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.

Isomer-specific analysis of nonylphenol and their transformation products in environment: A review.

Nonylphenols (NPs) are crucial fine chemicals widely employed in producing industrial and consumer surfactants that ultimately enter the environment through various pathways, leading to environmental pollution. NPs are suspected endocrine-disrupting chemicals that may accumulate in the body over time, resulting in unusual reproductive function. Due to limitations in analytical methods, NPs have typically been quantified as a whole in some studies. However, NPs are a mixture of multibranched structures, and different NP isomers exhibit distinct environmental behaviors and toxic effects. Therefore, it is critical to analyze environmental and human biological samples at the isomer-specific level to elucidate the contamination characteristics, human exposure load, and toxic effects of NPs. Accurately analyzing NP samples with various isomers, metabolites, and transformation products presents a significant challenge. This review summarizes recent advances in analytical research on NPs in technical products, environmental, and human biological samples, particularly emphasizing the synthesis and separation of standards and the transformation of NP homolog isomers in samples. Finally, the review highlights the research gaps and future research directions in this domain.

Oxidation of simulated wastewater by Fe2+-catalyzed system: The selective reactivity of chlorine radicals and the oxidation pathway of aromatic amines.

Aromatic amines (AAs), a characteristic pollutant with electron-donating groups in textile industry, having high reactivity with reactive chlorine free radicals, is probably the precursor of chlorinated aromatic products in advanced oxidation treatment. In this study, Fe2+/peroxydisulfate (PDS)/Cl- and Fe2+/H2O2/Cl-systems were used to treat four kinds of AAs (5-Nitro-o-toluidine (NT), 4-Aminoazobenzol (AAB), O-Aminoazotoluene (OAAT), 4,4'-Methylene-bis(2-chloroaniline) (MBCA)) in simulated wastewater, and the selectivity of various reactive species to AAs, the oxidation law and pathway of AAs were explored. The results showed that dichloride anion radical (Cl2·-) could effectively oxidize four AAs, and chlorine radical (·Cl) was strongly reactive to AAB and MBCA, especially MBCA. The largest f - (Fukui function) of MBCA is 0.0822, which is the lowest of the four AAs, so ·Cl might be more sensitive to electrophilic point than hydroxyl radical (·OH). The oxidation pathway of NT and MBCA showed that ·Cl mainly played the role of electron transfer to AAs instead of generating chlorinated products, but the addition of ·OH to -NH2 generated aromatic nitro compounds with higher toxicity than NT and MBCA. Therefore, the electron transfer of ·Cl and Cl2·- could not only improve the removal of AAs but also reduce the generation of toxic products. This study found that the reactivity of reactive chlorine free radicals was not necessarily related to chlorination, which provided a theoretical basis for the further studies into the formation mechanism of chlorination products.

Recovery of iron from iron tailings by suspension magnetization roasting with biomass-derived pyrolytic gas.

A major industrial solid waste, iron tailings occupy a large area and pose long-term pollution risks. The pyrolysis gas of biomass was used as reducing agent to suspension magnetize and roast iron tailings to recover iron in this study. The process conditions, phase transformation and microstructure evolution of the iron tailings, pyrolysis gas production, and reaction regulations were investigated to explain the mechanism of iron recovery by suspension magnetization roasting (SMR) under the action of biomass pyrolysis gas. These studies were conducted using X-ray diffraction, scanning electron microscopy, vibrating sample magnetometer, thermo-gravimetric and differential scanning calorimetry, brunauer-emmett-teller specific surface area, and gas chromatography. The results showed that, after the grinding-magnetic separation process, the iron recovery rate was 93.32 %; the iron grade of the iron concentrate was 61.50 %. The optimal process conditions were determined as follows: fast pyrolysis temperature of 600 °C, SMR temperature of 700 °C, biomass dosage of 10 %, and SMR time of 4-5 min. The formation of Fe3O4 from the surface to the interior of the particles during the reduction process, and formation of pores and cracks led to an increase in the specific surface area. The SMR temperature not only improved the heat and mass transfer effect in the reduction process but also generated more CO and H2 through the reverse reaction of methanation, which work together to increase the saturation magnetisation of the unit sample. This method can be used to efficiently recover high quality iron from refractory iron ores.

