Construction of enhanced multi-polarization and high performance electromagnetic wave absorption by self-growing ZnFe_(2)O_(4)on Cu_(9)S_(5)

The development of 3D structural composites with electromagnetic(EM)wave absorption could attenuate EM waves.Herein,magnetized flower-like Cu_(9)S_(5)/ZnFe_(2)O_(4)composites were fabricated through a multistep hydrothermal method.The crystallographic and surface phase chemical information,morphological structure,and magnetic and EM parameters of the composites were analyzed.The prepared Cu_(9)S_(5)/ZnFe_(2)O_(4)composites have multiple loss paths for EM waves and present an overall 3D flower-like structure.The Cu_(9)S_(5)/ZnFe_(2)O_(4)composites exhibit a minimum reflection loss of-54.38 dB and a broad effective absorption bandwidth of 5.92 GHz.Through magnetization,ZnFe_(2)O_(4)particles are self-assembled and grown on the surfaces of Cu_(9)S_(5).Such a modification is conducive to the generation of additional cross-linking contact sites and the effective introduction of a large number of phase interfaces,crystalline defects,special three-dimensional flower-like structures,and magneto-electrical coupling loss effects.Moreover,the synergistic effect of multiple loss strategies effectively improves EM wave absorption by the material.This work can provide a strategy for the use of magnetizationmodified sulfide composite functional materials in EM wave absorption.

Increasing nitrogen absorption and assimilation ability under mixed NO_(3)^(–)and NH_(4)^(+) supply is a driver to promote growth of maize seedlings

Compared with sole nitrate (NO_(3)^(-)) or sole ammonium (NH_(4)^(+)) supply,mixed nitrogen (N) supply may promote growth of maize seedlings.Previous study suggested that mixed N supply not only increased photosynthesis rate,but also enhanced leaf growth by increasing auxin synthesis to build a large sink for C and N utilization.However,whether this process depends on N absorption is unknown.Here,maize seedlings were grown hydroponically with three N forms (NO_(3)^(-)only,75/25 NO_(3)^(-)/NH_(4)^(+) and NH_(4)^(+) only).The study results suggested that maize growth rate and N content of shoots under mixed N supply was little different to that under sole NO_(3)^(-)supply at 0–3 d,but was higher than under sole NO_(3)^(-)supply at 6–9 d.^(15)N influx rate under mixed N supply was greater than under sole NO_(3)^(-) or NH_(4)^(+) supply at 6–9 d,although NO_(3)^(-) and NH_(4)^(+) influx under mixed N supply were reduced compared to sole NO_(3)^(-) and NH_(4)^(+) supply,respectively.qRT-PCR determination suggested that the increased N absorption under mixed N supply may be related to the higher expression of NO_(3)^(-) transporters in roots,such as ZmNRT1.1A,ZmNRT1.1B,ZmNRT1.1C,ZmNRT1.2 and ZmNRT1.3,or NH_(4)^(+) absorption transporters,such as Zm AMT1.1A,especially the latter.Furthermore,plants had higher nitrate reductase (NR)glutamine synthase (GS) activity and amino acid content under mixed N supply than when under sole NO_(3)^(-) supply.The experiments with inhibitors of NR reductase and GS synthase further confirmed that N assimilation ability under mixed N supply was necessary to promote maize growth,especially for the reduction of NO_(3)^(-) by NR reductase.This research suggested that the increased processes of NO_(3)^(-)and NH_(4)^(+) assimilation by improving N-absorption ability of roots under mixed N supply may be the main driving force to increase maize growth.

Dielectric loss enhancement induced by the microstructure of CoFe_(2)O_(4) foam to realize broadband electromagnetic wave absorption

