Microplastic removal

  • 文章类型: Journal Article
    由于它们对降解的抵抗力,分布广泛,容易扩散和潜在的生物吸收,微塑料(MPs)污染已成为主要的环境问题。在这项研究中,与其他吸附剂(裸Fe3O4,PEI/Fe3O4和CA/Fe3O4)相比,PEG修饰的Fe3O4磁性纳米颗粒对聚乙烯(PE)微球表现出优异的吸附效率。通过吸附等温线分析发现PE的最大吸附容量为2203mg/g。PEG/Fe3O4即使在低温(5°C,2163毫克/克),而中性pH有利于MP吸附。阴离子的存在(Cl-,SO42-,HCO3-,NO3-)和腐殖酸抑制了MP的吸附。提出吸附过程主要由分子间氢键驱动。总的来说,这项研究表明,PEG/Fe3O4可以潜在地用作对MP的有效控制,从而改善水环境和水资源的质量。
    Due to their resistance to degradation, wide distribution, easy diffusion and potential uptake by organisms, microplastics (MPs) pollution has become a major environmental concern. In this study, PEG-modified Fe3O4 magnetic nanoparticles demonstrated superior adsorption efficiency against polyethylene (PE) microspheres compared to other adsorbents (bare Fe3O4, PEI/Fe3O4 and CA/Fe3O4). The maximum adsorption capacity of PE was found to be 2203 mg/g by adsorption isotherm analysis. PEG/Fe3O4 maintained a high adsorption capacity even at low temperature (5°C, 2163 mg/g), while neutral pH was favorable for MP adsorption. The presence of anions (Cl-, SO42-, HCO3-, NO3-) and of humic acids inhibited the adsorption of MPs. It is proposed that the adsorption process was mainly driven by intermolecular hydrogen bonding. Overall, the study demonstrated that PEG/Fe3O4 can potentially be used as an efficient control against MPs, thus improving the quality of the aquatic environment and of our water resources.
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  • 文章类型: Review
    微塑料是塑料分子的小碎片,它们在各种常规产品如美容产品中找到了应用。稍后,人们意识到它对海洋和陆地生物有几种毒性作用。这篇综述是一种理解微塑料的方法,他们的起源,在水生系统中扩散,它们的生物降解和影响生物降解的因素。此外,本文讨论了微生物生物技术中应用的主要工程方法。具体来说,它回顾了微生物基因工程,如PET酶工程,MHET-ase工程,和固定方法。此外,通过评估最近的报告,提出了与塑料去除相关的主要挑战。
    Microplastics are the small fragments of the plastic molecules which find their applications in various routine products such as beauty products. Later, it was realized that it has several toxic effects on marine and terrestrial organisms. This review is an approach in understanding the microplastics, their origin, dispersal in the aquatic system, their biodegradation and factors affecting biodegradation. In addition, the paper discusses the major engineering approaches applied in microbial biotechnology. Specifically, it reviews microbial genetic engineering, such as PET-ase engineering, MHET-ase engineering, and immobilization approaches. Moreover, the major challenges associated with the plastic removal are presented by evaluating the recent reports available.
