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Exploring highly selective and stable electrocatalysts is of great significance for the electrochemical conversion of CO 2 into fuel. Herein, a three-dimensional (3D) nanostructure catalyst was developed by doping Pb single-atom (Pb SA ) in-situ on carbon paper (Pb SA100 -Cu/CP) through a low-energy and economical method. The designed catalyst exhibited abundant active sites and was beneficial to CO 2 adsorption, activation, and subsequent conversion to fuel. Interestingly, Pb SA100 -Cu/CP showed a prominent Faraday efficiency (FE) of 97 % at -0.9 V versus reversible hydrogen electrode (vs. RHE) and a high partial current density of 27.9 mA·cm -2 for formate. Also, the catalyst remained significantly stable for 60 h during the durability test. The reaction mechanism was investigated by density functional theory (DFT), demonstrating that the doping Pb SA induced the electrons redistribution, promoted the formate generation, reduced the rate-determining step (RDS) energy barrier, and inhibited the hydrogen evolution reaction. The study aims to provide a new strategy for developing of single-atom catalysts with high selectivity and stability, which will help reduce environmental pressure and alleviate energy problems., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

In this paper, the strength development of a pure steel slag (SS) system with various concentrations of N,N,N',N'-Tetrakis-(2-hydroxyethyl) ethylenediamine (THEED) was investigated. The hydration kinetics, pore structure and microstructure of SS pastes with and without THEED were characterized to underscore the working mechanism of THEED. Results show that THEED additions significantly increase the 3, 7 and 28 days compressive strength of hardened SS pastes. The enhancement effect increases with the dosage of THEED. At a concentration of 2000 ppm, THEED increased the compressive strength by 733%, 665%, and 545% at 3, 7 and 28 days, respectively. It is confirmed that THEED additions improve the hydration degree of SS by accelerating hydration of the aluminum phase (C 3 A, PDF-38-1429; C 12 A 7 , PDF-48-1882) and C 2 F,( PDF 38-0408) to generate Mc (PDF-41-0219) and Pa (PDF-30-0222) in the presence of CaCO 3 . Also, the hydration degree of silicates is increased by THEED. In this way, THEED additions refine the pore structure of hardened SS paste by increasing the pore volume with a diameter below 300 nm to achieve enhancement. The chelating effect of THEED results in promoting dissolution of SS, which provides the driving force for accelerating SS hydration.

Collaborative disposal of sludge has been applied extensively in cement industry kilns, but the influence of organic components in sludge on the selective non-catalytic reduction (SNCR) denitrification is still in highly demanding. This paper focuses the influence of ethanol, n-octane, benzene, and acetone on the SNCR denitrification, and the influence of ethanol are analyzed on SNCR denitrification under different flue gas condition. The result showed that the presence of organic components reduces the reaction temperature of SNCR. When the temperature of SNCR reaction is at 750 ~ 800 ℃, the denitrification rate of four organic components is ethanol > benzene > n-octane > acetone. The optimum denitrification rate on SNCR can reach as high as 90.377% when the reaction condition is the NH 3 /NO is 1; the ethanol concentration is 1000 ppm; O 2 concentration is 2%; and temperature is 750 ℃. The presence of carbon dioxide inhibits the denitrification reaction. With the increase of temperature, the influence of SO 2 on the denitrification reaction first increases and then decreases. In this paper, the influence of organic components in sludge on SNCR denitrification will be analyzed, which provides a theoretical basis for the selection of sludge dosing method for cement kiln collaborative disposal., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

NOx emission from the cement industry have received much attention. In order to reduce the NOx emission in cement kilns, nickel slag was used to prepare the non-ammonia denitrification material, and a denitrification mechanism was proposed in this study. The results showed that the denitrification material prepared at pH 7 exhibited the best denitrification performance. At low temperature, the highest denitrification performance was achieved between 200 and 300 °C with a NO decomposition rate of approximately 40%. Then, the NO decomposition rate increased as the temperature increased, reaching over 95% above 700 °C. The physicochemical characteristics showed that the material had the highest specific surface area and the highest relative Fe content, which benefited the denitrification performance. The divalent iron of the denitrification material was considered the active site for the reaction, and trivalent iron was not conducive to denitrification performance at a low temperature range. After the denitrification reaction, the Fe 3+ /Fe 2+ increased from 0.89 to 1.31. The proposed denitrification mechanism was the redox process between divalent iron and trivalent iron. This study not only recycles industrial waste to reduce solid waste pollution but also efficiently removes nitrogen oxides from cement kilns without ammonia.

In this study, two types of liquid alkali-free accelerators were prepared by aluminum sulfate (AF 1 ) and aluminum mud wastes (AF 2 ), and the life cycle assessment (LCA) in the preparation of AF 1 and AF 2 was compared. The LCA was considered from cradle to gate including raw materials used, transportation, and accelerator preparation based on the method ReCiPe2016. The results indicated that AF 1 had a higher environmental impact in all midpoint impact categories and endpoint indicators than that of AF 2 , and AF 2 reduced 43.59% emission of CO 2 , 59.09% emission of SO 2 , 71% consumption of mineral resources, and 46.67% consumption of fossil resources than that of AF 1 respectively. As an environment-friendly accelerator, AF 2 had a better application performance than traditional accelerator AF 1. When the dosage of accelerators was 7%, the initial setting times of cement pastes containing AF 1 and AF 2 were 4 min 57 s and 4 min 04 s respectively, the final setting times of cement pastes containing AF 1 and AF 2 were 11 min 49 s and 9 min 53 s respectively, and the compressive strengths at 1 d of mortars containing AF 1 and AF 2 were 7.35 MPa and 8.33 MPa respectively. This study aims to provide technical feasibility and environmental impact assessment for exploring new avenues of preparing environment-friendly liquid alkali-free accelerators with aluminum mud solid wastes. It has great potential in reducing carbon and pollution emissions and has a greater competitive advantage due to great application performance., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

