Method and device for cutting Fischer-Tropsch synthesis light oil by using bulkhead tower
Technical Field
The invention relates to a method and a device for cutting Fischer-Tropsch synthesis light oil by a bulkhead tower to obtain products of each carbon number fraction section, which are particularly suitable for cutting Fischer-Tropsch synthesis light oil mainly containing C6-C10 fractions.
Background
Fischer-Tropsch synthesis, i.e. an indirect coal liquefaction process, in the presence of a catalyst, gasifying the synthesis gas (CO, H)2) Converting into gasoline, diesel oil and other hydrocarbon products. The crude reaction products mainly comprise light oil, heavy oil and heavy wax. The Fischer-Tropsch synthesis product is usually used for further producing products such as gasoline, diesel oil, naphtha and the like, and olefin in the products needs to be subjected to hydrotreating, so that waste of alpha-olefin components with higher added values is caused. The main substances in the Fischer-Tropsch synthesis light oil are normal paraffin and normal olefin of C6-C10, the olefin component is mostly alpha-olefin, and the Fischer-Tropsch synthesis light oil has the characteristics of low sulfur content, almost no aromatic hydrocarbon and the like. If the substances in the Fischer-Tropsch synthesis product can be separated and refined by adopting a proper method, high value-added products can be further produced, the diesel oil is reduced, the products are refined, and the economic benefit is greatly improved.
The patent CN107267212A provides a separation process of Fischer-Tropsch synthesized crude products, which comprises a plurality of process steps of raw oil crude separation, oil hydrogenation, light hydrocarbon fine separation, wax hydrogenation, wax fine separation and the like, and according to the difference of the synthesis temperature of the Fischer-Tropsch synthesized crude products, various high value-added products such as naphtha, n-pentane, n-hexane, n-heptane, n-octane, C50, C70, C80 series wax, H1, H105 series wax and the like with different quantities can be obtained. Firstly, crude separation is carried out on raw oil products to obtain C5-C8 fraction, and the fraction is sent to a light component separation tower to carry out fine separation on light hydrocarbon; distilling C5 and C6 from the top of the light component separation tower, distilling C7 and C8 from the bottom of the tower, respectively feeding the material flows from the top of the tower and the bottom of the tower into a C5 separation tower and a C7 separation tower to obtain C5, C6, C7 and C8 components, respectively feeding the C5, C6, C7 and C8 components into alkane purification towers with carbon number, and finally obtaining products of n-pentane, n-hexane, n-heptane and n-octane with the purity of more than 99.9 wt%, and simultaneously obtaining byproducts of isopentane, isohexane, isoheptane, isooctane and the like. The patent CN107325838A is similar to the flow of the above patent, crude separation of raw oil products is carried out to obtain C5-C7 fraction, then products of n-pentane, n-hexane and n-heptane with purity of more than 99.9 wt% are obtained by fine separation of light hydrocarbon, and byproducts of isopentane, isohexane, isoheptane and the like are obtained at the same time.
The patent CN107916127A relates to a rectification process for Fischer-Tropsch synthesis product separation, and the rectification process adopts three-stage separation and then realizes five-stage fraction separation through four-tower rectification. Separating the oil phase from the water phase by the Fischer-Tropsch product raw material respectively passing through a first-stage condenser, a first-stage separator, a second-stage water cooler, a second-stage separator, a third-stage deep cooler and a third-stage separator, wherein upper liquid phases of the first-stage separator, the second-stage separator and the third-stage separator are respectively heavy hydrocarbon, light hydrocarbon and respectively enter a dry gas rectifying tower; the crude oil sequentially passes through four rectifying towers, namely a dry gas rectifying tower, a liquefied petroleum gas rectifying tower, a C5-C10 rectifying tower, a C11-C19 rectifying tower and the like to respectively obtain five products, namely dry gas (C1-C2), liquefied petroleum gas (C3-C4), C5-C10 fraction section, C11-C19 fraction section, C20+ fraction section and the like.
