Effective and selective recovery of Au(III) from WPCBs using quaternary phosphonium adsorbent synthesized by adjusting steric hindrance.

With the gradual depletion of natural gold ore, waste printed circuit boards (WPCBs) have become one of the most attractive alternatives to gold ore. Here, a series of quaternary phosphonium adsorbents with a large size were successfully synthesized by adjusting the number of functional groups and carbon chain length of functional monomers, which can be used for selective recovery of gold(III) from WPCBs leaching solution. The quaternary phosphonium adsorbent (PS-TEP) prepared by the nucleophilic substitution reaction between triethyl phosphine with the smallest volume and chloromethylated polystyrene (PS-Cl) exhibited the best gold loading capacity (617.90 mg g-1). The adsorption mechanism of gold(III) on PS-TEP surface mainly involves anion exchange between AuCl4- and Cl- in the adsorbent. The charge level of the H atom closest to -CH2-P+ group directly determines the strength of the interaction between the adsorbent and the gold ion. Multiwfn and VMD programs visually confirm the weak interaction between PS-TEP+ and AuCl4-. After 5 adsorption-stripping cycles, the adsorption rate of gold(III) in solution remained at about 99 %. In addition, PS-TEP exhibited good gold(III) selectivity in both simulated and actual WPCBs gold leaching solutions. These results indicate that the large-particle PS-TEP with high capacity is suitable for selective gold recovery from WPCBs leaching solution.

Effectively adsorb Au(S2O3)23- using aminoguanidine as trapping group from thiosulfate solutions.

Thiosulfate gold leaching is one of the most promising green cyanide-free gold extraction processes; however, the difficulty of recovering Au(I) from the leaching system hinders its further development. This study prepared aminoguanidine-functionalized microspheres (AGMs) via a one-step reaction involving nucleophilic substitution between aminoguanidine hydrochloride and chloromethylated polystyrene microspheres and used AGMs to adsorb Au(I) from thiosulfate solutions. Scanning electron microscopy, Brunauer-Emmett-Teller analysis, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy were used to analyze the structure and properties of AGMs. Experiments were designed to investigate the effects of pH, temperature, initial Au(I), and thiosulfate concentrations on the gold adsorption performance of AGMs. Results demonstrated that AGMs can efficiently adsorb Au(I) from thiosulfate solutions in a wide pH range. The adsorption process conforms to the pseudo-second-order kinetic model and Langmuir isotherm model, with a maximum capacity of 22.03 kg/t. Acidic thiourea is an effective desorbent, and after four adsorption-desorption cycles, the adsorption rate of Au(I) by AGMs is 78.63%, which shows AGMs have good cyclic application potential. Based on the results of characterization, experiments, and density functional theory calculations, the mechanism for the adsorption of [Au(S2O3)2]3- on AGMs involves anion exchange. Importantly, AGMs exhibited satisfactory adsorption property for Au(I) in practical Cu2+-NH3(en)-S2O32- systems. This study provided experimental reference for the recovery of Au(I) from thiosulfate solution.

Highly Efficient Recovery of Au(I) from Gold Leaching Solution Using Sodium Dimethyldithiocarbamate.

As a sustainable, nontoxic and environmentally friendly cyanide-free gold leaching agent, thiosulfate has been applied to some extent in the field of hydrometallurgy. However, the difficult recovery of gold ions in gold leaching solutions limits further application of thiosulfate gold leaching technology. This study demonstrated the feasibility of gold recovery by sodium dimethyldithiocarbamate (SDD) precipitation and recycling of ammonia and a lixiviant in solution. SDD achieved the purpose of recovering gold by forming granular precipitates with gold ions in solution. It can almost completely recover gold ions in 2.5-17.34 mg/L of gold leaching solution within 1 min at 25 °C, in which a gold recovery capacity of 7.99 kg/t is achieved. The leaching rate of gold ore did not change significantly after recycling the residual ammonia and thiosulfate in the leaching solution after gold recovery by SDD, and its leaching rate basically remained at 81%. The mechanism of SDD recovering Au was determined to involve the ligand exchange of SDD- and Au[(S2O3)2]3-. Moreover, the interaction mechanism between SDD and Au(I) was further validated by density functional theory calculations. Considering its low cost, simple technology, and environmental friendliness, the SDD precipitation process has the potential for large-scale application in gold recovery from thiosulfate gold leaching solutions.

