EP4259573A1

EP4259573A1 - Liquid formulation for hydrogen storage

Info

Publication number: EP4259573A1
Application number: EP21840654.4A
Authority: EP
Inventors: Jérôme BLANC
Original assignee: Arkema France SA
Current assignee: Arkema France SA
Priority date: 2020-12-09
Filing date: 2021-12-07
Publication date: 2023-10-18
Also published as: FR3117114B1; US20230348263A1; WO2022123166A1; CA3180890A1; CN115989190A; FR3117114A1; JP2023553230A; AU2021397854A1

Abstract

The present invention relates to a liquid formulation comprising an amount greater than or equal to 50 wt% benzyltoluene and an amount of less than 0.5 mol% diphenylmethane. The invention also relates to the use of said formulation as LOHC for the production of hydrogen comprising less than 0.5 mol% diphenylmethane.

Description

LIQUID FORMULATION FOR HYDROGEN STORAGE

The present invention relates to the field of liquid formulations capable of transporting hydrogen, and more particularly the field of formulations based on benzyltoluene capable of transporting hydrogen.

[0002] Hydrogen today represents an alternative to fossil, natural or electrical energy sources. However, the storage and transport of this energy source, hydrogen, remains a major challenge for the rapid and accessible development of this energy source.

[0003] Various approaches have been studied to store and transport this very volatile and highly explosive gas more easily, and, among these, mention may be made of storage under pressure, cryogenic storage, storage on a support. Among the types of support that can be envisaged, the technology based on organic liquid hydrogen carriers (technology known as LOHC for "Liquid Organic Hydrogen Carrier" in English) is a promising and particularly interesting technology for long-distance transport, at very low costs. fully compatible with large-scale development.

The principle of this LOHC technology consists in fixing hydrogen on a support molecule, which is preferably and most often liquid at room temperature, in a hydrogenation step, then in releasing the fixed hydrogen, at near the place of consumption, in a dehydrogenation step.

[0005] Among the LOHC molecules studied today, aromatic liquids with two or three rings, such as for example benzyltoluene (BT) and/or dibenzyltoluene (DBT) which have already been the subject of numerous studies and patent applications, represent molecules particularly well suited to this use. Patent EP2925669 thus shows the use of BT and/or DBT in LOHC technology, and describes the hydrogenation and dehydrogenation operations of these fluids for the storage and release of hydrogen.

[0006] Beyond the instantaneous performance of the hydrogenation and dehydrogenation steps, the sequence of cycles and the maintenance of performance (yield of hydrogen fixation/release) as well as the purity of the destocked hydrogen (or released) during the dehydrogenation step, are key points for the economic aspect of this technology. [0007] Indeed, the hydrogen resulting from this LOHC technology finds uses in very many fields, such as for example in fuel cells, as well as in various industrial processes, or even as fuel for all means of transport, such as trains, ships, trucks, motor cars, planes, and others. Any impurity present in the hydrogen, even in trace amounts, could have a negative impact, both on the hydrogenation/dehydrogenation process in terms of yield, and on the quality of the products manufactured or even on the yields in end uses. hydrogen produced by this technique.

[0008] In order to overcome these possible problems, one of the solutions is for the hydrogen released during the dehydrogenation step to be as pure as possible. However, the hydrogen released during the dehydrogenation step inevitably brings with it impurities from organic compounds often present in the organic liquid to be dehydrogenated.

These impurities are of various natures, and can be present in greater or lesser quantities, on the one hand in the starting LOHC fluid, but also in the LOHC fluid after it has undergone numerous hydrogenation/dehydrogenation cycles. (called "LOHC fluid" in the remainder of this presentation).

[0010] Among the most widely studied and most promising LOHC fluids today, benzyltoluene (BT) is a compound of choice, in particular because of its physico-chemical properties which are entirely compatible with the operations of hydrogenation/dehydrogenation and existing industrial preparation capacities. Indeed, BT is a well-known compound, commercially available and the method of preparation of which is also well known to those skilled in the art. For example, BT can easily be prepared by catalytic reaction of toluene with chlorotoluene, according to techniques now well known to those skilled in the art and in particular as described in patent EP0435737.

