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Evaluation of steel metallurgical dust management: combining treatment methods and resource attributes 钢铁冶金粉尘管理评估:处理方法与资源属性相结合
IF 6.9 2区 环境科学与生态学 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-19 DOI: 10.1016/j.psep.2024.09.052
The escalating challenges of resource scarcity and environmental pressures have drawn significant attention to heavy metal-containing dust generated during steel production. While previous research on heavy metals in steel manufacturing has primarily focused on emission inventories, health and ecological risks, and recycling technologies, the assessment of steel metallurgical dust management has been largely overlooked. To address this research gap, this study employed statistical entropy analysis to evaluate the effectiveness of dust treatment in the steel production process, aiming to identify potential issues in dust management. Furthermore, an evaluation framework was established to systematically assess the resource attributes of steel metallurgical dust, thereby supporting evidence-based decision-making in dust management. Results indicate that Cd, Pb, As, Zn, Cr, and Hg tend to accumulate in dust during steel production. Given its high resource attribute, converter dust should be prioritized for recovery. Further analysis suggests that the rotary kiln process plays a transitional role in dust recovery. This study provides a scientific foundation for dust management in the steel industry and offers guidance for the sustainable development of dust utilization.
资源匮乏和环境压力带来的挑战不断升级,使钢铁生产过程中产生的含重金属粉尘备受关注。以往对钢铁生产过程中重金属的研究主要集中在排放清单、健康和生态风险以及回收技术方面,而对钢铁冶金粉尘管理的评估在很大程度上被忽视了。针对这一研究空白,本研究采用统计熵分析法评估钢铁生产过程中粉尘处理的有效性,旨在找出粉尘管理中的潜在问题。此外,还建立了一个评估框架,用于系统评估钢铁冶金粉尘的资源属性,从而为粉尘管理中的循证决策提供支持。结果表明,在钢铁生产过程中,镉、铅、砷、锌、铬和汞容易在粉尘中积累。鉴于转炉粉尘的高资源属性,应优先对其进行回收。进一步分析表明,回转窑工艺在粉尘回收中起着过渡作用。这项研究为钢铁行业的粉尘管理提供了科学依据,并为粉尘利用的可持续发展提供了指导。
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引用次数: 0
Study on the radon exhalation rate of phyllite under thermal effects 热效应下辉绿岩的氡呼出速率研究
IF 6.9 2区 环境科学与生态学 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-19 DOI: 10.1016/j.psep.2024.09.076

As a result of human underground mining activities, phyllite has been extensively reused to make raw ceramic materials and concrete aggregates. Building materials are a significant source of indoor radon, and radon gas emitted from phyllite poses radiation risks to humans. High temperatures can alter the structural properties of rocks, impacting radon exhalation. Thus, this study examined phyllite's radon exhalation rate after heat treatment ranging from 25 °C to 1000 °C. The effects of changes in pore structure and mineral composition on phyllite's radon exhalation were analyzed in detail using nuclear magnetic resonance (NMR), polarizing optical microscopy (POM), three-dimensional microscopy (3DM), and scanning electron microscopy (SEM). Results indicate that the radon exhalation rate initially increases and then decreases with rising temperature. This rate correlates positively with both total porosity and micropore porosity. Processes such as free water evaporation, pyrite oxidation, quartz phase transformation, and chlorite dehydroxylation within phyllite contribute to pore development and the movement of free radon within pore spaces. The highest total porosity and radon exhalation rate occur at 700 °C, measuring 8.6 % and 6.14 Bq/m2·h, respectively—4.30 times and 1.18 times higher than at 25 °C. Additionally, mineral decomposition and melting reduce pore connectivity and effective porosity, hindering radon migration. These findings offer guidance for assessing radon radiation risks and indoor radon potential in phyllite-based building materials.

