Heavy Ion Research Articles

Research on chromium removal mechanism by electrochemical method from wastewater

Cr (VI), a heavy metal ion in electroplating wastewater, poses a significant environmental challenge due to its high toxicity and recalcitrance to degradation. This paper used copper plates, stainless steel, foam carbon, and carbon paper as electrodes to research the chromium removal mechanism from electroplating wastewater by a fast electrochemical method. The effect of the electrode materials and reaction conditions on removing Cr (VI) from wastewater was investigated. The analysis of the Cr (VI) removal rate during electrolysis revealed that the optimal electrode materials used the copper plate as the cathode and foam carbon as an anode. The optimal reaction conditions were determined: the electrolysis time is 30 min, the plate spacing is 2.0 cm, the operating voltage is 1.8 V, and the reaction temperature is 50 °C, achieving a maximum Cr (VI) recovery of 91.30 %. The proposed optimization of stirring instead of heating was found to be feasible. At 300 r/min, the energy consumption can be significantly reduced, and the removal rate of Cr (VI) can reach 87.82 %. The intrinsic mechanism behind the removal of Cr (VI) was studied by calculating the adsorption performance of the two electrodes on Cr (VI) and Cr (III) using the density functional theory (DFT), providing an in-depth understanding of the action mechanism and industry applications.

Large radial shift experiments in RHIC and their implications for EIC design

The Hadron Storage Ring (HSR) in the future Electron-Ion Collider (EIC) (EIC collaboration, 2020; Montag et al., 2022; Liu et al., 2022) must operate over a broad range of design circumferences. In 2018 preliminary beam studies on the circumference adjustment capabilities of the Relativistic Heavy Ion Collider (RHIC) (Accelerator Division, 2006) were performed by applying a small momentum offset to the circulating bunches without adjusting any bending magnets (Robert-Demolaize et al., 2019). The off-momentum linear optics were corrected back to on-momentum conditions. Applying a similarly small deviation to the dipole fields of a select set of bending magnets provides a large radial shift over much of the RHIC (or HSR) circumference while leaving the design trajectory unchanged in the insertion regions.This paper presents the design of the different lattice configurations foreseen as the most viable options for the required HSR circumference changes, and highlights the modifications necessary for regular operations and to allow for testing these new settings in RHIC. Experimental results from 2021 and 2022 are reviewed and compared to model predictions obtained from both MAD-X and Bmad (MAD, 0000; Bmad, 0000). The implications of these results for HSR design are discussed.

Fabrication of tight polyamide nanofiltration membrane by using a pyridine-diamine precursor for heavy metal ions removal

Nanofiltration offers a promising solution for removing heavy metal ions from wastewater, thereby mitigating ecological and environmental risks. In this study, we synthesized a novel pyridine-diamine precursor 2,6-dipiperazine pyridine (PyBPIP), and employed it as the sole aqueous monomer to fabricate tight polyamide (PA) nanofiltration (NF) membranes via interfacial polymerization (IP) method with trimesoyl chloride for the separation of heavy metals. The resulting membrane features an ultrathin PA functional layer (approximately 60 nm), a lower molecular weight cut-off of 251 Da, and a weakly negatively charged surface. This NF membrane exhibits competitive water permeance of approximately 7.67 LMH/bar and excellent rejection rates exceeding 98 % for various heavy metals ions including Zn2+, Mn2+, Cu2+, along with outstanding separation performance for other divalent cations. Additionally, the NF membrane also exhibits robust stability during the 72-h operational test. In summary, this study demonstrates the feasibility of designing suitable monomers for the preparation of highly perm-selective NF membranes for the removal of heavy metal ions in wastewater.

