The present application claims benefit of European patent application n° 10183593.2 filed on September 30, 2010, the content of which is incorporated herein by reference for all purposes.

Should the disclosure of any of the patents, patent applications, and publications which are incorporated herein by reference conflict with the description of the present application to the extent that it may render a term unclear, the present description shall take precedence.

The present invention relates to a derivative of epichlorohydrin, to the use of epichlorohydrin for manufacturing such derivative, to a process for manufacturing such a derivative and to the use of such a derivative. The present invention relates more specifically to a derivative of epichlorohydrin of natural origin, to the use of epichlorohydrin of natural origin for

manufacturing such a derivative, to a process for manufacturing such a derivative and to the use of such a derivative.

Epoxy resins are an important class of derivatives of epichlorohydrin.

Nowadays, almost 90 % of the world production of epoxy resins is based on the reaction between Bisphenol A (2,2-bis(4'-hydroxyphenyl)propane) and epichlorohydrin. Health issues have recently been raised linked to the estrogenic properties of Bisphenol A which might be released in epoxy resins derived articles due to polymer decay with time.

International application WO 2008/147473 discloses a process for the preparation of isosorbide diglycidyl ether as substitute to Bisphenol A diglycidyl ether (DGEBA), by reacting isosorbide with epichlorohydrin. Such a compound and derived products may however contain impurities which may render them unsuitable for certain applications. Those impurities can remain in the final products and possibly degrade with a concomitant deterioration of the properties of the final products. They can exhibit or degrade in

compounds exhibiting some toxicity leading to safety issues especially when the final products are intended to be in contact with food and drink.

Moreover, they can accumulate in and contaminate industrial process waters such as wastewaters for instance. The goal of the present invention is to solve those problems by

providing a new derivative of epichlorohydrin suitable in all known

applications.

The invention therefore relates in a first embodiment to a derivative of epichlorohydrin of natural origin, selected from the group consisting of glycidyl ethers presenting an epoxide equivalent weight higher than or equal to

50 g/equivalent and lower than or equal to 15000 g/equivalent, of glycidyl esters, of glycidyl amides, of glycidyl imides, of glycidyl amines, and any mixture thereof, and of which the ¹⁴ C mass content is such that the ratio ¹⁴ C / ¹² C is higher than 0.70 10 ^"12 .

One of the essential characteristics of the present invention resides in the ¹⁴ C / ¹² C ratio. When such a ratio is obtained, the amount of detrimental impurities can be lowered in the derivative, in the streams of the process for making the derivative and in the final articles that can be obtained from such derivatives.

By epichlorohydrin of natural origin, one intends to denote an

epichlorohydrin of which at least 10 % has been obtained from renewable raw materials, preferably of which at least 50 % has been obtained from renewable raw materials, more preferably of which at least 75 % has been obtained from renewable raw materials, still more preferably of which at least 90 % has been obtained from renewable raw materials, yet more preferably of which at least 95 % has been obtained from renewable raw materials, and most preferably at least 99 % has been obtained from renewable raw materials. An

epichlorohydrin of which at most 99.99 % has been obtained from renewable raw materials is also suitable. An epichlorohydrin which has been obtained only from renewable raw materials is particularly convenient.

By epichlorohydrin obtained from renewable raw materials one intends to denote an epichlorohydrin of which at least part of the carbon backbone, preferably all the carbon backbone, originates from renewable raw materials, whatever the process and the starting materials used for manufacturing such an epichlorohydrin.

The derivative of epichlorohydrin of natural origin according to the invention is selected from the group consisting of glycidyl ethers presenting an epoxide equivalent weight higher than or equal to 50 g/equivalent and lower than or equal to 15000 g/equivalent, of glycidyl esters, of glycidyl amides, of glycidyl imides, of glycidyl amines, and of any mixture thereof. The derivative of epichlorohydrin of natural origin can be selected from the group consisting of, a glycidyl ester, a glycidyl ether, a glycidyl amide, a glycidyl amine, a glycidyl imide, any mixture thereof and any combination thereof. The glycidyl ester can be a monoester or a polyester, often a diester. The glycidyl ester can be selected from the group consisting of a monomer, a polymer, and any mixture thereof. The glycidyl ester is preferably a monomer and more preferably a polymer. A glycidyl ester is frequently encountered. The glycidyl ether can be a monoether or a polyether, often a diether. The glycidyl ether can be selected from the group consisting of a monomer, a polymer, and any mixture thereof. The glycidyl ether is preferably a monomer and more preferably a polymer. A glycidyl ether is often encountered. The glycidyl amide can be a monoamide or a polyamide, often a diamide. The glycidyl amide can be selected from the group consisting of a monomer, a polymer, and any mixture thereof. The glycidyl amide is preferably a monomer and more preferably a polymer. A glycidyl amide is often encountered. The glycidyl amine can be a monoamine of a polyamine, preferably a diamine. The glycidyl amine can be selected from the group consisting of a monomer, a polymer, and any mixture thereof. The glycidyl amine is preferably a monomer and more preferably a polymer. A glycidyl amine is often encountered. The glycidyl imide can be a monoimide or a polyimide, often a dimide. The glycidyl imide can be selected from the group consisting of a monomer, a polymer, and any mixture thereof. The glycidyl imide is preferably a monomer and more preferably a polymer. A glycidyl imide is often encountered. The glycidyl imine can be a monoimine or a polyimine, often a diimine. The glycidyl imine can be selected from the group consisting of a monomer, a polymer, and any mixture thereof. The glycidyl imine is preferably a monomer and more preferably a polymer. A glycidyl imine is often encountered. The combination can be selected from the group consisting of a glycidyl ether-ester, a glycidyl amino-ester, a glycidyl amido-ether, a glycidyl imido-ether, or any mixture thereof.

The derivative of epichlorohydrin of natural origin according to the invention is preferably selected from the group consisting of glycidyl ethers presenting an epoxide equivalent weight higher than or equal to 50 g/equivalent and lower than or equal to 15000 g/equivalent.

The derivative of epichlorohydrin of natural origin according to the invention can be selected from the group consisting of a resin, a product that can be used as coagulant, a wet-strength resin, a cationization agent, a flame retardant, an ingredient for detergents, an elastomer and any mixture thereof.

The derivative of epichlorohydrin of natural origin according to the invention is preferably a polyglycidyl ether. The polyglycidyl ether can be selected from the group consisting of a monomer, a polymer, and any mixture thereof. The polyglycidyl ether is preferably a monomer and more preferably a polymer.

