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Bio-physical pre-treatments in anaerobic digestion of organic fraction of municipal solid waste to optimize biogas production and digestate quality for agricultural use 对城市固体废物的有机部分进行厌氧消化的生物物理预处理,以优化沼气生产和沼渣质量,供农业使用。
IF 7.1 2区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-08-24 DOI: 10.1016/j.wasman.2024.08.023

This study optimized the anaerobic digestion (AD) of separated collected organic fractions of municipal solid waste (OFMSW) to produce energy and digestate as biofertilizer. Due to OFMSW’s partial recalcitrance to degradation, enzymatic (UPP2, MCPS, USC4, USE2, A. niger) and physical (mechanical blending, heating, hydrodynamic cavitation) pre-treatments were tested. Experimental and modeling approaches were used to compare AD performance regarding energy sustainability and digestate quality. Digestate was separated into solid and liquid fractions, and then chemically and physically characterized by investigating the nutrient release mechanisms. Principal Component Analysis was applied, equally weighing energy and digestate productions. Unlike previous studies focusing only on biogas, this study evaluated the effects of pre-treatments on both biogas and digestate production, viewing AD as a biorefinery process for urban waste valorization. Results showed that all pre-treatments were energetically sustainable, but enzymatic pre-treatments yielded digestates richer in nutrients (increase of 80% N, 200% P and 150% K as compared to OFMSW) and with greater organic matter degradation compared to physical pre-treatments. The liquid fraction of digestate from enzymatic pre-treatments had higher nutrient concentrations, while those from physical pre-treatments had more balanced nutrient content, making them more suitable for fertigation.

本研究优化了城市固体废物(OFMSW)中分离收集的有机组分的厌氧消化(AD),以生产能源和作为生物肥料的沼渣。由于 OFMSW 部分不耐降解,因此测试了酶法(UPP2、MCPS、USC4、USE2、A. niger)和物理(机械混合、加热、流体动力空化)预处理方法。实验和建模方法用于比较厌氧消化(AD)在能源可持续性和沼渣质量方面的性能。沼渣被分离成固体和液体馏分,然后通过研究营养物质的释放机制对其进行化学和物理表征。应用主成分分析法对能源和沼渣产量进行了同等权衡。与以往只关注沼气的研究不同,本研究评估了预处理对沼气和沼渣产量的影响,将厌氧消化(AD)视为城市垃圾价值化的生物精炼过程。结果表明,所有预处理方法在能量上都是可持续的,但与物理预处理方法相比,酶预处理方法产生的沼渣营养成分更丰富(与 OFMSW 相比,氮增加了 80%,磷增加了 200%,钾增加了 150%),有机物降解程度更高。酶法预处理产生的沼渣液态部分养分浓度更高,而物理预处理产生的沼渣液态部分养分含量更均衡,更适合施肥。
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引用次数: 0
Solid waste detection, monitoring and mapping in remote sensing images: A survey 遥感图像中的固体废物检测、监测和绘图:调查
IF 7.1 2区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-08-24 DOI: 10.1016/j.wasman.2024.08.003

The detection and characterization of illegal solid waste disposal sites are essential for environmental protection, particularly for mitigating pollution and health hazards. Improperly managed landfills contaminate soil and groundwater via rainwater infiltration, posing threats to both animals and humans. Traditional landfill identification approaches, such as on-site inspections, are time-consuming and expensive. Remote sensing is a cost-effective solution for the identification and monitoring of solid waste disposal sites that enables broad coverage and repeated acquisitions over time. Earth Observation (EO) satellites, equipped with an array of sensors and imaging capabilities, have been providing high-resolution data for several decades. Researchers proposed specialized techniques that leverage remote sensing imagery to perform a range of tasks such as waste site detection, dumping site monitoring, and assessment of suitable locations for new landfills. This review aims to provide a detailed illustration of the most relevant proposals for the detection and monitoring of solid waste sites by describing and comparing the approaches, the implemented techniques, and the employed data. Furthermore, since the data sources are of the utmost importance for developing an effective solid waste detection model, a comprehensive overview of the satellites and publicly available data sets is presented. Finally, this paper identifies the open issues in the state-of-the-art and discusses the relevant research directions for reducing the costs and improving the effectiveness of novel solid waste detection methods.

