• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention relates to a process for staining cellulose in a supercritical CO2 medium with a hydrophobic and unfilled dye, comprising at least the steps of: (i) providing cellulose fibers, (ii) bringing said cellulose fibers into contact with one another with: a) an effective amount of at least one unloaded primary mono-urea organo-urea substituted with a linear or branched, saturated or unsaturated hydrocarbon chain and having at least 3 carbon atoms or a cyclic hydrocarbon radical, saturated or unsaturated, bound directly or via a methylene or ethylene group to the nitrogen atom, where appropriate substituted, under conditions conducive to the establishment of a covalent carbamate bond between the cellulose and the molecules of said urea; and b) at least one hydrophobic dye, in a supercritical CO2 medium, under conditions conducive to the immobilization of said dye on said fibers.
    公开号:FR3018832A1
    申请号:FR1452406
    申请日:2014-03-21
    公开日:2015-09-25
    发明作者:Aurelien Auger；Olivier Poncelet
    申请人:Commissariat a lEnergie Atomique CEA；Commissariat a lEnergie Atomique et aux Energies Alternatives CEA；
    IPC主号:
    专利说明:

    [0001] The present invention relates to a novel process for coloring paper cellulose. The processes for coloring cellulose in the paper industry or the textile industry are conventionally carried out in an aqueous medium. In general, fixing the dye to the cellulose fibers requires the use of large amounts of salts and ammonia to overcome the anionic repulsion between the dye and the cellulose. However, these salts and ammonia, as well as secondary products formed together, are commonly removed by washing at the end of the reaction. The large quantities of water required for this washing operation are therefore highly polluted and their complex treatment raises, for obvious reasons, a major economic and environmental problem. There is therefore a strong need for a more environmentally friendly cellulose fiber coloring process. The use of supercritical CO2 is an interesting alternative to replace water in cellulose fiber staining processes. In the remainder of the text, "supercritical CO2" and "sCO2" will be used interchangeably. Supercritical CO2 has many advantages over other solvents. It is low cost, non-toxic, non-flammable, chemically inert, and environmentally friendly. It is a very good solvent for hydrophobic and non-polar chemical compounds. Because of its high diffusivity, high density, and low viscosity, it facilitates penetration of the dye into the cellulose fibers, thereby reducing the reaction time. The colored cellulose obtained does not require drying which saves a large amount of energy. Advantageously, the required dye concentration is lower than that required for a coloring process in an aqueous medium. In addition, the dye, not attached to a cellulosic fiber, can be easily separated and recovered at the end of the reaction by simply reducing the supercritical CO2 pressure. CO2 and dye can be reused. However, since supercritical CO2 is a good solvent for hydrophobic and uncharged compounds, it has little affinity for cellulose, which is rather hydrophilic and polar.
    [0002] To overcome this lack of affinity, alternatives have already been proposed. Thus, US Pat. No. 6,620,211 describes a textile material dyeing method, in sCO2 medium, with dyes reactive with respect to the textile fibers in the presence of a hydration agent.
    [0003] No. 6,010,542, for its part, describes a method of coloring a substrate, in particular textile fibers, in sCO2 medium and in the presence of a surfactant. This method does not require high temperatures or high pressures, but requires an acidic reaction medium by the use of additives such as carboxylic acid. However, acidic conditions damage the cellulose fibers and are even incompatible with the cellulose of the paper. Another alternative is to synthesize new cellulose derivatives, with distinct physicochemical properties and in particular hydrophobic properties, unlike native cellulose. Thus, different ways have already been explored to try to modify the properties of cotton cellulose fibers, for example, and make them more hydrophobic. A first route is to form a cellulose xanthogenate, but the process also forms dangerous side products such as C52, H25 and heavy metals. A second way is to associate cellulose with copper and ammonia, but this process also faces environmental obstacles. Another, more environmentally friendly way is NMMO technology. It consists of a solvent system comprising cyclic amine oxides, in particular N-methylmorpholine N-oxide (NMMO), capable of dissolving not only the cellulose but also other polymers.
    [0004] Yin, C. et al. [1] propose, for their part, to take advantage of the properties of supercritical CO2 to synthesize a cotton cellulose carbamate, product of the esterification of cellulose with urea. No. 5,578,088 also describes a method for coloring the cellulose fibers of a textile, in supercritical CO2 medium, by modifying them in advance by covalent coupling with amino derivatives. These groups make it possible to make the cellulose compatible with hydrophobic dyes. Nevertheless, the amino compounds considered are of very complex chemical formulas.
