Gomez-Bolivar Jaime, Mikheenko Iryna P, Orozco Rafael L, Sharma Surbhi, Banerjee Dipanjan, Walker Marc, Hand Rachel A, Merroun Mohamed L, Macaskie Lynne E
Department of Microbiology, Faculty of Sciences, University of Granada, Granada, Spain.
School of Biosciences, University of Birmingham, Birmingham, United Kingdom.
Front Microbiol. 2019 Jun 20;10:1276. doi: 10.3389/fmicb.2019.01276. eCollection 2019.
cells support the nucleation and growth of ruthenium and ruthenium-palladium nanoparticles (Bio-Ru and Bio-Pd/Ru NPs). We report a method for the synthesis of these monometallic and bimetallic NPs and their application in the catalytic upgrading of 5-hydroxymethyl furfural (5-HMF) to 2,5 dimethylfuran (DMF). Examination using high resolution transmission electron microscopy with energy dispersive X-ray microanalysis (EDX) and high angle annular dark field (HAADF) showed Ru NPs located mainly at the cell surface using Ru(III) alone but small intracellular Ru-NPs (size ∼1-2 nm) were visible only in cells that had been pre-"seeded" with Pd(0) (5 wt%) and loaded with equimolar Ru. Pd(0) NPs were distributed between the cytoplasm and cell surface. Cells bearing 5% Pd/5% Ru showed some co-localization of Pd and Ru but chance associations were not ruled out. Cells loaded to 5 wt% Pd/20 wt% Ru showed evidence of core-shell structures (Ru core, Pd shell). Examination of this cell surface material using X-ray photoelectron spectroscopy (XPS) showed Pd(0) and Pd(II) and Ru(IV) and Ru(III), with confirmation by analysis of bulk material using X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) analyses. Both Bio-Ru NPs and Bio-Pd/Ru NPs were active in the conversion of 5-HMF into 2,5-DMF but commercial Ru on carbon catalyst outperformed 5 wt% bio-Ru by fourfold. While 5 wt% Pd/20 wt% Ru achieved 20% yield of DMF the performance of the 5 wt% Pd/5 wt% Ru bio-catalyst was higher and comparable to the commercial 5 wt% Ru/C catalyst in a test reaction using commercial 5-HMF (>50% selectivity). 5-HMF was prepared by thermochemical hydrolysis of starch and cellulose with solvent extraction of 5-HMF into methyltetrahydrofuran (MTHF). Here, with MTHF as the reaction solvent the commercial Ru/C catalyst had little activity (100% conversion, negligible selectivity to DMF) whereas the 5 wt% Pd/5 wt% Ru bio-bimetallic gave 100% conversion and 14% selectivity to DMF from material extracted from hydrolyzates. The results indicate a potential green method for realizing increased energy potential from biomass wastes as well as showing a bio-based pathway to manufacturing a scarcely described bimetallic material.
细胞支持钌和钌 - 钯纳米颗粒(生物Ru和生物Pd/Ru NPs)的成核和生长。我们报告了一种合成这些单金属和双金属纳米颗粒的方法及其在将5 - 羟甲基糠醛(5 - HMF)催化升级为2,5 - 二甲基呋喃(DMF)中的应用。使用高分辨率透射电子显微镜结合能量色散X射线微分析(EDX)和高角度环形暗场(HAADF)进行的检测表明,仅使用Ru(III)时,Ru NPs主要位于细胞表面,但只有在预先用Pd(0)(5 wt%)“播种”并负载等摩尔Ru的细胞中才能看到小的细胞内Ru - NPs(尺寸约为1 - 2 nm)。Pd(0) NPs分布在细胞质和细胞表面之间。含有5% Pd/5% Ru的细胞显示出Pd和Ru的一些共定位,但不排除偶然关联。负载至5 wt% Pd/20 wt% Ru的细胞显示出核壳结构(Ru核,Pd壳)的证据。使用X射线光电子能谱(XPS)对这种细胞表面材料进行检测,显示出Pd(0)、Pd(II)、Ru(IV)和Ru(III),通过使用X射线吸收近边结构(XANES)和扩展X射线吸收精细结构(EXAFS)分析对块状材料进行分析得到了证实。生物Ru NPs和生物Pd/Ru NPs在将5 - HMF转化为2,5 - DMF方面均具有活性,但商业碳载Ru催化剂的性能比5 wt%的生物Ru高四倍。虽然5 wt% Pd/20 wt% Ru实现了20%的DMF产率,但在使用商业5 - HMF的测试反应中(>50%选择性),5 wt% Pd/5 wt% Ru生物催化剂的性能更高,与商业5 wt% Ru/C催化剂相当。5 - HMF通过淀粉和纤维素的热化学水解制备,并通过溶剂萃取将5 - HMF萃取到甲基四氢呋喃(MTHF)中。在此,以MTHF作为反应溶剂时,商业Ru/C催化剂几乎没有活性(100%转化,对DMF的选择性可忽略不计),而5 wt% Pd/5 wt% Ru生物双金属催化剂对水解产物中萃取的物质实现了100%转化和14%的DMF选择性。结果表明了一种潜在的绿色方法,可从生物质废物中实现更高的能源潜力,同时展示了一条基于生物的途径来制造一种鲜有描述的双金属材料。