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Volatile methyl siloxanes (VMS), which are considered to be the most troublesome impurities in current biogas-cleaning technologies, need to be removed. In this study, we fabricated a series of Fe3O4–urea-modified reduced graphene-oxide aerogels (Fe3O4–urea–rGOAs) by using industrial-grade graphene oxide as the raw material. A fixed-bed dynamic adsorption setup was built, and the adsorption properties of the Fe3O4–urea–rGOAs for hexamethyldisiloxane (L2, as a VMS model pollutant) were studied. The properties of the as-prepared samples were investigated by employing various characterization techniques (SEM, TEM, FTIR, XRD, Raman spectroscopy, and N2 adsorption/desorption techniques). The results showed that the Fe3O4–urea–rGOA–0.4 had a high specific surface area (188 m2 g−1), large porous texture (0.77 cm3 g−1), and the theoretical maximum adsorption capacity for L2 (146.5 mg g−1). The adsorption capacity considerably increased with a decrease in the bed temperature of the adsorbents, as well as with an increase in the inlet concentration of L2. More importantly, the spent Fe3O4–urea–rGOA adsorbent could be readily regenerated and showed an excellent adsorption performance. Thus, the proposed Fe3O4–urea–rGOAs are promising adsorbents for removing the VMS in biogas. [ABSTRACT FROM AUTHOR]

The critical need to enhance the quality of indoor air leads to the improvement of catalyst activity for the removal of formaldehyde. Sepiolite can be utilized in catalytic reactions for its unique structure, composition and high surface area. The adhesion between sepiolite fibers and the blocked microporous channel (by impurities) demands the activation of natural sepiolite through acid treatment. This treatment successfully produces acid-modified sepiolite Pt-supported samples. The impacts of different acid concentrations, Pt loading content and calcination temperature on catalytic activity for formaldehyde (HCHO) oxidation are studied. The catalytic activity of HCHO is characterized and evaluated by techniques including specific surface area, X-ray diffraction, Fourier transform infrared spectrum, X-ray photoelectron spectroscopy and transmission electron microscopy. The results show the maximum specific area of sepiolite at the optimized 0.06 M acid concentration. Among all the prepared samples, the 0.02Pt/Sep catalyst calcined at 500 °C exhibits the highest catalytic activity for the oxidation of HCHO. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Volatile methyl siloxanes (VMSs) as a trace impurity in biogas decreases its energy utilization, and thus need to be removed. In this paper, a one-step hydrothermal reduction was performed to produce three-dimensional reduced graphene oxide aerogels (rGOAs) using industrial-grade graphene oxide (IGGO) as raw material and vitamin C (VC) as a reductant to facilitate the fabrication of rGOAs. The synthesis of rGOAs was a simple, green, and energy-efficient process. The developed rGOAs were characterized using the Brunauer–Emmett–Teller method, Raman spectrometry, scanning electron microscopy, Fourier-transform infrared spectroscopy, X-ray diffraction measurements and contact angle. The results obtained showed that rGOA-1 with a VC/IGGO ratio of 1/1 (m/m) exhibited a hierarchical porous structure and super-hydrophobicity, yielding a high specific surface area (137.9 m2 g−1) and superior water contact angle (143.8°). The breakthrough adsorption capacity of rGOA-1 for hexamethyldisiloxane (L2, a VMS model) was 11 times higher than that of IGGO. Low inlet concentration and bed temperature were considered beneficial for the L2 adsorption. Interestingly, rGOA-1 was less sensitive to water, and it was readily regenerated for reuse by annealing at 80 °C. The rGOAs have been demonstrated to have great potential for the removal of siloxanes from biogas. [ABSTRACT FROM AUTHOR]

To expand the applications of graphene-based materials to biogas purification, a series of reduced graphene oxide aerogels (rGOAs) were prepared from industrial grade graphene oxide using a simple hydrothermal method. The influences of the hydrothermal preparation temperature on the textural properties, hydrophobicity and physisorption behavior of the rGOAs were investigated using a range of physical and spectroscopic techniques. The results showed that the rGOAs had a macro-porous three-dimensional network structure. Raising the hydrothermal treatment temperature reduced the number of oxygen-containing groups, whereas the specific surface area (SBET), micropore volume (Vmicro) and water contact angle values of the rGOAs all increased. The dynamic adsorption properties of the rGOAs towards hexamethyldisiloxane (L2) increased with increasing hydrothermal treatment temperature and the breakthrough adsorption capacity showed a significant linear association with SBET, Vmicro and contact angle. There was a significant negative association between the breakthrough time and inlet concentration of L2, and the relationship could be reliably predicted with a simple empirical formula. L2 adsorption also increased with decreasing bed temperature. Saturated rGOAs were readily regenerated by a brief heat-treatment at 100 °C. This study has demonstrated the potential of novel rGOA for applications using adsorbents to remove siloxanes from biogas. [ABSTRACT FROM AUTHOR]

CaCO3-TiO2 composite particles were prepared with calcium carbonate (CaCO3) and TiO2 in stirred mill according the wet grinding method. The pigment properties, morphology, and structure of CaCO3-TiO2 composite particles and the interaction behaviors between CaCO3 and TiO2 particles were explored. In the CaCO3-TiO2 composite particles, TiO2 is uniformly coated on the surface of CaCO3 and the firm combination between CaCO3 and TiO2 particles is induced by the dehydration reaction of surface hydroxyl groups. CaCO3-TiO2 composite particles have similar pigment properties to pure TiO2. The hiding power, oil absorption, whiteness and ultraviolet light absorption of composite particles are close to those of pure TiO2. The application performance of CaCO3-TiO2 composite particles in the paint is consonant with their pigment properties. The contrast ratio of the exterior paint containing CaCO3-TiO2 composite particles is equivalent to that of the paint containing the same proportion of pure TiO2. [ABSTRACT FROM AUTHOR]

TiO2-coated wollastonite composite pigments were prepared by the mechano-chemical grinding of wollastonite and TiO2 powder together in a wet ultrafine stirred mill. X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and infrared spectra were used to investigate the microstructures and morphologies of the composite and the reaction mechanism. The results indicate that the TiO2-coated wollastonite composite pigments have similar properties to titanium dioxide pigment, showing much better properties than dry and wet mixing of wollastonite and TiO2. The hiding power of TiO2-coated wollastonite composite pigments (45% TiO2) is 17.97 g/m2, reaching 81.08% of titanium dioxide. A firm combination between wollastonite and TiO2 is obtained through a surface dehydroxylation reaction during the mechano-chemical method. [ABSTRACT FROM AUTHOR]