Exogenous plant growth regulator and foliar fertilizers for phytoextraction of cadmium with Boehmeria nivea [L.] Gaudich from contaminated field soil.

As a enrichment plant, ramie can be used for the phytoremediation of cadmium (Cd)-contaminated soil. However, it is worth exploring the role of plant growth regulators and foliar fertilizers in the process of plant growth and development and Cd adsorption. By measuring the agronomic traits, Cd content of aboveground and underground ramie, calculating the Cd transfer coefficient (TF) and Cd bioconcentration factors (BCF), and the correlation between various indicators. This study examined the effects of plant growth regulators and foliar fertilizers on ramie's capacity for Cd accumulation and transportation. Plant growth regulators and foliar fertilizers increased the Cd content of the aboveground ramie, reduced the Cd content of the underground ramie, and increased the TF. Among them, GA-1 increased the Cd content of the aboveground ramie to 3 times more than that of the control and reduced the Cd content of the underground ramie by 54.76%. Salicylic acid (SA) increased the Cd content of the aboveground ramie to three times more than that of the control. The combination of GA and foliar fertilizer reduced the Cd content of the aboveground and underground ramie and the TF and BCF of the underground ramie. After the hormones were sprayed, the TF of ramie had a significant positive correlation with the Cd content of the aboveground ramie; the BCF of the aboveground ramie had a significant positive correlation with the Cd content and TF of the aboveground ramie. The results indicate that Brassinolide (BR), gibberellin (GA), ethephon (ETH), polyamines (PAs), and salicylic acid (SA) have different effects on the enrichment and transport of Cd in ramie. This study provided an effective method to improve the capacity for ramie to adsorb heavy metals during cultivation.

Microbial Sensing and Removal of Heavy Metals: Bioelectrochemical Detection and Removal of Chromium(VI) and Cadmium(II).

The presence of inorganic pollutants such as Cadmium(II) and Chromium(VI) could destroy our environment and ecosystem. To overcome this problem, much attention was directed to microbial technology, whereas some microorganisms could resist the toxic effects and decrease pollutants concentration while the microbial viability is sustained. Therefore, we built up a complementary strategy to study the biofilm formation of isolated strains under the stress of heavy metals. As target resistive organisms, Rhizobium-MAP7 and Rhodotorula ALT72 were identified. However, Pontoea agglumerans strains were exploited as the susceptible organism to the heavy metal exposure. Among the methods of sensing and analysis, bioelectrochemical measurements showed the most effective tools to study the susceptibility and resistivity to the heavy metals. The tested Rhizobium strain showed higher ability of removal of heavy metals and more resistive to metals ions since its cell viability was not strongly inhibited by the toxic metal ions over various concentrations. On the other hand, electrochemically active biofilm exhibited higher bioelectrochemical signals in presence of heavy metals ions. So by using the two strains, especially Rhizobium-MAP7, the detection and removal of heavy metals Cr(VI) and Cd(II) is highly supported and recommended.

Thermal characteristics and cadmium binding behavior of EC-ELP fusion polypeptides.

Elastin-like polypeptides (ELPs) are stimulus-responsive protein-based biopolymers that exhibit phase transition behavior. By joining them to synthetic phytochelatin (EC), EC-ELP fusion proteins with temperature sensitivity and metal-binding functionality were generated to remove heavy metal ions biologically. Three different EC domains (EC10, EC20, EC30) were incorporated into the ELP, and the EC-ELP fusion proteins were expressed in E. coli. Their thermal properties and metal binding abilities were then investigated according to the EC length. In addition, the feasibility of reusing EC-ELPs and the cadmium ion binding affinity of reused EC-ELPs were explored.

Toxic heavy metal cadmium removal using chitosan and polypropylene based fiber composite.

