铝工业链中铝灰渣的危险废物特性与管理建议

为了明确铝灰渣的环境危害特征,于2019年4月和9月分别对广西典型铝冶炼、加工、再生企业进行了调查。利用铝灰渣与水反应的氨气释放率测定分光光度法等方法,对不同环节产生铝灰渣的浸出毒性、反应性、腐蚀性、易燃性进行评价分析。结果表明,铝灰渣浸出液中主要危害因子是氟化物,而非金属元素。氟化物质量浓度为2~1370 mg/L,原铝冶炼环节所产生的铝灰渣质量浓度最高。铝合金加工原辅料和末端处理方式会改变氟化物浸出质量浓度。铝灰渣反应性的氨气释放率为3.3~6.0 mg/kg,释放率和环境风险属于较低水平。铝灰渣在纯水中浸出液pH值为8.65~11.98,不具备腐蚀性;在1200℃条件下无法点燃,不具备易燃性。氟化物浸出和氨气释放是铝灰渣最需防范的环境危害,可作为其分类管理和无害化处置的依据。     

Effects of Al3+ on pollutant removal and extracellular polymeric substances (EPS) under anaerobic,anoxic and oxic conditions

The highest removal efficiencies of COD and TN were achieved under 10 mg/L of Al³⁺. The highest TP removal efficiency occurred under 30 mg/L of Al³⁺. EPS, PS and PN concentrations increased with the addition of Al³⁺. Sludge properties significantly changed with the addition of Al³⁺. Aluminum ions produced by aluminum mining, electrolytic industry and aluminum-based coagulants can enter wastewater treatment plants and interact with activated sludge. They can subsequently contribute to the removal of suspended solids and affect activated sludge flocculation, as well as nitrogen and phosphorus removal. In this study, the effects of Al³⁺ on pollutant removal, sludge flocculation and the composition and structure of extracellular polymeric substances (EPS) were investigated under anaerobic, anoxic and oxic conditions. Results demonstrated that the highest chemical oxygen demand (COD) and total nitrogen (TN) removal efficiencies were detected for an Al³⁺ concentration of 10 mg/L. In addition, the maximal dehydrogenase activity and sludge flocculation were also observed at this level of Al³⁺. The highest removal efficiency of total phosphorus (TP) was achieved at an Al³⁺ concentration of 30 mg/L. The flocculability of sludge in the anoxic zone was consistently higher than that in the anaerobic and oxic zones. The addition of Al³⁺ promoted the secretion of EPS. Tryptophan-like fluorescence peaks were detected in each EPS layer in the absence of Al³⁺. At the Al³⁺ concentration of 10 mg/L, fulvic acid and tryptophan fluorescence peaks began to appear, while the majority of protein species and the highest microbial activity were also detected. Low Al³⁺ concentrations (<10 mg/L) could promote the removal efficiencies of COD and TN, yet excessive Al³⁺ levels (>10 mg/L) weakened microbial activity. Higher Al³⁺ concentrations (>30 mg/L) also inhibited the release of phosphorus in the anaerobic zone by reacting with PO₄^3-.     

植物铝胁迫发生机制及其内在缓解途径研究进展

本文总结了土壤中铝的存在形式及其化学行为,分析了以针叶人工林为例的诱发植物铝胁迫效应的内外部机制,以及铝胁迫在不同生态水平上对植物生长的影响。比较了环境铝胁迫下,植物体自身缓解环境铝威胁的不同途径。     

Phosphorus transformation under the influence of aluminum,organic carbon,and dissolved oxygen at the water-sediment interface: A simulative study

• The three simulation factors caused various changes in both water and sediment. • Responses to simulations differed with the reported natural lakes and wetlands. • Al has dominant effects on sediment P release control among the three factors. • Adding sediment Al can be effective and safe under the simulated conditions. • Polyphosphates were not generated, while added phytate was rather stable. The effects of sediment aluminum (Al), organic carbon (OC), and dissolved oxygen (DO) on phosphorus (P) transformation, at the water-sediment interface of a eutrophic constructed lake, were investigated via a series of simulative experiments. The above three factors had various influences on dissolved P concentration, water pH, water and surface sediment appearance, and P fractions. Additions of Al had the greatest effect on suppressing P release, and the water pH remained alkaline in the water-sediment system under various OC and DO conditions. No dissolution of the added Al was detected. ³¹P-NMR characterization suggested that OC addition did not promote biological P uptake to polyphosphates under oxic conditions. The simulation result on the added phytate indicated the absence of phytate in the original lake sediment. As compared to the reported natural lakes and wetland, the water-sediment system of the constructed lake responded differently to some simulative conditions. Since Al, OC, and DO can be controlled with engineering methods, the results of this study provide insights for the practical site restorations.     

铝箔复合膜集气袋对有机废气的适用性研究

通过在不同的时间段,测定存放于铝箔复合膜集气袋和玻璃注射器的丙酮,醋酸乙酯,苯,异丙醇标准气的浓度,气体浓度与贮存时间的关系,本次试验结果表明,丙酮,醋酸乙酯,苯,异丙醇在铝箔气袋中的稳定性明显优于在玻璃注射器中,应尽可能在８－２４ｈ内测定。     

Oxidative stress is an early symptom triggered by aluminum in Al-sensitive potato plantlets

