Formation of organic chloride in the treatment of textile dyeing sludge by Fenton system.

In the oxidation treatment of textile dyeing sludge, the quantitative and transformation laws of organic chlorine are not clear enough. Thus, this study mainly evaluated the treatment of textile dyeing sludge by Fenton and Fenton-like system from the aspects of the influence of Cl-, the removal of polycyclic aromatic hydrocarbons (PAHs) and organic carbon, and the removal and formation mechanism of organic chlorine. The results showed that the organic halogen in sludge was mainly hydrophobic organic chlorine, and the content of adsorbable organic chlorine (AOCl) was 0.30 mg/g (dry sludge). In the Fenton system with pH=3, 500 mg/L Cl-, 30 mmol/L Fe2+ and 30 mmol/L H2O2, the removal of phenanthrene was promoted by chlorine radicals (•Cl), and the AOCl in sludge solid phase increased to 0.55 mg/g (dry sludge) at 30 min. According to spectral analysis, it was found that •Cl could chlorinate aromatic and aliphatic compounds (excluding PAHs) in solid phase at the same time, and eventually led to the accumulation of aromatic chlorides in solid phase. Strengthening the oxidation ability of Fenton system increased the formation of organic chlorines in liquid and solid phases. In weak acidity, the oxidation and desorption of superoxide anion promoted the removal and migration of PAHs and organic carbon in solid phase, and reduced the formation of total organic chlorine. The Fenton-like system dominated by non-hydroxyl radical could realize the mineralization of PAHs, organic carbon and organic chlorines instead of migration. This paper builds a basis for the selection of sludge conditioning methods.

Biomass waste as a clean reductant for iron recovery of iron tailings by magnetization roasting.

The magnetization roasting with coal as primary reductants adds cost and causes environmental pollution. Therefore, it is of great importance to investigate the biomass application as a reductant for magnetization roasting to recover iron from low-utilization iron tailings for emission mitigation and green utilization. This study systematically investigated the impact of biomass (pyrolysis gas from agricultural and forestry waste) as a reductant on the conversion of iron tailings to magnetite in magnetization roasting. Additionally, the thermal decomposition of biomass, phase transformation and microstructure evolution of iron tailings were analyzed by TG, XRD, BET, and other methods to elucidate the conversion mechanism for facilitating magnetized hematite in iron tailings with biomass-derived gas. The results showed that woody biomass was a more appropriate reductant for magnetization roasting; 650 °C was the optimal temperature for the complete transformation of hematite to magnetite by reduction roasting with biomass waste. Through magnetic separation, the concentrate with an iron grade of 62.04% and iron recovery of 95.29% was obtained, and the saturation magnetization was enhanced from 0.60 emu/g to 58.03 emu/g of iron tailings. During the magnetization roasting, CO and H2 generated from biomass reduced the hematite in tailings particles from interior to exterior, forming a loose structure with rich microfissures, facilitating the subsequent separation operations. This study offers a novel reference for applying biomass to exploit hematite minerals and shows the potential of biomass for energy savings and emission reduction in the utilization of iron tailing resources.

Nitrogen-enriched micro-mesoporous carbon derived from polymers organic frameworks for high-performance capacitive deionization.

Nitrogenization is an effective method for improving the capacitive deionization (CDI) performance of porous carbon materials. In particular, polymer organic frameworks with heteroatom doping, containing an ordered pore structure and excellent electrochemical stability, are ideal precursors for carbon materials for high-performance CDI. In this study, a nitrogen-enriched micro-mesoporous carbon (NMC) electrode was fabricated by carbonizing a Schiff base network-1 at 500, 600, and 700 °C. Scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, N2 adsorption-desorption, the contact angle of water, cyclic voltammetry, and electrochemical impedance spectroscopy were used to characterize the morphological structure, wettability, Brunauer-Emmett-Teller surface areas, and electrochemical performance of the NMCs. The results showed that the NMC carbonized at 600°C achieved the best specific capacitance (152.33 F/g), as well as a high electrosorption capacity (25.53 mg/g) because of its chemical composition (15.57% N) and surface area (312 m2/g). These findings prove that NMC is viable as an electrode material for desalination by high-performance CDI applications.

