Patent Application
20250146186
The invention falls within the general field of valorization of renewable resources, in particular cellulose.
More particularly, the invention relates to a method of preparing multi-functionalized cellulose fibers. The invention also relates to a more global method of preparing multi-functionalized nanofibrillated cellulose, as well as to multi-functionalized nanofibrillated cellulose obtainable by such a method, and the use thereof in composite materials.
Valorization of cellulose, the most abundant renewable resource on Earth, is considered as one of the most effective ways towards sustainability. Due to its high abundance, low cost and biodegradability, cellulose is indeed a high-value candidate for the preparation of bio-based materials, in replacement of fossil resources.
Many methods have been proposed by the prior art for modifying cellulose in order to adapt its surface properties to the applications for which it is intended to be used. Most of these methods achieve the grafting of a single functional group, for example a hydrophobic group, on the cellulose surface. As many applications require cellulose to have multiple functions, a few methods have also been proposed for grafting two different functional groups thereon. One of these methods, comprising providing cellulose fibers with a carboxymethyl function and an aldehyde function, is for example described in the publication of Sichinga et al., 2022, Cellulose, 29(2): 799-815. However, all the methods developed up to now for preparing multi-functionalized cellulose are costly and time-consuming. There remains a need for a method for preparing multi-functionalized cellulose fibers within short reaction times, at low cost and with a high yield. This need is all the more important that multi-functionalized cellulose fibers can be used for preparing multi-functionalized nanofibrillated cellulose, which find applications in many fields.
Nanofibrillated cellulose, also called cellulose nanofibers or cellulose nanofibrils (CNF), consisting of nanosized cellulose fibers with a width in the nanometric range, typically of between 5 and 15 nm, and a length in the micrometric range, has attracted much interest scientifically and commercially because of its high abundancy, renewability and recyclability, as well as its attractive properties such as high aspect ratio, high strength and stiffness, low density, transparency, high surface area and low thermal expansion. These outstanding properties have triggered the fabrication and use of nanofibrillated cellulose for a wide range of applications including packaging, paper and board, composite materials, adhesives, absorbents, electronics, medical, pharmaceutical and cosmetic products.
Despite its outstanding properties, nanofibrillated cellulose remains underemployed because of several constraints associated to its manufacture. Generally, nanofibrillated cellulose is prepared by disintegration, into fine fragments, of cellulose fibers, typically in the initial form of delignified wood pulp. However, the mechanical treatment methods implemented for this purpose, generally homogenization or high-pressure micro-fluidization, involve high-energy consumption in order to break the fibers to a nanometric scale and tend to damage the nanofiber structure by reducing its molar mass and crystallinity. In order to facilitate the nanofibrillation process and limit the energy requirement thereof, two main types of strategies of pretreating cellulose fibers have been developed by the prior art: an enzymatic strategy and a chemical strategy. Enzymatic cellulose pretreatment involves the use of endoglucanases or cellulases solutions, the hydrolyzing effect of which disrupts the cellulose structure, thereby promoting the subsequent mechanical treatment steps. However, the energy required for shearing the fibers is still high and multiple passes through the homogenizer or high-pressure micro-fluidizer are required. Furthermore, the quality of the nanofibers obtained, in particular their dispersion capacity, is often poor.
Chemical pretreatment of the cellulose fibers aims to introduce ionic groups on the surface of the fibers, for creating electrostatic repulsion phenomena and thereby improving the colloidal stability of the nanofibrils dispersion. Mechanical shearing is then highly facilitated. Two main methods have been proposed for this purpose: oxidation catalyzed by the radical 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) and carboxyalkylation, in particular carboxymethylation.
The TEMPO-catalyzed oxidation was proposed as one of the most promising methods for the production of cellulose nanofibers. Indeed, TEMPO transforms the primary hydroxyl at C6 in the cellulose chain into a carboxylate group, thereby creating electrostatic repulsions and facilitating the separation of cellulose nanofibers during the subsequent mechanical treatment. The use of the TEMPO oxidation reduces the energy cost of the process. However, it results in high quantities of toxic wastes, which are difficult to handle on an industrial scale, and significant decreases in degree of polymerization (DP) occur on the cellulose chains during oxidation. In addition, the presence of toxic residual reactive species in the reaction product obtained limits the use of the latter and adversely affects the properties of the CNF over time.
Traditionally developed for the complete solubilization of the cellulose fibers, controlled carboxymethylation can be viewed as a strategy to facilitate nanofibrillation. For this purpose, cellulose fibers are first impregnated with monochloroacetic acid (MCA), and then their hydroxyl groups are activated by concentrated sodium hydroxide (NaOH) solutions to perform Williamson etherification of hydroxyl groups of the cellulose chain. The degree of substitution (DS), which is the average number of functional groups, more particularly carboxymethyl groups, introduced in the cellulose polymer, can be controlled by experimental conditions such as MCA and NaOH ratios, temperature and reaction time. The carboxyl groups thus introduced in the cellulose chain facilitate fibers disruption and obtention of CNF, in particular as the formation of irreversible hydrogen bonds within the cellulose polymer is reduced by the replacement of hydroxyl groups with carboxymethyl groups.
A barrier to the industrial use of CNF is the difficulty to adapt their surface properties to specific applications. Carboxymethylated CNF is generally marketed without any further modification, which limits its use for applications where a high compatibility and/or interaction with some other components, such as organic components, is required, for example as reinforcing material in hydrophobic polymer matrices in the field of composite materials. Many industrial applications of nanofibrillated cellulose, e.g., in the field of composite materials, in the packaging industry, in separation technologies such as filtration and purification, as hydrogels or aerogels, etc., require indeed the introduction on the cellulose surface of additional functionalities, such as additional functions, additional properties, additional reactivity, etc. For most of such applications, it is currently proposed to functionalize the nanofibrillated cellulose by chemical post-treatment after the nanofibrillation has taken place, generally resulting in increased production costs and environmental impact.
It has been proposed by the prior art, illustrated by the publication of Kaldéus et al., Cellulose, 2018, 25: 7031-7042, to prepare bi-functional cellulose nanofibrils by a process comprising, before a nanofibrillation step, the one-pot preparation of bi-functional cellulose fibers bearing a carboxymethyl function and an additional function, more particularly an allyl function or a propargyl function. To this end, cellulose fibers are first subjected to a carboxymethylation step, then to an etherification reaction by contacting them with allyl bromide or propargyl bromide in an alkaline medium. However, this method requires high amounts of reactants, a long reaction time and it does not enable to graft on the cellulose surface more than 0.3-0.5 mmol of carboxymethyl groups per gram of cellulose. This document also discloses that adding allyl bromide or propargyl bromide concurrently with monochloroacetic acid led to extremely low values of the total fiber charge, and was therefore discarded. The present invention aims to propose a method for preparing multi-functionalized cellulose fibers, as well as, from the latter, multi-functionalized nanofibrillated cellulose, within short reaction times, at low cost and preferably with a high yield.
