首页 > 最新文献

Environmental Chemistry Letters最新文献

英文 中文
Transforming low-quality cotton fibers into dye adsorbents 将劣质棉纤维转化为染料吸附剂
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-01-31 DOI: 10.1007/s10311-023-01692-1
Zhen Zhang, Shaida Sultana Rumi, Lucian A. Lucia, Noureddine Abidi

Low-quality cotton fibers are a low-value waste material within the cotton industry. Upcycling and transforming into high-value materials are highly desired. This study investigates upcycling fibers into hydrogel biosorbents and assesses their efficacy in dye adsorption. An effective gelation approach was employed via simply dropping droplets of suspension mixture of sodium alginate and fibers into acidic bath. Resulting composite hydrogel beads were utilized for dye removal. Composite beads successfully immobilized less than 70 wt% of fibers and achieved a significant improvement in thermal stability. Composite beads with 50 wt% fibers and alginate showed no decrease in methylene blue adsorption capacity. This outcome was unexpected considering the lower dye adsorption capacity of fibers than alginate, particularly notable since it indicated that reduced quantities of the more costly sodium alginate were sufficient to achieve comparable dye adsorption capacity. Mechanistic study unveiled that both the loose crosslinking structure and the electrostatic forces were responsible for the unexpected high adsorption capacity of 50% fiber-alginate. This study reports a promising, innovative and effective upcycle strategy for the first time that can transform fibers into high-value biosorbents without compromising dye adsorption capability.

低质棉纤维是棉花产业中的低价值废料。人们非常希望将其升级再造并转化为高价值材料。本研究调查了将纤维升级再造为水凝胶生物吸附剂的情况,并评估了其在染料吸附方面的功效。研究采用了一种有效的凝胶化方法,只需将海藻酸钠和纤维的悬浮混合物滴入酸性水浴中。由此产生的复合水凝胶珠被用于去除染料。复合珠成功固定了低于 70 wt% 的纤维,并显著提高了热稳定性。含 50% 纤维和海藻酸盐的复合珠对亚甲蓝的吸附能力没有下降。考虑到纤维的染料吸附能力低于海藻酸盐,这一结果出乎意料,尤其值得注意的是,它表明减少成本较高的海藻酸钠的用量就足以达到相当的染料吸附能力。机理研究表明,松散的交联结构和静电力是 50% 纤维-海藻酸盐具有意想不到的高吸附能力的原因。本研究首次报道了一种前景广阔、创新而有效的循环利用策略,可在不影响染料吸附能力的前提下将纤维转化为高价值的生物吸附剂。
{"title":"Transforming low-quality cotton fibers into dye adsorbents","authors":"Zhen Zhang,&nbsp;Shaida Sultana Rumi,&nbsp;Lucian A. Lucia,&nbsp;Noureddine Abidi","doi":"10.1007/s10311-023-01692-1","DOIUrl":"10.1007/s10311-023-01692-1","url":null,"abstract":"<div><p>Low-quality cotton fibers are a low-value waste material within the cotton industry. Upcycling and transforming into high-value materials are highly desired. This study investigates upcycling fibers into hydrogel biosorbents and assesses their efficacy in dye adsorption. An effective gelation approach was employed via simply dropping droplets of suspension mixture of sodium alginate and fibers into acidic bath. Resulting composite hydrogel beads were utilized for dye removal. Composite beads successfully immobilized less than 70 wt% of fibers and achieved a significant improvement in thermal stability. Composite beads with 50 wt% fibers and alginate showed no decrease in methylene blue adsorption capacity. This outcome was unexpected considering the lower dye adsorption capacity of fibers than alginate, particularly notable since it indicated that reduced quantities of the more costly sodium alginate were sufficient to achieve comparable dye adsorption capacity. Mechanistic study unveiled that both the loose crosslinking structure and the electrostatic forces were responsible for the unexpected high adsorption capacity of 50% fiber-alginate. This study reports a promising, innovative and effective upcycle strategy for the first time that can transform fibers into high-value biosorbents without compromising dye adsorption capability.</p></div>","PeriodicalId":541,"journal":{"name":"Environmental Chemistry Letters","volume":"22 3","pages":"981 - 987"},"PeriodicalIF":15.0,"publicationDate":"2024-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140475153","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
Biomaterials technology and policies in the building sector: a review 建筑领域的生物材料技术和政策:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-01-29 DOI: 10.1007/s10311-023-01689-w
Lin Chen, Yubing Zhang, Zhonghao Chen, Yitong Dong, Yushan Jiang, Jianmin Hua, Yunfei Liu, Ahmed I. Osman, Mohamed Farghali, Lepeng Huang, David W. Rooney, Pow-Seng Yap

Traditional building materials have some drawbacks in the construction industry, particularly in terms of greenhouse gas emissions and energy consumption. Biomaterials derived from renewable sources are a promising alternative, significantly reducing the greenhouse effect and enhancing energy efficiency. However, traditional materials still dominate the construction sector, and there is a lack of understanding among some policymakers and developers regarding biomaterials. Here, we review building biomaterials and their policies and life cycle assessment through case studies. Bio-based materials have the potential to reduce over 320,000 tons of carbon dioxide emissions by 2050. They also exhibit advantages like decreasing water absorption by 40%, reducing energy consumption by 8.7%, enhancing acoustic absorption by 6.7%, and improving mechanical properties. We summarize recent advancements in mycelial materials, bioconcrete, natural fibers, and fiber-reinforced composites. We also explore the contributions of nanotechnology and microalgae technology in enhancing biomaterials' thermal insulation and eco-friendliness.

