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    • 专利摘要:
    The present invention relates to a process for preparing a protein-reduced algae powder, a bioplastic composition formulated from such a powder, a process for manufacturing a plastic product obtained from such a powder of algae and the plastic product thus obtained. Process for the preparation of an algae powder, in particular intended for the manufacture of a plastic product, comprising the successive stages of: - cultivation and / or harvesting of an algal biomass, - reduction of at least 10% the intrinsic quantity of proteins of the algae, preferably at least 40%, more preferably at least 70%, more preferably still at least 75%, by weight relative to the mass of proteins of the biomass harvested, - drying, - reduction to powder or granules.
    公开号:FR3041351A1
    申请号:FR1558743
    申请日:2015-09-17
    公开日:2017-03-24
    发明作者:Philippe Lavoisier；Ronan Pierre；Maud Benoit
    申请人:Ideas；
    IPC主号:
    专利说明:

    The present invention belongs to the technical field of materials formulated from natural materials, more specifically plastic materials, and relates to a process for the preparation of a reduced-protein algae powder, a bioplastic composition formulated from such a powder, a method of manufacturing a plastic product obtained from such an algae powder and the plastic product thus obtained.
    A plastic product is a product obtained from a composition containing polymers to which are added various additives, such as plasticizers. Traditional plastic is composed of polymers from the oil industry. But the depletion of oil resources and the preservation of the environment have motivated the search for non-petroleum compounds and plastics formulated with natural compounds are an interesting alternative to traditional plastics.
    Plastic products are often made by extrusion. The starting material which is in the form of granules or powder is passed through an extruder which makes it possible to continuously produce parts such as profiles, cables, tubes, sheets, films, fibers, plates, rods, etc.
    Algae are today considered as sources of valuable polymers. These have proved their effectiveness in various fields such as food, pharmacy, fuel or cosmetics. In addition, the proliferation of algae along marine coasts is becoming a disturbing and widespread phenomenon.
    In the field of plastic products, algae are a source of interesting raw materials because of their high polymer content.
    Bioplastic compositions made from macroalgae or microalgae are usually produced by grinding the dried algal material and then blending with other components such as plasticizers. In this respect, mention may be made of published patent application US 2013/0220173.
    The bioplastic compositions based on algae are then generally used in the form of granules, after passing through a screw extruder.
    The plastic products that can be manufactured from these granules are injected products, thermoformed, extruded into bubbles, extruded in inflation.
    The microalgae or macroalgae used for the preparation of the bioplastic compositions are generally green or brown algae. It is interesting to be able to use them in their entirety, ie with all the components of the algae: proteins, polysaccharides, minerals, etc .... indeed, many bioplastic compositions are known which are formulated from of algae polysaccharides extracted, purified and concentrated. For example, many plastic products include alginates as components. Such methods are expensive, time consuming and require fine extraction steps.
    Compositions made from powdered whole algae confer reduced mechanical properties to the formed plastic products. These are relatively brittle. In addition, the algae powders are used as fillers generally up to about 15% by weight, at most. In the sectors of valorisation of the algae, it would be advantageous to be able to increase the rate of algae in the plastic products.
    Another major disadvantage of bioplastic compositions based on microalgae or macroalgae is that they have a strong odor and a color, for example brown, very pronounced. In addition, it is noted that the problems of odor and color become more pronounced during the manufacture of plastic products, in particular during the processes of extrusion, molding, injection, thermo-compression, etc., of bioplastic compositions.
    To overcome this problem, some processes include the addition of compounds able to absorb or mask the odor, such as activated carbon, and dyes. It is necessary in this case to proceed with a selection of both the origin and the amount of the component to add in order to obtain stable, effective, natural mixtures and to avoid any incompatibility between components. The results obtained are not always satisfactory and the selection work is an additional constraint.
    Recent research has led to technical advances in improving bioplastic compositions formulated from algae components, including increasing the algal content in these compositions and obtaining plastic products with high molecular weight. good mechanical properties. In this respect, the French patent application FR 3,012,817 describes bioplastic compositions formulated from a component of algae, plasticizers of natural origin, such as glycerol, and polymers of plant origin, such as starch. Preferably, the algae component is in the form of an algae residue containing polysaccharides described as semi-refined, because not completely extracted and not purified. It has been observed a better plasticization of the starch in the bioplastic compositions made from the residues containing semi-refined polysaccharides, compared to refined extracts, thus purified, of the same polysaccharides.
    Furthermore, it has been demonstrated in the French patent application FR 3,012,817 that by using culture conditions specific to algal biomass, it was possible to increase the endogenous synthesis of starch. It has also been demonstrated that the use of an algal biomass in which the endogenous synthesis of starch has been accentuated before the preparation of an algae residue containing semi-refined polysaccharides, made it possible to obtain plastic products. advantageous mechanical properties, including good resistance to breakage. The mechanical properties of these bioplastics realized because of the starch richness are superior to those of the bioplastics obtained by simple drying and grinding of the micro or macroalgae.
    However, the bioplastic compositions and bioplastic products described in the aforementioned patent application, although having good mechanical characteristics, also have poor odor characteristics and a dark or brown color that is persistent, unlike transparency or light color. sought in plastic products. It is in this context that the applicant company has conducted research to address the color and odor problems of bioplastic compositions and bioplastic products obtained from algae.
