十二烷基硫酸钠（SDS）对铜电沉积行为的影响

在酸性体系中采用阴极扫描伏安和计时电流等电化学测试方法，研究添加十二烷基硫酸钠（SDS）对铜电沉积过程的影响机理。结果表明：SDS的添加使沉积电位正移，降低了阴极极化。SDS浓度低于临界胶束浓度1g/L时，铜的成核弛豫时间延长，形核速率降低。SDS浓度高于临界胶束浓度时，形成SDS球状胶束，铜的成核弛豫时间减少，形核速率加快。铜晶核形成过程符合Scharitker?Hill 三维成核/生长机制，当SDS为1g/L时，在-0.2V的低过电位区，铜结晶按渐进成核方式进行，在-0.23--0.28V的高过电位区，铜结晶按瞬时成核方式进行。而当SDS为0.5g/L时，铜在-0.2V--0.25V的低电位区和在-0.28V的高电位区均符合渐进成核。     

喷射沉积2195铝锂合金轧制板材晶粒组织及性能控制研究

研究了喷射沉积制备2195铝锂合金锭坯挤压板坯经不同终轧温度热轧至6mm厚度板材,以及经不同中间退火后再冷轧至6mm厚度板材固溶后的晶粒组织。结果表明,终轧温度290℃时,热轧板固溶后表层为粗大再结晶晶粒,而中心层为细长纤维状晶粒;终轧温度降低至220℃时,虽然表层再结晶晶粒尺寸减小,但中心层转变为尺寸粗大的长条状再结晶晶粒。板材中尺寸1μm以上的富Cu第二相粒子数量随中间退火(空冷)温度的增加(从330℃提高至450℃)而增加;冷轧固溶后表层等轴状再结晶晶粒尺寸增加,而中心层晶粒逐渐由粗大长条状再结晶晶粒转变为细小等轴状再结晶晶粒。适当温度中间退火、随炉冷却并冷轧、固溶后表层和中心层全部为细小等轴状再结晶晶粒。优化中间退火后的冷轧板材T8时效态强度最高,而终轧温度220℃的热轧板材T8时效态强度最低。     

高Cr镍基合金脱氮反应热力学与动力学研究

Cr作为抗热腐蚀性元素铬在高温合金中广泛添加，因其可增大氮元素溶解度，故高铬合金的冶金脱氮难度较大。合金氮含量升高可引发氮化物析出进而影响材料组织质量与力学性能，因此，非常必要澄清高Cr合金的脱氮行为与规律。本文以高Cr镍基合金为实验对象，对其在真空感应熔炼脱氮过程的热力学与动力学进行研究。结果表明，氮在高Cr镍基合金中的热力学平衡溶解度较高且主要受真空压力控制，为实现[N]≤10 ppm的纯净度指标，合金冶炼真空压力不可高于0.1Pa。脱氮反应初期氮含量迅速下降，但反应中后期需较长时间才可接近氮平衡溶解度，提高精炼温度有助于缩短脱氮平衡反应时间。动力学分析表明高Cr镍基合金脱氮符合二级反应规律，受界面化学反应过程控制，1500℃、1550℃和1600℃条件下的脱氮表观速率常数分别为0.0184m?s-1、0.0233 m?s-1和0.0397 m?s-1，表观活化能为211.4 kJ?mol-1。     

超细晶纯钛的微动疲劳特性

利用自行设计的微动疲劳实验夹具装置研究超细晶纯钛在柱面-平面接触下的微动疲劳特性,分析循环应力对其微动疲劳寿命的影响,通过观察接触区磨损和断口形貌,分析其微动损伤机制。结果表明,当法向载荷不变时,超细晶纯钛的微动疲劳寿命随着循环应力的增加而减小,比常规疲劳寿命更小。微动疲劳裂纹于接触区边缘萌生,磨损区破裂严重且附着有磨粒,在磨粒磨损作用下加速了试样的疲劳失效。断口同时呈现出疲劳形貌和微动形貌,形貌从平滑转向粗糙直至断裂,裂纹由小变大,裂纹扩展速率也逐渐增加,且在裂纹扩展区存在二次裂纹；由于受力不均在裂纹扩展区与断裂区之间存在山脊状形貌。     

圆盘类精锻件顺序转向输送方法的研究及应用

针对圆盘类精锻件输送问题,提出了一种圆盘类精锻件顺序转向输送方法,对圆盘类精锻件多排变单排的输送形式及多排布局方案进行研究。输送过程分为两个阶段:第1阶段,第1输送装置进行多排输送;第2阶段,经自动落料装置按顺序依次落料至第2输送装置,实现了转向、单排输送。其中,第1输送装置的多排布局分别为由远及近、由近及远两种形式,第2输送装置的输送速度分别设置为ΔL/P、2ΔL/P、3ΔL/P、4ΔL/P,通过对以上8种组合的位置仿真分析得到了合理方案。研究及应用表明,若第2输送装置输送速度设置为4ΔL/P,则由近及远多排布局方案的布局形式满足了顺序转向的输送要求。     

