Influence of Different Types of Surfactants on the Flotation of Natural Quartz by Dodecylamine.

The synergistic effect among flotation agents is why combined flotation agents exhibit superior performance compared to single flotation agents. This research investigates the influence of three surfactants with different charges of polar groups, sodium dodecyl sulfate (SDS), cetyltrimethylammonium bromide (CTAB), and octanol, combined with dodecylamine (DDA), on quartz flotation. Through the implementation of flotation tests, bubble-particle adhesion induction time testing, gas-liquid two-phase foam properties testing, and surface tension testing, it is revealed that substituting part of the DDA with these surfactants can either enhance or at least maintain the quartz recovery, affect the adhesion induction time, reduce the surface tension of the flotation system, and change the foaming performance and foam stability, depending on their mole ratio in the combined collector. Compared to DDA alone, combining CTAB or OCT with DDA can significantly increase quartz recovery, while SDS with DDA only yields an approximate recovery. Combining SDS or OCT with DDA can reduce the foam stability, while CTAB with DDA enhances the foam stability. The effect of the combination of surfactants and DDA on the adhesion induction time of quartz grains of different sizes with bubbles is the same; furthermore, there is a negative correlation between the adhesion induction time and the recovery, while the foaming properties and stability of foam are positively correlated with the recovery.

UV irradiation induced simultaneous reduction of Cu(II) and degradation of EDTA in Cu(II)-EDTA in wastewater containing Cu(II)-EDTA.

Decomplexation of Cu(II)-EDTA followed by chemical precipitation of free Cu(II) ions can effectively degrade EDTA in Cu(II)-EDTA and remove Cu(II), but requires large precipitant dosage and inevitably produces a large amount of copper-containing sludge that is difficult to deal with. Herein, we demonstrated that simultaneous reduction of Cu(II) and degradation of EDTA in Cu(II)-EDTA can be achieved by UV irradiation of wastewater containing Cu(II)-EDTA without adding reagent. 93.65% of Cu(II) was reduced to Cu(0) with a high purity of 99.93 wt%, which can be recycled, thus avoiding the generation of copper-containing sludge. 96.67% of EDTA in Cu(II)-EDTA was degraded, and the final products were HCHO, NH4+, NO3- and low-molecular acids. In depth, the dominant degradation mechanism of EDTA in Cu(II)-EDTA was photo-induced successive decarboxylation through homolysis of C-O and C-C bond of -CH2-COOH group, followed by ligand to metal charge transfer (LMCT) and hydrolysis reactions. The minor degradation mechanism of EDTA in Cu(II)-EDTA was successive decarboxylation by •OH radicals. Simultaneously, Cu(II) was reduced to Cu(0) by H• and eaq- produced by UV irradiation of Cu(II)-EDTA. This study provided an approach of simultaneous removal of heavy metals and degradation of EDTA in Cu(II)-EDTA in wastewater containing heavy metal-EDTA complex.

Rolling circle transcription: A new system to produce RNA microspheres for improving RNAi efficiency in an agriculturally important lepidopteran pest (Mythimna separate).

