Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
  • B01D3/14—Fractional distillation or use of a fractionation or rectification column
  • B01D3/143—Fractional distillation or use of a fractionation or rectification column by two or more of a fractionation, separation or rectification step
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
  • C07C29/62—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by introduction of halogen; by substitution of halogen atoms by other halogen atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
  • C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
  • C07C29/76—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
  • C07C29/80—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation
  • C07C29/82—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation by azeotropic distillation
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
  • C07C31/34—Halogenated alcohols
  • C07C31/36—Halogenated alcohols the halogen not being fluorine
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
  • C07C31/34—Halogenated alcohols
  • C07C31/42—Polyhydroxylic acyclic alcohols
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D301/00—Preparation of oxiranes
  • C07D301/02—Synthesis of the oxirane ring
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D301/00—Preparation of oxiranes
  • C07D301/02—Synthesis of the oxirane ring
  • C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
  • C07D301/04—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with air or molecular oxygen
  • C07D301/06—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with air or molecular oxygen in the liquid phase
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D301/00—Preparation of oxiranes
  • C07D301/02—Synthesis of the oxirane ring
  • C07D301/24—Synthesis of the oxirane ring by splitting off HAL—Y from compounds containing the radical HAL—C—C—OY
  • C07D301/26—Y being hydrogen
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
  • C07D303/02—Compounds containing oxirane rings
  • C07D303/08—Compounds containing oxirane rings with hydrocarbon radicals, substituted by halogen atoms, nitro radicals or nitroso radicals

Definitions

• the present invention relates to a process for preparing chlorohydrin by conversion of polyhydroxylated aliphatic hydrocarbons, more specifically by chlorination of polyhydroxylated aliphatic hydrocarbons
• Chlorohydrins are reaction intermediates in the manufacture of epoxides.
• Dichloropropanol for example, is a reaction intermediate in the manufacture of epichlorohydrin and epoxy resins (Kirk-Othmer Encyclopedia of Chemical Technology, Fourth Edition, 1992, Vol 2, page 156, John Wiley & Sons, Inc.). .
• dichloropropanol can be obtained in particular by hypochlorination of allyl chloride, by chlorination of allyl alcohol and by hydrochlorination of glycerol.
• the latter process has the advantage that dichloropropanol can be obtained from fossil raw materials or renewable raw materials, and it is known that petrochemical natural resources, from which fossil fuels are derived, for example petroleum, natural gas or coal, available on the earth are limited.
• the application WO 2005/054167 of Solvay SA describes a process for the manufacture of dichloropropanol by reaction between glycerol and hydrogen chloride in the presence of an acid such as adipic acid, as catalyst.
• the dichloropropanol is separated from the other products of the reaction and these are recycled to the glycerol chlorination reactor.
• a fraction of these other reaction products can be withdrawn via a purge and subjected to various treatments before disposal.
• Landfill is not an environmentally acceptable solution.
• the additional cost of treatment prior to landfill can be prohibitive for the economy of the process.
• the object of the invention is to provide a process for the preparation of chlorohydrin which does not have these disadvantages.
• the invention therefore relates to a process for producing a chlorohydrin in which a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon, or a mixture thereof, of which the total content of expressed metals, is reacted. in the form of elements is greater than or equal to 0.1 ⁇ g / kg and less than or equal to 1000 mg / kg, with a chlorinating agent.
• polyhydroxylated aliphatic hydrocarbon refers to a hydrocarbon that contains at least two hydroxyl groups attached to two different saturated carbon atoms.
• the polyhydroxylated aliphatic hydrocarbon may contain, but is not limited to, from 2 to 60 carbon atoms.
• Each of the carbons of a polyhydroxylated aliphatic hydrocarbon bearing the functional hydroxyl (OH) group can not have more than one OH group, and must be of sp3 hybridization.
• the carbon atom carrying the OH group may be primary, secondary or tertiary.
• the polyhydroxylated aliphatic hydrocarbon used in the present invention must contain at least two sp3 hybridization carbon atoms carrying an OH group.
• the polyhydroxylated aliphatic hydrocarbon includes any hydrocarbon containing a vicinal diol (1,2-diol) or a vicinal triol (1,2,3-triol) including higher orders of these repetitive, vicinal or contiguous units.
• the definition of the polyhydroxylated aliphatic hydrocarbon also includes, for example, one or more 1,3-, 1,4-, 1,5- and 1,6-diol functional groups.
• the polyhydroxylated aliphatic hydrocarbon may also be a polymer such as polyvinyl alcohol. Geminated diols, for example, are excluded from this class of polyhydroxylated aliphatic hydrocarbons.
• the polyhydroxylated aliphatic hydrocarbons may contain aromatic entities or hetero atoms including, for example, hetero atoms of the halogen, sulfur, phosphorus, nitrogen, oxygen, silicon and boron type, and mixtures thereof.
• Polyhydroxylated aliphatic hydrocarbons for use in the present invention include, for example, 1,2-ethanediol (ethylene glycol), 1,2-propanediol (propylene glycol), 1,3-propanediol, 1-chloro-2, 3- propanediol (chloropropanediol), 2-chloro-1,3-propanediol (chloropropanediol), 1,4-butanediol, 1,5-pentanediol, cyclohexanediols, 1,2-butanediol, 1,2-butane diol cyclohexanedimethanol, 1,2,3-propanetriol (also known as "glycerol” or "glycerin”), and mixtures thereof.
