在线教学的实践与反思*——以有机化学课程为例

以有机化学课程在线教学开展情况为背景,通过与传统教学模式对比,分析了在线教学的优势与不足。在此基础上,将笔者所在课程组开展在线教学以来在教学内容重构、教学环节设计、考核方式改革等方面的探索与尝试进行了总结与分享。     

化工原理问题导向式线上教学的探索与实践*

以化学制药专科专业化工原理课程为例,阐述问题导向式线上教学的课程设计思路及框架,探索由被动教到主动学的线上教学途径。通过对“流体流动与输送单元”的教学设计,从课前、课中和课后论述了以“问题”为中心的线上教学过程和实施情况,并说明了线上授课的教学效果。     

Real‐Time Monitoring of Transport of Chlorinated Hydrocarbons from Industrial Areas Using Open‐Path FTIR Spectrometry with COL1SB

Abstract

Open‐path Fourier transform infrared (FTIR) spectrometry was used to continuously monitor 11 chlorinated hydrocarbon species in the region connecting two different industrial complexes for 24 hr. The single‐beam spectra obtained from open‐path FTIR were analyzed by newly developed software named COL1SB, which generates site‐specific background spectra as well as path‐averaged water vapor concentrations in addition to performing regression analyses. The path‐averaged water vapor concentrations calculated by the COL1SB agreed very well with those measured by a thermo‐hygrometer. In addition, site‐specific background spectra were generated by accounting for chemical absorption of 50 chemical species. The accurate estimation of path‐averaged water vapor concentrations, as well as the usage of site‐specific background spectra, enables chlorinated hydrocarbons to be measured by open‐path FTIR spectrometry at the ppb level. Among 11 chlorinated hydrocarbons considered here, trichlorofluoromethane, carbon tetrachloride, trichloroethylene, and tetrachloroethylene were identified as major chlorinated hydrocarbons having concentrations above 1 ppb. Wind affected the temporal variations of these chlorinated hydrocarbons, indicating the importance of local transport. However, the effect of wind differed from one species to another because of different source characteristics.     

Dynamic Ion Speciation during the Hydrolysis of Aryltrifluoroborates**

Organotrifluoroborates serve as coupling partners during transmetalation in the Suzuki–Miyaura reaction but require hydrolysis prior to the coupling reaction. Their anionic nature allows study of their hydrolysis by electrospray ionization mass spectrometry (ESI-MS) through real-time monitoring, complemented by pH analysis. The induction period varied according to the borates employed, and a dynamic series of equilibria for numerous ions was observed during hydrolysis. We found that the induction periods and reaction rates were sensitive to the R group of the borates, the shape of the reaction vessel, and stir rate.     

Identification and quantification of the antipsychotics risperidone,aripiprazole, pipamperone and their major metabolites in plasma using ultra‐high performance liquid chromatography–mass spectrometry

The antipsychotics risperidone, aripiprazole and pipamperone are frequently prescribed for the treatment in children with autism. The aim of this study was to validate an ultra‐high performance liquid chromatography–mass spectrometry method for the quantification of these antipsychotics in plasma. An ultra‐high performance liquid chromatography–mass spectrometry assay was developed for the determination of the drugs and metabolites. Gradient elution was performed on a reversed‐phase column with a mobile phase consisting of ammonium acetate, formic acid in methanol or in Milli‐Q ultrapure water at a flow rate of 0.5 mL/min. The method was validated according to the US Food and Drug Administration guidelines. The analytes were found to be stable enough after reconstitution and injection of only 5 μL improved the accuracy and precision in combination with the internal standard. Calibration curves of all five analytes were linear. All analytes were stable for at least 72 h in the autosampler and the high quality control of 9‐OH‐risperidone was stable for 48 h. The method allows quantification of all analytes. The advantage of this method is the combination of a minimal injection volume, a short run‐time, an easy sample preparation method and the ability to quantify all analytes in one run. Copyright © 2015 John Wiley & Sons, Ltd.     

A simple,rapid and reliable liquid chromatography–mass spectrometry method for determination of methotrexate in human plasma and its application to therapeutic drug monitoring

A simple, rapid and reliable liquid chromatography–electrospray ionization tandem mass spectrometry method was established and validated for the determination of methotrexate in human plasma. After a straightforward protein precipitation by acetonitrile–water (70:30, v/v), methotrexate (MTX) and p‐aminoacetophenone (used as internal standard, IS) were separated on a Column C₁₈ column (50 × 2.1 mm, 3 µm; Column Technology, Fremont, CA, USA) using a gradient elution with mobile phase of acetonitrile and 0.03% acetic acid aqueous solution at a flow rate of 0.5 mL/min. The total chromatographic runtime was 5 min for each injection. Quantification detection was performed in a triple‐quadruple tandem mass spectrometer under positive mode monitoring the following mass transitions: m/z 455.3 → 308.3 for MTX and m/z 136.1 → 94.4 for IS. The calibration curve was linear over the range of 0.05–25.0 µmol/L with a lower limit of quantification of 0.05 µmol/L. The intra‐ and interday precisions were <5.2%, the accuracy varied from ?4.1 to 4.5%. The recovery was >94%. The LC‐MS/MS method showed an excellent agreement with the existing HPLC‐UV method using Passing–Bablok regression and Bland–Altman difference plot analysis. The validated LC‐MS/MS can be successfully applied to the routine therapeutic drug monitoring of MTX in clinical laboratories. Copyright © 2015 John Wiley & Sons, Ltd.     

