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Evidence of Chemical Reaction in Binary Blends of Polycarbonate and a Semi-Flexible Liquid Crystal Polymer 聚碳酸酯与半柔性液晶聚合物二元共混物化学反应的证据
Pub Date : 2021-07-19 DOI: 10.6000/1929-5995.2021.10.8
H. Hakemi
In this study, we provide the experimental results of the binary blends of a semi-flexible nematic liquid crystal polymer (LCP1) and polycarbonate (PC) within their phase diagram. The LCP1/PC blends were investigated by Differential Scanning Calorimetry (DSC), Optical Microscopy (OM), Wide-angle X-Ray Diffraction (WXRD), Fourier Transfer Infrared (FTIR), Gel Permeation Chromatography (GPC), and Nuclear Magnetic Resonance (NMR) techniques and observed the evidence of chemical reaction between LCP1 and PC in their heat-treated blends possibly by transesterification mechanism.
在本研究中,我们提供了半柔性向列液晶聚合物(LCP1)和聚碳酸酯(PC)二元共混物在相图中的实验结果。采用差示扫描量热法(DSC)、光学显微镜(OM)、广角x射线衍射(WXRD)、傅里叶转移红外(FTIR)、凝胶渗透色谱(GPC)和核磁共振(NMR)等技术对LCP1/PC共混物进行了研究,并观察了LCP1与PC在热处理共混物中可能通过酯交换机制发生化学反应的证据。
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引用次数: 0
Synthesis and Applications of Polymeric Reagent p-Substituted Triphenylamine 聚合试剂对取代三苯胺的合成及应用
Pub Date : 2021-06-08 DOI: 10.6000/1929-5995.2021.10.7
I. Abu-Abdoun
Chemical modification of chloromethylstyrene - styrene copolymer throughout reaction of p-substituted carboxylic acid group of bis-(4,4`-dibromo)-4``-triphenylamine carboxylic acid with the chloromethyl group attached to a phenyl group was carried out on soluble copolymer and polymeric cross-linked copolymer. Chemical oxidation of the neutral p-substituted triphenylamine with antimony pentachloride in dichloromethane solvent gives the corresponding cation - radical salt with the counter ion antimony hexachloride (SbCl6-). The isolated deep blue color cation radical salt is soluble or in insoluble (resin) form in the copolymer was used as a thermal cationic initiator for the polymerization of epoxy and vinyl monomers at room temperature. The cation radical resin showed good activity and stability compared to the soluble polymeric cation radical, both can initiate the cationic polymerization of cyclohexene oxide and N-vinylcarbazole in dichloromethane at room temperature.
通过双-(4,4′-二溴)-4′-三苯胺羧酸对取代羧基与氯甲基连接苯基的反应,对氯甲基苯乙烯-苯乙烯共聚物进行了化学改性。中性对取代三苯胺在二氯甲烷溶剂中与五氯化锑化学氧化得到相应的阳离子盐与反离子六氯化锑(SbCl6-)。分离出的深蓝色阳离子自由基盐在共聚物中可溶或以不溶(树脂)形式存在,用作室温下环氧和乙烯基单体聚合的热阳离子引发剂。与水溶性高分子阳离子自由基相比,阳离子自由基树脂表现出良好的活性和稳定性,两者都能在室温下在二氯甲烷中引发环氧环己烯和n -乙烯基咔唑的阳离子聚合。
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引用次数: 0
Low-Density Polyethylene Nanocomposite Containing Zn/Ti Layered Double Hydroxide 含锌/钛层状双氢氧化物的低密度聚乙烯纳米复合材料
Pub Date : 2021-02-26 DOI: 10.6000/1929-5995.2021.10.5
S. Jaerger, Daiane Nogueira, Douglas Santos de Oliveira, M. V. Machado, R. Marangoni
The presented work shows the synthesis and characterization of Zn/Ti layered double hydroxide (LDH) intercalated with carbonate and dodecyl sulfate ions following its application as a functional filler in LDPE in order to improve the thermal properties and resistance degradation in UV-Vis radiation. X-ray diffractogram patterns of Zn/Ti LDH-CO3 and Zn/Ti LDH-DDS present basal spacing value in the order of 6.81 Å and 38.09 Å, respectively, indicating success in layered compound synthesis. LDPE nanocomposite containing hydrophobic and hydrophilic LDH presented a very well dispersed nanocomposite, as demonstrated in XRD and DSC results. The addition of only 1 % of LDH as filler into LDPE causes an increase of 5.43 C in the thermal property. Zn/Ti LDH-DDS absorbs more light compared to the Zn/Ti LDH-CO3 due to the enhanced interlayer distance in the presence of DDS in the basal space of LDH, which further the intercalation process of polymer chains within the interlayer regions of LDH.