• 1,2-ethanediol ethylene glycol
• 1,2-propanediol propylene glycol
• 1,3-propanediol 1-ch
• the polyhydroxylated aliphatic hydrocarbon used in the present invention includes, for example, 1,2-ethanediol, 1,2-propanediol, 1,3-propanediol, chloropropanediol and 1,2,3-propanetriol, and mixtures of at least two of them. More preferably, the polyhydroxylated aliphatic hydrocarbon used in the present invention includes, for example, 1,2-ethanediol, 1,2-propanediol, chloropropanediol and 1,2,3-propanetriol, and mixtures thereof. least two of them. 1,2,3-propanetriol or glycerol is the most preferred.
• esters of the polyhydroxylated aliphatic hydrocarbon may be present in the polyhydroxylated aliphatic hydrocarbon and / or may be produced in the process for the manufacture of chlorohydrin and / or may be manufactured prior to the process for producing the chlorohydrin.
• examples of polyhydroxylated aliphatic hydrocarbon esters include ethylene glycol monoacetate, propanediol monoacetates, glycerol monoacetates, glycerol monostearates, glycerol diacetates, and mixtures thereof.
• chlorohydrin is used here to describe a compound containing at least one hydroxyl group and at least one chlorine atom attached to different saturated carbon atoms.
• a chlorohydrin that contains at least two hydroxyl groups is also a hydrocarbon - AT -
• the starting material and the product of the reaction can each be chlorohydrins.
• the "produced" chlorohydrin is more chlorinated than the starting chlorohydrin, that is to say that it has more chlorine atoms and fewer hydroxyl groups than the starting chlorohydrin.
• Preferred chlorohydrins are chloroethanol, chloropropanol, chloropropanediol, dichloropropanol and mixtures of at least two of them. Dichloropropanol is particularly preferred.
• chlorohydrins are 2-chloroethanol, 1-chloropropan-2-ol, 2-chloropropane-1-ol, 1-chloropropane-2,3-diol, 2-chloropropane-1,3-diol. 1,3-dichloropropan-2-ol, 2,3-dichloropropan-1-ol and mixtures of at least two of them.
• the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them, in the process according to the invention can be obtained starting from fossil raw materials or starting from renewable raw materials, from preferably from renewable raw materials.
• Fossil raw materials are understood to mean materials from the processing of petrochemical natural resources, for example, petroleum, natural gas, and coal. Of these materials, organic compounds having 2 and 3 carbon atoms are preferred.
• the polyhydroxylated aliphatic hydrocarbon is glycerol, allyl chloride, allyl alcohol and "synthetic" glycerol are particularly preferred.
• synthetic glycerol is meant a glycerol generally obtained from petrochemical resources.
• the polyhydroxylated aliphatic hydrocarbon is ethylene glycol
• ethylene and “synthetic" ethylene glycol are particularly preferred.
• polyhydroxylated aliphatic hydrocarbon is propylene glycol
• propylene and synthetic propylene glycol are particularly preferred.
• synthetic propylene glycol is meant a propylene glycol generally obtained from petrochemical resources.
• Renewable raw materials are defined as materials derived from the treatment of renewable natural resources.
• “natural” ethylene glycol, “natural” propylene glycol and “natural” glycerol are preferred.
• Ethylene glycol, propylene glycol and For example, “natural” glycerol is obtained by sugar conversion via thermochemical processes, which sugars can be obtained from biomass, as described in “Industrial Bioproducts: Today and Tomorrow, Energetics, Incorporated for the US Department of Energy, Office of Energy Efficiency and Renewable Energy, Office of the Biomass Program, July 2003, pages 49, 52 to 56 ".
• One of these processes is, for example, the catalytic hydrogenolysis of sorbitol obtained by thermochemical conversion of glucose.
• Another method is for example the catalytic hydrogenolysis of xylitol obtained by hydrogenation of xylose.
• the xylose can for example be obtained by hydrolysis of the hemicellulose contained in the corn fibers.
• natural glycerol or “glycerol obtained from renewable raw materials” is meant in particular glycerol obtained during the manufacture of biodiesel or glycerol obtained during transformations of fats or oils of plant or animal origin in general such as saponification, trans-esterification or hydrolysis reactions.
• oils that can be used to make natural glycerol are all common oils, such as palm, palm kernel, copra, babassu, old or new rapeseed, sunflower, maize, castor oil and cotton oils. , peanut, soybean, flax and crambe oils and all oils derived for example from sunflower or rapeseed plants obtained by genetic modification or hybridization.
• oils such as fish oils, tallow, lard and even rendering fats.
• partially modified oils for example by polymerization or oligomerization, for example the "standolies" of linseed oil, sunflower oil and blown vegetable oils.
• a particularly suitable glycerol can be obtained during the processing of animal fats. Another particularly suitable glycerol can be obtained during the manufacture of biodiesel.
• a third particularly suitable glycerol can be obtained during the transformation of fats or oils, animal or vegetable by trans-esterification in the presence of a heterogeneous catalyst, as described in documents FR 2752242, FR 2869612 and FR More specifically, the heterogeneous catalyst is chosen from mixed oxides of aluminum and zinc, and mixed oxides of zinc. and titanium, mixed oxides of zinc, titanium and aluminum, and mixed oxides of bismuth and aluminum, and the heterogeneous catalyst is implemented in the form of a fixed bed. The latter process may be a biodiesel manufacturing process. In the process according to the invention, it is preferred to use a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon, or a mixture of them, obtained from renewable raw materials.