The aim of the present work was to evaluate the performance of polypropylene (PP)/sisal fiber (SF)/banana fiber (BF) and chitosan-based hybrid (chitosan(CS)/SF)/BF) composite materials for the adsorptive removal of cadmium (Cd) ions from water waste. Polypropylene is harnessed for its importance in forming strong composite materials for various applications. Chitosan biopolymer encloses a great deal of amino and hydroxyl groups, which provide effective removal of Cd ions from wastewater. The batch adsorption studies proved that the removal of Cd ions was pH-dependent and attained optimum at pH 5.5 for both the composites. Langmuir and Freundlich models were applied for the obtained experimental values. Based on the R2 values, it was evidenced that the adsorption process was best fitted with the Freundlich isotherm than Langmuir. The sorption capacity of CS/SF/BF hybrid composite (Cmax = 419 mg/g) is higher than PP/SF/BF composite (Cmax = 304 mg/g), and allows multilayer adsorption. Kinetics studies revealed that the pseudo-second-order model was followed during the removal of Cd ion from wastewater. The overall evaluation proved that though both the adsorbents are suitable for the removal of Cd ions, the efficiency of CS-based ternary composite material is better than PP-based composite.

Properties and adsorption mechanism of magnetic biochar modified with molybdenum disulfide for cadmium in aqueous solution.

In this paper, we present the preparation of MoS2-modified magnetic biochar (MoS2@MBC) as a novel adsorbent by a simple hydrothermal method. MoS2@MBC contains abundant S-containing functional groups that facilitate efficient Cd(II) removal from aqueous systems. We employed various characterization techniques to explore the morphology, surface area, and chemical composition of MoS2@MBC; these included Brunauer-Emmett-Teller analysis scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and X-ray diffraction,. The results indicated the successful decoration of the surface of MoS2@MBC with iron and MoS2, and a higher surface area of MoS2@MBC than that of unmodified biochar. Moreover, adsorption properties including thermodynamics and kinetics were investigated along with the effects of pH, humic acid, and ionic strength on the Cd(II) adsorption onto MoS2@MBC. The O-, C-, S-, and Fe-containing functional groups on the surface of MoS2@MBC led to an electrostatic attraction of Cd(II) and strong Cd-S complexation. The Langmuir and pseudo second-order models fitted best for the batch adsorption experiments results. The adsorption capacity of MoS2@MBC (139 mg g-1 on the basis of the Langmuir model) was 7.81 times higher than that of pristine biochar. The adsorption process was found to be pH-dependent. The experimental results indicated that MoS2@MBC is an effective adsorbent for removing Cd(II) from water solutions. Further, the adsorption process involved the complexation of Cd(II) with oxygen-based functional groups, ion exchange, electrostatic attraction, Cd(II)-π interactions, metal-sulfur complexation, and inner-surface complexation. This work provides new insights into the Cd(II) ions removal from water via adsorption. It also demonstrates that MoS2@MBC is an efficient and economic adsorbent to treat Cd(II)-contaminated water.

Cadmium binding characterization and mechanism of a newly isolated strain Cystobasidium oligophagum QN-3.

The aim of this study was to screen a strain for the removal of Cd2+ from aqueous solution and investigate the characterization and mechanism of the Cd2+ binding process. A novel strain of yeast showed high tolerance of cadmium, namely Cystobasidium oligophagum QN-3, was isolated from soils, which could resist 22,000 mg/L and 18,000 mg/L Cd2+ on PDA (potato dextrose agar) plate and in PDA liquid medium, respectively. Cd2+ binding experiment showed that the strain could remove Cd2+ from aqueous solution effectively, the maximum Cd2+ removal rate of 84.45% was achieved at initial Cd2+ concentration 30 mg/L. Scanning electron microscopy (SEM) analysis revealed that sorption of Cd2+ by cells could be associated with changes in the cell surface morphology. Fourier transform-infrared spectroscopy (FTIR) analysis confirmed the important role of the functional groups OH, CO, NH2 , COO, PO, and CH on the cell surface in the binding of Cd2+ . The comparison of the binding ability of different cellular parts indicated a significant role of the cell wall played in the Cd2+ binding process. Pretreatment of the cells by boiling or ultrasonication could improve the biosorption capacity of QN-3. In addition, QN-3 exhibited selective and preferential property of binding capacity for other heavy metals, such as Pb2+ , Cu2+ , Cd2+ , Zn2+ , and Ni2+ . These data suggested the promising use of Cystobasidium oligophagum QN-3 as an effective and friendly biosorbent for cadmium or other heavy metals decontamination in the environment.

