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排序方式: 共有306条查询结果,搜索用时 31 毫秒
1.
Temperature effects on deposition rate of silicon nitride films were characterized by building a neural network prediction model. The silicon nitride films were deposited by using a plasma enhanced chemical vapor deposition system and process parameter effects were systematically characterized by 26−1 fractional factorial experiment. The process parameters involved include a radio frequency power, pressure, temperature, SiH4, N2, and NH3 flow rates. The prediction performance of generalized regression neural network was drastically improved by optimizing multi-valued training factors using a genetic algorithm. Several 3D plots were generated to investigate parameter effects at various temperatures. Predicted variations were experimentally validated. The temperature effect on the deposition rate was a complex function of parameters but N2 flow rate. Larger decreases in the deposition rate with the temperature were only noticed at lower SiH4 (or higher NH3) flow rates. Typical effects of SiH4 or NH3 flow rate were only observed at higher or lower temperatures. A comparison with the refractive index model facilitated a selective choice of either SiH4 or NH3 for process optimization. 相似文献
2.
Enhancing the organic dye adsorption on porous xerogels 总被引:4,自引:0,他引:4
Zhijian Wu Ik-Sung Ahn Chang-Ha Lee Jung-Hyun Kim Yong Gun Shul Kangtaek Lee 《Colloids and surfaces. A, Physicochemical and engineering aspects》2004,240(1-3):157-164
We investigate the adsorption of four different organic dyes (i.e., methyl orange, alizarin red S, brilliant blue FCF, and phenol red) on porous xerogels. To understand the factors affecting the adsorption capacity of the xerogels, we vary the hydrophobicity and the textural properties of the xerogels as well as the solution pH. We control the hydrophobicity by mixing two different precursors (i.e., vinyltriethoxysilane (VTES) and tetraethoxysilane (TEOS)) and the textural properties by using cetyltrimethylammonium bromide (CTAB) as a templating agent. We find that the adsorption capacity is enhanced as the organic/inorganic hybrid xerogel or the templated xerogel is used instead of the purely inorganic or the untemplated xerogel. In all the cases studied, adsorption decreases as the pH is increased due to the electrostatic repulsion between the dyes and the xerogel surface. We find that both the hydrophobic surface and larger pore size/volume are required to enhance the adsorption capacity significantly. 相似文献
3.
The enzyme catalyzed conversion of R/S-(±)-2-octanol with hexanoic acid to R/S-(±)-2-octyl hexanoate has been studied in
different microenvironments and in the presence of the competing substrate ethanol. The reactions were performed in various
gels made from aqueous gelatin solutions and liposome dispersions or isotropic liquid solutions, with or without oil and ethanol.
The lipase Candida sp. (SP 525) was dissolved in the dispersions or solutions stabilized by the naturally occurring zwitterionic surfactant
soybean lecithin. The sectioned porous gel was immersed in hexane containing 0.33 mol dm-3 of racemic 2-octanol and hexanoic acid. Since ethanol acts both as a substrate and as a part of the gel it is of fundamental
interest to know the phase behaviour of the used systems. Partial phase diagrams for the systems ethanol–water–soybean lecithin
and ethanol/water (7:3)–oil–soybean lecithin were determined at 298.2 K. The oil was either castor oil or hexadecane. The
conversion of R-2-octyl hexanoate was about 0.45 when no or small amounts of ethanol was present, but decreased considerably
with high amounts of ethanol present and ethyl hexanoate became the main product. Hydrolysis of R-2-octyl hexanoate was favoured
in the latter systems and hexanoic acid formed was immediately esterified to ethyl hexanoate. The conversion of R-2-octyl
hexanoate and ethyl hexanoate depends only on the ethanol content present in the systems and is thus independent of the environment
of the enzyme. However, the chiral esters synthesized from racemic 2-octanol and hexanoic acid showed high optical purities
regardless of the ethanol content.
Received: 1 July 1996 Accepted: 30 August 1996 相似文献
4.
Gun Wirtanen Timo Alanko Tiina Mattila-Sandholm 《Colloids and surfaces. B, Biointerfaces》1996,5(6):319-326
Biofilm growth of Bacillus subtilis, Pseudomonas fragi, Pediococcus inopinatus and Listeria monocytogenes was studied on stainless steel surfaces at room and low temperatures to evaluate the results of traditional hygiene measures. The results were compared with those of image analysis of stainless steel surfaces in an epifluorescence microscope. Statistical analyses were carried out to determine the variations between the conventional cultivation swab method, the glycocalyx amount obtained using swabbing, and the values of the areas of the biofilm, slime and cells. As a general rule, old biofilms showed total counts at approximately the same levels as the young biofilm. The results showed that temperature affected the results for all strains except B. subtilis. The strains of Pe. inopinatus and Ps. fragi showed increased attachment at 6°C and L. monocytogenes at 25°C. The biofilm slime was more easily detached than the cells. The results indicated that the traditional swab method is not reliable for the measurement of biofilm formation on surfaces. 相似文献
5.
