Ethylenediaminetetraacetic Acid Disodium Salt Research Articles

Bimetallic PdCu Nanoparticles for Electrocatalysis: Multiphase or Homogeneous Alloy?

Crystal phase structure of bimetallic alloy is an important factor determining the electrocatalytic activity toward oxidation of energy molecules. In this paper, PdCu bimetallic NPs with similar element composition and different crystal phase structural features have been synthesized hydrothermally by adjusting the content of ethylenediaminetetraacetic acid disodium salt (EDTA-2Na). Multiphase PdCu NPs composed of pure Pd and alloy phase are obtained with a low concentration (even as low as zero) of EDTA-2Na in synthetic systems while homogeneous PdCu alloy NPs are formed in the presence of EDTA-2Na with a high concentration. The catalytic activity of ethanol electrooxidation is increased from 3.1 mA·cm-2 of pure Pd NPs, to 3.6 mA·cm-2 of multiphase PdCu NPs, and to 5.0 mA·cm-2 of homogeneous PdCu alloy NPs (about 2360 mA mgPd-1). The surface composition and structural stability of homogeneous PdCu NPs were much less damaged during electrochemical measurements. Based on the experimental data, the formation mechanism of multiphase and homogeneous PdCu NPs and their structure-property relationship have been discussed.

Reusable Magnetic Nanoparticle Immobilized Nitrogen-Containing Ligand for Classified and Easy Recovery of Heavy Metal Ions.

Functionalized Tris[2-(dimethylamino) ethyl] amine (Me6TREN) ligands tethered-Fe3O4@Me6TREN nanoparticles (NPs) with a size of 150 nm were prepared to achieve classified and easy recovery of heavy metal ions in wastewater. The preparation of such NPs related to sequential silane ligand exchange and a following cure and Schiff base reactions for Fe3O4 NPs. Fe3O4@Me6TREN NPs as an effective nano-adsorbent of heavy metals exhibited significant differences in maximum adsorption capacity for Cr(III) (61.4 mg/g), Cu(II) (245.0 mg/g), Pb(II) (5.3 mg/g), and Cd(II) (1136.2 mg/g), in favor of classified removal of heavy metals from wastewater. Furthermore, Fe3O4@Me6TREN NPs can be regenerated by desorbing metal ions from NP surfaces eluted with ethylenediaminetetraacetic acid disodium salt (EDTA-Na2) aqueous, which endows such NPs promising potency as new nano-vectors for the removal of heavy metals.

Highly luminescent Cit/CaF2: Ce3+, Tb3+ nanoparticles and detection of Cu2+ ions

Terbium doped calcium fluoride (CaF2:Tb3+) and cerium co-doped CaF2:Tb3+ (CaF2:Ce3+, Tb3+) nanoparticles were synthesized by the hydrothermal method by using citric acid (Cit) as surfactant. The as-synthesized nanoparticles have good dispersibility in water to form an aqueous transparent dispersion at a concentration of 20 mg/mL. The nanoparticles have the CaF2-type cubic structures. Photoluminescence (PL) investigation showed that energy transfer can be occurred effectively from Ce3+ ions to Tb3+ ions in Cit/CaF2: Ce3+, Tb3+ nanoparticles. And the PL intensity of Cit/CaF2: Ce3+, Tb3+ nanoparticles is very strong at a low concentration of 1 mg/mL, which is 16-fold as high as that of Cit/CaF2: Tb3+ nanoparticles. The strong green emission from Cit/CaF2: Ce3+, Tb3+ nanoparticles can selectively be quenched by Cu2+ ions in comparison to other metal ions and its detection limit is 1.02 × 10−5 M in an aqueous solution. The PL quenching is reversible by the addition of ethylenediaminetetraacetic acid disodium salt (EDTA-2Na) with the recovery of almost 80% of the original PL. The results revealed that Cit/CaF2: Ce3+, Tb3+ nanoparticles could find a promising application for the detection of Cu2+ ions in an aqueous solution.

