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用于控制纳米微晶羟基磷灰石晶体学参数以增强光催化活性的不同溶剂和有机改性剂。

Different solvents and organic modifiers for the control of crystallographic parameters in nano-crystallite hydroxyapatite for amplification of photocatalytic activity.

作者信息

Kawsar Md, Sahadat Hossain Md, Tabassum Sumaya, Bahadur Newaz Mohammed, Ahmed Samina

机构信息

Glass Research Division, Institute of Glass & Ceramic Research and Testing, Bangladesh Council of Scientific and Industrial Research (BCSIR) Dhaka-1205 Bangladesh

Department of Applied Chemistry and Chemical Engineering, Noakhali Science and Technology University Noakhali Bangladesh.

出版信息

Nanoscale Adv. 2024 Apr 10;6(10):2682-2700. doi: 10.1039/d3na01122d. eCollection 2024 May 14.

DOI:10.1039/d3na01122d
PMID:38752133
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11093264/
Abstract

In this research, HAp nanocrystals were synthesized using conventional wet chemical precipitation methods using various organic modifiers, including urea, palmitic acid, and naphthalene. Ethanol and isopropyl alcohol (IPA) were used as solvents in this process. Different characterization techniques, namely X-ray diffraction (XRD), scanning electron microscopy (SEM), and UV-vis absorption spectroscopy, were employed to ascertain the formation of HAp nanocrystals. Numerous structural parameters, including lattice parameters, unit cell size, volume of the unit cell, specific surface area, degree of crystallinity, dislocation density, macrostrain, and crystallinity index, were assessed using XRD data. The linear straight-line method of Scherrer's equation, Monshi-Scherrer's method, the Williamson-Hall method, the size-strain plot method, the Halder-Wagner method, and Sahadat-Scherrer's model were applied to compute the crystallite size of the synthesized HAp samples. All the synthesized HAp has crystalline structures within the permissible range of 1-150 nm which were estimated from the XRD data using the mentioned models. However, the values for strain (from -3 × 10 to 6.4 × 10), strain (from -9.599 × 10 to 7 × 10 N m), and energy density (from -11 × 10 to 2 × 10 J m) were also calculated for the synthesized samples. In addition, the optical band gap energy of the synthesized HAp was computed (5.89 to 6.19 eV). The synthesis media have a control on the crystallographic planes, in the case of the ethanol medium, the (110) plane exhibited significant intensity (which could potentially serve as a driving force for enhancing photocatalytic activity). The use of 100% ethanol HAp yields the most favorable outcome regarding both the degradation percentage (91.79%) and degradation capacity (7%) for the Congo red dye.

摘要

在本研究中,使用包括尿素、棕榈酸和萘在内的各种有机改性剂,通过传统的湿化学沉淀法合成了羟基磷灰石(HAp)纳米晶体。在此过程中,使用乙醇和异丙醇(IPA)作为溶剂。采用不同的表征技术,即X射线衍射(XRD)、扫描电子显微镜(SEM)和紫外可见吸收光谱,来确定HAp纳米晶体的形成。利用XRD数据评估了许多结构参数,包括晶格参数、晶胞尺寸、晶胞体积、比表面积、结晶度、位错密度、宏观应变和结晶度指数。应用谢乐方程的线性直线法、蒙希-谢乐法、威廉姆森-霍尔法、尺寸-应变图法、哈尔德-瓦格纳法和萨哈达特-谢乐模型来计算合成的HAp样品的微晶尺寸。所有合成的HAp都具有1-150nm允许范围内的晶体结构,这是使用上述模型根据XRD数据估算得出的。然而,还计算了合成样品的应变值(从-3×10到6.4×10)、应变值(从-9.599×10到7×10 N m)和能量密度(从-11×10到2×10 J m)。此外,计算了合成的HAp的光学带隙能量(5.89至6.19eV)。合成介质对晶体学平面有控制作用,在乙醇介质的情况下,(110)平面显示出显著强度(这可能潜在地作为增强光催化活性的驱动力)。对于刚果红染料,使用100%乙醇HAp在降解率(91.79%)和降解能力(7%)方面产生了最有利的结果。

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