The patent CN101275080A relates to a separation method of Fischer-Tropsch reaction products, and mainly solves the problem that the separation of gasoline and diesel oil which are the products of the existing Fischer-Tropsch synthesis reaction is difficult. The hydrocarbon product obtained after the Fischer-Tropsch reaction is introduced into a separation device; and separating the product by a separating device to obtain a hydrocarbon and heavy hydrocarbon product containing gasoline and diesel oil, wherein the separating device comprises a hot trap tower and a heater, the heater is arranged at the lower part of the hot trap tower, the temperature control range of the bottom of the hot trap tower is 120-400 ℃, and the temperature control range of the top of the hot trap tower is 25-150 ℃.
The above documents generally have the problems of unclear fractionation section of the obtained product, difficulty in fine utilization of the product, and the like, and have the defects of complicated flow, and high energy consumption and equipment cost. The invention provides a novel process method and a novel device for separating products of each carbon number fraction section from Fischer-Tropsch oil with high efficiency and energy saving.
Disclosure of Invention
The invention aims to overcome the defects of the prior art and provides a high-efficiency and energy-saving method and device for separating and purifying products in each carbon number fraction section in Fischer-Tropsch synthesis light oil.
The technical method provided by the invention adopts a bulkhead tower technology to cut products of each carbon number fraction section of Fischer-Tropsch synthesis light oil, so as to respectively obtain products of C6-C10 fraction sections.
The process can adopt the flow of three single partition wall towers, and also can adopt the flow of two double partition wall towers or one five partition wall tower. Wherein, the flow of three single-partition towers and the flow of two double-partition towers can adopt different separation sequences, and the specific flow is as follows.
(1) Three single dividing wall tower process
(a) First separation sequence (see FIG. 1-1)
Feeding a Fischer-Tropsch synthesis light oil raw material (S01) into a T11 pre-separation tower, taking a fraction lighter than C6 from the top of the T11 (S02), taking a fraction heavier than C10 from the bottom of the T11 tower (S08), taking a C6-C10 fraction (S09) from the main tower side line of the T11, and feeding the fraction into the T12 pre-separation tower; c6 fraction (S03) is extracted from the top of the T12 tower, C10 fraction (S07) is extracted from the bottom of the T12 tower, and C7-C9 fraction (S10) is extracted from the main tower side line of the T12 and enters a T13 pre-separation tower; a C7 fraction (S04) is extracted from the top of the T13 tower, a C9 fraction (S06) is extracted from the bottom of the T13 tower, and a C8 fraction (S05) is extracted from the side of the T13 main tower.
(b) Second separation sequence (see FIGS. 1-2)
Feeding a Fischer-Tropsch synthesis light oil raw material (S01) into a T11 pre-separation tower, taking a fraction lighter than C6 from the top of the T11 (S02), taking a fraction C9 and heavier from the bottom of the T11 tower (S11), taking a fraction C6-C8 (S12) from the main tower side line of the T11, feeding the fraction into the T12 pre-separation tower, and feeding the fraction into a T13 pre-separation tower; a C6 fraction section (S03) is extracted from the top of the T12 tower, a C8 fraction section (S05) is extracted from the bottom of the tower, and a C7 fraction section (S04) is extracted from the side of the T12 main tower; the top of the T13 column was taken as a C9 cut (S06), the bottom was taken as a heavier than C10 cut (S08), and the side of the T13 column was taken as a C10 cut (S07).
(c) Third separation sequence (see FIGS. 1-3)
Feeding a Fischer-Tropsch synthesis light oil raw material (S01) into a T11 pre-separation tower, taking a fraction (S13) lighter than C7 at the top of the T11 tower, feeding the fraction into a T12 pre-separation tower, taking a fraction (S08) heavier than C10 at the bottom of the T11 tower, taking a C8-C10 fraction (S14) from the side line of the T11 main tower, and feeding the fraction into a T13 pre-separation tower; the T12 takes a fraction lighter than C6 at the top (S02), takes a C7 fraction section (S04) at the bottom, and takes a C6 fraction section (S03) from the main column side of the T12; the top of the T13 column was taken as the C8 cut (S05), the bottom was taken as the C10 cut (S07), and the C9 cut was taken from the main side of the T13 column (S06).