本文介绍了碳酸盐和十二烷基硫酸盐离子插层的Zn/Ti层状双氢氧化物(LDH)的合成和表征,并将其作为功能填料应用于LDPE中,以改善其热性能和抗紫外-可见辐射降解性。Zn/Ti LDH-CO3和Zn/Ti LDH-DDS的x射线衍射图显示基底间距值分别为6.81 Å和38.09 Å,表明层状化合物合成成功。XRD和DSC结果表明,含有疏水性和亲水性LDH的LDPE纳米复合材料具有很好的分散性。在LDPE中加入1%的LDH作为填料,其热性能提高了5.43℃。与Zn/Ti LDH- co3相比,DDS的存在增加了LDH基空间的层间距离,使得LDH层间区域内聚合物链的插层过程进一步加快。
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引用次数: 1
Introduction to the Study of Mechanical Properties of Terpolymer PP/EPDM Mixtures 聚丙烯/三元乙丙橡胶共混物力学性能研究简介
Pub Date : 2021-02-26 DOI: 10.6000/1929-5995.2021.10.1
S. Scagliusi, Elizabeth C.L. Carvalho, A. B. Lugão
: Thermoplastic elastomers (TPEs), based in PP (Polypropylene) / EPDM (Ethylene Propylene Diene Monomer) have as purpose improving PP resistance and impact, aiming to a more comprehensive use in automotive market, among edifications, construction and packaging sectors, due to their recyclability properties. PP is a commodity, with a high melting point, high mechanical resistance and low density, posing a balance between physical and mechanical properties; in addition, it shows an easy processing, at low cost. In order to minimize this deficiency, EPDM, an impact modifier, can be used. Nevertheless, most of polymeric blends are incompatible and immiscible, i.e., show a mutual and limited solubility and in most of cases, a high interfacial tension. However, there is a relatively low interfacial tension (force which acts on transformation of a continuous structure in a dispersion) between PP and EPDM (approximately 0.3 mN.m -1 ), reducing the rate of breakup and facilitating the build-up of a continuous structure. This work aims to the study of compatibility of PP and EPDM blends and variation of mechanical properties, emphasizing that many properties of thermoplastic elastomers can be processed according with conventional thermoplastics methods: herein, PP/EPDM blends, 90/10, 80/20, 70/30 and 50/50 were characterized according to: Mechanical essays, Differential Scanning Calorimetry, Thermogravimetric Analyses, Melt Flow Index, Izod Impact Strength and Dynamic mechanical Analyses.