By polymer, one intends to denote molecules with many units joined to each other through chemical covalent bonds, often in a repeating manner, those units being referred as repeat units. The number of repeat units is higher than zero. A polymer contains at least one type of repeat units. When the polymer contains only one type of repeat units, it is called a homopolymer. When the polymer contains more than one type of repeat units, it is called a copolymer. The copolymers can be of the random type, of the alternating type or of the block type, such as described in "Polymer Science Dictionary, M.S.M., Elsevier Applied Science, London and New York 1989, page 86".

The polyglycidyl ether of the present invention is preferably a resin and more preferably an epoxy resin.

By epoxy resin, one intends to denote a polyglycidyl ether polymer, the chemical formula of which contains at least two 2,3-epoxypropyloxy groups.

The ¹⁴ C content of a product is an indication of the use of natural and renewable raw materials to manufacture the product. Indeed, contrary to fossil raw materials, all materials composed of renewable raw materials contain ¹⁴ C. All carbon samples derived from living organisms (animals or plants) are made of a mixture of 3 isotopes : ¹² C (representing ~ 98.892 %), ¹³ C (~ 1.108 %) and ¹⁴ C (traces : 1.2 10 ^"10 %). The ratio ¹⁴ C/ ¹² C of living tissues is identical to that of the atmosphere. In the environment, ¹⁴ C exists under two major forms : mineral that is to say carbon dioxide (C0 ₂ ) and organic, that is to say carbon integrated in organic molecules.

In a living organism, the ratio ¹⁴ C/ ¹² C is kept constant by the metabolism because the carbon is continuously exchanged with the environment. The proportion of ¹⁴ C being roughly constant in the atmosphere, it is the same in the organism, when still living, because it absorbs that ¹⁴ C as it absorbs ¹² C. The average ¹⁴ C/ ¹² C ratio is equal to 1.2 10 ^"12 . 12 C is stable that is to say that the number of 12 C in a given sample is constant with time. ¹⁴ C is radioactive and each gram of ¹⁴ C of living being contains enough ¹⁴ C to give 13.6 disintegrations per minute.

The half-life time (period) Tm _, linked to the disintegration constant of ¹⁴ C is of 5730 years. Taking this duration into account, one can consider that the ¹⁴ C content is practically constant from the extraction of renewable raw materials (animal or plant origin) to the manufacture of the final product.

Today, there exist at least two different techniques for measuring the ¹⁴ C content of a sample :

" by liquid scintillation spectrometry

^■ by mass spectrometry : the sample is converted into graphite or gaseous C0 ₂ , analyzed by mass spectrometry. This technique uses accelerator and a mass spectrometer to separate ¹⁴ C and ¹² C ions and therefore to determine the ratio of the two isotopes.

All those methods for measuring the ¹⁴ C content of a sample are precisely described in standards ASTM D 6866 (notably D 6866-06 and D 6866-08) and in standards ASTM 7026 (notably D 7026-04). The method preferably used is the mass spectrometry described in standard ASTM D6866-08 ("accelerator mass spectroscopy").

In the derivative of epichlorohydrin of natural origin according to the invention, the ¹⁴ C mass content is such that the ratio ¹⁴ C / ¹² C is preferably higher than to or equal to 0.75 10 - ^" 12 , more preferably higher than to or equal to 0.8 10 - ^" 12 , still more preferably higher than to or equal to 0.9 10 - ^" 12 , yet more preferably higher than to or equal to 1.0 10 - ^" 12 , most preferably higher than or equal to 1.1 10 - ^" 12 and could reach a value equal 1.2 10 - ^" 12. In this last case, all the carbon elements used to manufacture the derivative of the invention will be of renewable (i.e. non fossil) natural origin.

A derivative of epichlorohydrin of natural origin according to the invention, of which the ¹⁴ C mass content is such that the ratio ¹⁴ C / ¹² C is equal to 1.2 10 ^"12 is convenient.

When the derivative of epichlorohydrin of natural origin is a glycidyl ether, specifically a polyglycidyl ether, more specifically when the polyglycidyl ether is a polymer and most preferably when the polyglycidyl ether is an epoxy resin, it can further exhibit at least one of the four following characteristics.

Its epoxide equivalent weight (EEW) expressed in g/equivalent is usually higher than or equal to 100, often higher than or equal to 150, frequently higher than or equal to 500, in many cases higher than or equal to 1000, and more specifically higher than or equal to 5000 and its epoxide equivalent weight is usually lower than or equal to 12000, often lower than or equal to 10000, frequently lower than or equal to 8000, in many cases lower than or equal to 7000, and more specifically lower than or equal to 6000. The epoxide equivalent weight is the weight of resin required to obtain 1 equivalent of epoxide functional group and it is obtained according to ASTM Standard D 1652.

Its epoxy value in equivalent per 100 g of derivative is generally higher than or equal to 0.008, usually higher than or equal to 0.009, often higher than or equal to 0.01, frequently higher than or equal to 0.013, in many cases higher than or equal to 0.014, and more specifically higher than or equal to 0.017 and its epoxy value is generally lower than or equal to 1.0, usually lower than or equal to 0.8, often lower than or equal to 0.7, frequently lower than or equal to 0.2 and in many cases lower than or equal to 0.1. The epoxy value in equivalent per 100 g is the number of epoxy groups per 100 g of resin and it is obtained according to ASTM Standard D 1652.

Its dynamic viscosity at 25°C is generally higher than or equal to 50 mPa.s, usually higher than or equal to 100 mPa.s, often higher than or equal

to 500 mPa.s, frequently higher than or equal to 1000 mPa.s, in many cases higher than or equal to 5000 mPa.s, and more specifically higher than or equal to 10000 mPa.s and its dynamic viscosity is generally lower than or equal to 50000 mPa.s, usually lower than or equal to 30000 mPa.s, often lower than or equal to 20000 mPa.s, frequently lower than or equal to 17000 mPa.s, in many cases lower than or equal to 15000 mPa.s, and more specifically lower than or equal to 10000 mPa.s. The viscosity at 25°C is obtained according to

ASTM Standard D 445.