• the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester or the mixture of them may have an alkali metal and / or alkaline content. -terreux less than or equal to 1 g / kg as described in the application entitled "Process for producing a chlorohydrin by chlorination of a polyhydroxylated aliphatic hydrocarbon" deposited in the name of Solvay SA the same day as the present application, including the content is here incorporated by reference.
• the alkali metals may be selected from lithium, sodium, potassium, rubidium and cesium and the alkaline earth metals may be selected from magnesium, calcium, strontium and barium.
• the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them may contain other metals than the alkali metals and alkaline earth metal. These include iron, nickel, chromium, copper, lead, arsenic, cobalt, titanium, vanadium, tin, tellurium, cadmium, antimony, mercury, selenium, zinc, aluminum and bismuth.
• the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them may also contain other elements than metals such as, for example, sulfur and nitrogen.
• the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them has a metal content preferably less than or equal to 500 mg / kg, more preferably less than or equal to 150 mg / kg, even more preferably less than or equal to 50 mg / kg and very particularly preferably less than 15 mg / kg.
• the iron content in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is less than or equal to 100. mg / kg, preferably less than or equal to 10 mg / kg and particularly preferably less than or equal to 1 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the nickel content in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is less than or equal to 10. mg / kg, preferably less than or equal to 1 mg / kg and particularly preferably less than or equal to 0.1 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the chromium content in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is less than or equal to 10. mg / kg, preferably less than or equal to 1 mg / kg and particularly preferably less than or equal to 0.1 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the copper content in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is less than or equal to 10. mg / kg, preferably less than or equal to 1 mg / kg and particularly preferably less than or equal to 0.25 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the cumulative content of lead, arsenic and cobalt in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is less than or equal to 5 mg / kg, preferably less than or equal to 3 mg / kg and particularly preferably less than or equal to 0.1 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the titanium content in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is less than or equal to 10 mg / kg, preferably less than or equal to 5 mg / kg and particularly preferably less than or equal to 1 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the cumulative content of titanium, vanadium, tin and tellurium in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is less than or equal to 10 mg / kg, preferably less than or equal to 5 mg / kg and particularly preferably less than or equal to 0.1 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the cumulative content of cadmium and antimony in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is lower or equal to 5 mg / kg, preferably less than or equal to 1 mg / kg and particularly preferably less than or equal to 0.1 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the content of mercury in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is less than or equal to 1 mg / kg, preferably less than or equal to 0.5 mg / kg and particularly preferably less than or equal to 0.04 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the zinc content in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is less than or equal to 10. mg / kg, preferably less than or equal to 2 mg / kg and particularly preferably less than or equal to 1 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the cumulative content of selenium and zinc in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is lower or equal to 12 mg / kg, preferably less than or equal to 1 mg / kg and particularly preferably less than or equal to 0.2 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the cumulative sodium and calcium content in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is lower or equal to 50 mg / kg, preferably less than or equal to at 30 mg / kg and particularly preferably less than or equal to 2.5 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the aluminum content in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is less than or equal to 10. mg / kg, preferably less than or equal to 5 mg / kg and particularly preferably less than or equal to 1 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the bismuth content in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is less than or equal to mg / kg, preferably less than or equal to 1 mg / kg and particularly preferably less than or equal to 0.2 mg / kg. This content is generally greater than or equal to 0.1 ⁇ g / kg.
• the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them has a content of heavy compounds other than the polyhydroxylated aliphatic hydrocarbon. and whose boiling point at a pressure of 1 bar absolute is at least 15 ° C higher than the boiling point of the chlorohydrin, less than or equal to 50 g / kg.
• the heavy compounds can be selected from fatty acids, their salts, their esters, and their mixtures
• the fatty acids preferably contain at least 12 carbon atoms.
• Fatty acids and fatty acid mixtures derived from vegetable oils and animal fats are preferred.
• Fatty acids and mixtures of fatty acids derived from rapeseed, sunflower, soy and palm oils are particularly preferred.
• Oleic, linoleic, linolenic, palmitic and stearic acids, and mixtures thereof, are particularly preferred.
• Oleic, linoleic and linolenic acids and mixtures thereof are particularly suitable.
• the fatty acid salts are often alkaline salts, alkaline earth salts and ammonium salts or mixtures thereof, and more particularly sodium, potassium and calcium salts.
• the fatty acid esters may be selected from mono-, di- and triglycerides, and fatty acid methyl esters and mixtures thereof. Without wishing to be bound by any theoretical explanation, it is believed that the heavy compounds present in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them, accumulate in the recycles and require increase the frequency of purging operations.
• the content of heavy compounds in the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them is preferably lower or equal to 30 g / kg, more preferably less than or equal to 10 g / kg, even more preferably less than or equal to 1 g / kg and very particularly preferably less than or equal to 0.5 g / kg; kg.
• the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them may be as specifically disclosed in application WO 2005/054167 from SOLVAY SA, page 2, line 8, to page 4, line 2.
• the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them may or may not have undergone purification treatment (s) between its manufacture and its use in the process according to the invention.
• purification treatment s
• Such treatments may be as described in SOLVAY SA application WO 2005/054167, page 3, lines 4 to 14 and lines 30 to 33.
• purification treatments such as distillation, evaporation, extraction, adsorption or concentration operations followed by separation operations such as decantation, filtration or centrifugation.
• separation operations such as decantation, filtration or centrifugation.