Treatment of simulated textile sludge using the Fenton/Cl- system: The roles of chlorine radicals and superoxide anions on PAHs removal.

The main content of this work is to investigate the removal of polycyclic aromatic hydrocarbons (PAHs: phenanthrene, anthracene, and fluoranthene) from simulated sludge solid phase employing an Fenton/Cl- system under various Cl- contents and pH values. The steady-state concentrations of the hydroxyl, chlorine, and dichloride anion radicals ([·OH]ss, [·Cl]ss, and [Cl2·-]ss) in heterogeneous system were first measured using tert-butanol, nitrobenzene, and benzoic acid. The outcomes exhibited that increasing the Cl- content from 50 to 2000 mg/L (pH = 3.0) or raising the pH from 3.0 to 5.0 (1000 mg/L Cl-) caused [·OH]ss to continuously decrease and [Cl2·-]ss and the concentration of superoxide anions (HO2·/O2·-) to continuously increase. When the pH was 3.0 and the Cl- concentration was 1000 mg/L, [·Cl]ss had a maximum value of 9.27 × 10-14 M. Combining the results of PAH removal, radical quenching, and product analysis, it was found that ·Cl in the Fenton/Cl- system promoted the oxidative degradation of phenanthrene without forming chlorination byproducts. Furthermore, HO2·/O2·- was helpful in removing anthracene and fluoranthene. Under the environment of high Cl- content (≥1000 mg/L), PAHs could be removed more effectively by using HO2·/O2·-. This investigation underpins further study on the regulation of reactive species and the efficient degradation of target organic matter in Fenton/Cl- system, and provides a basis for studying the formation of chlorinated or toxic byproducts in the process of treating textile dyeing sludge by Fenton.

Simultaneous reduction of antibiotics and antibiotic resistance genes in pig manure using a composting process with a novel microbial agent.

In recent years, in order to promote animal growth and reduce the risk of disease, a variety of antibiotics are frequently added to the animal feed of livestock and poultry. However, these antibiotics can not be fully digested by animals and most of them are excreted with feces, consequently causing the enrichment of antibiotic resistance genes (ARGs) and huge environmental risks. Nowadays, composting is a better option to solve these problems. Accordingly, this study explored the effects of co-composting swine manure with different inoculants dominated by Phanerochaete chrysosporium (p), Aspergillus niger (a), and Bacillus licheniformis (b) on the simultaneous removal of multiple antibiotics and resistance genes and evolution of the bacterial community. The results showed that the highest removal extent of tetracycline and oxytetracycline occurred in pile D (p:b:a=1:5:5, biomass) reaching 89.2% and 87.8%, respectively, while the highest removal extent of doxycycline and enrofloxacin occurred in pile A (p:b:a=1:0:0, biomass) reaching 98.6% and 89%, respectively. Compared with the levels in pile B (control check), in pile D, ARGs, except those for sulfonamides, decreased by 1.059 × 10-3-6.68 × 10-2 gene copies/16S rRNA copies. Inoculation with p alone effectively reduced intI1 and intI2. Canonical correspondence analysis (CCA) that microbial community structure evolution had a greater influence on ARGs than environmental factors. In summary, this study provided a feasible way to efficiently remove the antibiotics and antibiotic resistance genes in pig manure.

Chlorobenzene levels, component distribution, and ambient severity in wastewater from five textile dyeing wastewater treatment plants.