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.

Redox properties of nano-sized biochar derived from wheat straw biochar.

Nano-sized biochar (NBC) has received increasing attention due to its unique physicochemical characteristics and environmental behaviour, but an understanding of its redox properties is limited. Herein, the redox properties of NBC derived from wheat straw were investigated at two pyrolysis temperatures (400 and 700 °C). These NBC materials were prepared from bulk-biochar by grinding, ultrasonication and separation treatments. The resulting NBC had average particle sizes of 78.8 ± 1.9 and 122.0 ± 2.1 nm after 400 and 700 °C treatments, respectively. The physicochemical measurements demonstrated that both the NBC prepared at 400 °C (NBC-400) and the NBC prepared at 700 °C (NBC-700) were enriched in carboxyl and phenolic oxygen-content groups. Electrochemical analyses showed that both NBC-400 and NBC-700 were redox active and had an electron transfer capacity (ETC) of 196.57 µmol-1 gC -1 and 363.47 µmol-1 gC -1, respectively. On the basis of its redox activity of NBC, the NBC was capable of mediating the reduction of iron and manganese minerals as well as the degradation of methyl orange (MO) by sulfide. The NBC-700 could stimulate these reactions better than the NBC-400 due to its higher redox activity. Meanwhile, the NBC was more active in stimulating these reactions than bulk-biochar. Our results highlight the importance of size in evaluating the redox reactivity of biochar and related environmental processes and improve our understanding of the redox properties of biochar.

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.

Chlorophenols in textile dyeing sludge: Pollution characteristics and environmental risk control.

Chlorophenols (CPs) are toxic contaminants that tend to accumulate in textile dyeing sludge and pose a threat to the environment through the disposal process. To comprehensively evaluate CPs in sludge, the characteristics and risks of CPs from five textile dyeing plants (TDPs) were investigated in this study. The total concentration of 19 CPs (Σ19 CPs) varied from 170.90 to 6290.30 ng g-1 dry weight (dw), among which high-chlorine phenols accounted for the greatest proportion. The ecological screening level (ESL) of CPs was used to judge their pollution levels, while the risk quotient (RQ) value and dioxin conversion rate were used to analyze their potential risk. The results indicated that CPs may pose a moderate to high risk to the environment. The Fenton process was used to condition the hazardous sludge, and a higher content of CPs was found after conditioning. A lower rate of CP increase was achieved with a reagent dose of 180 mmol/L, H2O2:Fe2+ = 1:1, pH of 3-4 and reaction time of 30 min. In summary, the work helps to address the general knowledge gap in the textile dyeing industry and provides a reference for further research.

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.

Comparison of the Fe2+/H2O2 and Fe2+/PMS systems in simulated sludge: Removal of PAHs, migration of elements and formation of chlorination by-products.

In this study, polycyclic aromatic hydrocarbons (PAHs) at practical concentrations in the simulated sludge treated by the Fe2+/H2O2 and Fe2+/peroxymonosulfate (PMS) systems were evaluated in terms of the PAHs (phenanthrene, anthracene, fluoranthene) removal, element migration, Cl- effect, and chlorination by-product formation. The results indicated that according to the removal rate of PAHs, the optimal dosage of the Fe2+/PMS system (∑PAHs removal rate was 64.66 ±â€¯2.82 %) was 1/30 of that for the Fe2+/H2O2 system (∑PAHs removal rate was 78.63 ±â€¯0.38 %). The elemental contents in the simulated sludge were mainly affected by the extent of advanced oxidation and the amount of generated iron flocs. By studying the PAHs removal, free chlorine formation, total organochlorine content, and PAHs products in Fe2+/H2O2/Cl- and Fe2+/PMS/Cl- systems, it was found that chlorine radicals (·Cl) had high reactivity with phenanthrene and fluoranthene, whereas dichloride anion radicals (Cl2·-) exhibited the opposite behavior. Furthermore, PAHs were oxidized by ·Cl and hydroxyl radical in the Fe2+/H2O2/Cl- system, whereas PAHs and their products were chlorinated by free chlorine and ·Cl in the Fe2+/PMS/Cl- system to six chlorinated by-products such as Cl-PAHs (9-Cl-phenanthrene, 2-Cl-anthracene, 9,10-Cl2-anthracene, 3-Cl-fluoranthene). These results provide some useful suggestions for the safe advanced oxidation process treatment of textile dyeing sludge.

