scholarly journals Stan i perspektywy wykorzystania biogazu jako nośnika energii do zastosowań stacjonarnych i środków transportu

2012 ◽  
Vol 10 (3) ◽  
pp. 97-118
Author(s):  
Krzysztof Biernat ◽  
Izabela Różnicka

Both governmental and international programs support the promotion of biofuels and aim to increase the limit of renewable energy used in the fuel energy balance. Biogas is produced during the anaerobic methane fermentationprocess and it is known as a significant source of renewable energy, contributing to agriculture and environmental protection. Three types of biogas can be distinguished: biogas from sewage sludge, biogas collected from land`fils, andagricultural biogas. There are several possibilities of using upgraded biogas. Biogas can be used in cogeneration systems to provide heat and electricity, in transportation as a motor fuel and in the production of biohydrogen. Biogas upgrading process leads to a product which is characterized by the same parameters as compressed natural gas. Direct biogas use in the production of hydrogen is possible because of prior purification from traces like hydrogen sulfide, except carbon dioxide, by which the reaction can proceed in the desired manner.

Author(s):  
Koji Hashimoto ◽  
Zenta Kato ◽  
Naokazu Kumagai ◽  
Koichi Izumiya

Extrapolation of primary energy consumption of the world between 1990 and 2005 to the future revealed the complete exhaustion of oil, uranium, natural gas and coal reserves on the Earth in 2034, 2040, 2040 and 2054, respectively. We have been proposing global carbon dioxide recycling to use renewable energy for all people in the whole world. The electricity converted from renewable energy will be used for production of hydrogen by seawater electrolysis. Hydrogen, for which no infrastructures of transportation and combustion exist, will be converted to methane by the reaction with carbon dioxide captured by energy consumers. Among systems in global carbon dioxide recycling, seawater electrolysis and carbon dioxide methanation have not been performed industrially. We created energy-saving cathodes for hydrogen production and anodes for oxygen evolution without chlorine formation in seawater electrolysis, and ideal catalysts for methane formation by the reaction of carbon dioxide with hydrogen. This paper reviews the characteristics and performance of these materials in the systems.


2013 ◽  
Vol 67 (2) ◽  
pp. 326-332 ◽  
Author(s):  
A. Makaruk ◽  
M. Miltner ◽  
M. Harasek

Membrane gas permeation using glassy membranes proved to be a suitable method for biogas upgrading and natural gas substitute production on account of low energy consumption and high compactness. Glassy membranes are very effective in the separation of bulk carbon dioxide and water from a methane-containing stream. However, the content of hydrogen sulfide can be lowered only partially. This work employs process modeling based upon the finite difference method to evaluate a hybrid membrane system built of a combination of rubbery and glassy membranes. The former are responsible for the separation of hydrogen sulfide and the latter separate carbon dioxide to produce standard-conform natural gas substitute. The evaluation focuses on the most critical upgrading parameters like achievable gas purity, methane recovery and specific energy consumption. The obtained results indicate that the evaluated hybrid membrane configuration is a potentially efficient system for the biogas processing tasks that do not require high methane recoveries, and allows effective desulfurization for medium and high hydrogen sulfide concentrations without additional process steps.


2016 ◽  
Vol 9 (1) ◽  
pp. 126-136 ◽  
Author(s):  
Dionisio H. Malagón-Romero ◽  
Alexander Ladino ◽  
Nataly Ortiz ◽  
Liliana P. Green

Hydrogen is expected to play an important role as a clean, reliable and renewable energy source. A key challenge is the production of hydrogen in an economically and environmentally sustainable way on an industrial scale. One promising method of hydrogen production is via biological processes using agricultural resources, where the hydrogen is found to be mixed with other gases, such as carbon dioxide. Thus, to separate hydrogen from the mixture, it is challenging to implement and evaluate a simple, low cost, reliable and efficient separation process. So, the aim of this work was to develop a polymeric membrane for hydrogen separation. The developed membranes were made of polysulfone via phase inversion by a controlled evaporation method with 5 wt % and 10 wt % of polysulfone resulting in thicknesses of 132 and 239 micrometers, respectively. Membrane characterization was performed using scanning electron microscopy (SEM), differential scanning calorimetry (DSC), atomic force microscopy (AFM), and ASTM D882 tensile test. Performance was characterized using a 23 factorial experiment using the time lag method, comparing the results with those from gas chromatography (GC). As a result, developed membranes exhibited dense microstructures, low values of RMS roughness, and glass transition temperatures of approximately 191.75 °C and 190.43 °C for the 5 wt % and 10 wt % membranes, respectively. Performance results for the given membranes showed a hydrogen selectivity of 8.20 for an evaluated gas mixture 54% hydrogen and 46% carbon dioxide. According to selectivity achieved, H2 separation from carbon dioxide is feasible with possibilities of scalability. These results are important for consolidating hydrogen production from biological processes.


1986 ◽  
Vol 39 (5) ◽  
pp. 757 ◽  
Author(s):  
DN Furlong ◽  
D Wells ◽  
WHF Sasse

The photooxidation of ethylenediaminetetraacetic acid ( edta ) and related glycine derivatives, at Pt/TiO2/aqueous solution interfaces, has been monitored via the production of hydrogen and carbon dioxide. Yields are consistent with the exhaustive oxidation of methoxycarbonyl groups and the rate varied with the number and distribution of such groups. A photooxidation pathway is proposed which involves the oxidation of intermediate carbonium ions. Plausible molecular intermediates, such as formic acid and formaldehyde in the case of edta , have been shown in separate experiments to be photooxidized according to the proposed pathway. The maximum rate of oxidation for each donor depends on its oxidation potential and its tendency to adsorb on TiO2 surfaces. Desorption due to pH increase, as well as consumption of the donor, causes the rate to decline rapidly with illumination time. Acetic and malonic acids gave some hydrogen but underwent mainly (> c. 80%) photo-Kolbe decarboxylation to yield carbon dioxide and methane. By contrast the oxidation of oxomalonic, pyruvic and lactic acids proceeded mainly via a H2 producing pathway similar to that established for edta. The oxidation of pyruvic and lactic acids ceased at a yield of one mole of CO2 per mole of acid.


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