The inventors have now discovered that such objectives can be achieved by a specific method, which enables grafting two or even more functionalities onto the cellulose polymer in the form of solid fibers by one-pot simultaneous functionalization reactions. One of these functionalities may be a carboxyl-containing function, facilitating a subsequent nanofibrillation step when needed. In the context of a more global method of preparing multi-functionalized nanofibrillated cellulose, the inventors have in particular applied this specific method for multi-functionalizing cellulose fibers simultaneously by a carboxyl-containing group, for example a carboxymethyl group, and by one or several additional functional group(s), before submitting them to a nanofibrillation treatment. They have discovered that, unexpectedly and contrarily to the teaching of the above-mentioned publication of Kaldéus et al., in specific conditions, more particularly when implementing specific reactant concentrations, multi-functional cellulose fibers can be obtained by carrying out this specific method for realizing simultaneously a carboxylation, for example a carboxymethylation and an additional functionalization of the cellulose fibers, and that this simultaneous additional functionalization then does not hinder the carboxylation, for example the carboxymethylation, so that there is no significant decrease in the total carboxyl, for example carboxymethyl, charge grafted on the cellulose fibers, compared to cellulose fibers which have undergone only carboxylation, for example carboxymethylation. This simultaneous additional functionalization of the cellulose fibers does not interfere with the subsequent nanofibrillation step of an overall method of producing multi-functionalized CNF from cellulose fibers. This nanofibrillation step is still facilitated compared to the nanofibrillation of non-carboxylated, for example non-carboxymethylated, cellulose fibers.
Thus, according to a first aspect, the invention relates to a method of preparing multi-functionalized cellulose fibers, comprising subjecting cellulose fibers, preferably unmodified, i.e., non-functionalized, cellulose fibers, to:
According to the invention, the first functionalization step and the second functionalization step are carried out concomitantly, in one-pot, in an alkaline reaction medium, and each of the first reactant and the second reactant are present in said reaction medium in an amount of between 0.015 and 10 mmol per gram of cellulose.
The method of the invention yields multi-functionalized cellulose fibers much more quickly than the methods of the prior art, in a single step carried out under suitable conditions for covalently grafting the first functional group and the second functional group to the cellulose polymer.
The method of the invention makes it possible to functionalize cellulose fibers simultaneously with all combinations of functional groups, even simultaneously with a carboxyl function and a primary and/or secondary amine function. However, in that latter case the degree of substitution of the cellulose polymer is quite low.
Therefore, in particular embodiments of the invention, the first reactant and the second reactant do not simultaneously comprise a carboxyl function and a primary or secondary amine function. It is thereby meant that, if the first reactant comprises a carboxyl function, then neither the first reactant nor the second reactant comprises a primary or secondary amine function, and if the second reactant comprises a carboxyl function, then neither the first reactant nor the second reactant comprises a primary or secondary amine function. Similarly, if the first reactant comprises a primary or secondary amine function, then neither the first reactant nor the second reactant comprises a carboxyl function, and if the second reactant comprises a primary or secondary amine function, then neither the first reactant nor the second reactant comprises a carboxyl function. More generally, in particular embodiments of the method of the invention, the first reactant and the second reactant do not comprise simultaneously two or more functions that are likely to react with one another under the operating conditions, so as not to compete with the reactions of those reactants with cellulose.
The term carboxyl as used in this description encompasses both the acid form and the carboxylate ion form.
By functional group, it is herein meant a group having at least one function, of any kind, conferring it a specific characteristic/property/capacity. The term “functional group” as used in this description encompasses a functional group by itself, but also a larger organic chemical moiety containing at least one functional group.
The functional groups grafted onto the cellulose polymer according to the invention can be any group showing a function which may be of interest for a given application of the multi-functionalized cellulose fibers. These functional groups are preferably chosen so as to broaden the fields of application of cellulose fibers to applications requiring specific mechanical properties and/or functionalities, for example requiring tuning the surface properties of cellulose, such as polarity and/or charge. The functional groups may for example contain a polymerization initiating function, such as of the benzophenone type or of the α-bromoisobutyryl type, for forming, on the fibers surface, polymer chains such as acrylates, styrenes, etc., a chromophore, a hydrophobic group, a group bearing a positive or a negative charge, an alkene or an alkyne group for performing click chemistry such as by azide-alkyne cycloaddition, etc. By way of examples, the functional groups can be selected in the group comprising a carbonyl or carboxylate/carboxyl function, an alkyl, allyl, alkylol or alkyne chain, an aromatic ring, a specific functionality such as benzophenone, etc.
In particular embodiments of the invention, one of the functional groups, for example the first functional group, is a carboxyl-containing group, in particular a carboxyl (or carboxylate) group or carboxyalkyl group, preferably of the type containing a C1-C6 alkyl, for example methyl or ethyl. Such a feature is highly advantageous in the context of the more global preparation of multi-functionalized nanofibrillated cellulose. The first reactant can then be a haloformic acid, such as chloroformic acid, or an haloacetic acid, such as monochloroacetic acid, or an halopropionic acid, such as chloropropionic acid, or more generally an alkyl-haloacetic acid, such as an alkyl-chloroacetic acid. The first functionalization step can then be qualified as a carboxylation step, more particularly a carboxyalkylation step, for example a carboxymethylation step when a carboxymethyl group is grafted on the cellulose polymer.
A carboxyl-containing group can also for example be grafted on the cellulose fibers using a reactant which is devoid of halogen atom, but comprises a vinyl group, such as acrylic acid or a salt thereof, for example sodium acrylate, and/or comprises a phenyl group, optionally substituted, such as cinnamic acid or a salt thereof.
In particular embodiments of the invention, at least one of the first functional group and the second functional group is of the hydrophobic type. The multi-functionalized cellulose fibers obtained by the method of the invention are then advantageously compatible with matrices based on hydrophobic polymers. Hydrophobic groups that can be used in the context of the invention are for example alkyl, allyl or alkyne chains, aromatic rings, or polymerization initiators, such as benzophenone that enables the polymerization of acrylates or styrene on the surface of the cellulose fibers.
As an example, the second functional group can then be a dye.
