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The working fluids at supercritical pressures will experience abnormal heat transfer compared with those in a sub-critical state. In particular, the heat transfer deterioration (HTD) can make the wall temperature increase sharply in the tube, posing a challenge for the design of heat exchangers in the supercritical organic Rankine cycle (SORC). It is generally acknowledged that the effects of buoyancy and flow acceleration lead to abnormal heat transfer. However, a clear understanding of the interactions between the turbulent flow and heat transfer characteristics still needs to be further improved by obtaining the internal flow mechanism. The current study analyses the contours of the turbulent flow information under the different boundary conditions by means of validated CFD numerical simulation based on the previous experimental data and reveals the main causes of HTD and the impact mechanism of boundary conditions. The results reveal that two deteriorated extreme points are generated in a vertical upward tube with uniform heat flux for hexamethyldisiloxane at supercritical pressures. The buoyancy and flow acceleration effects caused by the drastic variation in fluid density near the pseudo-critical temperature can deform the velocity profile, thus reducing the local shear stress and turbulence intensity, and leading to the HTD. Moreover, HTD gets worse with the increase in heat flux and moderate with the rise in supercritical pressure. This study should support the data and theory for the refined design of heaters applied to the SORC in the future.

The paper was devoted to the results of the study of methods to obtain superhydrophobic film based on the plasma polymerisation of hexamethyldisiloxane (HMDSO) inside the plasma jet at atmospheric pressure. The 3D printing technology was intended for film deposition, which has the advantage of producing superhydrophobic surfaces over a wide range of scales. The effect of synthesis parameters on the hydrophobic properties of the film has been studied. The obtained superhydrophobic films demonstrated stability and resistance in chemical solutions, at high temperatures, under the influence of UV-irradiation and in various weather conditions. The results can be used in various fields, including automotive, construction, electronics, medicine and others, where surface protection against moisture, contamination and corrosion is required.

This study evaluated the effect of hexamethyldisiloxane (HMDSO) plasma on the fabrics surface to produce masks. Samples of 400-thread count cotton fabric were used. The fabrics was covered with a layer of HMDSO employing plasma enhanced chemical vapor deposition. Optical Microscopy, helium ion beam microscopy (HIM) and atomic force microscopy (AFM) were used for topographic analysis. Fourier transformed infrared spectroscopy technique was used to analyze the chemical modifications on surface. The level of hydrophobicity was evaluated using contact angle measurements. To evaluate the effect of washing cycle on the plasma coating, a protocol proposed by the World Health Organization was used. All experiments were performed in triplicate. For the statistical analysis, the Mann–Whitney, Kruskal–Wallis and Dunn tests were used. AFM showed that, after HMDSO plasma coating, a layer of small granules agglomerated on the original surface of the fabric was visualized. The fabric, which initially had a 0° contact angle value, presented angles of 120° after the plasma coating. It was concluded that the use of cotton fabric coated with HMDSO plasma proved to be adequate for the manufacture of protective masks, since the coating made the surface hydrophobic and this property is maintained even after washing cycles.

Volatile methyl siloxanes (VMS) must be removed because the formation of silica in the combustion process seriously affects the resource utilization of biogas. Herein, a series of APTMS ((3–aminopropyl)trimethoxysilane)-modified activated porous carbon (APC) adsorbents (named APTMS@APC) were prepared for VMS efficient removal. The as-prepared adsorbents were characterized using SEM, FTIR, Raman, X-ray diffraction analyses, and N2 adsorption/desorption. The results showed that the surface modification with APTMS enhanced the hydrophobicity of APC with the water contact angle increasing from 74.3° (hydrophilic) to 127.1° (hydrophobic), and meanwhile improved its texture properties with the SBET increasing from 981 to 1274 m2 g−1. The maximum breakthrough adsorption capacity of APTMS@APC for hexamethyldisiloxane (L2, model pollutant) was 360.1 mg g−1. Effects of an inlet L2 concentration (31.04–83.82 mg L−1) and a bed temperature (0–50 °C) on the removal of L2 were investigated. Meanwhile, after five adsorption–desorption cycles, the APTMS@APC demonstrated a superior cycling performance. This indicated that the hydrophobic APTMS@APC has a great significance to remove VMS.

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.

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.

Plasma enhanced chemical vapor deposition is a promising process for the generation of tailor-made polymer coatings on medical devices in order to improve their implant/ host interaction. The ultra-thin coatings can fulfil a variety of purposes, depending on the monomers used, the process conditions and the location of the coated implants in the human body. In addition, even complex geometries can be coated easily and without the application of solvents. Particularly hydrophilic and hydrophobic plasma polymer coatings can improve biocompatibility, especially in blood contact. Furthermore, the selection of the monomers used enables the generation of specific functional groups for further surface immobilization of drugs, such as proteins, by chemical crosslinking. The release of toxic residues from polymeric implants, such as monomers, additives or degraded components, can also be avoided. The aim of our investigation was the generation of plasma polymer films, their characterization and application as coatings for biodegradable metallic biomaterials in order to retard the degradation process. Metallic biomaterials, in various forms are frequently used in orthopaedics, dentistry, cardiovascular and neurosurgical equipment, because of their tensile strength, fracture toughness, fatigue strength and electrical conductivity. Plasma polymerization was performed using the monomers hexamethyldisiloxane and allylamine. The resulting plasma polymers were analysed in an accelerated degradation test. Both plasma polymers appear to be promising, while polyHMDSO appears to degrade over time and polyallylamine indicates to be stable.

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.

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.