Pub Date : 2026-01-05DOI: 10.1016/j.cep.2026.110699
Shengxuan Zhao , Enpei Zhu , Chao Luo , Li Zhu , Zhiqi Chen , Macong Duan , Xiaoyuan Li , Linqing Dai , Gengwei Zhang , Likang Fu , Libo Zhang , Yonggang Zuo , Bingguo Liu
Lithium extraction from spodumene conventionally requires complex, energy-intensive processes involving high-temperature conversion of α-spodumene to β-spodumene, followed by acid roasting and leaching. Inspired by alkali fusion, we achieved microwave-assisted alkaline roasting of spodumene at only 250 °C, producing water- and acid-soluble salts and thereby substantially reducing the roasting temperature. However, efficient lithium recovery during subsequent leaching remains challenging. Here, we report an ultrasonic leaching (UL) strategy applied to microwave-roasted slag after water washing in a sulfuric acid medium. Under optimized conditions, lithium leaching efficiency reached 99.9%, representing a 27% improvement over conventional leaching (CL). Kinetic analysis revealed that ultrasound reduced the apparent activation energy from 32.61 kJ·mol-1 (CL) to 20.68 kJ·mol-1. Mechanistic studies showed that ultrasound disrupts diffusion boundary layers, decreases particle size, and enhances interfacial mass transfer and infiltration, thereby accelerating lithium dissolution. This microwave-ultrasound synergistic strategy provides a highly efficient, sustainable, and environmentally friendly approach for lithium extraction, establishing a promising paradigm for process intensification in green hydrometallurgy.
{"title":"Ultrasonic-enhanced complete lithium extraction from alkaline roasting slag of spodumene: kinetics and mechanism","authors":"Shengxuan Zhao , Enpei Zhu , Chao Luo , Li Zhu , Zhiqi Chen , Macong Duan , Xiaoyuan Li , Linqing Dai , Gengwei Zhang , Likang Fu , Libo Zhang , Yonggang Zuo , Bingguo Liu","doi":"10.1016/j.cep.2026.110699","DOIUrl":"10.1016/j.cep.2026.110699","url":null,"abstract":"<div><div>Lithium extraction from spodumene conventionally requires complex, energy-intensive processes involving high-temperature conversion of α-spodumene to β-spodumene, followed by acid roasting and leaching. Inspired by alkali fusion, we achieved microwave-assisted alkaline roasting of spodumene at only 250 °C, producing water- and acid-soluble salts and thereby substantially reducing the roasting temperature. However, efficient lithium recovery during subsequent leaching remains challenging. Here, we report an ultrasonic leaching (UL) strategy applied to microwave-roasted slag after water washing in a sulfuric acid medium. Under optimized conditions, lithium leaching efficiency reached 99.9%, representing a 27% improvement over conventional leaching (CL). Kinetic analysis revealed that ultrasound reduced the apparent activation energy from 32.61 kJ·mol<sup>-1</sup> (CL) to 20.68 kJ·mol<sup>-1</sup>. Mechanistic studies showed that ultrasound disrupts diffusion boundary layers, decreases particle size, and enhances interfacial mass transfer and infiltration, thereby accelerating lithium dissolution. This microwave-ultrasound synergistic strategy provides a highly efficient, sustainable, and environmentally friendly approach for lithium extraction, establishing a promising paradigm for process intensification in green hydrometallurgy.</div></div>","PeriodicalId":9929,"journal":{"name":"Chemical Engineering and Processing - Process Intensification","volume":"221 ","pages":"Article 110699"},"PeriodicalIF":3.9,"publicationDate":"2026-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145923455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-03DOI: 10.1016/j.cep.2026.110697
Saravana Kannan Thangavelu
The global transition toward low-carbon and sustainable energy systems has intensified research on bioethanol production from lignocellulosic and waste biomass, yet large-scale deployment remains limited by process complexity, feedstock heterogeneity, and fragmented optimization strategies that inadequately capture nonlinear interactions and multi-objective trade-offs. This review critically synthesizes recent advances in process intensification and optimization across the entire bioethanol production chain, encompassing pretreatment, hydrolysis, fermentation, and product recovery. Conventional statistical tools, including Response Surface Methodology, Central Composite Design, and Box–Behnken Design, remain valuable for structured experimentation and identification of local optima with minimal experimental effort; however, their predictive robustness diminishes in highly nonlinear, multivariable systems. In contrast, artificial intelligence and machine learning approaches such as Artificial Neural Networks, Support Vector Machines, Genetic Algorithms, Particle Swarm Optimization, and the Non-dominated Sorting Genetic Algorithm II enable accurate nonlinear modeling, global optimization, and explicit handling of conflicting objectives related to yield, energy consumption, inhibitor formation, and cost. Particular emphasis is placed on emerging hybrid frameworks that integrate statistical design, AI-based surrogate models, and metaheuristic optimization to enhance prediction fidelity, process efficiency, and scalability. Furthermore, advances in omics-guided metabolic engineering, green solvent pretreatments, lignin valorization, and digital twins, coupled with real-time AI-driven process control.
