Preparation method of flexible optical/electric-thermal dual-response phase change cloth
A dual-response and flexible technology, applied in chemical instruments and methods, heat exchange materials, textiles and papermaking, etc., can solve the problem that carbon cloth cannot load storage heat transfer performance phase change core materials, etc., to ensure continuity and structure Integrity, improving light-to-heat conversion efficiency, improving the effect of poor light absorption
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment example 1
[0026] (1) Preparation of carbon cloth @MOF-5 carrier material:
[0027] Soak 2cm*3cm carbon cloth in 30mL concentrated HNO 3 In the solution, after reacting at 100°C for 3 hours, dry it in vacuum for 24 hours to obtain activated carbon cloth; place the activated carbon cloth (2cm*3cm) in 25mL DMF solvent containing 0.743g zinc nitrate hexahydrate and 0.207g terephthalic acid , and put it into a 50mL reactor. After reacting at 120 °C for 10 h, filter and wash with DMF three times, and dry at 80 °C for 24 h to obtain the carbon cloth @MOF-5 support material.
[0028] (2) Preparation of composite phase change materials:
[0029] Vacuumize the carbon cloth @MOF-5 (2cm*3cm) carrier material prepared above at 120°C for 8 hours to completely open the pores of the substrate. Dissolve 0.18g PEG2000 in 20mL ethanol to obtain a homogeneous phase change material solution. Then the carrier material was placed into the prepared phase change material solution, and then dried in an oven ...
Embodiment example 2
[0032] (1) Preparation of carbon cloth @IRMOF-3 carrier material:
[0033] Soak 2cm*3cm carbon cloth in 30mL concentrated HNO 3In the solution, after reacting at 100°C for 3 hours, vacuum-dried for 24 hours to obtain activated carbon cloth; put the activated carbon cloth (2cm*3cm) in a 30mL solution containing 0.892g zinc nitrate hexahydrate and 0.181g 2-aminoterephthalic acid DMF solvent, and put it into a 50mL reaction kettle. After reacting at 100 °C for 24 h, it was filtered and washed with DMF for 3 times, and dried at 80 °C for 24 h to obtain the carbon cloth @IRMOF-3 support material.
[0034] (2) Preparation of composite phase change materials:
[0035] Vacuumize 0.25g of the above-prepared carbon cloth @IRMOF-3 (2cm*3cm) carrier material at 120°C for 8 hours to completely open the pores of the matrix. 0.25 g octadecanoic acid was dissolved in 20 mL ethanol to obtain a uniform phase change material solution. Then the carrier material was put into the prepared phase...
Embodiment example 3
[0038] (1) Carbon cloth@MIL-101(Cr)-NH 2 Preparation of carrier material:
[0039] Soak 2cm*3cm carbon cloth in 30mL concentrated HNO 3 In the solution, after reacting at 100°C for 3 hours, vacuum-dried for 24 hours to obtain activated carbon cloth; place the activated carbon cloth (2cm*3cm) in a solution containing 1.6g of chromium nitrate nonahydrate and 0.72g of 2-aminoterephthalic acid and 0.4 g NaOH in 30 mL deionized water and place it in a 50 mL reaction kettle. After reacting at 150°C for 12h, filter and wash with DMF for 3 times, and dry at 80°C for 24h to obtain carbon cloth @MIL-101(Cr)-NH 2 carrier material.
[0040] (2) Preparation of composite phase change materials:
[0041] The above-prepared carbon cloth @MIL-101(Cr)-NH 2 (2cm*3cm) carrier material is vacuumized at 120° C. for 8 hours to completely open the pores of the substrate. 0.20 g octadecanoic acid was dissolved in 20 mL ethanol to obtain a uniform phase change material solution. Then the carrier...
PUM
| Property | Measurement | Unit |
|---|---|---|
| melting point | aaaaa | aaaaa |
| melting point | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