We applied a new RNA interference (RNAi) system using rolling circle transcription (RCT) technology to generate RNA microspheres (RMS) for targeting two key chitin synthetic pathway genes [chitin synthase A (CHSA), chitin synthase B (CHSB)] in the larvae of the oriental armyworm (Mythimna separate), a RNAi-unsusceptible agriculturally important lepidopteran pest. Feeding the third-instar larvae with the RMS-CHSA- or RMS-CHSB-treated corn leaf discs suppressed the expression of CHSA by 81.7% or CHSB by 88.1%, respectively, at 72 h. The silencing of CHSA consequently affected the larval development, including the reduced body weight (54.0%) and length (41.3%), as evaluated on the 7th day, and caused significant larval mortalities (51.1%) as evaluated on the 14th day. Similar results were obtained with the larvae fed RMS-CHSB. We also compared RNAi efficiencies among different strategies: 1) two multi-target RMS [i.e., RMS-(CHSA + CHSB), RMS-CHSA + RMS-CHSB], and 2) multi-target RMS and single-target RMS (i.e., either RMS-CHSA or RMS-CHSB) and found no significant differences in RNAi efficiency. By using Cy3-labeled RMS, we confirmed that RMS can be rapidly internalized into Sf9 cells (<6 h). The rapid cellular uptake of RMS accompanied with significant RNAi efficiency through larval feeding suggests that the RCT-based RNAi system can be readily applied to study the gene functions and further developed as bio-pesticides for insect pest management. Additionally, our new RNAi system takes the advantage of the microRNA (miRNA)-mediated RNAi pathway using miRNA duplexes generated in vivo from the RMS by the target insect. The system can be used for RNAi in a wide range of insect species, including lepidopteran insects which often exhibit extremely low RNAi efficiency using other RNAi approaches.

DRAGen - A deep learning supported RVE generator framework for complex microstructure models.

In this study an improved version of the Discrete RVE Automation and Generation Framework, also called DRAGen, is presented. The Framework incorporates a generator for Representative Volume Elements (RVEs). Several complex microstructure features, extracted from real microstructures, have been added to the generator, to enable it to generate RVEs with realistic microstructures. DRAGen is now capable of reading trained neural networks as well as .csv-files as input data for the microstructure generation. Furthermore, features such as pores and inclusions, martensite bands, hierarchical substructures, and crystallographic textures can be reconstructed in the RVEs. Besides the features, the functionality for different solvers was introduced. Therefore, the code was extended by modules for the generation of Finite Element (FE) and spectral solver input files. DRAGen now has the ability to create models for three powerful multiphysics frameworks used in the community: DAMASK, Abaqus and MOOSE. The evaluation of the features, as well as the simulations performed on sample models, show that the new version of DRAGen is a very powerful tool with flexible applicability for scientists in the ICME community. Also, due to the modular architecture of the project, the code can easily be expanded with features of interest. Therefore, it delivers a variety of functions and possible outputs, which offers researchers a broad spectrum of microstructures that can be used in microstructure studies or microstructure design developments.

Mechanistic insights into Sb(III) and Fe(II) co-oxidation by oxygen and hydrogen peroxide: Dominant reactive oxygen species and roles of organic ligands.

Sole O2 or H2O2 oxidant hardly oxidize Sb(III) on a time scale of hours to days, but Sb(III) oxidation can simultaneously occur in Fe(II) oxidation by O2 and H2O2 due to the generation of reactive oxygen species (ROS). However, Sb(III) and Fe(II) co-oxidation mechanisms regarding the dominant ROS and effects of organic ligands require further elucidation. Herein, the co-oxidation of Sb(III) and Fe(II) by O2 and H2O2 was studied in detail. The results indicated that increasing the pH significantly increased Sb(III) and Fe(II) oxidation rates during Fe(II) oxygenation, while the highest Sb(III) oxidation rate and oxidation efficiency was obtained at pH 3 with H2O2 as the oxidant. HCO3- and H2PO4-anions exerted different effects on Sb(III) oxidation in Fe(II) oxidation processes by O2 and H2O2. In addition, Fe(II) complexed with organic ligands could improve Sb(III) oxidation rates by 1 to 4 orders of magnitude mainly due to more ROS production. Moreover, quenching experiments combined with the PMSO probe demonstrated that .OH was the main ROS at acidic pH, whereas Fe(IV) played a key role in Sb(III) oxidation at near-neutral pH. In particular, the steady-state concentration of Fe(IV) ([Fe(IV)]ss) and kFe(IV)/Sb(III) were determined to be 1.66×10-9 M and 2.57×105 M-1 s-1, respectively. Overall, these findings help to better understand the geochemical cycling and fate of Sb in Fe(II)- and DOM-rich subsurface environments undergoing redox fluctuations and are conductive to developing Fenton reactions for the in-situ remediation of Sb(III)-contaminated environments.