{"title":"From response surface methodology to artificial intelligence: process intensification frameworks for sustainable bioethanol production","authors":"Saravana Kannan Thangavelu","doi":"10.1016/j.cep.2026.110697","DOIUrl":"10.1016/j.cep.2026.110697","url":null,"abstract":"<div><div>The global transition toward low-carbon and sustainable energy systems has intensified research on bioethanol production from lignocellulosic and waste biomass, yet large-scale deployment remains limited by process complexity, feedstock heterogeneity, and fragmented optimization strategies that inadequately capture nonlinear interactions and multi-objective trade-offs. This review critically synthesizes recent advances in process intensification and optimization across the entire bioethanol production chain, encompassing pretreatment, hydrolysis, fermentation, and product recovery. Conventional statistical tools, including Response Surface Methodology, Central Composite Design, and Box–Behnken Design, remain valuable for structured experimentation and identification of local optima with minimal experimental effort; however, their predictive robustness diminishes in highly nonlinear, multivariable systems. In contrast, artificial intelligence and machine learning approaches such as Artificial Neural Networks, Support Vector Machines, Genetic Algorithms, Particle Swarm Optimization, and the Non-dominated Sorting Genetic Algorithm II enable accurate nonlinear modeling, global optimization, and explicit handling of conflicting objectives related to yield, energy consumption, inhibitor formation, and cost. Particular emphasis is placed on emerging hybrid frameworks that integrate statistical design, AI-based surrogate models, and metaheuristic optimization to enhance prediction fidelity, process efficiency, and scalability. Furthermore, advances in omics-guided metabolic engineering, green solvent pretreatments, lignin valorization, and digital twins, coupled with real-time AI-driven process control.</div></div>","PeriodicalId":9929,"journal":{"name":"Chemical Engineering and Processing - Process Intensification","volume":"221 ","pages":"Article 110697"},"PeriodicalIF":3.9,"publicationDate":"2026-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145923454","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-02DOI: 10.1016/j.cep.2025.110692
Muhammad Ammar Jaya , Musabbikhah , Ahmad Imam Rifa’i , Tri Widodo Besar Riyadi , Pranowo , Budi Kristiawan , Agung Tri Wijayanta
This study presents a computational analysis aimed at intensifying heat transfer in tubular heat exchangers through a combined passive enhancement strategy. The approach integrates twisted-tape inserts with an Al2O3/R134a nanorefrigerant at 0.1 vol% concentration to improve thermohydrodynamic performance. The novelty of this work lies in (i) establishing an entropy-based assessment framework that couples vortex generation with twisted-tape augmentation, and (ii) providing design-oriented insights for compact and multifunctional heat exchangers. Simulations were performed across Reynolds numbers ranging from 1750 to 18,000, encompassing both laminar and turbulent regimes, with twisted tapes featuring a twist ratio of 8.3, which promotes the formation of secondary vortices and enhances fluid mixing. Results indicate significant thermal enhancement: the Nusselt number increased by 106.7 % in laminar flow and 16.8 % in turbulent flow compared to the baseline. Incorporating the nanorefrigerant further amplified performance, achieving improvements of 238.3 % and 91.2 % in laminar and turbulent regimes, respectively. Entropy generation analysis revealed regime-dependent trends, with friction factors decreasing from 0.067 in laminar flow to 0.037 in turbulence due to intensified momentum transport. The superior performance under turbulence is attributed to enhanced thermal conductivity and augmented mixing mechanisms. The proposed framework offers practical guidelines for optimizing heat exchanger designs, contributing to sustainable process intensification in chemical engineering applications.
