强变形工艺对2519A铝合金组织与性能的影响

通过硬度测试、拉伸性能测试、透射电镜观察等分析手段研究了不同强变形工艺下2519A铝合金的力学性能与微观组织。结果表明,经50%的冷轧变形和165 ℃人工时效后,2519A合金的力学性能明显提高,其抗拉强度、屈服强度和伸长率分别为522 MPa、468 MPa和8.5%。而在冷变形前添加165 ℃×2 h预时效处理,合金的力学性能进一步提高,其抗拉强度、屈服强度和伸长率分别达到535 MPa、497 MPa和8%。预时效处理可以提高合金中θ′相的密度,使析出相分布更加均匀,有助于提高合金的力学性能。     

Synthesis,Anticancer Activity,Structure-Activity Relationship and Mechanistic Investigations of Falcarindiol Analogues

Forty samples of optically active falcarindiol analogues are synthesized by using the easily available C2 symmetric (R)- and (S)-1,1’-binaphth-2-ol (BINOL) in combination with Ti(OⁱPr)₄, Zn powder and EtI. Their anticancer activities on Hccc-9810, HepG2, MDA-MB-231, Hela, MG-63 and H460 cells are assayed to elucidate their structure-activity relationships. These results showed that the falcarindiol analogue (3R,8S)- 2 i with the terminal double bond has the most potent anti-proliferation effect on Hccc-9810 cells with IC₅₀ value of 0.46 μM. The falcarindiol analogue (3R,8S)- 2 i can induce obvious Hccc-9810 cell apoptosis in a concentration-dependent manner by Hoechst staining and flow cytometry analysis. The proposed mechanism suggests that the falcarindiol analogue (3R,8S)- 2 i increases LDH release and MDA content, and reduces the levels of SOD activity, which lead to the accumulation of oxidative stress and induce apoptosis in Hccc-9810 cells.     

镍基MOF电极材料物理超声改性及电化学性能

采用水热法合成了以4,4′-联苯二甲酸(BPDC)为配体的Ni-金属有机框架(MOF),利用低成本、无污染的物理超声法在不改变Ni-MOF晶体结构的前提下对其进行改性,使块状Ni-MOF表面产生孔隙,改善Ni-MOF表面微/纳米结构,提高其电化学性能。通过扫描电子显微镜(SEM)图、X射线衍射(XRD)谱、循环伏安(CV)曲线和恒电流充放电(GCD)曲线分析了改性前后Ni-MOF的微结构形貌和电化学性能。结果表明,经过超声处理后,Ni-MOF的比表面积从40.6 m^2·g^-1增加到65.8 m^2·g^-1,平均孔径从12 nm增加到22 nm。在0.5 A·g^-1电流密度下,超声处理后Ni-MOF电极比电容从420 F·g^-1增加到515 F·g^-1,提高了22.6%,电荷转移电阻明显降低,从25.11Ω降低到15.51Ω。因此,物理超声法可有效改善Ni-MOF表面微/纳米结构,提高其电化学性能。     

热等静压处理对K439B高温合金显微组织的影响

对K439B合金进行了1165 ℃/150 MPa,4 h热等静压处理,采用光学显微镜和扫描电镜对比研究了铸态和热等静压态K439B合金的显微组织。结果表明:铸态K439B合金存在0.25%的显微疏松,热等静压后显微疏松基本消除(0.013%)。与铸态相比,经过热等静压处理后合金中的γ/γ′共晶组织体积分数和尺寸减小,各元素分布更加均匀,凝固偏析系数均更接近1。铸态K439B合金枝晶干处γ′相尺寸和体积分数分别是116.9 nm和17.8%,枝晶间部位γ′相尺寸和体积分数分别为244.4 nm和24.9%。热等静压后合金枝晶干部位的γ′相尺寸及体积分数分别为148.0 nm和17.5%,枝晶间部位γ′相尺寸和体积分数分别为159.1 nm和22.8%。热等静压处理使合金枝晶干、枝晶间部位的γ′相尺寸、体积分数和形貌接近,同时γ′相分布变得均匀。     

GC-MS法测定塑胶跑道面层中的6种有害物质

建立了检测塑胶跑道面层中6种有害物质(环己基异氰酸酯(CHI)、2,4-甲苯二异氰酸酯(2,4-TDI)、2,6-甲苯二异氰酸酯(2,6-TDI)、六亚甲基二异氰酸酯(HDI)、萘-1,5-二异氰酸酯(NDI)和4,4'-二苯基甲烷二异氰酸酯(4,4'-MDI))含量的GC-MS检测方法,分别讨论了定量方式和萃取时间对6种有害物质回收率的影响。将样品剪碎至10~20目(0.85~2.00 mm)的颗粒,用10 mL乙酸乙酯萃取,室温下超声20 min,提取液用DB-17MS石英毛细管色谱柱(30 m×0.25 mm×0.25μm)分离,采用GC-MS法并选择离子检测,内标法定量。结果表明,在0.5~100.0 mg/L(4,4'-MDI在1.0~100.0 mg/L)浓度范围内,线性良好,相关系数均大于0.998,方法检出限范围为2.0~10.0 mg/kg,定量限范围为6.0~20.0 mg/kg;加标平均回收率在80.1%~100.8%之间,相对标准偏差(n=6)小于5.2%。该方法快速、准确,适用于塑胶跑道面层中有害物质的测定。     