非法固体废物处理场的检测和定性对于环境保护,特别是减轻污染和健康危害至关重要。管理不当的垃圾填埋场会通过雨水渗透污染土壤和地下水,对动物和人类造成威胁。传统的垃圾填埋场识别方法,如现场检查,既耗时又昂贵。遥感技术是识别和监测固体废弃物处理场的一种经济有效的解决方案,可实现广泛覆盖和长期重复采集。地球观测(EO)卫星配备了一系列传感器和成像功能,几十年来一直在提供高分辨率数据。研究人员提出了利用遥感图像执行一系列任务的专门技术,如垃圾场探测、倾倒场监测和新垃圾填埋场合适地点评估。本综述旨在通过描述和比较各种方法、已实施的技术和使用的数据,详细说明与固体废物场地检测和监测最相关的建议。此外,由于数据源对于开发有效的固体废物检测模型至关重要,因此本文对卫星和公开可用的数据集进行了全面概述。最后,本文指出了最新技术中尚未解决的问题,并讨论了降低成本和提高新型固体废物检测方法有效性的相关研究方向。
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引用次数: 0
Exploring artificial intelligence role in improving service building engagement in sorting 探索人工智能在提高分类服务建设参与度中的作用。
IF 7.1 2区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-08-22 DOI: 10.1016/j.wasman.2024.07.031

Waste management researchers have identified that the correct disposal of solid waste is better addressed upstream, where people properly sort their solid waste. Sorting solid waste is a practice that requires a behaviour friendly to sorting and willingness to continuously comply with waste management policies. However, the dynamic and ever-changing nature of service buildings’ users makes fostering such behaviour challenging, potentially jeopardizing solid waste sorting efforts. Therefore, in this paper, we explore the possible role of artificial intelligence in alleviating the cumbersome process of sorting solid waste, by developing a virtual assistant that interacts with tenants via verbal and visual inputs to provide them with waste management services and instructions. The virtual assistant utilizes Natural Language Processing and computer vision techniques to enable voice and image recognition functionalities and achieved accuracy levels of 85% and 88% for verbal and visual inputs, respectively. The present work can be a solid foundation to investigate further implementation of virtual assistants to support sustainability practices in Facility Management.

废物管理研究人员发现,正确处理固体废物最好在上游进行,即人们对固体废物进行适当分类。对固体废物进行分类是一种行为习惯,需要人们对分类持友好态度,并愿意持续遵守废物管理政策。然而,服务楼宇用户的动态性和不断变化性使得培养这种行为具有挑战性,有可能危及固体废物分类工作。因此,在本文中,我们探讨了人工智能在减轻繁琐的固体废物分类过程中可能发挥的作用,开发了一个虚拟助手,通过语言和视觉输入与租户互动,为他们提供废物管理服务和说明。该虚拟助手利用自然语言处理和计算机视觉技术实现了语音和图像识别功能,语言和视觉输入的准确率分别达到 85% 和 88%。本研究成果可为进一步研究虚拟助手的实施奠定坚实的基础,以支持设施管理中的可持续发展实践。
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引用次数: 0
Estimating energy left in discarded alkaline batteries: Evaluating consumption and recovery opportunities 估算废弃碱性电池的剩余能量:评估消耗和回收机会
IF 7.1 2区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-08-22 DOI: 10.1016/j.wasman.2024.08.016

Each year, a significant number of single-use alkaline batteries with untapped energy are discarded. This study aims to analyze the usage patterns of alkaline batteries based on a dataset of 1021 used batteries, ranging from Size AA to 9V, collected from households in the State of New York. We measure the energy loss resulting from underutilized batteries and examine the corresponding environmental and economic impacts on a national scale. Discarded AA alkaline batteries maintain about 13 % of their initial energy, that results in an estimated annual energy loss of 660 MWh for all AA alkaline batteries in the U.S., and about 40 MWh in New York State. Annually in the U.S., consumers discard AA alkaline batteries with approximately $80 million worth of unused energy, including $4.8 million in New York State alone. We also show that the lifecycle impact of batteries should be multiplied by 1.25 to account for their underutilization. To address these issues, we propose actionable recommendations for improving battery consumption practices and facilitating End-of-Life/Use (EoL/U) recovery processes. The findings show the need for policy interventions to better manage battery usage and disposal toward reducing energy waste and mitigating environmental impacts.