Examples of functional groups which can be grafted on the cellulose by the method of the invention are:
More generally, in preferred embodiments of the invention, the first reactant and/or said second reactant has the general formula (I):
Y—R (I)
In particular, when Y represents a phenyl group, said phenyl group can be substituted, by one or several groups selected from:
In particular embodiments of the invention, in formula (I), R represents a functional group-containing linear, branched and/or cyclic C2-C20 hydrocarbon radical, saturated and/or unsaturated, aromatic or not, optionally substituted, optionally interrupted by one or more heteroatoms and/or by one or more groups comprising at least one heteroatom, R being devoid of hydroxyl group.
In particular, R can represent a benzophenone derivative, such as (4-methylphenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone, an allyl group, an alkyl acetate group, wherein the alkyl group preferably comprises from 1 to 20, in particular from 1 to 12, carbon atoms, an alkyl chain, preferably C1-C20, in particular C1-C12, an alkoyl chain, preferably C2-C20, in particular C2-C12, a benzoic acid group, optionally substituted, etc.
The method according to the invention may further respond to one or more of the features described below, implemented individually or in each of their technically operating combinations.
The first functionalization step and the second functionalization step of the method of the invention both preferably consist of Williamson etherification reactions, involving hydroxyl groups of the cellulose polymer. The functionalization steps are carried out by contacting the cellulose with the reactants in the alkaline reaction medium, in conditions enabling the etherification reaction of hydroxyl groups of the cellulose polymer to occur.
The cellulose fibers used in the method of the invention are preferably wood-derived fibers. They can be obtained by disintegrating delignified wood pulp, for example by stirring a dispersion thereof in water.
In preferred embodiments of the invention, the method comprises a step of dispersing the cellulose fibers in water before subjecting them to the first functionalization step and the second functionalization step. It is then preferably devoid of any intermediate solvent exchange step between this dispersing step and the first functionalization step and second functionalization step. It has in particular been noticed by the inventors that such an intermediate solvent-exchange step, from water to ethanol then from ethanol to isopropanol, which is typically performed in the methods of carboxymethylating cellulose fibers of the prior art, such as the method disclosed in the above-mentioned publication of Kaldéus et al., is not necessary to achieve successful carboxymethylation, or more generally functionalization, of the cellulose polymer in the framework of the method of the invention. Avoiding such a step in the context of the invention advantageously reduces the production cost of the multi-functionalized cellulose and limits the volume of organic effluents generated thereby.
In preferred embodiments of the invention, after dispersing the cellulose fibers in water, the method comprises separating them from the water, preferably by filtration, before proceeding to the next step of the method.
The method of the invention can then optionally comprise a step of spacing apart the cellulose fibers, which can be carried out by any technique known to the person skilled in the art.
The method of the invention can be implemented to prepare bi-functionalized cellulose fibers, using two reactants each of which comprises a functional group to be grafted on the cellulose polymer. It can also use more of such reactants, for example three of such reactants, each containing a different functional group, in order to prepare cellulose fibers having three functionalities, or even more, still in a one-pot manner.
In particular embodiments of the invention, the method comprises at least one further functionalization step for grafting at least one further organic functional group, i.e., a functional group different from the first functional group and the second functional group, on the cellulose polymer, by reacting the cellulose fibers with at least one further reactant comprising a halogen atom and said further functional group, and devoid of hydroxyl function, the further functionalization step(s) being carried out concomitantly with the first functionalization step and the second functionalization step, in one-pot, in the alkaline reaction medium, in suitable conditions to covalently attach the further functional group(s) to the cellulose polymer. Such a further reactant is then present in the reaction medium in an amount of between 0.015 and 10 mmol per gram of cellulose.
In particular embodiments of the invention, the first reactant, the second reactant and the further reactant(s) do not simultaneously comprise a carboxyl function and a primary or secondary amine function, or, more generally, functions that are likely to react together in the operating conditions.
The further functional group(s), the further reactant(s), and the further functionalization step(s) in general, can have one or more of the features described above or below regarding, respectively, the first and second functional groups, the first and second reactants and the first and second functionalization steps of the method of the invention. The further reactant(s) can in particular have the general formula (I).
In particular embodiments of the invention, each of the first reactant and the second reactant, and, when appropriate, the further reactant(s), is present in the reaction medium in an amount of between 0.03 and 2 mmol of reactant per gram of cellulose and more preferably of between 0.03 and 1 mmol of reactant per gram of cellulose. In such a concentration range, simultaneous grafting of all the functional groups onto the cellulose polymer is successfully achieved in the context of the invention of multi-functionalization of cellulose fibers.
The method of the invention does not comprise first dispersing the cellulose fibers in the alkaline medium, so as to induce their swelling, then adding therein the reactants for the functionalization steps. Multi-functionalized cellulose in a solubilized state would then indeed be obtained, which is not compatible with the objective of the invention of forming multi-functionalized cellulose fibers.
For obtaining multi-functionalized cellulose fibers, i.e., cellulose in the solid state, as required by the invention, such a prior dispersion of the cellulose fibers in the alkaline reaction medium is to be avoided. In such embodiments, the method of the invention then preferably comprises, before the first functionalization step and second functionalization step, and, when appropriate, the further functionalization step(s), steps of impregnating the cellulose fibers, preferably successively, with, respectively, a first impregnating solution comprising the first reactant, a second impregnating solution comprising the second reactant, and, when appropriate, one or several further impregnating solution(s) each comprising a further reactant. Each of these impregnating steps is then preferably carried out for a period of between 10 minutes and 1 hour, preferably between 10 and 40 minutes, more preferably between 20 and 40 minutes, for example of about 30 minutes, and preferentially at room temperature.
The volume of each impregnating solution is preferably of between 5 and 50 ml per gram of cellulose. In these solutions, the reactant may be contained in any suitable solvent thereof, in the concentration required to achieve a rate of between 0.015 and 10 mmol of reactant per gram of cellulose, preferably of between 0.03 and 2 mmol of reactant per gram of cellulose and more preferably of between 0.03 and 1 mmol of reactant per gram of cellulose.
Therefore, in particular embodiments of the invention, the method comprises, before the functionalization steps, a step of impregnating the cellulose fibers with a first impregnating solution comprising the first reactant, then a step of impregnating the cellulose fibers with a second impregnating solution comprising the second reactant, and then, optionally, one or more further steps of impregnating the cellulose fibers with further impregnating solution(s) each comprising a further reactant.
Each of the impregnating steps is preferably carried out by wetting the cellulose fibers with the impregnating solution.
