Metal ion adsorbability of electrospun wool keratose/silk fibroin blend nanofiber mats

In this study, electrospun wool keratose (WK)/silk fibroin (SF) blend nanofiber was prepared and evaluated as a heavy metal ion adsorbent which can be used in water purification field. The WK, which was a soluble fraction of oxidized wool keratin fiber, was blended with SF in formic acid. The electrospinnability was greatly improved with an increase of SF content. The structure and properties of WK/SF blend nanofibers were investigated by SEM, FTIR, DMTA and tensile test. Among various WK/SF blend ratios, 50/50 blend nanofiber showed an excellent mechanical property. It might be due to some physical interaction between SF and WK molecules although FTIR result did not show any evidence of molecular miscibility. As a result of metal ion adsorption test, WK/SF blend nanofiber mats exhibited high Cu²⁺ adsorption capacity compared with ordinary wool sliver at pH 8.5. It might be due to large specific surface area of nanofiber mat as well as numerous functional groups of WK. Consequently, the WK/SF blend nanofiber mats can be a promising candidate as metal ion adsorption filter.     

Metal adsorption of tannin based rigid foams

Tannin based rigid foams are structures in which flavonoids are randomly cross-linked with furanic units throughout covalent bonds. The use of these aromatic substrates from natural materials to trap some heavy metal ions dissolved in water solutions is described. Interesting results have been achieved using different mimosa bark tannin (Acacia mearnsii formerly mollissima, De Wildt) and pine bark tannin (Pinus radiata) mixed foams. Capability to catch Pb²⁺ and Cu²⁺ ions at different concentrations has been verified throughout ICP-OES analysis of the foams. A reliable proportionality has been found between initial concentration and percentage of metal ions adsorbed. These foams were able to adsorb up to 12.5% of Cu(II) and 20.1% of Pb(II) with respect to the concentration of these ions in solution.     

Application of electrospun silk fibroin nanofibers as an immobilization support of enzyme

Silk fibroin (SF) nanofibers were prepared by electrospinning and their application as an enzyme immobilization support was attempted. By varying the concentration of SF dope solution the diameter of SF nanofiber was controlled. The SF nanofiber web had high capacity of enzyme loading, which reached to 5.6 wt%. The activity of immobilizedα-chymotrypsin (CT) on SF nanofiber was 8 times higher than that on silk fiber and it increased as the fiber diameter decreased. Sample SF8 (ca. 205 nm fiber diameter) has excellent stability at 25°C by retaining more than 90 % of initial activity after 24 hours, while sample SF11 (ca. 320 nm fiber diameter) shows higher stability in ethanol, retaining more than 45% of initial activity. The formation of multipoint attachment between enzyme and support might increase the stability of enzyme. From these results, it is expected that the electrospun SF nanofibers can be used as an excellent support for enzyme immobilization.     

Preparation of amidoxime-modified polyacrylonitrile nanofibers immobilized with laccase for dye degradation

A novel approach to preparing multifunctional composite nanofibrous membrane was developed. Polyacrylonitrile (PAN) nanofibrous membrane was fabricated by electrospinning and then the nitrile groups in PAN copolymer was chemically modified to obtain amidoxime modified PAN (AOPAN) nanofiber membrane which was further used as a functional support for laccase immobilization. During the process of reactive dye degradation catalyzed by the AOPAN nanofiber membrane immobilized with laccase, metal ion adsorption occurred at the same time. The chemical modification was confirmed by Fourier transform spectroscopy (FTIR). Scanning electron microscope (SEM) was employed to investigate the surface morphologies of the electrospun nanofibers before and after laccase immobilization. The effects of environmental factors on laccase activity were studied in detail. It was found that the optimum pH and temperature for the activity of immobilized laccase was 3.5 and 50 °C. The relative activity retention of the immobilized laccase decreased dramatically during the initial four repeated uses. After 20 days’ storage, the activity retention of immobilized laccase was still high above 60 %. It has also proved that laccase immobilized on AOPAN nanofiber membrane performed well in dye degradation and metal ion adsorption.     