Preparation and characterization of PAN nanofibers containing boehmite nanoparticles for the removal of microbial contaminants and cadmium ions from water.

Nanofibers of polyacrylonitrile (PAN)/boehmite were prepared by electrospinning a homogeneous solution of PAN/DMF (dimethyl formamide). Enhancing the amount of boehmite nanoparticles (NPs) led to increase in the nanofibers' diameter. Samples had high pure water flux, which did not change significantly with boehmite concentration, but decreased with increasing electrospinning duration. Escherichia coli bacteria removal was remarkably more efficient, as it was enhanced from 72.33% to 97.37% with increase in the boehmite NPs' concentration from 0 to 10% wt. High bacterial removal efficiency could be attained by the large surface area of NPs, as well as the electrostatic force of attraction between NPs and microorganisms. The increase in boehmite concentration from 10 to 30 and 50% did not noticeably affect bacterial removal. Prolonging electrospinning time significantly enhanced bacteria removal. Hence, it was shown that 6-hour electrospinning of PAN/boehmite nanofiber layers composed of 50% boehmite led to 99.7%, 99.39%, 99.8%, and 74% E. coli, Staphylococcus aureus bacteria removal, particles' separation efficiency of 2 µm and cadmium adsorptivity, respectively, which were better than those obtained by using pure PAN nanofibers. E. coli bacterial removal efficiency of the sample was increased to 99.99% by repeating filtering four times. Considering the results, this PAN/boehmite nanofibers' membrane has potential application to purification of drinking water.

Genetic Engineering-Facilitated Coassembly of Synthetic Bacterial Cells and Magnetic Nanoparticles for Efficient Heavy Metal Removal.

Heavy-metal pollution is becoming a worldwide problem severely threatening our health and ecosystem. In this study, we constructed a genetic-engineering-driven coassembly of synthetic bacterial cells and magnetic nanoparticles (MNPs) for capturing heavy metals. The Escherichia coli cells were genetically engineered by introducing a de novo synthetic heavy-metal-capturing gene (encoding a protein SynHMB containing a six-histidine tag, two cystine-rich peptides, and a metallothionein sequence) and a synthetic type VI secretory system (T6SS) cluster of Pseudomonas putida, endowing the synthetic cells (SynEc2) with high ability of displaying the heavy-metal-capturing SynHMB on cell surface. MNPs were synthesized by a coprecipitation method and further modified by polyethylenimine (PEI) and diethylenetriaminepentaacetic acid (DTPA). Owing to the surface exposure of six-histidine tag on the synthetic bacteria and carboxyl groups on the modified MNPs (MNP@SiO2-PEI-DTPA), the synthetic bacterial cells and MNPs coassembled to form biotic/abiotic complex exhibiting a self-developing characteristic. In the culture medium containing both Cd2+ and Pb2+, the coassemblies captured these heavy metals with high removal efficiency (>90% even at 50 mg/L of Cd2+ and 50 mg/L of Pb2+) and were conveniently recycled by artificial magnetic fields. Moreover, the coassemblies realized coremoval of organic carbon pollutants with the removal efficiency of >80%. This study builds a novel biotic/abiotic coassembling platform facilitated by genetic engineering and sheds light on development of artificial magnetic biological systems for efficient treatment of environmental pollution.

Salicylaldehyde derivative of nano-chitosan as an efficient adsorbent for lead(II), copper(II), and cadmium(II) ions.