[0011] However, the synthesis of BT can lead, in particular due to the presence of traces of benzene in the starting toluene, to the formation of a by-product which is diphenylmethane (DPM) resulting from the coupling between the benzene and chlorotoluene. It is also possible that diphenylmethane is formed, undesirably, during the hydrogenation/dehydrogenation cycles of BT.

[0012] Thus, synthetic crudes from BT, but also LOHC fluids based on BT that have been engaged in hydrogenation/dehydrogenation cycles can thus contain variable amounts of diphenylmethane which can prove to be troublesome when present in excessive amounts. in an LOHC fluid, such as BT. There therefore remains a need for high-performance LOHC fluids, both from the point of view of yield in terms of storage (hydrogenation/dehydrogenation cycles) and from the point of view of the purity of the hydrogen released during the step of dehydrogenation. Still other objectives will become apparent in the remainder of the description of the invention which is set out in more detail below.

[0014] The Applicant has now discovered a formulation of LOHC fluid that is entirely suitable for the storage and transport of hydrogen capable of releasing, during the dehydrogenation step, hydrogen of high purity.

Thus, and according to a first aspect, the present invention relates to a liquid formulation based on benzyltoluene (BT) containing low levels of diphenylmethane (DPM). This type of formulation makes it possible in particular to overcome all or part of the drawbacks noted in the prior art for LOHC liquids, by meeting in particular the requirements for storage, transport and release of hydrogen, under optimal industrial and economic conditions, and in allowing the release, during the dehydrogenation step of said formulation, of high purity hydrogen, and in particular of hydrogen having very low contents of undesirable products, in particular DPM and its possible degradation products, such as benzene , this being particularly detrimental for the uses of hydrogen in fuel cells for example.

[0016] In addition, diphenylmethane has a melting point (25° C.) much higher than that of benzyltoluene (-80° C.), but also of another LOHC fluid, dibenzyltoluene (-38.5° C.). VS). Consequently, the DPM can form a cloudiness or even precipitate, when it is present in too large quantities in the BT, which can prove to be annoying or even prohibitive, in particular during the operations of transport and transfer of the LOHC fluid through pipes. , pumps, valves and other equipment necessary for the use of said LOHC fluid envisaged in the present invention, and in particular during transport and during use in the hydrogenation/dehydrogenation cycles.

[0017] Furthermore, the presence of DPM in a liquid formulation based on benzyltoluene results mainly from the presence of benzene in the raw materials used during the synthesis of BT and makes it possible to fear possible traces of benzene in the product. end, this benzene can then contaminate the hydrogen released during the dehydrogenation step.

[0018] Similarly, the inevitable degradation of DPM at high temperature and in contact with the catalysts used during the hydrogenation/dehydrogenation cycles can lead to the formation of non-negligible quantities of benzene, which benzene can then contaminate the hydrogen released during the dehydrogenation step.

More specifically, the present invention relates to a liquid formulation comprising:

- an amount equal to or greater than 50%, preferably equal to or greater than 60%, more preferably equal to or greater than 70%, better still equal to or greater than 80% and most preferably equal to or greater than 90% by weight of benzyltoluene (BT), relative to the total weight of the formulation, and

- a quantity of less than 0.5 molar % of diphenylmethane (DPM), relative to the total number of moles BT + DPM.

The formulation according to the present invention is a liquid formulation at ambient temperature and pressure, that is to say at 25° C. and 1 atmosphere (1013 mbar or 1013 hPA).

As indicated previously, the formulation according to the present invention comprises an amount equal to or greater than 50% by weight of BT, preferably equal to or greater than 60%, more preferably equal to or greater than 70%, better still equal to or greater than greater than 80% and quite preferably equal to or greater than 90% by weight of BT. In a very particularly preferred embodiment, the formulation according to the present invention comprises an amount equal to or greater than 98% by weight of benzyltoluene (BT).

