nanocomposite

纳米复合材料
  • 文章类型: Journal Article
    在目前的工作中,使用Fe和MoS2的纳米混合材料的合成已通过具有成本效益和环境友好的途径进行可持续制造创新。制备了稻草提取物,并将其与二硫化钼(MoS2)和硝酸铁[Fe(NO3)3·9H2O]混合,作为还原和螯合剂合成了纳米杂化材料,然后加热和煅烧。X射线衍射(XRD)图证实了由单斜晶Fe2(MoO4)3,立方Fe2.957O4和正交FeS组成的纳米杂化物的形成,其中86%由Fe2(MoO4)3组成。通过傅里叶变换红外光谱(FTIR)对其性能进行了分析,原子力显微镜(AFM),扫描电子显微镜(SEM),和透射电子显微镜(TEM)。动态光散射(DLS)研究的结果表明,尺寸分布不均匀,18%的颗粒的平均粒径为48.42nm,82%的颗粒的平均粒径为384.54nm。此外,zeta电位测量为-18.88mV,表明适度的稳定性。X射线光电子能谱(XPS)结果证实了Fe2和Fe3氧化态的存在以及钼(Mo)的存在,氧(O),和硫(S)。制备的纳米杂化材料的带隙为2.95eV,光致发光强度几乎是裸露MoS2的两倍。本工作在生物医学应用的光致发光纳米平台中具有潜在的应用。
    In present work, synthesis of a nanohybrid material using Fe and MoS2 has been performed via a cost-effective and environmentally friendly route for sustainable manufacturing innovation. Rice straw extract was prepared and used as a reducing and chelating agent to synthesize the nanohybrid material by mixing it with molybdenum disulfide (MoS2) and ferric nitrate [Fe (NO3)3.9H2O], followed by heating and calcination. The X-ray diffraction (XRD) pattern confirms the formation of a nanohybrid consisting of monoclinic Fe2(MoO4)3, cubic Fe2.957O4, and orthorhombic FeS with 86% consisting of Fe2(MoO4)3. The properties were analyzed through Fourier-transformed infrared spectroscopy (FTIR), atomic force microscopy (AFM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The results of the dynamic light scattering (DLS) study revealed a heterogeneous size distribution, with an average particle size of 48.42 nm for 18% of particles and 384.54 nm for 82% of particles. Additionally, the zeta potential was measured to be -18.88 mV, suggesting moderate stability. X-ray photoelectron spectroscopy (XPS) results confirmed the presence of both Fe2+ and Fe3+ oxidation states along with the presence of Molybdenum (Mo), oxygen (O), and Sulphur (S). The prepared nanohybrid material exhibited a band gap of 2.95 eV, and the photoluminescence intensity increased almost twice that of bare MoS2. The present work holds potential applications in photo luminescent nanoplatform for biomedical applications.
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  • 文章类型: Journal Article
    设计了一种确定微藻中叶绿素含量的独特方法,该方法采用了具有10µm间隙的金叉指状电极(G-IDE),由纳米分子印迹聚合物(纳米MIP)和二氧化钛/多壁碳纳米管(TiO2/MWCNT)纳米复合材料增强。纳米MIP,使用叶绿素模板空隙产生,成功捕获叶绿素,而TiO2/MWCNT纳米复合材料,通过溶胶-凝胶技术合成,表现出一致的分布和锐钛矿晶体结构。采购的叶绿素粉的重新结合,用作纳米MIP合成的模板,确定系数高(R2=0.9857)。通过将TiO2/MWCNT纳米复合材料与纳米MIP相结合,G-IDE传感方法检测微藻中叶绿素的R2值略好,为0.9892。与市售叶绿素粉相比,所提供的G-IDE传感器在叶绿素检测方面显示出显着的三倍增强。它的检出限为0.917mL(v/v),线性范围为10-6至1mL。通过验证其可重复性和可重用性,证实了该传感器检测微藻叶绿素的有效性。
    A unique method for determining chlorophyll content in microalgae is devised employing a gold interdigitated electrode (G-IDE) with a 10-µm gap, augmented by a nano-molecularly imprinted polymer (nano-MIP) and a titanium dioxide/multiwalled carbon nanotube (TiO2/MWCNT) nanocomposite. The nano-MIP, produced using chlorophyll template voids, successfully trapped chlorophyll, while the TiO2/MWCNT nanocomposite, synthesized by the sol-gel technique, exhibited a consistent distribution and anatase crystalline structure. The rebinding of procured chlorophyll powder, which was used as a template for nano-MIP synthesis, was identified with a high determination coefficient (R2 = 0.9857). By combining the TiO2/MWCNT nanocomposite with nano-MIP, the G-IDE sensing method achieved a slightly better R2 value of 0.9892 for detecting chlorophyll in microalgae. The presented G-IDE sensor showed a significant threefold enhancement in chlorophyll detection compared with commercially available chlorophyll powder. It had a detection limit of 0.917 mL (v/v) and a linear range that spanned from 10-6 to 1 mL. The effectiveness of the sensor in detecting chlorophyll in microalgae was confirmed through validation of its repeatability and reusability.
