US20010019015A1 - Novel photochemical gas-liquid process for halogenating alkylbenzenes - Google Patents
Novel photochemical gas-liquid process for halogenating alkylbenzenes Download PDFInfo
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- US20010019015A1 US20010019015A1 US09/785,317 US78531701A US2001019015A1 US 20010019015 A1 US20010019015 A1 US 20010019015A1 US 78531701 A US78531701 A US 78531701A US 2001019015 A1 US2001019015 A1 US 2001019015A1
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- 238000000034 method Methods 0.000 title claims abstract description 65
- 239000007788 liquid Substances 0.000 title claims abstract description 29
- 150000004996 alkyl benzenes Chemical class 0.000 title claims abstract description 9
- 230000002140 halogenating effect Effects 0.000 title claims abstract description 6
- 230000005855 radiation Effects 0.000 claims abstract description 16
- 239000012295 chemical reaction liquid Substances 0.000 claims abstract description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 44
- 239000007789 gas Substances 0.000 claims description 39
- 238000005660 chlorination reaction Methods 0.000 claims description 28
- 230000000630 rising effect Effects 0.000 claims description 6
- 239000007792 gaseous phase Substances 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 description 42
- 239000012530 fluid Substances 0.000 description 17
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 16
- XEMRAKSQROQPBR-UHFFFAOYSA-N (trichloromethyl)benzene Chemical compound ClC(Cl)(Cl)C1=CC=CC=C1 XEMRAKSQROQPBR-UHFFFAOYSA-N 0.000 description 14
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 14
- 229940073608 benzyl chloride Drugs 0.000 description 13
- 229910052801 chlorine Inorganic materials 0.000 description 12
- 239000000460 chlorine Substances 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 11
- CAHQGWAXKLQREW-UHFFFAOYSA-N Benzal chloride Chemical compound ClC(Cl)C1=CC=CC=C1 CAHQGWAXKLQREW-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 5
- 230000002093 peripheral effect Effects 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 238000004821 distillation Methods 0.000 description 4
- 238000005658 halogenation reaction Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000026030 halogenation Effects 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- -1 benzyl chloro-chlorides Chemical class 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 150000001804 chlorine Chemical class 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000005297 pyrex Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical class C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical group 0.000 description 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910021652 non-ferrous alloy Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000006552 photochemical reaction Methods 0.000 description 1
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/10—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms
- C07C17/14—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms in the side-chain of aromatic compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J19/12—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electromagnetic waves
- B01J19/122—Incoherent waves
- B01J19/123—Ultraviolet light
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00051—Controlling the temperature
- B01J2219/00074—Controlling the temperature by indirect heating or cooling employing heat exchange fluids
- B01J2219/00087—Controlling the temperature by indirect heating or cooling employing heat exchange fluids with heat exchange elements outside the reactor
- B01J2219/0009—Coils
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/19—Details relating to the geometry of the reactor
- B01J2219/194—Details relating to the geometry of the reactor round
- B01J2219/1941—Details relating to the geometry of the reactor round circular or disk-shaped
- B01J2219/1946—Details relating to the geometry of the reactor round circular or disk-shaped conical
Definitions
- the present invention relates to a novel photochemical gas-liquid process for halogenating alkylbenzenes, particularly a process for chlorination of toluene.
- Photochemical chlorination, or in broader terms halogenation, of hydrocarbon derivatives is currently employed on a wide scale. Nevertheless, in reactions involving substituting hydrogen atoms by chlorine atoms, numerous problems of selectivity occur.
- One representative example of photochemical chlorination is the chlorination of alkyl-benzene, particularly toluene.
- JP-A-85 25153 discloses a benzene chlorination reactor, but this chlorination reaction does not involve in any critical way the problems of selectivity listed above for toluene.
- This reactor is a special reactor, having fluid convection.
- the vertical cylindrical reaction vessel has an internal cylindrical wall with a mirror surface.
- An internal fluid circulation is achieved by means of a rising flow inside the cylinder, and a descending flow between the outer casing of said cylindrical wall and the said internal wall.
- the reaction vessel is fed with gas from the bottom, and the light source is disposed inside the reactor.
- the present invention provides a photochemical gas-liquid process for halogenating alkylbenzenes enabling high yield and high selectivity to be achieved together with other advantages.
- FIG. 1 is a general view of a reactor for carrying out the process according to the invention
- FIG. 2 is a diagrammatical view illustrating one embodiment of a reactor for carrying out the process of the, invention
- FIG. 3 is a diagrammatical view showing a second embodiment of a reactor for carrying out the present process
- FIG. 4 shows an alternative embodiment of the reactor for carrying out the present process
- FIG. 5 shows another embodiment of the reactor for carrying out the present process
- FIG. 6 shows a distributor
- FIG. 7 shows a further embodiment of a reactor for carrying out the process according to the present invention
- FIG. 8 shows an example of a plant or production line comprising several reactors
- FIG. 9 shows a further embodiment of the invention.
- the present invention provides a process for halogenating alkylbenzenes which is carried out in an axially symmetric photochemical gas/liquid reactor, comprising:
- At least one gas distributor at the bottom of said reactor
- inner sleeve means arranged concentrically between the source of radiation and the vessel, said inner sleeve means allowing internal recirculation of reaction liquid, said recirculation comprising a rising movement in the space located between the source and the inner sleeve means and a descending movement in the space situated between the vessel and the inner sleeve means.
- the present process is particularly useful for chlorinating toluene. This process allows a selectivity towards benzyl chloride or benzylidene chloride or phenylchloroform, depending upon the desired product.
- This reactor for carrying out the process enables three concentric zones to be defined inside the reactor:
- annular reaction zone disposed around the central zone and including, at its lower portion, a gas distribution system with calibrated orifices making it possible to impose a certain size on the gas bubbles.
- the originality of the reaction zone i.e. the area between the source and the inner sleeve means, lies in the controlled rising recirculation of the liquid therein, along the source;
- a peripheral zone in which there is controlled descending circulation of liquid that has undergone exchange in the reaction zone.
- This zone further provides the heat exchange necessary to maintain suitable temperatures via heat exchange surfaces (with heating, or more frequently cooling, provided on the outer wall of the reactor).
- the cross-section of the reaction zone of an internal-recirculation reactor is some three times smaller than that of a conventional reactor, without recirculation, for the same gas flow rate;
- the presence of the inner sleeve means close to the reactor wall enables a considerable, up to threefold, increase in overall heat exchange coefficient. This increase in exchange coefficient is particularly useful when designing large-capacity reactors;
- the inner sleeve means extends down to the level of the distributor or down to an intermediate level situated between the distributor and the bottom of the vessel.
- the inner sleeve means extend down to the bottom of the vessel and includes a series of orifices located at an intermediate level between the distributor and the bottom of the vessel
- the inner sleeve means can have any form provided it fulfils the recirculation function. Its shape can notably be a scaled-down version of the reactor wall. Viewed in cross-section, it can have a straight section or segment, at the upper or lower, or both, ends of which one or more other segments or curved sections making an angle with the straight segment can be present.
- the inner sleeve means can also be subdivided into sub-sections, either arranged horizontally in line thus forming calibrated sleeve means or alternately offset with respect to each other, in other words when viewed in cross-section, the sub-sections are arranged in line but making an angle with the general direction of the sleeve member.
- the sleeve means can also consist of sub-sections arranged generally vertically but with gaps of varying dimensions between them. They can also be offset from each other in the radial direction of the reactor. Last, it should be noted that this inner sleeve means can also be mirror-like so as to reflect inwards the radiation emitted by the source.