{"title":"Process intensification in tubular heat exchangers: Thermohydrodynamic analysis and entropy generation of Al2O3/R134a nanorefrigerant with twisted-tape enhancement across flow regimes","authors":"Muhammad Ammar Jaya , Musabbikhah , Ahmad Imam Rifa’i , Tri Widodo Besar Riyadi , Pranowo , Budi Kristiawan , Agung Tri Wijayanta","doi":"10.1016/j.cep.2025.110692","DOIUrl":"10.1016/j.cep.2025.110692","url":null,"abstract":"<div><div>This study presents a computational analysis aimed at intensifying heat transfer in tubular heat exchangers through a combined passive enhancement strategy. The approach integrates twisted-tape inserts with an Al<sub>2</sub>O<sub>3</sub>/R134a nanorefrigerant at 0.1 vol% concentration to improve thermohydrodynamic performance. The novelty of this work lies in (i) establishing an entropy-based assessment framework that couples vortex generation with twisted-tape augmentation, and (ii) providing design-oriented insights for compact and multifunctional heat exchangers. Simulations were performed across Reynolds numbers ranging from 1750 to 18,000, encompassing both laminar and turbulent regimes, with twisted tapes featuring a twist ratio of 8.3, which promotes the formation of secondary vortices and enhances fluid mixing. Results indicate significant thermal enhancement: the Nusselt number increased by 106.7 % in laminar flow and 16.8 % in turbulent flow compared to the baseline. Incorporating the nanorefrigerant further amplified performance, achieving improvements of 238.3 % and 91.2 % in laminar and turbulent regimes, respectively. Entropy generation analysis revealed regime-dependent trends, with friction factors decreasing from 0.067 in laminar flow to 0.037 in turbulence due to intensified momentum transport. The superior performance under turbulence is attributed to enhanced thermal conductivity and augmented mixing mechanisms. The proposed framework offers practical guidelines for optimizing heat exchanger designs, contributing to sustainable process intensification in chemical engineering applications.</div></div>","PeriodicalId":9929,"journal":{"name":"Chemical Engineering and Processing - Process Intensification","volume":"221 ","pages":"Article 110692"},"PeriodicalIF":3.9,"publicationDate":"2026-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145923576","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01DOI: 10.1016/j.cep.2026.110695
Khush Karan Gadra, Gaurav Ashok Bhaduri
Ex-situ CO₂ mineralisation is limited by slow CO₂ hydration rates and inefficient separation of precipitated carbonates, often requiring multiple reaction and solid–liquid handling steps. In this study, a Spiral Internal Draft Tube Reactor (SIDTR) is developed to intensify CO₂ mineralisation by integrating carbonation and CaCO₃ precipitation within a single hydrodynamic system. The reactor features an external spiral channel that establishes controlled circulation and pH zoning, enabling in-situ precipitation and settling of CaCO₃ while maintaining continuous CO₂ hydration in the draft-tube riser. The influence of spiral configuration, gas flow rate, and CO₂ concentration was systematically investigated. The six-turn spiral configuration (6SIDTR) yielded the highest mineralisation rate, achieving effective conversion even at 10% CO₂, representative of flue gas conditions. In continuous operation, the 6SIDTR achieved a 27.7 ± 0.08 % mineralisation efficiency, representing a 3.6-fold enhancement compared to a conventional bubble column under identical conditions. This reactor design reduces the conventional three-step mineralisation process to two units and offers a scalable route for process-intensified CO₂ mineralisation systems.