The first functionalization step, the second functionalization step, and, when appropriate, the further functionalization step(s), of the method of the invention are then conducted simultaneously, in the same reaction medium, according to any conventional operating protocol. The etherification reactions are preferentially triggered by contacting the cellulose fibers with the reactants in the presence of an alkali such as sodium hydroxide, preferably at a rate of between 4 and 40 mmol of sodium hydroxide per gram of cellulose. In preferred embodiments of the invention, wherein the cellulose fibers have previously been impregnated with the reactants, the fibers are then introduced in a reaction medium containing an alkaline compound, such as sodium hydroxide, dissolved in a suitable vehicle, together with the possible remainder of the impregnating solutions which would not have impregnated the fibers during the impregnating steps of the method.
In particular embodiments of the invention, the reaction medium for the functionalization steps is in an alcoholic medium, preferably a mild alcoholic medium, such as containing, or consisting of, isopropanol or a mixture of isopropanol and methanol. Preferably, the reaction medium is devoid of methanol.
The first functionalization step and the second functionalization step, and, when appropriate, the further functionalization step(s), are preferentially carried out for a period of between 30 and 90 minutes, more preferably of between 50 and 70 minutes, for example of about 60 minutes. Such a short reaction time is advantageously sufficient to ensure a high degree of functionalization of the cellulose polymer by all the functional groups.
In preferred embodiments of the invention, the first functionalization step and the second functionalization step, and, when appropriate, the further functionalization step(s), are carried out at a temperature of between 60 and 82° C., preferably of between 65 and 82° C. They are preferentially carried out at a temperature of between 65 and 75° C., thereby reducing even more the energy requirement of the method.
As indicated above, in particular embodiments of the invention, particularly suited for preparing multi-functionalized nanofibrillated cellulose from the multi-functionalized cellulose fibers prepared by the method of the invention, the first functional group is a carboxyl-containing group, in particular a carboxyl group or a carboxyalkyl group, preferably containing a C1-C6 alkyl, for example a carboxymethyl or carboxyethyl group. The first reactant is then preferably an alkyl-haloacetic, preferably a C1-C5 alkyl-haloacetic acid, such as a haloacetic acid, for example monochloroacetic acid, or a halopropionic acid, for example chloropropionic acid. The first reactant can also be devoid of halogen atom, and comprise a vinyl group, such as acrylic acid or a salt thereof, for example a sodium salt, or a phenyl group, optionally substituted, such as cinnamic acid.
A method according to the invention then comprises subjecting cellulose fibers to concomitant:
The carboxylation/carboxyalkylation, in particular carboxymethylation, step and the second functionalization step, and optionally further functionalization step(s), of the method of the invention, carried out concomitantly, advantageously yield, in a single step, multi-functionalized cellulose fibers on the surface of which are grafted both carboxyl-containing groups, in particular carboxyalkyl, for example carboxymethyl, groups and the second functional group. The degree of substitution of the cellulose polymer by carboxyl-containing groups, in particular carboxyalkyl, for example carboxymethyl, groups, which, for example, can be measured by conductimetry, as described in a detailed way herein below, is not significantly different from that obtained when solely applying the carboxylation/carboxyalkylation, in particular carboxymethylation, step to the cellulose fibers. The second functionalization step of the method of the invention advantageously has no impact on the carboxylation/carboxyalkylation, in particular carboxymethylation, of the cellulose fibers, nor on their morphology and colloidal stability.
The method of the invention then advantageously provides a straightforward synthetic route to introduce, on the surface of the cellulose fibers, several functionalities, including negative charges deriving from the carboxyl functions, in particular from the carboxymethyl groups, by one-pot simultaneous reactions. The carboxyalkylation, in particular carboxymethylation, step is preferably carried out by contacting the cellulose fibers, in the alkaline reaction medium, in conditions enabling the etherification reaction of hydroxyl groups of the cellulose polymer to occur, with a reactant containing:
Preferably, a ratio of between 0.1 and 10 mmol of such reactant, in particular monochloroacetic acid, per gram of cellulose is applied.
When the second reactant is used in an amount of between 0.015 and 10 mmol per gram of cellulose, preferably of between 0.03 and 2 mmol and more preferably of between 0.03 and 1 mmol per gram of cellulose, the grafting of the second functional group on the cellulose fibers is successfully achieved without significantly impeding the carboxylation, in particular carboxyalkylation, more particularly carboxymethylation, step.
The impregnation of the cellulose fibers with the impregnating solution containing the reactant for the carboxylation/carboxyalkylation step, in particular monochloroacetic acid, and the impregnation of the cellulose fibers with the second impregnating solution containing the second reactant, are preferably carried out successively, in any order. Preferably, the cellulose fibers are first impregnated with the reactant for the carboxylation/carboxyalkylation step, in particular monochloroacetic acid, before being impregnated with the second reactant for the second functionalization step.
In particular embodiments of the invention, the method comprises, successively:
Bi-functionalized cellulose fibers containing a carboxyl-containing function and an additional function are thereby obtained, by one-pot simultaneous reactions. As an example, the second functionalization step of the method of the invention can be implemented to introduce simultaneously in the cellulose polymer, in addition to carboxyl-containing, in particular carboxymethyl, groups, an ethyl acetate group, an allyl group, a decane group or a benzophenone derivative, such as (4-methylphenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone, an alkoyl group, a benzoic acid group, etc.
In other particular embodiments of the invention, the method comprises, successively:
Tri-functionalized cellulose fibers, containing a carboxyl-containing function and two additional functions, are thereby obtained, by one-pot simultaneous reactions.
The same process can be applied for the introduction of even more functionalities on the cellulose polymer, simply by adding a step of impregnating the cellulose fibers with an additional further reactant, before their immersion in the alkaline reaction medium.
As an example, the second functionalization step and the further functionalization step of the method of the invention can be implemented to introduce simultaneously an ethyl acetate group and an allyl group, or an allyl group and an alkyl group, in the cellulose polymer, in addition to carboxyl-containing groups, in particular carboxyalkyl groups, for example carboxymethyl groups.
Another aspect of the invention relates to multi-functionalized cellulose fibers, obtainable by a method according to the invention. The functional groups carried by such multi-functionalized cellulose fibers can have any of the features or combination of features described above in relation with the method of the invention.
Examples of such multi-functionalized cellulose fibers are functionalized with carboxyl-containing groups, such as carboxyalkyl groups, in particular containing a C1-C6 alkyl, for example carboxymethyl or carboxyethyl groups, or alkylcarboxyl groups, in particular containing a C1-C16 alkyl, for example methylcarboxyl, or else phenyl- and carboxyl-containing groups, such as a cinnamyl group, and with one or several of the following groups:
Examples of such multi-functionalized cellulose fibers according to the invention are tri-functionalized cellulose fibers functionalized with carboxyalkyl groups, in particular containing a C1-C6 alkyl, for example carboxymethyl groups, together with at least two of ethyl acetate groups, alkyl groups and allyl groups.