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  • 文章类型: Journal Article
    污泥是微塑料(MPs)向环境扩散的重要载体,因此,从污泥中高效去除MPs是迫切需要的。在这项研究中,提出了热液碳化(HTC),并评估了其从污水污泥中去除MP的潜力。光学显微镜和显微FTIR分析表明,污泥中MPs的浓度显著降低,在HTC温度为260°C时显示79%的降低。通过HTC实验研究了缩聚物和加成聚合物的潜在分解机理,使用聚对苯二甲酸乙二醇酯-微塑料(PET-MPs)和聚丙烯-微塑料(PP-MPs)。在HTC的过程中,PET-MPs的崩解效率显著高于PP-MPs,由于PET酯键容易通过水解被单体化。此外,残余PP-MPs的物理化学性质分析表明,暴露于热导致PP进行热解反应,导致聚合物分子链的随机断裂。总的来说,这些结果为HTC在去除污水污泥中的MPs的关键作用提供了初步的见解,为未来降低污水污泥中MP带来的风险提供了一种新的解决方案。
    Sewage sludge is an important vehicle for the diffusion of microplastics (MPs) into the environment, and thus, efficient removal of MPs from sludge is in urgent need. In this study, hydrothermal carbonization (HTC) is proposed and its potential for the removal of MPs from sewage sludge is assessed. Optical microscopy and micro-FTIR analysis showed that the concentrations of MPs in sewage sludge decreased significantly, exhibiting a 79% reduction with a HTC temperature of 260 °C. The potential decomposition mechanism of condensation polymers and addition polymers were investigated through HTC experiments, using polyethylene terephthalate-microplastics (PET-MPs) and polypropylene-microplastics (PP-MPs). During the HTC process, the disintegration efficiency of PET-MPs was significantly higher than PP-MPs, due to the PET ester bond being easily monomerized by hydrolysis. Furthermore, analyses of physicochemical properties of the residual PP-MPs indicated that exposure to heat cause PP to undergo pyrolysis reaction, resulting in the random rupture of polymer molecular chains. Overall, these results provide the first insight into the critical role of HTC in the removal of MPs from sewage sludge, providing a novel solution for reducing the risk posed by MPs in sewage sludge in the future.
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  • 文章类型: Journal Article
    Microplastics (MPs) derived from plastic wastes have attracted wide attention throughout the world due to the wide distribution, easy transition, and potential threats to organisms. This study proposes efficient Mg/Zn modified magnetic biochar adsorbents for microplastic removal. For polystyrene (PS) microspheres (1 µm, 100 mg/mL) in aqueous solution, the removal efficiencies of magnetic biochar (MBC), Mg modified magnetic biochar (Mg-MBC), and Zn modified magnetic biochar (Zn-MBC) were 94.81%, 98.75%, and 99.46%, respectively. It is supposed that the adsorption process was a result of electrostatic interaction and chemical bonding interaction between microplastics and biochar. The coexisting H2PO4- and organic matters in real water significantly affected the removal efficiency of Zn-MBC due to competitive adsorption effect. Microplastic degradation and adsorbent regeneration were accomplished by thermal treatment simultaneously. The degradation of adsorbed MPs was promoted by the catalytic active sites originated from Mg and Zn, releasing adsorption sites. Thermal regeneration maintained the adsorption capability. Even after five adsorption-pyrolysis cycles, MBC (95.02%), Mg-MBC (94.60%), and Zn-MBC (95.79%) showed high microplastic removal efficiency. Therefore, the low-cost, eco-friendly, and robust Mg/Zn-MBCs have promising potential for application in microplastic removal.
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  • 文章类型: Journal Article
    Microplastic (MP) contamination in water has garnered significantly global concerns. The MP removal particularly challenges when the particle size decreases to several microns and other contaminants co-exist. This study used the coagulative colloidal gas aphrons (CCGAs) to simultaneously remove the micron-scale MP particles (~5 µm in diameter) and dissolved organic matter (DOM). Carboxyl-modified poly-(methyl methacrylate) (PMMA) and unsurface-coated polystyrene (PS) were chosen as target MPs. Over 94% of PS particles and almost 100% of color were simultaneously removed with lower CCGA consumption than the scenarios with either contaminant in water. The PMMA removal was not as high as the PS removal since the HA polyanions could compete with the negatively-charged PMMA for CCGAs. High salinity reduced the removal of HA by changing its interfacial behaviors without impacting the MP separation. In river water or influent of wastewater treatment plant, the MP particles were almost completely eliminated whereas the DOM (tyrosine-like or tryptophan-like) was partially removed. The fluorescence quenching titration revealed that CCGAs preferably captured the free DOM and the DOM-coated MP particles through complexation interaction. The study denoted that the CCGA system could be a robust tool for efficiently and synergistically removing micron-scale MPs and DOM from different water matrixes.
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