Weathering mechanism of red discolorations on Limestone object: a case study from Lingyan Temple, Jinan, Shandong Province, China

Red discolorations are an effloresce phenomenon detect on the surface of stone objects and considered as damage factor in both esthetic and conservation points of view. It is very difficult to remove and seldom report about their weathering mechanism. Recently, numerous of red discolorations have affected the limestone objects of Lingyan Temple in Shandong province, one of the most important building materials in China. In order to set up the appropriate conservation remedy, it is essential to identify the origin, characteristics, composition, and the formation process of red discolorations. Several analytical and investigation techniques, such as X-ray fluorescence spectroscopy (XRF), X-ray diffraction (XRD), Micro-Raman spectroscopy (Raman), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) equipped with energy dispersive spectrometer (EDS) were used to better understand the red discolorations. The results demonstrated that the discolorations on limestone surface have been caused by carbonic acid weathering process. The red discolorations consisted mainly of kutnohorite (Ca(Fe,Mg,Mn)CO3) and iron oxides. They showed tabular, lamellar, and granular morphologies, which originated from the in situ carbonic acid weathering of kutnohorite. After rainfall, the Ca, Mg, Mn ions with relatively high solubility were primarily leached from carbonatite phases. It was resulting in the sedimentation of red iron oxides through a chemical reaction and physical adhesion. Based on those analyses, a chelating agent (ethylenediamine tetraacetic acid disodium salt) was chosen to remove theses red discolorations on the stone object.

Safety and efficacy of DSP® (Na2EDTA, tannin-rich extract of Castanea sativa, thyme oil and origanum oil) for pigs for fattening.

Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety for the environment and efficacy of DSP ® (a mixture of disodium salt of ethylenediaminetetraacetic acid (Na2 EDTA), tannin‐rich extract of Castanea sativa, thyme oil and origanum oil) as a zootechnical feed additive for pigs for fattening. The European Commission request followed an inconclusive opinion of the FEEDAP Panel published in 2016. The applicant submitted additional information to allow the FEEDAP Panel to complete its assessment; these additional data, related to the safety for the environment and the efficacy of the additive, were the subject of this opinion. Concerning safety for the environment, the risk quotient (PEC/PNEC) value for aquatic organisms was < 1, indicating no concerns of DSP ® for the aquatic compartment; no toxicity data for terrestrial organisms were provided and consequently no conclusion on the safety of DSP ® for the terrestrial compartment could be reached, as well as on the risk for groundwater contamination. Based on the results from three studies in pigs for fattening in which final body weight and average daily weight gain were increased, and feed to gain ratio was improved, the FEEDAP Panel concluded that DSP ® has the potential to be efficacious as a zootechnical additive in pigs for fattening.

Preparation of CaF2 Microspheres with Nanopetals for Water Vapor Adsorption

The hierarchically structured flower-like CaF2 microspheres with nanopetals, named FL-CaF2, were synthesized via a hydrothermal method using calcium acetate Ca(Ac)2 and NaBF4 as calcium and fluorine sources, respectively, assisted by the chelating reagent trisodium citrate (Na3Cit) with the optimal pH of the synthesis solution. Meanwhile, a reference sample, named FL-CaF2-R, was reproduced using ethylenediaminetetraacetic acid disodium salt (Na2EDTA) as the chelating reagent, based on the recipe and synthesis procedure from the literature. Various techniques such as X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Fourier transform-infrared spectroscopy, and N2 adsorption-desorption at 77 K were then used to characterize the synthesized samples. The results show that FL-CaF2 with a larger diameter has a much higher thermal stability than FL-CaF2-R because the larger the nanocrystallite size, the higher the thermal stability. The adsorption of water vapor on CaF2 is irreversible because CaF2 can interact with the adsorbed water molecules strongly. The dual-site Langmuir model was used to describe the measured adsorption isotherms of water vapor on FL-CaF2 at low water vapor pressures and 298, 308, and 318 K. FL-CaF2 has a much higher water-adsorption capacity than those reported in the literature. Furthermore, the isosteric heat of adsorption as a function of loading, derived from the measured isotherms, varies from ca. 46 to 43 kJ mol-1 in the whole loading range investigated. Finally, the applications of FL-CaF2 are anticipated in the dehydration of hydrogen fluoride gas as well as in catalysis.

