Search

A series of aromatic polyesters were prepared by the reaction of bisphenol‐A and bis(hydroxyphenyl)butane with diacyl chloride monomers by phase transfer interfacial polycondensation in order to improve the processability of the bisphenol A‐based polyarylate. The microstructure, molecular weight, crystallinity, solubility, thermal properties, mechanical properties, and optical properties of the prepared copolyesters were investigated. Inherent viscosities of the copolyesters are in the range of 0.14–0.53 dl g−1, and their average molecular weights are 7362–44,413 g mol−1, respectively. The feed compositions and copolymer compositions were nearly identical. The results show that with the increase in the content of side ethyl units, the copolyester gradually transforms into an amorphous structure, which is also verified by the improvement in dissolution properties. When the copolyester backbone was introduced into the side ethyl units, the thermal decomposition temperature was less affected and varied in the range of about 10°C, while the value of glass transition temperature reduced from 196.5°C to 165.1°C. The mechanical properties of the polymers are similar to those of the industrial commodity U‐100. In addition, the copolyester films have good optical properties, and the transmittance reached the maximum value of 98.41% when the content of bis(hydroxyphenyl)‐butane was 10%. [ABSTRACT FROM AUTHOR]

In this work, the synthesis of Nylon‐6.6 together with silver nanoparticles (presumably Ag2O, Ag NPs) was carried out at a polarized liquid‐liquid interface (LLI). The reduction of silver ions to Ag‐NPs was driven by an electrochemically controlled electron transfer reaction between silver cations initially dissolved in the aqueous phase and ferrocene species present in the organic phase. The formation of Ag2O is assumed to originate from Ag+ precipitation to AgOH further converted into Ag2O. The polyamide formation was derived from the interfacial polycondensation reaction happening between 1,6‐diaminohexane and adipoyl chloride. We studied the possibility to form given material simultaneously (interfacial polycondensation and Ag+ reduction occurring in one step) and sequentially (electrochemical Ag+ reduction by ferrocene from the organic phase was performed after polyamide deposition). The Ag‐based NPs‐polyamide material was synthesized at the macroscopic and microscopic LLI. As the support for the latter, fiberglass membranes was used. The resulting material was characterized by infra‐red (IR) spectroscopy and scanning electron microscopy (SEM). [ABSTRACT FROM AUTHOR]

It was tried to form Pickering emulsion by use of paraffin wax as a phase change material (PCM) and SiC as solid powder and to apply to the preparation of the hybrid microcapsules with the interfacial polycondensation reaction. Pickering emulsion could be formed by stirring PCM and SiC in the continuous water phase. The mean diameter of PCM droplets in the (O/W) emulsion decreased with the added amount of SiC. The SiC weight adhered on the surface of PCM droplets become the maximum in the continuous phase with pH 6.8. The hybrid microcapsules with the shell made of SiC and polyurea resin film could be prepared by using Pickering emulsion. There was a critical adhesion weight of SiC, above which the hybrid microcapsules could not be formed. Thermal conductivity of hybrid microcapsules could be improved as compared with the PCM microcapsules. Copyright © 2015 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

A novel dinaphthodioxocin-containing diol monomer, 8,16-methano-16H-dinaphtho[2,1-d:1′,2′-g][1,3] dioxocin-2,14-diol (MDDD) was synthesized in high yield and purity through the condensation of 2,7-dihydroxynaphthalene with malonaldehydetetramethyl acetal at room temperature. It is used as a new monomer for the synthesis of a series of novel dinaphthodioxocin-containing aliphatic polyesters by interfacial polycondensation method. The new diol monomer was fully characterized by IR, NMR, mass spectroscopies, and elemental analysis. Optimal conditions for polyesterification were obtained via study of the model compounds. Polyesters derived from MDDD and four aliphatic diacid chlorides had inherent viscosities ranging from 0.26 to 0.38 dL/g. The chemical structure of the polymers was fully characterized by IR, NMR spectroscopies, and elemental analysis. The physical properties of the polymers were studied. All the new polymers show good thermal stability and very good solubility in most organic solvents. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 [ABSTRACT FROM AUTHOR]

This work provides a better understanding for effective control of the nanocapsules wall thickness. Polyamides based nanocapsules are prepared by interfacial polymerization combined with spontaneous emulsification. A clear guideline of how factors such as monomer concentration, diffusion, interfacial reaction, or water swelling influence the capsule formation is very important to the control of capsule wall structure and release performance. In this goal, the macroscopic planar models of the interfacial polycondensation between diethylenetriamine and sebacoyle chloride are studied experimentally and theoretically. This planar model is developed to examine the kinetics of the reaction and to perform the estimation of parameters thanks to the experiment measurements. The effect of the operating conditions on the wall thickness is also studied. The model is shown to be consistent with the experimental data. Next, the spherical model is deduced from the first one. The results obtained with this model are in accordance with some observations of wall thickness. From this model, the increase of the wall thickness is predicted for several operating conditions. [ABSTRACT FROM AUTHOR]