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原始类水滑石层状双氢氧化物与二氧化碳的相互作用。

Interaction of Pristine Hydrocalumite-Like Layered Double Hydroxides with Carbon Dioxide.

作者信息

Narayanappa Anand N, Kamath P Vishnu

机构信息

Department of Chemistry, Central College, Bangalore University, Bangalore 560 001, India.

出版信息

ACS Omega. 2019 Feb 13;4(2):3198-3204. doi: 10.1021/acsomega.9b00083. eCollection 2019 Feb 28.

Abstract

The layered double hydroxides (LDHs) of Ca and trivalent cations, Al and Fe, are single-source precursors to generate supported CaO, which picks up CO from the gas phase in the temperature range 350-550 °C. The supports are ternary oxides, mayenite, and CaFeO. The uptake capacity of the Fe-containing LDH at 1.9 mmol g is two times the capacity of the Al-containing LDH. The product of CO uptake is calcite CaCO. It is observed that the intercalated chloride ions reduce the thermal penalty by inducing the early decomposition of CaCO. In the case of the chloride-intercalated LDHs of Ca and Fe, the CaCO formed is completely decomposed at 900 °C. This is in contrast with the CaCO formed from bare CaO, which shows no sign of decomposition at 900 °C under similar conditions. This work shows that the hydrocalumite-like LDHs are candidate materials for CO mineralization.

摘要

钙与三价阳离子(铝和铁)的层状双氢氧化物(LDHs)是生成负载型CaO的单源前驱体,该负载型CaO在350 - 550°C的温度范围内从气相中捕获CO。载体是三元氧化物、钙钛矿和CaFeO。含铁LDH在1.9 mmol g时的吸收容量是含铝LDH容量的两倍。CO吸收的产物是方解石CaCO。观察到插层的氯离子通过诱导CaCO的早期分解来降低热损失。在钙和铁的氯化物插层LDHs的情况下,形成的CaCO在900°C时完全分解。这与由纯CaO形成的CaCO形成对比,在类似条件下,纯CaO形成的CaCO在900°C时没有分解迹象。这项工作表明类水滑石LDHs是CO矿化的候选材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5db6/6648629/51b31a04f008/ao-2019-00083j_0001.jpg

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