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Journal articles on the topic 'Hydrogenolysis of cellulose'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Filatova, A. "Physical and chemical research of hydrogenolysis cellulose in subcritical water using Ru–containing catalysts new type." Bulletin of Science and Practice 398, no. 10(11) (2016): 47–55. https://doi.org/10.5281/zenodo.160918.

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The most appropriate parameters of the reaction of hydrogenolysis of cellulose: the temperature of 205 °C, a partial hydrogen pressure of 60 bar, reaction time 60 min, the ratio Ru/cellulose (mmol Ru in the composition of the composite per 1 g of cellulose) 0.042/1, the percentage content of ruthenium in the composite is 3% (mass.). Under these conditions, the conversion of cellulose amounted to 64.0%, the selectivity to sorbitol 43.5%. In addition, were synthesized Ru–containing catalysts. The obtained catalysts were investigated using a wide range of physical and chemical research. In additi

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2

Manaenkov, Oleg, Yuriy Kosivtsov, Valentin Sapunov, et al. "Kinetic Modeling for the “One-Pot” Hydrogenolysis of Cellulose to Glycols over Ru@Fe3O4/Polymer Catalyst." Reactions 3, no. 1 (2021): 1–11. http://dx.doi.org/10.3390/reactions3010001.

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Despite numerous works devoted to the cellulose hydrogenolysis process, only some of them describe reaction kinetics. This is explained by the complexity of the process and the simultaneous behavior of different reactions. In this work, we present the results of the kinetic study of glucose hydrogenolysis into ethylene- and propylene glycols in the presence of Ru@Fe3O4/HPS catalyst as a part of the process of catalytic conversion of cellulose into glycols. The structure of the Ru-containing magnetically separable Ru@Fe3O4/HPS catalysts supported on the polymeric matrix of hypercrosslinked poly

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3

Filatova, A., E. Shimanskaya, M. Sulman, and D. Gakipova. "The full catalytic processing of biomass components." Bulletin of Science and Practice, no. 12 (December 11, 2017): 50–56. https://doi.org/10.5281/zenodo.1101147.

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In this work, experimental studies aimed at the study of the hydrogenolysis of components of plant biomass with the production of valuable chemical substances have been conducted. Research aimed at the finding of the effective catalytic system allows obtaining a high degree of conversion of the substrate with high selectivity in the processing of all components of the biomass. On the basis of experimental data, it can be concluded that 3% Ru/MN270 catalyst is active in the hydrogenolysis of lignin, cellulose and hemicellulose, and it can be used in a complex processing of biomass. The catalyti

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4

Kumaniaev, Ivan, Elena Subbotina, Maxim V. Galkin, et al. "A combination of experimental and computational methods to study the reactions during a Lignin-First approach." Pure and Applied Chemistry 92, no. 4 (2020): 631–39. http://dx.doi.org/10.1515/pac-2019-1002.

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AbstractCurrent pulping technologies only valorize the cellulosic fiber giving total yields from biomass below 50 %. Catalytic fractionation enables valorization of both cellulose, lignin, and, optionally, also the hemicellulose. The process consists of two operations occurring in one pot: (1) solvolysis to separate lignin and hemicellulose from cellulose, and (2) transition metal catalyzed reactions to depolymerize lignin and to stabilized monophenolic products. In this article, new insights into the roles of the solvolysis step as well as the operation of the transition metal catalyst are gi

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5

Li, Naixu, Yu Zheng, Lingfei Wei, Hongcheng Teng, and Jiancheng Zhou. "Metal nanoparticles supported on WO3 nanosheets for highly selective hydrogenolysis of cellulose to ethylene glycol." Green Chemistry 19, no. 3 (2017): 682–91. http://dx.doi.org/10.1039/c6gc01327a.

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6

Chai, Jiachun, Shanhui Zhu, Youliang Cen, Jing Guo, Jianguo Wang, and Weibin Fan. "Effect of tungsten surface density of WO3–ZrO2 on its catalytic performance in hydrogenolysis of cellulose to ethylene glycol." RSC Advances 7, no. 14 (2017): 8567–74. http://dx.doi.org/10.1039/c6ra27524a.

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7

Manaenkov, Oleg V., Olga V. Kislitsa, Ekaterina A. Ratkevich, and Mikhail G. Sulman. "MAGNETICALLY RECOVERABLE POLYMER CATALYST FOR CELLULOSE HYDROGENOLYSIS." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 63, no. 2 (2020): 59–63. http://dx.doi.org/10.6060/ivkkt.20206302.6062.

