Composition and Refractory Properties of Mixtures of Moroccan Silica-Alumina Geomaterials and Alumina

Five mixtures (M1 to M5) of silica-alumina geomaterials and two varieties of alumina (AP and AR) were used for the elaboration of mullite refractory materials between 1500℃ and 1600℃. An X-ray diffraction (XRD) analysis showed that the refractory samples are composed of mullite, corundum and silica. The length of the mullite crystals was measured by a method of image analysis of scanning electron microscopy (SEM). Chemical and mechanical properties of these materials were investigated and correlated with their microstructure. Resistance towards Acid Attack test showed that the refractory samples present good resistance, as well as, the alumina powder AR obtained from waste of silica-alumina bricks proves to be efficient for an eventual use.

D.C.Plasma-Sprayed Coatings of Nanostructured Alumina-Titania-Silica

Nanocrystalline powders of w(Al2O3)=95%, w(TiO2)=3%, and w(SiO2)=2%, were reprocessed into agglomerated particles for plasma spraying, by using consecutive steps of ball milling, slurry forming, spray drying, and heat treatment. D. C. plasma was used to spray the agglomerated nanocrystalline powders, and resultant coatings were deposited on the substrate of stainless steel. Scanning electron microscopy (SEM) was used to examine the morphology of the agglomerated powders and the cross section of the alumina-titania-silica coatings. Exper-imental results show that the agglomerated nanocrystalline particles are spherical, with a size from (10 - 90)μm. The flow ability of the nanocrystalline powders is greatly improved after the reprocessing. The coatings deposited by the plasma spraying are mainly of nanostructure. Unlike conventional plasma-sprayed coatings, no laminar layer could be found in the nanostructured coatings. Although the nanostructured coatings have a lower microhardness than conventional microstructured coatings, the toughness of the nanostructured ceramic coatings is significantly improved.

Preparation of Silica–Alumina Hollow Spheres with a Single Surface Hole by Co-axial Microchannel

Si/Al composite hollow spheres with a surface hole were prepared with the co-axial microchannel in a one-step method. It is easy to use the technique for size control and continuous operation. At Si/Al ratio between 4 and 5, a hole forms on the surface, due to the fast gelation process and high viscosity of the sol. Scanning electron microscopy, nitrogen adsorption–desorption isotherms, and mercury intrusion method are used to characterize the samples. The hole size is 40–150 μm and the particle size is 450–600 μm. The size can be adjusted by the flow rate of the oil phase.

Phase and microstructure of CVD alumina-silica coating deposited at relative low temperature

Alumina-silica composite coatings were prepared on the surface of graphite paper by CVD using AlCl3/SiCl4/H2/CO2 as precursor in the temperature range of 300 to 550℃. XRD and SEM were used to examine the phase composition and the microstructure of the coating, respectively. The results indicate that the dense, uniform and adherent alumina-silica composite coating can be prepared on graphite paper substrate by CVD at 550℃ using SiCl4/AlCl3/CO2/H2. The alumina-silica composite coating is composed of a number of spherical particles. Each particle is composed of a number of fine-particle. The phase of the 550℃ composite coating includes γ-alumina containing amorphous silica. The content of Cl element in composite coating decreases with the increase of the deposition temperature. The analysis results of morphology and growth mechanisms of the CVD alumina-silica indicate that the condensation within the boundary layer will be more likely to lead to the formation of gel-particles. The gel-particles size decreases with the increase of deposition temperature in the range of 300550℃. Surface reaction is the main path to generate deposition products at 550℃.