Chlorobenzenes (CBs) present in synthetic dyes are discharged into natural waters during the treatment of textile dyeing wastewater, which may have adverse effects on human and environment. In this study, the existence and removal of 12 CBs in different units of five treatment plants were examined. The ecological risk of CBs in textile dyeing wastewater was assessed by ambient severity (AS) and risk quotients (RQs). The results showed that trichlorobenzene, tetrachlorobenzene, pentachlorobenzene and hexachlorobenzene were ubiquitous in textile dyeing wastewater, and their distribution was similar. In one of the plants, the content of hexachlorobenzene was found to be as high as 9.277 µg/L in the raw water, which was an oil-water mixture. In other plants, there was no significant difference in the content and composition of CBs among influent and effluent suggesting that the conventional wastewater treatment plants cannot improve the existence of them. Monochlorobenzene and dichlorobenzene were not detected, which may have been related to strong volatility, biochemical properties, and weak instrument sensitivity. In the treatment process and effluent, trichlorobenzene is the main pollutant and accounted for 39.51% of all CB. CB removal was found only in the anaerobic system, while the aerobic system did not have the corresponding removal effect on CB and total organic carbon. According to ecological risk assessment, CBs in effluent has not been found the significant potential harm to human health (AS < 1), but posed moderate ecological risk to aquatic ecosystem (RQs > 0.1).

Algal toxicity induced by effluents from textile-dyeing wastewater treatment plants.

This research aimed to evaluate the alga Scenedesmus obliquus toxicity induced by textile-dyeing effluents (TDE). The toxicity indicator of TDE in alga at the physiological (algal growth), biochemical (chlorophyll-a (Chl-a) synthesis and superoxide dismutase (SOD) activity) and structural (cell membrane integrity) level were investigated. Then we further study the relationship among toxicity indicators at physiological and biochemical level, and supplemented by research on algal biomacromolecules. According to the analysis of various endpoints of the alga, the general sensitivity sequence of toxicity endpoints of Scenedesmus obliquus was: SOD activity > Chl-a synthesis > algal growth. The stimulation rate of SOD activity increased from day 3 (57.25%~83.02%) to day 6 (57.25%~103.81%), and then decreased on day 15 (-4.23%~-32.96%), which indicated that the antioxidant balance system of the algal cells was destroyed. The rate of Chl-a synthesis inhibition increased gradually, reaching 19.70%~79.39% on day 15, while the rate of growth inhibition increased from day 3 (-12.90%~10.16%) to day 15 (-21.27%~72.46%). Moreover, the algal growth inhibition rate was positively correlated with the inhibition rate of SOD activity or Chl-a synthesis, with the correlation coefficients were 0.6713 and 0.5217, respectively. Algal cells would be stimulating to produce excessive reactive oxygen species, which would cause peroxidation in the cells, thereby destroying chloroplasts, inhibiting chlorophyll synthesis and reducing photosynthesis. With increasing exposure time, irreversible damage to algae can lead to death. This study is expected to enhance our understanding of the ecological risks through algal tests caused by TDE.

Ion-exchange polymers modified bacterial cellulose electrodes for the selective removal of nitrite ions from tail water of dyeing wastewater.

Ion-exchange polymer and modified carbonization bacterial cellulose (CBC) electrodes were fabricated using varying amounts of cation-exchange polymers (glutaric acid (GA) and sulfosuccinic acid (SSA)) and assembled within an asymmetric capacitive deionization unit (p-CDI). The performance of selective NO2- electro-adsorption was studied. The AC/CBC-SSA group showed a better salt adsorption capacity (14.56 mg/g) and nitrite removal efficiency (71.01%) than the AC/CBC-GA (10.72 mg/g, 47.83%) and AC/AC (4.81 mg/g, 12.74%) groups. It was confirmed that the CBC-SSA/GA electrodes enhanced nitrite selectivity and increased the adsorption capacity, and the total amounts of adsorbed anions increased when the applied voltage was increased from 0.8 to 1.2 V, while the molar fraction of nitrate decreased. The competitive and preferential adsorption of anions was further investigated using different binary solutions of anions and occurred in the following sequence: NO2- >SO42- >NO3- >F-≈ Cl-. Furthermore, the p-CDI units were applied to remove nitrite in real wastewater samples, and the results showed that they had excellent reusability and application for use in dyeing wastewater treatment.

Current situation and forecast of environmental risks of a typical lead-zinc sulfide tailings impoundment based on its geochemical characteristics.

