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Benzoic acid-functionalized α-Fe2O3 nanoparticles: synthesis, characterization, magnetic and optical properties 苯甲酸功能化α-Fe2O3纳米颗粒:合成、表征、磁性和光学性质
Pub Date : 2021-04-01 DOI: 10.26655/AJNANOMAT.2021.2.4
A. D. Khalaji, Z. P. Sangdevini, S. M. Mousavi, M. Jarošová, P. Machek
In this work, a new iron precursor was prepared, calcinated at 500 °C and 600 °C. The final α-Fe2O3 products (named Fe-500 and Fe-600) were characterized using the Fourier transformed infrared spectroscopy (FT-IR), UV-Vis, X-ray diffraction (XRD), transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM) analysis. The results of the FT-IR analysis demonstrated thet the sharp peaks at wavenumbers 450-650 cm-1 confirmed the stretching vibration of Fe-O. The XRD results revealed that the product prepared at 500 °C was a mixture of 59% rhombohedral and 41% cubic phases of Fe2O3 with only 11% of cubic phase Fe2O3 in the sample processed at 600 °C. TEM images showed a slight increase in particle size by increasing the calcination temperature. The magnetic properties of the products depicted a weak ferromagnetic behavior.
本文制备了一种新的铁前驱体,分别在500℃和600℃煅烧。采用傅里叶变换红外光谱(FT-IR)、紫外-可见光谱(UV-Vis)、x射线衍射(XRD)、透射电镜(TEM)和振动样品磁强计(VSM)对α-Fe2O3最终产物Fe-500和Fe-600进行了表征。FT-IR分析结果表明,波数450 ~ 650 cm-1处的尖峰证实了Fe-O的拉伸振动。XRD结果表明,500℃时制备的产物为59%的菱形相和41%的立方相Fe2O3的混合物,而600℃时制备的样品中立方相Fe2O3的含量仅为11%。TEM图像显示,随着煅烧温度的升高,颗粒尺寸略有增加。产物的磁性表现为弱铁磁性。
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引用次数: 4
Synergistic effect of ionic liquid on additive performance of octyl acrylate-vinyl acetate copolymer and their comparison when added to lube oil 离子液体对丙烯酸辛酯-醋酸乙烯酯共聚物添加剂性能的增效作用及其在润滑油中的比较
Pub Date : 2021-04-01 DOI: 10.26655/AJNANOMAT.2021.2.5
P. Ghosh, S. Yeasmin
Ionic liquids (ILs) have come out as a promising lubricant additive in base oil during the past few years due to their low volatility, non–flammability, thermal stability, moisture stability and miscibility with organic compounds. In the present work, an investigation was carried out to determine whether the flow improvement property and shear stability of a polymeric additive can be affected when blended with an ionic liquid. We prepared a copolymer of vinyl acetate and octyl acrylate and blended it with imidazolium–based IL. Their performance as pour point depressant (PPD), viscosity index improver (VII) and also their stability against the mechanical shear in terms of permanent shear stability index (PSSI) were determined when added to the base oil as solo additive or as blend. The results revealed that the blend outweighs the polymer and the IL in all respect as a lubricant additive. As PPD, the best result was obtained in case of the blend at 4% concentration in both the base oils i.e. –12.1 °C and –13.7 °C in BO1 and BO2 respectively. Kinematic viscosity loss was least when the base oils were doped with the blend. This was supported by the PSSI data: 24.22 at 1% concentration in BO1 and 11.82 at 3% concentration in BO2.
