Edible medicinal ink
A technology of medicinal ink and cellulose acetate, which is applied in the fields of ink and pharmacy, can solve the problems of quick drying, increase the controllability of production and processing, easy entanglement and clumping, etc., and achieves the effect of meeting the requirements of capsule printing.
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Embodiment 1
[0014] White ink composition one:
[0015] Various raw materials (parts by weight):
[0016] Cellulose acetate succinate 10
[0017] Titanium dioxide 10
[0018] Tween-20 0.05
[0019] Span -80 0.05
[0020] Glycerin 3
[0021] Acetone 5
[0022] Ethanol make up to 100
[0023] Implementation process:
[0024] In the production environment with the required purification degree, during the stirring process, dissolve the cellulose acetate succinate in the solvent (absolute ethanol), and let the resulting solution stand for 48 hours. When the impurities in the solution settle, take it out The upper transparent liquid is the resulting connecting material; the connecting material, pigment, Tween-20, Span-80, glycerin, acetone and the remaining ethanol are mixed and placed in a sand mill for grinding at a grinding speed of 3000 revolutions, 90 minutes, you can get the finished edible ink.
[0025] Three concentrations of binder are selected, 45%, 30%, 20% (that is, binder obtained by dissolving c...
Embodiment 2
[0034] White ink composition two (parts by weight):
[0035] Cellulose acetate titanate 3
[0036] Titanium dioxide 3
[0037] Span-80 0.04
[0038] Glycerin 0.5
[0039] Acetone 20
[0040] Isopropyl alcohol to make up to 100
[0041] The preparation process is the same as in Example 1.
[0042] Comparison of printing effect between the ink of the present invention (referred to as this product) and imported ink
[0043] Ink
Embodiment 3
[0045] White ink composition three (parts by weight):
[0046] Cellulose acetate succinate and cellulose acetate titanate (1:1) 3-4
[0047] Titanium dioxide 7
[0048] Tween-20 0.02
[0049] Span-80 0.02
[0050] Glycerin 1.5
[0051] Acetone 10
[0052] N-Butanol Make up to 100
[0053] The preparation process is as in Example 1.
[0054] The ink performance is as follows
[0055] Smooth edges
Uniformity
Smearing
Plumpness
Initial dryness (mm)
excellent
excellent
excellent
good
50
[0056] The overall performance index of the finished medicinal ink and its comparison with similar foreign products (colorcon's OPACODE series ink)
[0057] Comparison of printing effect between the ink of the present invention (referred to as this product) and imported ink
[0058] Ink
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