基于棱镜扫描法的太阳光谱仪光谱定标

为了标定扫描式棱镜太阳光谱仪的棱镜不同转动角度对应的中心波长和光谱带宽,利用了一种棱镜扫描方法对太阳光谱仪的光谱响应函数进行测量。该方法使用固定的单色光波长,控制棱镜转动实现单色光的像在探测器位置扫描,并通过坐标映射得到响应位置的光谱响应函数。文中根据光谱响应函数的定义,推导出棱镜扫描法与单色仪波长扫描方法波长定标原理上的等效性。之后分别以532 nm固体激光器和632.8 nm氦氖激光器为光源,使用棱镜扫描法测量太阳光谱仪对应波长位置的光谱响应函数,并以单色仪波长扫描法实验作为对比。实验结果表明,对于扫描式棱镜太阳光谱仪,棱镜扫描法测量的中心波长分别为531.86和632.67 nm,其准确度优于单色仪波长扫描法测得的531.39和631.97 nm。由于不受单色仪性能的限制,前者测量的光谱带宽值也优于后者。最后以汞灯为光源使用棱镜扫描法对太阳光谱仪进行了光谱定标实验,实现了特征光谱定标法结合棱镜扫描法对中心波长及光谱带宽的标定。该方法同样可以应用于扫描式光栅光谱仪以及单色仪的光谱定标。     

Comparison of different gas models to calculate the spring force of a hydropneumatic suspension

When developing any simulation model some compromise must be made between computational efficiency and the accuracy of the model. This study compares the performance of three ideal gas (IG) law variations (IG with the energy equation (EE), isothermal and adiabatic), and two real gas approaches (Benedict Webb Rubin (BWR) equation with and without the EE) to model the spring force of a hydropneumatic suspension. These models are compared with experimental data obtained from laboratory tests on a single hydropneumatic suspension unit. Both the BWR and IG models with the EE offer a significant improvement in correlation compared to the models without the EE. The real gas BWR approach offers a small improvement over the IG approach under the test conditions. The best (BWR with EE) and worst (IG isothermal) models are then used to model the spring forces in a full vehicle model of a 4 × 4 Sports Utility vehicle (SUV). The data is again compared with experimental results and the BWR model with the EE correlates significantly better than the IG isothermal model. It is thus concluded that the inclusion of the EE will yield significantly better results and it should only be omitted if the parameters investigated are not sensitive to errors in the spring model.     

One-dimensional and two-dimensional nanomaterials for the detection of multiple biomolecules

The complexity of biological samples determines that the detection of a single biomolecule is unable to satisfy actual needs. Moreover, the “false positives” results caused by a single biomolecule detections easily leads to erroneous clinical diagnosis and treatment. Thus, it is important for the homogenous quantification of multiple biomolecules in not only basic research but also practical application. As a consequent, a large number of literatures have been exploited to monitor multiple biomolecules in homogenous solution, enabling facilitating the development of the disease diagnosis, treatment as well as drug discovery. One-dimensional nanomaterials and two-dimensional nanomaterials have special physical and chemical properties, such as good electrochemical properties, stable structure, large specific surface area, and biocompatibility, which are widely used in electrochemical and fluorescent detection of biomolecules. This tutorial review highlights the recent development for the detection of multiple biomolecules by using nanomaterials including one-dimensional materials (1DMs) as well as two-dimensional materials (2DMs).     

In Situ Incorporation of Praziquantel in Polymer Microparticles through Suspension Polymerization for Treatment of Schistosomiasis

Schistosomiasis is one of the major public health problems worldwide. Even though this is a common illness among preschool children in poor countries, treatment is carried out mainly through the administration of praziquantel tablets, which has some disadvantages, such as the strong bitter taste. As an alternative to overcome this problem, the development of new encapsulated praziquantel formulations is demanded. For this reason, suspension polymerizations are carried out for the in situ encapsulation of praziquantel into polymer microparticles, using methyl methacrylate (MMA) and cationic compounds (diethylaminoethyl methacrylate, DEAEMA, and dimethylaminoethyl methacrylate, DMAEMA) as comonomers. This technique allows for the preparation of polymer microparticles with high encapsulation efficiencies (>90%) with characteristic sizes ranging from 0.5 to 1500 µm. Drug release profiles show that praziquantel is released from poly(methyl methacrylate) microparticles slowly due to the existence of strong diffusional resistance. On the other hand, the addition of cationic comonomers renders polymer particles sensitive to pH variations, allowing for faster release of praziquantel in acidic environments, as found in the stomach.     

砂粒与复杂流体压裂液在裂缝中的流动特性研究

在矩形裂缝通道中,应用高速摄像技术,研究了复杂流体压裂液水平流动过程中砂粒的沉降速度,测试了复杂流体的流变学特性,分析了复杂流体的水平流动如何影响砂粒的沉降.研究结果表明,流性指数不等于1的复杂流体,其水平流速影响砂粒的沉降规律,砂粒在裂缝中水平流动过程的沉降速度不仅随复杂流体表观粘度的减小而增大,同时随复杂流体水平流速的增大而增大,是静止沉降速度的数倍至十数倍.     

