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1.
Kwang-Hee Lim 《Korean Journal of Chemical Engineering》2005,22(2):228-233
An experiment for five stages of a biofilter-run was performed to investigate the effect of hydrophilic ethanol and hydrophobic
toluene on the biodegradation of hydrophobic toluene and hydrophilic ethanol, respectively, when waste-air containing toluene
and ethanol was treated by a biofilter. Removal efficiencies of toluene and ethanol began to decrease when inlet load surpassed
90 g/m3/h and 100 g/m3/h consistent with maximum elimination capacities of toluene and ethanol, respectively. At the end of the biofilter-run, removal
efficiencies for toluene and ethanol were decreased and maintained at 65% and 40%, respectively. The concentration of toluene
at 1st sampling port was raised by factor of two in the 3rd stage of the biofilter run when the inlet load of ethanol co-feed
was increased by 1.5 times, while the process conditions of toluene were maintained the same as those of the 2nd stage of
biofilter-run. According to the result of Mohseni and Allen, it may be interpreted that removal efficiency of hydrophobic
toluene was affected by the presence of hydrophilic ethanol when high load of hydrophobic toluene was applied like that of
the 1st sampling port of the biofilter. However it was not the case when a low load of hydrophobic toluene was applied like
those of the 2nd, 3rd and 4th sampling ports since hydrophobicity of toluene is much less that of α-pinene. Thus, it may be
suggested that biodegradation of hydrophobic VOC was interfered by hydrophilic VOC dissolved in the biolayer and the degree
of interference was proportional to the inlet load of hydrophobic VOC as well as that of hydrophilic VOC and was inversely
proportional to the solubility of hydrophobic VOC. However, it was inferred that the existence of hydrophobic toluene from
waste-air can hardly inversely hinder the removal of hydrophilic ethanol in the biofilter when timeevolutions of hydrophilic
ethanol concentrations of this experiment were compared with those of the previous experiment of biofilter to treat waste-air
containing ethanol only. 相似文献
2.
3.
《The Journal of Adhesion》2008,84(3):231-239
A process to fabricate stretchable gold tracks on silicone rubber substrates is studied by XPS, static water contact angle measurement, AFM, and SEM. The process involves several steps: removing uncured oligomers by hexane Soxhlet extraction; pre-stretching the substrate; activating the strained silicone surface by an oxygen plasma treatment; coating the strained substrate with 5 nm titanium and 80 nm gold layers; and finally releasing the sample. The plasma treatment creates a thin brittle silica-like layer that temporarily increases the substrate's surface energy. Indeed, the plasma treatment is followed by a hydrophobic recovery. As a consequence, the delay between plasma treatment and metal deposition has to be reduced as much as possible. The silica-like layer can be nicely observed after release. The entire process allows us to obtain stretchable metallized samples that remain conductive even after an excessive deformation leading to electrical failure. 相似文献
4.
The present work is to study the possibility for controlled distribution of the impurities when they are decomposed by sulphuric acid to wet phosphoric acid and phosphogypsum, as well as generating technological conditions for production of clean wet phosphoric acid and its derivatives - phosphoric fertilizers, food phosphates and other phosphoric products.A coefficient of distribution DA is introduced as a general criterion for elements dispersion. The study includes relationships between the weight ratio sulphuric acid/natural phosphate and DA; the period of decomposition and DA; the particle's size content of the natural phosphate and DA. The obtained experimental data and relationships about the influence of the above discussed technological parameters on dispersion of more than 23 elements allow for control of that process in wet phosphoric acid and phosphogypsum by selecting specific technological conditions. Thus, depending on the requirements of acid's consumers and procedures for secondary processing of phosphogypsum to end-products, a selective decomposition of the natural phosphates to phosphoric acid and phosphogypsum can be carried out with content of the impurities in those products varying in narrow limits. 相似文献
5.
基于卡尔曼滤波改进的精子图像序列分割方法 总被引:1,自引:0,他引:1
图像分割是精子图像识别的一项关键技术,在精子运动能力分析中起着至关重要的作用。本文对采集的连续精子图像序列进行灰度化、去噪等预处理后,采用Otsu算法对首幅动物精子图像二值化,对后续图像采用Kalman Filter确定二值化阈值范围,改进Otsu算法求出每一幅图像的适当阈值并进行二值化,缩短算法时间并能保证分割精度。应用形态学消除精子尾部和部分精子之间的粘连现象,通过计算和比较目标面积、形状因子,去除小颗粒杂质以及形状及灰度和精子相似的杂质,为精子运动能力检测提供高质量的分割图像。 相似文献
6.
