功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2014年
19期
19015-19019,19025
,共6页
贾洪声%鄂元龙%李海波%季思航%马根龙%贾晓鹏%马红安%郑友进
賈洪聲%鄂元龍%李海波%季思航%馬根龍%賈曉鵬%馬紅安%鄭友進
가홍성%악원룡%리해파%계사항%마근룡%가효붕%마홍안%정우진
高温高压%BiMnO 3%结构%磁性
高溫高壓%BiMnO 3%結構%磁性
고온고압%BiMnO 3%결구%자성
HPHT%BiMnO3%structure%magnetic property
利用国产六面顶液压机,以 Bi2 O 3、MnO 2和Mn 粉末为原料(n (Bi2 O 3)/n (MnO 2)/n (Mn )=2∶3∶1),在高温高压条件下(3~5 GPa,600~800℃),制备了钙钛矿结构 BiMnO 3烧结体.利用 X 射线衍射仪(XRD)、扫描电子显微镜(SEM)、振动样品磁强计(VSM)对烧结样品进行了测试分析,考察了烧结温度、压力对样品结构、组织形貌及磁性的影响.实验结果表明,当烧结温度为600℃时,钙钛矿结构BiMnO 3晶粒开始形成,随着温度的升高,其相对含量增加,比饱和磁化强度逐渐增大,而比饱和磁化强度随着压力增大,先增大后减小;样品矫顽力随晶粒尺寸减小而减小.合成钙钛矿结构 BiMnO 3单相最佳实验条件为4 GPa,800℃,1 h,其居里温度为99 K,在90 K的测试温度条件下,最大的比饱和磁化强度为35 A??m2/kg,最小的矫顽力为37.6×79.6 A/m.
利用國產六麵頂液壓機,以 Bi2 O 3、MnO 2和Mn 粉末為原料(n (Bi2 O 3)/n (MnO 2)/n (Mn )=2∶3∶1),在高溫高壓條件下(3~5 GPa,600~800℃),製備瞭鈣鈦礦結構 BiMnO 3燒結體.利用 X 射線衍射儀(XRD)、掃描電子顯微鏡(SEM)、振動樣品磁彊計(VSM)對燒結樣品進行瞭測試分析,攷察瞭燒結溫度、壓力對樣品結構、組織形貌及磁性的影響.實驗結果錶明,噹燒結溫度為600℃時,鈣鈦礦結構BiMnO 3晶粒開始形成,隨著溫度的升高,其相對含量增加,比飽和磁化彊度逐漸增大,而比飽和磁化彊度隨著壓力增大,先增大後減小;樣品矯頑力隨晶粒呎吋減小而減小.閤成鈣鈦礦結構 BiMnO 3單相最佳實驗條件為4 GPa,800℃,1 h,其居裏溫度為99 K,在90 K的測試溫度條件下,最大的比飽和磁化彊度為35 A??m2/kg,最小的矯頑力為37.6×79.6 A/m.
이용국산륙면정액압궤,이 Bi2 O 3、MnO 2화Mn 분말위원료(n (Bi2 O 3)/n (MnO 2)/n (Mn )=2∶3∶1),재고온고압조건하(3~5 GPa,600~800℃),제비료개태광결구 BiMnO 3소결체.이용 X 사선연사의(XRD)、소묘전자현미경(SEM)、진동양품자강계(VSM)대소결양품진행료측시분석,고찰료소결온도、압력대양품결구、조직형모급자성적영향.실험결과표명,당소결온도위600℃시,개태광결구BiMnO 3정립개시형성,수착온도적승고,기상대함량증가,비포화자화강도축점증대,이비포화자화강도수착압력증대,선증대후감소;양품교완력수정립척촌감소이감소.합성개태광결구 BiMnO 3단상최가실험조건위4 GPa,800℃,1 h,기거리온도위99 K,재90 K적측시온도조건하,최대적비포화자화강도위35 A??m2/kg,최소적교완력위37.6×79.6 A/m.
The BiMnO 3 sintered body with perovskite structure was prepared,using Bi2 O 3 ,MnO 2 and Mn pow-ders as starting materials (n (Bi2 O 3 )/n (MnO 2 )/n (Mn)=2∶3∶1),under high temperature and high pressure (HPHT,3-5 GPa,600-800 ℃)conditions in a China CS-IV type cubic-anvil high pressure apparatus (CHPA). The sintered samples were tested and analyzed by using X-ray diffraction (XRD),scanning electron microscopy (SEM)and vibrating sample magnetometer (VSM),and the effects of sintering temperature and pressure on the sample structure,morphology and magnetic properties were studied.The experimental results show that:when the sintering temperature was 600 ℃,the grains of perovskite BiMnO 3 begin to form;with the increase of temperature,the relative content of BiMnO 3 increases and the saturation magnetization increases gradually. While the saturation magnetization increases first and then decreases with the pressure increases;the coercivity decreases with decreasing of grain size.The optimum experimental synthesis conditions of BiMnO 3 single-phase with perovskite structure are 4 GPa,800 ℃,1 h,and its Curie temperature was 99 K.Under the test-tempera-ture of 90 K, the maximum saturation magnetization and minimum coercivity were 35 A ?? m2/kg and 37.6×79.6 A/m respectively.