Dual surfactants coassisted synthesis of CuO nanoleaves for activation of peroxymonosulfate to degrade acid orange 7

A facile and effective approach for synthesis of CuO with regular leaf structure and superior performance on activating peroxymonosulfate was reported. Polyvinylpyrrolidone and ethylenediaminetetraacetic acid disodium salt were used as structure-directing agents, whose synergistic effect was systematically investigated. Furthermore, it was found that the surface of CuO possessed abundant oxygen vacancies, which were ascribed to the collaborative action of dual agents and could enhance catalytic activity by facilitating the formation of active species and improving electron transfer. This research provides an effective strategy for injecting oxygen vacancies into metal oxides and will promote the application in water/environment cleaning.

Performance and toxicity of different absorption enhancers used in the preparation of Poloxamer thermosensitive in situ gels for ketamine nasal administration

The purpose of this study was to investigate the nasal absorption rate and nasal mucosal toxicity of thermosensitive ketamine in situ gels containing various absorption enhancers. The optimal composition ratio for the gel matrix was determined to be 17.2% Poloxamer 407 and 2% Poloxamer 188, as this combination resulted in solutions with a gelation point within the range found in the nasal cavity. Ketamine gels containing the tested enhancers, namely, ethylenediaminetetraacetic acid disodium salt, hydroxypropyl-β-cyclodextrin, propylene glycol, or Tween-80, were compared with enhancer-free counterparts to determine the absorption of the drug, in vivo by measuring its plasma levels in rats and in vitro using a Franz diffusion cell. Moreover, the toxicity of each gel type was assessed by microscopic observation of the morphology of rat nasal mucosa as well as by determining the mobility of the mucosal cilia using an established toad model. The results showed that gels containing hydroxypropyl-β-cyclodextrin could promote the absorption of ketamine without added toxicity compared to enhancer-free gels. Thus, we consider hydroxypropyl-β-cyclodextrin as the most promising absorption enhancer for the nasal administration of ketamine using in situ gels.

Co-doping effect of Amaranth and EDTA on bulk growth, optical, structural properties and second harmonic generation of KDP crystals grown by Sankaranarayanan-Ramasamy (SR) technique

KDP (Potassium dihydrogen phosphate) single crystals co-doped with Amaranth dye and EDTA (Ethylenediaminetetraacetic acid disodium salt) with concentrations of 0.005 mol% and 1 mol% respectively in the solution were grown from seeds by the method of temperature reduction and Sankaranarayanan-Ramasamy (SR) technique. The seeds were mounted vertically and in a direction of 59° from the vertical. The latter orientation of the seed made second harmonic generation (SHG) efficiency of KDP crystal with the 1064 nm laser reach its maximum value. Bulk growth, optical, and structural properties of the crystals were assessed by UV–Vis spectroscopy, X-ray diffraction (XRD) analysis, and photoluminescence. The elemental composition of crystals was also determined by Energy-dispersive X-ray (EDX) spectroscopy. Amaranth and EDTA additives have improved the SHG performance of pure KDP crystals by up to 168%, which probably could not be achieved by doping either with Amaranth or EDTA. Finally, three different parts of the crystal rods grown by SR technique were not homogeneous in the optical, structural properties and the degree of being dyed.

Multianalyte voltammetric determination of traffic-linked metals in marine organisms employed as pollution bio-monitors

ABSTRACT A new procedure is proposed for the voltammetric determination of ultra-trace cadmium(II), copper(II), lead(II), platinum(II), palladium(II), rhodium(III) and zinc(II) by a single run of square wave adsorptive catalytic stripping voltammetry. The voltammetric cell was based on a typical three-electrodes set-up: working electrode (stationary hanging mercury drop), reference electrode (Ag|AgCl|KClsat) and auxiliary electrode (platinum). The supporting electrolyte contained the formazone complex together with dimethylglyoxime and the disodium salt of ethylenediaminetetraacetic acid. Validation of the analytical procedure was obtained by the analysis of standard reference materials (Mussel Tissue BCR-CRM 278, Oyster Tissue NIST-SRM 1566a). Comparison with spectroscopic measurements was performed. Good accuracy was achieved. The analytical procedure was finally applied to mussels and clams sampled on the mouth of Po river, employed as bio-monitors.

