17（Cu-10Ni）-（NiFe2O4-10NiO）基金属陶瓷在铝电解过程中的相演变（英文）

采用冷压气氛烧结制备17(Cu-10Ni)-(NiFe2O4-10NiO)金属陶瓷,并作为阳极在960°C下分别进行10和40h的铝电解试验。对电解前后金属陶瓷的显微结构、物相成分进行分析检测。对电解质及阴极金属中的杂质含量进行分析,研究阳极组成中Fe、Ni和Cu元素的腐蚀行为。研究发现:在电解过程中,在材料表面形成NiFe2O4相致密层,该致密层随电解时间的延长而增厚。在NiFe2O4相致密层形成与增厚过程中,出现NiFe2O4相吞噬NiO相和金属相氧化的现象,金属陶瓷中Cu元素优先腐蚀溶解。并着重讨论NiFe2O4相致密层形成与增厚过程中金属相的腐蚀形式及NiO相向NiFe2O4相的转变机制。     

铁酸镍基金属陶瓷的强化烧结与熔盐腐蚀行为

采用气氛烧结方法制备NiFe2O4基金属陶瓷材料,并进行960℃的铝电解腐蚀实验.通过分析烧结体的显微结构和物相组成、电解试样的表层形貌与成分以及电解质和阴极铝的杂质含量等,研究BaO、Yb2O3和CoO的添加以及金属相的组成对NiFe2O4基金属陶瓷烧结性能的影响;表征J该金属陶瓷强化烧结体作为铝电解惰性阳极的电解腐蚀性能;并对材料强化烧结机制和熔盐腐蚀行为进行探讨.结果表明烧结过程中,BaO和Yb2O3与该金属陶瓷中的陶瓷相反应生成新的物相,CoO与陶瓷相形成固溶体,并加快烧结致密化进程;以Cu-Ni取代纯Cu和纯Ni作为金属陶瓷的金属相,可提高材料的相对密度;NiFe2O4基金属陶瓷的高致密度可抑制电解过程中金属相的流失和陶瓷相的腐蚀,阳极表层也转变为致密的NiFe2O4相.     

氧化银对惰性阳极耐熔盐腐蚀性能的影响

以Fe2O3、NiO和Ag2O为主要原料,采用固相烧结工艺制备了NiFe2O4/Ag惰性阳极,用X射线衍射和扫描电子显微镜对材料的组成和微观结构进行了研究,采用水冷法测量了样品的抗热震性,并测量了其在冰晶石熔盐中的电解腐蚀速率。结果表明:Ag2O的加入提高了样品的抗热震性,降低了惰性阳极试样在冰晶石熔盐中的电解腐蚀速率,当Ag2O含量为6%时,试样的电解腐蚀速率最低。     

铝电解用NiFe2O4-Cu金属陶瓷惰性阳极的制备

以高温固相合成法合成的NiFe2O4陶瓷粉体和金属Cu粉为原料, 采用冷压-烧结法制备了Cu含量在5%～20%之间的NiFe2O4-Cu金属陶瓷惰性阳极, 研究了烧结气氛和烧结温度对其物相组成、微观形貌和基本物理性能的影响. 结果表明 通过控制烧结气氛中氧分压在NiO和Cu2O的离解反应平衡氧分压之间, 可以制备出具有目标物相组成的NiFe2O4-Cu金属陶瓷; 烧结温度和保温时间对所得NiFe2O4-Cu金属陶瓷的相对密度有较大影响; NiFe2O4和Cu之间的不润湿性限制了NiFe2O4-Cu金属陶瓷烧结温度的提高和保温时间的延长, 在保证金属相分布均匀且不溢出的前提下, 所制备的NiFe2O4-Cu金属陶瓷的相对密度较小; 金属相Cu含量越高, NiFe2O4-Cu金属陶瓷最高烧结温度越低、最长保温时间越短, 从而相对密度越低、孔隙率越高; 除了尽量降低金属相含量外, 还可向NiFe2O4-Cu金属陶瓷中添加其他金属如Ni和Co等, 以改善陶瓷相与金属相之间的润湿性, 以提高烧结温度, 进而提高其相对密度和耐腐蚀性能.     

