Summary: Polystyrene (PS)/epoxy‐amine (DGEBA‐MDEA) is a thermoplastic/thermoset precursor blend which is miscible at high temperature (177 °C), and which phase separates under the polymerization of the epoxy‐amine system. Previous studies have shown that the morphology of this blend polymerized under shear is coarse and irregular because the dispersed epoxy‐amine domains coalesce before they gel. Several styrene‐methyl methacrylate and a styrene‐butadiene‐styrene block copolymers have been added to the PS/DGEBA‐MDEA 60/40 blend in order to limit the coalescence and thus obtain a finer morphology. Two of the copolymers used were reactive either with the epoxy or with the amine. It was shown that the addition of 15 wt.‐% of non reactive copolymer had a positive but limited effect on the size of the final epoxy‐amine particles. The copolymer remained at the interface at the early stages of the polymerization. However, it was pulled out by the shear forces around the gel point of the epoxy domains. Most of the non reactive copolymer was present in the shape of micelles at the end of the process. On the other hand, the reactive copolymers were able to establish covalent bonds with the epoxy‐amine drops and hence were not extracted at all. Consequently they allowed the decrease the size of the particles by a factor of 15. Despite this, the observation of the morphology at different stages of the polymerization has revealed that the copolymer moved at the interface of the epoxy domains during the collision of two droplets. The movements of fluids into the epoxy domains pushed the copolymer out of the inter‐droplet zone so that it could not prevent the drainage of the liquid film between the droplets and consequently their coalescence.
TEM showing that the layer of copolymer (in dark grey) has moved along the interface of epoxy‐amine drops during their successful collision in a polystyrene‐rich matrix. 相似文献
Understanding the phase transformation in glass and the morphology of related nanostructure after femtosecond laser irradiation is of great importance for fabricating functional optics, in which glass crystallization is involved to obtain nonlinear optical properties. We report on the crystallization inside lithium niobium silicate glass induced by fs laser irradiation. Energy‐dispersive X‐ray spectroscopy coupled to scanning transmission electron microscopy (STEM/EDS) and transmission electron microscopy confirm a nanoscale phase separation whereby LiNbO3 crystals are embedded in lamella‐shaped frames of amorphous SiO2. The obtained nanostructure may have applications in fabricating second‐order nonlinear optical devices. 相似文献
Prussian blue CsNiCr nanoparticles are used to decorate selected portions of a Si substrate. For successful grafting to take place, the Si surface needs first to be chemically functionalized. Low‐dose focused ion beam patterning on uniformly functionalized surfaces selects those portions that will not participate in the grafting process. Step‐by‐step control is assured by atomic force and high‐resolution scanning electron microscopy, revealing a submonolayer distribution of the grafted nanoparticles. By novel scanning Hall‐probe microscopy, an in‐depth investigation of the magnetic response of the nanoparticles to varying temperature and applied magnetic field is provided. The magnetic images acquired suggest that low‐temperature canted ferromagnetism is found in the grafted nanoparticles, similar to what is observed in the equivalent bulk material. 相似文献
Oxidation of Metals - The oxidation of a Ni–30Cr alloy at 700 °C in impure argon was studied in order to provide new elements of understanding on chromia scale growth in low... 相似文献
Alkenyl succinic anhydrides (ASA) were obtained by reaction between maleic anhydride and high‐oleic sunflower oil (HOSO) esters. A kinetics study of the maleinization of alkyl esters indicated that the maleinization reaction was second order overall and first order with respect to the individual reactants, and the activation energy was 77.2 ± 3.3 kJ/mol in the investigated temperature range (185–225 °C). These results showed that the cis configuration and the central position of the double bond in HOSO esters facilitate the maleinization of the latter. On the contrary, the length of the linear ester moiety had no influence on the course of the maleinization reaction. Moreover, new evidence demonstrates that there are two different reaction mechanisms: ene‐reaction and addition in allylic position with a 2 : 1 ratio, respectively. This ratio was constant throughout the reaction, thus indicating that these mechanisms are independent. 相似文献