每年都有大量能量尚未开发的一次性碱性电池被丢弃。本研究旨在根据从纽约州家庭收集的 1021 节废旧电池数据集分析碱性电池的使用模式,这些电池的规格从 AA 到 9V 不等。我们测量了未充分利用电池造成的能源损失,并在全国范围内研究了相应的环境和经济影响。废弃的 AA 碱性电池可保持约 13% 的初始能量,因此估计美国所有 AA 碱性电池的年能量损失为 660 兆瓦时,纽约州约为 40 兆瓦时。在美国,消费者每年丢弃的 AA 碱性电池未使用的能量价值约为 8000 万美元,其中仅纽约州就有 480 万美元。我们还表明,电池的生命周期影响应乘以 1.25,以考虑其利用不足的情况。为解决这些问题,我们提出了可操作的建议,以改进电池消费实践,促进报废/使用(EoL/U)回收流程。研究结果表明,有必要采取政策干预措施,以更好地管理电池的使用和处置,从而减少能源浪费,减轻对环境的影响。
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引用次数: 0
Hydrothermal carbonization of combined food waste: A critical evaluation of emergent products 混合食物垃圾的水热碳化:对新兴产品的重要评估
IF 7.1 2区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-08-21 DOI: 10.1016/j.wasman.2024.08.012

Hydrothermal carbonization (HTC) increasingly appears as an eco-friendly method for managing food waste (FW). In this work, a combination of FW was subjected to HTC, and products were critically evaluated. This involved a lab-scale pressure reactor and optimization of HTC conditions: temperature (220–340 °C) and residence time (90–260 min) via central composite design type of response surface methodology (CCD-RSM). Results showed varying temperatures and residence time to impact the hydrochar (HC) and hydrothermal carbonization aqueous phase (HTC-AP) properties. Although HC produced through HTC exhibited lower ash content (<2%) despite higher fixed carbon (>55 %) with respect to the raw FW, the heating value of HC ranged from 19.2 to 32.5 MJ/kg. Temperature primarily influenced FW conversion, affecting carbonaceous properties. Saturated fatty acids (SFA) were found to be predominant in the HTC-AP under all tested operating conditions (77.3, 48.4, and 37.1 wt% for HTC at 340, 280, and 220 °C in 180 min, respectively). Total phosphorus recovery in HC and HTC-AP respectively peaked at 340 °C and 220 °C in 180 min. The study concludes that HTC holds promise for energy-dense biofuel production, nutrient recovery, and fostering a circular economy.

水热碳化(HTC)作为一种管理食物垃圾(FW)的生态友好型方法日益受到重视。在这项工作中,对 FW 组合进行了氢化热处理,并对产品进行了严格评估。这涉及到一个实验室规模的压力反应器,以及通过响应面方法的中央复合设计类型(CCD-RSM)优化 HTC 条件:温度(220-340 °C)和停留时间(90-260 分钟)。结果表明,不同的温度和停留时间会影响水炭(HC)和水热碳化水相(HTC-AP)的特性。虽然通过水热碳化法生产的碳化炭灰分含量较低(2%),但固定碳含量(55%)却高于原料纤维素,碳化炭的热值介于 19.2 到 32.5 兆焦/千克之间。温度主要影响纤维素的转化,并影响碳质的特性。在所有测试的操作条件下,饱和脂肪酸(SFA)在 HTC-AP 中均占主导地位(180 分钟内,HTC 在 340、280 和 220 °C 下的饱和脂肪酸含量分别为 77.3、48.4 和 37.1 wt%)。HC 和 HTC-AP 的总磷回收率分别在 340 ℃ 和 220 ℃ 的 180 分钟内达到峰值。研究得出结论,HTC 有望用于高能量生物燃料的生产、营养物质的回收以及促进循环经济的发展。
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引用次数: 0
Efficient biodiesel production by sulfonated carbon catalyst derived from waste glycerine pitch via single-step carbonisation and sulfonation 利用从废甘油沥青中提取的磺化碳催化剂,通过一步碳化和磺化法高效生产生物柴油
IF 7.1 2区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-08-21 DOI: 10.1016/j.wasman.2024.08.011

