Pyrolysis and co-pyrolysis of Laminaria japonica and polypropylene over mesoporous Al-SBA-15 catalyst

The catalytic co-pyrolysis of a seaweed biomass, Laminaria japonica, and a typical polymer material, polypropylene, was studied for the first time. A mesoporous material Al-SBA-15 was used as a catalyst. Pyrolysis experiments were conducted using a fixed-bed reactor and pyrolysis gas chromatography/mass spectrometry (Py-GC/MS). BET surface area, N₂ adsorption-desorption isotherms, and NH₃ temperature programmed desorption were measured to examine the catalyst characteristics. When only L. japonica was pyrolyzed, catalytic reforming slightly increased the gas yield and decreased the oil yield. The H₂O content in bio-oil was increased by catalytic reforming from 42.03 to 50.32 wt% due to the dehydration reaction occurring on the acid sites inside the large pores of Al-SBA-15. Acids, oxygenates, mono-aromatics, poly aromatic hydrocarbons, and phenolics were the main components of the bio-oil obtained from the pyrolysis of L. japonica. Upon catalytic reforming over Al-SBA-15, the main oxygenate species 1,4-anhydro-d-galactitol and 1,5-anhydro-d-manitol were completely removed. When L. japonica was co-pyrolyzed with polypropylene, the H₂O content in bio-oil was decreased dramatically (8.93 wt% in the case of catalytic co-pyrolysis), contributing to the improvement of the oil quality. A huge increase in the content of gasoline-range and diesel-range hydrocarbons in bio-oil was the most remarkable change that resulted from the co-pyrolysis with polypropylene, suggesting its potential as a transport fuel. The content of mono-aromatics with high economic value was also increased significantly by catalytic co-pyrolysis.     

石墨炉原子吸收光谱法测定奶粉中的六价铬

基于Cr(Ⅲ)与噻吩甲酰三氟丙酮(TTA)生成的络合物在石墨炉中的挥发性,建立一种前处理简单、灵敏度高的测定奶粉中六价铬的分析方法。对样品的消化方式、Cr(Ⅲ)与TTA络合的酸度、试剂的加入量、超声波水浴的温度和时间、静置时间与石墨炉挥发Cr(Ⅲ)的原子化条件进行探讨。结果表明,Cr(Ⅵ)在0.002~0.010mg·L-1浓度内呈良好线性关系(r=0.9995)。奶粉样品中Cr(Ⅵ)不同加入量的平均回收率为78%~93%,其相对标准偏差为3.8%~9.4%,检出限为0.4 mg·L-1。方法具有分析速度快、灵敏度高、干扰少、操作简便等特点,应用于奶粉中六价铬的测定获得了满意的结果。     

钴铬铜复合离子掺杂黑色玻璃的制备及光吸收特性研究

以钠硼硅玻璃为基质,引入过渡金属离子为着色剂制备了单一离子着色玻璃和复合离子掺杂黑色玻璃,测定了各玻璃样品的透射光谱。结果表明,不同过渡金属离子对不同波段的太阳光产生吸收,钴铬铜复合离子掺杂黑色玻璃对到达地表的所有太阳光波段的吸收率可达到99%以上。     

固溶温度对Ti-5Mo-5V-2Cr-3Al钛合金棒材组织和性能的影响规律

研究了固溶温度对Ti-5Mo-5V-2Cr-3Al钛合金棒材显微组织和力学性能的影响。结果表明,钛合金固溶处理温度在相变点以下,空冷后,显微组织由β相、初生α相以及次生α相组成。随着固溶温度的升高,显微组织中β相晶粒尺寸增大,晶界α相厚度减小,产生有序化现象,而次生α相数量和尺寸减小,使合金的强度降低,塑性升高,但固溶处理温度为800℃时,网状晶界α相使塑性迅速下降;当固溶处理温度在相变点以上,Ti-5Mo-5V-2Cr-3Al钛合金重新形核并长大,随着固溶温度的升高,β相晶粒尺寸增大,初生α相数量减少,强度和塑性都下降,过冷β相晶粒发生应力诱发马氏体现象。     

Effects of the Thickness Ratio of CrN vs Cr2O3 Layer on the Properties of Double-layered CrN/Cr2O3 Coatings Deposited by Arc Ion Plating

In this study, CrN/Cr2O3 double-layered coatings with various thickness ratios of CrN vs Cr2O3 layer were prepared by arc ion plating technology. The influences of the thickness ratio of CrN vs Cr2O3 layer on the microstructural characteristics as well as the mechanical and tribological properties of the CrN/Cr2O3 doublelayered coatings were investigated. The corresponding mechanisms were also discussed. The results indicated that the insertion of CrN layer between the Cr2O3 layer and substrate can effectively decrease the internal stress level of the coating. With increasing the thickness ratio of CrN vs Cr2O3 layer, the surface roughness of double-layered coatings decreased gradually, which had a certain influence on the friction coefficient. In addition, the microhardness also declined gradually, the adhesive strength almost increased linearly, whereas the wear rate declined firstly and then increased slightly. As the thickness ratio was 2：1, the double-layered coating exhibited the best wear resistance.     

