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Supramolecular deep eutectic solvents in extraction processes: a review 萃取工艺中的超分子深共晶溶剂:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-11-23 DOI: 10.1007/s10311-024-01795-3
Patrycja Makoś-Chełstowska, Edyta Słupek, Sophie Fourmentin, Jacek Gębicki

Solvent selection is essential for industrial and analytical extraction processes to ensure environmental safety and neutrality. Nevertheless, toxic and hazardous solvents are often used, due to their cost-effectiveness and ready availability. In green chemistry, alternative solvents such as supramolecular deep eutectic solvents are gaining attention due to their superior performance compared with traditional non-green solvents in certain applications. Here we review the use of supramolecular deep eutectic solvents as a green solvent for analytical and industrial liquid–liquid extraction processes, with focus on physicochemical properties, extraction conditions, the capacity factor, the enrichment factor, fuel desulfurization, extraction of biological active compounds, lignin valorization, and sample preparation.

溶剂的选择对于工业和分析萃取过程至关重要,以确保环境安全和中立性。然而,有毒和有害溶剂因其成本效益高且随时可用而经常被使用。在绿色化学领域,超分子深共晶溶剂等替代溶剂因其在某些应用中优于传统的非绿色溶剂而备受关注。在此,我们回顾了超分子深共晶溶剂作为绿色溶剂在分析和工业液-液萃取过程中的应用,重点介绍了其理化性质、萃取条件、容量因子、富集因子、燃料脱硫、生物活性化合物萃取、木质素价值化以及样品制备。
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引用次数: 0
Iron-modified biochar for enhanced removal of ciprofloxacin and amoxicillin in wastewater 铁改性生物炭用于提高废水中环丙沙星和阿莫西林的去除率
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-11-10 DOI: 10.1007/s10311-024-01792-6
Sumita, Yong Wang, Jianping Yu, Cong Li

Antibiotic contamination in wastewater is an urgent environmental and public health concern because conventional treatment methods are ineffective in completely removing these pollutants. Iron-modified biochar, synthesized from agricultural waste, is proposed as an efficient and sustainable media for removal of ciprofloxacin and amoxicillin from wastewater. Iron-modified biochar was synthesized using a simple pyrolysis process with corn and ferrous sulfate as feedstock. Adsorbents were characterized by fourier transform infrared spectroscopy, X-Ray diffraction, and scanning electron microscopy. Removal performance of antibiotics was evaluated under different conditions, including antibiotic dosage, concentration of hydrogen peroxide, pH, and amount of humic acid. The results demonstrated high removal efficiencies of 87% for ciprofloxacin and 83% for amoxicillin within 25 min. Mechanistic studies revealed the generation of hydroxyl radicals (OH) and singlet oxygen (1O₂), and confirmed the activation of hydrogen peroxide in the system. These findings highlight the potential of iron-modified biochar as a sustainable and effective catalyst for antibiotic removal, offering a promising solution for reducing pharmaceutical contamination in wastewater.

废水中的抗生素污染是一个紧迫的环境和公共卫生问题,因为传统的处理方法无法完全去除这些污染物。利用农业废弃物合成的铁改性生物炭被认为是去除废水中环丙沙星和阿莫西林的高效且可持续的介质。铁改性生物炭是以玉米和硫酸亚铁为原料,通过简单的热解工艺合成的。傅立叶变换红外光谱、X 射线衍射和扫描电子显微镜对吸附剂进行了表征。在抗生素用量、过氧化氢浓度、pH 值和腐植酸用量等不同条件下,对抗生素的去除性能进行了评估。结果表明,在 25 分钟内,环丙沙星和阿莫西林的去除率分别高达 87% 和 83%。机理研究揭示了羟基自由基(-OH)和单线态氧(1O₂)的产生,并证实了系统中过氧化氢的活化。这些发现凸显了铁改性生物炭作为一种可持续、有效的抗生素去除催化剂的潜力,为减少废水中的药物污染提供了一种前景广阔的解决方案。
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引用次数: 0
Hydrothermal liquefaction for producing liquid fuels and chemicals from biomass-derived platform compounds: a review 水热液化法利用生物质衍生平台化合物生产液体燃料和化学品:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-11-10 DOI: 10.1007/s10311-024-01791-7
Bingbing Qiu, Xuedong Tao, Yanfang Wang, Donghui Zhang, Huaqiang Chu

Biomass offers a promising alternative for producing biofuels and chemicals through hydrothermal liquefaction, a process known for its ability to convert complex organic materials into valuable liquid products. Optimizing hydrothermal liquefaction for large-scale application involves understanding the underlying mechanisms and addressing key scientific and technical issues. We review hydrothermal liquefaction of biomass-derived chemicals, focusing on the breakdown and depolymerization of cellulose, hemicellulose, lignin, lipids, and proteins under hydrothermal conditions. We examine critical parameters such as reaction temperature, pressure, solvent selection, and catalyst choice, and their impact on product yield and quality. Catalytic routes transform key intermediates, such as 5-hydroxymethylfurfural and levulinic acid, into high-value liquid fuels and chemicals, offering significant potential for sustainable fuel production. Recent advances in process optimization are discussed.

