低碳微合金钢中的晶内铁素体及组织控制

回顾和评述了晶内铁素体的发现、发展及其与组织控制的关系.介绍了晶内铁素体的形核机制和影响晶内铁素体形成的因素,讨论了晶内铁素体的三维形态和长大动力学,并从以上几方面分析了晶内铁素体对低碳微合金钢组织细化的重要作用和影响.     

LF软吹时间对硅脱氧弹簧钢氧化物夹杂控制影响

 对于一些采用硅锰脱氧冶炼工艺的特殊钢,为保证钢水洁净度,常会选择较长时间的LF软吹处理,导致过程能耗增加。通过工业试验,借助FEI Explorer 4自动扫描电镜检测,研究不同LF精炼软吹时间对硅脱氧弹簧钢55SiCr铸坯氧化物夹杂成分、数量的影响;并采用夹杂物极值统计法,对比评价不同LF精炼软吹时间对应成品盘条横截面最大夹杂物尺寸控制情况。结果表明,在LF软吹10 min与软吹40 min 两种工艺条件下,铸坯中尺寸大于5 μm的氧化物夹杂成分接近,均在CaO-SiO₂-Al₂O₃相图中假硅灰石、钙长石和钙铝黄长石共晶低熔点区,其中软吹10 min工艺铸坯氧化物夹杂组成落入低熔点区的数量所占比例更大。LF软吹10 min与软吹40 min铸坯中尺寸大于5 μm的氧化物夹杂数量密度分别为11.70个/100 mm2和14.59个/100 mm2,尺寸大于15 μm 的氧化物夹杂数量密度分别为0.53个/100 mm2和1.65个/100 mm2,LF软吹10 min工艺铸坯大尺寸氧化物夹杂数量密度略低于LF软吹40 min工艺。当预测面积为30 000 mm2时,两种LF软吹时间对应成品盘条横截面最大夹杂物尺寸分别为27.1 μm和28.1 μm,盘条最大夹杂物尺寸控制无显著差别。结合硅锰脱氧钢中大尺寸低熔点CaO-SiO₂-Al₂O₃系夹杂物主要源自钢包渣乳化卷入,具有与钢水和氩气泡界面接触角很小、难以通过吹氩上浮去除的特点,建议硅锰脱氧钢LF软吹过程按短时间快节奏进行控制。     

Evolution of carbides and carbon content in matrix of an ultra-high carbon sintered steel during heat treatment process

DTA, thermal expansion, XRD, and SEM were used to evaluate the effect of quenching temperature on the mechanical properties and microstructure of a novel sintered steel Fe-6Co-1Ni-5Cr-5Mo-1C. Lattice parameters and the mass fraction of carbon dissolved in the matrix of the steel quenched were investigated. It is discovered that the hardness of the steel increases with quench-ing temperature in the range of 840-900℃ and remains constant in the range of 900 to 1100℃. It decreases rapidly when the tem-perature is higher than 1100℃. The mass fraction of carbon dissolved in the matrix of the steel quenched at 840℃ is 0.38, but when the quenching temperature is increased to 1150℃, it increases to 0.98. The carbides formed during sintering are still present at grain boundaries and in the matrix of the steel quenched at low quenching temperatures, such as 840℃. When the quenching temperature is increased to 1150℃, most of the carbides at grain boundaries are dissolved with just a small amount of spherical M23C6 existing in the matrix of the quenched steel.     

季铵型稻草木质素的合成及其对\[PdCl4\]2-的吸附性能

为经济高效和无污染提取钯,采用硫酸法从稻草中提取木质素,经3-氯-2-羟丙基三甲基氯化铵(CHMAC)化学改性后合成季铵型稻草木质素,并利用其从溶液中吸附[PdCl_4]~(2-).利用扫描电镜(SEM)、傅立叶红外光谱(FTIR)和差热-热重分析(TG-DSC)对木质素及其衍生物进行表征,同时考察pH值、[PdCl_4]~(2-)初始浓度和吸附时间对季铵型稻草木质素吸附性能的影响,并对[PdCl_4]~(2-)的选择性进行研究.实验结果表明,季铵型稻草木质素为表面多孔且不规则的块状体,在200℃内具有良好的热稳定性,1 469 cm~(-1)处出现季铵离子的弯曲振动特征峰.最佳吸附pH值为2,吸附平衡时间为8 h,在[PdCl_4]~(2-)初始浓度为4 mmol·L~(-1)时,季铵型稻草木质素对[PdCl_4]~(2-)的吸附达到饱和,饱和吸附容量为1.120 mmol·g~(-1),吸附过程遵循准二级动力学方程,吸附等温模型与Freundlich方程拟合较好,表明吸附过程为单分子层非均质化学吸附,盐酸浓度低于1 mol·L~(-1)时,季铵型稻草木质素对[PdCl_4]~(2-)具有良好的选择性.降低盐酸浓度,提高[PdCl_4]~(2-)初始浓度和延长吸附时间均有利于提高季铵型稻草木质素对[PdCl_4]~(2-)的吸附容量和选择性.     