(d) Fourth separation sequence (see FIGS. 1-4)
The Fischer-Tropsch synthesis light oil raw material (S01) enters a T11 pre-separation tower, C7 and lighter fractions (S13) are extracted from the top of the T11 and enter a T12 pre-separation tower, C9 and heavier fractions (S11) are extracted from the bottom of the T11 tower and enter a T13 pre-separation tower, and C8 fractions (S05) are extracted from the side line of the T11 main tower; the T12 takes a fraction lighter than C6 at the top (S02), takes a C7 fraction section (S04) at the bottom, and takes a C6 fraction section (S03) from the main column side of the T12; a C9 fraction (S06) is taken from the top of the T13 column, a fraction heavier than C10 is taken from the bottom of the T3578 column (S08), and a C10 fraction (S07) is taken from the main column side of the T13 column.
(2) Two double dividing wall tower flow
(a) First separation sequence (see FIG. 2-1)
Feeding a Fischer-Tropsch synthesis light oil raw material (S01) into a T21 pre-separation tower, extracting a fraction lighter than C6 from the top of the T21 (S02), extracting a C6-C9 fraction (S15) from the upper side line of a T21 main tower, feeding the fraction into a T22 pre-separation tower, extracting a C10 fraction section (S07) from the lower side line of the T21 main tower, and extracting a fraction heavier than C10 from the bottom of a T21 tower (S08); the top of the T22 is provided with a C6 fraction (S03), the upper side and the lower side of the T22 main column are provided with a C7 fraction (S04), a C8 fraction (S05) and the bottom of the T22 column is provided with a C9 fraction (S06).
(b) Second separation sequence (see FIG. 2-2)
Feeding a Fischer-Tropsch synthesis light oil raw material (S01) into a T21 pre-separation tower, extracting a fraction lighter than C6 (S02) from the top of the T21 tower, extracting a C6 fraction section (S03) from the upper side line of a T21 main tower, extracting a C7-C10 fraction (S16) from the lower side line of a T21 main tower, feeding the fraction into the T22 pre-separation tower, and extracting a fraction heavier than C10 from the bottom of a T21 tower (S08); the top of the T22 is provided with a C7 fraction (S04), the upper side and the lower side of the T22 main column are provided with a C8 fraction (S05), a C9 fraction (S06) and the bottom of the T22 column is provided with a C10 fraction (S07).
(c) Third separation sequence (see FIGS. 2-3)
Feeding a Fischer-Tropsch synthesis light oil raw material (S01) into a T21 pre-separation tower, extracting a fraction (S02) lighter than C6 from the top of the T21 tower, extracting a C6 distillation section (S03) and a C7 distillation section (S04) from the upper side line and the lower side line of a T21 main tower respectively, extracting a C8 fraction and a heavier fraction (S17) from the bottom of the T21 tower, and feeding the fractions into a T22 pre-separation tower; a C8 fraction (S05) is taken out from the top of the T22 column, a C9 fraction (S06) and a C10 fraction (S07) are taken out from the upper side line and the lower side line of the T22 main column, and a fraction heavier than C10 is taken out from the bottom of the T22 column (S08).
(d) Fourth separation sequence (see FIGS. 2-4)
The Fischer-Tropsch synthesis light oil raw material (S01) enters a T21 pre-separation tower, C6 and lighter fractions (S18) are extracted from the top of the T21 pre-separation tower and enter a T22 pre-separation tower, C9 distillation sections (S06) and C10 distillation sections (S07) are extracted from the upper side line and the lower side line of a T21 main tower respectively, and fractions heavier than C10 are extracted from the bottom of a T21 tower (S08); the top of the T22 column is provided with lighter fractions than C6 (S02), C6 fraction (S03) and C7 fraction (S04) are provided from the upper side and the lower side of the T22 main column, and C8 fraction (S05) is provided from the bottom of the T22 column.
(3) A five-compartment tower process (as shown in figure 3)
The Fischer-Tropsch synthesis light oil raw material (S01) enters a T3 pre-separation tower, is separated by a plurality of clapboards w11, w21-22, w31-33, w41-44 and w51-55 in the tower, finally, a component lighter than C6 is obtained at the top of the T3 tower (S02), products of C6-C10 fractional segments (S03-S07) are respectively obtained from five side lines from top to bottom, and a component heavier than C10 is obtained at the bottom of the tower (S08).