由于人类的地下采矿活动,辉绿岩被广泛地重新用于制造陶瓷原料和混凝土骨料。建筑材料是室内氡的一个重要来源,辉绿岩释放的氡气对人类构成辐射风险。高温会改变岩石的结构特性,影响氡的散发。因此,本研究考察了辉绿岩在经过 25 °C 至 1000 °C 的热处理后的氡呼出率。利用核磁共振、偏振光学显微镜、三维显微镜和扫描电子显微镜详细分析了孔隙结构和矿物成分变化对辉绿岩氡呼出的影响。结果表明,随着温度的升高,氡的呼出速率先是增加,然后减少。该速率与总孔隙率和微孔孔隙率呈正相关。辉绿岩中的游离水蒸发、黄铁矿氧化、石英相变和绿泥石脱羟基等过程促进了孔隙发育和游离氡在孔隙中的移动。总孔隙率和氡呼出率在 700 °C 时最高,分别为 8.6 % 和 6.14 Bq/m2-h,比 25 °C 时分别高出 4.30 倍和 1.18 倍。此外,矿物分解和熔化降低了孔隙连通性和有效孔隙度,阻碍了氡的迁移。这些发现为评估基于辉绿岩的建筑材料的氡辐射风险和室内氡潜力提供了指导。
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引用次数: 0
Experimental study on emissions and particulate characteristics of diesel engine fueled with plastic waste oil, acetone-butanol-ethanol and diesel blends 以塑料废油、丙酮-丁醇-乙醇和柴油混合物为燃料的柴油发动机的排放和颗粒特性实验研究
IF 6.9 2区 环境科学与生态学 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.psep.2024.09.060

Plastic waste poses a significant environmental challenge due to its non-biodegradable nature and accumulation in landfills. Converting plastic waste into usable fuel could offer a promising solution for mitigating these issues while addressing the emission-related challenges of diesel engines. This study investigates the impact of plastic waste oil (WPO) obtained through pretreatment and catalytic pyrolysis, blended with acetone-butanol-ethanol (ABE) and diesel fuel, on diesel engine. The aim was to evaluate how these blends affect gaseous emissions, organic compounds, and particle-bound carbon, focusing on their potential to reduce harmful pollutants compared to pure diesel fuel. The results indicated that the ABE5W15D blend significantly reduced smoke and CO emissions by 35.7 % and 17.43 %, respectively, with a slight decrease in HC emissions. However, the ABE20W blend showed elevated NOx levels due to higher ignition delay and increased cylinder pressure. Compared to pure diesel (D100), ABE10W10D and ABE5W15D blends reduced total polycyclic aromatic hydrocarbons (PAHs) emissions by 26.8 % and 37.4 %, respectively. Naphthalene was the dominant PAH, remarkably increasing with W20D use, while longer-chain alkanes associated with lubricant oil had higher W20D emissions. The ABE5W15D blend notably reduced organic carbon (OC) emissions by approximately 38.26 % compared to D100. ABE20D exhibited lower elemental carbon (EC) emissions than D100, although it had higher EC than OC. The W20D blend resulted in larger particle diameters, whereas ABE10W10D showed lower particle counts in the 7–15 nm range. In conclusion, blending plastic waste oil with ABE and diesel fuel can effectively mitigate certain pollutants, depending on the blend composition.

塑料废弃物由于其不可生物降解的特性以及在垃圾填埋场的堆积,给环境带来了巨大的挑战。将塑料废弃物转化为可用燃料可以为缓解这些问题提供一个很有前景的解决方案,同时解决柴油发动机排放相关的难题。本研究调查了通过预处理和催化热解获得的塑料废油(WPO)与丙酮-丁醇-乙醇(ABE)和柴油混合后对柴油发动机的影响。目的是评估这些混合燃料对气体排放、有机化合物和颗粒结合碳的影响,重点是与纯柴油相比,它们减少有害污染物的潜力。结果表明,ABE5W15D 混合燃料可显著减少烟雾和 CO 排放,分别减少 35.7% 和 17.43%,HC 排放也略有减少。然而,由于点火延迟和气缸压力增加,ABE20W 混合燃料的氮氧化物水平升高。与纯柴油(D100)相比,ABE10W10D 和 ABE5W15D 混合燃料的多环芳烃(PAHs)排放总量分别减少了 26.8% 和 37.4%。萘是主要的多环芳烃,随着使用 W20D 而显著增加,而与润滑油相关的长链烷烃的 W20D 排放量更高。与 D100 相比,ABE5W15D 混合物显著减少了约 38.26% 的有机碳 (OC) 排放量。ABE20D 的元素碳 (EC) 排放量低于 D100,尽管其 EC 高于 OC。W20D 混合物的颗粒直径更大,而 ABE10W10D 在 7-15 纳米范围内的颗粒数量更少。总之,将塑料废油与 ABE 和柴油混合可有效减少某些污染物,具体取决于混合成分。
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引用次数: 0
PbSO4 decomposition kinetic and phase transformation mechanism during lead waste recycling 铅废物回收过程中 PbSO4 的分解动力学和相变机制
IF 6.9 2区 环境科学与生态学 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.psep.2024.09.074
PbSO4 is the main component of lead paste, lead smoke and other lead-containing solid wastes. It usually matches with the primary lead concentrate to co-smelt for lead extraction, mostly in the oxidation smelting stage. The lead waste quickly experiences different temperature and atmosphere fields from feeding the furnace to the completion of the reactions. This work investigated PbSO4 decomposition kinetic and phase transformation mechanism during lead waste pyrometallurgical recycling. The results show that the activation energy of the decomposition reaction of PbSO4 at 800 ℃∼1000 ℃ in Ar atmosphere is 121.35 kJ/mol. The PbSO4 decomposition reaction in Ar and Air is a multi-step decomposition process, which may undergo PbSO4 → PbO·PbSO4 → 2PbO·PbSO4 → 4PbO·PbSO4 → PbO. PbO is not generated through direct decomposition of PbSO4. The results are expected to provide guidance for the lead wastes co-smelting process to achieve a target PbSO4 decomposition product.
