
FTIR, SEM and XRD analysis of activated carbon from sago wastes using acid modification
Author(s) -
Wiwin Rewini Kunusa,
Hendrik Iyabu,
Rawand S. Abdullah
Publication year - 2021
Publication title -
journal of physics. conference series
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 85
eISSN - 1742-6596
pISSN - 1742-6588
DOI - 10.1088/1742-6596/1968/1/012014
Subject(s) - activated carbon , carbonization , nuclear chemistry , adsorption , fourier transform infrared spectroscopy , chemistry , extraction (chemistry) , cellulose , dehydration , muffle furnace , carbon fibers , raw material , materials science , calcination , organic chemistry , chemical engineering , catalysis , composite material , biochemistry , composite number , engineering
Activated charcoal bio adsorbent is a method that can be developed because the raw material is easy to obtain and does not require large costs such as processing sago. The stages of making activated carbon include the stages of dehydration, carbonization, and extraction of silica using 4% NaOH solution (1:10). The activation stage successively used 250 mL of 1M NaCl, 1M MgCl 2 , 1M CaCO 3 , 1M K 2 Cr 2 O 7 and the addition of 100 mL of 1M HNO 3 , 3% H 2 O 2 , 1M H 3 PO 4 and 4NH 2 SO 4 respectively. The activation process uses a water bath at 700°C for 3 hours. In the conventional carbonization stage in a vacuum used drum for 1x24 hours. Physicochemical analysis of activated carbon products, namely moisture content, ash content, pH, Activated Carbon Adsorption Test against Iod Test and methylene blue. FT-IR analysis showed a wide band of 3442.94 cm ‒1 to 3415.93 cm ‒1 which showed the free O-H strain vibrations of the OH group in the cellulose molecule. 1178.51 cm ‒1 , –1039.53 cm ‒1 , -1024.20 cm ‒1 , C-C and C-O-C glycosidic ether band. SEM data describes the differences in the surface morphological structure of each sample and is supported by XRD data.