CN101108782A - Separation method of diene hydrocarbon in five fractions of petroleum cracked carbon - Google Patents
Separation method of diene hydrocarbon in five fractions of petroleum cracked carbon Download PDFInfo
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Abstract
The invention relates to a separation method of the diolefin in the petroleum cracking C5 fraction, which mainly solves the problems that the cracking C5 fraction in the past technology generates the dicyclopentadiene via the thermal dimerization reactor, the isoprene does self-polymerization and does copolymerization with the cyclopentadiene to cause great loss of the isoprene and the cyclopentadiene, at the same time the dicyclopentadiene has low product purity and low utilization value. The invention better solves the problem through the technical proposal that the isoprene in the C5 fraction is separated with the cyclopentadiene and the cyclopentadiene enters the thermal dimerization reactor to generate the dicyclopentadiene and separate with the m-pentadiene, which can be used in the industrial production of the diolefin separation in the cracking C5 fraction.
Description
Technical field
The present invention relates to the separation method of diolefin in a kind of five fractions of petroleum cracked carbon.
Background technology
Dienes such as isoprene, m-pentadiene and cyclopentadiene are rich in the C5 fraction of the quite a lot of quantity of by-product in the petroleum cracking process of producing ethylene in the C5 fraction.These diolefin chemical property are active, are important chemical material.Because the difference on raw material, cracking severity and the separation degree of petroleum hydrocarbon cracking, the diolefin content in the C5 fraction is different, but total amount is between 40～60%.Therefore, separate and utilize C5 fraction for the economic benefit that improves ethylene unit, the comprehensive utilization petroleum resources have profound significance.
Cracked C 5 fraction is close by more than 20 kinds of boiling points, and the component that easily forms azeotrope is to each other formed, and therefrom isolating purity, to meet the C 5 diene difficulty of application requiring higher, and technology is comparatively complicated, generally adopts extraction fractional distillation in the prior art.Selective solvent commonly used has dimethyl formamide (DMF) and acetonitrile, as disclosed processing methodes such as patent JP63101338, JP74019245, US3510405, US3535260.Wherein the DMF solvent have that selectivity to C 5 diene is good, solubleness big,, plurality of advantages such as corrodibility low and toxicity little five easily separated with carbon.
Because the isoprene market development is comparatively extensive than morning and application in isoprene, m-pentadiene and three kinds of C 5 dienes of cyclopentadiene, so C5 fraction separation process scheme early only is a separation utilization isoprene wherein.With petrochemical complex, the particularly development of fine chemistry industry, the market requirement of m-pentadiene and dicyclopentadiene increases day by day, and the method that further rectifying separation obtains m-pentadiene and dicyclopentadiene from the isolating heavy constituent of isoprene also comes into one's own day by day.
The key of C 5 diene sepn process is an isoprene and the separating of cyclopentadiene, and the boiling-point difference under both normal pressures is 7.45 ℃, and also can increase both separating difficulties with the azeotropic of other carbon five hydrocarbon.
The patent US3510405 of Nippon Zeon Co., Ltd. disclose a kind of from C5 fraction the processing method of separating high-purity isoprene, comprise the steps: the C5 fraction that will obtain by hydro carbons steam cracking or other high-temperature cracking method, through overheated dimerization reaction and therefrom isolate cyclopentadiene; With DMF is that solvent carries out the extractive distillation first time in the presence of stopper, and solvent is by the stripping tower recycling use; Material takes off heavy rectifying tower through one and carries out rectifying, therefrom separates the heavy constituent that contain cyclopentadiene and m-pentadiene; With DMF is that solvent carries out the extractive distillation second time in the presence of stopper, and solvent reclaims by stripping tower and uses; Material obtains highly purified isoprene product by the tower still after through a lightness-removing column rectifying.
Chinese patent CN1160035A discloses the method that a kind of liquid phase feeding extraction rectification method is separated five fractions of petroleum cracked carbon, and the flow process of isoprene separation and purification part is similar with US3510405, has improved wherein first, second extracting rectifying feed process; The tower still material of the dicyclopentadiene heavy constituent material of separation removal and weight-removing column behind the hot dimerization reaction removes processes such as carbon six hydrocarbon components by other carbon five hydrocarbon components of rectifying separation, rectifying, obtains highly purified m-pentadiene and dicyclopentadiene product.
Chinese patent CN1412165A discloses a kind of separation method of cracked C 5 fraction, principal character is after hot dimerization, rectifying separation dicyclopentadiene, carbon five materials remove alkynes by selective catalytic hydrogenation technology before carrying out extracting rectifying, thereby have saved second section extracting rectifying in traditional isoprene flow process.
A principal character of above-mentioned separating technology process is for earlier the hot dimerization of cyclopentadiene being converted into dicyclopentadiene, then separating in the Rich in isoprene material of heavy constituent such as dicyclopentadiene.But in the hot dimerization of cyclopentadiene, isoprene also has polymerization to a certain degree, and can and cyclopentadiene copolymerization is largely arranged.The generation of the dipolymer beyond these dicyclopentadiene has caused a large amount of losses of isoprene and cyclopentadiene, causes the yield raising of isoprene and dicyclopentadiene to be restricted.
Because the boiling point of the codimerization thing of isoprene dipolymer and isoprene and m-pentadiene is close with the boiling point of dicyclopentadiene, be difficult to separate, make the purity of dicyclopentadiene be subjected to influence, also just influenced the utility value of dicyclopentadiene.In order to improve the purity of dicyclopentadiene, just must increase the stage number or the bed stuffing height of rectifying tower or increase quantity of reflux, thereby increase facility investment or energy consumption.
In order to remedy above-mentioned technical disadvantages, Chinese patent CN1253130A disclose a kind of from C5 fraction the method for separating diolefin, reactive distillation is carried out in C5 fraction, when making cyclopentadiene generation dimerization reaction by reactive distillation, isoprene is separated by cat head, and material is through rectifying separation m-pentadiene, dicyclopentadiene.Reactive distillation cat head product obtains highly purified isoprene through operations such as first, second extractive distillations.It is said that this method can obtain purity and reach dicyclopentadiene more than 97%.
Chinese patent CN1490286A discloses a kind of separation method of cracked C 5 fraction, mainly on patent CN1253130A basis in conjunction with selective catalytic hydrogenation technology, carry out the extractive distillation front-end hydrogenation at carbon five and remove alkynes in the cut, saved common second section extractive distillation adopting.But because hydrogenation reaction, the saturated loss of diolefine is inevitable, and this method also must increase and faces hydrogen and hydrogen separation system simultaneously.
The principal character of CN1253130A and the disclosed method of CN1490286A is that cyclopentadiene dimerization in reaction fractionating tower becomes in the dicyclopentadiene, with the cat head feed separation that is rich in isoprene.But the residence time of material is difficult to control in the tower, also with regard to the transformation efficiency of uncontrollable cyclopentadiene, so the concentration of cat head cyclopentadiene is generally higher.The kind of stopper and consumption can directly influence the operation of reaction fractionating tower in addition, so this tower operation is difficult for.To the research situation of diolefin dimerization reaction mechanism and the poly-mechanism of resistance, the engineering design difficulty that finish this method is bigger, does not also have the report of through engineering approaches at present in view of at present.
In sum, all be earlier the hot dimerization of cyclopentadiene to be converted into dicyclopentadiene in the prior art, utilize the high boiling point of dicyclopentadiene to finish and the separating of isoprene then.This method can reduce the separating difficulty of isoprene and cyclopentadiene to a certain extent, but has a shortcoming: all isoprene all will be through overheated dipolymer reactor.Research and actually operating show that all isoprene has very high activity, in hot dipolymer reactor nearly 2～10% isoprene autohemagglutination or with the cyclopentadiene copolymerization, not only caused the loss of isoprene, also influence the purity (mass concentration is generally about 80%) of dicyclopentadiene to a great extent, reduced the use value of dicyclopentadiene.
Summary of the invention
Technical problem to be solved by this invention is in the conventional art during diolefin in the separating cracked carbon-5 fraction, raw material is earlier when hot dipolymer reactor generates dicyclopentadiene with the separating ring pentadiene, isoprene generation autohemagglutination and with cyclopentadiene generation copolymerization, cause isoprene and cyclopentadiene to lose in a large number; Simultaneously the dicyclopentadiene product purity is low, and the problem that utility value is little provides the method for diolefin in a kind of new separating cracked carbon-5 fraction.This method has isoprene yield height, dicyclopentadiene purity height, cyclopentadiene utilization ratio height, and the while can be reduced the characteristics of the temperature control requirement of hot dipolymer reactor.