PbSO4 是铅膏、铅烟和其他含铅固体废物的主要成分。它通常与原生铅精矿相匹配,共同熔炼提炼铅,主要是在氧化熔炼阶段。铅废料从进炉到反应结束,会迅速经历不同的温度场和气氛场。这项工作研究了铅废料火法冶炼回收过程中 PbSO4 的分解动力学和相变机理。结果表明,在 800 ℃∼1000 ℃ 的 Ar 大气中,PbSO4 分解反应的活化能为 121.35 kJ/mol。PbSO4 在 Ar 和空气中的分解反应是一个多步骤分解过程,可能经历 PbSO4 → PbO-PbSO4 → 2PbO-PbSO4 → 4PbO-PbSO4 → PbO。PbSO4 的直接分解不会产生 PbO。预计研究结果将为铅废物共熔工艺提供指导,以实现目标 PbSO4 分解产物。
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引用次数: 0
A large-scale-outdoor continuous release of cryogenic liquid onto ground 向地面连续释放大规模室外低温液体
IF 6.9 2区 环境科学与生态学 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-17 DOI: 10.1016/j.psep.2024.09.070

The accidental release of cryogenic liquids can cause several hazards to humans, assets, and the environment. Therefore, this phenomenon has drawn significant attention and has been investigated as part of quantitative risk assessment associated with the use of cryogenic liquids. However, the effects of release conditions on pool spread have not been thoroughly studied, and the mechanism of pool retraction has not been discussed. In this study, an attempt was made to address these gaps by both experimental and numerical analyses. Firstly, large-scale-outdoor release tests with a systematic measurement system were performed using liquid nitrogen to compare with large-scale release tests of liquid hydrogen. The release height and orientation were varied. It was observed that the pool shape was affected by the release orientation. However, the maximum pool size and average vaporization rate were insensitive to both the release height and orientation. The conductive heat from the ground was confirmed to be the major heat source for pool vaporization, accounting for over 90 % of the total heat transferred into the liquid pool. Subsequently, release scenarios were simulated using integral source models. Especially, several hypotheses were thoroughly discussed, implemented in the source models, and validated against experimental results to determine the most appropriate mechanism for pool retraction. The findings of this study are expected to be beneficial for the consequence estimation of cryogenic release scenarios and for the validation and improvement of source models.

