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1.
对在原渣系中加入不同质量分数的BaO、Li2O、B2O3和CaF2形成的新渣系,通过正交实验法进行脱硫实验分析。结果表明,对新渣系脱硫率影响从大到小依次是B2O3、Li2O、CaF2、BaO,加入添加剂之后的新渣系脱硫率都在80%以上;添加剂含量为w(BaO)=4%~6%、w(Li2O)=7%~10%、w(B2O3)=3%~4%和w(CaF2)≤3%时,渣系的脱硫效果最佳,实验室条件下能将钢中硫降至0.002%以内。  相似文献   

2.
高铝钢连铸过程中,为了避免或减轻钢液中Al与保护渣中SiO2发生反应,设计了低SiO2、高Al2O3含量的高铝钢连铸保护渣,通过添加适量的酸性氧化物B2O3协调熔渣酸碱性,利用实验分析了B2O3含量对高铝钢保护渣熔融特性、黏度特性及渣膜传热特性的影响。结果表明,B2O3含量在4%~10%时,随着B2O3含量增加,保护渣熔化温度、黏度、黏流活化能均降低,渣膜热流密度增加;保护渣的等温转变曲线(TTT曲线)向孕育时间增加的方向移动,晶体生长速率降低;实验条件下,增加B2O3含量可抑制保护渣中CaF2的析出。  相似文献   

3.
BaO,B2O3对CaO基精炼渣熔化性能及脱硫能力的影响   总被引:8,自引:0,他引:8  
在CaO基精炼渣中加入BaO和B2O3进行改质,对改质后的精炼渣进行熔化性能和脱硫性能的实验研究.结果表明,BaO可以降低精炼渣的熔点和粘度,有效地改善钢-渣反应的动力学条件,同时增强精炼渣的脱硫能力.当BaO含量为15%~25%时,脱硫率稳定在90%以上;而B2O3对精炼渣的脱硫率无明显影响,可取代CaF2作为助熔剂加入.  相似文献   

4.
助熔剂种类与配比对高磷铁水脱磷渣高温性能的影响   总被引:1,自引:0,他引:1  
分别以CaF2和B2O3为助熔剂,在实验室条件下研究了助熔剂种类与配比对脱磷渣熔点的影响,并测定了脱磷渣在不同温度下的黏度值.结果表明,以CaF2为助熔剂时,在保证脱磷渣熔点较低和流动性较好的同时,为了减轻设备腐蚀和环境污染程度,脱磷渣中CaF2与CaO的质量分数比值以0.50为最佳;以B2O3作为助熔剂时,只有当脱磷渣中B2O3与CaO的质量分数比值达到0.16时,助熔效果才比较明显.  相似文献   

5.
以炉渣离子、分子共存理论为基础,1Cr21Ni5Ti钢为研究对象,Al为脱氧剂,根据熔渣-金属中各个组元的平衡反应和质量守恒,建立了脱氧热力学模型,并在脱氧基础上设计了渣系.在脱氧剂Al不同的加入量条件下对1Cr21Ni5Ti钢中的Si,Al,Mn的平衡质量分数和渣中Ti O2的需求量进行了计算,Ti O2的加入保证了钢中Ti的含量.结果表明:随脱氧剂Al的增加,Si,Al,Mn,Al2O3的平衡质量分数呈上升的趋势,Si O2,Fe O,Mn O以及渣系中Ti O2的设计量呈下降的趋势;当Al加入量达到0.2%后,渣中不稳定氧化物含量很低,大部分Al进入到钢液中,造成钢液增[Al].根据1Cr21Ni5Ti的Si,Al,Mn的成分要求,得到Al的最大加入量为0.15%/吨钢,此时渣系中Ti O2的设计量为4%,达到保钛的目的.  相似文献   

6.
利用热丝法熔化温度测定仪研究了保护渣结晶温度的影响因素,得到各种成分对保护渣结晶温度的影响规律及影响程度·研究表明,随着碱度及渣中NaF和CaF2含量的增大,保护渣结晶温度逐渐升高;随着渣中Al2O3,MgO,Na2O,K2O,BaO,MnO,B2O3含量的增大,保护渣结晶温度逐渐降低;随着渣中Li2O含量的增大,保护渣结晶温度先降低,2%时结晶温度最低,而后逐渐升高·  相似文献   