The combined utilization of mineral accelerators and nano-seeding materials is a novel method to promote the early strength of cement-based materials. In this paper, the effects of nano-C-S-H seed (NCS) on the early compressive strength of the Portland cement (PC)- calcium sulfoaluminate cement (CSA) binder were investigated. The results showed that NCS and CSA synergistically contributed to the early strength of PC. In detail, a 326.3% increase in the 10 h compressive strength of PC paste was obtained through the addition of NCS (2 wt%) and CSA (5%) in common. This was higher than the sum of the increases observed with the single additions of CSA (157.9%) or NCS (87.6%), with the same above dosage, in PC. Meanwhile, the early strength enhancement effects of NCS and CSA, when used together in PC, lasted longer than the effects of either used alone. Moreover, the synergetic effect mechanism was analyzed by isothermal calorimeter, QXRD, TGA, MIP, and SEM techniques. The calorimetry, XRD, and TGA results demonstrated that the synergistic mechanism was associated with the synergistic promotion effects of CSA and NCS on the hydrates. The fast hydration of CSA produced large amounts of ettringite and also consumed partial free water to promote the performance of the seeding effect of NCS which, simultaneously, further accelerated the precipitation of C-S-H gel and CH. The high alkie environment was also beneficial for the continuous generation of ettringite. In addition, the results of MIP and SEM measurements showed that the micro-filling effect of NCS significantly optimized the pore structure of a PC-CSA blend-hardened paste. Thus, the synergistic strength enhancement effects of CSA and NCS on PC were attributed to the matching of the promotion of hydration generation and the optimization of pore structures in hardening cement paste. The results of this article provide a new approach to achieving the rapid development of the early strength of cementitious materials, with potential applications in precast concrete and low-temperature construction.

Contamination of leafy vegetables grown in heavy metal(loid)-polluted mining areas pose serious health risks. This study aimed to explore the heavy metal(loid) contamination of leafy vegetables near two mining areas, by collecting samples from 14 different leafy vegetable species in Yunnan Province, China. The lead (Pb), cadmium (Cd), arsenic (As), and copper (Cu) contents of the samples were determined, and risks to human health were calculated using the hazard quotient and hazard index (HI). Moreover, Malabar spinach was identified as a leafy vegetable that exhibits low accumulation of heavy metal(loid)s. The accumulation capacity of different Malabar spinach varieties was verified, and a Cd soil safety threshold was determined using a pot experiment. Overall, Pb and Cd were the main soil and vegetable contaminants found in both study sites. The HI values for all leafy vegetables, apart from Malabar spinach, were greater than 1, indicating the presence of risks to human health; moreover, the health risks were greater for children than adults. The Malabar spinach pot experiment results showed that only some Cd forms exceeded China's maximum permissible standards. Furthermore, Malabar spinach varieties A (instant Malabar spinach), C (extra-large leaf green vine Malabar spinach), and F (large leaf Malabar spinach) displayed the lowest Cd accumulation. We calculated Cd total and bioavailable soil safety thresholds of 4.75 and 0.77 mg kg -1 , respectively. However, further research is required to validate soil heavy metal safety thresholds for different vegetables. Ultimately, the heavy metal(loid) contamination of leafy vegetables described here was more serious than anticipated. Finally, the results of this study can inform residents living near these mining areas of a low-risk leafy vegetable, which will reduce the harm caused by heavy metal(loid) contamination in the area., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

A field survey and pot experiment were carried out to screen tolerant plants growing in cadmium (Cd)-polluted mining areas which were co-polluted with acid in soil, and the related physiological and biochemical mechanisms were also analyzed. Thirty-seven species of wild plants and their corresponding soil were collected from a farmland around the mining areas. Ageratum (Ageratum conyzoides L.) with strong Cd-accumulative ability was selected, and its tolerance experiment for acid and Cd with different levels were carried out separately or orthogonally, respectively. Furthermore, the activities of superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT), and the contents of malondialdehyde (MDA), photosynthetic pigments, soluble sugar and proline in its leaves were determined. The results showed that the Cd accumulation in ageratum and sticktight (Bidens pilosa L.) was relatively high, but the latter has been well documented, so we focused on ageratum in the present work. In pot experiment, ageratum grew normally at 100 mg kg -1 Cd in soil, and the Cd concentrations in its roots, stems and leaves were 75.37 ± 7.37, 31.01 ± 3.76 and 53.92 ± 10.05 mg kg -1 , respectively. In the case of acid tolerance experiment, all plant individuals of ageratum grew normally when soil pH was over 3.5. In the orthogonal experiment, the Cd accumulation in this plant increased with the decrease of soil pH under the same Cd treatment. Under strong acid conditions, the activity of SOD in leaves of ageratum was increased significantly. When the Cd concentration was 10 mg kg -1 and the soil pH was 5.5 or 3.5, the activities of POD and CAT were significantly increased. In addition, based on stepwise regression analysis, the leaf Cd concentration was significantly positive correlated with the activities of SOD and POD in leaves of ageratum. Therefore, ageratum not only had a strong tolerance for Cd and acid pollution in soil, but also had a strong ability to accumulate Cd. As a common plant in the mining area, it has a great potential for the phytoremediation of Cd and acid co-contaminated soil., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Concrete cracking has a negative impact on the durability of the structure. Pre-implanting microcapsules containing healing agents into the concrete are expected to induce the cracks to self-heal. However, the self-healing effect can potentially be influenced by several environmental conditions, thus limiting its applications. To address these challenges, we developed a new type of water-absorbing microcapsules, using calcium alginate hydrogel as the wall material and an adhesive epoxy polymer as the core material, to improve the self-healing adaptability in complex and changing environments. We explored the healing properties and mechanism of cementitious materials containing microcapsules under various environmental conditions. The experimental results showed that the water-absorbent microcapsules exhibit multiple self-healing effects under different external conditions: (1) in an anhydrous environment, fissures prompted the activation of microcapsules, and the epoxy polymer flowed out to seal the cracks. (2) When exposed to water, the microcapsules inflated to form a seal around the fissures. (3) The microcapsules facilitated the autogenous healing of cracks in the cementitious material when wet and dry conditions were alternated. The three self-healing mechanisms worked synergistically and contributed to the effective restoration of the impermeability and strength of concrete under different environments. Particularly, the recovery of compressive strength and impermeability exceeded 100% when the microcapsule content was 4% and the pre-pressure was 40% of f max .