Its content of hydrolysable chloride is generally higher than or equal to 0.01 %, usually higher than or equal to 0.02 %, often higher than or equal to 0.05 %, frequently higher than or equal to 0.07 %, in many cases higher than or equal to 0.1 %, and more specifically higher than or equal to 0.15 %, and its content of hydrolysable chloride is generally lower than or equal to 2.2 %, usually lower than or equal to 1 %, often lower than or equal to 0.8 %, frequently lower than or equal to 0.6 %, in many cases lower than or equal to 0.5 %, and more specifically lower than or equal to 0.4 %. The hydrolysable content is obtained according to ASTM Standard D 1726. When the derivative of epichlorohydrin of natural origin is a glycidyl ether, specifically a polyglycidyl ether, more specifically when the polyglycidyl ether is a polymer and most preferably when the polyglycidyl ether is an epoxy resin, it can further exhibit at least one of the following characteristics wherein the glycidyl ether exhibits in addition at least one of the following characteristics :

^■ an epoxy value in equivalent per 100 g of derivative higher than or equal to 0.008 and lower than or equal to 1.0,

^■ a dynamic viscosity at 25°C higher than or equal to 50 mPa.s and lower than or equal to 50000,

" a content of hydrolysable chloride higher than or equal to 0.01 % and lower than or equal to 2.2 %.

When the derivative of epichlorohydrin of natural origin is a glycidyl ether, specifically a polyglycidyl ether, more specifically when the polyglycidyl ether is a polymer and most preferably when the polyglycidyl ether is an epoxy resin, it generally exhibits exhibits an epoxy value in equivalent per 100 g of derivative higher than or equal to 0.008 and lower than or equal to 1.0.

When the derivative of epichlorohydrin of natural origin is a glycidyl ether, specifically a polyglycidyl ether, more specifically when the polyglycidyl ether is a polymer and most preferably when the polyglycidyl ether is an epoxy resin, it usually exhibits a dynamic viscosity at 25°C higher than or equal to 50 mPa.s and lower than or equal to 50000.

When the derivative of epichlorohydrin of natural origin is a glycidyl ether, specifically a polyglycidyl ether, more specifically when the polyglycidyl ether is a polymer and most preferably when the polyglycidyl ether is an epoxy resin, it frequently exhibits a content of hydrolysable chloride higher than or equal to 0.01 % and lower than or equal to 2.2 %.

The invention also relates in a second embodiment to the use of

epichlorohydrin of natural origin in the manufacture of a derivative of epichlorohydrin of natural origin, selected from the group consisting of glycidyl ethers presenting an epoxide equivalent weight higher than or equal to

50 g/equivalent and lower than or equal to 15000 g/equivalent, of glycidyl esters, of glycidyl amides, of glycidyl imides, of glycidyl amines, and of any mixture thereof, and of which the ¹⁴ C mass content is such that the ratio ¹⁴ C / ¹² C is higher than 0.70 10 ^"12 .

This use according to the invention generally comprises reacting epichlorohydrin of natural origin with at least one compound comprising at least one active hydrogen atom, wherein the epichlorohydrin of natural origin ratio ¹⁴ C

12 14 12

/ C and the said compound ratio C I C are such that

[Xepi ( ¹⁴ C / ¹² C) _epi + X _cpd ( ¹⁴ C / ¹² C) _cpd ] > 0.70 10 ^"12 wherein

■ X _e pi is the fraction of C atoms from epichlorohydrin of natural origin in the derivative of epichlorohydrin of natural origin,

^■ X _C pd is the fraction of C atoms from the said compound in the derivative of epichlorohydrin of natural origin,

^■ ( ¹⁴ C / ¹² C) _e pi is the carbon 14 to carbon 12 isotopic ratio in the epichlorohydrin of natural origin,

^■ ( ¹⁴ C / ¹² C) _C pd is the carbon 14 to carbon 12 isotopic ratio in the said compound.

This use according to the invention presents usually at least one of the following features :

^■ the ( ¹⁴ C / ¹² C) _ep i is higher than or equal to 0.2 10 ^"12 ,

■ the ( ¹⁴ C / ¹² C) _C pd is higher than or equal to 0.2 10 ^"12 .

In the use according to the invention, the ( ¹⁴ C / ¹² C) _ep i ratio is generally

-12 -12 higher than or equal to 0.2 10 ^" , preferably higher than or equal to 0.4 10 ^" ,

-12

more preferably higher than or equal to 0.6 10 ^" , yet more preferably higher than

-12 -12 or equal to 0.8 10 ^" , still more preferably higher than or equal to 1.1 10 ^" and

-12

most preferably equal to 1.2 10 ^" . In this last case, all the carbon elements used to manufacture the epichlorohydrin will be of non fossil natural origin.

In the use according to the invention, the ( ¹⁴ C / ¹² C) _cp d ratio is generally

-12 -12 higher than or equal to 0.2 10 ^" , preferably higher than or equal to 0.4 10 ^" ,

-12

more preferably higher than or equal to 0.6 10 ^" , yet more preferably higher than

12 12 or equal to 0.8 10 ^" , still more preferably higher than or equal to 1.1 10 ^" and

-12

most preferably equal to 1.2 10 ^" . In this last case, all the carbon elements used to manufacture the said compound will be of non fossil natural origin.

This use according to the invention presents preferably the following features :

■ the ( ¹⁴ C / ¹² C) _ep i is equal to 1.2 10 ^"12 , and

^■ the ( ¹⁴ C / ¹² C)cpd is equal to 1.2 10 ^"12 .

In a very preferred embodiment of the use according to the invention, the ( ¹⁴ C / ¹² C) _ep i ratio and the ( ¹⁴ C / ¹² C) _cpd ratio are both equal to 1.2 10 ^"12 .

In the use according to the invention, it is preferred that at least one part of the compound containing at least one active hydrogen atom, has been obtained from renewable raw materials. It is more preferred that at least 10 % of said compound has been obtained from renewable raw materials, and still more preferred that at least 33 % has been obtained from renewable raw materials, yet more preferred that at least 50 % has been obtained from renewable raw materials, most preferred at least 75 % has been obtained from renewable raw materials, still most preferred that at least 90 % has been obtained from renewable raw materials, yet most preferred that at least 95 % has been obtained from renewable raw materials, and particularly most preferred that at least 99 % has been obtained from renewable raw materials. A compound containing at least one active hydrogen atom of which less than 99.99 % has been obtained from renewable raw materials is also suitable. A compound containing at least one active hydrogen atom which has been obtained only from renewable raw materials is particularly convenient.

In the use according to the invention, the at least one compound which reacts with epichlorohydrin contains often at least two active hydrogen atoms, and frequently more than 3 active hydrogen atoms. That compound contains more preferably two active hydrogen atoms. A compound with more than three active hydrogen atoms is also convenient.

In the use according to the invention, the epichlorohydrin of natural origin can be obtained by any process from any starting materials provided that the carbon backbone of at least one part of the epichlorohydrin originates from renewable raw materials and preferably that the carbon backbone of all of the epichlorohydrin originates from renewable raw materials.