传统建筑材料在建筑业中存在一些弊端,尤其是在温室气体排放和能源消耗方面。从可再生资源中提取的生物材料是一种很有前途的替代品,可以显著减少温室效应,提高能源效率。然而,传统材料仍在建筑领域占据主导地位,一些政策制定者和开发人员对生物材料缺乏了解。在此,我们通过案例研究回顾了建筑生物材料及其政策和生命周期评估。到 2050 年,生物基材料有望减少超过 32 万吨的二氧化碳排放量。生物基材料还具有吸水率降低 40%、能耗降低 8.7%、吸音率提高 6.7%、机械性能改善等优势。我们总结了菌丝材料、生物混凝土、天然纤维和纤维增强复合材料的最新进展。我们还探讨了纳米技术和微藻技术在增强生物材料的隔热性和生态友好性方面的贡献。
{"title":"Biomaterials technology and policies in the building sector: a review","authors":"Lin Chen,&nbsp;Yubing Zhang,&nbsp;Zhonghao Chen,&nbsp;Yitong Dong,&nbsp;Yushan Jiang,&nbsp;Jianmin Hua,&nbsp;Yunfei Liu,&nbsp;Ahmed I. Osman,&nbsp;Mohamed Farghali,&nbsp;Lepeng Huang,&nbsp;David W. Rooney,&nbsp;Pow-Seng Yap","doi":"10.1007/s10311-023-01689-w","DOIUrl":"10.1007/s10311-023-01689-w","url":null,"abstract":"<div><p>Traditional building materials have some drawbacks in the construction industry, particularly in terms of greenhouse gas emissions and energy consumption. Biomaterials derived from renewable sources are a promising alternative, significantly reducing the greenhouse effect and enhancing energy efficiency. However, traditional materials still dominate the construction sector, and there is a lack of understanding among some policymakers and developers regarding biomaterials. Here, we review building biomaterials and their policies and life cycle assessment through case studies. Bio-based materials have the potential to reduce over 320,000 tons of carbon dioxide emissions by 2050. They also exhibit advantages like decreasing water absorption by 40%, reducing energy consumption by 8.7%, enhancing acoustic absorption by 6.7%, and improving mechanical properties. We summarize recent advancements in mycelial materials, bioconcrete, natural fibers, and fiber-reinforced composites. We also explore the contributions of nanotechnology and microalgae technology in enhancing biomaterials' thermal insulation and eco-friendliness.</p></div>","PeriodicalId":541,"journal":{"name":"Environmental Chemistry Letters","volume":"22 2","pages":"715 - 750"},"PeriodicalIF":15.0,"publicationDate":"2024-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10311-023-01689-w.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140018885","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Microplastic migration in porous media at various scales: a review 多孔介质中各种尺度的微塑料迁移:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-01-25 DOI: 10.1007/s10311-023-01688-x
Chunxiang Geng, Yanyan Gao, Hao Zhang, Dongxing Xue, He Shan, Bin Wang, Xiaopu Wang, Jian Zhao

Migration of microplastics in porous media is an important, yet overlooked phenomenon because most microplastic research has focused mainly on microplastic behavior in aquatic environments. Here we review experimental advances of microplastic migration in porous media, with emphasis on factors influencing microplastic migration. We observed that microplastic migration is influenced by environmental factors and microplastic properties. The effect of microplastic surface charge and functional groups, and of soil organisms on microplastic migration is unclear. Research at the macro-scale, higher than 1 m, predominantly starts with field sampling, and then carries out measurements or mathematical modeling to explore migration patterns. At the meso-scale, below 1 cm, studies often employ filled sand columns as proxies for porous media to generate breakthrough curves and retention profiles. At the micro-scale, below 1 mm, visualization of microplastic migration in pores is done by lab-on-a-chip devices to build transparent micromodels. Current research predominantly relies on industrially produced regular spherical microplastics, with limited focus on macro- and micro-scale studies.

微塑料在多孔介质中的迁移是一个重要但却被忽视的现象,因为大多数微塑料研究主要集中于微塑料在水生环境中的行为。在此,我们回顾了微塑料在多孔介质中迁移的实验进展,重点关注影响微塑料迁移的因素。我们观察到,微塑料迁移受环境因素和微塑料特性的影响。微塑料表面电荷和功能基团以及土壤生物对微塑料迁移的影响尚不清楚。宏观尺度(1 米以上)的研究主要从实地取样开始,然后通过测量或数学建模来探索迁移模式。在中尺度(1 厘米以下)的研究中,通常采用填充沙柱作为多孔介质的替代物,以生成突破曲线和滞留剖面图。在 1 毫米以下的微观尺度上,微塑料在孔隙中迁移的可视化研究则是通过芯片上的实验室设备来建立透明的微模型。目前的研究主要依赖于工业生产的规则球形微塑料,对宏观和微观尺度的研究关注有限。
{"title":"Microplastic migration in porous media at various scales: a review","authors":"Chunxiang Geng,&nbsp;Yanyan Gao,&nbsp;Hao Zhang,&nbsp;Dongxing Xue,&nbsp;He Shan,&nbsp;Bin Wang,&nbsp;Xiaopu Wang,&nbsp;Jian Zhao","doi":"10.1007/s10311-023-01688-x","DOIUrl":"10.1007/s10311-023-01688-x","url":null,"abstract":"<div><p>Migration of microplastics in porous media is an important, yet overlooked phenomenon because most microplastic research has focused mainly on microplastic behavior in aquatic environments. Here we review experimental advances of microplastic migration in porous media, with emphasis on factors influencing microplastic migration. We observed that microplastic migration is influenced by environmental factors and microplastic properties. The effect of microplastic surface charge and functional groups, and of soil organisms on microplastic migration is unclear. Research at the macro-scale, higher than 1 m, predominantly starts with field sampling, and then carries out measurements or mathematical modeling to explore migration patterns. At the meso-scale, below 1 cm, studies often employ filled sand columns as proxies for porous media to generate breakthrough curves and retention profiles. At the micro-scale, below 1 mm, visualization of microplastic migration in pores is done by lab-on-a-chip devices to build transparent micromodels. Current research predominantly relies on industrially produced regular spherical microplastics, with limited focus on macro- and micro-scale studies.</p></div>","PeriodicalId":541,"journal":{"name":"Environmental Chemistry Letters","volume":"22 2","pages":"691 - 713"},"PeriodicalIF":15.0,"publicationDate":"2024-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139595692","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
Cobalt-doped CdS quantum dots enhanced photoelectroreduction of CO2 to formic acid with high selectivity 掺钴 CdS 量子点增强了 CO2 对甲酸的光电还原,具有高选择性
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-01-20 DOI: 10.1007/s10311-023-01691-2
Shengqi Liu, Zhenyan Guo, Ying Yang, Pei-dong Wu, Zhengyi Li, Keping Wang, Heng Zhang, Hu Li, Song Yang