For solving the problems of the technologies described above, the technical solution used in the present invention is as follows: the separation method of diolefin in a kind of five fractions of petroleum cracked carbon may further comprise the steps:
A) raw material cracked C 5 fraction (13) enters isoprene knockout tower (2) middle part, and cat head separates the stream I that obtains being rich in isoprene; The tower still separates the stream I I that obtains being rich in cyclopentadiene and m-pentadiene;
B) stream I enters first extractive distillation column (3) middle part, contacts with the solvent orange 2 A that enters from tower top and carries out extracting rectifying, and cat head obtains containing the light constituent logistics of alkane and monoolefine, and the tower still obtains being rich in the solvent orange 2 A base stream I II of isoprene;
C) solvent base stream I II enters first stripping tower (4) and carries out solvent orange 2 A and reclaim, and cat head obtains being rich in the stream I V of isoprene, and the solvent orange 2 A logistics that the tower still obtains is back to first extractive distillation column (3) top;
D) stream I V enters cyclopentadiene recovery tower (5) middle and lower part, a small amount of cyclopentadiene among the stream I V is carried out Separation and Recovery, cat head obtains removing the isoprene logistics V behind the cyclopentadiene, and the tower still contains the cyclopentadiene logistics and is circulated to isoprene knockout tower (2) middle part;
E) logistics V enters second extractive distillation column (6) middle part, contacts with the solvent B that enters from tower top and carries out extracting rectifying, and cat head obtains isoprene solvent B base logistics VI, and the tower still obtains containing the solvent B logistics VII of a small amount of diolefin and alkynes;
F) logistics VI enters isoprene treating tower (8) middle part, and overhead stream is discharged out-of-bounds, and tower still side line obtains the polymerization grade isoprene product in the position that calculating from top to bottom accounts for total stage number 90～99%;
G) logistics VII enters second stripping tower (7) and carries out solvent recuperation, and cat head obtains containing the logistics of diolefin and alkynes, and the solvent B logistics that the tower still obtains is back to second extractive distillation column (6) top and recycles;
H) stream I I enters hot dipolymer reactor (9), generates the logistics VIII that is rich in dicyclopentadiene;
I) logistics VIII enters decarburization five towers (10), and cat head obtains being rich in the stream I X of m-pentadiene, and the tower still obtains being rich in the logistics X of dicyclopentadiene;
J) stream I X enters m-pentadiene treating tower (11) and makes with extra care, and the tower still obtains the m-pentadiene product of purity greater than 65 weight %;
K) logistics X enters dicyclopentadiene treating tower (12) middle part, and the tower still obtains purity greater than 90% dicyclopentadiene product;
Wherein solvent orange 2 A in first extractive distillation column and the solvent B in second extractive distillation column all are selected from least a in dimethyl formamide, N,N-DIMETHYLACETAMIDE, acetonitrile, n-formyl sarcolysine base pyrrolidone and the acetonitrile solution.
In the technique scheme, the operational condition of isoprene knockout tower 2: the stage number preferable range is 60～160, and tower still temperature preferable range is 70～110 ℃, and the tower top temperature preferable range is 35～70 ℃, the reflux ratio preferable range is 5～60, and the working pressure preferable range is 0.01～0.3MPa.The operational condition of first extractive distillation column 3: the stage number preferable range is 70～160, tower still temperature preferable range is 100～150 ℃, the tower top temperature preferable range is 35～80 ℃, the reflux ratio preferable range is 2～13, the working pressure preferable range is 0.01～0.3MPa, and the weight ratio preferable range of solvent orange 2 A and stream I is 3～11.The operational condition of first stripping tower 4: the stage number preferable range is 20～60, and tower still temperature preferable range is 120～220 ℃, and the tower top temperature preferable range is 30～60 ℃, and the reflux ratio preferable range is 1～5, and the working pressure preferable range is 0.01～0.3MPa.The operational condition of cyclopentadiene recovery tower 5: the stage number preferable range is 60～150, tower still temperature preferable range is 55～100 ℃, the tower top temperature preferable range is 35～55 ℃, and the reflux ratio preferable range is 5～30, and the working pressure preferable range is 0.01～0.25MPa.The operational condition of second extractive distillation column 6: the stage number preferable range is 90～190, tower still temperature preferable range is 100～150 ℃, the tower top temperature preferable range is 35～80 ℃, the reflux ratio preferable range is 2～10, the working pressure preferable range is 0.01～0.3MPa, and the weight ratio preferable range of solvent B and logistics V is 2～10.The operational condition of second stripping tower 7: the stage number preferable range is 20～60, and tower still temperature preferable range is 120～220 ℃, and the tower top temperature preferable range is 30～70 ℃, and the reflux ratio preferable range is 1～5, and the working pressure preferable range is 0.01～0.3MPa.The operational condition of isoprene treating tower 8: the stage number preferable range is 70～140, tower still temperature preferable range is 55～90 ℃, the tower top temperature preferable range is 35～55 ℃, and the reflux ratio preferable range is 100～600, and the working pressure preferable range is 0.02～0.3MPa.Hot dipolymer reactor 9 reaction conditionss: the temperature of reaction preferable range is 60～150 ℃, and the reaction pressure preferable range is 0.3～1.3MPa.The operational condition of decarburization five towers 10: stage number is 15～70, and tower still temperature preferable range is 80～130 ℃, and the tower top temperature preferable range is 35～60 ℃, and the reflux ratio preferable range is 0.5～5, and the working pressure preferable range is 0.01～0.05MPa.The operational condition of m-pentadiene treating tower 11: the stage number preferable range is 70～140, tower still temperature preferable range is 50～100 ℃, the tower top temperature preferable range is 40～60 ℃, and the reflux ratio preferable range is 10～90, and the working pressure preferable range is 0.02～0.2MPa.The operational condition of dicyclopentadiene treating tower 12: the stage number preferable range is 10～90, tower still temperature preferable range is 80～130 ℃, the tower top temperature preferable range is 5～50 ℃, and the reflux ratio preferable range is 0.5～5, the working pressure preferable range is-0.05～-0.1MPa.Before the raw material cracked C 5 fraction entered isoprene knockout tower 2, preferred version carried out rectifying separation for being introduced into lightness-removing column 1 middle part, removed overhead carbon four and carbon four following components, and tower still carbon five logistics XI enter isoprene knockout tower 2 middle parts.The operational condition of lightness-removing column 1: the feeding temperature preferable range is 30～75 ℃, the stage number preferable range is 50～100, tower still temperature preferable range is 70～100 ℃, the tower top temperature preferable range is 35～60 ℃, reflux ratio is a preferable range 15～35, and the working pressure preferable range is 0.1～0.3MPa.The extracting rectifying preferred version of step b) and step e) is for to carry out in the presence of stopper A, and described stopper A preferred version is to be selected from least a in ONP, oil of mirbane, furfural, n-formyl sarcolysine base pyrrolidone, thanomin or the Sodium Nitrite; More preferably scheme is Sodium Nitrite and thanomin composite polymerzation inhibitor, and wherein the mass ratio of Sodium Nitrite and thanomin is 0.25～15: 1, and the carbon five basic concentration of thanomin are 100～800ppm.The rectifying preferred version of solvent-free existence is for to carry out in the presence of stopper, and described stopper preferred version is to be selected from least a in ONP, tert-butyl catechol, diethyl azanol or the acid of dihydroxyl dihydro cinnamon.
The inventive method was separated isoprene earlier before raw material enters hot dipolymer reactor, had avoided autohemagglutination and the copolymerization loss of isoprene in hot dipolymer reactor, can improve 2～10% isoprene yield; Reduce the content of dimerization impurity in the dicyclopentadiene product simultaneously, made dicyclopentadiene product purity ratio reach 90 weight %, improved the use value of dicyclopentadiene product.The logistics that the inventive method will be rich in isoprene recycles the isolating logistics that contains cyclopentadiene again behind stripping behind the first time extracting rectifying and for the first time, can avoid the loss of cyclopentadiene, improves the utilization ratio of cyclopentadiene.The inventive method enters in the logistics that is rich in isoprene of cyclopentadiene recovery tower, and isoprene is dense, reclaims the Tata still and does not have any concentration control requirement, so design of cyclopentadiene recovery tower and operation easier are little, process cost is low.The present invention advances in the material of hot dipolymer reactor to have separated isoprene and most alkane and monoolefine, because the increase of cyclopentadiene concentration in the reactor makes the hot dimerization reaction of cyclopentadiene be more prone to carry out, transformation efficiency is also higher simultaneously; Can not consider the existence of isoprene in the hot dimerization reaction, reaction just can be carried out under higher temperature, help improving the transformation efficiency of cyclopentadiene, also can reduce simultaneously the temperature control requirement of reactor, and under identical temperature, pressure operation condition, can further reduce the volume of reactor, obtain better technical effect.
Description of drawings
Fig. 1 is the inventive method process flow diagram.
