Factors influencing hydroquinone degradation in aqueous solution using a modified microelectrolysis method

2014 ◽  
Vol 71 (3) ◽  
pp. 397-404 ◽  
Author(s):  
Tong Li ◽  
Tingting Li ◽  
Houfeng Xiong ◽  
Donglei Zou

The discharge of hydroquinone (HQ), an important chemical raw material, to natural waters poses different ecological threats to aquatic organisms. In this study, we investigated the removal performance of traditional and modified microelectrolysis methods in aqueous solutions. The traditional microelectrolysis packing was modified by adding manganese (Mn), zinc (Zn), and copper (Cu) powder as additives. The factors affecting the removal performance of HQ, such as catalytic metal type, mass fraction of additive, reaction time, and initial pH, were examined. The results showed that the Mn modified packing exhibited the best performance compared to Zn and Cu powder. The removal rate of HQ using Mn modified packing can reach 94% after 4 h. In addition, 9% of Mn packing has a higher removal rate than other mass fractions. The acidic solution pH shows a more favorable degradation than a neutral and alkaline solution. The intermediates of HQ degradation by modified microelectrolysis were identified and then the pathway of HQ degradation was proposed. Our result indicates that Mn as catalytic metal holds promising potential to enhance HQ removal in water using the microelectrolysis method.

2021 ◽  
Author(s):  
Sofia Manimanaki ◽  
Dimitris Mitrogiannis ◽  
Ioannis Baziotis ◽  
Maria Psychoyou ◽  
Ioannis Papanikolaou ◽  
...  

<p>Phosphorus (P) is an essential nutrient for plant growth. According to the vision of circular bioeconomy, the management of nutrient-rich wastewaters should include both treatment and utilization goals (Battista & Bolzonella, 2019). Consequently, the application of in-situ resources utilization (ISRU), using typical Martian soil (e.g., Yen et al., 2005), is vital for the sustainability of future long-term settlements on Mars.</p><p>Martian soil simulants, provided by The CLASS Exolith Lab from the University of Central Florida, were tested for their phosphorus sorption capacity. Sorption of phosphate anions (PO<sub>4</sub>-P) from aqueous solutions (AS) of KH<sub>2</sub>PO<sub>4</sub> and sodium bicarbonate, as well as from hydrolyzed human urine (HU) was examined at a preliminary stage, using three Martian soil simulants (MGS-1; Rocknest soil, MGS-1S; M-WIP Reference Case B and MGS-1C; M-WIP Reference Case C; Cannon et al. 2019). In particular, isothermal, kinetic, pH, temperature, initial sorbent concentration (5 g soil simulant/L AS or HU, 10 g/L and 15 g/L) and desorption experiments were carried out, the duration of which ranged from five days to three weeks.</p><p>The percentage of phosphorus removal was up to 60 % for the aqueous solutions and 24 % for the hydrolyzed human waste. The sulfate-rich simulant (MGS-1S) exhibited the best results. The major phases of MGS-1S are: gypsum, plagioclase, basaltic glass, pyroxene, and olivine. Temperature and the initial pH seem to be the dominant factors affecting P sorption. Equilibrium between sorbent and AS was achieved between five and seven days, as indicated by kinetic experiments. Isothermal experiments at 25 ⁰C with AS of different P concentrations displayed a linear correlation between adsorption capacity (q) and P-concentration (r<sup>2</sup>=0.98). Maximum q was observed at 8.5 and 27 mg/g for AS and HU experiments respectively, when 5 g/L of initial sorbent concentration was used. X-ray diffraction (XRD) of the sorbents treated with AS showed the presence of the newly formed phases berlinite and brushite. Perhaps due to hydrolysis of the pre-existing illite, aluminum bound with the solution’s phosphates, forming berlinite and buffering AS’s pH to lower values. Formation of brushite is possibly indicative of gypsum (predominant phase in the raw material) dissolution subsequently releasing sulfate anions. In a similar approach, XRD evaluation of the sorbents treated with HU revealed the newly formed phases calcite and hannayite. Phosphate and ammonia ions were likely to bind to the sample and were precipitated within newly formed calcium-bearing phases.</p><p>These experiments form a preliminary study of Martian soil simulants, and initial results indicate a possible use of Martian soils as waste recipients or as fertilizers in future missions.</p><p><strong>References</strong></p><p>Battista, F., & Bolzonella, D. (2019). Waste and Biomass Valorization, 10(12), 3701-3709.<br>Cannon, K. M., Britt, D. T., Smith, T. M., Fritsche, R. F., & Batcheldor, D. (2019). Icarus, 317, 470-478.<br>Yen, A. S., Gellert, R., Schröder, C., Morris, R. V., Bell, J. F., Knudson, A. T., ... & Blaney, D. (2005). Nature, 436(7047), 49-54.</p>