Flame retardant modification of leaf fibers was carried out to solve the technical problem of poor fire resistance of plant fibers and improve the utilization rate of urban fallen leaves in building materials. The modification scheme adopts three flame retardants, i.e., ammonium polyphosphate (APP), magnesium hydroxide (MH), and aluminum hydroxide (ATH), and two covering layers, i.e., pure acrylic polymer lotion and water glass (Na 2 O · nSiO 2 ) solution. The modified leaf fiber's combustion behavior and pyrolysis properties were tested and analyzed. The physical and mechanical characteristics, as well as the thermal insulation qualities, of leaf fiber cement-based composites (LFCC) were studied at high temperatures. The findings revealed that the three flame retardants had an effect on the chemical structure of leaf fibers. In comparison to leaf fibers without flame-retardant modification, flame-retardant-modified leaf fibers have a much greater thermal stability. and its LOI is greater than 27.0%, which is a fire-retardant material. Except for the sample with water glass as the modified cover layer, at high temperatures, the composite flame-retardant fiber LFCC's mass-loss rate is lower compared with fibers without flame-retardant modification or fibers modified with only one kind of flame-retardant. In the composite flame-retardant modified fiber LFCC, the samples with better strength at high temperature are those with ATH replacing 30% and 50% MH. The thermal conductivity of LFCC is negatively correlated with the range of temperature change., Competing Interests: The authors declare no conflict of interest., (© 2022 The Author(s).)

Reducing or eliminating cracks caused by shrinkage of cementitious materials remains a daunting challenge for construction engineers. Drying shrinkage and autogenous shrinkage are the main shrinkage types in the service process of cement-based materials, which have a great impact on engineering applications. If cracks in concrete generate by drying or autogenous shrinkage, the mechanical properties, water resistance and durability of concrete will be also affected. It is an effective method to use chemical admixtures to inhibit the shrinkage of cement-based materials. Polycarboxylate plasticizer (PCE) is an important chemical admixture in cement-based materials and is widely used in practical engineering. It can bring great value by reducing the shrinkage effect through molecular design. Through our innovative design, a series of shrinkage-reducing polycarboxylate superplasticizers (SRPs) were synthesized, their molecular structures were confirmed by Fourier transform infrared spectroscopy (FTIR) and their molecular properties were determined by gel permeation chromatography (GPC). Furthermore, the shrinkage performances at different ages of the mortars containing the synthesized SRPs with different structures were systematically evaluated. The results showed that compared with the blank sample, the dry shrinkage rate and free shrinkage rate of the mortars containing SRP decreased by over 20% and 15%, respectively. Additionally, the shrinkage rates of the mortars containing SRP were significantly lower than that of the mortar containing conventional PCE, and moreover, the water-reducing performance was improved compared to conventional PCE. Based on the experimental results of surface tension and evaporation rate of different SRP solutions, the mechanism of the shrinkage-reducing effect was probed, as expected to provide guidance for the design and development of new shrinkage-reducing admixtures.

Background: Triple-negative breast cancer (TNBC) is a common hypotype of breast cancer. Circular RNAs (circRNAs) are burgeoning serve as vital controllers in numerous tumors. Nevertheless, the expression and regulatory mode of circRNAs in TNBC are still indistinct. This paper aimed to reveal the function and molecular mechanism of circular RNA dehydrodolichyl diphosphate synthase (circDHDDS) in TNBC., Methods: The contents of circDHDDS, DHDDS mRNA, microRNA-362-3p (miR-362-3p) and DEAD (Asp-Glu-Ala-Asp) box polypeptide 5 (DDX5) were indicated by quantitative real-time polymerase chain reaction (qRT-PCR) and western blot. The colony formation assay and 5-ethynyl-2'-deoxyuridine (EdU) assay were executed to assess cell proliferation. The flow cytometry assay was utilized to detect cell apoptosis. The transwell assay and tube formation assay were applied to measure cell migration, invasion and angiogenesis. The targeted relationships of miR-362-3p and circDHDDS or DDX5 were forecasted and detected by dual-luciferase reporter assay. The in vivo test was implemented to confirm the effect of circDHDDS., Results: The contents of circDHDDS and DDX5 were increased, and miR-362-3p level was decreased in TNBC. CircDHDDS deficiency reserved cell proliferation, migration, invasion and angiogenesis, while facilitated cell apoptosis in TNBC cells. Furthermore, miR-362-3p was validated to exert a tumor repressive effect in TNBC cells by suppressing DDX5. Moreover, DDX5 could regulate the development of TNBC. The experimental data exposed that levels of miR-362-3p presented noteworthy negative correlation with circDHDDS and DDX5, while circDHDDS and DDX5 exhibited significant positive correlation. In mechanism, circDHDDS bound to miR-362-3p to modulate DDX5 expression. In addition, circDHDDS knock-down also attenuated tumor growth., Conclusion: CircDHDDS expedited TNBC by swelling DDX5 via adapting miR-362-3p., (© 2022 Wiley Periodicals LLC.)