    [0005] As for EP 1 809 806, it describes a method for staining cellulose fibers of a textile, in supercritical CO2 medium, by pre-treating with a hydrogen bond acceptor compound, preferably an alcohol. This method does not require a surfactant, but requires the use of an acid medium, for example H3PO4, which damages the cellulose and is incompatible with the cellulose of the paper in particular. Consequently, the techniques currently available are not entirely satisfactory and there remains a need for a simple method for efficiently staining cellulose fibers, especially paper, in supercritical sCO2, and under conditions compatible with their integrity. . The present invention aims precisely to provide a method that satisfies the aforementioned requirements. Thus, the present invention relates to a process for dyeing cellulose in a supercritical CO2 medium with a hydrophobic dye, comprising at least the steps of: (i) disposing cellulose fibers, (ii) bringing said cellulose fibers into contact with: a) an effective amount of at least one unloaded primary mono-urea organo-urea and substituted by a saturated or unsaturated, linear or branched hydrocarbon chain and having at least 3 carbon atoms or a cyclic hydrocarbon radical, saturated or unsaturated, directly attached or via a methylene or ethylene group to the nitrogen atom, optionally substituted, under conditions conducive to the establishment of covalent carbamate bond between the cellulose and each molecule of said organourea; and b) at least one hydrophobic dye, in supercritical CO2 medium, under conditions conducive to the immobilization of said dye on said fibers. According to a first embodiment, the interfacing considered in steps (a) and (b) are carried out successively.
    [0006] According to this embodiment, two variants can be considered.
    [0007] According to a first variant, the bringing together of the cellulose fibers with the primary organo-urea during step a) is also carried out in supercritical CO2 medium. According to a second variant, it is carried out in a solvent medium other than supercritical CO2. This variant can in particular be carried out in a solvent medium in the presence, for example, of DMSO. According to a second embodiment, the bringing into contact with the fibers of the cellulose with the primary organo-urea is carried out concomitantly with bringing into contact the hydrophobic dye concerned.
    [0008] The invention further relates to a material formed wholly or partly of cellulose, colored according to the process of the invention, in particular a paper. Unexpectedly, the inventors have discovered that it is possible to fix, with improved efficacy, one or more hydrophobic dyes on the cellulose fibers in a supercritical CO2 medium, provided that said fibers are used in a modified form. with an uncharged primary organo-urea substituted with a linear or branched, saturated or unsaturated hydrocarbon-based chain and having at least 3 carbon atoms or with a saturated or unsaturated cyclic hydrocarbon radical bonded directly or via a methylene or ethylene group to the nitrogen atom, optionally substituted, under conditions conducive to the establishment of covalent carbamate bond between the cellulose and each molecule of said organourea. The process of the invention is advantageous in several ways. Firstly, it is carried out at a non-acidic pH and, in particular, at a pH greater than or equal to 7. Thus, the process according to the invention does not require acidic conditions to activate the dye and accelerate its reaction with cellulose and, as such, is particularly advantageous for the staining of cellulosic fibers of paper. The process according to the invention also does not require the use of a surfactant The use of an organo-urea according to the invention makes it possible, by interacting with the cellulose fibers, to confer on it a hydrophobic nature. The nitrogen atoms of the organo-urea are also potential sites for the immobilization of the dye. In addition, by binding to the cellulose fibers, the organo-urea molecules also help to facilitate the accessibility of these fibers to the dye. The process is ecological. It takes place in sCO2 environment, and does not require the use of water. It advantageously makes it possible to avoid the formation of environmentally dangerous secondary products and to dispense with the necessary washing step according to the conventional method described above. Because of its high diffusivity, high density, and low viscosity, sCO2 facilitates penetration of the dye into cellulose fibers, thereby reducing reaction time. The colored cellulose obtained does not require drying, which also saves a large amount of energy. Finally, the required dye concentration is lower than that required for an aqueous dyeing process. Moreover, the dye, which has not been fixed, can be easily separated and recovered at the end of the reaction by simply reducing the supercritical CO2 pressure. CO2 and this excess of dye can be reused.