电流密度对铝电解NiFe_2O_4基金属陶瓷惰性阳极腐蚀的影响

在Na3AlF6-K3AlF6-AlF3-Al2O 3熔体中,研究电流密度对22(Ni+Cu)/(NiFe2O4-10NiO)金属陶瓷惰性阳极腐蚀速率的影响,并分析腐蚀后阳极的微观结构。结果表明,随着电流密度的升高,NiFe2O4基金属陶瓷惰性阳极腐蚀从以化学溶解腐蚀为主逐渐转变为以电化学腐蚀为主,腐蚀率先降低而后增大。当电流密度从1.0 A/cm2增大至1.6 A/cm2时,阳极年腐蚀率从1.22 cm/a降低至0.137 cm/a;进一步提高电流密度至4.0 A/cm2时,阳极年腐蚀率增大到4.96 cm/a。     

Yb2O3或Y2O3掺杂Cu-(NiFe2O4-10NiO)惰性阳极的导电性和耐蚀性

在氧分压约为100 Pa的氮气氛下烧结制备了掺杂Y2O3、Yb2O3的10Cu-(NiFe2O4-10NiO)金属陶瓷,并对其进行导电性能测试和10h(Na3A1F6-Al2O3体系中)铝电解实验.采用XRD、SEM和EDS分析稀土氧化物以及其与陶瓷基体反应产物的分布,考查电解实验后材料表层显微结构变化尤其是金属相的流失情况,评价稀土氧化物的添加对金属陶瓷电解初期腐蚀行为的影响.结果表明:掺杂稀土氧化物均使NiO相呈连通迹象,掺杂Yb2O3金属陶瓷晶粒较未掺杂的粗大,其与陶瓷相反应生成物成点线状分布于NiFe2O4相晶界,Y2O3与陶瓷相反应生成物则分布于NiO与NiFe2O4相间;所制备材料具有半导体特征,随着稀土氧化物的掺杂,材料导电性呈下降趋势;掺杂稀土氧化物尤其是Yb2O3有利于提高材料的耐蚀性能.     

大尺寸NiFe2O4-10NiO/17Ni型金属陶瓷惰性阳极的制备

研究以PVA为主要成分的粘结剂体系的热分解特性对大尺寸粉末压坯脱脂行为的影响,发现PVA的不均匀热分解是造成大尺寸粉末压坯脱脂失效的原因之一,开发一种具有稳定热分解反应特性的新型粘结剂体系,实现大尺寸粉末压坯的无缺陷热脱脂;研究烧结气氛、金属相的添加对NiFe2O4-10NiO致密化行为的影响。结果表明：N2气氛烧结及加入Ni可有效提高NiFe2O4-10NiO陶瓷基体的烧结致密度,1350℃时于N2气氛中烧结的NiFe204．10NiO／5Ni型金属陶瓷材料的相对密度达到97．28％。采用优化工艺实现d120mmX140mm深杯状NiFe2O4-10NiO／17Ni金属陶瓷惰性阳极脱脂预烧坯的烧结,所得烧结坯平均相对密度为95．21％。     

基于GA-BP的NiFe2O4基金属陶瓷阳极优化设计

采用BP神经网络对铝电解NiFe2O4基金属陶瓷惰性阳极的电解腐蚀过程进行了系统辨识。建立了以Al2O3质量浓度、电解温度、分子比、面积比和电流密度为输入,腐蚀率为输出的网络模型。在材料的设计中,采用了GA-BP优化方法,BP网络参与GA迭代计算时对个体的评价。应用结果表明,NiFe2O4基金属陶瓷惰性阳极的电解腐蚀率预测结果与实测值吻合;优化设计的结果与实验值很接近。     

