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生物乙醇制高级醇催化剂研究进展

王文文 逯炀炀 李治宇 张玉春 付鹏

王文文, 逯炀炀, 李治宇, 张玉春, 付鹏. 生物乙醇制高级醇催化剂研究进展[J]. 燃料化学学报(中英文). doi: 10.19906/j.cnki.JFCT.2023061
引用本文: 王文文, 逯炀炀, 李治宇, 张玉春, 付鹏. 生物乙醇制高级醇催化剂研究进展[J]. 燃料化学学报(中英文). doi: 10.19906/j.cnki.JFCT.2023061
WANG Wen-wen, LU Yang-yang, LI Zhi-yu, ZHANG Yu-chun, FU Peng. Research progress in catalysts for producing higher alcohols from bioethanol[J]. Journal of Fuel Chemistry and Technology. doi: 10.19906/j.cnki.JFCT.2023061
Citation: WANG Wen-wen, LU Yang-yang, LI Zhi-yu, ZHANG Yu-chun, FU Peng. Research progress in catalysts for producing higher alcohols from bioethanol[J]. Journal of Fuel Chemistry and Technology. doi: 10.19906/j.cnki.JFCT.2023061

生物乙醇制高级醇催化剂研究进展

doi: 10.19906/j.cnki.JFCT.2023061
基金项目: 国家自然科学基金面上项目(No.51976112);国家自然科学基金青年项目(52206264)
详细信息
    通讯作者:

    Tel: 15689002285, E-mail: lizhiyu@sdut.edu.cn

    Tel: 15064314128, E-mail: fupengsdut@163.com

  • 中图分类号: O643.3

Research progress in catalysts for producing higher alcohols from bioethanol

Funds: The project was supported by General Program of the National Natural Science Foundation of China (No.51976112); National Natural Science Foundation Project (52206264)
  • 摘要: 与乙醇相比,高级醇具有高的十六烷值、高能量密度、对发动机部件无腐蚀性、与水不混溶、稳定性好等直接作为燃料或燃料添加剂的优势,将发酵产生的生物乙醇转化为更有价值的高级醇受到了广泛关注。本文综述了近年来国内外有关生物乙醇制高级醇的研究进展,包括金属氧化物、羟基磷灰石(HAP)和负载型金属催化剂的研究开发现状,并比较了不同类型催化剂参与下乙醇转化率和高级醇选择性,结合乙醇经缩合反应制备高级醇的机理进行了讨论,最后对当前生物乙醇制高级醇的挑战以及未来研究趋势进行了总结与展望,指出多功能催化剂的开发是未来研究重点,羟醛缩合是进一步提高生物乙醇制高级醇转化率与选择性的有效策略。
  • 图  1  乙醇的转化途径[11]

    Figure  1  Conversion pathway of ethanol (with permission from Nat. Rev. Chem. Publications)

    图  2  木质纤维素生物质发酵制生物乙醇[14]

    Figure  2  Fermentation of Lignocellulose Biomass to Produce Bioethanol (with permission from Industrial Ind Crops Prod Publications)

    图  3  采用CO2/NH3-TPD对催化剂的酸碱度进行表征[21]

    Figure  3  Characterization of the acidity and alkalinity of the catalyst using CO2/NH3-TPD (a) MA: MgAlOx catalysts; (b) CMA: CuMgAlOx catalysts (with permission from J. Fuel Chem. Technol. Publications)

    图  4  Co0.15Mg2.85AlOx催化剂的催化性能[23]

    Figure  4  Catalytic performance of Co0.15Mg2.85AlOx catalyst (with permission from Green Chem. Publications)

    图  5  OM-CuxLayAl100催化剂的反应路径和机理[24]

    Figure  5  Reaction Path and Mechanism of OM-CuxLayAl100 Catalyst (with permission from Appl. Surf. Sci. Publications)

    图  6  Cu-HAP催化剂的催化性能和反应路径[29]

    Figure  6  Catalytic performance and reaction pathway of Cu HAP catalyst (with permission from ACS Catal Publications)

    图  7  (A)多孔BAP-Ni上的反应途径; (B)无孔BAP-Ni催化剂[30]