手性Salen-Co配合物在纳米Silica和壳核纳米Silica上的接枝及环氧化催化性能的研究

通过共价键将手性Salen-Co(Ⅲ)配合物接枝到纳米Silica和壳-核纳米Silica表面上制备固相催化剂,并且用红外光谱(FT-IR)、热重分析(TG-DTA)、透射电镜等表征手段对已制备的催化剂进行了表征,结果证实手性Salen-Co配合物成功接枝到了纳米Silica和壳-核纳米Silica表面。以反式二苯乙烯为反应底物,考察了所得固相催化剂的环氧化催化活性、选择性、e.e.值(对映体过量)和重复使用性能,从催化结果来看所得固相催化剂有一定的不对称催化活性,重复使用性能也比较好。

Catalytic performances of kaoline and silica alumina in the thermal degradation of polypropylene

Polypropylene was cracked thermally and catalytically in the presence of kaoline and silica alumina in a semi batch reactor in the temperature range 400℃～550℃ in order to obtain suitable liquid fuels.The dependencies between process temperatures,types of catalyst,feed compositions and product yields of the obtained fuel fractions were found.It was observed that up to 450℃ thermal cracking temperature,the major product of pyrolysis was liquid oil and the major product at other higher temperatures(475℃～550℃) are viscous liquid or wax and the highest yield of pyrolysis product is 82.85% by weight at 500℃.Use of kaoline and silica alumina decreased the reaction time and increased the yield of liquid fraction.Again the major pyrolysis product in catalytic pyrolysis at all temperatures was low viscous liquid oil.Silica alumina was found better as compared to kaoline in liquid yield and in reducing the reaction temperature.The maximum oil yield using silica alumina and kaoline catalyst are 91% and 89.5% respectively.On the basis of the obtained results hypothetical continuous process of waste polypropylene plastics processing for engine fuel production can be presented.

Effect of Plasma Spheroidization Process on the Microstructure and Crystallographic Phases of Silica, Alumina and Nickel Particles

During the plasma spheroidization process powders undergo different changes in their microstructures and crystal phases. In this paper, simple calculation of heat transfer between the plasma and a suspended particle was performed based on three hypotheses for the purpose of guiding experiments. Experimental investigation of the crystal phases and microstructural changes during the plasma processing was made using silica, alumina and nickel powders as starting materials. It has been revealed from the experimental results that these materials undergo different changes in crystal phases and microstructures, and these changes are essentially determined by the structures, properties and aggregate states of the starting materials.

Intensifying digestion of diaspore and separation of alumina and silica

It was found that there lies a linear relationship among the thermodynamic data of complicate inorganic compounds with similar components. A method for estimating the thermodynamic data of complicate compound and a thermodynamic database involving alumina production were developed. It was found that the alumina digestion rate of activated diasporic bauxite by means of heat field increased much due to the structure aberration, i.e, from perfect structure to unstable corundum. The results from thermodynamic calculation and experiments showed that it was feasible for desilication at atmospheric pressure, and the effects on equilibrium concentration of SiO 2 included temperature, mole ratio of Na 2O/Al 2O 3 ( α k), caustic and Na + concentration. The technology of desilication of green liquor at atmosphere and separation of alumina and silica in aluminate solution with high concentration were established. The reaction activity of compounds containing silica and the converting law among compounds were studied, and the prototype technology of desilication products by hydrotreatment was also developed.

Oxidative desulfurization of model and real oil samples using Mo supported on hierarchical alumina–silica: Process optimization by Box–Behnken experimental design