:热塑性弹性体(TPEs),基于PP(聚丙烯)/ EPDM(乙丙二烯单体)的目的是提高PP的耐冲击性,旨在更全面地应用于汽车市场,在教育,建筑和包装领域,由于其可回收性。PP是一种商品,具有高熔点、高机械阻力和低密度,在物理性能和机械性能之间取得平衡;此外,它还表现出加工简单、成本低的特点。为了尽量减少这一缺陷,可以使用抗冲击改性剂EPDM。然而,大多数聚合物共混物是不相容和不混溶的,即表现出相互和有限的溶解度,在大多数情况下,具有很高的界面张力。然而,PP和EPDM之间的界面张力(作用于分散中连续结构转变的力)相对较低(约0.3 mN)。M -1),减少了破裂的速度,促进了连续结构的建立。本工作旨在研究PP和EPDM共混物的相容性和力学性能的变化,强调热塑性弹性体的许多性能可以按照传统的热塑性塑料方法加工:在这里,PP/EPDM共混物、90/10、80/20、70/30和50/50分别根据:力学论文、差示扫描量热法、热重分析、熔体流动指数、Izod冲击强度和动态力学分析进行表征。
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引用次数: 0
Effect of Ionizing Radiation Applied to PLA Used as Compatibilizing Agent in Reinforced eGG Shell PBAT/PLA Bio-Based Composites 电离辐射对聚乳酸增容剂在增强蛋壳PBAT/PLA生物基复合材料中的作用
Pub Date : 2021-02-26 DOI: 10.6000/1929-5995.2021.10.4
E. Cardoso, D. F. Parra, S. Scagliusi, L. G. H. Komatsu, A. B. Lugão
: Bio-filler from eggshells as reinforcement of bio-based polymers are based on their benefits as adequate strength and stiffness, besides friendly, degradable and renewable environment. Eggshell is an agricultural waste considered as garbage, contributing to pollution; nevertheless, it can be transformed into bio-calcium carbonate, acquiring new values. As biodegradable polymers, there were chosen PLA (poly-lactic-acid) and PBAT (butylene adipate co-terephthalate), thermoplastics capable to be processed via conventional methods. PLA is a linear, aliphatic thermoplastic polyester, high in strength and modulus, but brittle. PBAT is a synthetic polymer, very flexible, based on fossil resources with high elongation at break, but low strength. It will be required the use of compatibilizers, for reducing interfacial tension exhibited by PLA/PBAT immiscible blend, considering their extreme glass transition temperatures: 62 o C for PLA and – 30 o C for PBAT. Herein it was used ionizing radiation for inducing compatibilization by free radicals, improving dispersion and adhesion of blend phases, without using chemical additives, at room temperature. PLA, acting as compatibilizer, was previously e-beam and gamma radiated, at 150 kGy. PBAT/PLA 50/50 blend with 15 phr of bio- filler from avian eggs 125 µ m particle size and both compatibilizers were homogeneized in a co-rotating twin-screw extruder, within a temperature profile 120 to 145 o C, from hopper to die. Characterization involved: Differential Scanning Calorimeter, Thermogravimetric Analyses, Fourier Transform Infrared Spectroscopy, Wide Angle X-Ray Diffraction, Tensile Strength and Elongation at Break.
蛋壳生物填料作为生物基聚合物的增强材料,其优点是具有足够的强度和刚度,并且环境友好、可降解和可再生。蛋壳是一种农业废弃物,被认为是垃圾,造成污染;然而,它可以转化为生物碳酸钙,获得新的价值。作为可生物降解的聚合物,有选择的PLA(聚乳酸)和PBAT(己二酸丁烯共对苯二甲酸酯),热塑性塑料能够通过常规方法加工。聚乳酸是一种直线型、脂肪族热塑性聚酯,强度和模量高,但易碎。PBAT是一种合成聚合物,非常灵活,基于化石资源,具有高断裂伸长率,但强度低。考虑到PLA/PBAT的极端玻璃化转变温度:PLA为62℃,PBAT为- 30℃,因此需要使用增容剂来降低PLA/PBAT非混相共混物所表现出的界面张力。在室温下,在不使用化学添加剂的情况下,利用电离辐射诱导自由基相容,改善共混相的分散性和附着力。PLA,作为相容剂,以前是电子束和γ辐射,在150 kGy。PBAT/PLA 50/50共混物与15 phr的125µm粒径的禽蛋生物填料和两种增容剂在同向旋转双螺杆挤出机中均匀化,从料斗到模具的温度范围为120至145℃。表征涉及:差示扫描量热计、热重分析、傅立叶变换红外光谱、广角x射线衍射、拉伸强度和断裂伸长率。
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引用次数: 0
Processing Characterization of Sisal/Epoxy Prepregs 剑麻/环氧预浸料的工艺表征
Pub Date : 2021-02-26 DOI: 10.6000/1929-5995.2021.10.6
Sayra Oliveira Silva, L. A. Teixeira, A. Gontijo, S. Luz
: Quality control to obtain composite laminates is frequently applied to synthetic fibers/epoxy prepregs. The gel time test, resin, volatiles and fiber content, drape measurement and tack tests together with water absorption capacity are methods currently employed. However, for natural fibers prepregs there is a gap in the literature, which makes their application difficult. Thus this work will investigate sisal fibers, which have low cost, high biodegradability and low specific weight, following the common methods to manufacture composites from natural fibers/epoxy prepregs. First, the prepregs were prepared by hand lay-up, aligning the fibers with epoxy, keeping 15% by weight content of fiber. After the quality control characterization, 3 mm thickness composite was prepared by using a press, and tensile tests and scanning electron microscopy (SEM) were applied. As a result, the resin fraction values and the solid content of the matrix showed little variation between the different samples. The natural fibers prepregs absorbed water quickly in the initial stage until reaching the saturation level. The NaOH-treated sisal/epoxy prepreg had a tension of 71.06 ± 8.28 kPa for the tack test and tensile strength of 69.24 ± 11.69 MPa. Finally, the NaOH-treated sisal 15 wt%/epoxy resulted in composites with a better performance than the neat epoxy resin. There was good adhesion between the fibers and matrix, as confirmed by SEM and mechanical tests.
