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Fabrication of astaxanthin‐loaded nanoparticles and their neuroprotective effects on C6 cell lines 制作虾青素负载纳米颗粒及其对 C6 细胞系的神经保护作用
IF 0.9 Q3 Chemistry Pub Date : 2024-03-28 DOI: 10.1002/vjch.202300299
H. Oanh, Hoang Thi Minh Hien, Nguyen Van Tru, T. T. Hien, Mai Ha Hoang
Astaxanthin (AST), a well‐known carotenoid primarily extracted from the green microalgae Haematococcus pluvialis, exhibits notable pharmacological properties, including anticancer, antioxidation, anti‐inflammatory, and neuroprotective effects. However, its practical application in pharmaceuticals, food, and cosmetics is hindered by its limited water solubility and poor bioavailability. To address these challenges, this study aims to fabricate astaxanthin‐loaded nanoparticles and evaluate their neuroprotective potential. Nanoparticles of astaxanthin were synthesized by the freeze‐drying method using the surfactants Tween 80 and lecithin, the β‐cyclodextrin encapsulating agent. The nanoparticles possessing high AST loading (up to 9.6 wt%) had a spherical shape with an average particle size of 98 nm and negative surface potentials (ζ = −36.8 mV). The neuroprotective effects of the astaxanthin nanoparticles were thoroughly determined. Nanoastaxanthin (NA) exhibited excellent dispersibility and stability in aqueous solutions, thereby remarkably improving its absorption into the C6 glial cell line. Furthermore, nanoastaxanthin protected C6 cells against Aβ25‐35‐induced neurotoxicity by inhibiting the activity of acetylcholinesterase and the expression of genes (iNOS, COX, TNF‐α, and IL‐6) involved in the inflammatory pathway. In general, these results suggest that nanoparticles of astaxanthin in this work may be appropriate ingredients for functional foods.
虾青素(AST)是一种著名的类胡萝卜素,主要从绿色微藻类 Haematococcus pluvialis 中提取,具有显著的药理特性,包括抗癌、抗氧化、抗炎和神经保护作用。然而,由于其水溶性有限且生物利用率低,阻碍了其在药品、食品和化妆品中的实际应用。为了应对这些挑战,本研究旨在制造虾青素负载纳米颗粒,并评估其神经保护潜力。研究人员利用表面活性剂吐温80和卵磷脂以及β-环糊精包裹剂,通过冷冻干燥法合成了虾青素纳米颗粒。高AST负载量(高达9.6 wt%)的纳米颗粒呈球形,平均粒径为98 nm,表面电位为负(ζ = -36.8 mV)。对虾青素纳米颗粒的神经保护作用进行了深入研究。纳米虾青素(NA)在水溶液中表现出优异的分散性和稳定性,从而显著提高了C6神经胶质细胞系对其的吸收。此外,纳米虾青素通过抑制乙酰胆碱酯酶的活性和炎症通路相关基因(iNOS、COX、TNF-α和IL-6)的表达,保护C6细胞免受Aβ25-35诱导的神经毒性的影响。总之,这些结果表明,本研究中的虾青素纳米颗粒可能是功能性食品的适当成分。
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引用次数: 0
Biosurfactant production by a crude oil‐utilizing bacterium towards petroleum hydrocarbon biodegradation applications 一种利用原油的细菌生产生物表面活性剂,用于石油烃的生物降解
IF 0.9 Q3 Chemistry Pub Date : 2024-03-28 DOI: 10.1002/vjch.202300297
T. Kieu, Thi Yen Nguyen, Van Tho Nguyen, Thi Ngoc Quynh Nguyen
Biosurfactants produced by microorganisms are green amphiphilic biomolecules. They have numerous advantages compared to chemical surfactants including a lower toxicity, better environmental compatibility and effective and stable properties under extreme conditions such as a wide range of temperature, pH and salinity. A highly bio‐surfactant‐producing strain of Bacillus, VTVK15 was selected among the Bacillus isolates from marine environment and oil contaminated sites in Ba Ria—Vung Tau. Sequence analysis of 16S rDNA showed that the VTVK15 strain was 99% similar with 16s rDNA sequence of Bacillus megaterium. The suitable conditions for the bio‐surfactant production by the strain VTVK15 were 37 °C, pH 7; 2% w/v and 0.4% w/v for temperature, initial solution pH, concentration of carbon substrate (crude oil), and concentration of nitrogen substrate ((NH4)2SO4), respectively. The emulsification index (E24) increased from 51.8% to 67.7% with suitable conditions. The petroleum hydrocarbon degradation (TPH) efficiency by the strain Bacillus megaterium VTVK15 in crude oil estimated using TPH analysis was 72% after 14 days. These results revealed that the strain VTVK15 exhibited a tremendous potential for bioremediation of petroleum hydrocarbon contaminants.