Glycerine pitch is a highly alkaline residue from the oleochemical industry that contains glycerol and contaminants, such as water, soap, salt and ash. In this study, acidic heterogeneous glycerol-based carbon catalysts were synthesised for biodiesel production via single-step partial carbonisation and sulfonation using pure glycerol and glycerine pitch, producing products labelled as SGC and SGPC, respectively. Carbon materials were obtained by heating glycerol and concentrated sulfuric acid (1:3) at 200℃ for 1 h. The produced SGC and SGPC displayed high densities of sulfonic group (–SO3H), i.e. 1.49 and 1.00 mmol·g−1, respectively, alongside carboxylic (–COOH) and phenolic (–OH) acid. In the catalytic evaluation, excellent oleic acid conversions of 96.0 ± 0.4 % and 92.4 ± 0.5 % were achieved using SGC and SGPC, respectively, under optimised reaction conditions: 1:10 M ratio of oleic acid to methanol, 5 % (w/w) catalyst, 64℃ and 5 h. SGPC was found to be recyclable with 68.5 % conversion after the 6th cycle, which was attributed to the loss of –SO3H and catalyst deactivation by the deposition of oleic acid on its surface. Remarkably, despite the impurities present in the glycerine pitch, the obtained results demonstrated that the reactivity of SGPC is comparable to SGC and superior to that of commercial solid acid catalysts, which demonstrated that the presence of impurities appears to have minimal impact on the production of carbon materials and their properties.

甘油沥青是油脂化学工业的一种高碱性残留物,含有甘油和水、肥皂、盐和灰分等污染物。本研究使用纯甘油和甘油沥青,通过单步部分碳化和磺化合成了酸性异相甘油基碳催化剂,用于生产生物柴油,生成的产品分别称为 SGC 和 SGPC。碳材料由甘油和浓硫酸(1:3)在 200℃加热 1 小时获得。生成的 SGC 和 SGPC 与羧酸(-COOH)和酚酸(-OH)一起显示出较高的磺酸基(-SO3H)密度,即分别为 1.49 和 1.00 mmol-g-1。在催化评估中,在优化的反应条件下,使用 SGC 和 SGPC 的油酸转化率分别达到 96.0 ± 0.4 % 和 92.4 ± 0.5 %:在第 6 个循环后,SGPC 的转化率为 68.5%,可回收利用,这归因于 -SO3H 的损失以及油酸沉积在催化剂表面导致的催化剂失活。值得注意的是,尽管甘油沥青中存在杂质,但所得结果表明 SGPC 的反应活性与 SGC 相当,优于商用固体酸催化剂,这表明杂质的存在似乎对碳材料的生产及其性能影响甚微。
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引用次数: 0
Enhanced reducing capacity of citric acid for lithium-ion battery recycling under microwave-assisted leaching 在微波辅助浸出条件下提高柠檬酸在锂离子电池回收中的还原能力。
IF 7.1 2区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-08-14 DOI: 10.1016/j.wasman.2024.08.004

The management and sustainable recycling of spent lithium-ion batteries (LIBs) holds critical importance from both economic and environmental standpoints. H2O2 and ascorbic acid are widely used inorganic and organic reductants in the hydrometallurgical process for battery recycling. In this study, citric acid, as a reductant, was found to have superior metal leaching efficiencies under microwave-assisted leaching than H2O2 and ascorbic acid. The enhanced performance was attributed not only to the inherent reducing property of citric acid but also to the chelation of citric acid with Cu and Fe, resulting in the formation of reductive radicals under microwave. The effect of acid type, H2SO4 concentration, citric acid concentration, solid-liquid (S/L) ratio, reaction time, and temperature were investigated. 99.5 % of Li, 99.7 % of Mn, 99.5 % of Co, and 99.3 % of Ni were leached from spent lithium nickel manganese cobalt oxides (NCM) battery black mass using 0.2 mol/L H2SO4 and 0.05 mol/L citric acid at 120 °C for 20 min with a fixed S/L ratio of 10 g/L in the microwave-assisted leaching process. Leaching kinetic results were best fitted with the Avrami model, suggesting that the microwave-assisted leaching process was controlled by diffusion. The leaching activation energies of Li, Mn, Co, and Ni were 30.11 kJ/mol, 27.48 kJ/mol, 21.32 kJ/mol, and 33.29 kJ/mol, respectively, providing additional evidence that supports the proposed diffusion-controlled microwave-assisted leaching mechanism. This method provided a green and efficient solution for spent LIBs recycling.

