Darryn W. Rackemann
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Darryn W. Rackemann has a total of 89 co-authors. Here are the top co-authors by number of shared publications:
- William Orlando Sinclair Doherty
Centre for Agriculture and the Bioeconomy, Faculty of Science, Queensland University of Technology, Brisbane, QLD 4000, Australia
15 shared publications - Lalehvash Moghaddam
Centre for Agriculture and the Bioeconomy, Faculty of Science, Queensland University of Technology, Brisbane, Australia
11 shared publications William O.S. Doherty
Faculty of Science and Engineering, Southern Cross University, Lismore, New South Wales 2480, Australia
6 shared publicationsJohn P. Bartley
School of Chemistry and Physics, Faculty of Science, Queensland University of Technology, Brisbane, Queensland 4001, Australia
5 shared publicationsZhanying Zhang
5 shared publicationsChalani Marasinghege
Queensland Univ Technol, Brisbane, Australia
4 shared publications
Latest Publications
- Open Access
- 1 April 2026
- Published by Elsevier in Industrial Crops and Products
- Vol. 244
Synergistic improvement of mechanical and barrier properties of paper using a hemicellulose-based composite coating for high humidity kiwifruit preservation
- 1 April 2026
- Published by Elsevier in Industrial Crops and Products
- Vol. 244
Open AccessSynergistic improvement of mechanical and barrier properties of paper using a hemicellulose-based composite coating for high humidity kiwifruit preservation
- Top Cited PapersOpen Access
- 23 March 2026
- Published by Elsevier in Bioresource Technology
- Vol. 450, 134477
Advances in porous activated carbon-based solid acid catalysts for biomass conversion
- 23 March 2026
- Published by Elsevier in Bioresource Technology
- Vol. 450, 134477
Top Cited PapersOpen AccessAdvances in porous activated carbon-based solid acid catalysts for biomass conversion
- 20 February 2026
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 28 (11) , 4924-4935
Production of furanics from sugarcane bagasse via the 5-chloromethylfurfural pathway: techno-economics and greenhouse gas assessment
This study investigated the commercial-scale production of furan-based chemicals (furanics) from sugarcane bagasse, using 5-chloromethylfurfural (CMF) as an intermediate platform molecule for the production of bio-based chemicals and materials. A process was developed to convert sugarcane bagasse from a co-located sugar mill to CMF and subsequently upgrade it to 5-methylfurfural (5-MF) or 2,5-dimethylfuran (DMF) to recover the chlorine and recycle as HCl back into the process. The economics and environmental factors for a production facility processing 237,600 t bagasse per annum were investigated. The total capital investment for CMF production is estimated at $63 million, for 5-methylfurfural production at $104 million, and for 2,5-dimethylfuran production at $135 million. The minimum selling price (MSP) for CMF is $0.97/kg; for 5-methylfurfural is $1.68/kg; and for 2,5-dimethylfuran is $2.76/kg. Sensitivity analysis reveals that the minimum selling price of CMF is significantly influenced by the CMF yield, costs of hydrochloric acid (HCl), feedstock, and utilities. The use of HCl also poses a technical and environmental challenge for recycling due to the existence of an azeotrope with water. Greenhouse gas (GHG) emissions of production were calculated to be 1.63 kgCO2-eq/kg CMF, 1.28 kgCO2-eq/kg 5-methylfurfural and 2.50 kgCO2-eq/kg 2,5-dimethylfuran, largely contributed to by HCl use. Therefore, process improvements targeting HCl use reduction are recommended. Solvent-free upgrading to furanic derivatives is proposed to reduce separation costs and improve process efficiency. Despite current challenges, the results demonstrate that CMF can serve as a sustainable and economically attractive route for producing bio-based furanics, showing potential for competitiveness with 5-(hydroxymethyl)furfural-based pathways.