由微生物产生的生物表面活性剂是一种绿色两亲性生物分子。与化学表面活性剂相比,生物表面活性剂具有许多优点,包括毒性较低、环境兼容性较好、在温度、pH 值和盐度等极端条件下具有有效和稳定的特性。从巴里亚-榜头的海洋环境和石油污染场地分离的芽孢杆菌中,筛选出了一株高产生物表面活性剂的芽孢杆菌 VTVK15。16S rDNA 序列分析表明,VTVK15 菌株与大型芽孢杆菌的 16s rDNA 序列有 99% 的相似性。VTVK15 菌株生产生物表面活性剂的适宜条件为 37 °C、pH 7;温度、初始溶液 pH 值、碳底物(原油)浓度和氮底物((NH4)2SO4)浓度分别为 2% w/v 和 0.4% w/v。在合适的条件下,乳化指数(E24)从 51.8%提高到 67.7%。用 TPH 分析法估算,14 天后,巨大芽孢杆菌 VTVK15 菌株在原油中的石油烃降解(TPH)效率为 72%。这些结果表明,VTVK15 菌株在石油烃污染物的生物修复方面具有巨大潜力。
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引用次数: 0
Investigation of the effect of lithium salt doping in gel polymer electrolytes for symmetrical solid‐state supercapacitors 研究凝胶聚合物电解质中的锂盐掺杂对对称固态超级电容器的影响
IF 0.9 Q3 Chemistry Pub Date : 2024-03-26 DOI: 10.1002/vjch.202300289
Hop Tran Thi Thanh, Mai Dang Thi, Tung Ngo Trinh, Son Pham Tung, T. Cong, T. T. Y. Nhi, Phuoc Anh Le, Do Thi Mai Huong
Stable and high‐mechanical‐strength gel polymer electrolytes have been investigated by doping lithium salts (LiBr, LiClO4, and Li2SO4) as additive factors into PVA‐CH3COONa systems and highly activated carbon electrodes for symmetrical solid‐state supercapacitors (SSCs). The investigation of the supercapacitors with the presence of lithium salts in the electrolyte not only enhances the mechanical property of gel polymer electrolytes (GPEs) but also improves the energy capability of supercapacitor devices. The electrode‐specific capacitance of supercapacitor‐doped LiClO4 salt was at its maximum value at 100 F g−1 (current density: 1.5 A g−1). These symmetrical SSCs are considered to have potential for developing eco‐friendly energy storage devices.