Effective reduction and recovery of As(III) and As(V) from alkaline wastewater by thiourea dioxide: Efficiency and mechanism.

For alkaline wastewater with high arsenic concentration, the traditional lime precipitation inevitably produces large amounts of hazardous waste. Herein, a heat-activated reduction method employing thiourea dioxide (TDO) as the reductant was proposed to efficiently remove and recover As(III)/As(V) from alkaline wastewater in the form of valuable As(0). More than 99.9% of As(III)/As(V) (2-400 mM) were reduced to As(0) with a high purity of more than 99.5 wt% by TDO within 30 min. The highly reductive eaq- and SO2- radical generated during TDO decomposition contribute to the arsenic reduction, and the contribution ratios of eaq- and SO2- radical were estimated to be approximately 57.6% and 42.4% for As(III) removal and 62.2% and 37.8% for As(V) removal, respectively. The arsenic reduction was greatly improved by increasing pH and temperature, which could accelerate the cleavage of C-S bond in TDO for the eaq- and SO2- formation. The presence of dissolved oxygen, which can not only scavenge eaq-/SO2- but also directly oxidize SO22-, had a negative effect on the arsenic removal. The presence of CO32- slightly suppressed the arsenic removal due to the eaq- scavenging effect while SiO32-, PO43-, Cl-, SO42- and NH4+ had negligible effects. The proposed method was a potential technology for the efficient removal and reduction of arsenic in alkaline wastewater.

Linking chromatin acylation mark-defined proteome and genome in living cells.

A generalizable strategy with programmable site specificity for in situ profiling of histone modifications on unperturbed chromatin remains highly desirable but challenging. We herein developed a single-site-resolved multi-omics (SiTomics) strategy for systematic mapping of dynamic modifications and subsequent profiling of chromatinized proteome and genome defined by specific chromatin acylations in living cells. By leveraging the genetic code expansion strategy, our SiTomics toolkit revealed distinct crotonylation (e.g., H3K56cr) and ß-hydroxybutyrylation (e.g., H3K56bhb) upon short chain fatty acids stimulation and established linkages for chromatin acylation mark-defined proteome, genome, and functions. This led to the identification of GLYR1 as a distinct interacting protein in modulating H3K56cr's gene body localization as well as the discovery of an elevated super-enhancer repertoire underlying bhb-mediated chromatin modulations. SiTomics offers a platform technology for elucidating the "metabolites-modification-regulation" axis, which is widely applicable for multi-omics profiling and functional dissection of modifications beyond acylations and proteins beyond histones.

Selective recovery of Cu(II) from strongly acidic wastewater by zinc dimethyldithiocarbamate: Affecting factors, efficiency and mechanism.

The selective recovery of copper from strongly acidic wastewater containing mixed metal ions remains a significant challenge. In this study, a novel reagent zinc dimethyldithiocarbamate (Zn(DMDC)2) was developed for the selective removal of Cu(II). The removal efficiency of Cu(II) reached 99.6% after 120 min reaction at 30°C when the mole ratio Zn(DMDC)2/Cu(II) was 1:1. The mechanism investigation indicates that the Cu(DMDC)2 products formed as a result of the displacement of Zn(II) from the added Zn(DMDC)2 by Cu(II) in wastewater, due to the formation of stronger coordination bonds between Cu(II) and the dithiocarbamate groups of Zn(DMDC)2. Subsequently, we put forward an innovative process of resource recovery for strongly acidic wastewater. Firstly, the selective removal of Cu(II) from actual wastewater using Zn(DMDC)2, with a removal efficiency of 99.7%. Secondly, high-value CuO was recovered by calcining the Cu(DMDC)2 at 800°C, with a copper recovery efficiency of 98.3%. Moreover, the residual As(III) and Cd(II) were removed by introducing H2S gas, and the purified acidic wastewater was used to dissolve ZnO for preparation of valuable ZnSO4·H2O. The total economic benefit of resource recovery is estimated to be 11.54 $/m3. Accordingly, this study provides a new route for the resource recovery of the treatment of copper-containing acidic wastewater.

