Biomimic modification of graphene oxide. (24th August 2015)
- Record Type:
- Journal Article
- Title:
- Biomimic modification of graphene oxide. (24th August 2015)
- Main Title:
- Biomimic modification of graphene oxide
- Authors:
- Fu, Lihua
Shi, Yingge
Wang, Ke
Zhou, Ping
Liu, Meiying
Wan, Qing
Tao, Lei
Zhang, Xiaoyong
Wei, Yen - Abstract:
- Abstract : Synthetic polymer modified graphene oxide was prepared via combination of mussel inspired chemistry and Michael addition reaction in aqueous solution. Abstract : Surface modification of graphene oxide has attracted increasing attention in recent years. In this article, a green, facile and efficient method was developed to modify graphene oxide with polymers via combination of mussel inspired chemistry and Michael addition reaction. Graphite powder was first oxidized and exfoliated into a single layer of slices through a modified Hummers method, then coated with polydopamine, which was formed via self-polymerization of dopamine in alkaline solution. Next, the intermediate (GO–PDA) was grafted by polyacrylic acid, which was synthesized via reversible addition–fragmentation chain transfer polymerization, through Michael addition reaction. The resulting products were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, transmission electron microscopy and X-ray photoelectron spectrometry. The characterization results indicated the success of adhesion and grafting of PDA and polyacrylic acid, respectively. The resulting products also exhibited sensitivity to pH. Apart from the polymer demonstrated in this work, many other polymers may also be grafted onto graphene oxide through this strategy when different monomers were adopted. Furthermore, this strategy can also be extended to surface modification of many other materials for theAbstract : Synthetic polymer modified graphene oxide was prepared via combination of mussel inspired chemistry and Michael addition reaction in aqueous solution. Abstract : Surface modification of graphene oxide has attracted increasing attention in recent years. In this article, a green, facile and efficient method was developed to modify graphene oxide with polymers via combination of mussel inspired chemistry and Michael addition reaction. Graphite powder was first oxidized and exfoliated into a single layer of slices through a modified Hummers method, then coated with polydopamine, which was formed via self-polymerization of dopamine in alkaline solution. Next, the intermediate (GO–PDA) was grafted by polyacrylic acid, which was synthesized via reversible addition–fragmentation chain transfer polymerization, through Michael addition reaction. The resulting products were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, transmission electron microscopy and X-ray photoelectron spectrometry. The characterization results indicated the success of adhesion and grafting of PDA and polyacrylic acid, respectively. The resulting products also exhibited sensitivity to pH. Apart from the polymer demonstrated in this work, many other polymers may also be grafted onto graphene oxide through this strategy when different monomers were adopted. Furthermore, this strategy can also be extended to surface modification of many other materials for the versatility of mussel inspired chemistry. It is therefore recommended that the novel strategy developed in this work should be a general strategy for fabrication of various functional nanocomposites, which can exhibit better performance for different applications. … (more)
- Is Part Of:
- New journal of chemistry. Volume 39:Number 10(2015:Oct.)
- Journal:
- New journal of chemistry
- Issue:
- Volume 39:Number 10(2015:Oct.)
- Issue Display:
- Volume 39, Issue 10 (2015)
- Year:
- 2015
- Volume:
- 39
- Issue:
- 10
- Issue Sort Value:
- 2015-0039-0010-0000
- Page Start:
- 8172
- Page End:
- 8178
- Publication Date:
- 2015-08-24
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c5nj02055g ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 350.xml