    Macro algae and microalgae are mainly composed of carbohydrates, proteins, pigments and minerals. Depending on the species and their harvest period, the contents of these components can vary widely. For example, depending on the season, algae produce more protein that makes up their reserves and will be used during their growing season.
    During the formation of bioplastics, the materials are subjected to high temperatures and high shear rates. At such temperatures, the amino acids of the proteins react with the polysaccharides following a reaction called Maillard reaction. The Maillard reaction is a known reaction that has been and is the subject of many studies to try to identify all the mechanisms. Many books describe in detail the principles which, therefore, will not be explained in the present description.
    The applicant company has shown that Maillard reactions were also responsible for the phenomena of coloration and release of undesirable odors during bioplastic manufacturing processes, due to the synthesis of aromatic and odorous compounds. She has worked to solve this technical problem.
    The object of the present invention is to overcome the aforementioned drawbacks and, in particular, to propose a process for obtaining an algae powder suitable for use in the preparation of bioplastic compositions and odorless bioplastic products and unwanted color.
    Another object of the invention is to propose such an algae powder which is also suitable for use in the preparation of plastic compositions having optimum plasticizing characteristics and in the preparation of plastic products having optimum mechanical properties, such as resistance to breakage, tension, tension and elongation at break.
    Finally, another object of the invention is to provide a bioplastic composition and bioplastic products made from an algae powder according to the invention. To this end, the invention relates to a process for preparing an algae powder, especially for the manufacture of a plastic product, comprising the successive steps of: - cultivation and / or harvesting of a biomass of algae - At least 10% reduction in the intrinsic protein content of the algae, in mass relative to the protein mass of the harvested biomass, - drying, - reduction to powder or granules.
    The reduction of the intrinsic protein content in the cells composing the algal biomass makes it possible to reduce the Maillard reaction phenomena and makes it possible to obtain a powder that can be used for the preparation of compositions and bioplastic products having good characteristics. in terms of reduction, or even absence of odors and undesirable colorations.
    Preferably, the reduction step is a reduction step of at least 40%, preferably at least 70%, more preferably at least 75%, of the intrinsic amount of algae proteins, in mass relative to the mass of proteins of the biomass harvested.
    The process according to the invention makes it possible to reduce up to more than 75% the amount of protein initially present in the algae biomass. By the same token, it makes it possible to obtain an algae powder having a protein content, relative to the total mass of the powder, which is very small.
    According to a preferred embodiment of the invention, the reduction of the amount of intrinsic protein of the harvested algae comprises: - the enzymatic hydrolysis of the intrinsic proteins by mixing the harvested biomass, preferably milled, and one or more proteases then, - the separation of a hydrolyzate enriched in protein material and a residue of algae.
    The method according to the preferred embodiment of the invention consists in carrying out an enzymatic hydrolysis of the proteins of the algae and the separation of the protein material obtained, rich in peptides and amino acids, of an algae residue in which the rate of protein is significantly decreased. The bioplastic compositions made from this algae residue are colorless or unstained and odorless. Products extruded and injected by processing bioplastic granules are also devoid of odor and color. Surprisingly, these products have superior mechanical properties to plastic products obtained from dried algae powders or algae powders prepared according to a process described in the French patent application FR 3,012,817.
    According to such an enzymatic hydrolysis process, the amount of algae proteins can be reduced by at least 40%, preferably between 40 and 80%, more preferably between 50 and 75%, by weight relative to the initial total weight of the proteins. .
    Furthermore, the hydrolysates of recovered protein material have a significant economic value for applications such as applications of cosmetics, fertilizers, nutrition, including animal nutrition. This valorization of by-products with a high added value of the process which is the subject of the invention, resulting from this enzymatic treatment, reinforces the economic model of the algal culture.
    Advantageously, the enzymatic hydrolysis of the proteins is carried out using one or more proteases, in particular one or more endopeptidases and / or exopeptidases, of bacterial or fungal origin, such as one or more enzymes obtained from from Bacillus licheniformis. Bacillus subtilis, Bacillus amyloliquefaciens or Aspergillus oryzae, preferentially Bacillus licheniformis.
    Depending on the nature of the enzyme used and / or the nature of the treated algae, the rate of reduction in the amount of protein will vary. The enzymes of bacterial or fungal origin used in the context of the present invention are all commercially available. For example, as an enzyme obtained from Bacillus licheniformis, mention will be made of Alcalase marketed by Novozymes. As an enzyme of fungal origin obtained from Aspergillus oryzae, Flavourzyme also marketed by the company Novozymes. Generally, the enzyme is added at a concentration of between 0.1 and 10% relative to the mass of proteins to be hydrolysed, preferably between 0.8 and 3%, more preferably between 1 and 2%.
    According to an advantageous embodiment of the invention, the method further comprises a step of: depigmenting algae with or without treatment with a chemical agent, following the step of harvesting a biomass of algae and prior to the reduction of the intrinsic amount of protein harvested algae.
    The purpose of the depigmentation is to whiten and / or reduce the level of natural pigments, for example chlorophyll, of the algae.
    The natural depigmentation of algae can be obtained for example by distributing the algae in layers outside of any building during the day and then washing them during the night. These steps can be repeated for approximately three days.
    For chemical depigmentation, for example, a chlorine bleaching agent will be used.
    Preferably, the depigmentation will be carried out by alcohol extraction, by means of one or more stages of maceration of the biomass in alcohol solutions, advantageously ethanol.
