Kobylinska Natalia, Klymchuk Dmytro, Shakhovsky Anatolij, Khainakova Olena, Ratushnyak Yakiv, Duplij Volodymyr, Matvieieva Nadiia
A. V. Dumansky Institute of Colloid and Water Chemistry, NAS of Ukraine Ak. Vernadsky blv. 42 Kyiv 03142 Ukraine
M. G. Kholodny Institute of Botany, NAS of Ukraine 2 Tereshchenkivska Str Kyiv 02000 Ukraine.
RSC Adv. 2021 Aug 9;11(43):26974-26987. doi: 10.1039/d1ra04080d. eCollection 2021 Aug 2.
The "green" synthesis of magnetite and cobalt ferrite nanoparticles (FeO-NPs and CoFeO-NPs) using extracts of L "hairy" roots was proposed. In particular, the effect and role of important variables in the 'green' synthesis process, including the metal-salt ratio, various counter ions in the reaction mixture, concentration of total flavonoids and reducing power of the extract, were evaluated. The morphology and size distribution of the magnetic nanoparticles (MNPs) depended on the metal oxidation state and ratio of Fe(iii) : Fe(ii) in the initial reaction mixture. MNPs obtained from divalent metal salts in the reaction mixture were non-uniform in size with high aggregation level. Samples obtained by the FeCl/FeSO mixture with a ratio of Fe(iii) : Fe(ii) = 1 : 2 showed an irregular shape of the nanoparticles and high aggregation level. MNPs obtained by the FeCl/FeSO/CoCl mixture showed a regular shape with slight aggregation, and were in the nanosize range (10-17 nm). Thus, this mixture as a metal-precursor was used for MNP biosynthesis in the subsequent experiments. The XRD data showed that the magnetic specimens contained mainly spinel type phase. The data of EDX and XPS analysis indicated that the product of the "green" synthesis was magnetite with some impurities, owing to the obtained ratio of Fe : O being similar to the theoretical atomic ratio of magnetite (3 : 4). The FeO-NP samples were superparamagnetic with high magnetization (until 68 emu g). The Co-containing MNPs demonstrated low ferromagnetic properties. The MNPs with pure magnetite phase, very good magnetization and uniform size distribution ( 12-14 nm) were prepared by the "hairy" root extract characterized by the highest amount of total flavonoids. According to the FTIR data, the synthesized FeO-NPs had a core-shell like structure, in which the core was composed of FeO, and the shell was formed by bioactive molecules. The presence of several organic compounds (such as flavonoids or carboxylic acids) plays a key role in the suppression of FeO-NP aggregation without addition of a stabilizing agents. Synthesized FeO-NP samples effectively removed Cu(ii) and Cd(ii) with the maximum adsorption capacity, reaching 29.9 mg g and 33.5 mg g, respectively. It is probable that the presence of organic components in extracts plays an important role in the adsorption properties of biosynthesised MNPs. The obtained MNPs were successfully applied to the removal of heavy metal ions in the environmental water samples. FeO-NPs also negatively affected plant growth in the case of using "hairy" roots as a test model, and the greatest inhibitory activity (99.56 wt%) was possessed by MNPs with high magnetic properties.
提出了利用“毛状”根提取物“绿色”合成磁铁矿和钴铁氧体纳米颗粒(FeO-NPs和CoFeO-NPs)的方法。特别评估了“绿色”合成过程中重要变量的影响和作用,包括金属盐比例、反应混合物中的各种抗衡离子、总黄酮浓度和提取物的还原能力。磁性纳米颗粒(MNPs)的形态和尺寸分布取决于初始反应混合物中金属的氧化态和Fe(iii) : Fe(ii)的比例。从反应混合物中的二价金属盐获得的MNPs尺寸不均匀,聚集程度高。通过Fe(iii) : Fe(ii) = 1 : 2的FeCl/FeSO混合物获得的样品显示纳米颗粒形状不规则且聚集程度高。通过FeCl/FeSO/CoCl混合物获得的MNPs呈规则形状,聚集轻微,且在纳米尺寸范围内(10-17 nm)。因此,该混合物作为金属前体用于后续实验中的MNP生物合成。XRD数据表明磁性样品主要包含尖晶石型相。EDX和XPS分析数据表明,“绿色”合成产物是含有一些杂质的磁铁矿,这是由于获得的Fe : O比例与磁铁矿的理论原子比(3 : 4)相似。FeO-NP样品具有超顺磁性和高磁化强度(高达68 emu g)。含钴的MNPs表现出低铁磁性能。通过具有最高总黄酮含量的“毛状”根提取物制备了具有纯磁铁矿相、非常好的磁化强度和均匀尺寸分布(12-14 nm)的MNPs。根据FTIR数据,合成的FeO-NPs具有核壳状结构,其中核由FeO组成,壳由生物活性分子形成。几种有机化合物(如黄酮类化合物或羧酸)的存在在不添加稳定剂的情况下对抑制FeO-NP聚集起关键作用。合成的FeO-NP样品分别以29.9 mg g和33.5 mg g的最大吸附容量有效去除了Cu(ii)和Cd(ii)。提取物中有机成分的存在可能在生物合成的MNPs的吸附性能中起重要作用。所获得的MNPs成功应用于环境水样中重金属离子的去除。以“毛状”根作为测试模型时,FeO-NPs对植物生长也有负面影响,具有高磁性的MNPs具有最大抑制活性(99.56 wt%)。