The effect of surfactants on the particle size of iron, cobalt and nickel nanopowders

This paper studies the effect of surfactants on the particle size of metal nanopowders (NPs): iron, cobalt and nickel synthesized using chemical-metallurgy method – hydrogen reduction of hydroxide compounds FeOOH, Co(OH) 2 and Ni(OH) 2 at 400, 285, and 280 °С, respectively. These hydroxides were pre-synthesized via chemical deposition from the corresponding nitrate solutions with NaOH alkali solution (10 wt.%) using sodium dodecyl sulfate (SDS) (0.1 %) and ethylenediaminetetraacetic acid disodium salt (EDTA) (0.3 %). The obtained NPs were studied using such methods as X-ray diffractometry (XRD), scanning electron microscopy (SEM), and measurements of the specific surface area by low-temperature nitrogen adsorption. According to XRD shows that all the obtained samples of NPs Fe, Co and Ni contain pure metallic phases. The results of electron microscopic analysis and measurement of the specific surface area of powder samples show that the addition of various surfactants to the initial synthesis medium of hydroxide compounds has a significant effect on the size and morphology of the obtained NPs. It was found that the addition of 0.1 % SDS leads to a decrease in the average size of the obtained particles, and the presence of 0.3 % EDTA contributes to the formation of larger metal particles. It was shown that the use of 0.3 % EDTA in deposition of initial hydroxide precursors makes it possible to obtain metal NPs with the narrowest crystallite size distributions.

Maltobionic acid accelerates recovery from iron deficiency-induced anemia in rats.

In experiments 1 and 2, effect of ingestion of maltobionic acid calcium salt (MBCa) on recovery of rats from a latent iron deficiency and from iron deficiency anemia was examined, respectively. After grouping rats into control and iron-deficiency groups, a latent iron deficiency or iron-deficiency anemia was induced in the latter group. And recovery from these states by MBCa containing diets (0%, 3%, and 6% MBCa in diet, classified into MBCa-0, MBCa-3, and MBCa-6 groups) was compared for convalescence period in light of iron sufficient control group. In experiment 1, MBCa ingestion significantly increased the iron concentration in the serum and liver, and promoted recovery from a latent iron deficiency. In experiment 2, hemoglobin and hematocrit levels increased significantly with MBCa intake, and recovery from iron-deficiency anemia was promoted. MBCa effectively promoted the recovery of rats from a subclinical iron deficiency and iron-deficiency anemia.Abbreviations: ANOVA: analysis of variance; DMT1: divalent metal transporter 1; EDTA-2Na: disodium salt of ethylenediaminetetraacetic acid; Fpn: feroportin; Hb: hemoglobin; Ht: hematocrit; ICP-OES: inductivity coupled plasma optical emission spectrometer; MBCa: maltobionic acid calcium salt; nitroso-PSAP: 2-nitroso-5-[N-n-propyl-N-(3-sulfopropyl)amino]phenol; SE: standard error; SI: serum-iron concentration; TSAT: transferrin saturation; TIBC: total iron-binding capacity; UIBC: unsaturated iron-binding capacity.

Functional rGO aerogel as a potential adsorbent for removing hazardous hexavalent chromium: adsorption performance and mechanism.

