Electrochemical Performance and Capacity Fading Mechanism of LiFePO4 at Different pH Aqueous Electrolyte Solutions

The electrochemical stability of LiFePO4 in a Li＋-containing aqueous electrolyte solution is critically dependent on the pH value of the aqueous solution. It shows a considerable decay in capacity of LiFePO4 upon cycling when the pH value is increased to 11. The mechanism responsible for the capacity fading is extensively investigated by means of cyclic voltammogram, ac impedance, charge/discharge, ex situ X-ray diffraction, and chemical analysis. LiFePO4 is relatively electrochemically stable in LiNO3 aqueous solution with pH=7. But the electrochemical performance of LiFePO4 in aqueous electrolyte is inferior to that in organic electrolyte. It is attributed to the loss of Li and the Fe, P dissolution during prolonged charge-discharge in aqueous medium. A precipitate is formed on the surface of LiFePO4 electrodes. It results in the change of crystalline structure, a large electrode polarization, and capacity fading.

Experiment and Analysis on the Treatment of Gaseous Benzene Using Pulsed Corona Discharge Plasma

An experiment and analysis on removal of gaseous benzene by pulse corona induced-plasma is presented in this article. Important parameters effecting removal efficiency have been investigated, such as pulse peak voltage, pulse frequency, gas inlet concentration, gas flow rate and reactor temperature. The result shows that the removal efficiency increases with the increase in pulse peak voltage, pulse frequency and reactor temperature, but decreases in the rise of gas inlet concentration and gas flow rate. On the condition of Vp= 36 kV, f= 80 Hz, C=1440 mg/m3 and Q=640 ml/min, the largest removal efficiency is 98%. Finally, the reacted products are qualitatively analysed and the reaction processes are deduced in combination with plasma-chemistry theory.

Monitoring and Prediction of the Vibration Intensity of Seismic Waves Induced in Underwater Rock by Underwater Drilling and Blasting

All underwater drilling and blasting operations generate seismic waves.However,due to a lack of suitable vibration sensing instruments,most studies on the propagation of seismic waves have been limited to shorelines near construction areas or wharfs,whereas comparatively few studies have beerconducted on the larger seafloor itself.To address this gap,a seafloor vibration sensor system was developed and applied in this study that consists of an autonomous acquisition storage terminal,soft-ware platform,and hole-plugging device that was designed to record the blasting vibration intensities received through submarine rocks at a given measurement point.Additionally,dimensional analyses were used to derive a predictive equation for the strength of blast vibrations that considered the in fluence of the water depth.By combining reliable vibration data obtained using the sensor system in submarine rock and the developed predictive equation,it was determined that the water depth was ar important factor influencing the measured vibration strength.The results using the newly derivedequation were compared to those determined using the Sadowski equation,which is commonly used on land,and it was found that predictions using the derived equation were closer to the experimental values with an average error of less than 10%,representing a significant improvement.Based on these results the developed sensor system and preliminary theoretical basis was deemed suitable for studying the propagation behavior of submarine seismic waves generated by underwater drilling and blasting operations.

Photodegradation of Methylene Blue in a Batch Fixed Bed Photoreactor Using Activated Carbon Fibers Supported TiO2 Photocatalyst

A batch fixed bed photoreactor,using felt-form activated carbon fibers(ACF)supported TiO2 photocatalyst(TiO2/ACF),was developed to carry out photocatalytic degradation of methylene blue(MB)solution.The effects of TiO2 particle size,loaded TiO2 amount,initial MB concentration,airflow rate and successive run on the decomposition rate were investigated.The results showed that photodegradation process followed a pseudo-first-order reaction kinetic law.The apparent first-order reaction constant kapp was larger than 0.047 min- 1 with half reaction time t1/2 shorter than 15 min,which was comparable to reported data using suspended Degussa P-25 TiO2 particles.The high degradation rate was mainly attributed to adsorption of MB molecules onto the surface of TiO2/ACF.The photocatalytic efficiency still remained nearly 90%after 12 successive runs,showing that successive usage of the designed photoreactor was possible.The synergic enhancement effect in combination of adsorption with ACF and photodegradation with TiO2 was proved by comparing MB removal rates in the successive degradation and adsorption runs,respectively.