A highly selective rhodamine based color turn on and fluorescence turn off sensor toward late IB metal ions

A fluorescence “turn-off” and color “turn-on” probe for late IB metal ions (Fe³⁺/Co²⁺/Ni²⁺/Cu²⁺/Zn²⁺) was developed based on rhodamine B. The probe was synthesized by condensation between rhodamine B and 8-hydroxyjulolidine-9-carboxaldehyde, which provided excellent selectivity function for late IB metal ions detection. It binds Cu²⁺ in a 1:1 stoichiometry in acetonitrile solution. This probe displays distinct color and fluorescence change upon the addition of late IB metal ions and little interference with other biologically relevant metal ions. Limit of detection for Cu²⁺, Fe³⁺, and Co²⁺ is higher than that of Zn²⁺ and Ni²⁺. In addition, the limit of detection toward Cu²⁺ is about 312 times lower than the World Health Organization (WHO) recommended level in drinking water.     

Preparation and BSA Adsorption Behavior of Chitosan-arginine Based Nanofiber Membranes

In this work, an affinity nanofiber membrane was successfully prepared by solution blowing of arginine-modified chitosan (CS-Arg) for bovine serum albumin (BSA) adsorption. CS-Arg was firstly synthesized by coupling L-arginine onto chitosan backbone. Then, CS-Arg nanofiber membranes (CANFs) were fabricated using solution blowing process with Polylactide (PLA) as assistant polymer. The results showed that CANFs effectively adsorbed BSA, and the adsorption capacities were influenced by the degrees of substitution (DS) of arginine in CS, pH value, contact time, and initial protein concentration. The highest adsorption capacity of 445.19 mg/g was achieved uvnder the following conditions: DS of 43.7 %, pH of 7.14, and initial concentration of 3.0 mg/ml. BSA adsorbed on the CANFs membrane conformed to Langmuir model, and the adsorption rate was consistent with the second-order kinetics model. This work implies that an arginine-modified chitosan nanofiber-based novel biomaterial has a potential application in adsorption of BSA.     

Synthesis of poly(hydroxamic acid) ligand from polymer grafted khaya cellulose for transition metals extraction

A cellulose-graft-poly(methyl acrylate) was synthesized by free radical initiating process and the ester functional groups were converted into the hydroxamic acid ligand. The intermediate and final products are characterized by FT-IR, FE-SEM, HR-TEM and XPS technique. The pH of the solution acts as a key factor in achieving optical color signals of metalcomplexation. The reflectance spectra of the [Cu-ligand]n+ complex was found to be a highest absorbance at 99.8 % at pH 6 and it was increased upon increasing of Cu²⁺ ion concentrations and a broad peak at 700 nm was observed which indicated the charge transfer (π-π transition) metals-Cu complex. The adsorption capacity of copper was found to be superior (336 mg g^?1) rather than other transition metals such as Fe³⁺, Co³⁺, Cr³⁺, Ni²⁺, Mn²⁺ and Zn²⁺ were 310, 295, 288, 250, 248 and 225 mg g^-1, respectively at pH 6. The experimental data of all metal ions fitted significantly with the pseudo-second-order rate equation. The transition metal ions sorption onto ligand were well fitted with the Langmuir isotherm model (R²>0.99), which suggested that the cellulose-based adsorbent known as poly(hydroxamic acid) ligand surface is homogenous and monolayer. The reusability of the poly(hydroxamic acid) ligand was checked by the sorption/desorption process up to ten cycles without any significant loss in its original sensing and removal performances.     

Detector for rapid detection of trace Cu<Superscript>2+</Superscript> in paddy water based on dual-wavelength quantum dot fluorescent probe

A novel device is designed for rapid detection of trace Cu²⁺ residues in paddy water using dual-wavelength quantum dot fluorescence probe. It includes three operation procedures: synthesis of dual-wavelength quantum dot, fluorescence excitation and acquisition of weak signal and signal conditioning. Based on the quenching principle of Cu²⁺ on quantum dot fluorescence, dual-wavelength quantum dot fluorescent probe can get lower limitation of detection. In addition, to improve the accuracy of testing results, two-channel detection was developed for avoiding interference. Experiment results demonstrate that the limitation for detection of trace Cu²⁺ in paddy water is 1.4 nM. The relationship between the Cu²⁺ concentration (x) and the ratio variation of dual wavelength (y) is y?=?2.15?×?exp(x/5.862)???1.154 with the coefficient of determination (R²) of 0.997 and the detection time of 4 min. Meanwhile, compared to other heavy metal ions, nutrient and organic compounds, the presented detector is of good selectivity for Cu²⁺ in paddy water. The repetitive detection experiments show that the developed device has high repeatability with relative standard deviation of 0.14%. The device can be used for quick and accurate detection of trace Cu²⁺ residues in paddy water with some specific advantages of high sensitivity, excellent selectivity and high repeatability.     