2020 ◽  
Vol 20 (3) ◽  
pp. 1072-1082
Author(s):  
Qianshu Sun ◽  
Shuang Zhao ◽  
Yubo Yan ◽  
Wenlin Jia ◽  
Weihua Yang

Abstract As one of the drinking water sources for Xuzhou city, Yuquan River has been polluted seriously in recent years. In this paper, enhanced coagulation technology was selected and various parameters (coagulant species, dosage, solution pH and coagulant aid species) were optimized for Yuquan River water treatment. Turbidity and UV254 removal rate were calculated to assess coagulation efficiencies, and meanwhile floc generation kinetics, zeta potential and scanning electron microscope (SEM) spectra were measured to study the coagulation mechanism. Results indicated that the coagulation effect of polyaluminium chloride (PAC) on Yuquan River water was better than that of aluminium sulphate (AS), and its optimal dosage was 20 mg/L. Flocs produced by PAC also exhibited larger size and faster growth velocity than those of AS. Moreover, the applicable initial pH range for Yuquan River was 6.0–9.0, and the optimal coagulation efficiency was observed at pH 7.0. When PAC or AS was selected as coagulant, the application of sodium alginate (SA) could improve turbidity and UV254 removal due to its adsorption bridging role. In addition, coagulation efficiency could be enhanced in an AS coagulation system when polyacrylamide (PAM) was dosed as coagulant aid.


2014 ◽  
Vol 5 (2) ◽  
pp. 149-156 ◽  
Author(s):  
Mang Lu ◽  
Yue Cheng ◽  
Jian-min Pan ◽  
Wen-jing Fan ◽  
Chuang Jiao ◽  
...  

In this study, MCM-41 stabilized nano zero-valent iron (M-NZVI) is synthesized using the rheological phase reaction method. Characterization with transmission electron microscopy validates the hypothesis that the introduction of MCM-41 leads to a decrease in aggregation of iron nanoparticles. X-ray diffraction confirms the existence of Fe0 and the strong antioxidant activity of Fe0 nanoparticles. Batch Cr(VI) reduction experiments exhibit that solution pH, M-NZVI dosage, and reaction time have significant effects on Cr(VI) removal. A high removal efficiency of Cr(VI) (84.5%) is obtained within 60 min for 100 mg/L of Cr(VI) solution at an initial pH of 6.0 and M-NZVI dosage of 0.5 g/L at 35 °C. The Cr(VI) removal rates follow modified pseudo-first-order kinetic equations. The observed removal rate constant was 0.0168/min for the M-NZVI dosage of 1.0 g/L. Our study suggests that the introduction of an innocuous stabilizer such as MCM-41 can significantly improve the performance of Fe0 nanoparticles for environmental remediation applications.


2020 ◽  
Vol 12 (3) ◽  
pp. 344-349 ◽  
Author(s):  
Xiaolei Teng ◽  
Junfeng Li ◽  
Zhaoyang Wang ◽  
Weiwei Liu ◽  
Dongbao Song ◽  
...  

The particle electrode was prepared by using industrial waste slag as raw material, and the surface morphology of the particle electrode was characterized by scanning electron microscopy. The comparison experiments showed that under the same experimental conditions, the efficiency of removing the methyl blue from the three-dimensional electrode of the steel slag particles was 23.48% higher than that of the two-dimensional electrode, and the energy consumption was reduced by 36.2%. The results showed that the primary and secondary factors affecting the methyl blue wastewater of steel slag particles are electrolyte concentration, voltage, initial waste concentration and particle volume. Under the optimal combination of pH 3, voltage 12 V, initial methyl blue concentration of 15 mg/L and electrolyte concentration of 0.3 mol/L, the removal rate of methyl blue reached 91.41%.


