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石油泄漏事故及工业含油废水排放等严重破坏了人类赖以生存的生态环境,如何有效分离油水混合物成了当前的研究热点。传统的油水分离材料的不可回收性带来材料的二次污染极大限制了它们的广泛应用。纤维素是地球上最丰富的天然聚合物,并且具有生物相容性、生物降解性、化学稳定性和低成本等特点,因此纤维素基油水分离材料亦受到广泛关注。本文系统总结了近年来过滤型和吸附型纤维素基油水分离材料的研究进展,重点围绕纤维素类物质作材料基底(滤纸、棉布等)、用其进行表面改性(纤维素纳米晶体、纤维素衍生物等)以及全纤维素基油水分离材料等方面进行详细分析和介绍,对纤维素基油水分离材料存在的问题进行了探讨,并对其未来发展进行了展望。 相似文献
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气体分离膜技术与传统的气体分离技术(如胺吸收、变压吸附、深冷分离等)相比,具有无相变、高效、节能、操作简便、无二次污染等特点,在空气中氧、氮的富集、石油炼制、化学品生产及二氧化碳的捕获等领域中具有极大的应用前景。分离膜作为气体膜分离技术的核心,获得高透过性及高选择性的膜材料是气体分离膜研究中的目标。聚甲基硅氧烷由于具有优异的高气体透过性、较低的获得成本、结构可变性较强等特点,已成为气体分离膜材料的一个重要研究方向。对目前用于气体分离膜的聚甲基硅氧烷基气体分离膜的种类及合成进行了研究,分析并讨论了各种聚甲基硅氧烷基气体分离膜在分离过程中的机理和作用,对聚甲基硅氧烷基气体分离膜的未来研究方向进行了展望。 相似文献
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相较于传统聚酰胺薄层复合(TFC)膜,金属有机骨架/聚酰胺薄层纳米复合(TFN)膜得益于MOFs材料的高比表面积、有序可控的孔隙结构、良好的聚合物相容性和可定制的化学功能,展现出更高的渗透选择性,在工业应用中显示出巨大的分子和离子分离潜力。本文首先简述了MOFs聚酰胺复合膜的研究背景,然后从MOFs材料的特性和MOFs聚酰胺复合膜的制备策略两个方面出发,总结了MOFs聚酰胺膜研究的最新进展。讨论了MOFs的物化特征在TFN膜的微观结构和分离性能中起的作用;介绍了MOFs聚酰胺复合膜的制备策略,重点对MOFs负载方法及效率进行了分析。最后简述了MOFs聚酰胺复合膜在气、液体系分离中的应用;对MOFs聚酰胺膜在应用过程中的稳定性问题进行了分析,并对未来MOFs聚酰胺复合膜优化MOFs负载和功能性设计的研究进行了展望。 相似文献
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多孔材料如金属有机框架材料(MOFs)、共价有机框架材料(COFs)、有机多孔聚合物(POPs)等由于构筑单元的多样性、可设计性,孔道的可调控性和功能化,已经被广泛用于分离、催化、气体储存以及药物释放等领域。尽管如此,这些多孔材料固有的结构特征让它们普遍对水气非常敏感,最严重时多孔结构在水溶液环境下会坍塌。为解决此类问题,制备疏水的多孔材料是一个非常好的策略。然而,设计超疏水多孔材料具有一定的挑战。介绍了具有(超)疏水性能的MOFs、COFs和POPs的发展现状,对超疏水多孔材料合成思路和结构特点进行了分析,对这类材料在催化、油水分离、气体吸附和分离等方面的应用进行了总结,并进一步探讨了此类材料存在的问题和发展方向。 相似文献
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Shahid Iqbal Sohail Nadeem Razia Bano Ali Bahadur Zahoor Ahmad Mohsin Javed Murefah Mana AL-Anazy Asif Ali Qasier Amel Laref Muhammad Shoaib Guocong Liu Muhammad Abdul Qayyum 《应用聚合物科学杂志》2021,138(25):50604
As to control the increased rate of environmental pollution there is an urgent need to develop improved biodegradable materials regarding the old polymeric packaging materials. It has been done by the incorporation of carbon nanomaterials to the biodegradable starch terpolymers of acrylic acid, methyl methacrylate (MMA), acrylonitrile (AN), 2-Ethylhexyl acrylate (2-EHA), and Ethyl acrylate (EA). The starch-terpolymers were prepared through the free radical polymerization technique using AA, MMA, AN, 2-EHA, EA as monomers. Two different starch-terpolymers were further mixed with carbon nanoparticles (NPs) to form a biodegradable nanocomposite. The biodegradable starch-grafted terpolymers-carbon nanocomposites (STPC NCs) were characterized through scanning electron microscopy, Fourier-transform infrared spectroscopy, thermogravimetric analysis, differential scanning calorimeter, and UV–Visible spectrophotometry. Further, resistivity, electrical conductivity, and biodegradability tests were performed to check its properties for packing materials. The biodegradation of SGCP-composites recorded using the soil burial method was up to 78%. Starch-terpolymers were prepared via free-radical polymerization The biodegradation capability of starch-grafted terpolymers was found to be 78% The decrease in water vapor permeability and solubility proves their utilization as food packaging material 相似文献
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Biodegradation process of a blend of thermoplastic unripe banana flour—polyethylene under composting: Identification of the biodegrading agent
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Horacio Vieyra Eduardo San Martín‐Martínez Esmeralda Juárez Ulises Figueroa‐López Miguel A. Aguilar‐Méndez 《应用聚合物科学杂志》2015,132(29)
Starch‐based biodegradable polymers are obtained by incorporating plant‐derived polymers into plastics. This blending allows for a reduction in the polymer's resistance to microbial degradation. Assessing biodegradability is a key step in the characterization of newly designed polymers. Composting has been taken into consideration in waste management strategies as an alternative technology for plastic disposal. This study analyzed the biodegradability of an injection‐molded plastic material in which thermoplastic unripe banana flour (TPF) acts as a matrix (70%) and metallocene catalyzed polyethylene acts as a reinforcing filler (30%). This plastic was termed 70 TPF, and the structural, physical, and mechanical changes associated with its degradation were analyzed. The characterization of the microorganism that contributes to 70 TPF biodegradation was also performed. After composting, 70 TPF decreased in tensile strength and the TPF moiety in the blend was lost, greatly affecting the microstructure of the sample. Based on these indicators of degradation, this study identified the fungus Mortierella elongata as the microorganism responsible for the degradation of the plastic, a finding that supports the role of fungal communities in the biodegradation of designed materials. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42258. 相似文献