Evaluation of substrates for zinc negative electrode in acid PbO_2–Zn single flow batteries

An investigation was performed on the suitability of carbon materials, metallic lead and its alloys as substrates for zinc negative electrode in acid PbO2-Zn single flow batteries. The zinc deposition process was carried out in the mediumofl mol.L 1H2SO4 at room temperature. No maximum current appears on the potentiostatic current transients for the zinc deposition on lead and its alloys. With increasing overpotential, the progressive nucleation turns to be a 3D-instantaneous nucleation process for the resin-graphite composite. Hydrogen evolution on the graphite composite is effectively suppressed with the doping of a polymer resin. The hydrogen evolution reaction on the lead is relatively weak, while on the lead alloys, it becomes serious to a certain degree. Although the ex- change current density of zinc deposition and dissolution process on the graphite composite is relatively low, the zinc corrosion is weakened to a great extent. With the increase of deposition time, zinc deposits are more compact. The cyclings of zinc galvanostatic charge-discharge on the graphite composite provide more than 90% of coulombic and 80% of energy efficiencies, and exhibit superior cycling stability during the first 10 cycles.

Calculation of the reactor neutron time of flight spectrum by convolution technique

It is a very complex and time-consuming process to simulate the nuclear reactor neutron spectrum from the reactor core to the export channel by applying a Monte Carlo program. This paper presents a new method to calculate the neutron spectrum by using the convolution technique which considers the channel transportation as a linear system and the transportation scattering as the response function. It also applies Monte Carlo Neutron and Photon Transport Code （MCNP） to simulate the response function numerically. With the application of convolution technique to calculate the spectrum distribution from the core to the channel, the process is then much more convenient only with the simple numerical integral numeration. This saves computer time and reduces some trouble in re-writing of the MCNP program.

Satellite-based detection of 16.76 MeV γ-ray from H-bomb D-T fusion

Based on the high energy γ-ray yield from the H-bomb D-T fusion reaction, it brings forward the idea applying the 16.76 MeV γ-ray to judge whether the H-bomb happens or not, and to deduce the explosion TNT equivalent accurately. The Monte Carlo N-Particle was applied to simulate the high energy γ-ray radiation characteristics reaching the geosynchronous orbit satellite, and the CVD diamond detector suit for the requirements was researched. A series of experiments were carried out to testify the capabilities of the diamond detector. It provides a brand-new approach to satellite-based nuclear explosion detection.

Comparative Toxicity of Nanomaterials to Air-blood Barrier Permeability Using an In Vitro Model

Objective To comparatively study the toxicity of four metal-containing nanoparticles(MNPs) and their chemical counterparts to the air-blood barrier(ABB) permeability using an in vitro model.Methods ABB model, which was developed via the co-culturing of A549 and pulmonary capillary endothelium, was exposed to spherical CuO-NPs(divided into CuO-40, CuO-80, and CuO-100 based on particle size), nano-Al2O3(sheet and short-rod-shaped), nano-ZnO, nano-Pb S, CuSO4, Al2(SO4)3, Zn(CH3COO)2, and Pb(NO3)2 for 60 min.Every 10 min following exposure, the cumulative cleared volume(ΔTCL) of Lucifer yellow by the model was calculated.A clearance curve was established using linear regression analysis of ΔTCL versus time.Permeability coefficient(P) was calculated based on the slope of the curve to represent the degree of change in the ABB permeability.Results The results found the increased P values of CuO-40, CuO-80, sheet, and short-rod-shaped nano-Al2O3, Al2(SO4)3, and Pb(NO3)2.Among them, small CuO-40 and CuO-80 were stronger than CuO-100 and CuSO4;no difference was observed between Al2(SO4)3 and sheet and short-rod-shaped nano-Al2O3;and nano-Pb S was slightly weaker than Pb(NO3)2.So clearly the MNPs possess diverse toxicity.Conclusion ABB permeability abnormality means pulmonary toxicity potential.More studies are warranted to understand MNPs toxicity and ultimately control the health hazards.

Coupling leaching of sphalerite concentrate

Coupling process of sphalerite concentrate leaching in H2SO4-HNO3 and tetrachloroethylene extracting of sulfur was investigated. Effects of leaching temperature, leaching time, mass ratio of liquid to solid and tetrachloroethylene addition on zinc leaching processes were examined separately. SEM images of sphalerite concentrate and residues were performed by using JEM-6700F field emission scanning electron microscope. The relationship between the number of recycling and extraction ratio of zinc was studied. The results indicate that 99.6% zinc is obtained after leaching for 3 h at 85 ℃ and pressure of （0.1 MPa O2,） with 20 g sphalerite concentrate in 200 mL leaching solution containing 2.0 mol/L H2SO4 and 0.2 mol/L HNO3, in the presence of 10 mL C2Cl4. The leaching time of zinc is 50% shorter than that in the common leaching. The coupling effect is distinct. The recycled C2Cl4 exerts little influence on extraction ratio of zinc.