Diversified competitive sulfuration behaviors of concomitant heavy metal ions on copper recovery from copper smelting waste acid

Currently, sulfuration is widely used for the Cu(II) recovery from copper smelting waste acids (CSWA). However, the abundant concomitant heavy metal ions (HMIs) seriously obstruct Cu(II) recovery. In this paper, we find that the precipitation difficulty of HMI sulfide is determined by solubility product constant (Ksp), H+ concentration and S(−II) concentration, resulting in the diversified competitive sulfuration behaviors of concomitant HMIs on Cu(II) recovery. For concomitant HMIs without S(−II)-consuming ability, the positive-side competitive sulfuration behaviors on Cu(II) recovery are in the order of In(III) > Zn(II) > Ni(II) > Fe(II) > Mn(II). However, with the formation of concomitant HMIs sulfides, the negative-side competitive sulfuration behaviors on Cu(II) recovery are in the order of Fe(III) > As(III) > Bi(III) > Cd(II). According to the results of diffusion-growth-dissolution model, the S(−II)-combining process on HMIs surface is divided into S(−II)-capturing and S(−II)-consuming stages, related to Ksp value and HMIs precipitation, respectively. In actual CSWA, 5000 ∼ 15000 mg/L As(III) seriously inhibits the recovery efficiency of 500 ∼ 2000 mg/L Cu(II), and other concomitant HMIs (e.g., 250 ∼ 1200 mg/L Zn(II), 300 ∼ 450 mg/L Cd(II), 10 ∼ 200 mg/L Bi(III) and 20 ∼ 200 mg/L Fe(II)) will further affect Cu(II) recovery. Besides, ignoring these diversified competitive sulfurations of concomitant HMIs induces unreasonable S(−II) concentration for complete Cu(II) recovery, resulting in Cu(II) recovery issues: As(III) precipitation and Cu(II) residue. Thus, timely information in instantaneous Cu(II) concentration is a feasible strategy to accurately adjust S(−II) concentration via Cu(II) quantitative model. This work is devoted to the efficient and controllable recovery of Cu resources and the reduction of As-containing hazardous wastes in sulfuration treatment of actual CSWA.

PE/PP fibrous adsorbents with bifunctional groups of tertiary amine and phosphate prepared by electron beam induced co-grafting for heavy metal adsorption of both cationic and anionic forms in acidic conditions.

A novel fabric adsorbent having bifunctional groups of tertiary amine and phosphate was prepared by co-graft polymerization of 2-diethylaminoethyl methacrylate (NMA) and 2-hydroxyethyl methacrylate phosphate (PMA) onto a polyethylene/polypropylene nonwoven fabric (PE/PP NF) under low-energy electron beam acceleration. The process involved pre-irradiating the fabric and immersing it in the comonomer solution for grafting. The kinetics of radiation-induced graft polymerization at a total dose of 100 kGy was investigated. For pre-irradiation at 100 kGy, the optimum condition offering highest degree of grafting was at 12 wt% of NMA, 8 wt% of PMA and 4 h of reaction time. The adsorption of anions using hydrogen chromate (HCrO4−) or Cr(VI) and cations using lead (Pb(II)), cadmium (Cd(II)) and copper (Cu(II)) in aqueous solution was carried out. The results demonstrated that the bifunctional adsorbent was able to adsorb both heavy metal anionic and cationic ions from water. The co-grafted adsorbents with tertiary amine and phosphate were able to adsorb 85% Cr(VI) anion and 29% Pb(II) cations from mixed Cr(VI) and Pb(II) solution at pH 3.0 and 71% Pb(II), 13% Cd(II) and 31 % Cu(II) from mixed Pb(II), Cd(II) and Cu(II) solution at pH 5.0. The unique achievement of this study is its hypothesis that a bifunctional adsorbent can be prepared from radiation-induced graft polymerization of two different monomers onto NF, along with proof that the prepared bifunctional adsorbent can actually absorb both cationic or anionic heavy metals forms. Additionally, the adsorbent's preparation offers a rapid and straightforward one-step grafting technique. Therefore, the new bifunctional adsorbents can remove heavy metal ions in aqueous solution, either in the cation or anion form, thus offering highly promising applications in industrial wastewater treatment.

