化工进展
化工進展
화공진전
CHEMICAL INDUSTRY AND ENGINEERING PROGRESS
2015年
5期
1401-1405
,共5页
陶玉贵%郑洁%朱龙宝%葛飞%梁敏东
陶玉貴%鄭潔%硃龍寶%葛飛%樑敏東
도옥귀%정길%주룡보%갈비%량민동
纳米TiO2%磷酸根%金红石%锐钛矿%表面羟基密度
納米TiO2%燐痠根%金紅石%銳鈦礦%錶麵羥基密度
납미TiO2%린산근%금홍석%예태광%표면간기밀도
TiO2 nanoparticle%phosphate%rutile%anatase%surface hydroxyl density
以冰乙酸作诱导剂,研究磷酸盐在溶胶-凝胶法合成纳米二氧化钛过程中对其微结构及其表面羟基密度的影响,并利用XRD、BET、EDS、SEM、FT-IR和TGA等方法对二氧化钛相变过程和表面结构变化进行表征。结果表明:合成过程中添加磷酸根可增加纳米二氧化钛的表面羟基密度,500℃、700℃煅烧6h,其表面羟基密度分别为10.74nm?2、4.03nm?2,而对照样在500℃煅烧条件下其表面羟基密度为4.95nm?2;同时磷酸根的添加,有利于锐钛型晶相结构的热稳定性,锐钛型向金红石转变的相变温度达800℃。这可能是由于PO43?与TiO2晶相生长基元[TiO6]八面体易发生多齿螯合,不利于金红石相形成。
以冰乙痠作誘導劑,研究燐痠鹽在溶膠-凝膠法閤成納米二氧化鈦過程中對其微結構及其錶麵羥基密度的影響,併利用XRD、BET、EDS、SEM、FT-IR和TGA等方法對二氧化鈦相變過程和錶麵結構變化進行錶徵。結果錶明:閤成過程中添加燐痠根可增加納米二氧化鈦的錶麵羥基密度,500℃、700℃煅燒6h,其錶麵羥基密度分彆為10.74nm?2、4.03nm?2,而對照樣在500℃煅燒條件下其錶麵羥基密度為4.95nm?2;同時燐痠根的添加,有利于銳鈦型晶相結構的熱穩定性,銳鈦型嚮金紅石轉變的相變溫度達800℃。這可能是由于PO43?與TiO2晶相生長基元[TiO6]八麵體易髮生多齒螯閤,不利于金紅石相形成。
이빙을산작유도제,연구린산염재용효-응효법합성납미이양화태과정중대기미결구급기표면간기밀도적영향,병이용XRD、BET、EDS、SEM、FT-IR화TGA등방법대이양화태상변과정화표면결구변화진행표정。결과표명:합성과정중첨가린산근가증가납미이양화태적표면간기밀도,500℃、700℃단소6h,기표면간기밀도분별위10.74nm?2、4.03nm?2,이대조양재500℃단소조건하기표면간기밀도위4.95nm?2;동시린산근적첨가,유리우예태형정상결구적열은정성,예태형향금홍석전변적상변온도체800℃。저가능시유우PO43?여TiO2정상생장기원[TiO6]팔면체역발생다치오합,불리우금홍석상형성。
Titanium dioxide was prepared by adding phosphate in the sol-gel process and acetic acid used as an inducer. The effect of phosphate on nano-titanium dioxide micro-structure and surface hydroxyl density were studied in this paper. The process of phase transition and surface structural change were investigated by powder X-ray diffraction(XRD),Brunauer–Emmett–Teller (BET),X-ray energy-dispersive (EDS),scanning electron microscope (SEM),fourier-transformed infrared (FT-IR) and thermogravimetric analysis (TGA). The results showed that the surface hydroxyl groups of nano-titanium dioxide were significantly increased with the adding amount of phosphate. The surface hydroxyl densities were 10.74nm?2 and 4.03nm?2 of the samples calcined at the temperature of 500℃ and 700℃,respectively. However,the control sample with none phosphate was 4.95 DOH/nm2 at 500℃. Moreover,the thermal stability of the phase transition was enhanced by adding phosphate in sol-gel process. Until the phase change temperature reached 800℃ did it have been begun to ransform anatase to rutile. The may be due to the bonding of PO43? in these multidentate modes occupy one full face of [TiO6] octahedra and inhibit the growing of chain along the opposite edges and hence inhibit the formation of rutile.