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  • 文章类型: Journal Article
    以有效且可回收的方式将亚硝酸盐选择性还原为气态氮(N2)是处理相关废水的有吸引力的替代方案。在这里,通过将Pd(0)纳米颗粒封装到多孔聚苯乙烯载体中,巧妙地组装了基于Pd的纳米复合材料(Pd@EDA-CMPS),先前用乙二胺(EDA)作为内源性电子供体进行了官能化。系统宏观实验证实,预接枝的EDA基团可以充分激发负载的Pd(0)纳米颗粒的催化活性,具有较高的去除效率和Pd@EDA-CMPS对亚硝酸盐的N2选择性;具体而言,Pd@EDA-CMPS实现了高N2选择性(86%),对竞争阴离子具有出色的抗干扰能力和广泛的pH范围适用性(4-11),而没有检测到其对应的N2产生(CMPS,EDA-CMPS,和Pd@CMPS)。光谱分析表明,接枝的EDA基团在多孔基底内部负载H的Pd(0)纳米颗粒的形成中起着决定性的作用。与EDA独特的pH缓冲能力相结合,促使反应产生氮气(N2)而不是氨(NH3)。耗尽的Pd@EDA-CMPS可以通过NaOH(洗脱)和NaBH4(恢复)溶液进行有希望的再生,而处理能力和N2选择性没有明显损失。这项工作提供了一种可行的策略,可以将亚硝酸盐催化还原为N2,而无需提供外源还原剂,例如氢气。
    Selectively reducing nitrite to gaseous nitrogen (N2) with an effective and recyclable fashion stands as an attractive alternative for treating the relevant wastewater. Herein, a Pd-based nanocomposite (Pd@EDA-CMPS) was subtly assembled by encapsulating Pd(0) nanoparticles into a porous polystyrene carrier, which was aforehand functionalized with ethylenediamine (EDA) as the endogenous electron donator. Systematical macroscopic experiments confirm that the pre-grafted EDA groups can substantially stimulate the catalytic activity of the laden Pd(0) nanoparticles with high removal efficiency and N2 selectivity of Pd@EDA-CMPS toward nitrite; specifically, high N2 selectivity (86 %) was achieved by Pd@EDA-CMPS with an excellent anti-interference ability against competing anion and a broad pH-range applicability (4-11), whereas no N2 production was detected for its counterparts (CMPS, EDA-CMPS, and Pd@CMPS). Spectroscopic analyses reveal that the grafted EDA groups played a decisive role in the formation of H-loaded Pd(0) nanoparticles inside the porous substrate, which joint with the unique pH-buffering ability of EDA drove the reaction to the production of nitrogen (N2) rather than ammonia (NH3). The exhausted Pd@EDA-CMPS can be promisingly regenerated by NaOH (eluting) and NaBH4 (restoring) solution without obvious loss in treatment capacity and N2 selectivity. This work provides a feasible strategy for catalytically reducing nitrite into N2 without the provision of exogenous reductor such as hydrogen.
