Studies of Adsorption of Cadmium Ions by Biowaste Adsorbent from Aqueous Solutions with Ion-Selective Electrodes and ICP-OES

Using environment-friendly and low-cost biowaste adsorbents as toxic metal ion removal substrates from aqueous solutions has a great economic advantage. This work evaluated pumpkin and potato peel biowastes for the adsorption of cadmium ions. The biowastes were treated with acid or base. Batch experiments were carried out by introducing a known concentration of metal ion solution into the biowaste sorbent at various pH levels. The pH and metal ion concentration was monitored with pH and cadmium ion-selective electrode continuously for two hours, and the final concentration for the metal ion after 24 hours was measured with the cadmium electrode and then confirmed with ICP-OES. L-type isotherms were obtained that fit to Freundlich model. Adsorption isotherms showed chemical adsorption and the kinetics following the second order model. Equilibrium adsorption capacity is higher than 29 mg/g at pH 5.6 when the initial concentration is 220 ppm. Dynamic cadmium adsorption capacity is 17 mg/g from aqueous solution when the feed solution is 220 ppm with pumpkin peel biowaste sorbent. The biowaste materials can be regenerated with acid washing.

Direct Determination of Potassium-Sodium Activity Ratio in Soil Suspension with Two Ion-Selective Electrodes

A K+-selective electrode and a Na+-selective electrode were used to construct a measuring cell without liquid-junction for the determination of the ion activity ratio of K+ to Na+ in soil suspensions. The measured cell potential was not affected by the total electrolyte concentration when the total cation concentration was 10-1-10-3 mol L-1 and the concentration ratio CK+ / CNa+. was 10:1 to 1:50. When the concentration ratios were equal to 1and the total electrolyte concentrations were 10-2 and 10-3 mol L-1, the ion activity ratio measurement would not be affected by pH in the pH range of 3.5 to 11.5 and 4.4 to 11 respectively. Ions other than H+ have no remarkable influence on the measurement. The ion activity ratio of K+ to Na+ measured directly in soil suspension agree well with those in centrifuged supernant solution. The relative deviation was within 4%. From the measured ion activity ratio, the difference of the bonding energies of K+ and Na+ ions was calculated.

Hetero-interfacial nickel nitride/vanadium oxynitride porous nanosheets as trifunctional electrodes for HER,OER and sodium ion batteries

The development of single electrode with multifunctional purposes for electrochemical devices remains a symbolic challenge in recent technology.This work explores interfacially-rich transition metal nitride hybrid that consist of nickel nitride and vanadium oxynitride(VO_(0.26)N_(0.52))on robust carbon fiber(denoted CF/Ni_(3)N/VON)as trifunctional electrode for hydrogen evolution reaction(HER),oxygen evolution reaction(OER),and sodium ion batteries(SIBs).The as-prepared CF/Ni_(3)N/VON exhibits low HER overpotential of 48 m V@10 m A cm^(-2),OER overpotential of 287 m V@10 m A cm^(-2),and sodium-ion anode storage reversible capacity of 555 m A h g^(-1)@0.2 C.Theoretical analyses reveal that the Ni_(3)N effectively facilitates hydrogen desorption for HER,increases the electrical conductivity for OER,and promotes the Na-ion storage intercalation process,while the VON substantially elevates the water dissociation kinetics for HER,accelerates the adsorption of OH*intermediate for OER and enhances the Na-ion surface adsorption storage process.Owing to the excellent HER and OER performances of the CF/Ni_(3)N/VON electrode,an overall water splitting device denoted as CF/Ni_(3)N/VON//CF/Ni_(3)N/VON was not only assembled showing an operating voltage of 1.63 V at current density of 10 m A cm^(-2)but was also successfully self-powered by the assembled CF/Ni_(3)N/VON//CF/Na_(3)V_(2)(PO_(4))_(3) flexible sodium ion battery.This work will contribute to the development of efficient and cost-effective flexible integrated electrochemical energy devices.