In the process (1), the theoretical plate number of a pre-separation tower (area a in figure 4-1) of a T11 single-partition wall tower is 10-200, the theoretical plate number of a main tower (area b in figure 4-1) is 10-200, the theoretical plate number of a common rectification section (area c in figure 4-1) is 0-100, the theoretical plate number of a common stripping section (area d in figure 4-1) is 0-100, the mass fraction of a liquid phase reflux entering the pre-separation tower is 0.01-0.99, the mass fraction of a gas phase reflux entering the pre-separation tower is 0.01-0.99, the reflux ratio is 0.1-20, and the operation pressure is 0.05-5 atm; the number of theoretical plates of a pre-separation tower (area a in figure 4-1) of the T12 single-partition wall tower is 10-200, the number of theoretical plates of a main tower (area b in figure 4-1) is 10-200, the number of theoretical plates of a common rectification section (area c in figure 4-1) is 0-100, the number of theoretical plates of a common stripping section (area d in figure 4-1) is 0-100, the mass fraction of a liquid phase reflux entering the pre-separation tower is 0.01-0.99, the mass fraction of a gas phase reflux entering the pre-separation tower is 0.01-0.99, the reflux ratio is 0.1-20, and the operating pressure is 0.05-5 atm; the number of theoretical plates of a pre-separation tower (area a in figure 4-1) of the T13 single-partition wall tower is 10-200, the number of theoretical plates of a main tower (area b in figure 4-1) is 10-200, the number of theoretical plates of a common rectification section (area c in figure 4-1) is 0-100, the number of theoretical plates of a common stripping section (area d in figure 4-1) is 0-100, the mass fraction of a liquid phase reflux entering the pre-separation tower is 0.01-0.99, the mass fraction of a gas phase reflux entering the pre-separation tower is 0.01-0.99, the reflux ratio is 0.1-20, and the operating pressure is 0.05-5 atm.
In the flow (2), the number of theoretical plates of a pre-separation column (region e in FIG. 4-2) of a T21 double-dividing-wall column is 10 to 200, the number of theoretical plates of a first main column (region f in FIG. 4-2) is 10 to 200, the number of theoretical plates of a first common rectification section (region g in FIG. 4-2) is 0 to 100, the number of theoretical plates of a first common stripping section (region h in FIG. 4-2) is 0 to 100, the mass fraction of a liquid phase reflux entering the pre-separation column is 0.01 to 0.99, the mass fraction of a gas phase reflux entering the pre-separation column is 0.01 to 0.99, the number of theoretical plates of a second main column (region 5 in FIG. 4-2) is 10 to 200, the number of theoretical plates of a third main column (region j in FIG. 4-2) is 10 to 200, the number of theoretical plates of a second common column (region k in FIG. 4-2) is 0 to 100, and the number of theoretical plates of l in a second common stripping section (region 4-2) is 0 to 100, the mass fraction of the liquid phase reflux entering the pre-separation tower and the first main tower is 0.01-0.99, the mass fraction of the gas phase reflux entering the pre-separation tower and the first main tower is 0.01-0.99, the reflux ratio is 0.1-20, and the operating pressure is 0.05-5 atm; t22 double dividing wall column has a pre-separation column (region e in FIG. 4-2) theoretical plate number of 10-200, a first main column (region f in FIG. 4-2) theoretical plate number of 10-200, a first common rectification section (region g in FIG. 4-2) theoretical plate number of 0-100, a first common stripping section (region h in FIG. 4-2) theoretical plate number of 0-100, a liquid phase reflux entering the pre-separation column of 0.01-0.99, a gas phase reflux entering the pre-separation column of 0.01-0.99, a second main column (region 5 in FIG. 4-2) theoretical plate number of 10-200, a third main column (region j in FIG. 4-2) theoretical plate number of 10-200, a second common rectification section (region k in FIG. 4-2) theoretical plate number of 0-100, a second common stripping section (region l in FIG. 4-2) theoretical plate number of 0-100, the mass fraction of the liquid phase reflux entering the pre-separation tower and the first main tower is 0.01-0.99, the mass fraction of the gas phase reflux entering the pre-separation tower and the first main tower is 0.01-0.99, the reflux ratio is 0.1-20, and the operating pressure is 0.05-5 atm.
