Chain elastic modulus of polyethylene: A spectroscopically determined force field (SDFF) study

Our SDFF for linear saturated hydrocarbon chains has been used to calculate the chain modulus of isolated and crystalline chains of n-alkanes of varying lengths. This has been done for static deformations and for the dynamic deformation in the longitudinal acoustic mode (LAM). Extrapolation to infinite chain length gives a common value of the room-temperature crystal modulus of 303 GPa (also obtained in an infinite chain calculation). Experimental Raman LAM measurements, corrected for chain-end interactions, give a modulus of 305 GPa, in excellent agreement. Problems with the experimental values obtained by inelastic neutron scattering and x-ray diffraction are discussed. © 1996 John Wiley & Sons, Inc.     

高压下碱卤晶体的三参量等温状态方程

 由等温体积弹性模量的定义及其与压强关系的假设出发,导出了一个新的适用于高压下碱卤晶体的三参量等温状态方程。计算了室温下NaCl晶体在0～30 GPa压强范围内、CsCl晶体在0～40 GPa压强范围内的相对体积以及NaCl晶体在0～30 GPa压强范围内的等温体积弹性模量,计算结果与实验值一致。对等温体积弹性模量及其对压强的一阶、二阶导数与压强的关系进行了讨论,指出压强趋于无穷大时的等温体积弹性模量是常数。     

4种等温物态方程适用性的比较研究

 通过分析现有文献,认为4种两参数的物态方程在高压物理研究中较为流行,它们是Vinet、Baonza、Morse和Born-Meyer（BM）方程。将这4种方程用于拟合50种材料的实验压缩数据,得出了零压下压缩模量及其一阶压力导数的优化取值,并计算了4种方程的平均压力误差。结果表明,Morse方程的精度最高,对50种材料的平均拟合误差为0.557 6%;BM方程次之,平均误差为0.615 1%;Vinet和Baonza方程的误差大一些,分别为0.788 9%和0.833 3%。对8种典型材料计算了压力误差随压强变化的曲线,所得结果与平均误差的趋势一致,也是Morse方程的精度最高。在宽广压力范围的高压物态方程研究中,推荐使用Morse方程。     

显微动态图像分析技术及其在生物物理中的应用

介绍了一种可实时监测细胞生命活动的显微动态图像分析技术。该技术把显微光学成像技术、数字处理技术和动态图像分析技术结合为一体,可实现对活细胞的结构功能、生长过程和环境变化的影响等进行非侵入性连续监测。通过在细胞膜弹性模量测量中的应用表明,该技术不仅原理可靠,实现容易,应用方便,而且检测速度快,测量精度高,稳定性能好。此项技术可望在生物物理学的实验研究中获得广泛的应用。     

表面波在表面活性剂流变学研究中的应用

论述了表面波的原理及其发展,文中进一步讨论了毛细波和纵向波的特点,较为详细地介绍了纵向波的实验方法和装置以及在表面活性剂流学变性质研究中的应用。     

超拉伸聚乙烯的弹性模量和导热性能

为了揭示聚合物分子链伸展、取向的本征特性，发展了两个新的测量方法和实验装置，用于研究拉伸比高达２００的超拉伸聚乙烯凝胶的弹性性能、传热性能和聚合物结构的关系．应用激光脉冲热致超声法给出材料拉伸方向和横向杨氏模量，应用激光脉冲光热辐射法给出拉伸方向，横向和厚度方向的导热系数．随拉伸比λ的增加，轴向杨氏模量急剧的增加，而横向的仅有少许减小．导热系数具有相似的特性．本文发现当λ＝２００时，这种拉伸取向聚乙烯的轴向模量可达钢的８０％，而导热系数甚至可达２倍，直至成为热的良导体，这是由于在高拉伸比时形成了相当数量的伸展分子链构成的针状晶体———晶桥．本文提出晶桥作为短纤维分散相的取向聚合物的结构模型，对于超拉伸聚乙烯的上述特性可以进行统一描述和定量化分析，和实验结果很好符合．     

