Zn(II) removal from wastewater by an alkali-activated material prepared from steel industry slags: optimization and modelling of a fixed-bed process.

Removal of dissolved zinc (Zn) from water by a novel alkali-activated material (AAM) prepared from steel industry slags in a fixed-bed column was investigated. Design of experiments was used to find the optimum operation parameters [flow rate (Q), adsorbent mass, (mads), and initial Zn concentration (C0)] for the removal of Zn2+ from a ZnCl2 solution. Regression models for the breakthrough (qb), and saturation (qsat) capacities of the bed and three other response parameters as functions of Q, mads and C0 were fitted with coefficients of determination (R2) ranging from 0.48 to 0.99. Experimental values of qb and qsat varied within 1.42-7.03 mg Zn/g and 10.57-17.25 mg Zn/g, respectively. The optimum operation parameters were determined to be Q= 1.64 ml/min and mads= 4.5 g, whereas C0 had negligible effect on the response parameters in the range 73-107 mg Zn/l. Finally, three empirical breakthrough curve (BTC) models were employed to describe the individual BTCs of which the modified dose - response model was found to give the best fit (0.960 ≤ R2 ≤ 0.998). The results of the present work demonstrate that the novel AAM has considerable potential to be utilized in water purification applications.

Ibuprofen degradation using a Co-doped carbon matrix derived from peat as a peroxymonosulphate activator.

The wider presence of pharmaceuticals and personal care products in nature is a major cause for concern in society. Among pharmaceuticals, the anti-inflammatory drug ibuprofen has commonly been found in aquatic and soil environments. We produced a Co-doped carbon matrix (Co-P 850) through the carbonization of Co2+ saturated peat and used it as a peroxymonosulphate activator to aid ibuprofen degradation. The properties of Co-P 850 were analysed using field emission scanning electron microscopy, energy filtered transmission electron microscopy and X-ray photoelectron spectroscopy. The characterization results showed that Co/Fe oxides were generated and tightly embedded into the carbon matrix after carbonization. The degradation results indicated that high temperature and slightly acidic to neutral conditions (pH = 5 to 7.5) promoted ibuprofen degradation efficiency in the Co-P 850/peroxymonosulphate system. Analysis showed that approx. 52% and 75% of the dissolved organic carbon was removed after 2 h and 5 h of reaction time, respectively. Furthermore, the existence of chloride and bicarbonate had adverse effects on the degradation of ibuprofen. Quenching experiments and electron paramagnetic resonance analysis confirmed that SO4·-, ·OH and O2·- radicals together contributed to the high ibuprofen degradation efficiency. In addition, we identified 13 degradation intermediate compounds and an ibuprofen degradation pathway by mass spectrometry analysis and quantum computing. Based on the results and methods presented in this study, we propose a novel way for the synthesis of a Co-doped catalyst from spent NaOH-treated peat and the efficient catalytic degradation of ibuprofen from contaminated water.

Characterization of lignin enforced tannin/furanic foams.

Worldwide, tons of lignin is produced annually in pulping plants and it is mainly considered as a waste material. Usually lignin is burned to produce energy for the pulping reactors. The production of value-added materials from renewable materials like lignin, has proved to be challenging. In this study, the effects of addition of three different types of lignin in the production of tannin/furanic foams is investigated. The foams were matured, first at 373 K and finally carbonized at 1073 K and the properties of them including mechanical strength, specific surface area and pore development are investigated before and after thermal treatment. According to the results, higher mechanical strength is obtained if samples are carbonized at 1073K compared to matured ones at 373K. Up to 10 times stronger materials are achieved this way, which makes them promising as insulating or constructive materials. With physical activation, it is possible to obtain specific surface areas and pore volumes close to 1200 m2/g and 0,55 cm3/g respectively. Mainly micropores are developed during the steam activation which makes these foams more suitable and selective to be used as catalyst support materials in the catalytic conversion of small molecules or in adsorption or gas storage application.