Polyethylene/montmorillonite clay nanocomposites were obtained via direct
melt intercalation. The clay was organically modified with four different
types of quaternary ammonium salts. The objective of this work is to study
the use of montmorillonite clay in the production of nanocomposites by means
on rheological, mechanical and crystallization properties of nanocomposites
and to compare to the properties of the matrix and PE/unmodified clay nanocomposites.
In general, the tensile test showed that the yield strength and modulus of
the nanocomposites are close to the pure PE. Apparently, the mixture with
Dodigen salt seems to be more stable than the pure PE and PE/unmodified clay. 相似文献
The chemical fixation of CO2 with mono-substituted terminal epoxides or cyclohexene oxide to form cyclic carbonates under the ZnCl2/[BMIm]Br catalyst system without using additional organic solvents was achieved in excellent selectivity (>98%) and TOF (5410 h−1) and the catalyst could be used six times almost without losing its catalytic activity and selectivity. Besides, the pure cis-cyclic carbonate of cyclohexene oxide was obtained in this catalyst system. 相似文献
The vapor-phase catalytic alkylation of phenol with methanol and dimethyl carbonate on a series of differently prepared CrPO4 (Cr/P=1) and CrPO4-AlPO4 (CrAIP) catalysts, has been studied at different temperatures (473–673 K). The reaction is first order in phenol, giving
a mixture of O- and C-alkylated products (C-alkylation taking place preferentially at theortho-position). Moreover, dimethyl carbonate is a better methylating agent than methanol. 相似文献
Stability constants and thermodynamic data for complex formation of silver(I) with noncyclic, macrocyclic, and macrobicyclic ligands have been measured in propylene carbonate using potentiometric and calorimetric methods. All ligands containing two nitrogen donor atoms form extremely stable complexes. Only if substituents reduce the basicity of the nitrogen donor atoms, the stability of the complexes decreases drastically. However, the cryptand (221) forms the most stable complex of all ligands examined. In this case, the dimensions of the ligand cavity and of the cation are nearly identical. 相似文献
The direct enzymatic synthesis of a cyclic trimethylene carbonate (1,3‐dioxane‐2‐one) monomer with/without a methyl substituent was carried out using dimethyl or diethyl carbonate and 1,3‐diol with the objective of producing aliphatic poly(trimethylene carbonate), a typical biodegradable synthetic plastic. The lipase‐catalyzed condensation of dimethyl or diethyl carbonate with aliphatic 1,3‐diols using immobilized Candida antarctica lipase (lipase CA) in an organic solvent at 70 °C afforded the corresponding methyl‐substituted and unsubstituted cyclic trimethylene carbonates. The cyclic trimethylene carbonates obtained by the reaction of dimethyl or diethyl carbonates with 1,3‐propanediol and 2‐methyl‐1,3‐propanediol were polymerized by lipase to produce the corresponding polycarbonates.
Total TMC yield as a function of the reaction time. 相似文献
A supercritical fluid (SCF) route for facile and homogeneous introduction of silver nanoparticles into polymer hosts is described. Our focus is on ultra-high molecular weight polyethylene (UHMWPE). We demonstrate that the metallic nanoparticles have a substantial effect upon the wear and tribochemical properties of the polymer substrate. 相似文献