A high temperature and high strength flexible zirconia-silica fiber membrane and its preparation method and application
A technology of silica fiber and zirconia, applied in the chemical characteristics of fibers, rayon manufacturing, rayon of inorganic raw materials, etc., can solve the problem that the mechanical properties of the fiber membrane cannot be guaranteed, the growth of zirconia grains cannot be inhibited, and the high strength cannot be guaranteed. And high flexibility and other issues, to achieve the effect of simple and controllable preparation method, easy industrial production, excellent high temperature flexibility
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Embodiment 1
[0048] A method for preparing a high-temperature and high-strength flexible zirconia-silica fiber membrane, comprising the following preparation steps:
[0049] (1) Add 200g of PAZ to 1000g of absolute ethanol, stir until completely dissolved, add 25g of yttrium nitrate, stir until completely dissolved, add 2g of polyethylene oxide, drop 60g of deionized water, heat to 45°C, stir until completely dissolved , followed by adding 172g of ethyl orthosilicate and stirring for 8h to obtain a precursor spinning solution.
[0050] (2) Spinning the precursor spinning liquid described in step (1) with spinning parameters as humidity 45%, temperature 25°C, voltage 11KV, propulsion speed 1.5ml / h, receiving distance 20cm, drum receiving speed 80r / min Electrospinning is carried out under the conditions to obtain the precursor fiber membrane; the physical photos are shown in the accompanying drawings figure 1 shown.
[0051] (3) heat-treat the precursor fiber membrane spun in step (2) to o...
Embodiment 2
[0054] As described in Example 1, the difference is:
[0055] In step (1), add 200g of PAZ into 667g of absolute ethanol, stir until completely dissolved, then add 25g of yttrium nitrate, stir until completely dissolved; add 2g of polyethylene oxide, add 60g of deionized water dropwise, heat to 45°C, stir until it was completely dissolved, then 172 g of ethyl orthosilicate was added and stirred for 2 hours to obtain a precursor spinning solution.
[0056] The obtained precursor spinning solution has good spinnability, the precursor fiber is longer than that of Example 1, and the fiber diameter is more uniform, and the ZrO 2 -SiO 2 The nanofiber membrane has a high degree of orientation, and the SEM pictures of the ordered fiber membrane are as follows: image 3 shown.
Embodiment 3
[0058] As described in Example 1, the difference is:
[0059] In step (1), add 200g of PAZ to 1000g of absolute ethanol, stir until completely dissolved, add 2g of polyethylene oxide, dropwise add 60g of deionized water, heat to 45°C, stir until completely dissolved, then add 172g of ethyl orthosilicate ester, stirred for 8h to obtain the precursor spinning solution;
[0060] No yttrium nitrate added, ZrO 2 No phase change, SiO 2 Always amorphous, ZrO 2 -SiO 2 Nanofibrous membranes have equally high strength and excellent flexibility.
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