As a kind of volatile organic compound (VOC), methyl tert-butyl ether (MTBE) is hazardous to human health and destructive to the environment if not handled properly. MTBE should be removed before the release of wastewater. The present work supported the methyl-modified silica layer (MSL) on porous α-Al 2 O 3 ceramic membranes with methyltrimethoxysilane (MTMS) as a precursor and pre-synthesized mesoporous silica microspheres as dopants by the sol-gel reaction and dip-coating method. MTMS is an environmentally friendly agent compared to fluorinated alkylsilane. The MSL-supported Al 2 O 3 ceramic membranes were used for MTBE/water separation by pervaporation. The NMR spectra revealed that MTMS evolves gradually from an oligomer to a highly cross-linked methyl-modified silica species. Methyl-modified silica species and pre-synthesized mesoporous silica microspheres combine into hydrophobic mesoporous MSL. MSL makes the α-Al 2 O 3 ceramic membranes transfer from amphiphilic to hydrophobic and oleophilic. The MSL-supported α-Al 2 O 3 ceramic membranes (MSL-10) exhibit an MTBE/water separation factor of 27.1 and a total flux of 0.448 kg m -2 h -1 , which are considerably higher than those of previously reported membranes that are modified by other alkylsilanes via the post-grafting method. The mesopores within the MSL provide a pathway for the transport of MTBE molecules across the membranes. The presence of methyl groups on the external and inner surface is responsible for the favorable separation performance and the outstanding long-term stability of the MSL-supported porous α-Al 2 O 3 ceramic membranes.

Self-healing cementitious materials are a promising means for ensuring sustainable concrete infrastructure and promoting long-term service lives. To obtain microcapsules that are versatile in varying environments, in this study, absorbing microcapsules with calcium alginate as the shell and epoxy resin as the core were prepared. The absorbing microcapsules exhibit self-healing and can reduce the shrinkage of cementitious materials. Volume changes of the microcapsules in the hardened paste with increasing hydration age were observed using three-dimensional X-ray computed tomography. In the hardened cement paste with a water-cement ratio of 0.29, the absorption of the microcapsules lasted for several days, and the release of water lasted for 28 days. The absorption of microcapsules affected the fluidity of cement paste, and it was significantly weakened and delayed due to the lower absorption rate. The addition of absorbing microcapsules significantly reduced the autogenous and drying shrinkage of mortars. For microcapsules with a core content of 55% added at 3.5% of cement weight, autogenous shrinkage was almost eliminated. Most importantly, the addition of absorbing microcapsules could achieve a certain degree of recovery of compressive strength as well as satisfactory recovery of impermeability in dry and wet environments.

The application of cement-based materials in engineering requires the understanding of their characteristics and subsequent deformation and fracture process of C-S-H gel in service. In this work, three types of amine molecules including tetraethylenepentamine (TEPA), polyacrylamide (PAM), and triethanolamine (TEA) were intercalated into C-S-H gel in an unsaturated status successfully. Systematical analysis was performed on the structures and properties for both C-S-H gel and corresponding amine molecules/C-S-H gel. It was found that the unsaturated intercalation of amine molecules into C-S-H gel plays a key role in the geometry and therein density of nanocomposites. Subsequently, radial distribution function (RDF), time-correlated function (TCF), and mean square displacement (MSD) were applied to characterize the structure and dynamic information of the as-generated nanocomposites, demonstrating the occurrence of interaction between amine molecules with Ca-Si layer and acceleration of water diffusion by unsaturated intercalation of amine molecules into the interlayer region in C-S-H gel. Finally, the deformation and fracture process of C-S-H gel and amine molecules/C-S-H gel under uniaxial tensile loads were given by molecular dynamics simulation. It was indicated that the tangent modulus of nanocomposites demonstrates a strain-softening nature, indicating a visco-elastic behavior. The breakage of Ca-O bonds and hydrogen bonds dominates the fracture of C-S-H gel. Weak interaction for TEPA/C-S-H gel or TEA/C-S-H gel leads to a decreased tensile strength. Local stress concentration in other interlayer region governs the deformation and fracture process in spite of the formation of strong interaction between double bonded polar oxygen atoms in PAM molecules and Ca atoms in C-S-H gel., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

In this work, a novel intumescent flame retardant (IFR) system was fabricated by the introduction of chitin as a green charring agent, ammonium polyphosphate (APP) as the acid source, and melamine (MEL) as the gas source. The obtained chitin-based IFR was then incorporated into a polylactic acid (PLA) matrix using melt compounding. The fire resistance of PLA/chitin composites was investigated via the limiting oxygen index (LOI), UL-94 vertical burning, and cone calorimeter (CONE) tests. The results demonstrated that the combination of 10%APP, 5%chitin and 5%MEL could result in a 26.0% LOI, a V-0 rating after UL and a 51.2% reduction in the peak heat release rate during the CONE test. Based on the mechanism analysis from both the morphology and the chemical structure of the char, it was suggested that chitin was a promising candidate as a charring agent for chitin reacted with APP and MEL with the formation of an intumescent layer on the surface.