    [0009] Other characteristics, advantages, and modes of application of the method according to the invention will emerge more clearly on reading the description which follows, given for illustrative and non-limiting purposes. In the rest of the text, the expressions "included between .. and ... "," ranging from ... to ... "and" varying from ... to ... "are equivalent and mean to mean that the limits are included, unless otherwise stated. Unless otherwise indicated, the expression "comprising / including a" shall be understood as "comprising / including at least one". Cellulose Cellulose is a natural linear polysaccharide. It is the most abundant and regenerable biopolymer. It is the main constituent of plants and in particular of the wall of their cells. This biopolymer consists of the succession of 13-D-glucopyranoside units linked together by 3-1,4-glycosidic linkages. The associated cellulose macromolecules form microfibrils, which themselves are layered together, forming macrofibrils and then cellulose fibers. Hydrogen bonds are established between the glucose molecules of the different chains.
    [0010] Its properties are determined by the presence of numerous intramolecular hydrogen bonds and by its partially crystalline and partially amorphous structure. Thus, because of the presence of its very numerous hydroxyl groups, the cellulose is polar and hydrophilic.
    [0011] Moreover, because of its structural characteristics, cellulose is not soluble in conventional organic solvents, and has no intrinsic affinity for dyes, most of them hydrophobic. The modification of the cellulose, considered according to the invention, makes it possible precisely to confer on it an affinity for the hydrophobic dye molecules, without altering the integrity of its fibers. In the case of paper in particular, the cellulose fibers are, in fact, more fragile than in cotton, for example, and their treatment proves more delicate. The cellulose of the paper is, for example, incompatible with acid treatment. In the context of the invention, this hydrophobic character is established via the formation of cellulose carbamate units, R-NH-00-O-Cellulose, products of the reaction between cellulose and a primary organo-urea with R representing the residue. of the organourea considered. Primary organo-urea In the context of the present invention, the organo-urea necessary for modifying the properties of cellulose is a primary mono-urea organo-urea. Unexpectedly, the inventors have indeed found that this type of urea is more advantageous than secondary and tertiary organo-urea. Advantageously, the primary organo-urea is substituted with a carbon unit capable of conferring on the modified cellulose a sufficiently hydrophobic character allowing it to be soluble in sCO2 and to interact with the hydrophobic dye molecules.
    [0012] A mono-organo-urea suitable for the invention may be of formula R-NH-CO-NH 2 in which R represents a linear or branched hydrocarbon chain, saturated or unsaturated, and having at least 3 carbon atoms or a cyclic hydrocarbon radical, saturated or unsaturated, directly attached or via a methylene or ethylene group to the nitrogen atom, optionally substituted. For the purposes of the invention, the term "hydrocarbon" qualifies the fact that the considered pattern consists essentially of carbon and hydrogen atoms. Where appropriate, heteroatoms may, however, also be present. According to a first variant, R represents an alkyl chain having at least 6 carbon atoms and preferably at least 8 carbon atoms. Preferably, the hydrocarbon chain R has a saturated linear skeleton comprising from 6 to 12 carbon atoms. Where appropriate, the hydrocarbon chain R may comprise one or more heteroatoms such as oxygen. According to a second variant, R represents an at least C6 cyclic radical and preferably an aromatic radical. It may especially be a heterocycle or a heteroaromatic ring, the heteroatom may be an oxygen atom, sulfur or nitrogen. The substituents which may be present may in particular be chosen from halogen atoms, alkyl or alkoxy radicals, in particular C 1 to C 5 radicals, saturated or unsaturated C 4 to C 6 rings or heterocycles. Of course, these substituents are chosen for their inertia with regard to the interactions, on the one hand, between the cellulose and the organo-urea, and, on the other hand, between the cellulose thus modified and the dyes to be immobilized, required according to the invention. The skilled person is able to make this choice. According to another of its specificities, the organo-urea according to the invention is uncharged or in other words is not in the ionic state. Advantageously, the organo-ureas able to modify the cellulose according to the process of the invention are chosen from: 1-octylurea, 30-1-octadecylurea, 4-methoxyphenylurea, N-phenylurea, benzylurea, butylurea, allylurea, and 3-fluorophenylurea.
    [0013] Some of these products, such as 4-methoxyphenylurea, are commercially available products. In any case, they are accessible by synthesis. In particular, it is possible to refer to the method described by Wertheim, E. [2].
