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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Ammonia-rich solution production from coal gasification gray water using Chemical-free Flow-Electrode capacitive deionization coupled with a monovalent cation exchange membrane

Taoqin Chen,Longqian Xu,Sheng Wei,Zhiqiang Fan,Ruibo Qian,Xueli Ren,Guo Zhou,Hongquan Yang,Jiayun Wu,Hongbin Chen

The conventional technologies for ammonia recovery from wastewaters usually requires high chemicals and energy input. And if the wastewater contains hardness, there is a risk of scaling with increasing in cost. Flow electrode capacitive deionization (FCDI) coupled with monovalent cation exchange membrane (MCEM) was employed to solve abovementioned problem.   Our method was an effective strategy for the selective production of an ammonia-rich solution from coal gasification gray water by simply adjusting the charging and discharging processes. During the charging process, both NH 4 + and Na + were transported to the cathode due to electrosorption of the electrical double layers (EDLs) on charged carbon particles and electrodialysis of potential gradient, while Ca 2+ was retained by the MCEM. The Faradaic reactions induced the generation of OH - and led to the conversion of charged NH 4 + into uncharged NH 3 . When the electrode polarity was reversed, charged species such as Na + would be mostly pushed back into the spacer chamber, yet NH 3 was more likely to be trapped in the cathode due to sluggish pH variations, thereby producing an ammonia-rich solution. Under optimal operating conditions (i.e., a carbon content of 5 wt%, charge and discharge voltages of 4.5 and 0.2 V, respectively, charge 80 min and discharging 15 min, and six continuous cycles), a stable recovery efficiency (∼205 mg/L per cycle) and product purity of 70.4% were attained at a relatively low electrical energy consumption (11.1 kWh/kg N). Additionally, Ca scale was effectively avoided by MCEM. These results demonstrated that FCDI coupled with MCEM could be a promising technology for efficient NH 4 + removal, recovery as an ammonia-rich solution and TOC removal from industry wastewaters with alleviation of scaling.

研究领域: 环境工程 · 化学工程
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CONSTRUCTION AND BUILDING MATERIALS · 2024 · IF 7.4

Optimizing the content of Li2CO3, Na2SO4 and TEA in fly ash–cement system by response surface methodology

Jixi Chen,Jinqing Jia,Mengyu Zhu

With an optimized dosage, hardening accelerators become a vital means of modifying fly ash-cement system (FAC). This study comprehensively investigated the mechanical properties of FAC modified by Li 2 CO 3 , Na 2 SO 4 , and triethanolamine (TEA) under different dosages, and optimized the dosage of accelerators through the response surface method (RSM). The synergistic effect of accelerators on the hydration of FAC was characterized by thermogravimetric differential scanning calorimetry (TG-DSC), X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The results demonstrated that the factors and response value followed a quadratic polynomial model. The regression coefficients R 2 of the model were all greater than 0.9, indicating good agreement with the experimental data. The content of Li 2 CO 3 and Na 2 SO 4 had an extremely significant effect on the compressive strength of 1d and 3d, followed by TEA. The optimal mix ratio predicted by RSM was 0.12 % Li 2 CO 3 , 0.47 % Na 2 SO 4 , and 0.40 % TEA. Early hydration stages revealed that the combined action of these accelerators increased the formation of CH, CaCO 3 , and amorphous C-(A)-S-H gel. Microscopically, the surface of fly ash exhibited alkali-induced corrosion, thereby enhancing its pozzolanic reactivity.

CAS / MDL: 102-71-6
研究领域: 材料科学 · 化学工程
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