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A new type of Ru-containing magnetically recoverable catalyst based on a polymer matrix of hypercrosslinked polystyrene (HPS) for the reaction of the hydrogenolysis of microcrystalline cellulose to ethylene and propylene glycol (EG and PG) is proposed. The catalyst is synthesized sequentially in two stages. At the first stage, by means of thermal decomposition of iron (III) salts in the presence of polyols, magnetite particles (Fe3O4) are formed in the pores of the HPS. At the second stage, Ru-containing nanoparticles of the active phase of the catalyst are synthesized on the surface of Fe3O4/

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8

Hamdy, Mohamed S., Murad A. Eissa, and Sherif M. A. S. Keshk. "New catalyst with multiple active sites for selective hydrogenolysis of cellulose to ethylene glycol." Green Chem. 19, no. 21 (2017): 5144–51. http://dx.doi.org/10.1039/c7gc02122d.

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Three different active sites were incorporated in 3-D silica matrix. One pot procedure was applied without using solvents or surfactants. The prepared material exhibited superior catalytic activity in the hydrogenolysis of cellulose to ethylene glycol.

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9

Manaenkov, O. V., O. V. Kislitza, V. Yu Doluda, et al. "KINETICS OF THE CELLULOSE HYDROGENOLYSIS IN SUBCRITICAL WATER." Scientific and Technical Volga region Bulletin 6, no. 4 (2016): 20–22. http://dx.doi.org/10.24153/2079-5920-2016-6-4-20-22.

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10

Fan, Guifang, De Chen, Shizhong Li, Mingde Yang, and Yulong Wu. "Effect of metal oxides on reaction route and product distribution of catalytic cellulose hydrogenolysis." BioResources 18, no. 4 (2023): 7367–90. http://dx.doi.org/10.15376/biores.18.4.7367-7390.

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The effects of CeO2, ZrO2, Nb2O5, and ZnO catalysts supported on carbon nanotubes (CNT) relative to cellulose hydrothermal hydrogenolysis in the presence of Ni/CNT and pressured H2 was studied in this work. The catalysts were characterized by inductively coupled plasma – optical emission spectrometry, X-ray diffraction, X-ray photoelectron spectrometry, transmission electron microscopy, NH3 temperature programmed desorption (TPD), and CO2-TPD. Glucose and its isomers were detected by mass spectrometry. The results showed that redox active CeO2/CNT with strong Lewis acid and strong Lewis base s

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11

Wang, Haiyong, Caihong Zhang, Qiying Liu, et al. "Direct Hydrogenolysis of Cellulose into Methane under Mild Conditions." Energy & Fuels 32, no. 11 (2018): 11529–37. http://dx.doi.org/10.1021/acs.energyfuels.8b02235.

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12

Palkovits, Regina, Kameh Tajvidi, Joanna Procelewska, Roberto Rinaldi, and Agnieszka Ruppert. "Hydrogenolysis of cellulose combining mineral acids and hydrogenation catalysts." Green Chemistry 12, no. 6 (2010): 972. http://dx.doi.org/10.1039/c000075b.

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13

Манаенков, Олег Викторович, Юрий Юрьевич Косивцов, Ольга Витальевна Кислица, Екатерина Алексеевна Раткевич, and Валентина Геннадьевна Матвеева. "KINETICS OF GLUCOSE HYDROGENOLYSIS IN THE PRESENCE OF A MAGNETICALLY RECOVERABLE POLYMERIC CATALYST." Вестник Тверского государственного университета. Серия: Химия, no. 4(46) (December 27, 2021): 37–48. http://dx.doi.org/10.26456/vtchem2021.4.5.

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В данной работе приводятся результаты исследования кинетики реакции гидрогенолиза глюкозы до этилен- и пропиленгликоля - как части общего процесса каталитической трансформации целлюлозы в гликоли в присутствии Ru-содержащих гетерогенных катализаторов. В качестве последнего в работе был использован разработанный ранее катализатор на полимерной основе 3 % Ru-FeO/СПС, обладающий магнитными свойствами. В ходе исследования получено формальное описание кинетики гидрогенолиза глюкозы, предложена математическая модель реакции гидрогенолиза глюкозы до гликолей в присутствии синтезированного катализатор

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14

Fabičovicová, Katarína, Martin Lucas, and Peter Claus. "From microcrystalline cellulose to hard- and softwood-based feedstocks: their hydrogenolysis to polyols over a highly efficient ruthenium–tungsten catalyst." Green Chemistry 17, no. 5 (2015): 3075–83. http://dx.doi.org/10.1039/c5gc00421g.

