In this study, a novel biochar-supported zero valent iron (BC-nZVI) was synthesized through a green method. A high performance on the simultaneous removal of Cu²⁺ and bisphenol A (BPA) by a combination of BC-nZVI with persulfate (BC-nZVI/PS) system was successfully achieved. The simultaneous efficiencies of Cu²⁺ and BPA could reach 96 and 98% within 60 min, respectively. Both HO• and SO₄•⁻ were two major reactive species in BC-nZVI/PS system, and SO₄•⁻ was primary radical responsible for the degradation of BPA. Four kinds of Cu species, such as Cu(OH)₂, CuO, Cu₂O and Cu⁰ were generated via the adsorption and reduction of the BC-nZVI, whereas six kinds of products of BPA including p-isopropenyl phenol and 4-isopropylphenol were generated via the combined oxidation of SO₄•⁻ and HO•. The possible reaction mechanism for the simultaneous removal of Cu²⁺ and BPA by BC-nZVI/PS system contained a synergistic effect between the reduction of Cu²⁺ and the oxidation of BPA. This is the first report on the feasibility of the remediation of coexistence of heavy metal and organic compound in aquatic environment using the BC-nZVI/PS system.

Bulk Cu compounds such as Cu(OH)₂ are extensively used as pesticides in agriculture. Recent investigations suggest that Cu-based nanomaterials can replace bulk materials reducing the environmental impacts of Cu. In this study, stress responses of alfalfa (Medicago sativa L.) seedlings to Cu(OH)₂ nanoparticle or compounds were evaluated. Seeds were immersed in suspension/solutions of a Cu(OH)₂ nanoform, bulk Cu(OH)₂, CuSO₄, and Cu(NO₃)₂ at 25 and 75 mg/L. Six days later, the germination, seedling growth, and the physiological and biochemical responses of sprouts were evaluated. All Cu treatments significantly reduced root elongation (average = 63%). The ionic compounds at 25 and 75 mg/L caused a reduction in all elements analyzed (Ca, K, Mg, P, Zn, and Mn), excepting for S, Fe and Mo. The bulk-Cu(OH)₂ treatment reduced K (48%) and P (52%) at 75 mg/L, but increased Zn at 25 (18%) and 75 (21%) mg/L. The nano-Cu(OH)₂ reduced K (46%) and P (48%) at 75 mg/L, and also P (37%) at 25 mg/L, compared with control. Confocal microscopy images showed that all Cu compounds, at 75 mg/L, significantly reduced nitric oxide, concurring with the reduction in root growth. Nano Cu(OH)₂ at 25 mg/L upregulated the expression of the Cu/Zn superoxide dismutase gene (1.92-fold), while ionic treatments at 75 mg/L upregulated (∼10-fold) metallothionein (MT) transcripts. Results demonstrated that nano and bulk Cu(OH)₂ compounds caused less physiological impairments in comparison to the ionic ones in alfalfa seedlings.

Alkali-leaching residual wire sludge (AWRS) is an abundant by-product in the harmless disposal process of wire rope sludge. In this study, we modified AWRS through thermal treatment to produce a low-cost and highly efficient adsorbent for the removal of Cu²⁺ and Ni²⁺ from wastewater. The results indicated that AWRS calcinated at 700 °C exhibited maximum Cu²⁺ and Ni²⁺ removal capacities (36.48 mg/g and 46.58 mg/g, respectively). The adsorption process was observed to follow the Elovich kinetic model and the Langmuir–Freundlich isotherm model. The sorption of Cu²⁺ and Ni²⁺ on AWRS700 was highly pH dependent and behaved optimally at the solution pH values of 6 and 5, respectively. Column studies and physicochemical analyses (XRD, SEM-EDS, and XPS) indicated that the sorption of Cu²⁺ and Ni²⁺ on AWRS700 was mainly governed by the chemisorption mechanism, and this was attributed to active metal oxides (Fe₂O₃, CaO, and Al₂O₃) in AWRS700. Specifically, Cu²⁺ is mainly adsorbed on AWRS700 in the form of Cu(OH)₂, CuO₂, and CuFeO₂, and Ni²⁺ is mainly adsorbed in the form of NiAlO₄, Ni₂O₃, and Ni(OH)₂. Given the low-cost and high adsorption efficiency of AWRS700, the developed AWRS700 is a promising adsorbent for Cu²⁺ and Ni²⁺ removal from wastewater.

