Effect of interaction from the reaction of carboxyl/epoxy hyperbranched polyesters on properties of feedstocks for metal injection molding

The purpose of this study is to improve the properties of the feedstocks and shape retention of debinded parts by the reaction between 17-4PH stainless steel powders. Carboxyl-terminated hyperbranched polyester (CTHP) and epoxy-terminated hyperbranched polyester (ETHP) were used to treat the powders, and termed as CTHP-m and ETHP-m with carboxyl and epoxy group, respectively. Comparing with pristine, CTHP-m and ETHP-m, feedstock prepared from equal amount of CTHP-m and ETHP-m (CTHP-m/ETHP-m) possessed more excellent properties. The experimental results showed that the critical solids loading, flexural modulus, density and melt flow index of CTHP-m/ETHP-m feedstock were 63.8 vol.%, 2800 Mpa, 5.06 g/cm3 and 62 g/10min, respectively, which were obviously higher than that of others. Also, the shape retention of CTHP-m/ETHP-m debinded parts was the best of all the samples. The improved properties of CTHP-m/ETHP-m feedstock were attributed to the powder interaction between CTHP-m and ETHP-m formed by the chemical reaction between epoxy and carboxyl group.

Effect of Terminal Groups on Thermomechanical and Dielectric Properties of Silica–Epoxy Composite Modified by Hyperbranched Polyester

To study the effect of hyperbranched polyester with different kinds of terminal groups on the thermomechanical and dielectric properties of silica–epoxy resin composite, a molecular dynamics simulation method was utilized. Pure epoxy resin and four groups of silica–epoxy resin composites were established, where the silica surface was hydrogenated, grafted with silane coupling agents, and grafted with hyperbranched polyester with terminal carboxyl and terminal hydroxyl, respectively. Then the thermal conductivity, glass transition temperature, elastic modulus, dielectric constant, free volume fraction, mean square displacement, hydrogen bonds, and binding energy of the five models were calculated. The results showed that the hyperbranched polyester significantly improved the thermomechanical and dielectric properties of the silica–epoxy composites compared with other surface treatments, and the terminal groups had an obvious effect on the enhancement effect. Among them, epoxy composite modified by the hyperbranched polyester with terminal carboxy exhibited the best thermomechanical properties and lowest dielectric constant. Our analysis of the microstructure found that the two systems grafted with hyperbranched polyester had a smaller free volume fraction (FFV) and mean square displacement (MSD), and the larger number of hydrogen bonds and greater binding energy, indicating that weaker strength of molecular segments motion and stronger interfacial bonding between silica and epoxy resin matrix were the reasons for the enhancement of the thermomechanical and dielectric properties.

Thermomechanical properties of silica–epoxy nanocomposite modified by hyperbranched polyester: A molecular dynamics simulation

In this article, pure epoxy resin and silica–epoxy nanocomposite models were established to investigate the effects of hyperbranched polyester on microstructure and thermomechanical properties of epoxy resin through molecular dynamics simulation. Results revealed that the composite of silica can improve the thermomechanical properties of nanocomposites, including the glass transition temperature, thermal conductivity, and elastic modulus. Moreover, the thermomechanical properties were further enhanced through chemical modification on the silica surface, where the effectiveness was the best through grafting hyperbranched polyester on the silica surface. Compared with pure epoxy resin, the glass transition temperature of silica–epoxy composite modified by silica grafted with hyperbranched polyester increased by 38 K. The thermal conductivity increased with the increase of temperature and thermal conductivity at room temperature increased to 0.4171 W/(m·K)−1 with an increase ratio of 94.3%. Young’s modulus, volume modulus, and shear modulus all fluctuated as temperature rise with a down overall trend. They increased by 44.68%, 29.52%, and 36.65%, respectively, when compared with pure epoxy resin. At the same time, the thermomechanical properties were closely related to the microstructure such as fractional free volume (FFV), mean square displacement (MSD), and binding energy. Silica surface modification by grafting hyperbranched polyester reduced the FFV value and MSD value most and strengthened the combination of silica and epoxy resin matrix the best, resulting in the best thermomechanical properties.

POLYDENTATE ADSORBENT BASED ON LINEN CELLULOSE MODIFIED BY HYPERBRANCHED POLYESTER POLYBENZOYLTHIOCARBAMATE

A highly efficient hybrid adsorbent based on an industrially available, biodegradable, non-toxic linencellulose modified with hyperbranched polyesterpolybenzoylthiocarbamate has been synthesized.The synthesis was carried out using as a linkertoluene diisocyanate.The second-generation hyperbranched polyesterpolybenzoylthiocarbamate according to 1H, 13C NMR and IR spectroscopy contains 8 terminal benzoylthiocarbamate and 8 hydroxyl groups.In the first stage, the reaction of toluene diisociant with linen cellulose was carried out. By potentiometric titration, the content of toluene diisociant was found to be 27%. Then, hyperbranched polyesterpolybenzoylthiocarbamate was added to the modified linen cellulose. The content of hyperbranched polymer in cellulose, determined by the weight method, is 5%. Unreacted isocyanate groups are neutralized with isobutyl alcohol. The structure of the hybrid material is proven by IR spectroscopy. The adsorption properties of the polydentate adsorbent were studied with respect to Cu(II) ions. It was found that the adsorption capacity of the adsorbent is 6.93 mg/g. Using DSC and TGA analysis, the temperature characteristics, thermal effects, and mass loss of the obtained polydentate compound and its complexes were determined.It was shown that in an acidic medium at pH 3-4, desorption of Cu (II) and Co (II) ions occurs with the regeneration of a hybrid adsorbent.