The invention also relates to the use of multi-functionalized cellulose fibers according to the invention for preparing composite materials which can be useful for many applications, for example in the field of textiles, in the field of packaging, in the field of pulp and paper industry, etc.
The multi-functionalized cellulose fibers according to the invention can also be used to prepare microfibrillated multi-functionalized cellulose and/or multi-functionalized nanofibrillated cellulose.
Another aspect of the invention is a method of preparing multi-functionalized microfibrillated cellulose, comprising subjecting cellulose fibers to a method of preparing multi-functionalized cellulose fibers according to the invention, preferably comprising a carboxylation/carboxyalkylation step as described above, then subjecting the multi-functionalized cellulose fibers thus obtained to a microfibrillation step.
Microfibrillated cellulose is defined in this description as consisting mainly of microsized cellulose fibers with a width typically of between 20 and 50 nm, and a length in the micrometric range. A small amount of nanosized cellulose particles can also be found in microfibrillated cellulose, mixed with these microsized cellulose fibers.
The microfibrillation step can be carried out in any way known to the person skilled in the art, in particular by mild agitation of the multi-functionalized cellulose fibers in an aqueous vehicle, for example at ambient temperature, for example for a period of 12 to 36 hours, in particular of about 24 hours.
Another object of the invention is multi-functionalized microfibrillated cellulose, obtainable by a method of preparing microfibrillated cellulose according to the invention, which is functionalized by two or more different functional groups, which can have any of the features or combination of features described above in relation with the method of preparing multi-functionalized cellulose fibers according to the invention, excluding the combinations of t-butylcarboxamide with any of the following functional groups:
Examples of such multi-functionalized microfibrillated cellulose are functionalized with carboxyl-containing groups, in particular carboxyalkyl groups, in particular containing a C1-C6 alkyl, for example carboxymethyl or carboxyethyl groups, and with one or several of the following groups:
Other examples of multi-functionalized microfibrillated cellulose according to the invention are tri-functionalized microfibrillated cellulose functionalized with carboxyl-containing groups, in particular carboxyalkyl groups, for example carboxymethyl, groups, together with ethyl acetate groups and allyl groups.
The invention also relates to the use of multi-functionalized microfibrillated cellulose according to the invention for preparing composite materials which can be useful for many applications, for example in the field of textiles, in the field of packaging, in the field of pulp and paper industry, etc.
The multi-functionalized microfibrillated cellulose according to the invention can also be used to prepare multi-functionalized nanofibrillated cellulose.
Another aspect of the invention is a method of preparing multi-functionalized nanofibrillated cellulose, comprising subjecting cellulose fibers to:
The presence on the multi-functionalized cellulose fibers of a high amount of negative charges, deriving from the carboxyl groups grafted on their surface, facilitates fiber disruption to the nanometric scale during the subsequent nanofibrillation step, thereby reducing the energy required for nanofibrillation. Multi-functionalized nanofibrillated cellulose is then obtained without any additional step compared to the methods of the prior art for preparing nanofibrillated cellulose implementing the sole carboxymethylation of the cellulose fibers, with the same degree of nanofibrillation and without any additional energy requirement.
In particular, it has been observed by the inventors that the multi-functionalized cellulose fibers obtained by the concomitant first functionalization step for grafting a carboxyl-containing functional group on the cellulose fibers, in particular a carboxyalkylation step, and more particularly a carboxymethylation step, and second functionalization step of the method of the invention, have particularly good dispersion properties in aqueous vehicles, which can be confirmed by dynamic rheology analysis. After a microfibrillation step, achieved by soft stirring of the fibers in water, dispersions of such multi-functionalized cellulose fibers in water show a gel-like behavior at least in the 0.5 to 4.5% w/w concentration range. In the 2 to 4.5% w/w concentration range, these dispersions do not even flow, demonstrating a high dispersion capacity of the cellulose microfibrils in water. Such a high dispersion capacity promotes the subsequent nanofibrillation step of the method of the invention.
The method of preparing multi-functionalized nanofibrillated cellulose of the invention can comprise, after the steps of functionalizing the cellulose fibers, for example the concomitant carboxymethylation step and second functionalization step, and before the nanofibrillation step, a step of purifying the multi-functionalized cellulose fibers, for example by filtration, optionally followed by a step of washing them, for example with isopropanol then with water, until a neutral pH is reached.
It can also optionally comprise, before the nanofibrillation step, a step of disrupting the cellulose fibers to the micrometric scale, i.e., a microfibrillation step. Such a step is particularly easy to carry out, and energy-efficient, due to the high degree of substitution of the fibers by carboxyl groups. It may in particular be carried out by mild agitation of the cellulose fibers in an aqueous vehicle, for example at ambient temperature, for example for a period of 12 to 36 hours, in particular of about 24 hours.
The nanofibrillation step of the method of the invention can be carried out by any conventional technique of mechanical breaking of cellulose fibers to the nanometric scale. It can for example be carried out by homogenization or high-pressure micro-fluidization. For example, the multi-functionalized cellulose fibers can be passed through a piston pump that applies high pressure, and then passed several times by Z-shaped interaction chambers, for example with internal diameters of 400, 200 and 100 μm, preferably at a constant flow rate, for example of about 350 mL·min−1, and for example at pressures of 100, 1500 and 2000 bar, respectively.
In this context of preparing multi-functionalized nanofibrillated cellulose, the second functional group is preferably chosen so as to broaden the field of application of nanofibrillated cellulose to applications requiring specific mechanical properties and/or functionalities, in particular requiring tuning the surface properties of cellulose, such as polarity and/or charge, for example for use in filtration media, for reinforcing composite materials, as emulsions stabilizers in water in oil (w/o) or oil in water (o/w) systems, etc. The second functional group may for example contain a polymerization initiating function, such as of the benzophenone type or of the α-bromoisobutyryl type, for forming, on the fibers surface, polymer chains such as acrylates, styrenes, etc., a chromophore, a hydrophobic group, a group bearing a positive or a negative charge, an alkene or an alkyne group for performing click chemistry such as by azide-alkyne cycloaddition, etc. Byway of examples, the second functional group can be selected in the group comprising a carbonyl or carboxylate/carboxylic acid function, an alkyl, allyl, alkoyl or alkyne chain, an aromatic ring, a specific functionality such as benzophenone, a benzoic group, etc.