A novel functional rGO aerogel was synthesized by a facile hydrothermal method. In this process, graphene oxide (GO) was used as the precursor and oxidant to synthesize the aerogels. Ethylenediaminetetraacetic acid disodium salt (EDTA-2Na) and pyrrole monomer (reducing agent) were selected to use as hole scavenger and nitrogen sources. The obtained EDTA-2Na/polypyrrole (Ppy)/rGO aerogel (EPGA) has a high adsorption capacity for Cr(VI) anions, and the maximum adsorption capacity reached 361mg/g at 298K at pH of 2. In addition, EPGA exhibited a good ability to selectively remove Cr(VI) anions under the effect of coexisting ions (Cl-, NO3-, SO42-, PO43-, Ni+, Cu2+, Zn2+, and Cd2+) and good regeneration ability. The kinetics process and adsorption isotherm can be fitted well with the pseudo-second-order kinetic model and Freundlich isotherm model, respectively. The removal mechanism involved electrostatic interaction, reduction, ion exchange, and chelation process. This work provides a simple and environmentally friendly synthetic route for EPGA, which will be a potential candidate for efficient removal Cr(VI) anions from industrial wastewater.

Synergetic activation of persulfate by heat and Fe(II)-complexes for hydrolyzed polyacrylamide degradation at high pH condition: Kinetics, mechanism, and application potential for filter cake removal during cementing in CO2 storage wells

The long-term integrity of the interface between cement and formation rock in CO2-capture and storage wells is crucial to avoid leakage of CO2 in/along wells. However, the interface can be easily damaged by the filter cake, which is a compressed composite of bentonite, polymers such as hydrolyzed polyacrylamide (HPAM), and barite, on the wellbore rock. Therefore, removing the filter cake during the cementing process by degrading HPAM in an efficient way is essential. In this study, chelated-Fe2+ activated potassium persulfate (KPS) was used for HPAM degradation and filter-cake removal. Ethylenediaminetetraacetic acid disodium salt dihydrate (EDTA-2Na) and diethylenetriaminepentaacetic acid (DTPA) were adopted to control the precipitation of Fe2+/Fe3+. A mixture of 0.4 mM Fe2+, 0.8 mM DTPA, and 4 mM KPS at a pH of 10.0 at 70 °C reduced the molecular weight of HPAM significantly from 3.0 × 106 to (3.6–10) × 104 Da. Electron paramagnetic resonance (EPR) analysis suggested that HO was the dominant radical and that SO4− and O2− were responsible for the degradation. The reactions conformed to continuous distribution kinetics with an activation energy of 38.36 kJ mol−1. A possible degradation pathway was proposed based on analyses via infrared spectroscopy (IR) and time-of-flight liquid chromatography-mass spectrometry (TOF-LC/MS). >90 wt% of the filter cake was removed by the system. The results suggest that the proposed DTPA-Fe2+ activated KPS system exhibits promising potential for in situ degradation of high molecular weight HPAM and for the removal of filter cake in downhole wells.

Дослідження процесів озонолізу органічних компонентів модельних розчинів рідких радіоактивних відходів реакторів ВВЕР

The article highlights the problem of reprocessing of liquid radioactive waste (LRW) from the Ukrainian nuclear power plants with VVER reactors. The main method of these LRW treatment is distillation (evaporation) and ion exchange sorption. The final products of LRW processing by distillation are distillation residues, spent sorbents and sludges, and salt melt with significant radioactivity accumulated in large volumes, which do not meet the long-term storage and disposal criteria. So, it is necessary to develop a new, more efficient LRW treatment scheme that can solve the problems of large volumes of LRW and transfer waste to a state suitable for long-term storage and disposal. One of the important and challenging problems of LRW treatment is the presence of organic components (ethylenediaminetetraacetic acid (EDTA), oxalic acid, synthetic surfactants (SPAR) in the waste, since these substances complicate removal of radionuclides from the LRW. The results of investigation of ozonolysis conditions of LRW organic components are presented on the example of a model solution with imitated solutions of disodium salt of ethylenediaminetetraacetic acid and ethane diacid. It was established, that ozonation of organic components of LRW results in decreasing of pH value, which causes reduction of their destruction efficiency. Control of the pH values at the initial level (11−12 units) by permanent alkalifying can increase the ozonolysis efficiency of LRW organic components in 30%. EDTA is better destructed by ozone than ethane diacid. Destruction of LRW organic components progresses in two stages: the first is fast and second is low. The maximum of EDTA destruction degree, in the experimental conditions, was 86%; destruction degree of ethane diacid — 51%; maximum of LRW model solution organic components (EDTA, ethane diacid, synthetic surface-active reagent) destruction degree was 67%. Due to co-precipitation and adsorption during the solution ozonizing, decrease in Mn concentration in LRW model solution reaches 94.3%, 137Cs activity decreases by 26%, and 90Sr — 15.7%, concentration of Co decreases only by 6%.