Monitoring the manufacturing process of glass fiber reinforced composites with carbon nanotube buckypaper sensor

Buckypapers are free-standing porous mats of entangled CNT ropes cohesively bounded by van der waals interactions, and can be used to monitor the manufacturing process of glass fiber reinforced composite. In this paper, the buckypaper (BP) was fabricated with monodispersion of multi-wall carbon nanotubes via spray-vacuum filtration, and its morphology and pore size distribution were characterized by scanning electron microscope and nitrogen adsorption/desorption. The resistance of the BP sensor was obtained using a four-point probe method, and the resistance changes could be related to phase changes of the resin matrix,. Experimental results show that the BP sensor embedded in the glass/epoxy composite laminates has indicated a relative resistance change from −2.9% to 226.5% during the manufacturing process. In addition, the temperature sensitivity of a pristine BP sensor and a BP sensor embedded in composite were also characterized. The results demonstrate that the effect of resin phase changes on the resistance changes of a BP sensor is greater than that of the temperature during composite manufacturing.     

Study of blood collection and sample preparation for analysis of vitamin D and its metabolites by liquid chromatography–tandem mass spectrometry

The analysis of vitamin D status, with special emphasis on 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D, is gaining interest in clinical studies due to the classical and non-classical effects attributed to this prohormone. In this research, the influence of the two steps preceding determination (viz. sample collection and preparation) on the quantitative analysis of vitamin D and its more important metabolites has been studied. Two preparation approaches, deproteination and solid-phase extraction (SPE), have been evaluated in terms of sensitivity to delimit their application, thus establishing that detection of 1,25-dihydroxyvitamin D cannot be addressed by protein precipitation. Concerning sample collection, serum and plasma reported high accuracy (above 83.3%) for vitamin D and metabolites, while precision, expressed as relative standard deviation, was below 12.9% for all analytes in both samples. Statistical analysis revealed that serum and plasma provided similar physiological levels for vitamin D₃, 24,25-dihydroxyvitamin D₃ and 25-hydroxyvitamin D₃, while significantly different levels were obtained for 1,25-dihydroxyvitamin D₃, always higher in plasma than in serum. Sample collection and treatment have proved to be significant in the analysis of vitamin D and its relevant metabolites.     

Comparison of scale factor estimators for ultrasonic temperature monitoring: Application to structural health monitoring

In Structural Health Monitoring (SHM) of materials, estimating the effects of environmental and operational conditions such as temperature is important. Indeed, temperature changes induce modifications of the mechanical properties of the material and therefore cause a dilation of the acoustic signals characterized by a scale factor. This paper described four scale factor estimators able to monitor changes in temperature: The short-time cross-correlation (STXC) method, the stretching method (STRE), the Minimum Variance Based Estimator method (MVBE) and the Scale Transform Based Estimator method (STBE). The first two methods have already been assessed in the literature while the latter two have been specifically developed for this study. First, closed-form for the Cramer-Rao bound on the estimates of the scale factor, from a simplified deterministic signal, are derived and simplified expressions are given. Then, a statistical evaluation of the quality of estimates is conducted through Monte-Carlo simulations using synthetic signals, based on a model taking into account the influence of temperature. A raw estimate of the computational complexity of signal processing methods also completes this evaluation phase. Finally, the experimental validation of estimation methods is conducted on an aluminum plate subjected to temperatures variations in a controlled thermal environment. The temperature estimates are then faced with an analytical model describing the material behavior.     

Vibrational spectroscopy in the development of surface hydrophilic elastomer latex (SHEL)

An illustrative example is given to show how various vibrational spectroscopy techniques coupled with two-dimensional (2D) correlation analysis can be effectively utilized in the development of a novel and functional material. Surface-hydrophilic elastomer latex (SHEL) is a material exhibiting rather unusual permanently water-wettable surface feature despite having a soft and rubbery bulk property, which can be successfully analyzed with vibrational spectroscopy. 2D photoacoustic (PAS) IR spectra of a SHEL film indicate the localized surface segregation of long-chain ethoxylate moiety of the oligomeric surfactant used in the preparation of this material. The accumulation of the hydrophilic long-chain ethoxylate produces the high energy polar surface over the hydrophobic bulk phase of SBR copolymer. The persistence of very low water contact angle, even after repeated washing of a SHEL film with an excess amount of water, indicates permanent covalent attachment of long-chain ethoxylate group to the SBR copolymer. 2D Raman spectra generated from the process monitoring of the emulsion copolymerization of SHEL reveal the mechanism of the covalent attachment of long-chain ethoxylate. The reaction involves a separate step of oleyl moiety of the block surfactant reacting with 1,3-butadiene prior to the onset of copolymerization to produce the SBR latex product.