Constructing Bidirectional Fluorine-Rich Electrode/Electrolyte Interphase Via Solvent Redistribution toward Long-Term Sodium Battery

The high concentration electrolytes with specific solvation structure could passivate the electrodes to prolong battery cycle life but at the expense of increased cost,which limits the wide application in commercialization.The regular concentration(1_(M))electrolytes with suitable properties(viscosity,ionic conductivity,etc.)are cost-guaranteed,but undesired reactions would always occur and lead to battery degradation during long cycles.To promote the long-term cycle stability in a cost-effective way,this work constructs bidirectional fluorine-rich electrode/electrolyte interphase(EEI)by redistribution of solvents and electrochemical induction.The fluorinated effect with reasonable zoning planning restricts morphological disintegration,meanwhile,forms spatial confinement on cathode.In particular,the obtained cathode electrolyte interphase(CEI)gets the ample ability of Na^(+)transport,which benefits from the fluorinated organics arranged in the epitaxy and the hemi-carbonate content acting on the thickness.Thus,the electrochemical long cycling performance of F-NVPOFⅡF-CC full cells is significantly enhanced(the decay rate at 1 C per cycle is as low as 0.01%).Such a fluorine-rich EEI engineering is expected to take transitional layers against the degradation of cells and make ultra-long cycle batteries possible.

Preparation of CeO_2 Nanoparticles and Its Application to Ion-selective Electrodes Based on Acetyl Cellulose

CeO2 nanoparticles with an average diameter of about 30 nm were prepared by sol-gel method at lower temperature. The gel, transformed from the aqueous solution of metal nitrate and citric acid, can be combusted completely at lower temperature. The redox behavior and the crystallization process of the dried gel were studied by thermogravimetric analysis and infrared spectroscopy. The synthesized powders were characterized by X-ray powder diffraction and transmission electron microscopy. In addition, rare earth elements ion-selective electrodes based on acetyl cellulose were prepared using ultra fine cerium oxide powders.

Construction and Application of a PVC Membrane Enoxacin Ion-selective Electrode Based on a Needle-shaped Inner Reference Electrode

A PVC membrane enoxacin ion-selective electrode based on a needle-shaped inner reference electrode was prepared. A Ag/AgCl wire was used as the substrate of this electrode. It was previously coated with a thin sheet of urea-formaldehyde resin containing Cl - ions to form a needle-shaped inner reference electrode, then the inner reference electrode was coated with a thin sheet of a PVC membrane containing an enoxacin tetraphenylborate ion-pair complex. The influences of various ion-pair complexes, concentrations of the active components in the membrane and the plasticizers on the performance of the electrode were studied by orthogonal design. The linear response range of the electrode was 7.9×10 -5 -1.0×10 -2 mol/L. The detection limit was 2.0×10 -5 mol/L. The slope was 30.4 mV/decade(25 ℃). The electrode can be used for the potentiometric determination of enoxacin tablets directly. The average recovery was 100.4%, and the RSD was 0.9%. The results agreed with those determined by the method in Chinese Pharmacopoeia.

Potentiometric Urea Biosensor Based on Ion-Selective Electrode by Different Immobilization Procedures

Enzyme was immobilized on an ammonium ion-selective electrode by different methods.An ion-selective electrode is not completely ion-specific,and interfering ions react with the ion-selective electrode membrane,altering the measured potential.Therefore,the characteristics of the effect of other ions on ammonium ion-selective electrode-based urea biosensors are considered.Based on the experimental results,the urea biosensor based on entrapment had a high response voltage of around 189 mV and fast response time of around 16 sec.Moreover,selectivity of the urea biosensor in different interfering ions was considered to elucidate the characteristics of ammonium ion-selective electrode-based biosensors.

STUDY OF CALCIUM ION-SELECTIVE ELECTRODE BASED ON A NEW NEUTRAL CARRIER

A calcium ion-setective eletrode based on a new neutral carrier was studied.The electrode gives a Nernstian response in the rang 5.9-1 Pa and the response is stable in a wide pH range.Logarithms of setectivity coefficents are -2.3 Li(+),-3.5 Na(+),-4.0 K(+),-3.7NH_4(+),-4.5 Mg(2+) and -4.4Zn(2+).

Research progress on carbon materials as negative electrodes in sodium-and potassium-ion batteries

Carbon materials,including graphite,hard carbon,soft carbon,graphene,and carbon nanotubes,are widely used as high-performance negative electrodes for sodium-ion and potassium-ion batteries(SIBs and PIBs).Compared with other materials,carbon materials are abundant,low-cost,and environmentally friendly,and have excellent electrochemical properties,which make them especially suitable for negative electrode materials of SIBs and PIBs.Compared with traditional carbon materials,modifications of the morphology and size of nanomaterials represent effective strategies to improve the quality of electrode materials.Different nanostructures make different contributions toward improving the electrochemical performance of electrode materials,so the synthesis of nanomaterials is promising for controlling the morphology and size of electrode materials.This paper reviews the progress made and challenges in the use of carbon materials as negative electrode materials for SIBs and PIBs in recent years.The differences in Na+and K+storage mechanisms among different types of carbon materials are emphasized.