With the rapid development of the construction industry, it is necessary to synthesize environment-friendly functional polymers, especially when developing "green" construction industry types. Herein a novel solid-state polycarboxylate superplasticizer (PCE) with low energy-consumption was designed and synthesized. In industrial application, solid-state PCE has exhibited better cement paste fluidity and concrete slump compared to liquid-state PCE. A life cycle assessment (LCA) of the PCE synthesis, the packaging materials used, and the transportation of the PCE were conducted based on the ReCiPe method. The results indicated that liquid-state PCE has a far greater environmental impact at >60% than solid-state PCE, which is less significant at <40%. The inventory data that are associated with the production of the new polymer are disclosed for the first time to enrich the related database in this field. This study demonstrates the optimization of the state and synthesis technique of a functional polymer, improving the performance and lowering the environmental impacts involved in producing the polymer, while reducing the risks to human health and protecting the ecosystem at the same time., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

In order to understand the mechanisms of arsenic (As) accumulation and detoxification in aquatic plants exposed to different As species, a hydroponic experiment was conducted and the three aquatic plants (Hydrilla verticillata, Pistia stratiotes and Eichhornia crassipes) were exposed to different concentrations of As(III), As(V) and dimethylarsinate (DMA) for 10 days. The biomass, the surface As adsorption and total As adsorption of three plants were determined. Furthermore, As speciation in the culture solution and plant body, as well as the arsenate reductase (AR) activities of roots and shoots, were also analyzed. The results showed that the surface As adsorption of plants was far less than total As absorption. Compared to As(V), the plants showed a lower DMA accumulation. P. stratiotes showed the highest accumulation of inorganic arsenic but E. crassipes showed the lowest at the same As treatment. E. crassipes showed a strong ability to accumulate DMA. Results from As speciation analysis in culture solution showed that As(III) was transformed to As(V) in all As(III) treatments, and the oxidation rates followed as the sequence of H. verticillata>P. stratiotes>E. crassipes>no plant. As(III) was the predominant species in both roots (39.4-88.3%) and shoots (39-86%) of As(III)-exposed plants. As(V) and As(III) were the predominant species in roots (37-94%) and shoots (31.1-85.6%) in As(V)-exposed plants, respectively. DMA was the predominant species in both roots (23.46-100%) and shoots (72.6-100%) in DMA-exposed plants. The As(III) contents and AR activities in the roots of P. stratiotes and in the shoots of H. verticillata were significantly increased when exposed to 1 mg·L -1 or 3 mg·L -1 As(V). Therefore, As accumulation mainly occurred via biological uptake rather than physicochemical adsorption, and AR played an important role in As detoxification in aquatic plants. In the case of As(V)-exposed plants, their As tolerance was attributed to the increase of AR activities., (Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.)

A series of novel comb-like poly(butyl acrylate)-g-poly(dimethylaminoethyl methacrylate) (PBA-g-PDMAEMA) with different side chain lengths were designed and successfully synthesized by the "first main chain then side chain" method. Infrared Spectroscopy (IR), 1 H Nuclear Magnetic Resonance ( 1 H NMR), and gel permeation chromatography (GPC) were used for structural confirmation and molecular weight characterization. This polymer exhibited responsive behavior from hydrophilicity to hydrophobicity under the alkaline environment of cement-based materials, with the contact angle of 105.6°, a decreased evaporation rate, and a hydrophile-lipophile balance (HLB) value. A significant internal hydrophobic effect on cement mortar was shown in the water absorption rate, which decreased by 75.2%, and a dry shrinkage-reducing rate of more than 30%. Furthermore, this polymer can effectively slow the exothermic rate, reduce the heat release, and delay the exothermic peak of cement hydration. It was interesting that these properties showed a direct correlation with the side chain length of the comb polymer. The aims of this study are to provide a new avenue to synthesize polymers with the spontaneous hydrophilicity-hydrophobicity transition in the cement system, achieving excellent internal hydrophobicity of cement-based materials, and to offer a promising alternative to resist external erosion for improving the durability and service life of cement-based materials.

Mn-based catalysts are expected to be applied for removing NO x due to its excellent low-temperature activity. However, the practical use of these catalysts is extremely restricted with the co-poisoning of alkali metal and SO 2 in the flue gas. Here the MnO 2 /TiO 2 catalyst was employed to elucidate the co-poisoning mechanisms of K and SO 2 for the low temperature selective catalytic reduction (SCR) of NO. The physicochemical properties of catalysts under different toxicity conditions were studied by experiments. The adsorption of NH 3 , SO 2 , NO, and K on active component (MnO 2 ) and support (TiO 2 ) was studied by density functional theory. This work unravels a promotion effect of support on the alkali and sulfur resistance. The SO 2 &K co-poisoning catalyst had higher SCR activity than the SO 2 -poisoned and K-poisoned catalyst alone. For a single toxic condition: (1) SO 2 was preferentially bonded with the terminated O site of MnO 2 inhibiting the dehydrogenation of NH 3 and redox cycle. (2) The presence of Lewis base (K atom) on the catalyst decreased the binding energy of a Lewis base (NH 3 ) and hindered the adsorption of NH 3 . For the synergistic effect of K and SO 2 , the majority of K adsorbed on the support (TiO 2 ) lead to increase alkalinity, which could promote the adsorption of SO 2 on the TiO 2 and reduce the toxicity of the active component (MnO 2 )., (Copyright © 2021 Elsevier B.V. All rights reserved.)

In order to obtain low-cost and excellent adsorption materials, this paper used calcium acetate and water glass as raw materials to synthesis hydrated calcium silicate gel by precipitation method. The performance and structure of hydrated calcium silicate gel were systematically studied by X-ray photoelectron spectroscopy, fourier transform infrared spectroscopy, specific surface area analyzer and scanning electron microscope. Studies have shown that, non-crystal hydrated calcium silicate gel (CSH) were successfully prepared, and the removal rate of lead ion using CSH reached more than 90%. The adsorption process is consistent with the pseudo-second-order kinetic model and Langmuir adsorption isotherm model, and the limit adsorption capacity reaches 263.17 mg·g -1 . The acid treatment experiment proved that the adsorption capacity of lead ion using CSH was satisfactory, and the adsorption rate remained at >60% after 5 cycles. The research may provide a low-cost, high-efficiency and high stability adsorbent.