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  • 文章类型: Journal Article
    具有ABX3结构的氧化物和卤化物钙钛矿材料表现出许多优异的性能,包括高介电常数,电化学性能,宽带隙,和大的吸收系数。这些属性导致了一系列的应用,包括可再生能源和光电子,需要高性能催化剂的地方。然而,单一结构的钙钛矿很难单独同时满足多种应用的多样化需求,例如高性能和良好的稳定性。因此,钙钛矿纳米复合材料已经开发,以解决当前的限制和增强其功能,通过结合钙钛矿与两种或更多的材料,以创建互补的材料。这篇综述论文根据其结构组成对钙钛矿纳米复合材料进行了分类,并概述了其合成方法,以及它们在各个领域的应用。这些包括燃料电池,电化学水分解,CO2缓解,超级电容器,和光电设备。此外,这篇综述总结了他们的研究现状,实际挑战,以及可再生能源和电子领域的未来前景。
    The oxide and halide perovskite materials with a ABX3 structure exhibit a number of excellent properties, including a high dielectric constant, electrochemical properties, a wide band gap, and a large absorption coefficient. These properties have led to a range of applications, including renewable energy and optoelectronics, where high-performance catalysts are needed. However, it is difficult for a single structure of perovskite alone to simultaneously fulfill the diverse needs of multiple applications, such as high performance and good stability at the same time. Consequently, perovskite nanocomposites have been developed to address the current limitations and enhance their functionality by combining perovskite with two or more materials to create complementary materials. This review paper categorizes perovskite nanocomposites according to their structural composition and outlines their synthesis methodologies, as well as their applications in various fields. These include fuel cells, electrochemical water splitting, CO2 mitigation, supercapacitors, and optoelectronic devices. Additionally, the review presents a summary of their research status, practical challenges, and future prospects in the fields of renewable energy and electronics.
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  • 文章类型: Journal Article
    这项研究提出了一种创新的方法,通过引入一种新型的ZnO-蜂胶纳米复合材料(ZnO-PNC)来对抗细菌中抗生素耐药性不断升级的威胁。抗生素的过度使用,特别是在像COVID-19大流行这样的事件中,增强了细菌耐药性,需要创新的解决方案。该研究采用具有成本效益和可控的生物合成方法来生产ZnO纳米颗粒(ZnO-NP),蜂胶提取物对减少和稳定Zn2离子至关重要。然后通过掺入ZnO-NP来创建可生物降解的纳米蜂胶基质,形成ZnO-PNC。通过FT-IR和Zeta电位分析证实了结构稳定性,虽然通过TEM验证了纳米级特性,SEM,和XRD分析。各种物质的抗菌功效,包括蜂胶,纳米蜂胶,乙醇蜂胶提取物,ZnO-NP,和ZnO-PNC,针对革兰氏阴性和革兰氏阳性细菌进行评估,与28种抗生素进行比较。在测试的细菌中,铜绿假单胞菌PAO1ATCC15692对生物合成的纳米复合材料ZnO-PNC比对ZnO-NP(38毫米)和纳米胶(32毫米)更敏感(40毫米),而大肠杆菌对纳米蜂胶(0毫米)的抗性高于对ZnO-NP(31毫米)的抗性,和ZnO-PNC(34毫米)。该研究揭示了当蜂胶与绿色合成的ZnO-NPs以ZnO-PNCs的形式结合时的协同效应,显著提高了它们对所有测试细菌的效率,包括大肠杆菌等抗生素耐药菌株。纳米复合材料优于其他材料和抗生素,表现出显著的抗菌效果。SEM成像证实了ZnO-NP和ZnO-PNC对细菌细胞膜的破坏。该研究强调了整合到可生物降解材料中的ZnO-NPs的潜在应用,并强调了氧化锌-蜂胶纳米复合材料在对抗抗菌耐药性方面的重要性。总的来说,这项研究为对抗多重耐药细菌提供了一个全面的解决方案,为感染控制的新方法开辟了道路。
    This study proposes an innovative approach to combat the escalating threat of antibiotic resistance in bacteria by introducing a novel ZnO-propolis nanocomposite (ZnO-P NCs). The overuse of antibiotics, particularly during events like the COVID-19 pandemic, has intensified bacterial resistance, necessitating innovative solutions. The study employs a cost-effective and controllable biosynthesis method to produce ZnO nanoparticles (ZnO-NPs), with propolis extract crucially contributing to the reduction and stabilization of Zn2+ ions. A biodegradable nano-propolis matrix is then created by incorporating ZnO-NPs, forming the ZnO-P NCs. Structural stability is confirmed through FT-IR and Zeta potential analysis, while nanoscale properties are validated via TEM, SEM, and XRD analyses. The antimicrobial efficacy of various substances, including propolis, nano propolis, ethanolic propolis extract, ZnO-NPs, and ZnO-P NCs, is assessed against Gram-negative and Gram-positive bacteria, alongside a comparison with 28 antibiotics. Among the bacteria tested, Pseudomonas aeruginosa PAO1 ATCC15692 was more sensitive (40 mm) to the biosynthesized nanocomposite ZnO-P NCs than to ZnO-NPs (38 mm) and nanopropolis (32 mm), while Escherichia coli was resistant to nanopropolis (0 mm) than to ZnO-NPs (31 mm), and ZnO-P NCs (34 mm). The study reveals a synergy effect when combining propolis with green-synthesized ZnO-NPs in the form of ZnO-P NCs, significantly improving their efficiency against all tested bacteria, including antibiotic-resistant strains like E. coli. The nanocomposite outperforms other materials and antibiotics, demonstrating remarkable antibacterial effectiveness. SEM imaging confirms the disruption of bacterial cell membranes by ZnO-NPs and ZnO-P NCs. The study emphasizes the potential applications of ZnO-NPs integrated into biodegradable materials and underscores the significance of the zinc oxide-propolis nanocomposite in countering antimicrobial resistance. Overall, this research offers a comprehensive solution to combat multidrug-resistant bacteria, opening avenues for novel approaches in infection control.