    According to one embodiment of the invention, the method also comprises, directly after the step of reducing the amount of intrinsic protein of the algae: a step of destructuring the cell walls of the algae, by mixing the residue of the algae; algae and an agent solubilizing polysaccharides, such as a chelating agent or an inorganic acid, preferably selected from citric acid, citric acid monohydrate, sodium oxalate, hydrochloric acid, sodium carbonate more preferably the citric acid, heating the mixture at a temperature between 80 and 100 °, preferably 90 ° C, for 1 to 4 hours, preferably 2 hours, then cooling and concentration of the algae residue, it being understood that said step does not involve any removal or separation of organic and inorganic components.
    Such a step makes it possible to obtain an extract of so-called "semi-refined" or solubilized polysaccharides. During this step, the chelating solubilizing agents, such as citric acid or oxalic acid, will capture certain ions present in the cell wall and thus promote the solubilization of certain ionic polysaccharides and the destructuration of the cell walls. Alternatively, when the solubilizing agent is an inorganic agent such as hydrochloric acid, it will also modify the solubility of the polysaccharides, or even partially hydrolyze, and modify the interactions within the cell wall. They thus also produce an effect of destructuring the cell walls.
    In the residue obtained, the polysaccharides are solubilized for a large part, but are not separated from the other non-polysaccharide constituents of the algae. The residue obtained at the end of this step indeed contains all the components of the alga present before its implementation, that is to say, the semi-refined polysaccharides, the fibers, the rest of the protein material not eliminated at all. the previous step. There is no extraction / separation / purification of the polysaccharides as in the case of a "refined" polysaccharide extract. This step makes the polysaccharides, in particular parietal, accessible and functional in comparison with the same polysaccharides contained in cells with structured walls. For this reason, the expression "activated algae" or "algal activation step" will also be used in the present application. This step is advantageous in terms of cost and time, because it does not include a total extraction process polysaccharides including parietal, said refined process, but a semi-extraction process or semi-refined process.
    Advantageously, the step of destructuring the cell walls of the algae comprises the successive steps of: - obtaining a ground material of the algal biomass, - mixing said ground material and water to obtain a paste, - adding an agent solubilizing, in particular citric acid, to a pH of between 2.5 and 3.5, preferably 3, - heating the mixture at a temperature of between 80 and 100 °, preferably 90 ° C., for 1 to 4 hours preferably 2 hours, - cooling to a temperature of less than or equal to 45 ° C., concentration in a vacuum at a temperature of between 45 and 50 ° C., adjustment of the pH of the residue obtained to a value of between 7 and 8, preferably 7. , 7 using a base such as sodium hydroxide.
    The choice of the polysaccharide solubilizer must take into account the compatibility between this agent and any other compound that will be added in the preparation of bioplastic compositions, such as plasticizers. The applicants have thus demonstrated that the molecular weight of the solubilizing agent was a preponderant element so that this agent could for example be thermo-stabilizing, as will be illustrated in what follows.
    According to one embodiment, the method according to the invention further comprises, after the step of reducing the amount of intrinsic protein of the algae and, when the process comprises a step of destructuring the cell walls of the algae, directly after that a step of obtaining a paste comprising the steps of: - precipitation with alcohol, - alcohol and precipitate separation, - drying of the precipitate.
    According to a preferred embodiment of the invention, the method further comprises, immediately before the step of obtaining a paste, a step of adding starch to the algae residue comprising the steps of: mixing a starch dispersion and the previously ground algae residue; heating the mixture at a temperature of between 80 and 100 ° C. for 1 to 3 hours; cooling to a temperature of between 45 and 50; ° C, Starch is a natural and biodegradable compound that is today considered as an interesting raw material for the production of biobased plastics. It can be plasticized easily using a plasticizer, such as water or glycerol, and is particularly suitable for the manufacture of films. The starch may be selected from native starches such as corn starch, wheat starch, potato starch, tapioca starch, pea starch, rice starch or mixtures thereof, or a polymer derived from starch.
    Advantageously, the method comprises a step of cultivating algae under favorable conditions for the biosynthesis of starch, said culture comprising the installation in the pond of a biomass of algae and the cultivation for four to six weeks, preferably four weeks, in a culture medium of seawater without fertilizer inputs, especially without nitrogen inputs.
    A biomass of algae containing up to 30%, or even up to 40% starch, by weight relative to the weight of the biomass, can be obtained from culture conditions favoring the synthesis of starch by the alga. Such aquaculture conditions are defined in the scientific publication entitled "Tuning the polysaccharide profile in Ulvacea through Controlled Tank Aquaculture Conditions", CEVA, Alg'n'Chem, Montpellier, November 2011, as well as the published doctoral thesis entitled " Influence of the seaweed culture conditions of the order of Ulvales on their growth and composition ", 2009. In this thesis, it is established that when the algae of the species Ulvaria obscura and Ulva armoricana are cultivated in depleted environment conditions , their total sugar content increases considerably. This is due to the increase of glucose content in the tissues, to the detriment of other constituent sugars. Nitrogen-restricted algae begin to make sugars, including storage sugars such as starch (Gomez Pinchetti et al., 1998, Andersen, 2005). Similarly, it is known that the degradation of starch is accelerated in the dark, especially when the culture media are enriched in nitrogen (Rosenberg et al., 1982, Williams et al., 1985, Ekman et al., 1991; Rincones et al., 1993, Wiencke et al., 2007). Thus, under conditions of controlled cultures, that is to say control of the culture time, brightness and enrichment or not of the culture medium using a fertilizer composition, including supplementing the medium in nitrogen, it is possible to influence the metabolism of algae so as to lead to the synthesis of certain compounds. As regards the increase of starch synthesis by the alga, it has therefore been found that it was useful not to supplement the culture medium with fertilizers, especially nitrogen. In addition, the absence of darkness during the cultivation is to favor. However, in order to obtain a high biomass with a starch content of up to 40% of the dry matter, the culture conditions can be defined as follows: a first culture phase in the presence of seawater supplemented with materials fertilizers (composition of Conway or Walne), so as to promote the growth of biomass, followed by a culture phase in the presence of seawater not supplemented with fertilizing materials, especially nitrogen, so as to favor the production of starch by the seaweed. In a practical way, algae are harvested in a marine environment rich in nutrients. This may be, for example, a known area of algal blooming. The algae are then transferred to basins without nutrients in which they will then transform the proteins into starch which corresponds to a starch enrichment for a loss in protein levels. For example, more than 20% (by weight) of glucose is obtained after four days of maturation and nearly 40% after nine days.