The process can be selected from the group consisting of dichloropropanol dehydrochlorination, allyl chloride epoxidation, and combination thereof. It is preferred that at least one part of the epichlorohydrin is obtained by

dehydrochlorination of dichloropropanol, preferably by dehydrochlorination of dichloropropanol with a basic compound. The dichloropropanol can be obtained by any process. That process can be selected from the group consisting of allyl chloride hypochlorination, glycerol hydrochlorination, allyl alcohol chlorination, 1,3-dichloroacetone reduction, 2,3-dichloropropanal reduction, and any combination thereof. It is preferred that at least one part of the dichloropropanol is produced by reaction between glycerol and hydrogen chloride. The glycerol can be obtained by any process. That process can be starting from renewable raw materials, fossil raw materials, or any combination thereof. It is preferred that at least one part of said glycerol has been prepared in a conversion process of renewable raw materials. In one embodiment of the use according to the invention at least one part of the epichlorohydrin of natural origin has been obtained by

dehydrochlorination of dichloropropanol, at least one part said dichloropropanol has been produced by reaction between allyl chloride and hypochlorous acid, at least one part of said allyl chloride has been obtained from propylene, and at least one part of said propylene has been prepared in a conversion process of renewable raw materials.

In another embodiment of the use according to the invention, at least one part of the epichlorohydrin of natural origin has been obtained by epoxidation of allyl chloride with hydrogen peroxide, at least one part of said allyl chloride has been obtained from propylene, and at least one part of said propylene has been prepared in a conversion process of renewable raw materials.

In still another embodiment of the use according to the invention, at least one part of the epichlorohydrin of natural origin has been obtained by dehydrochlorination of dichloropropanol, at least one part said dichloropropanol has been produced by chlorination of allyl alcohol, at least one part of said allyl alcohol has been obtained by isomerisation of propylene oxide, at least one part of the propylene oxide has been obtained from propylene, and at least one part of said propylene has been prepared in a conversion process of renewable raw materials.

In a more preferred embodiment of the use according to the invention, at least one part of the epichlorohydrin of natural origin has been obtained by dehydrochlorination of dichloropropanol, at least one part said dichloropropanol has been produced by reaction between glycerol and hydrogen chloride, and at least one part of said glycerol has been prepared in a conversion process of renewable raw materials.

In a most preferred embodiment of the use according to the invention, epichlorohydrin of natural origin has been obtained by dehydrochlorination of dichloropropanol, said dichloropropanol having been produced by reaction between glycerol and hydrogen chloride, and at least one part of said glycerol having been prepared in a conversion process of renewable raw materials.

By glycerol which has been prepared in a conversion process of renewable raw materials, one intends to denote glycerol obtained in the process selected from the group consisting of hydrolysis, saponification, transesterification, aminolysis and hydrogenation of oils and/or fats of animal and/or plant and/or algae origin, of fermentation, hydrogenation and hydrogenolysis of mono- and polysaccharides and derived alcohols, derived from or occurring naturally in the biomass, and any combination thereof.

Glycerol which has been obtained during the manufacture of biodiesel, i.e. during the transesterification of oils and/or fats of animal and/or plant and/or algae, and preferably during the transesterification of oils and/or fats of plant origin, is particularly convenient.

Glycerol which has been obtained in the manufacture of biodiesel is more particularly convenient.

Glycerol which has been obtained during the manufacture of soaps i.e. during the saponification of oils and/or fats of animal and/or plant and/or algae, and preferably during the saponification of oils and/or fats of plant origin, is particularly convenient.

Glycerol which has been obtained in the manufacture of soap is more particularly convenient.

Glycerol which has been obtained during the manufacture of fatty acids i.e. during the hydrolysis of oils and/or fats of animal and/or plant and/or algae, and preferably during the hydrolysis of oils and/or fats of plant origin, is particularly convenient.

Glycerol which has been obtained in the manufacture of fatty acids is more particularly convenient.

Glycerol which has been obtained during the manufacture of fatty alcohols i.e. during the hydrolysis and/or transesterification of oils and/or fats of animal and/or plant and/or algae, and preferably during the hydrolysis and/or transesterification of oils and/or fats of plant origin, is particularly convenient.

Glycerol which has been obtained in the manufacture of fatty alcohols is more particularly convenient.

Glycerol which has been obtained in at least one of the manufacture of soaps, fatty acids and fatty alcohols is more particularly convenient.

In the use according to the invention, the compound containing at least one active hydrogen atom can be of any type. It is preferably selected from the group consisting of a monoalcohol, a polyol, preferably containing more than three carbon atoms, a monocarboxylic acid, a polycarboxylic acid, a monoamine, a polyamine, an amino alcohol, a polyimide, a polyamide, a polyaminoamide, a polyimine, an acid mono- or polyphenol and mixtures of at least two of these compounds. In the use according to the invention, the polyol, preferably containing more than three carbon atoms, is preferably selected from the group consisting of a polyphenol, a sugar, a polyol derived from a sugar, an acid polyphenol, any derivative thereof, and any mixture thereof.

In the use according to the invention, when the polyol is a polyphenol, the polyphenol is preferably selected from the group consisting of a naturally occurring polyphenol extracted from the cashew nut shell liquid, a lignan, a lignin, a stilbene, a flavonoid, a polyphenol present in the bio-oil from lignin feedstocks, and any mixture thereof.

In the use according to the invention, when the polyphenol is a naturally occurring polyphenol extracted from the cashew nut shell liquid, it is preferably selected from the group consisting of cardanol, cardol, 2-methyl-cardol, and any mixture thereof.

In the use according to the invention, when the polyphenol is a lignan, it is preferably selected from the group consisting of pinoresinol, lariciresinol, matairesinol and alpha-conidentrin, and any mixture thereof.

In the use according to the invention, when the polyphenol is a stilbene, it is usually a 1,2-diarylethene with one ring having usually two hydroxyl groups in the meta position and the second ring is substituted by hydroxyl and methoxy groups in the ortho, meta and/or para position. The stilbene is preferably selected from the group consisting of resveratrol, pinosylvin, piceatannol, and any mixture thereof.

In the use according to the invention, when the polyphenol is a flavonoid, it is preferably selected from the group consisting of flavones, flavonols, flavanones, dihydroflavonols and chalcones. The flavonoids are usually in form of monomers, dimers, oligomers and polymers like non hydrolysable tannins.