- the inner sleeve means should be considered in this invention to mean any means capable of ensuring internal liquid recirculation.
- the inner sleeve means includes slots of a calibrated size along part or all of its length.
- Internal recirculation which is a feature of the reactor for carrying out the process according to the invention, preferably starts at a point below the distributor, in the vicinity of the bottom of the vessel, the liquid flow thus passing through the space defined by the distributor.
- the central radiation source can be arranged in several alternative ways inside the reactor.
- the source extends right through the reactor from one end to the other.
- the source passes through the reactor cover only.
- the central source preferably consists of one or several transparent tube(s) arranged in axial symmetry, a single tube being employed advantageously.
- Any suitable gas distributor can be employed, such as a grid, concentrically perforated toroidal members or any other embodiment readily accessible to the person skilled in the art.
- the distributor(s) consist(s) of one or several concentric toroidal members provided with calibrated holes in their upper halves.
- the reactor comprises one single distributor at the bottom of the reactor.
- the reactor comprises at least two distributors, situated at different levels inside said reactor.
- the velocity of the liquid in the rising movement occurring in the space situated between said source and said inner sleeve member is comprised between 0.1 and 0.8 m/s and preferably between 0.25 and 0.60 m/s.
- the velocity of the gas relative to the reactor is U+V.
- the velocity of the gas U+V is comprised between 0.3 and 1.1 m/s.
- the velocity of the liquid in the descending movement situated in the space between said inner sleeve means and said vessel is comprised between 0.5 and 3 m/s, preferably between 1 and 2.5 m/s.
- the fraction of the volume occupied by the gaseous phase represents 10 to 50%, preferably 20 to 40% by volume, of the volume of the vessel defined between the source and the inner sleeve means.
- the diameter of the bubbles generated by the distributor is comprised between 3 and 15 mm, preferably 6 and 10 mm.
- the reactor for carrying out the process of the present invention is one having axial symmetry, and is preferably a body of revolution. It can be cylindrical or cylindroconical.
- FIG. 1 shows a general view of a reactor for carrying out the process according to the present invention.
- Reactor 1 comprises several individual parts manufactured from materials that are appropriate to the chemical reaction considered. For example, for the chlorination of toluene, the parts of the reactor are manufactured from non-ferrous alloys, for example nickel or alloys thereof.
- Reactor 1 comprises a vessel 2 , a central source of radiation 3 which conventionally is a transparent tube, and a distributor 4 .
- the dimensions of the reactor, defined by its vessel are typically: length: 1 to 4 m, advantageously 1.5 to 3 m, diameter: 0.5 to 2 m, advantageously 0.7 to 1.5 m.
- the transparent tube or tubes are generally in pyrex glass or quartz, or in any other material which is transparent within the range covering the radiation wavelength employed.
- the wavelength corresponds to the ultraviolet (U.V.) part of the spectrum.
- This tube can be made of a material that is transparent to the wavelength employed, for example U.V., and which is substantially opaque to other wavelengths in order to limit the formation of by-products or the breakdown of the desired products, which could possibly happen at wavelength different from the working wavelength.
- This result is achieved for example with pyrex glass which is transparent to U.V., in other words a radiation of about 250 to 400 nm wavelength, but which is substantially opaque to radiation below 200 nm.
- the number of lamps and their power vary with the desired production capacity.
- the number of lamps is generally comprised between 1 and 10, and most frequently between 2 and 4, one lamp being however one of the preferred embodiments.
- Their individual power varies between 0.1 kW and 20 kW, most frequently between 0.2 and 4 kW.
- the individual power of the lamps varies between 0.1 kW and 20 kW, most frequently between 0.2 and 4 kW.
- These lamps can be arranged around a central rod which acts as a support, or be disposed within several tubes.
- the lamps can be at the same level or on different levels.
- the tube or tubes have quite conventional dimensions and their length substantially corresponds to the length of the reactor. Actually, the tube length is such that the tube or tubes are substantially completely immersed in the reaction fluid.
- the diameter of the central tube, when only one tube is employed, is conventionally comprised between 50 and 500 mm, advantageously 100 to 200 mm.
- the reactor moreover comprises, according to the invention, inner sleeve means 5 providing recirculation.
- the cylindrical or cylindricoconical reactor arranged in correspondence to the present invention comprises, moving from the axis towards the periphery:
- a central transparent tube designed to house the radiation source
- a peripheral zone (b) around the reaction zone the purpose of which is to ensure recirculation of the fluid from the reaction zone, and to facilitate heat exchange.
- zone (a) the direction of recirculation is indicated by the solid arrow whereas the direction of circulation in zone (b) is indicated by the dashed arrow as shown in FIG. 1.
- the entrained fluid overflows into the peripheral recycling and heat exchange zone, whereas the gas consisting of gas introduced that has not reacted and, possibly, gas produced by the reaction is evacuated from the top portion of the reactor. Nevertheless, the gas that has not reacted is frequently negligible in view of the efficiency of the reactors described here.
- the flow of unfixed chlorine becomes negligible at the end of chlorination, during chlorination of the substituting methyl group on the aromatic ring.
- the reactor also comprises an outer jacket 6 of the doublewall type preferably in the form of half-shells, ensuring heat exchange.
- the existence of the inner sleeve means or intermediate wall enables a significant increase in heat exchange coefficients to be obtained, thus significantly reducing the surface area required for heat exchange, when compared to the-areas needed in a conventional reactor without internal recirculation.
- the inner sleeve means 5 can be located inside the reactor according to several possible dispositions.
- FIGS. 2 and 3 give two embodiments.
- FIG. 2 shows an embodiment in which the intermediate inner sleeve means stops at distributor level, or at a level between the distributor and the bottom of the reactor.
- S′ which determines the recirculation velocity and flow rate and consequently the velocity of flow in the reaction zone having a surface area of S.
- the section S′ is calculated so that the specified velocity of the fluid in the reaction zone is comprised between 0.1 and 0.8 m.s ⁇ 1 , and that the fraction of the volume occupied by the gas represents 10 to 50%, preferably 20 to 40% of the volume of the reaction zone.
- the velocity of flow in the recirculation zone between the inner sleeve means and the vessel is then generally comprised between 1 and 3 m.s ⁇ 1 .
- This embodiment, where the inner sleeve means stops at distributor level, or at a level comprised between the distributor and the bottom of the reactor, is recommended but is not limited-to the case where reaction-kinetics are fast and requires efficient heat exchange, rendered possible by the high velocity of the fluid in the reaction zone.
- FIG. 2 shows the specific embodiment in which the inner sleeve means stops at distributor level, on FIG. 5 a.
- FIG. 3 shows another embodiment in which the inner sleeve means extends down to the bottom of the reactor.
- Orifices 7 are provided at the lower portion of the intermediate inner sleeve means. Preferably their outlet is oriented towards the gas distributor so as to ensure permanent renewal of fluid at this level. This orientation is shown on FIG. 3.
- These orifices may be jets, circular holes, rectangular slots, or of other types. The number and cross-sectional area of these orifices are determined so as to adjust the fluid flow rate/gas flow rate ratio to the selected value. Adjustment of this ratio enables the velocity of flow in the reaction zone to be varied.
- the surface area S′ or section of the recirculation peripheral zone no longer determines the fluid flow rate, and can be increased at will.
- This configuration is recommended for reactions having a relatively slow reaction rate and where it is desired to preserve a sufficient mass of liquid in the peripheral zone for operational stability, but is not limited to such-reactions. Operating conditions, regarding velocity of flow and the fraction of the volume occupied by the gaseous phase are similar to those in the previous embodiment.