反相悬浮聚合法制备硫氰酸根阴离子印迹微球及其离子识别性质

利用反相悬浮聚合法, 成功制备了微米级硫氰酸根(SCN^-)阴离子印迹微球。 以溶有分散剂Span-60的环已烷为分散介质, 以溶有模板阴离子SCN^-、阳离子单体丙烯酰氧乙基三甲基氯化铵(DAC)及交联剂N, N'-亚甲基双丙烯酰胺(MBA)的水溶液为分散相, 构成反相悬浮聚合体系, 在水相液滴中使DAC发生交联聚合, 成功制备了粒径约为200 μm的离子印迹微球(IIPMs)。 以同为一价阴离子的NO₃^-和I^-为对比离子, 深入考察研究了该离子印迹微球的离子识别与结合特性。 研究结果表明, 凭借强静电相互作用, 在水相液滴中, 阳离子单体DAC与模板阴离子SCN^-紧密相结合, 故在DAC交联聚合的同时, 实现了阴离子SCN^-的印迹。 所制备的阴离子印迹微球IIPMs对模板阴离子SCN^-具有很高的结合能力(结合容量为3.3 mmol/g(192 mg/g))和特异的识别选择性。 该印迹微球可选择性地识别与结合离子混合溶液中的SCN^-离子, 相对于NO₃^-和I^-阴离子, IIPMs对SCN^-阴离子的选择性系数分别为3.24和6.78。 该印迹微球还具有优良的重复使用性能。     

莠灭净悬浮剂物理稳定性

通过颗粒平均粒径测定和形貌表征研究了分散剂种类和用量对莠灭净悬浮剂物理稳定性的影响。 结果表明,相同条件下,双子型分散剂马来松香聚氧丙烯-氧乙烯醚磺酸盐（SC-3）可以在农药颗粒表面形成双层吸附,产生双层屏蔽结构,有效阻隔了颗粒与水的接触,抑制了颗粒团聚和奥氏熟化引起的结晶长大。 其用量(质量分数)大于4.0%时,所制备的莠灭净悬浮剂热贮前后颗粒粒径及形貌基本不变,其结晶长大现象得到有效地抑制,体系物理稳定性较好。     

悬浮聚合法制备罗丹明B磁性分子印迹微球及其性能

以罗丹明B（RhB）为模板分子,采用悬浮聚合法制备了罗丹明B磁性印迹微球（M-MIPs）,对其进行了结构表征,并与本体聚合的印迹材料进行了对比。 结果表明,2种聚合物中的Fe3O4均呈现良好的晶形。 悬浮法制得的M-MIPs呈球形,粒径在50 μm左右,其饱和磁化强度(5.406 emu/g)比本体法制得的M-MIP（1.772 emu/g）更大,有利于快速磁性分离。 悬浮法所得M-MIPs的吸附量是本体法所得M-MIPs吸附量的近1.8倍,且在吸附速率、选择性、重复使用性能等方面,均明显优于后者。 2种材料均符合Langmuir吸附模型;悬浮法所得M-MIPs对RhB的吸附过程更符合二级动力学方程,而本体法所得M-MIPs较符合一级动力学方程。 悬浮法制得的M-MIPs更适合于RhB的识别、富集与分析应用。     

高效液相色谱法同时测定双酚伪麻干混悬剂中的盐酸伪麻黄碱和氢溴酸右美沙芬

建立了可同时测定双酚伪麻干混悬剂中盐酸伪麻黄碱和氢溴酸右美沙芬含量的反相高效液相色谱方法。样品先经甲醇溶解,过滤,然后以Lichrospher C6H6化学键合硅胶为固定相、乙腈-水-H3PO4（体积比为50∶50∶0.1,pH 2.5,内含1 g/L十二烷基硫酸钠)为流动相进行色谱分离,在220 nm处定量测定。结果表明,氢溴酸右美沙芬、盐酸伪麻黄碱的质量浓度分别为1.03~206 mg/L和5~200 mg/L时,其峰面积与质量浓度的线性关系良好;批内(n=7)测定的平均相对标准偏差（RSD）分别为1.8%和1.0%,批间(n=5)测定的RSD分别为2.2%和1.5%;对双酚伪麻干混悬剂中氢溴酸右美沙芬、盐酸伪麻黄碱测定回收率分别为100.0%~101.8%和95.7%~98.7%。该法适用于双酚伪麻干混悬剂中氢溴酸右美沙芬和盐酸伪麻黄碱的质量控制及含量测定,方法准确,操作简便。     

Van der Pol type self-excited micro-cantilever probe of atomic force microscopy

A technique for dimensional reduction of nonlinear delay differential equations (DDEs) with time-periodic coefficients is presented. The DDEs considered here have a canonical form with at most cubic nonlinearities and periodic coefficients. The nonlinear terms are multiplied by a perturbation parameter. Perturbation expansion converts the nonlinear response problem into solutions of a series of nonhomogeneous linear ordinary differential equations (ODEs) with time-periodic coefficients. One set of linear nonhomogeneous ODEs is solved for each power of the perturbation parameter. Each ODE is solved by a Chebyshev spectral collocation method. Thus we compute a finite approximation to the nonlinear infinite-dimensional map for the DDE. The linear part of the map is the monodromy operator whose eigenvalues characterize stability. Dimensional reduction on the map is then carried out. In the case of critical eigenvalues, this corresponds to center manifold reduction, while for the noncritical case resonance conditions are derived. The accuracy of the nonlinear Chebyshev collocation map is demonstrated by finding the solution of a nonlinear delayed Mathieu equation and then a milling model via the method of steps. Center manifold reduction is illustrated via a single inverted pendulum including both a periodic retarded follower force and a nonlinear restoring force. In this example, the amplitude of the limit cycle associated with a flip bifurcation is found analytically and compared to that obtained from direct numerical simulation. The method of this paper is shown by example to be applicable to systems with strong parametric excitations.