In particular embodiments of the invention, the second functional group is of the hydrophobic type. The multi-functionalized nanofibrillated cellulose obtained by the method of the invention is then advantageously compatible with matrices based on hydrophobic polymers. Hydrophobic groups that can be used in the context of the invention are for example alkyl, allyl or alkyne chains, aromatic rings, or polymerization initiators, such as benzophenone that enables the polymerization of acrylates or styrene on the surface of the cellulose fibers. Examples of second functional groups which can be grafted on the cellulose fibers in the second functionalization step of the method of the invention are: benzophenone derivatives, such as (4-methylphenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone, allyl, alkyl acetates, wherein the alkyl group preferably comprises from 1 to 20, in particular from 1 to 12, carbon atoms, for example ethyl acetate or octyl acetate, alkyl chains, preferably C1-C20, in particular C1-C12, alkyl chains, for example decane, alkoyl chains, preferably C2-C20, in particular C2-C12, for example a lauroyl chain, benzoic acid groups, etc. Another aspect of the invention relates to multi-functionalized nanofibrillated cellulose, more particularly bi-functionalized nanofibrillated cellulose, obtainable by a method according to the invention, which is functionalized by covalent grafting, on the cellulose polymer, of carboxyl-containing groups, in particular carboxyalkyl groups, preferably carboxyalkyl groups containing a C1-C6 alkyl, for example carboxymethyl or carboxyethyl groups, and one additional functional group, preferably devoid of hydroxyl functions, and optionally also devoid of primary and secondary amine functions, excluding an allyl group, a propargyl group, a methyl-triazole-disperse red 13 group and a methyl 3-ethylthiopropionate group.
In particular embodiments of the invention, this multi-functionalized nanofibrillated cellulose comprises between 0.5 and 0.8 mmol of carboxyl groups, in particular carboxyalkyl groups, preferably carboxyalkyl groups containing a C1-C6 alkyl, for example carboxymethyl or carboxyethyl groups, per gram of cellulose.
The additional functional group may respond to any of the features described above in relation with the second functional group.
It can in particular be selected in the group consisting of benzophenone derivatives, such as (4-methylphenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone, allyl, alkyl acetates wherein the alkyl group preferably comprises from 1 to 20, in particular from 1 to 12, carbon atoms, for example ethyl acetate or octyl acetate, and alkyls, preferably C1-C20, in particular C1-C12, alkyls, such as decane, alkoyl chains, preferably C2-C20, in particular C2-C12, alkoyl chains, for example a lauroyl chain, benzoic acid groups.
Another aspect of the invention relates to multi-functionalized nanofibrillated cellulose, in particular tri, or more, -functionalized nanofibrillated cellulose, obtainable by a method according to the invention, which is functionalized by covalent grafting, on the cellulose polymer, of carboxyl-containing groups, in particular carboxyalkyl groups, preferably carboxyalkyl groups containing a C1-C6 alkyl, for example carboxymethyl or carboxyethyl groups, and at least two additional functional groups, preferably devoid of hydroxyl functions, and optionally also devoid of primary and secondary amine functions.
The additional functional groups may respond to any of the features described above in relation with the second functional group and the further functional group(s).
Tri-functionalized nanofibrillated cellulose according to the invention can for example carry, simultaneously, carboxymethyl groups, ethyl acetate groups or alkyl groups, and allyl groups.
As indicated above, the multi-functionalized nanofibrillated cellulose of the invention, either bi-functionalized, tri-functionalized, or even more functionalized, can have any functionality(ies) required for a desired application.
It can for example carry a functional group that changes the nature of its interactions with other compounds, i.e., that may be involved in hydrogen bonds, electrostatic interactions, etc., or that changes its polarity from hydrophilic to hydrophobic, in particular so as to favor a better dispersion of the nanofibrillated cellulose in hydrophobic polymer matrices, in the context of the fabrication of composite materials.
Another aspect of the invention relates to the use of multi-functionalized nanofibrillated cellulose according to the invention, in particular bi-functionalized or tri-functionalized nanofibrillated cellulose, for the preparation of composite materials, in particular for the reinforcement of materials based on hydrophobic polymer matrices, one of the functionalities grafted on the cellulose polymer then being a hydrophobic group, such as an alkyl chain, or a polymerization initiator, such as a benzophenone-containing group, the multi-functionalized nanofibrillated cellulose then being treated, before their use, by forming, on the surface thereof, polymer chains such as an acrylate chain.
Multi-functionalized nanofibrillated cellulose according to the invention may also be used for the manufacture of new cellulose-based products intended for many applications, in particular in the following fields, the functionality or functionalities of the nanofibrillated cellulose being appropriately selected according to each specific application:
The features and advantages of the invention will emerge more clearly in the light of the following examples of implementation, provided for illustrative purposes only and in no way limitative of the invention, with the support of
and
Delignified bleached softwood Kraft pulp was used as starting cellulose material. Monochloroacetic acid (MCA), (4-(Bromomethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone, ethyl chloroacetate, allyl bromide, 3-mercaptopropionic acid, 4,4-azobis(4-cyanovaleric acid), methanol, sodium hydroxide, methyl methacrylate, dodecyl methacrylate, styrene and tetrahydrofuran were purchased from Sigma Aldrich and used without further purification. Isopropanol and diethyl ether were supplied by VWR International.
Optical microscopy: cellulose samples (0.1 g·L−1 in milliQ water) were deposited onto a glass slide, dried at 40° C., and observed by a BX51 polarizing microscope (Olympus France S.A.S.) with a 4× objective. Images were captured by a U-CMAD3 camera displaying a U-TV0.5XC-3 adaptor (Olympus).
Rheology: rheological measurements were performed using stress-controlled rheometer AR-2000 (TA Instruments). Plate geometry (40 mm) was selected. All measurements were performed at 20° C. Samples were covered with paraffin oil to prevent evaporation during measurements. The elastic (G′) and viscous (G″) moduli were measured within the linear response regime meaning. Measurements were performed twice and the average of values was reported in the graphs.
Infrared analysis (FT-IR, Fourier Transform infrared spectroscopy): infrared spectra were obtained from potassium bromide (KBr) pellets containing freeze-dried cellulose samples placed directly in a Nicolet® iS50 FTIR spectrometer (Thermo Scientific) in absorbance mode. All spectra were collected, with a 4 cm−1 resolution, after 200 continuous scans from 400 to 4000 cm−1.
Conductometry: the surface charge of cellulose was measured by conductometric titration with a 0.01 M NaOH solution by a TIM900 titration manager and a CDM230 conductivity meter equipped with a CDC749 conductivity cell. The degree of substitution (DS) was then calculated by the following equation:
where nCOOH is the number of equivalents of —COOH groups calculated from conductometric titration, mfibers is the mass of cellulose pulp (dry basis), 162 accounts for the molecular weight of the anhydroglucose unit of cellulose, and 58 is the net increase in the weight of the anhydroglucose unit of cellulose for each sodium carboxymethyl group substituting a hydrogen atom of a hydroxyl group.