These polyphenols are preferentially used as a mixture. The polyphenols can also be hydrolyzable tannins like tannic acid, partially hydrolyzed tannins or the polyphenol acids resulting from a complete hydrolysis like gallic acid and ellagic acid. The flavonoid is preferably selected from the group consisting of quercetin, epicatechin, flavan-3,4-diols, and any mixture thereof.

In the use according to the invention, the polyphenol can be present in the bio-oil from lignin feedstocks and it is preferably selected from the group consisting of resorcinol, hydroquinone, catechol, 4-ethyl-catechol, pyrogallol, and any mixture thereof. In the use according to the invention, when the polyol is a sugar, the sugar is preferably selected from pentoses, hexoses, oligosaccharides, polysaccharides, and any mixture thereof. The hexoses are preferably selected from D-allose, D-altrose, D-glucose, D-mannose, D-gulose, D-idose, D-galactose, D-talose and mixtures thereof. The hexoses are more preferably selected from D-glucose, D-mannose, and mixture thereof.

In the use according to the invention, the sugars can be used as such or after a chemical modification. Such modifications are for example reactions with ethylene oxide, propylene oxide or butylene oxide to produce an oxy alkylated sugar and hydrogenation followed by oxylkylation.

In the use according to the invention, the polyol can be derived from other polyols derivatives prepared from sugars. Anhydrosugars like isosorbide, isomannide, isoidide are examples of such polyols. The products of reduction of hydroxymethylfurfural (HMF), 2,4-bis-(hydroxymethyl)-furan and

2,5-bis-(hydroxymethyl)-tetrahydrofuran and more particularly the cis isomer are other examples of such polyols. The hydromethylfurfural can be obtained from hexoses (mainly fructose and glucose) but also from oligosaccharides

(e.g. saccharose and cellobiose), from polysaccharides (xylans, chitine, mannans, glucans like starch and cellulose, galactans like agar-agar and fructans like inuline), from lignocellulose and from lignocellulosic biomass.

In the use according to the invention, when the polyol is a product derived from a sugar, the product derived from a sugar is preferably selected from the group consisting of an anhydrosugar, a reduction product from sugar, a reduction product of hydroxymethylfurfural, a difuran derivative of furfural and any mixture thereof.

In the use according to the invention, when the product derived from a sugar is an anhydrosugar, it is preferably selected from the group consisting of isosorbide, isomannide, isoidide and any mixture thereof. The anhydrosugar is more preferably isosorbide.

In the use according to the invention, when the product derived from a sugar is a reduction product from sugar, it is preferably selected from sorbitol, mannitol, xylitol, iditol and any mixture thereof.

In the use according to the invention, when the product derived from a sugar is a reduction product of hydroxymethylfurfural, it is preferably selected from the group consisting of 2,5-bis-(hydroxymethyl)-furan, 2,5-bis- (hydroxymethyl)-tetrahydrofuran, and any mixture thereof. In the use according to the invention, when the product derived from a sugar is a oxidation product of hydroxymethylfurfural, it is preferably selected from the group consisting of 2,5-furane dicarboxylic acid, 2,5- tetrahydrofuran, dicarboxylic acid and any mixture thereof.

In the use according to the invention, when the product derived from a sugar is a difuran derivative of furfural, it is preferably selected from the group consisting of 5,5'-methylene-bis-2-furanmethanol, 5,5'-isopropylidene-bis-2- furanmethanol, and any mixture thereof.

In the use according to the invention, when the product derived from a sugar is a difuran derivative of furfural, it is preferably selected from the group consisting of 5,5'-methylene-bis-2-furan carboxylic acid, 5,5'-isopropylidene- bis-2-furan carboxylic acid, and any mixture thereof.

In a more preferred embodiment of the use according to the invention, the derivative of epichlorohydrin of natural origin is obtained by reacting

epichlorohydrin of natural origin with at least isosorbide.

In the use according to the invention, when the compound containing at least one active hydrogen atom is an acid mono- or polyphenol, it is preferably selected from the group of trans-cinnamic acid mono- or poly-phenol like p- coumaric acid, cafeic acid, ferrulic acid, 5-hydroxy-ferrulic acid, sinapic acid, and mixtures thereof.

In the use according to the invention the compound containing at least one active hydrogen atom can be obtained from lignin containing feedstocks like lignocellulosic biomass feedstocks, lignin-enriched biomass fractions and lignin. The feedstocks can be for example woods like softwood bark, ground softwood, pine, sawdust woodchips, hardwood, mixed hardwoods. Other possible feedstocks are forest residues and agricultural residues like bark waste, peat moss, treetops, limbs, bagasse, bamboo sticks, cashew nut shell, corn bran, cereal straw, coffee husks, stems of corn, sorghum, cotton or hemp, reeds, papyrus, coconut husks, byproducts from the palm oil production like oil palm fronds, roots, trunks, empty fruit bunch and fiber shells. The feedstocks can also be industrial residues and industrial lignins like lignin from newspaper, paper waste, creosote treated wood waste, birch wood waste, wood industry residues, black pulping liquor, lignin from steam explosion of birch, lignosulphonate, Kraft lignin, hydrolysis lignin, soda lignin, filamentous fungi-treated wood materials, Organosolv lignin, Funaoka lignin and hydrotopic lignin. The lignin containing feedstocks can be used as such. The lignin containing feedstocks can be modified before reaction with epichlorohydrin. The modification is for example esterification with an alcohol, esterification with a mono carboxylic acid or a monoester of a dicarboxylic acid, etherification with an alkylating reagent. The modification can also enhance the reactional ability of the lignin derivatives with epichlorohydrin. Such modifications are for example reactions with ethylene oxide or propylene oxide to produce chain extended hydroxyalkyl lignin, reaction with formaldehyde to produce chain extended hydroxymethyl lignin, reaction with a dicarboxylic acid or an anhydride of a dicarboxylic acid.