Multiple Concurrent Causal Relationships and Multiple Governance Pathways for Non-Pharmaceutical Intervention Policies in Pandemics: A Fuzzy Set Qualitative Comparative Analysis Based on 102 Countries and Regions.

The global outbreak of COVID-19 has been wreaking havoc on all aspects of human societies. In addition to pharmaceutical interventions, non-pharmaceutical intervention policies have been proven to be crucial in slowing down the spread of the virus and reducing the impact of the outbreak on economic development, daily life, and social stability. However, no studies have focused on which non-pharmaceutical intervention policies are more effective; this is the focus of our study. We used data samples from 102 countries and regions around the world and selected seven categories of related policies, including work and school suspensions, assembly restrictions, movement restrictions, home isolation, international population movement restrictions, income subsidies, and testing and screening as the condition variables. A susceptible-exposed-infected-quarantined-recovered (SEIQR) model considering non-pharmaceutical intervention policies and latency with infectiousness was constructed to calculate the epidemic transmission rate as the outcome variable, and a fuzzy set qualitative comparative analysis (fsQCA) method was applied to explore the multiple concurrent causal relationships and multiple governance paths of non-pharmaceutical intervention policies for epidemics from the configuration perspective. We found a total of four non-pharmaceutical intervention policy pathways. Among them, L1 was highly suppressive, L2 was moderately suppressive, and L3 was externally suppressive. The results also showed that individual non-pharmaceutical intervention policy could not effectively suppress the spread of the pandemic. Moreover, three specific non-pharmaceutical intervention policies, including work stoppage and school closure, testing and screening, and economic subsidies, had a universal effect in the policies grouping for effective control of the pandemic transmission.

Records of trace metals since the Holocene in sediments of Laizhou Bay, Bohai Sea, China.

Trace metal (Cu, Pb, Zn, Cr, Cd, As, Hg, Ni, Li, and Co) concentration profiles along a sediment core were investigated to obtain background values, assess depositional trends and contamination levels in the Laizhou Bay, China. The enrichment factors of the metals indicated no anthropogenic enrichment, except for Pb, Cd, and Hg, which have been influenced by human activities since 7 ka. The mean concentrations of trace metals in the 10-7 ka phase can be considered as the background values in the study area. Principal component analysis indicated that the metals were mainly naturally sourced throughout the observed depositional period. Their geoaccumulation indices indicated that the sediments were not contaminated by Cu, Zn, Cr, Ni, and Co, but were contaminated by Pb, Cd, and Hg during the 7-0 ka period.

Reductive removal of As(V) and As(III) from aqueous solution by the UV/sulfite process: Recovery of elemental arsenic.

The removal of arsenic (As(V) and As(III)) from contaminated water has attracted great attention. However, the generation of arsenic-containing hazardous waste by traditional methods has become an inevitable environmental problem. Herein, a UV/sulfite advanced reduction method was proposed to remove As(V) and As(III) from aqueous solution in the form of valuable elemental arsenic (As(0)), thus avoiding the generation of arsenic-containing hazardous waste. The results showed that greater than 99.9% of As(V) and As(III) were reduced to the high purity As(0) (> 99.5 wt%) with the residual arsenic concentration below 10 µg L-1. The hydrated electrons (eaq-), H• and SO3•- radicals are generated by the UV/sulfite process, of which eaq- and H• serve as reductants of As(V) and As(III) while the SO3•- radicals inhibit arsenic reduction by oxidizing arsenic. The effective quantum efficiency (Φ) for the formation of As(0) in the As(V) and As(III) removal process is approximately 0.0078 and 0.0055 mol/Einstein, respectively. The reduction of arsenic is favorable under alkaline conditions (pH > 9.0) due to the higher photolysis efficiency of SO32- than HSO3- (pKa = 7.2) and higher stability of eaq-/H• under alkaline conditions. The presence of dissolved oxygen (O2), NO2-, NO3-, CO32-, PO43- and humic acid (HA) inhibited arsenic reduction through light blocking or eaq-/H• scavenging effects while Cl-, SO42-, Ca2+ and Mg2+ had negligible effects on arsenic reduction. The proposed method can effectively remove and recover arsenic from contaminated water at a low cost, demonstrating feasibility for practical application. This study provides a novel technology for the reductive removal and recovery of arsenic from contaminated water.

