Preparation method and application of laponite bioceramics
A bioceramic and hectorite technology, applied in medical science, prosthesis, etc., to achieve the effect of simple operation, good biocompatibility, and low cost of LAP
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[0049] The preparation method of laponite bioceramics provided by the present invention includes:
[0050] Step 1. Press synthetic laponite powder into tablets to obtain laponite tablets; the amount of synthetic laponite powder per laponite tablet is 0.3-0.6g; the compression pressure is 8-15 MPa; The tableting process is to compress the tablet by uniaxial compression in the mold (uniaxial compression refers to the method of pressing powder along an axial direction).
[0051] Step 2, sintering the obtained laponite flakes to obtain a laponite bioceramic; the sintering temperature is 600-800 ℃, and the sintering time is 2-6 h. The sintering process is carried out in a muffle furnace. During the process of heating up to the sintering temperature during sintering, the heating rate is 2-15 ℃ / min.
[0052] The method for preparing laponite bioceramics provided by the present invention also includes using scanning electron microscopy (SEM), X-ray diffraction (XRD), contact angle test, an...
Embodiment 1
[0075] Take 0.45 g of LAP powder, place it in a mold with a diameter of 14 mm, and compress tablets under a pressure of 10 MPa by a uniaxial compression method to obtain LAP tablets. Four LAP sheets were placed in a muffle furnace and sintered under the conditions shown in Table 1 to prepare LAP bioceramics, which were recorded as samples 2-5.
[0076] The diameter of the sample before and after sintering was measured with a micrometer, and the calculated diameter shrinkage rate is shown in Table 1. The density of all samples was measured using Archimedes' principle and divided by the original LAP powder to get the relative density change (see Table 1). The hydrophilicity of all samples was measured by contact angle. 1 μL of distilled water was dropped on the surface of the sample, and then measured with a contact angle meter. The results are shown in Table 1. The morphological changes of the LAP sheet prepared by the present invention are observed by SEM, as shown in Fig. 1. Th...
Embodiment 2
[0080] Take the LAP tablets and LAP bioceramics prepared in Example 1 respectively to test their XRD patterns (see attached figure 2 ). XRD test results show that at a lower sintering temperature (600 o C) There is no crystalline phase transformation before and after LAP sintering. And at higher sintering temperature (800 o C) The characteristic diffraction peaks of sodium mica and enstatite appear in the spectrum, indicating that the resulting LAP bioceramic contains crystal components such as LAP, sodium mica and enstatite.
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