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【Ten Years of Rapid Development in Chemical Equipment】The world’s first bio-based 1,5-pentanediol production process was successfully tested at the Zhoushan facility from 2645 to 2025

2025-09-01View Original

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Give praise and encouragement to the achievements made in China’s chemical technology and equipment sector; your participation in discussions is the greatest encouragement. **********************【Ten Years of Progress in Chemical Equipment】Continuous updates and summaries available – feel free to join the discussions: https://bbs.hcbbs.com/thread-3576046-1-1.html ***************** Recently, Sebel Corporation announced that its world’s first bio-based 1,5-pentanediol production process was successfully tested at its base in Zhoushan, using the world’s first one-step hydrogenation process. Tests have shown that the purity of its bio-based 1,5-pentanediol is over 99.5%, the colority is less than 5, and the moisture content is less than 0.1%; all these parameters meet or even exceed international standards. Currently, two main technical approaches are used in industrial production, both of which require strict control of reaction conditions to ensure product purity. The petroleum-based route uses **furfuryl alcohol as the starting material, and the target product is obtained through two steps of transformation. The specific process is as follows: First, **furfuryl alcohol is dehydrated under acidic conditions to produce a dihydropyran intermediate; during this step, the temperature must be kept within 50°C, and the reaction time should be maintained at 30–40 minutes ; Subsequently, the dihydropyran was converted into 5-hydroxyvaleraldehyde through a hydration reaction; a hydrogenation reaction was carried out using a nickel catalyst at 120–150°C and a pressure of 6 MPa. Finally, the fraction at 119–120°C (0.4 kPa) was collected by vacuum distillation, with a yield of the product exceeding 85%. The key quality control points are pH adjustment during the neutralization process and temperature control during the distillation stage. The bio-based route uses cyclopentadiene as a starting material; through a photooxidation reaction, an epoxypentenal intermediate is formed, which is then subjected to catalytic hydrogenation at temperatures of 70–100°C and pressures of 7 MPa. The advantage of this process lies in the renewability of its raw materials, but it requires a sophisticated reactor design, including specialized photochemical reaction equipment and a high-pressure hydrogenation system. The final products of both process routes must meet the standards for cosmetic ingredients, with key parameters including purity of ≥99%, moisture content of ≤0.1%, and heavy metal residues of ≤10ppm. Sebel’s production technology for bio-based 1,5-pentanediol represents the world’s first one-step hydrogenation process that utilizes special catalysts, and it holds significant demonstrative value. During the design and testing processes, the requirements for environmental protection, safety, and efficient production were fully taken into account. An advanced automated control system is employed to ensure precise control and stable operation of the production process. Bio-based 1,5-pentanediol, as an important raw material in organic chemistry, is widely used in various fields. In the high-end cosmetics industry, 1,5-pentanediol is the preferred ingredient for many well-known brands due to its excellent moisturizing and preservative properties. 1,5-Pentanediol of bio-based origin better meets today’s consumers’ demand for natural and green cosmetics, resulting in strong market demand. In the field of cosmetic ingredients, the purity of 1,5-pentanediol directly affects its efficacy and safety. According to industry standards, the purity requirement for cosmetic-grade 1,5-pentanediol is not less than 99%, a standard that is equivalent to that for its isomer, 1,2-pentanediol. In the field of biomedicine: 1,5-pentanediol can be used to synthesize various drug intermediates, and it is of great significance for the research, development, and production of drugs. Its high purity and stability meet the strict requirements of the biopharmaceutical industry for raw materials, providing strong support for the development of innovative drugs. High-end polyurethanes, electric vehicle industry: 1,5-pentanediol also plays a key role in the production of high-performance polymers such as high-end polyurethanes and polyesters. By using bio-based 1,5-pentanediol, high-performance polymer materials with improved properties and environmental benefits can be produced, such as advanced PCDL, valerolactone, and new types of PA56 fibers. These materials are exported to Japan, Thailand, and Malaysia, and are widely used in pharmaceutical intermediates, coating materials for electric vehicle lithium batteries, high-end clothing materials, as well as in the construction and packaging industries.
Reply #22025-09-01
