Nguyen Trung Dien, Ngo Sang Thanh, Hoang Yen Hai, Thai Nhung Thi Tuyet, Nguyen Huong Thi Thu, Trinh Gia Thi Ngoc
Can Tho University 3/2 Street, Ninh Kieu Can Tho 94000 Vietnam
Nanoscale Adv. 2024 Nov 19;7(2):477-494. doi: 10.1039/d4na00449c. eCollection 2025 Jan 14.
This study presents a synthesis method for environmentally friendly copper nanoparticles using ascorbic acid and gelatin as key components. The influence of precursor concentration, reductant amount, and stabilizer on the process was systematically investigated to obtain optimal results for the synthesis. The optimal parameters for forming copper nanoparticles, including 20 g per L gelatin, 19.3 mM (AcO)Cu, and 41.5 mM ascorbic acid, were determined using a central composite design of the response surface methodology. Successful generation of pure copper nanoparticles with both spherical and cylindrical shapes, whose sizes were 43.1 and 105.2 nm, respectively, was confirmed by X-ray diffraction analysis and transmission electron microscopy. The synthesized nanomaterial was stable for a two-week storage time after which they gradually oxidized into Cu ions. During antimicrobial activity testing, the synthesized nanoparticles displayed distinctive ability to inhibit the growth of Gram-positive bacteria (, , and ), Gram-negative bacteria (), and cancer cells (A549, Hep-G2, KB, and MCF7). Copper nanoparticles synthesized by chemical reduction demonstrated notable inhibitory activity against various pathogenic fungi that affect plants, including , , and . Additionally, the catalytic activity of the produced nanomaterial with a bandgap energy of 2.14 eV and a specific surface area of 40.6 m g was explored in the degradation of phenol, a common dye used in laboratories and industries. An optimized phenol red removal of 94.4% was achieved after a 540 second reaction time using response surface methodology, specifically a central composite design with an optimal dosage of copper nanoparticles at 31.5 ppm, a NaBH concentration of 53.1 mM, and a pH of 7.5.
本研究提出了一种以抗坏血酸和明胶为关键成分的环保型铜纳米颗粒合成方法。系统研究了前驱体浓度、还原剂用量和稳定剂对该过程的影响,以获得合成的最佳结果。使用响应面法的中心复合设计确定了形成铜纳米颗粒的最佳参数,包括每升20克明胶、19.3毫摩尔(醋酸根)铜和41.5毫摩尔抗坏血酸。通过X射线衍射分析和透射电子显微镜证实成功生成了尺寸分别为43.1纳米和105.2纳米的球形和圆柱形纯铜纳米颗粒。合成的纳米材料在储存两周内稳定,之后逐渐氧化成铜离子。在抗菌活性测试中,合成的纳米颗粒表现出独特的抑制革兰氏阳性菌(、和)、革兰氏阴性菌()和癌细胞(A549、Hep-G2、KB和MCF7)生长的能力。通过化学还原合成的铜纳米颗粒对影响植物的各种致病真菌,包括、和,表现出显著的抑制活性。此外,还研究了带隙能量为2.14电子伏特、比表面积为40.6平方米/克的所制备纳米材料在实验室和工业中常用染料苯酚降解中的催化活性。使用响应面法,特别是中心复合设计,在540秒反应时间后实现了94.4%的苯酚红优化去除率,其中铜纳米颗粒的最佳用量为31.5 ppm,硼氢化钠浓度为53.1毫摩尔,pH值为7.5。