铝电解NiFe2O4基惰性阳极材料纤维增强体的选择

以NiO和Fe2O3为原料采用固相烧结法合成NiFe2O4尖晶石,通过向其中添加短纤维制备纤维/NiFe2O4惰性阳极材料。为选择适合于NiFe2O4基惰性阳极材料的纤维增强体,对几种纤维在NiFe2O4基体中的高温稳定性进行考察。结果表明,高温下碳纤维、玻璃纤维、氧化铝纤维和碳化硅纤维与NiFe2O4基体是热力学不相容的;1 200℃时镀镍碳纤维和镍纤维不能在基体中稳定存在;1 400℃时ZrO2(f)与NiFe2O4基体具有良好的物理和化学相容性,添加3%ZrO2(f)(质量分数)阳极试样的力学性能得到明显改善。因此,ZrO2(f)可作为NiFe2O4基惰性阳极的纤维增强体。     

铝电解惰性阳极基体材料的研究

本论文选用ZnO和Fe2O3、Ni2O3和Fe2O3与NiO和Fe2O3等不同氧化物，采用高温固相烧结法制备铝电解惰性阳极基体材料，通过对其烧结性能、导电性能及耐蚀性能的综合分析，得出试验结论为：采用NiO和Fe2O3合成的NiFe2O4尖晶石材料，其综合性能最好，且试样理论尖晶石含量为85％左右时，其热腐蚀率最低。     

Preliminary testing of NiFe2O4-NiO-Ni cermet as inert anode in Na3AlF6-AlF3 melts

1 Introduction It is well known that the current aluminum reduction cell with carbon consumable anode has many disadvantages. So the concept of inert anode was introduced, with which the disadvantages can be avoided completely. A lot of research work has…     

添加剂BaO对铝电解用xCu/（10NiO-NiFe_2O_4）金属陶瓷惰性阳极腐蚀性能的影响

制备铝电解用xCu/（10NiO-NiFe2O4）和1BaO-xCu/（10NiO-NiFe2O4）（x=5,10,17）金属陶瓷惰性阳极,在传统电解质中以电流密度1.0A/cm2进行实验室电解腐蚀实验。结果表明：金属Cu被腐蚀,在阳极表面留下了许多孔洞从而导致在电解过程中电解质向阳极内部渗透;金属陶瓷5Cu/（10NiO-NiFe2O4）,10Cu/（10NiO-NiFe2O4）,17Cu/（10NiO-NiFe2O4）,1BaO-5Cu/（10NiO-NiFe2O4）,1BaO-10Cu/（10NiO-NiFe2O4）和1BaO-17Cu/（10NiO-NiFe2O4）的腐蚀速率分别为2.15,6.50,8.30,4.88,4.70和4.48cm/a;添加剂BaO对10Cu/（10NiO-NiFe2O4）和17Cu/（10NiO-NiFe2O4）金属陶瓷的抗腐蚀性能是有利的,因为添加剂BaO能有效提高其致密度从而提高其抗腐蚀性能;但BaO对5Cu/（10NiO-NiFe2O4）金属陶瓷的抗腐蚀性能是不利的,可能是因为聚集在晶界的添加剂BaO加速了金属陶瓷的腐蚀。     

Preparation and preliminary testing of cermet inert anode for aluminum electrolysis

1　INTRODUCTIONAluminumhasthelargest productivityamongthenonferrousmetals ,2 4Mtperyearintheworld .Whilegreatprogresshavebeenmadeintheprimaryaluminum production ,theindustrycontinuestopur sueresearchtosolvesomeformidablechallenges ,suchas quitealargeenergyintensity(14 0 0 0 15 0 0 0kW·hpertonaluminum) ,highcon sumptionofcarbonanode(5 0 0 6 0 0kgpertonalu minum) ,significantemissionsofgreenhousegas(1.71tpertonaluminum )andotherdetrimentalgases ,highcapitalinvestmentandcost[1] .Inertelectr…     

Effect of NiO content on corrosion behaviour of Ni-xNiO-NiFe2O4 cermets in Na3AlF6-Al2O3 melts

5Ni-xNiO-NiFe2O4 cermets with different NiO contents were prepared and the corrosion behaviour in Na3AlF6-Al2O3 melts was investigated in laboratory electrolysis tests. The results indicate that adding NiO is unfavorable to the densifieation of NiFe2O4-xNiO ceramics, while small Ni doping can greatly improve the sintering property. The electrolysis tests show that excess NiO is beneficial to the reduction of Fe while has little effects on that of Ni in the bath; the steady-state concentrations of Ni, Fe are below the corresponding solubilities of NiFe2O4-xNiO, implying that corrosion mechanism changes while electrifying. Post-electrolysis examination of anodes shows that Ni metal leaches at the anode surface, yet the substrate ceramic prevents the penetration of bath and the further loss of metal phase.     

