Synthesis of pumice and medical waste incinerator fly ash based phosphate geopolymers for methylene blue dye adsorption: co-valorization, parameters and mechanism†

IF 5.2 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Materials Advances Pub Date : 2024-10-08 DOI:10.1039/D4MA00779D
Collins Onyango, Wilfrida Nyairo, Bowa Kwach, Victor Shikuku, Tome Sylvain, Hermann Dzoujo Tamaguelon and Claus Rüscher
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Abstract

In this study, four geopolymer composites, GP-0, GP-10, GP-20 and GP-30, were synthesized from pumice, an abundant and inexpensive volcanic rock precursor, substituted with fractions of 0, 10, 20 and 30% by weight of medical waste incinerator fly ash (MWI-FA), respectively. The materials were characterized by standard methods (FTIR, XRF, BET surface area measurement, XRD, SEM-EDX and TGA). The materials were morphologically distinct and the specific surface areas (SSA) decreased with an increase in MWI-FA fraction. The adsorption performances of the geocomposites were evaluated in batch mode for the removal of methylene blue (MB), a toxic dye, from water. The study determined that the dye was optimally removed at circumneutral pH, 303 K temperature, 0.6 g/40 mL adsorbent dosage and 30 min contact time. The equilibrium data were best described using the Sips isotherm model. The geopolymers had ∼30 times higher adsorption capacities than pristine pumice. The maximum adsorption capacities of the geopolymers, ∼31 mg g−1, were indistinguishable despite an increase in MWI-FA indicating that MWI-FA provided new energetically favorable adsorption sites compensating diminished SSA. The adsorption kinetics was best described using the pseudo-second order kinetic model wherein the rate constant (K2) increased with the MWI-FA fraction suggesting porosity structures with reduced tortuosity. Thermodynamically, the adsorption process was exothermic (ΔH < 0), physical (ΔH and Ea < 40 kJ mol−1) spontaneous (ΔG < 0) and enthalpy-driven. Adsorption diminished in a saline environment. The exhausted adsorbent was recoverable and recycled twice using hot water before significant loss of adsorption potential. The composite geopolymers present a plausible strategy for stabilization of up to 30% MWI-FA without compromising the adsorptive properties for dye removal from water.

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基于浮石和医疗废物焚烧炉飞灰的磷酸盐土工聚合物的合成:亚甲基蓝染料吸附:共价、参数和机理†。
在这项研究中,利用浮石(一种丰富而廉价的火山岩前体)合成了四种土工聚合物复合材料,即 GP-0、GP-10、GP-20 和 GP-30,并分别添加了 0、10、20 和 30% (按重量计)的医疗废物焚化炉飞灰(MWI-FA)。这些材料采用标准方法(傅立叶变换红外光谱、X 射线荧光光谱、BET 表面积测量、X 射线衍射、扫描电镜-电子显微镜和热重分析)进行表征。这些材料形态各异,比表面积(SSA)随着 MWI-FA 部分的增加而减小。以批处理模式评估了土工复合材料对水中有毒染料亚甲基蓝(MB)的吸附性能。研究结果表明,在 pH 值为中性、温度为 303 K、吸附剂用量为 0.6 克/40 毫升、接触时间为 30 分钟的条件下,染料的去除效果最佳。用 Sips 等温线模型对平衡数据进行了最佳描述。土工聚合物的吸附容量是原始浮石的 30 倍。尽管 MWI-FA 增加了,但土工聚合物的最大吸附容量(∼31 mg g-1)并无差别,这表明 MWI-FA 提供了新的能量有利吸附位点,弥补了 SSA 的减少。使用伪二阶动力学模型对吸附动力学进行了最佳描述,其中速率常数(K2)随着 MWI-FA 分数的增加而增加,这表明孔隙结构的迂回度降低。从热力学角度看,吸附过程是放热(ΔH < 0)、物理(ΔH 和 Ea < 40 kJ mol-1)自发(ΔG < 0)和焓驱动的。在盐水环境中,吸附作用减弱。用完的吸附剂可回收,并在吸附潜能显著丧失之前用热水循环使用两次。复合土工聚合物为稳定多达 30% 的 MWI-FA 提供了一种可行的策略,同时又不影响从水中去除染料的吸附特性。
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来源期刊
Materials Advances
Materials Advances MATERIALS SCIENCE, MULTIDISCIPLINARY-
CiteScore
7.60
自引率
2.00%
发文量
665
审稿时长
5 weeks
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