离子液体由于其低挥发性、不可燃性、热稳定性、湿稳定性以及与有机化合物的混溶性等优点,近年来在基础油中成为一种很有前途的润滑剂添加剂。本文研究了一种聚合物添加剂与离子液体共混时,是否会影响聚合物添加剂的流动改善性能和剪切稳定性。制备了一种醋酸乙烯酯和丙烯酸辛酯共聚物,并与咪唑基IL共混,测定了它们作为降凝剂(PPD)、粘度指数改进剂(VII)的性能,以及作为单独添加剂和共混剂加入基础油时的抗机械剪切稳定性(PSSI)。结果表明,作为润滑剂添加剂,该共混物在各方面都优于聚合物和IL。作为PPD,当基础油在BO1和BO2中分别为-12.1°C和-13.7°C的浓度为4%时,获得的效果最好。当基础油掺入共混物时,运动粘度损失最小。PSSI数据支持了这一点:BO1浓度为1%时为24.22,BO2浓度为3%时为11.82。
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引用次数: 0
Effects of fluorodeoxyglucose magnetic nanoparticles on NCI-H727 and SH-SY5Y cancer cells. 氟脱氧葡萄糖磁性纳米粒子对 NCI-H727 和 SH-SY5Y 癌细胞的影响。
Pub Date : 2021-01-01 Epub Date: 2020-12-19 DOI: 10.26655/AJNANOMAT.2021.1.5
Perihan Unak, Rumbidzai Cheryl Budiyo, Alex Horsnzky, Volkan Yasakci, Gillian Pearce, Steve Russell, Omer Aras, Oguz Akin, Julian Wong

We present a report regarding the cytotoxic effects of iron-based magnetic nanoparticles conjugated with fluorodeoxyglucose (FDG-mNPs) on the viability of NCI-H727 and SH-SY5Y cancer cells. MTT assays were performed to determine cell viability in treated cancer cells grown under standard 2D culture conditions. FDG-mNP concentrations of 0.075 mg/mL, 0.15 mg/mL, and 0.3 mg/mL decreased mean cell viability of NCI-H727 cells to 92.5%, 82.9%, and 75% respectively. FDG-mNPs was also shown to have a detrimental effect on the viability of SY5Y cells: a decrease of 5.7%, 18.6%, and 36.4% was found for SY5Y cells treated with 0.075 mg/mL, 0.15 mg/mL, and 0.3 mg/mL concentrations of FDG-mNPs, respectively. When NCI-H727 and SH-SY5Y cancer cells were grown as 3D spheroids, morphology was visibly changed and the number of viable cells was decerased in spheroids treated with FDG-mNPs compared with untreated spheroids. The results of our study demonstrated that FDG-mNP has toxic effects on NCI-H7272 and SY5Y cancer cells, and we conclude that conjugated FDG-mNPs are promising in the development of clinical applications for the destruction of cancer cells.

我们报告了缀有氟脱氧葡萄糖的铁基磁性纳米粒子(FDG-mNPs)对 NCI-H727 和 SH-SY5Y 癌细胞活力的细胞毒性作用。在标准二维培养条件下,对经处理的癌细胞进行 MTT 检测,以确定细胞活力。FDG-mNP 浓度分别为 0.075 毫克/毫升、0.15 毫克/毫升和 0.3 毫克/毫升时,NCI-H727 细胞的平均存活率分别下降至 92.5%、82.9% 和 75%。研究还表明,FDG-mNPs 对 SY5Y 细胞的活力也有不利影响:用 0.075 毫克/毫升、0.15 毫克/毫升和 0.3 毫克/毫升浓度的 FDG-mNPs 处理 SY5Y 细胞,其活力分别下降了 5.7%、18.6% 和 36.4%。当 NCI-H727 和 SH-SY5Y 癌细胞生长为三维球形时,与未处理的球形细胞相比,经 FDG-mNPs 处理的球形细胞形态发生了明显变化,存活细胞数量减少。我们的研究结果表明,FDG-mNP 对 NCI-H7272 和 SY5Y 癌细胞具有毒性作用。
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引用次数: 0
Electrochemical deposition of tin doped zinc selenide (SnZnSe) thin film material 电化学沉积掺锡硒化锌(SnZnSe)薄膜材料
Pub Date : 2020-06-01 DOI: 10.26655/AJNANOMAT.2020.3.3
I. Ikhioya, D. Okoli, Azibuike J. Ekpunobic
In this research study, the growth of SnZnSe thin film materials was carried out using the cationic precursor, which was an aqueous solution of 0.035 mol solution of ZnSO4.7H2O while the anionic precursor was 0.1 mol solution of selenium metal powder was prepared by dissolving with 4 mL of hydrogen chloride (HCl). The XRD of the films deposited on FTO substrates at different dopant concentration 1%, 2%, 3% and 4% showed the reflection peaks at (220), (221), (300), (310), (311), (222) and (320) with the lattice constant of a=7.189 Ǻ.  The SEM results revealed the random distribution of tiny nano-grains on the substrate, the nano-grains were observed to agglomerate due to the presence of large free energy characteristics of small particles. The optical bandgap of the deposited material enhanced from 2.0-2.3 eV as the dopant concentration increased.
