电子显微学报
電子顯微學報
전자현미학보
JOURNAL OF CHINESE ELECTRON MICROSCOPY SOCIETY
2014年
4期
343-348
,共6页
钢渣%强碱性%高温%水化产物%微观形貌%化学结合水
鋼渣%彊堿性%高溫%水化產物%微觀形貌%化學結閤水
강사%강감성%고온%수화산물%미관형모%화학결합수
steel slag%high alkalinity%elevated temperature%hydration products%microstructure%non-evaporable water content
本文选用浓度为1?2 mol/L和1?6 mol/L的NaOH溶液为激发剂,研究强碱性环境对钢渣水化1 d和7 d的水化产物、微观形貌及水化结合水的影响,并与钢渣在60℃时的水化性能进行了比较。结果表明:强碱性环境和高温能够促进钢渣活性组分( C2 S、C3 S和C12 A7)的早期水化,但钢渣中的非活性组分( RO和Fe3 O4)的水化程度很低;强碱环境和高温对钢渣水化的水化产物种类的影响差异很小;钢渣水化产物的化学结合水量随着碱度的增加而增大,相比于高温,强碱环境对钢渣早期水化的促进作用较大。
本文選用濃度為1?2 mol/L和1?6 mol/L的NaOH溶液為激髮劑,研究彊堿性環境對鋼渣水化1 d和7 d的水化產物、微觀形貌及水化結閤水的影響,併與鋼渣在60℃時的水化性能進行瞭比較。結果錶明:彊堿性環境和高溫能夠促進鋼渣活性組分( C2 S、C3 S和C12 A7)的早期水化,但鋼渣中的非活性組分( RO和Fe3 O4)的水化程度很低;彊堿環境和高溫對鋼渣水化的水化產物種類的影響差異很小;鋼渣水化產物的化學結閤水量隨著堿度的增加而增大,相比于高溫,彊堿環境對鋼渣早期水化的促進作用較大。
본문선용농도위1?2 mol/L화1?6 mol/L적NaOH용액위격발제,연구강감성배경대강사수화1 d화7 d적수화산물、미관형모급수화결합수적영향,병여강사재60℃시적수화성능진행료비교。결과표명:강감성배경화고온능구촉진강사활성조분( C2 S、C3 S화C12 A7)적조기수화,단강사중적비활성조분( RO화Fe3 O4)적수화정도흔저;강감배경화고온대강사수화적수화산물충류적영향차이흔소;강사수화산물적화학결합수량수착감도적증가이증대,상비우고온,강감배경대강사조기수화적촉진작용교대。
NaOH solutions with concentration of 1?2 mol/L and 1?6 mol/L were used as activators in the hydration of steel slag. The hydration products, microstructure and non-evaporable water content of steel slag hydrating for 1 d and 7 d were investigated. The hydration properties of steel slag under the alkaline condition were compared with those under the temperature of 60 ℃. The results show that both the conditions of high alkalinity and elevated temperature can promote the early hydration of steel slag ’ s active components ( e. g. C2 S, C3 S and C12 A7 ) , but the hydration degree of low-active components ( e. g. RO phase and Fe3 O4 ) was very low. High alkalinity and elevated temperature had little influence on the kinds of hydration products of steel slag. The non-evaporable water content of steel slag increases with an increase in alkalinity. The promoting effect of high alkalinity on the early hydration of steel slag was stronger than that of elevated temperature.