Observation of the Emission Spectra of an Atmospheric Pressure Radio-frequency Plasma Jet

An atmospheric pressure plasma jet （APPJ） using radio-frequency （13.56 MHz） power has been developed to produce homogeneous glow discharge at low temperature. With optical emission spectroscopy, we observed the excited species （atomic helium, atomic oxygen and metastable oxygen） generated in this APPJ and their dependence on gas composition ratio and RF power. O and O2（b1∑g^＋） are found in the effluent outside the jet by measuring the emission spectra of effluent perpendicular to the jet. An interesting phenomenon is found that there is an abnormal increase of O emission intensity （777.4 nm） between 10 mm and 40 mm away from the nozzle. This observation result is very helpful in practical operation.

Study on the Surface Acoustic Wave Sensor with Self-Assembly Imprinted Film of Calixarene Derivatives to Detect Organophosphorus Compounds

The molecularly imprinted technology and the self-assembly technique were used together on the calixarene surface acoustic wave (SAW) chemical sensors to detect organophosphorus compounds. 25-(thioalkyl-alkoxy)-p-tertbutylcalix[4] arene with self-assembled monolayer character was the sensitive coating of the sensors. The sensors had a special response to organophosphorus compounds and the response frequency shift of this sensor to organophosphorus compounds in 0.1 mg/m3 was 350 Hz. The response frequency increased linearly with the increase of the concentration of DMMP in the range from 0.1 to 0.6 mg/m3. The possible explanation of the interaction between the coatings and organophosphorus compounds was discussed.

Identification of N-Methyl Bis(2-(Alkyloxy-Alkylphosphoryloxy)Ethyl) Amines by LC-HRMS/MS

N-Methyl bis(2-(alkyloxy-alkylphosphoryloxy)ethyl)amines, which are abbreviated as PNPs, are a series of new skeleton chemicals belonging to schedule 2.B.04 chemicals of Chemical Weapons Convention (CWC). PNPs are important markers of chemical warfare agents because they are structurally relative to both nerve agents and N-mustards. In this study, fragmentation pathways of the most characteristic fragment ions in Q-TOF mass spectrometry were proposed based on the information from accurate mass and secondary fragmentations of product ions scan experiments. Results indicated that the base ion in LC/HRMS was the quasi-molecular ion [M+H]+. In LC-HRMS/MS, it was [M+H-CnH2n+1P(O)(OH)CmH2m+1O]+ fragment ion which was formed by losing an alkyloxy alkylphosphoryloxy group from the quasi-molecular ion. The diagnostic ion m/z84.0814 was identified as [C5H10N]+, which was the group of (CH2=CH)2N+(H)CH3. PNPs have two protonated centers. One is on the N atom, the other is on the O atom (P=O). O-n-propyl PNPs generally exhibited two fragmentation pathways. Firstly, the quasi-molecular ion [M+H]+ lost a propoxy alkylphosphoryloxy group to produce [R1P(OH+)(O-n-C3H7)OCH2CH2N(CH3)CH=CH2]+, which could be fragmented further to produce [C5H10N]+ ion. Secondly, [R1P(OH+)(O-n-C3H7) OCH=CH2]+ ions were produced from [M+H]+ and fragmented further to produce the abundant ions [R1P(OH+)(OH)OCH =CH2]. However, O-isopropyl PNPs characteristically produced weak fragment ions [M+H-C3H6]+, which were presumably formed via loss of CH3CH=CH2 from [M+H]+. Other PNPs showed similar fragmentation pathways as O-n-propyl PNPs. On the summarization of the MS fragmentation pathways of PNPs, LC-HRMS/MS quantitative and qualitative methods were developed and applied to analyze N-Methyl bis(2-(butoxy-methylphosphoryloxy)ethyl]amine in high background organic samples. The analytical results had successfully supported the sample preparation for the 33rd official proficiency test of Organization for Prohibition of Chemical Weapons (OPCW).

