TY - JOUR
T1 - Synthesis of cristobalite from silica sands of Tuban and Tanah Laut
AU - Nurbaiti, U.
AU - Pratapa, S.
N1 - Publisher Copyright:
© Published under licence by IOP Publishing Ltd.
PY - 2018/4/6
Y1 - 2018/4/6
N2 - Synthesis of SiO2 cristobalite powders has been successfully carried out by a coprecipitation method by making use of local silica sands from districts of Tuban and Tanah Laut, Indonesia. Cristobalite is a phase of SiO2 polymorphs which can be used as a composite filler, a coating material, a surface finishing media, and structural ceramics. In the first stage of the synthesis, the as-received sands were processed by a magnetic separation, grinding, and soaking with HCl to increase the purity of silica content. X-ray fluorescence (XRF) spectroscopy showed that the atomic content of Si (excluding oxygen) in both powders reached 95.3 and 97.4%. A coprecipitation process was then performed by dissolving the silica powders in a 7M NaOH solution followed by a titration with 2M HCl to achieve a normal pH and to form a gel. Furthermore, the silica gel is washed, dried and then calcined at a temperature of between 950-1200 °C with a variation of holding time for 1, 4 dan 10 hrs to produce white powders. X-ray diffraction (XRD) data analyses showed that the powder with calcination temperature of 1150 °C for 4 hrs exhibited the highest cristobalite content of up to 95wt%. Its scanning electron microscopy (SEM) image showed that its grain morphology was relatively homogeneous.
AB - Synthesis of SiO2 cristobalite powders has been successfully carried out by a coprecipitation method by making use of local silica sands from districts of Tuban and Tanah Laut, Indonesia. Cristobalite is a phase of SiO2 polymorphs which can be used as a composite filler, a coating material, a surface finishing media, and structural ceramics. In the first stage of the synthesis, the as-received sands were processed by a magnetic separation, grinding, and soaking with HCl to increase the purity of silica content. X-ray fluorescence (XRF) spectroscopy showed that the atomic content of Si (excluding oxygen) in both powders reached 95.3 and 97.4%. A coprecipitation process was then performed by dissolving the silica powders in a 7M NaOH solution followed by a titration with 2M HCl to achieve a normal pH and to form a gel. Furthermore, the silica gel is washed, dried and then calcined at a temperature of between 950-1200 °C with a variation of holding time for 1, 4 dan 10 hrs to produce white powders. X-ray diffraction (XRD) data analyses showed that the powder with calcination temperature of 1150 °C for 4 hrs exhibited the highest cristobalite content of up to 95wt%. Its scanning electron microscopy (SEM) image showed that its grain morphology was relatively homogeneous.
UR - http://www.scopus.com/inward/record.url?scp=85045685420&partnerID=8YFLogxK
U2 - 10.1088/1742-6596/983/1/012014
DO - 10.1088/1742-6596/983/1/012014
M3 - Conference article
AN - SCOPUS:85045685420
SN - 1742-6588
VL - 983
JO - Journal of Physics: Conference Series
JF - Journal of Physics: Conference Series
IS - 1
M1 - 012014
T2 - 4th International Conference on Mathematics, Science, and Education, ICMSE 2017
Y2 - 18 September 2017 through 19 September 2017
ER -