CN106431359A - 一种压电纳米材料的制备工艺 - Google Patents
一种压电纳米材料的制备工艺 Download PDFInfo
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Abstract
本发明公开了一种压电纳米材料的制备工艺,包括以下步骤:1)、将原料按比列混匀成混合物,所述原料包括以下重量份组分:氧化铝70‑75重量份,钛酸盐20‑30重量份,长石7‑10重量份,二硼化锆5‑10重量份,五氧化二铌5‑8重量份,三氧化二铋5‑8重量份,聚铝硅氧烷6‑8重量份,聚碳硅烷6‑8重量份,纳米氧化镁2‑3重量份;碳化硅泡沫2‑3重量份;2)、将步骤1)获得的混合物加入研磨机中研磨15‑30分钟,得到胚体,将所得胚体在惰性气氛下进行烧结,得到纳米压电材料。本发明所述的压电纳米材料具有较高的压电系数,能够有效提高压电纳米材料的使用寿命。
Description
技术领域
本发明涉及压电材料技术领域,具体涉及一种压电纳米材料的制备工艺。
背景技术
压电材料是指受到压力作用时会在两端面见出现电压的晶体材料。压电纳米材料是指具有纳米结构的压电材料。压电效应的机理是:具有压电性的晶体对称性较低,当受到外力作用发生形变时,晶胞中正负离子的相对位移使正负电荷中心不再重合,导致晶体发生宏观极化,而晶体表面电荷面密度等于极化强度在表面法向上的投影,所以压电材料受到压力作用变形时两端面会出现异号电荷。反之,压电材料在电场中发生极化时,会因电荷中心的位移导致材料变形。
压电纳米材料主要用作压电驱动元件、电容器等。
现有的压电材料的压电系数较低、使用寿命较短。
发明内容
本发明的目的在于提供一种压电纳米材料的制备工艺,通过本发明所述工艺制备的压电纳米材料具有较高的压电系数、且使用寿命较高。
本发明通过下述技术方案实现:
一种压电纳米材料的制备工艺,包括以下步骤:
1)、将原料按比列混匀成混合物,所述原料包括以下重量份组分:
氧化铝70-75重量份,钛酸盐20-30重量份,长石7-10重量份,二硼化锆5-10重量份,五氧化二铌5-8重量份,三氧化二铋5-8重量份,聚铝硅氧烷6-8重量份,聚碳硅烷6-8重量份,纳米氧化镁2-3重量份;碳化硅泡沫2-3重量份;
2)、将步骤1)获得的混合物加入研磨机中研磨15-30分钟,在80-85℃下混合均匀,得到胚体,将所得胚体在惰性气氛下进行烧结,得到纳米压电材料所述烧结分为3个阶段,第一个阶段在1000-1100℃下烧结2-3小时,第二阶段在1200-1300℃下烧结1-2小时;第3阶段在1000-1100℃下烧结2-3小时。
通过上述工艺制备的压电纳米材料具有较高的压电系数,能够有效提高压电纳米材料的使用寿命;并且,本发明制备的压电纳米材料具有良好的稳定性和耐候性,能够适用于不同的环境,提高压电纳米材料的应用范围,进而提高了压电纳米材料的经济利用和商业价值。
通过将烧结分为3个阶段进行提高了压电纳米材料的烧结效果,确保材料的使用性能。
进一步地,钛酸盐至少包括钛酸钡、钛酸锂中的一种。
进一步地,所述原料还包括三氧化二锑2-3重量份。
进一步地,,所述原料还包括2-3重量份的纳米磁性氧化物。
通过加入纳米磁性氧化物提高了压电纳米材料的磁性,进而提高了其使用性能。
进一步地,纳米磁性氧化物至少包括含铁磁性氧化物、含钴磁性氧化物、含镍磁性氧化物中的一种。
本发明与现有技术相比,具有如下的优点和有益效果:
1、本发明所制备的压电纳米材料具有较高的压电系数,能够有效提高压电纳米材料的使用寿命。
2、本发明制备的压电纳米材料具有良好的稳定性和耐候性,能够适用于不同的环境,提高压电纳米材料的应用范围,进而提高了压电纳米材料的经济利用和商业价值。
具体实施方式
为使本发明的目的、技术方案和优点更加清楚明白,下面结合实施例,对本发明作进一步的详细说明,本发明的示意性实施方式及其说明仅用于解释本发明,并不作为对本发明的限定。
实施例1:
一种压电纳米材料的制备工艺,包括以下步骤:
1)、将原料按比列混匀成混合物,所述原料包括以下重量份组分:
氧化铝70重量份,钛酸钡8重量份,钛酸锂12重量份,长石7重量份,二硼化锆5重量份,五氧化二铌5重量份,三氧化二铋5重量份,聚铝硅氧烷6重量份,聚碳硅烷6重量份,纳米氧化镁2重量份;碳化硅泡沫2重量份;三氧化二锑2重量份;含铁磁性氧化物2重量份;
2)、将步骤1)获得的混合物加入研磨机中研磨15分钟,在80℃下混合均匀,得到胚体,将所得胚体在惰性气氛下进行烧结,得到纳米压电材料所述烧结分为3个阶段,第一个阶段在1000℃下烧结2小时,第二阶段在1200℃下烧结1小时;第3阶段在1000℃下烧结2小时。
实施例2:
一种压电纳米材料的制备工艺,包括以下步骤:
1)、将原料按比列混匀成混合物,所述原料包括以下重量份组分:
氧化铝75重量份,钛酸钡15重量份,钛酸锂15重量份,长石10重量份,二硼化锆10重量份,五氧化二铌8重量份,三氧化二铋8重量份,聚铝硅氧烷8重量份,聚碳硅烷8重量份,纳米氧化镁3重量份;碳化硅泡沫3重量份;三氧化二锑3重量份;含钴磁性氧化物3重量份;
2)、将步骤1)获得的混合物加入研磨机中研磨30分钟,在85℃下混合均匀,得到胚体,将所得胚体在惰性气氛下进行烧结,得到纳米压电材料所述烧结分为3个阶段,第一个阶段在100℃下烧结3小时,第二阶段在1300℃下烧结2小时;第3阶段在1100℃下烧结3小时。
实施例3:
一种压电纳米材料的制备工艺,包括以下步骤:
1)、将原料按比列混匀成混合物,所述原料包括以下重量份组分:
氧化铝72重量份,钛酸钡12重量份,钛酸锂10重量份,长石8重量份,二硼化锆9重量份,五氧化二铌7重量份,三氧化二铋7重量份,聚铝硅氧烷7重量份,聚碳硅烷7重量份,纳米氧化镁2重量份;碳化硅泡沫3重量份;三氧化二锑3重量份;含钴磁性氧化物1重量份,镍磁性氧化物1重量份;
2)、将步骤1)获得的混合物加入研磨机中研磨20分钟,在83℃下混合均匀,得到胚体,将所得胚体在惰性气氛下进行烧结,得到纳米压电材料所述烧结分为3个阶段,第一个阶段在1100℃下烧结3小时,第二阶段在1300℃下烧结2小时;第3阶段在1100℃下烧结3小时。
实施例4:
一种压电纳米材料的制备工艺,包括以下步骤:
1)、将原料按比列混匀成混合物,所述原料包括以下重量份组分:
化铝72重量份,钛酸钡12重量份,钛酸锂10重量份,长石8重量份,二硼化锆9重量份,五氧化二铌7重量份,三氧化二铋7重量份,聚铝硅氧烷7重量份,聚碳硅烷7重量份,纳米氧化镁2重量份;碳化硅泡沫3重量份;三氧化二锑3重量份;
2)、将步骤1)获得的混合物加入研磨机中研磨20分钟,在83℃下混合均匀,得到胚体,将所得胚体在惰性气氛下进行烧结,得到纳米压电材料所述烧结分为3个阶段,第一个阶段在1100℃下烧结3小时,第二阶段在1300℃下烧结2小时;第3阶段在1100℃下烧结3小时。
将实施例1至实施例4所制备的压电纳米材料分别进行性能测试,试验结果分别如表1:
表1
将实施例3进行稳定性试验,将实施例3所述的压电纳米材料应用于零下10摄氏度、50摄氏度、30摄氏度下使用,在1个月、3个月、6个月、9个月、12个月进行介电常数、耐压强度和断裂韧性检测,在1个月时,介电常数、耐压强度和断裂韧性均没有变化,在3个月时,介电常数下降了0.5%左右,而耐压强度和断裂韧性均没有变化;在6个月时,介电常数下降了0.8%左右,而耐压强度和断裂韧性均没有变化;在9个月时,介电常数下降了1..1%左右,耐压强度和断裂韧性均下降了0.5%左右,在12个月时,介电常数下降了1.2%左右,耐压强度和断裂韧性均下降了0.7%左右。上述实验结果说明本发明所述的压电纳米材料具有较好的稳定性、使用寿命较高,能够适用于不同温度下的环境,耐寒寒热性较好。
以上所述的具体实施方式,对本发明的目的、技术方案和有益效果进行了进一步详细说明,所应理解的是,以上所述仅为本发明的具体实施方式而已,并不用于限定本发明的保护范围,凡在本发明的精神和原则之内,所做的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
Claims (5)
1.一种压电纳米材料的制备工艺,其特征在于,包括以下步骤:
1)、将原料按比列混匀成混合物,所述原料包括以下重量份组分:
氧化铝70-75重量份,钛酸盐20-30重量份,长石7-10重量份,二硼化锆5-10重量份,五氧化二铌5-8重量份,三氧化二铋5-8重量份,聚铝硅氧烷6-8重量份,聚碳硅烷6-8重量份,纳米氧化镁2-3重量份;碳化硅泡沫2-3重量份;
2)、将步骤1)获得的混合物加入研磨机中研磨15-30分钟,在80-85℃下混合均匀,得到胚体,将所得胚体在惰性气氛下进行烧结,得到纳米压电材料;所述烧结分为3个阶段,第一个阶段在1000-1100℃下烧结2-3小时,第二阶段在1200-1300℃下烧结1-2小时;第3阶段在1000-1100℃下烧结2-3小时。
2.根据权利要求1所述的一种压电纳米材料的制备工艺,其特征在于,所述钛酸盐至少包括钛酸钡、钛酸锂中的一种。
3.根据权利要求1所述的一种压电纳米材料的制备工艺,其特征在于,所述原料还包括三氧化二锑2-3重量份。
4.根据权利要求1所述的一种压电纳米材料的制备工艺,其特征在于,所述原料还包括2-3重量份的纳米磁性氧化物。
5.根据权利要求4所述的一种压电纳米材料的制备工艺,其特征在于,所述纳米磁性氧化物至少包括含铁磁性氧化物、含钴磁性氧化物、含镍磁性氧化物中的一种。
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