Method for preparing 3D printing wax
A 3D printing, wax layer technology, applied in petroleum wax refining, wax physical treatment, petrochemical modification and other directions, which can solve the problems of declining product yield, inability to produce wax products, and long production cycle.
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Embodiment 1
[0072] This embodiment includes: (1) hydrogenation, (2) distillation, (3) emulsification, (4) sweating, (5) blending, and silk extrusion.
[0073] (1) Hydrogenation
[0074] Using the wax oil product (n-alkane content of 95.50wt%) of the low-temperature F-T synthesis experimental device of China Petrochemical Corporation as raw material, the FHJ-2 catalyst (a Ni / Al 2 o 3 Commercial catalyst, developed and produced by Fushun Petrochemical Research Institute, the active metal content is 40% based on oxides, and the catalyst is subjected to conventional reduction treatment before use), under the action of reaction pressure 5.0MPa, reaction temperature 200℃, volume space velocity 1.0h -1 Hydrogenation is carried out under the condition of 500:1 volume ratio of hydrogen to liquid to convert olefins and oxygenates in it. The weight content of normal paraffins in the hydrogenation product is 97.36%.
[0075] Chromatography-mass spectrometry analysis, no olefins, alcohols, acids an...
Embodiment 2
[0106] This embodiment includes: (1) hydrogenation, (2) distillation, (3) emulsification, (4) sweating, (5) blending, and silk extrusion.
[0107] (1) Hydrogenation
[0108] With embodiment 1.
[0109] (2) Distillation
[0110] With embodiment 1.
[0111] (3) Emulsification
[0112] This part includes (A1) oil phase material preparation, (A2) water phase material preparation, (A3) emulsion preparation three steps.
[0113] (A1) Oil phase material preparation
[0114] Take 82.0Kg of the fraction prepared in process (2), heat to 84°C and melt, add 1.9Kg of sorbitan monooleate, 0.8Kg of diethylene glycol monolaurate and 0.3 Kg of sodium butylnaphthalenesulfonate, stir uniform.
[0115] (A2) Preparation of aqueous phase materials
[0116] 0.12Kg of CO at 24.3 to 24.5 atmospheres 2 Dissolve in 14.88Kg of water and heat to 92°C.
[0117] (A3) Emulsion preparation
[0118] Pressurize the oil phase material to 24.3-24.5 atmospheres, and stir at a speed of 800r / min; add the w...
Embodiment 3
[0127] This embodiment includes: (1) hydrogenation, (2) distillation, (3) emulsification, (4) sweating, (5) blending, and silk extrusion.
[0128] (1) Hydrogenation
[0129] With embodiment 1.
[0130] (2) Distillation
[0131] With embodiment 1.
[0132] (3) Emulsification
[0133] This part includes (A1) oil phase material preparation, (A2) water phase material preparation, (A3) emulsion preparation three steps.
[0134] (A1) Oil phase material preparation
[0135] Take 78.0Kg of the distillate prepared in process (2), heat to 88°C and melt, add 2.3Kg of sorbitan monostearate, 0.9Kg of tetraethylene glycol monostearate and 0.6Kg of triacetamide oleate , stir well.
[0136] (A2) Preparation of aqueous phase materials
[0137] With 27.5% H 2 o 2 solution, solid NaOH and H 2 O formulated with H 2 o 2 0.5%, NaOH 3.0 mg / Kg aqueous solution, take 18.2Kg, pressurize to 18.6-18.8 atmospheric pressure under nitrogen condition, and heat to 93°C.
[0138] (A3) Emulsion pr...
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