Mohammad A. Khan
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Mohammad A. Khan has a total of 146 co-authors. Here are the top co-authors by number of shared publications:
- Husam N. Alshareef
Materials Science and Engineering, Physical Science and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia
13 shared publications - Hicham Idriss
Department of Chemistry, University College London, London WC1E 6BT, UK
12 shared publications - Golam Kibria
Department of Chemical and Petroleum Engineering, University of Calgary, 2500 University Drive, NW, Calgary, Alberta T2N 1N4, Canada
11 shared publications Unnat S. Bhansali
9 shared publications- Jinguang Hu
Department of Chemical and Petroleum Engineering, University of Calgary, 2500 University Dr. NW, Calgary, AB T2N 1N4, Canada
7 shared publications - Tareq Ali Al-Attas
Department of Chemical and Petroleum Engineering University of Calgary 2500 University Drive, NW Calgary Alberta T2N 1N4 Canada
5 shared publications
Latest Publications
- Open Access
- 28 April 2026
- Published by Royal Society of Chemistry (RSC) in Sustainable Energy & Fuels
- Vol. 10 (10) , 2548-2562
An integrated techno-economic-environmental-policy assessment of supercritical biodiesel production: pathway to competitiveness
Despite its promise, biodiesel production via the supercritical methanol (SCM) process has stalled due to limited understanding of interactions among key operating parameters and process-modeling gaps, resulting in contradictory techno-economic (TEA) and life-cycle carbon footprint assessments. In the present study, we integrate experimental optimization with techno-economic, carbon footprint, and policy analyses to identify the path to economic competitiveness for SCM biodiesel production from waste cooking oil (WCO). Response surface modeling based on experimental data was used to quantify interactions among operating parameters and develop a predictive yield model. Under optimal conditions (282.8 °C, 125 bar, methanol-to-oil ratio of 39.17, and reaction time of 43.3 min), biodiesel yield exceeded 92%, and a detailed process flowsheet was developed in Aspen Plus® to quantify material and energy requirements. TEA results indicate that under optimized conditions, SCM biodiesel remains economically challenged, with levelized production costs of 0.9–1.4 $ per kg-biodiesel, depending on plant scale. These costs are driven primarily by high WCO consumption (0.99 kg kg−1-biodiesel) and high-pressure steam demand (3 kg kg−1-biodiesel), required for stoichiometric conversion and energy-intensive distillation, respectively. In contrast, life cycle carbon footprint analysis demonstrates a strong environmental advantage: under renewable electricity and heat supply, SCM biodiesel achieves a carbon intensity of ∼0.28–0.30 kgCO2eq per kg-biodiesel, substantially lower than fossil diesel (∼4 kgCO2eq per kg-diesel). Finally, yet most importantly, by quantitatively linking process performance, economics, emissions, and policy, this study identifies carbon pricing (∼100 $ per t-CO2) and scale-up as critical levers to reconcile the environmental benefits of SCM biodiesel with commercially viable deployment.- 28 April 2026
- Published by Royal Society of Chemistry (RSC) in Sustainable Energy & Fuels
- Vol. 10 (10) , 2548-2562
Open AccessAn integrated techno-economic-environmental-policy assessment of supercritical biodiesel production: pathway to competitiveness
Despite its promise, biodiesel production via the supercritical methanol (SCM) process has stalled due to limited understanding of interactions among key operating parameters and process-modeling gaps, resulting in contradictory techno-economic (TEA) and life-cycle carbon footprint assessments. In the present study, we integrate experimental optimization with techno-economic, carbon footprint, and policy analyses to identify the path to economic competitiveness for SCM biodiesel production from waste cooking oil (WCO). Response surface modeling based on experimental data was used to quantify interactions among operating parameters and develop a predictive yield model. Under optimal conditions (282.8 °C, 125 bar, methanol-to-oil