CoFe_(2)O_(4)has been widely used for electromagnetic wave absorption owing to its high Snoek limit,high anisotropy,and suitable saturation magnetization;however,its inherent shortcomings,including low dielectric loss,high density,and magnetic agglomeration,limit its application as an ideal absorbent.This study investigated a microstructure regulation strategy to mitigate the inherent disadvantages of pristine CoFe_(2)O_(4)synthesized via a sol–gel auto-combustion method.A series of CoFe_(2)O_(4)foams(S0.5,S1.0,and S1.5,corresponding to foams with citric acid(CA)-to-Fe(NO_(3))_(3)·9H_(2)O molar ratios of 0.5,1.0,and 1.5,respectively)with two-dimensional(2D)curved surfaces were obtained through the adjustment of CA-to-Fe^(3+)ratio,and the electromagnetic parameters were adjusted through morphology regulation.Owing to the appropriate impedance matching and conductance loss provided by moderate complex permittivity,the effective absorption bandwidth(EAB)of S0.5 was as high as 7.3 GHz,exceeding those of most CoFe_(2)O_(4)-based absorbents.Moreover,the EAB of S1.5 reached 5.0 GHz(8.9–13.9 GHz),covering most of the X band,owing to the intense polarization provided by lattice defects and the heterogeneous interface.The three-dimensional(3D)foam structure circumvented the high density and magnetic agglomeration issues of CoFe_(2)O_(4)nanoparticles,and the good conductivity of 2D curved surfaces could effectively elevate the complex permittivity to ameliorate the dielectric loss of pure CoFe_(2)O_(4).This study provides a novel idea for the theoretical design and practical production of lightweight and broadband pure ferrites.

Initiating Binary Metal Oxides Microcubes Electromagnetic Wave Absorber Toward Ultrabroad Absorption Bandwidth Through Interfacial and Defects Modulation

Cobalt nickel bimetallic oxides(NiCo_(2)O_(4))have received numerous attentions in terms of their controllable morphology,high temperature,corrosion resistance and strong electromagnetic wave(EMW)absorption capability.However,broadening the absorption bandwidth is still a huge challenge for NiCo_(2)O_(4)-based absorbers.Herein,the unique NiCo_(2)O_(4)@C core-shell microcubes with hollow structures were fabricated via a facile sacrificial template strategy.The concentration of oxygen vacancies and morphologies of the three-dimensional(3D)cubic hollow core-shell NiCo_(2)O_(4)@C framework were effectively optimized by adjusting the calcination temperature.The specially designed 3D framework structure facilitated the multiple reflections of incident electromagnetic waves and provided rich interfaces between multiple components,generating significant interfacial polarization losses.Dipole polarizations induced by oxygen vacancies could further enhance the attenuation ability for the incident EM waves.The optimized NiCo_(2)O_(4)@C hollow microcubes exhibit superior EMW absorption capability with minimum RL(RLmin)of-84.45 dB at 8.4 GHz for the thickness of 3.0 mm.Moreover,ultrabroad effective absorption bandwidth(EAB)as large as 12.48 GHz(5.52-18 GHz)is obtained.This work is believed to illuminate the path to synthesis of high-performance cobalt nickel bimetallic oxides for EMW absorbers with excellent EMW absorption capability,especially in broadening effective absorption bandwidth.

Non‑Magnetic Bimetallic MOF‑Derived Porous Carbon‑Wrapped TiO2/ ZrTiO4 Composites for Efficient Electromagnetic Wave Absorption

Modern communication technologies put forward higher requirements for electromagnetic wave(EMW)absorption materials.Metal-organic framework(MOF)derivatives have been widely concerned with its diverse advantages.To break the mindset of magneticderivative design,and make up the shortage of monometallic non-magnetic derivatives,we first try non-magnetic bimetallic MOFs derivatives to achieve efficient EMW absorption.The porous carbon-wrapped TiO2/ZrTiO4 composites derived from PCN-415(TiZr-MOFs)are qualified with a minimum reflection loss of−67.8 dB(2.16 mm,13.0 GHz),and a maximum effective absorption bandwidth of 5.9 GHz(2.70 mm).Through in-depth discussions,the synergy of enhanced interfacial polarization and other attenuation mechanisms in the composites is revealed.Therefore,this work confirms the huge potentials of nonmagnetic bimetallic MOFs derivatives in EMW absorption applications.