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  • 文章类型: Journal Article
    甘蔗基产品本身就含有丰富的硅等元素,碳和氮。因此,这些成为在广泛的应用领域中使用的理想前体。吸引人的领域之一是将它们转化为具有高度兴趣的纳米材料,可用于几种突出的应用。在纳米材料中,基于二氧化硅纳米颗粒(SNP)的甘蔗产品,碳点(CD),基于金属/金属氧化物的NP,纳米纤维素,纤维素纳米纤维(CNFs),和纳米生物炭的报道越来越多。通过操纵实验条件和选择合适的起始前体和元素,有可能设计这些纳米材料具有适合特定应用的高度期望的性质。本综述提供了来自最近文献的发现,其中已经努力传达用于合成上述纳米材料的基于甘蔗的产品领域的新发展。就各种纳米材料的合成和应用前景进行了系统的讨论。只要有可能,进行了比较分析,以突出甘蔗产品与其他基于生物质的材料相比,用于预期目的的潜力。这篇评论有望在提供最新的文献调查中脱颖而出,并为读者提供未来研究的必要方向。
    这篇综述的重点是甘蔗衍生的纳米材料,如二氧化硅,纳米纤维素,纳米纤维,纳米晶体和金属/非金属纳米粒子及其在各种能源和环境领域的应用。
    Sugarcane-based products are inherently rich in elements such as silicon, carbon and nitrogen. As such, these become ideal precursors for utilization in a wide array of application fields. One of the appealing areas is to transform them into nanomaterials of high interest that can be employed in several prominent applications. Among nanomaterials, sugarcane products based on silica nanoparticles (SNPs), carbon dots (CDs), metal/metal oxide-based NPs, nanocellulose, cellulose nanofibers (CNFs), and nano biochar are becoming increasingly reported. Through manipulation of the experimental conditions and choosing suitable starting precursors and elements, it is possible to devise these nanomaterials with highly desired properties suited for specific applications. The current review presents the findings from the recent literature wherein an effort has been made to convey new development in the field of sugarcane-based products for the synthesis of the above-mentioned nanomaterials. Various nanomaterials were systematically discussed in terms of their synthesis and application perspectives. Wherever possible, a comparative analysis was carried out to highlight the potential of sugarcane products for the intended purpose as compared to other biomass-based materials. This review is expected to stand out in delivering an up-to-date survey of the literature and provide readers with necessary directions for future research.
    This review focuses on sugarcane-derived nanomaterials such as silica, nano cellulose, nanofibers, nanocrystals and metal/nonmetal nanoparticles and their application in various energy and environmental fields.