• Purification operations by treatment with resins, preferably ion exchangers are also mentioned.
• a polyhydroxylated aliphatic hydrocarbon an ester of a polyhydroxylated aliphatic hydrocarbon, or a mixture thereof, which has not undergone such treatments.
• the polyhydroxylated aliphatic hydrocarbon is glycerol
• glycerol can be obtained for example during the transformation of fats or oils, animal or vegetable, by trans-esterification in the presence of a heterogeneous catalyst, as described in documents FR 2752242, FR 2869612 and FR 2869613.
• the heterogeneous catalyst is selected from mixed oxides of aluminum and zinc, mixed oxides of zinc and titanium, mixed oxides of zinc, titanium and aluminum, and mixed oxides of bismuth and aluminum.
• aluminum, and the heterogeneous catalyst is implemented in the form of a fixed bed. The latter process may be a biodiesel manufacturing process.
• a glycerol obtained by a trans-esterification process starting from renewable raw materials in the presence of a heterogeneous catalyst selected from mixed oxides of aluminum and zinc, mixed oxides of zinc and titanium, the mixed oxides of zinc, titanium and aluminum, and the mixed oxides of bismuth and aluminum, supported and unsupported, and the heterogeneous catalyst is implemented in the form of a fixed bed.
• a first advantage is that the contamination of glycerol by metals is reduced.
• the latter may be alkali and / or alkaline-earth metals originating, for example, basic reagents used in the saponification reactions (alkaline bases), in neutralization operations, with alkaline bases or metals derived from the acidic acid catalysts used. during trans-esterification or acid hydrolysis reactions or metals from corrosion of glycerol manufacturing equipment.
• MONG non-glycerinous organic matter
• [GLC] is the glycerol content of glycerol (in%) as in ISO Standard method 2879 (1975) [H 2 O] is the water content (in%) in glycerol as determined by the Karl-Karl method. Fisher described in the standardized method ISO 2098 (1972) [dry residue] is the dry residue content (in%) of the glycerol obtained after calcination according to the standardized method ISO 2098 (1972).
• the non-glycerol organic matter content of glycerol is generally less than or equal to 5%, preferably less than or equal to 1%, and more preferably less than or equal to 0.5%.
• the quantity of caustic soda consumed for determining the content of fatty acids and esters of fatty acids according to the USP24 / NF19 standard is generally less than or equal to 30 milliequivalents / kg, preferably less than or equal to 3 milliequivalents / kg and particularly preferably less than or equal to 2 milliequivalents / kg. This content is generally greater than or equal to 0.2 milliequivalents / kg.
• a third advantage is that the water content of glycerol is reduced.
• the water content of the glycerol is generally less than or equal to 100 g / kg, preferably less than or equal to 50 g / kg, more preferably less than or equal to 20 g / kg. g / kg and very particularly preferably less than or equal to 10 g / kg. This content is generally greater than or equal to 500 mg / kg.
• the chlorinating agent may be as described in the application WO 2005/054167 of SOLVAY SA, of page 4, line 25, on page 6, line 2 .
• the chlorinating agent may be hydrogen chloride may be as described in the application WO 2005/054167 of SOLVAY SA, from page 4, line 30, to page 6, line 2.
• a chlorinating agent which may be aqueous hydrochloric acid or preferably anhydrous hydrogen chloride.
• Hydrogen chloride may be derived from a process for pyrolysis of chlorinated organic compounds such as vinyl chloride production, a process for the manufacture of 4,4-methylenediphenyl diisocyanate (MDI) or toluene diisocyanate (TDI), metal stripping processes or a reaction between an inorganic acid such as sulfuric or phosphoric acid and a metal chloride such as sodium chloride, potassium chloride or calcium chloride.
• MDI 4,4-methylenediphenyl diisocyanate
• TDI toluene diisocyanate
• metal stripping processes or a reaction between an inorganic acid such as sulfuric or phosphoric acid and a metal chloride such as sodium chloride, potassium chloride or calcium chloride.
• the chlorinating agent is gaseous hydrogen chloride or an aqueous solution of hydrogen chloride or a combination of both.
• the hydrogen chloride may be an aqueous solution of hydrogen chloride or preferably anhydrous hydrogen chloride, resulting from a chlorine-producing plant. allyl and / or manufacture of chloromethanes and / or chlorinolysis and / or high temperature oxidation of chlorinated compounds as described in the application entitled "Process for producing a chlorohydrin by reaction between a polyhydroxylated aliphatic hydrocarbon and a chlorinating agent "filed on behalf of SOLVAY SA on the same day as the present application, the contents of which are hereby incorporated by reference.
• a process for producing a chlorohydrin from a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon, or a mixture of them, and a chlorinating agent the latter containing at least one of the following compounds: nitrogen, oxygen, hydrogen, chlorine, an organic hydrocarbon compound, a halogenated organic compound, an oxygenated organic compound and a metal.
• an organic hydrocarbon compound which is selected from aromatic hydrocarbons, saturated or unsaturated aliphatic and mixtures thereof.
• an unsaturated aliphatic hydrocarbon which is selected from acetylene, ethylene, propylene, butene, propadiene, methylacetylene, and mixtures thereof, of a saturated aliphatic hydrocarbon which is selected from methane, ethane, propane, butane, and mixtures thereof, and an aromatic hydrocarbon which is benzene.