    [0014] According to a particular embodiment, the concentration of primary organo-urea suitable for modifying the cellulose is between 1 and 20% by weight relative to the weight of cellulose to be treated. The dye According to one particular embodiment, the dye molecule is hydrophobic, uncharged, and has a chromophoric group. In particular, the dyes that can be considered according to the invention are the triazine dyes, for example the 4.4 acid. 4, -s-triazine-2,4,6-triyltribenzoic acid, - carbonyl dyes, for example 1,4-bis (pentylamino) anthraquinone sold under the name Oil Blue Ne., By the company Sigma Aldrich, sulphidic dyes, for example the cyclic anhydride of 2-sulphobenzoic acid, or the red of phenol for example marketed by Sigma Aldrich, the anthraquinone dyes, for example 1-amino-9,10-dihydro-9, Sodium dioxo-4- (2,4,6-trimethylanilino) anthracene-2-sulphonate as sold by Sigma Aldrich under the name Acid Blue 129®, 1-aminoanthraquinone, or 3,4-Dihydroxy Sodium 9,10-dioxo-2-anthracenesulphonate sold under the name Alizarin Red Se by Sigma Aldrich, and azo dyes, for example N-ethyl-N- (2-hydroxyethyl) -4- (4-nitrophenylazo) aniline as sold under the name Disperse Red 1 by Sigma Aldrich, 2,2 '- [[4 - [(4-nitrophenyl) azo] phenyl] imino] bisethanol sold under the name Disperse Red 19 by the company Sigma Aldrich, 24442-Chloro-4-nitrophenyl azo) -N-ethylphenylaminoethanol sold under the name Disperse Red 13 by Sigma Aldrich, 4- (4-nitrophenylazo) aniline as sold under the name Disperse Orange 3 by the company Sigma Aldrich, or the N- Ethyl-1- (4- (phenylazo) phenylazo) -2-naphthylamine sold under the name Sudan Red 7B® by the Sigma Aldrich company. More particularly, the dye is chosen from the Blue Foron RDE® marketed by the Clariant company, the 244 - (2-Chloro-4-nitrophenylazo) -N-ethylphenylamino] ethanol marketed under the name Dis Persia Red 13® by Sigma Aldrich, and 4- (2-hydroxy-5-methylphenylazo) acetanilide as sold under the name Disperse Yellow 3® by Sigma Aldrich The concentration of dye is advantageously between 1% and 20% by weight relative to the weight of cellulose to be treated. Supercritical CO2 Due to its properties, supercritical CO2 has many advantages over other solvents. In particular, the critical point of CO2 is at 31 ° C, it is possible to work at low temperatures and thus avoid denaturation of the product to be treated. Its solubility can be modulated according to its temperature and its pressure. Because of its high diffusivity, high density, and low viscosity, it facilitates penetration of the dye molecules into the cellulose fibers, thereby reducing the reaction time, but also the amount of dye required to color the cellulose. compared to a conventional method in a liquid solvent medium. Moreover, at the end of the reaction, the reaction products and the CO2 can be easily separated and recovered by simply reducing the pressure of the supercritical CO2, which becomes CO2 gas again. Thus, the CO2 and the excess dye can be reused. CO2 in particular can be reusable almost infinitely.
    [0015] The present invention relates to a process for coloring cellulose in supercritical CO2 with a hydrophobic dye, comprising at least the steps of: (i) having cellulose fibers (ii) bringing into the presence of said cellulose fibers with: a) an effective amount of at least one unloaded primary mono-urea organo-urea and substituted with a linear or branched, saturated or unsaturated hydrocarbon chain and having at least 3 carbon atoms or by a cyclic hydrocarbon radical, saturated or unsaturated, bonded directly or via a methylene or ethylene group to the nitrogen atom and, where appropriate, substituted, under conditions conducive to the establishment of a covalent carbamate bond between the cellulose and each molecule said organo-urea; and b) at least one hydrophobic dye, in supercritical CO2 medium, under conditions conducive to the immobilization of said dye on said fibers. Preferably, the supercritical CO2 medium is generated in situ by heating under pressure of liquid CO2. Furthermore, the connections considered in steps a) and b) are advantageously carried out within the same reactor. According to a first embodiment, the interfacing considered in steps (a) and (b) are carried out successively. Under these circumstances, the cellulose is first treated with the primary organo-urea, in sCO2 medium or not, to form a cellulose carbamate R-NH-00-O-Cellulose. The alkyl chains R thus introduced at the surface of the cellulose fibers have the advantage of giving the cellulose hydrophobic properties and also represent dye-accessible sites on which said dye can come to rest, by Van der Waals interactions. . If the interaction is carried out in a supercritical CO2 medium, it is generally carried out in an autoclave. This type of reactor is loaded with cellulose and a primary organo-urea as defined above. The reactor is sealed and charged with liquid CO2. In particular, the temperature and pressure conditions are adjusted inside the reactor to a temperature and pressure for which the liquid CO 2 is converted to supercritical CO 2. After stabilization of the system, the reactor is kept under these conditions in order to allow a good diffusion and a homogeneous distribution of the hydrophobic organo-urea molecules in the heart of the cellulose substrate, and to form the cellulose carbamate R-NH-00-0 -Cellulose expected. After this pre-treatment, the dye is introduced into the reactor, in which the temperature and pressure conditions used previously in step a) are applied a second time. The properties of supercritical CO2 allow it to homogeneously diffuse, transport, and distribute dye molecules within the "mattress" of cellulosic fibers. The dye molecules are then adsorbed on the hydrocarbon units, that is to say the hydrocarbon chains or the cyclic hydrocarbon radicals of the cellulose carbamate. The pressure is then slowly decreased and the heating stopped. A cellulose substrate, colored at heart, is then obtained. According to a second variant embodiment, the treatment of the cellulose with the primary organo-urea may be carried out in a solvent medium, in particular a water medium, especially in the presence of dimethylsulfoxide (DMSO).