{"title":"Boosting CO2 mineralisation reaction with a spiral internal draft tube reactor: from concept to continuous operation","authors":"Khush Karan Gadra, Gaurav Ashok Bhaduri","doi":"10.1016/j.cep.2026.110695","DOIUrl":"10.1016/j.cep.2026.110695","url":null,"abstract":"<div><div>Ex-situ CO₂ mineralisation is limited by slow CO₂ hydration rates and inefficient separation of precipitated carbonates, often requiring multiple reaction and solid–liquid handling steps. In this study, a Spiral Internal Draft Tube Reactor (SIDTR) is developed to intensify CO₂ mineralisation by integrating carbonation and CaCO₃ precipitation within a single hydrodynamic system. The reactor features an external spiral channel that establishes controlled circulation and pH zoning, enabling in-situ precipitation and settling of CaCO₃ while maintaining continuous CO₂ hydration in the draft-tube riser. The influence of spiral configuration, gas flow rate, and CO₂ concentration was systematically investigated. The six-turn spiral configuration (6SIDTR) yielded the highest mineralisation rate, achieving effective conversion even at 10% CO₂, representative of flue gas conditions. In continuous operation, the 6SIDTR achieved a 27.7 ± 0.08 % mineralisation efficiency, representing a 3.6-fold enhancement compared to a conventional bubble column under identical conditions. This reactor design reduces the conventional three-step mineralisation process to two units and offers a scalable route for process-intensified CO₂ mineralisation systems.</div></div>","PeriodicalId":9929,"journal":{"name":"Chemical Engineering and Processing - Process Intensification","volume":"220 ","pages":"Article 110695"},"PeriodicalIF":3.9,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145880886","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31DOI: 10.1016/j.cep.2025.110693
Diana Carolina Barriga-Gómez , Juan Federico Herrera-Ruiz , Ricardo Morales-Rodriguez , Oscar Andrés Prado-Rubio
Succinic acid (SA) is a high-value platform chemical increasingly produced via microbial fermentation of renewable biomass. However, conventional biotransformations often face challenges such as low productivity, carbon utilization inefficiency, and energy-intensive downstream separation processes. Process Intensification (PI) offers a transformative framework to overcome these limitations, enabling more efficient, scalable, and sustainable production systems. To evidence how PI has shaped research in this area, a bibliometric analysis was first conducted, revealing PI as a central driver that connects strains, substrates, and reactor strategies within the field. This mapping provided the foundation for the second part of the study, a critical synthesis of the literature organized around the four PI domains: spatial, thermodynamic, functional, and temporal. Dominating technologies include membrane bioreactors, immobilized cell systems, in situ product recovery (ISPR), consolidated bioprocessing (CBP), and dynamic feeding operations. These approaches not only enhance key performance indexes such as yield, titer, and resource efficiency but also position bioprocessing as a convergent field integrating advanced materials, AI-based control, and solvent-free separations. Special attention is given to assessing technology readiness levels (TRLs), industrial scalability, and circular economic implications. Here in, it is shown how PI enables the transition to cleaner and more efficient bioprocesses, by aligning SA production with climate targets and the broader objectives of the United Nations 2030 Agenda for Sustainable Development.
{"title":"Innovative technologies for succinic acid fermentation: A path to sustainable production","authors":"Diana Carolina Barriga-Gómez , Juan Federico Herrera-Ruiz , Ricardo Morales-Rodriguez , Oscar Andrés Prado-Rubio","doi":"10.1016/j.cep.2025.110693","DOIUrl":"10.1016/j.cep.2025.110693","url":null,"abstract":"<div><div>Succinic acid (SA) is a high-value platform chemical increasingly produced via microbial fermentation of renewable biomass. However, conventional biotransformations often face challenges such as low productivity, carbon utilization inefficiency, and energy-intensive downstream separation processes. Process Intensification (PI) offers a transformative framework to overcome these limitations, enabling more efficient, scalable, and sustainable production systems. To evidence how PI has shaped research in this area, a bibliometric analysis was first conducted, revealing PI as a central driver that connects strains, substrates, and reactor strategies within the field. This mapping provided the foundation for the second part of the study, a critical synthesis of the literature organized around the four PI domains: spatial, thermodynamic, functional, and temporal. Dominating technologies include membrane bioreactors, immobilized cell systems, <em>in situ</em> product recovery (ISPR), consolidated bioprocessing (CBP), and dynamic feeding operations. These approaches not only enhance key performance indexes such as yield, titer, and resource efficiency but also position bioprocessing as a convergent field integrating advanced materials, AI-based control, and solvent-free separations. Special attention is given to assessing technology readiness levels (TRLs), industrial scalability, and circular economic implications. Here in, it is shown how PI enables the transition to cleaner and more efficient bioprocesses, by aligning SA production with climate targets and the broader objectives of the United Nations 2030 Agenda for Sustainable Development.</div></div>","PeriodicalId":9929,"journal":{"name":"Chemical Engineering and Processing - Process Intensification","volume":"221 ","pages":"Article 110693"},"PeriodicalIF":3.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145923579","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31DOI: 10.1016/j.cep.2025.110689
Carmen M. Sánchez-Arévalo , Laura García-Suarez , Maria Salud Camilleri-Rumbau , Jörg Vogel , Silvia Álvarez-Blanco , M. Cinta Vincent-Vela , Beatriz Cuartas-Uribe
The concerning and abundant textile wastewater can be treated by forward osmosis (FO) in order to reduce its volume and simultaneously recover clean water. However, the productivity of FO depends on the concentration of the draw solution that is used. In this work, a simultaneous application of FO and reverse osmosis (RO) is proposed. The HFFO14® FO membrane (Aquaporin, Denmark) was employed to concentrate a real textile wastewater, whereas the SW30-2540 (DuPont, USA) RO membrane was employed to simultaneously regenerate the draw solution, which consisted in a 0.7 M NaCl solution, and to obtain a clean water stream. The concentration of the textile wastewater increased until 90% water recovery was achieved. The rejection values obtained for the chemical oxygen demand and total organic carbon were in the range 99 – 100%. Afterwards, the previously concentrated textile wastewater was again processed until a volume concentration factor of 16.5 was reached. Stable values of permeate flux (around 4 L/h·m2) were obtained in the FO process, whereas the reverse osmosis step permitted the maintenance of a stable conductivity in the draw solution and provided clean water as permeate.
利用正向渗透技术处理大量的纺织废水,既可以减少废水的体积,又可以回收清洁水。然而,FO的生产效率取决于所使用的拉伸溶液的浓度。在这项工作中,提出了FO和反渗透(RO)的同时应用。采用HFFO14®FO膜(丹麦Aquaporin公司)对真实纺织废水进行浓缩,同时采用SW30-2540(美国杜邦公司)反渗透膜对含有0.7 M NaCl溶液的提取液进行再生,获得干净的水流。纺织废水的浓度不断提高,直至水回收率达到90%。化学需氧量和总有机碳的截留值在99 ~ 100%之间。然后再对先前浓缩的纺织废水进行处理,使其体积浓度系数达到16.5。在FO过程中获得了稳定的渗透通量值(约4 L/h·m2),而反渗透步骤允许在抽取溶液中保持稳定的电导率,并提供清洁的水作为渗透。
{"title":"Continuous regeneration of the draw solution in textile wastewater treatment using a combination of simultaneous forward osmosis and reverse osmosis","authors":"Carmen M. Sánchez-Arévalo , Laura García-Suarez , Maria Salud Camilleri-Rumbau , Jörg Vogel , Silvia Álvarez-Blanco , M. Cinta Vincent-Vela , Beatriz Cuartas-Uribe","doi":"10.1016/j.cep.2025.110689","DOIUrl":"10.1016/j.cep.2025.110689","url":null,"abstract":"<div><div>The concerning and abundant textile wastewater can be treated by forward osmosis (FO) in order to reduce its volume and simultaneously recover clean water. However, the productivity of FO depends on the concentration of the draw solution that is used. In this work, a simultaneous application of FO and reverse osmosis (RO) is proposed. The HFFO14® FO membrane (Aquaporin, Denmark) was employed to concentrate a real textile wastewater, whereas the SW30-2540 (DuPont, USA) RO membrane was employed to simultaneously regenerate the draw solution, which consisted in a 0.7 M NaCl solution, and to obtain a clean water stream. The concentration of the textile wastewater increased until 90% water recovery was achieved. The rejection values obtained for the chemical oxygen demand and total organic carbon were in the range 99 – 100%. Afterwards, the previously concentrated textile wastewater was again processed until a volume concentration factor of 16.5 was reached. Stable values of permeate flux (around 4 L/h·m<sup>2</sup>) were obtained in the FO process, whereas the reverse osmosis step permitted the maintenance of a stable conductivity in the draw solution and provided clean water as permeate.</div></div>","PeriodicalId":9929,"journal":{"name":"Chemical Engineering and Processing - Process Intensification","volume":"221 ","pages":"Article 110689"},"PeriodicalIF":3.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145923577","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31DOI: 10.1016/j.cep.2025.110690
Hao CHENG , Yongli LI , Dominique TARLET , Lingai LUO , Yilin FAN
The power-to-gas (PtG) process converts surplus renewable electricity into hydrogen via electrolysis, followed by methanation to produce synthetic methane. This integrated approach enhances the flexibility of hydrogen energy storage and transportation while achieves valorization, supporting and advancing the UN's sustainable development goals. Traditional methanation in large fixed-bed equipment suffers from limited heat and mass transfer efficiency, leading to the catalyst deactivation and compromised methanation performance. To overcome these challenges, microchannel-based reactors have been proposed as an alternate solution, offering enhanced heat and mass transfer performance, compact system volume, higher volumetric productivity and improved energy efficiency.
This paper presents a comprehensive literature review on research advances of the microchannel reactor technology for methanation. The review covers various aspects, including catalysts configuration, effects of operating factors, and strategies to intensify the methanation performance. In addition, special attention was given to integrated process coupling within methanation reaction, improving both reaction regulation and thermal energy management in methanation systems. The work provides a useful reference for developing high-efficiency microchannel reactor systems for methanation, offering fundamental insights for future industrial-scale implementation.
{"title":"Microreactor technology for CO2 methanation: A review on process intensification and system integration","authors":"Hao CHENG , Yongli LI , Dominique TARLET , Lingai LUO , Yilin FAN","doi":"10.1016/j.cep.2025.110690","DOIUrl":"10.1016/j.cep.2025.110690","url":null,"abstract":"<div><div>The power-to-gas (PtG) process converts surplus renewable electricity into hydrogen via electrolysis, followed by <span><math><mrow><mi>C</mi><msub><mi>O</mi><mn>2</mn></msub></mrow></math></span> methanation to produce synthetic methane. This integrated approach enhances the flexibility of hydrogen energy storage and transportation while achieves <span><math><mrow><mi>C</mi><msub><mi>O</mi><mn>2</mn></msub></mrow></math></span> valorization, supporting and advancing the UN's sustainable development goals. Traditional <span><math><mrow><mi>C</mi><msub><mi>O</mi><mn>2</mn></msub></mrow></math></span>methanation in large fixed-bed equipment suffers from limited heat and mass transfer efficiency, leading to the catalyst deactivation and compromised methanation performance. To overcome these challenges, microchannel-based reactors have been proposed as an alternate solution, offering enhanced heat and mass transfer performance, compact system volume, higher volumetric productivity and improved energy efficiency.</div><div>This paper presents a comprehensive literature review on research advances of the microchannel reactor technology for <span><math><mrow><mi>C</mi><msub><mi>O</mi><mn>2</mn></msub></mrow></math></span> methanation. The review covers various aspects, including catalysts configuration, effects of operating factors, and strategies to intensify the <span><math><mrow><mi>C</mi><msub><mi>O</mi><mn>2</mn></msub></mrow></math></span> methanation performance. In addition, special attention was given to integrated process coupling within methanation reaction, improving both reaction regulation and thermal energy management in methanation systems. The work provides a useful reference for developing high-efficiency microchannel reactor systems for <span><math><mrow><mi>C</mi><msub><mi>O</mi><mn>2</mn></msub></mrow></math></span> methanation, offering fundamental insights for future industrial-scale implementation.</div></div>","PeriodicalId":9929,"journal":{"name":"Chemical Engineering and Processing - Process Intensification","volume":"221 ","pages":"Article 110690"},"PeriodicalIF":3.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145923581","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Currently, Mexican sugar mills, in addition to producing saccharose as their main product, obtain molasses as a byproduct and bagasse as an agro-industrial waste. Molasses is marketed or used in distilleries within the mill to produce anhydrous ethanol, but with low profitability. Bagasse is burned to produce steam and electricity, generating environmental problems. Therefore, from a circular economy perspective, the objective of this study is to propose a strategy for the modernization and adaptation of a sugar mill to a biorefinery to diversify the commercialization of its products, improving the economics and sustainability of the industrial process. The proposed methodology considers the design, simulation, and technoeconomic evaluation of a sugarcane biorefinery to produce citric acid and biofertilizer using two scenarios: one using bagasse and the other using molasses as feedstocks. The study first considers an analysis of the Mexican market to determine the availability of feedstocks and the installed capacity of the proposed biorefinery. Next, the operation mode of the fermentation reactor (i.e., batch or fed-batch) is studied as a strategy to increase citric acid productivity. Finally, the biorefinery is technically and economically evaluated under different operating conditions to determine the feasibility and profitability of the industrial process.
{"title":"Citric acid production: A comprehensive assessment from a fermentation strategy to a circular economy process","authors":"Teresa Lopez-Arenas , Kevin Palacios-Samano , Hector Hernandez-Escoto , Mauricio Sales-Cruz","doi":"10.1016/j.cep.2025.110694","DOIUrl":"10.1016/j.cep.2025.110694","url":null,"abstract":"<div><div>Currently, Mexican sugar mills, in addition to producing saccharose as their main product, obtain molasses as a byproduct and bagasse as an agro-industrial waste. Molasses is marketed or used in distilleries within the mill to produce anhydrous ethanol, but with low profitability. Bagasse is burned to produce steam and electricity, generating environmental problems. Therefore, from a circular economy perspective, the objective of this study is to propose a strategy for the modernization and adaptation of a sugar mill to a biorefinery to diversify