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  • 文章类型: Journal Article
    植物基材料和可食用薄膜已成为传统包装材料的有希望的替代品,提供可持续和环保的解决方案。这篇小型评论强调了源自多糖的植物基材料的重要性,蛋白质,和脂质,展示其可再生和可生物降解的性质。可食薄膜的性质,包括机械强度,阻隔性能,光学特性,热稳定性,和延长保质期,正在探索,展示其对食品包装和其他应用的适用性。此外,3D打印技术的应用允许定制设计和复杂的几何形状,为个性化营养铺平道路。功能化策略,如主动和智能包装,生物活性化合物的掺入,和抗菌性能,还讨论了,提供额外的功能和好处。确定了挑战和未来方向,强调可持续性的重要性,可扩展性,regulation,和性能优化。强调了植物基材料和可食用薄膜的潜在影响,从减少对化石燃料的依赖到减少塑料废物和促进循环经济。总之,以植物为基础的材料和可食用薄膜在彻底改变包装工业方面具有巨大潜力,为传统材料提供可持续的替代品。拥抱这些创新将有助于减少塑料废物。促进循环经济,创造一个可持续和有弹性的星球。
    Plant-based materials and edible films have emerged as promising alternatives to conventional packaging materials, offering sustainable and environmentally friendly solutions. This mini-review highlights the significance of plant-based materials derived from polysaccharides, proteins, and lipids, showcasing their renewable and biodegradable nature. The properties of edible films, including mechanical strength, barrier properties, optical characteristics, thermal stability, and shelf-life extension, are explored, showcasing their suitability for food packaging and other applications. Moreover, the application of 3D printing technology allows for customized designs and complex geometries, paving the way for personalized nutrition. Functionalization strategies, such as active and intelligent packaging, incorporation of bioactive compounds, and antimicrobial properties, are also discussed, offering additional functionalities and benefits. Challenges and future directions are identified, emphasizing the importance of sustainability, scalability, regulation, and performance optimization. The potential impact of plant-based materials and edible films is highlighted, ranging from reducing reliance on fossil fuels to mitigating plastic waste and promoting a circular economy. In conclusion, plant-based materials and edible films hold great potential in revolutionizing the packaging industry, offering sustainable alternatives to conventional materials. Embracing these innovations will contribute to reducing plastic waste, promoting a circular economy, and creating a sustainable and resilient planet.
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  • 文章类型: Journal Article
    纤维素纳米纤维(CNF)产生防止与腐蚀性物质接触并改善防腐蚀的物理屏障。油棕叶(OPF),种植园未充分利用的生物质废物的主要来源,被加工成CNF。OPF-CNF,与羟乙基纤维素混合为基质,形成纳米复合材料。使用电化学方法的腐蚀分析表明,用含有5%CNF的富含纤维素的纳米复合材料涂覆的铜具有显着降低的腐蚀速率,效率为97.92%。这种基于CNF的涂层,结合屏障和钝化机制,提高性能,提供有竞争力的,环保替代传统涂料。
    Cellulose nanofibers (CNF) create a physical barrier preventing contact with corrosive substances and improving corrosion prevention. Oil palm fronds (OPF), the primary source of underused biomass waste from plantations, were processed into CNF. The OPF-CNF, mixed with hydroxyethyl cellulose as the matrix, forms a nanocomposite. Corrosion analysis using electrochemical methods demonstrated that copper coated with cellulose-rich nanocomposite containing 5 % CNF had a significantly decreased corrosion rate with an efficiency of 97.92 %. This CNF-based coating, combining barrier and passivation mechanisms, enhances performance, providing a competitive, eco-friendly alternative to conventional coatings.
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  • 文章类型: Journal Article
    脱碳合成方法的发展是制造氨的关键步骤,不可或缺的化学品和潜在的碳中和能源载体。在这方面,光催化生产技术作为能源密集型和对环境有害的Haber-Bosch工艺的可持续替代方法已经获得了广泛的关注。这里,我们提出了负载在微孔ZSM-5型硅酸铁沸石上的钴铁氧体纳米颗粒作为用于氨生成的理想新型光催化剂。作为微孔载体引入的沸石增加了催化活性位点。使用简单的一锅溶胶-凝胶法合成了各种重量百分比(10、25和50%)的CoFe2O4的铁氧体钴(CoFe2O4)和CoFe2O4/硅酸铁(CF/FS)纳米复合材料。在可见光照射下,研究了样品在氨生产中的光催化性能。使用CF50%/FS光催化剂可实现最高的NH4生成率(484.74µmolL-1h-1)。<50nm大小的CoFe2O4纳米颗粒在沸石表面的分布,如TEM图像所示,和广泛的BET表面积被提出为在CF50%/FS光催化剂中提高光催化活性的令人信服的证据。
    The development of decarbonized synthesis approaches is a critical step in the fabrication of ammonia, an indispensable chemical and a potential carbon-neutral energy carrier. In this regard, the photocatalytic production technology has gained ample attention as a sustainable alternative to energy-intensive and environmentally detrimental Haber-Bosch process. Here, we present cobalt ferrite nanoparticles supported on microporous ZSM-5 type ferrisilicate zeolite as a desirable novel photocatalyst for the ammonia generation. The zeolite introduced as a microporous support increasing the catalytically active sites. A straightforward one-pot sol-gel method was used to synthesize cobalt ferrite (CoFe2O4) and CoFe2O4/ferrisilicate (CF/FS) nanocomposites with various weight percentages (10, 25 and 50%) of CoFe2O4. The photocatalytic performances of the samples in the production of ammonia were investigated under visible light irradiation. The highest rate of NH4+ production (484.74 µmol L-1 h-1) was achieved using the CF50%/FS photocatalyst. The distribution of < 50 nm-sized CoFe2O4 nanoparticles on the surface of the zeolite, as demonstrated by TEM images, and extensive BET surface areas are presented as convincing evidences for the improved photocatalytic activity paticularly in CF50%/FS photocatalyst.