- FIG. 4 shows an embodiment in which the tube constituting the source of radiation passes right through the reactor, the tube then being open at both ends. It can pass through the central end pipe fittings of the cover and base, 8 a and 8 b respectively of the reactor when such end pipe fittings are present. These end pipe fittings, for introducing gas at the bottom and drawing it off at the top of the reactor can obviously also be provided laterally just like in any other of the embodiments according to the present invention.
- a retaining grid 9 rigidly fixed to the bottom end fitting of the reactor prevents the tube from changing position, and simultaneously acts as a support for a central rod designed to support the lamps.
- Sealing at the bottom of the reactor is provided by a sliding assembly comprising, notably, an annular seal 10 generally in PTFE or any other material, which is resistant to the reaction medium and a clamping arrangement for the annular seal mounted on a non-rigid support.
- Sealing at cover level of the reactor is obtained using the same principle but with the addition of an expansion concertina arrangement 11 designed to compensate variation in expansion between the transparent tube and the reactor.
- the tube end fittings at the cover and bottom of the reactor are connected to a circuit so that, in the unlikely case that the transparent tube breaks, there can be no danger of a breakdown of confinement and escape to the outer medium.
- the opening in the transparent tube at the two ends thereof allows regulated and pressurized circulation of inert gas inside the transparent tube.
- FIG. 5 shows an embodiment in which the tube only passes through the cover.
- the tube is blind, in other words is closed at its lower portion.
- the lower rounded end of the tube rests on a stopper 12 , preferably of PTFE, placed in the tube end fitting at the bottom of the reactor.
- the hollow shape of the stopper allows the transparent tube to slide sufficiently to absorb variations in expansion between the transparent tube and the reactor. The need to fit the concertina arrangement counteracting expansion at the reactor cover level then becomes superfluous.
- FIGS. 6 a and 6 b are a sectional view of a distributor according to one embodiment of the invention, FIG. 6 a showing a distributor and FIG. 6 b being a cross-sectional view thereof.
- This distributor consists of one or several concentric rings 13 a and 13 b adapted to the size of the reactor and carrying holes 14 scaled up to specific dimensions generally comprised between 3 and 15 mm and, most frequently, between 6 and 10 mm. A free space is left between the rings, representing from 40 to 80% of the cross-section of the reaction zone and this is designed to allow the recycled liquid to flow below the distributor.
- the calibrated holes are generally arranged on the upper half of the ring in two rows separated by a central angle which can vary but is most frequently comprised between 60 and 180°and, preferably, 90 to 135° to facilitate gas bubble entrainment in the flow of recirculation fluid.
- Several smaller holes 15 are also provided at the bottom portion to ensure fluid can flow out when the reactor is shut down, and then started up.
- the reactor is dimensioned so as to obtain a velocity of fluid circulation comprised between 0.1 and 0.8 m/s, preferably 0.25 and 0.60 m/s and the gaseous phase constituting from 10 to 50%, preferably 20 to 40% of the volume of the reaction zone.
- FIG. 7 shows one alternative embodiment of the present invention in which several distributors are present and in which the reactor has a cylindro-conical shape.
- Three distribution levels, 4 a , 4 b and 4 c are shown in this figure at levels O, H 1 and H 2 .
- H is the total height of the reaction zone.
- the dimensions of the cylindro-conical reactor are given by D 1 ib which is the inside diameter at the bottom of the vessel, D 1 ih, the inner diameter at the top part of the vessel, and D 2 eh is the outside diameter of the inner sleeve means at the top thereof.
- D 1 ib is the inside diameter at the bottom of the vessel
- D 1 ih the inner diameter at the top part of the vessel
- D 2 eh is the outside diameter of the inner sleeve means at the top thereof.
- the gas flow from the lower distributors gets added to the flow from the upper distributors.
- the reactor is provided with this particular shape so as to substantially
- FIG. 8 is a diagrammatical representation of an installation comprising several reactors according to the invention. The mode of operation of the plant is detailed in example 2.
- FIG. 9 shows another alternative embodiment of a reactor in which the inner ring member is a plate provided with calibrated slots 5 a . These slots may be present on only a part of the tubular member. This enables recirculation to be primed and maintained regardless of the level to which the reactor is filled.
- the other reference numerals are identical to those employed in FIGS. 1 to 3 .
- the invention thus provides a halogenation process carried out in the above-described reactor.
- the following are examples which should not be considered as limiting, of typical reactions:
- methylbenzene (toluene, xylenes, tri- and polymethylbenzenes);
- polycyclic aromatic hydrocarbons methyl-naphthalenes, for example
- Reactors used with these processes can be employed singly or coupled, for example in series, with other reactors which may be conventional or in accordance with the present invention.
- the chlorination reaction of toluene can be mentioned by way of example, in which three desired products can be obtained, benzyl chloride (monosubstitution), benzylidene chloride (disubstitution) and phenylchloroform (trisubstitution or complete substitution).
- FIG. 8 illustrates an example of a plant or production line for phenyl-chloroform.
- the first reactor is fed with toluene.
- the necessary chlorine is distributed by means of a multi-stage feed, in a calculated manner between the various reactors so as to ensure regular progression of chlorination from the first up to the last reactor.
- the first reactor is moreover supplied with the gaseous effluent from the reactors that follow it so as to recycle unfixed chlorine originating from the intermediate reactions, and the final reaction, implemented in the remainder of the reactors.
- This plant enables phenylchloroform in a 98% guaranteed content to be obtained at the outlet from the last reactor. Moreover, this plant allows mixtures rich in benzylchloride and/or benzylidene chloride to be drawn off at other stages, and particularly at the first stage. After distillation of these mixtures, benzyl chloride or benzylidene chloride of high purity can be obtained.
- the reactor of the present invention furthermore makes it possible to reduce the number of reactors in series in a production line, notably one producing phenylchloroform.
- a cylindro-conical reactor having three injection levels as shown in FIG. 7 was employed.
- the dimensions of this reactor, with reference to FIG. 7 were:
- the final stage is discontinuous.
- the last reactor fulfils the multiple functions of regulating the end of chlorination as well as the temporary storage reservoir for supplementary analytic analyses. Its dimensions are as follows:
- the inner sleeve means defining the recirculation zone was provided with calibrated slots in accordance with FIG. 9, enabling recirculation to be primed regardless of the level to which the discontinuous reactor was filled.
- the last reactor can advantageously be replaced by a continuous reactor the inner sleeve means of which, defining the recirculation zone, descends down to the bottom of the reactor as in FIG. 3, the respective dimensions of which are:
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Abstract
The invention provides a process for carrying out a photochemical gas-liquid process for halogenating alkyl-benzenes, said process being carried out in a photochemical gas-liquid reactor comprising a vessel, a central source of radiation, a gas distributor, and additionally, inner sleeve means arranged concentrically between the source of radiation and the vessel, said inner sleeve means providing for internal recirculation of reaction liquid.
Description
- The present invention relates to a novel photochemical gas-liquid process for halogenating alkylbenzenes, particularly a process for chlorination of toluene.
- Photochemical chlorination, or in broader terms halogenation, of hydrocarbon derivatives is currently employed on a wide scale. Nevertheless, in reactions involving substituting hydrogen atoms by chlorine atoms, numerous problems of selectivity occur. One representative example of photochemical chlorination is the chlorination of alkyl-benzene, particularly toluene.
