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71.
《Surface and interface analysis : SIA》2003,35(3):310-317
Carbonate is a somewhat enigmatic anion in static secondary ion mass spectrometry (SIMS) because abundant ions containing intact CO32? are not detected when analyzing alkaline‐earth carbonate minerals common to the geochemical environment. In contrast, carbonate can be observed as an adduct ion when it is bound with alkali cations. In this study, carbonate was detected as the adduct Na2CO3·Na+ in the spectra of sodium carbonate, bicarbonate, hydroxide, oxalate, formate and nitrite and to a lesser extent nitrate. The appearance of the adduct Na2CO3·Na+ on hydroxide, oxalate, formate and nitrite surfaces was interpreted in terms of these basic surfaces fixing CO2 from the ambient atmosphere. The low abundance of Na2CO3·Na+ in the static SIMS spectrum of sodium nitrate, compared with a significantly higher abundance in salts having stronger conjugate bases, suggested that the basicity of the conjugate anions correlated with aggressive CO2 fixation; however, the appearance of Na2CO3·Na+ could not be explained simply in terms of solution basicity constants. The oxide molecular ion Na2O+ and adducts NaOH·Na+ and Na2O·Na+ also constituted part of the carbonate spectral signature, and were observed in spectra from all the salts studied. In addition to the carbonate and oxide ions, a low‐abundance oxalate ion series was observed that had the general formula Na2?xHxC2O4·Na+, where 0 < x < 2. Oxalate adsorption from the laboratory atmosphere was demonstrated but the oxalate ion series also was likely to be formed from reductive coupling occurring during the static SIMS bombardment event. The remarkable spectral similarity observed when comparing the sodium salts indicated that their surfaces shared common chemical speciation and that the chemistry of the surfaces was very different from the bulk of the particle. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
72.
C.?GarciaEmail author A.?Durán R.?Moreno 《Journal of Sol-Gel Science and Technology》2005,34(3):211-217
Functional coatings incorporating different types of particles developed by the sol–gel method have been proposed in the last few years for diverse applications. This work focuses on the preparation of homogeneous coatings prepared from stable suspensions with 10 wt% of glass and glass ceramic particles in a hybrid organic–inorganic solution as dispersing media. For this purpose, the pH was shifted up to 6–7 by adding tetrapropylammonium hydroxide (TPAH) which behaves as a cationic surfactant being probably adsorbed on the particles surface, while the sol maintains stable. Rheological measurements were performed to study the stability of the suspensions prepared at different conditions such as the kind and concentration of dispersant and the pH conditions. After sintering at 450∘C/30 min, coatings around 2 μ m in thickness were obtained. 相似文献
73.
Exfoliated polystyrene (PS)/laponite nanocomposites were prepared successfully. The characteristic doo1 diffraction peak of organo-laponite disappeared in the XRD patterns of nanocomposites, indicating that the laponite layers were exfoliated and the ordered crystal structure of laponite was destroyed because of the styrene polymerization. TEM observations showed that the exfoliated laponite primary particles were dispersed randomly in the PS matrix with lateral dimensions from 1 nm to 10 rim. SEM results showed that the PS/laponite nanocomposite particles were almost monodispersed spheres with the size of about 120 rim. Because of the interaction between PS and laponite nanolayers, the nanocomposites exhibited higher thermal stability and glass transition temperature when compared to pure PS. 相似文献
74.
Photokilling Squamous Carcinoma Cells SCCVII with Ultrafine Particles of Selected Metal Oxides 总被引:1,自引:0,他引:1
Ivanković Siniša Gotić Marijan Jurin Mislav Musić Svetozar 《Journal of Sol-Gel Science and Technology》2003,27(2):225-233
The ability of ultrafine particles of TiO2, WO3 and iron-doped TiO2 to kill cancer cells in the presence of UV irradiation was investigated. The best photokilling effect on carcinoma cells SCVII cultured in vitro showed iron-doped TiO2 ultrafine particles synthesized by the sol-gel procedure with starting chemicals Ti(IV)-isopropoxide and anhydrous Fe(II)-acetate. It was found that a small particle size and high dispersity influenced citotoxicity and photocatalytic efficiency. The remarkable photokiling effect of highly iron-doped TiO2 ultrafine particles (the molar ratio Fe/Ti = 0.136) in the presence of UV irradiation was observed. The influence of ultrafine metal oxide particles on the inhibition of cancer cell proliferation was measured using a 3H-thymidine incorporation test. The possible mechanism involved in the photokilling of carcinoma cells with ultrafine particles of selected metal oxides was discussed. 相似文献
75.