Among Fig. 1,1 is lightness-removing column, and 2 is the isoprene knockout tower, 3 is first extractive distillation column, and 4 is first stripping tower, and 5 is the cyclopentadiene recovery tower, 6 is second extractive distillation column, and 7 is second stripping tower, and 8 is the isoprene treating tower, 9 is hot dipolymer reactor, and 10 are decarburization five towers, and 11 is the m-pentadiene treating tower, 12 is the dicyclopentadiene treating tower, and 13 is the raw material cracked C 5 fraction, and 14 is the isoprene product, 15 is the m-pentadiene product, and 16 is the dicyclopentadiene product.
Among the present invention, raw material five fractions of petroleum cracked carbon 13 enters lightness-removing column 1 middle part and carries out the rectifying separation, removed overhead carbon four and following light component thereof and part alkynes, and the tower reactor separation obtains carbon five logistics XI. Polymerization inhibitor advances tower with carbon Wuyuan material.
Carbon five logistics XI enter isoprene knockout tower 2 middle parts, and cat head separates the stream I that obtains being rich in isoprene; Tower reactor is separated the stream I I that obtains being rich in cyclopentadiene and pentadiene.
Stream I enters the first extractive distillation column 3 middle parts, contacts with the solvent orange 2 A that enters from tower top and carries out extracting rectifying, and cat head obtains containing the light component logistics of alkane and monoolefine, and tower reactor obtains being rich in the solvent orange 2 A base stream I II of isoprene.
Solvent orange 2 A base stream I II enters the first stripper 4 and carries out solvent recovery, and cat head obtains being rich in the stream I V of isoprene, and the solvent orange 2 A logistics that tower reactor obtains is back to the first extractive distillation column 3 tops and recycles.
Stream I V enters cyclopentadiene recovery tower 5 middle and lower parts, a small amount of cyclopentadiene among the stream I V is separated recovery, cat head obtains removing the isoprene logistics V behind the cyclopentadiene, can be used as the extraction of chemical grade isoprene product, also can further process entering to generate the polymerization grade isoprene product. Tower reactor obtains cyclopentadiene, isoprene and recombinates to divide being back to isoprene knockout tower 2 middle parts.
Logistics V enters the second extractive distillation column 6 middle parts, contacts with the solvent B that enters from tower top and carries out extracting rectifying, and cat head obtains isoprene solvent B base logistics VI, and tower reactor obtains containing the solvent stream VII of a small amount of diolefin and alkynes.
Logistics VI enters isoprene treating column 8 middle parts, and overhead stream is discharged out-of-bounds, obtains the polymerization grade isoprene product by the column plate side line.
Logistics VII enters the second stripper 7 and carries out solvent recovery, and cat head obtains containing the logistics of diolefin and alkynes, and the solvent B logistics that tower reactor obtains is back to the second extractive distillation column 6 tops and recycles.
Stream I I enters hot dipolymer reactor 9, generates the logistics VIII that is rich in dicyclopentadiene.
Logistics VIII enters decarburization five towers 10, and cat head obtains being rich in the stream I X of pentadiene, and tower reactor obtains being rich in the logistics X of dicyclopentadiene.
Stream I X enters pentadiene treating column 11 and makes with extra care, and tower reactor obtains purity greater than the pentadiene product of 65 % by weight.
Logistics X enters dicyclopentadiene treating column 12 middle parts, and tower reactor obtains purity greater than 90% dicyclopentadiene product.
The present invention is further elaborated below by embodiment.
Embodiment
[embodiment 1]
Press the technical process of Fig. 1, raw material five fractions of petroleum cracked carbon 13 enters isoprene knockout tower 2 middle parts by the 55th block of column plate, and cat head separates the stream I that obtains being rich in isoprene, and the tower still separates the stream I I that obtains being rich in cyclopentadiene and m-pentadiene.Isoprene knockout tower 1 feeding temperature is 50 ℃, and stage number is 110, and tower still temperature is 79 ℃, and tower top temperature is 52 ℃, and tower top pressure is 0.09MPa, and tower still pressure is 0.17MPa, and reflux ratio is 11.Stopper is the diethyl azanol.
Stream I enters the 80th block of column plate in first extractive distillation column, 3 middle parts, carry out extracting rectifying with contacting from the 6th solvent dimethylformamide that column plate enters of tower, cat head obtains containing the light constituent logistics of alkane and monoolefine, and the tower still obtains being rich in the solvent base stream I II of isoprene.The extracting rectifying stopper is Sodium Nitrite and thanomin composite polymerzation inhibitor, and wherein the mass ratio of Sodium Nitrite and thanomin is 1.4, and the carbon five basic concentration of thanomin are 400ppm.First extractive distillation column, 3 stage number are 140, and tower still temperature is 123 ℃, and tower top temperature is 38 ℃, and tower top pressure is 0.04MPa, and tower still pressure is 0.13MPa, and reflux ratio is 3.5, and solvent ratio is 4.
Solvent base stream I II enters first stripping tower 4 and carries out solvent recuperation, and cat head obtains being rich in the stream I V of isoprene, and the solvent stream that the tower still obtains is back to the 6th column plate place, first extractive distillation column, 3 tops and recycles.First stripping tower, 4 stage number are 40, and tower still temperature is 169 ℃, and tower top temperature is 42 ℃, and tower top pressure is 0.03MPa, and tower still pressure is 0.05MPa, and reflux ratio is 1.3.
Stream I V enters the 60th column plate place of cyclopentadiene recovery tower 5, a small amount of cyclopentadiene among the stream I V is carried out Separation and Recovery, cat head obtains removing the isoprene logistics V behind the cyclopentadiene, can be used as the extraction of chemical grade isoprene product, also can further handle entering to generate the polymerization grade isoprene product.The tower still obtains cyclopentadiene, isoprene and heavy constituent and is back to the 57th column plate place, isoprene knockout tower 2 middle parts.Cyclopentadiene recovery tower 5 stage number are 110, and tower still temperature is 61 ℃, and tower top temperature is 44 ℃, and tower top pressure is 0.04MPa, and tower still pressure is 0.12MPa, and reflux ratio is 9.Stopper is the diethyl azanol.
Logistics V enters the 127th column plate place, second extractive distillation column, 6 middle parts, contact with the solvent dimethylformamide that enters from tower top and to carry out extracting rectifying, cat head obtains isoprene solvent base logistics VI, and the tower still obtains containing the solvent stream VII of a small amount of diolefin and alkynes.The extracting rectifying stopper is Sodium Nitrite and thanomin composite polymerzation inhibitor, and wherein the mass ratio of Sodium Nitrite and thanomin is 1.4, and the carbon five basic concentration of thanomin are 400ppm.Second extractive distillation column, 6 stage number are 180, and tower still temperature is 119 ℃, and tower top temperature is 44 ℃, and tower top pressure is 0.04MPaG, and tower still pressure is 0.14MPaG, and reflux ratio is 3.5, and solvent ratio is 4.
Logistics VI enters the 38th column plate place, isoprene treating tower 8 middle parts, and stage number is 85, and tower still temperature is 59 ℃, and tower top temperature is 45 ℃, and tower top pressure is 0.05MPa, and tower still pressure is 0.12MPa, and reflux ratio is 100.Overhead stream is discharged out-of-bounds, obtains the polymerization grade isoprene product by the 80th column plate side line.Stopper is the diethyl azanol.
Logistics VII enters second stripping tower 7 and carries out solvent recuperation, and cat head obtains containing the logistics of diolefin and alkynes, and the solvent stream that the tower still obtains is back to the 10th column plate place, second extractive distillation column, 6 tops and recycles.Second stripping tower, 7 stage number are 40, and tower still temperature is 169 ℃, and tower top temperature is 41 ℃, and tower top pressure is 0.03MPa, and tower still pressure is 0.05MPa, and reflux ratio is 4.
Stream I I enters hot dipolymer reactor 9, generates the logistics VIII that is rich in dicyclopentadiene.Temperature of reaction is 100 ℃, and reaction pressure is 0.6MPa.
Logistics VIII enters decarburization five towers 10, and cat head obtains being rich in the stream I X of m-pentadiene, and the tower still obtains being rich in the logistics X of dicyclopentadiene.The stage number of decarburization five towers 10 is 45, and tower still temperature is 104 ℃, and tower top temperature is 51 ℃, and tower top pressure is 0.03MPa, and tower still pressure is 0.05MPa, and reflux ratio is 2.6.
Stream I X enters m-pentadiene treating tower 11 and makes with extra care, and the tower still obtains the m-pentadiene product that purity is 65.10 weight %.M-pentadiene treating tower 11 stage number are 95, and tower still temperature is 62 ℃, and tower top temperature is 47 ℃, and tower top pressure is 0.02MPa, and tower still pressure is 0.08MPa, and reflux ratio is 40.Stopper is the diethyl azanol.