Excessive carbon dioxide (CO2) emission has caused problems associated with environmental pollution and climate deterioration. As a consequence, the selective conversion of CO2 into liquid fuels by artificial photosynthesis has gained increasing attention. However, the rational design of photocathode to achieve selective CO2 photoelectroreduction is challenging. Here, we sensitized cuprous oxide (p-nCu2O) loaded on hydroxyl iron oxide (FeOOH) with cobalt-doped cadmium sulfide (Co:CdS) quantum dots to prepare a novel photocathode FeOOH/p-nCu2O/Co:CdS by sequential electrodeposition and chemical bath deposition. The composite photocathode exhibited a larger photovoltage, which is 1.9 times higher than the pristine counterpart, and was efficient for CO2 reduction to produce formic acid with high selectivity of up to 82.9% (Faradaic efficiency). Theoretical calculations revealed that the photocathode out-layer Co:CdS quantum dots had increased binding energy toward the key intermediate *OOCH through additional hybridization orbitals to exclusively favor the formation of formic acid. An impurity energy level was revealed to form by doping Co to the CdS-containing composite, which could reduce the photocathode band gap with improved absorption toward visible light, thus remarkably increasing the photoelectrochemical properties. This is the first work undertaking the energy band structure optimization of the photocathode enabled by elemental doping to improve its photoelectrocatalytic performance.

过量的二氧化碳(CO2)排放造成了与环境污染和气候恶化相关的问题。因此,通过人工光合作用将二氧化碳有选择地转化为液体燃料越来越受到人们的关注。然而,如何合理设计光电阴极以实现二氧化碳的选择性光电还原是一项挑战。在这里,我们通过顺序电沉积和化学沉积的方法,将负载在羟基氧化铁(FeOOH)上的氧化亚铜(p-nCu2O)与掺杂钴的硫化镉(Co:CdS)量子点敏化,制备出一种新型光电阴极 FeOOH/p-nCu2O/Co:CdS。这种复合光电阴极的光电压比原始光电阴极高出 1.9 倍,并能高效地还原 CO2 生成甲酸,选择性高达 82.9%(法拉第效率)。理论计算显示,光电阴极外层 Co:CdS 量子点通过额外的杂化轨道增加了与关键中间体 *OOCH 的结合能,从而完全有利于甲酸的形成。通过在含 CdS 的复合材料中掺入 Co,发现形成了一个杂质能级,它可以降低光电阴极带隙,改善对可见光的吸收,从而显著提高光电化学性能。这是第一项通过元素掺杂优化光电阴极能带结构以提高其光电催化性能的研究。
{"title":"Cobalt-doped CdS quantum dots enhanced photoelectroreduction of CO2 to formic acid with high selectivity","authors":"Shengqi Liu,&nbsp;Zhenyan Guo,&nbsp;Ying Yang,&nbsp;Pei-dong Wu,&nbsp;Zhengyi Li,&nbsp;Keping Wang,&nbsp;Heng Zhang,&nbsp;Hu Li,&nbsp;Song Yang","doi":"10.1007/s10311-023-01691-2","DOIUrl":"10.1007/s10311-023-01691-2","url":null,"abstract":"<div><p>Excessive carbon dioxide (CO<sub>2</sub>) emission has caused problems associated with environmental pollution and climate deterioration. As a consequence, the selective conversion of CO<sub>2</sub> into liquid fuels by artificial photosynthesis has gained increasing attention. However, the rational design of photocathode to achieve selective CO<sub>2</sub> photoelectroreduction is challenging. Here, we sensitized cuprous oxide (p-nCu<sub>2</sub>O) loaded on hydroxyl iron oxide (FeOOH) with cobalt-doped cadmium sulfide (Co:CdS) quantum dots to prepare a novel photocathode FeOOH/p-nCu<sub>2</sub>O/Co:CdS by sequential electrodeposition and chemical bath deposition. The composite photocathode exhibited a larger photovoltage, which is 1.9 times higher than the pristine counterpart, and was efficient for CO<sub>2</sub> reduction to produce formic acid with high selectivity of up to 82.9% (Faradaic efficiency). Theoretical calculations revealed that the photocathode out-layer Co:CdS quantum dots had increased binding energy toward the key intermediate *OOCH through additional hybridization orbitals to exclusively favor the formation of formic acid. An impurity energy level was revealed to form by doping Co to the CdS-containing composite, which could reduce the photocathode band gap with improved absorption toward visible light, thus remarkably increasing the photoelectrochemical properties. This is the first work undertaking the energy band structure optimization of the photocathode enabled by elemental doping to improve its photoelectrocatalytic performance.</p></div>","PeriodicalId":541,"journal":{"name":"Environmental Chemistry Letters","volume":"22 2","pages":"463 - 470"},"PeriodicalIF":15.0,"publicationDate":"2024-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139505021","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
Synthesis of green nanoparticles for energy, biomedical, environmental, agricultural, and food applications: A review 合成用于能源、生物医学、环境、农业和食品应用的绿色纳米粒子:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-01-20 DOI: 10.1007/s10311-023-01682-3
Ahmed I. Osman, Yubing Zhang, Mohamed Farghali, Ahmed K. Rashwan, Abdelazeem S. Eltaweil, Eman M. Abd El-Monaem, Israa M. A. Mohamed, Mai M. Badr, Ikko Ihara, David W. Rooney, Pow-Seng Yap