The formulation according to the present invention preferably comprises benzyltoluene alone, or optionally with one or more other LOHC fluids as indicated below, that is to say without component other than DPM present in an amount less than 0, 5% molar. Thus, and in a preferred embodiment, the formulation according to the invention comprises an amount at most equal to 99.99% by weight of BT, preferably at most equal to 99.95% by weight of BT, more preferably at most equal to 99.9% by weight of BT.

[0023] As indicated above, the formulation may also comprise one or more other LOHC fluids well known to those skilled in the art, such as those derived from petroleum products and/or products synthesized from petroleum products, or even derived from petroleum products. renewables and/or products synthesized from renewable products. DPM is not considered to be an LOHC fluid of interest within the meaning of the present invention.

[0024] Such other LOHC fluids are, for example and without limitation, those chosen from dibenzyltoluene (DBT), diphenylethane (DPE), ditolyl ether (DT), phenylxylylethane (PXE), mono- and bi-xylylxylenes, 1,2,3,4-tetrahydro-(1-phenyl-ethyl)naphthalene, di-isopropylnaphthalene, mono-isopropylbiphenyl, phenylethyl-phenylethane (PEPE) , N-ethylcarbazole, phenylpyridines, tolylpyridines, diphenylpyridines, dipyridylbenzenes, dipyridinetoluenes, as well as mixtures of two or more of them, in all proportions, to cite only the main organic fluids known and usable in the scope of the present invention.

According to a preferred embodiment of the present invention, the formulation comprises at least 50% by weight of benzyltoluene (BT), and dibenzyltoluene (DBT). According to an embodiment of the present invention, the formulation comprises from 70% to 80% by weight of BT and from 20% to 30% by weight of DBT (relative to the total weight of BT + DBT). According to another embodiment, the formulation comprises from 80% to 99.9% by weight of BT and from 0.1% to 20% by weight of DBT (relative to the total weight of BT + DBT), preferably the formulation comprises from 90% to 99.9% by weight of BT and from 0.1% to 10% by weight of DBT (based on the total weight of BT + DBT), and more preferably the formulation comprises from 90% to 99.5% by weight of BT and 0.5% to 10% by weight of DBT (based on the total weight of BT + DBT).

As indicated above, the formulation according to the present invention comprises an amount of less than 0.5% molar, preferably equal to or less than 0.4% molar, advantageously equal to or less than 0.3% molar, more preferably equal to or less than 0.1 mol% of DPM, relative to the total number of moles BT + DPM. As indicated above, it has in fact been established that DPM very often leads to numerous drawbacks, whether during the hydrogenation/dehydrogenation operations to which the LOHC formulations are subjected, but also in the hydrogen released during the dehydrogenation operations, hydrogen which may then not have the degree of purity required for the applications for which it is intended.

[0027] Indeed, if the LOHC fluid formulations are particularly well suited to the transport of hydrogen, in the form of liquid, and in a safe manner, these formulations must ensure that the hydrogen, released during the step of dehydrogenation, a purity at least as great as that of the hydrogen used for the hydrogenation of the support.

Thus, the hydrogen transported thanks to the formulation according to the present invention has a degree of purity that is entirely compatible in particular with applications such as, for example, fuel cells, and all other industrial applications requiring the use of high purity hydrogen, such as the electronics sector for the production of microprocessors, semiconductors, and others. In a preferred embodiment of the present invention, the DPM is present in the formulation at a content of between 1 ppm molar and 0.5% molar, limits excluded, preferably greater than 1 ppm molar and equal to or less than at 0.3% molar, more preferably still greater than 1 ppm molar and equal to or less than 0.1% molar, relative to the total number of moles BT+DPM.

[0030] The formulation according to the invention may further, although this does not form a preferred embodiment, comprise one or more additives and/or fillers well known to those skilled in the art, and for example, and in such a way non-limiting, selected from antioxidants, pigments, colorants, flavors, odor masking agents, viscosity modifiers, passivators, pour point depressants, decomposition inhibitors and mixtures thereof.

