Co-reporter:Wenqi Yu, Jifang Fu, Liya Chen, Peisong Zong, Jintao Yin, Dapeng Shang, Qi Lu, Hua Chen, Liyi Shi
Composites Science and Technology 2016 Volume 125() pp:90-99
Publication Date(Web):23 March 2016
DOI:10.1016/j.compscitech.2016.01.005
Multi-walled carbon nanotubes (MWCNTs) have been widely used as thermal conductive filler for polymers during the past decades. However, the high electrical conductivity and serious agglomerate phenomenon of MWCNTs hamper their applications in some specific fields. In this work, multi-walled carbon nanotubes (MWCNTs) were coated with insulated inorganic nanosilica (nano-SiO2) via the Stober method and further modified by the organic 1,1′-(Methylene di-4,1-phenelene) bismaleimide (BMI) via nucleophilic addition reaction to prepare MWCNTs@SiO2-g-BMI nanocomposite and then used it to modify the epoxy resin (EP). The new chemical-functionalization method can improve the homogeneous dispersion of MWCNTs in many organic solvents. The MWCNTs@SiO2-g-BMI/EP nanocomposites at a low loading fraction of 1.25 wt % showed a 125.5% higher thermal conductivity compared to the neat EP composite. Moreover, an excellent electrical volume resistivity (about 2.9076 × 1015 Ω cm) of MWCNTs@SiO2-g-BMI/EP nanocomposite was also realized. The high thermal conductivity and electrical resistivity can be explained in terms of the reduced thermal boundary resistance and restrictive inter-tube charge transport by the nano-SiO2 shell. Besides, the well-chosen BMI can enhance the dispersity and interfacial interaction between MWCNTs and EP matrix. This approach provides a strategy to enhance the thermal conductivity and simultaneously possess electrical insulation of EP materials with ultra-low filler content.
Co-reporter:Peisong Zong, Jifang Fu, Liya Chen, Jintao Yin, Xing Dong, Shuai Yuan, Liyi Shi and Wei Deng
RSC Advances 2016 vol. 6(Issue 13) pp:10498-10506
Publication Date(Web):21 Jan 2016
DOI:10.1039/C5RA24885J
In order to obtain homogeneous dispersion and strong interfacial interaction in epoxy nanocomposites, an effective approach is proposed to prepare aminopropylisobutyl polyhedral oligomeric silsesquioxane (ApPOSS) covalently grafted graphene (ApPOSS–graphene) enhancement epoxy (EP) hybrids with high thermal conductivity and electrical insulating property. The chemically converted ApPOSS–graphene 2D sheet with amine groups and rigid Si–O–Si cages is a versatile starting platform to prepare nanohybrids, which conduce to uniform dispersion and well compatibility of graphene in polymer matrix. Compared to pristine GO/EP, the interfacial interactions between ApPOSS–graphene and epoxy matrix through non-covalent and covalent bonds promote well dispersibility, compatibility and interfacial quality in composites, which contribute to improving thermal conductivity through forming effective heat conduct networks and decreasing thermal interfacial resistance. With the incorporation of only 0.25 and 0.5 wt% ApPOSS–graphene, the thermal conductivities of the ApPOSS–graphene/EP composites increase by 37.6% and 57.9% compared with neat EP, while maintaining high electrical resistivity. We believe that using ApPOSS chemically reducing and functionalized modifying GO may open a novel interface design strategy for extending applications of POSS and GO to fabricate high performance composites with high thermally conductive and electrically insulating properties.
Co-reporter:Dr. Jifang Fu;Peisong Zong;Liya Chen;Dr. Xing Dong;Dapeng Shang;Wenqi Yu; Liyi Shi; Wei Deng
ChemNanoMat 2016 Volume 2( Issue 8) pp:830-839
Publication Date(Web):
DOI:10.1002/cnma.201600131
Abstract
Homogeneous dispersion and a good interface between polymer and filler is crucial to obtain high-performance polymer composites. In this work, we use a novel method employing organic aminopropyl-functionalized nanosilica sols (OAS-sols) to functionalize graphene oxide (GO) and thereby synthesize OAS covalently grafted graphene hybrid nanosheets (OAS-graphene). The spherical OAS covalently attached on the two-dimensional (2D) nanosheet GO surfaces creates OAS-graphene hybrids, which have large surface areas and homogeneous amino active sites distributed on the nanosheets. The OAS-graphene gave an improved dispersion and interface compatibility as well as a decreased thermal interfacial resistance. As a result, the thermal conductivity and mechanical properties of the epoxy nanocomposites were significantly improved at low loading while maintaining high electrical insulative properties.