In the use according to the invention the compound containing at least one active hydrogen atom can be a phenolic s -rich product preferentially produced as bio-oil from the lignin feedstocks described here-above by treatment like slow, fast and flash pyrolysis, hydro-pyrolysis, vacuum pyrolysis, liquefaction and solvolysis (phenol, resorcinol...). The bio-oil can be produced by a catalytic pyrolysis of biomass not containing lignin like vegetable oil or starchy feedstocks. The bio-oil can also be produced by pyrolysis of biosludges (for example biosludges from fructose-manufacturing factory, milk derivative factory or beer brewing factory). The bio-oil contains aliphatic hydrocarbons, acids, esters, alcohols, ketones, aldehydes, furans and phenolics. The phenolics are constituted of phenol, p-cresol, ortho-cresol, meta-cresol, ethyl phenol,

2,3-dimethyl phenol, 2,4-dimethyl phenol, 2,5-dimethyl phenol, 2,6-dimethyl phenol, 3,5-dimethyl phenol, resorcinol, hydroquinone, catechol,

4-ethyl-catechol, pyrogallol, 2-methoxy-4-methyl-phenol, guaiacol,

4-methyl-guaiacol, 4-ethyl-guaiacol, 4- propyl-guaiacol, 4-allyl-guaiacol, 4-(l-propenyl)-guaiacol, syringol, 4-methyl-syringol, 4-ethyl-syringol,

4-allyl-syringol, 4-(l-propenyl)-syringol, 4-hydroxybenzoic acid, 4-hydroxy benzoic acid methyl ester and 3-hydroxy-4-methoxy benzoic acid. The bio-oil can be used as such or can be processed to a purified or enriched phenolics fraction by the means of an additional chemical treatment, a physical

fractionation treatment or any combination of these two types of treatment. The additional chemical treatment can be for example an hydrolysis, a dehydratation, an hydrogenolysis, an oxydehydroxygenation, etc. The fractionation treatment can be an evaporation, a distillation, a cristallisation, an extraction, a

chromatography, etc.

In the use according to the invention, when the alcohol is a phenol, it can be used as such or in a mixture. It can also be modified before the reaction with epichlorohydrin of natural origin. The coupling with ketones, the coupling with aldehydes and the oxidative coupling are examples of such modifications. The ketones and aldehydes used can be of non renewable or of renewable origin. Acetone, levulinic acid and formaldehyde are examples of ketones and aldehydes that can be of renewable origin. Levulinic acid is in particular produced from polysaccharides, hemicellulose and glucans, dissacharides or monomeric sugars like glucose and fructose. Diphenolic acid [4,4-bz ^' s-(4'-hydroxyphenyl)pentanoic acid] is prepared by the reaction of levulinic acid with two molecules of phenol.

In the use according to the invention, when the compound containing at least one active hydrogen atom is an acid, it is preferably a rosin acids selected from the group consisting of abietic acid, neoabietic acid, dehydroabietic acid, palustric acid, levopimaric acid, pimaric acid, isopimaric acids, and any mixture thereof and more preferably acids derived from abietic acid and from abietic acid derived imide diacid.

The reaction conditions for the use according to the invention are not critical. The reaction can be carried out under conditions described in prior art for derivatives of epichlorohydrin.

In the use according to the invention it preferred that the epichlorohydrin and the at least one compound comprising at least one active hydrogen atom are both obtained from renewable materials only.

The invention relates in a third embodiment to a process for

manufacturing a derivative of epichlorohydrin of natural origin selected from the group consisting of glycidyl ethers presenting an epoxide equivalent weight higher than or equal to 50 g/equivalent and lower than or equal to 15000 g/equivalent, of glycidyl esters, of glycidyl amides, of glycidyl imides, of glycidyl amines, and of any mixture thereof, and of which the ¹⁴ C mass

14 12 -12

content is such that the ratio C I C is higher than 0.7 10 ^" , comprising reacting epichlorohydrin of natural origin with at least one compound

comprising at least one active hydrogen atom, wherein the epichlorohydrin of natural origin ratio ¹⁴ C / ¹² C and said compound ratio ¹⁴ C / ¹² C are such that

[X _e pi ( ¹⁴ C / ¹² C) _epi + X _cpd ( ¹⁴ C / ¹² C) _cpd ] > 0.7 10 ¹²

wherein

X _e pi is the fraction of C atoms from epichlorohydrin of natural origin in the derivative of epichlorohydrin of natural origin,

X _C p _d is the fraction of C atoms from said compound in the derivative of epichlorohydrin of natural origin, ( C / C)e _P i is the carbon 14 to carbon 12 isotopic ratio in the

epichlorohydrin of natural origin, and

( ¹⁴ C / ¹² C) _C pd is the carbon 14 to carbon 12 isotopic ratio in said compound.

In a preferred variant of the process according to the invention, the said process presents at least one of the following features:

^■ the ( ¹⁴ C / ¹² C) _ep i is higher than or equal to 0.2 10 ^"12 ,

^■ the ( ¹⁴ C / ¹² C) _cpd is higher than or equal to 0.2 10 ^"12 .

In another preferred variant of the process according to the invention,

14 12 -12 the ( C I C) _e pi in the said process is higher than or equal to 0.2 10 ^" .

In still another preferred variant of the process according to the

14 12 -12

invention, the ( C I C) _cp d is higher than or equal to 0.2 10 ^" .

In yet another preferred variant of the process according to the invention, the ( ¹⁴ C / ¹² C) _ep i in the said process is higher than or equal to 0.2 10 ^"12 and the ( ¹⁴ C / ¹² C) _cpd is higher than or equal to 0.2 10 ^"12 .

In a more preferred variant of the process according to the invention, the said process presents the following features:

^■ the ( ¹⁴ C / ¹² C) _ep i is equal to 1.2 10 ^"12 , and

^■ the ( ¹⁴ C / ¹² C)cpd is equal to 1.2 10 ^"12 .

Detailed information concerning the derivative of epichlorohydrin of natural origin, natural epichlorohydrin, the compound comprising at least one active hydrogen atom, as well as preferred embodiments concerning the process, can be taken from the previous detailed description relating to the product and the use in accordance with the instant invention, to which reference is made.

The processes for preparing the derivative of epichlorohydrin, dichloropropanol and epichlorohydrin can be such as disclosed in International applications WO2005/054167, WO2006/100311, WO2006/100312,

WO2006/100313, WO2006/100314, WO2006/100315, WO2006/100316, WO2006/100317, WO2006/106153, WO2007/054505, WO 2006/100318, WO2006/100319, WO2006/100320, WO 2006/106154, WO2006/106155, WO 2007/144335, WO 2008/107468, WO 2008/101866, WO 2008/145729, WO 2008/1 10588, WO 2008/152045, WO 2008/152043, WO 2009/000773, WO 2009/043796, WO 2009/121853, WO 2008/152044, WO 2009/077528, WO 2010/066660, WO 2010/029039, WO 2010/029153, WO 201 1/054769 and WO 2011/054770, filed in the name of SOLVAY, the contents of which are incorporated herein by reference.