The potential environmental implications of a Pb (Lead)-Zn (Zinc) sulfide tailing impoundment were found to be dependent on its geochemical characteristics. One typical lead-zinc sulfide tailing impoundment was studied. Ten boreholes were set with the grid method and 36 tailings were sampled and tested. According to the results of metal content analysis, the tailing samples contained considerably high contents of heavy metals, ranging from 6.99 to 89.0 mg/kg for Cd, 75.3 to 602 mg/kg for Cu, 0.53% to 2.63% for Pb and 0.30% to 2.54% for Zn. Most of the heavy metals in the sample matrix showed a uniform concentration distribution, except Cd. Cd, Pb, Zn, and Mn were associated with each other, and were considered to be the dominant contributors based on hierarchical cluster analysis. XRD, SEM and XPS were employed for evaluation of the tailing weathering characteristics, confirming that the tailings had undergone intensive weathering. The maximum potential acidity of the tailings reached 244 kg H2SO4/ton; furthermore, the bioavailability of heavy metals like Pb, Cd, Cr, Cu, and Zn was 37.8%, 12.9%, 12.2%, 5.95%, and 5.46% respectively. These metals would be potentially released into drainage by the weathering process. Analysis of a gastrointestinal model showed that Pb, Cr, Ni and Cu contained in the tailings were high-risk metals. Thus, control of the heavy metals' migration and their environmental risks should be planned from the perspective of geochemistry.

The agricultural use potential of the detoxified textile dyeing sludge by integrated Ultrasound/Fenton-like process: A comparative study.

Enhancing industrial sludge detoxification is of scientific and practical significance in confronting urban development and stringent environmental regulations. A strategy combining ultrasound (US) with the zero-valent iron/EDTA/Air (ZEA) process was proven to be eco-friendly, being efficient in the removal of toxic compounds from textile dyeing sludge in our previous studies. In this paper, therefore, the detoxification effects of three advanced oxidation processes (US, ZEA, US/ZEA) on textile dyeing sludge were comparatively evaluated for the first time through alteration of the sludge's physico-chemical parameters (e.g., macronutrients, heavy metals, and persistent organic pollutants) and toxicity (plants and aquatic biota), by which the appropriateness of industrial sludge's agricultural use was assessed. The results showed that US led to the least alteration of the physico-chemical properties, and the treated sludge became less biodegradable, as demonstrated by XPS. With ZEA treatment, persistent organic pollutants (POPs) were degraded by oxidation, and heavy metals were more leachable, leading to effective detoxification with a relatively low sludge dose, but an excessive amount of EDTA would negatively change the fertilizing properties of the sludge. However, the integration of US and ZEA could avoid this situation, as US promoted the degradation of EDTA and POPs, thus causing the least inhibition or even a noticeable stimulation of plant growth when the sludge dosage was 7.5 tdw/ha (recommended dosage by the latest legislation in China). Aquatic organism toxicity tests further confirmed that US/ZEA treatment realized the most significant toxicity reduction, leading to the slightest environmental disruption. This study could be instructive in providing guidance for industrial sludge management considering agricultural use.

Treatment of 3,3'-dimethoxybenzidine in sludge by advance oxidation process: Degradation products and toxicity evaluation.

Studies on the oxidation products of organic pollutants and their toxicity in textile dyeing sludge after the sludge was treated by the advance oxidation processes were limited, since textile dyeing sludge was a complicated mixture. For the first time, simulated sludge was used to study the degradation mechanism of 3,3'-dimethoxybenzidine (DMB) during the combined ultrasound-Mn(VII) treatment. The toxicity of DMB and its products was also evaluated. The results indicated that the compositions and microstructures of polyaluminium chloride (PAC)- and polyferric sulphate (PFS)-based simulated sludge were similar to those of real textile dyeing sludge. The optimum conditions of ultrasound-Mn(VII) treatment were: a KMnO4 dosage of 40 µM, an ultrasound power density of 0.36 W cm-3, and a reaction time of 20 min. 98.24% of DMB and 63.04% of total organic carbon (TOC) in the simulated sludge were removed. Six products, that is, 2-nitroanisole, 3-methoxy-4-nitrophenol, vanillylmandelic acid, vanillyl alcohol, m-anisic acid, and benzoic acid, were identified by GC-MS and LC-MS-MS. It was noted that all of these identified products were also detected in the real textile dyeing sludge after the ultrasound-Mn(VII) treatment. All of them were less toxic than DMB. Moreover, 53.30% and 54.80% of toxicity toward the alga Desmodesmus subspicatus and the bacterium Vibrio fischeri were removed in simulated sludge, respectively. Therefore, simulated sludge was helpful for studying a pollutant's degradation mechanism in the complex sludge mixtures. The results would also provide some useful suggestions for the sludge disposal after the sludge was treated by the advance oxidation processes.

