Image analysis of atmospheric corrosion of field exposure high strength aluminium alloys

The corrosion morphology image acquisition system which can be used in the field was established. In Beijing atmospheric corrosion exposure station, the image acquisition system was used to capture the early stage corrosion morphology of five types of high strength aluminium alloy specimens. After the denoise treatment, wavelet-based image analysis method was applied to decompose the improved images and energies of sub-images were extracted as character information. Based on the variation of image energy values, the corrosion degree of aluminium alloy specimens was qualitatively and quantitatively analyzed. The conclusion was basically identical with the result based on the corrosion weight loss. This method is supposed to be effective to analysis and quantify the corrosion damage from image of field exposure aluminium alloy specimens.     

Functionalized-multiwalled carbon nanotubes as a preconcentrating probe for rapid monitoring of cationic dyestuffs in environmental water using AP-MALDI/MS

A simple and sensitive method was developed for the rapid analysis of cationic dyestuffs from river and industrial wastewater using functionalized-multiwalled carbon nanotubes (f-MWCNT) with atmospheric pressure-matrix assisted laser desorption/ionization mass spectrometry (AP-MALDI/MS). The separation and preconcentration of analytes from sample solution was based on electrostatic force of attraction between positive dyestuffs and negatively charged f-MWCNT. The optimum enrichment of the three dyestuffs was observed at pH 5.0 for 3 min contact time and using 1 mg f-MWCNT in 1 mL water sample. The developed method has been successfully applied for the determination of three cationic dyestuffs namely neutral red (NR), brilliant cresyl blue (BB), and methylene blue (MB) in real world samples including river and industrial wastewater. The relative recoveries of dyestuffs from water sample were in the range 88.6-98.4%, indicating that the matrix had little effect on enrichment of analytes. The LOD and LOQ for cationic dyestuffs in water were 0.5-1.9 and 1.6-6.0 microg/L, respectively. All the results indicated that the proposed method could be used for the simultaneous determination of the three cationic dyestuffs in river and industrial wastewater at trace levels without the need of any chromatographic separation techniques.     

Multivariate optimization of a GC-MS method for determination of sixteen priority polycyclic aromatic hydrocarbons in environmental samples

This paper describes the development and optimization, by using multivariate analysis, of a GC-MS-SIM method for evaluation of the 16 polyaromatic hydrocarbons considered as priority pollutants in atmospheric particulate material by the US EPA. In order to assure an adequate separation in the shortest analysis time, a multivariate design was used to set the conditions of the oven temperature program. The optimization process was carried out using factorial fractional design and Box-Behnken design. The following factors were evaluated: initial temperature, temperature rate #1, intermediary temperature, temperature rate #2, and final temperature. The optimized conditions were set at: 70 degrees C (2 min) --> 200 degrees C (30 degrees C/min, 5 min) --> 300 degrees C (5 degrees C/min, 1.67 min). Moreover, we have also optimized the injector temperature as 310 degrees C and sampling time as 0.8 min. The total analysis time was 33 min. Validation of GC-MS-SIM yielded satisfactory results for repetitivity of the detector response and retention times, and linearity of calibration curves. LOD were established as 0.13-0.34 ng/mL (peak area) and 0.18-0.72 ng/mL (peak height). The method has been shown to be appropriate for the analysis of samples of atmospheric particulate material and/or other environmental matrices.     

Dechlorination of poly(vinyl chloride) using NaOH in ethylene glycol under atmospheric pressure

A solution of NaOH dissolved in ethylene glycol (EG) was effective in the dechlorination of poly(vinyl chloride) (PVC) at atmospheric pressure. The degree of dechlorination increased with increasing temperature, reaching a maximum of 97.8% at 190 °C. The dechlorination proceeded under chemical control and exhibited first-order kinetics with an apparent activation energy of 170 kJ mol⁻¹. The apparent rate constant for dechlorination in 1.0 M NaOH/EG was approximately 150 times greater than that in 1.0 M NaOH/H₂O. In addition, dechlorination was faster at atmospheric pressure in NaOH/EG than under high pressure in NaOH/H₂O. The dechlorination reaction occurs via a combination of E2 and S_N2 mechanisms.     

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通过测量大气压介质阻挡放电等离子体辐射信号,建立偶极子辐射模型,利用快速傅立叶变换,计算了大气压介质阻挡放电等离子体中离子速度分布。计算结果表明,速度分布偏离麦克斯韦分布,并且随着放电过程的进行,离子速度及相对离子数进行有规律的变化。     

单臂压缩感知鬼成像的光强扩散函数分析法

为了提高单臂压缩感知鬼成像的成像质量,减少成像系统本身和外部环境的干扰,提出了一种光强扩散函数分析方法.在单臂压缩感知鬼成像原理的基础上分析了成像过程,指出降低成像质量的主要因素是菲涅尔衍射和大气湍流.针对这两个因素,推导并分析了光强度扩散函数的公式,研究透镜的焦距与口径之比和照明光源的波长对鬼成像的影响.仿真结果表明:在单臂压缩感知鬼成像中,使用焦距与尺寸半径之比在2~5范围内的成像投影透镜可以消除衍射效应的影响;短波长光源适用于大气湍流较弱时的成像,长波长光源在大气湍流较强时对干扰有更好的耐受能力.该方法可以有效地提高成像质量并优化成像系统.     