In this study, a biodegradable natural polymer chitosan was modified with salicylaldehyde to prepare salicylaldehyde functionalized chitosan nanoparticles (N-Ch-Sal). The N-Ch-Sal was characterized by atomic force microscopy (AFM), scanning electron microscopy-energy-dispersive X-ray (SEM-EDX), Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA). The salicylaldehyde functionalized chitosan nanoparticles (N-Ch-Sal) (~80 nm) were then used for the adsorption of three heavy metals viz., Cu(II), Cd(II) and Pb(II) ions. The above-mentioned techniques were also employed for evaluation of changes in N-Ch-Sal after metal adsorption. The parameters affecting the adsorption of metal ions including pH, contact time, amount of adsorbent, initial metal ion concentration and the effect of interfering ions, were studied thoroughly and optimized. The concentration of metal ions remaining in the aqueous system after adsorption experiments was analyzed by ICP-MS. At optimal conditions, sorption capacity of Pb(II) ion was found to be highest i.e., 123.67 followed by Cu(II) (84.60) and Cd(II) (63.71 mg/g). The adsorption process followed the pseudo-second-order kinetic model and fitted well with the Langmuir adsorption isotherm. The adsorption method was applied to a real tap water sample for the quantification and removal of Pb(II) ions. The concentration of Pb(II) ions in the tested sample was 4.88 ppb.

Inoculation of Cd-contaminated paddy soil with biochar-supported microbial cell composite: A novel approach to reducing cadmium accumulation in rice grains.

Bioremediation of heavy metal-contaminated soil using metal-resistant microbes is a promising remediation technology. However, as exogenous bacteria sometimes struggle to survive and grow when introduced to new soils, it is important to develop appropriate carriers for microbial populations. In this study, we report a novel approach to remediating Cd-contaminated rice paddy soil using biochar-supported microbial cell composites (BMCs) produced from agricultural waste (cornstalks). Pot experiments showed that amendment with BMC was more efficient at reducing root and grain Cd content than pure bacteria, while improving soil Cd fractionation toward more stabilized and less labile forms. Bacteria in the BMC medium grew more readily with more abundant metabolites than those raised in free cells, probably because biochar provides shelter via porous structures (as confirmed by scanning electron microscopy) as well as additional nutrients. Overall, the improved long-term production of microbial biomass caused by BMC inoculation results in a higher remediation efficiency. Our results demonstrate the feasibility of using biochar as an appropriate carrier for metal-tolerant bacteria to remediate Cd-contaminated paddy fields.

Simultaneous immobilization of the cadmium, lead and arsenic in paddy soils amended with titanium gypsum.

In situ immobilization of heavy metals in contaminated soils using industrial by-products is an attractive remediation technique. In this work, titanium gypsum (TG) was applied at two levels (TG-L: 0.15% and TG-H: 0.30%) to simultaneously reduce the uptake of cadmium (Cd), lead (Pb) and arsenic (As) in rice grown in heavy metal contaminated paddy soils. The results showed that the addition of TG significantly decreased the pH and dissolved organic carbon (DOC) in the bulk soil. TG addition significantly improved the rice plants growth and reduced the bioavailability of Cd, Pb and As. Particularly, bioavailable Cd, Pb and As decreased by 35.2%, 38.1% and 38.0% in TG-H treatment during the tillering stage, respectively. Moreover, TG application significantly reduced the accumulation of Cd, Pb and As in brown rice. Real-time PCR analysis demonstrated that the relative abundance of sulfate-reducing bacteria increased with the TG application, but not for the iron-reducing bacteria. In addition, 16S rRNA sequencing analysis revealed that the relative abundances of heavy metal-resistant bacteria such as Bacillus, Sulfuritalea, Clostridium, Sulfuricella, Geobacter, Nocardioides and Sulfuricurvum at the genus level significantly increased with the TG addition. In conclusion, the present study implied that TG is a potential and effective amendment to immobilize metal(loid)s in soil and thereby reduce the exposure risk of metal(loid)s associated with rice consumption.

Hybrid ash/biochar biocomposites as soil amendments for the alleviation of cadmium accumulation by Oryza sativa L. in a contaminated paddy field.