- 20 February 2026
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 28 (11) , 4924-4935
Production of furanics from sugarcane bagasse via the 5-chloromethylfurfural pathway: techno-economics and greenhouse gas assessment
This study investigated the commercial-scale production of furan-based chemicals (furanics) from sugarcane bagasse, using 5-chloromethylfurfural (CMF) as an intermediate platform molecule for the production of bio-based chemicals and materials. A process was developed to convert sugarcane bagasse from a co-located sugar mill to CMF and subsequently upgrade it to 5-methylfurfural (5-MF) or 2,5-dimethylfuran (DMF) to recover the chlorine and recycle as HCl back into the process. The economics and environmental factors for a production facility processing 237,600 t bagasse per annum were investigated. The total capital investment for CMF production is estimated at $63 million, for 5-methylfurfural production at $104 million, and for 2,5-dimethylfuran production at $135 million. The minimum selling price (MSP) for CMF is $0.97/kg; for 5-methylfurfural is $1.68/kg; and for 2,5-dimethylfuran is $2.76/kg. Sensitivity analysis reveals that the minimum selling price of CMF is significantly influenced by the CMF yield, costs of hydrochloric acid (HCl), feedstock, and utilities. The use of HCl also poses a technical and environmental challenge for recycling due to the existence of an azeotrope with water. Greenhouse gas (GHG) emissions of production were calculated to be 1.63 kgCO2-eq/kg CMF, 1.28 kgCO2-eq/kg 5-methylfurfural and 2.50 kgCO2-eq/kg 2,5-dimethylfuran, largely contributed to by HCl use. Therefore, process improvements targeting HCl use reduction are recommended. Solvent-free upgrading to furanic derivatives is proposed to reduce separation costs and improve process efficiency. Despite current challenges, the results demonstrate that CMF can serve as a sustainable and economically attractive route for producing bio-based furanics, showing potential for competitiveness with 5-(hydroxymethyl)furfural-based pathways.
- Open Access
- 3 May 2025
- Published by Elsevier in Materials Today Communications
- Vol. 46
Furan modified lignin: Advancing rigid, open polyurethane foam production from agricultural waste
- 3 May 2025
- Published by Elsevier in Materials Today Communications
- Vol. 46
Open AccessFuran modified lignin: Advancing rigid, open polyurethane foam production from agricultural waste
- Open Access
- 4 February 2025
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 13 (10) , 7445-7460
Reduction of RuO 2 nanoparticles supported on silica by organic molecules: a strategy for nanoparticle redispersion
A detailed study of reduction of supported RuO 2 nanoparticles by organic molecules. The relationship between reduction heat, reaction products, nanoparticle dispersion, and catalytic activity was investigated.
- 4 February 2025
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 13 (10) , 7445-7460
Open AccessReduction of RuO 2 nanoparticles supported on silica by organic molecules: a strategy for nanoparticle redispersion
A detailed study of reduction of supported RuO 2 nanoparticles by organic molecules. The relationship between reduction heat, reaction products, nanoparticle dispersion, and catalytic activity was investigated.
- Open Access
- 25 June 2024
- Published by Elsevier in Journal of Analytical and Applied Pyrolysis
- Vol. 181, 106606
Unveiling sustainable synergy and ageing stability of bio-oils from cotton gin trash and plastic waste co-liquefaction for an integrated waste-to-energy solution
- 25 June 2024
- Published by Elsevier in Journal of Analytical and Applied Pyrolysis
- Vol. 181, 106606
Open AccessUnveiling sustainable synergy and ageing stability of bio-oils from cotton gin trash and plastic waste co-liquefaction for an integrated waste-to-energy solution
- Open Access
- 7 March 2024
- Published by Elsevier in Journal of Food Engineering
- Vol. 374
One pot two-alkali clarification process to minimize sucrose degradation of clarified sugarcane juice during evaporation
- 7 March 2024
- Published by Elsevier in Journal of Food Engineering
- Vol. 374
Open AccessOne pot two-alkali clarification process to minimize sucrose degradation of clarified sugarcane juice during evaporation
- 26 February 2024
- Published by Verlag Dr. Albert Bartens KG in Sugar Industry
- Vol. 149 (3) , 201-207
Optimisation of pH for minimising juice degradation during evaporation