Logistics X enters the 24th column plate place, dicyclopentadiene treating tower 12 middle parts, and it is 90.14% dicyclopentadiene product that the tower still obtains purity.Dicyclopentadiene treating tower 12 stage number are 38, and tower still temperature is 110 ℃, and tower top temperature is 17 ℃, and tower top pressure is-0.09MPa that tower still pressure is-0.08MPa that reflux ratio is 1.3.
The weight percent composition of raw material and each unit component sees Table 1.
Table 1
| Component | |
First |
First stripping tower 4 | |||
| Charging | Eject material | End discharging | Charging | Eject material | Eject material | |
| Below carbon four reaches | 3.78 | 6.60 | 6.60 | 11.57 | ||
| Iso-pentane | 3.78 | 6.60 | 6.60 | 11.57 | ||
| 3-methyl butene-1 | 0.86 | 1.50 | 1.50 | 2.62 | ||
| Skellysolve A | 5.72 | 9.98 | 9.98 | 17.50 | ||
| Amylene-1 | 4.00 | 6.99 | 6.99 | 12.25 | ||
| 2-methyl butene-1 | 4.67 | 8.14 | 0.00 | 8.14 | 14.28 | 0.00 |
| Anti-amylene-2 | 2.71 | 4.27 | 0.61 | 4.27 | 7.48 | 0.02 |
| Along amylene-2 | 1.85 | 2.50 | 0.98 | 2.50 | 4.37 | 0.02 |
| Pentadiene-1,4 | 2.56 | 4.47 | 0.00 | 4.47 | 7.80 | 0.05 |
| 2-methyl butene-2 | 2.95 | 4.14 | 1.34 | 4.14 | 6.78 | 0.65 |
| Pentamethylene | 0.99 | 0.00 | 2.33 | 0.00 | 0.00 | 0.00 |
| Isoprene | 24.40 | 41.98 | 0.80 | 41.98 | 3.75 | 92.69 |
| Cyclopentenes | 3.86 | 0.00 | 9.03 | 0.00 | 0.00 | 0.01 |
| Crotonylene | 0.82 | 1.43 | 0.00 | 1.43 | 0.03 | 3.28 |
| Anti-pentadiene-1,3 | 10.43 | 0.00 | 24.43 | 0.00 | 0.00 | |
| Along pentadiene-1,3 | 5.70 | 0.00 | 13.34 | 0.00 | 0.00 | |
| Cyclopentadiene | 12.08 | 1.28 | 26.56 | 1.28 | 2.98 | |
| Pentadiene-1,2 | 0.32 | 0.00 | 0.75 | 0.00 | 0.01 | |
| Valylene | 0.07 | 0.12 | 0.00 | 0.12 | 0.28 | |
| Total carbon six | 2.82 | 6.61 | ||||
| Benzene/methylbenzene | 0.59 | 1.39 | ||||
| Dicyclopentadiene | 4.61 | 10.79 | ||||
| CP-IP | 0.18 | 0.41 | ||||
| CP-PD | 0.00 | 0.00 | ||||
| X1 | 0.08 | 0.18 | ||||
| X2 | 0.19 | 0.43 | ||||
Continuous table 1
| Component | |
Second |
|
|
||||||
| Charging | Eject material | End discharging | Charging | Eject material | Eject material | Charging | Eject material | End discharging | Side line | |
| Below carbon four reaches | ||||||||||
| Iso-pentane | ||||||||||
| 3-methyl butene-1 | ||||||||||
| Skellysolve A | ||||||||||
| Amylene-1 | ||||||||||
| 2-methyl butene-1 | 0.00 | 0.00 | 0.00 | 0.01 | 0.01 | 0.03 | 0.00 | 5ppm | ||
| Anti-amylene-2 | 0.02 | 0.02 | 0.04 | 0.02 | 0.02 | 0.00 | 0.02 | 0.01 | 0.03 | 250ppm |
| Along amylene-2 | 0.02 | 0.02 | 0.05 | 0.02 | 0.02 | 0.00 | 0.02 | 0.01 | 0.02 | 213ppm |
| Pentadiene-1,4 | 0.05 | 0.06 | 0.00 | 0.06 | 0.07 | 0.00 | 0.07 | 0.37 | ||
| 2-methyl butene-2 | 0.65 | 0.31 | 3.57 | 0.31 | 0.37 | 0.02 | 0.37 | 0.05 | 0.52 | 0.44 |
| Pentamethylene | 0.00 | 0.00 | 0.00 | |||||||
| Isoprene | 92.69 | 95.41 | 69.63 | 95.41 | 96.04 | 92.42 | 96.04 | 82.20 | 99.43 | 99.51 |
| Cyclopentenes | 0.01 | 0.00 | 0.06 | |||||||
| Crotonylene | 3.28 | 3.67 | 0.00 | 3.67 | 3.47 | 4.61 | 3.47 | 17.33 | 0.00 | 28ppm |
| Anti-pentadiene-1,3 | 0.00 | 0.00 | 0.01 | |||||||
| Along pentadiene-1,3 | 0.00 | 0.00 | 0.03 | |||||||
| Cyclopentadiene | 2.98 | 0.21 | 26.54 | 0.21 | 1.18 | 0.00 | 5ppm | |||
| Pentadiene-1,2 | 0.01 | 0.00 | 0.07 | |||||||
| Valylene | 0.28 | 0.31 | 0.00 | 0.31 | 1.77 | |||||
| Total carbon six | ||||||||||
| Benzene/methylbenzene | ||||||||||
| Dicyclopentadiene | ||||||||||
| CP-IP | ||||||||||
| CP-PD | ||||||||||
| X1 | ||||||||||
| X2 | ||||||||||
Continuous table 1
| Component | Hot dipolymer reactor 9 | Decarburization five towers 10 | M-pentadiene treating tower 11 | Dicyclopentadiene treating tower 12 | |||||||
| Charging | Discharging | Charging | Eject material | End discharging | Charging | Eject material | End discharging | Charging | Eject material | End discharging | |
| Below carbon four reaches | |||||||||||
| Iso-pentane | |||||||||||
| 3-methyl butene-1 | |||||||||||
| Skellysolve A | |||||||||||
| Amylene-1 | 0.00 | 0.01 | |||||||||
| 2-methyl butene-1 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | |||||
| Anti-amylene-2 | 0.61 | 0.61 | 0.61 | 1.05 | 1.05 | 2.42 | |||||
| Along amylene-2 | 0.98 | 0.98 | 0.98 | 1.69 | 1.69 | 3.89 | |||||
| Pentadiene-1,4 | 0.00 | 0.00 | 0.00 | ||||||||
| 2-methyl butene-2 | 1.34 | 1.34 | 1.34 | 2.31 | 0.00 | 2.31 | 5.29 | 0.00 | 0.00 | 0.00 | |
| Pentamethylene | 2.33 | 2.33 | 2.33 | 4.00 | 0.03 | 4.00 | 0.96 | 6.34 | 0.03 | 0.08 | |
| Isoprene | 0.80 | 0.75 | 0.75 | 1.29 | 0.00 | 1.29 | 2.95 | 0.00 | 0.00 | 0.00 | |
| Cyclopentenes | 9.03 | 9.03 | 9.03 | 15.52 | 0.08 | 15.52 | 8.29 | 21.11 | 0.08 | 0.24 | |
| Crotonylene | 0.00 | 0.00 | 0.00 | 0.00 | |||||||
| Anti-pentadiene-1,3 | 24.43 | 23.76 | 23.76 | 40.88 | 0.07 | 40.88 | 53.80 | 30.89 | 0.07 | 0.20 | |
| Along pentadiene-1,3 | 13.34 | 12.98 | 12.98 | 22.32 | 0.07 | 22.32 | 6.17 | 34.81 | 0.07 | 0.22 | |
| Cyclopentadiene | 26.56 | 4.15 | 4.15 | 7.14 | 0.02 | 7.14 | 15.08 | 1.00 | 0.02 | 0.05 | |
| Pentadiene-1,2 | 0.75 | 0.75 | 0.75 | 1.30 | 0.00 | 1.30 | 1.14 | 1.42 | 0.00 | 0.00 | |
| Valylene | |||||||||||
| Total carbon six | 6.61 | 6.61 | 6.61 | 2.50 | 25.99 | 2.50 | 0.00 | 4.43 | 25.99 | 78.30 | |
| Benzene/methylbenzene | 1.39 | 1.39 | 1.39 | 0.00 | 6.96 | 0.00 | 0.00 | 6.96 | 20.89 | 0.04 | |
| Dicyclopentadiene | 10.79 | 31.84 | 31.84 | 60.23 | 60.23 | 0.00 | 90.14 | ||||
| CP-IP | 0.41 | 0.48 | 0.48 | 0.91 | 0.91 | 1.36 | |||||
| CP-PD | 0.00 | 2.03 | 2.03 | 3.84 | 3.84 | 5.75 | |||||
| X1 | 0.18 | 0.18 | 0.18 | 0.35 | 0.35 | 0.52 | |||||
| X2 | 0.43 | 0.77 | 0.77 | 1.46 | 1.46 | 2.19 | |||||
CP-IP: the codimerization thing of cyclopentadiene and isoprene;
CP-PD: the codimerization thing of cyclopentadiene and m-pentadiene;
X1: isoprene or m-pentadiene from dipolymer;
X2: other heavy constituent.