低温液体的意外泄漏会对人体、资产和环境造成多种危害。因此,这一现象引起了人们的极大关注,并作为与使用低温液体相关的定量风险评估的一部分进行了调查。然而,释放条件对池扩散的影响尚未得到深入研究,池回缩的机理也未得到讨论。本研究试图通过实验和数值分析来弥补这些不足。首先,利用系统测量系统,使用液氮进行了大规模室外释放试验,以便与液氢的大规模释放试验进行比较。释放的高度和方向是变化的。结果表明,池的形状受释放方向的影响。但是,最大池体尺寸和平均汽化率对释放高度和方向都不敏感。经证实,来自地面的传导热是液池汽化的主要热源,占传入液池总热量的 90% 以上。随后,利用积分源模型模拟了释放情景。特别是,对几种假设进行了深入讨论,并在源模型中实现了这些假设,还根据实验结果进行了验证,以确定最合适的液池回缩机制。预计本研究的结果将有助于低温释放情景的后果估计以及源模型的验证和改进。
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引用次数: 0
Strategies for effective foam mitigation in industrial biodigestors: A state-of-the-art analysis 在工业生物消化器中有效减少泡沫的策略:最新分析
IF 6.9 2区 环境科学与生态学 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-17 DOI: 10.1016/j.psep.2024.09.059

In the renewable energies scenario, biogas has several advantages, such as reducing greenhouse gas emissions, the possibility of decentralized production, and using a wide variety of substrates. Many operational factors significantly impact biogas production efficiency, and failure to ideally align them can lead to adverse situations in the production process. In this context, uncontrolled foam formation is one of these main negative factors. To obtain a better understanding of foam formation during biogas production, this article carried out a survey of the most likely causes. The most relevant factors found are the inefficient agitation system, the excess organic loading rate into the equipment, and the stress of the microbial community. In addition, ways of mitigating the formed foam were investigated, and this work provides effective guidelines to overcome this problem, such as maintaining the agitation efficiently, regulating temperature and pH within ideal ranges, and controlling the microbial community with the application of antifoams being the most relevant action. Therefore, understanding the mechanisms of foam formation and mitigation methods will help develop more efficient forms of industrial operation. Finally, future research directions were proposed for anaerobic digestion and foam formation.

在可再生能源领域,沼气具有多种优势,如减少温室气体排放、可分散生产以及可使用多种基质。许多操作因素都会对沼气生产效率产生重大影响,如果不能理想地调整这些因素,就会导致生产过程中出现不利情况。在这种情况下,不受控制的泡沫形成就是这些主要负面因素之一。为了更好地了解沼气生产过程中泡沫的形成,本文对最可能的原因进行了调查。发现最相关的因素是搅拌系统效率低下、设备中有机物负载率过高以及微生物群落的压力。此外,文章还研究了缓解泡沫形成的方法,为解决这一问题提供了有效的指导,如保持高效搅拌、在理想范围内调节温度和 pH 值以及控制微生物群落,其中应用消泡剂是最相关的措施。因此,了解泡沫的形成机制和缓解方法将有助于开发更有效的工业运行形式。最后,提出了厌氧消化和泡沫形成的未来研究方向。
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引用次数: 0
Cost-efficient electrosynthesis of hydrogen peroxide in acidic and neutral solutions 在酸性和中性溶液中经济高效地电合成过氧化氢
IF 6.9 2区 环境科学与生态学 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-17 DOI: 10.1016/j.psep.2024.09.056
Oxygen reduction reaction is considered a green and low-carbon approach for H2O2 production. Low space-time yield and high energy consumption are serious challenges to the implementation of a commercial scale now. A cost-efficient H2O2 electrosynthesis using a recycled gold catalyst is developed here. The carbon-supported gold catalyst is synthesized using electroplating gold wastewater, which indicates good catalysis performances for both sulfite oxidation and H2O2 production. The sulfite/air fuel cell adopting the bifunctional gold catalyst can directly produce 8.70±0.53 g L−1 H2O2 in 0.5 mol L−1 Na2SO4 solution, with a good current efficiency of 71.56 %±2.13 % and a remarkable space-time yield of 27.20±1.17 mg cm−2 h−1. Adopting the desulfurization solution from flue gas as the anodic sacrificial agent, the electricity costs for acidic and neutral H2O2 electrosynthesis are only 2.09–3.82 kWh kg−1. The reported H2O2 electrosynthesis performances, especially for power consumption, are also summarized and compared.
