Radio wave treatment is considered as an alternative for steam treatment of soil in glasshouse horticulture for pathogen suppression. In principle, radio wave treatment can be selectively focused on localized infestations, as well as accommodate renewable energy sources. It may therefore help to significantly reduce fossil fuel consumption for soil treatment in greenhouse horticulture. A prototype treatment system has been developed prior to this study. Following this system’s development, the next step is to develop optimum treatment strategies for its application. To this end, this study presents the development of an experimental method to perform quantified experimentation at laboratory scale on pathogen infested soil samples. The study is an interdisciplinary approach that merges respective contributions from microwave engineering, control engineering, and phytopathology. The design requirements for the experimental system are outlined. The design of the layout of the apparatus, computer simulations to optimize its geometry, and the design of power and temperature control are discussed. The study is finalized by reporting a demonstration of the experimental method.

Thermal pathogen suppression in glasshouse horticulture by treatment with steam generated through combustion of fossil fuel will become progressively less desirable. Radio wave treatment could be an alternative. It has several advantages, the most notable is that it generates heat where it is needed in soil, so that it avoids heat losses and long process duration associated with heat transport. Radio wave treatment is a more dynamic and more complex process though, therefore more advanced development tools are needed to apply it effectively. To this end, this study describes the development of a framework for numerical simulation of this process to aid in the development of the radio wave treatment process. The modeling framework is COMSOL Multiphysics in combination with MATLAB, and the computational requirements are constrained to workstation grade hardware. Simulation results are presented to demonstrate the simulation.

Three-dimensional mathematical model was developed for a rectangular TE _10n microwave heating cavity system, working at 2.45 GHz. Energy/heat, momentum equations were solved together with Maxwell's electromagnetic field equations using COMSOL MULTIPHYSICS® simulation environment. The dielectric properties, ε' and ε'', of NaY zeolite (Si/Al = 2.5) were evaluated as a function of temperature. Considering these values, the microwave heating of a porous fixed-bed made of dry NaY zeolite was simulated. Electric field distribution, axial and radial temperature profiles and temperature evolution with time were obtained. The zeolite fixed bed was heated up to 180 °C in 5 min, with 30 W power. The fixed-bed temperature evolution under non-steady state conditions showed the same trend as the one observed experimentally with only an average deviation of 10.3%. The model was used to predict microwave heating of other materials improving energy efficiency of the microwave cavity. Furthermore, the developed model was able to predict thermal runaway for zeolites.

In this work, we report on air/N₂ gasification of a byproduct stream from an industrial fermenter in a tubular microwave plasma reactor to investigate the feasibility of the technology for organic compounds valorization, given the limited number of relevant works in the literature. In this context, an operating window regarding air/N₂/biomass flow rates and power input has been identified to enable stable and efficient operation. Up to 89% carbon conversion efficiency and 41% cold gas efficiency have been attained with syngas product composition H₂:CO:CO₂ = 41:53:6 on molar basis, fairly close to the calculated equilibrium composition values in the temperature range 973 K to 2173 K.

A series of ruthenium-doped strontium titanate (SrTiO₃) perovskite catalysts were synthesized by conventional and microwave-assisted hydrothermal methods. The structure was analyzed by X-Ray diffraction (XRD) confirming the formation of the perovskite phase with some TiO₂ anatase phase in all the catalysts. Microwave irradiation decreases the temperature and time of synthesis from 220 °C for 24 h (conventional heating) to 180 °C for 1h, without affecting the formation of perovskite. A 7 wt. % ruthenium-doped SrTiO₃ catalyst showed the best dielectric properties, and thus its catalytic activity was evaluated for the methane dry reforming reaction under microwave heating in a custom fixed-bed quartz reactor. Microwave power, CH₄:CO₂ vol. % feed ratio and gas hourly space velocity (GHSV) were varied in order to determine the best conditions for performing dry reforming with high reactants conversions and H₂/CO ratio. Stable maximum CH₄ and CO₂ conversions of ∼99.5% and ∼94%, respectively, at H₂/CO ∼0.9 were possible to reach with the 7 wt. % ruthenium-doped SrTiO₃ catalyst exposed to maximum temperatures in the vicinity of 940 °C. A comparative theoretical scale-up study shows significant improvement in H₂ production capability in the case of the perovskite catalyst compared to carbon-based catalysts.