Solid-state 13C CP/MAS NMR (Cross-Polarization Magic-Angle-Spinning Nuclear Magnetic Resonance): Cellulose samples (100 mg) were rehydrated in 50 μL H2O and water excess was absorbed using an adsorbent. About 80-100 mg of each sample was packed into 4 mm NMR rotor. Cross-polarization magic angle (CP/MAS) NMR experiments were acquired on a Bruker Avance III 400 spectrometer operating at a 13C frequency of 100.62 MHz equipped with a double resonance H/X CP/MAS 4 mm probe. Measurements were conducted at room temperature with a MAS spinning rate of 9 kHz. The CP pulse sequence parameters were: 3.5 μs proton 90° pulse, 1.75 ms CP contact time at 67.5 kHz. and 9 s recycle time. The number of acquisitions for the CP/MAS 13C spectra was typically 5.120 scans. 13C NMR spectra were referenced to the carbonyl peak of glycine at 176.03 ppm. All spectra were processed with Gaussian multiplication parameters of LB=−5 Hz and GB=0.1. NMR spectra were deconvoluted as described in Villares et al., Sci. Rep., 2017, 7, 40262.
Cellulose fibers were bi-functionalized with a carboxymethyl group and a benzophenone-derived moiety, carrying a benzophenone functional group according to the following reaction scheme:
wherein n is an integer between 200 and 5000.
Cellulose fibers (delignified bleached softwood Kraft pulp) (100 mg) were firstly dispersed in water with a blender. The fibers were filtrated using a vacuum filtration system and washed with ethanol. The fibers were then impregnated with monochloroacetic acid (10 mg) dissolved in 0.5 mL of isopropanol for 30 min at room temperature. Then, (4-(bromomethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone (10 mg) dissolved in diethyl ether (2 mL) was added to the fibers. The fibers were impregnated with this solution for 30 min at room temperature. After impregnation, the fibers were added to a solution of sodium hydroxide (16 mg) in isopropanol (1 mL) heated at 60° C. in a two-neck round-bottom flask. 2.5 mL of isopropanol were added to achieve a total isopropanol reaction volume of 5 mL. Reaction was allowed to proceed for 60 min at 70° C. under reflux. The fibers were purified by filtration and washing steps were carried out with isopropanol (×3) then water (×3) until reaching neutral pH.
Fibrillation was achieved by magnetic stirring overnight in water, to yield cellulose microfibrils.
For the purpose of comparison, fibers were separately impregnated with monochloroacetic acid or (4-(bromomethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone, to introduce only one functionality (carboxymethyl or benzophenone derivative), and processed as described above.
The aspect and microscopy images of native cellulose fibers (“Cell”, a1/, b1/), benzophenone derivative-functionalized cellulose fibers (“Cell-BP”, a2/, b2/), carboxymethylated cellulose fibers (“CMC”, a3/, b3/) and benzophenone derivative-functionalized carboxymethylated cellulose fibers (“CMC-BP”, a4/, b4/) are shown in
The carboxymethylated samples CMC and CMC-BP were analyzed by conductometric titration to determine the carboxyl content after carboxymethylation. The total charge of CMC was 0.745±0.019 mmol·g−1, which corresponds to a degree of substitution (DS) of 0.13±0.01. When fibers were simultaneously carboxymethylated and functionalized with the benzophenone derivative (CMC-BP), the total charge was 0.709±0.037 mmol·g−1, and the corresponding DS was 0.12±0.01. No significant decrease in the total charge was therefore observed when both reactions occurred concomitantly, which indicates that both functionalities, carboxymethyl and benzophenone, were successfully grafted.
Solid-state 13C CP/MAS NMR experiments were performed to demonstrate the covalent grafting of carboxymethyl and benzophenone derivative functionalities on the cellulose fibers. The spectra obtained are shown in
As indicated above, the presence of charge from carboxymethyl groups on the cellulose fibers impacts their mechanical and viscoelastic properties and confers them a gel-like behavior. Dynamic rheology was used to assess the properties of CMC-BP dispersions in water at different concentrations (0.5%, 1%, 2%, 4.5% w/w) and characterize the gel behavior of these carboxymethylated bi-functionalized cellulose fibers. The results are shown in
The loss tangent (tan δ=G′/G″) was calculated. The results are shown in
Benzophenone is one of the most well-known photoinitiators for radical polymerization. Benzophenone abstracts hydrogen from H-donors such as monomers, and forms two types of radicals: a ketyl radical on the benzophenone moiety and an alkyl radical generated on the H-donor that starts polymerization. Therefore, the benzophenone functionalities grafted at the cellulose surface may act as initiators to graft polymer chains on the cellulose surface. The resultant polymers are therefore tethered by one chain end to the benzophenone moieties at the cellulose surface and can adopt various conformations depending on grafting density.
Three different monomers, methyl methacrylate, dodecyl methacrylate or styrene, were used and polymerization was achieved by UV irradiation. The bi-functionalized fibers CMC-BP were impregnated with the monomers (20 mmol per gram of cellulose). After irradiation at 365 nm (UV Lightningcure, 4500 mW·cm−2) for 30 min, the fibers were washed with tetrahydrofuran to remove the monomer excess.
The growth of hydrophobic uncharged polymer chains on the cellulose fibers was monitored by FT-IR. The spectra obtained for each monomer are shown in
Conversely, when, as a comparative example, native cellulose fibers were incubated with the monomers, after washing with THF and water, the FT-IR spectra did not show any trace of any of the monomers, which discarded the hypothesis of monomer adsorption on the fiber surface.
The same protocol as described in Example A was applied using allyl bromide (11 μL dissolved in 0.5 mL isopropanol) instead of the benzophenone derivative as a reactant for the functionalization of the cellulose fibers.
Bi-functionalized cellulose fibers containing carboxymethyl groups and allyl groups were obtained.
They were analyzed by conductometric titration to determine their carboxyl content. The total charge was 0.53±0.04 mmol·g−1, which corresponds to a degree of substitution (DS) of 0.09±0.01.
The same protocol as described in Example A was applied using ethyl chloroacetate (11 μL dissolved in 0.5 mL isopropanol) instead of the benzophenone derivative as a reactant for the functionalization of the cellulose fibers.
Bi-functionalized cellulose fibers containing carboxymethyl groups and ethyl acetate groups were obtained.