Synthesis of azole-functionalized microspheres and their adsorption properties for gold(I) thiosulfate complex.

Gold is an essential precious metal with exceptional properties. Thus, azole-functionalized microspheres (PS-3-AT) were prepared by grafting 3-amino-1,2,4-triazole (3-AT) into chloromethyl polystyrene beans (PS-Cl) and used as a novel adsorbent for the gold(I)-thiosulfate complex. The effects of initial gold concentration, thiosulfate concentration, temperature, and pH on the Au(S2O3)23- adsorption process over PS-3-AT were investigated. In this study, PS-3-AT was considered an effective adsorbent for Au(I) recovery from a thiosulfate solution, demonstrating that PS-3-AT completely adsorbed Au(S2O3)23- with an adsorption capacity of 39.8 kg t-1 achieved during multistage adsorption testing. Through adsorption kinetics and isotherm studies, the pseudo-second-order and Freundlich models well describe the adsorption process of PS-3-AT for Au(I), also suggesting the exothermic nature. Furthermore, SEM, FT-IR spectroscopy, BET, and XPS techniques were used to characterize the surface and structural properties of the samples. Notably, a reliable adsorption mechanism was developed that proposed the formation of the -NH+Cl- group during the grafting process and Cl- exchange with Au(S2O3)23- to achieve Au(I) capture. Moreover, quantum chemistry calculations and the independent gradient model (IGM) were adopted to visualize the interaction between PS-3-AT and Au(S2O3)23- at an atomic level. The desorption ratio was 97.9% while 2 M NaCl was used as the desorbent, and regeneration with PS-3-AT was achieved after five cycles. Therefore, the facile synthetic method and adsorption properties of PS-3-AT for the gold(I)-thiosulfate complex are satisfactory, which is valuable for the development of thiosulfate gold leaching technologies.

Interactions Between Phenolic Acids and Microorganisms in Rhizospheric Soil From Continuous Cropping of Panax notoginseng.

Large-scale intensive cultivation has made continuous cropping soil sickness more serious for Panax notoginseng in Yunnan. Autotoxic substances can promote the occurrence of continuous cropping soil sickness. Phenolic acids exert a strong autotoxic effect on P. notoginseng. Based on UPLC-MS/MS, the levels of six phenolic acids with the strongest autotoxicity of P. notoginseng rhizospheric soil were tested. Based on Illumina MiSeq high-throughput sequencing technology, the variation in the microbial diversity in the rhizospheric soil was used as an index to explore the interactions between phenolic acids and the soil microorganisms of the P. notoginseng rhizosphere. (1) Continuous P. notoginseng cropping significantly changed the microbial community structure. Continuous cropping increased bacterial Chao1 index and Shannon index and decreased fungal Shannon index. After P. notoginseng disease, bacterial Shannon index reduced and fungal Chao1 index decreased. (2) Phenolic acid significantly changed the bacterial community structure. VA significantly reduced the bacterial Shannon index. Exogenous p-HA, FA, SA, and VA significantly increased the fungal Chao1 index and p-HA showed the most significant effect. Para-HA affected bacterial specificity, and VA affected fungal specificity. (3) VA was positively correlated with most fungi and bacteria. Para-HA was positively correlated with Lelliottia and Flavobacterium. Para-HA was also positively correlated with plant pathogens (Fusarium and Ilyonectria). Para-HA and VA were able to promote the growth of primary pathogenic bacteria. Thus, p-HA and VA are the main phenolic acid-autotoxin substances in P. notoginseng under continuous cropping. (4) A correlation analysis of soil environmental factors associated with fungal and bacterial communities showed that AK, TN, OM, and HN were most strongly correlated with soil microorganisms. (5) The microorganisms in the rhizosphere of 3-year-old soil planted with P. notoginseng exhibited obvious effects on the degradation of the four phenolic acids. The effect of soil microorganisms on phenolic acids was first-order kinetic degradation with a high degradation rate and a half-life of less than 4.5 h. The results showed that phenolic acids could promote the growth of pathogenic bacteria. And the interaction between rhizospheric soil microorganisms and phenolic acids was the main cause of the disturbance of P. notoginseng rhizosphere microflora.