In the flow (3), the theoretical plate number of a pre-separation tower (area 1 in fig. 4-3) of a T3 five-partition wall tower is 10-200, the theoretical plate number of a first main tower (area 2 in fig. 4-3) is 10-200, the theoretical plate number of a first common rectification section (area 3 in fig. 4-3) is 0-100, the theoretical plate number of a first common stripping section (area 4 in fig. 4-3) is 0-100, the mass fraction of a liquid phase reflux entering the pre-separation tower is 0.01-0.99, and the mass fraction of a gas phase reflux entering the pre-separation tower is 0.01-0.99; the theoretical plate number of the second main tower (5 regions in fig. 4-3) is 10-200, the theoretical plate number of the third main tower (6 regions in fig. 4-3) is 10-200, the theoretical plate number of the second common rectification section (7 regions in fig. 4-3) is 0-100, the theoretical plate number of the second common stripping section (8 regions in fig. 4-3) is 0-100, the mass fraction of the liquid phase reflux entering the pre-separation tower and the first main tower is 0.01-0.99, and the mass fraction of the gas phase reflux entering the pre-separation tower and the first main tower is 0.01-0.99; the theoretical plate number of the fourth main tower (area 9 in fig. 4-3) is 10-200, the theoretical plate number of the fifth main tower (area 10 in fig. 4-3) is 10-200, the theoretical plate number of the sixth main tower (area 11 in fig. 4-3) is 10-200, the theoretical plate number of the third common rectification section (area 12 in fig. 4-3) is 0-100, the theoretical plate number of the third common stripping section (area 13 in fig. 4-3) is 0-100, the mass fraction of the liquid phase reflux entering the pre-separation tower, the first main tower and the second main tower is 0.01-0.99, and the mass fraction of the gas phase reflux entering the pre-separation tower, the first main tower and the second main tower is 0.01-0.99; the theoretical plate number of the seventh main tower (14 regions in fig. 4-3) is 10-200, the theoretical plate number of the eighth main tower (15 regions in fig. 4-3) is 10-200, the theoretical plate number of the ninth main tower (16 regions in fig. 4-3) is 10-200, the theoretical plate number of the tenth main tower (17 regions in fig. 4-3) is 10-200, the theoretical plate number of the fourth common rectification section (18 regions in fig. 4-3) is 0-100, the theoretical plate number of the fourth common rectification section (19 regions in fig. 4-3) is 0-100, the mass fraction of the liquid phase reflux entering the pre-separation tower plate, the first main tower, the second main tower and the fourth main tower is 0.01-0.99, and the mass fraction of the gas phase reflux entering the pre-separation tower, the first main tower, the second main tower and the fourth main tower is 0.01-0.99; the number of theoretical plates of an eleventh main column (20 regions in FIGS. 4-3) is 10 to 200, the number of theoretical plates of a twelfth main column (21 regions in FIGS. 4-3) is 10 to 200, the number of theoretical plates of a thirteenth main column (22 regions in FIGS. 4-3) is 10 to 200, the number of theoretical plates of a fourteenth main column (23 regions in FIGS. 4-3) is 10 to 200, the number of theoretical plates of a fifteenth main column (24 regions in FIGS. 4-3) is 10 to 200, the number of theoretical plates of a fifth common rectification section (25 regions in FIGS. 4-3) is 0 to 100, the number of theoretical plates of a fifth common stripping section (26 regions in FIGS. 4-3) is 0 to 100, the mass fraction of a liquid phase reflux into the pre-separation column, the first main column, the second main column, the fourth main column and the eleventh main column is 0.01 to 0.99, and a gas phase reflux into the pre-separation column, the first main column, The mass fractions of the second main tower, the fourth main tower and the eleventh main tower are 0.01-0.99; the reflux ratio is 0.1-20, and the operation pressure is 0.05-5 atm.
The device mainly comprises three single-partition towers or two double-partition towers or a five-partition tower.
The method and the device for separating the products of each carbon number fraction section from the Fischer-Tropsch synthesis light oil have the advantages that the products of each carbon number fraction section can be clearly separated from the Fischer-Tropsch synthesis light oil, the products are finely utilized, meanwhile, the energy consumption and the equipment cost are low, higher economic benefits can be created, and further, the market competitiveness of industries and enterprises is improved.