通过将锂盐(LiBr、LiClO4 和 Li2SO4)作为添加剂掺入 PVA-CH3COONa 系统和高活性碳电极中,研究了用于对称固态超级电容器(SSC)的稳定且高机械强度的凝胶聚合物电解质。对电解质中含有锂盐的超级电容器的研究不仅增强了凝胶聚合物电解质(GPEs)的机械性能,还提高了超级电容器装置的能量能力。超级电容器掺杂的 LiClO4 盐的电极特异电容在 100 F g-1 时达到最大值(电流密度:1.5 A g-1)。这些对称的 SSCs 被认为具有开发环保型储能设备的潜力。
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引用次数: 0
Nitidine from Zanthoxylum rhetsa and its cytotoxic activities in vitro and in silico ADMET properties 来自 Zanthoxylum rhetsa 的氮苷及其体外细胞毒性活性和硅学 ADMET 特性
IF 0.9 Q3 Chemistry Pub Date : 2024-03-26 DOI: 10.1002/vjch.202300278
Tran Thi Tuyen, Pham Minh Quan, D. H. Nghi, Pham Cao Bach, Dang Hoang Hiep, Nguyen Thanh Duong, Nguyen Nhat Linh, Trinh Anh Vien, Phạm Thị Hồng Minh, Nguyen Thi Hong Van
Nitidine, a potential medicinal natural benzophenanthridine alkaloid, has expressed various bioactivities such as antibacterial, antifungal, antiviral, anti‐inflammatory, analgesic, and notably cytotoxicity. In this study, nitidine was isolated from trunk of Zanthoxylum rhetsa (Rutaceae) and its structure was elucidated by spectral data (1D and 2D NMR; and MS). The cytotoxicity of nitidine was assessed in vitro against five cancer cell lines, and normal cell line Vero. As the results, nitidine exhibited potent inhibitory activity against KB, LU‐1, HepG2, LNCaP and MCF7 cell lines with IC50 values of 0.28, 0.26, 0.27, 0.25 and 0.28 µm, respectively, while low‐cytotoxicity against normal cell line Vero with IC50 value of 140.65 µm. Comparing cytotoxic activity of nitidine with docking analysis in previous study, nitidine formed hydrogen bonds with residues Asn101 and Ala317 of tubulin and had a docking score of −14.45 kcal/mol, all the data proved nitidine would be a potential candidate for inhibiting the function of tubulin at the active site regarding binding affinity, dock pose, and ADMET—where ADMET stands for absorption, distribution, metabolism, excretion and toxicity—properties analysis.
硝啶是一种潜在的药用天然二苯并菲啶类生物碱,具有多种生物活性,如抗菌、抗真菌、抗病毒、消炎、镇痛和显著的细胞毒性。本研究从芸香科植物 Zanthoxylum rhetsa 的树干中分离出了硝啶,并通过光谱数据(1D 和 2D NMR 以及 MS)阐明了其结构。在体外评估了硝啶对五种癌细胞株和正常细胞株 Vero 的细胞毒性。结果显示,硝啶对 KB、LU-1、HepG2、LNCaP 和 MCF7 细胞株具有强效抑制活性,IC50 值分别为 0.28、0.26、0.27、0.25 和 0.28 µm,而对正常细胞株 Vero 的毒性较低,IC50 值为 140.65 µm。将硝啶的细胞毒性活性与之前研究中的对接分析进行比较,发现硝啶与小管蛋白的残基 Asn101 和 Ala317 形成氢键,对接得分为 -14.45 kcal/mol,所有数据都证明,从结合亲和力、对接姿态和 ADMET(ADMET 是吸收、分布、代谢、排泄和毒性的缩写)特性分析来看,硝啶是抑制小管蛋白活性位点功能的潜在候选化合物。
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引用次数: 0
Xanthine oxidase and nitric oxide inhibitory activities of compounds isolated from Gomphrena celosioides 从 Gomphrena celosioides 中分离的化合物的黄嘌呤氧化酶和一氧化氮抑制活性
IF 0.9 Q3 Chemistry Pub Date : 2024-03-26 DOI: 10.1002/vjch.202300269
Ngo Van Quang, Nguyen Thi Mai Phuong, D. V. Luong, Nguyen Thi Trang Huyen, Do Thi Thanh Xuan, Thanh Thi Thu Thuy
In this study, the investigation of xanthine oxidase and nitric oxide formation inhibitory activities of three compounds isolated from aerial part of Gomphrena celosioides, a folk medicinal plant for treatment of gout disease, is reported. The isolated compounds were determined based on NMR and ESI‐MS spectra, they are umbellatosides B, 20‐hydroxyecdysone, and 20‐hydroxyecdysone‐20,22‐monoacetonide. Biological activity results indicated that three compounds showed great activities, in which, umbellatosides B has good activity with IC50 value of 33.78 ± 0.49 and 19.55 ± 0.61 µm for xanthine oxidase and nitric oxide inhibitory activities, respectively. This is the report on the xanthine oxidase and nitric oxide inhibitory activities of three compounds that were first time isolated from the G. celosioides.