A novel ash/biochar (A/B) biocomposite composed of 90% biomass bottom ash from agroforestry biomass direct-fired power plants, 5% animal-derived biochar from carcass pyrolysis, and 5% bentonite as an adhesive was amended in cadmium (Cd)-polluted paddy soil to alleviate cadmium accumulation by Oryza sativa L. Ash increased the soil pH and contributed exogenous available silicon. Biochar with high Ca/P components played an important role in soil cadmium immobilization. A 1-year field experiment with consecutive rice growing seasons (early and late rice) was conducted in Xiangtan, China, to examine the effects of A/B amendment in Cd-contaminated paddy soil. The A/B biocomposite was amended into soil through one-time addition at three application rates (1, 5, and 10 kg/m2). When A/B amendment was ≥5 kg/m2, the soil pH increased from 4.11 to more than 6. The available silicon content in the soil even increased by 22.9 times. For early rice soil, the CaCl2-extractable Cd(II) and toxicity characteristic leaching procedure (TCLP)-extractable Cd(II) decreased by 77.9%-96.1% and 52.4%-70.7%, respectively. A/B remarkably reduced Cd accumulation in rice organs, and this observation was related to A/B treatment rates. Ash and biochar contributed to the inhibition of Cd accumulation in rice organs and Cd translocation from roots to stems. The Cd concentrations in brown rice decreased to 0.11 and 0.12 mg/kg in early and late rice, respectively, and these values were lower than the national food safety standard limit value of China (0.2 mg/kg).

Phosphorus influence Cd phytoextraction in Populus stems via modulating xylem development, cell wall Cd storage and antioxidant defense.

The soils in mining lands with cadmium (Cd) contamination usually are deficient in nutrients. Disclosing how P nutrition and N:P stoichiometric ratio influences Cd accumulation and stress tolerance in stems of Populus spp. will facilitate the phytoremediation of mining sites polluted by Cd. In this study, investigations at the anatomical and physiological levels were conducted using a clone of Populus × euramericana. Both phosphorus deficiency and cadmium exposure inhibited xylem development via reducing cell layers in the xylem. Under P-sufficient condition, appropriate P status and balanced N:P ratio in stem promoted xylem development under Cd exposure via stimulating cell division, which enhanced Cd accumulation in stems. Cd accumulation in cell walls of collenchyma tissues of the stem was enhanced by P application due to increased polysaccharide production and cell wall affinity for Cd. The low P concentrations (0.3-0.4 mg g-1) and imbalanced N:P ratio under P deficiency inhibited the production of APX and ascorbate-GSH cycle, which increased oxidative stress and lipid peroxidation as indicated by high MDA concentration in stem. Under P-sufficient condition, the interactions between phytohormones and antioxidants play crucial roles in the process of antioxidant defense under Cd exposure. In conclusions, appropriate P addition and balanced N:P ratio enhanced secondary xylem development and promoted cadmium accumulation and stress tolerance in Populus stems, which can benefit the phytoextraction of Cd from Cd-contaminated soil.

Goethite-modified biochar restricts the mobility and transfer of cadmium in soil-rice system.

Cadmium (Cd) contamination of paddy soils has raised serious concerns for food safety and security. Remediation and management of Cd contaminated soil with biochar (BC) and modified biochar is a cost-effective method and has gained due attention in recent years. Goethite-modified biochar (GB) can combine the beneficial effects of BC and iron (Fe) for remediation of Cd contaminated soil. We probed the impact of different BC and GB amendments on Cd mobility and transfer in the soil-rice system. Both BC and GB effectively reduced Cd mobility and availability in the rhizosphere and improved the key growth attributes of rice. Although BC supply to rice plants enhanced their performance in contaminated soil but application of 1.5% GB to the soil resulted in prominent improvements in physiological and biochemical attributes of rice plants grown in Cd contaminated soil. Sequential extraction results depicted that BC and GB differentially enhanced the conversion of exchangeable Cd fractions to non-exchangeable Cd fractions thus restricted the Cd mobility and transfer in soil. Furthermore, supplementing the soil with 1.5% GB incremented the formation of iron plaque (Fe plaque) and boosted the Cd sequestration by Fe plaque. Increase in shoot and root biomass of rice plants after GB treatments positively correlates with incremented chlorophyll contents and gas exchange attributes. Additionally, the oxidative stress damage in rice plants was comparatively reduced under GB application. These findings demonstrate that amending the soil with 1.5% GB can be a potential remediation method to minimize Cd accumulation in paddy rice and thereby can protect human beings from Cd exposure.