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  • 文章类型: Journal Article
    使用聚(醚-嵌段-酰胺)(PEBA)弹性体作为共混物对应物,制备了基于高性能聚(乳酸)(PLA)共混物的复合材料。证实了增容剂(ADR)增强了PLA和PEBA之间的相互作用。将碳纳米管(CNT)和有机粘土(30B)单独且同时添加到共混物中以产生生物纳米复合材料。形态学结果表明,碳纳米管主要分散在PEBA区域,而30B主要位于PLA和PEBA相的界面区域。添加的CNT和30B的选择性定位导致相容化的PLA/PEBA共混物的性质的显著改变。形成生物纳米复合材料后,PLA的脆性和可燃性得到了明显改善。差示扫描量热法结果表明,CNTs和30B有助于复合材料中PLA和PEBA的结晶,CNT提供优于30B的成核效率。热重分析揭示了在添加CNT和/或30B之后共混物的热稳定性增强,在包含2phr30B的情况下,损失20重量%时增加高达16°C。CNTs和/或30B的添加改善了共混物在燃烧试验期间的抗滴落性能,和CNT表现出更好的抗滴落效率。在形成相容化共混物后,PLA的延展性得到了极大的改善,并且随着CNT和/或30B的并入而进一步改善(从纯PLA的9%增加到含有CNT/30B的杂化复合材料的252%)。添加1phrCNTs的复合材料的冲击强度约为PLA的3倍。流变特性表明添加的填料的(伪)网络形成,导致电阻率的显著降低,添加3份量的碳纳米管,最高可达6个数量级。
    High-performance poly(lactic acid) (PLA) blend-based composites were fabricated with a poly(ether-block-amide) (PEBA) elastomer acting as the blend counterpart. It was confirmed that a compatibilizer (ADR) enhanced the interaction between PLA and PEBA. Carbon nanotubes (CNTs) and organoclay (30B) were added individually and simultaneously into the blend to produce bionanocomposites. Morphological results showed that CNTs were mainly dispersed in PEBA domains, whereas 30B was mainly localized at the interfacial region of PLA and PEBA phases. The selective localization of added CNTs and 30B led to significant modification of the properties of the compatibilized PLA/PEBA blend. The brittleness and flammability of PLA were evidently improved after forming the bionanocomposites. Differential scanning calorimetry results revealed that CNTs and 30B assisted the crystallization of both PLA and PEBA in the composites, with CNTs providing superior nucleation efficiency to 30B. Thermogravimetric analysis revealed the thermal stability enhancement of the blend after adding CNTs and/or 30B, with up to 16 °C increase at 20 wt% loss with inclusion of 2 phr 30B. Addition of CNTs and/or 30B improved the blend\'s anti-dripping performance during burning tests, and CNT exhibited better anti-dripping efficiency. Ductility of PLA was drastically improved after forming the compatibilized blend, and further improved with incorporation of CNTs and/or 30B (increased from 9 % for neat PLA to 252 % for the hybrid composite containing CNT/30B). The impact strength of 1 phr CNTs-added composite was about 3 times that of PLA. Rheological properties indicated the (pseudo)network formation of added filler(s), leading to a significant reduction in electrical resistivity, up to six orders of magnitude with addition of 3 phr CNTs.
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