Electrochemical methanol reformation (ECMR) is an alternative promising technology for producing hydrogen at low energy consumption compared to water electrolysis. In this process, solid polymer electrolyte Nafion (R) is widely employed, due to its superior proton conductivity. However, major limitations are the utilisation of expensive platinum based catalysts, high cost of the above membrane and the crossover of methanol through the polymer electrolyte membrane. In the present work, attempt has been to made to use low cost polymer electrolyte membrane and less noble electro catalyst. A series of Anion Exchange Membranes (AEM) are synthesized from Poly (2, 6-dimethyl-1, 4-phenylene oxide) (PPO) for its application in ECMR. PPO is successfully made into anion conducting by chloromethylation followed by quaternization. Two AEM's are synthesized by optimizing chloromethylation reaction time to 5 h and quaternization time to 5 and 8 h and are labelled as QPPO (C5, Q5) and QPPO (C5, Q8) respectively. Further, with the view to improve the anion conductivity further, composite AEMs are prepared by incorporating inorganic anion conducting quaternized graphene oxide particles in the matrix of PPO and QPPO (C5, Q8) polymers separately to obtain two polymers PPO/QGO and QPPO/QGO. The anionic conductivity of PPO/QGO and QPPO/QGO polymer is 1.2 x 10(-4) and 1.5 x 10(-4) S cm(-1) respectively. Both the membranes are subjected as electrolyte for ECMR application using membrane electrode assembly made by with in house synthesized nitrogen doped graphene supported Pd catalyst (Pd/NG) as anode catalyst and commercial Pt/C as cathode catalyst. The performance of composite membrane was compared with the commercial Fumasep (R) FAA anion exchange membrane. The polarization studies of ECMR cell with composite membrane shows comparable performance with that of commercial Fumasep (R) FAA-2 FAA membrane. The durability of the membrane(s) in the electrolysis environment was tested for about 20 h. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.