Author:
Marlina H A,Sebayang K,Gea S,Noer Z,Septawendar R,Sunendar B
Abstract
Abstract
This current study successfully synthesized Na2Mn3O7 in two steps. Firstly, the synthesis of MnO from NaCl and MnCl2.4H2O precursors. NaCl was mixed with citric acid as a chelating agent, while MnCl2.4H2O was mixed with two types of chelating agents (citric acid and 1% chitosan). The solutions of [NaCl-a chelating agent] and [MnCl2.4H2O-a chelating agent] were stirred for ±2 hours. The solutions were hydrothermally heated at 150°C for 6 hours and then calcined at 800°C for 1 hour in a nitrogen condition. The MnO presence was then analyzed using an XRD method. As a comparison, another sample was water leached. Then, it was examined by an XRD method. Secondly, the synthesis of Na2Mn3O7 from MnO and Na2CO3 powder was carried out through a solid method. The calcination was carried out at 800°C for ±3 hours in an oxidizing atmosphere. The XRD results showed the presence of Na2Mn3O7 in the final products of both samples. Based on these experimental results, the sample [NaCl-citric acid; MnCl2.4H2O-1%chitosan] showed higher purity than the sample [NaCl-citric acid; MnCl2.4H2O-citric acid], so that it had a higher intensity of the Na2Mn3O7 phase than the sample [NaCl-citric acid; MnCl2.4H2O-citric acid]. Besides, the Cl- ions removal after calcination greatly affected the intensity of the MnO and Na2Mn3O7 formed.
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