生物质为通过水热液化生产生物燃料和化学品提供了一种前景广阔的替代方法,水热液化是一种以能够将复杂的有机材料转化为有价值的液体产品而著称的工艺。要优化水热液化以实现大规模应用,就必须了解其基本机制并解决关键的科学和技术问题。我们回顾了生物质衍生化学品的水热液化,重点是纤维素、半纤维素、木质素、脂质和蛋白质在水热条件下的分解和解聚。我们研究了反应温度、压力、溶剂选择和催化剂选择等关键参数及其对产品产量和质量的影响。催化路线可将 5- 羟甲基糠醛和乙酰丙酸等关键中间产物转化为高价值的液体燃料和化学品,为可持续燃料生产提供了巨大潜力。本文讨论了工艺优化方面的最新进展。
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引用次数: 0
Graphene oxide composites for dye removal in textile, printing and dyeing wastewaters: a review 氧化石墨烯复合材料在纺织印染废水中除染的研究进展
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-11-08 DOI: 10.1007/s10311-024-01794-4
Haodong Ma, Lingjie Yu, Limeng Yang, Yijun Yao, Guodong Shen, Yongzhen Wang, Bo Li, Jiaguang Meng, Menghe Miao, Chao Zhi

The textile, printing and dyeing industries are producing wastewater containing hazardous dye contaminants, which require advanced remediation methods to avoid environmental pollution. Here we review graphene oxide-based materials for the removal of dye contaminants in waters and wastewater, with focus on the properties of graphene oxide, adsorption mechanisms, factors controlling the adsorption, and applications. Dye adsorption is controlled by temperature, adsorbent and dye concentrations, and adsorption time. Graphene oxide composites include membranes and aerogels. Graphene oxide displays suitable hydrophilicity, acid‐alkali resistance, and strong adsorption capabilities. Increasing the surface activity and specific surface area of graphene oxide promotes the adsorption of graphene oxide on textile wastewater and dyeing wastewater.

纺织、印染行业产生的废水中含有有害的染料污染物,需要先进的修复方法来避免环境污染。本文综述了氧化石墨烯基材料去除水中和废水中的染料污染物的研究进展,重点介绍了氧化石墨烯的性质、吸附机理、控制吸附的因素及其应用。染料吸附受温度、吸附剂和染料浓度以及吸附时间的控制。氧化石墨烯复合材料包括膜和气凝胶。氧化石墨烯具有良好的亲水性、耐酸碱性和较强的吸附能力。提高氧化石墨烯的表面活性和比表面积,促进氧化石墨烯在纺织废水和印染废水上的吸附。
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引用次数: 0
Possible formation of long-lived photo-oxidants by photolysis of organic matter phenols in sunlit waters 日照水域中有机物酚类的光解可能形成长寿命光氧化物
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-11-05 DOI: 10.1007/s10311-024-01786-4
Marcello Brigante, Davide Vione

Photodegradation in sunlit waters is a major process of contaminant abatement, yet underlying chemical processes in the presence of dissolved organic matter are poorly known. Long-lived photo-oxidants are reactive species formed when the chromophoric dissolved organic matter absorbs sunlight, and they are involved in the degradation of contaminants. Previous works identified long-lived photo-oxidants with phenoxy radicals, which could be formed upon oxidation of natural phenols by the excited triplet states of chromophoric dissolved organic matter. Here, we generated reactive phenoxy radicals by direct ultraviolet-A photolysis of 2-nitrophenol and 4-nitrophenol. We measured the second-order rate constants for reaction of these phenoxy radicals with 2,4,6-trimethylphenol, a model electron-rich phenol. Results show rate constants of 9.39 × 108(M−1s−1) for the 2-nitrophenoxyl radical, and 1.56 × 108(M−1s−1) for the 4-nitrophenoxyl radical. These values are slightly lower than the typical rate constant of the reaction between 2,4,6-trimethylphenol and the excited triplet states of chromophoric dissolved organic matter, of 3 × 109(M−1s−1). This means that 2,4,6-trimethylphenol would not be degraded to comparable extents by the excited triplet states of chromophoric dissolved organic matter and by long-lived photo-oxidants, if long-lived photo-oxidants were generated solely by the triplet states of chromophoric dissolved organic matter. Overall, findings suggest the occurrence of new pathway involving the direct photolysis of organic matter phenols that generates long-lived photo-oxidants.