在本研究中,SnZnSe薄膜材料的生长采用阳离子前驱体(0.035 mol ZnSO4.7H2O水溶液)和阴离子前驱体(0.1 mol金属硒粉溶液,用4 mL氯化氢溶解)进行。在掺杂浓度为1%、2%、3%和4%的FTO衬底上沉积的薄膜的XRD显示,反射峰位于(220)、(221)、(300)、(310)、(311)、(222)和(320),晶格常数为a=7.189 Ǻ。扫描电镜结果显示,纳米颗粒在衬底上随机分布,由于小颗粒存在较大的自由能特征,纳米颗粒呈团聚状。随着掺杂浓度的增加,沉积材料的光学带隙从2.0 eV增大到2.3 eV。
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引用次数: 4
Electrochemical determination of Vitamin B6 in fruit juices using a new nanostructure voltammetric sensor 新型纳米结构伏安传感器电化学测定果汁中维生素B6
Pub Date : 2020-06-01 DOI: 10.26655/ajnanomat.2020.4.5
Farzaneh Mehri-Talarposhti, A. G. Saraei, L. Golestan, S. Shahidi
In this study, MgO/CNTs nanocomposite was synthesized using a simple approach according to the hydrogen bonding between the oxygen atom in MgO and hydrogen atom in SWCNTs-COOH. The nanocomposite was characterized using the FESEM and EDS methods. The MgO/CNTs nanocomposite was used for amplification of the paste electrode (PE) at the presence of 1-methyl-3-buthyl imizazolonium tetrafluoroborate (MBITF) as the binder. The MgO/CNTs/MBITF/PE was used as an electroanalytical tool for electro-oxidation determination of vitamin B6 in food samples. In comparison to PE, the oxidation signal of vitamin B6 was improved up to 3.2 times at the surface of MgO/CNTs/MBITF/PE. At pH=6 as optimum condition, the MgO/CNTs/MBITF/PE revealed linear dynamic range of 0.1-400 µM for determination of vitamin B6 with the detection limit of 30.0 nM. In the final step, the MgO/CNTs/MBITF/PE showed acceptable recovery data for the determination of vitamin B6 in fruit juices samples, confirming the ability of the sensors in real sample analysis.
本研究利用MgO中的氧原子与SWCNTs-COOH中的氢原子之间的氢键,采用一种简单的方法合成了MgO/CNTs纳米复合材料。采用FESEM和EDS对复合材料进行了表征。利用MgO/CNTs纳米复合材料在1-甲基-3-丁基咪唑唑四氟硼酸铵(MBITF)作为粘结剂的情况下扩增浆状电极(PE)。采用MgO/CNTs/MBITF/PE作为电氧化测定食品样品中维生素B6的电分析工具。与PE相比,MgO/CNTs/MBITF/PE表面维生素B6的氧化信号提高了3.2倍。在pH=6的最佳条件下,MgO/CNTs/MBITF/PE测定维生素B6的线性动态范围为0.1 ~ 400µM,检出限为30.0 nM。在最后一步中,MgO/CNTs/MBITF/PE在果汁样品中维生素B6的测定中显示出可接受的回收率数据,证实了传感器在实际样品分析中的能力。
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引用次数: 8
Eco-friendly 2,4-D dimethylamine herbicide delivery system using synthesized nano-matrix 合成纳米基质的生态友好型2,4- d二甲胺除草剂输送系统
Pub Date : 2020-06-01 DOI: 10.26655/AJNANOMAT.2020.3.2
I. Happiness, R. Wuana, N. Lami, S. Rufus
This study used chitosan as a capping agent and L-ascorbic acid as reducing agent to prepare copper nanoparticles encapsulated with 2,4-D dimethylamine herbicide via a green chemical reduction method to improve its herbicidal activity and reduce the negative environmental impacts associated with its application. Characterization of the synthesized CuCtsNPs and 2,4-D-CuCtsNPs was carried out using the following techniques; transmission electron microscopy (TEM), fourier transform- infra-red (FT-IR), scanning electron microscopy (SEM), energy-dispersive x-ray (EDX), powder x-ray diffraction (PXRD), differential scanning calorimeter (DSC), thermogravimetric  and differential thermal analysis (TGA/DTA). The maximum absorption peak of CuCtsNPs was observed