[embodiment 2]
Technical process by [embodiment 1], before just the raw material cracked C 5 fraction enters isoprene knockout tower 2, enter by the 44th column plate place, lightness-removing column 1 middle part earlier, carry out rectifying separation, removed overhead carbon four and carbon four following components, tower still carbon five logistics XI enter isoprene knockout tower 2 middle parts.Lightness-removing column 1 stage number is 75, and feeding temperature is 50 ℃, and tower still temperature is 76 ℃, and tower top temperature is 49 ℃, and tower top pressure is 0.15MPa, and tower still pressure is 0.20MPa, and reflux ratio is 20.The stopper ONP advances tower with carbon Wuyuan material.
Solvent B in the solvent orange 2 A in first extractive distillation column and second extractive distillation column is acetonitrile, and stopper is n-formyl sarcolysine base pyrrolidone; Stopper in the sepn process of other solvent-free existence is an ONP.
The purity of m-pentadiene is 68.12%, and the purity of dicyclopentadiene is 89.27%.
Each unitary operational condition sees Table 2, and the weight percent composition of raw material and each unit component sees Table 3.
Table 2
| Operational condition | Lightness-removing column 1 | |
First |
First stripping tower 4 |
| Feeding temperature (℃) | 50 | - | - | - |
| Charging place stage number (piece) | 44 | 66 | 46 | 30 |
| Total stage number (piece) | 75 | 130 | 90 | 56 |
| Tower still temperature (℃) | 76 | 86 | 102 | 108 |
| Tower top temperature (℃) | 49 | 63 | 54 | 56 |
| Tower still pressure (MPa) | 0.2 | 0.22 | 0.18 | 0.15 |
| Tower top pressure (MPa) | 0.15 | 0.15 | 0.11 | 0.1 |
| Solvent ratio | - | - | 3.3 | - |
| Reflux ratio | 20 | 8.5 | 9 | 6 |
| The reactor reaction temperature (℃) | - | - | - | - |
| Reactor reaction pressure (MPa) | - | - | - | - |
Continuous table 2
| Operational condition | |
Second |
|
|
| Feeding temperature (℃) | - | - | - | - |
| Charging place stage number (piece) | 52 | 87 | 30 | 29 |
| Total stage number (piece) | 80 | 120 | 55 | 130 |
| Tower still temperature (℃) | 72 | 111 | 112 | 64 |
| Tower top temperature (℃) | 63 | 63 | 59 | 52 |
| Tower still pressure (MPa) | 0.21 | 0.25 | 0.14 | 0.15 |
| Tower top pressure (MPa) | 0.15 | 0.15 | 0.12 | 0.08 |
| Solvent ratio | - | 2 | - | - |
| Reflux ratio | 20 | 8 | 4 | 200 |
| The reactor reaction temperature (℃) | - | - | - | - |
| Reactor reaction pressure (MPa) | - | - | - | - |
Continuous table 2
| Operational condition | Hot dipolymer reactor 9 | Decarburization five towers 10 | M- |
|
| Feeding temperature (℃) | - | - | - | - |
| Charging place stage number (piece) | - | 16 | 31 | 27 |
| Total stage number (piece) | - | 30 | 110 | 50 |
| Tower still temperature (℃) | - | 98 | 66 | 116 |
| Tower top temperature (℃) | - | 46 | 52 | 20 |
| Tower still pressure (MPa) | - | 0.03 | 0.1 | -0.07 |
| Tower top pressure (MPa) | - | 0.01 | 0.04 | -0.08 |
| Solvent ratio | - | - | - | - |
| Reflux ratio | - | 4 | 80 | 3.5 |
| The reactor reaction temperature (℃) | 90 | - | - | - |
| Reactor reaction pressure (MPa) | 0.5 | - | - | - |
Table 3
| Component | Lightness-removing column 1 | Isoprene knockout tower 2 | First extractive distillation column 3 | First stripping tower 4 | |||||
| Charging | Eject material | End discharging | Charging | Eject material | End discharging | Charging | Eject material | Eject material | |
| Below carbon four reaches | 3.88 | 31.55 | |||||||
| Iso-pentane | 3.88 | 27.59 | 0.55 | 0.53 | 0.98 | 0.98 | 2.05 | ||
| 3-methyl butene-1 | 0.88 | 6.95 | 0.03 | 0.03 | 0.05 | 0.05 | 0.11 | ||
| Skellysolve A | 5.87 | 0.29 | 6.65 | 6.38 | 11.70 | 11.70 | 24.63 | ||
| Amylene-1 | 4.11 | 5.65 | 3.89 | 3.74 | 6.85 | 6.85 | 14.42 | ||
| 2-methyl butene-1 | 4.79 | 3.12 | 5.02 | 4.82 | 8.84 | 0.00 | 8.84 | 18.60 | 0.00 |
| Anti-amylene-2 | 2.78 | 0.01 | 3.17 | 3.04 | 5.30 | 0.33 | 5.30 | 11.15 | 0.01 |
| Along amylene-2 | 1.90 | 0.00 | 2.17 | 2.08 | 3.33 | 0.58 | 3.33 | 6.99 | 0.01 |
| Pentadiene-1,4 | 2.63 | 17.40 | 0.56 | 0.54 | 0.98 | 0.00 | 0.98 | 2.06 | 0.01 |
| 2-methyl butene-2 | 2.93 | 0.00 | 3.34 | 3.35 | 5.83 | 0.37 | 5.83 | 11.51 | 0.88 |
| Pentamethylene | 1.02 | 0.00 | 1.16 | 1.12 | 0.00 | 2.45 | 0.00 | 0.00 | 0.00 |
| Isoprene | 23.19 | 0.64 | 26.35 | 28.83 | 52.22 | 0.80 | 52.22 | 0.37 | 96.23 |
| Cyclopentenes | 3.96 | 0.00 | 4.52 | 4.34 | 0.02 | 9.51 | 0.02 | 0.00 | 0.02 |
| Crotonylene | 0.84 | 6.72 | 0.02 | 0.01 | 0.03 | 0.00 | 0.03 | 0.00 | 0.04 |
| Anti-pentadiene-1,3 | 10.71 | 0.00 | 12.21 | 11.71 | 0.00 | 25.75 | 0.00 | 0.00 | |
| Along pentadiene-1,3 | 5.85 | 0.00 | 6.67 | 6.40 | 0.01 | 14.05 | 0.01 | 0.00 | |
| Cyclopentadiene | 11.69 | 0.00 | 13.33 | 13.05 | 3.50 | 24.49 | 3.50 | 1.17 | |
| Pentadiene-1,2 | 0.33 | 0.00 | 0.38 | 0.36 | 0.02 | 0.78 | 0.02 | 0.01 | |
| Valylene | 0.07 | 0.08 | 0.07 | 0.07 | 0.12 | 0.00 | 0.12 | 0.07 | |
| Total carbon six | 2.90 | 3.31 | 3.17 | 6.97 | |||||
| Benzene/methylbenzene | 0.61 | 0.70 | 0.67 | 1.47 | |||||
