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31.
Alberto Giaconia Giuseppe Filardo Onofrio Scialdone Alessandro Galia 《Journal of polymer science. Part A, Polymer chemistry》2006,44(13):4122-4135
A laboratory‐scale continuous reaction system using a stirred tank reactor was assembled in our laboratory to study the dispersion polymerization of vinyl monomers in supercritical carbon dioxide (scCO2). The apparatus was equipped with a suitable downstream separation section to collect solid particles entrained in the effluent stream from the reactor, whose monomer concentration could be measured online with a gas chromatograph. The dispersion polymerization of methyl methacrylate in scCO2 was selected as a model process to be investigated in the apparatus. The experiments were performed at 65 °C and 25 MPa with 2,2′‐azobisisobutyronitrile as the initiator and a reactive polysiloxane macromonomer as a surfactant to investigate the effect of the mean residence time of the reaction mixture on the monomer conversion, polymerization rate, polymer molecular weight, and particle size distribution. The results were compared with those obtained in batch polymerizations carried out under similar operative conditions. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4122–4135, 2006 相似文献
32.
为了求解各向异性接合材料界面端部奇异性应力场,建立了一种新型杂交元模型.该模型的独特之处在于:基于有限元特征法得到的奇异性场数值特征解建立了一种新型界面端奇异单元.通过算例证明,新型杂交元模型能够利用较少的单元数获得较为精确的数值结果.当前模型应用范围广泛,能够用于复杂结构的界面端部场求解. 相似文献
33.
P. Guenoun M. Delsanti D. Gazeau J.W. Mays D.C. Cook M. Tirrell M. Tirrell L. Auvray 《The European Physical Journal B - Condensed Matter and Complex Systems》1998,1(1):77-86
Aqueous micellar solutions of ionic/neutral block copolymers have been studied by light scattering, small angle neutron scattering
and small angle X-ray scattering. We made use of a polymer comprised of a short hydrophobic block (polyethylene-propylene)
PEP and of a long polyelectrolytic block (polystyrene-sulfonate) PSSNa which has been shown previously to micellize in water.
The apparent polydispersity of these micelles is studied in detail, showing the existence of a few large aggregates coexisting
with the population of micelles. Solutions of micelles are found to order above some threshold in polymer concentration. The
order is liquid-like, as demonstrated by the evolution with concentration of the peak observed in the structure factor (), and the degree of order is found to be identical over a large range of concentrations (up to 20 wt%). Consistent values
of the aggregation number of the micelles are found by independent methods. The effect of salt addition on the order is found
to be weak.
Received: 19 June 1997 / Received in final form: 4 September 1997 / Accepted: 9 October 1997 相似文献
34.
Peng Z 《Angewandte Chemie (International ed. in English)》2004,43(8):930-935
Hybrid materials based on covalently linked inorganic polyoxometalates (POMs) and organic species containing a delocalized pi system have drawn increasing attention. These hybrids, traditionally prepared by cluster assembly approaches that lack predictability and controllability, can now be synthesized through common organic reactions by using organically functionalized POM clusters as building blocks. This minireview highlights some of the most recent advances on a particular type of hybrids where the organic and inorganic components are connected by an imido linkage. 相似文献
35.
J. Goworek W. Stefaniak Agnieszka Kierys Mariola Iwan 《Journal of Thermal Analysis and Calorimetry》2007,87(1):217-222
Mesoporous silica material of MCM-41 type was synthesized by co-condensation
of highly concentrated octyltriethoxysilane (OTEOS), octadecyltriethoxysilane
(ODTEOS) and tetraethoxysilane (TEOS). The obtained hybrid materials were
characterized using XRD, TG-DSC and low temperature adsorption/desorption
of nitrogen. It was shown that the applied method of synthesis allows to obtain
silica of MCM-41 type with a high degree of hydrocarbon saturation. 相似文献
36.
