Thermal behaviour and phases evolution during the sintering of porous inorganic membranes

Anorthite-based highly porous membranes were successfully produced using calcined oyster shell to enhance the pore network. The calcined oyster shells produce CaO responsible for the crystallisation of gehlenite and anorthite at relatively low temperature. While the crystallisation produced nano and meso size of intergranular pores, vitrification of feldspar is responsible for development of the capillary porosities. The increasing sintering temperature from 1200 °C to 1300 °C implies the increase in average pores radius from 1.2 μm to 14.3 μm due to the formation of spherical pores from vitrification. The combination of different class of porosities in the matrices results in the interconnection with improvement of the permeability of the porous network. Porosity, permeability and chemical stability were improved with 20 wt.% of calcined oyster shell addition allowing the possible development of high strength porous network which is promising for the membranes support and other applications including liquid separation as well as liquid filtration where high pressure is used.     

硅疏水改性聚胺阻垢剂的制备及其性能

用γ-缩水甘油醚氧丙基三甲氧基硅烷(KH560)、1-氯辛烷对低相对分子质量聚乙烯亚胺(PEI)进行疏水接枝改性,得到了含硅疏水改性聚胺阻垢剂。通过FTIR、TG、粒径分析、Zeta电位测试等分析改性后聚胺阻垢剂的结构与性能。结果表明,改性后产物热稳定性提高、黏度增大、表面张力降低、溶液粒径增大。将改性聚胺阻垢剂用于分散铝硅酸钠颗粒,对处理前后的颗粒进行红外光谱表征,并通过对悬浮分散液进行稳定性、颗粒沉降等测试,评价聚胺阻垢剂的阻垢分散性能并初步讨论其分散机理。当m(PEI, M_w=10000)∶m(KH560)∶m(1-氯辛烷)=10∶2∶0.5,反应时间6 h,反应温度75℃时,合成的阻垢剂分散性能最佳。当结疤的质量浓度为30 g/L时,悬浮液颗粒沉降速度达到最低值0.047 cm/d,沉降速率减小程度达到94.8%,分散性显著提高。经过改性后的PEI在氧化铝工业生产中具有高效的阻垢作用,可通过在工厂进行条件优化,进一步替代传统的强酸型阻垢剂,减小管道腐蚀程度,降低能耗。     

Relationship between the microstructure and reaction performance of aluminosilicate

A systematic study was conducted to comprehend the mechanism of thermal activation of silica-alumina materials by using 29 Si and 27 Al magnetic angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy.The reaction performance of silica-alumina-based materials with different molar ratios of Si/Al,which were thermally activated,was also investigated.With the increase in calcining temperature,the coordination of Al in metakaolin becomes four,five,and six firstly,and then transforms completely to four ...     

SiO_2/Al_2O_3 RATIO OF HYDRATED SODIUM ALUMINOSILICATE IN ALUMINA PRODUCTION

ＳｉＯ２／Ａｌ２Ｏ３ＲＡＴＩＯＯＦＨＹＤＲＡＴＥＤＳＯＤＩＵＭＡＬＵＭＩＮＯＳＩＬＩＣＡＴＥＩＮＡＬＵＭＩＮＡＰＲＯＤＵＣＴＩＯＮ①ＤｅｎｇＨｏｎｇｍｅｉ，ＺｅｎｇＷｅｎｍｉｎｇ，ＣｈｅｎＮｉａｎｙｉＳｈａｎｇｈａｉＩｎｓｔｉｔｕｔｅｏｆＭｅｔａｌｕ...     

硅酸铝/铝硅合金梯度复合材料的研究

采用挤压铸造技术制备硅酸铝短纤维增强铝硅合金梯度复合材料，研究了这类材料的凝固组织和基本热物理性能。结果表明，在复合材料中，基体组织细小，纤维与基体结合良好，并呈梯度状无序分布；梯度复合材料的热物理性能优异。     

