炭素技术
炭素技術
탄소기술
CARBON TECHNIQUES
2014年
6期
10-14
,共5页
焦剑%崔永红%蔡宇%汪雷%吕盼盼
焦劍%崔永紅%蔡宇%汪雷%呂盼盼
초검%최영홍%채우%왕뢰%려반반
介孔炭%三嵌段共聚物%线性酚醛树脂%溶剂挥发诱导自组装
介孔炭%三嵌段共聚物%線性酚醛樹脂%溶劑揮髮誘導自組裝
개공탄%삼감단공취물%선성분철수지%용제휘발유도자조장
Mesoporous carbon%triblock copolymer%linear phenolic resin%solvent evaporation-induced self-assembly
以三嵌段共聚物F127为模板剂,线性酚醛树脂(PF)为炭前驱体,在F127与PF的质量比mF127∶mPF=1∶1时,利用溶剂挥发诱导自组装制备介孔炭材料,对在不同焙烧温度下制备的介孔材料进行表征,研究焙烧温度对所得介孔材料结构的影响。采用XRD、TEM、N2吸附/脱附等方法对介孔材料的结构进行了表征,研究了焙烧温度对上述介孔炭结构的影响。结果表明:介孔材料的晶面间距随着温度的升高而降低,当焙烧温度为600℃时,介孔材料的骨架从高分子材料转变为炭材料。其比表面积和C/H摩尔比均随着焙烧温度升高而增加,但其孔壁厚度和孔径却随着焙烧温度的升高而降低。孔径大小和孔壁厚度在600℃以后降低的幅度较小,基本上趋于稳定,碳骨架的收缩变得缓慢。随着焙烧温度的升高,其介观结构基本不发生改变。
以三嵌段共聚物F127為模闆劑,線性酚醛樹脂(PF)為炭前驅體,在F127與PF的質量比mF127∶mPF=1∶1時,利用溶劑揮髮誘導自組裝製備介孔炭材料,對在不同焙燒溫度下製備的介孔材料進行錶徵,研究焙燒溫度對所得介孔材料結構的影響。採用XRD、TEM、N2吸附/脫附等方法對介孔材料的結構進行瞭錶徵,研究瞭焙燒溫度對上述介孔炭結構的影響。結果錶明:介孔材料的晶麵間距隨著溫度的升高而降低,噹焙燒溫度為600℃時,介孔材料的骨架從高分子材料轉變為炭材料。其比錶麵積和C/H摩爾比均隨著焙燒溫度升高而增加,但其孔壁厚度和孔徑卻隨著焙燒溫度的升高而降低。孔徑大小和孔壁厚度在600℃以後降低的幅度較小,基本上趨于穩定,碳骨架的收縮變得緩慢。隨著焙燒溫度的升高,其介觀結構基本不髮生改變。
이삼감단공취물F127위모판제,선성분철수지(PF)위탄전구체,재F127여PF적질량비mF127∶mPF=1∶1시,이용용제휘발유도자조장제비개공탄재료,대재불동배소온도하제비적개공재료진행표정,연구배소온도대소득개공재료결구적영향。채용XRD、TEM、N2흡부/탈부등방법대개공재료적결구진행료표정,연구료배소온도대상술개공탄결구적영향。결과표명:개공재료적정면간거수착온도적승고이강저,당배소온도위600℃시,개공재료적골가종고분자재료전변위탄재료。기비표면적화C/H마이비균수착배소온도승고이증가,단기공벽후도화공경각수착배소온도적승고이강저。공경대소화공벽후도재600℃이후강저적폭도교소,기본상추우은정,탄골가적수축변득완만。수착배소온도적승고,기개관결구기본불발생개변。
Ordered mesoporous carbon had been synthesized through solvent evaporation induced organic-organic self-assembly method (EISA), by using triblock copolymer F127 as template and novalac phenolic resin (mF127∶mPF=1∶1) as carbon precursor. The structure of ordered mesoporous carbon was characterized by X-ray diffraction, transmission electron microscopy and N2 adsorption/desorption measurements. Influence of calcination temperatures on the pore structures of ordered mesoporous carbon was investigated. The results showed that, when the calcination temperatur was 600℃, the skeleton of mesoporous matter was transformed from polymer material to carbon material. As the calcination temperature increased from 400℃to 900℃, the interplanar spacing of ordered mesoporous materials decreased, both the pore wall thickness and pore size reduced, but the surface area and molar ratio of C/H increased. The shrink-age of carbon skeleton became slow above 600℃. The mesostructure retained well with the increase of carbon temperature.