TY - JOUR
T1 - Hydrothermal synthesis temperature induces sponge-like loose silica structure
T2 - A potential support for Fe2O3-based adsorbent in treating As(V)-contaminated water
AU - Numpilai, Thanapha
AU - Ng, Kim Hoong
AU - Polsomboon, Nutkamaithorn
AU - Cheng, Chin Kui
AU - Donphai, Waleeporn
AU - Chareonpanich, Metta
AU - Witoon, Thongthai
N1 - Funding Information:
The TEM and HRTEM images of Fe2O3 and Fe2O3 supported on silica materials prepared with different hydrothermal temperatures are shown in Fig. 3. As shown in Fig. 3a, primary Fe2O3 nanoparticles with about 20 nm in size were stuck tightly to neighboring nanoparticles, forming sub-micrometer-sized particles. The samples subjected to hydrothermal treatment at 60 °C and 100 °C displayed close-contact nanoparticle aggregates without macrovoids (Fig. 3b and c). Cleary, increasing the hydrothermal temperature from the low-temperature region (60 °C and 100 °C) to the high temperature of 140 °C caused a notable change in the structural appearance to a foam-like network morphology with large cavities (Fig. 3d). This structure was still well-preserved and enlarged gaps resulted when the treatment temperature increased to 180 °C (Fig. 3e). It was noteworthy that a substantial decrease in the Fe2O3 particle size to ∼4–5 nm was observed whether applying a dense or loose silica structure (Fig. 3b–e).This project was funded by: the Kasetsart University Research and Development Institute (KURDI), FF(KU)2.65 and the National Research Council of Thailand (N42A640324). C.K. Cheng would like to acknowledge the Khalifa University (RC2-2018-024) Phase 2 fund (project reference number 8474000133).
Funding Information:
This project was funded by: the Kasetsart University Research and Development Institute (KURDI), FF(KU)2.65 and the National Research Council of Thailand ( N42A640324 ). C.K. Cheng would like to acknowledge the Khalifa University ( RC2-2018-024 ) Phase 2 fund (project reference number 8474000133 ).
Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/12
Y1 - 2022/12
N2 - Low cost Fe2O3-based sorbents with an exceptional selectivity toward the targeted As(V) pollutant have gained extensive attention in water treatment. However, their structural features often influence removal performance. In this respect, we present herein a rational design of silica-supported Fe2O3 sorbents with an enhanced morphological structure based on a simple temperature-induced process. Low-hydrothermal temperature synthesis (60 and 100 °C) provided a large silica-cluster size with a close packed structure (S-60 and S-100), contributing to an increase in mass transport resistance. Fe2O3/S-60 with 6.2-nm pore width silica achieved a maximum As(V) uptake capacity (qm) of only 3.5 mg g−1. Supporting Fe2O3 on S-100 with an approximately two-fold increase in the pore size (13 nm) did not lead to any evident enhancement in qe (3.7 mg g−1). However, expanding the pore window up to 22.6 nm (S-140) and 39.5 nm (S-180), along with changing from close-packed to sponge-like loose structures induced by high-temperature synthesis (140 °C and 180 °C), resulted in substantial increases in qm. Fe2O3/S-140 had 1.7 and 1.6 times higher qm (5.9 mg g−1) than Fe2O3/S-100 and Fe2O3/S-60, respectively. The highest qm (7.4 mg g−1) was achieved for Fe2O3/S-180, which was attributed to its relatively small-sized silica cluster and the largest cavities that facilitated easier access by As(V) to adsorbing sites.
AB - Low cost Fe2O3-based sorbents with an exceptional selectivity toward the targeted As(V) pollutant have gained extensive attention in water treatment. However, their structural features often influence removal performance. In this respect, we present herein a rational design of silica-supported Fe2O3 sorbents with an enhanced morphological structure based on a simple temperature-induced process. Low-hydrothermal temperature synthesis (60 and 100 °C) provided a large silica-cluster size with a close packed structure (S-60 and S-100), contributing to an increase in mass transport resistance. Fe2O3/S-60 with 6.2-nm pore width silica achieved a maximum As(V) uptake capacity (qm) of only 3.5 mg g−1. Supporting Fe2O3 on S-100 with an approximately two-fold increase in the pore size (13 nm) did not lead to any evident enhancement in qe (3.7 mg g−1). However, expanding the pore window up to 22.6 nm (S-140) and 39.5 nm (S-180), along with changing from close-packed to sponge-like loose structures induced by high-temperature synthesis (140 °C and 180 °C), resulted in substantial increases in qm. Fe2O3/S-140 had 1.7 and 1.6 times higher qm (5.9 mg g−1) than Fe2O3/S-100 and Fe2O3/S-60, respectively. The highest qm (7.4 mg g−1) was achieved for Fe2O3/S-180, which was attributed to its relatively small-sized silica cluster and the largest cavities that facilitated easier access by As(V) to adsorbing sites.
KW - Adsorption
KW - Arsenic removal
KW - Hydrothermal treatment temperature
KW - Porous silica materials
KW - Sponge-like structure
UR - https://www.scopus.com/pages/publications/85137040943
U2 - 10.1016/j.chemosphere.2022.136267
DO - 10.1016/j.chemosphere.2022.136267
M3 - Article
C2 - 36055586
AN - SCOPUS:85137040943
SN - 0045-6535
VL - 308
JO - Chemosphere
JF - Chemosphere
M1 - 136267
ER -