超声萃取-酶标仪-微量法测定污染土壤中的总石油烃

石油的开采、运输、泄漏及石油产品使用量的不断增加,导致了严重的土壤石油污染,改变了土壤的理化性质,引起土壤中的微生物大量死亡,影响植物的正常生长,并能通过皮肤、呼吸、饮食等方式进入人体,危害健康。因此,土壤石油污染的修复刻不容缓,但修复效果的评价离不开土壤中残留石油的提取和检测,建立快速高效的石油提取和分析测定方法是非常重要的。该研究讨论了检测波长、提取剂种类、提取剂用量以及超声萃取次数、萃取时间、超声萃取功率等影响污染土壤中总石油烃提取的参数和变量,最终建立了一种超声萃取-酶标仪-微量法提取检测污染土壤中总石油烃的方法。确定优化的提取和检测条件为：紫外检测波长为304 nm,用石油醚作提取剂,土液比为1∶4,超声萃取2次,每次萃取时间为20 min,超声萃取功率为100 W。该优化条件下,土壤石油添加回收率是88.4%～101.6%,相对标准偏差均小于4.7%,提取测定结果符合环境分析化学检测要求。利用酶标仪代替紫外分光光度计进行检测,能更方便快速的得出结果,且测定溶液用量少,可以更好地推广应用于微量石油污染环境样品的定量检测。此外,该方法用石油醚和乙醇作为提取和定容试剂,克服了采用二氯甲烷、四氯化碳等有机试剂提取而造成溶剂消耗量大、易产生二次污染、不利于环境友好发展等缺点,是一种快速、高效、绿色的提取和测定污染土壤中总石油烃的方法。     

基于平行活动围道模型的高分辨率遥感影像城区主干道路段提取

为了提取并表示高分辨率遥感影像中的主干道路段,提出了一种多分辨框架下的平行活动围道模型的算法.该算法在活动围道模型原理的基础上,重新定义各能量项:采用抛物线做为道路段的先验模型,增加了平行性能量,并采用多分辨框架下的梯度做为外部能量.该模型的优化过程实现了道路的定位,得到的结果是平行抛物线的参数,实现了道路的矢量表示.实验结果表明,能有效提取高分辨率遥感影像中的主干道路段.     

基于视差自相关特征水深反演

提出了一种基于视差自相关特征模拟水深的新方法。这种方法利用不同摄站获取的同一物体的两幅图像,在水的折射影响下,造成的视觉上的偏差计算水深,可以得到相关区域三维显示中各点的水深数值。以数码相机所拍摄两张照片为例,实现相关区域水深三维显示。结果表明此算法具有一定的可行性,可以进行更深层次的研究,并应用于浅海、河流等地的资源探测开发。     

Ultrasound-assisted extraction,analysis and antioxidant activity of polysaccharide from the rinds of Garcinia mangostana L.

According to response surface methodology (RSM), the extraction conditions of ultrasound-assisted extraction of polysaccharide from the rinds of Garcinia mangostana L. (GMRP) were optimized and determined. The optimal conditions obtained through optimization were: the liquid to material ratio was 40 mL/g, ultrasonic power was 288 W and extraction time was 65 min. The average extraction rate of GMRP was 14.73%. Ac - GMRP was obtained by acetylation of GMRP, and the antioxidant activities of the two polysaccharides were compared in vitro. The results indicated that the antioxidant capacity of polysaccharide obtained after acetylation was significantly improved compared with that of GMRP. In conclusion, chemical modification of polysaccharide is an effective measure to improve its properties to a certain extent. Meanwhile, it implies that GMRP has great research value and potential.     

基于宽光谱干涉系统的拼接主镜共相位检测技术

 针对拼接式大口径望远镜主镜,提出一种基于迈克尔逊干涉原理基础上的宽带光谱（白光）干涉检测方法,对拼接子镜间相位误差进行实时检测,进而对失调子镜进行相应校正,以实现拼接子镜的共面排布。子镜间相位误差通过干涉图形间的不匹配性进行提取。应用双中心波长组合白光源来提高白光中心条纹的可见度,通过理论仿真,对不同中心波长组合的白光中心条纹可见度进行比较,结果表明：该双中心波长组合白光源系统的应用,可以提高白光干涉中心条纹的信号分辨能力,借以提高检测精度,使得该白光干涉检测系统对拼接子镜间的相位失调误差进行高精度提取。     

Improved extraction of vegetable oils under high-intensity ultrasound and/or microwaves

Ultrasound-assisted extraction (UAE) and microwave-assisted extraction (MAE) techniques have been employed as complementary techniques to extract oils from vegetable sources, viz, soybean germ and a cultivated marine microalga rich in docosahexaenoic acid (DHA). Ultrasound (US) devices developed by ourselves, working at several frequencies (19, 25, 40 and 300 kHz), were used for US-based protocols, while a multimode microwave (MW) oven (operating with both open and closed vessels) was used for MAE. Combined treatments were also studied, such as simultaneous double sonication (at 19 and 25 kHz) and simultaneous US/MW irradiation, achieved by inserting a non-metallic horn in a MW oven. Extraction times and yields were compared with those resulting from conventional procedures. With soybean germ the best yield was obtained with a ‘cavitating tube’ prototype (19 kHz, 80 W), featuring a thin titanium cylinder instead of a conventional horn. Double sonication, carried out by inserting an immersion horn (25 kHz) in the same tube, improved the yield only slightly but halved the extraction time. Almost comparable yields were achieved by closed-vessel MAE and simultaneous US/MW irradiation. Compared with conventional methods, extraction times were reduced by up to 10-fold and yields increased by 50–500%. In the case of marine microalgae, UAE worked best, as the disruption by US of the tough algal cell wall considerably improved the extraction yield from 4.8% in soxhlet to 25.9%. Our results indicate that US and MW, either alone or combined, can greatly improve the extraction of bioactive substances, achieving higher efficiency and shorter reaction times at low or moderate costs, with minimal added toxicity.     

