镧
煅烧
纳米颗粒
碳酸镧
正交晶系
材料科学
水合物
核化学
粉末衍射
氧化镧
无机化学
矿物学
氧化物
结晶学
纳米技术
化学
晶体结构
冶金
有机化学
高磷血症
钙
催化作用
作者
Sentienla Imsong,Punazungba Imsong,Swapnali Hazarika,M. Indira Devi
标识
DOI:10.1515/zpch-2023-0396
摘要
Abstract This study could present the size and morphology of two synthesized nanoparticles (NPs) by observing their smallest possible dimensions. Lanthanum carbonate nanoparticles were synthesized by sonochemical method through the interaction of lanthanum acetate hydrate and sodium carbonate in an aqueous medium with a probe sonicator. After rigorous washing followed by drying, the La 2 (CO 3 ) 3 ·8H 2 O(S1) NPs were calcined at a temperature of 600 °C to obtain lanthanum oxide nanoparticles (S2). Both NPs were characterised through various instrumental techniques. PXRD study showed orthorhombic with space group of Pccn (56) and hexagonal phases with space group of P 3 ‾ m 1 $P\overline{3}m1$ (164) for S1 and S2 respectively whose morphology and elemental analysis were studied through FESEM and EDX. High resolution TEM image of La 2 (CO 3 ) 3 ·8H 2 O and La 2 O 3 showed spherical shapes of the nanoparticles. Further study of XPS and FTIR conveyed detailed information of both nanoparticles whose TGA-DSC showed three step decomposition curves. The size and morphology of the synthesized nanoparticles have been found to have a distinct morphology and are found comparatively smaller in size than those observed in the earlier reported works (Table 1 Table 1: Comparative study of synthesized lanthanum carbonate and lanthanum oxide NPs with various techniques applied by other researchers. Sl. no. Name of NPs Methods Conditions Size of NP Reference 1 La 2 (CO 3 ) 3 ·8H 2 O Sonochemical method Time: 25 min XRD: Pccn (56) a = 8.9840 Å b = 9.5800 Å c = 17.0000 Å This work Temperature: 301 K Size : 24.102 nm Starting materials: (a) La(CH 3 COO) 2 : 0.050 M (b) Na 2 CO 3 :0.050 M TEM : Size : 4–30 nm La 2 (CO 3 ) 3 Reverse micelles Time: 1 h XRD : Size : nanoparticles absent [20] Temperature: 303 K Starting materials: (a) Triton X-100 (b) Cyclohexane (c) n-butylalcohol (d) La(NO 3 ) 3(aq) e) NaCO 3(aq) La 2 (CO 3 ) 3 ·8H 2 O Hydrothermal Time: 2–5 days XRD : Pccn a = 8.984 Å b = 9.580 Å c = 17.00 Å [21] Temperature: 773 K Size : nanoparticles absent Prepared by slow hydrolysis of La(CCl 3 COO) 3 La 2 (CO 3 ) 3 ·1.4H 2 O Hydrothermal Time: 1 h 30 min Structure unknown [22] Temperature: 368 K Starting material: (a) La 2 O 3 (b) HNO 3 (c) Urea La 2 (CO 3 ) 3 ·1.7H 2 O Sonochemical Time: 30 min XRD: a = 8.990 Å c = 9.675 Å [23] Temperature: not specified Size : not specified (a) La(OAC) 3 (b) Na 2 CO 3 TEM : Size: 25–35 nm Concentration: (a) La(OAC) 3 : 0.051 M (b) Na 2 CO 3 : 0.251 M La 2 (CO 3 ) 3 ·5H 2 O Hydrothermal Time: XRD: Pbca a = 9.0167 Å b = 12.842 Å c = 9.6331 Å [24] Temperature: Size : not specified Starting materials: (a) La 2 O 3 (b) HCl (c) Na 2 CO 3 La 2 (CO 3 ) 3 ·3.4H 2 O Hydrothermal Time: 3–4 h XRD: P 2 1 2 1 2 a = 9.57 Å b = 12.65 Å c = 8.94 Å [25] Temperature: 298–308 K Size : not specified Starting materials: (a) LaCl 3 (b) NH 4 HCO 3 2 La 2 O 3 Thermal decomposition Time: 2 h P 3 m 1 a = 3.973 Å b = 3.9373 Å c = 6.129 Å [26] Temperature: 1073 K Size : 15 nm Starting material: La(OH) 3 nanorods TEM : Size : 23 nm La 2 O 3 Thermal decomposition Time: 2 h XRD : a = 11.347 Å [23] Temperature: 873 K Size: 30 nm Starting material: La 2 (CO 3 ) 3 ·1.7H 2 O TEM : Size : 30 nm La 2 O 3 Thermal decomposition Time: not specified Not specified [27] Temperature: 1198 K Starting material: (a) La(NO 3 ) 3 ·9H 2 O (b) NH 4 HCO 3 La 2 O 3 Thermal decomposition Time: 4 h Not specified [28] Temperature: 1073 K Starting material: La(OH) 3 La 2 O 3 Thermal decomposition Time: 2 h P 3 ‾ m 1 $P\overline{3}m1$ a = 3.973 Å b = 3.9373 Å c = 6.129 Å This work Temperature: 873 K XRD : Size : 43.26 nm Starting material: La 2 (CO 3 ) 3 ·8H 2 O TEM: Size : 17–34 nm ).
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