Drawings
FIGS. 1-1 to 1-4 are schematic diagrams of separation processes of different separation sequences of three single-wall towers, respectively.
FIGS. 2-1 to 2-4 are schematic diagrams of the separation processes of two double-wall towers in different separation sequences.
FIG. 3 is a schematic diagram of a separation process for a five-divided wall column.
FIGS. 4-1 to 4-3 are schematic structural views of a single-divided wall column, a double-divided wall column and a five-divided wall column, respectively.
T11-first single dividing wall column, T12-second single dividing wall column, T13-third single dividing wall column, T21-first double dividing wall column, T22-second double dividing wall column, T3-five dividing wall column.
S01 Fischer-Tropsch synthesis light oil raw material, S02-the fraction lighter than C6, S03-C6 fraction section, S04-C7 fraction section, S05-C8 fraction section, S06-C9 fraction section, S07-C10 fraction section, S08-the fraction heavier than C10, S09-C6-C10 fraction, S10-C7-C9 fraction, S11-C9 and heavier fraction, S12-C6-C8 fraction, S13-C7 and lighter fraction, S14-C6-C9 fraction, S15-C7-C10 fraction, S16-C8 and heavier fraction, S17-C8 and lighter fraction.
Detailed Description
The method and apparatus provided by the present invention will be further described with reference to the accompanying drawings, but the scope of the present invention is not limited to the embodiments.
The Fischer-Tropsch synthesis light oil raw material (S01) adopted by the invention mainly comprises hydrocarbons with the carbon number range of C6-C10 and a trace amount of oxygen-containing compounds. The hydrocarbons mainly comprise normal paraffin and alpha-olefin, and also comprise some isoparaffin, internal olefin, branched olefin, and small amount of naphthene, aromatic hydrocarbon and cyclic olefin.
Example 1
The invention is used in the narrow cut cutting process of Fischer-Tropsch synthesis light oil, and comprises a first single-wall tower (T11), a second single-wall tower (T12), a third single-wall tower (T13), a condenser, a reboiler, a pump, related feed lines and lines connecting the above devices, as shown in figure 1-1. The raw material is 1000g of Fischer-Tropsch synthetic oil light oil, and the light oil comprises hydrocarbons with the carbon number ranging from C6 to C10 and a trace amount of oxygen-containing compounds. The hydrocarbons mainly comprise normal paraffin and alpha-olefin, and also comprise some isoparaffin, internal olefin, branched olefin, and small amount of naphthene, aromatic hydrocarbon and cyclic olefin. The oxygen-containing compound comprises one or more of alcohol, aldehyde, ketone, acid and ester compounds. The theoretical plate number of a pre-separation tower (area a in figure 4-1) of a first single-partition wall tower (T11) is 10, the theoretical plate number of a main tower (area b in figure 4-1) is 200, the theoretical plate number of a common rectification section (area c in figure 4-1) is 0, the theoretical plate number of a common stripping section (area d in figure 4-1) is 100, the mass fraction of a liquid phase reflux entering the pre-separation tower is 0.01, the mass fraction of a gas phase reflux entering the pre-separation tower is 0.01, the reflux ratio is 0.1, and the operating pressure is 0.05 atm; the theoretical plate number of the pre-separation column (region a in fig. 4-1) of the second single-dividing wall column (T12) was 200, the theoretical plate number of the main column (region b in fig. 4-1) was 10, the theoretical plate number of the common rectification section (region c in fig. 4-1) was 100, the theoretical plate number of the common stripping section (region d in fig. 4-1) was 0, the mass fraction of the liquid phase reflux entering the pre-separation column was 0.99, the mass fraction of the gas phase reflux entering the pre-separation column was 0.99, the reflux ratio was 20, and the operating pressure was 5 atm; the theoretical plate number of the pre-separation column (region a in fig. 4-1) of the third single-dividing wall column (T13) was 100, the theoretical plate number of the main column (region b in fig. 4-1) was 100, the theoretical plate number of the common rectification section (region c in fig. 4-1) was 50, the theoretical plate number of the common stripping section (region d in fig. 4-1) was 50, the mass fraction of the liquid phase reflux entering the pre-separation column was 0.5, the mass fraction of the gas phase reflux entering the pre-separation column was 0.5, the reflux ratio was 10, and the operating pressure was 2.5 atm. The purities of C6-C10 fraction products (S05, S08, S10, S09 and S06) are respectively 99.1%, 99.5%, 99.2%, 99.7% and 99.0%, and the yields are respectively 95.1%, 95.0%, 95.9%, 95.1% and 96.0%. Wherein the product purity refers to the total mass content of all hydrocarbons of that carbon number.