- Photochemical chlorination of toluene principally leads to the formation of benzyl chloride, benzylidene chloride and phenylchloroform.
- It is also known that apart from this principal chlorination of the methyl group of the toluene molecule, unwanted small amounts of chlorinated derivatives on the aromatic ring always form, particularly chlorotoluenes and homologous compounds thereof: benzyl chloro-chlorides, benzylidene chloro-chlorides and chlorophenylchloroforms.
- It is moreover known that the proportion of chlorine derivatives on the aromatic ring increases substantially as the degree of chlorination of the mixture increases. Starting from 0.1 to 0.5%, when limited to benzyl chloride, the proportion of chlorine derivatives on the aromatic ring can reach or even exceed 5% when it is desired to achieve complete chlorination of the methyl group, for the purposes of producing essentially phenylchloroform.
- For this reason, it is difficult to obtain high-purity phenylchloroform by direct chlorination without having recourse to distillation of the reaction mixture. Certain patents hence consider carrying out incomplete chlorination in order to limit the formation of derivatives, and to then subsequently distil the mixtures obtained with a subsequent increase in cost price.
- Numerous photochemical reactors have been developed, some of them for a specific use. Thus JP-A-85 25153 discloses a benzene chlorination reactor, but this chlorination reaction does not involve in any critical way the problems of selectivity listed above for toluene. This reactor is a special reactor, having fluid convection. The vertical cylindrical reaction vessel has an internal cylindrical wall with a mirror surface. An internal fluid circulation is achieved by means of a rising flow inside the cylinder, and a descending flow between the outer casing of said cylindrical wall and the said internal wall. The reaction vessel is fed with gas from the bottom, and the light source is disposed inside the reactor.
- The documents “Reaktionsapparate für Gas-Flüssig-Reaktionen”, p. 372, and “Chemischtechnisches Lexikon” describe reactors of the type convection reactor using the air-lift principle and/or which include an entraining flow which is injected at the base of the apparatus. The example of implementation concerns oxidation of n-butane.
- None of these documents discloses the process according to the present invention.
- The present invention provides a photochemical gas-liquid process for halogenating alkylbenzenes enabling high yield and high selectivity to be achieved together with other advantages.
- FIG. 1 is a general view of a reactor for carrying out the process according to the invention;
- FIG. 2 is a diagrammatical view illustrating one embodiment of a reactor for carrying out the process of the, invention;
- FIG. 3 is a diagrammatical view showing a second embodiment of a reactor for carrying out the present process;
- FIG. 4 shows an alternative embodiment of the reactor for carrying out the present process;
- FIG. 5 shows another embodiment of the reactor for carrying out the present process;
- FIG. 6 shows a distributor;
- FIG. 7 shows a further embodiment of a reactor for carrying out the process according to the present invention;
- FIG. 8 shows an example of a plant or production line comprising several reactors;
- FIG. 9 shows a further embodiment of the invention.
- The present invention provides a process for halogenating alkylbenzenes which is carried out in an axially symmetric photochemical gas/liquid reactor, comprising:
- a vessel;
- a central source of radiation;
- at least one gas distributor, at the bottom of said reactor;
- inner sleeve means arranged concentrically between the source of radiation and the vessel, said inner sleeve means allowing internal recirculation of reaction liquid, said recirculation comprising a rising movement in the space located between the source and the inner sleeve means and a descending movement in the space situated between the vessel and the inner sleeve means.
- The present process is particularly useful for chlorinating toluene. This process allows a selectivity towards benzyl chloride or benzylidene chloride or phenylchloroform, depending upon the desired product.
- This reactor for carrying out the process enables three concentric zones to be defined inside the reactor:
- a central zone where the source of radiation is provided;
- an annular reaction zone disposed around the central zone and including, at its lower portion, a gas distribution system with calibrated orifices making it possible to impose a certain size on the gas bubbles. The originality of the reaction zone, i.e. the area between the source and the inner sleeve means, lies in the controlled rising recirculation of the liquid therein, along the source;
- a peripheral zone in which there is controlled descending circulation of liquid that has undergone exchange in the reaction zone. This zone further provides the heat exchange necessary to maintain suitable temperatures via heat exchange surfaces (with heating, or more frequently cooling, provided on the outer wall of the reactor).
- Reactors for carrying out the present process also enable the following aims to be met:
- the cross-section of the reaction zone of an internal-recirculation reactor is some three times smaller than that of a conventional reactor, without recirculation, for the same gas flow rate;
- a two to three-fold reduction in the height of liquid through which the gas needs to pass in order to achieve the same degree of chlorine or halogen fixation;
- recirculation of liquid along the source of radiation enables the latter to be used much more efficiently. The number and power of the lamps can be reduced, and they can all be housed in a single central tube, even for high-capacity reactors;
- the presence of the inner sleeve means close to the reactor wall enables a considerable, up to threefold, increase in overall heat exchange coefficient. This increase in exchange coefficient is particularly useful when designing large-capacity reactors;
- the combination of the above advantages enables reactors to be designed which are much smaller and compact when compared to conventional reactors of equivalent production capacity, or individual production capacities to be obtained which are well above those obtainable in conventional reactors not employing recirculation.
- In one embodiment, the inner sleeve means extends down to the level of the distributor or down to an intermediate level situated between the distributor and the bottom of the vessel.
- In another embodiment, the inner sleeve means extend down to the bottom of the vessel and includes a series of orifices located at an intermediate level between the distributor and the bottom of the vessel
- Regarding the inner sleeve means, this can have any form provided it fulfils the recirculation function. Its shape can notably be a scaled-down version of the reactor wall. Viewed in cross-section, it can have a straight section or segment, at the upper or lower, or both, ends of which one or more other segments or curved sections making an angle with the straight segment can be present. The inner sleeve means can also be subdivided into sub-sections, either arranged horizontally in line thus forming calibrated sleeve means or alternately offset with respect to each other, in other words when viewed in cross-section, the sub-sections are arranged in line but making an angle with the general direction of the sleeve member. The sleeve means can also consist of sub-sections arranged generally vertically but with gaps of varying dimensions between them. They can also be offset from each other in the radial direction of the reactor. Last, it should be noted that this inner sleeve means can also be mirror-like so as to reflect inwards the radiation emitted by the source.
- Thus any arrangement of the inner sleeve means is possible, provided it is able to fulfil the recirculation function. Thus, the inner sleeve means should be considered in this invention to mean any means capable of ensuring internal liquid recirculation.
- In one embodiment, the inner sleeve means includes slots of a calibrated size along part or all of its length.
- Internal recirculation, which is a feature of the reactor for carrying out the process according to the invention, preferably starts at a point below the distributor, in the vicinity of the bottom of the vessel, the liquid flow thus passing through the space defined by the distributor.
- The central radiation source can be arranged in several alternative ways inside the reactor.
- In one embodiment, the source extends right through the reactor from one end to the other.
- In another embodiment, the source passes through the reactor cover only.
- The central source preferably consists of one or several transparent tube(s) arranged in axial symmetry, a single tube being employed advantageously.
- Any suitable gas distributor can be employed, such as a grid, concentrically perforated toroidal members or any other embodiment readily accessible to the person skilled in the art.
- Preferably, the distributor(s) consist(s) of one or several concentric toroidal members provided with calibrated holes in their upper halves.
- In one embodiment, the reactor comprises one single distributor at the bottom of the reactor.
- In another embodiment, the reactor comprises at least two distributors, situated at different levels inside said reactor.
- The operating conditions of the reactor as regards temperature, pressure and so on are those conventionally employed for the particular reaction.