Young Gun Ko Ung Su Choi Yong Sung Park Je Wan Woo 《Journal of polymer science. Part A, Polymer chemistry》2004,42(8):2010-2018
The role of hydrogen bonding in the chemistry of transition‐metal complexes remains a topic of intense scientific and technological interest. Poly(acrylo‐amidino diethylenediamine) was synthesized to study the effects of hydrogen bonding on complexes at different pHs. The polymer was synthesized through the coupling of diethylene triamine with polyacrylonitrile fiber in the presence of AlCl3 · 6H2O addition. The adsorption capacity of this polymer was 11.4 mequiv/g. The ions used for the adsorption test were CrO, PO, Cu2+, Ni2+, Fe2+, and Ag+. All experiments were confirmed with Fourier transform infrared. In the study of anion adsorption, at low pHs, only ionic bonds existed, whereas at high pHs, no bonds existed. However, in the middle pH region, both ionic bonds and hydrogen bonds formed between poly(acrylo‐amidino diethylenediamine) and the chromate ion or phosphate ion. When poly(acrylo‐amidino diethylenediamine) and metal ions (Cu2+, Ni2+, Fe2+, and Ag+) formed complexes, a hydrogen‐bonding effect was not observed with Fourier transform infrared. The quantity of metal ions adsorbed onto poly(acrylo‐amidino diethylenediamine) followed the order Ag+ > Cu2+ > Fe2+ > Ni2+. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2010–2018, 2004 相似文献
6.
A polyacrylonitrile (PAN) fiber was adopted for the backbone of a chelate polymer and poly(acrylo‐amidino ethylene amine) (PAEA) was prepared through a one‐step reaction between the PAN fiber and ethylenediamine (EDA). The maximum removal capacity and degree of substitution were 7.8 meq per gram of dried PAEA and 98%, respectively. The PAEA was tested as an adsorbent in single and two‐component metal aqueous solutions under changing pH. The Cu2+ ion accomplished maximum adsorption amount at pH 3 and the order of maximum adsorbed amounts on PAEA is Cu2+ > Ag+ > Zn2+ > Ni2+ > Pb2+ in molar basis. FT‐IR spectroscopy was employed to characterize the chemical bonding in metal aqueous solutions and surface morphology was examined using atomic force microscopy (AFM) and scanning electron microscopy (SEM). Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
7.
Redox‐responsive core cross‐linked micelles of poly(ethylene oxide)‐b‐poly(furfuryl methacrylate) by Diels‐Alder reaction for doxorubicin release
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Cuong M. Q. Le Hai Ha Pham Thi Xuan Thang Cao Gun‐Do Kim Chul‐Woong Oh Kwon Taek Lim 《Journal of polymer science. Part A, Polymer chemistry》2016,54(23):3741-3750
Redox‐responsive core cross‐linked (CCL) micelles of poly(ethylene oxide)‐b‐poly(furfuryl methacrylate) (PEO‐b‐PFMA) block copolymers were prepared by the Diels‐Alder click‐type reaction. First, the PEO‐b‐PFMA amphiphilic block copolymer was synthesized by the reversible addition‐fragmentation chain transfer polymerization. The hydrophobic blocks of PFMA were employed to encapsulate the doxorubicin (DOX) drug, and they were cross‐linked using dithiobismaleimidoethane at 60 °C without any catalyst. Under physiological circumstance, the CCL micelles demonstrated the enhanced structural stability of the micelles, whereas dissociation of the micelles took place rapidly through the breaking of disulfide bonds in the cross‐linking linkages under reduction environment. The core‐cross‐linked micelles showed fine spherical distribution with hydrodynamic diameter of 68 ± 2.9 nm. The in vitro drug release profiles presented a slight release of DOX at pH 7.4, while a significant release of DOX was observed at pH 5.0 in the presence of 1,4‐dithiothreitol. MTT assays demonstrated that the block copolymer did not have any practically cytotoxicity against the normal HEK293 cell line while DOX‐loaded CCL micelles exhibited a high antitumor activity towards HepG2 cells. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 3741–3750 相似文献
8.
9.
Hanna Hedström Henrik Ramebäck Christian Ekberg 《Journal of Radioanalytical and Nuclear Chemistry》2013,298(2):847-852
Co-precipitation of radium, barium and strontium is an important process in many contexts, such as uranium mining, oil extraction and in the safety assessment of a final repository for used nuclear fuel. Co-precipitation to a solid solution is possible since radium, barium and strontium act as chemical analogues. In this work the co-precipitation of radium, barium and strontium was studied and the kinetic behavior of the co-precipitation process was investigated. It was shown that radium, barium and strontium co-precipitate congruently and that the precipitation followed an Arrhenius behavior and the Arrhenius parameters for the systems was determined. When studying the differences of the Arrhenius constants by using a student t test (95 % confidence interval) it was observed that the only significant difference in the activation energy, E a, is between radium and barium and between radium and strontium respectively, the pure strontium having the larger activation energy in comparison. This is most likely coupled to the metal ion size; since the hydration waters are more strongly bound, which leads to them having a slower exchange rate, which in turn effects the rate of co-precipitation to the metal these reactions will be slower. 相似文献
10.
Capacitive Sensor to Monitor Enzyme Activity by Following Degradation of Macromolecules in Real Time
Bergdahl Gizem Ertürk Hedström Martin Mattiasson Bo 《Applied biochemistry and biotechnology》2019,189(2):374-383
Applied Biochemistry and Biotechnology - A capacitive sensor was developed to analyze the presence and enzymatic activity of a model protease from standard solutions by following the degradation of... 相似文献