The catalytic performance of Mo supported on hierarchical alumina–silica(Si/Al = 15) with Mo loadings of 3, 6 and 15 wt% was investigated for the oxidative desulfurization(ODS) of model and real oil samples. Hierarchical alumina–silica(h Al–Si) was synthesized by economical and ecofriendly silicate-1 seed-induced route using cetyltrimethylammonium bromide(CTAB) as mesoporogen. The effect of CTAB on the structure of catalyst was studied by characterization techniques. The results revealed that 6%Mo/h Al–Si had the highest sulfur removal compared to the other catalyst loadings. The effect of operating parameters was evaluated using Box–Behnken experimental design. The optimal desulfurization conditions with the 6%Mo/h Al–Si catalyst were determined at oxidation temperature of 67 ℃, oxidation time of 42 min, H2O2/S molar ratio of 8 and catalyst dosage of 0.008 g·ml^-1 for achieving a conversion of 95%. Under optimal conditions, different sulfur-containing compounds with initial concentration of 1000 ppm, Dibenzothiophene(DBT), Benzothiophene(BT) and Thiophen(Th), showed the catalytic oxidation reactivity in the order of DBT > BT>Th. According to the regeneration experiments, the 6%Mo/h Al–Si catalyst was reused 4 times with a little reduction in the performance. Also, the total sulfur content of gasoline and diesel after ODS process reached 156.6 and 4592.2 ppm, respectively.

Effect of Microsilica Addition on Properties of CMA72 Bonded Al2O3-MgO Castables

CMA72 bonded Al2 O3 - MgO castable is promising for application of steel ladle wall, because of unique combination of thermo-mechanical properties, slag corro- sion resistance and cost benefit. In these castables, mi- crosilica can be introduced to counterbalance the expan- sion generated by spinel formation. In this paper, the of microsilica dosage on properties of eastables was evaluated. Expansion, expressed by the permanent linear change （PLC）, is highly dependent on the dosage of microsilica. Unexpected expansion occurs when the dos- age of microsilica is too low due to dominant effect of spinel and CA6 formation. Too high dosage results in sintering shrinkage, which is related to amount of liquid phase generated by microsilica addition. In addition, HMOR declines dramatically with increasing microsilica dosage. Considering the balance between expansion con- trol and hot property retention, 1.0 mass% of microsili- ca is recommended for the castable containing 4 mass% of magnesia.

无有机胺醇水体系低硅铝比ZSM-5沸石的一步合成

研究了无有机胺醇水体系低硅铝比ZSM-5沸石的绿色合成方法。在无有机胺模板剂和不加晶种的醇水体系中,一步合成了形貌均一的小晶粒聚集体低硅铝比ZSM-5沸石,考察了合成体系中各配料的含量以及晶化温度对合成低硅铝比ZSM-5沸石的影响。利用XRD、FTIR、SEM、N_(2)吸附-脱附、^(27)Al MAS NMR和^(29)Si MAS NMR等方法对合成的ZSM-5沸石进行表征。实验结果表明,当n(Si)∶n(Al)=20,n(Na_(2)O)∶n(SiO_(2))=0.071,n(C_(2)H_(5)OH)∶n(SiO_(2))=1.77,晶化温度为160℃时,可合成具有高结晶度的纯相ZSM-5沸石。^(27)Al MAS NMR表征结果显示,合成的ZSM-5沸石主要含有骨架四配位铝,无非骨架铝。合成的ZSM-5沸石的比表面积和微孔孔体积分别为384 m^(2)/g和0.14 cm^(3)/g,总酸量达到789μmol/g,骨架n(Si)∶n(Al)=14.4。

New Process for Preparation Alumina and Silica White from Coal Fly Ash

Fly ash was used to prepare alumina and silica white, The 3 stages of the process are as follows: ammonium sulfate calcining, acid leaching and alkali dissolution. The optimum conditions for the experiments to determine are as follows: molar ratio of (NH4)2SO4/Al2O3 is 6, the calcining time is 2h, he H2SO4 concentration is 20%, the leaching temperature is 80℃ and dissolution duration is 2h, the ratio of solution and solid reaction material is 6 for ammonium sulfate calcining and acid leaching stage, reaction time 30min, ratio of liquid to ore 5∶1, alkali concentration 45% and reaction temperature 95 ℃for the alkali dissolution stage. Under these conditions, the total leaching efficiencies of Al2O3 and SiO2 are 78.86% and 95%, respectively. The quality of the main products alumina and silica white can meet the national standards of GB/T24487-2009 and GB10517-89, respectively.