During juice evaporation, sucrose loss can occur due to degradation reactions that are influenced by heat, pH, residence time, and dry substance content. The impacts of heat can be controlled through process and equipment design, and juice pH could be optimised to reduce its effects on degradation reactions. A factory sampling program was conducted with…
- 26 February 2024
- Published by Verlag Dr. Albert Bartens KG in Sugar Industry
- Vol. 149 (3) , 201-207
Optimisation of pH for minimising juice degradation during evaporation
During juice evaporation, sucrose loss can occur due to degradation reactions that are influenced by heat, pH, residence time, and dry substance content. The impacts of heat can be controlled through process and equipment design, and juice pH could be optimised to reduce its effects on degradation reactions. A factory sampling program was conducted with…
- 18 December 2023
- Published by American Chemical Society (ACS) in ACS Sustainable Chemistry & Engineering
- Vol. 12 (1) , 480-489
Thermochemically Treated Tin-Doped Nanocarbon Composite Structures for the High Catalytic Performance in the One-Step Synthesis of 5-Methyl Furfural
- 18 December 2023
- Published by American Chemical Society (ACS) in ACS Sustainable Chemistry & Engineering
- Vol. 12 (1) , 480-489
Thermochemically Treated Tin-Doped Nanocarbon Composite Structures for the High Catalytic Performance in the One-Step Synthesis of 5-Methyl Furfural
- Open Access
- 20 October 2023
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 8 (43) , 40442-40455
High Conversion of Concentrated Sugars to 5-Hydroxymethylfurfural over a Metal-free Carbon Catalyst: Role of Glucose–Fructose Dimers
To reduce the production cost of chemicals from renewable resources, the feedstock loading must be high and the catalyst must be of low cost and efficient. In this study, at a very short reaction time of 10 min at 125 °C, concentrated sugar solutions (20 wt %, 101 wt % on solvent) were converted to 5-hydroxymethylfurfural (HMF) over a cotton gin trash (CGT)-derived sulfonated carbon catalyst in a 1-butyl-3-methyl-imidazolium chloride ([BMIM]Cl) and 2-methyltetrahydrofuran (MeTHF) biphasic system. We report, for the first time, that the presence of glucose either as a covalently bonded monomer in sucrose or in a mixture with fructose achieved yields of HMF up to 62 mol % compared to a value of only 39 mol % obtained with fructose on its own. In the concentrated reaction medium, glucose, fructose, and sucrose molecules produce difructose anhydrides, dimers/reversion products, and sucrose isomers. The glucose-fructose dimers formed in sucrose and glucose/fructose reaction systems play a critical role in the transformation of the sugars to a higher-than-expected HMF yield. Thus, a strategy of using cellulosic glucose, where it is partially converted to fructose content and the high sugar concentration sugar mixture is then converted to HMF, should be exploited for future biorefineries.
- 20 October 2023
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 8 (43) , 40442-40455
Open AccessHigh Conversion of Concentrated Sugars to 5-Hydroxymethylfurfural over a Metal-free Carbon Catalyst: Role of Glucose–Fructose Dimers
To reduce the production cost of chemicals from renewable resources, the feedstock loading must be high and the catalyst must be of low cost and efficient. In this study, at a very short reaction time of 10 min at 125 °C, concentrated sugar solutions (20 wt %, 101 wt % on solvent) were converted to 5-hydroxymethylfurfural (HMF) over a cotton gin trash (CGT)-derived sulfonated carbon catalyst in a 1-butyl-3-methyl-imidazolium chloride ([BMIM]Cl) and 2-methyltetrahydrofuran (MeTHF) biphasic system. We report, for the first time, that the presence of glucose either as a covalently bonded monomer in sucrose or in a mixture with fructose achieved yields of HMF up to 62 mol % compared to a value of only 39 mol % obtained with fructose on its own. In the concentrated reaction medium, glucose, fructose, and sucrose molecules produce difructose anhydrides, dimers/reversion products, and sucrose isomers. The glucose-fructose dimers formed in sucrose and glucose/fructose reaction systems play a critical role in the transformation of the sugars to a higher-than-expected HMF yield. Thus, a strategy of using cellulosic glucose, where it is partially converted to fructose content and the high sugar concentration sugar mixture is then converted to HMF, should be exploited for future biorefineries.