Towards the Optimization of a Photovoltaic/Membrane Distillation System for the Production of Pure Water.

The production of pure water plays a pivotal role in enabling sustainable green hydrogen production through electrolysis. The current industrial approach for generating pure water relies on energy-intensive techniques such as reverse osmosis. This study unveils a straightforward method to produce pure water, employing real-world units derived from previously simulated and developed laboratory devices. This demonstrated system is cost-effective and boasts low energy consumption, utilizing membrane distillation (MD) driven by the waste heat harnessed from photovoltaic (PV) panels. In a previous study, modeling simulations were conducted to optimize the multi-layered MD system, serving as a blueprint for the construction of prototype devices with a suitable selection of materials, enabling the construction of field-testable units. The most efficient PV-MD device, featuring evaporation and condensation zones constructed from steel sheets and polytetrafluoroethylene (PTFE) membranes, is capable of yielding high-purity water with conductivity levels below 145 µS with high flux rates.

Realistic operation of two residential cordwood-fired outdoor hydronic heater appliances-Part 2: Particle number and size.

The use of wood as a fuel for home heating is a concern from an environmental health and safety perspective as biomass combustion appliances emit high concentrations of particulate matter. Wood burning significantly contributes to wintertime particulate matter concentrations in many states in the northern United States. Of particular concern are outdoor wood-fired hydronic heaters. These devices are concerning as they tend to have very large combustion chambers and typical use patterns can result in long periods of low output, which result in an increased particulate matter emission rate relative to high heat output operating conditions. In this study, the performance of two hydronic heaters operating under different combustion conditions, including four different heat output categories approximately corresponding to categories I-IV denoted in Environmental Protection Agency Method 28 Outdoor Wood-fired Hydronic Heaters, and during start-up and reloading events were investigated. Measurements of flue gas particulate number concentration and size for particles with aerodynamic diameters between 0.006 and 10 µm were made using a dilution sampling system. The measured particle number concentration in the flue gas was between 0.71 and 420 million particles per cubic centimeter and was dependent on fuel loading and heat output. For each hydronic heater tested, the highest average particle concentration was found at the beginning of each test during the cold-start condition. Additionally, the majority of the particles had aerodynamic diameters less than 0.100 µm (particles of this size made up between 64% and 97% of all particles) and less than 1% of all particles had aerodynamic diameters greater than 1 µm for all phases. For particles in the accumulation mode, between 0.100 and 1 µm, the mean particle diameter was dependent on fuel loading and heat output.Implications: In this work, we provide information on the particle number concentration and particle size of emissions from outdoor cord- wood-fired hydronic heaters. Wood-fired hydronic heater data is sparsely available compared to wood stove data. Thus, additional data from this source help to inform the work of modelers and policy makers interested in hydronic heaters. The test method used in this work is also novel, as it is more inclusive of real-world use cases than the current certification method. Our data helps to validate the test method and allows for comparisons between real-world use case scenarios, and idealized test cases.

Realistic operation of two residential cordwood-fired outdoor hydronic heater appliances-Part 3: Optical properties of black and brown carbon emissions.

Residential biomass combustion is a source of carbonaceous aerosol. Inefficient combustion, particularly of solid fuels produces large quantities of black and brown carbon (BC and BrC). These particle types are important as they have noted effects on climate forcing and human health. One method of measuring these quantities is by measurement of aerosol light-absorption and scattering, which can be performed using an aethalometer and nephelometer, respectively. These instruments are widely deployed in the study of ambient air and are frequently used in air quality modeling and source apportionment studies. In this study, we will describe (1) a method for measuring primary BC and BrC emissions from two residential log-fired wood hydronic heaters and (2) the BC and BrC emission from these devices over a wide range of operating conditions, such as cold-starts, warm-starts, four different levels of output ranging from 15% to 100% maximum rated output, and periods of repeated cycling. The range in flue-gas BC concentrations, measured using an aethalometer at the 880 nanometer (nm) wavelength, were between 5.09 × 102 and 2.24 × 104 micrograms per cubic meter (µg/m3) while the scattering coefficient of the flue-gas, measured by a nephelometer at 880 nm, ranged between 2.20 × 103 and 8.56 × 105 inverse megameters (Mm-1). The BrC concentrations, measured using the 370 nm wavelength of an aethalometer, were between 9.10 × 101 and 3.56 × 104 µg/m3. The calculated Angstrom Absorption Exponent (AAE) of the flue-gas aerosol ranged between 1.54 and 3.63. Performing a comparison between the measured BC concentration and an external particulate matter (PM) concentration showed that overall BC makes up roughly a quarter of the PM emitted by either of the two appliances. Further for both appliances, the cold-start and the test phase immediately following it had the highest BC and BrC concentrations, the highest measured scattering coefficient, as well as a low AAE.Implications: In this work we provide information on the black and brown carbon emissions from outdoor cordwood-fired hydronic heaters. Aethalometer based black carbon measurements are common in atmospheric science, but are uncommonly used in laboratory studies. This work helps to bridge that gap. This data helps to inform the work of modelers and policy makers interested in hydronic heaters and source apportioning biomass combustion emissions.