Temperature-Driven Metalloprotein-Based Hybrid Hydrogels for Selective and Reversible Removal of Cadmium(II) from Water.

To develop biomaterials that easily and reversibly remove trace amounts of metal ions, we synthesized PNIPAM-co-CadRP, a thermally sensitive hybrid hydrogel by immobilizing a reconstituted cadmium binding peptide (CadRP) derived from the metalloregulatory protein CadR in a poly(N-isopropylacrylamide) (PNIPAM) gel network. The hybrid hydrogel retains the properties of the immobilized peptide and highly sensitively and selectively binds Cd(II) ions. The thermally sensitive properties of the hybrid hydrogel, which swells at low temperatures (<34 °C) and shrinks at high temperatures, provides a driving force sufficient to alternate the conformation of the immobilized CadRP such that the peptide captures and releases metal ions at high and low temperatures, respectively. Using this novel hybrid gel, we captured nanomolar Cd(II) from samples of environmental water in a highly efficient manner, leading to a practical and repeatedly reusable material to remediate our environment.

Effects of soaking, acidity and temperature on cadmium and lead removal from rice.

In this research, effect of soaking time, acidity and temperature on the removal of lead and cadmium from rice was investigated. Different rice treatments were involved i.e. three soaking times (0, 15, and 30 min), three temperatures (20, 25, and 30 °C) and four concentrations of glacial acetic acid (0.5%, 1%, 2%, and 3%). Results showed that few samples have shown lead concentrations above the maximum limit set by the World Health Organization (WHO) and the UN Food and Agriculture Organization (FAO) of 0.2 mg/kg, whereas, all cadmium concentrations were below the limit of 0.4 mg/kg. A decrease in lead and cadmium concentrations were observed with increasing time of soaking. Lead had the lowest concentration at 20 °C, while cadmium had the lowest concentration at 30 °C. Cadmium concentration decreased with increasing water acidity, while the lead concentration reached the lowest concentration with 1% acidity.

Insight into the mechanisms of plant growth promoting strain SNB6 on enhancing the phytoextraction in cadmium contaminated soil.

Plant growth-promoting rhizobacteria (PGPR) assisted accumulator has been proposed as a phytoextraction method to clean cadmium (Cd) in contaminated soil, while the mechanisms were few studied regrading PGPR-soil-accumulator as an assemble. In this study, we revealed the possible mechanisms of the plant growth-promotion strain SNB6 on enhancing the Cd phytoextration of vetiver grass by the analysis of the whole genome of SNB6, soil biochemical properties and plant growth response. Results showed that SNB6 encoded numerous genes needed for Cd tolerance, Cd mobilization and plant growth promotion. SNB6 increased HOAc-extractable Cd that showed a positive correlation with Cd uptake in accumulator. In addition, SNB6 improved the biochemical activities (bioavailability of nutritional substances, bacterial count, soil respiration and enzyme activity) in rhizosphere soil. Moreover, the antioxidative enzymes activities of accumulator were significantly enhanced by SNB6. Consequently, SNB6 promoted Cd uptake and biomass of accumulator, thus enhancing the Cd phytoextraction. The maximum Cd extractions in root, stem and leaf reached to 289.47 mg/kg, 88.33 mg/kg and 59.38 mg/kg, respectively. Meanwhile, the total biomass of accumulator was increased by 9.68-45.99% in SNB6 treatment. These findings could be conducive to the understanding the mechanisms of PGPR on enhancing the Cd phytoextraction of accumulator.

Efficiency and mechanisms of cadmium removal via core-shell zeolite/Zn-layer double hydroxides.