    [0016] According to this embodiment, the pre-treated cellulose in the form of cellulose carbamate is then brought into contact with the dye in a reactor supplied with supercritical CO2. The temperature and pressure conditions applied, identical to those described above, are also maintained in order to allow good diffusion and a homogeneous distribution of hydrophobic organourea and dye molecules in the heart of the cellulose substrate. This treatment makes it possible to obtain a colored substrate at heart with the dye molecules adsorbed on the hydrocarbon chains or the cyclic hydrocarbon radicals of the cellulose carbamate. The pressure is then slowly decreased and the heating stopped. The colored substrate is then removed from the autoclave.
    [0017] According to a second embodiment, steps (a) and (b) are performed concomitantly. According to this embodiment, the autoclave is loaded with a cellulose substrate, the primary organo-urea, as well as the chosen hydrophobic dye. The autoclave is sealed and loaded with liquid CO2. The temperature and pressure are adjusted to convert the liquid CO2 to supercritical CO2, which diffuses and transports the organo-urea as well as the dye in the cellulosic fiber mat. After stabilization of the system, the reactor is kept under these conditions in order to allow a good diffusion and a homogeneous distribution of hydrophobic molecules of organo-urea and dye in the heart of the cellulose substrate. The pressure is then slowly decreased and the heating stopped. A cellulose substrate, colored at heart, is then obtained.
    [0018] The temperature applied during steps a) and b) is advantageously between 100 and 140 ° C, preferably between 120 ° C and 130 ° C. Moreover, the pressure applied during steps a) and b) is advantageously between 250 bar and 350 bar, preferably between 280 bar and 320 bar. In particular, the temperature and pressure conditions applied during steps a) and b), carried out successively or concomitantly, are maintained for a time varying from 1 minute to 60 minutes, more particularly from 10 minutes to 40 minutes. In particular, the process according to the invention is advantageously carried out under anhydrous conditions. For the purposes of the invention, "anhydrous conditions" means that the reaction media are not supplemented with water. Water naturally contained in cellulose remains present. Advantageously, the method according to the invention does not require the use of surfactant. In particular, the cellulose substrate is a paper. Applications The method according to the invention can be used to treat cellulose fibers forming different substrates. Thus, it can in particular be papers, or textiles. In the paper and textile industries, such a process makes it possible to color the paper according to an ecological implementation, and to obtain a colored substrate at heart, having good color fastness over time.
    [0019] In particular, a textile obtained according to the process of the invention has a very good hold especially in washing and scrubbing.
    [0020] With regard to its functionalization with carbamate units, the paper obtained according to the invention can advantageously lend itself to additional modifications. Thus, it may be possible to confer further hydrophobic properties, or oleophobic by consecutive grafting with suitable chemical reasons.
    [0021] A colored and hydrophobic cellulosic substrate is particularly interesting in the textile industry. This property can be used for making protective gowns. This property can for example be useful in the navy for making cards, likely to be in contact with water.
    [0022] In the same way, a colored and oleophobic cellulosic substrate may be particularly interesting for example in the field of catering for cookbooks and protective clothing. The method according to the invention can also be implemented during the manufacture of tracing papers for example.
