Petroleum resin hydrogenation catalyst and preparation method and application thereof
A technology for hydrogenation catalysts and petroleum resins, applied in chemical instruments and methods, organic compound/hydride/coordination complex catalysts, physical/chemical process catalysts, etc., can solve the problems of low softening point of resin products, high reaction temperature, Affect the application range of the resin and other issues, to achieve the effect of increasing sulfur resistance, mild reaction conditions, and improved thermal stability
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Embodiment 1
[0023] Preparation of framework nickel catalyst:
[0024] Gradually add 50g of 100 mesh Ni-Al alloy powder (1:1 mass ratio) into aqueous sodium hydroxide solution (30wt%) at 90°C, stir for 4h, wash with deionized water until the pH value is neutral, and obtain skeleton nickel Catalyst A (specific surface area is 67m 2 / g).
[0025] 50g of Ni-Al alloy powder (2:1 mass ratio) was gradually added to sodium hydroxide (40wt%) at 90°C, stirred for 4h, washed with deionized water until the pH value was neutral, and the skeleton nickel catalyst B ( The specific surface area is 61m 2 / g).
[0026] 50g of 100-mesh Ni-Al alloy powder (1:1 mass ratio) was gradually added to potassium hydroxide (20wt%) at 90°C, stirred for 4h, washed with deionized water until the pH value was neutral, and a skeleton nickel catalyst was prepared C (the specific surface area is 85m 2 / g).
Embodiment 2
[0028] Preparation of heteropolyacids:
[0029] Dissolve 10g of phosphomolybdenum heteropolyacid (H3PO4·12MoO3) in deionized water, then add 1.2g of cobalt carbonate, dry at 120°C for 4h after complete dissolution, and roast at 400°C for 3h to obtain heteropolyacid salt D.
[0030] Dissolve 10g of phosphomolybdenum heteropolyacid (H3PO4·12MoO3) in deionized water, then add 1.5g of zinc carbonate, dry at 120°C for 4h after complete dissolution, and roast at 400°C for 3h to obtain heteropolyacid salt E.
[0031] Dissolve 13.5g of phosphotungstic heteropolyacid (H3PO4·12WO3) in deionized water, then add 1.2g of manganese carbonate, dry at 120°C for 4h after complete dissolution, and roast at 400°C for 3h to obtain heteropolyacid salt F.
[0032] Dissolve 13.5g of phosphotungstic heteropolyacid (H3PO4·12WO3) in deionized water, then add 0.9g of iron carbonate, dry at 120°C for 4h after complete dissolution, and roast at 400°C for 3h to obtain heteropolyacid salt G.
Embodiment 3
[0034] Preparation of heteropoly acid salt modified framework nickel catalyst:
[0035]Get 4 parts of every part of 10g framework nickel catalyst A, add respectively in 1.5g heteropolyacid salt D, E, F, G solution (solution mass concentration is 3%), stir 12h under room temperature, make heteropolyacid respectively Salt-modified skeleton nickel catalysts A1, A2, A3, A4.
[0036] Under the same conditions as above, the skeleton catalysts were replaced with B and C to prepare modified skeleton catalysts B1-B4, C1-C4, respectively.
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