Polystyrene/magnesium hydroxide nanocomposite particles prepared by surface-initiated in-situ polymerization

In order to avoid their agglomeration and incompatibility with hydrophobic polystyrene substrate, magnesium hydroxide nanoparticles were encapsulated by surface-initiated in-situ polymerization of styrene. The process contained two steps: electrostatic adsorption of initiator and polymerization of monomer on the surface of magnesium hydroxide. It was found that high adsorption ratio in the electrostatic adsorption of initiator could be attained only in acidic region, and the adsorption belonged to typical physical process. Compared to traditional in-situ polymerization, higher grafting ratio was obtained in surface-initiated in-situ polymerization, which can be attributed to weaker steric hindrance. Both Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM) indicated that polystyrene/magnesium hydroxide nanocomposite particles had been successfully prepared by surface-initiated in-situ polymerization. The resulting samples were also analyzed and characterized by means of contact angle testing, dispersibility evaluation and thermogravimetric analysis.     

用按需滴定技术制备聚合物微透镜阵列

采用高分子聚合物-单体混合溶液按需滴定-原位热聚合的新方法制作折射微透镜及其阵列.制备透镜的主要材料是甲基丙烯酸甲酯及其聚合物.制备的微透镜直径在1 mm～3 mm范围内,矢高为100 μm～400 μm,透镜焦距在1 mm～4 mm之间.所得微透镜在波长λ=1.55 μm处有很好的光学透过率(90%),适于作光通信耦合器件.用AFM-Ⅱ型原子力显微镜测得微透镜阵列的表面粗糙度Ra约等于0.9 nm,并通过液体的表面张力理论分析了微透镜的形成机理.     

基于原位反应合成的一个锌的配位聚合物

A coordination polymer of Zn(IBT)2 (2) (HIBT=5-(4-((1H-imidazol-1-yl)methyl)phenyl)-2H-tetrazole) has been prepared by hydrothermal method and characterized by IR spectroscopy,elemental analysis and single-crystal X-ray diffraction structure analysis. Compound 2 has one-dimensional (1D) hinged chain structure and displays strong photoluminescent emission at room temperature.     

原位固相接枝改性碳酸钙/聚丙烯复合材料的制备

用马来酸酐（MAH）在碳酸钙（CaCO3）表面引入双键,通过原位固相接枝法将聚丙烯蜡（PPW）化学键合在CaCO3表面,制得3种接枝率的CaCO3-MAH-PPW。 将这3种改性CaCO3填充聚丙烯（PP）制备复合材料,研究了PP/CaCO3界面作用对复合材料强度的影响。 结果表明,CaCO3表面经PPW接枝改性后在PP中的分散性提高,与PP相容性变好;随着改性CaCO3表面PPW接枝率的提高,CaCO3与PP之间界面作用逐渐增强。 当PPW接枝率为4.48 mg PPW/g CaCO3时,CaCO3与PP之间的界面作用最强,复合材料拉伸强度下降最小,杨氏模量提升最大,当m(PP)∶m(CaCO3)=100∶50时,杨氏模量达0.86 GPa,是纯PP的1.63倍;而PPW化学接枝率为2.49 mg PPW/g CaCO3时,CaCO3与PP之间的界面作用适中,复合材料缺口冲击强度提升最大,且当m(PP)∶m(CaCO3)=100∶10时,缺口冲击强度达3.91 kJ/m2,是纯PP的1.35倍。     

聚甲基丙烯酸甲酯/苯乙烯-丙烯腈无规共聚物薄膜表面原位原子力显微镜相图

采用原位原子力显微镜在线跟踪方法,研究了聚甲基丙烯酸甲酯/苯乙烯 丙烯腈无规共聚物共混体系表面相分离行为,得到了具有下临界共溶温度（临界温度约为175 ℃）原位相图。 与文献报道的用离位方法所得结果的主要差别是原位的临界相分离温度稍有提高,以及离位结果中存在的组成对称性。 这些差别主要来源于离位和原位实验方法上的差别,薄膜厚度减小导致的相容性,热力学历史的变化以及基底效应的加剧。     

基于原位等离子体氮化及低压化学气相沉积-Si_3N_4栅介质的高性能AlGaN/GaN MIS-HEMTs器件的研究

通过对低压化学气相沉积(LPCVD)系统进行改造,实现在沉积Si_3N_4薄膜前的原位等离子体氮化处理,氮等离子体可以有效地降低器件界面处的氧含量和悬挂键,从而获得了较低的LPCVD-Si_3N_4/GaN界面态,通过这种技术制作的MIS-HEMTs器件,在扫描栅压范围V_(G-sweep)=(-30 V,+24 V)时,阈值回滞为186 mV,据我们所知为目前高扫描栅压V_(G+)(20 V)下的最好结果.动态测试表明,在400 V关态应力下,器件的导通电阻仅仅上升1.36倍(关态到开态的时间间隔为100μs).     