本研究报告了从一种治疗痛风病的民间药用植物 Gomphrena celosioides 的气生部分分离出的三种化合物对黄嘌呤氧化酶和一氧化氮形成的抑制活性。根据 NMR 和 ESI-MS 图谱确定了分离出的化合物,它们分别是伞形酮苷 B、20-羟基蜕皮激素和 20-羟基蜕皮激素-20,22-单丙酮苷。生物活性结果表明,这三种化合物具有很高的活性,其中伞形酮苷 B 具有很好的活性,其抑制黄嘌呤氧化酶和一氧化氮活性的 IC50 值分别为 33.78 ± 0.49 µm 和 19.55 ± 0.61 µm。这是关于首次从 G. celosioides 中分离出的三种化合物的黄嘌呤氧化酶和一氧化氮抑制活性的报告。
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引用次数: 0
Degradation of trimethoprim by advanced oxidation process using UV/TiO2 and H2O2: Kinetic and economic aspects 利用紫外线/二氧化钛和 H2O2 的高级氧化工艺降解三甲氧苄啶:动力学和经济方面
IF 0.9 Q3 Chemistry Pub Date : 2024-03-26 DOI: 10.1002/vjch.202300274
Dang Hong Minh, Nguyen Thanh Huyen, P. D. Chinh, Nguyen Thi Lan Phuong, Nguyen Thanh Dong, Nguyen Minh Tan, Nguyen Thi Thu Trang
Trimethoprim (TMP) is an effective antibiotic for treating many different infections, but it can lead to water pollution and pose a threat of generating antibiotic‐resistant bacteria through waste in the drug manufacturing process, use, and excretion of humans as well as animals. Due to its strong and non‐selective oxidizing ability, advanced oxidation processes (AOPs) utilizing UV/TiO2 and H2O2 are more efficient in removing them than conventional wastewater treatment. This work investigates TMP degradation in different water substrates by AOPs using UV/TiO2 and H2O2. The results show that the apparent reaction rate constant to the TMP's degradation in the de‐ion water matrix is 0.0379; 0.1937; and 0.209 min−1 for UV/TiO2, UV/H2O2, and UV/TiO2/H2O2 processes. The rate of degradation of TMP in hospital wastewater is lower than that of lake water and de‐ion water. The major intermediate products obtained from the degradation of TMP in de‐ion water by UV/TiO2/H2O2 process were recognized as C14H19O4N4 (m/z: 307), C5H7ON4 (m/z: 139), and C5H6O2N4 (m/z: 155). Finally, the cost of TMP treatment in de‐ion water by several AOPs using photocatalyst and hydrogen peroxide was calculated, it is 0.88 $/m3 for UV/H2O2; 33.01 $/m3 for UV/TiO2 process, and 18.77 $/m3 for UV/TiO2/H2O2 process.
三甲氧苄啶(TMP)是一种有效的抗生素,可用于治疗多种不同的感染,但在药物生产、使用和人类及动物排泄过程中产生的废物会导致水污染,并造成产生抗生素耐药菌的威胁。由于其氧化能力强且无选择性,利用紫外线/二氧化钛和 H2O2 的高级氧化工艺(AOPs)比传统的废水处理方法更有效地去除它们。本研究利用 UV/TiO2 和 H2O2 的高级氧化工艺研究了不同水基质中 TMP 的降解情况。结果表明,UV/TiO2、UV/H2O2 和 UV/TiO2/H2O2 工艺在去离子水基质中降解 TMP 的表观反应速率常数分别为 0.0379、0.1937 和 0.209 min-1。医院废水中 TMP 的降解率低于湖水和去离子水。紫外/二氧化钛/H2O2 工艺降解去离子水中的 TMP 得到的主要中间产物为 C14H19O4N4(m/z:307)、C5H7ON4(m/z:139)和 C5H6O2N4(m/z:155)。最后,计算了采用光催化剂和过氧化氢的几种 AOP 处理去离子水中 TMP 的成本,UV/H2O2 为 0.88 美元/立方米,UV/TiO2 为 33.01 美元/立方米,UV/TiO2/H2O2 为 18.77 美元/立方米。
{"title":"Degradation of trimethoprim by advanced oxidation process using UV/TiO2 and H2O2: Kinetic and economic aspects","authors":"Dang Hong Minh, Nguyen Thanh Huyen, P. D. Chinh, Nguyen Thi Lan Phuong, Nguyen Thanh Dong, Nguyen Minh Tan, Nguyen Thi Thu Trang","doi":"10.1002/vjch.202300274","DOIUrl":"https://doi.org/10.1002/vjch.202300274","url":null,"abstract":"Trimethoprim (TMP) is an effective antibiotic for treating many different infections, but