Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff CF10 3AT, UK.
The UK Catalysis Hub, Research Complex at Harwell, Harwell, Oxon OX11 0FA, UK.
Nature. 2016 Mar 3;531(7592):83-7. doi: 10.1038/nature16935. Epub 2016 Feb 15.
Copper and zinc form an important group of hydroxycarbonate minerals that include zincian malachite, aurichalcite, rosasite and the exceptionally rare and unstable--and hence little known and largely ignored--georgeite. The first three of these minerals are widely used as catalyst precursors for the industrially important methanol-synthesis and low-temperature water-gas shift (LTS) reactions, with the choice of precursor phase strongly influencing the activity of the final catalyst. The preferred phase is usually zincian malachite. This is prepared by a co-precipitation method that involves the transient formation of georgeite; with few exceptions it uses sodium carbonate as the carbonate source, but this also introduces sodium ions--a potential catalyst poison. Here we show that supercritical antisolvent (SAS) precipitation using carbon dioxide (refs 13, 14), a process that exploits the high diffusion rates and solvation power of supercritical carbon dioxide to rapidly expand and supersaturate solutions, can be used to prepare copper/zinc hydroxycarbonate precursors with low sodium content. These include stable georgeite, which we find to be a precursor to highly active methanol-synthesis and superior LTS catalysts. Our findings highlight the value of advanced synthesis methods in accessing unusual mineral phases, and show that there is room for exploring improvements to established industrial catalysts.
铜和锌形成了一类重要的羟基碳酸盐矿物,包括锌孔雀石、铜氨矾、蓝铜矿和极为罕见且不稳定的——因此鲜为人知且基本被忽视的——砷铜锌矿。前三种矿物广泛用作甲醇合成和低温水气变换(LTS)反应等工业重要反应的催化剂前体,前体相的选择强烈影响最终催化剂的活性。首选相通常为锌孔雀石。这种方法是通过共沉淀法制备的,其中涉及砷铜锌矿的短暂形成;除了少数例外,该方法都使用碳酸钠作为碳酸盐源,但这也引入了钠离子——一种潜在的催化剂毒物。在这里,我们表明,使用二氧化碳的超临界抗溶剂(SAS)沉淀(参考文献 13、14)——一种利用超临界二氧化碳的高扩散率和溶解能力快速膨胀和过饱和溶液的过程——可用于制备含钠量低的铜/锌羟基碳酸盐前体。这些前体包括稳定的砷铜锌矿,我们发现它是高活性甲醇合成和优越 LTS 催化剂的前体。我们的发现强调了先进合成方法在获取不常见矿物相方面的价值,并表明在改进现有工业催化剂方面还有改进的空间。