    Figure  7  Reaction pathway on (A) porous BAP-Ni; (B) nonporous BAP-Ni catalyst (with permission from ACS Sustain. Chem. Eng. Publications)

    图  8  (A)8h后的产物选择性:负载量分别为2.5g/L(白色)和10g/L(紫色)HAP, 2.5g/L(黄色), 10g/L(棕色); (B)8h后的产物分布:Cu/MgAl (蓝色); Ru/MgAl (黄色); Pd/MgAl (绿色); Pt/MgAl (灰色)[38]

    Figure  8  (A)Product selectivity after 8 hours: loading amounts of 2.5g/L (white) and 10g/L (purple) HAP, 2.5g/L (yellow), and 10g/L (brown), respectively; (B)Product distribution after 8 hours: Cu/MgAl (blue); Ru/MgAl (yellow); Pd/MgAl (green); Pt/MgAl (gray) (with permission from Green Chem. Publications)

    图  9  催化剂的制备工艺示意图和SEM图像[50]

    Figure  9  Schematic diagram of catalyst preparation process and SEM diagram(a)NiSn@C-5/1-500, (b)NiSn@C-1/2-500, (c)NiSn@C-1/5-500, (d)NiSn@C-1/2-300, (e)NiSn@C-1/2-600, (f)NiSn@C-1/2-800 (with permission from Energy Convers. Manag Publications)

    图  10  Ni20Sn1@NC催化剂的催化性能[51]

    Figure  10  Ni20Sn1@NC Catalytic performance of catalysts (with permission from Ind. Eng. Chem. Res. Publications)

    图  11  催化剂制备示意图和表征分析[52]

    Figure  11  Schematic diagram and characterization analysis of catalyst preparation (with permission from ACS Catal Publications)

    图  12  乙醇在Ni和Sn-Ni上解离的结构图以及偶联机制[53]

    Figure  12  Structure diagram and coupling mechanism of ethanol dissociation on Ni and Sn-Ni (with permission from Appl. Catal. B Publications)

    图  13  电荷密度分布以及Bader电荷转移[54]

    Figure  13  Charge density distribution and Bader charge transfer (with permission from Chem. Eng. J Publications)

    图  14  不同碳化温度下的XRD图以及演化示意图[55]

    Figure  14  XRD patterns and evolution diagrams at different carbonization temperatures (with permission from Fuel Publications)

    图  15  a.乙醇生成正丁醇的直接机理; b.间接机理示意图; c.主要机理; d和e.次要机理

    Figure  15  a.Direct mechanism of ethanol producing n-butanol; b.Schematic diagram of indirect mechanism;c.Main mechanism; d and e.Secondary mechanisms

    表  1  金属氧化物催化剂

    Table  1  Metal oxide catalysts

    CatalystsReaction conditionsConv.(%)Sel.(%)Reference
    MgO450 ℃,0.5 g catalyst,N2 10 ml/min,7 h56.132.715
    MgO400 ℃,0.2 g catalyst,6% ethanol,1.3atm23.034.016
    Mg-ZrO2400 ℃52.035.017
    Mg-Al(Mg/Al=3)350 ℃,0.3 g catalyst,12% ethanol,
    atmospheric pressure,12 h
    35.040.018
    Cu1MgAl3O200 ℃,0.5 g catalyst,39.5 g ethanol,
    autogenic pressure,5 h
    2.543.020
    Cu5MgAl3O200 ℃,0.5 g catalyst,39.5 g ethanol,
    autogenic pressure,5 h
    4.140.020
    Cu10MgAl3O200 ℃,0.5 g catalyst,39.5 g ethanol,
    autogenic pressure,5 h
    4.528.020
    Cu20MgAl3O200 ℃,0.5 g catalyst,39.5 g ethanol,
    autogenic pressure,5 h
    3.818.020
    Pd5MgAlO200 ℃,0.5 g catalyst,39.5 g ethanol,
    autogenic pressure,5 h
    3.872.720
    Ag5MgAlO200 ℃,0.5 g catalyst,39.5 g ethanol,
    autogenic pressure,5 h
    1.638.820
    Mn5MgAlO200 ℃,0.5 g catalyst,39.5 g ethanol,
    autogenic pressure,5 h
    0.753.320
    Fe5MgAlO200 ℃,0.5 g catalyst,39.5 g ethanol,
    autogenic pressure,5 h
    0.339.220
    Sm5MgAlO200 ℃,0.5 g catalyst,39.5 g ethanol,
    autogenic pressure,5 h
    1.366.320
    Yb5MgAlO200 ℃,0.5 g catalyst,39.5 g ethanol,
    autogenic pressure,5 h
    1.253.020
    CuMgAlOx260 ℃,0.1 MPa,GHSV=750 mL·gcat−1·h−1,
    LHSV=2 mL·gcat−1·h−1
    43.948.021
    CuMgAlOx350 ℃,0.15 g catalyst,5 h79.632.022
    Co0.15Mg2.85AlOx250 ℃,0.1 MPa,0.2 g catalyst,WHSV=0.96 h−132.995.423
    OM-Cu4La2.6Al100260 ℃,3 MPa (N2),LHSV=2 ml/(h·gcat),12 h52.272.224
    Conv-conversion of ethanol; Sel-selectivity of higher alcohol
    下载: 导出CSV