it can lead to water pollution and pose a threat of generating antibiotic‐resistant bacteria through waste in the drug manufacturing process, use, and excretion of humans as well as animals. Due to its strong and non‐selective oxidizing ability, advanced oxidation processes (AOPs) utilizing UV/TiO2 and H2O2 are more efficient in removing them than conventional wastewater treatment. This work investigates TMP degradation in different water substrates by AOPs using UV/TiO2 and H2O2. The results show that the apparent reaction rate constant to the TMP's degradation in the de‐ion water matrix is 0.0379; 0.1937; and 0.209 min−1 for UV/TiO2, UV/H2O2, and UV/TiO2/H2O2 processes. The rate of degradation of TMP in hospital wastewater is lower than that of lake water and de‐ion water. The major intermediate products obtained from the degradation of TMP in de‐ion water by UV/TiO2/H2O2 process were recognized as C14H19O4N4 (m/z: 307), C5H7ON4 (m/z: 139), and C5H6O2N4 (m/z: 155). Finally, the cost of TMP treatment in de‐ion water by several AOPs using photocatalyst and hydrogen peroxide was calculated, it is 0.88 $/m3 for UV/H2O2; 33.01 $/m3 for UV/TiO2 process, and 18.77 $/m3 for UV/TiO2/H2O2 process.","PeriodicalId":23525,"journal":{"name":"Vietnam Journal of Chemistry","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2024-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140380216","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis, studies on properties of Eu3+/Dy3+ co–doped BaMoO4 nanophosphors via hydrothermal method 水热法合成 Eu3+/Dy3+ 共掺杂 BaMoO4 纳米磷酸盐并研究其性质
IF 0.9 Q3 Chemistry Pub Date : 2024-03-21 DOI: 10.1002/vjch.202300266
Nhuong Chu Manh, Truong Mai Xuan, Lan Nguyen T. Hien, Huong Tra, Anh Duong T. Tu, Toan Tran Quoc
The article shows the outstanding properties and luminescence ability of Eu3+/Dy3+ co–doped BaMoO4 (BMED) materials, which have been successfully fabricated by the hydrothermal method. The crystalline structure analysis of BMED nanophosphor by X–ray diffraction (XRD) shows that it has a structure single–phase structure, with tetragonal BaMoO4 (JCPDS 029–0193), consist of spherical nanoparticles with a size diameter of 31.79–52.99 nm. The characteristic vibrational modes of molybdate lattice in the Raman spectroscopy confirmed the successful Eu3+/Dy3+ co–doped into the host matrix. The field emission scanning electron microscopy (FE–SEM) image shows that the BMED consists of quite uniform nanoparticle with sizes less than 50 nm. The energy dispersive spectra (EDS) confirm the purity and uniform distribution of elements Eu, Dy, Mo, O, Ba throughout in the solid sample. The BMED nanophosphor has is small bandgap from 2.83 to 3.00 eV. The photoluminescence spectra show that BMED have strong red emission at 616 nm of the transition (5D0 → 7F2) with luminescence lifetime from 0.330 to 1.429 ms. The BMED nanophosphor have potential application for the production of warm wLEDs, agricultural lighting and biomedical marking.
