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21.
Microcapsules containing healing agents have been used to develop the self-healing polymeric composites. These microcapsules
must possess special properties such as appropriate strength and stability in surrounding medium. A new series of microcapsules
containing dicyclopentadiene (DCPD) with melamine–formaldehyde (MF) resin as shell material were synthesized by in situ polymerization
technology. These microcapsules may satisfy the requirements for self-healing polymeric composites. The chemical structure
of microcapsule was identified by using Fourier transform infrared (FTIR) spectrometer. The morphology of microcapsule was
observed by using optical microscope (OM) and scanning electron microscope. Size distribution and mean diameter of microcapsules
were determined with OM. The thermal properties of microcapsules were investigated by using thermogravimetric analysis and
differential scanning calorimetry. Additionally, the self-healing efficiency was evaluated. The results indicate that the
poly(melamine–formaldehyde) (PMF) microcapsules containing DCPD have been synthesized successfully, and their mean diameters
fall in the range of 65.2∼202.0 μm when the adjusting agitation rate varies from 150 to 500 rpm. Increasing the surfactant
concentration can decrease the diameters of microcapsules. The prepared microcapsules are thermally stable up to 69 °C. The
PMF microcapsules containing DCPD can be applied to polymeric composites to fabricate the self-healing composites. 相似文献
22.
磷系阻燃环氧树脂研究 总被引:2,自引:0,他引:2
本文对近年来国内外9,10-二氢-9-氧杂-10-磷杂菲-10-氧化物(DOPO)衍生物的合成及其应用于阻燃环氧树脂的方法进行介绍,并对所显示的阻燃性、热性能等作了概述和比较。将反应型磷系阻燃剂DOPO衍生物引入环氧树脂基体结构中形成阻燃持久、无卤、低烟、无毒、热稳定性好的新型含磷环氧树脂。 相似文献
23.
Zhen-zhong Yang 《高分子科学》2007,(2):137-143
In this review, our recent work in phase inversion emulsification (PIE) for polymer (especially epoxy resin) waterborne dispersions is summarized. Based on experimental results about PIE process, the physical model is proposed which can guide the synthesis of the waterborne dispersions such as polymer/nanoparticle composite dispersion. In the presence of a latent curing catalyst, PIE can give a crosslinkable epoxy resin waterborne dispersion. The dispersions can form cured transparent coatings with some unique properties such as UV shielding. They are promising in functional coatings, waterborne resin matrices for composites, and sizing for high performance fibers. 相似文献
24.
用自制的带甲基侧基的环氧树脂(TMBP)作为界面增容剂, 从拉伸性能、键合胶含量、动态性能、扫描电镜和流变性能等方面, 研究了TMBP对炭黑在丁苯橡胶中分散度的影响, 并与市售通用双酚A型环氧树脂(E-51)和橡胶工业常用软化剂邻苯二甲酸二辛酯(DOP)进行了比较. 结果表明, 带甲基侧基的环氧树脂TMBP在提高炭黑分散性方面的效果远比E-51好, 其作用模式具有典型的增容特性. 相似文献
25.
Microgel-epoxy resin two-phase polymers were prepared by in situ copolymerization of ethylenic monomers with unsaturated polyesters. The choice of monomers and the effect of monomer concentration on microgel particle size were discussed. Agglomeration of particles played a significant role in the early stage of polymerization. The microgel dispersion in epoxy resin was stable after the finish of polymerization. Upon curing the particles remained well dispersed. 相似文献
26.