日照水域中的光降解是污染物消减的一个主要过程,但人们对溶解有机物存在时的基本化学过程知之甚少。长寿命光氧化物是发色性溶解有机物吸收阳光后形成的活性物种,它们参与了污染物的降解过程。之前的研究发现,长寿命光氧化物与苯氧自由基有关,后者可能是由发色性溶解有机物的激发三重态氧化天然酚时形成的。在这里,我们通过直接紫外线-A 光解 2-硝基苯酚和 4-硝基苯酚生成了活性苯氧自由基。我们测量了这些苯氧自由基与 2,4,6-三甲基苯酚(一种富电子模型苯酚)反应的二阶速率常数。结果显示,2-硝基苯氧基自由基的速率常数为 9.39 × 108(M-1s-1),4-硝基苯氧基自由基的速率常数为 1.56 × 108(M-1s-1)。这些数值略低于 2,4,6-三甲基苯酚与发色性溶解有机物激发三重态反应的典型速率常数 3 × 109(M-1s-1)。这意味着,如果长寿命光氧化剂仅由发色性溶解有机物的三重态产生,则发色性溶解有机物的激发三重态和长寿命光氧化剂对 2,4,6- 三甲基苯酚的降解程度不相上下。总之,研究结果表明存在一种新的途径,涉及有机物酚类的直接光解,从而产生长寿命光氧化物。
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引用次数: 0
Microplastics alter crystal growth in coral skeleton structures 微塑料改变了珊瑚骨骼结构中的晶体生长
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-11-01 DOI: 10.1007/s10311-024-01790-8
Pei-Ying Lin, Shu-Ling Hsieh, De-Sing Ding, Chen-Tung Arthur Chen, David E. Beck, Shuchen Hsieh

Microplastics have emerged as a global environmental issue, inducing harmful effects on marine ecosystems and biodiversity. Their small size allows them to easily disperse across different ecosystems and enter the marine food chain, increasingly threatening coral ecosystems. This study hypothesizes that exposure to polyethylene microplastics alters the structure of coral skeletons. To test this, Briareum violacea corals were cultured under controlled conditions and exposed to polyethylene microplastics at concentrations of 0, 5, 10, 50, 100, and 300 mg/L for seven days. Skeletal structures were analyzed using X-ray diffraction, while inductively coupled plasma mass spectrometry was employed to assess changes in skeletal solubility and measure total calcium ion concentrations in seawater. The results revealed a transformation of coral skeletons from aragonite calcium carbonate crystals to amorphous calcium carbonate, as observed through X-ray diffraction analysis, with polyethylene microplastics causing this transformation to begin at a concentration of 10 mg/L. Additionally, skeletal solubility increased by 7.4-fold, as inferred from calcium ion concentrations measured by inductively coupled plasma mass spectrometry. Here we demonstrate that polyethylene microplastic exposure directly drives the degradation of coral skeletons, emphasizing the urgency of mitigating plastic pollution to safeguard coral ecosystems.

微塑料已成为一个全球环境问题,对海洋生态系统和生物多样性造成有害影响。微塑料体积小,很容易分散到不同的生态系统中,并进入海洋食物链,日益威胁着珊瑚生态系统。本研究假设,接触聚乙烯微塑料会改变珊瑚骨骼的结构。为了验证这一假设,在受控条件下培养了 Briareum violacea 珊瑚,并将其暴露于浓度为 0、5、10、50、100 和 300 毫克/升的聚乙烯微塑料中七天。利用 X 射线衍射分析了骨骼结构,同时采用电感耦合等离子体质谱法评估了骨骼溶解度的变化,并测量了海水中钙离子的总浓度。X 射线衍射分析结果表明,珊瑚骨骼从文石碳酸钙晶体转变为无定形碳酸钙,聚乙烯微塑料在浓度为 10 毫克/升时开始导致这种转变。此外,根据电感耦合等离子体质谱法测得的钙离子浓度推断,骨骼溶解度增加了 7.4 倍。在这里,我们证明了接触聚乙烯微塑料会直接导致珊瑚骨骼退化,从而强调了减轻塑料污染以保护珊瑚生态系统的紧迫性。
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引用次数: 0
Anaerobic digestion of agricultural waste for biogas production and sustainable bioenergy recovery: a review 厌氧消化农业废弃物以生产沼气和实现可持续生物能源回收:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-10-26 DOI: 10.1007/s10311-024-01789-1
Ahmed Alengebawy, Yi Ran, Ahmed I. Osman, Keda Jin, Mohamed Samer, Ping Ai