微波合成PMMA胶乳粒子 总被引:2,自引:0,他引:2
在常压微波辐照下合成聚甲基丙烯酸甲酯(PMMA)单分散的胶体微粒。体系中未加表面活性剂和稳定剂,在透射电镜下观察粒子的形状和直径大小,并得出在引发剂浓度一定的条件下,微粒的体积与单体的浓度呈现线性关系,为我们合成一定大小的超细微粒提供了选择的条件。功力学实验表明,微波场下反应速度大大加快,反应是突变的,无恒速阶段。 相似文献
76.
Catherine J. Murphy 《Journal of Cluster Science》1996,7(3):341-350
One of the most exciting frontiers in materials chemistry in recent years is the optoelectronics of quantum-confined semiconductor nanoclusters. These nanoclusters are 10–200 A in diameter, and in this size regime exhibit extra-ordinarily interesting quantum mechanical effects. Cadmium sulfide is a popular semiconductor for these studies, and reviewed here is the synthesis and charac-terization of such CdS nanoclusters, with emphasis on how chemical control of the surface by thiolates influences product formation and properties. Also described are the syntheses and structures of true molecular clusters of CdS capped with thiolate ligands. 相似文献
77.
Summary Polyethylene oxide (PEO)-based polymers with hydroxy, methoxy, and aminopropoxy terminal groups were coated on diol functionalized and hexamethyldisilazane end-capped silica particles. Proton-donor and proton-acceptor test solutes, including carboxylic acids, hydroxy-containing compounds, arylamines, and alkylamines were used to evaluate the chromatographic performances of these polymer coated particles under SFC conditions with neat CO2 as mobile phase. It was found that the particles coated with hydroxy-terminated PEO were suitable for the separation of proton-donor compounds such as hydroxy-containing compounds and carboxylic acids, and the particles coated with aminopropoxy-terminated PEO could be used for the separation of amines. That is, the proton-accepting stationary phase is suitable for the separation of proton accepting solutes, including strong basic alkylamines (pKb4), using neat CO2 as mobile phase, while the protondonating stationary phase is suitable for the separation of proton-donating compounds such as carboxylic acids (pKa4). Hydrogen bond basicity was found to be a critical factor for the chromatography of basic amines. Low volatility acidic and basic drugs were chromatographed using the new stationary phases. The stability of the PEO coated particles was determined by measuring the loss of organic carbon under SFC conditions. It was found that approximately 18 % of the coating (average molecular weight of 15,000) was washed out of the particles by supercritical CO2 after 7 h at 350 atm and 50°C 相似文献
78.
Recently, we reported that multi-hollow polymer particles can be prepared from carboxylated polymer particles by the stepwise
alkali/acid method. In this article, an attempt was made to prepare similar particles from acid-swellable polymer particles
by the stepwise treatment with acid and alkali, which was named the stepwise acid/alkali method. The acid-swellable particles
were produced by emulsion terpolymerization of styrene, butyl acrylate, and dimethyl 2-amino ethyl methacrylate. The effects
of initial pH value, temperature, and time in the acid and alkali treatment processes on the multi-hollow structure were examined.
Received: 18 December 1996 Accepted: 11 March 1997 相似文献
79.
A new reactor and a novel in-situ sampling technique were developed for the study of the synthesis of CeO2 powders produced from dissolved cerium nitrate salts. The conical reactor minimized particle recirculation and provided a
highly symmetrical and undisturbed plasma flow suitable for the analysis of the phenomena affecting the formation of CeO2 powders. Both a calorimetric study of the reactor and a thermodynamic analysis of CeO2 formation were conducted. The sampling probe is described and near-isokinetic sampling was achieved. The sampled particles
were collected using a miniature wet collection system, i.e. a mist atomizer and a custom-made spray chamber. A numerical
simulation of the velocity and temperature fields of the plasma gas in the reactor was done using Fluent. A comprehensive
droplet-to-particle formation mechanism presented elsewhere is revisited and expanded based on calorimetry, thermodynamics
of CeO2 formation, numerical simulations and collected particles. No traces of other oxidation states other than CeO2 were found. 相似文献
80.
J. Lédé 《Journal of Thermal Analysis and Calorimetry》1996,46(1):67-84
This paper deals with models describing the thermal and chemical behaviour of solid particles undergoing fast endothermic reactions under the influence of an external heat flux. The heat source temperature is supposed to be constant, to increase with time, or to deliver a simple thermal flash. It is shown that the pyrolysis conditions (reaction temperature, conversion, etc.) depend on the chemical characteristics of the reaction and also to a large extent on the external heating conditions. Relationships are proposed to take into account these parameters. The results are applied to the thermal decomposition of NaHCO3. The pyrolysis of cellulose is finally chosen in order to show how these operating parameters can also affect the selectivity of a more complex reaction. 相似文献