To investigate the removal mechanisms of cadmium (Cd) by Zn-layer double hydroxides-modified zeolites substrates in constructed rapid infiltration systems (CRIS), the ZnAl-LDHs and ZnFe-LDHs were synthesized and in-situ coated on the original zeolites through co-precipitation method. The prepared Zn-LDHs-modified and original zeolites were characterized by scanning electron microscope (SEM) and energy dispersive spectroscopy (EDS) methods, whose results provided the evidences that the Zn-LDHs were successfully coated on the original zeolites. From the results of purification experiments, the average Cd removal rates of ZnAl-LDHs-modified, ZnFe-LDHs-modified and original zeolites were 88.40, 86.00 and 32.52%, respectively; demonstrating that the removal rates of zeolites could significantly improve. Additionally, the modification of Zn-LDHS could enhance the theoretical adsorption ability. According to the results of isothermal adsorption and desorption tests, the desorption rates of Zn-LDHs-modified zeolites were higher than that of original zeolites. Cd adsorption capacity of ZnFe-LDHs-modified zeolites was 1428.57 mg kg-1 and original zeolites was 434.783 mg kg-1. In the adsorption kinetic studies, the pseudo-second-order models were used to well describe the experimental results of Zn-LDHs-modified zeolites, indicating that their adsorption types were attributed to be more stable chemisorption. Besides, the relevant microbial tests also confirmed that microbial enzymatic activity and extracellular polymeric substances (EPS) were significantly promoted on surface of Zn-LDHs-modified zeolites. The contents of EPS on the surface of zeolites were as following: ZnAl-LDHs-modified zeolites (78.58128 µg/g) > ZnFe-LDHs-modified zeolites (71.85445 µg/g) > original zeolites (68.69904 µg/g). Meanwhile, the results of high-throughput sequencing showed that modification by Zn-LDHs improved microbial diversity and relative abundance. The Proteobacteria was the dominant phylum and the Acidobacteria was conducive to Cd removal. Overall, it could be concluded that ZnAl-LDHs-modified zeolites might be applied as an efficient substrate for Cd removal in CRIS.

A water-soluble peptide fluorescent chemosensor for detection of cadmium (II) and copper (II) by two different response modes and its application in living LNcap cells.

A novel peptide-based fluorescent chemosensor (DGC) based on dansyl-appended dipeptide (Gly-Cys-NH2) was synthesized using SPPS technology. DGC exhibited highly sensitive detection of Cadmium (II) ions in 100% aqueous solutions through fluorescent "turn on" response and the detection limits of 14.5 nM. On the other hand, the fluorescence of DGC was almost completely quenched with fast response time when the addition of Cu2+ ions to DGC solutions, the detection limits for Cu2+ was 26.3 nM. In addition, the 2:1 binding stoichiometry of DGC with Cd2+ and Cu2+ were confirmed by Job's plot, fluorescent titration and HR-MS data. More importantly, MTT assays and fluorescence imaging experiments suggested that DGC has outstanding membrane permeability and hypotoxicity, and could be an efficient fluorescent chemosensor for Cd2+ and Cu2+ detection by two different response modes in living LNcap cells.

Role of concentration polarization in cross flow micellar enhanced ultrafiltration of cadmium with low surfactant concentration.

Concentration polarization is an important issue in micellar enhanced ultrafiltration (MEUF) of wastewater containing heavy metal ions at low surfactant concentrations. In this paper, we studied removal of Cd(Ⅱ) by cross flow MEUF at low sodium dodecyl sulfate (SDS) concentration levels, and the role of concentration polarization in flux decline and Cd(Ⅱ) rejection was emphasized. Concentration polarization resistance and SDS concentration near membrane were calculated to characterize concentration polarization. The results showed that SDS concentration near membrane was 13 mM when feed concentration was merely 0.8 mM. By combining phase diagram of SDS, structures of SDS micelles in concentration polarization layer were deduced and thin layer structure transformed to porous structure formed by accumulated globular micelles when SDS concentration increased. Although micelles formed in concentration polarization layer was responsible for flux decline, they also provided adsorption sites for Cd(Ⅱ).