Nanomaterials have been rapidly developed during the last decades, yet many nanoparticles synthesized by classical methods are toxic and their synthesis procedure is not sustainable. Here we review the green synthesis of nanoparticles from biomass and waste with a focus on synthetic mechanisms and applications in energy production and storage, medicine, environmental remediation, and agriculture and food. Biomass use for synthesis include microorganisms, fungi, plants, and agro-industrial bio-waste. Compared to conventional synthesis, green synthesis allows a 30% reduction in energy consumption, cost savings of up to 40%, and a 50% increase in production output. Biomedical applications comprise antibacterials, anticancers, antioxidants, and drug delivery mechanisms. Carbon quantum dots and photovoltaics are discussed in the energy section. Agricultural and food applications focus on nanofertilization, pest control, and food quality. Environmental remediation includes water and soil purification.

过去几十年来,纳米材料得到了快速发展,然而许多用传统方法合成的纳米粒子都是有毒的,而且其合成过程也不是可持续的。在此,我们回顾了从生物质和废物中绿色合成纳米粒子的过程,重点关注合成机制以及在能源生产和储存、医药、环境修复、农业和食品领域的应用。用于合成的生物质包括微生物、真菌、植物和农工生物废弃物。与传统合成相比,绿色合成可减少 30% 的能源消耗,节约高达 40% 的成本,并提高 50% 的产量。生物医学应用包括抗菌、抗癌、抗氧化和药物输送机制。能源部分讨论了碳量子点和光伏技术。农业和食品应用侧重于纳米施肥、害虫控制和食品质量。环境修复包括水和土壤净化。
{"title":"Synthesis of green nanoparticles for energy, biomedical, environmental, agricultural, and food applications: A review","authors":"Ahmed I. Osman,&nbsp;Yubing Zhang,&nbsp;Mohamed Farghali,&nbsp;Ahmed K. Rashwan,&nbsp;Abdelazeem S. Eltaweil,&nbsp;Eman M. Abd El-Monaem,&nbsp;Israa M. A. Mohamed,&nbsp;Mai M. Badr,&nbsp;Ikko Ihara,&nbsp;David W. Rooney,&nbsp;Pow-Seng Yap","doi":"10.1007/s10311-023-01682-3","DOIUrl":"10.1007/s10311-023-01682-3","url":null,"abstract":"<div><p>Nanomaterials have been rapidly developed during the last decades, yet many nanoparticles synthesized by classical methods are toxic and their synthesis procedure is not sustainable. Here we review the green synthesis of nanoparticles from biomass and waste with a focus on synthetic mechanisms and applications in energy production and storage, medicine, environmental remediation, and agriculture and food. Biomass use for synthesis include microorganisms, fungi, plants, and agro-industrial bio-waste. Compared to conventional synthesis, green synthesis allows a 30% reduction in energy consumption, cost savings of up to 40%, and a 50% increase in production output. Biomedical applications comprise antibacterials, anticancers, antioxidants, and drug delivery mechanisms. Carbon quantum dots and photovoltaics are discussed in the energy section. Agricultural and food applications focus on nanofertilization, pest control, and food quality. Environmental remediation includes water and soil purification.</p></div>","PeriodicalId":541,"journal":{"name":"Environmental Chemistry Letters","volume":"22 2","pages":"841 - 887"},"PeriodicalIF":15.0,"publicationDate":"2024-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10311-023-01682-3.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139505090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact of humic substances on the bioremediation of polycyclic aromatic hydrocarbons in contaminated soils and sediments: A review 腐殖质对受污染土壤和沉积物中多环芳烃生物修复的影响:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-01-13 DOI: 10.1007/s10311-023-01678-z
Solmaz Gholami, Ali Behnami, Mohsen Hesami Arani, Roshanak Rezaei Kalantary

Polycyclic aromatic hydrocarbons (PAHs) are present in the environment due to both natural sources and human activities. They are abundant and resistant to decomposition. Humic substances, depicted as a significant component of soil organic matter, can influence the effectiveness of PAHs bioremediation in contaminated environments. We review bioremediation studies on soil contamination with PAHs in the presence of humic substances in reports published from 2000 to 2023. Around 36% of the studies indicated that the presence of humic substances enhances the bioavailability and biodegradation rate of PAHs in soils and sediments. This enhancement is attributed to the surfactant properties of humic substances, particularly humic acids, which display a micellar microstructure. In contrast, approximately 19% of the studies suggested that humic substances could diminish the bioavailability and biodegradation rate of PAHs due to the sequestration of PAHs within humic substances. Moreover, the impact of humic substances on the bioavailability of PAHs seems to be concentration-dependent. Humic acidx can function as a carrier for PAHs, aiding in their transfer to bacterial cells. In contrast, humin, a substantial component of soil organic matter, has the ability to adsorb more PAHs, potentially resulting in their long-term aging.