A systematic study of the conventional and microwave (MW) kinetics of an industrially relevant demethylation reaction is presented. In using industrially relevant reaction conditions the dominant influence of the solvent on the MW energy dissipation is avoided. Below the boiling point, the effect of MWs on the activation energy E_a and k₀ is found nonexistent. Interestingly, under reflux conditions, the microwave-heated (MWH) reaction displays very pronounced zero-order kinetics, displaying a much higher reaction rate than observed for the conventionally thermal-heated (CTH) reaction. This is related to a different gas product (methyl bromide, MeBr) removal mechanism, changing from classic nucleation into gaseous bubbles to a facilitated removal through escaping gases/vapors. Additionally, the use of MWs compensates better for the strong heat losses in this reaction, associated with the boiling of HBr/water and the loss of MeBr, than under CTH. Through modeling, MWH was shown to occur inhomogeneously around gas/liquid interfaces, resulting in localized overheating in the very near vicinity of the bubbles, overall increasing the average heating rate in the bubble vicinity vis-à-vis the bulk of the liquid. Based on these observations and findings, a novel continuous reactor concept is proposed in which the escaping MeBr and the generated HBr/water vapors are the main driving forces for circulation. This reactor concept is generic in that it offers a viable and low cost option for the use of very strong acids and the managed removal/quenching of gaseous byproducts.

The release of hydrogen from solid hydrides by thermolysis can be improved by nanoconfinement of the hydride in a suitable micro/mesoporous support, but the slow heat transfer by conduction through the support can be a limitation. In this work, a C/SiO₂ mesoporous material has been synthesized and employed as matrix for nanoconfinement of hydrides. The matrix showed high surface area and pore volume (386 m²/g and 1.41 cm³/g), which enabled the confinement of high concentrations of hydride. Furthermore, by modification of the proportion between C and SiO₂, the dielectric properties of the complex could be modified, making it susceptible to microwave heating. As with this heating method the entire sample is heated simultaneously, the heat transfer resistances associated to conduction were eliminated. To demonstrate this possibility, ethane 1,2-diaminoborane (EDAB) was embedded on the C/SiO₂ matrix at concentrations ranging from 11 to 31%wt using a wet impregnation method, and a device appropriate for hydrogen release from this material by application of microwaves was designed with the aid of a numerical simulation. Hydrogen liberation tests by conventional heating and microwaves were compared, showing that by microwave heating hydrogen release can be initiated and stopped in shorter times.

The complexity and challenges in noncontact temperature measurements inside microwave-heated catalytic reactors are presented in this paper. A custom-designed microwave cavity has been used to focus the microwave field on the catalyst and enable monitoring of the temperature field in 2D. A methodology to study the temperature distribution in the catalytic bed by using a thermal camera in combination with a thermocouple for a heterogeneous catalytic reaction (methane dry reforming) under microwave heating has been demonstrated. The effects of various variables that affect the accuracy of temperature recordings are discussed in detail. The necessity of having at least one contact sensor, such as a thermocouple, or some other microwave transparent sensor, is recommended to keep track of the temperature changes occurring in the catalytic bed during the reaction under microwave heating.

Gasification technology may combine waste treatment with energy generation. Conventional gasification processes are bulky and inflexible. By using an external energy source, in the form of microwave-generated plasma, equipment size may be reduced and flexibility as regards to the feed composition may be increased. This type of gasification may be combined with fuel cell technology to generate electricity for on-site microwave generation. In this paper, we present short gasification experiments with cellulose, as model biomass compound, in air plasma. In order to optimize reaction rates, gasification and plasma generation are combined in the same volume in order to expose the solids to plasma of maximum intensity. The heating value of the fuel gas yield exceeds, up to 84%, the net microwave energy transmitted into the reactor over a range of operating conditions. As the system has not been optimized, in particular regarding residence time, the results give confidence that this concept can eventually be developed into a viable small-scale decentralized gasification technology.