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.

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.

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).

Consequence of replacing nitrogen with carbon dioxide as atmosphere on suppressing the formation of polycyclic aromatic hydrocarbons in catalytic pyrolysis of sawdust.

This study evaluates the effect of replacement of N2 with CO2 as atmosphere in catalytic pyrolysis of waste lignocellulosics with acidic and metal-modified zeolites, respectively, on the 16 EPA priority pollutant polycyclic aromatic hydrocarbons (PAHs) in bio-oils. By coupling solid phase extraction pretreatment with single ion monitoring detection, it is found that the replacement alleviates PAHs in bio-oil concerning synchronously abating the 16 PAHs with low, medium and high molecular weights, and the benzo[a]pyrene equivalent toxicity of bio-oil decreases. Meanwhile, CO2 decreases the content of small oxygenates, e.g. furans, ketones, acids, and increases phenolics and aromatics affording more stable and valuable bio-oils. Moreover, CO2 enhances carbon conversion efficiency, especially in combination with Fe-modified zeolite, which presents a synergistic effect. This study indicates the practical application of CO2 as an atmosphere in catalytic pyrolysis to improve the bio-oil quality by suppressing PAHs formation and adjusting compound constituent.

Peptide-induced super-assembly of biocatalytic metal-organic frameworks for programmed enzyme cascades.

Despite the promise of metal-organic frameworks (MOFs) as functional matrices for enzyme stabilization, the development of a stimulus-responsive approach to induce a multi-enzyme cascade reaction in MOFs remains a critical challenge. Here, a novel method using peptide-induced super-assembly of MOFs is developed for programmed enzyme cascade reactions on demand. The super-assembled MOF particles containing different enzymes show remarkable 7.3-fold and 4.4-fold catalytic activity enhancements for the two-enzyme and three-enzyme cascade reactions, respectively, as compared with the unassembled MOF nanoparticles. Further digestion of the coiled-coil forming peptides on the MOF surfaces leads to the MOF superstructure disassembly and the programmed enzyme cascade reaction being "switched-off". Research on these stimuli-responsive materials with controllable and predictable biocatalytic functions/properties provide a concept to facilitate the fabrication of next-generation smart materials based on precision chemistry.

Effect of sintering temperature on mineral composition and heavy metals mobility in tailings bricks.

In this study, the mixing mechanism and phase transition process of different metals during the sintering of tailings bricks with four different metal oxides (CuO, PbO, ZnO, and CdO) at temperatures ranging from 700 to 1100 °C for 2 h were investigated. The properties of the sintered product was characterized and analyzed, and the results showed that the main crystalline phases are quartz, cristobalite, hematite, and mullite while the metal oxides are ascribed to copper ferrite spinel (CuFe2O4), gahnite (ZnAl2O4), zinc ferrite spinel (ZnFe2O4), lead feldspar (PbAl2Si2O8), and cadmium feldspar (CdAl2Si2O8). Further analysis indicates that the heavy metals were transited into spinel or silicate structures with favorable efficiency. This indicates a good heavy-metal fixation effect from the structural change after the sintering process. Finally, the leaching experiments of the sintered samples suggest that the metal leaching decreased to a low and stable value when the sintering temperature was higher than 950 °C, which meets the China standard (GB 5085.3-2007). The above results indicate that the sintering process facilitates the combination of Cu, Zn, Pb and Cd offering an effective and safe method for the application of materials that contain tailings.

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.