Rytterjarvis9168

Heterogeneous Fenton oxidation of trichloroethylene (TCE) catalyzed by sewage sludge biochar was studied. The highest TCE removal efficiency was 83% at pH 3.1, catalyzed by 300 W biochar. The biochars produced at higher microwave power levels provided better catalytic effect, due to higher iron contents and specific surface areas. Reactivity of sewage sludge biochar maintained after several uses, which provides an advantage for using as a permeable reactive barrier to remediate groundwater pollution. Chromium, copper, nickel, lead, and zinc were found in the leachate generated from sewage sludge biochar, and most of the concentrations were lower than the standards for non-drinking water use. Besides, copper, zinc, and iron were found in the reaction solutions of Fenton oxidation. Because of the highest dosage required for Fenton oxidation, the environmental impact caused by 200 W biochar is highest. The environmental impact caused by 300 W biochar is lowest. Among the four endpoint impact categories in the life cycle assessment (LCA), human health is the highest concern, whereas ecosystem quality is the least. According to experimental and LCA results, the optimum microwave power level would be 300 W. The primary impact source is microwave pyrolysis because of high energy usage. The enormous tourism boom raises concern about possible negative environmental impacts worldwide. One of the risks posed by tourism may be heavy metal pollution. On the example of the volcanic island of Santorini, a popular tourist destination, pollution of soils categorized according to the tourism load was monitored. Significant anthropogenic contamination by heavy metals, especially Cu, Cr and Pb, was found out. This contamination may constitute a moderate ecological risk to the island ecosystems. Calcitriol Tourism has been shown to be a significant pollution factor as evidenced by the contaminated soils near the airport. Simultaneously, airport traffic has been proved to be an important emitter of Co, Cr and especially Zn. The comparison with other volcanic islands has shown that on Santorini the content of heavy metals in soils is significantly lower, despite frequently higher tourism intensity. On this basis, it can be concluded that in case of volcanic islands the dominant factor determining the content of heavy metals in the soil is the parent rock. Given high and ever-increasing intensity of tourism on the island, it can be assumed that soil contamination will continue to rise rapidly. Therefore, without proper steps reducing tourism, increase in soil degradation, growing negative impacts on local ecosystems as well as on the quality of produced wine can be expected on Santorini. The BCR sequential extraction scheme (SES), initially developed for soils and sediments, is frequently adopted to evaluate the environmental risks of municipal solid waste incineration (MSWI) fly ash. Within the procedure, metals are liberated from the matrix hosting them relying on the selectivity of the chosen chemical reagents or operation conditions. However, the effect of the high content of alkaline substances in MSWI fly ash on the selectivity of acetic acid to acid-soluble fraction metals was ignored. In this study, the feasibility of the BCR SES for evaluating MSWI fly ash was assessed by adjusting the acetic acid washing times in the acid-soluble extraction step. The metal fractionation, as well as mineralogy, morphology, and surface chemistry of the residues after three successive acid washing processes, were analyzed. The results reveal that only easily soluble salts, but not hydroxides, are entirely extracted after the first acid washing (pH∼12.0). Importantly, carbonates (generally reported as an indicator of the complete release of acid-soluble metals) are mostly decomposed only after the third acid washing (pH∼3.8). The incomplete dissolution of calcium carbonates in a single-step acid washing may convey misleading results of metal fractionation and underestimates the environmental risk of potentially toxic elements. Therefore, complete removal of carbonates should be employed as the endpoint of the acid-soluble fraction extraction step in the evaluation of MSWI fly ash. This work can help in selecting proper strategies for fly ash management and developing proper sequential extraction schemes for similar high-alkalinity hazardous waste risk assessment. In this study, subcritical water-NaOH (CW-NaOH) and subcritical water-C2H5OH (CW-C2H5OH) processes were developed for diethylhexyl phthalate (DEHP) degradation and dechlorination of polyvinyl chloride (PVC) waste. The introduction of NaOH or C2H5OH in subcritical water had a noticeable influence on the mechanism of DEHP degradation and dechlorination. For both CW-NaOH and CW-C2H5OH treatments, the increase in temperature could increase dechlorination efficiency (DE) of PVC. The DE of CW-NaOH is much higher than that of CW-C2H5OH under the same conditions. The DE of CW-NaOH could exceed 95% at 300 °C. Hydroxyl nucleophilic substitution was the main dechlorination mechanism in CW-NaOH, while nucleophilic substitution and direct dehydrochlorination were equally important in CW-C2H5OH. In CW-NaOH treatment, 2-ethyl-1-hexanol, benzaldehyde, and toluene were obtained by hydrolysis and reduction reactions of DEHP. Acetophenone was produced by the further cyclization, dehydrogenation and rearrangement reactions of 2-ethyl-1-hexanol. Transesterification was the main degradation pathway of DEHP in CW-C2H5OH at 300 °C. The cyclization and dehydration of 2-ethyl-1-hexanol resulted in producing a high level of ethyl-cyclohexane and 1-ethyl-cyclohexene in CW-C2H5OH at 350 °C. Furthermore, high concentration of ethyl palmitate and ethyl stearate could be prepared in CW-C2H5OH system by the strong reactivity of C2H5OH with the lubricants in PVC. In order to harness the full capability of ultraviolet and visible light in the dielectric barrier discharge induced non-thermal plasma (DBD-NTP) process, g-C3N4/TiO2 catalysts were prepared and utilized in this process. Synergistic degradation of acid orange 7 (AO7) dye by DBD-NTP and g-C3N4/TiO2 was conducted, and the performance, degradation pathways and synergistic catalytic mechanism were investigated. The results showed that the degradation rate of AO7 in the DBD-NTP and g-C3N4-15/TiO2 process increased by 39.1% compared with that in the single DBD-NTP process at 12 min discharge time. At 20 W input power, initial concentration of AO7 was 5 mg/L, catalytic dosage was 0.5 g/L, initial pH value was 10.0 and air flow rate was 52 L/h, the degradation rate of AO7 reached 100.0% after 12 min discharge time. Higher discharge power and initial concentration of AO7 inhibited AO7 degradation, whereas increasing the air flow rate and initial pH value of the solution promoted AO7 degradation. The degradation pathways of AO7 consisted of azo structure destruction, ring opening reaction, hydroxylation, carboxylation and mineralization reaction.