around 560 nm while that of 2,4-D-CuCtsNPs at 558 nm. The yield of CuCtsNPs was at the range of 40-92% and encapsulation efficiency of the 2,4-D-CuCtsNPs formulationwas 93%. Debye- Scherer’s equation was used to calculate the average crystalline size of the synthesized CuCtsNPs and 2,4-D-CuCtsNPs. The values were 38.78 nm (CuCtsNPs) and 54.93 nm (2,4-D-CuCtsNPs) respectively. The SEM images revealed the particle size of 21-56 nm for CuCtsNPs and 25-69 nm for 2,4-D-CuCtsNPs. The results obtained from the DSC and TGA curves of CuCtsNPs and 2,4-D-CuCtsNPs showed that the formulations exist in crystalline state and were thermally stable up to 401.73 °C. Aqueous release studies for the formulation were carried out in three different pH media and two agricultural soils. Leaching profile of the loaded CuCtsNPs through the soil layer (UAM and CAPS) demonstrated that the UAM soil had higher value for 2,4-D (58.67%) than in CAPS soil 40.78%. This study formulated an environmentally friendly herbicide delivery nano-matrix (CuCtsNPs) for the successful slow release of 2,4-D Dimethylamine herbicide in aqueous medium and agricultural soils.
本研究以壳聚糖为封盖剂,l -抗坏血酸为还原剂,通过绿色化学还原法制备了包裹2,4- d二甲胺除草剂的铜纳米颗粒,以提高其除草活性,减少其使用对环境的负面影响。利用以下技术对合成的CuCtsNPs和2,4- d -CuCtsNPs进行表征;透射电子显微镜(TEM)、傅里叶变换-红外(FT-IR)、扫描电子显微镜(SEM)、能量色散x射线(EDX)、粉末x射线衍射(PXRD)、差示扫描量热计(DSC)、热重和差示热分析(TGA/DTA)。CuCtsNPs的最大吸收峰在560 nm左右,2,4- d -CuCtsNPs的最大吸收峰在558 nm左右。CuCtsNPs的产率为40 ~ 92%,2,4- d -CuCtsNPs的包封率为93%。采用Debye- Scherer方程计算合成的CuCtsNPs和2,4- d -CuCtsNPs的平均晶粒尺寸。分别为38.78 nm (CuCtsNPs)和54.93 nm (2,4- d -CuCtsNPs)。扫描电镜显示,CuCtsNPs的粒径为21 ~ 56 nm, 2,4- d -CuCtsNPs的粒径为25 ~ 69 nm。对CuCtsNPs和2,4- d -CuCtsNPs的DSC和TGA曲线分析结果表明,该配方以结晶形式存在,在401.73℃内热稳定。在三种不同pH介质和两种农业土壤中进行了该制剂的水释放研究。负载CuCtsNPs通过土层(UAM和CAPS)的淋溶曲线表明,UAM土壤的2,4- d值(58.67%)高于CAPS土壤的40.78%。本研究制备了一种环境友好型除草剂缓释纳米基质(CuCtsNPs),用于2,4- d二甲胺除草剂在水介质和农业土壤中的缓释。
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引用次数: 0
An efficient one-pot, four-component synthesis of a series of pyrazolo [3,4-b] pyridines in the presence of magnetic LDH as a nanocatalyst 以磁性LDH为纳米催化剂,一锅法合成一系列吡唑[3,4-b]吡啶
Pub Date : 2020-06-01 DOI: 10.26655/ajnanomat.2020.3.7
Fatemeh Majidi Arlan, Ramin Javahershenas, J. Khalafy
In this research study, one-pot, four-component reaction of 3-aryl-3-oxopropanenitriles, 1-aryl-3-methyl-1H-pyrazol-5 (4H) one, arylglyoxals and ammonium acetate using green solvent systems and different catalysts under the reflux conditions afforded a series of the corresponding 4-aroyl-3-methyl-1,6-diaryl-1H-pyrazolo [3,4-b] pyridine-5-carbonitrile derivatives. The best yields (70-85%) were obtained using the metal oxide silica based-matal bifunctional LDH (layered double hydroxide) as a magnet nanocatalyst in EtOH/H2O (1:1) under the reflux conditions. This protocol provided mild reaction conditions, good yields, simple workup procedure, easy preparation of nanocatalyst and, products to structurally diverse bicyclic pyrazolo [3,4-b] pyridines, demonstrating biological and pharmacological activities.
