Solid enzyme type time-temperature indicator and preparation method thereof
An indicator and time technology, applied in thermometers, material analysis by observing the influence of chemical indicators, thermometers with physical/chemical changes, etc., can solve the problems of wasting food safety, difficult temperature monitoring, hidden dangers, etc., to achieve Eliminate easy leakage, good visual effect, and easy production
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Embodiment 1
[0056] A preparation method of a solid enzyme type time-temperature indicator, the specific steps are as follows:
[0057] A. Preparation of PVA gel sheets embedded with laccase
[0058] 1. Preparation of PVA aqueous solution
[0059] Prepare a PVA aqueous solution with a concentration of 0.1 g / mL, and heat it in a water bath at 95°C for 1.5 hours while stirring magnetically to completely dissolve the PVA.
[0060] 2. Preparation of laccase PVA solution
[0061] 2-1. Preparation of buffer solution
[0062] 0.004g / mL sodium acetate aqueous solution was added to diluted acetic acid aqueous solution, and the pH was adjusted to 5.0 to obtain a buffer solution.
[0063] 2-2. Preparation of laccase solution
[0064] Add 0.010g laccase to 1mL buffer solution to obtain laccase buffer solution;
[0065] Add 0.001g stabilizer bovine serum albumin to 1mL laccase buffer solution and mix evenly. The stabilizer can increase the stability of the solution, colloid, solid and mixture, slo...
Embodiment 2
[0079] A preparation method of a solid enzyme type time-temperature indicator, the specific steps are as follows:
[0080] A. Preparation of PVA gel sheets embedded with laccase
[0081] 1. Preparation of PVA aqueous solution
[0082] Prepare a PVA aqueous solution with a concentration of 0.1 g / mL, and heat it in a water bath at 95°C for 1.5 hours while stirring magnetically to completely dissolve the PVA.
[0083] 2. Preparation of laccase PVA solution
[0084] 2-1. Preparation of buffer solution
[0085] 0.0041g / mL sodium acetate aqueous solution was added to diluted acetic acid aqueous solution, and the pH was adjusted to 5.0 to obtain a buffer solution.
[0086] 2-2. Preparation of laccase solution
[0087] Add 0.021g laccase to 1mL buffer solution to obtain laccase buffer solution;
[0088] Add 0.001g stabilizer bovine serum albumin to 1mL laccase buffer solution and mix evenly. The stabilizer can increase the stability of the solution, colloid, solid and mixture, sl...
Embodiment 3
[0102] A preparation method of a solid enzyme type time-temperature indicator, the specific steps are as follows:
[0103] A. The preparation method of the PVA gel sheet embedded with laccase is the same as that in Example 2.
[0104] B. Preparation of guaiacol-embedded PVA gel sheets
[0105] 1. Preparation of PVA aqueous solution
[0106] The preparation of PVA aqueous solution is consistent with step A,
[0107] 2. Preparation of guaiacol-PVA mixed solution
[0108] Add 0.2976g guaiacol to 40mL PVA aqueous solution to prepare a guaiacol-PVA mixed solution with a concentration of 60mM;
[0109] 3. Preparation of PVA gel sheets embedded with guaiacol
[0110] Fully stir the guaiacol-PVA mixed solution with a magnetic stirrer. The stirring speed should not be too fast. If the stirring speed is too fast, air will enter the solution and generate air bubbles, which will affect the preparation quality of subsequent gel sheets. Pour it into a grid-shaped plastic mold The lengt...
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