Ionochromism of Crystal Violet Lactone triggered by metal cations

The ionochromic properties of Crystal Violet Lactone(CVL), 3,3-bis(p-dimethylaminophenyl)-6-dimethylaminophthalate with metal cations were investigated. It showed interestingly ring open reaction with addition of several metal ions in CH₃CN solution. Upon addition of Hg²⁺, the CVL shows a new peak around 603nm in its absorption spectra, and the color of solution changed from colorless to blue. Whereas other ions including Fe³⁺, Cu²⁺, Fe²⁺, Al³⁺ and so on induced basically weakly spectral change, which makes it promising application in Hg²⁺ sensor.     

Antibacterial properties of silk fibroin/chitosan blend films loaded with plant extract

The silk fibroin (SF)/chitosan (CHI) blend films were prepared by dissolving them in formic acid. The morphology of the films was examined by scanning electron microscopy (SEM). The roughness of the membranes was determined by atomic force microscopy (AFM). These films were treated with the extracts of Pistacia terebinthus, Pistacia lentiscus, and Hypericum empetrifolium. Folin-Ciocalteu assay was used to determine the amount of total phenols adsorbed on these blend films. The antibacterial properties of films were tested using disc diffusion and turbidity measurement methods against Escherichia coli and Staphylococcus epidermidis. The release of adsorbed phenolics from the film surface resulted in antibacterial properties.     

Cadmium-Containing Carbonic Anhydrase CDCA1 in Marine Diatom Thalassiosira weissflogii

The Carbon Concentration Mechanism (CCM) allows phytoplakton species to accumulate the dissolved inorganic carbon (DIC) necessary for an efficient photosynthesis even under carbon dioxide limitation. In this mechanism of primary importance for diatoms, a key role is played by carbonic anhydrase (CA) enzymes which catalyze the reversible hydration of CO₂, thus taking part in the acquisition of inorganic carbon for photosynthesis. A novel CA, named CDCA1, has been recently discovered in the marine diatom Thalassiosira weissflogii. CDCA1 is a cambialistic enzyme since it naturally uses Cd²⁺ as catalytic metal ion, but if necessary can spontaneously exchange Cd²⁺ to Zn²⁺. Here, the biochemical and structural features of CDCA1 enzyme will be presented together with its putative biotechnological applications for the detection of metal ions in seawaters.     

Surface modified ployacrylonitrile nanofibers and application for metal ions chelation

Ployacrylonitrile (PAN) nanofibers were formed by electrospinning. Amidoxime ployacrylonitrile (AOPAN) nanofibers were prepared by reaction with hydroxylamine hydrochloride, which were used as the matrix for metal ions chelation. FTIR spectra of the PAN nanofibers and AOPAN nanofibers were recorded for analysis of the surface chemical structures. The AOPAN conventional fibers were also prepared for comparison, and surface morphologies of the modified PAN conventional fibers and PAN nanofibers were observed by FESEM. Metal ions concentrations were calculated by AAS. The chelated isothermal process and kinetics parameters of the modified PAN nanofibers and PAN conventional fibers were studied in this work. Results indicated that the saturated coordinate capacity of AOPAN nanofibers to Cu²⁺, Cd²⁺ was 3.4482 and 4.5408 mmol/g (dry fiber) respectively, nearly two times higher than that of AOPAN conventional fibers. Besides, the desorption rate of Cu²⁺ and Cd²⁺ from metal chelated AOPAN nanofibers was 87 and 92 % respectively in 1 mol/l nitric acid solution for 60 min. The isothermal processes were found to be in conformity with Langmuir model.     

