“…And it reached to 2.79 at the end of 6 consecutive reactions. The chromium could be removed as a hydroxide precipitate . However, it is not conducive to the precipitation of TCr in the condition of acidic pH .…”
Excessive consumption of Fe (II) and massive generation of sludge containing Fe (III) from classic Fenton process remains a major obstacle for its poor recycling of Fe (III) to Fe (II). Therefore, the MHACF‐MIL‐101(Cr) system, by introducing H2, Pd0 and MIL‐101(Cr) into Fenton reaction system, was developed at normal temperature and pressure. In this system, the reduction of FeIII back to FeII by solid catalyst Pd/MIL‐101(Cr) for the storage and activation of H2, was accelerated significantly by above 10‐fold and 5‐fold controlled with the H2‐MIL‐101(Cr) system and H2‐Pd0 system, respectively. However, the concentration of Fe (II) generated by the reduction of Fe (III) could not be detected with the only input of H2 and without the addition of MOFs material. In addition, the apparent consumption of Fe (II) in MHACF‐MIL‐101(Cr) system was half of that in classical Fenton system, while more Fe (II) might be reused infinitely in fact. Accordingly, only trace amount of Fe (II) vs H2O2 concentration was needed and hydroxyl radicals through the detection of para‐hydroxybenzoic acid (p‐HBA) as the oxidative product of benzoic acid (BA) by·OH could be continuously generated for the effective degradation of 4‐chlorophenol(4‐CP). The effects of initial pH, concentration of 4‐CP, dosage of Fe2+, H2O2 and Pd/MIL‐101(Cr) catalyst, Pd content and H2 flow were investigated, combined with systematic controlled experiments. Moreover, the robustness and morphology change of Pd/MIL‐101(Cr) were thoroughly analyzed. This study enables better understanding of the H2‐mediated Fenton reaction enhanced by Pd/MIL‐101(Cr) and thus, will shed new light on how to accelerate Fe (III)/Fe (II) redox cycle and develop more efficient Fenton system.
“…And it reached to 2.79 at the end of 6 consecutive reactions. The chromium could be removed as a hydroxide precipitate . However, it is not conducive to the precipitation of TCr in the condition of acidic pH .…”
Excessive consumption of Fe (II) and massive generation of sludge containing Fe (III) from classic Fenton process remains a major obstacle for its poor recycling of Fe (III) to Fe (II). Therefore, the MHACF‐MIL‐101(Cr) system, by introducing H2, Pd0 and MIL‐101(Cr) into Fenton reaction system, was developed at normal temperature and pressure. In this system, the reduction of FeIII back to FeII by solid catalyst Pd/MIL‐101(Cr) for the storage and activation of H2, was accelerated significantly by above 10‐fold and 5‐fold controlled with the H2‐MIL‐101(Cr) system and H2‐Pd0 system, respectively. However, the concentration of Fe (II) generated by the reduction of Fe (III) could not be detected with the only input of H2 and without the addition of MOFs material. In addition, the apparent consumption of Fe (II) in MHACF‐MIL‐101(Cr) system was half of that in classical Fenton system, while more Fe (II) might be reused infinitely in fact. Accordingly, only trace amount of Fe (II) vs H2O2 concentration was needed and hydroxyl radicals through the detection of para‐hydroxybenzoic acid (p‐HBA) as the oxidative product of benzoic acid (BA) by·OH could be continuously generated for the effective degradation of 4‐chlorophenol(4‐CP). The effects of initial pH, concentration of 4‐CP, dosage of Fe2+, H2O2 and Pd/MIL‐101(Cr) catalyst, Pd content and H2 flow were investigated, combined with systematic controlled experiments. Moreover, the robustness and morphology change of Pd/MIL‐101(Cr) were thoroughly analyzed. This study enables better understanding of the H2‐mediated Fenton reaction enhanced by Pd/MIL‐101(Cr) and thus, will shed new light on how to accelerate Fe (III)/Fe (II) redox cycle and develop more efficient Fenton system.