文章展示了水热法成功制备的Eu3+/Dy3+共掺杂BaMoO4(BMED)材料的优异性能和发光能力。X 射线衍射(XRD)对 BMED 纳米磷的晶体结构分析表明,其结构为单相结构,BaMoO4 为四方结构(JCPDS 029-0193),由直径为 31.79-52.99 nm 的球形纳米颗粒组成。拉曼光谱中钼酸盐晶格的特征振动模式证实了 Eu3+/Dy3+ 成功地掺杂到了宿主基质中。场发射扫描电子显微镜(FE-SEM)图像显示,BMED 由尺寸小于 50 nm 的非常均匀的纳米颗粒组成。能量色散光谱(EDS)证实了固体样品中 Eu、Dy、Mo、O、Ba 元素的纯度和均匀分布。BMED 纳米磷具有 2.83 至 3.00 eV 的小带隙。光致发光光谱显示,BMED 在跃迁(5D0 → 7F2)的 616 纳米波长处有强烈的红色发射,发光寿命为 0.330 至 1.429 毫秒。BMED 纳米荧光粉可用于生产暖色发光二极管、农业照明和生物医学标记。
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引用次数: 0
Identification of a new α‐glucosidase inhibitor: Alkyl ferulate ester derived from unripe fruits of Solanum torvum Swartz 鉴定一种新的α-葡萄糖苷酶抑制剂:从 Solanum torvum Swartz 未熟果实中提取的阿魏酸烷基酯
IF 0.9 Q3 Chemistry Pub Date : 2024-03-14 DOI: 10.1002/vjch.202300231
T. Le, Tien Hoang Nguyen, Vy Thuy Hoang Phan, H. Nguyen, Thang Quoc Truong, Thy Anh Nguyen, T. Van Do, Mai Thanh Thi Nguyen
In this study, the phytochemical compositions and α‐glucosidase inhibitory activity of the ethyl acetate extract derived from the unripe fruits of Solanum torvum Swartz have been investigated. The investigation led to the isolation of a new isoferulate fatty alkyl ester, solacanin B (1), in addition to eight known compounds, including lyciumol A (2), ethyl caffeate (3), caffeic acid (4), scopoletin (5), p‐hydroxybenzaldehyde (6), p‐hydroxybenzoic acid (7), vanillic acid (8) and 1‐O‐palmitoylglycerol (9). The structural elucidation of these compounds was achieved through extensive spectroscopic analyses and reference literature. Bioactivity assay of all compounds demonstrated that compounds 1–4, and 7 showed more potent α‐glucosidase inhibition activities, with IC50 values of 48.4, 29.3, 38.8, 95.0, and 186.6 µm, respectively, than that of positive control acarbose (IC50, 214.5 µm).
在这项研究中,研究人员调查了从 Swartz Solanum torvum 未熟果实中提取的乙酸乙酯萃取物的植物化学成分和 α-葡萄糖苷酶抑制活性。研究结果表明,除了八种已知化合物外,还分离出了一种新的异ferulate 脂肪烷基酯--茄素 B (1),这些化合物包括茄酚 A (2)、咖啡酸乙酯 (3)、咖啡酸 (4)、莨菪亭 (5)、对羟基苯甲醛 (6)、对羟基苯甲酸 (7)、香草酸 (8) 和 1-O-棕榈酰甘油 (9)。通过广泛的光谱分析和参考文献,这些化合物的结构得以阐明。对所有化合物进行的生物活性分析表明,化合物 1-4 和 7 显示出更强的α-葡萄糖苷酶抑制活性,其 IC50 值分别为 48.4、29.3、38.8、95.0 和 186.6 µm,高于阳性对照阿卡波糖(IC50,214.5 µm)。
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引用次数: 0
The effect of NaOH concentration on ferrate electrosynthesis NaOH 浓度对铁酸盐电合成的影响
IF 0.9 Q3 Chemistry Pub Date : 2024-03-14 DOI: 10.1002/vjch.202300270
Nguyen Thi Van Anh, Phan Thi Binh, Mai Thi Xuan, Mai Thi Thanh Thuy
This study investigated the electrochemical characteristics of mild steel anode in NaOH solutions with concentrations ranging from 8 to 16 m to elucidate their impact on the electrochemical synthesis of ferrate and determine the optimal electrolyte concentration for this process. The electrochemical properties of anode material were determined using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and the Tafel polarization. The ferrate concentration was determined by UV–vis method and the conductivity of electrolytes was evaluated through EIS measurement in the high‐frequent range. The results showed that a passive layer easily formed on the anode surface in NaOH solution with a concentration range of 8–12 m, preventing the formation of ferrate. Conversely, at higher electrolyte concentrations (14 and 16 m NaOH), the dissolution capability of the passive layer was enhanced, resulting in a better ability to synthesize ferrate.