原位反应烧结法制备MgAlON复合材料

实验原料选用高纯电熔镁砂(粒径3～1 mm);α-Al2O3(活性)微粉(粒径≤5μm);电熔镁铝尖晶石(粒径≤1mm);Al粉(粒径≤0.088 mm);化学纯MgO(粒径≤0.04 μ m)和少量的活性材料,氮化气氛下原位反应制备MgAlON复合材料,考察了氮化烧结后试样的常规性能、物相组成、显微结构.结果表明:1500℃下,氮化气氛中耐火基质料为Al-Al2O3-MgO系的混合粉可以通过原位反应制备MgAlON复合材料;骨料种类的不同,不影响MgAlON矿相的生成.且MgAl2O4-MgAlON材料的烧结性能及氮化效果较好,常温强度也较高.试样骨架结构是骨料大颗粒在烧结中形成的,骨架中填充着反应合成的MgAlON晶粒和骨料小颗粒,使得烧成后的试样内部结构致密;微晶结构以及晶须的存在有利于提高材料的常温力学性能.     

一种在线测量微机械薄膜残余应力的新结构

提出了一种利用临界屈曲法在线测量微机械薄膜残余应力的新结构，并采用表面微加工技术制作了两种测试样品.搭建了在线观测实验装置来实时监控释放过程中结构出现的临界屈曲变形模态，由此判断出结构内部的应力状态，同时在测得临界刻蚀深度的情况下，采用有限元方法计算出残余应力大小.借助有限元方法，先研究了多个参数对临界屈曲应力的影响，然后利用这种新结构对薄膜残余应力进行了实际测量，所得结果与微旋转结构的应力测量结果基本吻合.分析及实验表明，新结构在测量薄膜残余应力方面有许多优点，具有较高的实用价值，不仅能满足大量程的应力检测要求，而且只用一个结构就可以同时测量压应力和拉应力，从而极大提高了器件版图空间的利用率.     

激光熔覆原位合成Nb(C,N)陶瓷颗粒增强铁基金属涂层

采用预涂粉末激光熔覆技术,在42CrMo基体上制备出原位合成Nb(C, N)颗粒增强的铁基复合涂层。X射线及扫描电镜分析结果表明:激光熔覆获得的涂层基体为耐氧化、耐蚀性良好的Fe-Cr细晶组织及少量的-Fe相,原位合成的Nb（C, N）呈块状弥散分布在基体上。进一步的磨损试验表明:这些颗粒增强相极大增强了抗磨损性能,与未熔覆的母材相比,其磨损失重仅为母材的1/9左右; 涂层在750 ℃恒温氧化条件下具有较好的抗氧化性能,氧化层主要由NbO1.1,Cr2O3相组成; 母材的氧化产物为Fe2O3,容易脱落,保护性能较差; 激光熔覆涂层的氧化膜厚度仅为未涂层的1/5。     

A Single-Gallery Model for the In Situ Production of Polyethylene-Clay Nanocomposites

Polyolefin-clay nanocomposites are finding many new applications because of their improved properties, such as high modulus, elevated scratch resistance and low gas permeability. Currently, these composites are produced by melt blending organically modified clay with polyolefins. The most challenging step in this process is the intercalation and exfoliation of the clay to produce a homogenously dispersed phase at the nanoscale. A promising alternative to melt blending is in-situ polymerization, where the polymer is produced between the clay layers in the polymerization reactor. In-situ polymerization of olefins with metallocene catalysts supported on clay can produce nanocomposites using conventional polymerization reactors, provided that the clay can be used as a support for the olefin polymerization catalyst. In this approach, the clay fulfills the functions of catalyst support and dispersed phase in the final nanocomposite. In this work, a mathematical model describing particle growth during in-situ polymerization of ethylene with a metallocene catalyst supported on clay will be discussed. The model expands the approach of the multi-grain model used in heterogeneous olefin polymerization to account for the layered structure of clays.