- Preferably, the velocity of the liquid in the rising movement occurring in the space situated between said source and said inner sleeve member is comprised between 0.1 and 0.8 m/s and preferably between 0.25 and 0.60 m/s.
- With the liquid velocity designated as U and the velocity of the gas with respect to the velocity of the liquid designated by V, the velocity of the gas relative to the reactor is U+V. In one embodiment, the velocity of the gas U+V is comprised between 0.3 and 1.1 m/s.
- Preferably, the velocity of the liquid in the descending movement situated in the space between said inner sleeve means and said vessel is comprised between 0.5 and 3 m/s, preferably between 1 and 2.5 m/s.
- Preferably, the fraction of the volume occupied by the gaseous phase represents 10 to 50%, preferably 20 to 40% by volume, of the volume of the vessel defined between the source and the inner sleeve means.
- Preferably, the diameter of the bubbles generated by the distributor is comprised between 3 and 15 mm, preferably 6 and 10 mm.
- The reactor for carrying out the process of the present invention, is one having axial symmetry, and is preferably a body of revolution. It can be cylindrical or cylindroconical.
- The reactor and its implementation for carrying out the process of the invention will now be described in detail, with reference to the figures of the drawing.
- FIG. 1 shows a general view of a reactor for carrying out the process according to the present invention.
Reactor 1 comprises several individual parts manufactured from materials that are appropriate to the chemical reaction considered. For example, for the chlorination of toluene, the parts of the reactor are manufactured from non-ferrous alloys, for example nickel or alloys thereof.Reactor 1 comprises avessel 2, a central source ofradiation 3 which conventionally is a transparent tube, and a distributor 4. The dimensions of the reactor, defined by its vessel, are typically: length: 1 to 4 m, advantageously 1.5 to 3 m, diameter: 0.5 to 2 m, advantageously 0.7 to 1.5 m. The transparent tube or tubes are generally in pyrex glass or quartz, or in any other material which is transparent within the range covering the radiation wavelength employed. Conventionally, the wavelength corresponds to the ultraviolet (U.V.) part of the spectrum. This tube can be made of a material that is transparent to the wavelength employed, for example U.V., and which is substantially opaque to other wavelengths in order to limit the formation of by-products or the breakdown of the desired products, which could possibly happen at wavelength different from the working wavelength. This result is achieved for example with pyrex glass which is transparent to U.V., in other words a radiation of about 250 to 400 nm wavelength, but which is substantially opaque to radiation below 200 nm. The number of lamps and their power vary with the desired production capacity. The number of lamps is generally comprised between 1 and 10, and most frequently between 2 and 4, one lamp being however one of the preferred embodiments. Their individual power varies between 0.1 kW and 20 kW, most frequently between 0.2 and 4 kW. The individual power of the lamps varies between 0.1 kW and 20 kW, most frequently between 0.2 and 4 kW. These lamps can be arranged around a central rod which acts as a support, or be disposed within several tubes. Thus, it is possible to employ either a dual-lamp central light source or 3 single-lamp light sources, account should be taken of the influence of how the light sources are arranged on the hydraulic flow inside the reactor. Depending on the dimensions of the tube, the lamps can be at the same level or on different levels. The tube or tubes have quite conventional dimensions and their length substantially corresponds to the length of the reactor. Actually, the tube length is such that the tube or tubes are substantially completely immersed in the reaction fluid. The diameter of the central tube, when only one tube is employed, is conventionally comprised between 50 and 500 mm, advantageously 100 to 200 mm. The reactor moreover comprises, according to the invention, inner sleeve means 5 providing recirculation. Thus, the cylindrical or cylindricoconical reactor arranged in correspondence to the present invention comprises, moving from the axis towards the periphery: - a central transparent tube designed to house the radiation source;
- an annular reaction zone (a) around the central transparent tube;
- a peripheral zone (b) around the reaction zone, the purpose of which is to ensure recirculation of the fluid from the reaction zone, and to facilitate heat exchange. In zone (a), the direction of recirculation is indicated by the solid arrow whereas the direction of circulation in zone (b) is indicated by the dashed arrow as shown in FIG. 1. At the upper portion of the reaction zone, the entrained fluid overflows into the peripheral recycling and heat exchange zone, whereas the gas consisting of gas introduced that has not reacted and, possibly, gas produced by the reaction is evacuated from the top portion of the reactor. Nevertheless, the gas that has not reacted is frequently negligible in view of the efficiency of the reactors described here. For example, the flow of unfixed chlorine becomes negligible at the end of chlorination, during chlorination of the substituting methyl group on the aromatic ring. One can in fact consider that the gas flow is for the major part made up by gas introduced and vaporised organic compounds, regardless of the rate of fixation of the gas. The reactor also comprises an
outer jacket 6 of the doublewall type preferably in the form of half-shells, ensuring heat exchange. The existence of the inner sleeve means or intermediate wall enables a significant increase in heat exchange coefficients to be obtained, thus significantly reducing the surface area required for heat exchange, when compared to the-areas needed in a conventional reactor without internal recirculation. - The inner sleeve means 5 can be located inside the reactor according to several possible dispositions. FIGS. 2 and 3 give two embodiments.
- FIG. 2 shows an embodiment in which the intermediate inner sleeve means stops at distributor level, or at a level between the distributor and the bottom of the reactor.
-
-
- The section S′ is calculated so that the specified velocity of the fluid in the reaction zone is comprised between 0.1 and 0.8 m.s−1, and that the fraction of the volume occupied by the gas represents 10 to 50%, preferably 20 to 40% of the volume of the reaction zone. The velocity of flow in the recirculation zone between the inner sleeve means and the vessel is then generally comprised between 1 and 3 m.s −1. This embodiment, where the inner sleeve means stops at distributor level, or at a level comprised between the distributor and the bottom of the reactor, is recommended but is not limited-to the case where reaction-kinetics are fast and requires efficient heat exchange, rendered possible by the high velocity of the fluid in the reaction zone. FIG. 2 shows the specific embodiment in which the inner sleeve means stops at distributor level, on FIG. 5a.
- FIG. 3 shows another embodiment in which the inner sleeve means extends down to the bottom of the reactor. Orifices7 are provided at the lower portion of the intermediate inner sleeve means. Preferably their outlet is oriented towards the gas distributor so as to ensure permanent renewal of fluid at this level. This orientation is shown on FIG. 3. These orifices may be jets, circular holes, rectangular slots, or of other types. The number and cross-sectional area of these orifices are determined so as to adjust the fluid flow rate/gas flow rate ratio to the selected value. Adjustment of this ratio enables the velocity of flow in the reaction zone to be varied. In this embodiment, the surface area S′ or section of the recirculation peripheral zone no longer determines the fluid flow rate, and can be increased at will. This configuration is recommended for reactions having a relatively slow reaction rate and where it is desired to preserve a sufficient mass of liquid in the peripheral zone for operational stability, but is not limited to such-reactions. Operating conditions, regarding velocity of flow and the fraction of the volume occupied by the gaseous phase are similar to those in the previous embodiment.