SiO_(2)-Al_(2)O_(3)复合气凝胶常压干燥制备技术研究进展

SiO_(2)-Al_(2)O_(3)复合气凝胶(SAA)具有低密度、高比表面积、低热导率和耐高温等特点,可应用于航空航天、化工冶金、窑炉保温等领域。常压干燥具备制备成本低、可满足工业化大批量生产等优势,具有良好的实际应用前景。介绍了SAA的制备方法,重点对常压干燥制备SAA中前驱体、表面改性剂、纤维增强的研究现状进行了综述,并展望了常压干燥方法制备SAA的发展方向。

Effect of SiO2 Micropowder Addition on Properties of Alumina-magnesia Based Wet Gunning Mix for Working Layer

The magnesia - alumina based wet gunning mix was prepared using tabular corundum aggregates,fused mag- nesia aggregates, tabular corundum micropowder, silica mieropowder and pure calcium ahuninate cement as the main starting materials. Effects of silica micropowder ad- ditions （0, 0. 2% , 0. 5% , 1.0% , 1.5% , 2. 0% , and 2.5%, by mass, the same hewinafier） on properties oJ the gunning mix were researched. The results show that when ttze silica micropowder addition is i. 0% -2. 0% , the gunning mix has good .flou,ability and pumpability. Adding 2.5% silica micropowder, the nepheline forms at 1 600 ℃, which will reduce the high. temperature proper- ties of ntagnesia -ahtmina wet gunning mix. The intro- duction qf silica micropowder has obvious effects on cold mechanical properties of the gunning mix. For the speci- tnens dried at 110 ℃ , the strength increases slightly with the silica micropowder addition increasing. For the specimens heat-treated at 1 600 ℃ for 3 h, the strength in- creases nutrkedlv with the silica micropowder addition in- creasing. When keeping the water addition and particle size di, stribution constant, the residual linear expansion rate qf the specimen with 1.5% of silica micropowder is the lowest, ltot modulus tf rupture at 1 450 ℃ .for 0. 5 h oJ the specimens decreases gradually with the increase of silica fame addition. A small amount of silica micropow- der is beneficial for the slag penetration resistance.

Incorporation of Sphingosine 1-Phosphate Loaded Mesoporous Silica Nanoparticles into Poly ( L-lactic acid ) Nanofibrous Scaffolds for Bone Tissue Engineering

Controlled release of the functional factors is the key to improve clinical therapeutic efficacy during the tissue repair and regeneration. The thrce-dimensional （3D） scaffold can provide not only physical properties such as high strength and porosity hut also an optimal environment to enhance tissue regeneration. Sphingosine 1-phosphate （SIP）, an angiogenlc factor, was loaded into mesoporous silica nanoparticles （MSNs） and then incorporated into poly （ L-lactic add ） （ PLLA ） nanofibrons scaffold, which was fabricated by thermally induced phase separation （TIPS） method. The prepared scaffolds were examined by attenuated total reflection Fourier transform infrared spectroscopy （ATR-FTIR）, scanning electron microscopy （ SEM）, and transmission electron microscopy （TEM） and compressive mechanical test. The ATR-FTIR result demonstrated the existence of MSNs in the PLLA nanofibrous scaffold. The SEM images showed that PLLA scaffold had regular pore channel, interconnected pores and nanofibrous structure. The addition of MSNs at appropriate content had no visible effect on the structure of scaffold. The compressive modulus of scaffold containing MSNs was higher than that of the scaffold without MSNs. Furthermore, fluorescein isothiocyanate （FTTC） was used as model molecule to investigate the release behavior of SIP from MSNs- incorporated PLLA （MSNs/PLLA） nanofibrons scaffold. The result showed that the composite scaffold largely reduced the initial burst release and exhibited prolonged release of FITC than MSNs. Thus, these results indicated that SIP-loaded composite uanofibrons scaffold has potential applications for bone tissue engneering.