Free-conditioning dewatering of sewage sludge through in situ propane hydrate formation.

The propane hydrate formation was proposed to have potentials in realizing free-conditioning dewatering of sewage sludge with implications to simultaneous clean water extraction and highly efficient volume reduction. Primarily, the investigation on phase equilibrium of propane hydrates found that the organic components of sewage sludge promoted the propane hydrate formation in terms of decreasing equilibrium pressure by up to 19.2%, compared with that in pure water. Further, the feasibility of hydrate-based dewatering was verified through the observation of propane hydrate formation in sewage sludge and also the quality analysis of water generated from decomposition of up-floated formed hydrates. The formation of up-floated propane hydrates extracted water molecules from sewage sludge into homogeneous crystal phase, which actually excluded sludge particles from hydrate phase and realized the reduction of water in sludge phase. The efficiency of water conversion into hydrates was determined by monitoring propane pressure, which indicated that 14 batch runs decreased the water content of sludge from 98.81wt.% to 44.3wt.% under free-conditioning conditions. The chemical oxygen demand, total nitrogen and total phosphorus of hydrate-extracted water were measured to be 21 ±â€¯1 mg/L, 10.5 ±â€¯0.2 mg/L and 0.4 ±â€¯0 mg/L, respectively, which reflected the excellent separation performance and also indicated that the hydrate-extracted water can be directly discharged without further treatments. Finally, the unit energy consumption of hydrate-based dewatering process based on a continuous operation mode was calculated to be 2673.96 kW h/t dry solid of sewage sludge, which was nearly half of that in thermal drying process. Therefore, the propane hydrate-based process is believed to maximize the green operation of enhanced sludge dewatering while minimizing the energy and additional material consumption.

Solvent effect in sonochemical synthesis of metal-alloy nanoparticles for use as electrocatalysts.

Nanomaterials are now widely used in the fabrication of electrodes and electrocatalysts. Herein, we report a sonochemical study of the synthesis of molybdenum and palladium alloy nanomaterials supported on functionalized carbon material in various solvents: hexadecane, ethanol, ethylene glycol, polyethylene glycol (PEG 400) and Ionic liquids (ILs). The objective was to identify simple and more environmentally friendly design and fabrication methods for nanomaterial synthesis that are suitable as electrocatalysts in electrochemical applications. The particles size and distribution of nanomaterials were compared on two different carbons as supports: activated carbon and multiwall carbon nanotubes (MWCNTs). The results show that carbon materials functionalized with ILs in ethanol/deionized water mixture solvent produced smaller particles sizes (3.00 ±â€¯0.05 nm) with uniform distribution while in PEG 400, functionalized materials produced 4.00 ±â€¯1 nm sized particles with uneven distribution (range). In hexadecane solvents with Polyvinylpyrrolidone (PVP) as capping ligands, large particle sizes (14.00 ±â€¯1 nm) were produced with wide particle size distribution. The metal alloy nanoparticles produced in ILs without any external reducing agent have potential to exhibit a higher catalytic activity due to smaller particle size and uniform distribution.

Occurrence State and Molecular Structure Analysis of Extracellular Proteins with Implications on the Dewaterability of Waste-Activated Sludge.