从经济和环境角度来看,废旧锂离子电池(LIB)的管理和可持续回收利用都至关重要。H2O2 和抗坏血酸是电池回收湿法冶金工艺中广泛使用的无机和有机还原剂。本研究发现,在微波辅助浸出过程中,作为还原剂的柠檬酸比 H2O2 和抗坏血酸具有更高的金属浸出效率。性能提高的原因不仅在于柠檬酸固有的还原性,还在于柠檬酸与铜和铁螯合,从而在微波下形成还原自由基。研究了酸的种类、H2SO4 浓度、柠檬酸浓度、固液(S/L)比、反应时间和温度的影响。在微波辅助浸出过程中,使用 0.2 摩尔/升 H2SO4 和 0.05 摩尔/升柠檬酸,在 120 °C、20 分钟、固液比 10 克/升的条件下,从废旧锂镍锰钴氧化物(NCM)电池黑中浸出了 99.5%的锂、99.7%的锰、99.5%的钴和 99.3%的镍。浸出动力学结果与 Avrami 模型的拟合效果最佳,表明微波辅助浸出过程受扩散控制。锂、锰、钴和镍的浸出活化能分别为 30.11 kJ/mol、27.48 kJ/mol、21.32 kJ/mol 和 33.29 kJ/mol,为提出的扩散控制微波辅助浸出机制提供了更多证据。该方法为废锂电池的回收提供了一种绿色高效的解决方案。
{"title":"Enhanced reducing capacity of citric acid for lithium-ion battery recycling under microwave-assisted leaching","authors":"","doi":"10.1016/j.wasman.2024.08.004","DOIUrl":"10.1016/j.wasman.2024.08.004","url":null,"abstract":"<div><p>The management and sustainable recycling of spent lithium-ion batteries (LIBs) holds critical importance from both economic and environmental standpoints. H<sub>2</sub>O<sub>2</sub> and ascorbic acid are widely used inorganic and organic reductants in the hydrometallurgical process for battery recycling. In this study, citric acid, as a reductant, was found to have superior metal leaching efficiencies under microwave-assisted leaching than H<sub>2</sub>O<sub>2</sub> and ascorbic acid. The enhanced performance was attributed not only to the inherent reducing property of citric acid but also to the chelation of citric acid with Cu and Fe, resulting in the formation of reductive radicals under microwave. The effect of acid type, H<sub>2</sub>SO<sub>4</sub> concentration, citric acid concentration, solid-liquid (S/L) ratio, reaction time, and temperature were investigated. 99.5 % of Li, 99.7 % of Mn, 99.5 % of Co, and 99.3 % of Ni were leached from spent lithium nickel manganese cobalt oxides (NCM) battery black mass using 0.2 mol/L H<sub>2</sub>SO<sub>4</sub> and 0.05 mol/L citric acid at 120 °C for 20 min with a fixed S/L ratio of 10 g/L in the microwave-assisted leaching process. Leaching kinetic results were best fitted with the Avrami model, suggesting that the microwave-assisted leaching process was controlled by diffusion. The leaching activation energies of Li, Mn, Co, and Ni were 30.11 kJ/mol, 27.48 kJ/mol, 21.32 kJ/mol, and 33.29 kJ/mol, respectively, providing additional evidence that supports the proposed diffusion-controlled microwave-assisted leaching mechanism. This method provided a green and efficient solution for spent LIBs recycling.</p></div>","PeriodicalId":23969,"journal":{"name":"Waste management","volume":null,"pages":null},"PeriodicalIF":7.1,"publicationDate":"2024-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141989068","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
Selective removal of iron from sulfuric acid leaching solution of aerospace magnetic material scraps by jarosite process 用贾洛石工艺选择性去除航空航天磁性材料废料硫酸浸出液中的铁
IF 7.1 2区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-08-13 DOI: 10.1016/j.wasman.2024.08.007

