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In Situ Synthesized Hydroxyapatite-Cellulose Nanofibrils as Biosorbents for Heavy Metal Ions Removal

机译:原位合成羟基磷灰石纤维素纳米原纤维作为生物吸附剂去除重金属离子

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The synthesis of hydroxyapatite (HAp) in the presence of cellulose nanofibrils (CNF) or TEMPO-oxidized CNF (TCNF) was performed in situ by wet chemical precipitation process, using chemical precursors, to hybrid a low-cost biosorbents for removal of Co2+ as a model heavy metal ion. The removal is investigated by batch adsorption method depending on the pH value, the dosage of adsorbent, initial Co2+ concentration and the contact time of adsorption. The removal of Co2+ reached the maximum (87%) at pH 6 by using a dosage of 0.5 g L-1. The TCNFs is shown to increase the nucleation and growth of the HAp synthesized, providing higher surface area (138 m(2) g(-1)) with lower pore diameter (11.89 nm), compared to the CNFs based hybrid (135 m(2) g(-1), 14.42 nm) or pure HAp (118 m(2) g(-1), 13.32 nm), however, both resulting to a higher adsorption capacity (25 mg g(-1)) of Co2+ compared to HAp or TCNF (20-22 mg g(-1)). The adsorption is follows primarily by pseudo-first and Elovic order kinetic models which is due to the physisorption of Co2+ and surface ionic interactions with available negative phosphate (from HAp) and/or carboxylic (from TCNF) groups, fitting well with the Freundlich adsorption isotherm, and secondly due to the ion-exchange mechanism of Co2+ with Ca2+ from HAp. Both hybrid adsorbents show good adsorption (aeyen40%) capacity even after third reusing cycle, and high temperature stability (weight loss of 14%) up to 1000 A degrees C, however, the CNF-HAp hybrid represent a high-value alternative to relatively costly TCNF.
机译:在存在纤维素纳米原纤维(CNF)或TEMPO氧化CNF(TCNF)的情况下,羟基磷灰石(HAp)的合成是通过湿法化学沉淀工艺原位进行的,使用化学前体与低成本的生物吸附剂进行混合,以去除Co2 +。模型重金属离子。根据pH值,吸附剂的用量,初始Co2 +浓度和吸附的接触时间,采用间歇吸附法研究其去除效果。通过使用0.5 g L-1的剂量,在pH 6时,Co2 +的去除达到最大(87%)。与基于CNF的杂交体(135 m()相比,TCNFs显示出增加了合成HAp的成核和生长,提供了更高的表面积(138 m(2)g(-1))和更低的孔径(11.89 nm)。 2)g(-1),14.42 nm)或纯HAp(118 m(2)g(-1),13.32 nm),但是,二者均导致更高的Co2 +吸附容量(25 mg g(-1))与HAp或TCNF(20-22 mg g(-1))相比。吸附主要遵循伪一阶和Elovic阶动力学模型,这是由于Co2 +的物理吸附以及与可用负磷酸盐(来自HAp)和/或羧基(来自TCNF)的表面离子相互作用,非常适合Freundlich吸附等温线,其次是由于Co2 +与HAp中Ca2 +的离子交换机理。两种杂化吸附剂即使在第三次重复使用循环后仍显示出良好的吸附(ae <40%)容量,以及高达1000 A的高温稳定性(失重14%),但是,CNF-HAp杂化剂表现出很高的替代相对昂贵的TCNF的价值。

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