    According to one embodiment of the invention, the algae are microalgae or macroalgae, preferably green (chlorophyceae), brown (Phaeophyceae) or red (Rhodophyceae) algae, more preferably algae of the genus Ulva or of the Sargassaceae family. . As an example of green algae of the genus Ulva, mention may be made of Ulva armoricana or Ulva lactuca.
    The distinction between microalga and macroalga is imprecise. The algae classed among the macroalgae are the algae whose vegetative apparatus is visible to the naked eye, that of the microalgae being visible by means of a microscope.
    The microalgae may for example be chosen from chlorophyceae or diatoms. The invention also relates to an algae powder obtained by means of a process as described above, as well as a bioplastic composition, in particular intended for the manufacture of a plastic product, comprising an algae powder obtained at using a method as described above.
    Advantageously, the algae powder according to the invention contains less than 5% of proteins, in mass of proteins relative to the total mass of the powder. Generally it provides a powder containing between 1 and 4%, preferably between 1 and 2% of protein relative to the total amount of powder.
    The method according to the invention thus makes it possible to obtain a seaweed powder with a high added value given the small amount of protein in the powder obtained.
    Advantageously, the bioplastic composition comprises at least one other component such as a plasticizer compound, a natural polymer, a stabilizer, an antioxidant, an anti-ultraviolet agent, a dye, a filler, an agent promoting compatibility between compounds, water or a preservative.
    The plasticizers, providing more flexibility and promoting the plasticization of the algae powder, have been selected from polyols from vegetable triglycerides such as triols: glycerin (monoglycerol), diglycerine (diglycerol> 90%), polyglycerines 3 (triglycerol> 35%), polyglycerin 4 (tri and tetraglycerol> 65%); diols: ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol (1,2-propane diol), trimethylene glycol (1,3-propane diol), butylene glycol (1,3-butane diol), n-butylene glycol (butane 1,4-diol L-2,3-butylene glycol or cis-butylene glycol (butane-2,3-diol), tertaols: erythritol, pentols: Xylitol, Arabitol, Ribitol, hexols: sorbitol, galactitol, mannitol, heptols: Volemitol: The disaccharides polyols with nine functions OH: Maltitol, isomaltitol, lactitol and any combination of these compounds.
    GMO-free vegetable diglycerols, such as the product SP-PG3 from SPIGA, have been used preferentially. They will also be preferred to glycerine because less migrants. Indeed, glycerine tends to migrate to the surface of the plastic part produced and tends to provide a bold appearance to the product, with a loss of mechanical properties. The diglycerol molecule is more cumbersome than that of glycerin and therefore migrates much less in the polymer matrix. In addition, diglycerins provide better plasticization of bioplastics. These plasticizers are used at levels of 10%, by weight, of the algae powder and up to 10% of the bioplastic.
    Polymers other than starch can be added and are selected according to the characteristics they can bring to the desired plastic product. It may be characteristics of hydrophobicity, transparency, tensile strength, hardness, ability to allow printing, etc.
    Biodegradable thermoplastic polymers are chosen from polylactic acid (PLA) (produced by the company Natureworks), polybutylene succinate (PB S) and polybutylene succinate adipate (PB SA) (produced by Showa Denko under the BIONOLLE reference series 1000 (PB S) and 3000 (PB SA)), polybutylene adipate terephthalate (PBAT copolyester) (produced by BASF under the references ECOFLEX or DuPont under the reference BIOMAX), polyhydroxyalkanoates (PHA) (produced by METABOLIX), polyhydroxybutyrates (PHB), polyhydroxyvalerate (PHV), polyhydroxybutyratehydroxyvalerate coproplymers (PHBV), polycaprolacones (PCL) (CAPA company, series 6500 and 6800).
    Polyvinyl alcohols, or PVA, can be mixed with the algae powder in the compositions of the present invention and enhance the biodegradability, transparency and strength properties of the finished material, flexibility and allow good starch dispersion. PVA will be chosen with molecular weights between 20,000 to 80,000 Da. Among the PVAs available on the market, we can cite the product marketed under the trademark CELVOL E 205 from Sekishui; 87-90% hydrolyzed, having a molecular weight between 30,000 - 70,000 Da and a viscosity of between 4-6 cps to 4%, or the product marketed under the trademark MOWIOL 5-88 from Kuraray; 87% hydrolyzed, with a molecular weight of about 31,000 Da.