部分相干光在大气湍流中的到达角起伏

研究了部分相干高斯谢尔光束在大气湍流中的到达角起伏.主要采用湍流内外尺度的修正Von Karmon谱模型及广义惠更斯-菲涅尔原理和交叉谱密度函数推导出了部分相干光在大气湍流中的到达角起伏表达式.对比分析了湍流内外尺度、湍流强度、传输距离、源相干参数以及波长等参数对部分相干光在大气湍流水平路径上传输时的到达角起伏的影响.结果表明:随着传输距离的增加,到达角起伏越来越小;随着大气湍流内外尺度和源相干参数的增加,到达角起伏也越来越大;与部分相干光相比,完全相干光的到达角起伏受湍流影响很小;随着波长和湍流强度的减小,到达角起伏越来越小.     

High-performance liquid chromatographic/ion-trap mass spectrometric speciation of aquatic mercury as its pyrrolidinedithiocarbamate complexes

Mercury-pyrrolidinedithiocarbamate complexes are first time used for speciation of aquatic mercury with high-performance liquid chromatographic/ion trap-mass spectrometric method utilizing atmospheric pressure chemical ionization (APCI). The separation of the four mercury species was achieved in less than 5 min with a linear gradient profile of aqueous methanol from 70 up to 100% (v/v) in 4th min, isocratic elution at 100% up to 5th min and followed by a negative gradient to 70% in 6th min. The best separation was achieved on a reverse phase Zorbax Eclipse XDB C18 column (50 mm × 2.1 mm i.d., 1.8 μm particle size). The on-column limits of detection (injection volume 1 μL) were 370 pg for methylmercury (MeHg⁺), 280 pg for ethylmercury (EtHg⁺), 250 pg for phenylmercury (PhHg⁺) and 90 pg for inorganic mercury (Hg²⁺) when the data were collected in selective ion monitoring (SIM) mode. A method of isolation and preconcentration of the mercury species using a “home-made” C18 solid phase extraction (SPE) microcolumns was developed to enhance sensitivity of the method. The preconcentration factor as much as 2500 was achieved with on-column complex formation of mercury-pyrrolidinedithiocarbamate. Methanol (100%) was chosen for elution of preconcentrated mercury species. The method was applied for the determination of mercury species in river water samples.     

Atmospheric Plasma Sterilization and Deodorization of Dielectric Surfaces

A method is presented for rapid and uniform sterilization and deodorization of dielectric surfaces. The technology is applicable to the inside surface of PET or glass bottles, polymer caps, plastic tubes, etc. The treatment is based on a pulsed RF discharge in air at atmospheric pressure (eventually with addition of argon) creating a nonequilibrium plasma on the treated surface. The plasma effectively destroys microorganisms in vegetative or sporulent form. It also slightly etches the polymeric material, removing some atomic layers and, thereby, cleaning it from aromatic organic components (deodorization). The process is short: PET bottles 1.5 L, in particular, can be treated in about 20 msec. The results of surface analysis and microbiological, chromatography, and spectroscopy tests are discussed. A device has been developed and integrated into an industrial-filling machine for online sterilization and deodorization of the inside surface of PET bottles before filling, and for sterilization of caps and bottle necks before seaming. It allows cold asceptic filling at a rate of 36,000 bottles per hour.     

Synthesis of Ozone at Atmospheric Pressure by a Quenched Induction-Coupled Plasma Torch

The technical feasibility of using an induction-coupled plasma (ICP) torch to synthesize ozone at atmospheric pressure is explored. Ozone concentrations up to ~250 ppm were achieved using a thermal plasma reactor system based on an ICP torch operating at 2.5 MHz and ~11 kVA with an argon/oxygen mixture as the plasma-forming gas. The corresponding production rate and yield were ~20 g ozone/hr and ~2g ozone/kWh, respectively. A gaseous oxygen quench formed ozone by rapid mixing of molecular oxygen with atomic oxygen produced by the torch. The ozone concentration in the reaction chamber was measured by Fourier Transform infrared (FTIR) spectroscopy over a wide range of experimental conditions and configurations. The geometry of the quench gas flow, the quench flow velocity, and the quench flow rate played important roles in determining the ozone concentration. The ozone concentration was sensitive to the torch RF power, but was insensitive to the torch gas flow rates. These observations are interpreted within the framework of a simple model of ozone synthesis.