本研究以3-芳基-3-氧丙腈、1-芳基-3-甲基- 1h -吡唑-5 (4H) 1、芳基乙二醛和乙酸铵为原料,采用绿色溶剂体系和不同催化剂,在回流条件下进行一锅四组分反应,得到了一系列相应的4-芳基-3-甲基-1,6-二烷基- 1h -吡唑[3,4-b]吡啶-5-碳腈衍生物。在回流条件下,以金属氧化物二氧化硅基材料双功能LDH(层状双氢氧化物)为磁性纳米催化剂,在乙醇/水(1:1)条件下,得率最高(70-85%)。该工艺反应条件温和,产率高,工艺步骤简单,纳米催化剂制备方便,产物结构多样,具有良好的生物活性和药理活性。
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引用次数: 1
Bio-synthesis of iron oxide nanoparticles using neem leaf cake extract and its influence in the agronomical traits of vigna mungo plant 印楝叶饼提取物生物合成氧化铁纳米颗粒及其对芒果植物农艺性状的影响
Pub Date : 2020-01-01 DOI: 10.26655/AJNANOMAT.2020.1.4
R. Radhakrishnan, D. Lakshmi, F. Khan, Gopalakrishnan Ramalingam, K. Kaviyarasu, K. Kaviyarasu
In this work reports the synthesis of iron oxide along with the complex formation from the neem cake using the biosynthesis and precipitation method. Ferrous sulphate (FeSO4) and sodium hydroxide were used as the precursor precipitating agent, respectively. The resultant specimens were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), ultra-violet visible spectroscopy (UV-Vis), fourier-transform infrared spectroscopy (FT-IR), soil test, biochemical, and phytochemical analysis. To test the effect of the synthesized specimen as the nanofertilizer in the seed germination and the growth, the sample was incorporated in to the red soil and the agronomical traits including plant height. Number of leaves were studied over a survival period of 75 days of the selected plant species vigna mungo using POT analysis. The plant samples were harvested, and then the biochemical and phytochemical studies were carried out for alkaloids, glycosides, flavonoids, phenols, steroids, protein and total chlorophyll content. The results showed that the nanoparticles incorporation enhanced the plant growth and increased the concentration of the bioactive compounds in an appreciable level.
本文报道了用生物合成沉淀法从印楝饼中合成氧化铁并形成络合物。以硫酸亚铁(FeSO4)和氢氧化钠分别作为前驱体沉淀剂。通过x射线衍射(XRD)、扫描电镜(SEM)、能量色散x射线能谱(EDX)、紫外可见光谱(UV-Vis)、傅里叶变换红外光谱(FT-IR)、土壤测试、生化和植物化学分析对所得样品进行了表征。为了测试合成样品作为纳米肥料对种子萌发和生长的影响,将样品掺入红壤和株高等农艺性状中。采用POT分析方法,对所选植物芒戈(vigna mungo)在75 d的生存期内的叶片数量进行了研究。采集植物样品,进行生物碱、苷类、黄酮类、酚类、类固醇、蛋白质和总叶绿素含量的生化和植物化学研究。结果表明,纳米颗粒的掺入促进了植物的生长,并在一定程度上提高了生物活性化合物的浓度。
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引用次数: 10
Comparative investigations of synthesis TiO2 Nano-Particles from four different types of alcohols by Sol-Gel method and evaluation of their antibacterial activity 溶胶-凝胶法制备四种不同类型醇合成TiO2纳米粒子的比较研究及其抗菌活性评价
Pub Date : 2019-10-01 DOI: 10.26655/ajnanomat.2019.4.7
Mariam Farag Ambaraka, Fawzia Muftah Aljazwia, Randa Fawzi Alsupikhe
TiO2 nanoparticles were synthesized using a simple reaction of TiCl4 with different types of primary and secondary alcohols. Four different alcohols  (ethanol, isopropyl, isobutyl, and isobentyl alcohol) were investigated. The experiments were carried out to compare the products of the reactions with different precursors. The gelatine products were calcined at 400 °C and at 1000 °C in a box furnace and the effect of calcination temperature on the feature of nano-particles was studied. The synthesized TiO2 nanoparticles were characterized using X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results revealed that the average particle size was 8.9-18.4 nm. The antibacterial result of titanium dioxide nanoparticles at four types of  bacteria was two gram-positive (Staphylococcus aureus and Streptococcus sp.) and two gram-negative (Escherichia coli and Klebsiella sp.). Also, nanoparticles titanium dioxide did not have any effect on these types of bacteria. The sol-gel method could be used for applications that involve nano-crystalline TiO2 with anatase phase with low cost and simple preparation.