Synthesis and microwave absorption properties of graphene-oxide(GO)/polyaniline nanocomposite with Fe_3O_4 particles

In order to investigate the impedance matching properties of microwave absorbers,the ternary nanocomposites of GO/PANI/Fe3O4（GPF） are prepared via a two-step method,GO/PANI composites are synthesized by dilute polymerization in the presence of aniline monomer and GO,and GO/PANI/Fe3O4 is prepared via a co-precipitation method.The obtained nanocomposites are characterized by scanning electron microscopy（SEM）,X-ray diffraction（XRD）,and Fourier transform infrared spectroscopy（FTIR）,respectively.The microwave absorbability reveals enhanced microwave absorption properties compared with GO,PANI,and GO/PANI.The maximum reflection loss of GO/PANI/Fe3O4 is up to-27 dB at 14 GHz with its thickness being 2 mm,and its absorption bandwidths exceeding-10 dB are more than 11.2 GHz with its thickness values being in the range from 1.5 mm-4 mm.It provides that GO/PANI/Fe3O4 can be used as an attractive candidate for microwave absorbers.

Tip-induced directional charge separation on one-dimensional BiVO4 nanocones for asymmetric light absorption

One dimensional(1D)semiconductor is a class of extensively attractive materials for many emerging solar energy conversion technologies.However,it is still of shortage to assess the impact of 1D structural symmetry on spatial charge separation and understand its underlying mechanism.Here we take controllably-synthesized 1D BiVO_(4)nanocones and nanorods as prototypes to study the influence of 1D symmetry on charge separation.It is found that the asymmetric BiVO_(4)nanocones enable more effective charge separation compared with the symmetric nanorods.The unexpected spatial charge separation on the nanocones is mainly ascribed to uneven light absorption induced diffusion-controllable charge separation due to symmetry breaking of 1D nanostructure,as evidenced by spatial and temporal resolved spectroscopy.Moreover,the promotion effect of charge separation on the nanocones was quantitatively evaluated to be over 20 times higher than that in BiVO_(4)nanorods.This work gives the first demonstration of the influence of 1D structural symmetry on the charge separation behavior,providing new insights to design and fabricate semiconductor materials for efficient solar energy conversion.

Ti_(3)C_(2)T_(x)/Fe_(3)O_(4)纳米复合材料的吸波和电磁屏蔽性能与机制

在电磁屏蔽领域,铁氧体是常用的涂覆型吸波剂,但以Fe_(3)O_(4)为首的铁氧体存在一些不足。本研究采用冷冻干燥的方法成功制备了花苞状Ti_(3)C_(2)T_(x)/Fe_(3)O_(4)复合材料,Ti_(3)C_(2)T_(x)/Fe_(3)O_(4)复合材料的花苞状结构对电磁波的多重反射、界面极化和电磁耦合作用等使复合材料具有更好的微波吸收性能。当频率为6.74 GHz时,最小反射损耗达到-51.41 dB,对应的匹配厚度为2.8 mm,这意味着它可以吸收99.99928%的电磁波。本研究中特殊的花苞状Ti_(3)C_(2)T_(x)/Fe_(3)O_(4)复合材料表现出优异的吸波性能,在电磁屏蔽领域具有良好的应用前景。

Zr-4合金表面Cr涂层长期水腐蚀行为研究

采用等离子增强物理气相复合沉积技术在Zr-4合金包壳管材外表面制备Cr涂层,在360℃水中采用高温高压釜对Cr涂层Zr-4合金开展300天的长期耐腐蚀性能研究。研究结果表明:Cr涂层致密且与基体结合良好,涂层内无裂纹、孔洞等缺陷;经300天腐蚀后,对比试样Zr-4表面生成约6μm氧化层,而Cr涂层管材表面生成的纳米级超薄Cr2O3钝化层可阻碍O原子向基体扩散,大幅度提升了锆合金包壳材料的耐腐蚀性能。同时,Cr在中性氧化性水质中将以HCrO4-离子的形式释放于水中,腐蚀300天后,Cr涂层厚度由原来的15μm减薄为6.2μm;半涂层Zr-4管材腐蚀300天后,涂层区与非涂层区界面处生成的ZrO2氧化层厚度约为6.1μm,与对比试样Zr-4管材生成的氧化层厚度相当,Cr和基体Zr-4之间不存在电化学加速腐蚀;Cr涂层试样的腐蚀吸氢约为对比试样Zr-4的1/2,Cr涂层包壳中氢化物的析出明显减少,有利于包壳性能提升。

