柴达木盆地涩北地区第四系泥岩型生物气储层孔隙有效性评价

通过低场核磁共振实验分析了柴达木盆地涩北地区第四系泥岩型生物气储层在饱和水状态及渐变烘干温度状态下的T₂谱,明确了孔隙流体的核磁响应特征,以评价孔隙的有效性。研究结果表明： ①核磁共振实验是以饱和水状态T₂谱为基础,采用正态分布函数拟合构建了离心束缚水T₂谱,确定了可动流体和毛管束缚流体T₂截止值,用于划分出流体类型并开展了孔隙有效性评价。②研究区岩样饱和水状态T₂谱谱峰呈左小右大的形态,右峰幅度值远大于左峰,占T₂谱幅度值90%以上;随着烘干温度的升高,T₂谱幅度减小且左移趋势明显;束缚水T₂谱形态近似于正态分布,起始位置与饱和水状态的T₂谱基本重合。③研究区可动流体T₂截止值T_{2 C1}平均为3.3 ms,毛管束缚流体T₂截止值T_{2 C2}平均为1.8 ms;孔隙流体包括可动水、毛管束缚水和黏土束缚水,黏土束缚水T₂小于T_{2 C2},毛管束缚水T₂大于T_{2 C2}且小于T_{2 C1},可动流体T₂大于T_{2 C1};毛管束缚水含量最高,黏土束缚水其次,两者占总孔隙流体的84.43%～95.06%,可动水含量低。④研究区储层有效孔隙占总孔隙的54.99%,主要为毛管束缚孔,黏土束缚孔为无效孔隙;黏土含量越高,有效孔隙度越小。     

Sand corrosion,thermal expansion,and ablation of medium- and high-entropy compositionally complex fluorite oxides

Sand corrosion, thermal expansion, and ablation properties of a new class of medium- and high-entropy compositionally complex fluorite oxides (CCFOs) are examined as potential protective coating materials. Five binary oxides were mixed and sintered into dense, single-phase CCFOs of the general formula: [Hf_(1-2x)/3Zr_(1-2x)/3Ce_(1-2x)/3Y_xYb_x]O_2-δ (x = 0.2, 0.074, and 0.029). These CCFOs exhibit decreased molten sand infiltration and interaction at intermediate temperatures (1200-1300°C) in comparison with a cubic yttria-stabilized zirconia (YSZ) reference; however, at higher temperatures, the trend is reversed due to the increased chemical reactivity. The equimolar high-entropy (Hf_0.2Zr_0.2Ce_0.2Y_0.2Yb_0.2)O_2-δ exhibits no grain boundary penetration by molten sand at all examined temperatures (1200°C-1500°C), although reaction and precipitation are significant. Moreover, these CCFOs exhibit higher intrinsic thermal expansion coefficients (CTE) than the YSZ reference, thereby being more compatible with Ni-based superalloys. The 8YSZ-like (Hf_0.284Zr_0.284Ce_0.284Y_0.074Yb_0.074)O_2-δ exhibits the highest CTE in this series of CCFOs due to oxygen clustering effects. Finally, these CCFOs also exhibit lower emissivities and form unique faceted microstructures in ablative environments.     

High-temperature Na2SO4 interaction with air plasma sprayed Yb2Si2O7 + Si EBC system: Topcoat behavior

The high-temperature interaction between ~2.5 mg/cm² of Na₂SO₄ and an atmospheric plasma sprayed (APS) Yb₂Si₂O₇ topcoat–Si bond coat system on SiC CMC substrates was studied for times up to 240 h at 1000°C–1316°C in a 0.1% SO₂–O₂ gaseous environment. Yb₂Si₂O₇ reacted with Na₂SO₄ to form Yb₂SiO₅ and an intergranular amorphous Na-silicate phase. Below 1200°C, the reaction was sluggish, needing days to cause morphological changes to the “splat microstructure” associated with APS coatings. The reaction was rapid at 1200°C and above, needing only a few hours for the entire topcoat to transform into a granulated microstructure consisting of Yb₂SiO₅ and Yb₂Si₂O₇ phases. Na₂SO₄ deposits infiltrated the Yb₂Si₂O₇ topcoat and transformed into an amorphous Na-silicate in less than 1 h at all exposure temperatures. Quantitative assessment of the Yb₂SiO₅ area fraction in the topcoat showed a linear decrease over time at 1316°C, attributed to reaction with the SiO₂ thermally grown oxide (TGO) formed on the Si bond coat and rapid transport through the interpenetrating amorphous Na-silicate grain boundary phase. It was predicted that nearly 2 weeks is needed for complete removal of Yb₂SiO₅ from the topcoat at 1316°C for a single applied loading of Na₂SO₄.     