Quantitative Chemoproteomic Profiling of Protein Cross-Links Induced by Methylglyoxal.

Methylglyoxal (MGO) is a highly reactive metabolite mainly formed as a byproduct of glycolysis. Elevated MGO has been considered as a risk factor for several diseases including diabetes and neurodegeneration. While MGO modifications on proteins were globally profiled, the cross-links between proteins induced by MGO in proteomes are unexplored to date. Here, we reported a quantitative chemoproteomic platform based on mass shifts that enables identification of events of protein cross-links induced by MGO in proteomes. A total of 66 cross-linked targets were identified from the profiling experiments when cells were treated with MGO, among which the components of functional complexes such as spliceosomes and ribosomes were enriched. We found that inosine-5'-monophosphate dehydrogenase 2 (IMPDH2) was homocross-linked by MGO and the active-site Cys331 was critical for mediating the cross-link, which in turn affected IMPDH2's activity. Our study has provided new clues for the functional impact in proteomes by MGO, and the methodology can be, in principle, applied to profile protein cross-links induced by other reactive metabolites.

H2S release rate strongly affects particle size and settling performance of metal sulfides in acidic wastewater: The role of homogeneous and heterogeneous nucleation.

Sulfide precipitation is an extensively used method to precipitate metal and arsenic from acidic wastewater, whereas the tiny and negatively-charged metal sulfides with poor settling performance are generated. The factors and mechanisms that influence particle size and settling performance remain unclear. Herein, the effects of sulfuration factors, e.g., reagent dosage, acidity and H2S release rate on the particle size and settling performance of metal sulfides were investigated, and involved mechanisms were systematically revealed. The results showed that the reagent dosage and acidity had a limited effect on particle size and settling performance while the H2S release rate played a critical role. Under homogeneous conditions, the decrease in H2S release rate, which can reduce the initial supersaturation and supply the sustainable supersaturation, increased the particle size of metal sulfides generated using Na2S solution. Under heterogeneous conditions, the decrease in H2S release rate further increased the particle size of metal sulfides generated using low-solubility CaS/FeS and further improved settling performance, in which heterogeneous nucleation played a crucial role besides supersaturation. The developed dissolution-diffusion-growth model qualitatively explained the negative relationship between H2S release rate and particle growth. This work provides implications for improving the settling performance of metal sulfides in acidic wastewater.

Reductive Removal and Recovery of As(V) and As(III) from Strongly Acidic Wastewater by a UV/Formic Acid Process.

The removal of arsenic (As(V) and As(III)) from strongly acidic wastewater using traditional neutralization or sulfuration precipitation methods produces a large amount of arsenic-containing hazardous wastes, which poses a potential threat to the environment. In this study, an ultraviolet/formic acid (UV/HCOOH) process was proposed to reductively remove and recover arsenic from strongly acidic wastewater in the form of valuable elemental arsenic (As(0)) products to avoid the generation of hazardous wastes. We found that more than 99% of As(V) and As(III) in wastewater was reduced to highly pure solid As(0) (>99.5 wt %) by HCOOH under UV irradiation. As(V) can be efficiently reduced to As(IV) (H2AsO3 or H4AsO4) by hydrogen radicals (H•) generated from the photolysis of HCOOH through dehydroxylation or hydrogenation. Then, As(IV) is reduced to As(III) by H• or through its disproportionation. The reduction of As(V) to H4AsO4 by H• and the disproportionation of H4AsO4 are the main reaction processes. Subsequently, As(III) is reduced to As(0) not only by H• through stepwise dehydroxylation but also through the disproportionation of intermediate arsenic species As(II) and As(I). With additional density functional theory calculations, this study provides a theoretical foundation for the reductive removal of arsenic from acidic wastewater.