    [0023] A tracing paper is a particularly dense and hard paper compared to most other forms of paper. Therefore, it is a fragile paper that can tear easily when folded. Such treatment in the presence of a primary organo-urea in sCO2 medium makes it possible to obtain a paper having a better resistance to folding, to stretching, but also to water.
    [0024] References [1] Yin, C. et al. Carbohydrate Polymers, 2007, 67, 147-154 [2] Wertheim, E. JACS, 1931, 53 (1), 200 Example 1: Staining of a two-step blotting paper with Disperse Red 13® dye An autoclave, microreactor type, is loaded with 1.62 g of blotting paper and 162 mg of octadecylurea. The reactor is sealed and charged with liquid CO2.
    [0025] The temperature and pressure conditions are adjusted inside the reactor until a temperature of 130 ° C. and a pressure of 280 bar are reached. After stabilization of the system, the reactor is kept for 10 minutes under these conditions. At the end of this pre-treatment, the cellulose carbamate is obtained. 100 mg of Disperse Red 13® dye are then added to the reactor. The same temperature and pressure conditions as those used previously are applied a second time for 10 minutes. The pressure is then slowly decreased and the heating stopped. The obtained paper, stained to heart, is then removed from the autoclave. Liquid CO2 and excess dye are easily separated and can be reused.
    [0026] Example 2: Single-step blotting of paper by Disperse Red 13® dye An autoclave is loaded with 1.62 g of blotting paper, 162 mg of octadecyl urea, and 100 mg of Disperse Red 13® dye. The autoclave is sealed and loaded with liquid CO2.
    [0027] The temperature is adjusted to 130 ° C and the pressure to 280 bar to convert the liquid CO2 to supercritical CO2. After stabilization of the system, the reactor is kept under these conditions for 10 minutes. The pressure is then slowly decreased and the heating stopped. The obtained paper, stained to heart, is then removed from the autoclave.
    [0028] Liquid CO2 and excess dye are easily separated and can be reused. Example 3: Staining of blot paper with Blue Foron Stain RDE® An autoclave is loaded with 1.20 g of blotting paper, 100 mg of octadecyl urea, and 100 mg of Foron Blue RD-E®. The autoclave is sealed and loaded with liquid CO2. The temperature is adjusted to 120 ° C and the pressure to 310 bar to convert the liquid CO2 to supercritical CO2. After stabilization of the system, the reactor is kept under these conditions for 10 minutes. The pressure is then slowly decreased and the heating stopped. The obtained paper, stained to heart, is then removed from the autoclave.
    [0029] Example 4: Staining of a blotter paper with Disperse Red 13® dye An autoclave is loaded with 1.25 g of blotting paper, 100 mg of 4-methoxyphenyl urea, and 100 mg of Disperse Red 13® dye. The autoclave is sealed and loaded with liquid CO2.
    [0030] The temperature is adjusted to 120 ° C and the pressure to 260 bar to convert the liquid CO2 to supercritical CO2. After stabilization of the system, the reactor is kept under these conditions for 10 minutes. The pressure is then slowly decreased and the heating stopped. The obtained paper, stained to heart, is then removed from the autoclave.
    [0031] Example 5: Staining of a blotter paper with Disperse Red 19® dye An autoclave is loaded with 1.15 g of blotting paper, 100 mg of 4-methoxyphenyl urea, and 100 mg of Disperse Red 19® dye. The autoclave is sealed and loaded with liquid CO2.
    [0032] The temperature is adjusted to 140 ° C and the pressure to 280 bar to convert the liquid CO2 to supercritical CO2. After stabilization of the system, the reactor is kept under these conditions for 10 minutes. The pressure is then slowly decreased and the heating stopped. The paper obtained, colored at heart, is then removed from the autoclave.
    权利要求:
    Claims (14)
    [0001]
    REVENDICATIONS1. A process for dyeing cellulose in a supercritical CO2 medium with a hydrophobic dye, comprising at least the steps of: (i) providing cellulose fibers, (ii) contacting said cellulose fibers with: a) an effective amount of at least one primary mono-urea, not charged, and substituted with a linear or branched hydrocarbon chain, saturated or unsaturated, and having at least 3 carbon atoms or with a cyclic hydrocarbon radical, saturated or unsaturated, linked directly or via a methylene or ethylene group to the nitrogen atom, optionally substituted, under conditions conducive to the establishment of carbamate covalent linkage between the cellulose and each molecule of said organourea; and b) at least one hydrophobic dye, in supercritical CO2 medium, under conditions conducive to the immobilization of said dye on said fibers.
