中子,x射线衍射,DSC,拉曼,Mössbauer和磷酸铁玻璃和结晶相的浸出研究

IF 4.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
RSC Advances Pub Date : 2025-02-17 DOI:10.1039/D5RA00295H
Kajal Dadwal, Margit Fábián, Istvan Tolnai, Suruchi Sharma, Rajinder Kaur, Maria Gracheva, Krisztina Kovács, Zoltán Klencsár and Atul Khanna
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引用次数: 0

摘要

采用熔体淬火法制备了xFe2O3 -(100−x)P2O5玻璃,并对其进行了结构性能相关性研究。制备了Fe2O3含量为25 ~ 40 mol%的玻璃,而Fe2O3含量为50 mol%的样品在熔融淬火时形成了Fe32+Fe43+[PO4]63−和Fe22+[P2O7]4−相的结晶样品。当Fe2O3浓度从25 mol%增加到40 mol%时,玻璃化密度从2.98 g cm−3增加到3.20 g cm−3,离子填充分数在0.63 ~ 0.65之间,玻璃化转变温度从500℃降低到493℃。利用中子衍射数据集的对分布函数分析和反向蒙特卡罗模拟计算了原子对分布、原子间距离和配位环境。P-O配位数呈四面体结构,在3.9 ~ 3.7(±0.1)范围内,Fe-O配位数随Fe2O3浓度的增加从4.8降至4.2(±0.1),O-O配位数在6.6 ~ 6.3(±0.1)范围内,这些配位数的降低是由于Fe2O3摩尔%的增加导致玻璃网络中氧缺乏性的增加。Fe-O和P-O对分布是不对称的,这表明由于键长范围很广,最大键长分别在1.79 Å和1.45-1.51 Å之间,这表明了短程无序。Mössbauer在室温和80k下进行的研究发现,铁以2+和3+价态存在,并且玻璃和晶体样品至少在三个不同的位置含有Fe2+。Raman研究发现,在Fe2O3浓度为35 mol%时,偏磷酸盐和焦磷酸盐结构单元占主导地位,而在Fe2O3浓度为40 mol%时,正磷酸盐结构单元占多数。晶体样品是一种两相材料,含有正磷酸盐和焦磷酸盐单位,前者是优势种。在90℃的纯净水中对两种磷酸铁玻璃进行浸出研究发现,随着Fe2O3摩尔%的增加,玻璃的溶解度降低,化学耐久性显著提高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neutron, X-ray diffraction, DSC, Raman, Mössbauer and leaching studies of iron phosphate glasses and crystalline phases

Neutron, X-ray diffraction, DSC, Raman, Mössbauer and leaching studies of iron phosphate glasses and crystalline phases

xFe2O3–(100 − x)P2O5 glasses were synthesized by melt quenching and structure–property correlation studies were carried. Glasses containing 25 to 40 mol% Fe2O3 were prepared while the sample with 50 mol% Fe2O3 formed a crystalline sample containing Fe32+Fe43+[PO4]63− and Fe22+[P2O7]4− phases on melt-quenching. Glass density increases from 2.98 to 3.20 g cm−3, ionic packing fraction is in the range of 0.63–0.65 and the glass transition temperature decreases from 500 °C to 493 °C on increasing Fe2O3 concentration from 25 to 40 mol%. Pair distribution function analysis and Reverse Monte Carlo simulations of neutron diffraction datasets were used to calculate the atomic pair distributions, interatomic distances and co-ordination environments. The P–O co-ordination is essentially tetrahedral and is in the range: 3.9–3.7 (±0.1), the Fe–O co-ordination number decreases steadily from 4.8 to 4.2 (±0.1) with an increase in Fe2O3 concentration in the phosphate network, while O–O co-ordination is in the range: 6.6–6.3(±0.1), the decrease in these co-ordination numbers are due to an increase in oxygen deficiency in the glass network with an increase in Fe2O3 mol%. Fe–O and P–O pair distributions are asymmetrical indicating short-range disorder due to the existence of a wide range of bond-lengths with maxima at 1.79 Å and in the range: 1.45–1.51 Å respectively. Mössbauer studies carried out at room temperature and 80 K found that Fe exists in 2+ and 3+ valence states, and the glass and crystalline samples contained Fe2+ at least at three different sites. Raman studies found that the meta and pyrophosphate structural units are dominant species up to 35 mol% Fe2O3 concentration, while the orthophosphate units are in majority at 40 mol% of Fe2O3. The crystalline sample is a two phase material and contained both orthophosphate and pyrophosphate units with the former being the dominant species. Leaching studies on two iron phosphate glasses carried out in purified water at 90 °C found that dissolution of glasses decreases and the chemical durability increases drastically with an increase in Fe2O3 mol%.

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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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