Growth characteristics and kinetics of niobium carbide coating obtained on AISI 52100 by thermal-reactive diffusion technique

Niobium carbide coating was produced by thermal-reactive diffusion technique on AISI 52100 steel in salt bath at 1 123 K, 1 173 K, and 1 223 K for 1, 2, 4, and 6 hours. The salt consisted of borax, sodium fl uoride, boron carbide, and niobium pentoxide. The presence of NbC phase on the steel surface was confi rmed by X-ray diffraction analysis. Microscopic observation showed that niobium carbide coating formed on the substrate was smooth and compact. There was a distinct and fl at interface between the coating and substrate. The micro-hardness of niobium carbide coating was 2892±145HV. The thickness of coating ranged from 1.6 μm to 14μm. The forming kinetics of niobium carbide coating was revealed. Moreover, a contour diagram derived from experimental data was graphed for correct selection of process parameters. Some mathematical equations were built for predicting the coating thickness with predetermined processing temperature and time. The results showed that these mathematical equations are very practical as well as the kinetics equation.     

不锈钢粉尘内配煤团块高温自还原过程中金属铁的聚集

用不锈钢生产中的高碱度二次粉尘制备内配煤团块,在高温下自还原获得含铬、镍的金属铁粒.研究影响铁粒聚集长大的因素.研究表明：（1）内配煤团块的渣相碱度（w（CaO）/w（SiO2））小于2.8时,还原产物冷却过程中渣相与金属铁粒才能自然分离.碱度越低,渣量越大,越不利于金属铁聚集长大;（2）提高内配碳比,渣相残碳量明显升高,渣中过量的碳阻碍金属相聚集长大;（3）提高还原温度,直接还原铁的海绵状结构解体,逐渐聚集成颗粒状金属铁.还原温度越高,越有利于金属铁的聚集长大     

V的碳氮化合物析出对36Mn2V非调质钢组织性能的影响

在φ340机组上进行非调质36Mn2V和37Mn5油井管钢工艺试验,对比分析二者组织性能．研究36Mn2V钢中微合金元素V的碳氯化物析出对其组织性能的影响。结果表明。36Mn2V、37Mn5钢可分别用于高钢级N80-1和低钢级J55、K55油井管的生产,36Mn2V非调质钢在高温形变诱导下析出V（C、N）,促进了晶内细小铁素体和珠光体的析出,反之细晶铁素体析出促进了V（C、N）沿y／a界面弥散析出,故而显著改善了36Mn2V非调质钢组织性能。     

碳热还原氮化一步法制备钒氮合金工艺研究

对V2O5自还原氮化过程进行热力学分析,并以工业级V2O5和炭黑为原料,经过混料、研磨、压制成块后进行烧结和还原氮化,制得含氮量较高的钒氮合金。结果表明,为了避免V2O5在还原过程中挥发,预还原温度应控制在V2O5熔点（678℃）以下;经过650℃预还原4h,试样中的V2O5才能全部转化为低价态的钒氧化物;V2O5在N2气氛下自还原时,还原终温低于1 271℃时,还原产物优先生成VN,还原终温高于1 271℃时,还原产物中才会出现大量VC;为保证还原产物的高氮和低碳含量,应将还原氮化最终温度控制在1 200～1 300℃。     

低碳钢头坯洁净度研究

采用氧氮分析、金相分析、大样电解分析、扫描电镜及能谱分析等,研究LD—Ar站—CC生产的低碳钢头坯不同浇铸长度处的洁净度变化规律,并与正常坯洁净度水平进行对比分析。结果表明,头坯中T[O]和氮含量均随着浇铸长度的增加呈明显的下降趋势;头坯中显微夹杂物数量和大型夹杂物数量随着浇铸长度的增加大体都呈减少趋势;头坯中显微夹杂物主要来源于脱氧产物和二次氧化,大型夹杂物来源于二次氧化、结晶器卷渣、中间包卷渣和钢包引流砂;与正常坯洁净度相比较,头坯洁净度在浇铸长度大于3m以后与正常坯水平相一致。