山东科技大学学报:自然科学版
山東科技大學學報:自然科學版
산동과기대학학보:자연과학판
Journal of Shandong Univ of Sci and Technol: Nat Sci
2012年
1期
80-83
,共4页
钇铝石榴石%共沉淀法%前驱体%透明陶瓷%纳米粉体
釔鋁石榴石%共沉澱法%前驅體%透明陶瓷%納米粉體
을려석류석%공침정법%전구체%투명도자%납미분체
yttrium aluminum garnet%co-precipitation%precursor%transparent ceramics%nano-sized powder
以硝酸铝和硝酸钇为原料,以碳酸氢铵为沉淀剂,采用共沉淀法合成铝和钇的碳酸盐作为反应前驱体,同时借助IR、XRD和TEM等测试手段对不同浓度盐溶液所得前驱体和煅烧产物进行表征。结果表明:盐溶液浓度的升高不利于纯相YAG粉体的合成,当铝离子浓度达到0.05mol/L时,前驱体在900℃保温2h可以得到纯相YAG粉体,粉体分散性好,平均粒径为30~40nm,近球形;而当浓度大于0.5mol/L时,前驱体只有在1 200℃以上才可以形成纯相YAG。
以硝痠鋁和硝痠釔為原料,以碳痠氫銨為沉澱劑,採用共沉澱法閤成鋁和釔的碳痠鹽作為反應前驅體,同時藉助IR、XRD和TEM等測試手段對不同濃度鹽溶液所得前驅體和煅燒產物進行錶徵。結果錶明:鹽溶液濃度的升高不利于純相YAG粉體的閤成,噹鋁離子濃度達到0.05mol/L時,前驅體在900℃保溫2h可以得到純相YAG粉體,粉體分散性好,平均粒徑為30~40nm,近毬形;而噹濃度大于0.5mol/L時,前驅體隻有在1 200℃以上纔可以形成純相YAG。
이초산려화초산을위원료,이탄산경안위침정제,채용공침정법합성려화을적탄산염작위반응전구체,동시차조IR、XRD화TEM등측시수단대불동농도염용액소득전구체화단소산물진행표정。결과표명:염용액농도적승고불리우순상YAG분체적합성,당려리자농도체도0.05mol/L시,전구체재900℃보온2h가이득도순상YAG분체,분체분산성호,평균립경위30~40nm,근구형;이당농도대우0.5mol/L시,전구체지유재1 200℃이상재가이형성순상YAG。
Yttrium aluminum garnet(YAG) nano-sized powder was synthesized by means of the co-precipitation method taking the ammonium hydrogen carbonate as precipitant.The resulting precursor precipitant and calcined product were characterized with the test means of infrared radiation(IR),X-ray diffraction(XRD) and transmission electron microscope(TEM).The results show that high concentration of Al3+ is not good for the formation of YAG crystallites,and the pure phase YAG crystallites are obtained by calcining at 900 C for 2 h when the concentration of Al3+ is 0.05 mol/L.The synthesized product consists of highly dispersed nano-sized particles with the average size of 30 nm to 40 nm.Higher sintering temperature is needed for pure phase YAG crystallites when the concentration of Al3+ is above 0.5 mol/L.