Clean and effective removal of Cl(-I) from strongly acidic wastewater by PbO2.

Recycling strongly acidic wastewater as diluted H2SO4 after contaminants contained being removed was previously proposed, however, Cl(-I), a kind of contaminant contained in strongly acidic wastewater, is difficult to remove, which severely degrades the quality of recycled H2SO4. In this study, the removal of Cl(-I) using PbO2 was investigated and the involved mechanisms were explored. The removal efficiency of Cl(-I) reached 93.38% at 50℃ when PbO2/Cl(-I) mole ratio reached 2:1. The identification of reaction products shows that Cl(-I) was oxidized to Cl2, and PbO2 was reduced to PbSO4. Cl2 was absorbed by NaOH to form NaClO, which was used for the regeneration of PbO2 from the generated PbSO4. Cl(-I) was removed through two pathways, i.e., surface oxidation and •OH radical oxidation. •OH generated by the reaction of PbO2 and OH- plays an important role in Cl(-I) removal. The regenerated PbO2 had excellent performance to remove Cl(-I) after six-time regeneration. This study provided an in-depth understanding on the effective removal of Cl(-I) by the oxidation method.

Covalently Engineered Protein Minibinders with Enhanced Neutralization Efficacy against Escaping SARS-CoV-2 Variants.

The rapid emergence and spread of escaping mutations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has significantly challenged our efforts in fighting against the COVID-19 pandemic. A broadly neutralizing reagent against these concerning variants is thus highly desirable for the prophylactic and therapeutic treatments of SARS-CoV-2 infection. We herein report a covalent engineering strategy on protein minibinders for potent neutralization of the escaping variants such as B.1.617.2 (Delta), B.1.617.1 (Kappa), and B.1.1.529 (Omicron) through in situ cross-linking with the spike receptor binding domain (RBD). The resulting covalent minibinder (GlueBinder) exhibited enhanced blockage of RBD-human angiotensin-converting enzyme 2 (huACE2) interaction and more potent neutralization effect against the Delta variant than its noncovalent counterpart as demonstrated on authentic virus. By leveraging the covalent chemistry against escaping mutations, our strategy may be generally applicable for restoring and enhancing the potency of neutralizing antibodies to SARS-CoV-2 and other rapidly evolving viral targets.

A review on the removal of Cl(-I) with high concentration from industrial wastewater: Approaches and mechanisms.

Large quantities of wastewaters containing high concentrations of Cl(-I) can be generated in several industries when chloride-containing materials and additive agents are employed. Because Cl(-I) is unavailable to microorganisms, physicochemical methods are generally used for the removal of Cl(-I); however, as the most stable form of chlorine under aqueous conditions, Cl(-I) in wastewaters is difficult to remove to achieve low residual concentrations through common physicochemical methods. This paper provides new insights into traditional precipitation, oxidation, ion exchange and physical separation methods, as well as newly developed approaches, for Cl(-I) removal from various industrial wastewaters through analysis of the mechanisms, applicable conditions, optimum parameters, and method advantages and disadvantages. Moreover, the developmental trends and potential improvements to these approaches are also presented. Currently, precipitation is the most common and efficient Cl(-I) removal method, for which ultraviolet (UV) light is regarded as an effective means of improvement. Additionally, advanced oxidation processes (AOPs), where Cl(-I) can be oxidized to generate Cl radicals, Cl2- radicals, Cl2 gas, etc., show great promise for Cl(-I) removal. This review provides a theoretical foundation for the effective treatment and for the secondary utilization of industrial wastewaters containing Cl(-I).