Nicholas P. Petropolis Harrison M. Petropolis Nicole E. MacNeil Taylor M. Doucet D. Gerrard Marangoni 《Journal of surfactants and detergents》2021,24(1):51-66
The critical micelle concentrations (CMC) values and counterion dissociation (α values) have been determined for a number of mixed micellar systems consisting of two typical ionic surfactants and glycol ethers (glymes) as cosurfactants, namely diethylene glycol dimethyl ether, diethylene glycol diethyl ether, triethylene glycol dimethyl ether, and tetraethylene glycol dimethyl ether. Conductance experiments were used to determine the CMC and α values of the mixed micelles as a function of glyme concentration in the aqueous mixed solvent. Favorable interactions between sodium dodecyl sulfate micelles and glyme cosurfactants were deduced from the decreases in the CMC values and the large increase in the α values of these systems as a function of increasing glyme concentration in the mixed solvents. In contrast to the anionic surfactant/glyme systems, in general, there appeared to be little favorable interactions between the surfactant and glymes when micelles of the cationic surfactant dodecyltrimethylammonium bromide were formed in water/glyme solvent systems containing an increasing amount of the glymes. The interaction of glymes with the surfactant micelles was examined closely via 13C nuclear magnetic resonance (NMR) chemical shifts for both surfactant and glyme carbons; these chemical shifts changes were interpreted in terms of the distribution and the localization of the glymes in the aggregates. Finally, partition constants, determined from two-dimensional diffusion-oriented spectroscopy (2D-DOSY) experiments, were used to calculate thermodynamic quantities of transfer of the glymes between the bulk phase and the self-assembled aggregates. All these results are interpreted in terms of the key contributions that both the glyme ethoxylated groups and alkyl endgroups make to the hydrophobic interactions. 相似文献
7.
Quantification of trace amounts of impurities in high purity cobalt by high resolution inductively coupled plasma mass spectrometry 总被引:2,自引:0,他引:2
XIE Hualin HUANG Kelong NIE Xidu TANG Yougen 《稀有金属(英文版)》2007,26(3):286-291
An analytical method using high resolution inductively coupled plasma mass spectrometry (HR-ICP-MS) for rapid simultaneous determination of 24 elements (Be, Mg, Al, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Ge, As, Se, Mo, Ag, Cd, Sn, Sb, Ba, Pt, Au, and Pb) in high purity cobalt was described. Sample digestions were performed in closed microwave vessels using HNO3 and HCl. The matrix effects because of the presence of excess HCl and Co were evaluated. The usefulness of high mass resolution for overcoming some spectral interference was demonstrated. The optimum conditions for the deter- mination were tested and discussed. The standard addition method was employed for quantitative analysis. The detection limits were 0.016-1.50 μg?g?1, the recovery ratios were 92.2%-111.2%, and the RSD was less than 3.6%. The method was accurate, quick, and convenient. It was applied to the determination of trace impurities in high purity cobalt with satisfactory results. 相似文献
8.
9.
A.E. Elsherief 《Journal of Applied Electrochemistry》2003,33(1):43-49
The effects of cobalt concentration, temperature and the presence of zinc, copper and iron ions in the electrolyte on current efficiency and cathodic quality were investigated by cyclic voltammetry and galvanostatic methods during cobalt electrowinning. The results showed that high cathodic efficiency of cobalt deposition was obtained from solutions containing cobalt concentration in the range 30–60 g l–1. Current efficiency increased from 94% to 97% with increase in cobalt concentration to 60 g l–1 at 20 °C. It was also found that increase in temperature to 50 °C enhanced the cobalt deposition reaction, along with the rate of hydrogen evolution, resulting in little change in current efficiency. The presence of foreign cations in the electrolyte not only adversely affects current efficiency but also promotes cracking and peeling. 相似文献
10.
Selective modification by ozonation for the surface of polyvinyl chloride (PVC) was evaluated to separate PVC from the other plastics, polyethylene terephthalate (PET), polycarbonate (PC) and polymethyl methacrylate (PMMA), with almost the same density as PVC by the froth flotation process. Ozonation could selectively decrease the contact angles of flexible PVC from 87.5 degrees to 68.4 degrees and rigid PVC from 90.3 degrees to 66.9 degrees, whereas little decreases in the contact angle were observed for other plastics. This would be due to the replacement of the chloride group on the surface of PVC, into hydrophilic functional groups; carbonyl, carboxyl and ester group. The PVC was successfully separated from the other plastics by the froth flotation process after the selective surface modification by ozonation. 相似文献