Author(s):  
Jiwei Zhang ◽  
Jingjing Xu ◽  
Shuaixia Liu ◽  
Baoxiang Gu ◽  
Feng Chen ◽  
...  

Background: Coal gangue was used as a catalyst in heterogeneous Fenton process for the degradation of azo dye and phenol. The influencing factors, such as solution pH gangue concentration and hydrogen peroxide dosage were investigated, and the reaction mechanism between coal gangue and hydrogen peroxide was also discussed. Methods: Experimental results showed that coal gangue has the ability to activate hydrogen peroxide to degrade environmental pollutants in aqueous solution. Under optimal conditions, after 60 minutes of treatment, more than 90.57% of reactive red dye was removed, and the removal efficiency of Chemical Oxygen Demand (COD) up to 72.83%. Results: Both hydroxyl radical and superoxide radical anion participated in the degradation of organic pollutant but hydroxyl radical predominated. Stability tests for coal gangue were also carried out via the continuous degradation experiment and ion leakage analysis. After five times continuous degradation, dye removal rate decreased slightly and the leached Fe was still at very low level (2.24-3.02 mg L-1). The results of Scanning Electron Microscope (SEM), energy dispersive X-Ray Spectrometer (EDS) and X-Ray Powder Diffraction (XRD) indicated that coal gangue catalyst is stable after five times continuous reuse. Conclusion: The progress in this research suggested that coal gangue is a potential nature catalyst for the efficient degradation of organic pollutant in water and wastewater via the Fenton reaction.


J ◽  
2021 ◽  
Vol 4 (2) ◽  
pp. 193-205
Author(s):  
Opeyemi A. Oyewo ◽  
Sam Ramaila ◽  
Lydia Mavuru ◽  
Taile Leswifi ◽  
Maurice S. Onyango

The presence of toxic metals in surface and natural waters, even at trace levels, poses a great danger to humans and the ecosystem. Although the combination of adsorption and coagulation techniques has the potential to eradicate this problem, the use of inappropriate media remains a major drawback. This study reports on the application of NaNO2/NaHCO3 modified sawdust-based cellulose nanocrystals (MCNC) as both coagulant and adsorbent for the removal of Cu, Fe and Pb from aqueous solution. The surface modified coagulants, prepared by electrostatic interactions, were characterized using Fourier transform infrared, X-ray diffraction (XRD), and scanning electron microscopy/energy-dispersive spectrometry (SEM/EDS). The amount of coagulated/adsorbed trace metals was then analysed using inductively coupled plasma atomic emission spectroscopy (ICP-AES). SEM analysis revealed the patchy and distributed floccules on Fe-flocs, which was an indication of multiple mechanisms responsible for Fe removal onto MCNC. A shift in the peak position attributed to C2H192N64O16 from 2θ = 30 to 24.5° occurred in the XRD pattern of both Pb- and Cu-flocs. Different process variables, including initial metal ions concentration (10–200 mg/L), solution pH (2–10), and temperature (25–45 °C) were studied in order to investigate how they affect the reaction process. Both Cu and Pb adsorption followed the Langmuir isotherm with a maximum adsorption capacity of 111.1 and 2.82 mg/g, respectively, whereas the adsorption of Fe was suggestive of a multilayer adsorption process; however, Fe Langmuir maximum adsorption capacity was found to be 81.96 mg/g. The sequence of trace metals removal followed the order: Cu > Fe > Pb. The utilization of this product in different water matrices is an effective way to establish their robustness.


Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2741
Author(s):  
Pengcheng Lv ◽  
Ruihong Meng ◽  
Zhongyang Mao ◽  
Min Deng

In this study, the hydrated sodium aluminosilicate material was synthesized by one-step hydrothermal alkaline desilication using fly ash (FA) as raw material. The synthesized materials were characterized by XRD, XRF, FT-IR and SEM. The characterization results showed that the alkali-soluble desilication successfully had synthesized the sodium aluminosilicate crystalline (N-A-S-H) phase of sodalite-type (SOD), and the modified material had good ionic affinity and adsorption capacity. In order to figure out the suitability of SOD as an adsorbent for the removal of ammonium and phosphorus from wastewater, the effects of material dosing, contact time, ambient pH and initial solute concentration on the simultaneous removal of ammonium and phosphorus are investigated by intermittent adsorption tests. Under the optimal adsorption conditions, the removal rate of ammonium was 73.3%, the removal rate of phosphate was 85.8% and the unit adsorption capacity reached 9.15 mg/L and 2.14 mg/L, respectively. Adsorption kinetic studies showed that the adsorption of ammonium and phosphorus by SOD was consistent with a quasi-secondary kinetic model. The adsorption isotherm analysis showed that the equilibrium data were in good agreement with the Langmuir and Freundlich model. According to thermodynamic calculations, the adsorption of ammonium and phosphorus was found to be a heat-absorbing and spontaneous process. Therefore, the preparation of SOD by modified FA has good adsorption properties as adsorbent and has excellent potential for application in the removal of contaminants from wastewater.


2020 ◽  
Vol 13 (1) ◽  
pp. 126
Author(s):  
Guozhen Zhang ◽  
Xingxing Huang ◽  
Jinye Ma ◽  
Fuping Wu ◽  
Tianhong Zhou

Electrochemical oxidation technology is an effective technique to treat high-concentration wastewater, which can directly oxidize refractory pollutants into simple inorganic compounds such as H2O and CO2. In this work, two-dimensionally stable anodes, Ti/RuO2-IrO2-SnO2, have been developed in order to degrade organic pollutants from pharmaceutical wastewater. Characterization by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD) showed that the oxide coating was successfully fabricated on the Ti plate surface. Electrocatalytic oxidation conditions of high concentration pharmaceutical wastewater was discussed and optimized, and the best results showed that the COD removal rate was 95.92% with the energy consumption was 58.09 kW·h/kgCOD under the electrode distance of 3 cm, current density of 8 mA/cm2, initial pH of 2, and air flow of 18 L/min.


1955 ◽  
Vol 1 (5) ◽  
pp. 299-311 ◽  
Author(s):  
R. Steel ◽  
C. P. Lentz ◽  
S. M. Martin

Factors affecting the production of citric acid in the submerged fermentation of ferrocyanide-treated beet molasses by Aspergillus niger were studied in 2.5 and 36 liter fermenters. The small fermenters were used to determine the effects of changes in sterilization technique, phosphate supplement, ferrocyanide treatment, inoculum level, initial pH, fermentation temperature, and aeration rate. The relation between ferrocyanide concentration and inoculum level was also studied. Four different samples of molasses were fermented successfully. An average yield of 8.2% citric acid (64% conversion) was obtained from 51 small-scale fermentations. Comparable yields were obtained in the large fermenters under comparable conditions. Most of the information obtained with the small fermenters was applicable to the larger-scale fermenters, but in the latter the fermentation was significantly more stable. Aeration was the main problem in the scale-up and aeration rates approximately double those calculated on a fermenter cross-sectional area basis were required for comparable results in the large fermenters.


2014 ◽  
Vol 884-885 ◽  
pp. 190-194
Author(s):  
Wei Xiao ◽  
Ran Di Zhang ◽  
Yu Bing Song ◽  
Run Ping Han ◽  
Yan Qiang Li

The adsorption studies of 4-chloro-2,5-dimethoxy nitrobenzene (CDNB) from aqueous solution on pyrolytic char activated by ammonium dihydrogen phosphate from pine sawdust have been performed. Several experimental parameters like initial pH, NaCl concentration, contact time solution temperature were evaluated. Solution pH within 2-7 is favor of adsorption and it is advantage of adsorption at higher temperature. Langmuir, Freundlich and Temkin isotherm models were used to fit the experimental data and Temkin model was better. The adsorption capacity was up to 33.8 mg·g1at 323 K. The process is spontaneous and endothermic and physical action is major mechanism.


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