    Bioplastic compositions derived from biobased materials can also be produced by mixing the algae powder with polyolefins produced from plant resources such as polyethylenes derived from sugarcane, such as those from the company BRASKEM.
    Hybrid bioplastic compositions may include algae powders and non-biodegradable and non-biosourced polymers such as polyolefins (polypropylene homopolypropylene (Homo PP) and polypropylene copolymer (CoPP), polyethylenes), polystyrenes, polyesters, Polyvinyl chloride (PVC), poly (acrylonitrile-co-butadiene-co-styrene (ABS), thermoplastic elastomers such as polyurethanes, block copolymers styrene (SAS, SBS) such as those produced by KRATON polymers LLC, Houston, Texas ethylene vinyl acetate (EVA), or mixtures thereof.
    The bioplastic compositions may also include additives such as anti-ultraviolet and antioxidants. These include the products sold under the Irganox 1010 brand, Irganox B-225, Irganox B-900, Irgastab from Ciba Specialty Chemicals, Cyanox LTDP from Cytec. These additives are added in amounts of up to 0.5% by weight of the total weight of the composition. As mineral fillers, mention will be made of talc, calcium carbonate and titanium dioxide (rutile or anatase). These fillers are used to add whiteness or opacity to the final plastic product. Carbon black can also be used to give opacity and black color to the final plastic product.
    The bioplastic compositions may also include thermo-reactive and / or photo-reactive oxo-biodegradable additives which, under the effect of light, temperature or the combination of the two, will oxidize the polyolefins such as polyethylenes and polypropylenes to render them biodegradable in the presence of microorganisms. By way of example, such additives are produced by Symphony in the series D2W - DG13-15.
    Odor absorbers may also be added, for additional action on odor problems in bioplastic formation, when especially odorous additives will be added such as vanillin (odor masking) or inorganic antimicrobial additives in PE matrices such as masterbatch 9655 from Symphony.
    Preferably, the composition comprises between 10 and 60%, by weight, preferably between 15 and 55%, by weight, of an algae powder obtained using a process as defined above and between 90 and 40% of at least one other component.
    The present invention also relates to a method of manufacturing a plastic product which includes a method for preparing an algae powder as defined above.
    Advantageously, the method of manufacturing said plastic product further comprises a step of preparing a bioplastic composition from said algae powder.
    Advantageously, the process for manufacturing said plastic product comprises a step of extruding said bioplastic composition into granules.
    Advantageously, the manufacturing process of said plastic product comprises a step of shaping a plastic product by injection molding, extrusion blow molding or extrusion in a flat die of said bioplastic composition. The invention finally relates to a plastic product obtained from such a manufacturing process.
    According to a preferred embodiment of the invention, the product is a food or non-food film, a molded or thermoformed object, such as a packaging for example multi-layer or sheets.
    The characteristics of the invention, as well as others, will emerge more clearly on reading the following embodiments that are intended to be illustrative and not restrictive.
    EXAMPLE 1 Obtaining a Sample Algae Powder
    Green algae of the species Ulva Armoricana were harvested, dried in flakes at 50 ° C and then reduced to particles of average size of 100 μm in diameter. A powder of 2 kg was thus obtained. The composition of the algae powder is given in Table 1.
    Table 1
    *% dry / crude mass of dry matter of the compound relative to the mass of dried algae "raw", that is to say without correction of the percentage of residual moisture still present in the dried seaweed.
    Note that the starch content is 4.1% dry / crude in this powder.
    EXAMPLE 2 Preparation of a control algae powder, called activated and enriched in starch:
    The method used implements, in order, the following steps, detailed in Example 3 to follow: 1- harvest of a biomass of green algae Ulva Armoricana and enrichment in conditions favoring the synthesis of starch, 2 depigmentation, 3-absent (step of reduction of intrinsic protein not achieved), 4-destructuration of the cell walls by treatment with citric acid (step of activation of algae), 5- addition of starch (final mixture 60% dry weight of activated algae and 40% dry mass of starch), 6-precipitation / filtration, 7- drying / powder reduction of average size of 100 μm in diameter.
    Steps 1, 2, 4, 5 and 6 are therefore carried out as those of Example 3 to follow.
    Example 3 Obtaining an Algae Powder According to the Invention, Said Activated, Deproteinated and Rich in Starch:
    The method used implements, in order, the following steps, developed in the following: 1 - harvesting a biomass of green algae Ulva armoricana and culture in conditions favoring the synthesis of starch, 2 - depigmentation, 3 - reduction of the intrinsic protein content, 4 - destruction of the cell walls by treatment with citric acid (algae activation step), 5 - addition of starch, 6 - precipitation / separation, 7 - drying and reduction in powder of average size of 100 μm in diameter. 1. Harvest and cultivation of biomass in starch enrichment condition:
    The Ulves, of the species Ulva armoricana, were harvested in France over a period stretching from September to October. At such a time, they have high initial glucose levels favorable for endogenous starch enrichment. The algae were grown for 1 month and 4 days in the pond and nitrogen deprivation conditions. The lighting conditions result from the natural lighting of the months of October and November in Brittany (France). A quantity of 18 kg of fresh material was obtained. The harvested algae were frozen under vacuum, without rinsing with fresh water. 15 kg of fresh algae were subsequently thawed and crushed by URSCHEL grinder on grid 66896. After defrosting and milling, 14.65 kg of crushed algae were obtained. The following data was measured:
    Dry matter content: 21.38%
    Mass of algae (MS: dry matter): 3.13 kg
    Protein content: 9.29% dry / dry, or 0.29 kg of protein
    Glucose (starch) content: 32.80% dry / dry
    The glucose content is representative of the starch content, the starch being converted into glucose during quantitative and qualitative analyzes. It is noted that the glucose level is 32.80% dry / dry, relative to the glucose level of Example 1 4.1% dry / crude. There has therefore been stimulation and increase of starch synthesis by the algae during its cultivation under favorable conditions for the synthesis of starch by the algae. 2, depigmentation with ethanol:
    After grinding, carry out four successive macerations, hydro-ethanolic, in order to remove a maximum of chlorophyll and bleach the seaweed. Each maceration is carried out by soaking crushed algae for 1 to 3 days in the presence of 25 L of ethanol. At the end of these maceration steps, the mixture is filtered on a fabric having pores 100 microns in diameter and the crushed and depigmented algae are recovered. The amount of discolored ulva obtained is 14.90 kg with an MS of 16.47%, ie 2.45 kg dry. The mass yield of this step is 78%.