- FIG. 4 shows an embodiment in which the tube constituting the source of radiation passes right through the reactor, the tube then being open at both ends. It can pass through the central end pipe fittings of the cover and base,8 a and 8 b respectively of the reactor when such end pipe fittings are present. These end pipe fittings, for introducing gas at the bottom and drawing it off at the top of the reactor can obviously also be provided laterally just like in any other of the embodiments according to the present invention. A
retaining grid 9 rigidly fixed to the bottom end fitting of the reactor prevents the tube from changing position, and simultaneously acts as a support for a central rod designed to support the lamps. Sealing at the bottom of the reactor is provided by a sliding assembly comprising, notably, anannular seal 10 generally in PTFE or any other material, which is resistant to the reaction medium and a clamping arrangement for the annular seal mounted on a non-rigid support. Sealing at cover level of the reactor is obtained using the same principle but with the addition of anexpansion concertina arrangement 11 designed to compensate variation in expansion between the transparent tube and the reactor. The tube end fittings at the cover and bottom of the reactor are connected to a circuit so that, in the unlikely case that the transparent tube breaks, there can be no danger of a breakdown of confinement and escape to the outer medium. The opening in the transparent tube at the two ends thereof allows regulated and pressurized circulation of inert gas inside the transparent tube. - FIG. 5 shows an embodiment in which the tube only passes through the cover. In this case, the tube is blind, in other words is closed at its lower portion. The lower rounded end of the tube rests on a
stopper 12, preferably of PTFE, placed in the tube end fitting at the bottom of the reactor. The hollow shape of the stopper allows the transparent tube to slide sufficiently to absorb variations in expansion between the transparent tube and the reactor. The need to fit the concertina arrangement counteracting expansion at the reactor cover level then becomes superfluous. - FIGS. 6a and 6 b are a sectional view of a distributor according to one embodiment of the invention, FIG. 6a showing a distributor and FIG. 6b being a cross-sectional view thereof. This distributor consists of one or several
concentric rings holes 14 scaled up to specific dimensions generally comprised between 3 and 15 mm and, most frequently, between 6 and 10 mm. A free space is left between the rings, representing from 40 to 80% of the cross-section of the reaction zone and this is designed to allow the recycled liquid to flow below the distributor. - As indicated in FIG. 6b, the calibrated holes are generally arranged on the upper half of the ring in two rows separated by a central angle which can vary but is most frequently comprised between 60 and 180°and, preferably, 90 to 135° to facilitate gas bubble entrainment in the flow of recirculation fluid. Several
smaller holes 15 are also provided at the bottom portion to ensure fluid can flow out when the reactor is shut down, and then started up. The bubbles of gas introduced entrain recycled fluid at a determined velocity and according to a well defined gas phase/fluid phase ration which is optimized in order to obtain the best reaction kinetic. Generally, the reactor is dimensioned so as to obtain a velocity of fluid circulation comprised between 0.1 and 0.8 m/s, preferably 0.25 and 0.60 m/s and the gaseous phase constituting from 10 to 50%, preferably 20 to 40% of the volume of the reaction zone. - FIG. 7 shows one alternative embodiment of the present invention in which several distributors are present and in which the reactor has a cylindro-conical shape. Three distribution levels,4 a, 4 b and 4 c are shown in this figure at levels O, H1 and H2. H is the total height of the reaction zone. Moreover, the dimensions of the cylindro-conical reactor are given by D1ib which is the inside diameter at the bottom of the vessel, D1ih, the inner diameter at the top part of the vessel, and D2eh is the outside diameter of the inner sleeve means at the top thereof. Here, the gas flow from the lower distributors gets added to the flow from the upper distributors. Thus, the reactor is provided with this particular shape so as to substantially maintain the same flow parameters at all levels in the reactor.
- FIG. 8 is a diagrammatical representation of an installation comprising several reactors according to the invention. The mode of operation of the plant is detailed in example 2.
- FIG. 9 shows another alternative embodiment of a reactor in which the inner ring member is a plate provided with calibrated
slots 5 a. These slots may be present on only a part of the tubular member. This enables recirculation to be primed and maintained regardless of the level to which the reactor is filled. The other reference numerals are identical to those employed in FIGS. 1 to 3. - The invention thus provides a halogenation process carried out in the above-described reactor. The following are examples which should not be considered as limiting, of typical reactions:
- aromatic hydrocarbon side chain chlorination:
- methylbenzene (toluene, xylenes, tri- and polymethylbenzenes);
- other alkylbenzenes; in this case it is chlorination of a carbon atom next to the aromatic ring which is obtained preferably,
- polycyclic aromatic hydrocarbons (methyl-naphthalenes, for example)
- aliphatic hydrocarbon chlorination;
- other halogenations;
- generally speaking:
- all gas-liquid alkylbenzene halogenation reactions in which significant gains in reaction kinetics and selectivity are required thanks to the implementation of optimized recirculation for the liquid velocity in the reaction zone, the volume fraction of gas in the reaction zone, diameter of the bubbles, and recirculation. Such reactors can thus implement any gas-liquid reaction by a suitable choice of optimal values associated with the three parameters above: velocity/fraction/diameter, recirculation being either internal or external with the provision of a recirculation loop.
- Reactors used with these processes can be employed singly or coupled, for example in series, with other reactors which may be conventional or in accordance with the present invention.
- Thus, it is possible to couple an external heat exchanger with recirculation means onto the reactors described. The exchanger can receive part or all the recirculating fluid in the reactor.
- The general principles described also allow current reactors to be modified so that they can be transformed with advantage, through the incorporation of an intermediate tubular member.
- The chlorination reaction of toluene can be mentioned by way of example, in which three desired products can be obtained, benzyl chloride (monosubstitution), benzylidene chloride (disubstitution) and phenylchloroform (trisubstitution or complete substitution).
- When it is desired to essentially produce benzyl chloride, in other words in a benzylidene/benzyl chloride ratio <0.15, a single reactor will generally be used. An incomplete chlorination can be carried out in order to obtain a mixture at the outlet from the reactor containing on average:
- toluene . . . 50 to 40%
- benzyl chloride . . . 46 to 53%
- benzylidene chloride . . . 2 to 7%
- Several smaller reactors can also be connected in series enabling a smaller proportion of benzylidene chloride to be obtained, which may proof to be advantageous.
- When it is desired to produce benzylidene chloride, one can operate as follows. Gaseous effluent from the second reactor is recycled back to the first reactor so as to rid it of the last residual amounts of unfixed chlorine.
- When it is desired to produce phenylchloroform, it is generally preferable to operate with several reactors in series. Two to six reactors in series are employed or even more, 3 to 5 reactors being advantageous. FIG. 8 illustrates an example of a plant or production line for phenyl-chloroform. The first reactor is fed with toluene. The necessary chlorine is distributed by means of a multi-stage feed, in a calculated manner between the various reactors so as to ensure regular progression of chlorination from the first up to the last reactor. The first reactor is moreover supplied with the gaseous effluent from the reactors that follow it so as to recycle unfixed chlorine originating from the intermediate reactions, and the final reaction, implemented in the remainder of the reactors. This plant enables phenylchloroform in a 98% guaranteed content to be obtained at the outlet from the last reactor. Moreover, this plant allows mixtures rich in benzylchloride and/or benzylidene chloride to be drawn off at other stages, and particularly at the first stage. After distillation of these mixtures, benzyl chloride or benzylidene chloride of high purity can be obtained. The reactor of the present invention furthermore makes it possible to reduce the number of reactors in series in a production line, notably one producing phenylchloroform.
- It is thus possible, thanks to the advantages reactors implementing the process provide, to obtain production capacities of 20 to 25000 metric tons/year, expressed of fixed chlorine, either from a single reactor if benzyl chloride is concerned or from a scaled-down production line if phenyl-chloroform is concerned. Moreover, the increase in chlorination velocity of the lateral chain of toluene and the corresponding reduction in residence time, notably of the liquid phase, are achieved to the detriment of chlorination of the ring, said chlorination being reduced to unobtainable limits when conventional reactors are employed. It is thus possible to obtain benzyl chloride containing less than 500 ppm of chloro-toluene, as well as phenylchloroform having purity higher than 98% at the output from the reactor. This makes it possible to dispense with costly distillation of these products.
