负载型双金属Pd-Sn (3.0)/ γ-Al2O3催化剂催化硬脂酸加氢制1-十八醇

Atina Sabila Azzahra, Elisa Hayati, Rodiansono Rodiansono
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引用次数: 0

摘要

γ-Al2O3上负载的双金属钯锡催化剂(表示为Pd–Sn(3.0)/γ-Al2O3;Pd=5%wt,Pd/Sn摩尔比为3.0)。样品的XRD图谱显示,载体γ-Al2O3、金属Pd、Sn和Pd-Sn合金相具有典型的衍射峰。在2θ=39.8°处观察到金属Pd的衍射峰;46.6°;和68.0°,可分别归属于Pd(111)、Pd(200)和Pd(220),而在2θ=39.8°和41.0°处的衍射峰可分别归因于Pd2Sn和Pd3Sn2,它们可能与Pd(11)物种重叠。氨解吸和吡啶吸附曲线显示出Lewis和Brönsted酸性位点。Pd–Sn(3.0)/γ-Al2O3催化剂的比表面积(SBET)为117.83 m2/g,主要为微孔结构。硬脂酸的最高转化率为99.1%,1-十八醇的产率为43.2%。在温度513K、初始H2压力2.0MPa、反应时间13h和2-丙醇/水(4.0:1.0v/v)溶剂中获得。
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Catalytic hydrogenation of stearic acid to 1-octadecanol using supported bimetallic Pd–Sn(3.0)/γ–Al2O3 catalyst
Supported bimetallic palladium-tin catalyst on gamma-alumina (γ-Al2O3) (denoted as Pd–Sn(3.0)/γ-Al2O3; Pd = 5%wt and Pd/Sn molar ratio is 3.0) has been synthesized via the hydrothermal method at a temperature of 423 K for 24 h and reduced with H2 at 673 K for 3 h. The XRD patterns of the samples showed typical diffraction peaks of support γ-Al2O3, metallic Pd, Sn, and Pd–Sn alloy phases. Diffraction peaks of metallic Pd were observed at 2θ = 39.8°; 46.6°; and 68.0°, which can be attributed to the Pd(111), Pd(200), and Pd(220), respectively, while the diffraction peaks at 2θ = 39.8° and 41.0° can be attributed to Pd2Sn and Pd3Sn2, respectively, which may overlap with the Pd(111) species. The ammonia desorption and pyridine adsorption profiles showed Lewis and Brönsted acid sites. The specific surface area (SBET) of Pd–Sn(3.0)/γ-Al2O3 catalyst was 117.83 m2/g which is dominated by a micropore structure. The highest conversion of stearic acid was 99.1% with a yield of 1-octadecanol 43.2% was obtained at temperature 513 K, initial H2 pressure of 2.0 MPa, a reaction time of 13 h, and in 2-propanol/water (4.0:1.0 v/v) solvent.
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