ratio of 39.17, and reaction time of 43.3 min), biodiesel yield exceeded 92%, and a detailed process flowsheet was developed in Aspen Plus® to quantify material and energy requirements. TEA results indicate that under optimized conditions, SCM biodiesel remains economically challenged, with levelized production costs of 0.9–1.4 $ per kg-biodiesel, depending on plant scale. These costs are driven primarily by high WCO consumption (0.99 kg kg−1-biodiesel) and high-pressure steam demand (3 kg kg−1-biodiesel), required for stoichiometric conversion and energy-intensive distillation, respectively. In contrast, life cycle carbon footprint analysis demonstrates a strong environmental advantage: under renewable electricity and heat supply, SCM biodiesel achieves a carbon intensity of ∼0.28–0.30 kgCO2eq per kg-biodiesel, substantially lower than fossil diesel (∼4 kgCO2eq per kg-diesel). Finally, yet most importantly, by quantitatively linking process performance, economics, emissions, and policy, this study identifies carbon pricing (∼100 $ per t-CO2) and scale-up as critical levers to reconcile the environmental benefits of SCM biodiesel with commercially viable deployment. - 5 March 2026
- Published by American Chemical Society (ACS) in ACS Catalysis
- Vol. 16 (7) , 6685-6698
A Bio-Photo/Electro Hybrid Catalytic Cell for Biomass Valorization Coupled with NADH-Driven Enzymatic Synthesis
- 5 March 2026
- Published by American Chemical Society (ACS) in ACS Catalysis
- Vol. 16 (7) , 6685-6698
A Bio-Photo/Electro Hybrid Catalytic Cell for Biomass Valorization Coupled with NADH-Driven Enzymatic Synthesis
- 16 September 2025
- Published by American Chemical Society (ACS) in Nano Letters
- Vol. 25 (39) , 14481-14488
Enhanced Reaction Kinetics of Highly Selective Oxidation of 5-Hydroxymethylfurfural to 2,5-Furandicarboxylic Acid over NiCo2S4
Selective valorization of biomass feedstocks and their derivatives, using renewable electricity to produce value-added chemicals, is a promising route to decarbonize the chemical industry. Herein, we demonstrate the selective production of 2,5-furandicarboxylic acid (FDCA) from the electrocatalytic oxidation of 5-hydroxymethylfurfural (HMF). NiCo2S4 as an anode electrode exhibits almost 100% yield of FDCA with >90% Faradaic efficiency (FE) and high stability at optimized conditions, which outperforms pure NiSx and CoSx. Theoretical calculations reveal that the enhanced reaction kinetics for HMF conversion to FDCA on NiCo2S4 arises from an optimal OH coverage and a more exergonic rate-limiting step compared with its monometallic counterparts. A techno-economic analysis (TEA) for a 100-ton/day FDCA industrial scale production facility reveals that the NiCo2S4 catalyst could drive economic feasibility of the process. This work provides an economically feasible approach to sustainably produce FDCA from HMF oxidation by electrocatalysis.
- 16 September 2025
- Published by American Chemical Society (ACS) in Nano Letters
- Vol. 25 (39) , 14481-14488
Enhanced Reaction Kinetics of Highly Selective Oxidation of 5-Hydroxymethylfurfural to 2,5-Furandicarboxylic Acid over NiCo2S4
Selective valorization of biomass feedstocks and their derivatives, using renewable electricity to produce value-added chemicals, is a promising route to decarbonize the chemical industry. Herein, we demonstrate the selective production of 2,5-furandicarboxylic acid (FDCA) from the electrocatalytic oxidation of 5-hydroxymethylfurfural (HMF). NiCo2S4 as an anode electrode exhibits almost 100% yield of FDCA with >90% Faradaic efficiency (FE) and high stability at optimized conditions, which outperforms pure NiSx and CoSx. Theoretical calculations reveal that the enhanced reaction kinetics for HMF conversion to FDCA on NiCo2S4 arises from an optimal OH coverage and a more exergonic rate-limiting step compared with its monometallic counterparts. A techno-economic analysis (TEA) for a 100-ton/day FDCA industrial scale production facility reveals that the NiCo2S4 catalyst could drive economic feasibility of the process. This work provides an economically feasible approach to sustainably produce FDCA from HMF oxidation by electrocatalysis.
