SiO_2气凝胶干燥技术现状

由于SiO_2气凝胶具有良好的性能被人们所广泛重视,SiO_2气凝胶制备技术的关键在于干燥技术的应用。本文总结了目前SiO_2气凝胶干燥技术的特点,指出了如果能够突破SiO_2气凝胶的低成本干燥,将会使SiO2气凝胶迅速商品化得到广泛的应用。

Preparation of TiO_2/SiO_2 Aerogels by Non-supercritical Drying Method and Their Photocatalytic Activity for Degradation of Pyridine

TiO2/SiO2 aerogels with different molar ratio of SiO2/TiO2 were prepared via non-supercritical method using tetrabutyl titanate and silica sols as raw materials. The samples were characterized by TEM, SEM, BET, IR, XRD and so on. The results indicate that the BET surface area of TiO2/SiO2 aerogels calcined at 550℃ which consisted of anatase structure of TiO2 with narrow distribution pores of 5-25 nm is as high as 357.89 m2·g-1. For the photocatalytic degradation of pyridine, the catalytic activities of TiO2/SiO2 aerogels are much higher than that of TiO2 powder. The photocatalytic activity of TiO2/SiO2 aerogels calcined at 800℃ is the optimum. The higher the content of SiO2, the higher the photocatalytic activity of TiO2/SiO2 aerogels. The cost for preparation of the aerogels is greatly reduced by using non-supercritical drying method, and the aerogels are hopefully applied in the treatment of industrial waste water such as coking effluent treatment.

THE FABRICATION OF CARBON AEROGELS BY GELATION IN ISOPROPANOL WITH BASIC CATALYST

A new method for the fabrication of carbon aerogels is reported in this paper. Resorcinol and furfural were gelated in isopropanol with basic catalysts and then dried directly under isopropanol supercritical condition, followed by carbonization under nitrogen atmosphere. The bulk densities of carbon aerogels obtained are in the range of 0.21g/cm3~0.27g/cm3 and the sizes of the interconnected carbon nano-particles are in the range of 20nm^30nm. All of the aerogel samples exhibit high BET surface areas in the range of 730m2/g^900m2/g. The bulk density, micro-pore volume, meso-pore volume and meso-pore diameter can be controlled by gelation conditions such as R/I ratio and R/C ratio.

Preparation and Application of the Sol–Gel Combustion Synthesis-Made CaO/CaZrO_3 Sorbent for Cyclic CO_2 Capture Through the Severe Calcination Condition

Calcium looping method has been considered as one of the efficient options to capture C02 in the combustion Ilue gas. CaO-based sorbent is the basis for application of calcium looping and should be subjected to the severe calcination condition so as to obtain the concentrated C02 stream. In this research, CaO/CaZrO3 sorbents were synthesized using the sol-gel combustion synthesis （SGCS） method with urea as fuel. The cyclic reaction performance of the synthesized sorbents was evaluated on a lab-scaled reactor system through calcination at 950 ℃ in a pure C02 atmosphere and carbonation at 650 ℃ in the 15% （by volume） C02. The mass ratio of CaO to CaZr03 as 8：2 （designated as CasZr2） was screened as the best option among all the synthesized CaO sorbents for its high CO2 capture capacity and carbonation conversion at the initial cycle. And then a gradual decay in the C02 capture capacity was observed at the following 10 successive cycles, but hereafter stabilized throughout the later cycles. Furthermore, structural evolution of the carbonated CasZr2 over the looping cycles was investigated. With increasing looping cycles, the pore peak and mean grain size of the carbonated CasZr2 sorbent shifted to the bigger direction but both the surface area （SA） ratio and surface fractal dimension Ds decreased. Finally, morphological transformation of the carbonated CasZr2 was observed. Agglomeration and edge rounding of the newly formed CaC03 grains were found as aggravated at the cyclic carbonation stage. As a result, carbonation of CasZr2 with C02 was observed only confined to the external active CaO by the fast formation of the CaC03 shell outside, which occluded the further carbonation of the unreacted CaO inside. Therefore, enough attention should be paid to the carbonation stage and more effective activation measures should be explored to ensure the unreacted active CaO fully carbonatPd river the extended Ioonin cycles.

Electrical Properties of NASICON-type Structured Li1.3Al0.3Ti1.7（PO4）3 Solid Electrolyte Prepared by 1,2-Propylene glycol-assisted Sol-gel Method

Lithium-ion conductor Liz.3Alo.3Ti1.7（P04）3 with an ultrapure NASICON-type phase is syn- thesized by a 1,2-propylene glycol （1,2-PG）-assisted sol-gel method and characterized by differential thermal analysis-thermo gravimetric analysis, X-ray diffraction, scanning elec- tron microscopy, electrochemical impedance spectroscopy, and chronoamperornetry test. Due to the use of 1,2-PG, a homogeneous and light yellow transparent precursor solu- tion is obtained without the precipitation of Ti4＋ and A13＋ with PO43- Well crystallized Lil.3Alo.3Til.7（PO4）3 can be prepared at much lower temperatures from 850 ~C to 950 ~C within a shorter synthesis time compared with that prepared at a temperature above 1000 ~C by a conventional solid-state reaction method. The lithium ionic conductivity of the sintered pellets is up to 0.3 mS/cm at 50 ℃ with an activation energy as low as 36.6 k J/tool for the specimen pre-sintered at 700 ℃ and sintered at 850 ℃. The high conductivity, good chemi- cal stability and easy fabrication of the Li1.3Al0.3Ti1.7（PO4）a provide a promising candidate as solid electrolyte for all-solid-state Li-ion rechargeable batteries.