含Co、Ni、Fe锂铝硅玻璃的析晶机制

以Li2O-Al2O3-SiO2（锂铝硅）微晶玻璃为研究对象,采用DTA、XRD、IR和SEM等测试技术研究含Fe2O3、Co2O3、Ni2O3锂铝硅玻璃的析晶动力学和晶化过程,分析着色剂成分Co2O3、Ni2O3对锂铝硅玻璃晶化过程及结构的影响机制。结果表明：着色剂成分不仅决定锂铝硅微晶玻璃的着色度,而且还影响锂铝硅玻璃的析晶过程和显微结构;着色剂的加入可提高锂铝硅玻璃的析晶温度,但降低析晶动力学参数,且高Co2O3含量的降幅大于高Ni2O3含量的。着色剂对锂铝硅玻璃析晶能力的影响主要与着色离子的离子半径、电场强度及对断裂硅氧四面体联结能力有关。     

Synthesis of γ-alkoxy-propylamines and their collecting properties on aluminosilicate minerals

1　INTRODUCTIONBayerprocessiswidelyusedtotreatthebauxitewithmoleratioofAl2 O3toSiO2 (n (Al) /n (Si) )morethan 8.AlthoughthereareabundantbauxiteresourcesinChina ,mostofthemarediasporicbaux itewithhighaluminumcontent ,butlown(Al) /n(Si) ,usually 5 8[1] .ThistypeofbauxiteisdifficulttobetreateddirectlybytheBayerprocess .Itisthereforehighlydesirabletoincreasen(Al) /n(Si)ofbauxitebyphysicalcleaning[2 ] .Forthisreason ,flotationdesilicate Bayerprocesswasdeveloped[3] .Flotationdesilicationc…     

钾/钠离子对水热合成铯榴石结构的影响

水热合成铯榴石能低温、晶格固化放射性废物¹³⁷Cs，但在放射性废物中Cs⁺通常与同族的K⁺/Na⁺共存，两者可能会对水热合成铯榴石组成和结构产生影响。基于此，参考铯榴石化学计量组成CsAlSi₂O₆，首先利用偏高岭土、纳米二氧化硅和CsOH•H₂O为原料水热合成了铯榴石。然后分别以不同摩尔质量的KOH或NaOH取代CsOH•H₂O，研究了K⁺/Na⁺对水热合成产物组成和结构的影响。结果表明，铯榴石水热晶化温度相对较低，产物微观下呈多晶微球态；K⁺与Cs⁺共存时，体系水热产物主要为铯榴石微球，微球尺寸随K⁺掺入比例的提高而增加，但K⁺主要存在于晶化程度较低的钾铝硅酸盐水合物中，并未参与铯榴石形成；Na⁺与Cs⁺共存时，体系水热产物主要由铯榴石和方沸石(NaAlSi₂O₆•H₂O)组成，Cs⁺和Na⁺各自存在于铯榴石或方沸石结构中。铯榴石相对较低的水热晶化温度及其结构中Cs⁺不能迁移和进行离子交换的特性，使得水热条件下K⁺/Na⁺不能进入先形成的铯榴石结构中的碱金属离子位点。尽管如此，K⁺或Na⁺的存在可降低铯榴石的水热晶化温度、促进铯榴石晶粒生长，且当K⁺或Na⁺与Cs⁺共存时，Cs⁺仍优先进入并稳定固化于铯榴石晶体结构中。     

ZnO·Al2O3·nSiO2玻璃抗裂纹萌生能力反常演化的结构起源探索

为探究ZnO·Al₂O₃·nSiO₂玻璃抗裂纹萌生能力(C_R)随SiO₂含量变化的演化规律,制备了一系列不同n值(n=2,2.35,2.5,2.65,3,3.5)的样品。基于C_R和结构表征发现,C_R随着n的增加呈先增大后减小的反常演化,并于n=2.5时出现极值(31.1 N)。这是源于随着n增大:(1)原子堆积份数逐渐减小,可致密化体积逐渐增加,从而导致C_R逐步提高;(2)Al—O多面体结构单元含量逐步减少,导致C_R逐步下降;(3)考虑到相界面对裂纹生长的强阻挡能力,中程异构分相(富Al和富Si相)致相界面数量呈先增多后减少的变化趋势,导致C_R产生类似的非单调演化。上述三个因素的竞争和协同作用是该体系中C_R呈反常演化的结构起源,但考虑到极值点附近较小的组分变化,中程异构致相界面数量随n增加呈现的非单调演变才应是C_R呈反常演化的主要结构根源。