大尺寸优质Cr^(3+)∶BeAl_(2)O_(4)晶体生长与性能研究

本文采用感应加热提拉法结合上称重自动控径技术,成功生长出大尺寸、高质量的翠绿宝石(Cr^(3+)∶BeAl_(2)O_(4))晶体。晶坯等径圆柱体尺寸达到ϕ70 mm×140 mm,晶坯质量超过2800 g。通过冷光源照射晶坯,发现晶坯中心区域ϕ10~15 mm存在气泡。采用5 mW绿光激光照射ϕ8 mm×130 mm的翠绿宝石晶体棒,晶体内部无散射颗粒。利用Zygo激光平面干涉仪对晶体棒进行测试,波前畸变为0.3λ@632.8 nm。用电感耦合等离子体原子发射光谱法测定了翠绿宝石晶体的铬离子掺杂浓度,并计算出轴向浓度梯度为0.5×10^(-4)~1.9×10^(-4)cm^(-1)(摩尔分数)。用Perkin Elmer Lambda-950紫外可见近红外分光光度计测试了不同掺杂浓度的翠绿宝石晶体在室温下的吸收光谱,并计算了吸收系数。这些研究结果为翠绿宝石晶体的应用提供了重要的基础数据。

Understanding the Pt-like Catalytic Activity of Transition Metal Carbide Ta4C_(3) for I_(3)^(-) Reduction

This paper attempts to understand the Pt-like catalytic activity of transition metal carbide Ta4C_(3) for IRR(I_(3)^(-)reduction reaction)based on the correlation of adsorption energy to d-band center(εd).Ta4C_(3) was prepared by carbothermal reduction method with a template.Its photoelectrochemical properties were investigated as a CE(counter electrode)in DSSC(dye-sensitized solar cell).Its surface electronic structures,including DOS(density of state)andεd,and adsorption energy were computed by first-principle DFT(density functional theory).In TMC(transition metal carbide)Ta4C_(3),the interaction between Ta and C atoms makes the d-band of Ta broaden and results in the downward shift of itsεd.A moderate absorption energy corresponding to theεd is achieved,which is the nature of the Pt-like catalytic activity of Ta4C_(3).Appropriate change of adsorption energy by adjustingεd is a promising strategy to improve catalytic activity.This work is of great significance to the fundamental and application researches.

Study of a mass transfer-reaction model for SO_2 absorption process using LAS/H_2SO_4 solution

A regenerative absorption process for removal of SOx from FCC off-gas using LAS/ H2SO4 solution as absorbant was studied and pilot-plant experiments were carried out. A mass transfer- reaction model for the SO2 absorption process was established based on pilot-plant experiments, and the concentration distribution of components in the liquid film, and the partial pressure and mass transfer rate of SO2 along the height of the absorption tower, was calculated from this model. The numerical simulation results were compared with the experimental results and proved that the model can be used for describing the SO2 absorption process.

ABSORPTION SPECTRA OF 4f ELECTRON TRANSITIONS IN THE SYSTEM OF NEODYMIUMSEMIXYLENOL ORANGE-CETYLPYRIDINIUM CHLORIDE

In this paper the absorption spectra of Nd-SXO-CPC complex by 4f electron transitions have been studied by zero-order and fourth-order derivative spectrophotome-try. The molar absorptivity is 2.6×10~3 1.mol^(-1).cm^(-1) at 585 nm, the fourth-order derivative molar absorptivity is 1.4×10~4 1.mol^(-1).cm^(-1) at 584.5(-) and 587(+) nm. They are 300 times and 1600 times greater than those of the chloride, respectively.

Nonlinear Intestinal Absorption of Fluorescein Isothiocyanate Dextran 4, 000 Caused by Absorptive and Secretory Transporting System

The mechanism of the nonlinear concentration dependence of the intestinal absorption of fluorescein isothiocyanate dextran 4,000 (FD-4) was studied using in situ rat intestinal loops and the in vitro Ussing-type chamber method. The intestinal absorption rate constant of FD-4, as evaluated by the intestinal loop method, increased significantly in a nonlinear fashion as the FD-4 concentration increased up to 0.2 mM and tended to decrease at concentrations higher than 0.2 mM. The mucosal-to-serosal permeation of FD-4 across rat ileal sheets, as evaluated by the in vitro Ussing-type chamber method, also increased in a nonlinear fashion in the low concentration range (0.01 - 0.02 mM), before decreasing as the concentration increased further, whereas serosal-to-mucosal permeation decreased in a concentration-dependent manner. In addition, mucosal-to-serosal flux and serosal-to-mucosal flux were increased and reduced in the presence of the metabolic inhibitor 2, 4-dinitrophenol, respectively. These results suggest that FD-4 is predominantly secreted into the intestinal lumen by an efflux transport system.