Therapeutic potential of xanthones from Swertia chirata in breast cancer cells.

Background & objectives:Medicinal plants like Swertia chirata are rich sources of different xanthones. This study was aimed to assess the cytotoxic potential of four most abundant xanthones present in S. chirata both in vivo and in vitro in Ehrlich ascites carcinoma (EAC), a mouse transplantable breast carcinoma cell line and two human breast carcinoma cell lines (MCF-7 and MDA-MB-231).Methods:Four xanthones derived from S. chirata namely 1-hydroxy-3,7,8-trimethoxyxanthone (XA), 1,8-dihydroxy-3,5-dimethoxyxanthone (XB), 1-hydroxy-3,5,8-trimethoxyxanthone (XC) and 1,5,8-trihydroxy-3-methoxyxanthone (XD) were used for determination of sub-lethal dose on the cell lines EAC, MCF-7, MDA-MB-231 and verified toxicity of sub-lethal dose on normal murine fibroblast cells. Cytotoxicity was measured in vivo and survivability of mice was plotted accordingly. Therapeutic efficacy of XD was evaluated both in vivo and in vitro by determination of lipid peroxidation (LPO), reactive oxygen species (ROS) generation and by quantitating the enzyme status (GSH, catalase, superoxide dismutase) in treated and untreated samples. DNA damage was evaluated using comet and DNA fragmentation assays. Furthermore, apoptotic effect was analyzed by flow cytometry and validated by TUNEL assay and Western blotting.Results:Among all the xanthones tested XD showed IC50 at the lowest dose, and normal cells were unaffected at this dose. Survivability of mice increased significantly when treated with XD compared to other xanthones and cisplatin. Significantly increased ROS and LPO were found in cancer cells as a result of XD treatment which was unaltered in normal cell line. XD induced DNA damage and apoptosis in cancer cell lines.Interpretation & conclusions:Our experimental data indicate that XD may potentially act as a chemotherapeutic agent by enhancing ROS in breast cancer cells thereby leading to apoptosis.

Acceleration and centralization of a back-diffusion process: Effects of EDTA-2Na on cadmium migration in high- and low-permeability systems

Pollutant accumulation in the low-permeability zones (LPZs) in groundwater systems is regarded as a secondary source, and its consequent back-diffusion can extend the timeframe of pump-and-treat remediation. However, the bioavailability and mobility of heavy metals and the medium characteristics can be changed during the process. This study investigated the accumulation and back-diffusion law of toxic metals and the effects of ethylenediaminetetraacetic acid disodium salt (EDTA-2Na) on them by implementing a series of tank experiments. In these experiments, a cadmium solution was injected first, and deionized water or EDTA-2Na constantly washed the system consisting of different medium layers. The experimental results showed that the cadmium breakthrough curves had some concentration gradient reverse points where the curves fluctuated with elution by deionized water, which did not exist when EDTA-2Na was the eluent. In these scenarios, the mass of accumulated cadmium in the media before elution was large, with a value of 931 mg (153 mg/kg), when the low-permeability medium was clay. However, when EDTA-2Na was injected together with cadmium, the value dropped to 319 mg (52.3 mg/kg), greatly reducing the cadmium accumulation. Additionally, the use of EDTA-2Na as an eluent resulted in the appearance of a secondary peak in the breakthrough curve, showing that EDTA-2Na accelerated and centralized the back-diffusion. Notably, the reduced cadmium accumulation in LPZs with the elution by EDTA-2Na was partly due to a reduced adsorption capacity of the clay minerals. The above results can advance the technology related to pump-and-treat remediation.