氧还原反应被认为是生产 H2O2 的绿色低碳方法。低时空产率和高能耗是目前实现商业规模的严峻挑战。本文开发了一种使用回收金催化剂的经济高效的 H2O2 电合成方法。碳支撑金催化剂是利用电镀金废水合成的,对亚硫酸盐氧化和 H2O2 生产均有良好的催化性能。采用双功能金催化剂的亚硫酸盐/空气燃料电池可在 0.5 mol L-1 Na2SO4 溶液中直接产生 8.70±0.53 g L-1 H2O2,电流效率为 71.56 %±2.13 %,时产率为 27.20±1.17 mg cm-2 h-1。采用烟气脱硫溶液作为阳极牺牲剂,酸性和中性 H2O2 电合成的电费仅为 2.09-3.82 kWh kg-1。此外,还总结并比较了已报道的 H2O2 电合成性能,尤其是耗电量。
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引用次数: 0
Investigation of microstructure, hydrogen storage performance of Re-Mg-based alloy modified by RE2O3 (RE = Dy, Er, Yb) 用 RE2O3(RE = Dy、Er、Yb)改性 Re-Mg 基合金的微观结构和储氢性能研究
IF 7.8 2区 环境科学与生态学 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-17 DOI: 10.1016/j.psep.2024.09.061
Hui Yong, Pei Yan, Yiwan Chen, Qianqian Zhang, Shuai Wang, Zhigao Sheng, Jifan Hu
In order to further study the hydrogen storage mechanism of Mg-based hydrogen storage materials, Mg90Ce5Y5 alloy was used as the basis, and three kinds of heavy rare earth oxides were doped into the alloy by ball milling technology. The microstructure and hydrogen storage properties were characterized by XRD, SEM, TEM and PCI. The results show that the hydrogen absorption rate and discharge rate of modified Mg90Ce5Y5 alloy are significantly increased, and the performance is Er2O3 > Dy2O3 > Yb2O3. The hydrogen storage capacity of Er2O3 catalyzed samples is 5.02 wt%, which is higher than 4.82 wt% and 4.80 wt% of Dy2O3 and Yb2O3 catalyzed samples. The hydrogen absorption saturation rate of the sample catalyzed by Er2O3 for 2 min is ∼90 %, the complete release of hydrogen only takes 50 min at 573 K, and the dehydrogenation activation energy is 76.9 kJ/mol. The hydrogen absorption and emission rate is fast, and the dehydrogenation activation energy is slightly lower than that of the other two catalysts. In the process of hydrogen absorption and desorption, the three catalysts exhibit different phase transitions, namely DyH2↔DyH3, ErH2↔ErH3 and irreversible YbH2. DyH2↔DyH3, ErH2↔ErH3 phase transitions have the "hydrogen pump" effect, which can effectively improve the hydrogen absorption and desorption kinetic rate of Mg90Ce5Y5 alloy. Some nano-rare earth compounds and phase transformation significantly improve the kinetic properties of the alloy. However, the enthalpy change of all three catalytic alloys is around 76 kJ/mol H2, which is considered only a slight improvement in thermodynamic properties.
为了进一步研究镁基储氢材料的储氢机理,以 Mg90Ce5Y5 合金为基础,通过球磨技术在合金中掺杂了三种重稀土氧化物。通过 XRD、SEM、TEM 和 PCI 对其微观结构和储氢性能进行了表征。结果表明,改性 Mg90Ce5Y5 合金的吸氢率和放电率显著提高,表现为 Er2O3 > Dy2O3 > Yb2O3.Er2O3 催化样品的储氢量为 5.02 wt%,高于 Dy2O3 和 Yb2O3 催化样品的 4.82 wt% 和 4.80 wt%。样品在 Er2O3 催化下 2 分钟的吸氢饱和率为 ∼90 %,在 573 K 下完全释放氢气只需 50 分钟,脱氢活化能为 76.9 kJ/mol。氢气吸收和释放速度快,脱氢活化能略低于其他两种催化剂。在吸氢和脱氢过程中,三种催化剂表现出不同的相变,即 DyH2↔DyH3、ErH2↔ErH3 和不可逆的 YbH2。DyH2↔DyH3、ErH2↔ErH3相变具有 "氢泵 "效应,能有效提高Mg90Ce5Y5合金的吸氢和解吸动力学速率。一些纳米稀土化合物和相变显著改善了合金的动力学特性。不过,这三种催化合金的焓变都在 76 kJ/mol H2 左右,只能算是热力学性质的轻微改善。
{"title":"Investigation of microstructure, hydrogen storage performance of Re-Mg-based alloy modified by RE2O3 (RE = Dy, Er, Yb)","authors":"Hui Yong, Pei Yan, Yiwan Chen, Qianqian Zhang, Shuai Wang, Zhigao Sheng, Jifan Hu","doi":"10.1016/j.psep.2024.09.061","DOIUrl":"https://doi.org/10.1016/j.psep.2024.09.061","url":null,"abstract":"In order to further study the hydrogen storage mechanism of Mg-based hydrogen storage materials, Mg<ce:inf loc=\"post\">90</ce:inf>Ce<ce:inf loc=\"post\">5</ce:inf>Y<ce:inf loc=\"post\">5</ce:inf> alloy was used as the basis, and three kinds of heavy rare earth oxides were doped into the alloy by ball milling technology. The microstructure and hydrogen storage properties were characterized by XRD, SEM, TEM and PCI. The results show that the hydrogen absorption rate and discharge rate of modified Mg<ce:inf loc=\"post\">90</ce:inf>Ce<ce:inf loc=\"post\">5</ce:inf>Y<ce:inf loc=\"post\">5</ce:inf> alloy are significantly increased, and the performance is