ABSORPTION SPECTRA OF 4f ELECTRON TRANSITIONS OF NEODYMIUM COMPLEX WITH 8-HYDROXYQUINOLINE AND OCTYLPHENOL POLY(ETHYLENEGLYCOL)ETHER

In this paper the absorption spectra of 4f electron transitions of the neodymlum complex with 8-hydroxyquinoline and octylphenol poly(ethyleneglycol)ether have been studied. The marked intensification of the band at low octylphenol poly(ethyleneglycol)ether concentration is found normally at 575 nm, and its resolution into three sharp bands centering at 572, 580 and 584 nm. The absorbances of the absorption maxima are 3.5 (at 572 nm), 7.2 (at 580 nm) and 10.2 (at 584 nm) times greater than that of the chloride.

杯[4]芳烃修饰Amberlite XAD-4树脂去除水中双氯芬酸

通过偶氮化反应将合成的去叔丁基杯[4]芳烃连接到Amberlite XAD-4树脂上,并且采用FTIR、SEM和TG/DTA法表征了杯[4]芳烃修饰Amberlite XAD-4树脂的结构.结果表明,水溶液中杯[4]芳烃修饰Amberlite XAD-4树脂对双氯芬酸的去除率远大于单独AmberliteXAD-4树脂和杯[4]芳烃.双氯芬酸的浓度为20mg/L时,随着杯[4]芳烃修饰AmberliteXAD-4树脂投加量的增加,双氯芬酸的去除率增加很快.当吸附剂量增加到80mg/L时,双氯芬酸的去除率为92.8%,并且达到吸附平衡,吸附的双氯芬酸量为34.02mg/g.Langmuir和Freundlich等温线与实验数据均有很好的拟合度.对热力学参数的计算表明,△H与△G负值显示出反应的放热和自发过程.

PA、H103及XAD-4树脂在茶多酚吸附工艺中的特性研究

本文主要研究了PA、H103及XAD-4树脂在茶多酚吸附分离体系中的吸附热力学特性及吸附动力学特性。热力学研究表明,三种吸附剂的吸附等温线都属于优惠型的吸附等温线,并可以用Langmiur 方程来描述,且与Langmiur方程高度相关;动力学特性研究表明,PA和H103树脂为中速吸附型的吸附剂,XAD-4为慢速吸附型的吸附剂。PA、H103及XAD-4树脂的吸附平衡速率常数依次为KPA=1.461h-1,KH103=1.198h-1,KXAD-4=0.498h-1。

胺化XAD-4螯合树脂的合成及其对Cu^(2+)的吸附

通过XAD-4树脂和氯代乙酰氯的Friedel-Crafts反应合成了氯乙酰化XAD-4树脂,再将氯乙酰化XAD-4树脂分别与二乙烯三胺、三乙烯四胺和四乙烯五胺反应制备了三种氨基螯合树脂,用电导率法研究了它们对Cu2+的吸附动力学。红外光谱和碱基全交换容量测定结果表明氯乙酰基被成功地引入到XAD-4树脂上以及二乙烯三胺、三乙烯四胺和四乙烯五胺被键合到氯乙酰化XAD-4树脂上。吸附动力学测试表明,螯合树脂对金属铜离子的吸附速率和吸附量与氨基含量密切相关,二级速率方程可用来描述螯合树脂对金属铜离子的吸附动力学。

XAD-4树脂对水相中邻氨基苯酚的吸附特性研究

研究了XAD-4大孔树脂对水相中邻氨基苯酚的吸附特性。研究内容包括接触时间、pH、吸附剂质量、吸附温度对吸附的影响。树脂能有效地除去水相中的邻氨基苯酚,在pH=3.2～5.2的范围内树脂对邻氨基苯酚均有较大的吸附,其最佳酸度为pH=4.0,吸附率可达97.3%。研究表明Langmuir等温吸附模型能较好地描述吸附过程。用1.5～2.0 mol/L HCl对吸附后的树脂进行再生试验,脱附率可达91.2%。