    The total protein content is determined by the Kjeldhal method (Nx6,25). The principle of this method is a multiplication of the mineral nitrogen content by a mean coefficient which represents the nitrogen richness of the animal or vegetable proteins. The total protein content is expressed as a percentage of protein (mass of dry matter) relative to the dry mass of "raw" dried depigmented eggs, that is to say without correction of the few percentages of moisture present in the product. dried seaweed.
    Balance sheet:
    Quantity of algae dry matter at the beginning of the stage: 3.13 kg
    Quantity of algal dry matter at the end of the stage: 2.45 kg
    Protein content: 10.4% dry / raw, or 0.25 kg of protein
    Starch content: 32.1% dry / crude 3, Intrinsic protein reduction:
    The principle of this step is to hydrolyze the proteins enzymatically and to extract the hydrolysates in a basic medium. 13.65 kg of depigmented ulva was used (MS 16.47%), ie 2.24 kg dry. 3.1 Watery maceration
    Suspension of 13.65 kg of depigmented ults from the previous step, ie 2.24 kg dry, in 47.8 kg of demineralized water and stirring with the Rayneri turbine for 30 minutes (MS 3.57% ). Then add 11.68 kg of demineralized water to obtain 3.02% DM.
    Maceration one night at a temperature of 7 ° C, then separation on sieve 100 pm in static. In a second step, manual pressing of the remaining algae residue on the 100 μm sieve with a 30 μm screen.
    Balance of this sub-step: quantity: 57 kg (MS: 0.47%) of filtrate and 14.8 kg (MS: 13.04%) is 1.92 kg dry of algae residue. The intermediate mass yield of this step is 85%. 3.2. First extraction with soda:
    This step promotes extraction and accessibility to the enzyme. It allows the extraction of soluble proteins to promote the action of the enzyme specifically on insoluble proteins.
    The residue from substep 3.1 is taken up (1.92 kg dry) in demineralised water and suspended at 3.5% DM. Then add 30% sodium hydroxide in sufficient quantity to be in final solution at 0.12 M concentration.
    Stirring with the Rayneri turbine during lh30. Sieve separation at 100 μm statically (dripping overnight at room temperature), then manual pressing of the remaining algae residue on the sieve 100 pm with a 30 μm screen.
    Assessment of this substep: amount: 40.2 kg (MS: 1.04%) of filtrate and 14.7 kg (MS: 12.68%) or 1.86 kg dry residue of algae. The intermediate mass yield of this step is 96%. 3.3, Enzymatic hydrolysis with an Alcalase® protease:
    Recovery of the algae residue from substep 3.2 (1.86 kg dry) in deionized water for suspension at 3.5% MS, ie 47.43 kg of demineralized water. Transfer the medium into a concentration ball and then adjust the pH to 8.0 with 140 g of 96% sulfuric acid (starting pH 12.3). Stirring on stirrer at maximum speed and heating at 55 ° C. Once at temperature, adding 3.28 g of Alcalase® enzyme from Novozymes, a protease from Bacillus lichenformis (Ref Sigma: P4860,> 2.4 U / boy Wut). Generally, the enzyme is added at a concentration of between 0.1 and 10% relative to the dry mass of proteins, preferably between 0.8 and 3%, more preferably between 1 and 2%. Stirring overnight (12h) at 55 ° C. 3.4, Second extraction with soda:
    After cooling to 30 ° C, pH adjustment to 12.0 with 498 g of 30% NaOH (initial pH 5.23). Sieve separation at 100 pm in static, then in a second time, manual pressing of algae residues remaining on the sieve 100 pm with a canvas 30 pm.
    Summary of this step: quantity: 47 kg (MS: 1.97%) filtrate and 14 kg (MS: 8.90%) is 1.24 kg dry residue of algae. The intermediate mass yield at this stage is 66%.
    The filtrate, rich in protein material (peptides and amino acids) is harvested for subsequent recovery. 3.5. Rinsing with water of algae residue
    Recovery of the residue obtained from sub-step 3.4 (1.24 kg dry) and rinsing with demineralized water for suspension at 3% MS, ie 27.53 kg of demineralised water added.
    Agitation one hour and sieving 100pm for one night (no pressing on canvas 30pm required).