| Dicyclopentadiene | 4.73 | 5.39 | 5.17 | 11.37 | |||||
| CP-IP | 0.18 | 0.21 | 0.20 | 0.43 | |||||
| CP-PD | 0.00 | 0.00 | 0.00 | 0.00 | |||||
| X1 | 0.08 | 0.09 | 0.09 | 0.19 | |||||
| X2 | 0.19 | 0.22 | 0.32 | 0.21 | 0.46 | 0.21 | 8.10 | 1.56 | |
Continuous table 3
| Component | |
Second |
|
|
||||||
| Charging | Eject material | End discharging | Charging | Eject material | Eject material | Charging | Eject material | End discharging | Side line | |
| Below carbon four reaches | ||||||||||
| Iso-pentane | ||||||||||
| 3-methyl butene-1 | ||||||||||
| Skellysolve A | ||||||||||
| Amylene-1 | 0.01 | |||||||||
| 2-methyl butene-1 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.06 | 0.00 | 12ppm | ||
| Anti-amylene-2 | 0.01 | 0.01 | 0.00 | 0.01 | 0.01 | 0.00 | 0.01 | 0.01 | 0.01 | 95ppm |
| Along amylene-2 | 0.01 | 0.01 | 0.01 | 0.01 | 0.01 | 0.00 | 0.01 | 0.01 | 0.01 | 108ppm |
| Pentadiene-1,4 | 0.01 | 0.01 | 0.00 | 0.01 | 0.01 | 0.00 | 0.01 | 0.61 | 1ppm | |
| 2-methyl butene-2 | 0.88 | 0.29 | 3.50 | 0.29 | 0.40 | 0.01 | 0.40 | 0.05 | 0.69 | 0.37 |
| Pentamethylene | 0.00 | 0.00 | 0.02 | |||||||
| Isoprene | 96.23 | 98.24 | 87.15 | 98.24 | 97.76 | 94.23 | 97.76 | 96.28 | 96.44 | 98.00 |
| Cyclopentenes | 0.02 | 0.00 | 0.12 | |||||||
| Crotonylene | 0.04 | 0.05 | 0.00 | 0.05 | 0.05 | 0.07 | 0.05 | 2.05 | 0.00 | 28ppm |
| Anti-pentadiene-1,3 | 0.00 | 0.00 | 0.00 | |||||||
| Along pentadiene-1,3 | 0.00 | 0.00 | 0.01 | |||||||
| Cyclopentadiene | 1.17 | 0.01 | 6.40 | 0.01 | 0.03 | 0.00 | 0ppm | |||
| Pentadiene-1,2 | 0.01 | 0.00 | 0.03 | |||||||
| Valylene | 0.07 | 0.08 | 0.00 | 0.08 | 0.18 | |||||
| Total carbon six | ||||||||||
| Benzene/methylbenzene | ||||||||||
| Dicyclopentadiene | ||||||||||
| CP-IP | ||||||||||
| CP-PD | ||||||||||
| X1 | ||||||||||
| X2 | 1.56 | 1.29 | 2.76 | 1.29 | 1.75 | 5.48 | 1.75 | 0.94 | 2.85 | 1.61 |
Continuous table 3
| Component | Hot dipolymer reactor 9 | Decarburization five towers 10 | M-pentadiene treating tower 11 | Dicyclopentadiene treating tower 12 | |||||||
| Charging | Discharging | Charging | Eject material | End discharging | Charging | Eject material | End discharging | Charging | Eject material | End discharging | |
| Below carbon four reaches | |||||||||||
| Iso-pentane | |||||||||||
| 3-methyl butene-1 | |||||||||||
| Skellysolve A | |||||||||||
| Amylene-1 | 0.00 | 0.00 | |||||||||
| 2-methyl butene-1 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | |||||
| Anti-amylene-2 | 0.33 | 0.33 | 0.33 | 0.56 | 0.56 | 1.88 | |||||
| Along amylene-2 | 0.58 | 0.58 | 0.58 | 0.99 | 0.99 | 3.33 | |||||
| Pentadiene 1,4 | 0.00 | 0.00 | 0.00 | ||||||||
| 2-methyl butene-2 | 0.37 | 0.37 | 0.37 | 0.63 | 0.00 | 0.63 | 2.10 | 0.00 | 0.00 | 0.00 | |
| Pentamethylene | 2.45 | 2.45 | 2.45 | 4.18 | 0.03 | 4.18 | 0.73 | 5.65 | 0.03 | 0.09 | |
| Isoprene | 0.80 | 0.73 | 0.73 | 1.26 | 0.00 | 1.26 | 4.20 | 0.00 | 0.00 | 0.00 | |
| Cyclopentenes | 9.51 | 9.51 | 9.51 | 16.23 | 0.07 | 16.23 | 6.87 | 20.21 | 0.07 | 0.21 | |
| Crotonylene | 0.00 | 0.00 | 0.00 | 0.00 | |||||||
| Anti-pentadiene-1,3 | 25.75 | 25.09 | 25.09 | 42.86 | 0.07 | 42.86 | 57.85 | 36.47 | 0.07 | 0.19 | |
| Along pentadiene-1,3 | 14.05 | 13.69 | 13 69 | 23.38 | 0 08 | 23.38 | 3.95 | 31.66 | 0.08 | 0.22 | |
| Cyclopentadiene | 24.49 | 3.57 | 3.57 | 6.09 | 0.01 | 6.09 | 18.03 | 1.00 | 0.01 | 0.04 | |
| Pentadiene-1,2 | 0.78 | 0.78 | 0.78 | 1.33 | 0.00 | 1.33 | 1.06 | 1.44 | 0.00 | 0.00 | |
| Valylene | |||||||||||
| Total carbon six | 6.97 | 6.97 | 6.97 | 2.50 | 27.44 | 2.50 | 0.00 | 3.57 | 27.44 | 78.38 | |
| Benzene/methylbenzene | 1.47 | 1.47 | 1.47 | 0.00 | 7.30 | 0.00 | 0.00 | 7.30 | 20.86 | 0.00 | |
| Dicyclopentadiene | 11.37 | 30.77 | 30.77 | 58.01 | 58.01 | 0.00 | 89.27 | ||||
| CP-IP | 0.43 | 0.50 | 0.50 | 0.94 | 0.94 | 1.45 | |||||
| CP-PD | 0.00 | 2.01 | 2.01 | 3.80 | 3.80 | 5.84 | |||||
| X1 | 0.19 | 0.19 | 0.19 | 0.36 | 0.36 | 0.56 | |||||
| X2 | 0.46 | 0.99 | 0.99 | 1.87 | 1.87 | 2.88 | |||||
CP-IP: the codimerization thing of cyclopentadiene and isoprene;
CP-PD: the codimerization thing of cyclopentadiene and m-pentadiene;
X1: isoprene or m-pentadiene from dipolymer;
X2: other heavy constituent.
[embodiment 3]
Technical process by [embodiment 2], just the solvent orange 2 A in first extractive distillation column is a N,N-DIMETHYLACETAMIDE, stopper is Sodium Nitrite and thanomin composite polymerzation inhibitor, and wherein the mass ratio of Sodium Nitrite and thanomin is 10: 1, and the carbon five basic concentration of thanomin are 160ppm.Solvent B in second extractive distillation column is a n-formyl sarcolysine base pyrrolidone, and stopper is an oil of mirbane, and the stopper in the sepn process of other solvent-free existence is a tert-butyl hydroquinone.
The purity of m-pentadiene is 68.99%, and the purity of dicyclopentadiene is 90.32%.
Each unitary operational condition sees Table 4, and the weight percent composition of raw material and each unit component sees Table 5.
