TY - JOUR
T1 - Esterification of p-hydroxybenzoic acid with glucose using a γ-Al2O3/SO4 catalyst
AU - putri, elfia siska yasa
AU - Wibowo, Widajanti
AU - Kosela, Soleh
PY - 2019
Y1 - 2019
N2 - Esterification of p-hydroxybenzoic acid with glucose can be expected to produce esters. The rate of esterification reaction is usually very slow and, therefore, needs an acid catalyst to accelerate it. This research examined the performance of a heterogeneous catalyst made of γ-Al2O3 impregnated with a protic acid, H2SO4. The heterogeneous catalyst, γ-Al2O3/SO4, was characterized using XRD, XRF, and BET methods. The esterification reactions were conducted using dimethyl sulfoxide (DMSO) solvent at a temperature of 1000C and observed after they lasted for 1 to 24 hours (reaction time). The esterification of p-hydroxybenzoic acid with glucose used two catalysts, namely 3% SO42-/Al2O3 and 5% SO42-/Al2O3. The reaction products were analyzed using HPLC, IR, and LC-MS methods. The % yield was the highest at Hour 24 for both catalysts, while the % conversion fluctuated during the esterification time. The LC-MS showed that the three produced esters had molecular weights of 300, 420, and 540.
AB - Esterification of p-hydroxybenzoic acid with glucose can be expected to produce esters. The rate of esterification reaction is usually very slow and, therefore, needs an acid catalyst to accelerate it. This research examined the performance of a heterogeneous catalyst made of γ-Al2O3 impregnated with a protic acid, H2SO4. The heterogeneous catalyst, γ-Al2O3/SO4, was characterized using XRD, XRF, and BET methods. The esterification reactions were conducted using dimethyl sulfoxide (DMSO) solvent at a temperature of 1000C and observed after they lasted for 1 to 24 hours (reaction time). The esterification of p-hydroxybenzoic acid with glucose used two catalysts, namely 3% SO42-/Al2O3 and 5% SO42-/Al2O3. The reaction products were analyzed using HPLC, IR, and LC-MS methods. The % yield was the highest at Hour 24 for both catalysts, while the % conversion fluctuated during the esterification time. The LC-MS showed that the three produced esters had molecular weights of 300, 420, and 540.
UR - http://journal.uad.ac.id/index.php/PHARMACIANA/article/view/11892
M3 - Article
SN - 2477-0256
JO - Pharmaciana
JF - Pharmaciana
ER -