河北联合大学学报(自然科学版)
河北聯閤大學學報(自然科學版)
하북연합대학학보(자연과학판)
Journal of Hebei United university natural sclence edition
2014年
2期
67-70
,共4页
豆贝贝%刘志刚%杨立荣%姚少威%白瑞英%封孝信
豆貝貝%劉誌剛%楊立榮%姚少威%白瑞英%封孝信
두패패%류지강%양립영%요소위%백서영%봉효신
纳米硅酸三钙%燃烧法%粒度分布%水化热
納米硅痠三鈣%燃燒法%粒度分佈%水化熱
납미규산삼개%연소법%립도분포%수화열
ricalcium silicate%combustion method%particle size distribution%hydration heat
以硅溶胶、硝酸钙为原料,尿素为燃料,采用燃烧法制备纳米硅酸三钙。研究了化学计量比、引燃温度对合成产物中游离氧化钙含量的影响。用乙二醇法测定产物中游离氧化钙的含量,X射线衍射仪、场发射扫描电镜、Zeta电位及纳米粒度分析仪和微量热仪表征合成样品的物相、微观形貌、粒度分布和水化热。结果表明:化学计量比为0.24,引燃温度为700℃时,合成产物中游离氧化钙含量达到最低值2.0%;合成的纳米硅酸三钙颗粒为不同结晶程度且呈现多种形貌的颗粒,平均粒度为225.9 nm;合成的纳米硅酸三钙水化放热峰值出现的时间为69.2 s,峰值为2.4368 mw/g,比传统水泥具有较高的水化活性。
以硅溶膠、硝痠鈣為原料,尿素為燃料,採用燃燒法製備納米硅痠三鈣。研究瞭化學計量比、引燃溫度對閤成產物中遊離氧化鈣含量的影響。用乙二醇法測定產物中遊離氧化鈣的含量,X射線衍射儀、場髮射掃描電鏡、Zeta電位及納米粒度分析儀和微量熱儀錶徵閤成樣品的物相、微觀形貌、粒度分佈和水化熱。結果錶明:化學計量比為0.24,引燃溫度為700℃時,閤成產物中遊離氧化鈣含量達到最低值2.0%;閤成的納米硅痠三鈣顆粒為不同結晶程度且呈現多種形貌的顆粒,平均粒度為225.9 nm;閤成的納米硅痠三鈣水化放熱峰值齣現的時間為69.2 s,峰值為2.4368 mw/g,比傳統水泥具有較高的水化活性。
이규용효、초산개위원료,뇨소위연료,채용연소법제비납미규산삼개。연구료화학계량비、인연온도대합성산물중유리양화개함량적영향。용을이순법측정산물중유리양화개적함량,X사선연사의、장발사소묘전경、Zeta전위급납미립도분석의화미량열의표정합성양품적물상、미관형모、립도분포화수화열。결과표명:화학계량비위0.24,인연온도위700℃시,합성산물중유리양화개함량체도최저치2.0%;합성적납미규산삼개과립위불동결정정도차정현다충형모적과립,평균립도위225.9 nm;합성적납미규산삼개수화방열봉치출현적시간위69.2 s,봉치위2.4368 mw/g,비전통수니구유교고적수화활성。
Nano tricalcium silicate ( nano-C3 S) was synthesized by a combustion method with silica sol and calcium nitrate as raw materials ,urea as fuel .Effects of stoichiometric ratio and ignition temperature on the content of f-CaO in synthesized nano-C3 S were investigated .The content of f-CaO in synthesized samples was measured by glycol method .The phase composition ,microstructure ,particle size distribution and hydration heat of samples were charac-terized by X-ray diffractometer (XRD),Field emission scanning electron microscope (FSEM),Zeta potential/sub-micron size analyzer and Digital display calorimeter .The results show that the content of f-CaO in the sample rea-ches the least value about 2 .0% under the synthesized condition of stoichiometric ratio at 0 .24 and the ignition temperature at 700℃.The synthesized nano-C3 S particles show various morphology and diverse degree of crystalli-zation with an average particle ’ size of 225.9 nm.The synthesized nano-C3 S shows a higher hydration reactivity in comparision with traditional cement because the value of the heat evolution peak of the product is 2 .4368 mw/g at a hydration time of 69 .2 seconds .