“…As a result of electrolysis, charged particles are neutralized in raw wastewater and subsequently form flocs. It is possible to remove phenol, anions such as nitrate and nitrite, cations such as ammonia, and metals as well as COD, TOC, color and turbidity [35,[38][39][40][41][42]. This method has been implemented for a pilot project at Shazand Oil Refinery in Arak, Iran [43].…”
The present article is an assessment of wastewater treatment processes in the oil refinery sector in Kazakhstan by comparing relevant experience of developed and developing countries. The legislation in this sphere, the treatment methods, the discharge process and the effect on the environment were evaluated following international and national regulations. In our study, the wastewater systems in three factories in Kazakhstan were assessed. Results show that, even though the environmental regulation in Kazakhstan promotes the polluter pays principle and follows the World Health Organization (WHO) recommendations, the oil refinery plants in Kazakhstan still contain exceeding concentrations of pollutants in their effluents. One issue is that the local legislation allows disposal of wastewater to natural or artificial ponds as long as the concentrations of pollutants in effluents are less than the already existing concentrations in the pond. Consequently, the factories can use ponds with an initially high concentration of contaminants. The high initial concentration of pollutants in the pond water is due to wastewater discharged before the implementation of current environmental regulations. This issue in the current legislation leads to the situation where there is no incentive for efficient wastewater treatment. The national law also lacks regulations regarding which methodology should be used to assess the pollutants in the wastewater. Thus, the control by national environmental office for each enterprise is negotiated separately between the factory and the governmental body. This gives the factory a strong position to define the parameters assessing the effluents. This has led to none of the factories measuring, e.g., heavy metals in discharged wastewater. Total petroleum hydrocarbons (TPH) concentration in wastewater is often exceeded at each factory and there is no analysis done for different hydrocarbon fraction. To overcome the issues described in the present study, we strongly recommended a unified and transparent methodology for the country’s oil refinery industry to assess important pollutants in discharged wastewater.
“…However, routinely available methods suffer from serious drawbacks, including high cost and the formation of hazardous byproducts requiring management and disposal. As an alternative, flocculation is an environmentally friendly, cost-effective, and an increasingly important process in pollution control [13][14][15][16]. Flocculation is a usual step in water treatment and the flocculant is the core of flocculation technology, so it is very important to choose a suitable The intrinsic viscosity (η), a major determinant in controlling P(AM-DMDAAC) performance [39], was used to assess the effectiveness of P(AM-DMDAAC) prepared in this study.…”
A composite flocculant P(AM–DMDAAC) was synthesized by the copolymerization of acrylamide (AM) and dimethyl diallyl ammonium chloride (DMDAAC). By using microwave (MV) assistance with ammonium persulfate as initiator, the synthesis had a short reaction time and yielded a product with good solubility. Fourier-transform infrared spectroscopy, scanning electron microscopy, and differential thermal analysis–thermogravimetric analysis were employed to determine the structure and morphology of P(AM–DMDAAC). The parameters affecting the intrinsic viscosity of P(AM–DMDAAC), such as MV time, mass ratio of DMDAAC to AM, bath time, reaction temperature, pH value, and the dosages of ammonium persulfate initiator, EDTA, sodium benzoate, and urea were examined. Results showed that the optimum synthesis conditions were MV time of 1.5 min, m(DMDAAC):m(AM) of 4:16, 0.5 wt‰ initiator, 0.4 wt‰ EDTA, 0.3 wt‰ sodium benzoate, 2 wt‰ urea, 4 h bath time, reaction temperature of 40 °C, and pH of 2. The optimal dimethyl phthalate (DMP) removal rate can reach 96.9% by using P(AM–DMDAAC), and the P(AM–DMDAAC) had better flocculation than PAM, PAC, and PFS.
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