    [0002]
    2. Method according to claim 1, in which the put in the presence considered in steps a) and b) are carried out successively.
    [0003]
    3. The method according to claim 1, wherein the pairings considered in steps a) and b) are carried out concomitantly.
    [0004]
    4. A process according to any one of the preceding claims, wherein the supercritical CO2 medium is generated in situ by heating under pressure of liquid CO2.
    [0005]
    5. Process according to any one of the preceding claims, in which the bringing into association considered in steps a) and b) are carried out within the same reactor.
    [0006]
    6. Method according to claim 2, wherein step a) is carried out in a solvent medium, especially in the presence of dimethylsulfoxide, and step b) is carried out in supercritical CO2 medium.
    [0007]
    7. Process according to any one of the preceding claims, in which the concentration of primary organourea is between 1% and 20% by weight relative to the weight of cellulose to be treated.
    [0008]
    8. Method according to any one of the preceding claims, wherein the dye concentration is between 1% and 20% by weight relative to the weight of cellulose to be treated.
    [0009]
    9. Process according to any one of the preceding claims, in which the organourea is chosen from 4-methoxyphenylurea, octadecylurea and octylurea, N-phenylurea, benzylurea, butylurea and allylurea. , and 3-fluorophenylurea.
    [0010]
    The process according to any one of the preceding claims, wherein the temperature applied in steps a) and b) is between 100 ° C and 140 ° C, preferably between 120 ° C and 130 ° C.
    [0011]
    11. A method according to any one of the preceding claims, wherein the pressure applied in steps a) and b) is between 250 bar and 350 bar, preferably between 280 bar and 320 bar.
    [0012]
    A process according to any one of the preceding claims, wherein the temperature and pressure conditions applied in steps a) and b), successively or concomitantly, are maintained for a period of time ranging from 1 minute to 60 minutes. more particularly from 10 minutes to 40 minutes.
    [0013]
    The process of any one of the preceding claims, wherein the cellulose is a paper cellulose.
    [0014]
    14. Colored paper obtained according to the method described according to any one of the preceding claims.
    类似技术:
    公开号 | 公开日 | 专利标题
    EP3119937B1|2018-05-16|Method for colouring cellulose
    JP3253649B2|2002-02-04|Method for dyeing hydrophobic fiber material with disperse dye
    CH637798A|1983-08-31|
    Abdel-Halim et al.2008|Utilization of hydroxypropyl cellulose and poly |-hydroxypropyl cellulose composite as thickeners for textile printing
    CA2803863A1|2014-07-25|Cellulose extraction process
    Phan et al.2014|Innovative pretreatment of sugarcane bagasse using supercritical CO2 followed by alkaline hydrogen peroxide
    CA2189796C|2000-08-22|Method for preparing delignified and bleached chemical paper pulps
    Kim et al.2007|Enzymatic polymerization on the surface of functionalized cellulose fibers
    MX2018013351A|2019-02-20|Methods, processes, and apparatuses for producing dyed and welded substrates.
    FR2610942A1|1988-08-19|LIQUID SULFUR DYE COMPOSITIONS AND THEIR PREPARATION
    TW201038655A|2010-11-01|Polyvinyl alcohol film composition, and polarizer plate employing the same
    Maradiya2012|Disperse dyes based on 2-aminothiazole derivatives for cellulose triacetate fabric
    FR2717481A1|1995-09-22|Novel platinum complexes useful, inter alia, as photoactivatable hydrosilylation catalysts and a method thereof.
    FR3015988A1|2015-07-03|IMPREGNATION OF A PAPER USING A SUPERCRITICAL FLUID
    Guo et al.2020|Reactive dyeing of silk using commercial acid dyes based on a three‐component Mannich‐type reaction
    Mondal et al.1998|Structure of nascent microbial cellulose I. Effects of methyl and methoxy groups of Direct Blue 1 and 53 on nascent microbial cellulose
    US1078504A|1913-11-11|Diazotizable disazo dyes for cotton.
    FR3067368B1|2019-07-26|METHOD FOR PRINTING A TEXTILE BY TRANSFER
    US864644A|1907-08-27|Sulfur dye and process of making same.