- The advantages highlighted in the case of chlorination of toluene are not specific to this particular reaction: they are a general feature of two-phase gas/liquid photochemical reactions.
- The following examples illustrate the invention without limiting it.
- A cylindro-conical reactor having three injection levels as shown in FIG. 7 was employed. The dimensions of this reactor, with reference to FIG. 7 were:
- D1ih . . . 1.35 m
- H1. . . 0.75 m
- D2ib . . . 0.75 m
- H2. . . 0.75 m
- D1ih-D2eh . . . 44 mm
- The reaction was carried out under the following operating conditions:
- liquid velocity in the reaction zone . . . 0.39 m.s−1
- liquid velocity in the recirculation zone . . . 1.82 m.s−1
- gas velocity in the reaction zone . . . 0.61 m.s−1
- volume percentage of gas phase . . . 28%
- temperature T) . . . 95° C.
- pressure (P) . . . 760 Torr (0.1 MPa)
- total gas flow at above T and P (Cl2+HCl+vaporized organic compounds) 0.184 m3.s−1
- chlorine flow rate . . . 900 kg.h−1
- The normal operating running conditions were established and the following results were obtained, on the basis of a duration of production of 3 days, after distillation of the mixture leaving the reactor:
Amount chloro-toluene (3 days) Purity content benzyl chloride 99.6 tons 99.85 <500 ppm benzylidene chloride 9.5 tons - A series of reactors having the following dimensions, with reference to FIG. 2 (the inner sleeve means stopping at an intermediate level between the single distributor and the bottom of the reactor):
- D1i. . . 0.99
- D2e. . . 0.91 m
- D2e. . . 0.904 m
- D3e. . . 0.125 m
- H . . . 0.9 m
- These reactors were connected in the arrangement shown in FIG. 8. The complete installation consisted of three continuous reactors (1, 2, 3) connected in series and a final discontinuous stage made up by two alternating reactors (4A, 4B), one being in service at a time. The chlorine was distributed between
reactors - The operating conditions were as follows:
Reactor 1Reactor 2Reactor 3velocity U of liquid in 0.55 0.33 0.30 reaction zone (m/s) % of gas phase gas 29 15 13 reaction zone (%) velocity U + V of gas in 0.9 0.8 0.8 reaction zone (m/s) temperature (° C.) 100 145 155 pressure (Torr(MPa)) 760 850 850 (0.1 MPA) (0.112 MPa) (0.112 MPa) total gas flow rate (m3/s) 0.16 0.07 0.05 fresh chlorine flow — 410 300 rate (kg/h) recovered chlorine flow 40 — — rate (kg/h) - At this stage in the chlorination, i.e. after the third reactor, the phenylchloroform content exceeded 90%, in other words the amount of chlorine fixed exceeded 95% of the total.
- In this particular example, the final stage is discontinuous. The last reactor fulfils the multiple functions of regulating the end of chlorination as well as the temporary storage reservoir for supplementary analytic analyses. Its dimensions are as follows:
- D1i. . . 1.58 m
- D2e. . . 1.48 m
- H (inner inner sleeve means) . . . 1.5 m
- reactor volume . . . 5 m3
- As the liquid level in the last discontinuous reactor was variable, the inner sleeve means defining the recirculation zone was provided with calibrated slots in accordance with FIG. 9, enabling recirculation to be primed regardless of the level to which the discontinuous reactor was filled.
- The operating conditions were as follows:
- Temperature (°C.) . . . 155
- Pressure Torr (MPa)) . . . 850 (0.112MPa)
- Average Cl2 flow rate (kg/h) 54
- The gaseous effluent containing the excess chlorine was recycled to
reactor 1 in conformity with FIG. 8. - The following results are obtained under normal operating conditions:
- Phenylchloroform:
- amount over 3 days . . . 50.03 metric tons
- purity . . . 98.41%
- The last reactor can advantageously be replaced by a continuous reactor the inner sleeve means of which, defining the recirculation zone, descends down to the bottom of the reactor as in FIG. 3, the respective dimensions of which are:
- D1i. . . 0.4 m D3e. . . 0.175 m
- D2e. . . 0.3 m H . . . 1.2 m
Claims (19)
1. A process for halogenating alkylbenzenes characterized in that said process is carried out in an axially symmetrical photochemical gas/liquid reactor (1), comprising:
a vessel (2);
a central source of radiation (3);
at least one distributor for gas (4), at the bottom of said reactor;
inner sleeve means (5) arranged-concentrically between the source of radiation (3) and the vessel (2), said inner sleeve means allowing internal recirculation of reaction liquid, said recirculation comprising a rising movement in the space situated between the source (3) and the inner sleeve means (5) and a descending movement in the space situated between the vessel (2) and the inner sleeve means (5).
2. The process according to wherein said process is a process for chlorination of toluene.
claim 1
3. The process according to , wherein said process is carried out in a reactor in which the inner sleeve means (5) extends down to the level of the distributor or down to an intermediate level situated between the distributor (4) and the bottom of the vessel (2).
claim 1
4. The process according to , wherein said process is carried out in a reactor in which the inner sleeve means (5) extend down to the bottom of the vessel (2) and includes a series of orifices (7) located at an intermediate level between the distributor (4) and the bottom of the vessel (2).
claim 1
5. The process according to , wherein said process is carried out in a reactor in which the inner sleeve means (5) includes slots of a calibrated size (5 a) along part or all of its length.
claim 1
6. The process according to , wherein said process is carried out in a reactor in which internal recirculation starts at a point below the distributor (4), in the vicinity of the bottom of said reactor (2).
claim 1
7. The process according to , wherein said process is carried out in a reactor in which the source (3) extends right through the reactor from one end to the other.
claim 1
8. The process according to , wherein said process is carried out in a reactor in which the source (3) passes through the reactor cover only.
claim 1
9. The process according to , wherein said process is carried out in a reactor in which the central source (3) consists of one or several transparent tube(s) arranged in axial symmetry.
claim 1
10. The process according to , wherein said process is carried out in a reactor in which the distributor(s) (4) is/are consist of one or several concentric toroidal members provided with holes in their upper halves.
claim 1
11. The process according to , wherein said process is carried out in a reactor comprising one single distributor (4) at the bottom of the reactor.
claim 1
12. The process according , wherein said process is carried out in a reactor comprising at least two distributors, situated at different levels inside said reactor.
claim 1
13. The process according , wherein said process is carried out in a reactor which is cylindrical in shape.
claim 1
14. The process according , wherein said process is carried out in a reactor which is cylindro-conical in shape.
claim 1
15. The process according to , wherein said process is carried out in a reactor in which the velocity U of the liquid in the rising movement occurring in the, space situated between said source (3) and said inner sleeve member (5) is comprised between 0.1 and 0.8 m/s and preferably between 0.25 and 0.60 m/s.
claim 1
16. The process according to , wherein said process is carried out in a reactor in which the velocity of the gas U+V is comprised between 0.3 and 1.1 m/s.
claim 1
17. The process according to , wherein said process is carried out in a reactor in which the velocity of the liquid in said descending movement situated in the space between said inner sleeve means (5) and said vessel (2) is comprised between 0.5 and 3 m/s, preferably between 1 and 2.5 m/s.