Electrospun SiO<Subscript>2</Subscript>/PMIA nanofiber membranes with higher ionic conductivity for high temperature resistance lithium-ion batteries

The nanofiber membrane prepared by electrospinning has been widely applied in lithium-ion batteries. A powerful strategy for designing, fabricating and evaluating Poly-m-phenylene isophthalamide (PMIA) nanofiber membrane with SiO₂ nanoparticles was developed by electrospinning in this paper. The morphology, crystallinity, thermal shrinkage, porosity and electrolyte uptake, and electrochemical performance of the SiO₂/PMIA nanofiber membranes were investigated. It was demonstrated that the nanofiber membrane with 6 wt% SiO₂ possessed notable properties, such as better thermal stability, higher porosity and electrolyte uptake, resulting in higher ionic conductivity (3.23×10^-3 S·cm^-1) when compared with pure PMIA nanofiber membrane. Significantly, the SiO2/PMIA nanofiber membrane based Li/LiCoO₂ cell exhibited more excellent cycling stability with capacity retention of 95 % after 50 cycles. The results indicated that the SiO₂-doped PMIA nanofiber membranes had a potential application as separator in high temperature resistance lithium-ion batteries.     

Synthesis of electrospun carbon nanofiber/WO<Subscript>3</Subscript> supported Pt,Pt/Pd and Pt/Ru catalysts for fuel cells

In the present study, nano-sized Pt/WO₃-carbon nanofiber, Pt-Pd/WO₃-carbon nanofiber and Pt-Ru/WO₃-carbon nanofiber electrocatalysts were synthesized and the performance of prepared catalysts were compared with catalysts coated carbon black for the oxygen reduction reaction (ORR). The morphology and structure of prepared catalysts were characterized using scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis. The SEM images showed that the catalyst nanoparticles were well dispersed on the both carbon nanofiber and carbon black supports. Electrochemical measurements including linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS) and chronoamperometry (CA) tests were applied to investigate the potential of the fabricated electrodes on the ORR. The results demonstrated that the catalysts based on carbon nanofibers showed a significant increase of activity toward the ORR. Also, the Pt/Pd coated carbon nanofibrous electrode showed the highest electrochemical activity.     

Effective removal of calcium ions from simulated hard water using electrospun polyelectrolyte nanofibrous mats

The development of easily separated from water, high effective mineral ion removal materials is quite required in the hard water treatment system. In this study, water-stable polyelectrolyte polyacrylic acid (PAA) nanofibrous mats were fabricated by electrospinning technology and subsequent thermal crosslinking. Influence factors such as contact time, mat content, temperature and interfering ions strength were experimentally examined. The results indicated that polyelectrolyte PAA nanofibrous mats could be used as high effective Ca(II) ions removal material via complexation to form PAA?COOCa ²⁺ complex, with a maximum Ca(II) ion removal capacity of 152.8 mg/g within 60 min at 25 °C. Both equilibrium and kinetic studies showed that the behaviors of Ca(II) ions removal by polyelectrolyte nanofibrous mats followed Freundlich model and fitted pseudo-second-order model, respectively.     

Preparation of electrospun affinity membrane and cross flow system for dynamic removal of anionic dye from colored wastewater

In this research, poly(vinyl alcohol) (PVA)/chitosan electrospun nanofibrous membrane (ENM) was prepared by electrospinning method in order to investigate its dye removal ability from colored wastewater. The morphology and average fiber diameter of the membranes were investigated by scanning electron microscopy (SEM), image analysis and atomic force microscopy (AFM). The chemical characterization was studied by Fourier transform infrared spectroscopy (FTIR). The permeability of the membranes was evaluated by measuring pure water flux (PWF). In order to investigate the performance of the prepared membranes they were used in the batch adsorption and membrane separation for dye removal from colored wastewater. The effect of pH, number of membranes and dye concentration on the dye removal ability of the ENM was investigated. Response surface methodology (RSM) was used to achieve multi-objective optimization and equations of adsorption capacity and breakthrough time regarding operating conditions. The results demonstrated the potential of using PVA/chitosan nanofiber membrane as a microfiltration (MF) membrane for dye removal. Moreover, the recoverability property of prepared membranes was noticeable.     

Cloning and Characterization of a Novel Endo-Type Metal-Independent Alginate Lyase from the Marine Bacteria Vibrio sp. Ni1

The applications of alginate lyase are diverse, but efficient commercial enzymes are still unavailable. In this study, a novel alginate lyase with high activity was obtained from the marine bacteria Vibrio sp. Ni1. The ORF of the algB gene has 1824 bp, encoding 607 amino acids. Homology analysis shows that AlgB belongs to the PL7 family. There are two catalytic domains with the typical region of QIH found in AlgB. The purified recombinant enzyme of AlgB shows highest activity at 35 °C, pH 8.0, and 50 mmol/L Tris-HCl without any metal ions. Only K⁺ slightly enhances the activity, while Fe²⁺ and Cu²⁺ strongly inhibit the activity. The AlgB preferred polyM as substrate. The end products of enzymatic mixture are DP2 and DP3, without any metal ion to assist them. This enzyme has good industrial application prospects.     