Among the antioxidants which can be advantageously used in the formulation of the invention, mention may be made, by way of non-limiting examples, of phenolic antioxidants, such as for example dibutylhydroxytoluene, butylhydroxyanisole, tocopherols, as well as the acetates of these phenolic antioxidants. Mention may also be made of antioxidants of the amine type, such as for example phenyl-o-naphthylamine, of the diamine type, for example N,N′-di-(2-naphthyl)-para-phenylenediamine, but also the acid ascorbic acid and its salts, esters of ascorbic acid, alone or in mixtures of two or more of them or with other components, such as for example green tea extracts, coffee extracts.

In one embodiment, the present invention relates to a formulation comprising:

- an amount equal to or greater than 50%, preferably equal to or greater than 60%, more preferably equal to or greater than 70%, better still equal to or greater than 80% and most preferably equal to or greater than 90% by weight of benzyltoluene (BT), and

- optionally at least one other LOHC fluid, other than BT, preferably optionally at least one other LOHC fluid which is dibenzyltoluene (DBT),

- an amount between 1 molar ppm and 0.5 molar %, limits excluded, preferably greater than 1 molar ppm and equal to or less than 0.3 molar %, more preferably greater than 1 molar ppm and equal to or less than 0 .1% molar, relative to the total number of moles BT + DPM,

- optionally at least one additive, as defined above.

In another embodiment, the present invention relates to a formulation comprising: - an amount equal to or greater than 50%, preferably equal to or greater than 60%, more preferably equal to or greater than 70%, better still equal to or greater than 80% and most preferably equal to or greater than 90% by weight of benzyltoluene (BT), and

- an amount of dibenzyltoluene (DBT) of between 0.1% and 30% by weight, relative to the total weight of the LOHC fluids present in said formulation,

- optionally at least one additive and/or filler, as defined previously.

Benzyltoluene (BT) is a well-known compound, commercially available and the method of preparation of which is also well known to those skilled in the art. For example, BT can easily be prepared by catalytic reaction of toluene with chlorotoluene, according to techniques now well known to those skilled in the art and in particular as described in patent EP0435737.

[0035] The synthetic crudes of BT, but also the LOHC liquids based on BT having been engaged in hydrogenation/dehydrogenation cycles can thus contain variable amounts of DPM, as described above. The formulation according to the present invention can therefore be prepared, for example and typically, from these synthetic raw materials or liquid LOHCs based on BT, according to any method well known to those skilled in the art.

[0036] Methods for preparing the formulation according to the present invention which could be envisaged and appear quite obvious to those skilled in the art, are for example the distillation of a formulation of BT in order to eliminate the DPM or any at least to lower the DPM content in the BT. However, this solution suffers from numerous drawbacks, among which may be mentioned high costs and complications of industrial installations implementing distillation stages (heating, placing under vacuum or partial pressure, etc.), especially since the quantities of DPM to be eliminated are often relatively low and the difference between the boiling points being relatively low (boiling point of BT = 280° C. boiling point of DPM = 264° C.).

Another method could consist in using a starting toluene of very high purity, in particular free or comprising only minute traces of benzene in order to minimize the formation of DPM. The “pure” BT formulation produced from this toluene ultra-pure would however be of a cost completely incompatible with use on an industrial scale.

According to a preferred embodiment, the formulation according to the present invention can advantageously be obtained from a synthetic crude of BT or a crude from distillation of BT or even from a formulation based on BT having already undergone a greater or lesser number of hydrogenation/dehydrogenation cycles, by one or more treatment(s) on filtering agents and/or adsorbents.

The filtering agents which can be used in the context of the present invention can be of all types and are well known to those skilled in the art. The filtering agents which have proved to be the most suitable are the adsorbent filtering agents, and more particularly the filtering agents comprising one or more compounds chosen from minerals based on silicates, carbonates, carbon, as well as mixtures of two or more of these minerals in all proportions.