• halogenated organic compound which is a chlorinated organic compound chosen from chloromethanes, chloroethanes, chloropropanes, chlorobutanes, vinyl chloride, vinylidene chloride, monochloropropenes, perchlorethylene, trichlorethylene, chlorobutadiene, chlorobenzenes and mixtures thereof.
• halogenated organic compound which is a fluorinated organic compound selected from fluoromethanes, fluoroethanes, vinyl fluoride, vinylidene fluoride, and mixtures thereof.
• an oxygenated organic compound which is chosen from alcohols, chloroalcohols, chloroethers and their mixtures
• a metal selected from alkali metals, alkaline earth metals, iron, nickel, copper, lead, arsenic, cobalt, titanium, cadmium, antimony, mercury, zinc, selenium, aluminum, bismuth, and mixtures thereof.
• the chlorinating agent is derived at least partially from a process for producing allyl chloride and / or a process for producing chloromethanes and / or a process chlorinolysis and / or a process for the oxidation of chlorinated compounds at a temperature greater than or equal to 800 ° C.
• the hydrogen chloride is an aqueous solution of hydrogen chloride and does not comprise gaseous hydrogen chloride.
• the reaction between the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them, and the chlorinating agent can be carried out in a reactor as described in SOLVAY SA application WO 2005/054167, on page 6, lines 3 to 23.
• the reaction between the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them, and the chlorinating agent can be carried out in equipment, made of or covered with chlorine-resistant materials, as described in the application entitled
• a process for chlorohydrin annealing comprising a step in which a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon or a mixture thereof is subjected to reaction with a polyhydroxylated aliphatic hydrocarbon.
• chlorinating agent containing hydrogen chloride and at least one other step performed in equipment, made of or coated with chlorinating agent resistant materials, under the conditions of carrying out this step.
• metallic materials such as enamelled steel, gold and tantalum and non-metallic materials such as high-density polyethylene, polypropylene, polyvinylidene fluoride, polytetrafluoroethylene, perfluoroalkoxyalkanes and poly (perfluoropropylvinylether), polysulfones and polysulfides, graphite and impregnated graphite.
• non-metallic materials such as high-density polyethylene, polypropylene, polyvinylidene fluoride, polytetrafluoroethylene, perfluoroalkoxyalkanes and poly (perfluoropropylvinylether), polysulfones and polysulfides, graphite and impregnated graphite.
• the reaction between the polyhydroxylated aliphatic hydrocarbon and the chlorinating agent may be carried out in a reaction medium, as described in the application entitled “Continuous process of manufacture of chlorohydrins "filed on behalf of SOLVAY SA on the same day as the present application, the contents of which are hereby incorporated by reference.
• a continuous process for the production of chlorohydrin in which a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon or a mixture of them is reacted with a chlorinating agent and an organic acid.
• a liquid reaction medium whose composition in the stationary state comprises polyhydroxylated aliphatic hydrocarbon and esters of the polyhydroxylated aliphatic hydrocarbon whose sum of the contents expressed in moles of polyhydroxylated aliphatic hydrocarbon is greater than 1, 1 mol% and less than or equal to 30 mol%, the percentage being related to the organic part of the liquid reaction medium.
• the reaction between the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them, and the chlorinating agent can be carried out in the presence of a catalyst as described in SOLVAY SA application WO 2005/054167, page 6, line 28, on page 8, line 5.
• a catalyst based on a carboxylic acid or on a carboxylic acid derivative having an atmospheric boiling point greater than or equal to 200 ° C. in particular adipic acid and derivatives of adipic acid.
• the reaction between the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them, and the chlorinating agent may be carried out at a catalyst concentration, a temperature, a pressure and for residence times as described in SOLVAY SA application WO 2005/054167, page 8, line 6 to page 10, line 10. Mention is especially made of a temperature of at least 20 ° C and at most 160 ° C, a pressure of at least 0.3 bar and at most 100 bar, and a residence time at least 1 hour and not more than 50 hours.
• the reaction between the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them, and the chlorinating agent may be carried out in the presence of a solvent as described in the application WO 2005/054167 of SOLVAY SA, on page 11, lines 12 to 36.
• an organic solvent such as a chlorinated organic solvent, an alcohol, a ketone, an ester or an ether, a non-aqueous solvent miscible with polyhydroxylated aliphatic hydrocarbon such as chloroethanol, chloropropanol, chloropropanediol. , dichloropropanol, dioxane, phenol, cresol, and mixtures of chloropropanediol and dichloropropanol, or heavy products of the reaction such as oligomers of at least partially chlorinated and / or esterified polyhydroxylated aliphatic hydrocarbon.
• a non-aqueous solvent miscible with polyhydroxylated aliphatic hydrocarbon such as chloroethanol, chloropropanol, chloropropanediol. , dichloropropanol, dioxane, phenol, cresol, and mixtures of chloropropanediol and dichloropropanol, or heavy products of the reaction such
• the reaction between the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them, and the chlorinating agent may be carried out in the presence of a liquid phase comprising heavy compounds other than the polyhydroxylated aliphatic hydrocarbon, as described in The application entitled “Process for manufacturing a chlorohydrin in a liquid phase" filed on behalf of SOLVAY SA on the same day as the present application, the contents of which are hereby incorporated by reference.
• a process for producing a chlorohydrin wherein a polyhydroxylated aliphatic hydrocarbon, a polyhydroxylated aliphatic hydrocarbon ester, or a mixture thereof is subjected to a reaction with a chlorinating agent. in the presence of a liquid phase comprising heavy compounds other than the polyhydroxylated aliphatic hydrocarbon and whose boiling point at a pressure of 1 bar absolute is at least 15 ° C higher than the boiling point of chlorohydrin under a pressure of 1 bar absolute.