Generation of sodium hypochlorite (NaOCl) from sodium chloride solution using C/PbO_2 and Pb/PbO_2 electrodes

Two modified electrodes （Pb/PbO2 and C/PbO2） were prepared by electrodepositing a lead oxide layer on lead and carbon sub- strates. These modified electrodes were used as anodes for the generation of sodium hypochlorite （NaOC1） from sodium chloride solution. Different operating conditions and factors affecting the treatment process of NaOC1 generation, including current density, pH values, con- ductive electrolytes, and electrolysis time, were studied and optimized. By comparison the C/PbO2 electrode shows a higher efficiency than the Pb/PbO2 electrode for the generation of NaOC1.

Advanced flexible electrode materials and structural designs for sodium ion batteries

With the spectacular rise of wearable and portable electronics,flexible power supplying systems with robust mechanical flexibility and high energy storage performance under various mechanical deformation conditions are imperative to be needed.Sodium ion batteries(SIBs)with sustainable natural abundance,low cost and superb properties similar to equivalent lithium ion batteries(LIBs),which have shown significant potentials as energy source for flexible electronic devices.In this review,the recent advances in flexible electrode materials based on different types of conductive substrates are addressed and the strategies underlying rational design for flexible structures are highlighted,as well as their applications in flexible SIBs.The remaining key challenges in rational electrodes design are discussed,and perspectives for practical applications of flexible SIBs are proposed as general guidance for future research of high-performance flexible SIBs.

New layered metal oxides as positive electrode materials for room-temperature sodium-ion batteries

In order to achieve better Na storage performance, most layered oxide positive electrode materials contain toxic and expensive transition metals Ni and/or Co, which are also widely used for lithium-ion batteries. Here we report a new quaternary layered oxide consisting of Cu, Fe, Mn, and Ti transition metals with O3-type oxygen stacking as a positive electrode for room-temperature sodium-ion batteries. The material can be simply prepared by a high-temperature solidstate reaction route and delivers a reversible capacity of 94 m Ah/g with an average storage voltage of 3.2 V. This paves the way for cheaper and non-toxic batteries with high Na storage performance.

A Molecular-Sieving Interphase Towards Low-Concentrated Aqueous Sodium-Ion Batteries

Aqueous sodium-ion batteries are known for poor rechargeability because of the competitive water decomposition reactions and the high electrode solubility.Improvements have been reported by saltconcentrated and organic-hybridized electrolyte designs,however,at the expense of cost and safety.Here,we report the prolonged cycling of ASIBs in routine dilute electrolytes by employing artificial electrode coatings consisting of NaX zeolite and NaOH-neutralized perfluorinated sulfonic polymer.The as-formed composite interphase exhibits a molecularsieving effect jointly played by zeolite channels and size-shrunken ionic domains in the polymer matrix,which enables high rejection of hydrated Na^(+)ions while allowing fast dehydrated Na^(+)permeance.Applying this coating to electrode surfaces expands the electrochemical window of a practically feasible 2 mol kg^(-1) sodium trifluoromethanesulfonate aqueous electrolyte to 2.70 V and affords Na_(2)MnFe(CN)_(6)//NaTi_(2)(PO_(4))_(3) full cells with an unprecedented cycling stability of 94.9%capacity retention after 200 cycles at 1 C.Combined with emerging electrolyte modifications,this molecular-sieving interphase brings amplified benefits in long-term operation of ASIBs.

ELECTRODE SELECTION OF ELECTROLYSIS WITH MEMBRANE FOR SODIUM TUNGSTATE SOLUTION

Xiao Liansheng Wang Wei Zhang Qixiu Gong Bofan Cao Jiashu (Department of Metallurgical Science and Engineering, Central South University of Technology, Changsha 410083, China) Abstrac By measuring the electrode polarization curves of many kinds of materials and life spans of electrodes through intensifying electrolysis in the process, the appropriate electrode materials for different stages of electrolysis of sodium tungstate solution with membrane have been selected The effects of the electrodes with different shapes on electrolysis have been investigated. The result shows that network electrode is more suitable to electrolysis of sodium tungstate solution.

The Electrooxidation of Tetracycline at Acetylene Black Electrode in the Presence of Sodium Dodecyl Sulfate

The electrooxidation of tetracycline (TC) at acetylene black electrode has been studied in the presence of sodium dodecyl sulfate (SDS). Tetracycline (TC) exhibited very sensitive oxidation peak in this system. The peak current was proportional to TC concentration, and the detection limit was 1.2×10-8 mol/L. The system was used to the determination of TC in Pharmaceuticals.