By way of non-limiting examples, mention may be made of inorganic or organic filtering agents, and in particular those chosen from clays, zeolites, diatomaceous earth, ceramics, carbonates, and carbon derivatives, as well as mixtures of two or more of them, in any proportion.

The following can be mentioned more particularly as filtering agents, adsorbents and filter-adsorbents:

• clays, including silicates, and for example magnesium silicates, such as and without limitation, attapulgites, montmorillonites, selenites, bentonites, talcs, and others,

• natural or synthetic aluminum silicates, in particular kaolins, kaolinites, zeolites,

• carbonates, for example of calcium and/or magnesium, and more particularly those known under the names of limestone or chalks,

• derivatives of charcoal, wood, shells, for example coconut shells, olive stones or pomace, and more generally those known under the name of activated carbon,

• and others and mixtures thereof.

[0042] Silicates, in particular clays and zeolites, have proved to be very particularly effective for the preparation of the formulation of the present invention. Silicates have in fact shown themselves to be particularly suitable for the elimination, or at least for the significant reduction of the quantities of DPM present in a formulation comprising an amount equal to or greater than 50% by weight of benzyltoluene (BT).

According to a very particularly preferred embodiment of the present invention, as examples of filtering agents advantageously usable for the preparation of the formulation of the present invention, mention may be made of attapulgite Microsorb® 16/30 LVM from BASF (example of alumino-magnesian clay with the chemical formula (Mg, Al) ₅ Si8O22(OH) ₄ , SiC>2), Amcol Rafinol 900 FF from Minerals Technologies, Amcol Rafinol 920 FF from Minerals Technologies, Amcol Mineral Bent (aluminum hydrosilicate) from Minerals Technologies), and Siliporite®, in particular MK30B0 and MK30B2, from ARKEMA (preparations based on zeolite of the alumino silicate type).

In a very particularly preferred embodiment, the filtering agent used for the preparation of the formulation according to the present invention is chosen from molecular sieves (also called "zeolitic adsorbents"), in particular molecular sieves allowing the adsorption , as selectively as possible, the DPM present in the formulation comprising at least 50% BT.

The most appropriate zeolite adsorbent materials, that is to say materials comprising one or more zeolites, are advantageously chosen from molecular sieves based on synthetic zeolites which, by virtue of their wide variety of preparation methods , a wide variety of parameters which can be finely adjusted, such as for example the thermal stability, the mechanical resistance or even the facilitation of regeneration, and this in order to meet the specific criteria required for the use of interest.

According to a preferred embodiment, among the most suitable zeolite adsorbent materials for use in the context of the present invention, mention may be made of natural or synthetic zeolites, and more particularly zeolite adsorbent materials chosen from natural zeolites, such as for example chabazite, and among synthetic zeolites, in particular LTA-type zeolites, FAU-type zeolites, EMT-type zeolites, MFI-type zeolites, and BEA-type zeolites.

[0047] The different types of zeolites mentioned above are easily accessible to a person skilled in the art commercially or can be easily synthesized using procedures known and available in the scientific literature and the patent literature. In addition, the different types of zeolite are clearly defined and exposed, for example, in “Atlas of Zeolite Framework Types”, 5th edition, ⁽ 2001), Elsevier. The treatments on filtering agents and/or adsorbents as they have just been described and in particular the treatments on zeolites as they have just been described, are effective and economical alternatives to the selection of a toluene ultra-pure as a raw material for the synthesis process, or even for costly and complex distillation operations. The preparation of the formulation according to the invention by treatment on a filtering agent and/or adsorbent, in particular on zeolite, has the great advantage of tolerating a greater variety of raw materials at acceptable costs while making it possible to provide a final product (the BT) of very high purity. Furthermore, the use of filtering agents and/or adsorbents, in particular zeolites, also makes it possible to eliminate all or part of one or more other impurities and undesired compounds inherently present in the preparation of BT, or produced during the numerous hydrogenation/dehydrogenation cycles of the formulation according to the present invention.

