Synthesis of Water-soluble Polyaniline by Using Different Types of Cellulose Derivatives
Source abstract
Abstract
Pure polyaniline (PAni) is insoluble in water. Water-soluble complexes of PAni with different of cellulose derivatives were successfully synthesized by using chemical oxidation polymerization of aniline in aqueous solution of cellulose derivatives. In this study, cellulose derivatives such as methylcellulose (MC), hydroxypropyl cellulose (HPC), and hydroxypropyl methylcellulose (HPMC) had been used as a steric stabilizer, aniline (Ani) as a monomer with hydrogen chloride (HCl) as an acidic dopant, and ammonium persulfate (APS) as an initiator. The chemical structure of PAni complexes were confirmed by using Fourier Transform Infrared Spectroscopy (FTIR). The interactions of PAni and cellulose derivatives were observable through Ultraviolet-Visible Spectroscopy (UV-Vis) in the wavelength range of 300 nm to 900 nm. The Standard Four-Point Probe Method was used for the conductivity measurements. In the electrical conductivity measurement, PAni in toluene was used as a control. The result showed that water-soluble PAni-cellulose derivatives gave higher conductivity value (9.47 × 10 −2 – 1.87 × 10 −1 S/cm) than the pristine PAni (1.60 × 10 −3 S/cm).
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Research context
OpenAlex topics: Conducting polymers and applications · Electrochemical sensors and biosensors · Polydiacetylene-based materials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia
Department of Physical Science, Faculty of Applied Sciences and Computing, Tunku Abdul Rahman University College, Jalan Genting Kelang, Setapak, 53300, Kuala Lumpur, Malaysia
References (21)
Show source-provided references
1. The Royal Swedish Academy of Sciences. The Nobel Prize in Chemistry, 2000: Conductive polymers. Retrieved from https://www.nobelprize.org/nobel_prizes/chemistry/laureates/2000/advanced-chemistryprize2000.pdf
2. 10.1016/j.trac.2012.06.00310.1016/j.trac.2012.06.003 ↗
3. 10.1016/j.mssp.2015.01.00810.1016/j.mssp.2015.01.008 ↗
4. 10.1016/j.synthmet.2006.10.00110.1016/j.synthmet.2006.10.001 ↗
5. 10.1016/j.synthmet.2011.02.00310.1016/j.synthmet.2011.02.003 ↗
6. 10.1016/S0379-6779(99)00179-410.1016/S0379-6779(99)00179-4 ↗
7. 10.1021/la950523y10.1021/la950523y ↗
8. 10.1002/app.2883610.1002/app.28836 ↗
9. 10.1021/ma020913910.1021/ma0209139 ↗
10. 10.1166/jnn.2010.251110.1166/jnn.2010.2511 ↗
11. 10.1016/S0379-6779(99)00185-X10.1016/S0379-6779(99)00185-X ↗
12. 10.1016/j.synthmet.2010.11.03610.1016/j.synthmet.2010.11.036 ↗
13. Harun M.H. · JASA · 2007 · 2 · 63
14. 10.1016/j.reactfunctpolym.2007.01.00510.1016/j.reactfunctpolym.2007.01.005 ↗
15. 10.1016/j.eurpolymj.2012.10.02610.1016/j.eurpolymj.2012.10.026 ↗
16. 10.1016/j.synthmet.2012.07.02010.1016/j.synthmet.2012.07.020 ↗
17. 10.1016/j.synthmet.2005.06.01010.1016/j.synthmet.2005.06.010 ↗
18. 10.1016/j.synthmet.2008.07.00510.1016/j.synthmet.2008.07.005 ↗
19. 10.1016/j.carbpol.2008.09.01010.1016/j.carbpol.2008.09.010 ↗
20. 10.1016/j.carbpol.2013.07.01710.1016/j.carbpol.2013.07.017 ↗
21. 10.1016/j.molstruc.2004.05.02110.1016/j.molstruc.2004.05.021 ↗