Comparison of Canola and Soy Flour with Added Isocyanate as Wood Adhesives

Canola is widely grown in the northern latitudes for its vegetable oil, generating large quantities of residual, low value canola flour used as animal feed. The common wood adhesive poly(diphenylmethylene diisocyanate) (pMDI) should react with the wide variety of functional groups in proteins. Therefore, it would seem that canola flour with added pMDI could be an effective adhesive. Two main questions are addressed in this study: How do the wood adhesive properties of canola flour compare to the better-studied soy flour? How well do proteins, which contain an abundance of functional groups, cure with the very reactive pMDI? These questions were addressed using the small-scale adhesive strength test ASTM D-7998, with various adhesive formulations and bonding conditions for canola flour plus pMDI compared to soy adhesives. The more challenging wet cohesive bond strength was emphasized because the dry strengths were usually very good. Generally, soy adhesives were better than canola ones, as was the polyamidoamine-epichlorohydrin cross-linker compared to pMDI, but these generalizations can be altered by the conditions selected. Three-ply plywood tests supported the small-scale test results.     

Isolation and characterization of components responsible for neuroprotective effects of Allium cepa outer scale extract against ischemia reperfusion induced cerebral injury in mice

The antioxidant-mediated neuroprotective effect of Allium cepa outer scale extract (ACE) in mice with cerebral ischemia-reperfusion (I-R) injury was demonstrated in our earlier work. The current investigation aimed at establishing the bioactive component(s) responsible for this activity. Thus ACE was fractionated into ethyl acetate (EF) and aqueous (AF) fractions. These fractions were evaluated against cerebral I-R injury in mice. I-R injury in mice was induced by bilateral common carotid artery occlusion followed by 24 hr reperfusion. Memory, sensorimotor functions, cerebral infarct size, and oxidative stress were measured to address the neuroprotective mechanism of test substances. EF showed marked improvement of memory and sensorimotor functions by reducing brain oxidative stress and infarct size in mice after I-R injury. The bioactive EF was subjected to chromatographic (HPLC-PDA, HPLC-MS, preparative HPLC) and spectroscopic studies to isolate and identify the neuroprotective compounds. This lead to separation of three components, namely quercetin, quercetin 4′-O-glucoside, and the remaining fraction, from EF. The separated components were biologically evaluated. These components showed improvement in mice with I-R injury. But, EF displayed more marked neuroprotective effects as compared to the isolated components. The distinct neuroprotective outcome of EF may be credited to the synergistic action of compounds present in EF. Further studies such as evaluation of neurotoxic effects and other possible neuroprotective mechanisms are required to develop EF as a neuroprotective drug.     

异料拼接对女装毛衫创新设计的影响

针对目前女装毛衫款式简单,缺乏前卫创新设计,难以充分满足毛衫市场时装化、外穿化的需求,结合2019秋冬国际品牌流行发布会上的毛衫设计实例,从点线面的视角阐述异料拼接在女装毛衫上的表现形式,将材料的多元组合思维引入女装毛衫设计,展示了异料拼接在女装毛衫设计中的应用形式及特征,总结出其对毛衫款式、造型、风格、功能4个层面设计的影响,指出在打破传统款式限制、改变毛衫空间廓形、提升毛衫风格美感与功能性等方面具有重要意义,为毛衫产业实现转型升级提出新的参考路径。     

The dependence of fatigue crack growth on hydrogen in warm-rolled 316 austenitic stainless steel

The fatigue crack growth rate of warm-rolled AISI 316 austenitic stainless steel was investigated by controlling rolling strain and temperature in argon and hydrogen gas atmospheres. The fatigue crack growth rates of warm-rolled 316 specimens tested in hydrogen decreased with increasing rolling temperature, especially 400 °C. By controlling the deformation temperature and strain, the influences of microstructure (including dislocation structure, deformation twins and α′ martensite) and its evolution on hydrogen-induced degradation of mechanical properties were separately discussed. Deformation twins deceased and dislocations became more uniform with the increase in rolling temperature, inhibiting the formation of dynamic α′ martensite during the crack propagation. In the cold-rolled 316 specimens, deformation twins accelerated hydrogen-induced crack growth due to the α′ martensitic transformation at the crack tip. In the warm-rolled specimens, the formation of α′ martensite around the crack tip was completely inhibited, which greatly reduced the fatigue crack growth rate in hydrogen atmosphere.     

Phase evolution of a novel silicon-alumina-fused mullite-containing Ti2O3 refractory at 1300 °C in N2

A novel silicon-alumina-fused mullite-containing Ti₂O₃ composite refractory is prepared and sintered in the presence of solid carbon at 1300 °C in N₂. The sintered samples exhibit a functional gradient characteristic. The phase evolution can be described as follows: Passive and active oxidation of Si to form SiO₂ and SiO to reduce the partial pressure of oxygen. SiO(g) and Si react with N₂ to form Si₃N₄ respectively. As the temperature increases and the partial pressure of oxygen decreases, Ti₂O₃ reacts with CO and N₂ to form Ti(C,N)ss, which is accompanied by the release of O₂. Si₃N₄ fixes the O₂ and reacts to form Si₂N₂O, and Si₂N₂O reacts with Al₂O₃ to form O′-Sialon, thereby realizing the transformation from Si₃N₄ to Sialon. CO and residual carbon from the pyrolysis of phenolic resin react with SiO(s) and Si to form SiC. The dense layer formed by SiC and SiO₂ blocks the diffusion of external gas to the central parts of the samples, there is still free Si which can continue to react and transform into a non-oxide reinforcing phase. In this paper, the reaction models are presented.