Toxicity evaluation of textile dyeing effluent and its possible relationship with chemical oxygen demand.

Textile dyeing wastewater was the focus of much research because of its adverse effect on aquatic biota. In the present research, textile dyeing influent and effluent samples were collected from four textile dyeing wastewater treatment plants (TDPs) in Guangdong province, China, and their conventional indicators and toxicity were examined to reveal relationships. The relationship between toxicity and chemical oxygen demand (COD) was clearly established at individual TDPs. Results indicated the highest removal efficiencies of 94.4%, 90.6%, 91.9%, 94.6%, 92.8% and 97.5% for TOC, mixed-liquor volatile suspended solids (MLVSS), COD, ammonia nitrogen (NH3-N), total phosphorus (TP) and colour, respectively. The primary clarifier used in TDP3 and TDP4 was beneficial for removing macromolecular organic substances, and membrane filtration and sedimentation basin employed at TDP1 and TDP2, respectively, helped to remove toxic substances. Toxicity to V. fischeri or D. subspicatus was found to be related to certain conventional indicators such as TOC, COD, TP, colour, and MLVSS, and was positively correlated with COD in different textile dyeing effluents (R2 > 0.84). It was recommended that the relationship between toxicity and COD in wastewater should be established individually at each plant. Therefore, this study could be useful in providing suggestions for guiding effluent management when no toxicity experiments were conducted.

Combined ultrasound with Fenton treatment for the degradation of carcinogenic polycyclic aromatic hydrocarbons in textile dying sludge.

To develop an effective method to remove the toxic and carcinogenic polycyclic aromatic hydrocarbons (CPAHs) from textile dyeing sludge, five CPAHs were selected to investigate the degradation efficiencies using ultrasound combined with Fenton process (US/Fenton). The results showed that the synergistic effect of the US/Fenton process on the degradation of CPAHs in textile dyeing sludge was significant with the synergy degree of 30.4. During the US/Fenton process, low ultrasonic density showed significant advantage in degrading the CPAHs in textile dyeing sludge. Key reaction parameters on CPAHs degradation were optimized by the central composite design as followed: H2O2 concentration of 152 mmol/L, ultrasonic density of 408 W/L, pH value of 3.7, the molar ratio of H2O2 to Fe2+ of 1.3 and reaction time of 43 min. Under the optimal conditions of the US/Fenton process, the degradation efficiencies of five CPAHs were obtained as 81.23% (benzo[a]pyrene) to 84.98% (benz[a]anthracene), and the benzo[a]pyrene equivalent (BaPeq) concentrations of five CPAHs declined by 81.22-85.19%, which indicated the high potency of US/Fenton process for removing toxic CPAHs from textile dyeing sludge.

Thermodynamic Equilibrium Calculations on Cd Transformation during Sewage Sludge Incineration.

Thermodynamic equilibrium calculations were performed to reveal the distribution of cadmium during the sewage sludge incineration process. During sludge incineration in the presence of major minerals, such as SiO2, Al2O3 and CaO, the strongest effect was exerted by SiO2 on the Cd transformation compared with the effect of others. The stable solid product of CdSiO3 was formed easily with the reaction between Cd and SiO2, which can restrain the emissions of gaseous Cd pollutants. CdCl2 was formed more easily in the presence of chloride during incineration, thus, the volatilization of Cd was advanced by increasing chlorine content. At low temperatures, the volatilization of Cd was restrained due to the formation of the refractory solid metal sulfate. At high temperatures, the speciation of Cd was not affected by the presence of sulfur, but sulfur could affect the formation temperature of gaseous metals.

