TY - JOUR
T1 - Response surface methodology applied to oxalic acid hydrolysis of oil palm
AU - Suryadi, Herman
AU - Yanuar, Arry
AU - Harmita,
AU - Rachmadani, Putri Winny
N1 - Publisher Copyright:
© 2020 The Authors. Published by Innovare Academic Sciences Pvt Ltd.
PY - 2020/3
Y1 - 2020/3
N2 - Objective: The study aimed to identify the best conditions using oxalic acid for hydrolysis of hemicellulose in oil palm empty fruit bunch (OPEFB) biomass. Methods: The analytical method of high-performance liquid chromatography (HPLC) was using a SUPELCOSIL LC-NH2 column, refractive index detection detector, and three compositions of the mobile phase. At first, the hydrolysis of hemicellulose in OPEFB powder was optimized by applying a response surface methodology. A three-variable, six-central composite design was used for the experiments. Temperature (between 95°C and 135°C), reaction time (between 10 and 110 min), and oxalic acid concentration (between 1% and 7% [w/v]) were evaluated by running 15 different experiments at constant biomass concentrations. Then, hydrolysis was optimized again at the constant temperature selected with three variables: OPEFB concentration, reaction time, and oxalic acid concentration. Hydrolysate samples were detoxified with carbon active, and furfural compound was analyzed by gas chromatography with flame ionization detector. Results: The optimum condition of HPLC was using acetonitrile: water (9:1) at a flow rate of 1.0 ml/min. The first hydrolysis results showed a high yield of D-xylose produced, which was 6.40 g D-xylose/100 g OPEFB biomass, with a xylose recovery of 93.8%. However, this result was not yet optimum. Further hydrolysis at constant temperature experiment produced the highest xylose yield of 13.13%, equivalent to 32 g/l D-xylose. Conclusion: The yield of D-xylose from mild hydrolysis using oxalic acid was similar to that using dilute sulfuric acid as used in the previous study by Rahman et al.
AB - Objective: The study aimed to identify the best conditions using oxalic acid for hydrolysis of hemicellulose in oil palm empty fruit bunch (OPEFB) biomass. Methods: The analytical method of high-performance liquid chromatography (HPLC) was using a SUPELCOSIL LC-NH2 column, refractive index detection detector, and three compositions of the mobile phase. At first, the hydrolysis of hemicellulose in OPEFB powder was optimized by applying a response surface methodology. A three-variable, six-central composite design was used for the experiments. Temperature (between 95°C and 135°C), reaction time (between 10 and 110 min), and oxalic acid concentration (between 1% and 7% [w/v]) were evaluated by running 15 different experiments at constant biomass concentrations. Then, hydrolysis was optimized again at the constant temperature selected with three variables: OPEFB concentration, reaction time, and oxalic acid concentration. Hydrolysate samples were detoxified with carbon active, and furfural compound was analyzed by gas chromatography with flame ionization detector. Results: The optimum condition of HPLC was using acetonitrile: water (9:1) at a flow rate of 1.0 ml/min. The first hydrolysis results showed a high yield of D-xylose produced, which was 6.40 g D-xylose/100 g OPEFB biomass, with a xylose recovery of 93.8%. However, this result was not yet optimum. Further hydrolysis at constant temperature experiment produced the highest xylose yield of 13.13%, equivalent to 32 g/l D-xylose. Conclusion: The yield of D-xylose from mild hydrolysis using oxalic acid was similar to that using dilute sulfuric acid as used in the previous study by Rahman et al.
KW - Acid hydrolysis
KW - D-xylose
KW - Hydrolysate
KW - Oil palm empty fruit bunch
KW - Oxalic acid
KW - Response surface methodology
UR - http://www.scopus.com/inward/record.url?scp=85084146894&partnerID=8YFLogxK
U2 - 10.22159/ijap.2020.v12s1.FF037
DO - 10.22159/ijap.2020.v12s1.FF037
M3 - Article
AN - SCOPUS:85084146894
SN - 0975-7058
VL - 12
SP - 172
EP - 176
JO - International Journal of Applied Pharmaceutics
JF - International Journal of Applied Pharmaceutics
IS - Special Issue 1
ER -