7.
结合某钢厂顶底复吹转炉冶炼含有铜、镍等成分耐候钢的生产过程,在实验室对铁碳熔体和纯铁液还原炼钢渣中铜、镍等氧化物进行研究.结果表明,在初始条件相同的情况下,1 300 ℃下铁碳熔体分别还原渣中Cu2O和NiO时,Cu2O比NiO更易还原,还原速度更快.1 600 ℃时在实验研究的碱度范围内,含有25% FeO的转炉终点渣中Cu2O、NiO能被纯铁液在10~20 min内还原完毕,尤其前10 min内w[Cu]、w[Ni]增长迅速.在相同碱度下,渣中Cu2O、NiO同时还原的速率基本相同;随着渣碱度的增大,Cu2O、NiO还原的速率及终还原率均有所降低.  相似文献   

8.
利用FactSage热力学软件Phase Diagram和Equilib模块分别计算了CaO含量对CaO-Al2 O3-22%MgO-1%SiO2-2%FeO系液相线的影响以及CaO、调渣剂CaF2和B2 O3单独或复合添加对Al2 O3-MgO-25%CaO-1%SiO2-2%FeO系1700℃液相量的影响。通过差热分析测定了现场实验炉渣的熔化开始温度和结束温度,验证了理论计算变化规律。结果发现:电铝热法生产FeV的炉渣中CaO质量分数应该控制在25%左右,此时熔化性能较好;调渣剂CaF2的调渣效果好于B2 O3,且Al2 O3/MgO质量比较高时二者不能复合使用;考虑到工业应用效果和环境保护,CaF2添加量应控制在2%~5%。  相似文献   

9.
0Cr18Ni9不锈钢中非金属夹杂物来源   总被引:1,自引:0,他引:1  
为了研究不锈钢连铸坯中非金属夹杂物的主要类型及其主要来源,用扫描电镜分析了0Cr18Ni9不锈钢连铸坯中的夹杂物成成,并分别在AOD渣、大包渣及中间包渣中加入示踪剂进行了三次示踪实验.实验结果表明,0Cr18Ni9不锈钢连铸坯中的非金属夹杂物主要为CaO-SiO2-Al2O3-MgO系夹杂物,其次为MgO-Al2O3类尖晶石和硫化物;非金属夹杂物的主要来源是AOD还原期的还原产物、脱硫产物和出钢时混入钢水中的AOD渣滴;AOD出钢后,大包顶渣、中间包覆盖剂和结晶器保护渣不会对钢液造成明显污染.  相似文献   

10.
真空铝热还原法制备金属锶的反应机理   总被引:2,自引:0,他引:2  
为提高锶还原率,研究了真空铝热还原法制备金属锶的反应机理.对锶还原率和渣相间关系进行了理论分析;对实际锶还原率进行了计量;并对实际渣相进行了XRD定量分析.理论分析认为,锶还原率越高,则渣相中SrO.A l2O3相数量越多.实验结果表明:制备的金属Sr纯度可达99.5%以上;实际渣相中SrO.A l2O3相质量分数大大高于理论值;且实际锶还原率越低,渣相中SrO.A l2O3相质量分数反而越高.分析认为,原料A l粉被氧化后生成A l2O3,会大量消耗原料SrO,生成SrO.A l2O3相.尽量减少原料A l粉被氧化,是保证高锶还原率的关键.  相似文献   

11.
LF炉合成精炼渣成分优化   总被引:2,自引:1,他引:2  
通过建立二次回归正交设计模型,考察了合成精炼渣碱度w(CaO)/w(SiO2),Al2O3和CaF2质量分数对LF深脱硫效果的影响.结果表明,当渣中w(FeO)为0.5%,w(MgO)为9%时,随渣中w(CaO)/w(SiO2)增加,脱硫率均先增大后减小.当w(CaO)/w(SiO2)不同时,Al2O3和CaF2质量分数对脱硫效果的影响程度不同,主要原因是渣中有效CaO含量变化引起的.随渣中w(FeO)降低和渣量增加,脱硫率明显增大.实验优化的最佳脱硫渣系组成为w(CaO)/w(SiO2)=9~11,w(Al2O3)=27%~29%,w(MgO)=9%,w(CaF2)=8%~10%,w(FeO...  相似文献   