Example 2
The invention is used in the narrow cut cutting process of Fischer-Tropsch synthesis light oil, and comprises a first double-wall tower (T21), a second double-wall tower (T22), a condenser, a reboiler, a pump, related feeding pipelines and pipelines for connecting the above devices, as shown in figure 2-1. The raw material is 1000g of Fischer-Tropsch synthetic oil light oil, and the light oil comprises hydrocarbons with the carbon number ranging from C6 to C10 and a trace amount of oxygen-containing compounds. The hydrocarbons mainly comprise normal paraffin and alpha-olefin, and also comprise some isoparaffin, internal olefin, branched olefin, and small amount of naphthene, aromatic hydrocarbon and cyclic olefin. The oxygen-containing compound comprises one or more of alcohol, aldehyde, ketone, acid and ester compounds. The theoretical plate number of the pre-separation column (region e in FIG. 4-2) of the first double divided wall column (T21) was 10, the theoretical plate number of the first main column (region f in FIG. 4-2) was 200, the theoretical plate number of the first common rectification section (region g in FIG. 4-2) was 0, the theoretical plate number of the first common stripping section (region h in FIG. 4-2) was 100, the mass fraction of the liquid phase reflux entering the pre-separation column was 0.99, the mass fraction of the gas phase reflux entering the pre-separation column was 0.01, the theoretical plate number of the second main column (region i in FIG. 4-2) was 200, the theoretical plate number of the third main column (region j in FIG. 4-2) was 10, the theoretical plate number of the second common rectification section (region k in FIG. 4-2) was 0, the theoretical plate number of the second common stripping section (region l in FIG. 4-2) was 100, the mass fraction of the liquid phase reflux entering the pre-separation tower and the first main tower is 0.01, the mass fraction of the gas phase reflux entering the pre-separation tower and the first main tower is 0.99, the reflux ratio is 0.1, and the operating pressure is 0.05 atm. The theoretical plate number of the pre-separation column (region e in FIG. 4-2) of the second double divided wall column (T22) was 200, the theoretical plate number of the first main column (region f in FIG. 4-2) was 10, the theoretical plate number of the first common rectification section (region g in FIG. 4-2) was 100, the theoretical plate number of the first common stripping section (region h in FIG. 4-2) was 0, the mass fraction of the liquid phase reflux entering the pre-separation column was 0.01, the mass fraction of the gas phase reflux entering the pre-separation column was 0.99, the theoretical plate number of the second main column (region i in FIG. 4-2) was 10, the theoretical plate number of the third main column (region j in FIG. 4-2) was 200, the theoretical plate number of the second common rectification section (region k in FIG. 4-2) was 100, the theoretical plate number of the second common stripping section (region l in FIG. 4-2) was 0, the mass fraction of the liquid phase reflux entering the pre-separation tower and the first main tower is 0.99, the mass fraction of the gas phase reflux entering the pre-separation tower and the first main tower is 0.01, the reflux ratio is 20, and the operating pressure is 5 atm. The purities of C6-C10 fraction products (S06, S07, S8, S09 and S04) are respectively 99.0%, 99.7%, 99.2%, 99.3% and 99.5%, and the yields are respectively 95.5%, 95.3%, 95.2%, 95.8% and 95.0%. Wherein the product purity refers to the total mass content of all hydrocarbons of that carbon number.
