聚合物共混改性原理纳米复合材料.ppt
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1、聚合物共混改性原理 聚合物纳米复合材料,张 琴,聚合物复合体系的分类,纳米概念的形成,早期,石墨、炭黑中的颗粒1959年,美国物理学家Richard Feynman提出“what would happen if we could arrange the atoms one by one the way we want them?”20世纪70年代康乃尔大学C.G.Granqvist&R.A.Buhrman 小组气相沉积制备纳米 20世纪80年代,原西德Gleiter首次制备金属纳米,提出纳米材料及其应用1981年,IBM发明AFM和STM,推动纳米技术发展20世纪80年代末期,日本丰田研究中心
2、制得PA6/粘土纳米复合材料,What nanocomposites are,Nanocomposites are made by mixing two or more phase,such as particles,layers or fibres,where at least one of the phases is in the nanometre size range.Because the building blocks making up the nanocomposites are therefore so close to the molecular scale,confine
3、ment and quantum effects result from the way that the blocks interact.Nanocomposites show properties not found in bulk materials,differentiating them from typical composites or filled-polymer systems.,Classification of nanocomposite,Polymer/inorganic nanocomposites,Polymer nanocomposites are general
4、ly defined as the combination of a polymer matrix resin and inorganic particles(particles,layers or fibres)which have at least one dimension(i.e.length,width,or thickness)in the nanometer size range,制备聚合物纳米复合材料的无机物的种类,纳米粒子(CaCO3、SiO2、TiO2、ZnO、Al2O3、Cr2O3)纳米纤维(碳纳米管、纤维素晶须、凹凸棒土)层状无机物,Layered host cryst
5、als susceptible to intercalation by a polymer,蒙脱土的化学通式:Nax(H2O)4(AL2xMgx)Si4O10(OH)2,分类:钠基蒙脱土(碱性土)钙基蒙脱土(碱土性土)天然漂白土(酸性土),蒙脱土的改性方法,人工钠化改型(悬浮液法、堆场钠化法、挤压法)酸活化方法(干法活化工艺、湿法活化工艺),湿法生产工艺:,干法生产工艺:,Structure of 2:1 layered silicates,蒙脱土的结构特征-天然的纳米结构,Cation-exchange reaction between the silicate and the alkyla
6、mmonium salt,蒙脱土族矿物具有离子交换性、吸水性、膨胀性、触变性、黏结性、吸附性等特性,插层剂的作用,利用离子交换的原理进入蒙脱土片层之间;扩张片层间距;改善层间的微环境;使蒙脱土的内外表面由亲水性转化为疏水性;增强蒙脱土片层与聚合物分子链之间的亲和性;降低硅酸盐材料的表面能。,常用的插层剂有烷基铵盐、季铵盐、吡啶类衍生物和其他阳离子型表面活性剂,聚合物/层状硅酸盐纳米复合材料特点,需要填料体积分数少;具有优良的热稳定性及尺寸稳定性;性价比高。,Polymer layered Nanocomposites preparation,In-situ intercalation poly
7、merization to intercalate the monomer and then take advantage of the hosts oxidising properties to induce polymerization Polymer intercalation from solution Polymer melt intercalation to mix the polymer and layered silicate together and then heat the mixture above the glass transition temperature(so
8、ftening point)of the polymer Exfoliation-adsorption Template synthesis,In situ Polymerization,Schematic representation of in-situ polymerization,聚合物大分子溶液插层工艺示意图,Schematic representation of melt intercalation,制备方法的改进,利用共聚物制纳米复合材料(PS、PMMA);利用聚合物催化剂制纳米复合材料(PS、PET);利用相容剂制纳米复合材料(PP);利用环状低聚物的开环聚合制纳米复合材料(P
9、C);硬质环氧树脂纳米复合材料的制备(硬质环氧树脂)。,Naoki Hasegawa,et al,Polymer 44(2003)29332937,a novel compounding process using Namontmorillonite water slurry for preparing novel nylon 6/Namontmorillonite nanocomposites,Naoki Hasegawa,et al,Polymer 44(2003)29332937,Layered Nanocomposite structure,PLS纳米复合材料微观结构的分类表,Sche
10、matic depicting the XRD patterns for various types of structures,The new properties of nanocomposites,Efficient reinforcement with minimal loss of ductility and impact strengthIncrease thermal stabilityIncrease flame retardant Improved gas barrier properties Improved ionic conductivityReduced therma
11、l expansion coefficientAltered electronic and optical properties,Properties of Nylon-6 layered silicate nanocomposites,Organoclay(wt%)dependence of HDT of neat PLA and various PLACNs.(b)Load dependence of HDT of neat PLA and PLACN7,TGA curves for polystyrene,PS and the nanocomposites,Proposed model
12、for the torturous zigzag diffusion path in an exfoliated polymerclay nanocomposite when used as a gas barrier,Comparison of combustion of Nylon 6,6 and Nylon6,6 nanocomposite with clay fraction of 5 wt.-%(Cloisite 15A)at external flux of 35 Kw/m2,PP及其纳米复合材料的热释放速率对比(热通量=35kW/m2),Real picture of biode
13、gradability of neat PLA and PLACN4 recovered from compost with time.Initial shape of the crystallizedsamples was 3*10*0.1 cm3.,Degree of biodegradation(i.e.CO2 evolution),and(b)time-dependent change of matrix Mw of neat PLA and PLACN4(MEE clay=4 wt%)under compost at(58+2)C,聚合物纳米复合材料的问题,无机相分布不规则;无机相形
14、态难控制;存在界面问题;分散方法需改进。,Morphology of layered silicate,Kinetics of polymer melt intercalation,Two steps for nanocomposite formation:Polymer transported from the agglomerate-polymer melt interface to the primary particlesPolymer melt penetrate to the edges of the crystallites The first step is limiting
15、step for polymer nanocomposites formation,Thermodynamic analysis,F=F(h)-F(h0)=E-TS F 0 indicate layer separation is favorable F 0 implies the initial unintercalated state is favorable S S chain+S polymer,Influence factors of polymer intercalation,Original properties of silicate Polymer architecturei
16、nteraction between surface and polymer a.Organically modified layered silicates surface b.Adding a fraction of functionalized polymersProcess condition,WAXD patterns of organically modified clay:(a)smectiteclay modified with C8,C12,and C16 phosphonium salt;(b)smectite,MMT,and mica clay modified with
17、 C16 phosphonium salt,Bright field TEM images of melt compounded nanocomposites containing,3 wt%MMT based on(a)HMW,(b)MMW,and(c)LMW N6,Schematic illustration of OMLS dispersion process in PP-g-MA matrix,Three cases involving the interplay during melt processing,Process condition,H.R.Dennis et al./Po
18、lymer 42(2001)95139522,Illustrates schematically how platelets peel apart under the action of shear,H.R.Dennis et al./Polymer 42(2001)95139522,The key of the formation of nanocomposites is:there are enough interaction between polymer and layer silicates so that the intercalation and exfoliation can
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