Chitosan/modified sidr (Ziziphus spina-christi) tree leaves biocomposite for removal of methylene blue dye: characterization, adsorption optimization, isotherms, and kinetics

被引:0
作者
Abdulhameed, Ahmed Saud [1 ,2 ]
Omari, Rima Heider Al [3 ]
Abualhaija, Mahmoud [4 ]
Algburi, Sameer [5 ]
机构
[1] Univ Anbar, Coll Pharm, Dept Pharmaceut Chem, Ramadi, Iraq
[2] Univ Warith Al Anbiyaa, Coll Engn, Karbala, Iraq
[3] Al Ahliyya Amman Univ, Fac Allied Med Sci, Med Lab Sci Dept, Amman, Jordan
[4] Univ Jordan, Water Energy & Environm Ctr, Amman 11942, Jordan
[5] Al Kitab Univ, Coll Engn Technol, Kirkuk 36015, Iraq
基金
英国科研创新办公室;
关键词
Chitosan; Biomass; Ziziphus spina-christi; Methylene blue dye; Response surface methodology; COMPOSITE; WATER;
D O I
10.1007/s13399-024-06268-9
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
This study targets the development of a sustainable and effective adsorbent (henceforth, CHA/STL-HS) for the removal of methylene blue (MB) by combining chitosan (CHA) with modified sidr (Ziziphus spina-christi) tree leaves (STL) using sulfuric acid (H2SO4, HS). The physicochemical properties of CHA/STL-HS were analyzed using techniques such as FESEM-EDX, CHNS-O, XRD, BET, and FTIR. Response surface methodology (RSM) was applied to optimize the adsorption efficiency of CHA/STL-HS, taking into account variables such as pH (4-10), CHA/STL-HS dose (0.02-0.08 g), and time (10-60 min). The acquired data of MB adsorption by CHA/STL-HS were well-matched with the Freundlich and pseudo-first-order models. Remarkably, CHA/STL-HS exhibited an outstanding adsorption ability of 546.98 mg/g. The significant adsorption of MB onto CHA/STL-HS is primarily attributed to electrostatic interaction between the MB cation and the acidic groups of CHA/STL-HS, alongside n-pi interactions and hydrogen bonding. The current research highlights the potential of integrating biomass (STL-HS) into biopolymer (chitosan) to generate an adsorbent that exhibits promise in eliminating cationic dye from contaminated aquatic environments.
引用
收藏
页码:15747 / 15761
页数:15
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