    Zhang et al.2021|Telechelic PEG‐polymers end‐capped with chromophores: Using as cationic reactive dyes and salt‐free dyeing properties on cotton fabrics
    FR3099481A1|2021-02-05|Multistate supramolecular polymer
    US665737A|1901-01-08|Process of dyeing.
    WO2008043764A1|2008-04-17|Method for processing an article containing a plastic material coated with a silicone material
    FR3085173A1|2020-02-28|PROCESS FOR THE HYDROPHOBIC TREATMENT OF A CELLULOSIC MATERIAL
    FR3102478A1|2021-04-30|Process for preparing a compound comprising at least one imine function by a specific condensation reaction and particular application of this process to the field of coloring
    同族专利:
    公开号 | 公开日
    EP3119937A1|2017-01-25|
    FR3018832B1|2016-04-01|
    US10557231B2|2020-02-11|
    WO2015140750A1|2015-09-24|
    EP3119937B1|2018-05-16|
    US20170096773A1|2017-04-06|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    DE4332219A1|1992-09-24|1994-03-31|Ciba Geigy|Dyeing woollen, silk and esp. cotton fabric with dispersion dyes - by pretreating with hydrophobic finishing agent and then dyeing with dispersion dye in supercritical carbon di:oxide.|
    CN102702364A|2012-06-19|2012-10-03|天津工业大学|Method for preparing cellulose carbamate|CN108289420A|2015-11-27|2018-07-17|斯道拉恩索公司|The covered ground mulch impregnated with the supercritical fluid comprising colorant|BE666801A|1964-07-14|
    US3788811A|1971-05-18|1974-01-29|Allied Chem|Solvent compositions for solvent dyeing and dyestuff solutions prepared therefrom|
    GB2259525B|1991-09-11|1995-06-28|Ciba Geigy Ag|Process for dyeing cellulosic textile material with disperse dyes|
    DE4422707A1|1994-06-29|1996-01-04|Hoechst Ag|Process for dyeing aminated cellulose / polyester blends with fiber-reactive disperse dyes|
    US6010542A|1997-08-29|2000-01-04|Micell Technologies, Inc.|Method of dyeing substrates in carbon dioxide|
    NL1014395C2|2000-02-16|2001-08-20|Stork Brabant Bv|Method for dyeing textile materials in a supercritical fluid.|
    EP1809806B1|2004-11-04|2009-12-23|Feyecon Development & Implementation B.V.|A method of dyeing a substrate with a reactive dyestuff in supercritical or near supercritical carbon dioxide|
    CN103541247B|2013-09-27|2017-11-14|浙江亿得化工有限公司|A kind of Dyeing with Disperse/Reactive one for polyester-cotton fabric bathes two step exhaust dyeing methods|FR3048982B1|2016-03-16|2020-09-25|Arjo Wiggins Fine Papers Ltd|METHOD OF MANUFACTURING PAPER IMPREGNATED BY A SUPERCRITICAL PRESSURE FLUID - IMPREGNATED PAPER, ESPECIALLY COLORED|
    FR3085173A1|2018-08-21|2020-02-28|Commissariat A L'energie Atomique Et Aux Energies Alternatives|PROCESS FOR THE HYDROPHOBIC TREATMENT OF A CELLULOSIC MATERIAL|
    FR3102478B1|2019-10-29|2021-09-24|Commissariat Energie Atomique|Process for preparing a compound comprising at least one imine function by a specific condensation reaction and particular application of this process to the field of coloring|
    法律状态:
    2015-01-30| PLFP| Fee payment|Year of fee payment: 2 |
    2016-03-31| PLFP| Fee payment|Year of fee payment: 3 |
    2017-03-30| PLFP| Fee payment|Year of fee payment: 4 |
    2018-03-30| PLFP| Fee payment|Year of fee payment: 5 |
    2020-03-31| PLFP| Fee payment|Year of fee payment: 7 |
    2021-03-30| PLFP| Fee payment|Year of fee payment: 8 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1452406A|FR3018832B1|2014-03-21|2014-03-21|PROCESS FOR COLORING CELLULOSE|FR1452406A| FR3018832B1|2014-03-21|2014-03-21|PROCESS FOR COLORING CELLULOSE|
    US15/128,001| US10557231B2|2014-03-21|2015-03-19|Method for coloring cellulose|
    PCT/IB2015/052018| WO2015140750A1|2014-03-21|2015-03-19|Method for colouring cellulose|
    EP15714954.3A| EP3119937B1|2014-03-21|2015-03-19|Method for colouring cellulose|
    [返回顶部]