In the cement industry, SO 2 and NOx are generally removed separately. There are many problems, such as large area, high investment cost, secondary pollution and so on. Desulfurization and denitrification technology have become a frontier research direction in the field of air pollution control. In this paper, rice husk ash and carbide slag were compounded and modified to prepare modified rice husk ash-carbide slag composite absorbent, and its desulfurization and denitrification performance and mechanism were studied. The results showed that the NO conversion and SO 2 conversion of the modified rice husk ash-carbide slag composite absorbent increased by 44% and 2%, respectively, at 700 °C. Fibrous calcium silicate and calcium silicoaluminate hydrates were formed during the hydration process, which made the specific surface area of the absorbent larger and provided more reactive sites. The hydration process increases the content of oxygen-containing functional groups, decreases the hydroxyl/ether C-O functional groups, and increases the content of carboxyl-COO functional groups are conducive to the denitrification reaction.

Sulphoaluminate cement has the advantage of low-temperature application performance, but its hydration mechanism at low temperatures is not yet clear. Anhydrous calcium sulfoaluminate (C 4 A 3 S) is the main mineral in the composition of sulfoaluminate cement clinkers. In this paper, C 4 A 3 S mixed with gypsum (CaSO 4 ∙2H 2 O) to form a C 4 A 3 S-CSH 2 cement system; X-ray diffraction (XRD), thermogravimetric analysis (TG-DTG), scanning electron microscopy (SEM) and mercury intrusion analysis (MIP) to clarify the effect of temperatures on the hydration properties of C 4 A 3 S-CSH 2 cement system. The results showed that hydration of the C 4 A 3 S-CSH 2 cement system could carry on at low temperatures, even at -15 °C. The main hydration product was ettringite. Low temperatures did not change the types of the hydration products, but the low temperature of 0 °C was more favorable for the formation of ettringite. The early hydration of the C 4 A 3 S-CSH 2 cement system was inhibited by the decrease in temperature. However, hydration of the cement at 0 °C continued at a high rate after one day. Morphologies of the ettringite for the C 4 A 3 S-CSH 2 cement system at -15 °C were needle-like structures, while they were of columnar structure at 0 °C. The compressive strength of samples at 0 °C reached 82 MPa, which is significantly higher than that at 20 °C.

The slag obtained in the process of pig iron smelting has been widely used, but the variational hydration activity always is a significant factor affecting its quality. In this experiment, the laboratory simulated slag was prepared by adjusting the chemical composition and cooling method. The experiment primary characterized the structure and hydration process with different types of slag by using MAS NMR, XRD, compressive strength, ICP, SEM, and hydration heat, then obtained the influence of the composition of the network former S/A (the mass ratio of SiO 2 and Al 2 O 3 in chemical composition) and amorphous phase content on its structure and hydration activity. The result shows that lowering the S/A value can reduce the degree of vitreous polymerization in the slag; reducing the S/A value of the slag can make the slag hydration time advance, and consequently, the cumulative exotherm increases, the liquid phase Ca/Si and Al/Si ionic ratio increases, and the hydration product changes from C-S-H gel to C-A-S-H gel, which ultimately leads to an increase in compressive strength. In the high S/A value slag, the formation of the trace crystal phase of gehlenite is beneficial to reduce the degree of polymerization of the amorphous.

A series of polycarboxylate superplasticizer (PCE) polymers were synthesized from acrylic acid (AA) and isoprenyloxy polyethylene glycol ether (IPEG) at the mole ratios of 3.0, 4.2, 5.0 and 6.0. In this study, the molecular weight properties of PCE polymers were recorded by size exclusion chromatography with the time interval of 1 h. Mini slump test was used to detect the dispersing effectiveness of PCE polymer in cement paste. The results indicated that the reaction rate of monomers, conversion of 52IPEG macromonomer and molecular weight of PCE polymers increased with the general adding ratio of AA to IPEG macromonomers while the side chain density of PCE polymers decreased. PCE polymers possessed molecular weight around 30,000 g/mol with low side chain density, and long main chain length presented high initial dispersing effectiveness at the low dosage around 0.12%. The majority of effective PCE polymers were formed during the adding period of acrylic acid in the first 3 h.

Background: MiR-493 promotes the proliferation of prostate cancer (PC) cells by targeting PHLPP2. We aimed to explore the relationship between miR-493 and autophagy in PC., Methods: qRT-PCR and western blotting were used to determine the mRNA levels and protein expression of miR-493, PHLPP2, autophagy gene BECN1 and ATG7 in PC cells. The autophagy gene expression was determined after PC cells transfected with miR-493 precursor or PHLPP2 precursor. Corresponding changes of autophagy phenotype and PC cell function were also studied., Results: The mRNA levels and protein expression of miR-493, PHLPP2, BECN1 and ATG7 in PC cells were significantly decreased in PC cells. Overexpression of miR-493 or PHLPP2 markedly upregulated the expression levels of BECN1 and ATG7 in PC cells. Overexpression of miR-493 and PHLPP2 markedly promoted autophagy, and inhibited the invasion and cloning formation of PC cells., Conclusion: MiR-493 is a potent inducer of cytotoxic autophagy that leads to prostate cancer inhibition by regulating on PHLPP2., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)

Nitrogen oxide (NOx) emissions have attracted much attention for increasing concern on the quality of the atmospheric environment. In view of NO decomposition in the cement production process, the preparation of Cu-Al/SiO 2 porous material and its effect on NO decomposition were studied, and the denitrification mechanism was proposed in this paper. The NO decomposition performance of the Cu-Al/SiO 2 porous material was tested via the experimental setup and infrared spectrometer and micro gas chromatography (GC). The result shows that the Cu-Al/SiO 2 porous material with the template of cetyltrimethylammonium bromide (CTAB) had a better NO decomposition rate than materials with other templates when the temperature was above 500 °C, and NO decomposition rate could approach 100% at high temperatures above 750 °C. Structure analysis indicates that the prepared Cu-Al/SiO 2 material structure was a mesoporous structure. The X-Ray Diffraction (XRD) and Ultraviolet-visible spectrophotometry (UV-Vis) results of the denitrification product show that the Cu-Al/SiO 2 material mainly decomposed to Cu 2 O and Si 2 O, and the CuO decomposed to Cu 2 O and O 2 at high temperature. The Cu(I)O was considered as the active phase. The redox process between Cu(II)O and Cu(I)O was thought to be the denitrification mechanism of the Cu-Al/SiO 2 porous material.