• the reaction between the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of them, and the chlorinating agent is preferably carried out in a liquid reaction medium.
• the liquid reaction medium may be mono- or multiphasic.
• the liquid reaction medium consists of all the dissolved or dispersed solid compounds, dissolved or dispersed liquids and gaseous dissolved or dispersed, at the reaction temperature.
• the reaction medium comprises the reactants, the catalyst, the solvent, the impurities present in the reagents, in the solvent and in the catalyst, the reaction intermediates, the products and the by-products of the reaction.
• reagents is meant the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester and the chlorinating agent.
• impurities present in the polyhydroxylated aliphatic hydrocarbon mention may be made of carboxylic acids, carboxylic acid salts, fatty acid esters with polyhydroxylated aliphatic hydrocarbon, esters of fatty acids with the alcohols used. during the trans-esterification, inorganic salts such as chlorides and sulphates alkali or alkaline earth.
• polyhydroxylated aliphatic hydrocarbon is glycerol
• the reaction intermediates mention may be made of polyhydroxylated aliphatic hydrocarbon monochlorohydrins and their esters and / or polyesters, esters and / or polyesters of polyhydroxylated aliphatic hydrocarbons and esters of polychlorohydrins.
• chlorohydrin is dichloropropanol
• products of the reaction is meant chlorohydrin and water.
• the water may be the water formed in the chlorination reaction and / or the water introduced into the process, for example via the polyhydroxylated aliphatic hydrocarbon and / or the chlorinating agent, as described in WO 2005 / 054167 of SOLVAY SA, on page 2, lines 22 to 28, on page 3, lines 20 to 25, on page 5, lines 7 to 31 and on page 12, lines 14 to 19.
• Examples of such products include partially chlorinated and / or esterified polyhydroxylated aliphatic hydrocarbon oligomers.
• the polyhydroxylated aliphatic hydrocarbon is glycerol
• the by-products mention may be made, for example, of partially chlorinated and / or esterified glycerol oligomers.
• the reaction intermediates and by-products may be formed in the various process steps such as, for example, during the chlorohydrin manufacturing step and during the chlorohydrin separation steps.
• the polyhydroxylated aliphatic hydrocarbon ester can therefore be, depending on the case, a reagent, a polyhydroxylated aliphatic hydrocarbon impurity or a reaction intermediate.
• the liquid reaction medium may thus contain polyhydroxylated aliphatic hydrocarbon, the dissolved or dispersed chlorination agent in the form of bubbles, the catalyst, the solvent, the impurities present in the reactants, the solvent and the catalyst, such as dissolved or solid salts. for example, the solvent, the catalyst, the reaction intermediates, the products and the by-products of the reaction.
• the method according to the invention can be carried out in batch mode or in continuous mode is preferred. Continuous mode is particularly preferred.
• the reaction between the polyhydroxylated aliphatic hydrocarbon and the chlorinating agent can be carried out in the presence of an organic acid.
• the organic acid can be a product from the process for producing the polyhydroxylated aliphatic hydrocarbon or a product not from this process. In the latter case, it may be an organic acid used to catalyze the reaction between the polyhydroxylated aliphatic hydrocarbon and the chlorinating agent.
• the organic acid may also be a mixture of organic acid from the process for producing the polyhydroxylated aliphatic hydrocarbon and an organic acid not originating from the process for producing the polyhydroxylated aliphatic hydrocarbon.
• the separation of the chlorohydrin and the other compounds from the reaction medium can be carried out according to the modes as described in the application WO 2005/054167 of SOLVAY SA, of page 12, line 1, to on page 16, line 35 and on page 18, lines 6 to 13.
• These other compounds are those mentioned above and comprise the reagents not consumed, the impurities present in the reagents, the catalyst and the solvent, the solvent, the catalysts, reaction intermediates, water and by-products of the reaction.
• the separation of the chlorohydrin and the other compounds from the reaction medium of chlorination of the polyhydroxylated aliphatic hydrocarbon can be carried out according to modes as described in the patent application EP 05104321.4 filed on behalf of SOLVAY SA on May 20, 2005, the contents of which are hereby incorporated by reference.
• a separation mode comprising at least one separation operation for removing salt from the liquid phase is particularly preferred.
• a process for producing a chlorohydrin in which (a) a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon, or a mixture thereof is subjected to a reaction with a chlorinating agent in a reaction medium, (b) a fraction of the reaction medium containing at least water and the chlorohydrin is withdrawn continuously or periodically, (c) at least part of the fraction obtained in step ( b) is introduced into a distillation step and (d) the reflux ratio of the distillation step is controlled by supplying water to said distillation step.
• a process for producing a chlorohydrin in which (a) a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon or a mixture thereof is subjected to a reaction with hydrogen chloride in a reaction medium, (b) a fraction of the reaction medium containing at least water and the chlorohydrin is withdrawn continuously or periodically, (c) at least a part of the fraction obtained in the step (b) is introduced into a distillation step, wherein the ratio between the hydrogen chloride concentration and the water concentration in the fraction introduced into the distillation step is smaller than the hydrogen chloride concentration ratio / water in the azeotropic hydrogen chloride / water binary composition at distillation temperature and pressure.