- 2 July 2025
- Published by Elsevier in Reliability Engineering & System Safety
- Vol. 264
Hydrogen Integration into Natural Gas Pipelines: Risk Analysis and Regulatory Recommendations
- 2 July 2025
- Published by Elsevier in Reliability Engineering & System Safety
- Vol. 264
Hydrogen Integration into Natural Gas Pipelines: Risk Analysis and Regulatory Recommendations
- 20 May 2025
- Published by American Chemical Society (ACS) in ACS Sustainable Chemistry & Engineering
- Vol. 13 (21) , 7915-7925
Electrification of Chemical Industry: a Case Study on Methanol Production
- 20 May 2025
- Published by American Chemical Society (ACS) in ACS Sustainable Chemistry & Engineering
- Vol. 13 (21) , 7915-7925
Electrification of Chemical Industry: a Case Study on Methanol Production
- Top Cited PapersOpen Access
- 14 February 2025
- Published by Royal Society of Chemistry (RSC) in Energy & Environmental Science
- Vol. 18 (6) , 2747-2790
Methane pyrolysis for hydrogen production: navigating the path to a net zero future
Hydrogen is a versatile energy vector, pivotal to a NetZero future, but will require the development of technologies for low-carbon hydrogen production like methane pyrolysis and new value chains that connect supply to demand.
- 14 February 2025
- Published by Royal Society of Chemistry (RSC) in Energy & Environmental Science
- Vol. 18 (6) , 2747-2790
Top Cited PapersOpen AccessMethane pyrolysis for hydrogen production: navigating the path to a net zero future
Hydrogen is a versatile energy vector, pivotal to a NetZero future, but will require the development of technologies for low-carbon hydrogen production like methane pyrolysis and new value chains that connect supply to demand.
- Open Access
- 2 November 2024
- Published by Elsevier in International Journal of Hydrogen Energy
- Vol. 138, 1201-1212
Strategic deployment of hydrogen fuel cell buses and fueling stations: Insights from fleet transition models
- 2 November 2024
- Published by Elsevier in International Journal of Hydrogen Energy
- Vol. 138, 1201-1212
Open AccessStrategic deployment of hydrogen fuel cell buses and fueling stations: Insights from fleet transition models
- 28 June 2024
- Published by American Chemical Society (ACS) in ACS Catalysis
- Vol. 14 (14) , 10614-10623
Uncovering Electrochemical Methane Oxidation Mechanism through the In Situ Detection of Reaction Intermediates
- 28 June 2024
- Published by American Chemical Society (ACS) in ACS Catalysis
- Vol. 14 (14) , 10614-10623
Uncovering Electrochemical Methane Oxidation Mechanism through the In Situ Detection of Reaction Intermediates
- Open Access
- 13 June 2024
- Published by Elsevier in International Journal of Hydrogen Energy
- Vol. 74, 136-150
Mitigating uncertainty: A risk informed approach for deploying hydrogen refueling stations
- 13 June 2024
- Published by Elsevier in International Journal of Hydrogen Energy
- Vol. 74, 136-150
Open AccessMitigating uncertainty: A risk informed approach for deploying hydrogen refueling stations
- Open Access
- 22 May 2024
- Published by Elsevier in Chemosphere
- Vol. 361, 142419
Coupling hydrothermal liquefaction and anaerobic digestion for waste biomass valorization: A review in context of circular economy
- 22 May 2024
- Published by Elsevier in Chemosphere
- Vol. 361, 142419
Open AccessCoupling hydrothermal liquefaction and anaerobic digestion for waste biomass valorization: A review in context of circular economy