Summary: The effect of impurities on the coordination polymerization has generally been classified and discussed in different ways and has been investigated in detail in the syndiospecific homo‐ and copolymerization of styrene. With regard to impurities of styrene, phenylacetylene as an unpolar impurity containing separate multiple bonds, 1‐phenyl‐1,2‐ethanediol and ω‐hydroxyacetophenone as examples of polar impurities, and ethylbenzene as an other unpolar impurity have been investigated regarding the effect on the polymerization rate and the influence on the molecular properties of the syndiotactic polystyrenes. In the syndiospecific copolymerization with p‐methylstyrene, indene shows a different behavior regarding the decrease of the polymerization conversion depending on the comonomer concentrations present in the monomer mixture. Additionally, the effect of impurities of the catalyst system on the syndiospecific styrene polymerization has been demonstrated, particularly of octahydrofluorene as a component of the transition metal compound and of trimethylaluminium as a component of the cocatalyst methylaluminoxane. All results have been discussed with respect to the mechanisms of the effects on polymerization behavior and on polymer properties.
Dependence of the relative polymerization conversion on the amount of indene added to the monomer mixture in styrene (ST)/p‐methylstyrene (PMS) copolymerization (catalyst n‐ratio: 0.5; molar ratio MAO:Ti = 110:1; polymerization temperature: 60 °C; polymerization time: 45 min). 相似文献
Colloidal silica particles are prepared via a sol gel technique carried out in an inverse microemulsion of water in a toluene solution of tetraethoxysilane (TEOS), stabilized by either an anionic surfactant AOT or isopropanol. Functionalized material was obtained using a functional coupling agent (RO)3Si(CH2)3X, X being a functional group such as methacryloyl, thiol, vinyl, amino group, or a chlorine atom. Functionalization can be carried out either directly via the direct copolycondensation of TEOS and the coupling agent, or in a two-step process involving a core-shell polycondensation of the coupling agent onto preformed silica particles. Kinetic studies of the copolycondensation are carried out using either29Si NMR analysis or liquid chromatography. They show that the consumption of TEOS is more rapid than that of the coupling agent. The materials are characterized both chemically (elemental analysis, FTIR,13C and29Si NMR CPMAS analysis), and by their particle size. The silica functionalized with a polymerizable methacryloyl group is encapsulated by a polymer layer in an inverse emulsion polymerization of acrylic acid. After inversion of the emulsion in water, the resulting material is covered with a layer of hydrophobic polymer in a conventional emulsion polymerization. 相似文献
This paper addresses the issue of studying a food complex system in a reverse engineering manner with the aim of identifying the set of all possible actions that makes it reach a quality target with respect to manufacturing constraints. Once the set of actions is identified, several criteria can be considered to identify interesting trajectories and control policies. A viability approach, coupling the viability theory and a geometric approach of robustness, is proposed to study complex dynamical systems. It can be implemented for several types of systems, from linear to non linear or hybrid systems. The proposed framework was adapted to a living food system: a ripening model of Camembert cheese to identify the set of states and actions (capture basin) from which it is possible to reach a predefined quality target. Within the set of viable trajectories, particular trajectories that improve the Camembert cheese ripening process are identified using the proposed approach. The results are applied at a pilot scale and are discussed in this paper. 相似文献
Previous published work has shown that hydroxyl terminated perfluoroether oligomers can be suitably modified and functionalised to make them miscible with epoxy resins in the uncured state. The reaction conditions can adjusted to induce phase separation either through spinodal decomposition to produce an IPN type morphology, or by nucleation and growth if a dispersed-particle microstructure is required.In the present work we examine the relative toughening enhancement efficiency of the two possible heterophase morphologies. Both systems show a sigmoidal increase in fracture toughness, with increasing concentration of the perfluoroether modifier. However, this takes place at much lower modifier concentrations for the systems with a particulate morphology (about 3.5% w/w) than for IPN systems (about 7.5% w/w). The maximum fracture toughness achievable for the two systems, on the other hand, is very similar and coincides with the concentration at which co-continuous phases are formed.These differences in morphology, however, are not reflected in the variation of modulus and compressive yield strength with increasing concentration of perfluoroether modifier, in so far as both systems exhibit a gradual and small reduction in property with increasing concentration. Furthermore, the dynamic mechanical spectra of the two systems are very different, but the changes resulting from increasing the concentration of toughening agent are relatively small in either case.Nanoindentation tests indicate that it is the local plasticity, brought about by the presence of the softer perfluoroether phase, which is responsible for the enhancement of fracture toughness. This is corroborated by AFM examinations, which reveal local plastic deformations in the regions surrounding the softer particles. 相似文献