首页> 外文期刊>Journal of Materials Science >Size-dependent hydration mechanism and kinetics for reactive MgO and Al2O3 powders with respect to the calcia-free hydraulic binder systems designed for refractory castables
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Size-dependent hydration mechanism and kinetics for reactive MgO and Al2O3 powders with respect to the calcia-free hydraulic binder systems designed for refractory castables

机译:关于反应MgO和Al2O3粉末的尺寸依赖性水化机理和动力学相对于为难熔铸件设计的无钙液粘合剂系统

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This work investigates the time-dependent hydration behavior of 1:1 molar ratio mixture of reactive alpha-Al2O3 nano- or micro-powder and reactive MgO in relation to the development of new hydraulic binder systems for in situ spinel refractory corundum castables. Mg-Al-CO3 hydrotalcite-like phases formed in the cementitious matrices cured in the corresponding curing condition up to 280 days of age at 50 A degrees C were subjected to morphological, chemical and structural characterization using XRD, FT-IR, NMR, SEM and TEM techniques. The observations indicate that both the short-term cured MgO-nano-Al2O3 cementitious matrix and the long-term cured one containing micro-Al2O3 contain mainly OH-(Mg-3) hydroxyl group, whereas the long-term cured MgO-nano-Al2O3 cementitious matrix is dominated by OH-(Mg2Al) hydroxyl group. The thermal stability of hydrotalcite-like compounds (Mg0.667Al0.333(OH)(2)(CO3)(0.167)(H2O)(0.5), Mg6Al2CO3(OH)(16)center dot 4H(2)O) (HTlcs) through combined DTA-TGA-EGA-MS analyses shows that HTlcs undergo dehydration first and then dehydroxylation overlapping with decarbonization processes. According to EGA-MS and FT-IR measurements, the Mg-Al cementitious matrices were progressively carbonated over curing time and then interlayer water molecules were preferably coordinated by interlayer CO3 (2-) ions that exist in a complex network of hydrogen bonds between octahedral layers. In the near-fully-hydrated binder paste, dehydration of crystalline water molecules occurs at 262 A degrees C and the thermal stability of hydroxyl groups in HTlcs is OH-(Mg2Al) (422 A degrees C) > OH-(Mg-3) (337 A degrees C) at a ramping rate of 10 A degrees C/min. The basic information provided by the microcalorimetric measurement is such that the starting grain size significantly affects the heat flow curve. From the SEM and TEM images, the hydrates are found to be hexagonal in shape.
机译:该作品研究了反应性α-Al2O3纳米或微粉和反应性MgO的1:1摩尔比混合物的时间依赖性水合行为,以及用于原位尖晶石难治性刚性刚胺碎屑的新液压粘合剂系统的开发。 Mg-Al-Co3在50℃下固化的水泥基质中形成的水​​泥基质中的水滑石状相,使用XRD,FT-IR,NMR,SEM进行形态,化学和结构表征。和水彩技巧。观察结果表明短期固化的MgO-NaNO-Al 2 O 3水泥基质和含有微Al2O3的长期固化的基质主要含有OH-(Mg-3)羟基,而长期固化的MgO-纳米 - Al 2O3水泥基质由OH-(Mg2Al)羟基支配。水滑石状化合物的热稳定性(Mg0.667Al0.333(OH)(2)(2)(2)(0.167)(0.5),Mg6Al 2CO 3(OH)(16)中心点4h(2)O)(HTLCS )通过组合的DTA-TGA-EGA-MS分析表明,HTLCS首先经历脱水,然后与脱碳过程重叠脱羟基化。根据EGA-MS和FT-IR测量,Mg-Al水泥基质在固化时间上逐渐碳酸化,然后层间水分子优选由中间层CO 3(2-)离子与八面体之间的氢键复合网络中存在的中间层CO 3(2-)离子协调层。在接近完全水合的粘合剂糊中,结晶水分子的脱水在262℃下发生,HTLC中羟基的热稳定性是OH-(Mg2Al)(422℃)> OH-(MG-3) (337℃)以10℃/ min的斜坡率。由微量微核测量提供的基本信息是使起始晶粒尺寸显着影响热流曲线。从SEM和TEM图像中,发现水合物是六边形的形状。

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