Aerospace magnetic material scraps are abundant in cobalt and nickel. Sulfuric acid leaching process is an efficient method for extracting them. But it is a non-selective process, a significant amount of iron dissolves in the solution. This study focuses on the selective removal of iron from this solution using the jarosite process. Eh-pH diagram of K-S-Fe-H2O system was established. Based on thermodynamic analysis, H2O2 is used to oxidize Fe2+ into Fe3+, achieving efficient and selective removal of iron from the solution containing cobalt and nickel. The optimal conditions are as follows: temperature 95°C, K2SO4 dosage coefficient 1.5, seed dosage 10 g/L, time 90 min, pH 1.76, and endpoint pH controlled at approximately 3. Under these conditions, the iron removal efficiency is above 99%, while the loss ratios of cobalt and nickel are below 2%. The product is characterized by XRD and SEM-EDS. Results indicate that the product is jarosite ((K,H3O)Fe3(SO4)2(OH)6), exhibiting an ellipsoid structure with the mean particle size in the range of 0.2–5.0 μm. Temperature, pH value and seed dosage significantly affect reaction rate, particle size and crystallinity, and K2SO4 dosage mainly affects reaction rate and the morphology of jarosite. The jarosite crystallization kinetics can be described by the Avrami equation, with an Avrami index (n) of approximately 2.5 and the apparent activation energy of 42.68 kJ/mol.

航天磁性材料废料中含有丰富的钴和镍。硫酸浸出法是提取这两种元素的有效方法。但这是一种非选择性工艺,大量的铁会溶解在溶液中。本研究的重点是利用贾拉特工艺从溶液中选择性地去除铁。建立了 K-S-Fe-H2O 系统的 Eh-pH 图。根据热力学分析,H2O2 可将 Fe2+ 氧化成 Fe3+,从而实现从含钴和镍的溶液中高效、选择性地去除铁。最佳条件如下:温度 95°C,K2SO4 用量系数 1.5,种子用量 10 g/L,时间 90 分钟,pH 值 1.76,终点 pH 值控制在 3 左右。在这些条件下,除铁效率高于 99%,而钴和镍的损失率低于 2%。产品通过 XRD 和 SEM-EDS 进行表征。结果表明,该产品为硬玉((K,H3O)Fe3(SO4)2(OH)6),呈椭圆形结构,平均粒径在 0.2-5.0 μm 之间。温度、pH 值和种子用量对反应速率、粒度和结晶度有显著影响,而 K2SO4 用量则主要影响反应速率和贾洛石的形态。贾洛石的结晶动力学可用阿夫拉米方程描述,阿夫拉米指数(n)约为 2.5,表观活化能为 42.68 kJ/mol。
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引用次数: 0
Preparation of high quality carbon nanotubes by catalytic pyrolysis of waste plastics using FeNi-based catalyst 使用镍铁基催化剂催化热解废塑料制备高质量纳米碳管
IF 7.1 2区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-08-13 DOI: 10.1016/j.wasman.2024.08.005

Plastic waste pollution is the serious environmental problem, and catalytic pyrolysis of waste plastics is an effective way to solve this problem. Carbon nanotubes (CNTs) are prepared by catalytic pyrolysis of low-density polyethylene (LDPE) waste plastics by one-stage method using iron nitrate and nickel nitrate as catalyst. The growth mechanism of CNTs is analyzed in detail. TPO, XRD, SEM and Raman analyses show that increasing Ni content contributes to the production of CNTs with good morphology and high graphitization degree. While the increasing Fe content contributes to improving the yield of CNTs. The outer and inner diameters of the FeNi12-CNTs-800 are about 21 nm and 8 nm with the length of 18.9 μm, respectively. LDPE pyrolysis gases are analyzed to determine that the primary carbon source required for CNTs growth is C2H4. The C2H4 adsorption and decomposition processes on FeNi alloys are performed to reveal the growth mechanism of CNTs, based on density functional theory calculation. Three kinds of the growth models are proposed to explain the difference of the CNTs tubular shape. FeNi12-CNTs-800 are used to remove microplastics from wastewater due to existence of magnetic. PVC can be quickly removed from wastewater with removal of 100 % at 20 min. This study provides an effective way for recycling and treatment of waste plastic.

