由相容性求任意阶非线性偏微分方程的决定方程

研究了求任意阶的非线性偏微分方程的决定方程,运用相容性方法,和运用传统的向量场及其延拓的方法求得的结果相同.但运用相容性方法不用再计算复杂的无穷小生成元的延拓的系数,这样在计算过程中既能提高计算的速度,又能提高计算的准确率,因此,这种方法比运用向量场及其延拓的方法更简便、快捷,并举例验证了这一事实.     

Compatibility studies between captopril and pharmaceutical excipients used in tablets formulations

Captopril (CAP) was the first commercially available angiotensine-converting enzyme (ACE) inhibitor. In the anti-hypertensive therapy is considered the selected drug has to be therapeutically effective together with reduced toxicity. CAP is an antihypertensive drug currently being administered in tablet form. In order to investigate the possible interactions between CAP and excipients in tablets formulations, differential scanning calorimetry (DSC) and thermogravimetric (TG) analysis completed by X-ray powder diffraction (XRPD) and Fourier transform infrared spectroscopy (FTIR) were used for compatibility studies. A possible drug-excipient interaction was observed with magnesium stearate by DSC technique.     

医院管理综合评价方法的组合与优化

针对医院管理中单一综合评价方法的不足,基于评价结果的一致性和评价方法的兼容性对四种评价方法进行比较、组合和优化,提出一种改进的平均值组合方法.使其评价结果更合理,兼容性更高.     

Siloxane photopolymer to replace polydimethylsiloxane in microfluidic devices for polymerase chain reaction

Herein, we describe the preparation and characterization of a material suitable for the fabrication of microfluidic devices. The material is a silicone acrylic polymer, obtained by photopolymerization. It is polymerase chain reaction (PCR) compatible, resistant to temperature, optically transparent, and dimensionally stable; it has a better water and solvent resistance if compared with polydimethylsiloxane. Production of microfluidic layouts is successfully tested: a simple photolithographic approach allows to accurately control the pattern transfer and to produce PCR compatible microfluidic devices. The polymer characterization suggests that the proposed material satisfies all the characteristics required for an ideal PCR chip, without further treatment. Moreover, the possibility for fast, accurate, and cheap reproducibility of microdevices by liquid phase photopolymerization increases the polymer attractiveness. The material is a good alternative with respect to polydimethylsiloxane for the fabrication of microfluidic chips for biological analysis purposes. Copyright © 2013 John Wiley & Sons, Ltd.     

Synthesis of all‐conjugated poly(3‐hexylthiophene)‐block‐ poly(3‐(4′‐(3″,7″‐dimethyloctyloxy)‐3′‐pyridinyl)thiophene) and its blend for photovoltaic applications

New all‐conjugated block copolythiophene, poly(3‐hexylthiophene)‐block‐poly(3‐(4′‐(3″,7″‐dimethyloctyloxy)‐3′‐pyridinyl)thiophene) (P3HT‐b‐P3PyT) was successfully prepared by Grignard metathesis polymerization. The supramolecular interaction between [6,6]‐phenyl‐C₆₁‐butyric acid methyl ester (PCBM) and P3PyT was proposed to control the aggregated size of PCBM and long‐term thermal stability of the photovoltaic cell, as evidenced by differential scanning calorimetry (DSC), transmission electron microscopy (TEM), and optical microscopy. The effect of different solvents on the electronic and optoelectronic properties was studied, including chloroform (CL), dichlorobenzene (DCB), and mixed solvent of CL/DCB. The optimized bulk heterojunction solar cell devices using the P3HT‐b‐P3PyT/PCBM blend showed a power conversion efficiency of 2.12%, comparable to that of P3HT/PCBM device despite the fact that former had a lower crystallinity or absorption coefficient. Furthermore, P3HT‐b‐P3PyT could be also used as a surfactant to enhance the long‐term thermal stability of P3HT/PCBM‐based solar cells by limiting the aggregated size of PCBM. This study represents a new supramolecular approach to design all‐conjugated block copolymers for high‐performance photovoltaic devices. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011.     

Compatible Polyethylene/Polyvinyl Chloride Particle Hybrids Prepared by in‐situ Polymerization

Polyethylene/polyvinyl chloride (PE/PVC) hybrids were successfully prepared by a polymerization‐filling method. The catalyst for ethylene polymerization was supported on PVC particles, and ethylene was then polymerized in‐situ on the surface of the activated PVC. PVC particles could be well segmented and dispersed during in‐situ polymerization, and the prepared hybrids had an additional tangent peak between the glass transitions of polyethylene and PVC, indicating the formation of a compatible interlayer between nascent polyethylene and PVC during polymerization.     