Table 4
| Operational condition | Lightness-removing column 1 | |
First |
First stripping tower 4 |
| Feeding temperature (℃) | 35 | - | - | - |
| Charging place stage number (piece) | 35 | 39 | 75 | 21 |
| Total stage number (piece) | 60 | 90 | 150 | 50 |
| Tower still temperature (℃) | 68 | 87 | 150 | 190 |
| Tower top temperature (℃) | 43 | 70 | 51 | 46 |
| Tower still pressure (MPa) | 0.16 | 0.26 | 0.15 | 0.08 |
| Tower top pressure (MPa) | 0.1 | 0.21 | 0.08 | 0.05 |
| Solvent ratio | - | - | 8.5 | - |
| Reflux ratio | 30 | 30 | 2.2 | 3 |
| The reactor reaction temperature (℃) | - | - | - | - |
| Reactor reaction pressure (MPa) | - | - | - | - |
Continuous table 4
| Operational condition | |
Second |
|
|
| Feeding temperature (℃) | - | - | - | - |
| Charging place stage number (piece) | 95 | 80 | 17 | 50 |
| Total stage number (piece) | 140 | 160 | 35 | 100 |
| Tower still temperature (℃) | 75 | 171 | 218 | 76 |
| Tower top temperature (℃) | 55 | 52 | 39 | 67 |
| Tower still pressure (MPa) | 0.22 | 0.20 | 0.04 | 0.25 |
| Tower top pressure (MPa) | 0.1 | 0.08 | 0.02 | 0.18 |
| Solvent ratio | - | 7 | - | - |
| |
15 | 5 | 2.5 | 260 |
| The reactor reaction temperature (℃) | - | - | - | - |
| Reactor reaction pressure (MPa) | - | - | - | - |
Continuous table 4
| Operational condition | Hot dipolymer reactor 9 | Decarburization five towers 10 | M- |
|
| Feeding temperature (℃) | - | - | - | - |
| Charging place stage number (piece) | - | 32 | 43 | 40 |
| Total stage number (piece) | - | 65 | 130 | 80 |
| Tower still temperature (℃) | - | 117 | 75 | 124 |
| Tower top temperature (℃) | - | 53 | 60 | 25 |
| Tower still pressure (MPa) | - | 0.06 | 0.16 | -0.06 |
| Tower top pressure (MPa) | - | 0.04 | 0.1 | -0.07 |
| Solvent ratio | - | - | - | - |
| Reflux ratio | - | 1.8 | 20 | 2.5 |
| The reactor reaction temperature (℃) | 127 | - | - | - |
| Reactor reaction pressure (MPa) | 1.1 | - | - | - |
Table 5
| Component | Lightness-removing column 1 | Isoprene knockout tower 2 | First extractive distillation column 3 | First stripping tower 4 | |||||
| Charging | Eject material | End discharging | Charging | Eject material | End discharging | Charging | Eject material | Eject material | |
| Below carbon four reaches | 2.10 | 24.77 | |||||||
| Iso-pentane | 2.10 | 22.98 | 0.17 | 0.16 | 0.33 | 0.33 | 0.66 | ||
| 3-methyl butene-1 | 1.24 | 14.27 | 0.03 | 0.03 | 0.07 | 0.07 | 0.13 | ||
| Skellysolve A | 1.43 | 0.37 | 1.53 | 1.49 | 3.04 | 3.04 | 6.06 | ||
| Amylene-1 | 7.15 | 12.60 | 6.64 | 6.46 | 13.20 | 13.20 | 26.30 | ||
| 2-methyl butene-1 | 6.68 | 6.38 | 6.71 | 6.52 | 13.32 | 0.00 | 13.32 | 26.55 | 0.00 |
| Anti-amylene-2 | 5.72 | 0.04 | 6.24 | 6.07 | 10.88 | 1.46 | 10.88 | 21.67 | 0.01 |
| Along amylene-2 | 2.67 | 0.01 | 2.92 | 2.84 | 4.00 | 1.73 | 4.00 | 7.96 | 0.01 |
| Pentadiene-1,4 | 1.43 | 12.97 | 0.36 | 0.35 | 0.72 | 0.00 | 0.72 | 1.42 | 0.01 |
| 2-methyl butene-2 | 2.86 | 0.00 | 3.13 | 3.17 | 4.90 | 1.52 | 4.90 | 9.12 | 0.65 |
| Pentamethylene | 0.76 | 0.00 | 0.83 | 0.81 | 0.00 | 1.58 | 0.00 | 0.00 | 0.00 |
| Isoprene | 20.51 | 1.23 | 22.29 | 23.36 | 46.93 | 0.80 | 46.93 | 0.12 | 94.08 |
| Cyclopentenes | 3.81 | 0.00 | 4.17 | 4.05 | 0.01 | 7.93 | 0.01 | 0.00 | 0.01 |
| Crotonylene | 0.32 | 3.71 | 0.01 | 0.01 | 0.01 | 0.00 | 0.01 | 0.00 | 0.02 |
| Anti-pentadiene 1,3 | 10.26 | 0.00 | 11.22 | 10.90 | 0.00 | 21.33 | 0.00 | 0.01 | |
| Along pentadiene-1,3 | 6.11 | 0.00 | 6.67 | 6.49 | 0.01 | 12.69 | 0.01 | 0.01 | |
| Cyclopentadiene | 18.72 | 0.00 | 20.46 | 20.88 | 2.06 | 38.89 | 2.06 | 4.13 | |
| Pentadiene-1,2 | 0.10 | 0.00 | 0.11 | 0.11 | 0.00 | 0.21 | 0.00 | 0.00 | |
| Valylene | 0.30 | 0.68 | 0.27 | 0.26 | 0.53 | 0.00 | 0.53 | 1.06 | |
| Total carbon six | 5.71 | 6.24 | 6.06 | 11.86 | |||||
| Benzene/methylbenzene | 0.00 | 0.00 | 0.00 | 0.00 | |||||
| Dicyclopentadiene | |||||||||
| CP-IP | |||||||||
| CP-PD | |||||||||
| X1 | |||||||||
| X2 | |||||||||
Continuous table 5
| Component | |
Second |
|
|
||||||
| Charging | Eject material | End discharging | Charging | Eject material | Eject material | Charging | Eject material | End discharging | Side line | |
| Below carbon four reaches | ||||||||||
| Iso-pentane | ||||||||||
| 3-methyl butene-1 | ||||||||||
| Skellysolve A | ||||||||||
| Amylene-1 | 0.00 | 0.00 | 0.00 | 1ppm | ||||||
| 2-methyl butene-1 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.02 | 0.00 | 19ppm | ||
| Anti-amylene-2 | 0.01 | 0.01 | 0.02 | 0.01 | 0.01 | 0.00 | 0.01 | 0.01 | 0.01 | 97ppm |
| Along amylene-2 | 0.01 | 0.00 | 0.02 | 0.00 | 0.01 | 0.00 | 0.01 | 0.00 | 0.01 | 52ppm |
| Pentadiene-1,4 | 0.01 | 0.01 | 0.00 | 0.01 | 0.01 | 0.00 | 0.01 | 0.89 | 9ppm | |
| 2-methyl butene-2 | 0.65 | 0.12 | 4.67 | 0.12 | 0.14 | 0.04 | 0.14 | 0.03 | 0.16 | 0.14 |
| Pentamethylene | 0.00 | 0.00 | 0.01 | 0.00 | ||||||
| Isoprene | 94.08 | 98.58 | 59.83 | 98.58 | 99.81 | 91.46 | 99.81 | 97.60 | 99.82 | 99.84 |
| Cyclopentenes | 0.01 | 0.00 | 0.11 | 0.00 | ||||||
| Crotonylene | 0.02 | 0.03 | 0.00 | 0.03 | 0.02 | 0.03 | 0.02 | 1.42 | 0.00 | 28ppm |
| Anti-pentadiene-1,3 | 0.01 | 0.00 | 0.07 | 0.00 | ||||||
| Along pentadiene-1,3 | 0.01 | 0.00 | 0.10 | 0.00 | ||||||
| Cyclopentadiene | 4.13 | 0.05 | 35.12 | 0.05 | 0.00 | 0.30 | 0.00 | 0.00 | 0.00 | 3ppm |
| Pentadiene-1,2 | 0.00 | 0.00 | 0.04 | 0.00 | ||||||
| Valylene | 1.06 | 1.20 | 0.00 | 1.20 | 0.00 | 8.16 | 0.00 | 0.02 | 0.00 | 5ppm |
| Total carbon six | ||||||||||
| Benzene/methylbenzene | ||||||||||
| Dicyclopentadiene | ||||||||||
| CP-IP | ||||||||||
| CP-PD | ||||||||||
| X1 | ||||||||||
| X2 | ||||||||||
Continuous table 5
| Component | Hot dipolymer reactor 9 | Decarburization five towers 10 | M-pentadiene treating tower 11 | Dicyclopentadiene treating tower 12 | |||||||
| Charging | Discharging | Charging | Eject material | End discharging | Charging | Eject material | End discharging | Charging | Eject material | End discharging | |
| Below carbon four reaches | |||||||||||
| Iso-pentane | |||||||||||
| 3-methyl butene-1 | |||||||||||
| Skellysolve A | |||||||||||
| Amylene-1 | 0.00 | 0.01 | 0.01 | 0.02 | |||||||
| 2-methyl butene-1 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.01 | |||||
| Anti-amylene-2 | 1.46 | 1.46 | 1.46 | 2.88 | 2.88 | 6.70 | |||||
| Along amylene 2 | 1.73 | 1.73 | 1.73 | 3.40 | 0.00 | 3.40 | 7.92 | 0.00 | 0.00 | ||
| Pentadiene-1,4 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | |||||
| 2-methyl butene-2 | 1.52 | 1.52 | 1.52 | 2.98 | 0.00 | 2.98 | 6.95 | 0.00 | 0.00 | 0.00 | |
| Pentamethylene | 1.58 | 1.58 | 1.58 | 3.09 | 0.02 | 3.09 | 0.51 | 5.03 | 0.02 | 0.10 | |
| Isoprene | 0.80 | 0.73 | 0.73 | 1.43 | 0.00 | 1.43 | 3.33 | 0.00 | 0.00 | 0.00 | |
| Cyclopentenes | 7.93 | 7.93 | 7.93 | 15.50 | 0.10 | 15.50 | 9.24 | 20.20 | 0.10 | 0.45 | |
| Crotonylene | 0.00 | 0.00 | 0.00 | 0.00 | |||||||
| Anti-pentadiene-1,3 | 21.33 | 20.20 | 20.20 | 39.68 | 0.06 | 39.68 | 48.44 | 33.08 | 0.06 | 0.27 | |
| Along pentadiene 1,3 | 12.69 | 12.02 | 12.02 | 23.58 | 0.07 | 23.58 | 7.18 | 35.91 | 0.07 | 0.33 | |
| Cyclopentadiene | 38.89 | 2.32 | 2.32 | 4.55 | 0.02 | 4.55 | 9.28 | 1.00 | 0.02 | 0.07 | |
| Pentadiene-1,2 | 0.21 | 0.21 | 0.21 | 0.41 | 0.00 | 0.41 | 0.43 | 0.39 | 0.00 | 0.00 | |
| Valylene | |||||||||||
| Total carbon six | 11.86 | 11.86 | 11.86 | 2.50 | 21.54 | 2.50 | 0.00 | 4.38 | 21.54 | 98.77 | |
| Benzene/methylbenzene | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | |
| Dicyclopentadiene | 0.00 | 34.71 | 34.71 | 70.62 | 70.62 | 0.00 | 90.32 | ||||
| CP-IP | 0.00 | 0.13 | 0.13 | 0.27 | 0.27 | 0.35 | |||||
| CP-PD | 0.00 | 3.53 | 3.53 | 7.18 | 7.18 | 9.19 | |||||
| X1 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.01 | |||||
| X2 | 0.00 | 0.05 | 0.05 | 0.11 | 0.11 | 0.14 | |||||
CP-IP: the codimerization thing of cyclopentadiene and isoprene;
CP-PD: the codimerization thing of cyclopentadiene and m-pentadiene;
X1: isoprene or m-pentadiene from dipolymer;
X2: other heavy constituent.