塑料垃圾污染是严重的环境问题,而催化热解废塑料是解决这一问题的有效途径。本研究以硝酸铁和硝酸镍为催化剂,采用一步法催化热解低密度聚乙烯(LDPE)废塑料,制备了碳纳米管(CNTs)。详细分析了 CNTs 的生长机理。TPO、XRD、SEM 和拉曼分析表明,镍含量的增加有助于生成具有良好形态和较高石墨化程度的 CNT。而增加铁的含量则有助于提高 CNT 的产量。FeNi12-CNTs-800 的外径和内径分别约为 21 nm 和 8 nm,长度为 18.9 μm。通过分析低密度聚乙烯热解气体,确定碳纳米管生长所需的主要碳源是 C2H4。基于密度泛函理论计算,研究了 C2H4 在铁镍合金上的吸附和分解过程,揭示了 CNTs 的生长机理。提出了三种生长模型来解释 CNTs 管状形状的差异。由于存在磁性,FeNi12-CNTs-800 可用于去除废水中的微塑料。废水中的 PVC 可在 20 分钟内被快速去除,去除率达 100%。这项研究为废塑料的回收和处理提供了一种有效的方法。
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引用次数: 0
Study on the effect of conditioner on NOx precursor control behavior from sewage sludge pyrolysis: Focusing on conditioner assessments and in-situ fixation mechanism 研究调节剂对污水污泥热解产生的氮氧化物前体控制行为的影响:重点关注调节剂评估和原位固定机制。
IF 7.1 2区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-08-12 DOI: 10.1016/j.wasman.2024.08.002

The nitrogen transformation during sludge pyrolysis is affected by the dewater conditioner. However, the comparative analysis of the conditioner under identical pyrolysis conditions has been previously absent. In this study, Ca-, Fe- and Al-based conditioners were selected as the representatives. A comprehensive evaluation considering the cost of the conditioners and the product characteristics was conducted. Additionally, the in-situ fixation mechanism of the conditioner on nitrogen-containing gas was concurrently revealed. Among the six conditioners, CaO and AlCl3 were identified as the top performers, ranking first and second, respectively. Furthermore, Fe/Ca-based conditioners reduced NH3 and HCN release by 1.5 ∼ 5.53 % and 0 ∼ 1.55 %, respectively, by facilitating the conversion of amine-N to a more stable form in condensable fraction. Fe promoted volatile amine-N cyclization, while Ca encouraged its dehydrogenation. Both Fe/Ca-based conditioners increased 7.5 ∼ 14.8 % nitrogen retention in char, by inhibiting the decomposition of protein-N. Al-based conditioners had little effect on NH3 and HCN, but contributed to 2.3 ∼ 2.8 % production of stabilized nitrogen in char. The introduction of Cl in Fe/Ca/Al chloride conditioners would promote the decomposition of inorganic ammonium salts to produce NH3 at 30 ∼ 185 °C. And Cl also reacted with volatiles through electrophilic substitution reaction, leading to the formation of halogenated hydrocarbons in condensable fraction and the release of more NH3, HCN, and HNCO at 30 ∼ 465 °C. The findings of this study provide a detailed comparative analysis of various conditioners under uniform conditions and reveal the in-situ fixation mechanism of nitrogen-containing gas. This will provide guidance for the sludge conditioning-dewatering-drying integrated treatment and disposal.

污泥热解过程中的氮转化受到脱水调节剂的影响。然而,此前一直缺乏在相同热解条件下对调节剂的比较分析。本研究选取了以钙、铁和铝为基础的调节剂作为代表。研究对调节剂的成本和产品特性进行了综合评估。此外,还同时揭示了调节剂对含氮气体的原位固定机制。在六种调节剂中,CaO 和 AlCl3 的性能最佳,分别排名第一和第二。此外,Fe/Ca 基调节剂通过促进胺-N 在可冷凝组分中转化为更稳定的形式,使 NH3 和 HCN 释放量分别减少了 1.5 ∼ 5.53 % 和 0 ∼ 1.55 %。铁促进挥发性胺-N 的环化,而钙则促进其脱氢。两种以铁/钙为基础的调节剂都通过抑制蛋白质-N的分解,提高了炭中 7.5 ~ 14.8 % 的氮保留率。铝基调节剂对 NH3 和 HCN 的影响很小,但却有助于提高炭中 2.3 ∼ 2.8 % 的稳定氮产量。在 Fe/Ca/Al 氯化调节剂中引入 Cl 会促进无机铵盐的分解,在 30 ∼ 185 °C 的温度下产生 NH3。Cl 还会通过亲电取代反应与挥发物发生反应,从而在可冷凝部分形成卤代烃,并在 30 ∼ 465 °C 时释放出更多的 NH3、HCN 和 HNCO。本研究结果提供了统一条件下各种调节剂的详细对比分析,并揭示了含氮气体的原位固定机制。这将为污泥调理-脱水-干化一体化处理和处置提供指导。
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