shows a reversible capacity of 557 mA h g^?1 even after 1000 cycles at 5 C rate with only 0.016% of capacity decay per cycle.     

铋精矿加压氧化氨浸高效分离铜、硫和铋

针对湖南柿竹园铋精矿火法冶炼过程中存在的成本高、低浓度SO₂和散烟排放污染环境、有价金属综合回收率低等问题, 以柿竹园铋精矿为原料, 提出了加压氧化氨浸分离铋与铜、硫的新工艺, 研究了氨水加入量、浸出温度、浸出时间、浸出压力及浸出液固比等因素对铜、硫、铋浸出率的影响。在氨水用量1.8 mL/g_铋精矿、液固比4∶1、釜压2.8 MPa、浸出温度160 ℃、浸出时间5 h、搅拌速度600 r/min的优化工艺条件下, 铜、硫浸出率分别达93.57%和92.87%, 铋不浸出并以氧化铋形态全部入渣, 实现了铜、硫与铋的高效分离。     

电化学反应器隔膜材料的分子设计与介尺度策略

电化学反应器中隔膜材料是将正极和负极在电子通路上隔开但在离子传输通路上保持畅通的特殊材料。作为电化学反应器三个关键材料之一，隔膜材料还需耐强酸/强碱和高电压等环境。围绕电化学反应器中隔膜材料，从分子设计的角度针对材料电化学性能与化学稳定性的调控、电化学装置的介观传质性能的促进和改善等研究思路与进展进行了综述，为相关研究提供性能导向的分子设计参考。     

提高Mn系低温脱硝催化剂抗硫抗水性能的国内外研究概述

介绍了氮氧化物的来源、SCR脱硝的反应机理和工艺流程、催化剂的硫和水中毒机理,重点介绍了国内外学术和工业界为提高催化剂抗硫和抗水性能所做的研究和尝试,旨在推动低温SCR技术的进展,促进该技术早日实现在工业上的大规模应用。     

高含硫气田集输系统增压模式优化研究

随着高含硫气田的持续开发,气井井口压力逐步低于集输压力,亟需实施集输系统增压运行。采用OLGA软件,以气液两相流、压降预测、耦合传热理论为基础,针对高含硫气田集输管网高程差、气体组分、液气比、管网全尺寸参数等工况条件,建立了复杂山地高含硫湿气集输系统生产运行的数值模型,以集输系统生产历史数据为基础,验证模型准确性并进行修正。考虑单井、多井或单线配置压缩机等情况,根据开发预测的各井压力变化情况,计算集输管网的压力分布及系统能耗,重点分析了单站增压、区域+单站增压、集输干线增压三种模式,最终优选出高含硫气田集输系统增压模式。     

连续蓄热式生物质气化/燃烧供热系统

生物质能源是一种环境友好的可再生能源,但也存在能量密度低、含水率高、碱金属含量高等缺点,导致其在热利用的过程中存在易结渣、堵灰及腐蚀、热效率不高等问题。本文结合生物质气化、炉内碱金属/硫固定、两级焦油裂解、蓄热式燃烧,以及冷凝热回收等多项先进技术,设计并搭建了连续蓄热式生物质气化/燃烧供热系统。以海洋贝壳类废弃物作为生物质成型燃料的添加剂和生物质焦油裂解过程的催化剂,在实现海洋废弃资源高值化利用的同时,克服了生物质热利用过程中的多项障碍,能够显著提高生物质能热利用效率,同时大幅度降低当前工业及民用供热过程中CO₂、SO_x、NO_x及烟尘的排放,具有良好的经济性与环保性。     

污泥生物炭中氮硫行为及环境效应研究进展

污泥生物炭中氮硫元素含量高，其氮硫行为和环境效应对全球气候变化的影响不容忽视。以往的研究中，研究者往往以富碳生物炭作为主要研究对象，关注碳对全球气候变化的行为和功效，而对氮硫元素的作用关注不够。本文从原始污泥基本性质到其热解过程，再到生物炭的老化，逐步对污泥生物炭整个生命周期内氮硫的行为及其环境效应研究进行综述，并对未来应注重开展的研究方向进行展望，为生物炭中氮硫元素固定、释放及与之关联的环境效应和温室气体排放控制研究提供理论基础。分析表明，污泥中氮元素含量普遍高于硫元素，且热解过程中氮比硫更容易转移至气相产物。氮硫元素随热解温度的增加，在三相产物中的分配都是炭中持续减少，油中先增后减，气中一直增加。高温（＞800℃）条件下，气相中的氮含量高于固相，而硫元素则仍然主要存在于固相中。污泥生物炭老化及其环境效应研究表明，污泥生物炭氮硫元素与土壤的相互作用及其温室效应问题在今后的研究中应引起重视。