• the separation of the chlorohydrin and the other compounds from the reaction medium of chlorination of the polyhydroxylated aliphatic hydrocarbon can be carried out according to the modes as described in the application entitled “Process of manufacture of a chlorohydrin "deposited in the name of SOLVAY SA, the same day as the present application, and the contents of which are hereby incorporated by reference.
• a process for the manufacture of a chlorohydrin comprising the following steps: (a) reacting a polyhydroxylated aliphatic hydrocarbon, an ester of an aliphatic hydrocarbon polyhydroxylate, or a mixture thereof, with a chlorinating agent and an organic acid so as to obtain a mixture containing chlorohydrin and chlorohydrin esters, (b) subjecting at least a portion of the resulting mixture to step (a) to one or more treatments in steps subsequent to step (a) and (c) adding polyhydroxylated aliphatic hydrocarbon to at least one of the steps subsequent to step (a), so that it reacts at a temperature greater than or equal to 20 ° C with the chlorohydrin esters so as to at least partially form esters of the polyhydroxylated aliphatic hydrocarbon.
• the polyhydroxylated aliphatic hydrocarbon is glycerol and the chlorohydrin is dichloropropanol.
• the separation of the chlorohydrin and of the other compounds from the reaction medium of chlorination of the polyhydroxylated aliphatic hydrocarbon can be carried out according to the modes as described in the application entitled "Process of manufacture of a chlorohydrin from a polyhydroxylated aliphatic hydrocarbon deposited in the name of SOLVAY SA on the same day as the present application, and the contents of which are hereby incorporated by reference.
• fraction taken in step (b) to a distillation and / or stripping operation in which polyhydroxylated aliphatic hydrocarbon is added so as to separate from the fraction taken in step (b) a mixture containing water and chlorohydrin having a reduced content of chlorinating agent compared to that of the fraction taken in step (b).
• the separation of the chlorohydrin and of the other compounds from the reaction medium of chlorination of the polyhydroxylated aliphatic hydrocarbon can be carried out according to the modes as described in the application entitled "Process of conversion of polyhydroxylated aliphatic hydrocarbons to chlorhydrins "deposited in the name of SOLVAY SA on the same day as the present application and the contents of which are hereby incorporated by reference.
• Particular mention is made of a process for preparing a chlorohydrin comprising the following steps:
• step (b) at least a fraction of the mixture obtained in step (a) is subjected to a distillation and / or stripping treatment so as to obtain a concentrated portion of water, chlorohydrin and chlorohydrin esters.
• step (c) at least a fraction of the part obtained in step (b) is subjected to a separation operation in the presence of at least one additive so as to obtain a concentrated portion of chlorohydrin and of chlorohydrin esters and which contains less than 40% by weight of water.
• the separation operation is more particularly a settling.
• the separation and the treatment of the other compounds of the reaction medium for chlorinating the polyhydroxylated aliphatic hydrocarbon, the polyhydroxylated aliphatic hydrocarbon ester, or the mixture of between them, may be carried out in the manner described in the application entitled
• a process for producing a chlorohydrin comprising the following steps: (a) reacting a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon, or a mixture of them, the alkali and / or alkaline-earth metal content is less than or equal to 5 g / kg, an oxidizing agent and an organic acid so as to obtain a mixture containing at least chlorohydrin and by-products, (b) subject to at least a part of the mixture obtained at step (a) to one or more treatments in steps subsequent to step (a) and (c) at least one of the steps subsequent to step (a) consists of an oxidation at a temperature greater than or equal to 800 ° C.
• step (b) is a separation operation chosen from among the operations of decantation, filtration, centrifugation, extraction, washing, evaporation, stripping, distillation, adsorption or combinations of at least two of them.
• the chlorohydrin when the chlorohydrin is chloropropanol, it is generally obtained in the form of a mixture of compounds comprising the isomers of 1-chloropropan-2-ol and 2-chloropropan-1-ol. .
• This mixture generally contains more than 1% by weight of the two isomers, preferably more than 5% by weight and more particularly more than 50%.
• the mixture usually contains less than 99.9% by weight of the two isomers, preferably less than 95% by weight and most preferably less than 90% by weight.
• the other constituents of the mixture may be compounds derived from chloropropanol production processes, such as residual reagents, reaction by-products, solvents and in particular water.
• the weight ratio between the isomers 1-chloropropan-2-ol and 2-chloropropane-1-ol is usually greater than or equal to 0.01, preferably greater than or equal to 0.4. This ratio is usually less than or equal to 99 and preferably less than or equal to 25.
• the chlorohydrin is chloroethanol
• This mixture generally contains more than 1% by weight of the isomer, preferably more than 5% by weight and especially more than 50%.
• the mixture usually contains less than 99.9% by weight of the isomer, preferably less than 95% by weight and most preferably less than 90% by weight.
• the other constituents of the mixture may be compounds from chloroethanol production processes, such as residual reagents, reaction byproducts, solvents and especially water.
• the chlorohydrin is dichloropropanol
• it is generally obtained in the form of a mixture of compounds comprising the isomers of dichloropropan-2-ol and 2,3-dichloropropan-1-ol.
• This mixture generally contains more than 1% by weight of the two isomers, preferably more than 5% by weight and more particularly more than 50%.
• the mixture usually contains less than 99.9% by weight of the two isomers, preferably less than 95% by weight and most preferably less than 90% by weight.
• the other constituents of the mixture may be compounds from dichloropropanol production processes, such as residual reagents, reaction by-products, solvents and in particular water.