    表  2  羟基磷灰石(HAP)催化剂

    Table  2  Hydroxyapatite (HAP) catalyst

    CatalystsReaction conditionsConv.(%)Sel.(%)Reference
    HAP Ca/P=1.64320 ℃,0.21 g catalyst,GHSV=10000 h−122.762.426
    HAP (Ca + Sr)/P=1.67400 ℃,flow=50 mL·min−1,
    GHSV=5000 mL·gcat−1·h−1,4 h
    13.076.427
    Ca-HAP-1(1.59)400 ℃,atmospheric pressure, GHSV=10000 h−116.222.228
    Ca-HAP-2(1.62)400 ℃,atmospheric pressure, GHSV=10000 h−120.850.428
    Ca-HAP-3(1.65)400 ℃,atmospheric pressure, GHSV=10000 h−121.262.428
    Ca-HAP-4(1.67)400 ℃,atmospheric pressure, GHSV=10000 h−115.856.228
    Sr-HAP-1(1.58)300 ℃,atmospheric pressure, W/Fethanol=130 h·g·mol−11.169.028
    Sr-HAP-2(1.64)300 ℃,atmospheric pressure, W/Fethanol=130 h·g·mol−15.978.128
    Sr-HAP-3(1.67)300 ℃,atmospheric pressure, W/Fethanol=130 h·g·mol−17.981.728
    Sr-HAP-4(1.70)300 ℃,atmospheric pressure, W/Fethanol=130 h·g·mol−111.386.428
    Cu-HAP250 ℃,0.1 g catalyst,
    H2 or N2 30 mL·min−1,0.5 h
    36.686.729
    Ni-HAP400 ℃,0.25 g catalyst,0.5 mL ethanol, 0.1 MPa N2,24 h55.667.730
    Conv-conversion of ethanol; Sel-selectivity of higher alcohol
    下载: 导出CSV

    表  3  单金属负载催化剂

    Table  3  Monometal Supported Catalysts

    CatalystsReaction conditionsConv.(%)Sel.(%)Reference
    5%Ru/Al2O3300 ℃,0.01−0.05 g catalyst,1.2 g ethanol, autogenic pressure,3 h12.09.034
    5%Rh/Al2O3300 ℃,0.01−0.05 g catalyst,1.2 g ethanol, autogenic pressure,3 h5.035.034
    5%Pd/Al2O3300 ℃,0.01−0.05 g catalyst,1.2 g ethanol, autogenic pressure,3 h9.021.034
    5%Pt/Al2O3300 ℃,0.01−0.05 g catalyst,1.2 g ethanol, autogenic pressure,3 h3.037.034
    0.8%Au/Al2O3300 ℃,0.01−0.05 g catalyst,1.2 g ethanol, autogenic pressure,3 h6.035.034
    6%Ag/Al2O3300 ℃,0.01−0.05 g catalyst,1.2 g ethanol, autogenic pressure,3 h2.020.034
    Ag/Mg-Al250 ℃53.713.835
    Ni/γ-Al2O3230 ℃,WHSV=1.42 h−1,100bar,10 h41.047.536
    Ni/γ-Al2O3240 ℃,2 g catalyst,70bar, LHSV=0.1 h−1,10 h14.069.037
    Cu/γ-Al2O3240 ℃,2 g catalyst,70bar, LHSV=0.1 h−1,10 h14.064.037
    Cu/CeO2260 ℃,1 mL·min−1CO2 and 0.05 mL·min−1EtOH,LHSV=1.97 h−139.035.038
    Ru/MgO400 ℃43.09.039
    Au/mTiO2250 ℃74.010.040
    Co/MgAlO350 ℃55.033.041
    Cu/MgAl230 ℃,0.5 or 2 g catalyst,200 mL ethanol, 30bar N2,8 h---81.942
    Ru/Mg3Al1-LDO350 ℃,0.5 g catalyst,P(N2)=0.1 MPa, WHSV=3.2 h−129.682.643
    Ni@C0.5 g catalyst,5 MPa H2 initial pressure, 10 h61.785.744
    Conv-conversion of ethanol; Sel-selectivity of higher alcohol
    下载: 导出CSV