Synthesis and evaluation of ion-imprinted composite membranes of Cr(vi) based on ß-diketone functional monomers.

Using Cr(vi) as the imprinted ions and 2-allyl-1,3-diphenyl-1,3-propanedione (ADPD) (a compound synthesized by independent design) as the functional monomer, a series of chromium ion-imprinted composite membranes (Cr(vi)-IICMs) and corresponding non-imprinted composite membranes (NICMs) were synthesized and tested. The results showed that the Cr(vi)-IICM10 membrane prepared under optimal experimental conditions exhibited a high adsorption capacity towards Cr(vi) (Q = 30.35 mg g-1) and a high imprinting factor (α = 2.70). The structural characteristics of Cr(vi)-IICM10 and NICM10 were investigated using FE-SEM, ATR-FTIR, and BET techniques combined with UV-Vis photometry and inductively coupled plasma emission spectrometry (ICP-OES) to evaluate the adsorption performance and permeation selectivity, while the effect on adsorption permeance of varying the experimental conditions including the solvent type, pH, and temperature was also investigated. The results showed that Cr(vi)-IICM10 is a mesoporous material with excellent permeation selectivity, reusability, and favorable pH response, and that its adsorption behavior is in accordance with the Langmuir model and pseudo-first-order kinetics. Thus, Cr(vi)-IICM10 shows great potential towards utilization as a "smart membrane" to control the separation and removal of Cr(vi) in wastewater, and also proved a reasonable design of the new functional monomer ADPD.

Interface Modulation of MoS2 /Metal Oxide Heterostructures for Efficient Hydrogen Evolution Electrocatalysis.

Developing efficient earth-abundant MoS2 based hydrogen evolution reaction (HER) electrocatalysts is important but challenging due to the sluggish kinetics in alkaline media. Herein, a strategy to fabricate a high-performance MoS2 based HER electrocatalyst by modulating interface electronic structure via metal oxides is developed. All the heterostructure catalysts present significant improvement of HER electrocatalytic activities, demonstrating a positive role of metal oxides decoration in promoting the rate-limited water dissociation step for the HER mechanism in alkaline media. The as-obtained MoS2 /Ni2 O3 H catalyst exhibits a low overpotential of 84 mV at 10 mA cm-2 and small charge-transfer resistance of 1.5 Ω in 1 m KOH solution. The current density (217 mA cm-2 ) at the overpotential of 200 mV is about 2 and 24 times higher than that of commercial Pt/C and bare MoS2 , respectively. Additionally, these MoS2 /metal oxides heterostructure catalysts show outstanding long-term stability under a harsh chronopotentiometry test. Theoretical calculations reveal the varied sensitivity of 3d-band in different transition oxides, in which Ni-3d of Ni2 O3 H is evidently activated to achieve fast electron transfer for HER as the electron-depletion center. Both electronic properties and energetic reaction trends confirm the high electroactivity of MoS2 /Ni2 O3 H in the adsorption and dissociation of H2 O for highly efficient HER in alkaline media.

Sensitive assay of Escherichia coli in food samples by microchip capillary electrophoresis based on specific aptamer binding strategy.

The rapid and cost-effective detection of bacteria is of great importance to ensuring food safety, preventing food poisoning. Herein, we developed a sensitive detection of Escherichia coli (E. coli) using bacteria-specific aptamer in conjunction with microchip capillary electrophoresis-coupled laser-induced fluorescence (MCE-LIF). Based on the differences between charge to mass ratios of free aptamer and bacteria-aptamer complex, which influence their electrophoretic mobilities, the separation of free aptamers and complex peaks by MCE could be achieved. Under optimal conditions, the sensitive detection of E. coli was achieved with a detection limit of 3.7 × 102 CFU mL-1, at a fast response of 135 s and a short detection length of 2.3 cm. The spiked recovery experiment showed that E. coli could be recovered from spiked drinking water and milk samples with recovery rates of 94.7% and 92.8%, respectively. This work demonstrates that the established detection strategy can be a useful tool for the detection and/or monitoring of E. coli in food and environment.