:合成纤维/环氧预浸料通常采用质量控制来获得复合层压板。凝胶时间试验、树脂、挥发物和纤维含量、垂度测量和粘性试验以及吸水能力是目前采用的方法。然而,对于天然纤维预浸料,文献中存在空白,这使得它们的应用变得困难。因此,本研究将根据天然纤维/环氧预浸料制备复合材料的常用方法,研究具有低成本、高生物降解性和低比重的剑麻纤维。首先,通过手工铺层制备预浸料,将纤维与环氧树脂对齐,保持纤维重量含量15%。在进行质量控制表征后,采用压片法制备了厚度为3 mm的复合材料,并进行了拉伸试验和扫描电镜(SEM)分析。结果表明,树脂分数值和基体固含量在不同样品间变化不大。天然纤维预浸料在初始阶段吸水速度较快,直至达到饱和水平。经naoh处理的剑麻/环氧预浸料在黏着试验中拉力为71.06±8.28 kPa,抗拉强度为69.24±11.69 MPa。最后,经naoh处理的剑麻/环氧树脂复合材料的性能优于纯环氧树脂。SEM和力学试验结果表明,纤维与基体具有良好的粘附性。
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引用次数: 2
Influence of Hybridization on Mechanical Properties and Water Absorption in Jute and Jute /E-Glass Reinforced Composites 杂化对黄麻及黄麻/ e -玻璃增强复合材料力学性能和吸水性的影响
Pub Date : 2021-02-26 DOI: 10.6000/1929-5995.2021.10.2
V. Lacerda, Salvador n Barbalho, Zip Code Brazil Ba, A. R. Conceição, Catarina da N. Scherer, Michel G. Santos, M. Leao
The use of composite materials is increasingly present not only in several industrial areas but also in daily life. With the escalating environmental concern, it is necessary the search for materials that prove to be ecologically sustainable and economically viable. Vegetable fibers have been presenting themselves as an excellent alternative, however, because their disadvantage of having a high moisture absorption capacity, the introduction of synthetic fibers, forming hybrid composites, is a good solution since it combines the characteristics of both types of reinforcements. The present research aims to carry out a comparative study between two types of laminated polymer composites, one reinforced with Jute fibers and the other hybrid, composed of Jute and E-glass fibers. The mechanical performances of the composites submitted to the Uniaxial Tensile, Three-point Flexural and Shear tests were evaluated, as well as fracture analyzes. A comparative study to analyze the influence of hybridization on moisture absorption was carried out. The results showed that the hybridized composite showed an increase in the elastic modulus, as well as in its resistance to flexion and shear, which shows the formation of a more rigid material. Hybridization also changed the moisture content of the composite.
