Abstract:As far as biodiesel economy and hydrogen production are concerned, steam reforming of glycerol, which is the main byproduct of the biodiesel plants, is an appealing policy. Despite hydrogen abundant application in various fields, the total energy efficiency of its production process is comparatively unpleasant. Thus, an upgrading of the outdated procedure is the vital key for consideration of hydrogen as the future fuel. In the current study, a new reactor configuration that integrates both chemical looping co… Show more
“…In CL-SR of glycerol on NiO/Alumina, a steam to carbon ratio of 3 produces a maximum H 2 selectivity of 88% at 550 °C. The 1:3 OC/sorbent ratio aids in improving catalytic activity as well as H 2 purity . Jiang et al synthesized and employed a Ni-based montmorillonite-Al mesoporous oxygen carrier for the first time in CL-SR.…”
Chemical looping-steam reforming
(CL-SR) is a prospective technology
for the simultaneous production of syngas and hydrogen (H2). The quality of syngas and hydrogen (H2) obtained from
CL-SR process has garnered the interest of the scientific society.
A recyclable oxygen storage material (oxygen carrier) is reacted through
an alternating cycle of fuel (reduction step) and steam (oxidation
step) at higher temperatures. Oxygen carrier (OC) plays a vital role
in directing the path of the reaction in the CL-SR process. Hence,
developing and selecting a proper OC is crucial. The current study
intends to address recent breakthroughs in the development and performance
of OCs subjected to different reacting fuel species such as methane
(CL-SMR), CO2 (CL-HG), and liquid fuels. The performance
of various classes of OCs such as metal oxide, mixed metal oxides,
and perovskites toward conversion and lattice oxygen selectivity is
investigated. The thermodynamic study and constraints related to the
performance of OCs in CL-SR are discussed along with the economic
evaluation of the CL-SR process and the conventional SMR process.
Further, the theoretical approaches involved in determining the kinetics
of the CL-SR process and kinetic models developed by the researchers
are reviewed. Finally, the scientific barriers and the suggestions
for optimized operation of the CL-SR process are listed.
“…In CL-SR of glycerol on NiO/Alumina, a steam to carbon ratio of 3 produces a maximum H 2 selectivity of 88% at 550 °C. The 1:3 OC/sorbent ratio aids in improving catalytic activity as well as H 2 purity . Jiang et al synthesized and employed a Ni-based montmorillonite-Al mesoporous oxygen carrier for the first time in CL-SR.…”
Chemical looping-steam reforming
(CL-SR) is a prospective technology
for the simultaneous production of syngas and hydrogen (H2). The quality of syngas and hydrogen (H2) obtained from
CL-SR process has garnered the interest of the scientific society.
A recyclable oxygen storage material (oxygen carrier) is reacted through
an alternating cycle of fuel (reduction step) and steam (oxidation
step) at higher temperatures. Oxygen carrier (OC) plays a vital role
in directing the path of the reaction in the CL-SR process. Hence,
developing and selecting a proper OC is crucial. The current study
intends to address recent breakthroughs in the development and performance
of OCs subjected to different reacting fuel species such as methane
(CL-SMR), CO2 (CL-HG), and liquid fuels. The performance
of various classes of OCs such as metal oxide, mixed metal oxides,
and perovskites toward conversion and lattice oxygen selectivity is
investigated. The thermodynamic study and constraints related to the
performance of OCs in CL-SR are discussed along with the economic
evaluation of the CL-SR process and the conventional SMR process.
Further, the theoretical approaches involved in determining the kinetics
of the CL-SR process and kinetic models developed by the researchers
are reviewed. Finally, the scientific barriers and the suggestions
for optimized operation of the CL-SR process are listed.
“…However, the price of pure glycerol is between 0.22 and 0.37£/ Lb. Approximate crude glycerol production will reach 50 billion liters in 2021 [ 30 ].…”
Section: Glycerol Production From the Biodiesel Industrymentioning
Graphic abstract
The rapid industrial and economic development runs on fossil fuel and other energy sources. Limited oil reserves, environmental issues, and high transportation costs lead towards carbon unbiased renewable and sustainable fuel. Compared to other carbon-based fuels, biodiesel is attracted worldwide as a biofuel for the reduction of global dependence on fossil fuels and the greenhouse effect. During biodiesel production, approximately 10% of glycerol is formed in the transesterification process in a biodiesel plant. The ditching of crude glycerol is important as it contains salt, free fatty acids, and methanol that cause contamination of soil and creates environmental challenges for researchers. However, the excessive cost of crude glycerol refining and market capacity encourage the biodiesel industries for developing a new idea for utilising and produced extra sources of income and treat biodiesel waste. This review focuses on the significance of crude glycerol in the value-added utilisation and conversion to bioethanol by a fermentation process and describes the opportunities of glycerol in various applications.
“…With the increasing potential reserves proven, methane (CH 4 ) conversion and utilization have gradually been given great attention to lab research and industrial applications. − However, the efficient activation of CH 4 remains a great challenge as a result of the high bond energy (439 kJ mol –1 ) and low polarizability of C–H bonds. Nowadays, the main industrial utilization of CH 4 is for hydrogen production, including high-temperature steam methane reforming at 700–1000 °C (SMR, CH 4 + H 2 O → 3H 2 + CO; Δ H 298 K = +206 kJ mol –1 ) and the subsequent low-temperature water–gas shift reaction below 300 °C (CO + H 2 O → H 2 + CO 2 ; Δ H 298 K = −41 kJ mol –1 ). , Although low-temperature steam reforming technologies based on alcohols (methanol, ethanol, and glycerol) have been reported, − a vast majority of current industrial hydrogen is still produced through the high-temperature SMR route as a result of the abundant reserves of methane. , High reaction temperatures will lead to massive energy inputs and carbon-deposition-induced deactivation through side reactions. − The development of advanced SMR driven by sustainable energy inputs at mild conditions has become a current research hotspot.…”
Steam methane reforming is one of the primary industrial hydrogen sources but depends upon high temperatures to activate the inert C−H bonds in methane, motivating novel methods to achieve more sustainable methane activation and hydrogen production. Here, we prepared a PdNi bimetallic catalyst derived from layered double hydroxides for light-driven steam methane reforming, achieving a hydrogen production rate of 82.9 mmol g −1 h −1 at 300 °C under xenon lamp illumination. Outdoor condensed sunlight irradiation further delivered a hydrogen production rate of up to 260.9 mmol g −1 h −1 . Both temperature-programmed desorption and density functional theory calculations indicated that Pd doping enhances the adsorption and activation of inert methane molecules, promoting hydrogen production via the reforming process. These results provide a reference for the direct utilization of solar energy to produce hydrogen from earth-abundant natural gas and water sources.
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