    Balance sheet:
    Quantity of algae dry matter at the beginning of the stage: 2.24 kg
    Quantity of dry matter of algae at the end of the stage: 1.11 kg
    Mass yield: 49%.
    Protein content: 5.6% dry / raw, or 0.06 kg of protein
    Starch content: 49.4% dry / crude
    The protein content of the algae residue determined by the Kjeldhal method (Nx6,25) is 5.6% dry / crude. The protein content in the residue (5.6% dry / crude) was reduced by 46% based on the protein content in the residue of the previous step (10.4% dry / crude).
    Based on the amount of total starting protein (0.29 kg), the final protein amount (0.06 kg) was reduced by 79% by mass.
    Enzymatic hydrolysis from another enzyme:
    An enzymatic hydrolysis of the proteins was carried out, for comparison, on a biomass of 2 kg in order to verify the feasibility of the process using other proteases, in particular from a protease derived from Aspergillus oryzae and marketed under the name Flavourzyme by the company Sigma. The algal biomass used underwent in this test the same steps as steps 1 to 3 described above. The protein content was reduced by 12% (amount of residual protein (in mass), compared to the amount of protein present initially.The color characteristics are the obtaining of a yellow-green residue as in the case of the use of Alcalase, however an unsatisfactory odor is detected Hydrolysis using TAlcalase is preferred 4. Activation of algae: destructuration of the cell walls:
    As a reminder, the principle is to destructure the cell walls with the aid of an agent solubilizing polysaccharides, in this case with the aid of a chelating agent, and more specifically to break the particularly ionic bonds involving the parietal polysaccharides. in order to make the parietal polysaccharides accessible, free and functional, therefore active, without being forced to extract them by means of refined and fine extraction processes. At the end of this step, the algae residue recovered contains the polysaccharides as well as all the non-polysaccharide components present before the implementation of this step.
    The algae residue from step 3 is taken again to be milled with the colloid mill very tight to have a smooth paste, with an addition of 12 kg of water to push the residues and rinse the mill. After grinding, obtaining 26.6 kg (MS: 4.07%) of a seaweed residue in the form of a thick puree, or 1.08 kg dry.
    Transfer the milled algae residue, ie 26.6 kg, into a 100 L enamelled reactor and add 11.4 kg of water for rinsing the equipment. A total of 38 kg of ground material (final MS calculated: 2.85%), ie 1.08 kg dry, used for activation with the aid of a chelating agent: citric acid monohydrate.
    The pH is adjusted to 3 with 436.5 g of citric acid monohydrate.
    The reaction medium is heated and maintained for 2 hours at 90 ° C. with stirring, and then cooled to ambient temperature (measurement of the pH after cooling: 3.06).
    Then, the entire medium (algae residue and liquid) is transferred directly into a concentration ball and concentrated under vacuum at 45 to 50 ° C. About 15 liters of water are then removed. At this stage, the absence of a separation or filtration step leading to the elimination of the non-polysaccharide compounds is noted. 22.2 kg, at 6.31% DM, ie 1.4 kg dry concentrate are recovered.
    Neutralization of the concentrate at pH 7.7 with 510 ml of 30% NaOH (MS after neutralization: 6.78%), ie 1.5 kg sec.
    The intermediate yield for this overall activation step is considered 100% because no source of loss is identified (1.08 kg + 0.487 kg of sodium citrate).
    Balance sheet:
    Quantity of algae dry matter at the beginning of the stage: 1.11 kg
    Quantity of dry matter of algae at the end of the stage: 1.54 kg
    Protein content: 4% dry / raw
    Starch content: 34.4% dry / crude 5- Addition of a starch dispersion
    The activated algae concentrate from the previous step is used at a rate of 22.2 kg (6.78%) or 1.5 kg dry.
    A starch dispersion was prepared so as to obtain a final mixture of 60% dry mass of activated algae and 40% dry mass of starch. To avoid adding too much water, prepare a dispersion of about 10% starch, ie 8.29 kg of water and 1.01 kg of starch. The starch dispersion is maintained at 90 ° C for 30 minutes (baking). The dispersion is very viscous, 10% is a limit that it is better not to exceed.
    Transfer the activated algae concentrate and the starch dispersion to 90 ° C in a container allowing stirring Rayneri. Stirring for three hours to mix and transfer the 34 kg of dispersion in 102 L of alcohol (80 L of new alcohol and 22 L of alcohol recycled at 90 °). Mix then rest the solution overnight for decantation. Separation of the precipitate on a cloth of 30 pm then manual pressing on canvas of 20pm. The amount of pressed mixture recovered is 13.1 kg.
    Drying in the oven, heating for 5h at 45 ° C. The yield of this step is 152%.
    Balance sheet:
    Quantity of dry matter of algae at the beginning of the stage: 1.5 kg
    Quantity of algal dry matter at the end of the step: 2.3 kg
    Protein content: 2.4% dry / raw, or 0.05 kg of protein
    Starch content: 53.4% dry / raw 6. Grinding:
    A first Forplex pin milling takes place, followed by a second Forplex 100 μm grid milling.
    Quantity after milling: 1.91 kg.
    Crushing yield: 83% by mass, related to the dead volumes of the grinders.
    The granulometric distribution of these crushed algae is as follows:
    It is noted that at the end of the process, an algal powder containing 2.4% of proteins and 53% of starch is obtained as a percentage of dry mass relative to the total dry mass of the powder.