复合材料的使用越来越多,不仅在几个工业领域,而且在日常生活中。随着对环境问题的日益关注,有必要寻找证明具有生态可持续性和经济可行性的材料。然而,由于植物纤维具有高吸湿能力的缺点,植物纤维一直是一种很好的替代材料,因此合成纤维的引入,形成混合复合材料,是一种很好的解决方案,因为它结合了两种增强材料的特点。本研究旨在对黄麻纤维增强层压聚合物复合材料和黄麻纤维与e -玻璃纤维混合复合材料进行对比研究。对复合材料进行了单轴拉伸、三点弯曲和剪切试验,并进行了断裂分析。通过对比研究,分析杂交对吸湿性的影响。结果表明,杂化复合材料的弹性模量增加,抗挠曲和抗剪切能力增强,材料刚性增强。杂交也改变了复合材料的含水量。
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引用次数: 0
A Review on Carbon Nanotubes: Preparation, Properties and Applications 碳纳米管的制备、性能及应用研究进展
Pub Date : 2020-12-30 DOI: 10.6000/1929-5995.2020.09.10
Md Nur Karim, M. Patwary, S. Abedin, Md Riaj Hossen, Md Saifur Rahman
Carbon nanotubes(CNTs) have achieved attention in recent times because of their extraordinary physicochemical properties like strength, flexibility, sensors, conducting etc. Carbon nanotubes(CNTs) are known as nano-architectured allotropes of carbon, having graphene sheets which are rolled up into cylinder that forms carbon nanotubes. In the field of nanotechnology, carbon nanotubes are the one of the most unique invention. The eye-catching features of carbon nanotubes are their electronic, mechanical, optical and chemical characteristics, which open a way to future applications. Carbon nanotubes can be single walled and multi walled which can be produced in various ways. The most common techniques used nowadays are: arc discharge, laser ablation and chemical vapour deposition. In this review article,the applications of CNTs in various technologically important fields are discussed in detail.
近年来,碳纳米管(CNTs)因其强度、柔韧性、传感器、导电性等优异的物理化学特性而受到广泛关注。碳纳米管(CNTs)被称为碳的纳米结构同素异形体,其石墨烯片卷成圆柱体形成碳纳米管。在纳米技术领域,碳纳米管是最独特的发明之一。碳纳米管引人注目的特点是其电子、机械、光学和化学特性,这为未来的应用开辟了一条道路。碳纳米管可以是单壁的,也可以是多壁的,制备方法多种多样。目前最常用的技术有:电弧放电、激光烧蚀和化学气相沉积。在这篇综述文章中,详细讨论了碳纳米管在各个技术重要领域的应用。
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引用次数: 1
Effect of Molybdenum Trioxide in the Behavior of Poly(vinyl alcohol) Nanocomposites Systems Focusing New Systems for Protection against COVID-19 三氧化钼对聚乙烯醇纳米复合材料性能的影响聚焦新型COVID-19防护体系
Pub Date : 2020-12-30 DOI: 10.6000/1929-5995.2020.09.09
M. Tavares, J. C. D. Filho, Tais Nascimento, G. Iulianelli, Pedro Paulo Merat
The purpose of this work was to study the molecular dynamics, morphology, mechanical and thermal performance of nanomaterials formed by poly(vinyl alcohol) and molybdenum trioxide (PVA/MoO3) obtained through solution casting method, focusing new materials with therapeutic applications since the molybdenum trioxide exhibit an excellent antibacterial activity and could be a pathway to prevent viruses. The obtaining materials were characterized by conventional techniques as X-ray diffraction, thermogravimetric and dynamical-mechanical analysis. The unconventional low-field NMR relaxometry was used to evaluate the molecular dynamic and morphology of these systems. The results obtained showed that the MoO3 addition into PVA matrix promote an increase on the thermal stability at higher temperatures and a progressive increase on the rigidity of the PVA systems. Also changes in the molecular mobility of nanomaterials determined through the proton spin-lattice relaxation time showed that low proportion of molybdenum trioxide increased the intercalation of the poly(vinyl alcohol) chains between oxide lamellae while higher quantity of molybdenum trioxide caused an inverse effect on the oxide lamellae delamination. From those results the nanomaterials presented a mixed structural organization as intercalated and exfoliated morphologies. According to these first results, the nanocomposites obtained promise to be antimicrobial and antiviral agent to prevent COVID-19 and similar viruses.