本研究调查了低碳钢阳极在浓度为 8 至 16 m 的 NaOH 溶液中的电化学特性,以阐明其对电化学合成铁酸盐的影响,并确定该过程的最佳电解质浓度。使用循环伏安法(CV)、电化学阻抗光谱法(EIS)和塔菲尔极化法测定了阳极材料的电化学特性。利用紫外可见光法测定了铁酸盐的浓度,并通过高频范围内的 EIS 测量评估了电解质的电导率。结果表明,在浓度范围为 8-12 m 的 NaOH 溶液中,阳极表面很容易形成被动层,从而阻止了铁酸盐的形成。相反,在电解质浓度较高(14 和 16 m NaOH)的情况下,被动层的溶解能力增强,从而提高了合成铁酸盐的能力。
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引用次数: 0
Magnetic Fe3O4/Fe‐Mn binary oxide/bentonite nanocomposite—a novel adsorbent for removal of reactive red 195 dye from water 磁性 Fe3O4/Fe-Mn 二元氧化物/膨润土纳米复合材料--去除水中活性红 195 染料的新型吸附剂
IF 0.9 Q3 Chemistry Pub Date : 2024-03-14 DOI: 10.1002/vjch.202300285
N. Duong, Q. T. Trang, Pham Van Lam, P. T. Bich
In this study, a nanocomposite, Fe3O4/Fe‐Mn binary oxide/bentonite (FFMB), was synthesized, characterized and evaluated its adsorption behavior of azo Reactive Red 195 dye (RR‐195) in aqueous solution. The results of characterization (X‐ray diffraction, Fourier transform infrared spectroscopy, field emission scanning and transmission electron microscopies, vibration‐sample magnetometer, etc.) demonstrate that FFMB consists of Fe3O4 core and Fe2O3‐MnO2 binary oxide shell, which are distributed relatively uniformly on the exfoliated bentonite support with BET surface area of about 188 m2 g−1. It exhibits superparamagnetic properties with saturation magnetization of 39.6 emu g−1. The results of batch adsorption experiments show that the material has high ability of RR‐195 adsorption in terms of both adsorption rate and capacity. The adsorption efficiency was highest at pH 2–3. The adsorption process followed the pseudo‐second‐order kinetics and Langmuir isotherm models with a rather high maximum adsorption capacity of 163.4 mg g−1. Besides, Weber–Morris kinetic and Temkin isotherm models also provide useful insight into the adsorption mechanism. The material shows a good reusability. After 5 adsorption–desorption cycles the adsorption efficiency reached about 75% of the first cycle and the saturation magnetization decreased insignificantly. These results reveal that FFMB can become an alternative adsorbent for azo dye removal from wastewaters.
本研究合成了一种纳米复合材料--Fe3O4/Fe-Mn 二元氧化物/膨润土(FFMB),对其进行了表征,并评估了其在水溶液中对偶氮活性红 195 染料(RR-195)的吸附行为。表征结果(X 射线衍射、傅立叶变换红外光谱、场发射扫描电子显微镜和透射电子显微镜、振动样品磁力计等)表明,FFMB 由 Fe3O4 内核和 Fe2O3-MnO2 二元氧化物外壳组成,二者相对均匀地分布在剥离膨润土载体上,BET 表面积约为 188 m2 g-1。它具有超顺磁性,饱和磁化率为 39.6 emu g-1。批量吸附实验结果表明,该材料在吸附速率和吸附容量方面都具有很高的 RR-195 吸附能力。在 pH 值为 2-3 时,吸附效率最高。吸附过程遵循伪二阶动力学和 Langmuir 等温线模型,最大吸附容量高达 163.4 mg g-1。此外,Weber-Morris 动力学模型和 Temkin 等温线模型也对吸附机理提供了有用的启示。该材料具有良好的重复使用性。经过 5 个吸附-解吸循环后,吸附效率达到了第一个循环的 75%,饱和磁化率下降不明显。这些结果表明,FFMB 可以成为去除废水中偶氮染料的替代吸附剂。
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引用次数: 0
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Vietnam Journal of Chemistry
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