Electrochemical oxidation of sodium sulfide on rotating ring-disc electrode

A rotating ring (Pt) disc (Pt) electrode was employed to investigate the oxidation process of sodium sulfide (Na 2S). It was reported that the oxidation intermediates and product of HS - were formed on the disc electrode and then reduced on the ring electrode. The results indicate that at a rotation rate of 20 Hz, when the disc electrode potential was -0.15 V (vs SHE) and higher, more extensive oxidation process took place via a series of electrochemical steps to produce sulfur (S). The products of oxidation intermediates (S 2- x , S 2- 2) and sulfur (S) reduced either on the ring electrode with a set potential of -0.8 V (vs SHE), or on disc electrode with negative going potential sweep at about -0.5～ 0.55 V (vs SHE). The experimental results of voltammogram of ring disc electrode at sodium sulfide solution demonstrated that the first step was the oxidation of HS - and produce S 2- x , and then the S 2- x adsorbed integrated itself and formed sulfur (S).

A comparative study of four 20-membered N_2S_4-crown ethers as ionophores for polymeric membrane silver selective electrodes

Four 20-membered N_2S_4-monoazathiacrown ethers have been synthesized and explored as neutral ionophores for Ag^+-selective electrodes.Potentiometric responses reveal that the flexibility of the ligands has great effect on the selectivity and sensitivity to Ag^+ ions.The electrode based on ionophore 9,10,20,25-tetrahydro-5H,12H-tribenzo[b,n,r][1,7,10,16,4,13]tetrathiadiaza cycloicosine 6,13-(7H,14H)-dione(C) with 2-nitrophenyl octyl ether(o-NPOE) as solvent in a poly(vinyl chloride)(PVC) membrane matrix sho...

Glassy carbon electrode modified with multi-walled carbon nanotubes sensor for the quantihication of antihistamine drug pheniramine in solubilized systems

A sensitive electroanalytical method for quantification of pheniramine in pharmaceutical formulation has been investigated on the basis of the enhanced electrochemical response at glassy carbon electrode modified with multi-walled carbon nanotubes in the presence of sodium lauryl sulfate.The experimental results suggest that the phcniramine in anionic surfactant solution exhibits electrocatalytic effect resulting in a marked enhancement of the peak current response.Peak current response is linearly dependent on the concentration of pheniramine in the range 200-1500 μg/mL with correlation coefficient 0.9987.The limit of detection is 58.31 μg/m L.The modified electrode shows good sensitivity and repeatability.

Determination of Boron Trifluoride in Boron Trifluoride Complex by Fluoride Ion Selective Electrode

A method was proposed to determine boron trifluoride in boron trifluoride complex using fluoride ion selective electrode(ISE). Hydroxide was chosen to mask aluminum for the determination of 0.01—0.1 mol/L of fluoride. The simulation indicated that the permissible aluminum masked at a certain p H value was limited and hardly related to F-concentration and boric acid. It is better to control p H value below 11.5 and the aluminum concentration within 0.025 mol/L to minimize the interference of hydroxide to the fluoride ISE. The decomposition conditions of boron trifluoride by aluminum chloride were investigated. It is found that the F-detection ratio will approach 1.0 if the Al/F molar ratio is 0.3—0.7 and aluminum concentration is no more than 0.02 mol/L when heated at 80 ℃ for 10 min. In one word, hydroxide is quite fit to mask aluminum for samples which contain high content of fluoride and aluminum and the BF3 content can be successfully determined by this method.

A Method of Preparation of Ag/AgCl Chloride Selective Electrode

We put forward a method of rapid preparation of chloride selective electrode（Ag/AgCl electrode） by dipping silver wire into sodium hypochlorite solution. The electrodes were prepared through different immersion time. The properties of the electrodes, such as Nernst response, response time and longterm stability, were tested in simulated concrete pore solutions（SCPS）. Moreover, the surface morphology of the electrodes was also detected after immersion in solutions over three months. The experimental results reveal that the Ag/AgCl electrode with the fabrication time of 20 minutes（E-20） which is recommended to work as the chloride ion selective electrode has the best performance. Compared to that fabricated by the electrolytic process（E-EP）, E-20 can be manufactured in mass. The method has almost the same good performance of Nernst response as E-EP, and has a better response time which is less than 25 seconds. The method also shows a better good long-term stability in SCPS containing chloride ions over three months.