NANOMECHANICAL MAPPING OF CARBON BLACK REINFORCED NATURAL RUBBER BY ATOMIC FORCE MICROSCOPY

Atomic force microscopy （AFM） has the advantage of obtaining mechanical properties as well as topographic information at the same time. By analyzing force-distance curves measured over two-dimensional area using Hertzian contact mechanics, Young＇s modulus mapping was obtained with nanometer-scale resolution. Furthermore, the sample deformation by the force exerted was also estimated from the force-distance curve analyses. We could thus reconstruct a real topographic image by incorporating apparent topographic image with deformation image. We applied this method to carbon black reinforced natural rubber to obtain Young＇s modulus distribution image together with reconstructed real topographic image. Then we were able to recognize three regions; rubber matrix, carbon black （or bound rubber） and intermediate regions. Though the existence of these regions had been investigated by pulsed nuclear magnetic resonance, this paper would be the first to report on the quantitative evaluation of the interfacial region in real space.     

STUDY ON THE PROPERTIES OF BLEND OF NATURAL RUBBER LATEX/METHYL METHACRYLATE GRAFTED RUBBER LATEX BY GAMMA RADIATION

Natural rubber latex(NRL)and methyl methacrylate(MMA)grafted rubber latex were blended in different ratios and irradiated at various absorbed doses by gamma rays from Co-60 source at room temperature.The tensile properties, swelling ratio and permanent set were measured.The maximum tensile strength and modulus at 500% elongation were obtained at an absorbed dose of 8 kGy.Modulus increases from 6.99 MPa to 9.87 MPa for an increase in proportion of MMA grafted rubber from 40% to 60% in the blend at similar absorbed dose.Elongation at break and swelling ratio decrease with increasing absorbed dose as well as the MMA grafted rubber content in the blends.The decreasing trend of permanent set is high up to 5 kGy absorbed dose,and beyond that dose,it becomes almost flat.     

羟基取代烷基苯磺酸盐界面扩张粘弹性质

研究了2-羟基-3,5-二癸基苯磺酸钠(C10C10OHphSO3Na)表面和正癸烷-水界面上的扩张粘弹性质, 考察了平衡时间对界面性质的影响. 研究结果表明, 羟基取代烷基苯磺酸钠具有十分特异的界面性质, 其扩张模量比一般表面活性剂大一个数量级, 达到平衡的时间较长, 形成的界面膜弹性较大. 界面张力弛豫测定结果表明, 平衡时界面上存在特征时间长达103 s的慢过程. 上述实验结果可能是由于羟基间形成氢键造成的.     

pH响应性P(MMA-co-MAA-co-HEMA)微凝胶的制备及其性能

利用预乳化乳液法制备了不同单体配比的聚(甲基丙烯酸甲酯-co-甲基丙烯酸-co-甲基丙烯酸羟乙酯)(P(MMA-co-MAA-co-HEMA))微凝胶分散液;采用透射电子显微镜、动态光散射仪研究了微凝胶的微观形态、粒径大小及其溶胀率;利用试管倒转法对微凝胶分散液的凝胶化相转变行为进行了研究,借助椎板流变仪考察了所形成胶态凝胶的储能模量与单体配比、微凝胶分散液浓度和温度的关系.结果表明,所制备的微凝胶的数均粒径为90 nm左右,当MMA与MAA的投料质量不变时,随着HEMA含量的增加,分散液凝胶化所需的临界最小浓度增大,临界最大pH值减小,胶态凝胶的储能模量增加.当保持单体MMA与HEMA的投料质量不变时,随着单体MAA投料质量的增多,微凝胶的数均粒径和溶胀率增大,胶态凝胶的储能模量先升高后降低;当MAA占单体总摩尔数的25%时,浓度为15 wt%的微凝胶分散液在扫描频率为100 rad/s时,胶态凝胶的储能模量最高可达2×104Pa.这类微凝胶分散液在组织工程支架材料方面有潜在的应用价值.