Amino acid-based nanoparticles-incorporated thin-film nanocomposite forward osmosis membranes for efficient desalination and heavy metal ions rejection

The current study explores potential applications of state-of-the-art thin-film nanocomposite forward osmosis (TFN-FO) membranes, modified with histidine-functionalized graphene quantum dots (His-GQDs) and MIP-202(Zr) nanoparticles (NPs), for sustainable desalination and heavy metal ions rejection. The porous and layered structure of the applied NPs, along with various hydrophilic functional groups on their surface, contribute to improving the fabricated membranes' ion/water separation performance. The successful preparation and incorporation of desired NPs into the polyamide layer was investigated using typical analytical methods. Under the common FO test conditions, the best-performing TFN-MQ2 membrane displayed a water flux of 21.8 LMH, which was over 1.5 times greater than the water flux of blank TFC. Simultaneously, the selectivity was found to be approximately 1.7 times greater than that of the unmodified TFC membrane. Moreover, the optimal TFN-MQ2 membrane exhibited superior rejection rates for Cu2+ ions (98.5 %) and Pb2+ ions (98.1 %), surpassing all other samples in heavy metal ion rejection. The findings of this study suggest that carefully choosing cost-efficient and eco-friendly nanofillers (such as amino acid-based NPs) can enhance the desalination performance of TFN-FO membranes and bolster their resistance to fouling and rejection of heavy metal ions. Not to mention, the overall costs of membrane production will be reduced.

Advanced solar-driven hydrogel sponge for efficient heavy metal wastewater purification and clean water production through interfacial evaporation

Solar-driven interfacial evaporation (SDIE) technology represents a promising solution for freshwater harvesting, characterized by its cost-effectiveness, eco-friendliness, and sustainability. Nevertheless, achieving efficient removal of heavy metal ions during the SDIE process remains a significant challenge. In this study, we present a cost-effective method to construct a hybrid hydrogel evaporator by incorporating the konjac glucomannan (KGM) and reduced graphene oxide (rGO) into a polyvinyl alcohol (PVA) network. The hybrid hydrogel evaporator features a three dimensional layered structure, full spectrum absorption capability, high stability and inherent salt diffusion ability. These characteristics enabling a evaporation rate of 1.61 kg m−2 h−1 from wastewater across varying pH values (2-12) and high salinity levels (1 kW m-2). Significantly, the hybrid polymer network within the hydrogel is rich in -OH groups, enabling concurrent wipe off heavy metal ions and organic dyes from wastewater. The results in a ten thousand times reduction in the concentration of heavy metals such as Cr3+, Mn2+, Cu2+, Zn2+, and Pb2+ in the wastewater. This study provides new insights into solar evaporation technology and contributes to addressing challenges related to water scarcity.

Microstructure evolution of CdZnTe crystals irradiated by heavy ions

Consideration of irradiation effects is important for in-orbit operation and radiation protection in aerospace applications. The configuration of irradiation defects and their impact on deteriorating the carrier transport properties of CZT crystals need to be clarified. In this study, the microdefect evolution mechanism of CdZnTe (CZT) crystals under 10 MeV Chlorine (Cl) ion irradiation at flux of 1×1010∼1×1012 n·cm-2 are investigated. The stacking faults first appear in the CZT crystal at 4.5×10-4 displacement per atom (dpa), which are categorized into slip-type, gap-type and vacancy-type. In order to hinder the further expansion of stacking fault, S-shaped stacking fault dipole appears. When the dpa reaches 4.5×10-2, the local phase transition occurs in the damage zone to form CuPt-A ordered phase with ZnTe/CdTe periodic arrangement because the fluctuation in local composition and strain caused by cascade collisions. The deterioration of electric field distribution and charge collection caused by irradiation damage layer leads to the decrease of γ-ray detection ability. The energy resolution (ER) of the CZT detector for γ-ray can be maintained at 30.6% when the ion flux accumulates to 1×1012 n·cm-2, revealing high irradiation hardness. Consequently, these findings provide a theoretical basis for the radiation damage recovery of CZT detectors, further demonstrating that CZT crystals are the most competitive new generation of room-temperature nuclear radiation detection materials, and can provide radiation protection strategies for similar compound semiconductor materials.