环境中的多环芳烃(PAHs)既有自然来源,也有人类活动。多环芳烃含量丰富且不易分解。腐殖质是土壤有机物的重要组成部分,可影响受污染环境中多环芳烃生物修复的效果。我们回顾了 2000 年至 2023 年期间发表的报告中有关多环芳烃污染土壤时腐殖质的生物修复研究。约 36% 的研究表明,腐殖质的存在提高了土壤和沉积物中多环芳烃的生物利用率和生物降解率。这种提高归因于腐殖质的表面活性剂特性,尤其是腐殖酸,它具有胶束状微结构。相反,约有 19% 的研究表明,由于 PAHs 封存在腐殖质中,腐殖质可能会降低 PAHs 的生物利用率和生物降解率。此外,腐殖质对 PAHs 生物利用率的影响似乎与浓度有关。腐殖酸可作为多环芳烃的载体,帮助它们转移到细菌细胞中。与此相反,腐殖质作为土壤有机物的重要组成部分,能够吸附更多的多环芳烃,从而可能导致多环芳烃的长期老化。
{"title":"Impact of humic substances on the bioremediation of polycyclic aromatic hydrocarbons in contaminated soils and sediments: A review","authors":"Solmaz Gholami,&nbsp;Ali Behnami,&nbsp;Mohsen Hesami Arani,&nbsp;Roshanak Rezaei Kalantary","doi":"10.1007/s10311-023-01678-z","DOIUrl":"10.1007/s10311-023-01678-z","url":null,"abstract":"<div><p>Polycyclic aromatic hydrocarbons (PAHs) are present in the environment due to both natural sources and human activities. They are abundant and resistant to decomposition. Humic substances, depicted as a significant component of soil organic matter, can influence the effectiveness of PAHs bioremediation in contaminated environments. We review bioremediation studies on soil contamination with PAHs in the presence of humic substances in reports published from 2000 to 2023. Around 36% of the studies indicated that the presence of humic substances enhances the bioavailability and biodegradation rate of PAHs in soils and sediments. This enhancement is attributed to the surfactant properties of humic substances, particularly humic acids, which display a micellar microstructure. In contrast, approximately 19% of the studies suggested that humic substances could diminish the bioavailability and biodegradation rate of PAHs due to the sequestration of PAHs within humic substances. Moreover, the impact of humic substances on the bioavailability of PAHs seems to be concentration-dependent. Humic acidx can function as a carrier for PAHs, aiding in their transfer to bacterial cells. In contrast, humin, a substantial component of soil organic matter, has the ability to adsorb more PAHs, potentially resulting in their long-term aging.</p></div>","PeriodicalId":541,"journal":{"name":"Environmental Chemistry Letters","volume":"22 2","pages":"889 - 918"},"PeriodicalIF":15.0,"publicationDate":"2024-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10311-023-01678-z.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139435462","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Prevalence of microplastics and fate in wastewater treatment plants: a review 废水处理厂中微塑料的盛行与归宿:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-01-11 DOI: 10.1007/s10311-023-01679-y
Shilpa Jose, Linson Lonappan, Hubert Cabana

Microplastics have multidimensional traits, as compared to other emerging contaminants, presenting a concern to terrestrial, aquatic life and humans through inhalation or ingestion. Hazardous chemicals adsorbed on microplastics could potentially be transferred to the environment or consumed by living organisms. We review the transformation of plastic waste in the environment, the origin and transportation of microplastics, the regulatory measures for plastic and microplastic pollution, and the fate of microplastics in wastewater treatment plants. Plastic debris is building up in the environment despite legislative attempts by many countries. Accumulated plastic waste from a range of sources breaks down into smaller fragments and microplastics through chemical, physiochemical and biodegradation mechanisms. This review also discusses personal protective equipment in relation to COVID-19 as a source of microplastics. Millions of microplastics are discharged into the environment through effluents and biosolids. Daily microplastic emissions to the environment from effluent range about 0.46 million to 140 billion. Previous studies had only explored the existence of microplastics in wastewater treatment plants, with limited visualization of how microplastics interact with the various treatment technologies used in wastewater treatment plants.

