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Surface acidity of calcium phosphate and calcium hydroxyapatite: FTIR spectroscopic study of low-temperature CO adsorption

机译:磷酸钙和羟基磷灰石的表面酸度:低温CO吸附的FTIR光谱研究

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摘要

The surface properties of calcium phosphate precursor (CP) and crystalline calcium hydroxyapatite (HA) prepared biomimetically have been studied by 1R spectroscopy of adsorbed CO. Both samples are characterized by the absence of Bronsted acidity. Low-temperature CO adsorption on CP evacuated at 523 K leads to formation of only one family of Ca~(2+)-CO species (2168 cm~(-1)). The analysis indicates that the respective calcium ions on the surface are not isolated. Similar spectra were obtained with HA evacuated at 573 K. In this case, however, the Ca~(2+)-CO band was detected at 2165 cm~(-1) due to enhanced lateral interaction between the adsorbed CO molecules. Another family of Ca~(2+) sites (Ca~(2+)-CO band at 2178 cm~(-1)) was created after evacuation of the HA sample at 673 K. These sites were assumed to be a result of sample dehydroxylation. The results demonstrate the absence of any protonic acidity of the samples (i.e. P-OH surface groups) and weak electrostatic Lewis acidity caused by coordinatively unsaturated Ca~(2+) cations.
机译:通过吸附CO的1R光谱研究了仿生制备的磷酸钙前体(CP)和结晶性羟基磷灰石钙(HA)的表面性能。这两个样品的特征都是不存在布朗斯台德酸度。在523 K下抽空的CP上的低温CO吸附导致仅形成一族Ca〜(2 +)-CO物种(2168 cm〜(-1))。分析表明表面上的各个钙离子未被分离。在573 K处抽空HA可获得相似的光谱。但是,在这种情况下,由于吸附的CO分子之间的横向相互作用增强,在2165 cm〜(-1)处检测到Ca〜(2 +)-CO带。在673 K下抽空HA样品后,创建了另一个Ca〜(2+)位点族(Ca〜(2 +)-CO带位于2178 cm〜(-1))。这些位点被认为是由于样品脱羟基。结果表明没有样品的质子酸度(即P-OH表面基团)和由配位不饱和的Ca〜(2+)阳离子引起的弱的静电路易斯酸度。

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