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生物可降解聚酯纤维进展 总被引:17,自引:0,他引:17
随着人们对废弃高分子材料造成环境污染的日益认识,对生物可降解材料的研究得到了重视和发展。本文对高分子材料的降解机理和目前在聚酯纤维方面已取得的进展进行了讨论。着重介绍了目前研究有所发展的聚乳酸(PLA)、聚(β-羟基丁酸酯)(PHB)和聚丁二酸酯类等近几年的工作。 相似文献
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Leonardo de Souza Vieira Larissa Stieven Montagna Ana Paula Bernardo da Silva Gleice Ellen Almeida Verginio Fabio Roberto Passador 《应用聚合物科学杂志》2021,138(33):50821
The use of biodegradable polymers is an interesting way to reduce the polymeric waste accumulation in the environment. However, the addition of fillers to biodegradable polymer matrices may decrease their biodegradability. Glassy carbon (GC) is a promising carbon material that can be employed as a filler in the production of antistatic packaging utilized to protect electronic components. The use of a biodegradable polymeric matrix such as poly (3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) can be an excellent alternative for the preparation of green composites to be used in these packages. This work aims to evaluate the effect of the GC addition and the GC particle size on the biodegradability of the PHBV matrix, as well as to study the result of the employment of a previous photodegradation treatment on the biodegradation in aqueous medium of PHBV/GC composites. Scanning electron microscopy, residual weight measurement (%) and surface roughness showed that GC does not interfere negatively with PHBV biodegradability. Differential scanning calorimetry analysis and residual weight measurement permitted to suggest that the increase in the crystallinity degree of PHBV and PHBV/GC samples occasioned by the ultraviolet radiation hindered the water and enzyme access to the bulk of the materials, decreasing the biodegradability. 相似文献
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塑料“白色污染”越来越引起人们的广泛关注,在自然界微生物的作用下能降解成为二氧化碳、水和无机物的生物降解材料是解决问题的一种有效途径。新型生物降解聚酯的开发离不开对材料生物降解性能的研究和评价方法的开发,为此,本文评述了生物降解聚酯的类型及其生物降解性能、聚酯降解微生物与酶的研究进展,介绍了土壤、堆肥和水体环境中的材料生物降解性评价方法。可以看到低成本、高性能是生物降解聚酯的发展方向;现有聚酯降解微生物和酶尚不能满足聚酯工业回收应用要求,需开发更高效、更稳定的酶;目前生物降解评价方法受接种环境影响大、评价周期长且难完全模拟材料在自然环境中生物降解行为,新型生物降解聚酯的开发也亟需可靠、快速的降解评价方法。 相似文献
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Biodegradability of biomass pyrolysis oils: Comparison to conventional petroleum fuels and alternatives fuels in current use 总被引:1,自引:0,他引:1
Joël Blin Ghislaine Volle Philippe Girard Tony Bridgwater Dietrich Meier 《Fuel》2007,86(17-18):2679-2686
Concern with environmental issues such as global climate change has stimulated research into the development of more environmentally friendly technologies and energy sources. One critical area of our economy is liquid fuels. Fast pyrolysis of lignocellulosic biomass for liquids production is of particular concern, as it is one of the most interesting ways to produce renewable liquid fuel for transport and heat and power production.The aerobic biodegradability of various pyrolysis oils from different origins and of a EN 590 diesel sample was examined using the Modified Sturm (OECD 301B). The results demonstrate that all fast pyrolysis oils assessed are biodegradable with similar shaped curves with 41–50% biodegradation after 28 days, whereas the diesel sample reached only 24% biodegradation. Since pyrolysis oils achieved biodegradability over 20% these are classified as inherently biodegradable. Modelling of biodegradation processes was successfully performed with a first-order chemical reaction.The biodegradability results obtained for biomass pyrolysis oils are compared to those of conventional and alternative fuels. 相似文献
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Biodegradable polymers are by definition those that degrade as a result of the action of microorganisms and/or enzymes. The rate of this biodegradation may vary from hours to years depending on the molecular architecture of the polymer in question. Biopolymers like lignin take years to degrade while many proteins and polysaccharides degrade within hours to days. The same is true for the synthetic biodegradable polymers where polyethylene is sometimes regarded as inert to biodegradation while polyanhydrides are rapidly biodegradable. The influence of structure, morphology, and surface area on the biodegradability are discussed, with polyesters and degradable polyethylene (with pro-oxidant and/or biodegradable additives) as examples. The rate of biodegradation is controllable by choosing the appropriate molecular architecture. In addition to this the environmental interaction of these polymers should be determined. The degradation product pattern of biodegradable polymers should be compatible with the natural degradation mechanisms (i.e., catabolisms). 相似文献