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Peptization of Nanoparticulate Titania Sols Prepared Under Different Water-Alkoxide Molar Ratios

机译:不同水-醇盐摩尔比制备的纳米二氧化钛溶胶的胶溶

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摘要

Particulate titania sols with water-alkoxide molar ratios (r) of r = 30:1 ([Ti~(4+)] = 1.146M), r = 50:l ([Ti~(4+)] = 0.818M), r = 75:1 ([Ti~(4+)] = 0.579M), and r = 100:1 ([Ti~(4+)] = 0.459M), have been synthesized. Both hydrolysis and peptization temperatures were maintained at 35℃ in all cases. HNO_3 was used as a catalyst and its amount was calculated to maintain the H~+/Ti molar ratio at 0.2. The combination of the data measured with optical techniques such as laser diffraction, dynamic light scattering (DLS), and multiple light scattering with a near-infrared light allows us to follow up the evolution of the peptization process and to unequivocally establish a procedure to quantify its time. This time increases as the water-alkoxide molar ratio increases. Stable monomodal nanoparticulate TiO_2 · xH_2O sols with an average particle size of ~ 20 nm, as measured by DLS were obtained after peptization, except for r = 30:1. However, TEM observations of the xerogels treated at 300℃ for 1 h show primary particles of ~ 10 nm. This suggests that the synthesized sols are formed by agglomerated particles and DLS measurements provide particle sizes larger than the actual primary size. The viscosity of the sols increases with the Ti concentration, but it is very low (<5 mPa·s), except that of the 30:1 sol, where a transient structured fluid is formed that breaks with time and by shearing. The sols have considerably long-term stability when preserved cool (< 10℃). The anatase phase is obtained as a major phase in the xerogels, although a small peak of brookite is also present. The xerogels calcined at 300℃ for 1 h show traces of rutile at r values of 50:1 and 30:1. This fact confirms that the anatase-rutile transformation is produced at lower temperatures when the molar ratio is lower, i.e., when the Ti concentration increases.
机译:水醇盐摩尔比(r)为r = 30:1([Ti〜(4+)] = 1.146M),r = 50:l([Ti〜(4+)] = 0.818M)的二氧化钛溶胶,r = 75∶1([Ti〜(4 +)] = 0.579M),r = 100∶1([Ti〜(4 +)] = 0.459M)。在所有情况下,水解和胶解温度均保持在35℃。使用HNO_3作为催化剂,并计算其含量以保持H〜+ / Ti摩尔比为0.2。用光学技术(例如激光衍射,动态光散射(DLS)和近红外光的多次散射)测量的数据相结合,使我们能够追踪肽化过程的发展,并明确地建立量化程序是时候了。随着水-醇盐摩尔比增加,该时间增加。胶溶后,获得了稳定的单峰纳米颗粒TiO_2·xH_2O溶胶,通过DLS测得的平均粒径为〜20 nm,除了r = 30:1。然而,在300℃下处理1 h的干凝胶的TEM观察显示,初级粒子约为10 nm。这表明合成的溶胶是由团聚的颗粒形成的,而DLS测量提供的粒度大于实际的初级粒度。溶胶的粘度随Ti浓度的增加而增加,但非常低(<5 mPa·s),除了30:1溶胶的粘度外,在溶胶中形成的瞬态结构化流体会随着时间的流逝和剪切作用而破裂。低温保存(<10℃)时,溶胶具有相当长的长期稳定性。锐钛矿相是干凝胶中的主要相,尽管板钛矿也有一个小的峰。在300℃煅烧1小时的干凝胶在r值为50:1和30:1时显示出金红石的痕迹。该事实证实当摩尔比较低时,即当Ti浓度增加时,在较低温度下产生锐钛矿-金红石相转变。

著录项

  • 来源
    《Journal of the American Ceramic Society》 |2010年第1期|59-64|共6页
  • 作者单位

    Instituto de Ceramica y Vidrio, CSIC, c/Kelsen, 5. Cantoblanco E-28049, Madrid, Spain;

    Instituto de Ceramica y Vidrio, CSIC, c/Kelsen, 5. Cantoblanco E-28049, Madrid, Spain;

    Instituto de Ceramica y Vidrio, CSIC, c/Kelsen, 5. Cantoblanco E-28049, Madrid, Spain;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-17 13:40:11

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