Effect of Ni content on corrosion behavior of Ni/（10NiO-90NiFe2O4） cermet inert anode

Ni/（10NiO-90NiFe2O4） cermet inert anodes with metal Ni content of 0, 5, 10, 15 and 20 （mass fraction, %） were prepared and their corrosion behavior in Na3AlF6-Al2O3 melts was investigated in laboratory electrolysis tests. The results indicate that the content of metal Ni in anodes has little effect on the steady-state concentration of impurities Ni and Fe in electrolyte and the values range in （114-173）×10^-6 and （287-385）×10^-6, but the content of impurities in the metal aluminum manifolds. There is preferential corrosion for metal Ni in NiO-NiFe2O4 based cermet anodes. Considering the corrosion resistance and electrical conductivity, the cermet containing 5%Ni （mass fraction） behaves best among NiO-NiFe2O4 based cermet anodes studied, and should be further studied.     

NiFe2O4基金属陶瓷惰性阳极的腐蚀研究进展

综述了近年来国内外铝电解用NiFe2O4基金属陶瓷惰性阳极在阳极组元的溶解与分布、腐蚀率的预测与测定以及氧化物和金属相对阳极腐蚀的影响三个方面所做的研究工作。     

EFFECT OF Cu-Ni CONTENT ON THE CORROSION RESISTANCE OF （Cu-Ni）/（10NiO-90NiFe204） CERMET INERT ANODE FOR ALUMINUM ELECTROLYSIS

（Cu-Ni）/（10NiO-90NiFe204） cermet inert anodes containing metal Cu-Ni0, 5, 10, 15 and 20 wt pct were prepared and their corrosion resistance to Na3AlF6-Al2O3 melts was investigated. The results indicate that the content of metal Cu-Ni has little effect on the steady-state concentration of Ni in the electrolyte and the values could not be used to effectively differentiate their corrosion resistance. The steady-state concentration of Fe decreases from 304×10^-6 to 168×10^-6 and that of Cu increases from 21×10^-6 to 71×10^-6 with the content of metal Cu-Ni increasing from 0 to 20 wt pct. Post-examination shows that metallic phase Cu-Ni is corroded preferentially during electrolysis and many pores are left at the anode surface. Considering the corrosion resistance and electrical conductivity, the cermet containing metal Cu-Ni 5 wt pct should be selected and studied further.     

EFFECT OF Cu-Ni CONTENT ON THE CORROSION RESISTANCE OF (Cu-Ni)/(10NiO-90NiFe2O4) CERMET INERT ANODE FOR ALUMINUM ELECTROLYSIS

(Cu-Ni)/(10NiO-9ONiFe2O4 ) cermet inert anodes containing metal Cu-Ni 0,5, 10, 15 and 20 wt pet were prepared and their corrosion resistance to Na3AlF6-Al2O3 melts was investigated. The results indicate that the content of metal Cu-Ni has little effect on the steady-state concentration of Ni in the electrolyte and the values could not be used to effectively differentiate their corrosion resistance. The steady-state concentration of Fe decreases from 304×10-8 to 168×10-6 and that of Cu increases from 21×10-6 to 71×10-6 with the content of metal Cu-Ni increasing from 0 to 20 wt pct. Post-examination shows that metallic phase Cu-Ni is corroded preferentially during electrolysis and many pores are left at the anode surface. Considering the corrosion resistance and electrical conductivity, the cermet containing metal Cu-Ni 5 wt pct should be selected and studied further.     

Results from 100 h electrolysis testing of NiFe2O4 based cermet as inert anode in aluminum reduction

1 Introduction Since the Hall-Héroult process was applied in aluminum production, an inert anode was always the target that the aluminum industry was seeking for in the new technology field[1]. Some selection criteria have been defined in order to ident…