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Polyols, a class of biomass-derived platform molecules, were obtained in high yields by hydrogenolysis of different cellulosic feedstocks using a bifunctional Ru–W catalyst, which exhibits a very high concentration of acid sites.

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15

You, Su Jin, In Gu Baek, and Eun Duck Park. "Hydrogenolysis of cellulose into polyols over Ni/W/SiO2 catalysts." Applied Catalysis A: General 466 (September 2013): 161–68. http://dx.doi.org/10.1016/j.apcata.2013.06.053.

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16

Yang, Chaojun, Zhili Miao, Fan Zhang, et al. "Hydrogenolysis of methyl glycolate to ethanol over a Pt–Cu/SiO2single-atom alloy catalyst: a further step from cellulose to ethanol." Green Chemistry 20, no. 9 (2018): 2142–50. http://dx.doi.org/10.1039/c8gc00309b.

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17

He, Jiayue, Kefeng Huang, Kevin J. Barnett та ін. "New catalytic strategies for α,ω-diols production from lignocellulosic biomass". Faraday Discussions 202 (2017): 247–67. http://dx.doi.org/10.1039/c7fd00036g.

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Catalytic strategies for the synthesis of 1,5-pentanediol (PDO) with 69% yield from hemicellulose and the synthesis of 1,6-hexanediol (HDO) with 28% yield from cellulose are presented. Fractionation of lignocellulosic biomass (white birch wood chips) in gamma-valerolactone (GVL)/H<sub>2</sub>O generates a pure cellulose solid and a liquid stream containing hemicellulose and lignin, which is further dehydrated to furfural with 85% yield. Furfural is converted to PDO with sequential dehydration, hydration, ring-opening tautomerization, and hydrogenation reactions. Acid-catalyzed cellulose dehydr

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18

Cai, Chiliu, Changhui Zhu, Haiyong Wang, et al. "Catalytic Hydrogenolysis of Biomass-derived Polyhydric Compounds to C2–C3 Small- Molecule Polyols: A Review." Current Organic Chemistry 23, no. 20 (2019): 2180–89. http://dx.doi.org/10.2174/1385272823666190913185618.

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Biomass energy has attracted much attention because of its clean and renewable characteristics. At present, C2–C3 polyols such as glycerol, 1,2-propanediol, and ethylene glycol, widely used as platforms for downstream chemicals or directly used as chemicals in diversified industries, mainly depend on the petrochemical industry. In terms of the feedstock for C2–C3 polyol production, the C3-derived glycerol is a side product during biodiesel synthesis, whereas the C5-derived xylitol and C6-derived sorbitol can be mainly obtained by hydrolysis–hydrogenation of hemicellulose and cellulose from lig

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19

Chu, Dawang, Yingying Xin, and Chen Zhao. "Production of bio-ethanol by consecutive hydrogenolysis of corn-stalk cellulose." Chinese Journal of Catalysis 42, no. 5 (2021): 844–54. http://dx.doi.org/10.1016/s1872-2067(20)63709-3.

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20

Zhu, Wenwen, Hanmin Yang, Jizhong Chen, et al. "Efficient hydrogenolysis of cellulose into sorbitol catalyzed by a bifunctional catalyst." Green Chemistry 16, no. 3 (2014): 1534. http://dx.doi.org/10.1039/c3gc41917g.

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21

Xiao, Zihui, Pengfei Ma, Shaohua Jin, and Changhai Liang. "Tailoring Catalytic Properties of CuMgAl Hydrotalcites for Selective hydrogenolysis of Cellulose." ChemistrySelect 4, no. 8 (2019): 2243–48. http://dx.doi.org/10.1002/slct.201803558.

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22

Lucas, Martin, Katarina Fabičovicová, and Peter Claus. "Hydrothermally Stable Ruthenium-Zirconium-Tungsten Catalyst for Cellulose Hydrogenolysis to Polyols." ChemCatChem 10, no. 3 (2017): 612–18. http://dx.doi.org/10.1002/cctc.201701113.

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23

Song, Jihuan, Dan Wang, Qiyuan Wang, Chenmeng Cui, and Ying Yang. "Selective Control of Catalysts for Glycerol and Cellulose Hydrogenolysis to Produce Ethylene Glycol and 1,2-Propylene Glycol: A Review." Catalysts 14, no. 10 (2024): 685. http://dx.doi.org/10.3390/catal14100685.