Polymethylene‐b‐polystyrene diblock copolymer: Synthesis,property, and application

The design and synthesis of well‐defined polymethylene‐b‐polystyrene (PM‐b‐PS, M_n = 1.3 × 10⁴–3.0 × 10⁴ g/mol; M_w/M_n (GPC) = 1.08–1.18) diblock copolymers by the combination of living polymerization of ylides and atom transfer radical polymerization (ATRP) was successfully achieved. The ¹H NMR spectrum and GPC traces of PM‐b‐PS indicated the successful extension of PS segment on the PM macroinitiator. The micellization behavior of such diblock copolymers in tetrahydrofuran were characterized by dynamic light scattering (DLS) and atomic force microscopy (AFM) techniques. The average aggregate sizes of PM‐b‐PS diblock copolymers with the same length of PM segment in tetrahydrofuran solution (1.0 mg mL^?1) increases from 104.2 nm to 167.7 nm when the molecular weight of PS segment increases. The spherical precipitated aggregates of PM‐b‐PS diblock copolymers with an average diameter of 600 nm were observed by AFM. Honeycomb porous films with the average diameter of 3.0 μm and 6.0 μm, respectively, were successfully fabricated using the solution of PM‐b‐PS diblock copolymers in carbon disulfide via the breath‐figure (BF) method under a static humid condition. The cross‐sections of low density polyethylene (LDPE)/polystyrene (PS)/PM‐b‐PS and LDPE/polycarbonate (PC)/PM‐b‐PS blends were observed by scanning electron microscope and reveal that the PM‐b‐PS diblock copolymers are effective compatilizers for LDPE/PS and LDPE/PC blends. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1894–1900, 2010     

基于电磁环境效应的无人机系统级电磁辐射指标制定

分析了实际电磁环境对无人机的影响,通过在实际飞行环境中对各地面发射机的辐射和场地电磁环境的测试,得到对无人机造成伤害的电磁环境场强极限值在0.1~8×103MHz频段中为60~200 V/m.将不同频段下传导干扰与辐射干扰进行结合分析,并根据无人机中存在的辐射干扰和传导干扰的共性特征,得到无人机系统级电磁辐射极限场强在0.1~2×103MHz频段中为10~60 V/m.依照国军标GJB3567-99《军用飞机雷电防护鉴定试验方法》,以及在实际飞行场地中采用410 A敏感度测试系统进行测试,结果显示:采用该指标的无人机各机载设备工作正常,未出现设备失灵或降级情况,说明该指标的制定为无人机系统的电磁兼容设计提供了一个有效的评估准则.     

HTPB/增塑剂玻璃化转变温度及力学性能的分子动力学模拟

为了预测高分子粘结剂端羟基聚丁二烯(HTPB)与增塑剂癸二酸二辛酯(DOS)、硝化甘油(NG)的相容性及HTPB/增塑剂共混物的玻璃化转变温度(Tg)和力学性能,在COMPASS力场条件下采用分子动力学(MD)模拟方法对相容体系(HTPB-DOS)和不相容体系(HTPB-NG)进行了研究.结果表明,通过比较溶度参数差值(Δδ)的大小可以预测HTPB与增塑剂的相容性,即HTPB与DOS属于相容体系,而HTPB与NG不相容.通过温度-比容曲线可以得到HTPB、HTPB/DOS与HTPB/NG的Tg分别为197.54,176.30和200.03K.力学性能分析结果表明,添加DOS增塑剂后使HTPB的弹性模量(E),体积模量(K)和剪切模量(G)下降,材料刚性减弱,柔性增强,力学性能得到改善.本模拟方法可以作为预测聚合物/增塑剂共混物性能的有利工具,也可以为固体推进剂和高聚物粘结炸药的配方设计提供理论指导.     

Removal of lipopolysaccharide and reactive oxygen species using sialic acid immobilized polysulfone dialyzer

Sialic acid (N‐acetylneuraminic acid, NANA) was covalently immobilized onto the surface of a polysulfone (PSF) hollow fiber membrane. Prior to the immobilization, the surface of PSF was treated with ozone, followed by grafting with acrylic acid, and then the esterification of NANA. The surface concentration of NANA was determined by 2‐thiobarbituric acid (TBA) test. Hemocompatibility, the capability of suppressing oxidative stress, and clearance of lipopolysaccharide (LPS) from the resulting hollow fiber membrane were evaluated. The results show that by immobilizing NANA onto PSF hollow fiber, the adhesion of platelet was reduced, while both APTT and PT were little affected. Furthermore, oxidative stress was suppressed by NANA‐immobilized PSF hollow fibers. The level of LPS was also greatly reduced. Copyright © 2009 John Wiley & Sons, Ltd.