Effects of crude oil spillage on growth and yield of maize (Zea mays L.) in soils of midwestern Nigeria

The effect of crude oil spillage on growth, productivity and nutrient uptake of maize (Zea mays L.) was assessed in a pot experiment using an Evwreni manifold sample of a petroleum development company, which had aspecific gravity of 0.8778. The Suwan 1 variety of maize was used in the experiment. In crude oil polluted soils, germination was delayed and the germination percentage was significantly affected by oil pollution. Growth was poor in polluted soils using parameters such as plant height, stem girth,ear height, leaf area at four weeks after planting, leaf area at maturity and average length of primary roots as growth indicators. Grain yield was significantly reduced at 95% level of probability with yield (when compared with the control) reduced by as much as 98.6%, 96.5% and 58.3% for preplant,five weeks after planting (5 WAP) and seven weeks after planting (7 WAP) treatments, respectively. Leaf analysis of the maize plants grown in soilscontaminated with crude oil a week before planting (preplant treatment) revealed mean levels of heavy metals (6.18 ppm Zn²⁺, 0.62 ppm Cu²⁺,26.24 ppm Fe²⁺, 10.84 ppm Mn²⁺, 2.96 ppm Pb²⁺ and 3.88 ppm Co²⁺) which are higher than the maximum permissible levels (MPL) for maize in tropical soils. Maize plants that were polluted at other time intervals showed no significant (p>0.05) variation in heavy metal concentrations when compared with the control, and were considered potentiallysafe for human consumption.     

Evaluation of a Thermophilic,Psychrostable, and Heavy Metal-Resistant Red Sea Brine Pool Esterase

Lipolytic enzymes catalyze the hydrolysis and synthesis of ester compounds. They are valuable in the pulp, food, and textile industries. This study aims to comprehensively evaluate the extreme properties of a hormone-sensitive lipase (EstATII-TM) isolated from the Red Sea Atlantis II brine pool. EstATII-TM was cloned, expressed, and its biochemical activities were assessed under different conditions. EstATII-TM catalytic properties and resistance to different metal ions were compared to commercial thermophilic esterases under different temperatures. Phylogenetically, EstATII-TM was assigned to the GDSAG motif subfamily of hormone-sensitive lipase. The optimal enzyme activity was evident at a temperature of 30 °C and pH 7–8. The enzyme retained 84.9% of its activity at 0.5 M NaCl. EstATII-TM maintained 93% to 97% activity at −40 and −20 °C, respectively. EstATII-TM activity was significantly enhanced, up to 10-fold, at temperatures ranging from 45 to 65 °C in the presence of 1 mM Cu²⁺, Cd²⁺, Ba²⁺, Mn²⁺, and Zn²⁺. EstATII-TM showed superior catalytic activity and resistance-to/enhancement-by metal ions compared to two commercial thermophilic esterases. The Red Sea Atlantis II brine EstATII-TM is characterized by tolerance to high temperatures, stability to hot and cold conditions, as well as toxic heavy metal contamination, making it an ideal candidate for industrial processes.     

Antimicrobial electrospun silk fibroin mats with silver nanoparticles for wound dressing application

In this report, silk fibroin (SF) mats coated with silver nanoparticles (AgNPs) were manufactured as a prototypic wound dressing and evaluated for antimicrobial properties. SF was extracted from cocoons of Thai silkworms Bombyx mori (variant Nangnoi Si Sa Ket) and fabricated into nonwoven mats by electrospinning. In a one-step synthesis method, colloidal AgNPs were prepared from silver nitrate by gamma irradiation and inspected by transmission electron microscopy. Using the in vitro disc diffusion and growth-inhibition assays, AgNP-coated SF mats effectively inhibited the growth of Staphyllococus aureus and Pseudomonas aeruginosa when the coating solution containing colloidal AgNPs was 4 mM, or equivalent to 50.4 ng/cm² of adsorbed AgNPs. Based on these results, the AgNP-coated SF mats can potentially be used as antimicrobial wound dressings.