The objective of this study was to evaluate whether the oxidative stress caused by aluminum (Al) toxicity is an early symptom that can trigger root growth inhibition in Macaca (Al-sensitive) and SMIC148-A (Al-tolerant) potato clones. Plantlets were grown in a nutrient solution (pH 4.00) with 0, 100 and 200 mg Al L⁻¹. At 24, 72, 120 and 168 h after Al addition, root length and biochemical parameters were determined. Regardless of exposure time, root length of the Macaca clone was significantly lower at 200 mg Al L⁻¹. For the SMIC148-A clone, root length did not decrease with any Al treatments. Al supply caused lipid peroxidation only in Macaca, in both roots (at 24, 72, 120 and 168 h) and shoot (at 120 and 168 h). In roots of the Macaca, catalase (CAT) and ascorbate peroxidase (APX) activity decreased at 72 and 120 h, and at 24, 72 and 120 h, respectively. At 168 h, both activities increased upon addition of Al. In roots of the SMIC148-A, CAT activity increased at 72 and 168 h, whereas APX activity decreased at 72 h and increased at 24, 12 and 168 h. The Macaca showed lower root non-protein thiol group (NPSH) concentration at 200 mg Al L⁻¹ in all evaluations, but the SMIC148-A either did not demonstrate any alterations at 24 and 72 h or presented higher levels at 120 h. This pattern was also observed in root ascorbic acid (AsA) concentration at 24 and 120 h. The cellular redox status of these potato clones seems to be affected by Al. Therefore, oxidative stress may be an important mechanism for Al toxicity, mainly in the Al-sensitive Macaca clone.     

Enhancement of phosphorus sorption onto light expanded clay aggregates by means of aluminum and iron oxide coatings

Phosphorus (P) loading from non-point or point sources increases the eutrophication risk of natural waters. The functioning of constructed wetlands (CWs) used as natural water treatment systems can be improved by means of additional materials adsorbing soluble P. In this study, light expanded clay aggregates (LECA) and LECA coated with aluminum (Al) oxide (Al-LECA) or iron (Fe) oxide (Fe-LECA) were tested for their efficiency as P sorbents in the pH range 3–8. The oxide coatings duplicated the actual sorption capacity calculated from the sorption isotherms at the P concentration in the equilibrium solution of 20 μg L⁻¹, assumed to be the allowable P level in purified water. In the oxide-coated LECAs the sorption was fast and followed both the first- and second-order Lagergren kinetic models, suggesting that the formation of a binuclear surface complex was feasible. In LECA, sorption was markedly slower and followed the first-order kinetic model, indicating that retention occurred through a monodentate attachment. These findings were in harmony with the degree of P saturation (DPS) of the sorbent surfaces at the highest P addition level (200 μg L⁻¹), DPS being decisively higher for LECA than for the oxide-coated sorbents. Accordingly, at higher pH values the competition by hydroxyl ions diminished the sorption in LECA relatively more than that in the coated sorbents. In agreement with the acidity of Al³⁺ being 100 times lower than that of Fe³⁺, at elevated pH the sorption by Al-LECA proved to be less reversible than that by Fe-LECA. The results provide evidence that in CWs Al-coated sorbents are superior to Fe-coated ones that are also redox-sensitive and may lose their sorption properties in anoxic conditions.     

Uptake of aluminum by lipid vesicles

Aluminium uptake and tight binding were studied in multilayered phospholipid liposomes, as a model for cellular uptake of aluminum ions. Most of these studies were conducted with an initial aluminum concentration of 10 μM, while aluminum superficially bound to liposomes was removed by citrate chelation. Maximum uptake and tight binding of aluminium were pH‐dependent. In dimyristoyl phosphatidylcholine (DMPC) liposomes, this maximum occurred in the neutral pH region, while it was shifted towards more acidic pH values in DMPC liposomes containing 20% of acidic phosphatidylserine. The initial rate of aluminum uptake was apparently dependent on the physical state of the liposome membrane. Prior formation of an aluminum‐citrate chelate prevented aluminum uptake and tight binding to DMPC liposomes.     

Regimes and critical conditions of detonation propagation in expanding channels in gas suspensions of ultrafine aluminum particles

Under study are the regimes of detonation propagation in channels with linear expansion filled with monodisperse mixtures of oxygen and ultrafine aluminum particles of various loading; the methods of numerical simulations are used. The detonation combustion of submicron aluminum particles is described within the semi-empirical model of reduced kinetics with due regard to the transition from the diffusion-limited regime of combustion to the kinetic one. Waves of both planar and developed cellular detonation are considered as initial conditions. The characteristics of the main flow regimes are obtained and described: the subcritical (detonation failure), critical (detonation failure in some part of the channel) and supercritical (continuous detonation propagation). The maps of flow regimes in suspensions of 200-nm – 400-nm particles are presented in the plane of parameters: the channel width, expansion angle. The obtained critical conditions are similar to those observed in the gas detonation. The critical channel width linearly depends on the expansion angle up to a first critical value (35°–38°). Behind the second critical value (50°), the channel width is independent on the expansion angle. Between these values, there is an interval of nonmonotonicity similar to the detonation of micro-sized suspensions of aluminum particles. The effect of particle loading on the critical conditions in poor mixtures appears in the form of a sharp increase in the critical channel width, if the mass concentration falls below 0.25.     

Twin-roll casting of aluminum–steel clad strips

The results of experiments on twin-roll casting of aluminum–steel clad strips are presented. For the first time this energy-saving production technology for a clad material of this metals combination was implemented. Besides the experimental equipment and processing details, the results of metallographic, electron microprobe and transmission electron microscopy analysis of the aluminum–steel interface are shown. The pack rolling and deep-drawing tests of the twin-roll cast clad strips were performed to check their applicability for a further processing using plastic deformation. In addition adhesive strength of the bond was tested. The performed analysis have shown the formation of a continuous, thin and uniform layer of intermetallic phases on the materials interface of approx. 3 μm thickness having an adhesive strength over 70 MPa.