Dependence of zeolite topology on alkane diffusion inside diverse channels

Zeolites have been widely used for the processes of adsorption, separation, and catalysis, which are strongly correlated with molecular diffusion. However, the correlation between pore dimension and diffusion properties has not been systematically investigated so far. In this work, the diffusion properties of alkanes in six zeolites with similar pore sizes but different pore dimension have been examined. It is found that the diffusion coefficients of alkanes in zeolites are 2–5 orders of magnitude smaller than that in gas phase. Moreover, the diffusion of alkanes inside zeolites is sensitive to the pore dimension, and can be differentiated by 1-D straight, 1-D tortuous, and 3-D intersecting channels, based on the derived quantitative correlation between the diffusion behavior and pore dimension. Our work may not only provide deep insights into the effects of pore dimension on diffusion, but also benefits for the future design and practical applications of zeolite catalysts.     

Immobilization of lipase onto metal–organic frameworks for enantioselective hydrolysis and transesterification

Enzyme immobilization enhances the catalytic activity and stability of the enzyme, and also improves reusability. Metal–organic frameworks (MOFs), which possess diversified structures and porosity, have been used as excellent carriers for enzyme immobilization. Pseudomonas fluorescens lipase (PFL) has been successfully immobilized onto MOFs by covalent cross-linking to obtain a series of immobilized lipase (PFL@MOFs). PFL@MOFs are used for catalytic enantioselective hydrolysis of 2-(4-hydroxyphenyl) propionic acid ethyl ester enantiomers (2-HPPAEE) in aqueous medium and transesterification of 4-methoxymandelic acid enantiomers (4-MMA) in organic medium. The experimental results indicated that PFL@Uio-66(Zr) exhibits excellent enzymatic catalysis performances and high enantioselectives. In addition, to improve catalytic activity and reusability, PFL is modified by the polyethylene glycol (PEG) to prepare PEG-modified lipase (PFL-PEG), then PFL-PEG is immobilized onto Uio-66(Zr) to prepare PFL-PEG@Uio-66(Zr), demonstrating better reusability and catalytic activity compared with PFL@Uio-66(Zr).     

A graphene oxide membrane with self-regulated nanochannels for the exceptionally stable bio-oil dehydration

The transport behaviors and nanochannel structures of a graphene oxide (GO) membrane were studied for pervaporation dehydration of bio-oil with a high acidity and a complex composition. The GO membrane showed an unprecedentedly stable water flux of approximately 0.43 kg m⁻² hr⁻¹, with a water content of 97 wt% in the permeate throughout 70 hr of pervaporation testing at 30°C. Both the calculated activation energy for water permeation and X-ray diffraction characterization results confirmed that the nanochannel structures of the GO membrane were temperature- and liquid media-responsive. The molecular intercalation-induced self-regulation of the size of laminar nanochannels in the GO membrane was suggested to be primarily responsible for the significantly reduced membrane fouling and the exceptionally stable pervaporation performance for the GO membrane. The mechanistic insights into the nanochannel structures and antifouling properties would provide important inspiration for the design of novel highly fouling-resistant membrane materials for practical applications.     

Effect of titanium chelating compound on hydration resistance of CaO material

The hydration resistance of CaO materials prepared by Ca(OH)₂ calcination with titanium chelating compounds is investigated in this paper. The crystalline phases and microstructure characteristics of sintered specimens were studied by X-ray diffraction (XRD), define FTIR spectroscopy, scanning electron microscopy (SEM), and energy dispersive spectrometer (EDS). The results showed that the hydration resistance of CaO samples was improved significantly, especially for samples with 9 wt% Ti chelating compound. The specimens with Ti chelating compound showed an increase in bulk density and a decrease in apparent porosity after heating when compared to the specimens without additive. The grain surface of CaO grain and the gaps between the CaO grain boundaries were covered with calcium phosphate glass phase, calcium phosphate showed two different shapes: irregular shape and rod shape. The formation and distribution of these two forms were the key factors that affecting the hydration resistance of CaO samples.     

Defect structure evolution and electrical properties of BaTiO3-based ferroelectric ceramics

Relaxor perovskite ferroelectric 0.1Bi(Zn_1/2Zr_1/2)O₃-0.9BaTiO₃(0.1BZZ-0.9BT) ceramics were successfully prepared, whose powders synthesized by the sol-gel process, with average grain size about 1.29 μm. 1.75 J/cm³ discharge energy density and good dielectric stability were obtained over a wide temperature range from 25°C to 140°C. The pulse discharge capability of 0.1BZZ-0.9BT ceramics was tested under different electric fields. The discharge time was 2.13 μs, which proved its ability to charge and discharge quickly. Complex impedance analysis and thermally stimulated depolarization current tests were applied to investigate the defect types and activation of 0.1BZZ-0.9BT ceramics. The evolution process of composite defects and oxygen vacancies profoundly affects the dielectric temperature stability of 0.1BZZ-0.9BT ceramics’ energy storage property.