Enhanced effects of reducing agent on oxalate chelated Fe(II) catalyzed percarbonate system for benzene degradation

The addition of hydroxylamine hydrochloride (HAH), ascorbic acid (ASC), sodium ascorbate (SAS) to the OA-Fe(II)/SPC system could promote the generation of HO• by accelerating Fe(II)/Fe(III) recycles and H2O2 decomposition. The enhancement of HAH on HO• generation surpasses ASC and SAS in the OA-Fe(II)/SPC system. The generation of O2•− was also enhanced by HAH, ASC and SAS, and more significant promotion of O2•− generation was observed with ASC and SAS addition. More effective benzene removal was achieved in an OA-Fe(II)/SPC system with suitable HAH, ASC and SAS addition, compared to the parent system. Excessive HAH, ASC or SAS had a negative effect on benzene removal. Results of scavenger tests showed that HO• is indeed the dominant free radical for benzene removal in every system, but the addition of HAH, ASC and SAS increased the contribution of O2•− to benzene degradation. HAH, ASC and SAS enhanced OA-Fe(II)/SPC systems could be well utilized to acidic and neutral conditions, while HCO3−, high concentration of HA and alkaline conditions were not favorable to benzene removal. Moreover, the addition of HAH, ASC and SAS are conducive to benzene removal in actual groundwater, and HAH was the optimal reducing agent for the enhancement of the OA-Fe(II)/SPC system.

A novel application of building demolition waste for removal benzene from aqueous solutions

A novel application of building demolition waste for removal benzene from aqueous solutions. In this research, demolition waste from buildings has been studied for possible use as benzene removal adsorbent from aquatic solution. The effect of adsorbent dosage, contact time, initial benzene concentration, and initial pH on benzene adsorption capacity have been investigated in the batch adsorption experiments. The adsorption effects initially happened very rapidly and achieved equilibrium within 180 min. Benzene removal was observed to decrease by an increase in the initial concentration of benzene of 300–700 mg·L–1, an increase in the adsorbent dose of 0.4–2.4 g per 100 mL, where an optimum adsorbent dose equal to 1.2 g per 100 mL was found. The potential of adsorption increases with pH 3.0–7.0 to reach the maximum removal efficiency at pH 6.0. The findings showed that equilibrium data were adequately adapted and correlated with the Freundlich isotherm models. The average percentage of the removal at room temperature was about 98%. Results suggest that building demolition waste can be used effectively in industrial wastewater treatment for the removal of aromatic hydrocarbon, benzene, as a low-cost option.

Use of NH4Cl for activation of carbon xerogel to prepare a novel efficacious adsorbent for benzene removal from contaminated air streams in a fixed-bed column

Background Ammonium chloride as an explosive salt has proved to be a prominent activation agent for adsorbents and increase the specific surface area and volume of cavities. In this work, the ability of this substance was scrutinized for activation of carbon aerogel to prepare an efficient adsorbent for benzene removal from air streams. Methods A carbon xerogel was fabricated from Novallac polymer and activated by ammonium chloride.The changes in structure and morphology were considered via Brunauer–Emmett–Teller (BET), scanning electron microscopy (SEM), Fourier transform infrared (FTIR), Barrett-Joyner-Halenda (BJH), and energy dispersive X-ray (EDX) analyses. Also, comprehensive studies were conducted to vouchsafe the properties of the new adsorbent for benzene removal, using a fixed-bed column mode. Results The results showed both the successful synthesis and the suitability of the activation process. ACX possessed a higher specific surface area (1008 g/m3), compared to the parent carbon xerogel (CX; 543.7 g/m3) and organic xerogel (OX; 47 g/m3), as well as a higher adsorption capacity. Conclusion NH4CL is a very beneficial for modifying the structure and morphology of carbon aerogel, and the dynamic behavior of the column with respect inlet benzene concentration can be explained by Yan-Nelson model.

Enhancement of benzene degradation by persulfate oxidation: synergistic effect by nanoscale zero-valent iron (nZVI) and thermal activation

The feasibility of an advanced oxidation process based upon sodium persulfate (SPS) activated simultaneously by heat (50 °C) and nanoscale zero-valent iron (nZVI) on benzene removal was investigated. The experimental results strongly showed the synergistic effect of thermal and nZVI activation to SPS and benzene removal was enhanced with the increase of SPS/nZVI/benzene molar ratio. Specifically, 94% of benzene could be removed in 1 hr at 50 °C at the SPS/nZVI/benzene molar ratio of 10/5/1. The radical scavenger tests and electron paramagnetic resonance (EPR) analysis confirmed that SO4•− was the predominant species contributing to benzene degradation. Further, the effects of the solution matrix on benzene elimination were investigated. The results indicated that benzene destruction in the thermally activated SPS/nZVI system performed better under acidic conditions, and the high concentration of both Cl− and HCO3− had adverse effects on benzene elimination. The test for the performance of benzene degradation in the actual groundwater demonstrated that benzene could be degraded entirely at SPS/nZVI/benzene molar ratio of 40/40/1 at 50 °C, indicating that the synergistic catalysis of thermal and nZVI activation to SPS is exploitable and the thermally activated SPS/nZVI system can be applicable to the remediation of benzene contaminated groundwater.

Using Biofilter Packed with Different Wood Waste Charges for Purification of Air Contaminated with Benzene

The main aim of this work was the analysis and assessment of benzene removal from air using bio-filter packed with a mixture of wood waste. The results of this work show that the small scale bio-filter with various coniferous and deciduous wood waste charges is capable of efficiently removing benzene from polluted air stream. The analysis of different mixtures of wood waste charge, while pH value was kept at neutral (pH = 7), determined, that the best wood waste mixture is consisted of 70% coniferous wood (45% pine trees, 25% fir trees), 30% deciduous wood (20% maple, 10% hazel) which was consisted of 10–20 mm fraction particles and had porosity value of 46%. This bio-media was best used for benzene removal from contaminated air stream (E = 93.86–74.78%).