INTEGRATION METHOD FOR THE DYNAMICS EQUATION OF RELATIVE MOTION OF VARIABLE MASS NONLINEAR NONHOLONOMIC SYSTEM

1.IntroductionMoreandmoreattentionhasbeenpaidtothestudyofdynamicsofcomplicatedsystemwiththedevelopmentofmodernscienceandtechnology.Thestudyoftherelativemotionofvariablemasssystembyusingthetheoryandmethodofanalyticalmechanicsnotonlycanunifytheexpressionformbutalsocandisplayitssuperioritytothecomplicatedsystem.In1961,thedynamicsofrelativemotionofholonomicsystemwasderivedbyLur'ell].Inrecehtyears,LiulZIandLuol3'4]havegiventhedynamicsequationsofrelativemotionofvariablemassnonholonomicsystem.Howe…     

大豆油煎炸过程理化指标与LF-NMR弛豫特性的相关性研究

在对大豆油无料/薯条煎炸过程[温度:(180±5)℃,持续36 h]中的酸价(AV)、粘度(V)、吸光值(A)及总极性化合物(TPC)含量等及低场核磁共振(LF-NMR)弛豫特性(峰起始时间T21、T22、T23、相应的峰面积比例S21、S22、S23、单组份弛豫时间T2W)变化规律研究的基础上,利用多元回归分析建立了理化指标与其LF-NMR检测结果的相关性模型,并进行验证。结果表明:大豆油的酸价、TPC含量及S21峰面积均随煎炸时间的延长而线性增大,T21、T22峰起始时间及T2W则随煎炸时间的延长而线性减小(r2>0.90),粘度、吸光值随煎炸时间的延长逐渐增加并符合二项式关系(r2>0.90),而T23峰起始时间及S22、S23与煎炸时间之间无明显规律性变化。煎炸薯条后,油样的酸价、粘度、TPC含量、吸光值及S21均较无料煎炸显著增大(P<0.05),而T21、T22峰起始时间及T2W显著缩短。多元回归分析表明,酸价及TPC含量与T2W、T21,粘度与T2W,吸光值与S21间均可建立良好的相关性模型(R2>0.93)。模型验证合理可靠,可通过油样的LF-NMR检测结果有效预测其理化指标的变化。     

Study on the activity and mechanism of skimmianine against human non-small cell lung cancer

The present research was to investigate the effects of skimmianine (SK) in four non-small cell lung cancer (NSCLC) cells. We found that SK can significantly inhibit the growth of NSCLC cells and markedly induce apoptosis in NSCLC cells. The effects of growth inhibition and apoptosis induction were in a concentration–response relationship and caspase-dependent manner.     

含有非圆形双孔的无限平板中应力的解析解研究

无限平板中含有任意形状单个孔的问题可以使用复变函数方法获得其应力解析解.对于无限平板中含有两个圆孔或两个椭圆孔的双连通域问题,也可以利用多种方法进行求解,比如双极坐标法、应力函数法、复变函数法以及施瓦茨交替法等.其中复变函数中的保角变换方法是获得应力解析解的一个重要方法.但目前尚未见到用此方法求解无限板中含有一个正方形孔和一个椭圆孔的问题.当板在无穷远处受有均布载荷和孔边作用垂直均布压力时,利用保角变换方法可以求解板中含有两个特定形状孔的问题.该方法将所讨论的区域映射成象平面里的一个圆环,其中最关键的一步是找出相应的映射函数.基于黎曼映射定理,提出了该映射函数一般形式,并利用最优化方法,找到了该问题的具体映射函数,然后通过孔边应力边界条件建立了求解两个解析函数的基本方程,获得了该问题的应力解析解.运用ANSYS有限单元法与结果进行了对比.研究了孔距、椭圆形孔大小和两孔布置方位对边界切向应力的影响,以及不同载荷下两孔中心线上应力分布规律.      

Distance versus Capillary Flow Dynamics-Based Detection Methods on a Microfluidic Paper-Based Analytical Device (μPAD)

In recent years, there has been high interest in paper-based microfluidic sensors or microfluidic paper-based analytical devices (μPADs) towards low-cost, portable, and easy-to-use sensing for chemical and biological targets. μPAD allows spontaneous liquid flow without any external or internal pumping, as well as an innate filtration capability. Although both optical (colorimetric and fluorescent) and electrochemical detection have been demonstrated on μPADs, several limitations still remain, such as the need for additional equipment, vulnerability to ambient lighting perturbation, and inferior sensitivity. Herein, alternative detection methods on μPADs are reviewed to resolve these issues, including relatively well studied distance-based measurements and the newer capillary flow dynamics-based method. Detection principles, assay performance, strengths, and weaknesses are explained for these methods, along with their potential future applications towards point-of-care medical diagnostics and other field-based applications.     

The extended Hulburt–Hirschfelder‐long‐range oscillator model for direct‐potential‐fit analysis

In the present work, an extended Hulburt–Hirschfelder oscillator model is proposed as a means of simplifying potential energy functions for direct‐potential‐fit analyses. The new potential energy function is joined smoothly to the long‐range inverse‐power dispersion energy expression. The new model is employed in direct‐potential‐fits using spectroscopic line positions that involve the ground electronic states of the principal isotopologues of hydrogen iodide and carbon monoxide, and the ground and first singlet‐sigma excited states of hydrogen fluoride and hydrogen chloride. The present methodology is found to lead to compact, flexible, and robust representations for the potential energy that compare favorably with the results of past work where more complicated models were employed.     

Corrigendum on ‘investigation on molecular interaction studies of binary mixture of Dehpa and Petrofin at 298.15 K’

Expressions of Redlich–Kister (RK) excess function using polynomials on difference of molar composition are used. Calculated values of excess properties from experimental values are well presented in some curves as a function of mole fraction (x₂) of the second pure component of the studied binary liquid mixture. Nevertheless, the authors presented values of adjustable parameters, not for the polynomial of the popular RK equation (i.e. vs. x₂–x₁), but for globally the excess property Y^E as an overall three degree polynomial on (x₂) including implicitly the molar fraction product (x₁·x₂) in their nonlinear regression, which can then induces some readers to probable confusion.