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The bioconversion of cellulose and the transformation of glycerol can yield various diols, aligning with environmental sustainability goals by reducing dependence on fossil fuels, lowering raw material costs, and promoting sustainable development. However, in the selective hydrogenolysis of glycerol to ethylene glycol (EG) and 1,2-propylene glycol (1,2-PG), challenges such as low selectivity of catalytic systems, poor stability, limited renewability, and stringent reaction conditions remain. The production of diols from cellulose involves multiple reaction steps, including hydrolysis, isomeriz

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24

Filatova, A., and E. Shimanskaya. "Modern catalysts for the process of converting cellulose to glycols." Bulletin of Science and Practice, no. 11 (November 13, 2017): 36–43. https://doi.org/10.5281/zenodo.1048286.

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Creation of highly efficient catalytic systems for industrial processes is closely connected with the active development of modern chemistry. An increase in the efficiency of the catalysts can be achieved by directional formation of metal particles exhibiting high catalytic activity. In this connection, the problems of obtaining catalytic systems with control over the size of metal-containing particles are topical; stabilization of particles by polymers; studying the physical and chemical properties of such catalysts; studies of the kinetics of the reaction and the establishment of specific fe

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25

Liu, Mingrui, Hua Wang, Jinyu Han, and Yufei Niu. "Enhanced hydrogenolysis conversion of cellulose to C2–C3 polyols via alkaline pretreatment." Carbohydrate Polymers 89, no. 2 (2012): 607–12. http://dx.doi.org/10.1016/j.carbpol.2012.03.058.

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26

Tajvidi, Kameh, Peter J. C. Hausoul, and Regina Palkovits. "Hydrogenolysis of Cellulose over Cu-Based Catalysts-Analysis of the Reaction Network." ChemSusChem 7, no. 5 (2014): 1311–17. http://dx.doi.org/10.1002/cssc.201300978.

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27

Chu, Dawang, Zhicheng Luo, Yingying Xin, et al. "One-pot hydrogenolysis of cellulose to bioethanol over Pd-Cu-WOx/SiO2 catalysts." Fuel 292 (May 2021): 120311. http://dx.doi.org/10.1016/j.fuel.2021.120311.

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28

Liu, Qiying, Haiyong Wang, Haosheng Xin, et al. "Selective Cellulose Hydrogenolysis to Ethanol Using Ni@C Combined with Phosphoric Acid Catalysts." ChemSusChem 12, no. 17 (2019): 3977–87. http://dx.doi.org/10.1002/cssc.201901110.

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29

Liu, Qiying, Haiyong Wang, Haosheng Xin, et al. "Selective Cellulose Hydrogenolysis to Ethanol Using Ni@C Combined with Phosphoric Acid Catalysts." ChemSusChem 12, no. 17 (2019): 3881. http://dx.doi.org/10.1002/cssc.201902299.

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30

Wu, Qiong, Zhuoyu Wang, Baozheng Zhao, Ruiyang Zhao, Shitao Yu, and Lang Huang. "Nickel-tungsten co-doped biochar catalyst boosting ethylene glycol production from cellulose hydrogenolysis." Industrial Crops and Products 207 (January 2024): 117752. http://dx.doi.org/10.1016/j.indcrop.2023.117752.

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31

Su, Tong, Daguo Wu, Xinghua Zhang, et al. "Directed hydrogenolysis of “cellulose-to-ethylene glycol” using a Ni–WO_x based catalyst." RSC Advances 15, no. 18 (2025): 14235–45. https://doi.org/10.1039/d5ra01528f.

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32

Espro, Claudia, Bianca Gumina, Tomasz Szumelda, Emilia Paone, and Francesco Mauriello. "Catalytic Transfer Hydrogenolysis as an Effective Tool for the Reductive Upgrading of Cellulose, Hemicellulose, Lignin, and Their Derived Molecules." Catalysts 8, no. 8 (2018): 313. http://dx.doi.org/10.3390/catal8080313.

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Lignocellulosic biomasses have a tremendous potential to cover the future demand of bio-based chemicals and materials, breaking down our historical dependence on petroleum resources. The development of green chemical technologies, together with the appropriate eco-politics, can make a decisive contribution to a cheap and effective conversion of lignocellulosic feedstocks into sustainable and renewable chemical building blocks. In this regard, the use of an indirect H-source for reducing the oxygen content in lignocellulosic biomasses and in their derived platform molecules is receiving increas

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33

LI, Si-chan, Yu-long DENG, Hai-yong WANG, Chen-guang WANG, Long-long MA, and Qi-ying LIU. "Production of acetol and lactic acid from cellulose hydrogenolysis over Sn-Fe@C catalysts." Journal of Fuel Chemistry and Technology 50, no. 3 (2022): 314–25. http://dx.doi.org/10.1016/s1872-5813(21)60153-6.