Example 3
The invention is used in the narrow cut cutting process of Fischer-Tropsch synthesis light oil, and comprises a five-wall column (T3), a condenser, a reboiler, a pump, related feed lines and lines connecting the above devices, as shown in FIG. 3. The raw material is 1000g of Fischer-Tropsch synthetic oil light oil, and the light oil comprises hydrocarbons with the carbon number ranging from C6 to C10 and a trace amount of oxygen-containing compounds. The hydrocarbons mainly comprise normal paraffin and alpha-olefin, and also comprise some isoparaffin, internal olefin, branched olefin, and small amount of naphthene, aromatic hydrocarbon and cyclic olefin. The oxygen-containing compound comprises one or more of alcohol, aldehyde, ketone, acid and ester compounds. The theoretical plate number of a pre-separation column (region 1 in fig. 4-3) of the five-divided wall column (T3) was 200, the theoretical plate number of the first main column (region 2 in fig. 4-3) was 10, the theoretical plate number of the first common rectification section (region 3 in fig. 4-3) was 100, the theoretical plate number of the first common stripping section (region 4 in fig. 4-3) was 100, the mass fraction of the liquid phase reflux entering the pre-separation column was 0.01, and the mass fraction of the gas phase reflux entering the pre-separation column was 0.01; the theoretical plate number of the second main column (5 regions in fig. 4-3) is 10, the theoretical plate number of the third main column (6 regions in fig. 4-3) is 200, the theoretical plate number of the second common rectification section (7 regions in fig. 4-3) is 50, the theoretical plate number of the second common stripping section (8 regions in fig. 4-3) is 50, the mass fraction of the liquid phase reflux entering the pre-separation column and the first main column is 0.2, and the mass fraction of the gas phase reflux entering the pre-separation column and the first main column is 0.2; the theoretical plate number of the fourth main column (region 9 in fig. 4-3) is 100, the theoretical plate number of the fifth main column (region 10 in fig. 4-3) is 100, the theoretical plate number of the sixth main column (region 11 in fig. 4-3) is 100, the theoretical plate number of the third common rectification section (region 12 in fig. 4-3) is 70, the theoretical plate number of the third common stripping section (region 13 in fig. 4-3) is 30, the mass fraction of the liquid phase reflux entering the pre-separation column, the first main column and the second main column is 0.5, and the mass fraction of the gas phase reflux entering the pre-separation column, the first main column and the second main column is 0.5; the theoretical plate number of the seventh main column (14 regions in fig. 4-3) was 30, the theoretical plate number of the eighth main column (15 regions in fig. 4-3) was 150, the theoretical plate number of the ninth main column (16 regions in fig. 4-3) was 60, the theoretical plate number of the tenth main column (17 regions in fig. 4-3) was 800, the theoretical plate number of the fourth common rectifying section (18 regions in fig. 4-3) was 20, the theoretical plate number of the fourth common stripping section (19 regions in fig. 4-3) was 90, the mass fraction of the liquid phase reflux into the pre-separation column, the first main column, the second main column and the fourth main column was 0.7, and the mass fraction of the gas phase reflux into the pre-separation column, the first main column, the second main column and the fourth main column was 0.7; the theoretical plate number of the eleventh main column (20 regions in FIGS. 4-3) was 30, the theoretical plate number of the twelfth main column (21 regions in FIGS. 4-3) was 70, the theoretical plate number of the thirteenth main column (22 regions in FIGS. 4-3) was 40, the theoretical plate number of the fourteenth main column (23 regions in FIGS. 4-3) was 100, the theoretical plate number of the fifteenth main column (24 regions in FIGS. 4-3) was 200, the theoretical plate number of the fifth common rectification section (25 regions in FIGS. 4-3) was 50, the theoretical plate number of the fifth common stripping section (26 regions in FIGS. 4-3) was 30, the mass fraction of the liquid phase reflux into the pre-separation column, the first main column, the second main column, the fourth main column and the eleventh main column was 0.9, the gas phase reflux into the pre-separation column, the mass fraction of the first main column, the second main column, the fourth main column and the eleventh main column is 0.9; the reflux ratio was 10 and the operating pressure was 1 atm. The purities of C6-C10 fraction products (S06, S07, S8, S09 and S04) are respectively 99.0%, 99.1%, 99.2%, 99.3% and 99.4%, and the yields are respectively 95.1%, 95.3%, 95.2%, 95.0% and 95.0%. Wherein the product purity refers to the total mass content of all hydrocarbons of that carbon number.