与其他新出现的污染物相比,微塑料具有多方面的特性,通过吸入或摄入会对陆生、水生生物和人类造成危害。吸附在微塑料上的有害化学物质有可能转移到环境中或被生物体消耗。我们回顾了塑料垃圾在环境中的转化、微塑料的来源和运输、针对塑料和微塑料污染的监管措施,以及微塑料在污水处理厂中的去向。尽管许多国家都在努力立法,但环境中的塑料垃圾仍在不断增加。各种来源的累积塑料垃圾会通过化学、物理化学和生物降解机制分解成更小的碎片和微塑料。本综述还讨论了与作为微塑料来源的 COVID-19 有关的个人防护装备。数百万微塑料通过污水和生物固体排放到环境中。每天从污水中排放到环境中的微塑料约为 46 万至 1400 亿个。以往的研究仅探讨了污水处理厂中是否存在微塑料,对微塑料如何与污水处理厂中使用的各种处理技术相互作用的直观了解有限。
{"title":"Prevalence of microplastics and fate in wastewater treatment plants: a review","authors":"Shilpa Jose,&nbsp;Linson Lonappan,&nbsp;Hubert Cabana","doi":"10.1007/s10311-023-01679-y","DOIUrl":"10.1007/s10311-023-01679-y","url":null,"abstract":"<div><p>Microplastics have multidimensional traits, as compared to other emerging contaminants, presenting a concern to terrestrial, aquatic life and humans through inhalation or ingestion. Hazardous chemicals adsorbed on microplastics could potentially be transferred to the environment or consumed by living organisms. We review the transformation of plastic waste in the environment, the origin and transportation of microplastics, the regulatory measures for plastic and microplastic pollution, and the fate of microplastics in wastewater treatment plants. Plastic debris is building up in the environment despite legislative attempts by many countries. Accumulated plastic waste from a range of sources breaks down into smaller fragments and microplastics through chemical, physiochemical and biodegradation mechanisms. This review also discusses personal protective equipment in relation to COVID-19 as a source of microplastics. Millions of microplastics are discharged into the environment through effluents and biosolids. Daily microplastic emissions to the environment from effluent range about 0.46 million to 140 billion. Previous studies had only explored the existence of microplastics in wastewater treatment plants, with limited visualization of how microplastics interact with the various treatment technologies used in wastewater treatment plants.</p></div>","PeriodicalId":541,"journal":{"name":"Environmental Chemistry Letters","volume":"22 2","pages":"657 - 690"},"PeriodicalIF":15.0,"publicationDate":"2024-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139431366","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
13C dicarboxylic acid signatures indicate temporal shifts in catchment sediment sources in response to extreme winter rainfall 13C 二羧酸特征显示集水区沉积物来源随极端冬季降雨而发生的时间变化
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-01-10 DOI: 10.1007/s10311-023-01684-1
Hari Ram Upadhayay, Adrian Joynes, Adrian L. Collins

Rainfall and land-use interactions drive temporal shifts in suspended sediment sources, yet the magnitude of such changes remains poorly understood due to the lack of land-use specific source tracers. We investigated α,ω-dicarboxylic fatty acid root-specific biomarkers, as diagnostic tracers for apportioning sources of time-integrated suspended sediment samples collected from a grassland dominated agricultural catchment in the southwest of England during the wet winter period. Applying fatty acids-specific stable carbon isotope analysis and a Bayesian isotope mixing model, we show that stream banks contributed most of the sediment in the early winter, i.e. October–December, while winter cereal-dominated arable land contributed more than half of the sediment during the late winter, i.e. January–March. The dominant sediment source shifted in conjunction with a period of prolonged consecutive rainfall days in the later period suggesting that intervention required to mitigate soil erosion and sediment delivery should adapt to changing rainfall patterns. Our novel findings demonstrate that isotopic signatures of α,ω-dicarboxylic fatty acids are promising tracers for understanding the resistance of agricultural soils to water erosion and quantifying the interactive effects of extreme rainfall and land use on catchment sediment source dynamics.

降雨和土地利用的相互作用推动了悬浮沉积物来源的时间变化,但由于缺乏特定土地利用的来源示踪剂,人们对这种变化的程度仍然知之甚少。我们研究了α,ω-二羧酸根特异性生物标记物,将其作为诊断示踪剂,用于划分冬季潮湿期间从英格兰西南部一个以草地为主的农业集水区采集的时间整合悬浮沉积物样本的来源。应用脂肪酸特异性稳定碳同位素分析和贝叶斯同位素混合模型,我们发现溪流河岸在初冬(即 10 月至 12 月)贡献了大部分沉积物,而以冬季谷物为主的耕地在晚冬(即 1 月至 3 月)贡献了一半以上的沉积物。随着后期连续降雨日数的延长,沉积物的主要来源也发生了变化,这表明减轻土壤侵蚀和沉积物输送所需的干预措施应适应不断变化的降雨模式。我们的新发现表明,α,ω-二羧酸的同位素特征是一种很有前途的示踪剂,可用于了解农业土壤的抗水蚀能力,以及量化极端降雨和土地利用对集水区沉积物来源动态的交互影响。
{"title":"13C dicarboxylic acid signatures indicate temporal shifts in catchment sediment sources in response to extreme winter rainfall","authors":"Hari Ram Upadhayay,&nbsp;Adrian Joynes,&nbsp;Adrian L. Collins","doi":"10.1007/s10311-023-01684-1","DOIUrl":"10.1007/s10311-023-01684-1","url":null,"abstract":"<div><p>Rainfall and land-use interactions drive temporal shifts in suspended sediment sources, yet the magnitude of such changes remains poorly understood due to the lack of land-use specific source tracers. We investigated α,ω-dicarboxylic fatty acid root-specific biomarkers, as diagnostic tracers for apportioning sources of time-integrated suspended sediment samples collected from a grassland dominated agricultural catchment in the southwest of England during the wet winter period. Applying fatty acids-specific stable carbon isotope analysis and a Bayesian isotope mixing model, we show that stream banks contributed most of the sediment in the early winter, i.e. October–December, while winter cereal-dominated arable land contributed more than half of the sediment during the late winter, i.e. January–March. The dominant sediment source shifted in conjunction with a period of prolonged consecutive rainfall days in the later period suggesting that intervention required to mitigate soil erosion and sediment delivery should adapt to changing rainfall patterns. Our novel findings demonstrate that isotopic signatures of α,ω-dicarboxylic fatty acids are promising tracers for understanding the resistance of agricultural soils to water erosion and quantifying the interactive effects of extreme rainfall and land use on catchment sediment source dynamics.</p></div>","PeriodicalId":541,"journal":{"name":"Environmental Chemistry Letters","volume":"22 2","pages":"499 - 504"},"PeriodicalIF":15.0,"publicationDate":"2024-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10311-023-01684-1.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139419999","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cardiovascular adverse effects and mechanistic insights of arsenic exposure: a review 砷暴露对心血管的不良影响和机理认识:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-01-09 DOI: 10.1007/s10311-023-01677-0
Yán Wāng, Ling Ma, Chunzhi Wang, Tiantian Gao, Yapeng Han, De-Xiang Xu