Er<ce:inf loc=\"post\">2</ce:inf>O<ce:inf loc=\"post\">3</ce:inf> &gt; Dy<ce:inf loc=\"post\">2</ce:inf>O<ce:inf loc=\"post\">3</ce:inf> &gt; Yb<ce:inf loc=\"post\">2</ce:inf>O<ce:inf loc=\"post\">3</ce:inf>. The hydrogen storage capacity of Er<ce:inf loc=\"post\">2</ce:inf>O<ce:inf loc=\"post\">3</ce:inf> catalyzed samples is 5.02 wt%, which is higher than 4.82 wt% and 4.80 wt% of Dy<ce:inf loc=\"post\">2</ce:inf>O<ce:inf loc=\"post\">3</ce:inf> and Yb<ce:inf loc=\"post\">2</ce:inf>O<ce:inf loc=\"post\">3</ce:inf> catalyzed samples. The hydrogen absorption saturation rate of the sample catalyzed by Er<ce:inf loc=\"post\">2</ce:inf>O<ce:inf loc=\"post\">3</ce:inf> for 2 min is ∼90 %, the complete release of hydrogen only takes 50 min at 573 K, and the dehydrogenation activation energy is 76.9 kJ/mol. The hydrogen absorption and emission rate is fast, and the dehydrogenation activation energy is slightly lower than that of the other two catalysts. In the process of hydrogen absorption and desorption, the three catalysts exhibit different phase transitions, namely DyH<ce:inf loc=\"post\">2</ce:inf>↔DyH<ce:inf loc=\"post\">3</ce:inf>, ErH<ce:inf loc=\"post\">2</ce:inf>↔ErH<ce:inf loc=\"post\">3</ce:inf> and irreversible YbH<ce:inf loc=\"post\">2</ce:inf>. DyH<ce:inf loc=\"post\">2</ce:inf>↔DyH<ce:inf loc=\"post\">3</ce:inf>, ErH<ce:inf loc=\"post\">2</ce:inf>↔ErH<ce:inf loc=\"post\">3</ce:inf> phase transitions have the \"hydrogen pump\" effect, which can effectively improve the hydrogen absorption and desorption kinetic rate of Mg<ce:inf loc=\"post\">90</ce:inf>Ce<ce:inf loc=\"post\">5</ce:inf>Y<ce:inf loc=\"post\">5</ce:inf> alloy. Some nano-rare earth compounds and phase transformation significantly improve the kinetic properties of the alloy. However, the enthalpy change of all three catalytic alloys is around 76 kJ/mol H<ce:inf loc=\"post\">2</ce:inf>, which is considered only a slight improvement in thermodynamic properties.","PeriodicalId":20743,"journal":{"name":"Process Safety and Environmental Protection","volume":null,"pages":null},"PeriodicalIF":7.8,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142275693","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Analysis of the effect of geometric and flow parameters on the separation efficiency of virtual impact separators: Optimization based on response surface methodology 分析几何参数和流动参数对虚拟冲击分离器分离效率的影响:基于响应面方法的优化
IF 6.9 2区 环境科学与生态学 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-17 DOI: 10.1016/j.psep.2024.09.071
Respiratory dust is the primary factor triggering pneumoconiosis. Accurately separating respiratory dust from total dust according to specific criteria are key aspects of respiratory dust monitoring and prevention technology. In this study, we numerically solve the gas-solid two-phase flow within a virtual impactor by coupling computational fluid dynamics (CFD) with the discrete element method (DEM). Here, we explored the air velocity and dust separation efficiency of each component of the virtual impactor to determine optimal structural scale parameters. Accurate 3D printing technology was employed to materialize the three-dimensional structure of the virtual impactor. The separation efficiency of the virtual impactor was evaluated and verified through simulated duct experiments. The results indicate that the weak flow ratio has the most significant effect on separation efficiency, followed by the effect of the ratio of separation chamber diameter to nozzle width (S/W), the ratio of the weak flow outlet size to nozzle width (D/W) aving the smallest degree of influence. When S/W is 1.8, D/W is 1.333, and the weak flow ratio is 0.1, the separation efficiency curves show optimal performance, as confirmed by experimental verification. The experimental verification matched the simulated separation efficiency data within a deviation range of 1.10–11.4 %.
