A compact X-band backward traveling-wave accelerating structure

Very high-energy electrons(VHEEs)are potential candidates for FLASH radiotherapy for deep-seated tumors.We proposed a compact VHEE facility based on an X-band high-gradient high-power technique.In this study,we investigated and realized the first X-band backward traveling-wave(BTW)accelerating structure as the buncher for a VHEE facility.A method for calculating the parameters of single cell from the field distribution was introduced to simplify the design of the BTW structure.Time-domain circuit equations were applied to calculate the transient beam parameters of the buncher in the unsteady state.A prototype of the BTW structure with a thermionic cathode-diode electron gun was designed,fabricated,and tested at high power at the Tsinghua X-band high-power test stand.The structure successfully operated with 5-MW microwave pulses from the pulse compressor and outputted electron bunches with an energy of 8 MeV and a pulsed current of 108 mA.

Design,fabrication,and testing of an X-band 9-MeV standing-wave electron linear accelerator

In this study,an X-band standing-wave biperiodic linear accelerator was developed for medical radiotherapy that can accel-erate electrons to 9 MeV using a 2.4-MW klystron.The structure works atπ/2 mode and adopts magnetic coupling between cavities,generating the appropriate adjacent mode separation of 10 MHz.The accelerator is less than 600-mm long and constitutes four bunching cells and 29 normal cells.Geometry optimizations,full-scale radiofrequency(RF)simulations,and beam dynamics calculations were performed.The accelerator was fabricated and examined using a low-power RF test.The cold test results showed a good agreement with the simulation and actual measurement results.In the high-power RF test,the output beam current,energy spectrum,capture ratio,and spot size at the accelerator exit were measured.With the input power of 2.4 MW,the pulse current was 100 mA,and the output spot root-mean-square radius was approximately 0.5 mm.The output kinetic energy was 9.04 MeV with the spectral FWHM of 3.5%,demonstrating the good performance of this accelerator.

Application and mechanism of Fenton-like iron-based functional materials for arsenite removal

Between the two major arsenic-containing salts in natural water, arsenite(As(Ⅲ)) is far more harmful to human and the environment than arsenate(As(V)) due to its high toxicity and transportability. Therefore, preoxidation of As(Ⅲ) to As(V) is considered to be an effective means to reduce the toxicity of arsenic and to promote the removal efficiency of arsenic. Due to their high catalytic activity and arsenic affinity, iron-based functional materials can quickly oxidize As(Ⅲ) to As(V) in heterogeneous Fenton-like systems, and then remove As(V) from water through adsorption and surface coprecipitation. In this review, the effects of different iron-based functional materials such as zero-valent iron and iron(hydroxy) oxides on arsenic removal are compared, and the catalytic oxidation mechanism of As(Ⅲ) in heterogeneous Fenton process is further clarified. Finally, the main challenges and opportunities faced by iron-based As(Ⅲ) oxidation functional materials are prospected.

Redox behavior and chemical species of arsenic in acidic aqueous system

Arsenic(As)removal from smelting acidic wastewater is an urgent task.The most common method is oxidation of trivalent As(III)to pentavalent As(V)subsequently precipitated by ferric(Fe(III))salts.Foundations of redox behavior and chemical species are of great importance for understanding As removal.In this work,cyclic voltammetry(CV)and UV?Vis spectroscopy were used for laboratory observation;meanwhile HSC and MINTEQ software were employed for theoretical analyses.It is found that As(III)oxidation,a multiple electron transfer reaction,is diffusion-controlled.The oxidation over-potential is very high(about0.9V)in sulfuric acid solutions(pH1.0).In addition,Fe(III)?As(V)complexes are evidenced by UV?Vis spectra and chemical species analyses in series of Fe(III)?As(V)?H2SO4?H2O solutions.Therefore,the Fe(III)and As(V)species distribution against pH values are determined and a newφ?pH diagram with inclusion of Fe?As complexes is consequently compiled based on thermodynamic data predicted by other researchers.

