首页> 外文期刊>ACS Sustainable Chemistry & Engineering >Development of Au and 1D Hydroxyapatite Nanohybrids Supported on 2D Boron Nitride Sheets as Highly Efficient Catalysts for Dehydrogenating Glycerol to Lactic Acid
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Development of Au and 1D Hydroxyapatite Nanohybrids Supported on 2D Boron Nitride Sheets as Highly Efficient Catalysts for Dehydrogenating Glycerol to Lactic Acid

机译:在2D氮化硼片上负载的Au和1d羟基磷灰石纳米胺的研制为高效催化剂,用于将甘油脱氢至乳酸的催化剂

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In this study, highly transparent and tightly packed two-dimensional boron nitride (2D BN NSs) nanosheets were prepared using an eco-friendly green-template-assisted synthesis method, where a banana stem powder was used as the bio template. Microscopic results indicated that 2D BN NSs mostly consisted of thin layers, with lateral sizes of 0.5 to 2 mu m. Further, strongly coupled dual catalytic sites of OD Au and c-axis oriented 1D hexagonal hydroxyapatite (HAp) nanorods were successfully immobilized and uniformly distributed on the surfaces of 2D BN NSs (Au/HAp/BN). A detailed study of Au/HAp/BN formation mechanism is presented in this paper. This study showed that due to the intriguing morphological, structural, and compositional features of Au/HAp/BN ternary nanohybrids, they can be used as an efficient heterogeneous catalytic oxidation system for oxidizing glycerol into lactic acid. In particular, the localized surface of BN was shown to exhibit high affinity toward adsorbing glycerol via higher adsorption affinity; therefore, an oxidizing reaction was obtained at the dual catalytic sites of Au and HAp in the heterogeneous catalytic system of Au/HAp/BN. On the Au/HAp/BN catalyst, 100% glycerol conversion yield was obtained with a high selective production of lactic acid (99.5%) in its base condition at a temperature of 100 degrees C. Different effects of the NaOH-glycerol molar ratio, reaction time of the catalytic activity, and selectivity of the Au/HAp/BN catalyst suggested that the dual-route reaction pathway was responsible for dehydrating glycerol to lactic acid; this has been elucidated in the paper. Reusability experiments showed the chemical stability and prolonged usage of the Au/HAp/BN catalyst, which can be beneficial for industrial applications.
机译:在该研究中,使用环融合的绿色模板辅助合成方法制备高度透明和紧密的二维氮化物(2D BN NSS)纳米晶片,其中使用香蕉茎粉作为生物模板。显微镜结果表明,2D BN NSS主要由薄层组成,横向尺寸为0.5至2μm。此外,成功地固定并均匀地分布在2D BN NSS(AU / HAP / BN)的表面上成功地固定并均匀地分布在2D BN NSS(Au / Hap / Bn)的表面上的强耦合的OD Au和C轴取向的1d六方羟基磷灰石(Hap)纳米末端。本文提出了对Au / Hap / Bn形成机制的详细研究。该研究表明,由于Au / Hap / Bn三元纳米嗜含量的有趣形态,结构和组成特征,它们可以用作氧化甘油氧化成乳酸的有效的异质催化氧化体系。特别地,显示BN的局部表面,以通过更高的吸附亲和力对吸附甘油的高亲和力;因此,在Au / Hap / Bn的异质催化系统的Au和Hap的双催化位点获得氧化反应。在Au / Hap / Bn催化剂上,在100℃的温度下,在其基础条件下,在100℃的碱条件下,获得100%甘油转化产率。催化活性的反应时间,Au / Hap / Bn催化剂的选择性表明,双途反应途径负责将甘油脱水至乳酸;这在纸上阐明了这一点。可重用性实验表明,AU / HAP / BN催化剂的化学稳定性和延长用途,可对工业应用有益。

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