GaMnN材料红外光谱中洛伦兹振子模型的遗传算法研究

利用红外反射光谱研究了蓝宝石衬底上用金属有机物化学气相淀积方法生长的稀磁半导体GaMnN材料的晶格振动特性. 并成功地将改进的遗传算法应用于其红外反射光谱洛伦兹振子模型参数的提取. 通过与GaN薄膜的洛伦兹振子模型参数的对比研究发现,GaN掺入Mn后,ω_TO向高频方向移动,γ,ε_∞和ε_s均增加,而ω_LO基本保持不变. 文中同时分析和讨论了Mn对晶格振动特性的影响及 关键词： 稀磁半导体GaMnN材料 遗传算法 洛伦兹振子模型 参数提取     

Effect of fluid properties on ultrasound assisted liquid-liquid extraction in a microchannel

When immiscible liquids are subjected to an ultrasonic field, they form emulsions. This principle has been used to improve the mass transfer characteristics of a liquid-liquid extraction process in microreactor systems. The formation of emulsion and its characteristics are prominently dependent on the properties of the liquids used and this also holds true for emulsion brought about by ultrasound. This paper focuses on the properties of fluids that are reported to have an influence on the cavitation behaviour, namely viscosity, interfacial tension and vapour pressure. These properties were examined by changing the solvent of the organic phase in the hydrolysis of p-nitrophenyl acetate. The study is performed by comparing pairs of solvents that are different in one property but similar in the other two. The pairs selected are toluene – chlorobenzene for viscosity, toluene – methyl Isobutyl ketone for interfacial tension and methyl isobutyl ketone – 2-Methyl tetrahydrofuran for vapour pressure effects. A qualitative study was performed with a high-speed camera in flow to understand the emulsification initiation mechanisms and behaviours. These findings were further explored by performing the sonicated emulsion in a batch-sonicated reactor. The quantitative analysis of the fluid properties was evaluated and compared based on the relative percentage increase in yield upon sonication with respect to their individual silent conditions. The quantitative results were further supported by the quantification of the emulsion performed with an FBRM probe. The results indicate a two times improvement in yield with solvent of lower viscosity as 2 times more droplets were formed in the emulsion. Both the solvent systems with higher interfacial tension and vapour pressure had an improved yield of 1.4 times owing to larger number of droplets formed.     

Liquid chromatographic determination of trace levels of nitrophenols in water samples after dispersive magnetic solid phase extraction

An efficient and fast dispersive magnetic solid phase extraction method was developed using MIL‐101(Cr)/poly (mercaptobenzothiazole)@magnetite nanoparticles for the preconcentration and determination of nitrophenols in river and rain water samples. High‐performance liquid chromatography‐Ultraviolet instrument was applied for the analysis of target nitrophenols. The effect of several variables on the extraction performance was explored via design of experiment approach. Limits of detection and linear dynamic ranges were attained in the range of 0.05–0.10 µg/L and 0.2–250 µg/L, respectively. The enrichment factors were in the range of 317–363. The precision (n = 3) of dispersive magnetic solid phase extraction method was in the range of 5.3–6.8%. Eventually, the method was utilized for the analysis of target nitrophenols in river and rain water samples.     

Quantification of fenoprofen in human plasma using UHPLC–tandem mass spectrometry for pharmacokinetic study in healthy subjects

A rapid, simple and sensitive ultra-performance liquid chromatography–tandem mass spectrometry (UHPLC–MS/MS) method has been developed to quantify fenoprofen, a nonsteroidal anti-inflammatory drug in human plasma for a pharmacokinetic study in healthy subjects. Owing to high levels of protein binding, protein precipitation followed by solid-phase extraction was employed for the extraction of fenoprofen and fenoprofen-d3 (used as internal standard) from 200 μL human plasma. Separation was performed on a BEH C₁₈ (50 × 2.1 mm, 1.7 μm) column using methanol−0.2% acetic acid in water (75:25, v/v) under isocratic elution. Electrospray ionization was operated in the negative mode for sample ionization. Ion transitions used for quantification in the selected reaction monitoring mode were m/z 241/197 and m/z 244/200 for fenoprofen and fenoprofen-d3, respectively. Under the optimized conditions, fenoprofen showed excellent linearity in the concentration range 0.02–20 μg/mL (r² ≥ 0.9996), adequate sensitivity, favorable accuracy (96.4–103.7%) and precision (percentage coefficient of variation ≤4.3) with negligible matrix effect. The validated method was successfully applied to a pharmacokinetic study of fenoprofen in healthy subjects. The significant features of the method include higher sensitivity, small plasma volume for processing and a short analysis time.