以二氧化钛为原料,与不同类型的伯、仲醇进行简单反应,合成了二氧化钛纳米颗粒。研究了四种不同的醇(乙醇、异丙基、异丁基和异戊醇)。通过实验对不同前驱体的反应产物进行了比较。在箱式炉中分别在400℃和1000℃下煅烧明胶制品,研究了煅烧温度对纳米颗粒形貌的影响。采用x射线衍射(XRD)和扫描电镜(SEM)对合成的TiO2纳米颗粒进行了表征。结果表明,平均粒径为8.9 ~ 18.4 nm。二氧化钛纳米颗粒对4种细菌的抑菌效果为2种革兰氏阳性菌(金黄色葡萄球菌和链球菌)和2种革兰氏阴性菌(大肠杆菌和克雷伯氏菌)。此外,纳米二氧化钛对这些类型的细菌没有任何影响。溶胶-凝胶法可用于锐钛矿相纳米TiO2的制备,成本低,制备简单。
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引用次数: 1
Antibacterial activity of magnesium oxide nanostructures prepared by hydrothermal method 水热法制备氧化镁纳米结构的抗菌活性研究
Pub Date : 2019-09-01 DOI: 10.26655/ajnanomat.2019.4.6
Shah Rukh, A. H. Sofi, M. A. Shah, S. Yousuf
In this research study, the magnesium oxide nanoparticles were synthesized using an inexpensive and simple hydrothermal method. A pure magnesium metal powder, de-ionized water, and hydrogen peroxide (H2O2) was utilized as the starting materials. The synthesized MgO was dense, uniformly distributed with a relatively spherical shape, without any cracks and voids as confirmed by the scaning electron microscopy (SEM) analysis. The structure was crystalline with a high purity. No other peak corresponding to any other material or metal could be ascertained from powder X-ray diffraction (XRD) pattern. The crystallite size of the prepared samples was found to be nearly 18 nm which was favorable for antibacterial activity. The antibacterial activity of MgO nanostructures was carried out by using disc diffusion method. The inhibition zones of diameters = 1 mm were observed in case of salmonella and Staphylococcus aureus, however, in case of E. Coli inhibition zones of diameter = 2 mm was obtained.
在本研究中,采用廉价、简单的水热法制备了氧化镁纳米颗粒。以纯金属镁粉、去离子水和过氧化氢(H2O2)为原料。经扫描电镜(SEM)分析,合成的MgO致密,分布均匀,呈相对球形,无裂纹和空洞。这种结构是结晶的,纯度很高。在粉末x射线衍射(XRD)图谱中没有发现与其他材料或金属相对应的峰。制备的样品晶粒尺寸接近18 nm,有利于抗菌活性。采用圆盘扩散法对MgO纳米结构的抑菌活性进行了研究。对沙门氏菌和金黄色葡萄球菌的抑制区直径为1 mm,对大肠杆菌的抑制区直径为2 mm。
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引用次数: 6
期刊
Asian Journal of Nanoscience and Materials
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