Synthesis of N-Glycyl-2,3,4,6-tetra-O-benzyl-1,5-dideoxy-1,5- imino-D-glucitol

1-Deoxynojirimycin (1,5-dideoxy-1,5-imino-D-glucitol, DNJ) and its derivatives have been found to have a number of biological activities, such as anti-HIV, anticancer, anti-diabetic, etc.[1] N-Hydroxylethyldeoxynojirimycin (Miglitol)has been used as a drug for treating diabetic. N-Butyl-1-deoxynojirimycin (NB-DNJ) has show potent anti-HIV-1 and HIV-2 activity without cytotoxicity.[2] Recently, NB-DNJ has been approved for clinical trials as a potential therapy for some glycosphingolipid (GSL) lysosomal storage diseases, which belong to a group of severe and fatal human diseases[3]Therefore, it is very significant to study N-substituted compounds of DNJ.……

Protective Effect of Cerium on Chloroplast in Wheat Seedling

The rates of Hill reaction and contents of MDA in chloroplast of wheat seedling under salinity stress or treated by ·O - 2 , which was produced by the system of xanthine and xanthine oxidase were studied. The results show that ·O - 2 can destroy structure and function of chloroplast, and cerium protects those of the cell organelle by cleaning ·O - 2 . The higher the concentration of cerium is, the stronger the protective effects of cerium is on chloroplast treated by ·O - 2 in the condition of the certain lower concentration of cerium. The function of cerium is as the same as SOD in scavenging ·O - 2 , and the effective time of protective effect is longer. This effect is more important as chloroplast is in photostage.

A Modified Qu EChERS-DART-MS/MS Technique for High-Throughput Detection of Organophosphate Nerve Agent Hydrolysis Products in Environmental Samples

Organophosphate nerve agents(OPNAs)are lethal chemical weapons(CWs)which hydrolyze rapidly to alkyl phosphate compounds in the environment.The identification of alkyl phosphate compounds in the environment is critical for the verification of OPNAs.Currently,due to the complex sample preparation and long detection process for organophosphate nerve agent hydrolysis products(OPNAHPs),their high-throughput determination is difficult.To simplify sample preparation and detection of OPNAHPs from environmental samples,a quick,easy,cheap,effective,rugged and safe(Qu ECh ERS)method for the simultaneous purification of the five OPNAHPs in environmental samples combined with detection through direct analysis in real-time ionization source coupled with tandem mass spectrometer(DART-MS/MS)was developed.An internal standard method was applied for the quantification.The method exhibited a good linearity(R^(2)>0.991)in the range of 1.00 ng/m L-4.00μg/m L.The limits of detection and limits of quantification were 1.00-7.00 ng/m L and 10.0-20.0 ng/m L,respectively.The recoveries of OPNAHPs in environmental samples were between 65.3%and 107%,with relative standard deviations ranged from 1.6%to 19%.In addition,the sample preparation and analysis process for OPNAHPs could be completed in less than 10 min.The results demonstrated that the modified Qu ECh ERS method could quickly and efficiently remove the matrix of environmental samples.Combined with DART-MS/MS,an accurate and high-throughput detection method of OPNAHPs in environmental samples was provided.The developed method has great potential in the fields of early warning,clinical treatment and environmental decontamination.

Preparation and characterization of microcapsule containing epoxy resin and its self-healing performance of anticorrosion covering material

Microencapsulated healing agents that possess adequate strength,long shelf-life,and excellent bonding to the host material are required for self-healing materials. The in situ encapsulation method is demonstrated over an order of magnitude size reduction for the preparation of urea-formaldehyde(UF) capsules filled with a healing agent,a mixture epoxy resin of the epoxy 711 and E-51. Capsules with diameters as small as about 100 μm are achieved under the agitation rate of 800 r min-1. The capsules possess a uniform UF shell wall(4 μm average thickness) . By using the analysis of scanning electronic microscope(SEM) ,thermal analysis(TG-DTA) and FTIR,the characteristics of the microcapsules were investigated respectively. Successful self-healing has been demonstrated for anticorrosion covering materials with microcapsules.

Analysis of the M~[X] /G/1 Queues with Second Multi-optional Service and Unreliable Server

A bulk-arrival single server queueing system with second multi-optional service and unreliable server is studied in this paper. Customers arrive in batches according to a homogeneous Poisson process, all customers demand the first ＂essential＂ service, whereas only some of them demand the second ＂multi-optional＂ service. The first service time and the second service all have general distribution and they are independent. We assume that the server has a service-phase dependent, exponentially distributed life time as well as a servicephase dependent, generally distributed repair time. Using a supplementary variable method, we obtain the transient and the steady-state solutions for both queueing and reliability measures of interest.

Mid-infrared absorption spectra of dimethyl methylphosphonate as molecular simulant of nerve agents

The fine mid-infrared absorption features of dimethyl methylphosphonate vapor have been characterized by using Fourier transforms infrared spectroscopy, and the nitrous oxide was used for calibration purpose. The results show that the main P--O--C and P=O bonds related absorption bands of dimethyl methylphosphonate vapor are peaked at 1050.01 and 1275.76 cm^-1 respectively, those two bands show continuous characteristics at resolution of 0.125 cm^-1.