EFFECT OF AGING ON HYDROGEN EMBRITTLEMENT SUSCEPTIBILITY OF STEEL Cr21Ni6Mn9N

Effects of 650℃ aging for 1—1000 h on structure and hydrogen embrittlement susceptibility(HES)of steel Cr21Ni6Mn9N have been investigated.The results show that M_(23)C_6 typecarbide precipitates at grain boundaries and Cr-depletive region appears beside them duringaging.The precipitates grow and connect each other as the aging time prolongs.Meanwhile,the degree of Cr-depletion aggravates first and then recovers gradually while the aging time isvery long,i.e.,1000 h.The HES of the steel increases with increasing aging time but does notreduce with the recovery of Cr content at the Cr-depletive region.That implies that the ex-isting of carbides at grain boundaries might be the main reason which promotes the HES ofsteel during aging.     

同轴电纺法TiO2/g-C3N4的制备及光催化性能研究

传统的静电纺丝法使用单一的毛细管状喷头喷丝,通常用于制备实心且表面光滑单一组分的纳米纤维,无法得到具有多种功能性结构的复合材料,应用范围较窄。以酞酸丁酯和尿素为原料,采用同轴静电纺丝法成功制备了TiO₂/g-C₃N₄复合材料,并用X射线衍射（XRD）、傅里叶变换红外光谱（FTIR）、紫外可见漫反射光谱（UV-vis DRS）、场发射扫描电子显微镜（SEM）和Brunauer-Emmett-Teller （BET）分析对样品进行了表征,通过光催化降解亚甲基蓝溶液（MB）研究了不同g-C₃N₄添加量对TiO₂/g-C₃N₄复合材料光催化性能的影响。实验结果表明,采用同轴静电纺丝法结合500℃煅烧工艺成功制备了大比表面积及高光催化性能的TiO₂/g-C₃N₄复合材料。当g-C₃N₄添加量为0.15 g时,TiO₂/g-C₃N₄复合材料对亚甲基蓝溶液（MB）的光催化降解效率可达93.8%,且经过5次重复实验后降解率仍可达80%以上。     

N,N−二甲基−二硫代甲酰胺丙磺酸钠对THPED体系化学镀铜的影响

研究了N,N?二甲基?二硫代甲酰胺丙磺酸钠(DPS)作为添加剂对以四羟丙基乙二胺(THPED)为单一配位剂的化学镀铜体系的沉积速率、镀层形貌和晶体结构的影响。结果发现,当DPS的质量浓度从0 mg/L增大到1.0 mg/L时,沉积速率从2.91μm/h提高到6.73μm/h,所得镀层结晶均匀、细致。线性扫描伏安测量结果表明,DPS是通过促进甲醛的阳极氧化来加速化学镀过程。本体系的Cu镀层主要呈面心立方多晶取向,DPS的添加会令晶面取向从(220)转变为(111)。     

Structural Studies of the Lipopolysaccharide of Aeromonas veronii bv. sobria Strain K133 Which Represents New Provisional Serogroup PGO1 Prevailing among Mesophilic Aeromonads on Polish Fish Farms

In the present work, we performed immunochemical studies of LPS, especially the O-specific polysaccharide (O-PS) of Aeromonas veronii bv. sobria strain K133, which was isolated from the kidney of carp (Cyprinus carpio L.) during an outbreak of motile aeromonad infection/motile aeromonad septicemia (MAI/MAS) on a Polish fish farm. The structural characterization of the O-PS, which was obtained by mild acid degradation of the LPS, was performed with chemical methods, MALDI-TOF mass spectrometry, and ¹H and ¹³C NMR spectroscopy. It was revealed that the O-PS has a unique composition of a linear tetrasaccharide repeating unit and contains a rarely occurring sugar 2,4-diamino-2,4,6-trideoxy-D-glucose (bacillosamine), which may determine the specificity of the serogroup. Western blotting and ELISA confirmed that A. veronii bv. sobria strain K133 belongs to the new serogroup PGO1, which is one of the most commonly represented immunotypes among carp and trout isolates of Aeromonas sp. in Polish aquacultures. Considering the increase in the MAI/MAS incidences and their impact on freshwater species, also with economic importance, and in the absence of an effective immunoprophylaxis, studies of the Aeromonas O-antigens are relevant in the light of epidemiological data and monitoring emergent pathogens representing unknown antigenic variants and serotypes.     

BiOI/g-C3N4光催化降解甲基橙研究

以三聚氰胺为前驱物采用热聚合法制备了石墨相氮化碳（g-C₃N₄）,并在其表面原位合成了碘氧化铋（BiOI）,构筑了石墨相氮化碳-碘氧化铋复合材料。采用X射线衍射仪（XRD）、傅里叶变换红外光谱仪（FT-IR）、紫外可见漫反射仪（UV-Vis-DRS）等对催化剂进行了表征。结果表明,当BiOI与g-C₃N₄物质的量比为0.5时,BiOI/g-C₃N₄催化剂具有高分散的BiOI颗粒及适中的禁带宽度,吸附和降解甲基橙性能最佳。回流温度为120 ℃时制备的BiOI/g-C₃N₄催化剂具有适中的粒径、比表面积和表面羟基浓度,吸附和降解甲基橙性能最佳,且该催化剂具有良好的重复使用性能。     