Recovery of valuable metals from zinc leaching residue by sulfate roasting and water leaching

Zinc leaching residue(ZLR),produced from traditional zinc hydrometallurgy process,is not only a hazardous waste but also a potential valuable solid.The combination of sulfate roasting and water leaching was employed to recover the valuable metals from ZLR.The ZLR was initially roasted with ferric sulfate at640°C for1h with ferric sulfate/zinc ferrite mole ratio of1.2.In this process,the valuable metals were efficiently transformed into water soluble sulfate,while iron remains as ferric oxide.Thereafter,water leaching was conducted to extract the valuable metals sulfate for recovery.The recovery rates of zinc,manganese,copper,cadmium and iron were92.4%,93.3%,99.3%,91.4%and1.1%,respectively.A leaching toxicity test for ZLR was performed after water leaching.The results indicated that the final residue was effectively detoxified and all of the heavy metal leaching concentrations were under the allowable limit.

Formation of arsenic−copper-containing particles and their sulfation decomposition mechanism in copper smelting flue gas

The heat recovery steam generator(HRSG)of copper smelting generates a large number of arsenic−coppercontaining particles,and the in-situ separation of arsenic and copper is of importance for cutting off environmental risk and realizing resource recovery.The formation of arsenic−copper-containing particles was simulated,the method of in-situ decomposition of arsenic−copper-containing particles by pyrite was proposed,and the decomposition mechanism was confirmed.It was found that particles with high arsenic content were formed in the simulated HRSG,and copper arsenate was liable for the high arsenic content.Pyrite promoted the sulfation of copper,leading to the in-situ decomposition of copper arsenate.In this process,gaseous arsenic was released,and thus the separation of arsenic and copper was realized.

A new mixed-valent iron arsenate black crystal

Scorodite（FeAsO4·2H2O）is the most popular phase for arsenic（As）immobilization while the reductive dissolution of Fe（Ⅲ）to Fe（Ⅱ）will promote As release.In the present study,an equilibrium between Fe（Ⅲ）and Fe（Ⅱ）was achieved in scorodite preparation system by introducing certain alcohol（methanol,ethanol,isopropanol or tert-butanol）,and thus a new mixed-valent iron arsenate black crystal formulated as Fe（Ⅱ）（5.2）Fe（Ⅲ）（8.8）（HAsO4）4（AsO4）8·H2O was prepared.In comparison with scorodite,the black crystal has higher As content（36.4%,mass fraction）and lower crystal water content（0.73%,mass fraction）.Additionally,the leaching concentration of As can be lower than the threshold value（5 mg/L）regulated by identification standards for hazardous wastes of China（GB 5080.3-2007）.Therefore,this new mixed-valent iron arsenate crystal could be classified as a non-hazardous and promising As-bearing phase in environmental applications.

Modular synthesis of 1,4-diketones through regioselective bis-acylation of olefins by merging NHC and photoredox catalysis

Efficient and modular synthesis of structurally diverse 1,4-diketones from readily available building blocks represents an essential but challenging task in organic chemistry.Herein,we report a multi-component,regioselective bis-acylation of olefins by merging NHC organocatalysis and photoredox catalysis.With this protocol,a broad range of 1,4-diketones could be rapidly assembled using bench-stable feedstock materials.The robustness of this method was further evaluated by sensitivity screening,and good reproductivity was observed.Moreover,the diketone products could be readily converted into functionalized heterocycles,such as multi-substituted furan,pyrrole,and pyridazine.Mechanistic investigations shed light on the NHC and photoredox dual catalytic radical reaction mechanism.

Palladium-catalysed stereoselective[3+2]annulation of vinylethylene carbonates and tryptanthrin-based ketones

The palladium-catalysed[3+2]annulation of vinylethylene carbonates(VECs)and ketones remains challenging in organic synthesis.Herein,we successfully achieved the[3+2]annulation of tryptanthrin-based ketones and VECs for the efficient synthesis of indoloquinazolinone derivatives with generally excellent yields and good diastereoselectivity.Notably,the asymmetric version of this[3+2]annulation can also be achieved by using a chiral spiroketal-based diphosphine ligand.In addition,preliminary biological studies reveal that some of the products exhibit promising antibacterial activity.