They were analyzed by conductometric titration to determine their carboxyl content. The total charge was 0.71±0.09 mmol·g−1, which corresponds to a degree of substitution (DS) of 0.12±0.02.
Similar results were obtained using ethyl bromoacetate instead of ethyl chloroacetate, demonstrating that the nature of the halide does not significantly impact the grafting.
Similar results were also obtained using octyl chloroacetate instead of ethyl chloroacetate, demonstrating that the alkyl chain length has no influence on the grafting.
The same protocol as described in Example A was applied using dibromodecane (20 μL dissolved in 0.5 mL isopropanol) instead of the benzophenone derivative as a reactant for the functionalization of the cellulose fibers.
Bi-functionalized cellulose fibers containing carboxymethyl groups and decane groups were obtained.
They were analyzed by conductometric titration to determine their carboxyl content. The total charge was 0.53±0.04 mmol·g−1, which corresponds to a degree of substitution (DS) of 0.09±0.01.
Cellulose fibers were tri-functionalized with a carboxymethyl group, an ethyl acetate group and an allyl group, according to the following reaction scheme:
wherein n is an integer between 200 and 5000.
The tri-functionalization proceeded by a similar procedure to the bi-functionalization described above in Example A, but performing three consecutive 30-min impregnations of the cellulose fibers (100 mg) with monochloroacetic acid (10 mg) dissolved in 0.5 mL of isopropanol, then ethyl chloroacetate (11 μL) in 0.5 mL of isopropanol and then allyl bromide (11 μL) in 0.5 mL of isopropanol. Then, the impregnated fibers were added to the sodium hydroxide solution and the same procedure as for bi-functionalization was followed.
The surface charge of the tri-functionalized fibers obtained (“CMC-EA-Allyl”), determined by conductometric titration, was 0.227±0.045 mmol·g−1.
These tri-functionalized fibers were analyzed by FT-IR, at neutral pH and at pH 2 (in order to obtain a pH equal to 2, samples were acidified with some 0.01 M HCl droplets). The spectra obtained are shown in
In order to detect the presence of the allyl group on the surface of the fibers, a post-modification by thiol-ene coupling with 3-mercaptopropionic acid was carried out. To this end, 100 mg of the tri-functionalized fibers were solvent-exchanged from water (100 mL), ethanol (100 mL, 99%) and then methanol (100 mL). The fibers were then dispersed in methanol (10 mL) and stirred for 60 min. Then, 4 μL of methyl 3-mercaptopropionate and 400 μg of 4,4′-azobis-(4-cyanovaleric acid) were added. The reaction was carried out at 60° C. for 18 h. The fibers were then washed with methanol.
The increase of surface charge due to the presence of propionic acid groups on the cellulose surface was quantified by conductometry. The total surface charge measured for the post-modified cellulose fibers was 0.314±0.068 mmol·g−1. The increase in the total surface charge of the propionic acid derivative (“CMC-EA-PA”) compared to the allyl derivative (“CMC-EA-Allyl”) clearly pointed at the successful coupling between allyl groups and 3-mercaptopropionic acid, and therefore, confirmed the allylation of the cellulose fibers.
FT-IR analysis was conducted on the post-modified fibers, both at neutral pH and at pH 2. The spectra are shown in
The bi-functionalized cellulose fibers obtained in Examples A, B, C and D and the tri-functionalized cellulose fibers obtained in Example E, can be subjected to a nanofibrillation treatment by homogenization.
To this end, the fibers can be passed through a piston pump at high pressure, and then passed several times, at a constant flow rate of 350 mL·min−1, by Z-shaped interaction chambers with internal diameters of 400, 200 and 100 μm, at pressures of 100, 1500 and 2000 bar, respectively.
For each sample, multi-functionalized nanofibrillated cellulose is thereby obtained.
Cellulose fibers were tri-functionalized with a carboxymethyl group, a decane group and an allyl group.
The tri-functionalization proceeded by a similar procedure to the bi-functionalization described above in Example A, but performing three consecutive 30-min impregnations of the cellulose fibers (100 mg) with monochloroacetic acid (0.10 mmol) dissolved in 0.5 mL of isopropanol, then 1,10-dibromodecane (0.10 mmol) in 0.5 mL of isopropanol and then allyl bromide (0.10 mmol) in 0.5 mL of isopropanol. Then, the impregnated fibers were added to the sodium hydroxide solution and the same procedure as for bi-functionalization was followed.
The introduction of monochloroacetic acid was demonstrated by surface charge of 0.618±0.030 mmol·g−1, compared to 0.218±0.024 mmol g−1 for native cellulose fibers.
The introduction of allyl functionalities was demonstrated by the post-functionalization with 3-mercaptopropionic acid via a thiol-ene coupling reaction, carried out as described in Example E. Thus, the surface charge increased to 0.713±0.065 mmol·g−1, demonstrating the introduction of 3-mercaptopropionic acid groups.
Finally, the cross-linked and plastic aspect of the fibers demonstrated the presence of decane after tri-functionalization, as shown in
Cellulose fibers were bi-functionalized with an acrylate group and a benzophenone-derived moiety, carrying a benzophenone functional group.
Cellulose fibers (delignified bleached softwood Kraft pulp) (100 mg) were firstly dispersed in water with a blender. The fibers were filtrated using a vacuum filtration system and washed with ethanol. The fibers were then impregnated with sodium acrylate (0.10 mmol) dissolved in 0.5 mL of water/isopropanol (1/4) for 30 min at room temperature. Then, (4-(bromomethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone (0.03 mmol) dissolved in diethyl ether (2 mL) was added to the fibers. The fibers were impregnated with this solution for 30 min at room temperature. After impregnation, the fibers were added to a solution of sodium hydroxide (16 mg) in isopropanol (1 mL) heated at 60° C. in a two-neck round-bottom flask. 2.5 mL of isopropanol were added to achieve a total isopropanol reaction volume of 5 mL. Reaction was allowed to proceed for 60 min at 70° C. under reflux. The fibers were purified by filtration and washing steps were carried out with isopropanol (×3) then water (×3) until reaching neutral pH.
Fibrillation was achieved by magnetic stirring overnight in water, to yield cellulose microfibrils.
The presence of acrylate functionalities was demonstrated by the surface charge determined by conductometric titration (0.633±0.166 mmol·g−1).
The presence of benzophenone functionalities was demonstrated by a post-polymerization assay using dodecyl methacrylate, carried out as described in Example A. The results are shown in
| Number | Date | Country | Kind |
|---|---|---|---|
| 22305166.5 | Feb 2022 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2023/053534 | 2/13/2023 | WO |