N含量对Nb微合金化HRB400E钢筋组织与性能的影响

摘要：为了更好地发挥N元素在Nb微合金化钢筋中的作用,降低生产成本以及为钢筋成分设计提供理论依据。利用金相显微镜、扫描电镜、透射电镜、力学试验机对不同N含量的Nb微合金化高强抗震钢筋进行显微组织表征及力学性能测试,探究N含量对Nb微合金化钢筋的组织与力学性能的影响。研究表明,轧制过程中的奥氏体组织,随着N含量的增加,平均奥氏体晶粒有所减小;最终组织为铁素体和珠光体,随着N含量的增加,铁素体平均晶粒尺寸而减小,片层状珠光体的连续性增加,片层间距减小;析出相Nb(C,N)随着N含量的增大,沉淀析出的第二项颗粒体积分数增大,颗粒尺寸随之减小;在力学性能方面,屈服强度逐渐增加,抗拉强度先增加后减少。     

控轧控冷工艺对高强度锚杆钢组织和性能的影响

随着矿井深度的增加,对锚杆支护强韧性的要求越来越高,为了应对这一情况,需要研发出更高强度的锚杆钢。利用锚杆钢研究了轧制工艺、冷却工艺与珠光体、铁素体相比例,析出相析出行为及力学性能的关系。研究结果表明,在中轧后、精轧前采用适当水冷+回复段处理的复合工艺可使晶粒更细小、组织更均匀。对超高强度锚杆钢进行热压缩变形试验,由热模拟试验结果确定相转变温度为A_c1=737 ℃、A_c3=886 ℃。最终筛选出入精轧温度为810 ℃、回复段温度为800 ℃时,可获得的晶粒尺寸达4 μm,珠光体体积分数为66.8%,铁素体体积分数为33.2%,珠光体片层间距达200 nm;另外调整V、Cr、N等析出以提高锚杆钢的强韧性,较低的回复温度有利于细小、弥散、V(C/N)析出相的析出,V(C/N)的析出可进一步改善锚杆钢的力学性能。由该控轧控冷工艺轧制的锚杆钢屈服强度为780 MPa、抗拉强度为930 MPa、硬度为291HV、伸长率为20%。     

冷却速率对N06625合金凝固过程微观偏析的影响

高温合金铸锭在凝固过程中各部分冷却条件不同,中心部分冷却速率缓慢。为了模拟铸锭内部的缓慢冷却速率,通过超高温激光共聚焦扫描显微镜(HT-CLSM)、钨灯丝扫描电子显微镜(SEM)、光学显微镜(OM)并结合相关计算,研究了N06625合金在不同冷却速率(10、20、30 ℃/min)下的凝固偏析和微观组织演变状况。结果表明,随着冷却速率升高,析出相的数量、尺寸和面积分数降低,且聚集程度降低,形状由大尺寸长条状和大块状转变为小条状和小块状;Laves相呈块状和条状在枝晶间析出,随着冷却速率降低,Laves相的尺寸和数量增大,聚集程度增加。枝晶干芯部Nb和Mo元素的质量分数以及Nb的有效分配系数(k_e[Nb])和Mo的有效分配系数(k_e[Mo])随冷却速率增大而增大,在所研究冷速范围内都表现出很强烈的偏析倾向,k_e[Nb]分别为0.46、0.55和0.62,k_e[Mo]分别为0.73、0.77和0.80,且k_e[Nb]的变化趋势更加明显。采用Clyne-Kurz偏析模型并结合试验中的数据,对Nb和Mo元素偏析程度的具体变化趋势进行定量表征,结果表明在N06625合金凝固过程中,冷却速率越低或固相分数越大,残余液相中Nb和Mo元素的质量分数上升速率越快。     

00Crl8Nil0N奥氏体不锈钢200 - 600℃高温疲劳性能的研究

试验用00Cr18Ni10N钢（/%:0.018C,0.41Si,1.68Mn,18.18Cr,10.38Ni,0.16N）经1t EAF-AOD-ESR冶炼,锻成Φ30 mm材和1 050℃固溶处理,进行了00Cr18Ni10N钢200～600℃光滑（K_t=1）、缺口（K_t=3）的轴向高周疲劳性能研究,绘制了疲劳S-N曲线、计算了疲劳极限,并对疲劳试样的典型断口进行了SEM观察。结果表明,光滑试样的疲劳极限随试验温度升高而降低,缺口试样的疲劳极限对试验温度变化不敏感。当应力集中系数由K_t=1提高到K_t=3时,00Cr18Ni10N钢的200、400、600℃下10⁷周次条件疲劳极限分别从530、506、410 MPa,降低到323、370、392 MPa。表明在高温下00Cr18Ni10N钢存在疲劳极限对应力集中敏感,且应力集中敏感性随着试验温度的升高而降低。疲劳试样的断口形貌由疲劳源区、疲劳裂纹扩展区和瞬断区组成,疲劳起源于表面加工刀痕的不连续位置,呈韧性断裂特征。     

Thermal stability behaviors of Cr(N,O)/CrN double-layered coatings by TGA/DTA analysis

In this study, Cr(N,O)/CrN double-layered coatings were synthesized using the cathodic arc deposition (CAD) process. CrN film was first deposited onto a substrate as an interlayer to ensure better adhesion, and Cr(N,O) film was subsequently deposited on top of the CrN layer as the surface layer. Variation in the Cr(N,O) coating composition was achieved through changing the O₂/N₂ flow ratio during the last stage of processing. Phase structure, chemical composition, and morphology of the resulting coatings were analyzed and observed using the X-ray diffractometer, Auger electron spectrometer and SEM. In addition, oxidation behavior of the coatings was investigated using TGA/DTA methods. The tests were carried out by increasing temperature up to 1000 °C in ambient air. With the introduction of oxygen gas during the CAD process, a superficial layer was produced in the Cr(N,O) constituent containing CrN and Cr₂O₃ phases. The formation of the oxide phase attributed to the reaction of chromium and oxygen was more favorable than that of chromium and nitrogen. The results also showed that Cr(N,O)/CrN double-layered coatings exhibited superior oxidation resistance at elevated temperature than that of CrN single-layer coated specimen (870 °C vs. 750 °C).