Synthesis and Characterization of Polystyrene/Nanosilica Organic-Inorganic Hybrid

A polystyrene（PS）/nanosilica organic-inorganic hybrid material was prepared from styrene monomer and commercial aqueous silica sol containing large amounts of Si-OH by means of emulsion polymerization. The nanosilica sol was modified by the addition of the reactive coupling agent methacrylexy propyltrimethoxysilane （ MPS）, and the resulting latex particles were protected by surfactants such as sodium dodecyl sulphonate（ SDS）, hydroxypropyl methyl cellulose （ HMPC）, and poly （vinylpyrrolidone） （PVP）. The effects of the type of surfactant, the amount of surfactant, and the coupling agent on the shape and stability of the resulting latex particles were investigated. The TEM observation indicates that among SDS, HMPC, and PVP, SDS is the best surfactant. When the content of SDS is 0. 5% and the amount of MPS is 7% in the system, the latex with obvious core-shell structure could be obtained. The average diameters of the monodispersed particles range from 182 to 278 nm, and the average number of silica beads for each composite are 1325 and 4409, respectively. The FrIR analysis shows that PS was chemically linked to silica through MPS. The thermal gravimetric analysis shows that when there is a higher silica content, the hybrid composites have a better heat resistance.

Silica Bricks GB/T 2608-2012

1 Scope This standard specifies the classifcation, technical requirements, test methods, quality appraisal procedure, packing, marking, transportation, storage and quality certificate of silica bricks.

硅胶-氧化铝层析柱-气相色谱法测定沉积物中邻苯二甲酸酯类有机物

建立了硅胶-氧化铝层析柱净化分离,GC-MS、GC-FID定性定量分析沉积物样品邻苯二甲酸酯类有机污染物Phthalate esters(PAEs)的方法.比较了Florisil、硅胶、氧化铝和硅胶-氧化铝层析柱对PAEs分离特征;优化了硅胶-氧化铝层析柱净化分离PAEs的条件.方法线性范围0.05～500 μg/g,回收率75.3%～113.6%,相对标准偏差2.74%～12.2%,检出限0.29～1.2 ng/g.内标法定量,应用于珠江口沉积物样品中PAEs测定,获得满意的结果.

硅铝凝胶粉结合SiAlON增强A1_2O_3-SiC-C浇注料

以电熔致密刚玉和碳化硅为骨料,硅铝凝胶粉、氮化硅粉、硅粉为细粉,制成SiAlON增强Al2O3-SiC-C浇注料,研究了硅铝凝胶粉的加入量分别为1%、3%、5%(质量分数,下同)时对此浇注料的烧结性能、力学性能的影响。结果表明:采用硅铝凝胶粉取代纯铝酸钙水泥作结合剂,可使SiAlON增强Al2O3-SiC-C浇注料在经中温、高温热处理后的常温抗折强度及耐压强度较大提高,中温、高温强度提高幅度更大。另外,随着硅铝凝胶粉加入量的增加,浇注料的常温及高温强度呈先增大而后减小的趋势。由X射线衍射和扫描电镜分析结果可知,硅铝凝胶粉的加入既有利于降低βSiAlON的生成温度,又可以减少材料中的低熔物质。分布均匀、发育良好的粒状βSiAlON的形成是SiAlON增强Al2O3-SiC-C浇注料较水泥结合浇注料强度高的根本原因。

高硅铝比ZSM-5分子筛的合成及催化裂化性能研究

在实验室以正丁胺为模板剂,在晶化温度160～180℃,晶化时间28～40h,投料硅铝摩尔比100～300的条件下,合成出高硅铝比的ZSM5分子筛,并制备了FCC催化剂。在重油微反装置上对FCC催化剂的评价结果表明,催化剂中HZSM5分子筛硅铝比的提高,可增加轻质油收率及汽油辛烷值,而液化气、干气及焦炭收率减少。