Unveiling characteristics of a bioelectrochemical system with polarity reversion for simultaneous azo dye treatment and bioelectricity generation.

A novel bioelectrochemical system (BES) operated with polarity reversion was explored for simultaneous anaerobic/aerobic treatment of azo dye and production of bioelectricity under extremely low buffer. The Congo red was first decolorized in anode, with completed color removal in 35 h. The resultant decolorization intermediates were then mineralized after the anode reversed to aerobic biocathode, evidenced by 55 % chemical oxygen demand (COD) removal in 200 h. The mineralization efficiency was further increased to 70 % when the period of the half-cycle was prolonged to 375 h. Meanwhile, the BES produced a continuous stable positive/negative alternate voltage output under 5 mM phosphate buffer because of the self-neutralization of the accumulated protons and hydroxyl ions in electrolyte. The electrode performance was significantly improved, which was indicated by alleviated electrode polarization, due to in situ use of accumulated protons and hydroxyl ions and enhanced electron transfer in the presence of Congo red and its degradation intermediates, which resulted in 1.05-fold increases in maximum power density (67.5 vs. 32.9 mW/m(2)). An analysis of the microbial diversity in the biofilm revealed that the biofilm was dominated by facultative bacteria with functional roles in contaminant degradation and electricity generation.

Enhanced dewaterability of textile dyeing sludge using micro-electrolysis pretreatment.

The effects of micro-electrolysis treatment on textile dyeing sludge dewatering and its mechanisms were investigated in this study. Capillary suction time (CST) and settling velocity (SV) were used to evaluate sludge dewaterability. Extracellular polymeric substances (EPS) concentration and sludge disintegration degree (DDSCOD) were determined to explain the observed changes in sludge dewaterability. The results demonstrated that the micro-electrolysis could significantly improve sludge dewaterability by disrupting the sludge floc structure. The optimal conditions of sludge dewatering were the reaction time of 20 min, initial pH of 2.5, Fe/C mass ratio of 1/1, and the iron powder dosage of 2.50 g/L, which achieved good CST (from 34.1 to 27.8 s) and SV (from 75 to 60%) reduction efficiency. In addition, the scanning electron microscope (SEM) images revealed that the treated sludge floc clusters are broken up and that the dispersion degree is better than that of a raw sludge sample. The optimal EPS concentration and DDSCOD to obtain maximum sludge dewaterability was 43-46 mg/L and 4.2-4.9%, respectively. The destruction of EPS was one of the primary reasons for the improvement of sludge dewaterability during micro-electrolysis treatment.

Effect of K2FeO4/US treatment on textile dyeing sludge disintegration and dewaterability.

The effect of potassium ferrate/ultrasonic (K2FeO4/US) treatment on the physicochemical features of textile dyeing sludge was studied. The soluble chemical oxygen demand (SCOD), deoxyribonucleic acid (DNA), sludge volume index (SVI), sludge viscosity, capillary suction time (CST) and particle size were measured to understand the observed changes in the sludge physicochemical features. The results showed that the combined K2FeO4/US treatment presented great advantages for disrupting the sludge floc structure over K2FeO4 or ultrasonic treatments alone. The optimal parameters of sludge disintegration were found to be a K2FeO4 treatment time of 60 min, a K2FeO4 dosage of 0.5936 g/g SS, an ultrasonic time of 15 min and an ultrasonic intensity of 0.72 W/mL. The initial median diameter of the sludge particles was 15.24 µm, and this value decreased by 35.89%. The CST was initially 59.6 s and increased by 231%, whereas the SVI was 97.78 mL/g and decreased by 25.89%. Scanning electron microscope (SEM) images indicated that the sludge surface was irregular and loose with a large amount of channels or voids during K2FeO4/US treatment. K2FeO4/US treatment synergistically enhanced the sludge solubilization and reached 668.67 mg/L SCOD, which is 31.81% greater than the additive value obtained with K2FeO4 treatment alone (215.95 mg/L) or with ultrasonic treatment alone (240 mg/L).