Degradation Under Low Drain Bias Induced by Heavy Ion in SiC MOSFETs

Degradation Under Low Drain Bias Induced by Heavy Ion in SiC MOSFETs

Synergistic and simultaneous removal of heavy metal ions over waste bamboo shoot particles encapsulated carboxymethyl cellulose/gelatin composite hydrogel

Synergistic and simultaneous removal of heavy metal ions over waste bamboo shoot particles encapsulated carboxymethyl cellulose/gelatin composite hydrogel

Microwave enhanced carbon dots synthesis from eggshell membrane: Versatile applications in heavy metal ion sensing, strain free detection of fingerprints, UV shielding, food packing and anti-counterfeiting

In this study, a one-step microwave irradiation process combined with a sodium hydroxide (NaOH) solution allowed for the quick and easy synthesis of carbon dots (CDs) from eggshell membrane (ESM) ashes. The resultant CDs demonstrated exceptional selectivity for Fe3+ and excellent fluorescence (FL) with a quantum yield (QY) of 15.3%. Utilizing synthetic CDs, a sensitive nanoprobe is utilized to identify free Fe3+ within the 0-350μM (R2 = 0.9976) range, with a 0.281μM limit of detection (LoD). Additionally, the CDs were shown to be useful for intracellular Fe3+ detection applications because of their low cytotoxicity and biocompatibility. Investigations using real samples at 420 and 500nm excitation wavelengths showed promising results in terms of real-world application. In order to transform molecular data into FL signal outputs, a multi-input logic gate is also constructed. In the UV-A (93%), UV-B (88%), UV-C (98%) and HEBL (79%) regions, blue colour-emitting CDs had the maximum UV blockage, but pure polyvinyl alcohol (PVA) absorbed less than 22–30% of the light in all UV regions. The integration of CDs into the polymer improved the thermal characteristics of the PVA film. Additionally, testing of in vitro cell viability demonstrated that the CDs, when embedded in the PVA, did not cause cytotoxicity to the Neuroblastoma cell line (SH-SY-5Y). As a paradigm for perishable commodities, the effects of CDs and PVA were assessed on the shelf life of tomatoes. When fresh tomatoes were coated with CDs@PVA and PVA, weight and moisture loss were effectively decreased, according to the results of the long-term monitoring study. Throughout almost 34 days at room temperature, it also dramatically reduced the growth of fungi and prevented spoiling, all the while maintaining the fruits original colour and appearance. The CDs FL under 365nm UV light excitation makes them well-suited for creating fluorescent inks to deter counterfeiting. Additionally, the study explored the CDs exceptional FL properties for use as a luminescent fingerprint powder, aiding in the detection of latent fingerprints (LFPs) on various surfaces. The findings from this study highlight the potential of cost-effective and safe CDs for a range of applications, including non-cytotoxic UV blocking, active packaging, Fe3+ sensing, fingerprint detection, anti-counterfeiting (AC) measures and flexible nanocomposite (NC) films.

Constructing SDBS-intercalated MoS2 nanosheets confined and near-vertically grown on network biochar adsorbent: Insights into highly efficient co-adsorption of ciprofloxacin and lead ions

