TY - JOUR
T1 - Structural study of geopolymers obtained from alkali-activated natural pozzolan feldspars
AU - González-García, D. M.
AU - Téllez-Jurado, L.
AU - Jiménez-Álvarez, F. J.
AU - Balmori-Ramírez, H.
N1 - Publisher Copyright:
© 2016 Elsevier Ltd and Techna Group S.r.l.
PY - 2017/2/1
Y1 - 2017/2/1
N2 - The structural evolution of geopolymers obtained by the alkaline activation of a natural pozzolan composed by a mixture of feldspars (albite and anorthite), calcite and quartz has been followed up to 28 days. The geopolymers have been synthesized using a sodium silicate solution as an activator with an activator/pozzolan volume ratio =0.6, and curing at room temperature or at 40 °C. The reaction has been followed by isothermal calorimetry and the structural evolution has been followed by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR) and scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS). The results show that the phases of albite and anorthite dissolve and that a gel is produced, which is identified by an increment of an amorphous halo observed in the XRD pattern at <10° and between 20 and 40° 2θ, characteristic of geopolymers. The albite and anorthite phases reappear after 14 days of curing. The FT-IR results show a decrease in the intensity of the OH-bands and a shift to the right of the Si-O-Si and Si-O-Al bands as the curing time increases due to the depolymerization and structural reorganization that occur during the curing, in accordance with a geopolymerization mechanism. The microstructure observed by SEM-EDS shows that the final product contains dense plates and has a compressive strength of 13.2 MPa after 28 days of curing.
AB - The structural evolution of geopolymers obtained by the alkaline activation of a natural pozzolan composed by a mixture of feldspars (albite and anorthite), calcite and quartz has been followed up to 28 days. The geopolymers have been synthesized using a sodium silicate solution as an activator with an activator/pozzolan volume ratio =0.6, and curing at room temperature or at 40 °C. The reaction has been followed by isothermal calorimetry and the structural evolution has been followed by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR) and scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS). The results show that the phases of albite and anorthite dissolve and that a gel is produced, which is identified by an increment of an amorphous halo observed in the XRD pattern at <10° and between 20 and 40° 2θ, characteristic of geopolymers. The albite and anorthite phases reappear after 14 days of curing. The FT-IR results show a decrease in the intensity of the OH-bands and a shift to the right of the Si-O-Si and Si-O-Al bands as the curing time increases due to the depolymerization and structural reorganization that occur during the curing, in accordance with a geopolymerization mechanism. The microstructure observed by SEM-EDS shows that the final product contains dense plates and has a compressive strength of 13.2 MPa after 28 days of curing.
KW - Alkali activation
KW - Feldspar
KW - Geopolymers
KW - Microstructure evolution
UR - http://www.scopus.com/inward/record.url?scp=85006515981&partnerID=8YFLogxK
U2 - 10.1016/j.ceramint.2016.11.070
DO - 10.1016/j.ceramint.2016.11.070
M3 - Artículo
SN - 0272-8842
VL - 43
SP - 2606
EP - 2613
JO - Ceramics International
JF - Ceramics International
IS - 2
ER -