Anaerobic digestion constitutes a sustainable method for waste management and renewable energy generation, addressing significant environmental and societal challenges. The growing global waste crisis and the increasing momentum toward sustainable energy solutions emphasize the critical need to enhance anaerobic digestion technology for improved efficiency and environmental advantages. This process mitigates waste accumulation, enhances energy security, and reduces greenhouse gas emissions, providing a feasible solution within the framework of a circular bioeconomy. Here, we review the principles of anaerobic digestion and biogas production, focusing on agricultural waste and the utilization of biogas for energy within a sustainable framework. We specifically explore biogas applications in rural and industrial settings, assess the environmental impacts, and discuss the regulatory landscape with insights from China and Europe. This study reveals that the strategic implementation of anaerobic digestion can markedly improve energy yield and sustainability, demonstrating how focused policies and advanced technological practices can optimize biogas utilization. The review enhances comprehension of environmental impacts, emphasizing insights from China and Europe as key examples.

厌氧消化是一种可持续的废物管理和可再生能源发电方法,可应对重大的环境和社会挑战。全球废物危机日益严重,可持续能源解决方案的势头日益强劲,这突出表明迫切需要加强厌氧消化技术,以提高效率和环境优势。这一工艺可以减少废物堆积,提高能源安全,减少温室气体排放,在循环生物经济的框架内提供可行的解决方案。在此,我们回顾了厌氧消化和沼气生产的原理,重点是农业废弃物和在可持续框架内利用沼气作为能源。我们特别探讨了沼气在农村和工业环境中的应用,评估了对环境的影响,并结合中国和欧洲的经验讨论了监管环境。本研究揭示了厌氧消化的战略实施可显著提高能源产量和可持续性,并展示了有针对性的政策和先进的技术实践如何优化沼气利用。本综述以中国和欧洲为例,强调了对环境影响的理解。
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引用次数: 0
4-Nonylphenol adsorption, environmental impact and remediation: a review 4-壬基酚吸附、环境影响和补救:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-10-15 DOI: 10.1007/s10311-024-01788-2
Ronaldo Antunes Funari Junior, Lucas Mironuk Frescura, Bryan Brummelhaus de Menezes, Marcelo Barcellos da Rosa

Endocrine-disrupting compounds such as 4-nonylphenol pose significant societal and environmental challenges due to their toxicity and estrogenic properties, adversely impacting human health, wildlife, and aquatic ecosystems. The complexity of 4-nonylphenol environmental behavior, its transport mechanisms, and the challenges in mitigating its impact through adsorption processes are critical. Here we review 4-nonylphenol contamination with focus on remediation by adsorption. We found that biofilms can accumulate 4-nonylphenol in aquatic environments; adsorption equilibrium in soils is influenced by temperature; and microplastics facilitate the transport of 4-nonylphenol through ecosystems. We present effective materials for 4-nonylphenol removal, including graphene oxides, silica, zeolites, and activated carbons. We analyze key variables influencing adsorption efficiency, offering a comprehensive database and insights into optimal removal strategies.

内分泌干扰化合物(如 4-壬基酚)因其毒性和雌激素特性,对人类健康、野生动物和水生生态系统造成了不利影响,给社会和环境带来了重大挑战。4- 壬基酚环境行为的复杂性、其迁移机制以及通过吸附过程减轻其影响所面临的挑战都至关重要。在此,我们回顾了 4-壬基酚的污染情况,并重点介绍了吸附修复方法。我们发现,生物膜可在水生环境中积累 4-壬基酚;土壤中的吸附平衡受温度影响;微塑料可促进 4-壬基酚在生态系统中的迁移。我们介绍了去除 4-壬基酚的有效材料,包括石墨烯氧化物、二氧化硅、沸石和活性炭。我们分析了影响吸附效率的关键变量,为最佳去除策略提供了一个全面的数据库和见解。
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引用次数: 0
Phototransformation and toxicity enhancement of silver chloride nanoparticles by polystyrenemicroplastics under sunlit 聚苯乙烯微塑料在阳光照射下对氯化银纳米颗粒的光转化和毒性增强作用
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-10-10 DOI: 10.1007/s10311-024-01783-7
Yonghao Sun, Jiaolong Huang, Zhen Wang, Peng Duan, Weicheng Zhang