An experimental and thermodynamic equilibrium investigation of the Pb, Zn, Cr, Cu, Mn and Ni partitioning during sewage sludge incineration.

The effects of different chlorides and operational conditions on the distribution and speciation of six heavy metals (Pb, Zn, Cr, Cu, Mn and Ni) during sludge incineration were investigated using a simulated laboratory tubular-furnace reactor. A thermodynamic equilibrium investigation using the FactSage software was performed to compare the experimental results. The results indicate that the volatility of the target metals was enhanced as the chlorine concentration increased. Inorganic-Cl influenced the volatilization of heavy metals in the order of Pb>Zn>Cr>Cu>Mn>Ni. However, the effects of organic-Cl on the volatility of Mn, Pb and Cu were greater than the effects on Zn, Cr and Ni. With increasing combustion temperature, the presence of organic-Cl (PVC) and inorganic-Cl (NaCl) improved the transfer of Pb and Zn from bottom ash to fly ash or fuse gas. However, the presence of chloride had no obvious influence on Mn, Cu and Ni. Increased retention time could increase the volatilization rate of heavy metals; however, this effect was insignificant. During the incineration process, Pb readily formed PbSiO4 and remained in the bottom ash. Different Pb compounds, primarily the volatile PbCl2, were found in the gas phase after the addition of NaCl; the dominant Pb compounds in the gas phase after the addition of PVC were PbCl2, Pb(ClO4)2 and PbCl2O4.

Levels, composition profiles and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in sludge from ten textile dyeing plants.

As components of synthetic dyes, polycyclic aromatic hydrocarbons (PAHs) are present as contaminants in textile dyeing sludge due to the recalcitrance in wastewater treatment process, which may pose a threat to environment in the process of sludge disposal. In order to evaluate PAHs in textile dyeing sludge, comprehensive investigation comprising 10 textile dyeing plants was undertaken. Levels, composition profiles and risk assessment of 16 EPA-priority PAHs were analyzed in this study. The total concentrations of 16 PAHs (∑16 PAHs) varied from 1463 ± 177 ng g(-1) to 16,714 ± 1,507 ng g(-1) with a mean value of 6386 ng g(-1). The composition profiles of PAHs were characterized by 3- and 4-ring PAHs, among which phenanthrene, anthracene and fluoranthene were the most dominant components. The mean benzo[a]pyrene equivalent (BaPeq) concentration of ∑16 PAHs in textile dyeing sludge was 423 ng g(-1), which was 2-3 times higher than concentrations reported for urban soil. According to ecological risk assessment, the levels of PAHs in the textile dyeing sludge may cause a significant risk to soil ecosystem after landfill or dumping on soil.

The enrichment and transformation mechanism of Pb and Cu in suspension magnetization roasting and magnetic separation from iron tailings.

Magnetic iron concentrate (MIC) and nonmagnetic tailings (NT) are obtained from magnetization roasting of iron tailings (IT). MIC containing Pb adversely affects blast furnace ironmaking, while Cu in NT poses leaching risks. This study utilizes fast pyrolysis-suspension magnetization roasting to recover iron from IT. The enrichment of Pb, Cu, and the phase transformation mechanism of Cu in the process of suspension magnetization roasting and magnetic separation were clarified. Results show 96.13 % of Cu in IT is in limonite and 47.23 % of Pb is associated with iron. At 750 °C, with 10 % dosage of biomass pyrolysis and 10 min roasting, Pb, Cu and Fe contents in MIC are 0.96, 2.14 and 3.17 times that of NT. Increasing roasting temperature enhances Cu associated with iron enrichment into the MIC, while oxidation of free copper oxide associated with iron forms magnetic copper ferrite. Increased pyrolyzed biomass leads to over-reduction of magnetite associated with Cu to FeO associated with Cu, promoting magnetic copper ferrite decomposition into FeO and free copper oxide. This research holds significant importance in controlling the quality of MIC and the storage risk of IT, and provides theoretical guidance for the regulation and recovery of valuable metals in subsequent processes.