The teams led by Liang Changhai and Chen Xiao from the School of Chemical Engineering have made new progress in the selective hydrogenation of furfural to produce 1,5-pentanediol. Date: 2024-12-06 Author: Clicks: The efficient and clean conversion of biomass is an important approach to achieving the **dual-carbon strategic goals. Furfural, as an important biomass platform compound, can be converted into various fine chemicals such as furfuryl alcohol, 2-methylfuran, cyclopentanol, cyclopentanone, 1,2-pentanediol, and 1,5-pentanediol. 1,5-Pentanediol can be widely used in polyester resins, synthetic lubricants, polyester polyols, and elastomer plasticizers; its global market value is expected to reach $42 million by 2027. Therefore, developing 1,5-pentanediol from bio-based furfural holds significant practical value. Recently, the team led by Professor Liang Changhai and Associate Professor Chen Xiao from the School of Chemical Engineering at our university reduced the activation energy required for the hydrogenation of furfural to 1,5-pentanediol significantly by regulating metal active sites and oxygen vacancies in the carrier, thereby increasing the yield of 1,5-pentanediol. This study provides an important reference for the development of catalysts for the selective hydrogenation of furfural, as well as theoretical support for the synthesis of bio-based 1,5-pentanediol. The relevant results were published in the journal Chemical Engineering Journal under the title “Insights on the Hydrogenation of Furfural and Its Derivatives to 1,5-Pentanediol over Ni/La-substituted CeO2 Catalysts”, and in the journal Fuel under the title “Selective Hydrogenolysis of Furfural-derived Tetrahydrofurfuryl Alcohol to 1,5-Pentanediol over Ni-Co/La(OH)x Bimetallic Catalysts”. Additionally, a Chinese invention patent titled “A Method for the One-Step Hydrogenation of Furfural to 1,5-Pentanediol” (ZL202211218391.5) was granted. The first author of the paper is Associate Professor Chen Xiao, while the corresponding authors are Professor Liang Changhai and Associate Professor Chen Xiao. The precise activation of specific bonds in furfural and its derivatives for the production of high-value fine chemicals and polymer monomers is of great significance, and the key lies in the development of efficient catalysts. This study investigated the structural properties of Ni-based bifunctional catalysts, as well as their catalytic activity and mechanism of action in the hydrogenation-hydrolysis of furfural derivatives to produce 1,5-pentanediol, from the perspectives of rare earth metal oxide carriers and active metal components ; The reaction mechanism for the catalytic conversion of furfural and its derivatives into 1,5-pentanediol using Ni-based bifunctional catalysts was revealed, the structure-activity relationship of the catalysts was established, and high-efficiency conversion was achieved through the optimization of reaction conditions.
Reply #32025-09-01
A La-substituted CeO2-supported Ni catalyst with tunable surface oxygen vacancies was developed via co-precipitation-hydrothermal method for the hydrogenation of furfural and its derivatives to produce 1,5-pentanediol. In La-substituted CeO2-supported Ni catalysts, Ni/3.0La2O3-CeO2 possesses interfacial Niδ+-OV-LaxCe sites, making it a non-precious metal catalyst with promise for the hydrogenolysis of furfural and its derivatives to produce 1,5-pentanediol. The kinetic results indicate that in the hydrogenation of furfural to 1,5-pentanediol over La-substituted CeO2-supported Ni catalysts, the cleavage of C-O bonds represents the greatest challenge compared to the hydrogenation of C=O and C=C bonds. In the hydrogenolysis of furfuryl alcohol catalyzed by Ni/3.0La2O3-CeO2, the yield of 1,5-pentanediol can reach 70%, which is much higher than that of catalysts based on non-precious metals. Under mild reaction conditions, the metal Ni0 sites for the dissociation of H2, the interfacial Niδ+-OV-LaxCe sites, and the basic sites for the adsorption/activation of C-O-C bonds play a crucial role in the hydrogenolysis of furfuryl alcohol to 1,5-pentanediol. Furthermore, Ni/3.0La2O3-CeO2 exhibits excellent stability. This work laid the foundation for the development of bio-based fine chemicals via the hydrogenation of furfural and its derivatives. Using Ni as the active component and introducing a second metal, Co, Ni-Co/La(OH)x bimetallic catalysts with different Ni/Co molar ratios were synthesized via co-precipitation-hydrothermal method. The effect of Co incorporation on the coordination environment of Ni and its mechanism of action in the hydrogenation-hydrolysis of furfuryl alcohol were investigated. It was found that La(OH)x rich in defect sites polarizes the Ni-Co alloy, thereby promoting the cleavage of hydrogen and further exposing more interfacial NiCo-OV-La3+ sites. By taking advantage of the synergistic effect between alloy sites and interfacial sites, the optimized Ni4Co1/La(OH)x bimetallic catalyst significantly enhanced the adsorption of –OH groups in furfuryl alcohol, and promoted the selective attack of active hydrogen species on the C-O-C bonds in the furan ring. This method significantly improved the efficiency of selective hydrogenolysis of furfuryl alcohol to 1,5-pentanediol, with a selectivity of 88.6% for 1,5-pentanediol and a conversion rate of 98.1% for furfuryl alcohol. Furthermore, the Ni4Co1/La(OH)x bimetallic catalyst exhibited excellent performance in the one-pot hydrogenation-hydrolysis reaction of furfural, showing an activation energy of 17.77 kJ/mol and a turnover frequency of 192.1 h−1. It is worth noting that the Ni4Co1/La(OH)x bimetallic catalyst also exhibits excellent stability. The above results provide theoretical support for the development of renewable diol monomers.
Reply #42025-09-03
【Ten Years of Rapid Development in Chemical Engineering Equipment】2647-2025: Zhejiang Zhongkong’s world’s first large-scale temporal model for the process industry is now available for use. https://bbs.hcbbs.com/thread-5700490-1-1.html (Source: Haichuan Chemical Industry Forum)

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