To overcome the problems of the weak adsorption ability of biochar to heavy metal ions (HMIs) and competitive adsorption between HMIs and antibiotics during co-adsorption, the adsorbent material in which 2D sodium dodecylbenzenesulfonate-intercalated molybdenum disulfide nanosheets confined and growing near-vertically on 3D network biochar (SDBS-MoS2/BC) was synthesized. The SDBS-MoS2/BC demonstrated good adsorption ability for ciprofloxacin (CIP) and lead ions (Pb2+). Notably, the adsorption capacity of SDBS-MoS2/BC for the target in the binary system remains higher than in the single system, even at elevated concentrations of the competing target (Qmax,CIP = 393.701 mg g−1, Pb2+: 100 mg/L; Qmax,Pb = 264.550 mg g−1, CIP: 100 mg/L). This may be due to the improvement in the utilization of edge/interlayer adsorption sites by the near-vertical SDBS interlayer expansion of MoS2 as a heavy metal ion anchor. Furthermore, the spatial difference between the upper edge site of near-vertical SDBS-MoS2 and the BC plane, that is, the “longitudinal steric effect”, can separate the CIP and Pb2+ adsorptions in a different horizontal plane to avoid competitive adsorption. The underlying adsorption mechanism was elucidated through a series of experiments and the analysis of characterization results. Furthermore, the load of the SDBS-MoS2/BC sponge-packed column can continuously remove contaminants from water. The rapid, anti-interference, multifunctional and reusable properties make SDBS-MoS2/BC promising for excellent environmental treatment.

The exploration of effect for nano-Al2O3 on solid waste based superfine tailings cemented paste backfill: Pyrolysis property, hydration mechanism and environmental risk

Resource utilization of superfine tailings has become a key research direction in filling mining. This study analyzes the mechanical properties, pyrolysis mechanism and hydration mechanism of nano-Al2O3(NA)-doped solid waste based superfine tailings cemented paste backfill (SWSCPB) by multiple microscopic characterization methods and pyrolysis kinetic theory. The results show that the main temperature interval for the pyrolysis of SWSCPB to happen is 280–900 °C, which is divided into two stages of dehydroxylation and decarbonization. The apparent activation energy(E) and pre-index factor(A) of pyrolysis are higher than those of NA0 and NA2 at 1 % NA dosage, indicating that NA increases the energy barrier of pyrolysis, the percentage of activated molecules, and the collision probability of hydration products in SWSCPB, but decreases due to agglomeration at exceeds 1 % NA dosage. NA can enhance macroscopic strength of SWSCPB, with the highest strength at 1 % NA dosage. Compared with NA0 and NA2, more hydration products such as AFt and C-(A)-S-H are present in NA1, and the distribution of Q2 and Q4 in C-(A)-S-H is more pronounced, with a higher degree of polymerization, a stronger tendency for the conversion of non-bridging to bridging oxygen bonds, and fewer pores in the microstructure of SWSCPB. The NA dosage can provide more nuclei for the formation of AFt, C-(A)-S-H in SWSCPB, and can also promote the replacement of Si by Al for the conversion of C-S-H to C-(A)-S-H with higher polymerization. In addition, the leaching risk and mechanism of heavy metal ions from SWSCPB are preliminarily explored in combination with leaching experiments. The results provide new insights and guidance for the application of SWSCPB in filling mining under cleaner production targets.

Study on the new slow-release carbon source biochemistry and its improvement of SRB on the acid mine drainage treatment

The content of sulfate and heavy metals in acidic mine drainage (AMD) exceeds the standard severely, and the acidity is extremely high, causing serious harm to the environment. SRB can efficiently remove sulfates through its own metabolism. The treatment of AMD by SRB faces problems such as carbon source scarcity and heavy metal ion toxicity to SRB. In this study, corn cob and polycaprolactone were embedded to prepare a novel slow-release carbon source (PSCL), which simultaneously achieves carbon source supply and metal ion removal. Through adsorption isotherms, kinetics, thermodynamics studies, and various characterization analyses, it is known that PSCL removes Cu2+ and Zn2+ through ion exchange, physical and chemical adsorption, electrostatic attraction, and surface complexation. PSCL carbon release experiments and characterization results confirm that its surface carbon distribution is dense, the molecular weight of DOM in the leachate is small, the degree of humification is low, and it has a porous structure, making it a good carbon release material and biological attachment. The experimental results of PSCL enhanced SRB treatment of AMD showed that the removal rates of SO42−, Cu2+ and Zn2+ could be increased to 97.48%, 98.11% and 90.42%, respectively, with a effluent pH of 7.05, effectively improving the water quality of AMD. This study provides new materials and methods to address the limitations of SRB in treating actual AMD.