A series of MCM-41 molecular sieves with different molar ratio of template to silicon were synthesized through hydrothermal synthesis method by using cetyltrimethylammonium bromide (CTAB) as the template, diatomite as the silicon source. By using impregnation method, the Mn-Ce/MCM-41 SCR molecular sieve-based catalysts were prepared. The results observed that when the molar ratio of template to silicon was 0.2:1, the MCM-41 as catalyst carrier has the highest surface area and largest pore volume, it also presented typically ordered hexagonal arrays of uniform channels. The denitration catalytic material based on this carrier has a high number of Lewis acidic sites, and the denitration efficiency can reach more than 93%.

Air quenched slag is processed by a fast air cooling method which is developed with the advantages of recovering heat from molten slag and water conservation compared to the water quenching method. Air quenched slags with different chemical compositions are synthesized in the lab by designing three chemical composition ratios: (CaO + MgO)/(SiO₂ + Al₂O₃), CaO/MgO and SiO₂/Al₂O₃, which are donated as CM/SA, C/M and S/A, respectively. The effect of different chemical compositions on the phase compositions of synthetic air quenched slag, the strength and hydration properties of slag blends were investigated by using various characterization techniques. The results show that the amorphous content of air quenched slag decreased with the increasing basicity CM/SA of slag. The S/A ratio of slag was the dominant factor for the compressive strength of slag blends at 28 days and negatively correlated with strength. Decreasing the S/A ratio of slag increased the reactivity of slag and its reaction degree indicated by higher hydration heat release, lower CH content, greater chemical combined water amount and denser microstructure. Moreover, thermodynamic modelling revealed that a higher S/A of slag leads to the increase of C-(A)-S-H and AFt contents, whilst decreasing the amounts of Ht, AFm-SO₄ phases and the total volume of hydrates.

Background: MicroRNA-493 (miR-493) was upregulated in prostate cancer (PCa). This study was designed to investigate the mechanism underlying miR-493 mediated pro-proliferation in PCa cells. Methods: Expression of miR-493 in PCa cell lines (DU145 and PC3) and control cells was determined using qRT-PCR. PCa cells were transfected with miR-493 mimics, inhibitor, negative control (NC), PH domain leucine-rich-repeats protein phosphatase 2 (PHLPP2), and Akt expressing plasmids and Akt inhibitor MK-2206. Cell proliferation, quantitative expression of miRNA and mRNA were detected. Protein expression was determined using western blotting analysis. Results: Results showed that miR-493 in PCa cells was upregulated compared with RWPE-1 cells. Cells transfected with miR-493 mimics or inhibitor significantly reduced or enhanced expression of PHLPP2 (p < 0.05), respectively. Cell proliferation was significantly enhanced by miR-493 overexpression, or inhibited by PHLPP2 overexpression. The administration of Akt inhibitor MK 2206 attenuated miR-493-enhanced cell proliferation. PCa cells transfected with Akt express vectors partially enhanced PHLPP2-reduced cell proliferation. Conclusions: These results demonstrated that miR-493 acted as a onco-miR in PCa cells and promoted PCa cell proliferation via inhibiting tumor suppresser PHLPP2 expression and activating Akt signaling pathway.

In this study, Multiwalled carbon nanotubes (MWCNTs) were oxidized by a mixture of sulfuric acid and nitric acid ( V : V = 3:1) at 70 °C for 1, 2, and 4 h, respectively. The oxidized MWCNTs were characterized by N₂ adsorption, Fourier-transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), thermal gravimetric analysis (TGA), and Raman spectroscopy to determine the oxidation degree. The dispersion of the MWCNTs was investigated by UV-vis-NIR, SEM, and dynamic light scattering measurements. Results show that sulfonitric treatment increased the surface area and total pore volume and reduced the average pore diameter of MWCNTs. The treatment promoted the formation of oxidized species on the surface MWCNTs, as identified by FT-IR, TGA, and X-ray photoelectron spectroscopy measurements, and more oxygen-containing functional groups were generated when treatment time was extended. Moreover, a general relationship between oxidation degree and dispersibility of MWCNTs in water was established. UV-vis-NIR and dynamic light scattering measurements and SEM images revealed that MWCNTs with higher oxidation degree showed better dispersibility in water., Competing Interests: The authors declare no conflict of interest.

The silica aerogels were prepared via a sol-gel technique and ambient pressure drying by using industrial solid wastes, dislodged sludges, as raw materials. A strategy was put forward to reduce the corrosion of equipment during the drying procedure. The pore structure, hydrophobicity, and thermal insulation property of the obtained samples were investigated in detail. The results show that the corrosion can be effectively avoided by using an equimolar mixture of trimethylchlorosilane (TMCS) and hexamethyldisilazane (HMDS) as silylation agents. At a Si:TMCS:HMDS molar ratio of 1:0.375:0.375, the silica aerogels possess a desirable pore structure with a pore volume of 3.3 ± 0.1 cm³/g and a most probable pore size of 18.5 nm, a high hydrophobicity with a water contact angle of 144.2 ± 1.1°, and a low thermal conductivity of 0.031 ± 0.001 W/(m∙K).