The invention relates in a fourth embodiment to the use of a derivative of epichlorohydrin of natural origin, selected from the group consisting of glycidyl ethers presenting an epoxide equivalent weight higher than or equal to 50 g/equivalent and lower than or equal to 15000 g/equivalent, of glycidyl esters, of glycidyl amides, of glycidyl imides, of glycidyl amines, and any mixture thereof, of which the ¹⁴ C mass content is such that the ratio ¹⁴ C / ¹² C is higher than 0.7 10 ^"

12 , more specifically as raw materials in the production of coatings or

composites. In that use, the derivative of epichlorohydrin of natural origin and the process for making that product are as described here above.

In a first aspect of that fourth embodiment, the coating obtained from derivative of epichlorohydrin of natural origin can be used in the fields of marine and industrial maintenance, of metal container, of coil coatings, of automotive coatings or of inks and resists.

The coating obtained from derivative of epichlorohydrin of natural origin can be used in the fields of marine and industrial maintenance (corrosion- resistant coatings for ships, shipping containers, offshore oil rigs and platforms, transportation infrastructures such as bridges, rail car coatings, coatings for industrial storage tanks, and primers for light industrial and agricultural equipment), of metal container (aluminum and steel food and beverage cans), of coil coatings (metal can ends, can bodies, building products, appliance panels, transportation, and metal furniture applications), of automotive coatings (primer surface coatings) and of inks and resists. Coating can be done using various technologies like low solids solvent borne coating, high solid solvent borne coating, solvent-free coating, waterborne coating, powder coating and radiation- curable coating.

In a first preferred variant of that first aspect the use of a derivative of epichlorohydrin of natural origin is in the production of coatings for marine and industrial maintenance comprising corrosion-resistant coatings for ships, shipping containers, offshore oil rigs and platforms, transportation infrastructures such as bridges, rail car coatings, coatings for industrial storage tanks, and primers for light industrial and/or agricultural equipment

In a second preferred variant of that first aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of coatings for metal containers comprising aluminum and steel food and beverage cans. In a third preferred variant of that first aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of coatings for coils coatings comprising metal can ends, can bodies, building products, appliance panels, transportation, and metal furniture applications.

In a fourth preferred variant of that first aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of coatings for automotive coatings comprising primer surface coatings.

In a fifth preferred variant of that first aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of coatings for inks and resists.

In a second aspect of that fourth embodiment, the composites can be used in the field of structural composites (fiber reinforcing materials based on glass, boron, graphite, aromatic polyaramides and natural fibers). The natural fibers can be of vegetable or of animal origin. The vegetable fibers can be bast fibers, leaf fibers, seed-hair fibers, grass fibers, straw fibers, root fibers or wood fibers. Bast fibers are produced for example by Flax, Hemp, Jute, Banana, China jute, Kenaf, Kudzu, Nettle, Paper Mulberry, Papyrus, Pennywort, Ramie, Roselle,

Seagrasses, Sunn hemp, Arundo Donax, Elephant Grass, Bamboo, Urena, Sunflower, Water Hyacinth and bagasse from Sugar Cane and Sorghum. Leaf fibers are produced for example by Abaca, Cantala, Caroa, Corn, Curaua, Fique, Henequen, Istle, Mauritius, Phormium, Pineapple, Sanseviera, Sisal, palm trees like Gomuti, Palmyra Palm, Piassava, Crin vegetal and Raffia. Seed-hair fibers are produced for example by African Palm, Coir, Cotton, Kapok and Milkweed floss. Grass fibers are produced for example by Alfalfa, Babhar grass, Esparto, Reed Canary grass, Sabai grass, switchgrass and Miscanthus. Straw fibers are produced for example by barley, rice, oat, rye and wheat. Root fibers are produced for example by Cassava and Broom root. The wood fibers can be issued from soft or hard wood. The animal fibers can be for example poultry feather, silk and wool.

In that second aspect, the composites can also be used in the field of civil engineering of flooring (floor paints, self-leveling floors, trowelable floors, and pebble-finished floors) and of construction, of electrical laminates (printed wiring boards and printed circuit boards), of other electrical and electronic applications, like casting, potting, encapsulation (switchgear components, transformers, insulators, high voltage cable accessories, and similar devices) and transfer molding (encapsulation of electronic components such as semiconductor chips, passive devices, and integrated circuits), of adhesives (cohesion between similar and dissimilar materials such as metals, glass, ceramics, wood, cloth, and many types of plastics) and of tooling (prototypes, master models, molds and other parts for aerospace, automotive, foundry, boat building, and various industrial molded items)

In a first preferred variant of that second aspect, the use of a derivative of epichlorohydrin of natural origin is in the fields of structural composites, of civil engineering, of flooring, of construction, of electrical laminates, of electrical and electronic applications, of transfer molding, of adhesives, of energy production or of tooling.

In a second preferred variant of that second aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of composites for structural composites comprising fiber reinforcing materials based on glass, boron, graphite, aromatic polyaramides and/or natural fibers.

In a third preferred variant of that second aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of composites for civil engineering comprising for instance adhesives. The adhesives applications are for example in the fields of air field runways and aprons, highway and bridge joints, bridge abutments, concrete lined canals, traverse and longitudinal joints, multilevel parking lot joints, underground tunnel construction joints and sections, attaching metal studs in concrete, bonding traffic markers on roadways and road dividers, bonding pancake lighting systems in airport runways, parking lots, etc.

In a fourth preferred variant of that second aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of composites for flooring comprising floor paints, self-leveling floors, trowelable floors, and/or pebble- finished floors.

In a fifth preferred variant of that second aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of composites for construction comprising among others adhesives applications and formed parts, obtained for instance by extrusion, pultrusion and any other forming techniques.

In a sixth preferred variant of that second aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of composites for energy production comprising windmill blade and/or turbine housing.

In a seventh preferred variant of that second aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of composites for electrical laminates comprising printed wiring boards and/or printed circuit boards.

In an eighth first preferred variant of that second aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of composites for electrical and electronic applications compring switchgear components, transformers, insulators, high voltage cable accessories, and/or similar devices.

In a ninth preferred variant of that second aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of composites for transfer molding comprising the encapsulation of electronic components such as semiconductor chips, passive devices, and/or integrated circuits.

In a tenth preferred variant of that second aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of composites for adhesive for cohesion between similar and dissimilar materials such as metals, glass, ceramics, wood, cloth, and many types of plastics.

In a eleventh preferred variant of that second aspect, the use of a derivative of epichlorohydrin of natural origin is in the production of composites for tooling comprising prototypes, master models, molds and/or other parts for aerospace, automotive, foundry, boat building, and/or various industrial molded items.

