Preparation of Epoxy Resin/Montmorillonite Composites by Monomer Insert In Situ Polymerization

2010 ◽  
Vol 178 ◽  
pp. 236-241
Author(s):  
Jing Xie ◽  
Shang Yue Shen ◽  
Yu Xia Luo ◽  
Meng Meng Zhang ◽  
Ying Chen

Epoxy resin/ montmorillonite (EP/MMT) composite was prepared via monomer insert in-situ polymerization. It was shown that the EP/MMT composites could be successfully synthesized from the raw materials only by one step, making it simpler than traditional in-situ intercalative polymerization method. The d001 spacing of montmorillonite was tested by XRD and increased to 4.30nm. The results showed that tensile strength and impact strength were improved by 98.11 and 93.69%, respectively. The glass transition temperature was increased by 17.3 °C.

2016 ◽  
Vol 7 (1) ◽  
pp. 36-43 ◽  
Author(s):  
Jin Won Yu ◽  
Jin Jung ◽  
Yong-Mun Choi ◽  
Jae Hun Choi ◽  
Jaesang Yu ◽  
...  

Epoxy nanocomposites are fabricated by using diamine-functionalized GO and exhibit high Tg, tensile strength, and crosslink density.


2005 ◽  
Vol 249 (1-4) ◽  
pp. 266-270 ◽  
Author(s):  
Xingwei Li ◽  
Xiaoxuan Li ◽  
Gengchao Wang

RSC Advances ◽  
2016 ◽  
Vol 6 (55) ◽  
pp. 49448-49458 ◽  
Author(s):  
Jiaojiao Ma ◽  
Ying Li ◽  
Xiande Yin ◽  
Yu Xu ◽  
Jia Yue ◽  
...  

A novel and one-stepin situpolymerization method for preparing the poly(vinyl alcohol) (PVA)/graphene oxide (GO) nanocomposites.


2020 ◽  
pp. 096739112093523
Author(s):  
Mohammad Ebrahim Karkhanehchin ◽  
Morteza Maghrebi ◽  
Majid Baniadam ◽  
Ali Dashti ◽  
Maryam Mokhtarifar

The aim of this study was to produce carbon nanotubes (CNTs)/polymer composite fibers by wet spinning without any solvent. The functionalized multiwalled-carbon nanotubes (F-MWNTs)/epoxy resin was synthesized by in situ polymerization method. Epoxy resin, F-MWNTs, and curing agent were mixed and injected by a syringe pump. The effects of operating parameters including the percentage of CNTs and the extrusion velocity of the syringe pump on the dispersion and alignment of F-MWNTs in the cross-section of F-MWNTs/polymer composite fibers were investigated. The composite fibers were characterized by tensile strength analysis, scanning electron microscopy (SEM), and electrical conductivity analysis. The experimental results showed that a decrease (30 ml/h to 15 ml/h) in extrusion velocity increased the electrical conductivity of composite fibers by more than 3%. This behavior was attributed to the higher alignment of F-MWNTs and improved conducting pathways along the composite fiber axis, as observed by SEM. In addition, by reducing extrusion velocity (30 ml/h to 15 ml/h), the tensile strength of composite fibers was enhanced just over twofold due to the better arrangement of CNTs which can be attributed to the further retention time of composite fibers and the pressure of the walled-needle. Moreover, the higher the processing time of spinning, the lower electrical conductivity of the fibers is which might be due to the higher coagulation of fibers.


2011 ◽  
Vol 130-134 ◽  
pp. 1528-1531
Author(s):  
Si Chen ◽  
Jian Ming Xu ◽  
Guo Dong Tang ◽  
Xu Wang

Gelator (G2-C12-G2) was synthesized successfully, the structure of which was confirmed by1H-NMR and Mass spectra (MS). And G2-C12-G2was used to modify PMMA by “in-situ” polymerization. The results of gel permeation chromatography (GPC) showed that Mn and Mw/Mnof the PMMA composite were barely influenced by the incorporation of gel. The results of dynamic mechanical analysis (DMA) showed that the modified PMMA had higher modulus, toughness and glass transition temperature (Tg) than pure PMMA. Furthermore the results of spectrophotometer showed that the transparency of modified PMMA was nearly the same as pure PMMA .


2021 ◽  
Vol 21 (3) ◽  
pp. 5-16
Author(s):  
Fayçal Dergal ◽  
Djahida Lerari ◽  
Khaldoun Bachari

Abstract A significant number of investigations have been reported on the elaboration and characterization of Polymer/Clays composites, via different methods. In our work, new composites materials were successfully prepared by in-situ polymerization of 4-vinylpyridine (4VP), in presence of two different types of Algerian modified clays (Maghnia and Mostaganem), noted (BC) and (MC), respectively. Different percentage clays (1 wt%, 3 wt% and 5 wt%) have been used. The differential scanning calorimetry analysis reveals the variation of glass transition temperature (Tg) of the copolymer in the composite materials. We show a decrease glass transition temperature (Tg) from 147°C to 131°C for P4VP-BC and from 147°C to 124°C for P4VP-MC according to the increase percentage of clays. Thermogravimetric analysis (TGA) shows good stability of composite materials at high temperature. Fourier Transformed Infrared (FTIR), Scanning Electron Microscopy coupled with Energy dispersive X-Ray Spectroscopy (SEM-EDX) and 1H NMR spectroscopy are used to show the presence of the clays in the materials.


2009 ◽  
Vol 66 ◽  
pp. 230-233 ◽  
Author(s):  
Tao Wei ◽  
Zhi Xiong Huang ◽  
Guo Rui Yang ◽  
Min Xian Shi

The PANI/PMN composite was prepared by one-step in-situ polymerization method and was characterized via FT-IR, XRD, SEM and TG. The results indicate that the best reaction conditions of in-situ polymerization are 0°C/24h.The PMN powder are entirely coated with PANI, when composite contains more than 60% PANI by volume. The steric hindrance effect of PMN powder decreases the crystallization degree of PANI which polymerizes on the surface of PMN powder in the process of in-situ polymerization. The main weight loss occurring between 300 and 480°C corresponds to the degradation of the PANI polymer chain.


Coatings ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 49
Author(s):  
Ana-Maria Mocioiu ◽  
Ioan Albert Tudor ◽  
Oana Cătălina Mocioiu

“In situ” polymerization method was used to develop PANI-PSSA /textile. Polyaniline doped with polystyrene sulfonic acid (PANI-PSSA) used as coatings for textiles were obtained by aqueous and emulsion route. The emulsion route uses chloroform as solvent. Polymerization has been achieved in one step on the wool or polyamide textiles. For coated and uncoated textiles, dried at room temperature, were characterized structurally by Infrared Spectroscopy with Attenuated Total Reflectance (ATR), morphologically by Scanning Electron Microscopy (SEM), and by Atomic Force Microscopy (AFM) and electrically. The synthesis methods lead to differences in structure, morphology and properties of the coated polyamide and wool textiles.


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