The utilisation of activated porous carbon (APC) for the removal of volatile methyl siloxane (VMS) has attracted significant research attention. However, the development of materials with high adsorption capacity remains a challenge. In this study, we successfully developed a high-specific-surface-area (2551 m2 g−1) APC material with a large porous texture (1.30 cm3 g−1) using coconut shell waste and NaOH as the activating agent. The performance of the APC material in the removal of hexamethyldisiloxane (L2) was evaluated using a fixed-bed dynamic adsorption setup. Notably, at 0 °C, the APC demonstrated a remarkable L2 removal ability, achieving a breakthrough adsorption capacity of 898.6 mg g−1. By increasing the inlet concentration of L2 and decreasing the temperature appropriately, the L2 adsorption capacity could be further improved. One advantage of APCs is their simple recycling process, which allows for sustained adsorption performance even after five consecutive cycles of adsorption and desorption. Therefore, the prepared APC material holds great promise as an efficient adsorbent for the removal of VMS.
In this study, β-cyclodextrin-modified reduced graphene oxide aerogels (β-CD-rGOAs) were synthesized via a one-step hydrothermal method and were used to remove hexamethyldisiloxane (L2) from biogas. The β-CD-rGOAs were characterized by the Brunner–Emmet–Teller technique, using Fourier-transform infrared spectroscopy, Raman spectrometry, scanning electron microscopy (SEM), contact angle measurements, and X-ray diffraction. The results of the characterizations indicate that β-CD was grafted onto the surface of rGOAs as a cross-linking modifier. The β-CD-rGOA had a three-dimensional, cross-linked porous structure. The maximum breakthrough adsorption capacity of L2 on β-CD-rGOA at 273 K was 111.8 mg g−1. A low inlet concentration and bed temperature facilitated the adsorption of L2. Moreover, the β-CD-rGOA was regenerated by annealing at 80 °C, which renders this a promising material for removing L2 from biogas.
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