• the mass ratio between the 1,3-dichloropropan-2-ol and 2,3-dichloropropan-1-isomers is usually greater than or equal to 0.01, often greater than or equal to 0.4, frequently greater than or equal to 1 , 5, preferably greater than or equal to 3.0, more preferably greater than or equal to 7.0 and most preferably greater than or equal to 20.0.
• This ratio is usually less than or equal to 99 and preferably less than or equal to 25.
• the chlorohydrin is dichloropropanol and the latter is obtained in a process starting from allyl chloride
• the The isomeric mixture has a weight ratio of 1,3-dichloropropan-2-ol: 2,3-dichloropropan-1-ol which is often 0.3 to 0.6, typically about 0.5.
• the weight ratio 1,3-dichloropropan-2-ol: 2,3-dichloropropan-1-ol is usually greater than or equal to 1.5, preferably greater than or equal to 3.0 and most preferably greater than or equal to 9.0.
• the weight ratio 1,3-dichloropropan-2-ol: 2,3-dichloropropane-1 -ol is often of the order of 0.1.
• the chlorohydrin when the chlorohydrin is dichloropropanol, the mixture of isomers has a weight ratio 1,3-dichloropropan-2-ol: 2,3-dichloropropan-1-ol generally greater than or equal to 0, 5, often greater than or equal to 3 and frequently greater than or equal to 20.
• the chlorohydrin may contain a high content of halogenated ketones, in particular chloroacetone, as described in FIG. patent application FR 05.05120 of 20/2017 filed in the name of the applicant, and the content of which is hereby incorporated by reference.
• the content of halogenated ketone can be reduced by subjecting the chlorohydrin obtained in the process according to the invention to azeotropic distillation in the presence of water or by subjecting the chlorohydrin to dehydrochlorination treatment as described in this application, from page 4, line 1, to page 6, line 35.
• a process for producing an epoxide in which halogenated ketones are formed as by-products and which comprises at least one treatment for removing at least a portion of the halogenated ketones formed Mention is more particularly made of a process for producing an epoxide by dehydrochlorination of a chlorohydrin of which at least one fraction is produced by chlorination of a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon, or a mixture thereof, a dehydrochlorination treatment and azeotropic distillation treatment of a halogenated water-ketone mixture for removing at least a portion of the halogenated ketones formed and a method of manufacture epichlorohydrin in which the halogenated ketone formed is chloroacetone.
• the chlorohydrin may be subjected to a dehydrochlorination reaction to produce an epoxide as described in the patent applications WO 2005/054167 and FR 05.05120 filed in the name of SOLVAY SA.
• epoxy is used herein to describe a compound having at least one oxygen bridged on a carbon-carbon bond.
• the carbon atoms of the carbon-carbon bond are adjacent and the compound may contain other atoms than carbon and oxygen atoms, such as hydrogen atoms and halogens.
• Preferred epoxides are ethylene oxide, propylene oxide, glycidol and epichlorohydrin, and mixtures of at least two of them.
• the dehydrochlorination of the chlorohydrin can be carried out as described in the application entitled "Process for producing an epoxide from a polyhydroxylated aliphatic hydrocarbon and a chlorinating agent" deposited in the name of SOLVAY SA on the same day as the present application, and the content of which is hereby incorporated by reference.
• a process for producing an epoxide in which a reaction medium resulting from the reaction between a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon, or a mixture of them, is subjected to and a chlorinating agent, the reaction medium containing at least 10 g of chlorohydrin per kg of reaction medium, to a subsequent chemical reaction without intermediate treatment.
• a chlorinating agent the reaction medium containing at least 10 g of chlorohydrin per kg of reaction medium
• a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon or a mixture thereof is reacted with a chlorinating agent and an organic acid to form chlorohydrin and chlorohydrin in a reaction medium containing polyhydroxylated aliphatic hydrocarbon, polyhydroxylated aliphatic hydrocarbon ester, water, the chlorinating agent and the organic acid, the reaction medium containing at least 10 g of chlorohydrin per kg of reaction medium
• step (b) at least one fraction of the reaction medium obtained in step (a), which fraction having the same composition as the reaction medium obtained in step (a), is subjected to one or more treatments in stages subsequent to step (a)
• step (c) adding a basic compound to at least one of the steps subsequent to step (a) to react at least partially with the chlorohydrin, the chlorohydrin esters, the chlorinating agent and the organic acid to form epoxide and salts.
• the process for the production of the chlorohydrin according to the invention can be integrated into an overall scheme for producing an epoxide as described in the application entitled "Process for producing an epoxide from a chlorohydrin" deposited in the name of SOLVAY SA the same day as the present application, and the contents of which are hereby incorporated by reference.
• a process for the production of an epoxide comprising at least one step of purifying the epoxide formed, the epoxide being at least partly produced by a process for the dehydrochlorination of a chlorohydrin, the latter being at least partly manufactured by a process for chlorinating a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon, or a mixture of them.
• the polyhydroxylated aliphatic hydrocarbon is preferably glycerol and the chlorohydrin is preferably dichloropropanol.
• chlorohydrin is dichloropropanol
• the process according to the invention can be followed by the manufacture of epichlorohydrin by dehydrochlorination of dichloropropanol and epichlorohydrin can be used in the manufacture of epoxy resins.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Epoxy Compounds (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Paints Or Removers (AREA)
• Catalysts (AREA)
• Epoxy Resins (AREA)

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