Human exposure to environmental arsenic induces cardiovascular diseases such as arrhythmias, hypertension, and arteriosclerosis. Here, we review the toxicological and cardiovascular impacts of arsenic in in vitro cardiac and vascular models. The mechanism of arsenic-induced cardiovascular impairments includes oxidative stress, epigenetic modifications, chromatin instability, subcellular damage, and premature aging. The different types of cardiac and vascular cells exhibit distinct responses to arsenic exposure. Arsenic causes arrhythmias, which involve alteration of cardiomyocyte potassium channels and, in turn, repolarization issues. This is mainly due to redox signals that cause epigenetic modifications of potassium channels. On the other hand, vascular lesions, such as damage to blood vessels, occur mainly due to an imbalance in redox levels. This imbalance leads to premature senescence of cells and stop the cell cycle. Furthermore, intracellular accumulation of calcium and ferrous ions plays a major role in arsenic-induced vascular cell apoptosis and cardiomyocyte ferroptosis, respectively.

人类接触环境中的砷会诱发心血管疾病,如心律失常、高血压和动脉硬化。在此,我们回顾了砷在体外心脏和血管模型中的毒理学和心血管影响。砷诱发心血管损伤的机制包括氧化应激、表观遗传修饰、染色质不稳定性、亚细胞损伤和早衰。不同类型的心脏和血管细胞对砷暴露表现出不同的反应。砷会导致心律失常,这涉及心肌细胞钾离子通道的改变,进而导致再极化问题。这主要是由于氧化还原信号导致钾通道的表观遗传学改变。另一方面,血管病变,如血管损伤,主要是由于氧化还原水平失衡造成的。这种失衡导致细胞过早衰老并停止细胞周期。此外,细胞内钙离子和亚铁离子的积累分别在砷诱导的血管细胞凋亡和心肌细胞铁凋亡中发挥了重要作用。
{"title":"Cardiovascular adverse effects and mechanistic insights of arsenic exposure: a review","authors":"Yán Wāng,&nbsp;Ling Ma,&nbsp;Chunzhi Wang,&nbsp;Tiantian Gao,&nbsp;Yapeng Han,&nbsp;De-Xiang Xu","doi":"10.1007/s10311-023-01677-0","DOIUrl":"10.1007/s10311-023-01677-0","url":null,"abstract":"<div><p>Human exposure to environmental arsenic induces cardiovascular diseases such as arrhythmias, hypertension, and arteriosclerosis. Here, we review the toxicological and cardiovascular impacts of arsenic in in vitro cardiac and vascular models. The mechanism of arsenic-induced cardiovascular impairments includes oxidative stress, epigenetic modifications, chromatin instability, subcellular damage, and premature aging. The different types of cardiac and vascular cells exhibit distinct responses to arsenic exposure. Arsenic causes arrhythmias, which involve alteration of cardiomyocyte potassium channels and, in turn, repolarization issues. This is mainly due to redox signals that cause epigenetic modifications of potassium channels. On the other hand, vascular lesions, such as damage to blood vessels, occur mainly due to an imbalance in redox levels. This imbalance leads to premature senescence of cells and stop the cell cycle. Furthermore, intracellular accumulation of calcium and ferrous ions plays a major role in arsenic-induced vascular cell apoptosis and cardiomyocyte ferroptosis, respectively.</p></div>","PeriodicalId":541,"journal":{"name":"Environmental Chemistry Letters","volume":"22 3","pages":"1437 - 1472"},"PeriodicalIF":15.0,"publicationDate":"2024-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139400573","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
Ecotoxicological response of algae to contaminants in aquatic environments: a review 藻类对水生环境中污染物的生态毒理学反应:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-01-08 DOI: 10.1007/s10311-023-01680-5
Van-Giang Le, Minh-Ky Nguyen, Hoang-Lam Nguyen, Van-Anh Thai, Van-Re Le, Q. Manh Vu, Perumal Asaithambi, S. Woong Chang, D. Duc Nguyen