本工作的目的是研究聚乙烯醇和三氧化钼(PVA/MoO3)通过溶液浇铸法制备的纳米材料的分子动力学、形态、力学和热性能,重点研究具有治疗应用价值的新材料,因为三氧化钼具有优异的抗菌活性,可能是预防病毒的途径。用常规的x射线衍射、热重和动力力学分析等方法对所得材料进行了表征。采用非常规的低场核磁共振弛豫法评价了这些体系的分子动力学和形态。结果表明,在PVA基体中加入MoO3,有利于提高PVA体系在高温下的热稳定性,并逐步提高体系的刚度。此外,通过质子自旋-晶格弛豫时间测定的纳米材料分子迁移率的变化表明,低比例的三氧化钼增加了氧化物片间聚乙烯醇链的插层,而高比例的三氧化钼则对氧化物片的分层产生相反的影响。这些结果表明,纳米材料呈现出夹层和剥离形态的混合结构组织。根据这些初步结果,获得的纳米复合材料有望成为预防COVID-19和类似病毒的抗菌和抗病毒药物。
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引用次数: 1
Interaction of Lipase with Lipid Model Systems 脂肪酶与脂质模型系统的相互作用
Pub Date : 2020-12-21 DOI: 10.6000/1929-5995.2020.09.08
S. Zaitsev, I. S. Zaitsev, I. Milaeva
The aim of this work was to study the interaction of lipases (as an important biopolymer) with models of biomembranes based on the phospholipid and cholesterol. Lipases (triacylglycerolacyl hydrolases) are widely distributed enzymes and well-known by their hydrolytic activity. The study of the lipase interactions with lipid vesicles in aqueous dispersions is of fundamental and practical interest. The pure phosphatidylcholine from egg yolk (ePC) and cholesterol (Chol) were obtained from Sigma-Aldrich. Lipase was obtained from hog pancreas. Measurements of the current and equilibrium surface tension (ST and eST) values were carried out using a BPA-1P device and ADSA program. The particle sizes in the prepared colloidal solutions were determined by the method of dynamic light scattering. An addition of lipase led to some decrease both, of ST and eST for the samples of ePC:Chol (in the ratios from19:1 to 1:1). The mean particle diameter (MPD) and effective particle diameter (EPD) values for the samples of ePC:Chol changed drastically by lipase addition. The EPD/MPD ratios increased from 1.7 to 2.0, from 1.8 to 2.6, from 2.3 to 6.5, from 1.5 to 2.9 for the samples of ePC:Chol at the ratios of 19:1, 14:1, 9:1, 7:1, respectively by lipase concentration increase. This general tendency can be explained by strong interaction of lipase with lipid membrane that leads to the formation of the mixed particles ePC:Chol:lipase with more narrow particle size distribution as compared to the initial EPD/MPD ratio (for the ePC:Chol mixture without lipase).
本研究的目的是研究脂肪酶(一种重要的生物聚合物)与基于磷脂和胆固醇的生物膜模型的相互作用。脂肪酶(三酰基甘油酰水解酶)是一种广泛分布的酶,以其水解活性而闻名。脂肪酶与水分散体中脂质囊泡相互作用的研究具有基础性和实践性的意义。用Sigma-Aldrich法从蛋黄中分离得到纯磷脂酰胆碱(ePC)和胆固醇(Chol)。脂肪酶是从猪胰腺中提取的。使用BPA-1P装置和ADSA程序测量电流和平衡表面张力(ST和eST)值。用动态光散射法测定了所制备胶体溶液的粒径。添加脂肪酶导致ePC:Chol样品的ST和eST(比例为19:1 ~ 1:1)均有所降低。添加脂肪酶后,ePC:Chol样品的平均粒径(MPD)和有效粒径(EPD)值发生了较大的变化。随着脂肪酶浓度的增加,EPD/MPD比值在19:1、14:1、9:1、7:1时分别由1.7增加到2.0、1.8增加到2.6、2.3增加到6.5、1.5增加到2.9。这种总体趋势可以通过脂肪酶与脂质膜的强烈相互作用来解释,这种相互作用导致混合颗粒ePC:Chol:脂肪酶的形成,与初始EPD/MPD比(对于没有脂肪酶的ePC:Chol混合物)相比,其粒径分布更窄。
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引用次数: 0
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Journal of Research Updates in Polymer Science
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