Na2SO4 deposit-induced hot corrosion of SiC fibers relevant for SiC CMCs

Hi Nicalon, Hi Nicalon S, Sylramic, and Sylramic iBN SiC fibers were exposed to ~60 μg/cm² of Na₂SO₄ in a 0.1% SO₂/O₂ gaseous environment for times between 0.75 and 24 h at 1000°C. After exposure, the corrosion products were characterized using SEM, EDS, ICP-OES, TEM, and EFTEM to determine their high-temperature resistance to Na₂SO₄ and key reaction mechanisms. All SiC fiber types tested in this work exhibited little resistance to Na₂SO₄ deposit-induced attack relative to their behavior in dry O₂ environments. It was found that Hi-Nicalon displayed the least resistance to Na₂SO₄ deposit-induced attack due to excess carbon content resulting in the formation of a highly porous crystalline oxide and promotion of basic corrosion conditions. All fiber types formed a crystalline SiO₂ reaction product, either cristobalite or tridymite. Sylramic and Sylramic iBN formed a crystalline SiO₂ reaction layer containing TiO₂ needles due oxidation of TiB₂ particles. Additionally, Na₂SO₄ deposits resulted in pitting of all fiber surfaces.     

An improved strategy to synthesize graphite oxide with controllable interlayer spacing as coatings for anticorrosion application

A facile method to synthesize nanoscale graphene oxide (GO) with controllable interlayer spacing was carried out using two-step oxidation process and much less acid to improve the efficiency of the oxidation. The X-ray diffraction results demonstrated that GO had been successfully prepared from graphite because of disappearance of characteristic peaks of pristine graphite at about 2θ = 26.5° along with appearance of a sharp major peak of GO at about 2θ = 9.4°. The increased basal spacing d₀₀₁ of as-prepared GO could reach as high as 9.39 Å, suggesting higher degree of oxidation than that prepared by the classical Hummers' synthesis, and characterization results from Fourier transform infrared spectrometer, X-ray photoelectron spectroscopy, Raman spectroscopy, scanning electron microscopy and transmission electron microscopy further confirmed this conclusion. The influence of GO on anti-corrosion performance of nanocomposite coatings composited with the 2,5-dimethoxyaniline (DMA) conductive polymer was examined via potentiodynamic polarization curve tests in 3.5 wt% NaCl aqueous solution. The results demonstrated that the incorporation of GO significantly decreased the corrosion current density (i_corr = 2.62 μA/cm²) in the case of GO-PDMA coating, reflecting excellent physical isolation of GO and its synergistic effect with PDMA against the infiltration of water and corrosive electrolyte.     

Use of acoustic emission technique for the early detection of aluminum alloys exfoliation corrosion

Exfoliation corrosion of aluminum alloys is a form of localized corrosion which affects many industries, specially aeronautics. The study of this corrosion mode using only electrochemical techniques is not fully efficient for the detection and control on line of this phenomenon. Therefore, we developed a non-destructive testing technique based on the acoustic emission recordings in order to follow-up this form of corrosion on aluminum alloys. Indeed, recent works have shown the interest of the acoustic emission for the detection, the monitoring and the localization of pitting corrosion on aluminum alloys. This pitting corrosion phenomenon is currently well understood and the experimental methodology acquired during that study is transposed to the study of exfoliation corrosion of aluminum alloys.The present study is conducted on two aluminum alloys: (Al 2024 T3, and Al 7449 T6 and T7). Samples are immersed 4 days in the modified ASTM STP 1134 saline solution. Observations of the structures after tests show that the exfoliation corrosion sensitivity of alloy 7449 T6 is more important than for alloy 7449 T7 which exhibits only the presence of small and non-occluded pits. Very severe exfoliation corrosion was also observed on Al 2024 T3, but after a longer immersion time or in a more acid solution.The recording of the acoustic emission activity shows evident links between this activity and the exfoliation corrosion rate. The analysis of the signal's characteristics reveals a population corresponding to the release of hydrogen bubbles. A few more energetic signals have also been observed. Their source can be either, the cracking resulting from the separation of sheets of metal, or the development and evolution of hydrogen bubbles formed inside blisters during exfoliation corrosion.     