The occurrence state and molecular structure of extracellular proteins were analyzed to reveal the influencing factors on the water-holding capacities of protein-like substances in waste-activated sludge (WAS). The gelation process of extracellular proteins verified that advanced oxidation processes (AOPs) for WAS dewaterability improvement eliminated the water affinity of extracellular proteins and prevented these macromolecules from forming stable colloidal aggregates. Isobaric tags for relative and absolute quantitation proteomics identified that most of the extracellular proteins were originally derived from the intracellular part and the proteins originally located in the extracellular part were mainly membrane-associated. The main mechanism of extracellular protein transformation during AOPs could be represented by the damage of the membrane or related external encapsulating structure and the release of intracellular substances. For the selected representative extracellular proteins, the strong correlation (R2 > 0.97, p < 0.03) between the surface hydrophilicity index and α-helix percentages in the secondary structure indicated that the water affinity relied more on the spatial distribution of hydrophilic functional groups rather than the content. Destructing the secondary structure represented by the α-helix and stretching the polypeptide aggregation in the water phase through disulfide bond removal might be the key to eliminating the inhibitory effects of extracellular proteins on the interstitial water removal from WAS.

Hydrate formation at the methane/water interface on the molecular scale.

We report the nucleation process of methane hydrate on the molecular scale. A stationary planar interface separating methane gas and liquid water was studied by using in situ neutron reflectivity. We found that the angstrom-scale surface roughening is triggered as soon as the water phase contacts methane gas under the hydrate forming conditions. In addition, it was found that the microscopic surface structure remains unchanged until a macroscopic hydrate film is developed at the interface. We therefore postulate that the angstrom-scale surface roughening is attributed to the formation of microscopic hydrate "embryos" in a "dynamic equilibrium" manner.

Sonolysis induced decomposition of metal carbonyls: kinetics and product characterization.

The decomposition kinetics of Fe(CO)5 and Mo(CO)6 induced by sonolysis in hexadecane solvent was studied as a function of temperature (303-343 K) under an inert atmosphere. The decomposition data, obtained over at least two half lives in most of the runs, yielded first-order rate constant (k) values with correlation co-efficient (R2) > 0.95. The products were characterized by various spectroscopic techniques. The transmission electron microscopy (TEM) yielded images from which the mean particle diameter (MPD) of approximately 10 nm for Fe and < 3 nm for Mo were estimated. The generation of amorphous Fe and semi-crystalline Mo particles was determined from line broadening and corresponding d-spacing values in the X-ray diffraction (XRD) spectra. The XAFS/XANES data were consistent with the production of Fe(0) metal but carbided Mo (Mo2C). The one-step production of high-yield pyrophoric products demonstrated the applicability of sonolysis to effectively produce gram-quantity of zero-valent metals.

H(2) production and carbon utilization by Thermotoga neapolitana under anaerobic and microaerobic growth conditions.

H(2) production by Petrotoga miotherma, Thermosipho africanus, Thermotoga elfii, Fervidobacterium pennavorans, and Thermotoga neapolitana was compared under microaerobic conditions. Contrary to these previously reported strains being strict anaerobes, all tested strains grew and produced H(2) in the presence of micromolar levels of O(2). T. neapolitana showed the highest H(2) production under these conditions. Microscopic counting techniques were used to determine growth curves and doubling times, which were subsequently correlated with optical density measurements. The Biolog anaerobic microtiter plate system was used to analyze the carbon source utilization spectrum of T. neapolitana and to select non-metabolized or poorly metabolized carbohydrates as physiological buffers. Itaconic acid was successfully used as a buffer to overcome pH-induced limitations of cell growth and to facilitate enhanced production of CO-free H(2).

Synthesis of zerovalent nanophase metal particles stabilized with poly(ethylene glycol).

Concurrent sonolysis of iron pentacarbonyl and poly(ethylene glycol)-400 (PEG-400) in hexadecane solvent proceeds via zero-order kinetics and results in Fe nanoparticles encapsulated in PEG-400 (Fe-PEG). The transmission electron microscopy images show Fe-PEG consisting of <3 nm Fe particles that are evenly dispersed in the PEG matrix. Mössbauer and X-ray absorption fine structure/X-ray absorption near-edge structure data reveal an ordered PEG assembly that helps protect the zerovalent Fe core. The Fe nanoparticles in Fe-PEG are superparamagnetic with a magnetization value of 45 emu/g-Fe at 10 KOe. The rheology of the synthesized material shows an unusual increase in viscosity with temperature that is likely due to lower critical saturation temperature phase segregation over 40 degrees C. The low-temperature mobility of the PEG-400 moiety in Fe-PEG would allow facile ligation of the Fe0 core with biologically and chemically active groups.