0IntroductionIncreasinginterestisfocusedonthestudyofmagnetic,electronicandoptoelectronicpropertiesoflow鄄dimensionalorganic鄄inorganichybridcompoun鄄ds[1~3].Studiesshowthatcomplexconsistingoforganicandinorganiccomponentshavegreatpotentialforthecreationoff… 相似文献
37.
Georgi E. Chernev Bisserka I. Samuneva Petar R. Djambaski Isabel M. M. Salvado Helena V. Fernandes 《Central European Journal of Chemistry》2006,4(1):81-91
In this work we present experimental results about the formation, properties and structure of sol — gel silica based biocomposite
containing Calcium alginate as an organic compound. Two different types of silicon precursors have been used in the synthesis:
tetramethylortosilicate (TMOS) and ethyltrimethoxysilane (ETMS). The samples have been prepared at room temperature. The hybrids
have been synthesized by replacing different quantitis of the inorganic precursor with alginate. The structure of the obtained
hybrid materials has been studied by XRD, IR Spectroscopy, EDS, BET and AFM. The results proved that all samples are amorphous
possessing a surface area from 70 to 290 m2/g. It has also been established by FT IR spectra that the hybrids containing TMOS display Van der Walls and Hydrogen bonding
or electrostatic interactions between the organic and inorganic components. Strong chemical bonds between the inorganic and
organic components in the samples with ETMS are present. A self-organized nanostructure has been observed by AFM. In the obtained
hybrids the nanobuilding blocks average in size at about 8–14 nm for the particles. 相似文献
38.
0IntroductionThefirstmolecule鄄basedmagnetswerereportedin1986[1].Duringthelasttwodecades,moreandmoreattentionhasbeenpaidtothesynthesisofmolecule鄄basedmagnets,especiallytoPrussianBlueanalogu鄄es[2].TheoldPrussianBlueanalogueshavebeenbroughtuptodateduetoth… 相似文献
39.
S. Dirè P. Egger M. L. Di Vona M. Trombetta S. Licoccia 《Journal of Sol-Gel Science and Technology》2004,32(1-3):57-61
The preparation of nanostructured organic-inorganic materials by assembling of nanobuilding blocks allows controlling the extent of phase interaction, which in its turn governs structure-properties relationships. We present here the synthesis of siloxane-based nanobuilding blocks prepared by reacting diphenylsilanediol with vinyltriethoxysilane and triethoxysilane. The reaction products were obtained by non-hydrolytic condensation between silanediol and ethoxide groups in inert atmosphere, in the presence of pyridine, triethylamine or butyl lithium. Different synthetic conditions were examined by means of ATR-FTIR and NMR spectroscopies, showing the formation of siloxane bonds. In the case of triethoxysilane the reaction carried out in the presence of pyridine leads to Si–H bond preservation in the final product. Air stable products with improved Si–O–Si hydrolytic stability can be obtained by removal of the base after the reaction completion. The condensation products can be described as a mixture of siloxane rings involving difunctional and trifunctional silicon units. 相似文献
40.
Joël J. E. Moreau Luc Vellutini Catherine Bied Michel Wong Chi Man 《Journal of Sol-Gel Science and Technology》2004,32(1-3):63-67
The acid-hydrolysis of an organo-bridged bisdiethoxysilylated molecular precursor bearing urea groups, (EtO)2MeSi(CH2)3NHCONH(CH2)12NHCONH(CH2)3SiMe(OEt)2, has been performed in pure aqueous medium. Scanning electron microscopy (SEM) analysis of the resulting insoluble solid revealed plate-like forms with a lamellar structure as determined by powder X-ray diffraction (PXRD) studies with a sharp peak at 28.5 Å. The solid state 29Si MAS-NMR spectrum of this bridged siloxane hybrid is consistent with a moderately condensed material with complete preservation of the Si–C bonds throughout the hybrid network. In comparison, the classical sol–gel hydrolysis-condensation of the molecular precursor in ethanol with stoichiometric amount of water and fluoride anion as catalyst produced an amorphous featureless solid. 相似文献