New insights into sustainable in-situ fixation of heavy metals in disturbed seafloor sediments

To address the issues of plume formation and heavy metal ion release during deep-sea mining operations, this study employed multi-sourced mineral composite roasting materials (MMCCM) of varying sizes. An in-situ capping technique was applied within a simulated system to immobilize heavy metals in contaminated sediments. The results demonstrated that capping with MMCCM of different sizes significantly suppressed the upward migration of Cu, Co, and Ni from sediments into the overlying seawater following disturbance. Ion diffusion was identified as a key mechanism driving heavy metal migration. By calculating the release rates of heavy metals during both the disturbed and undisturbed phases, it was found that the application of MMCCM induced a negative diffusion of heavy metals, indicating that the MMCCM-sediment layer functioned as a "sink" for heavy metals. FTIR and XPS analysis showed that the primary mechanisms for heavy metal removal by MMCCM were electrostatic attraction and complexation-precipitation. Additionally, capping with MMCCM facilitated the transition of heavy metals from labile to stable forms within the sediments. Through comprehensive evaluation, the long-term effectiveness of the fixed effects was demonstrated as follows: large MMCCM (L@MCM) > medium MMCCM (M@MCM) > small MMCCM (S@MCM) > powder MMCCM (P@MCM). Finally, we proposed future research directions and introduced the DQSE framework for the sustainable application of MMCCM. Based on the above findings, this study provides new insights and research references for the in-situ immobilization of heavy metals and plume reduction during future deep-sea mining processes.

Electrochemical activation of periodate with graphite electrodes for degradation of high concentrations of thiocyanogen (SCN−) in mineral processing tail liquid

Cyanide has been widely used in gold extraction due to its cost-effectiveness, high selectivity and recovery. Regrettably, its wide application also leads to the presence of a large amount of thiocyanogen (SCN−) in the tail liquid of mineral processing plants, which affects the quality of the effluent water, and thus poses a threat to the ecological environment and human health. This paper investigates the degradation of high concentration of SCN− in water using electrochemical oxidation/periodate (E-GP/PI) system. A degradation rate of 90.25 % of SCN− was achieved by optimising various operating parameters. The effects of organic matter and typical heavy metal ion concentrations on the degradation of SCN− were investigated, and it was found that Cu2+ was able to promote the degradation of SCN− through the formation of stable complexes with SCN−, which enhanced the degradation rate to 96.48 %. However, the presence of Octadecyltrimethylammonium bromide (OTAB) and butylxanthin hindered the degradation process, where 500 mg/L of OTAB reduced the degradation rate of SCN− to 80.88 %, while 100 mg/L of butylxanthin reduced the degradation rate to 78.66 %. On this basis, experiments were carried out using real wastewater samples and SCN− degradation efficiencies of about 90 % were obtained. Afterwards, through electron paramagnetic resonance analysis, free radical burst, ion chromatograph and other research techniques, IO3 and O2– were obtained as the main drivers of SCN− degradation and SCN− degradation pathways were elucidated. Finally, the E-GP/PI system was shown to be effective in reducing the ecotoxicity of SCN− by increasing the 24-h LC50 from 12.5 % to 48.5 % in a toxicity test with daphnia. This study provides a new idea for the green and efficient treatment of SCN− rich beneficiation tail liquid.