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34

Wang, Haiyong, Haosheng Xin, Chiliu Cai, et al. "Selective C3-C4 Keto-Alcohol Production from Cellulose Hydrogenolysis over Ni-WOx/C Catalysts." ACS Catalysis 10, no. 18 (2020): 10646–60. http://dx.doi.org/10.1021/acscatal.0c02375.

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35

Chu, Dawang, and Chen Zhao. "Reduced oxygen-deficient CuWO4 with Ni catalyzed selective hydrogenolysis of cellulose to ethylene glycol." Catalysis Today 351 (July 2020): 125–32. http://dx.doi.org/10.1016/j.cattod.2018.10.006.

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36

Xiao, Zhuqian, Qiuwei Ge, Chuang Xing, et al. "Self-reducing bifunctional Ni-W/SBA-15 catalyst for cellulose hydrogenolysis to low carbon polyols." Journal of Energy Chemistry 25, no. 3 (2016): 434–44. http://dx.doi.org/10.1016/j.jechem.2016.03.015.

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37

Wang, Haiyong, Xiaohong Hu, Siwei Liu, et al. "Selective (ligno) cellulose hydrogenolysis to ethylene glycol and propyl monophenolics over Ni–W@C catalysts." Cellulose 27, no. 13 (2020): 7591–605. http://dx.doi.org/10.1007/s10570-020-03340-1.

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38

Hilgert, Jakob, Niklas Meine, Roberto Rinaldi, and Ferdi Schüth. "Mechanocatalytic depolymerization of cellulose combined with hydrogenolysis as a highly efficient pathway to sugar alcohols." Energy Environ. Sci. 6, no. 1 (2013): 92–96. http://dx.doi.org/10.1039/c2ee23057g.

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39

Nguyen, Van Chuc, Sarah Kheireddine, Amar Dandach, Marion Eternot, Thi Thu Ha Vu, and Nadine Essayem. "Acid Properties of GO and Reduced GO as Determined by Microcalorimetry, FTIR, and Kinetics of Cellulose Hydrolysis-Hydrogenolysis." Catalysts 10, no. 12 (2020): 1393. http://dx.doi.org/10.3390/catal10121393.

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Graphene oxide addresses increasing interests as a solid acid catalyst working in water for carbohydrate conversion. If there is a general agreement to correlate its unique catalytic performances to its ability to adsorb sugars, the origin of its acidity remains controversial. In this article, we study the acid strength of graphene oxide (GO) prepared by modified Hummers method and that of reduced GO by calorimetry of NH3 adsorption and by FTIR of pyridine adsorption. Very strong acid sites are detected on GO by calorimetry, while reduced graphene oxide (reGO) is not very acidic. The FTIR of p

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40

Филатова, А. Е., А. М. Сульман, Е. И. Шиманская, О. В. Гребенникова, and М. А. Монжаренко. "INFLUENCE OF THE PROPERTIES OF THE POLYMER MATRIX OF THE CATALYST ON THE PROCESSING OF PLANT BIOMASS." Вестник Тверского государственного университета. Серия: Химия, no. 1(51) (March 13, 2023): 45–50. http://dx.doi.org/10.26456/vtchem2023.1.5.

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В настоящее время усилия многих научных коллективов сосредоточены на разработке новых, эффективных и экологически безопасных способов получения полиспиртов из растительной биомассы, в первую очередь, из целлюлозы. Огромные природные возобновляемые запасы данного биополимера способны полностью удовлетворить потребности современной промышленности в полиспиртах, что особенно актуально с учётом перспективы постепенного истощения запасов углеводородных ископаемых. Одностадийный гидрогенолиз целлюлозы до полиспиртов (one-pot процесс), в присутствии гетерогенных металлосодержащих катализаторов извест

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41

Fabičovicová, Katarína, Oliver Malter, Martin Lucas, and Peter Claus. "Hydrogenolysis of cellulose to valuable chemicals over activated carbon supported mono- and bimetallic nickel/tungsten catalysts." Green Chem. 16, no. 7 (2014): 3580–88. http://dx.doi.org/10.1039/c4gc00664j.