A novel star-shaped polycarboxylate superplasticizer (SPCE) was synthesized through a simple two-step method. 1 H Nuclear Magnetic Resonance ( 1 H NMR) and Infrared Spectroscopy (IR) measurements were used for structural characterization. SPCE and comb-shaped polycarboxylate superplasticizer (CPCE) with same molecular weights were designed and synthesized. The cement paste containing SPCE exhibited better fluidity, fluidity retention, water reduction, 25% lower saturated dosage of PCE, 10% longer setting time, lower hydration heat, more delayed hydration heat evolution and lower amount of hydration products at early ages. Furthermore, the adsorption behavior of SPCE and CPCE in cement pastes and the zeta potential were investigated, and then the working mechanism of SPCE was theoretically explained. It is interesting that changing topological structure from comb-shape to star-shape can achieve the optimization of dispersion effect, and further improve the working effectiveness. The aims of this study are to provide a new avenue to synthesize superplasticizer with novel structure achieving the chemical diversity of superplasticizer structure, and to verify the contribution of optimizing molecular shape. This new type of superplasticizer can be used as a rheology modifying agent in fresh cement-based materials., (Copyright © 2017 Elsevier Inc. All rights reserved.)

The hierarchical-structured superhydrophilic poly(ethylenimine)/poly(acrylic acid) (PEI/PAA)calcium silicate hydrate (CSH) multilayered membranes (PEI/PAA-CSH)n were prepared as aqueous nanofiltration (NF) membrane, and then they were transformed into superhydrophobic organic solvent nanofiltration (OSN) membranes by one-step modification of trimethylperfluorinatedsilane (PFTS). Investigation on surface structures and properties of these multilayered membranes (PEI/PAA-CSH)n indicated that the hierarchical-structured (PEI/PAA-CSH)n multilayered membrane produced by in situ incorporation of CSH aggregates into PEI/PAA multilayers facilitated its one-step transformation from superhydrophilicity into superhydrophobicity. Both of the superwetting membranes showed better nanofiltration performances for retention of dyes of water and ethanol solution, respectively. Moreover, the long-term performance and antifouling behaviors, investigated by retention of methyl blue (MB), bovine serum albumin (BSA), and humic acid (HA) aqueous water solution and nonaqueous ethanol solution indicated that both of the superhydrophilic and superhydrophobic membrane showed higher stability and excellent antifouling property.

Carotid body tumors (CBTs) are a rare type of extra-adrenal paraganglioma, which originate from the carotid body. A 29-year-old woman was admitted to the Department of Head and Neck Surgery, Beijing Tongren Hospital (Capital Medical University, Beijing, China) with hoarseness of the throat, which had progressively worsened over seven months. The patient had a family history of CBTs. Computed tomography and ultrasound imaging revealed multiple well-enhanced masses located at the bilateral carotid bifurcation and in the left parapharyngeal space. Surgery and pathological examination confirmed that the patient had developed regional lymph node metastasis. Significantly enhanced multiple pulmonary and hepatic lesions indicated that the patient had also developed distal metastasis. A genetic analysis performed on the family members of the patient revealed that the family carried a mutated succinate dehydrogenase D gene. In the present study, a systemic review of the literature indicated that extra vigilance is required in familial forms of CBT, in order to increase the standard of treatment for CBT patients.

A polycarboxylate superplasticizer (PCE) was synthesized in a non-solvent system with bulk polymerization and then was pulverized into powdered form to achieve a rapid transportation and convenient preparation. PCE synthesized by using isopentenyl polyethylene glycol (TPEG) or isobutenyl polyethylene glycol (IPEG) as a macromonomer exhibited the best fluidities and retaining properties at 80 °C and 75 °C, respectively. Besides, azobisisobutyronitrile (AIBN) was suitable as an initiator, and the fumaric acid was suitable as the third monomer. The test results of ¹H nuclear magnetic resonance (¹H NMR) confirmed the occurrences of polymerization, and the measurement results of molecular weight and distribution showed that PCE molecular weight characteristics were in accordance with their fluidity properties in cement paste. The application performances in cement showed that PCEs with the best paste fluidity retentions had the longest final setting time and the shortest setting time interval, and the PCEs with good fluidity properties can obviously delay the hydration process and lower the hydration heat. Accordingly, this is a novel, energy-saving and economical method to prepare powdered PCE in the field of concrete admixtures.

b-1,3-Glucanases are a group of pathogenesis related proteins that have been reported to be involved in plant defense against pathogens in many other plant pathogen systems. However, it was not clear if these genes play similar role in wheat (Triticum aestivum L.) against Puccinia striiformis f. sp. tritici (Pst), the stripe rust pathogen. To investigate the role of b-1,3-glucanase (EC3.2.1.39) in the resistance response of wheat (cv. Suwon11) to stripe rust, a wheat b-1,3-glucanase gene induced by Pst, designated as TaGlu, was cloned and characterized.TaGlu was predicted to encode a basic protein of 334 amino acids. Quantitative real-time PCR analyses revealed that the transcription of TaGlu was induced during both compatible and incompatible interactions with Pst, but the transcription level was much higher in the incompatible interaction than that in the compatible interaction. TaGlu also showed noticeable induction of gene expression in young green leaf tissues treated with salicylic acid, methyl jasmonate or ethylene. Immunogold labeling assays showed that the enzyme were localized mainly in the host cell wall and over the extra haustorial matrix, and the labeling densities were found significantly higher in the incompatible interaction than those in the compatible interaction.

Objective: To study the effect of radionuclide lymphoscintigraphy, a new method of localization diagnosis of chyluria., Methods: Radionuclide lymphoscintigraphy was used to examine 34 patients with chyluria and the results of radionuclide lymphoscintigraphy was compared with those of cystoscopy and lymphangiography., Results: Among the 34 patients 85.3% of unilateral localization diagnosis by radionuclide lymphoscintigraphy was coincident with that by cystoscopy. The positive rate of bilateral localization diagnosis was higher than that by cystoscopy., Conclusion: A less invasive technique, radionuclide lymphoscintigraphy can be used as a new option for the localization diagnosis of chyluria.