12.
A thermodynamic analysis of the carbothermic reduction of high-phosphorus oolitic iron ore (HPOIO) was conducted by the FactSage thermochemical software. The effects of temperature, C/O ratio, additive types, and dosages both on the reduction of fluorapatite and the formation of liquid slag were studied. The results show that the minimum thermodynamic reduction temperature of fluorapatite by carbon decreases to about 850°C, which is mainly ascribed to the presence of SiO2, Al2O3, and Fe. The reduction rate of fluorapatite increases and the amount of liquid slag decreases with the rise of C/O ratio. The reduction of fluorapatite is hindered by the addition of CaO and Na2CO3, thereby allowing the selective reduction of iron oxides upon controlled C/O ratio. The thermodynamic results obtain in the present work are in good agreement with the experimental results available in the literatures.  相似文献   

13.
To design optimal pyrometallurgical processes for nickel and cobalt recycling, and more particularly for the end-of-life process of Ni-Co-Fe-based end-of-life (EoL) superalloys, knowledge of their activity coefficients in slags is essential. In this study, the activity coefficients of NiO and CoO in CaO-Al2O3-SiO2 slag, a candidate slag used for the EoL superalloy remelting process, were measured using gas/slag/metal equilibrium experiments. These activity coefficients were then used to consider the recycling efficiency of nickel and cobalt by remelting EoL superalloys using CaO-Al2O3-SiO2 slag. The activity coefficients of NiO and CoO in CaO-Al2O3-SiO2 slag both show a positive deviation from Raoult's law, with values that vary from 1 to 5 depending on the change in basicity. The activity coefficients of NiO and CoO peak in the slag with a composition near B=(%CaO)/(%SiO2)=1, where B is the basicity. We observed that controlling the slag composition at approximately B=1 effectively reduces the cobalt and nickel oxidation losses and promotes the oxidation removal of iron during the remelting process of EoL superalloys.  相似文献   

14.
针对高镁高硅型中低品位红土镍矿,采用煤基自还原-细磨-磁选工艺制备镍铁粉,研究了内配碳比对红土镍矿中铁、镍氧化物自还原的影响,CaF_2对红土镍矿自还原过程中氧化物的还原、金属相的析出及聚集长大的影响规律。研究表明在CaF_2作用下通过降低内配碳比可抑制氧化铁的还原,从而获得镍品位较高的镍铁粉,但相应牺牲镍的回收率;CaF_2能与红土镍矿中高熔点的硅酸盐脉石通过固相反应生成低熔点的透闪石(Ca_2Mg_5(Si_4O_(11))_2F_2),使硅酸盐矿物结构由岛状转变为链状,提高硅酸盐矿物反应活性,促进镍、铁氧化物的还原;通过降低红土镍矿脉石相的熔化性温度,CaF_2能明显强化红土镍矿自还原过程中金属相的析出、聚集和长大,促进镍铁与脉石的有效分离,从而大幅度提高镍铁粉中镍和铁的品位及金属元素的回收率。  相似文献   

15.
随着优质铁矿资源的消耗,钢铁企业可利用的铁矿原料品位逐渐降低。因此,高铝质铁矿资源越来越受到钢铁企业的关注,但高铝原料在高炉冶炼过程中会带来渣铁黏稠、炉温偏低、冶炼安全等一系列问题。本研究中采用FactSage热力学软件分析Al2O3质量分数对高炉渣平衡物相、熔化温度、相析出温度的影响以及高铝渣液相区变化和黏度变化,旨在为高炉冶炼高铝原料提供一定的基础支撑。研究发现:炉渣为低铝(5%~10%)含量时,随着Al2O3含量增加,炉渣熔化温度升高,析出相为黄长石相和纯物质相,高炉渣黏度变化不大,炉渣中SiO2含量高,炉渣黏度过高,不适合高炉冶炼;炉渣为中铝(10%~15%)含量时,随着Al2O3含量增加,炉渣熔化温度升高,析出相为尖晶石相、黄长石相和纯物质相,高炉渣黏度增加幅度略有提高,Al2O3含量对高炉渣性质影响较小,增加炉渣二元碱度对炉渣黏度降低效果较明显;炉渣为高铝(15%~30%)含量时...  相似文献   

