Ma Xiaowei, Campbell Nicholas, Madec Lénaïc, Rankin Matthew A, Croll Lisa M, Dahn J R
Department of Physics and Atmospheric Science, Dalhousie University, Halifax, Nova Scotia B3H 3J5, Canada.
3M Canada Company, Brockville, Ontario K6V 5V8, Canada.
J Colloid Interface Sci. 2016 Mar 1;465:323-32. doi: 10.1016/j.jcis.2015.11.048. Epub 2015 Nov 22.
In this work, nanoporous manganese oxides (MnOx) were prepared by thermal decomposition of MnC2O4·2H2O at 225°C for 6h in air. The manganese oxalate dihydrate precipitate was made from manganese sulfate and ammonium oxalate during ultrasonication and stirring. The physical properties of the oxalate precursors and the resulting MnOx samples were characterized with SEM, TGA-DSC, FTIR and powder XRD. The specific surface areas and porosity of MnOx were studied by single-point BET and multi-point N2 adsorption-desorption measurements. The amorphous MnOx from oxalate prepared by sonication showed a specific surface area as large as 499.7m(2)/g. Dynamic SO2 and NH3 flow tests indicated that the adsorption capacity of MnOx, especially for SO2, can be increased by increased surface area. Compared to the best Mn3O4-impregnated activated carbon adsorbent, nanoporous MnOx could remove approximately three times as much SO2 and a comparable amount of NH3 per gram of adsorbent. This could lead to respirators of lower weight and smaller size which will be attractive to users.
在本工作中,通过在空气中于225°C将MnC2O4·2H2O热分解6小时制备了纳米多孔锰氧化物(MnOx)。在超声和搅拌过程中,由硫酸锰和草酸铵制得草酸锰二水合物沉淀。用扫描电子显微镜(SEM)、热重-差示扫描量热仪(TGA-DSC)、傅里叶变换红外光谱仪(FTIR)和粉末X射线衍射仪(XRD)对草酸盐前驱体和所得MnOx样品的物理性质进行了表征。通过单点BET和多点N2吸附-脱附测量研究了MnOx的比表面积和孔隙率。通过超声处理由草酸盐制备的无定形MnOx的比表面积高达499.7m²/g。动态SO2和NH3流动测试表明,MnOx的吸附容量,尤其是对SO2的吸附容量,可以通过增加表面积来提高。与最佳的Mn3O4浸渍活性炭吸附剂相比,每克纳米多孔MnOx吸附剂去除的SO2量约为其三倍,去除的NH3量相当。这可能会使呼吸器重量更轻、尺寸更小,对用户具有吸引力。