Co-reporter:Wenqi Yu, Jifang Fu, Xing Dong, Liya Chen, Haisen Jia, and Liyi Shi
ACS Applied Materials & Interfaces 2013 Volume 5(Issue 18) pp:8897
Publication Date(Web):August 28, 2013
DOI:10.1021/am402845d
An organic aminopropyl-functionalized nanosilica sol was synthesized in the presence of ethyl silicate, γ-(aminopropyl)triethoxysilane (KH550), and N,N-dimethylformamide (DMF) via a sol–gel technique and then used to prepare epoxy nanocomposites. Structure and morphology analyses of the obtained aminopropyl-functionalized nanosilicas were observed by dynamic light scattering (DLS), transmission electron microscopy (TEM), and high-resolution TEM (HRTEM). TEM and DLS showed that modified nanosilicas with an average diameter of 30 nm dispersed homogeneously in DMF. The effects of the aminopropyl-functionalized nanosilica particles on the flexural modulus, impact strength, glass transition temperature (Tg), and bulk resistivity (ρv) of the epoxy nanocomposites were investigated. The toughening mechanisms and microstructures were determined in terms of the impact fracture surface morphology using scanning electron microscopy.Keywords: bulk resistivity; epoxy; nanocomposites; nanosilica sol; sol−gel;
Co-reporter:Guojun Ding;Xing Dong;Liya Chen;Haisen Jia;Wenqi Yu;Liyi Shi
Polymer Composites 2013 Volume 34( Issue 10) pp:1753-1760
Publication Date(Web):
DOI:10.1002/pc.22579
Octaaminophenyl polyhedral oligomeric silsesquioxane (OAPS) was synthesized using three-step method and used to modify o-cresol-novolac epoxy resin (ECN) for printed circuit board. The influence of OAPS on the reactivity and the final properties of the hybrid networks were evaluated. The intercrosslinking reaction between ECN and OAPS was confirmed by Fourier transform infrared spectra. The ECN/OAPS hybrids have better impact strength, higher electrical resistivity and thermal stability, lower water absorption than the unmodified ECN. The volume resistivity and surface resistivity of the hybrids increase by an order of magnitude or more compared to the neat epoxy. The thermal stability of the hybrids improves by the incorporation of OAPS; the initial decomposition temperature and char yield show an increasing tendency up to 4 wt% loading of OAPS. The hybrids exhibit higher storage modulus and glass transition temperature (Tg) than the neat epoxy. The Tg of the hybrids greatly improves up to 153.3°C at 3 wt% content, much higher than 119.4°C of the neat epoxy. POLYM. COMPOS., 34:1753–1760, 2013. © 2013 Society of Plastics Engineers
Co-reporter:Ji-Fang Fu;Li-Ya Chen;Hui Yang;Qing-Dong Zhong;Li-Yi Shi;Wei Deng;Xing Dong;Yi Chen ;Guo-Zhang Zhao
Polymer Composites 2012 Volume 33( Issue 3) pp:404-411
Publication Date(Web):
DOI:10.1002/pc.22162
Abstract
Al2O3 nanoparticles were introduced to natural rubber (NR) to investigate its reinforcement effect on filled NR vulcanizates. The results show that Nano-Al2O3/NR nanocomposites exhibit significantly improved tensile strength, elongation at break, modulus, and tearing strength. Scanning electron microscopy analyses indicate that nanoparticles dispersed in NR matrix at nanoscale and show nano-reinforcement effect on NR vulcanizates. The aging resistances of filled NR vulcanizates improve. After aging test, tensile strength, tearing strength, and modulus improved, and elongation at break decreased. These attribute to the crosslink maturation reactions, which result in the conversion of polysulfidic linkages into disulfidic and monosulfidic ones. The acid and alkaline resistances of nano-Al2O3-filled NR vulcanizates improve compared with that of unfilled NR systems. After acid and alkaline test, tensile strength and elongation at break improve, and modulus decrease. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers