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Fallen leaves to sustainable energy solution: review on hydrogen production 从落叶到可持续能源解决方案:氢气生产回顾
Pub Date : 2024-08-27 DOI: 10.1039/D4SU00356J
Kyu Kyu Tin, Wirach Taweepreda, Akanksha Singh, Naresh Kumar Wagri and Anil Kumar

Fallen leaves represent a significant feedstock for hydrogen production due to their high cellulose content, abundance, and minimal sulfur content. These characteristics make them suitable for various hydrogen production technologies, including biohydrogen and biomass-derived liquid reforming processes, contributing to sustainable energy production. This comprehensive literature review explores fallen leaves as a low-cost biomass feedstock for hydrogen production in the pursuit of zero-carbon and sustainable energy solutions. Steam methane reforming, while cost-effective and possessing high production capacity, results in substantial carbon emissions. In contrast, electrolysis, leveraging renewable resources, is attractive but requires significant energy input. Biomass gasification and thermochemical processes show promise for sustainable hydrogen production, though further technological advancements are necessary. Additionally, anaerobic fermentation by microorganisms can directly produce hydrogen from biomass (including fallen leaves), offering an energy-efficient method that utilizes organic waste. This review evaluates hydrogen production concerning energy efficiency, economics, and environmental impact. The findings contribute to the global transition from fossil fuels to renewable energy sources, aligning with climate commitments and the goal of carbon neutrality.

落叶由于纤维素含量高、数量多且含硫量极低,是制氢的重要原料。这些特点使其适合各种制氢技术,包括生物氢和生物质衍生液体重整工艺,从而为可持续能源生产做出贡献。本综合文献综述探讨了落叶作为制氢的低成本生物质原料,以实现零碳和可持续能源解决方案。蒸汽甲烷转化虽然具有成本效益和高产能,但会导致大量碳排放。相比之下,利用可再生资源的电解法很有吸引力,但需要大量能源投入。生物质气化和热化学工艺显示了可持续制氢的前景,但还需要进一步的技术进步。此外,微生物厌氧发酵可直接从生物质(包括落叶)中制氢,提供了一种利用有机废物的节能方法。本综述对氢气生产的能效、经济性和环境影响进行了评估。研究结果有助于全球从化石燃料向可再生能源过渡,符合气候承诺和碳中和目标。
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引用次数: 0
Sustainable agro-waste pellets as granular slow-release fertilizer carrier systems for ammonium sulfate† 作为硫酸铵颗粒缓释肥料载体系统的可持续农业废弃物颗粒
Pub Date : 2024-08-27 DOI: 10.1039/D4SU00141A
B. G. K. Steiger, N. T. Bui, B. M. Babalola and L. D. Wilson

In this study, several granular biocomposite carrier systems were prepared that contain biomaterials (chitosan, torrefied wheat straw and avian eggshells) as additive components at variable composition. The biocomposites were loaded with ammonium sulfate (AS) by two methods: (1) in situ addition of AS during pellet preparation, and (2) an adsorption method of AS after pellet preparation. Characterisation was carried out via spectroscopy (XRD, FT-IR) and complementary methods (TGA, acid stability). The pellet system (C1) by method (1) contained ca. 22 mg per g NH4+, whereas pellet systems by method (2) contained up to ca. 40 mg per g NH4+. The mol-ratio of NH4+ : SO42− varied from 2.18 (C1) to 2.72 (CW72), 2.97 (CW20), 2.64 (CW21) and 3.20 (CW22). Release studies in water showed that C1 pellets released almost 100% NH4+ within 3 h, while release varied from ca. 60% (CW72), ca. 40% (C20), 20% (C21) to 10% (CW22). By comparison, the systems prepared through method (2) showed a marginal increase of the release profiles up to 96 h. Granular AS carrier systems prepared by method (2) displayed greater mechanical stability and AS content versus the systems prepared by method (1). We demonstrated the ability to tailor the physico-chemical properties of such biocomposite carriers and highlight their promising potential as slow-release fertilizer systems.

本研究制备了几种颗粒状生物复合材料载体系统,其中含有不同成分的生物材料(壳聚糖、干麦秆和禽蛋壳)作为添加剂。通过两种方法在生物复合材料中添加硫酸铵(AS):(1) 在制备颗粒时原位添加 AS,(2) 在制备颗粒后采用吸附法添加 AS。通过光谱(XRD、FT-IR)和补充方法(TGA、酸稳定性)进行了表征。采用方法(1)制备的颗粒体系(C1)每克含有约 22 毫克 NH4+,而采用方法(2)制备的颗粒体系每克含有约 40 毫克 NH4+。NH4+ :SO42- 的摩尔比从 2.18(C1)到 2.72(CW72)、2.97(CW20)、2.64(CW21)和 3.20(CW22)不等。在水中的释放研究表明,C1 颗粒在 3 小时内几乎释放了 100%的 NH4+,而释放量则从约 60%(CW72)、约 40%(C20)、20%(C21)到 10%(CW22)不等。与方法(1)相比,方法(2)制备的颗粒状 AS 载体系统具有更高的机械稳定性和 AS 含量。我们证明了定制此类生物复合载体物理化学特性的能力,并强调了其作为缓释肥料系统的巨大潜力。
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引用次数: 0
Greener nanobiopolymers and nanoencapsulation: environmental implications and future prospects 更环保的纳米生物聚合物和纳米封装:环境影响与未来前景
Pub Date : 2024-08-23 DOI: 10.1039/D4SU00411F
Shikha Gulati, Anoushka Amar, Lakshita Chhabra, Riya Katiyar, Meenakshi, Tanu Sahu and Rajender S. Varma

To minimize the consumption of nonrenewable resources and ensure environmental sustainability, there ought to be greater utilization of abundant and renewable greener nanobiopolymers, particularly those derived from various plants and microbes. This article discusses the various types, origins, and synthesis methods of biopolymers, including those that come from natural resources and microorganisms, with a focus on their properties in nanoformat; the most common and recently researched nanobiopolymers have been deliberated. In addition, discussion on various synthesis steps and structural characterization of green polymeric materials such as cellulose, chitin, and lignin is also incorporated. A comprehensive discussion of greener nanobiopolymers with illustrative examples has been presented for the last five years comprising their diverse types and topologies including the environmental improvements realized via the deployment of nanoencapsulation, especially the applications of polymer nanoencapsulated materials in wastewater and soil treatment. The emphasis on the use of greener nanobiopolymers for sustainable environmental remediation is specifically highlighted for the decontamination of soil, water, and air with the main objective being to offer an overview of their adaptability embracing nanotechnology. This effort could stimulate additional research in their deployment in practical environmental applications.

为了最大限度地减少不可再生资源的消耗,确保环境的可持续发展,应该更多地利用丰富的可再生绿色纳米生物聚合物,特别是那些从各种植物和微生物中提取的聚合物。本文讨论了生物聚合物(包括来自自然资源和微生物的生物聚合物)的各种类型、起源和合成方法,重点关注其在纳米格式中的特性;并讨论了最常见和最新研究的纳米生物聚合物。此外,还讨论了纤维素、甲壳素和木质素等绿色聚合物材料的各种合成步骤和结构特征。该书全面论述了过去五年中绿色纳米生物聚合物的各种类型和拓扑结构,包括通过部署纳米封装实现的环境改善,特别是聚合物纳米封装材料在废水和土壤处理中的应用,并列举了一些实例。重点强调了将更环保的纳米生物聚合物用于可持续的环境修复,特别是用于土壤、水和空气的净化,主要目的是概述纳米技术的适应性。这项工作可以促进在实际环境应用中使用纳米生物聚合物的更多研究。
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引用次数: 0
Introduction of the first commercial biobased benzoxazines for the manufacturing of fibre reinforced polymers† 推出首款用于制造纤维增强聚合物的商用生物基苯并恶嗪
Pub Date : 2024-08-22 DOI: 10.1039/D4SU00192C
Gideon Abels, Katharina Koschek, Paul Jones and Wendy Howarth

Benzoxazines are a promising material class due to their flexible molecular design, high thermomechanical properties, and inherent flame retardancy. Especially the latter makes them interesting for all kinds of applications, for example lightweight constructions in the transportation sector. The first commercial benzoxazines were based on bisphenol and aniline, petrochemical resources produced from crude oil. However, due to the growing demand for more sustainable materials the use of biobased resources for benzoxazine synthesis has been thoroughly investigated in the past years. In this work, we present the first commercial benzoxazines that consist of biobased compounds. After analysing the curing behaviour of these new resins using thermal analysis, polymers are manufactured and characterised from them. Finally, the resins were used for manufacturing fibre-reinforced polymers (FRP) for flame-retardant lightweight applications. Thermomechanical and combustion analysis showed that the polymers achieve high flexural moduli up to 2.8 MPa and glass transition temperatures of 100 °C and 141 °C. In addition, the biobased benzoxazines have promising flame-retardancy due to intumescence, resulting in high LOI values of 31.4 ± 0.2 and 33.3 ± 0.1%

苯并噁嗪具有灵活的分子设计、较高的热机械性能和固有的阻燃性,是一种前景广阔的材料。尤其是后者,使其在各种应用领域(如运输领域的轻质结构)中都具有很强的吸引力。最早的商用苯并噁嗪是基于从原油中提取的石化资源双酚和苯胺。然而,由于对更具可持续性材料的需求日益增长,过去几年中,人们对使用生物基资源合成苯并恶嗪进行了深入研究。在这项工作中,我们首次提出了由生物基化合物组成的商用苯并恶嗪。在利用热分析方法分析了这些新树脂的固化行为后,我们用它们制造了聚合物并对其进行了表征。最后,这些树脂被用于制造阻燃轻质应用的纤维增强聚合物(FRP)。热力学和燃烧分析表明,聚合物的弯曲模量高达 2.8 兆帕,玻璃化转变温度分别为 100 °C 和 141 °C。此外,生物基苯并噁嗪因膨胀而具有良好的阻燃性,其 LOI 值分别为 31.4 ± 0.2 和 33.3 ± 0.1%。
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引用次数: 0
Safe-and-sustainable-by-design roadmap: identifying research, competencies, and knowledge sharing needs 安全可持续的设计路线图:确定研究、能力和知识共享需求
Pub Date : 2024-08-19 DOI: 10.1039/D4SU00310A
Christina Apel, Akshat Sudheshwar, Klaus Kümmerer, Bernd Nowack, Klara Midander, Emma Strömberg and Lya G. Soeteman-Hernández

The European Chemicals Strategy for Sustainability introduces the Safe-and-Sustainable-by-Design (SSbD) concept. It goes beyond current regulatory compliance and aims to ensure the safety and sustainability of (novel) chemicals, materials, products, and processes. It starts at early-innovation stages and follows the chemicals and materials throughout their entire lifecycle. This perspective paper presents an SSbD roadmap that explores current needs and gives recommendations for the practical operationalization of SSbD in industrial operations and processes. This roadmap was co-created including different SSbD stakeholders and encompasses three interlinked agendas on (i) research needs, (ii) skills, competencies, and education needs, and (iii) knowledge and information sharing needs. An overarching need is the development of a common understanding of SSbD with clear definitions, terminology, and criteria. In addition, SSbD operationalisation needs to be pragmatic and applied as early as possible in the innovation process. From a research needs perspective, it is essential to integrate the different fields of innovation, safety, and sustainability. From a skills, competencies and education perspective, targeted training is needed that balances the depth and breadth of SSbD required for a specific audience. These trainings should not only convey hard/technical skills, but also soft/social skills to support more sustainability-oriented decisions on all levels. From a knowledge and information sharing perspective, a strategic plan and a trusted environment are needed to support dialogue between all SSbD stakeholders while at the same time protecting intellectual property (IP). The roadmap should help to coordinate planning for the implementation of SSbD at industrial, academic, policy, and regulatory level by defining actions and raise strategic efforts.

欧洲化学品可持续发展战略》引入了 "安全可持续设计"(SSbD)概念。它超越了当前的法规遵从性,旨在确保(新型)化学品、材料、产品和工艺的安全性和可持续性。它始于早期创新阶段,并贯穿化学品和材料的整个生命周期。本视角文件介绍了 SSbD 路线图,探讨了当前的需求,并就 SSbD 在工业运营和工艺流程中的实际操作提出了建议。该路线图由不同的 SSbD 利益相关者共同制定,包括三个相互关联的议程:(i) 研究需求;(ii) 技能、能力和教育需求;(iii) 知识和信息共享需求。最重要的需求是通过明确的定义、术语和标准形成对 SSbD 的共同理解。此外,SSbD 的可操作性需要务实,并在创新过程中尽早应用。从研究需求的角度来看,必须整合创新、安全和可持续性等不同领域。从技能、能力和教育的角度来看,需要开展有针对性的培训,以平衡特定受众所需的 SSbD 深度和广度。这些培训不仅要传授硬技能/技术技能,还要传授软技能/社会技能,以支持在各个层面做出更加以可持续发展为导向的决策。从知识和信息共享的角度来看,需要一个战略计划和一个值得信赖的环境,以支持所有 SSbD 利益相关者之间的对话,同时保护知识产权(IP)。路线图应通过确定行动和提高战略努力,帮助协调在工业、学术、政策和监管层面实施 SSbD 的规划。
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引用次数: 0
Electrocatalytic hydrogenation of the formyl group and heteroaromatic ring in furfural on activated carbon cloth-supported ruthenium† 在活性碳布支撑的钌上对糠醛中的甲酰基和杂芳环进行电催化加氢反应
Pub Date : 2024-08-19 DOI: 10.1039/D4SU00260A
Meheryar R. Kasad, James E. Jackson and Christopher M. Saffron

Electrocatalytic hydrogenation (ECH) was explored as a mild technique (≤50 °C under atmospheric pressure) to produce valuable products from furfural, a promising biomass-derived platform chemical. In situ hydrogen equivalents made by water splitting were used to reduce the formyl group and saturate the heteroaromatic ring of furfural on an activated carbon cloth-supported ruthenium electrocatalyst. A systematic study was conducted to understand the relationship between the reaction conditions and the products. The factors analyzed include catholyte solution organic co-solvent content, catholyte solution acid content, and temperature. Acidity of the catholyte solution had the most significant effect on the yield of tetrahydrofurfuryl alcohol (THFA). The highest THFA yield was obtained in mildly acidic catholyte solutions (0.02 M HCl and 0.002 M HCl–0.02 M NaCl). The low carbon mole balance closure in the experiments was attributed to the side reactions of the reactants, intermediates, and products. The effects of current density on faradaic efficiency and of the functional groups attached to the furan ring on the formation of saturated heterocyclic products were also explored.

电催化加氢(ECH)作为一种温和的技术(常压下温度≤50 °C),被用来从糠醛(一种有前景的生物质衍生平台化学品)中生产有价值的产品。利用水分裂产生的原位氢当量,在活性炭布支撑的钌电催化剂上还原糠醛的甲酰基并使其杂芳环饱和。为了解反应条件与产物之间的关系,进行了系统研究。分析的因素包括阴溶液中有机助溶剂的含量、阴溶液中酸的含量和温度。电解质溶液的酸度对四氢呋喃甲醇(THFA)的产率影响最大。在弱酸性的阴溶液(0.02 M HCl 和 0.002 M HCl-0.02 M NaCl)中,四氢糠醇的产量最高。实验中出现的低碳分子平衡闭合是由于反应物、中间产物和产物的副反应造成的。此外,还探讨了电流密度对法拉第效率的影响,以及呋喃环上的官能团对饱和杂环产物形成的影响。
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引用次数: 0
Addressing the persistence of per- and poly-fluoroalkyl substances (PFAS): current challenges and potential solutions 解决全氟烷基和多氟烷基物质(PFAS)的持久性问题:当前的挑战和潜在的解决方案
Pub Date : 2024-08-14 DOI: 10.1039/d4su00152d
Emeka J. Itumoh, Shailja Data, Jack L.-Y. Chen, Melanie Kah, Lokesh P. Padhye, Erin M. Leitao
The combined stability, mobility, and bioaccumulation of per- and poly-fluoroalkyl substances (PFAS) has prompted a global environmental crisis. PFAS have unique properties owing to their strong, hydrophobic C–F bonds, which result in their resistance to water, oil, chemicals, and heat. Applications of PFAS include their use as water-, grease-, and fire-proof coatings, emulsifiers, and surfactants, spanning most manufacturing sectors. The continued regulation of specific PFAS provides significant research opportunities for chemists and their collaborators across environmental, social, engineering, and materials sciences. Solutions in the areas of detection and analysis, immobilisation and destruction, and the creation of viable and safe alternatives are urgently needed. In this tutorial review, PFAS and their associated challenges are described, followed by a summary of existing solutions and future research opportunities.
全氟烷基和多氟烷基物质(PFAS)兼具稳定性、流动性和生物蓄积性,已引发全球环境危机。全氟辛烷磺酸具有独特的性质,因为它们具有很强的疏水性 C-F 键,从而具有耐水、耐油、耐化学品和耐热的特性。PFAS 的应用包括用作防水、防油和防火涂料、乳化剂和表面活性剂,遍及大多数制造行业。对特定 PFAS 的持续监管为化学家及其环境、社会、工程和材料科学领域的合作者提供了重要的研究机会。我们迫切需要在检测和分析、固定和销毁以及创造可行和安全的替代品方面找到解决方案。本教程综述介绍了全氟辛烷磺酸及其相关挑战,随后总结了现有的解决方案和未来的研究机会。
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引用次数: 0
Magnetic polyvinylpolypyrrolidone polymer composite-supported copper(i) catalyst: an efficient and easily reusable catalyst for sustainable synthesis of 1,2,3-triazoles in water†‡ 磁性聚乙烯基吡咯烷酮聚合物复合材料支撑的铜(I)催化剂:一种高效且易于重复使用的催化剂,可用于在水中可持续合成 1,2,3-三唑
Pub Date : 2024-08-14 DOI: 10.1039/D4SU00292J
Noura Aflak, Fatima-Ezzahraa Essebbar, Lahoucine Bahsis, Hicham Ben El Ayouchia, Hafid Anane, Miguel Julve and Salah-Eddine Stiriba

The development of sustainable products and processes involves the use of green chemistry principles. A new and facile synthesis of a recoverable copper(I) catalyst supported on magnetic crosslinked polyvinylpolypyrrolidone (Fe3O4-PVPP) for the synthesis of 1,2,3-triazole derivatives under copper-catalyzed azide–alkyne cycloaddition reactions (CuAAC) is presented in this study. The magnetic support was prepared by in situ co-precipitation of Fe3O4 in polyvinylpolypyrrolidone followed by immobilization of copper(I) on the magnetic support to afford a Cu(I)/PVPP-Fe3O4 composite, which was characterized using several techniques. Its catalytic efficiency in CuAAC working under low copper catalyst loading leads to the selective synthesis of 1,4-disubstituted-1,2,3-triazoles with good to excellent yields. The green aspect of this catalytic process relies on using water as catalytic reaction medium, working at room temperature, easy isolation of 1,2,3-triazoles and simple separation of the composite catalyst by exposure to an external magnet for recovery and further reuse. The greenness of the procedure was also assessed through the atom economy (AE), E-factor and EcoScale, showing low waste generation and better sustainability scores.

可持续产品和工艺的开发需要利用绿色化学原理。本研究提出了一种在磁性交联聚乙烯基聚吡咯烷酮(Fe3O4-PVPP)上支撑的可回收铜(I)催化剂的新型简便合成方法,用于在铜催化叠氮-炔环加成反应(CuAAC)中合成 1,2,3- 三唑衍生物。磁性支持物是通过在聚乙烯吡咯烷酮中原位共沉淀 Fe3O4 制备的,然后将铜(I)固定在磁性支持物上,得到 Cu(I)/PVPP-Fe3O4 复合材料。在低铜催化剂负载条件下,该复合材料在 CuAAC 中的催化效率高,可选择性地合成 1,4-二取代的-1,2,3-三唑,产率高至极佳。该催化过程的绿色环保性依赖于使用水作为催化反应介质,在室温下工作,易于分离 1,2,3-三唑,以及通过将复合催化剂暴露在外部磁铁下进行简单分离,以便回收和进一步再利用。此外,还通过原子经济(AE)、E-因子和 EcoScale 对该程序的绿色环保性进行了评估,结果显示废物产生量低,可持续性得分较高。
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引用次数: 0
Multi-functional syringol based epoxides and properties of their thermoset polymers 多功能丁香酚基环氧化物及其热固性聚合物的性能
Pub Date : 2024-08-13 DOI: 10.1039/D4SU00320A
Melissa Sanchez, Peter C. Ford and Mahdi M. Abu-Omar

Lignin-based syringol monomer, 2,6-dimethoxypropylphenol (DMPP), can be upgraded through two synthetic routes to multi-functional propylpyrogallol DMPPO. With three hydroxyl groups, DMPPO can serve as a renewable polymer building block. In this study, we describe the synthesis and characterization of DMPPO epoxide mixtures based on their synthesis methodology; one route uses HBr, another a greener methodology with Nb2O5 catalyst in water. Epoxy thermoset polymers using the two different epoxide preparations are synthesized, characterized, and contrasted. Optimization of reaction conditions, including temperature and catalyst concentration, to enhance the performance of epoxy thermosets is discussed. Through dynamic mechanical analysis (DMA) and thermogravimetric analysis (TGA), the thermo-mechanical behavior and thermal stability of the resulting epoxy thermoset networks are evaluated, shedding light on how structural differences impact performance.

木质素基丁香酚单体--2,6-二甲氧基丙基苯酚(DMPP)可通过两种合成路线升级为多功能丙基焦醛 DMPPO。DMPPO 具有三个羟基,可作为可再生聚合物的结构单元。在本研究中,我们介绍了基于其合成方法的 DMPPO 环氧化物混合物的合成和表征;一种方法是使用 HBr,另一种是在水中使用 Nb2O5 催化剂的更环保的方法。对使用两种不同环氧化物制备的环氧热固性聚合物进行了合成、表征和对比。讨论了如何优化反应条件,包括温度和催化剂浓度,以提高环氧热固性聚合物的性能。通过动态机械分析 (DMA) 和热重分析 (TGA),评估了所得环氧热固性网络的热机械行为和热稳定性,揭示了结构差异对性能的影响。
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引用次数: 0
On the synthesis of biorefineries for high-yield isobutanol production: from biomass-to-alcohol experiments to system level analysis† 关于合成高产异丁醇的生物精炼厂:从生物质转化为酒精的实验到系统级分析†。
Pub Date : 2024-08-13 DOI: 10.1039/D4SU00283K
Arthur E. Pastore de Lima, Jason Coplien, Larry C. Anthony, Trey K. Sato, Yaoping Zhang, Steven D. Karlen, Chris Todd Hittinger and Christos T. Maravelias

The production of isobutanol from lignocellulose has gained attention due to its favorable physical and chemical properties. The use of lignocellulosic biomass as a feedstock to produce isobutanol has substantial sustainability benefits, but the biological conversion to isobutanol faces challenges, such as low yields and by-product formation. In this work, we demonstrate the high-yield production of isobutanol through microbial fermentation of pulp hydrolysates. Three hydrolysates are produced from poplar, sorghum, and switchgrass using pretreatment based on γ-valerolactone. Furthermore, we synthesize a biomass-to-isobutanol biorefinery and perform technoeconomic analysis of three resulting processes using experimental results obtained from an engineered yeast strain which consumes most of the glucose available in the hydrolysate and produces isobutanol at 89–94% theoretical yields. The corresponding minimum fuel selling price (MFSP) is $14.40–$16.01 per gasoline gallon equivalent, with the sorghum-based biorefinery resulting in the lowest price. We identify that solvent/biomass ratio during pretreatment and enzyme loading during hydrolysis have the greatest impact on the MFSP; improvements in these parameters can reduce the MFSP by 46%.

利用木质纤维素生产异丁醇因其良好的物理和化学特性而备受关注。使用木质纤维素生物质作为原料生产异丁醇具有巨大的可持续发展优势,但生物转化异丁醇面临着产量低和副产品形成等挑战。在这项工作中,我们展示了通过微生物发酵纸浆水解物来高产生产异丁醇的方法。我们使用基于 γ-戊内酯的预处理方法从杨树、高粱和开关草中生产出三种水解物。此外,我们还合成了一种生物质制异丁醇的生物精炼技术,并利用一种工程酵母菌株的实验结果对由此产生的三种工艺进行了技术经济学分析,这种酵母菌株可消耗水解物中的大部分葡萄糖,并以 89-94% 的理论产量生产异丁醇。相应的最低燃料销售价格(MFSP)为每汽油加仑当量 14.40 美元至 16.01 美元,其中以高粱为原料的生物精炼厂的价格最低。我们发现,预处理过程中的溶剂/生物质比率和水解过程中的酶负荷对 MFSP 的影响最大;改善这些参数可将 MFSP 降低 46%。
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引用次数: 0
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RSC sustainability
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