Silver chloride nanoparticles and microplastics are polluting in surface waters, yet their interactions, associated toxicity and environmental risks are poorly known. Here we hypothesized that polystyrene microplastics could enhance the phototransformation of silver chloride nanoparticles and modify their toxicity. We conducted phototransformation of silver chloride nanoparticles with polystyrene microplastics under light irradiation. The photo-dissolution of silver chloride nanoparticles and photo-reduction of silver ions were determined in both double-distilled-water and environmental waters. We found that polystyrene microplastics highly enhanced the phototransformation of silver chloride nanoparticles by hydroxyl radicals, singlet oxygen, and triplet state microplastics, leading to the release of silver ions and chloride ions. Subsequently, the silver ions were reduced to silver nanoparticles by superoxide radicals. Consequently, the silver species transformation increased the toxicity of silver chloride nanoparticles even at environmental concentration, as evidenced by survival rate of zebrafish larvae reduced from 100% to 23.3%. This is the first study to show that polystyrene microplastics can enhance the phototransformation of silver chloride nanoparticles to silver nanoparticles, thereby increasing the environmental risks of silver chloride nanoparticles in environmental waters.

纳米氯化银颗粒和微塑料对地表水造成污染,但它们之间的相互作用、相关毒性和环境风险却鲜为人知。在此,我们假设聚苯乙烯微塑料可增强氯化银纳米粒子的光转化并改变其毒性。我们用聚苯乙烯微塑料在光照下进行了氯化银纳米粒子的光转化。在双蒸馏水和环境水体中测定了氯化银纳米粒子的光致溶解和银离子的光致还原。我们发现,聚苯乙烯微塑料高度增强了羟基自由基、单线态氧和三重态微塑料对氯化银纳米粒子的光转化,导致银离子和氯离子的释放。随后,银离子被超氧自由基还原成纳米银粒子。因此,即使在环境浓度下,银物种的转化也会增加氯化银纳米粒子的毒性,斑马鱼幼虫的存活率从 100%降至 23.3%就是证明。这是首次有研究表明,聚苯乙烯微塑料可促进氯化银纳米粒子向银纳米粒子的光转化,从而增加氯化银纳米粒子在环境水体中的环境风险。
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引用次数: 0
Remediation of tetracycline pollution using microplastics, green materials, membranes and sonocatalysts: a review 利用微塑料、绿色材料、膜和声波催化剂修复四环素污染:综述
IF 15 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-10-09 DOI: 10.1007/s10311-024-01777-5
Jothivel Sivanesan, Baskaran Sivaprakash, Natarajan Rajamohan, Vedula Sairama Srinivasa Phanindra, Christian Sonne, Rock Keey Liew, Su Shiung Lam

Tetracyclines are broad-spectrum antibiotics used as human and veterinary ailments, anticancer and antiviral agents, and for treating inflammations including arthritis and the Huntington’s disease. However, their inappropriate usage and disposal induce environmental pollution due to their persistency, hydrophilicity and limited volatility, requiring advanced remediation methods. Here, we review techniques for tetracycline removal, including adsorption, advanced oxidation and filtration. Materials to treat tetracycline pollution include aged microplastics, green materials, chemical compounds, sonocatalysts and membranes. Complete tetracycline removal is achieved by using membranes, sonocatalysis and composites. Green composites appear eco-friendly for wastewater treatment. Chemically-synthesized composites are mainly used in photocatalysis, oxidative and enzymatic degradation.

四环素是一种广谱抗生素,可用于治疗人类和兽类疾病、抗癌和抗病毒,以及治疗包括关节炎和亨廷顿氏病在内的炎症。然而,由于其持久性、亲水性和有限的挥发性,不当使用和处置会造成环境污染,因此需要先进的补救方法。在此,我们回顾了四环素的去除技术,包括吸附、高级氧化和过滤。处理四环素污染的材料包括老化微塑料、绿色材料、化合物、声催化剂和膜。利用膜、声催化和复合材料可以完全去除四环素。绿色复合材料在废水处理中显得非常环保。化学合成的复合材料主要用于光催化、氧化和酶降解。
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引用次数: 0
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Environmental Chemistry Letters
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