呼吸性粉尘是诱发尘肺病的主要因素。根据特定标准准确分离呼吸性粉尘和总粉尘是呼吸性粉尘监测和预防技术的关键环节。在这项研究中,我们通过将计算流体动力学(CFD)与离散元法(DEM)相结合,对虚拟冲击器内的气固两相流进行了数值求解。在此,我们探讨了虚拟冲击器各组件的气流速度和粉尘分离效率,以确定最佳结构比例参数。我们采用了精确的三维打印技术来实现虚拟冲击器的三维结构。通过模拟管道实验对虚拟冲击器的分离效率进行了评估和验证。结果表明,弱流比对分离效率的影响最大,其次是分离室直径与喷嘴宽度之比(S/W)的影响,弱流出口尺寸与喷嘴宽度之比(D/W)的影响程度最小。当 S/W 为 1.8,D/W 为 1.333,弱流比为 0.1 时,分离效率曲线表现出最佳性能,实验验证也证实了这一点。实验验证与模拟分离效率数据吻合,偏差范围在 1.10-11.4 % 之间。
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引用次数: 0
A strategy for treatment of low-grade ore: Efficient separation and purification of iron 低品位矿石处理战略:高效分离和提纯铁
IF 6.9 2区 环境科学与生态学 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-16 DOI: 10.1016/j.psep.2024.09.069

The gradual depletion of mineral resources has led to the emergence of a new engineering challenge in the field of mineral processing: the effective treatment of low-grade ores. In this study, the low-grade titanium ore leaching solution was employed as the raw material. The extraction ability of a series of hydroxyl extractants for the most common metal iron in minerals was investigated. As a result, a new high-quality processing system for low-grade ore with branched-chain octanol as the core component was constructed. In the treatment of mineral leaching solution, branched-chain octanol has high selectivity and large capacity (111.7 g/L) for iron. It was capable of efficiently removing a significant quantity of iron ions in low-grade ores that were not anticipated to be present. By employing quantum chemical (QC) methodologies, the mechanism for the high selectivity of branched-chain octanol for Fe(Ⅲ) has been elucidated by analyzing the frontier molecular orbital (FMO) energy of acid salts of common metals in minerals. Combined with spectral analysis and slope method, the structure of the extracted complex was confirmed to be [n-R8-OH]2·H·FeCl4. On the basis of system optimization, a three-stage countercurrent extraction and three-stage countercurrent stripping was employed to remove all the Fe(Ⅲ) in the mineral leaching solution. And after detecting, the purity of the obtained Fe(III) solution was greater than 99.5 %. In the treatment of low-grade minerals, especially those containing key metals, the branched-chain octanol extraction system demonstrates high selectivity and reliability, which is a effective means to improve the quality of mineral leaching solution.

随着矿产资源的逐渐枯竭,矿物加工领域出现了一项新的工程挑战:如何有效处理低品位矿石。本研究以低品位钛矿浸出液为原料。研究了一系列羟基萃取剂对矿物中最常见金属铁的萃取能力。由此,构建了以支链辛醇为核心成分的新型低品位矿石高质量处理系统。在处理矿物浸出液时,支链辛醇对铁具有高选择性和大容量(111.7 克/升)。它能够有效地去除低品位矿石中预计不会存在的大量铁离子。利用量子化学(QC)方法,通过分析矿物中常见金属酸盐的前沿分子轨道(FMO)能量,阐明了支链辛醇对铁(Ⅲ)的高选择性机理。结合光谱分析和斜率法,确认提取的配合物结构为[n-R8-OH]2-H-FeCl4。在系统优化的基础上,采用三级逆流萃取和三级逆流汽提,将矿物浸出液中的铁(Ⅲ)全部去除。经检测,得到的 Fe(III) 溶液纯度大于 99.5%。支链辛醇萃取系统在处理低品位矿物,尤其是含关键金属矿物时,具有高选择性和高可靠性,是提高矿物浸出液质量的有效手段。
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引用次数: 0
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Process Safety and Environmental Protection
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