    表  4  多金属负载催化剂

    Table  4  Multimetal Supported Catalysts

    CatalystsReaction conditionsConv.(%)Sel.(%)Reference
    Cu-CeO2/AC250 ℃,1.0 g catalyst, 2 MPa(N2), LHSV=4 ml/(h·gcat)39.155.245
    5Cu1Ce/AC250 ℃,1.0 g catalyst, 2 MPa(N2), LHSV=4 ml/(h·gcat)46.261.845
    4Cu1Ce/AC250 ℃,1.0 g catalyst, 2 MPa(N2), LHSV=4 ml/(h·gcat)45.662.745
    3Cu1Ce/AC250 ℃,1.0 g catalyst, 2 MPa(N2), LHSV=4 ml/(h·gcat)46.260.045
    2Cu1Ce/AC250 ℃,1.0 g catalyst, 2 MPa(N2), LHSV=4 ml/(h·gcat)46.358.745
    1Cu1Ce/AC250 ℃,1.0 g catalyst, 2 MPa(N2), LHSV=4 ml/(h·gcat)44.045.545
    3Cu1Ce/SiO2250 ℃,1.0 g catalyst, 2 MPa(N2), LHSV=4 ml/(h·gcat)23.312.345
    3Cu1Ce/A2O3250 ℃,1.0 g catalyst, 2 MPa(N2), LHSV=4 ml/(h·gcat)46.917.445
    Ni-Cu/HT310 ℃, Ni:Cu = 1:162.434.846
    Ni/La2O3/Al2O3230 ℃,30 g catalyst,
    reactor pressure=100bar
    41.074.047
    Ni/Cu/La2O3/β-Al2O3230 ℃,30 g catalyst,WHSV=2.06h−115%78%48
    NiSn/MgAlO250 ℃,1g NaOH,10 g H2O,10 g ethanol, 12 h66.993.849
    NiSn@C250 ℃,0.5 g catalyst,EtOH/H2O=1,24 h47.036.050
    NiSn@NC250 ℃,0.5 g catalyst,15g ethanol,
    15 g H2O,1 g NaOH,24 h
    68.531.851
    NiZn@NC250 ℃,0.5 g catalyst,15g ethanol,
    15 g H2O, 1 g NaOH,24 h
    75.2---52
    Sn-Ni/CS230 ℃,0.3 g catalysts,0.87 g NaOH,
    10 g EtOH,10 g H2O,12 h
    60.085.053
    NiMo@C240 ℃,0.6g catalyst,13.5 g C2H5OH,
    1.5 g fusel,15.0 g H2O,0.9 g NaOH,12 h
    89.444.754
    NiSn@C-MgO250 ℃,0.5 g catalyst,10 g ethanol,
    10 g H2O,0.5 g NaOH,12 h
    73.360.955
    Cu-La2O3/Al2O3250 ℃, 1.0 g catalyst,3 MPa(N2), LHSV=2 mL·gcat−1·h−156.776.19
    Conv-conversion of ethanol; Sel-selectivity of higher alcohol
    下载: 导出CSV
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  • 收稿日期:  2023-07-13
  • 修回日期:  2023-08-19
  • 录用日期:  2023-08-21
  • 网络出版日期:  2023-09-18

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