Subcellular and regional localization of mRNA translation in midbrain dopamine neurons.

Midbrain dopaminergic (mDA) neurons exhibit extensive dendritic and axonal arborizations, but local protein synthesis is not characterized in these neurons. Here, we investigate messenger RNA (mRNA) localization and translation in mDA neuronal axons and dendrites, both of which release dopamine (DA). Using highly sensitive ribosome-bound RNA sequencing and imaging approaches, we find no evidence for mRNA translation in mDA axons. In contrast, mDA neuronal dendrites in the substantia nigra pars reticulata (SNr) contain ribosomes and mRNAs encoding the major components of DA synthesis, release, and reuptake machinery. Surprisingly, we also observe dendritic localization of mRNAs encoding synaptic vesicle-related proteins, including those involved in exocytic fusion. Our results are consistent with a role for local translation in the regulation of DA release from dendrites, but not from axons. Our translatome data define a molecular signature of sparse mDA neurons in the SNr, including the enrichment of Atp2a3/SERCA3, an atypical ER calcium pump.

Improving removal rate and efficiency of As(V) by sulfide from strongly acidic wastewater in a modified photochemical reactor.

Employing ultraviolet light to enhance the removal of As(V) by sulfide (S(-II)) from strongly acidic wastewater is a potential method. However, we found the arsenic trisulfide (As2S3) and elemental sulfur (S8) particles formed in this method not only vastly hinder light transmission in the wastewater but also undergo light-induced redissolution, leading to a decrease in removal rate and efficiency of As(V). Herein, As(V) removal by sulfide from strongly acidic wastewater was performed in a modified photochemical reactor to weaken the effect of the formed particles on As(V) removal. It was found that in this study, the formed particles could be efficiently removed from the photoreactor by three operations, i.e. circulation-filtration, septum setting, and lamp sleeve cleaning. The removal of As(V) was approximately 11-fold faster than that without three operations, saving 90.9% of the reaction time and 89.4% of energy consumption. The removal efficiency of As(V) also increased through weakening the light-induced redissolution of the formed particles. This study facilitates the practical application of the UV light promoted As(V) removal technology and also provides a new method to lessen the light-blocking effect in the particle-forming photochemical reaction systems.

Calcium sulfide-organosilicon complex for sustained release of H2S in strongly acidic wastewater: Synthesis, mechanism and efficiency.

Sulfide precipitation is an efficient method to remove Cu(II) and As(III) from strongly acidic wastewater, but the instantaneous release of H2S from traditional sulfuration reagents causes serious H2S pollution. Moreover, the obtained precipitates are mixtures of CuS and As2S3, leading to difficulties in resource recovery. In this study, a calcium sulfide-organosilicon complex (CaS-OSCS), in which CaS was coated into a matrix of {[O1.5Si(CH2)3NH]CS}n (OSCS) via the coordination bonding, was developed. OSCS, as a matrix of CaS-OSCS, can ensure the sustained and stable release of H2S under strongly acidic conditions owing to its low swelling (1.75% swelling ratio) and excellent acid resistance. The release longevity of H2S from CaS-OSCS extended from 5 min up to 50 min compared with that from CaS because the hydrophobic OSCS prevented solution diffusing to the pores of CaS-OSCS and thus slowed down the hydrolysis of CaS in pores. 99% of Cu(II)/As(III) was precipitated without H2S escape, and the dosage of sulfuration reagents was reduced by 30%. In addition, CaS-OSCS improved the selective separation of copper from wastewater, and a separation factor between Cu(II) and As(III) reached 2376. This study provides a potential approach for the elimination of H2S pollution and selective recovery of copper.