the commercialization of its products, improving the economics and sustainability of the industrial process. The proposed methodology considers the design, simulation, and technoeconomic evaluation of a sugarcane biorefinery to produce citric acid and biofertilizer using two scenarios: one using bagasse and the other using molasses as feedstocks. The study first considers an analysis of the Mexican market to determine the availability of feedstocks and the installed capacity of the proposed biorefinery. Next, the operation mode of the fermentation reactor (i.e., batch or fed-batch) is studied as a strategy to increase citric acid productivity. Finally, the biorefinery is technically and economically evaluated under different operating conditions to determine the feasibility and profitability of the industrial process.</div></div>","PeriodicalId":9929,"journal":{"name":"Chemical Engineering and Processing - Process Intensification","volume":"221 ","pages":"Article 110694"},"PeriodicalIF":3.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145923578","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-30DOI: 10.1016/j.cep.2025.110688
Lei Zhang , Yuyao Lou , Liwei Meng , Tianxiang Li , Tongxun Liu , Xue Han , Yafei Wang
Pd-based membrane reactors (PMRs) offer a promising approach for on-board bioethanol reforming hydrogen production in fuel cell vehicles (FCVs). However, the model of the palladium membrane reactor (PMR) is urgently needed for on-board hydrogen supply. This study developed a kinetic model for single-tube Pd membrane reactors (PMRs) with autothermal reforming (ATR) to systematically evaluate key parameters: reactor length-to-diameter ratio (L/D), gas hourly space velocity (GHSV = 1, 000–3, 000 h-1), membrane insertion ratio (20–80 %), and catalyst stacking ratio (Volumetric catalyst stacking per unit palladium film area) (2–5 mL/cm2). When membrane insertion ratios ranged from 40 % to 50 %, hydrogen yield (∼5.7 mol/mol), hydrogen recovery (∼96 %), and hydrogen production rate (1.24 g/h) simultaneously reached peak values. In a 7-tube PMR configuration, the hydrogen production rate increased to 7.7 g/h, but hydrogen yield and recovery decreased. The incorporation of baffle plates as turbulence promoters enhanced hydrogen recovery from 80 % to 91 %. In the optimized four-layer PMR design with 37 tubes, the hydrogen production rate reached 41.3 g/h. Furthermore, the conceptual full-scale PMR for fuel cell vehicles is more compact than conventional high-pressure hydrogen storage tanks. This integrated ATR approach with multitubular designs and turbulence promoters enables efficient compact on-board hydrogen production.
{"title":"Enhancing hydrogen production in Pd-based membrane reactors via bioethanol autothermal reforming: Turbulence promoters and multitubular designs","authors":"Lei Zhang , Yuyao Lou , Liwei Meng , Tianxiang Li , Tongxun Liu , Xue Han , Yafei Wang","doi":"10.1016/j.cep.2025.110688","DOIUrl":"10.1016/j.cep.2025.110688","url":null,"abstract":"<div><div>Pd-based membrane reactors (PMRs) offer a promising approach for on-board bioethanol reforming hydrogen production in fuel cell vehicles (FCVs). However, the model of the palladium membrane reactor (PMR) is urgently needed for on-board hydrogen supply. This study developed a kinetic model for single-tube Pd membrane reactors (PMRs) with autothermal reforming (ATR) to systematically evaluate key parameters: reactor length-to-diameter ratio (L/D), gas hourly space velocity (GHSV = 1, 000–3, 000 h<sup>-1</sup>), membrane insertion ratio (20–80 %), and catalyst stacking ratio (Volumetric catalyst stacking per unit palladium film area) (2–5 mL/cm<sup>2</sup>). When membrane insertion ratios ranged from 40 % to 50 %, hydrogen yield (∼5.7 mol/mol), hydrogen recovery (∼96 %), and hydrogen production rate (1.24 g/h) simultaneously reached peak values. In a 7-tube PMR configuration, the hydrogen production rate increased to 7.7 g/h, but hydrogen yield and recovery decreased. The incorporation of baffle plates as turbulence promoters enhanced hydrogen recovery from 80 % to 91 %. In the optimized four-layer PMR design with 37 tubes, the hydrogen production rate reached 41.3 g/h. Furthermore, the conceptual full-scale PMR for fuel cell vehicles is more compact than conventional high-pressure hydrogen storage tanks. This integrated ATR approach with multitubular designs and turbulence promoters enables efficient compact on-board hydrogen production.</div></div>","PeriodicalId":9929,"journal":{"name":"Chemical Engineering and Processing - Process Intensification","volume":"220 ","pages":"Article 110688"},"PeriodicalIF":3.9,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145880887","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}