Claims (7)
1. the separation method of diolefin in the five fractions of petroleum cracked carbon may further comprise the steps:
A) raw material cracked C 5 fraction (13) enters isoprene knockout tower (2) middle part, and cat head separates the stream I that obtains being rich in isoprene; The tower still separates the stream I I that obtains being rich in cyclopentadiene and m-pentadiene;
B) stream I enters first extractive distillation column (3) middle part, contacts with the solvent orange 2 A that enters from tower top and carries out extracting rectifying, and cat head obtains containing the light constituent logistics of alkane and monoolefine, and the tower still obtains being rich in the solvent orange 2 A base stream I II of isoprene;
C) solvent base stream I II enters first stripping tower (4) and carries out solvent orange 2 A and reclaim, and cat head obtains being rich in the stream I V of isoprene, and the solvent orange 2 A logistics that the tower still obtains is back to first extractive distillation column (3) top;
D) stream I V enters cyclopentadiene recovery tower (5) middle and lower part, a small amount of cyclopentadiene among the stream I V is carried out Separation and Recovery, cat head obtains removing the isoprene logistics V behind the cyclopentadiene, and the tower still contains the cyclopentadiene logistics and is circulated to isoprene knockout tower (2) middle part;
E) logistics V enters second extractive distillation column (6) middle part, contacts with the solvent B that enters from tower top and carries out extracting rectifying, and cat head obtains isoprene solvent B base logistics VI, and the tower still obtains containing the solvent B logistics VII of a small amount of diolefin and alkynes;
F) logistics VI enters isoprene treating tower (8) middle part, and overhead stream is discharged out-of-bounds, and tower still side line obtains the polymerization grade isoprene product in the position that calculating from top to bottom accounts for total stage number 90～99%;
G) logistics VII enters second stripping tower (7) and carries out solvent recuperation, and cat head obtains containing the logistics of diolefin and alkynes, and the solvent B logistics that the tower still obtains is back to second extractive distillation column (6) top and recycles;
H) stream I I enters hot dipolymer reactor (9), generates the logistics VIII that is rich in dicyclopentadiene;
I) logistics VIII enters decarburization five towers (10), and cat head obtains being rich in the stream I X of m-pentadiene, and the tower still obtains being rich in the logistics X of dicyclopentadiene;
J) stream I X enters m-pentadiene treating tower (11) and makes with extra care, and the tower still obtains the m-pentadiene product of purity greater than 65 weight %;
K) logistics X enters dicyclopentadiene treating tower (12) middle part, and the tower still obtains purity greater than 90% dicyclopentadiene product;
Wherein solvent orange 2 A in first extractive distillation column and the solvent B in second extractive distillation column all are selected from least a in dimethyl formamide, N,N-DIMETHYLACETAMIDE, acetonitrile, n-formyl sarcolysine base pyrrolidone and the acetonitrile solution.
2. according to the separation method of diolefin in the described five fractions of petroleum cracked carbon of claim 1, it is characterized in that
The operational condition of isoprene knockout tower (2): stage number is 60～160, and tower still temperature is 70～110 ℃, and tower top temperature is 35～70 ℃, and reflux ratio is 5～60, and working pressure is 0.01～0.3MPa;
The operational condition of first extractive distillation column (3): stage number is 70～160, and tower still temperature is 100～150 ℃, and tower top temperature is 35～80 ℃, and reflux ratio is 2～13, and working pressure is 0.01～0.3MPa, and the weight ratio of solvent orange 2 A and stream I is 3～11;
The operational condition of first stripping tower (4): stage number is 20～60, and tower still temperature is 120～220 ℃, and tower top temperature is 30～60 ℃, and reflux ratio is 1～5, and working pressure is 0.01～0.3MPa;
The operational condition of cyclopentadiene recovery tower (5): stage number is 60～150, and tower still temperature is 55～100 ℃, and tower top temperature is 35～55 ℃, and reflux ratio is 5～30, and working pressure is 0.01～0.25MPa;
The operational condition of second extractive distillation column (6): stage number is 90～190, and tower still temperature is 100～150 ℃, and tower top temperature is 35～80 ℃, and reflux ratio is 2～10, and working pressure is 0.01～0.3MPa, and the weight ratio of solvent B and logistics V is 2～10;
The operational condition of second stripping tower (7): stage number is 20～60, and tower still temperature is 120～220 ℃, and tower top temperature is 30～70 ℃, and reflux ratio is 1～5, and working pressure is 0.01～0.3MPa;
The operational condition of isoprene treating tower (8): stage number is 70～140, and tower still temperature is 55～90 ℃, and tower top temperature is 35～55 ℃, and reflux ratio is 100～600, and working pressure is 0.02～0.3MPa;
Hot dipolymer reactor (9) reaction conditions: temperature of reaction is 60～150 ℃, and reaction pressure is 0.3～1.3MPa;
The operational condition of decarburization five towers (10): stage number is 15～70, and tower still temperature is 80～130 ℃, and tower top temperature is 35～60 ℃, and reflux ratio is 0.5～5, and working pressure is 0.01～0.05MPa;
The operational condition of m-pentadiene treating tower (11): stage number is 70～140, and tower still temperature is 50～100 ℃, and tower top temperature is 40～60 ℃, and reflux ratio is 10～90, and working pressure is 0.02～0.2MPa;
The operational condition of dicyclopentadiene treating tower (12): stage number is 10～90, and tower still temperature is 80～130 ℃, and tower top temperature is 5～50 ℃, and reflux ratio is 0.5～5, working pressure is-0.05～-0.1MPa.
3. according to the separation method of diolefin in the described five fractions of petroleum cracked carbon of claim 1, it is preceding to it is characterized in that the raw material cracked C 5 fraction enters isoprene knockout tower (2), be introduced into lightness-removing column (1) middle part and carry out rectifying separation, removed overhead carbon four and carbon four following components, tower still carbon five logistics XI enter isoprene knockout tower (2) middle part.
4. according to the separation method of diolefin in the described five fractions of petroleum cracked carbon of claim 3, the operational condition that it is characterized in that lightness-removing column (1): feeding temperature is 30～75 ℃, stage number is 50～100, tower still temperature is 70～100 ℃, tower top temperature is 35～60 ℃, reflux ratio is 15～35, and working pressure is 0.1～0.3MPa.
5. according to the separation method of diolefin in the described five fractions of petroleum cracked carbon of claim 1, the extracting rectifying that it is characterized in that step b) and step e) carries out in the presence of stopper A, and described stopper A is selected from least a in ONP, oil of mirbane, furfural, n-formyl sarcolysine base pyrrolidone, thanomin or the Sodium Nitrite.
6. according to the method for diolefin in the described separating cracked carbon-5 fraction of claim 5, it is characterized in that extracting rectifying stopper A is Sodium Nitrite and thanomin composite polymerzation inhibitor, wherein the mass ratio of Sodium Nitrite and thanomin is 0.25～15: 1, and the carbon five basic concentration of thanomin are 100～800ppm.
7. according to the method for diolefin in the described separating cracked carbon-5 fraction of claim 1, the rectifying that it is characterized in that solvent-free existence carries out in the presence of stopper B, and described stopper B is selected from least a in ONP, tert-butyl catechol, diethyl azanol or the acid of dihydroxyl dihydro cinnamon.
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Address after: 100029 Beijing City, Chaoyang District Hui Street No. 6 Patentee after: China Petrochemical Group Corp. Patentee after: SINOPEC Shanghai Engineering Company Limited Address before: 100029 Beijing City, Chaoyang District Hui Street No. 6 Patentee before: China Petrochemical Group Corp. Patentee before: Sinopec Shanghai Engineering Co., Ltd. |