咪唑啉型缓蚀剂的合成及其缓蚀机理的研究

以棕榈酸、二乙烯三胺、马来酸酐为原料合成了一种咪唑啉型缓蚀剂YQ-01,与YQ-02复配后得到能有效抑制二氧化碳腐蚀的缓蚀体系YQ-03。应用静态挂片失重法、电化学极化曲线、X射线光电子能谱分析研究了YQ-03抑制二氧化碳腐蚀的电化学特征,分析了腐蚀前、后及加入缓蚀体系YQ-03后A3钢的表面产物,探讨了YQ-03的缓蚀机理。结果表明,由主剂YQ-01和助剂YQ-02组成的复配缓蚀体系有良好的协同作用,腐蚀产物膜有3层,能有效抑制饱和CO2的高矿化度盐水对A3钢的腐蚀。     

Improvement of corrosion resistance of AZ91D magnesium alloy by gadolinium addition

Based on the previous investigation on beneficial introduction of holmium into magnesium alloy, the effect of gadolinium, an adjacent rare earth element, on corrosion resistance was examined. The corrosion behavior of two Mg-9Al-Gd alloys （Mg-9Al-0.45Gd and Mg-9Al-l.43Gd） was evaluated and compared with that of Mg-9Al alloy without Gd by means of specimen mass loss and hydrogen evolution in 3.5% NaCl solution saturated with Mg（OH）2. The Gd-containing alloys exhibit enhanced corrosion resistance with respect to the plain Mg-9Al alloy. The microstructures of Mg-9Al alloy and Mg-9Al-0.45 Gd alloy were observed by electron probe microanalysis （EPMA） and energy dispersion spectroscopy （EDS）. The alloys with Gd addition show a microstructure characterized by a phase solid solution, surrounded by minor amount of β phase and more grain-like Gd-containing phase. To illustrate the involved mechanism their polarization curves were recorded. The electrochemical investigations reveal that Gd addition shifts the corrosion potential of the alloy towards active, as Gd containing phase is more active and hence less cathodic. As a result, the micro-galvanic corrosion is suppressed. Moreover corrosion product films formed on the Gd containing alloys are more compact and provide a better protective effectiveness than that on the alloy without Gd against corrosion. Repassivation measurements in mixture solution of 0.21 mol/L K2CrO4＋0.6 mol/L NaCI also verify the beneficial role of Gd addition. Based on the present preliminary analysis, both the deposited Gd-containing phases and corrosion product films are believed to be responsible for the improved corrosion behaviour due to Gd addition.     

Quantitative determination of corrosion products and adsorbed water on copper in humid air containing SO2 by IR-RAS measurements

The time dependency of the amounts of corrosion products and co-existing adsorbed water on copper in humid air containing SO₂ was estimated from a series of in situ time-resolved IR-RAS spectra on the basis of the relations between the band intensities and the mass changes of the corrosion products, which were determined by simultaneous measurement of IR-RAS and QCM. The amounts of both corrosion products increased slowly at the initial stage and later increased rapidly. Although the relative humidity was kept constant, the amount of adsorbed water increased nearly the same behavior as that of corrosion products in the stage of relatively small amounts of corrosion products and later increased rapidly when the amounts of corrosion products increased. In humid air without SO₂, sulfite gradually decomposed and some of it changed into sulfate.     

X射线荧光光谱在铝矿石赤泥组分分析中的应用

文介绍X射线荧光光谱在铝矿石，赤泥等材料组分分析中的应用。采用熔融玻璃片和粉末压片法制样，用理论α系数和散射线内标法校正元素间的效应。使用PW2403x射线光谱仪对样品中的Al2O3、SiO2、Fe2O3、TiO2、K2O、NB2O、CaO、MgO、P2O5、灼减、MnO、S、Pb、Zn、Sr、Zr、V、Ga、Cr等19个元素进行测定，其分析结果的精密度和准确度可与化学法相媲美。