Mohammed Ali Hani S H, Anwar Yasir, Al-Ghamdi Youssef O, Fakieh Muhammad, Khan Shahid Ali
Department of Biological Sciences, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589, Saudi Arabia.
Princess Dr. Najla Bint Saud Al-Saud Center for Excellence Research in Biotechnology, King Abdulaziz University, P.O. Box 80203, Jeddah 21589, Saudi Arabia.
Polymers (Basel). 2022 Feb 6;14(3):627. doi: 10.3390/polym14030627.
MnO and MnO blended with 1 and 2 weight percent of activated carbon (AC), MnO/AC1 and MnO/AC2 were synthesized through the sol-gel method. The pure chitosan (CS) films were cast in the form of films. Similarly, 5 weight% of each MnO, AC, MnO/AC1 and MnO/AC2 was intermingled with the CS to produce different films, such as CS-AC, CS-MnO, CS-MnO/AC1 and CS-MnO/AC2. Zero-valent Co NPs were then supported on these films through the chemical reduction method and expressed as CS@Co, CS-AC@Co, CS-MnO@Co, CS-MnO/AC1@Co and CS-MnO/AC2@Co NPs. All the catalysts were characterized by field emission scanning electron microscopy (FESEM), energy-dispersive spectroscopy (EDS) and X-ray diffraction (XRD) techniques. The synthesized catalysts were used as a dip catalyst against the hydrogenation of 4-nitrophenol (4NP), and for the degradation of methyl orange (MO) and Congo red (CR) dyes. The and R values were deduced from pseudo-first-order kinetics for 4NP and MO and zero-order kinetics for CR dye. The values of CS-AC@Co and CS-MnO/AC1@Co NPs for 4NP hydrogenation were higher than those for any other member of the series, at 1.14 × 10 and 1.56 × 10 min respectively. Similarly, the rate of CR degradation was highest with CS-AC@Co. The R values for 4NP, MO and CR dyes were above 0.9, which indicated that the application of pseudo-first- and zero-order models were appropriate for this study. Furthermore, the antibacterial activity of all the catalysts was evaluated against and . The CS-AC@Co NPs exhibited the highest zone of inhibition compared to other catalysts against , while all the catalysts were inactive against . This study reveals that the catalyst can be used for the degradation of other pollutants and for microbial inhibition.
通过溶胶 - 凝胶法合成了MnO以及与1重量百分比和2重量百分比活性炭(AC)混合的MnO,即MnO/AC1和MnO/AC2。纯壳聚糖(CS)制成薄膜形式。同样,将5重量%的每种MnO、AC、MnO/AC1和MnO/AC2与CS混合,制成不同的薄膜,如CS - AC、CS - MnO、CS - MnO/AC1和CS - MnO/AC2。然后通过化学还原法将零价Co纳米颗粒负载在这些薄膜上,并表示为CS@Co、CS - AC@Co、CS - MnO@Co、CS - MnO/AC1@Co和CS - MnO/AC2@Co纳米颗粒。所有催化剂均通过场发射扫描电子显微镜(FESEM)、能量色散光谱(EDS)和X射线衍射(XRD)技术进行表征。合成的催化剂用作4 - 硝基苯酚(4NP)氢化以及甲基橙(MO)和刚果红(CR)染料降解的浸渍催化剂。从4NP和MO的准一级动力学以及CR染料的零级动力学推导出速率常数和R值。CS - AC@Co和CS - MnO/AC1@Co纳米颗粒对4NP氢化的速率常数分别为1.14×10和1.56×10 min,高于该系列的任何其他成员。同样,CS - AC@Co对CR的降解速率最高。4NP、MO和CR染料的R值均高于0.9,这表明准一级和零级模型适用于本研究。此外,评估了所有催化剂对大肠杆菌和金黄色葡萄球菌的抗菌活性。与其他催化剂相比,CS - AC@Co纳米颗粒对大肠杆菌表现出最高的抑菌圈,而所有催化剂对金黄色葡萄球菌均无活性。本研究表明,该催化剂可用于其他污染物的降解和微生物抑制。