Preparation of cellulose nanofiber/polyvinyl alcohol-based composite films for metal ion detection by starch/disodium calcium ethylenediaminetetraacetate synergistic complexation effect

Heavy metal pollution causes irreversible damage to plants, animals, and humans. Therefore, it is meaningful to develop facile, fast, and efficient strategies for heavy metal ion (HMI) detection. Here, a portable composite film (CPSE) was designed for HMI detection with high sensitivity and wide detection range. The CPSE was prepared by using cellulose nanofibers (CNF)/polyvinyl alcohol (PVA) as the matrix and utilizing modified starch (HPS) to assist disodium calcium ethylenediaminetetraacetate (EDTA-Ca) to form stable complexes with HMI. The R, G and B values (the three primary colors of light) were captured using an image acquisition system to produce an HMI standard color card successfully. Specifically, the composite film can effectively distinguish Cu2+, Pb2+ and Fe3+. The response time of the composite film to HMI was 2–4 s, and the detection ranges of Cu2+ and Fe3+ were 5–700 ppm and 10–1000 ppm, respectively. Additionally, the synergistic effect of HPS and EDTA-Ca led to the increase in tensile strength (1.59–1.71 times), tear strength (3.29–3.57 times), and glass transition temperature (~ 6 °C) compared to CNF/PVA/HPS and CNF/PVA/EDTA-Ca films. This study confirms the value of CPSE films as materials for HMI detection and suggests innovative ideas for designing similar biomass detection materials in the future.

Functionalizing heavy metal contained incinerated sewage sludge ash in recycled glass-based alkali-activated materials for sewer environment

This study evaluates the performance of alkali-activated cement (AAC) mortars in an artificial sewage environment. The mortars, initially prepared with waste glass powder (GP) and ground granulated blast furnace slag (GGBS) in a 50:50 mass ratio, were modified by replacing 10 wt% of GGBS with incinerated sewage sludge ash (ISSA) with the goal of offering a biocidal effect. Comparisons were made with calcium aluminate cement (CAC), metakaolin (MK), and MK combined with zinc ferrite nanoparticles, each at a similar GGBS replacement level. The results showed that only incorporating CAC improved the strength development, achieving compressive and flexural strengths of 62.7 MPa and 7.4 MPa, respectively, at 28 days, while introducing ISSA or MK reduced the compressive strength to 47 MPa and flexural strength to 4.5 MPa. Although heavy metal ions from ISSA or zinc ferrite nanoparticles minimized biofilm thickness, they could not compensate for the reduced strength and increased alkalis leaching. Among all the tested mixtures, the 50GP40GGBS10CAC mixture exhibited superior biogenic acid resistance, possibly due to its Al-rich C-N-A-S-H gel phases (Ca/Si = 0.4, Na/Al = 0.8, Si/Al = 3.4) and refined pore structure (porosity = 3.4 %), making it the most microbial acid-resistant option for sewer rehabilitation.

Magnetically separable and reusable Fe3O4/rGO photocatalyst synthesized through green approach for heavy metal ion reduction application

Magnetically separable and reusable Fe3O4/rGO photocatalyst synthesized through green approach for heavy metal ion reduction application

Multifunctional carbon nanotube arrays on kapok-derived carbon microtube composites for efficient electromagnetic wave absorption and Cu(II) removal

To cope with different environments of application, electromagnetic wave absorption (EWA) materials with multifunctionality have attracted a wide range of interests. And excessive heavy metal ions in aqueous solutions seriously affect people’s health and pose a major challenge to environmental safety. In this study, carbon microtube/carbon nanotube (CMT/CNT) composites were fabricated via carbonization and chemical vapor deposition (CVD) methods. The CNT wrapped with cobalt nanoparticles were grown in situ on the CMT which derived from kapok fiber. By varying the concentration of cobalt precursors, the EWA and Cu(II) adsorption performances of CMT/CNT can be efficiently tuned. Optimizing the cobalt content to 2 wt% resulted in a minimum reflection loss (RL) of −66.14 dB at a matching thickness of 1.91 mm, with an effective absorption bandwidth (EAB) of 5.35 GHz. The adsorption capacity of Cu(II) by the CMT/CNT composite can reach 102.01 mg/g when the initial Cu(II) concentration is 500 mg/L. This research not only shows great promise for applications in the field of EWA materials but also holds significant potential for heavy metal ion removal and as a catalyst carrier, among other areas.