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钙缺失羟磷灰石对酸性、碱性和水煤气分子的不可逆吸附。

Irreversible adsorption of acidic, basic, and water gas molecules on calcium-deficient hydroxyapatite.

机构信息

Tobacco Science Research Center, Japan Tobacco Inc., 6-2 Umegaoka, Aoba-ku, Yokohama, Kanagawa 227-8512, Japan.

出版信息

Dalton Trans. 2019 Dec 3;48(47):17507-17515. doi: 10.1039/c9dt03704g.

Abstract

Hydroxyapatite [Ca10(PO4)6(OH)2, HAP] has P-OH Brønsted acidic sites, Ca2+ Lewis acidic sites, and OH- and O2- basic sites on which acidic and basic gas molecules can be selectively adsorbed, and has no micropore onto which various molecules adsorb regardless of the chemical properties of gas molecules. The interaction between the surface sites and acidic and basic gas and water molecules has been investigated by evaluating the adsorption properties of various molecules on the surfaces of calcium-deficient HAP. The specific adsorption sites were assessed by examining the reversible and irreversible adsorption of NH3, CO2, aldehydes, and water vapor on HAP at the temperature of 298 K, using two HAP samples with different Ca/P ratios, but similar structures and surface areas: Ca-deficient HAP with an extreme lower Ca/P ratio (named P-HAP) and one with a higher Ca/P ratio (named C-HAP). Irreversible adsorption of NH3 on C-HAP is attributed to the adsorption on both Ca2+ Lewis acidic and P-OH Brønsted acidic sites. Irreversible adsorption on P-HAP is attributed to the adsorption on P-OH Brønsted acidic sites only. Irreversible adsorption of CO2 occurred on C-HAP only, and preferentially on OH- basic sites. Acetaldehyde undergoes a catalytic reaction over both OH- basic sites and surface P-OH Brønsted acidic sites at 298 K. Water irreversible adsorption was extensively observed for P-HAP, and water was barely desorbed at low pressures. In situ powder X-ray diffraction showed an asymmetric expansion of the lattice in the [100] direction, indicating that water was incorporated into P-HAP crystals, especially on structural OH- sites. Irreversible adsorption of acidic and basic molecules was therefore less observed on P-HAP than on C-HAP, but P-HAP had considerable irreversible adsorption of water vapor with associated asymmetric lattice expansion. The incorporation of water vapor was first observed and could be useful to improve adsorption or catalytic performance with the mediation of water vapor and/or hydration.

摘要

羟基磷灰石[Ca10(PO4)6(OH)2,HAP]具有 P-OH 布朗斯特酸性位、Ca2+路易斯酸性位以及 OH-和 O2-碱性位,酸性和碱性气体分子可被选择性地吸附在这些位上,且没有微孔,因此各种分子无论其化学性质如何都不会被吸附。通过评估缺钙羟基磷灰石表面上各种分子的吸附性质,研究了表面位与酸性和碱性气体及水分子之间的相互作用。通过在 298 K 下,使用两种具有不同 Ca/P 比但具有相似结构和表面积的 HAP 样品(Ca 缺乏 HAP,具有极低的 Ca/P 比(命名为 P-HAP)和具有较高 Ca/P 比的 HAP(命名为 C-HAP)),研究了 NH3、CO2、醛和水蒸气在 HAP 上的可逆和不可逆吸附,来评估特定的吸附位。在 C-HAP 上不可逆吸附的 NH3归因于对 Ca2+路易斯酸性和 P-OH 布朗斯特酸性位的吸附。在 P-HAP 上不可逆吸附的 NH3归因于仅对 P-OH 布朗斯特酸性位的吸附。CO2仅在 C-HAP 上发生不可逆吸附,且优先在 OH-碱性位上发生。在 298 K 时,乙醛在 OH-碱性位和表面 P-OH 布朗斯特酸性位上发生催化反应。水在 P-HAP 上发生广泛的不可逆吸附,且在低压下几乎不脱附。原位粉末 X 射线衍射显示晶格在[100]方向上的不对称扩展,表明水被掺入 P-HAP 晶体中,特别是在结构 OH-位上。因此,与 C-HAP 相比,P-HAP 上酸性和碱性分子的不可逆吸附较少,但 P-HAP 对水蒸气具有相当大的不可逆吸附,并伴随着不对称晶格膨胀。首次观察到水蒸气的掺入,并且可以通过水蒸气和/或水合的介导来改善吸附或催化性能。

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