Cheng Jiaqi, Poduska Kristin M
Department of Chemistry, Memorial University of Newfoundland, St. John's, NL A1B3X7, Canada.
Department of Physics and Physical Oceanography, Memorial University of Newfoundland, St. John's, NL A1B3X7, Canada.
Nanomaterials (Basel). 2013 Jun 24;3(3):317-324. doi: 10.3390/nano3030317.
We demonstrate a simple strategy to either prevent or enhance hydroxide incorporation in nanocrystalline solid-state metathesis reaction products prepared in ambient environments. As an example, we show that ZnCO (smithsonite) or Zn₅(CO₃)₂(OH)₆ (hydrozincite) forms extremely rapidly, in less than two minutes, to form crystalline domains of 11 ± 2 nm and 6 ± 2 nm, respectively. The phase selectivity between these nanocrystalline products is dominated by the alkalinity of the hydrated precursor salts, which may in turn affect the availability of carbon dioxide during the reaction. Thus, unlike traditional aqueous precipitation reactions, our solid-state method offers a way to produce hydroxide-free, nanocrystalline products without active pH control.
我们展示了一种简单的策略,可用于防止或增强在环境条件下制备的纳米晶固态复分解反应产物中氢氧化物的掺入。例如,我们表明碳酸锌(菱锌矿)或碱式碳酸锌(水锌矿)能在不到两分钟的时间内极快速地形成,分别形成11±2纳米和6±2纳米的晶畴。这些纳米晶产物之间的相选择性主要由水合前体盐的碱度决定,而碱度反过来可能会影响反应过程中二氧化碳的可得性。因此,与传统的水相沉淀反应不同,我们的固态方法提供了一种无需主动控制pH值就能制备无氢氧化物纳米晶产物的途径。