Constantinos D. Diakoumakos John A. Mikroyannidis Christoforos A. Krontiras Michael N. Pisanias 《Journal of polymer science. Part A, Polymer chemistry》1994,32(10):1915-1921
New thermosetting resins were prepared from the reaction of 1,4-bis(2,2-dicyanovinyl)benzene with aromatic diamines in varying molar ratios. The thermal stability of these resins was correlated with their composition and the curing conditions. They were stable in N2 up to 370–448°C and afforded anaerobic char yields of 73–84% at 800°C after curing at 300°C for 20–60 h. The temperature dependence of the electrical resistivity of all resins pyrolyzed at 700°C for 15 h was studied in the temperature range from ?173–327°C (100–600 K). The results showed that at room temperature the unpyrolyzed polymers have insulating properties, whereas a dramatic decrease in the electrical resistivity is observed following pyrolysis. The temperature dependence of the electrical resistivity suggests that all of the materials studied have semiconducting properties. The observed electrical conductivity is thermally activated with activation energies ranging from 0.03–0.06 eV. © 1994 John Wiley & Sons, Inc. 相似文献
27.
We report the first enzyme-catalysed kinetic resolution of epoxy enol esters. The lipase-promoted hydrolysis of these compounds provided α-hydroxyketones or α-hydroxyaldehydes (arising from the spontaneous rearrangement of the epoxy enols) and the residual esters with moderate to good enantioselectivity (E up to 100). 相似文献
28.
Cure kinetics of epoxy-amine resins used in the restoration of works of art from glass or ceramic 总被引:1,自引:0,他引:1
The cure kinetics of two epoxy/amine resins, Araldite 2020 and AY103-HY956 widely used as adhesives in the restoration of works of art from glass or ceramic was investigated using FTIR spectroscopy. These resins are two-part adhesives, consisting of a resin - A, based on a diglycidyl ether of bisphenol A, and a hardener - B which is either a cycloaliphatic amine (isophorone diamine) for Araldite 2020, or a mixture of three aliphatic amines in HY956. The study was based on the collection of IR spectra, in the middle range (4000-600 cm−1), of mixtures of resin and hardener at different proportions and isothermal temperatures (22-70 °C) as a function of curing time. A kinetic model was employed to simulate the experimental data using two kinetic rate constants. Diffusion control was incorporated to describe the cure behaviour at high degrees of conversion. From fitting to experimental data the kinetic and diffusional parameters were estimated, together with the activation energies of the kinetic and autocatalytic rate constants. It was found that higher degrees of curing are obtained at higher temperatures and increased amounts of hardener. Differences in the performance of the two adhesives are explained based on the type of the amines used as hardener. 相似文献
29.
Thermal
degradation of vinylidene chloride/[4-(t-butoxycarbonyloxy)phenyl]methyl
acrylate copolymers
B. A. Howell D. A. Spears P. B. Smith 《Journal of Thermal Analysis and Calorimetry》2006,85(1):115-117
Vinylidene chloride polymers containing comonomer
units capable of consuming evolved hydrogen chloride to expose good radical-scavenging
sites might be expected to display greater thermal stability than similar
polymers containing simple alkyl acrylates as comonomer. Incorporation of
a comonomer containing the phenyl t-butyl
carbonate moiety into a vinylidene chloride polymer has the potential to afford
a polymer with pendant groups which might interact with hydrogen chloride
to expose phenolic groups. Copolymers of vinylidene chloride with [4-(t-butoxycarbonyloxy)phenyl]methyl acrylate have been
prepared, characterized, and subjected to thermal degradation. The degradation
has been characterized by thermal and spectroscopic techniques. The degradation
of vinylidene chloride/[4-(t-butoxycarbonyloxy)phenyl]methyl
acrylate copolymers is much more facile than the same process for similar
copolymers containing either [4-(isobutoxycarbonyloxy)phenyl]methyl acrylate
or methyl acrylate, a simple alkyl acrylate, as comonomer. During copolymer
degradation, [4-(t-butoxycarbonyloxy) phenylmethyl
acrylate units are apparently converted to acrylic acid units by extensive
fragmentation of the sidechain. Thus, the phenyl t-butyl
carbonate moiety does function as a labile acid-sensitive pendant group but
its decomposition in this instance leads to the generation of a phenoxybenzyl
carboxylate capable of further fragmentation. 相似文献
30.