Method for preparing cyclopentadiene and methylcyclopentadiene
A technology of methylcyclopentadiene and cyclopentadiene, which is applied in the fields of depolymerization, organic chemistry, distillation purification/separation, etc. Purity and high yield and other issues to achieve the effect of preventing material coking and pipeline blockage, improving purity and yield
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Embodiment 1
[0035] This example is used to illustrate the method for preparing cyclopentadiene and methylcyclopentadiene of the present invention.
[0036] Such as figure 1 As shown, (1) carry out the first depolymerization and rectification in the first rectification tower 1 of the above-mentioned carbon nine cuts, and cool at the top of the tower at 38° C. to obtain cyclopentadiene;
[0037] (2) Pass the heavy component (the content of cyclopentadiene is 100PPM) obtained at the bottom of the tower in step (1) into the second rectification tower 2 to carry out the second depolymerization rectification, and cool at the top of the tower at 38° C. to obtain formazan Cyclopentadiene,
[0038] Wherein, the first depolymerization rectification and the second depolymerization rectification are all carried out under normal pressure, and other operating conditions are shown in Table 1 below, the purity and yield of cyclopentadiene and methylcyclopentadiene obtained Rates are shown in Table 2 be...
Embodiment 2
[0040] This example is used to illustrate the method for preparing cyclopentadiene and methylcyclopentadiene of the present invention.
[0041] Such as figure 1 As shown, (1) carry out the first depolymerization and rectification in the first rectification tower 1 of the above-mentioned carbon nine cuts, and obtain cyclopentadiene by cooling at the top of the tower at 40° C.;
[0042] (2) Pass the heavy component (the content of cyclopentadiene is 150PPM) that step (1) tower bottom obtains in the second rectification tower 2 and carry out the second depolymerization rectification, cool down at tower top 37 ℃ to obtain formazan Cyclopentadiene,
[0043]Wherein, the first depolymerization rectification and the second depolymerization rectification are all carried out under normal pressure, and other operating conditions are shown in Table 1 below, the purity and yield of cyclopentadiene and methylcyclopentadiene obtained Rates are shown in Table 2 below.
Embodiment 3
[0045] This example is used to illustrate the method for preparing cyclopentadiene and methylcyclopentadiene of the present invention.
[0046] Such as figure 1 As shown, (1) carry out the first depolymerization and rectification in the first rectification tower 1 of the above-mentioned carbon nine cuts, and cool at the top of the tower at 37° C. to obtain cyclopentadiene;
[0047] (2) the heavy component (the content of cyclopentadiene is 200PPM weight %) obtained at the bottom of the tower of step (1) is passed in the second rectification tower 2 and carries out the second depolymerization rectification, cooling at the top of the tower at 40°C to give methylcyclopentadiene,
[0048] Wherein, the first depolymerization rectification and the second depolymerization rectification are all carried out under normal pressure, and other operating conditions are shown in Table 1 below, the purity and yield of cyclopentadiene and methylcyclopentadiene obtained Rates are shown in Tab...
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Abstract
Description
Claims
Application Information
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