claim 1
18. The process according to , wherein said process is carried out in a reactor in which the fraction of the volume occupied by the gaseous phase represents 10 to 50%, preferably 20 to 40% by volume, of the volume of said vessel defined between said source (3) and said inner sleeve means (5).
claim 1
19. The process according , wherein said process is carried out in a reactor in which the diameter of the bubbles generated by the said distributor is comprised between 3 and 15 mm, preferably 6 and 10 mm.
claim 1
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/785,317 US6398922B2 (en) | 1993-01-28 | 2001-02-20 | Photochemical gas-liquid process for halogenating alkylbenzenes |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9300863 | 1993-01-28 | ||
FR9300863A FR2700714A1 (en) | 1993-01-28 | 1993-01-28 | New photochemical reactors and processes using them in particular halogenation process of alkylbenzenes. |
US18656494A | 1994-01-26 | 1994-01-26 | |
US09/785,317 US6398922B2 (en) | 1993-01-28 | 2001-02-20 | Photochemical gas-liquid process for halogenating alkylbenzenes |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US18656494A Continuation | 1993-01-28 | 1994-01-26 |
Publications (2)
Publication Number | Publication Date |
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US20010019015A1 true US20010019015A1 (en) | 2001-09-06 |
US6398922B2 US6398922B2 (en) | 2002-06-04 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/785,317 Expired - Fee Related US6398922B2 (en) | 1993-01-28 | 2001-02-20 | Photochemical gas-liquid process for halogenating alkylbenzenes |
Country Status (9)
Country | Link |
---|---|
US (1) | US6398922B2 (en) |
EP (1) | EP0609153B1 (en) |
JP (1) | JP2523100B2 (en) |
KR (1) | KR970000935B1 (en) |
CN (1) | CN1061026C (en) |
AT (1) | ATE170774T1 (en) |
CA (1) | CA2114383C (en) |
DE (1) | DE69413082T2 (en) |
FR (1) | FR2700714A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050040028A1 (en) * | 2001-04-05 | 2005-02-24 | Melanie Hebert | Semi-continuous photochemical method and device therefor |
DE102020114809A1 (en) | 2020-06-04 | 2021-12-09 | EKATO Rühr- und Mischtechnik GmbH | Stirring device and method for operating a stirring device |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL1006654C2 (en) * | 1997-07-24 | 1999-01-26 | Dsm Nv | Preparation of 3-Methoxymethyl-quinoline |
JP4886324B2 (en) * | 2006-03-02 | 2012-02-29 | 出光興産株式会社 | Secondary reactor for butanol production |
US20140221692A1 (en) | 2013-02-04 | 2014-08-07 | Chevron Phillips Chemical Company Lp | Flow Reactor Vessels and Reactor Systems |
JP6311946B2 (en) * | 2013-09-13 | 2018-04-18 | ファイニングス シーオー. エルティーディーFinings Co. Ltd | Method for preparing trichloromethyl substituted benzene |
CN107417490B (en) * | 2017-05-23 | 2021-09-10 | 方圆化工有限公司 | Tower type continuous photochlorination method for preparing chlorobenzyl |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE590772A (en) | 1959-05-12 | 1900-01-01 | ||
GB1084212A (en) * | 1963-11-19 | 1900-01-01 | ||
US3816287A (en) * | 1971-10-22 | 1974-06-11 | Bayer Ag | Photolytic process for the continuous production of benzotrichloride with a low benzal chloride content |
DE2305761C3 (en) | 1973-02-07 | 1975-08-28 | Alfred 7500 Karlsruhe Graentzel | Photochemical reactor |
DE2530094C2 (en) | 1975-07-05 | 1979-06-07 | Hoechst Ag, 6000 Frankfurt | Process for the continuous production of mono- or d-trichloromethyl) benzenes |
CA1048733A (en) | 1977-02-02 | 1979-02-20 | Anthony J. Last | Ozone/ultraviolet water purifier |
DE2961828D1 (en) | 1978-10-11 | 1982-02-25 | Bayer Ag | Process for the monohalogenation of alkylbenzenes in alpha position |
US4189363A (en) | 1979-02-21 | 1980-02-19 | Stuart Enterprises | Process of producing ozone in water |
US4348265A (en) | 1981-03-27 | 1982-09-07 | The Dow Chemical Company | Process for the selective aliphatic chlorination of alkylbenzenes |
FR2524875A1 (en) | 1982-04-07 | 1983-10-14 | Elf Aquitaine | PROCESS AND APPARATUS FOR PHOTOCHEMICAL PRODUCTION OF HALOGENO-ALKANES AND CYCLO-ALKANES |
DE3245312A1 (en) * | 1982-12-08 | 1984-06-14 | Hoechst Ag, 6230 Frankfurt | METHOD FOR CARRYING OUT (BIO-) CHEMICAL REACTIONS |
JPS61187930A (en) * | 1985-02-14 | 1986-08-21 | Ishikawajima Harima Heavy Ind Co Ltd | Photoreactor |
JPH01160476A (en) * | 1987-12-16 | 1989-06-23 | Nippon Sharyo Seizo Kaisha Ltd | Bubble tower-type reactor |
JPH1160476A (en) * | 1997-08-25 | 1999-03-02 | Taisho Pharmaceut Co Ltd | Compressed solid composition |
-
1993
- 1993-01-28 FR FR9300863A patent/FR2700714A1/en active Pending
-
1994
- 1994-01-27 CA CA002114383A patent/CA2114383C/en not_active Expired - Fee Related
- 1994-01-27 CN CN94102670A patent/CN1061026C/en not_active Expired - Fee Related
- 1994-01-28 KR KR1019940001595A patent/KR970000935B1/en not_active IP Right Cessation
- 1994-01-28 DE DE69413082T patent/DE69413082T2/en not_active Expired - Fee Related
- 1994-01-28 JP JP6026375A patent/JP2523100B2/en not_active Expired - Lifetime
- 1994-01-28 AT AT94400185T patent/ATE170774T1/en active
- 1994-01-28 EP EP94400185A patent/EP0609153B1/en not_active Expired - Lifetime
-
2001
- 2001-02-20 US US09/785,317 patent/US6398922B2/en not_active Expired - Fee Related
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050040028A1 (en) * | 2001-04-05 | 2005-02-24 | Melanie Hebert | Semi-continuous photochemical method and device therefor |
US7491299B2 (en) | 2001-04-05 | 2009-02-17 | Arkema France | Semi-continuous photochemical method and device therefor |
DE102020114809A1 (en) | 2020-06-04 | 2021-12-09 | EKATO Rühr- und Mischtechnik GmbH | Stirring device and method for operating a stirring device |
Also Published As
Publication number | Publication date |
---|---|
KR940018339A (en) | 1994-08-16 |
ATE170774T1 (en) | 1998-09-15 |
FR2700714A1 (en) | 1994-07-29 |
JP2523100B2 (en) | 1996-08-07 |
CN1061026C (en) | 2001-01-24 |
KR970000935B1 (en) | 1997-01-21 |
DE69413082D1 (en) | 1998-10-15 |
US6398922B2 (en) | 2002-06-04 |
CA2114383A1 (en) | 1994-07-29 |
CA2114383C (en) | 1999-11-09 |
CN1101907A (en) | 1995-04-26 |
JPH06293677A (en) | 1994-10-21 |
DE69413082T2 (en) | 1999-05-27 |
EP0609153B1 (en) | 1998-09-09 |
EP0609153A1 (en) | 1994-08-03 |
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