16.
The viscosity of CaF2-CaO-Al2O3-MgO-(TiO2) slag was measured using a rotating crucible viscometer. Raman spectroscopy analysis was performed to correlate the viscosity to slag structure. The viscosity of the slag was found to decrease with increasing TiO2 content in the slag from 0 to 9.73wt%. The activation energy decreased from 95.16 kJ/mol to 79.40 kJ/mol with increasing TiO2 content in the slag. The introduction of TiO2 into the slag played a destructive role in Al-O-Al structural units and Q4 units by forming simpler structural units of Q2 and Ti2O64- chain. The amount of Al-O-Al significantly decreased with increasing TiO2 content. The relative fraction of Q4 units in the[AlO4]5--tetrahedral units shows a decreasing trend, whereas the relative fraction of Q2 units and Ti2O64- chain increases with increasing TiO2 content accordingly. Consequently, the polymerization degree of the slag decreases with increasing TiO2 content. The variation in slag structure is consistent with the change in measured viscosity.  相似文献   

17.
A mathematical model was developed to describe the interaction of multiple physical fields in a slag bath during electroslag remelting (ESR) process with a current-conductive mould. The distributions of current density, magnetic induction intensity, electromagnetic force, Joule heating, fluid flow and temperature were simulated. The model was verified by temperature measurements during remelting 12CrMoVG steel with a slag of 50wt%-70wt% CaF2, 20wt%-30wt% CaO, 10wt%-20wt% Al2O3, and ≤ 10wt% SiO2 in a 600 mm diameter current-conductive mould. There is a good agreement between the calculated temperature results and the measured data in the slag bath. The calculated results show that the maximum values of current density, electromagnetic force and Joule heating are in the region between the corner electrodes and the conductivity element. The characteristics of current density distribution, magnetic induction intensity, electromagnetic force, Joule heating, velocity patterns and temperature profiles in the slag bath during ESR process with current-conductive mould were analyzed.  相似文献   

18.
Al-Ti-O inclusions always clog submerged nozzles in Ti-bearing Al-killed steel. A typical synthesized Al2TiO5 inclusion was immersed in a CaO-SiO2-Al2O3 molten slag for different durations at 1823 K. The Al2TiO5 dissolution paths and mechanism were revealed by scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS). Decreased amounts of Ti and Al and increased amounts of Si and Ca at the dissolution boundary prove that inclusion dissolution and slag penetration simultaneously occur. SiO2 diffuses or penetrates the inclusion more quickly than CaO, as indicated by the w(CaO)/w(SiO2) value in the reaction region. A liquid product (containing 0.7–1.2 w(CaO)/w(SiO2), 15wt%–20wt% Al2O3, and 5wt%–15wt% TiO2) forms on the inclusion surface when Al2TiO5 is dissolved in the slag. Al2TiO5 initially dissolves faster than the diffusion rate of the liquid product toward the bulk slag. With increasing reaction time, the boundary reaches its largest distance, the Al2TiO5 dissolution rate equals the liquid product diffusion rate, and the dissolution process remains stable until the inclusion is completely dissolved.  相似文献   

19.
The effect of B2O3 addition on the aqueous tape casting, sintering, microstructure and microwave dielectric properties of Li2O-Nb2O5-TiO2 ceramics has been investigated. The tape casting slurries exhibit a typical shear-thinning behavior without thixotropy, but the addition of B2O3 increases the viscosity of the slurries significantly. It was found that doping of B2O3 can decrease the tensile strength, strain to failure and density of the green tapes. The sintering temperature could be lowed down to 900℃ with the addition of 2 wt% B2O3 due to the liquid phase effect. No secondary phase is observed. The addition of B2O3 does not induce much degradation on the microwave dielectric properties. Optimum microwave dielectric properties of εr 67, Q×f 6560 GHz are obtained for Li2O-Nb2O5-TiO2 ceramics containing 2 wt% B2O3 sintered at 900 1C. It represents that the ceramics could be promising for multilayer low-temperature co-fired ceramics (LTCC) application.  相似文献   

20.
在实验室条件下采用钼丝挂渣法测量熔渣发泡高度,以相对发泡高度作为衡量指标,结合理论分析,系统研究了高碱度合成精炼渣的泡沫化性能.结果表明:熔渣相对发泡高度随着黏度的增大、表面张力和密度的减小而增大.在精炼渣成分一定时,随温度升高和吹气量增加,熔渣相对发泡高度都有先增加后降低的趋势.具有较好泡沫化性能的精炼渣组成范围是:ω(CaO)/ω(SiO_2)为5~8,ω(Al_2O_3):27%,ω(CaF_2)为3%~6%,ω(MgO)=8%,ω(FeO)<0.5%.  相似文献   

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