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42

Li, Yuping, Yuhe Liao, Xiaofeng Cao, et al. "Advances in hexitol and ethylene glycol production by one-pot hydrolytic hydrogenation and hydrogenolysis of cellulose." Biomass and Bioenergy 74 (March 2015): 148–61. http://dx.doi.org/10.1016/j.biombioe.2014.12.025.

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43

Манаенков, Олег Викторович, Ольга Витальевна Кислица, and Валентина Геннадьевна Матвеева. "CONVERSION OF CELLULOSE TO POLYHYDROAL ALCOHOLS IN WATER: A REVIEW OF CATALYSTS." Вестник Тверского государственного университета. Серия: Химия, no. 1(47) (April 5, 2022): 7–23. http://dx.doi.org/10.26456/vtchem2022.1.1.

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Целлюлоза - самый распространённый биополимер на Земле. Данный ресурс возобновляем, не имеет пищевой ценности для человека и ежегодно синтезируется в природе в огромных масштабах, способных полностью удовлетворить потребности в сырье современной химической и топливной промышленности. Благодаря наличию в структуре целлюлозы большого количества гидроксильных групп, одними из самых оптимальных вариантов её конверсии, обладающих высокой атомной эффективностью, являются процессы гидролитического гидрирования до гекситов (сорбита и маннита) и гидрогенолиза до гликолей (этилен- и пропиленгликоля). Об

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44

Chen, Tian-Ying, Cheng-Ye Ma, Dou-Yong Min, et al. "Aldehydes-Aided Lignin-First Deconstruction Strategy for Facilitating Lignin Monomers and Fermentable Glucose Production from Poplar Wood." Energies 13, no. 5 (2020): 1113. http://dx.doi.org/10.3390/en13051113.

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In this study, lignin with fine structures and facile enzymatic saccharifying residue were successively dissociated based on the lignin-first biomass deconstruction strategy. In the lignin-first process, aldehyde-protected lignin fractions were firstly isolated by acid-catalyzed dioxane extraction in the presence of formaldehyde (FA) and acetaldehyde (AA) and then analyzed by advanced nuclear magnetic resonance (NMR) spectroscopy and gel permeation chromatography (GPC). The optimized hydrogenolysis of the extracted lignin (LFA and LAA) resulted in a high yield (42.57% and 33.00%) of lignin mon

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45

Han, Shuangmei, Ruizhen Wang, Kui Wang, Jianchun Jiang, and Junming Xu. "Low-condensed lignin and high-purity cellulose production from poplar by synergistic deep eutectic solvent-hydrogenolysis pretreatment." Bioresource Technology 363 (November 2022): 127905. http://dx.doi.org/10.1016/j.biortech.2022.127905.

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46

Leal, Glauco F., Luiz A. Ramos, Dean H. Barrett, Antonio Aprígio S. Curvelo, and Cristiane B. Rodella. "A thermogravimetric analysis (TGA) method to determine the catalytic conversion of cellulose from carbon-supported hydrogenolysis process." Thermochimica Acta 616 (September 2015): 9–13. http://dx.doi.org/10.1016/j.tca.2015.07.017.

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Wang, Xicheng, Feng Wu, Shengxi Yao, Yijun Jiang, Jing Guan, and Xindong Mu. "Ni–Cu/ZnO-catalyzed Hydrogenolysis of Cellulose for the Production of 1,2-Alkanediols in Hot Compressed Water." Chemistry Letters 41, no. 5 (2012): 476–78. http://dx.doi.org/10.1246/cl.2012.476.

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Xiao, Zhuqian, Yaru Hu, Jiajing Hu, et al. "Coordination environment tuning of Ni-Sn catalysts by glu-carbon to optimize cellulose hydrogenolysis to oxygenated chemicals." Fuel 350 (October 2023): 128833. http://dx.doi.org/10.1016/j.fuel.2023.128833.

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Gao, Mengting, Zelin Li, Baozheng Zhao, Shitao Yu, Lang Huang, and Qiong Wu. "Nickel‑tungsten co-doped carbon-based catalyst for high selective production of ethylene glycol from cellulose hydrogenolysis." Fuel Processing Technology 247 (August 2023): 107816. http://dx.doi.org/10.1016/j.fuproc.2023.107816.

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Wang, Jie, Quanxing Zheng, Hongliang Lu, et al. "TiO2 layer coated MoO3 nanorod supported Ni catalyst for selective hydrogenolysis of cellulose to ketones and alcohols." Fuel 394 (August 2025): 135136. https://doi.org/10.1016/j.fuel.2025.135136.

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