By way of example, a BT formulation containing amounts greater than 0.5% molar of DPM, typically 0.7%, 0.8% and 0.9% molar, is advantageously passed over a bed of zeolite adsorbent, typically in the form of zeolite crystals agglomerated with a binder, generally a clay. The zeolite crystals preferably comprise one or more cations, advantageously chosen from alkali and alkaline-earth metal cations, more specifically from lithium, sodium, potassium, magnesium, calcium, strontium and barium cations. Examples of zeolite adsorbents include, but are not limited to, zeolite adsorbents from the Siliporite® range sold by ARKEMA.

The treatment on a bed of zeolite adsorbent can be carried out at any temperature, advantageously at a temperature between 5° C. and 80° C., typically around 40° C., and most often at atmospheric pressure, for obvious reasons. ease of the process, it being understood that the streams can be subjected to overpressures or depressions in order to promote and/or facilitate the passage of the stream through the bed of adsorbent.

The treatment on zeolitic adsorbent described above makes it possible in particular to lower the DPM content in a BT formulation to values below 0.20% molar, better still below 0.15% molar, even better still below 0.10% molars.

According to another aspect, the present invention relates to the use of a formulation as defined above as LOHC fluid for the production of hydrogen comprising a low level of impurities and in particular for the production of hydrogen comprising a quantity less than 0.5 mol% of diphenylmethane, relative to the total number of moles H ₂ + DPM. Thanks to the formulation of the present invention, the hydrogen stored and then released during the dehydrogenation step is a high purity hydrogen, and in particular a hydrogen containing no or only negligible amounts of benzene. The hydrogen thus produced can therefore find uses in a very large number of applications, in particular for fuel cells, and all other industrial applications requiring the use of high purity hydrogen, such as the electronics sector for the production of microprocessors, semiconductors, and others.

Claims

1. Liquid formulation comprising:

2. Formulation according to claim 1, comprising an amount equal to or greater than 98% by weight of benzyltoluene.

3. Formulation according to claim 1 or claim 2, comprising one or more other LOHC fluids derived from petroleum products and/or products synthesized from petroleum products, or also derived from renewable products and/or products synthesized from renewable products.

4. Formulation according to any one of the preceding claims, comprising one or more other LOHC fluids chosen from dibenzyltoluene, diphenylethane, ditolylether, phenylxylylethane, mono- and bi-xylylxylenes, 1, 2,3,4-tetrahydro-(1-phenyl - ethyl)naphthalene, di-isopropylnaphthalene, mono-isopropylbiphenyl, phenylethylphenylethane, N-ethylcarbazole, phenylpyridines, tolylpyridines, diphenylpyridines, dipyridylbenzenes, dipyridinetoluenes, as well as mixtures of two or more of them, in all proportions.

5. Formulation according to any one of the preceding claims, comprising at least 50% by weight of benzyltoluene and dibenzyltoluene, preferably from 70% to 80% by weight of benzyltoluene and from 20% to 30% by weight of dibenzyltoluene, by relative to the total weight of benzyltoluene + dibenzyltoluene.

6. Formulation according to any one of claims 1 to 4, comprising from 80% to 99.9% by weight of benzyltoluene and from 0.1% to 20% by weight of dibenzyltoluene (relative to the total weight of benzyltoluene + dibenzyltoluene ), preferably the wording comprises from 90% to 99.9% by weight of benzyltoluene and from 0.1% to 10% by weight of dibenzyltoluene, based on the total weight of benzyltoluene + dibenzyltoluene.

7. Formulation according to any one of the preceding claims, comprising an amount equal to or less than 0.4% molar, preferably equal to or less than

0.3% molar, more preferably equal to or less than 0.1% molar of DPM, relative to the total number of moles BT+DPM.

8. Use of a formulation according to any one of the preceding claims, as LOHC fluid for the production of hydrogen comprising a quantity of less than 0.5% molar of diphenylmethane.

9. Use according to the preceding claim, for the production of hydrogen usable in fuel cells, or in the electronics sector for the production of microprocessors, semiconductors, and others.