Mechanism study about the adsorption of Pb(II) and Cd(II) with iron-trimesic metal-organic frameworks

This study examined the effects of two kinds of iron-trimesic metal-organic frameworks (MOFs) [MIL-100(Fe) and Fe-BTC] on adsorption of Pb(II) and Cd(II). For both materials, adsorption of Pb and Cd nearly approached equilibriums in the initial 2 min with high pseudo-second-order kinetics rate constants (0.895 g·mg−1·min−1 for Pb and 1.416 g·mg−1·min−1 for Cd). Both materials showed better adsorption performance with the increase of solution pH (from 2 to 7). Adsorption processes were endothermic, entropy-increased and spontaneous. The higher enthalpy change (ΔH0) and entropy change (ΔS0) values for Cd adsorption reflected the more difficult adsorption of Cd compared with Pb, which is related with more negative hydration enthalpy (ΔHhydΘ) and larger ionic radius of Cd. Multilayer adsorption phenomena appeared with no maximum adsorptive capacity observed. Both Langmuir-Freundlich and Freundlich-BET models could well describe isotherms. Multilayer adsorption may be attributed to the formation of inner-sphere complexation and outer-sphere complexation. Bockris-Devanathan-Muller (BDM) electrical double layer theory was used for illustrating adsorption mechanism. The fixed-bed adsorption experiments with Fe-BTC showed outstanding elimination performance in initial operating period (>99.8% for Pb and >99.6% for Cd), with effective filtration volume of 980 mL for Pb and 300 mL for Cd. Recyclability test showed that Fe-BTC could be well regenerated by ethylenediamine tetraacetic acid disodium salt (EDTA-2Na). This study showed that MIL-100(Fe) and Fe-BTC are potential for practical heavy metal removal applications.

Recycling of Chemical Eluent and Soil Improvement After Leaching.

Ethylenediaminetetraacetic acid disodium salt (EDTA) was selected among various eluents due to its highest removal efficiency for lead (Pb) (43.7%) and zinc (Zn) (57.1%) leaching from Pb-Zn contaminated soil by soil column experiment. Compared with newly prepared EDTA eluent, using recycled EDTA eluent can still leaching down 71.1% of Pb and 63.2% of Zn respectively, which showed the reusable benefits of recycled EDTA eluent. After soils were leached by EDTA, soil quality decline, such as reducing of urease, catalase, invertase activities and microorganism numbers. However, adding 5% nutrition soil or earthworm fertilizer can significantly improve the quality of EDTA leached soil, and promote growth of peas and ryegrass compared with EDTA treatments. Overall, the improvement of EDTA leached soil by adding nutrition soil or earthworm fertilizer is important, and recycled EDTA eluent can recycle and re-use for Pb-Zn contaminated soil remediation.

Production, purification and biochemical characterization of the microbial protease produced by Lactobacillus fermentum R6 isolated from Harbin dry sausages

This study investigated the purification and biochemical characterization of the protease produced by Lactobacillus fermentum R6 isolated from Harbin dry sausages. The optimized fermentation conditions were as follows: a fermentation time of 48 h, an initial pH of 6 and a fermentation temperature of 37 °C. The 37.7 kDa extracellular protease was purified using ammonium sulphate deposition, an ion exchange layer system and gel filtration. The protease produced by L. fermentum R6 had the highest initial velocity and kcat/Km at pH 6, 40 °C. The microbial protease activity could be inhibited by ethylene diamine tetraacetic acid disodium salt (EDTA). The Vmax and Km of the protease were 58.2 ± 1.42 mg/min and 17.3 ± 0.85 mg/mL, respectively. Sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) reflected the ability of the protease to hydrolyse myofibrillar and sarcoplasmic proteins, in particular, myosin heavy chain, paramyosin, phosphorylase and creatine kinase-M type. In conclusion, L. fermentum R6 can be used as a starter culture or an enzyme-producing strain for the inoculation of Harbin dry sausages.