Mn18Cr18N护环钢静态再结晶组织及模型

在Gleeble-1500D热模拟机上,采用双道次热压缩试验研究Mn18Cr18N护环钢高温变形后不同停留时间内的静态软化行为,分析热变形温度、应变速率、变形程度以及初始奥氏体晶粒对静态再结晶行为的影响.通过应力补偿法计算静态再结晶软化率,并结合金相组织作了修正.建立其静态再结晶动力学模型,获得静态再结晶激活能249.3 k J/mol.研究表明:Mn18Cr18N钢静态再结晶软化曲线呈"S"形,符合Avrami方程.静态再结晶体积分数随着停留时间延长而增加,热变形温度越高,静态再结晶分数越大,而在较低温度和较小变形程度时,孕育时间较长,主要发生静态回复,将静态再结晶动力学模型的预测结果与实测值进行比较,二者吻合较好,为护环钢后续热镦粗工艺模拟提供更为详尽的模型.     

High-temperature corrosion behavior of Ni–50Cr coating deposited by high velocity oxygen–fuel technique on low alloy ferritic steel

Ni–50Cr coatings were deposited using the HVOF technique on low alloy ferritic steel (2.25Cr–1Mo) substrates to improve their performance in high temperature steam environments. Different thermal spray parameters were studied in order to optimize the corrosion resistance of the coatings. High temperature thermal tests at 650 °C in different CO₂ atmospheres (air with 0, 15 and 25 vol.% CO₂) and thermal cycling tests in air at 550 °C and 650 °C were conducted to study the effectiveness of the coating protection system. The uncoated specimens were severely corroded but no oxidation in the coated substrates was detected. A reduction of 10 times in terms of weight change per area unit in the coated steel was obtained after 360 h of testing respect to that of the uncoated steel.     

Magnetic and structural properties of nanostructured (Fe65Co35)100−xCrx (x = 0, 10) powders prepared by mechanical alloying process

This work focuses on the preparation of nanostructured (Fe₆₅Co₃₅)_100−xCr_x (x = 0, 10) powders by mechanical alloying. The powders are milled for different milling times (up to 90 h). Characterizations of the milled powders were carried out by X-ray diffraction (XRD), scanning electron microscopy (SEM) and vibratory sample magnetometer (VSM). It was observed that the formation of bcc-FeCo and bcc-FeCoCr phases were completely accomplished after 60 and 90 h of milling, respectively. The grain size decreases and the microstrain increases with increasing the milling time. In the initial stages of milling (up to 15 h) for the (Fe₆₅Co₃₅)₉₀Cr₁₀ powders, the saturation magnetization (M_s) decreased but further milling (up to 90 h) increased the M_s. However, the trend for coercivity was different and three stages were observed. An initial increasing stage (up to 15 h of milling), followed by a reducing middle stage (up to 60 h of milling) and then again an increasing final stage (up to 90 h milling). Besides, for the same milling time of 90 h, the addition of 10 at.% of Cr to Fe₆₅Co₃₅ powders leads to higher coercivity and lower saturation magnetization.     

A study of microstructure and performance of cast Fe–8Cr–2B alloy

The effects of quenching temperature on microstructure and hardness of cast Fe–8Cr–2B alloy containing 0.3 wt% C, 2.0 wt% B, 8.0 wt% Cr, 0.6 wt% Si, and 0.8 wt% Mn were investigated by optical microscopy (OM), scanning electron microscopy (SEM), X‐ray diffraction (XRD), Rockwell hardness and Vickers microhardness testers. The experimental results indicate that the as‐cast microstructure of cast Fe–8Cr–2B alloy consists of M₂B (M = Fe, Cr), M₇(C, B)₃, α‐Fe, and γ‐Fe. The dendritic matrix composed of lath martensite mixed with a small amount of retained austenite, and the netlike boride M₂B distribute in the grain boundary. After quenching between 950 °C and 1100 °C, the netlike eutectic boride are broken up and a new phase‐M₂₃(C, B)₆ which is distributed in the shape of sphere or short rod‐like are precipitated from the matrix. Both the macrohardness and microhardness of specimens increase with the increasing quenching temperature. At about 1050 °C, the hardness reaches the maximum value. However, when the temperature exceeds 1050 °C, the hardness will decrease slightly. With the increase of tempering temperature, the hardness of cast Fe–8Cr–2B alloy quenching from 1050 °C decreases gradually and its impact toughness increases slightly. Crusher hammer made of cast Fe–8Cr–2B alloy quenching from 1050 °C and tempering from 300 °C has good application effect, and its service life improves by 150–180% than that of high manganese steel hammer.     

开放体系下碳热还原氮化法制备(Cr,Ta)_2CN固溶体粉末的研究

以Cr2O3、Ta2O5和纳米碳黑为原料,在开放体系的流动N2气氛条件下,采用碳热还原氮化法制备出了(Cr,Ta)2CN固溶体粉末,利用XRD、SEM、EDS等分析测试手段对制备过程中的物相演变规律和微观形貌变化进行了研究。研究结果表明,碳热还原氮化法制备(Cr,Ta)2CN固溶体粉末过程中物相演变顺序为Cr2O3、Ta2O5、C→Cr2O3、Cr3C2、Cr7C3、Cr Ta O4、C→Cr2O3、Cr7C3、Cr Ta O4→(Cr,Ta)2CN。在N2流量为500 m L/min、烧结温度为1 500℃保温2 h的条件下,可制备出粒度约5μm、游离碳和氧含量分别为0.16%,0.085%的单相(Cr,Ta)2CN固溶体粉末。