The examples below are intended to illustrate the invention without, however, limiting it.

Example 1 (not according the invention)

The apparatus employed was a thermostatised flask equipped with a mechanical stirrer, with a jacket containing a thermocouple and with a

Dean-Stark separator surmounted by a water-cooled condenser. A pump has been used to inject a caustic soda aqueous solution at a constant rate in the flask.

The reaction flask has initially been loaded with a mixture of isosorbide (43.8 g, 0.3 mol) and the epichlorohydrin sample ECH1 coming from a propylene-chlorine plant (275.0 g, 3.0 mol). The epichlorohydrin ECH1 has been obtained by dehydrochlorination of dichloropropanol, the dichloropropanol having been obtained by hypochlorination of allyl chloride, the allyl chloride having been obtained by chlorination of propylene, a fossil raw material. The analysis of the epichlorohydrin ECH 1 is given in Table 1. The mixture has been heated at reflux under stirring to a temperature of 115°C. A 50 % aqueous solution of caustic soda (49.8 g, 0.6 mol) has been introduced at a rate of 3.276 ml/h during 10 hour. The temperature of the mixture in the flask has been maintained in the range 100°C - 115°C in order to assure a constant reflux. The epichlorohydrin rich organic phase which decanted during the reaction as a lower phase in the separator has been recycled regularly in the reaction flask and the aqueous rich phase collected as an upper phase in the separator has been regularly drawn off. The heating has been maintained for 15 min after the total introduction of the caustic soda solution to achieve the collect of the water phase in the decantor. 33.0 g of aqueous phase (Wl) have been collected with a composition given in Table 1.

The epichlorohydrin in excess has been removed from the reaction mixture by distillation under a vacuum of 30 torr and by a progressive heating of the mixture to 107°C. 199.7 g (2.1 mol) of epichlorohydrin have been recovered in this step. The composition of the distillate (ECH2) is given in Table 1.

The salt has been separated from the crude product (40.3 g) after addition of 78.0 g of acetone under agitation and by filtration. The cake of filtration has been washed with 50.0 ml of acetone. The acetone solutions have been mixed and evaporated at 60°C under a pressure of 20 torr.

The residual product of the evaporation (75.9 g) contained less than 1 %g/g of unconverted isosorbide. The residue contained 0.450 mol epoxy per 100 g and 0.32 % of hydrolysable chlorine.

The residual product had a ¹⁴ C mass content such that the ratio ¹⁴ C / ¹² C was 0.64 10 ^"12 (measured according to standard ASTM D6866).

Example 2 (according the invention)

The trial has been carried out in the apparatus described in example 1. The reaction flask has been initially charged with a mixture of isosorbide (43.8 g, 0.3 mol) and epichlorohydrin sample ECH 3 (278 g, 3.0 mol). The epichlorohydrin ECH3 has been obtained by dehydrochlorination of

dichloropropanol, the dichloropropanol having been obtained by

hydrochlorination of natural glycerol, the glycerol having been obtained from renewable raw materials. The analysis of the epichlorohydrin is given in Table 1. The mixture has been heated at reflux under stirring to a temperature of 115°C. A 50 % aqueous solution of caustic soda (49.8 g, 0.6 mol) has been introduced at a rate of 3.276 ml/h during 10 hour. The temperature of the mixture in the flask has been maintained in the range 104°C - 115°C in order to assure a constant reflux. The epichlorohydrin rich organic phase which decanted during the reaction as a lower phase in the separator has been recycled regularly in the reaction flask and the aqueous rich phase collected as an upper phase in the separator was regularly drawn off. The heating has been maintained for 15 min after the total introduction of the caustic soda solution to achieve the collect of the water phase in the decantor. 33.5 g of aqueous phase (W2) have been collected with a composition given in Table 1.

The epichlorohydrin in excess has been removed from the reaction mixture by distillation under a vacuum of 40 torr and by a progressive heating of the mixture to 70°C. 202.1 g (2.2 mol) of epichlorohydrin has been recovered in this step. The composition of the distillate (ECH4) is given in Table 1.

The salt has been separated from the crude product (38.4 g) after addition of 78 g of acetone under agitation and by filtration. The cake of filtration has been washed with 50 ml of acetone. The acetone solutions have been mixed and evaporated at 60°C under a pressure of 20 torr.

The residual product of the evaporation (73.8 g) contained less than 1 %g/g of unconverted isosorbide. The residue contained 0.457 mol epoxy per 100 g and 0.16 % of hydrolysable chlorine.

The residual product had a ¹⁴ C mass content such that the ratio ¹⁴ C / ¹² C was 1.2 10 - ^" 12 (measured according to standard ASTM D6866).

The High Performance Liquid Chromatography analyses of the residual products obtained in examples 1 and 2 are presented in Table 1.

Table 1

Component Example 1 Example 2

ECH1 ECH2 Wl ECH3 ECH4 W2

(g kg) (g kg) (mg/1) (g kg) (g/kg) (mg/1) acetaldehyde n.d. n.d 0.39 n.d n.d 0.4 acrolein n.d n.d 0.06 n.d n.d 0.07

2-propanol n.d n.d < 0.05 n.d n.d n.d allyl alcohol 0.002 n.d 0.28 0.005 0.003 0.28 hydroxyacetone 0.012 0.004 n.d 0.006 0.006 n.d chloroacetone + n.d n.d

(3,3 -dichloro- 1 -propene) 0.003 n.d 0.041 0.003

1 ,2-dichloropropane 0.019 0.011 n.d 0.003 n.d n.d

2,3-dichloro- 1 -propene 0.006 0.031 n.d n.d n.d n.d l-chloro-2, 3- Principal Principal Principal Principal epoxypropane product product (7.2g/kg ) product product (Hg/kg )

1 , 3 -dichloro- 1 -propene n.d n.d n.d cis maj. +

(C6H140 min.) 0.041 0.030 0.001

2-chloro-2-propene- 1 -ol 0.14 0.016 n.d 0.020 0.006 0.05

1 , 3 -dichloro- 1 -propene n.d

trans 0.014 0.01 0.009 0.006

C ₅ Hi ₀ O / C ₄ H ₇ C10 0.006 0.008 n.d n.d n.d n.d

C ₆ H ₁₂ 0 n.d n.d 0.17 n.d n.d 0.16

1,3-dichloropropane +

Ni 0.002 0.001 0.09 0.024 0.028 0.09

Cyclopentanone n.d n.d n.d 0.009 0.011 n.d

n.d. : not detected n.i. : unidentified product