Algae play a vital role in aquatic ecosystems, contributing to oxygen production and serving as a foundational component of the food chain. Environment stress and contamination can lead to harmful algal blooms, depleting oxygen levels and creating dead zones in water bodies. When exposed to contaminants such as industrial chemicals, pharmaceuticals, pesticides, heavy metals, and synthetic nano/microparticles, algae can exhibit adverse responses, disrupting the balance of aquatic ecosystems. Furthermore, environmental issues related to ecotoxicology responses of algae include the disruption of biodiversity and the loss of crucial habitats, which can lead to health issues. We reviewed the response of algae exposed to contaminants in the aquatic environments, including ecotoxicology and environmental stresses. The major points are: (1) The accumulation of polycyclic aromatic hydrocarbons in food chains and ecosystems and their uptake is widely revealed as a major concern for environmental health and human beings. (2) Bisphenol A can negatively impact algae by inhibiting biochemical and physiological processes, in which half maximal effective concentration varies from 1.0 mg L-1 to 100 mg L-1. (3) Though the level of per- and polyfluoroalkyl substances in the environment is generally low, ranging from ng L-1 to mg L-1, the combined contaminant exposure leads to significantly more significant toxic effects than individual compounds. (4) An exposure level of 1000ng L is unsafe for the ecosystems, and per- and polyfluoroalkyl substances could lead to algal growth inhibition, e.g., damage to the photosynthetic, inhibition of deoxyribonucleic acid replication, and reactive oxygen species metabolism. (5) The ecotoxicity of chemicals to algae is influenced by chemical, biological, and physical factors, creating complex effects at the biological community level. (6) This research indicated the importance of the ecotoxicology response of algae to contaminants, emphasizing the necessity for monitoring and strategic interventions to protect the sustainability of aquatic ecosystems.

藻类在水生生态系统中发挥着至关重要的作用,它有助于氧气的产生,是食物链的基本组成部分。环境压力和污染会导致有害的藻类大量繁殖,耗尽氧气并在水体中形成死区。当接触到工业化学品、药品、杀虫剂、重金属和合成纳米/微粒等污染物时,藻类会表现出不良反应,破坏水生生态系统的平衡。此外,与藻类生态毒理学反应有关的环境问题包括生物多样性的破坏和重要栖息地的丧失,这可能会导致健康问题。我们回顾了水生环境中藻类接触污染物后的反应,包括生态毒理学和环境压力。主要观点如下(1) 多环芳烃在食物链和生态系统中的积累及其摄入量已被广泛揭示为环境健康和人类的一个主要问题。(2) 双酚 A 可抑制藻类的生化和生理过程,从而对藻类产生负面影响,其半数最大有效浓度介于 1.0 毫克/升至 100 毫克/升之间。(3) 虽然环境中的全氟烷基和多氟烷基物质含量一般较低,从纳克/升到毫克/升不等,但与单个化合物相比,污染物的综合接触会导致更严重的毒性影响。(4) 1000ng L 的暴露水平对生态系统来说是不安全的,全氟和多氟烷基物质会导致藻类生长受抑制,如光合作用受损、脱氧核糖核酸复制受抑制、活性氧代谢受抑制等。(5) 化学品对藻类的生态毒性受化学、生物和物理因素的影响,在生物群落层面产生复杂的效应。(6) 这项研究表明了藻类对污染物的生态毒理学反应的重要性,强调了监测和战略干预的必要性,以保护水生生态系统的可持续性。
{"title":"Ecotoxicological response of algae to contaminants in aquatic environments: a review","authors":"Van-Giang Le,&nbsp;Minh-Ky Nguyen,&nbsp;Hoang-Lam Nguyen,&nbsp;Van-Anh Thai,&nbsp;Van-Re Le,&nbsp;Q. Manh Vu,&nbsp;Perumal Asaithambi,&nbsp;S. Woong Chang,&nbsp;D. Duc Nguyen","doi":"10.1007/s10311-023-01680-5","DOIUrl":"10.1007/s10311-023-01680-5","url":null,"abstract":"<div><p>Algae play a vital role in aquatic ecosystems, contributing to oxygen production and serving as a foundational component of the food chain. Environment stress and contamination can lead to harmful algal blooms, depleting oxygen levels and creating dead zones in water bodies. When exposed to contaminants such as industrial chemicals, pharmaceuticals, pesticides, heavy metals, and synthetic nano/microparticles, algae can exhibit adverse responses, disrupting the balance of aquatic ecosystems. Furthermore, environmental issues related to ecotoxicology responses of algae include the disruption of biodiversity and the loss of crucial habitats, which can lead to health issues. We reviewed the response of algae exposed to contaminants in the aquatic environments, including ecotoxicology and environmental stresses. The major points are: (1) The accumulation of polycyclic aromatic hydrocarbons in food chains and ecosystems and their uptake is widely revealed as a major concern for environmental health and human beings. (2) Bisphenol A can negatively impact algae by inhibiting biochemical and physiological processes, in which half maximal effective concentration varies from 1.0 mg L<sup>-1</sup> to 100 mg L<sup>-1</sup>. (3) Though the level of per- and polyfluoroalkyl substances in the environment is generally low, ranging from ng L<sup>-1</sup> to mg L<sup>-1</sup>, the combined contaminant exposure leads to significantly more significant toxic effects than individual compounds. (4) An exposure level of 1000ng L is unsafe for the ecosystems, and per- and polyfluoroalkyl substances could lead to algal growth inhibition, e.g., damage to the photosynthetic, inhibition of deoxyribonucleic acid replication, and reactive oxygen species metabolism. (5) The ecotoxicity of chemicals to algae is influenced by chemical, biological, and physical factors, creating complex effects at the biological community level. (6) This research indicated the importance of the ecotoxicology response of algae to contaminants, emphasizing the necessity for monitoring and strategic interventions to protect the sustainability of aquatic ecosystems.</p></div>","PeriodicalId":541,"journal":{"name":"Environmental Chemistry Letters","volume":"22 2","pages":"919 - 939"},"PeriodicalIF":15.0,"publicationDate":"2024-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139379473","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
期刊
Environmental Chemistry Letters
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1