Corrosion products have been takenfrom 130 copper or bronze outdoor objects all overEurope. Their chemical composition and crystalsymmetry have been determined by means of scanning electron microscopy (SEM/EDS) and X-ray powderdiffraction. Data on location, sampling, objectcharacteristics, general environment and air pollutionlevel; type, colour and chemical composition of thecorrosion layers have been obtained and evaluated by multivariate statistical analysis. The resultsverify that the highest air pollution levels are usually associated with the occurrence of thick,black or dark grey corrosion layers on copper orbronze objects, preferentially containing soot, ironoxide hydroxides, and antlerite,Cu₃(SO₄)(OH)₄. Pale green corrosionusually contains brochantite,Cu₄(SO₄)(OH)₆, and is rather associatedwith less polluted areas. Atacamite, a copper hydroxide chloride with the chemical formula Cu₂Cl(OH)₃, is preferentially observed in coastal regions.In addition, sulphur isotope analyses have beenperformed on eleven corrosion samples from citycenters. The δ³⁴S values are typically inthe region from +4 to +6‰ relative to the sulphurisotope standard CDT (Canyon Diablo Troilite) with amean value of 4.7±1.2 (1σ), therebyindicating that the sulphur in the corrosion layers,in the form of brochantite or antlerite, mainlyoriginates from a similar source despite geographicvariation, most likely sulphur contained in air pollutants.

In order to improve the heavy metal wastewater treatment by avoiding formation of amorphous sludge phase, we develop a faster formation of high crystalline layered double hydroxide (LDH) sludge to remove Cu and Zn from wastewater by controlled double-jet precipitation (CDJP) without hydrothermal or heat aging post-treatment. A series of experimental procedures are conducted to determine the optimal parameters. Results show that the optimal adding rate, pH value, and stirring rate is 0.5 mL min⁻¹, 9.0, and 500 rpm, respectively. The CuZnAl-LDH phase sludge is formed in a well-crystallized hexagonal platelet, which assembled into a flower-like architecture. Comparative studies show that the formation of amorphous LDH sludge in conventional precipitation (CP) could be divided roughly into two stages—from the mixed copper hydroxide, zinc hydroxide, and scarbroite to the mixed low crystallinity CuAl-LDH and ZnAl-LDH. However, in CDJP method, the high crystalline LDH sludge evolved from a new four-step evolution process that is the formation of an amorphous (quasi-)multinary metastable ternary CuZnAl-LDH phase, followed by the indiffusion of cations and substitution of anions to fabricate crystalline LDH, the integrated LDH hexagonal platelets assembled into a flower-like architecture by the screw dislocation growth mechanism, the coarsening growth of each ternary LDH platelet, respectively. Thereinto, the formation of (quasi-)multinary metastable LDH phase instead of metal hydroxide in initial stage would be an obvious advantage of the CDJP method compared to CP method due to the former skipping the sequential precipitation.

Storing and exhibiting cultural heritages are the basic social functions of museum. Since it is impossible to store or display objects without using containers, cases, or holders, the equipment quality is of great importance. Evaluating the suitability of the equipment should not only learn the mechanical behavior but also focus on the materials because some of them (such as woods) may do harm to the objects due to contaminants released. A convenient test by the deposited metal film method has been proposed previously in order to evaluate more potential museum materials in limited time. The conformance between this method and the Oddy test, the classic method for evaluating and selecting museum materials, is mainly studied in this work. The two testing systems were compared from several aspects such as sample appearance, corrosion product, surface morphology, and metallic content by naked eye and modern characterization measures like X-ray diffraction, scanning electron microscopy, and energy-dispersive spectroscopy. The corrosion mechanisms were deduced according to the corrosion products, including Cu → Cu₂O → CuO and Cu → Cu₂O → Cu(OH)₂·H₂O → Cu(HCOO)(OH). The suitability of potential materials for the conservation of metal objects was defined according to the metallic contents of coupons (calculated by atomic ratio) which were classified by the Oddy test. The critical values distinguishing permanently usable from temporarily usable are approximately determined as 70% for copper and 75% for silver, and those distinguishing temporarily usable from unusable are approximately determined as 55% for copper and 60% for silver. The corresponding metal films were classified based on the metallic content standard derived, and then typical appearances of the films assigned to different suitability levels were suggested. Special phenomena, such as the failure in detecting some corrosion products, is attributed to low yield and uneven distribution of ultrafine corrosion products on the films, the covering effect caused by other corrosion products on the copper coupons, and the weakening effect resulted from intensive metal peaks, while some unexpected corrosion conditions on the coupons and the films, are related to the characteristics of general corrosion and pitting corrosion. The results indicate the potential application of the deposited metal film method, giving an optional choice to evaluate and select museum materials with less time. The evaluation methods were preliminarily established from three aspects, such as artificial judgment, metallic content analysis, and corrosion product identification. The artificial judgment is generally applicable, and the other two are useful for verifying the result if possible. More actual cases and further calibration work are essential for further development of the deposited metal film method.