    Example 4 Bioplastic Compositions
    Bioplastic compositions were formulated by mixing the algae powders of Examples 1, 2 and 3 with other compounds. As a control, native corn starch is used. The formulated compositions are extruded as granules. A total of 49 compositions have been formulated. Table 2 below indicates the compositions of the mixtures made:
    Table 2:
    PBAT: (polybutylene adipate terephthalate)
    After :
    CoPP: polypropylene copolymer
    After
    PBS: Polybutylene succinate
    Formulas 34 to 37, 40 to 43 and 46 to 49 comprise between 25 and 55% by weight, relative to the total weight of the compositions, of an algae powder obtained according to Example 3. algae whose protein levels were reduced, the intrinsic starch level was increased, a starch supply was added and the parietal polysaccharides were made functional.
    EXAMPLE 5 Extrusion in the Form of Granules of the Compositions of Example 4
    The extrusion conditions are shown in Table 3
    Table 3:
    The odor, color and mechanical characteristics of the extruded compositions are presented in Table 4:
    Table 4:
    The extruded products obtained with the bioplastic compositions 34-37, 40-43, 46-49 containing algae powders according to the invention (Example 3) do not emit any annoying, nauseating or uncomfortable odor.
    The bioplastic compositions 16-19, 22-25, 28-32, containing algae powders according to Example 2, which were prepared according to a method identical to that of Example 3, but without a rate reduction step. of protein, have a weak odor.
    Extruded products obtained with bioplastic compositions made from the native starch powder (compositions 1-3) and those made from simply powdered algae of Example 1 (formulas 4-7, 8-11 , 12-15), without any treatment, have respectively a smell of bread and a strong smell of seaweed.
    The method according to the invention is therefore effective in suppressing odor phenomena.
    With regard to color, the extruded products obtained from powdered algae of Example 1 (formulas 4-7, 8-11, 12-15) have dark brown colors. Such colors do not make them usable in the manufacture of the majority of plastic products.
    The extruded products obtained with bioplastic compositions 16-19 and 22-25, 28-31 containing algae powders according to Example 2, have light to dark beige or light to dark green colors.
    Only the compositions 22 and 40 made it possible to obtain a semi-transparent color. In these formulas, the rate of algae is lower than in the compositions 23-25 and 41-43. The polymer is CoPP.
    In formula 34 which has the same amount of algae, the color is very light beige but less transparent, the polymer is PB AT.
    Bioplastic compositions 34-37 and 40-43 will yield plastic products whose colors will not be easy to predict. Addition of a polymer such as CoPP is recommended.
    The extruded products obtained with the bioplastic compositions 34-37 and 40-43, containing algae powders according to Example 3, have light beige colors or are semi-transparent. Formula 37 containing 55% by weight of algae powder according to the invention made it possible to obtain a beige extruded product, which is acceptable. Indeed, during the formation of films, the products are stretched and the final color rendered will depend on the thickness of the film.
    Here again, it is noted that the CoPP polymer is effective in enhancing transparency.
    Among the formulations using PBAT as a polymer, it should be noted that the compositions 34-36, made from reduced-protein algae powders, have lower modulus of elasticity than the moduli of the other compositions and deformations at break. much higher than with non-deproteinated algae powders (16-18). The materials are therefore more flexible with better deformation.
    In formulations using PBS as a polymer, it will be appreciated that compositions 47-48 with reduced protein algae powder have lower modulus of elasticity and much greater ultimate tensile strength than powders. non-deproteinized algae (28-30), the materials are therefore more flexible with better deformation.
    Moreover, materials with PB S and with the same algae levels are, however, much stiffer and less deformable than PBAT formulations.
    In formulations using CoPP, it will be appreciated that compositions (40-42) with reduced protein algae powder have equivalent modulus of elasticity and deformations at break such as non-deproteinized algae powders (22). -25). However, materials incorporating CoPP are much more rigid and less deformable than formulations incorporating PBAT.
    EXAMPLE 6 Bioplastic Compositions Formulated from Algae Powders Obtained by a Process According to the Invention Using Anti-UV Agents antioxidants, anti-odor.
    Bioplastic compositions were formulated by mixing the algae powders of Examples 2 and 3, PBAT and anti-UV, antioxidant and anti-odor agents. A total of four compositions were formulated containing 40% of seaweed powder.
    Table 5 below indicates the compositions of the mixtures made:
    Table 5
    The extrusion conditions were 120, 140, 170 ° C - 50 rpm and the injection conditions were 170 ° C - 8 bar.
    Compositions 64 and 65 are less colored and odorless compared to Formula 62. Formula 63 is more colored but the odor is improved over Formula 62. The addition of antioxidant and anti-UV enhances color relative to to the compositions of Example 4.
    The mechanical properties obtained are as follows (Table 6)
    Table 6:
    EXAMPLE 7 Bioplastic Compositions Formulated from Algae Powders Obtained by a Process According to the Invention Using Another Chelating Agent at the Cell Wall Destructuring Step
    The steps of the method according to Example 3 were carried out with in step 4 the following chelating agents: sodium oxalate, sodium carbonate and sodium chloride. The algae powders were mixed with plasticizers and polymers. The molar mass of each mixture was measured. The results are as follows: a) with sodium oxalate: 570,000 g / mol, b) with sodium carbonate: 600,000 g / mol, c) with sodium chloride: 474,000 g / mol, d) with citric acid : 295,000 g / mol.
    The molar mass is halved with citric acid.
    Thermal stability tests were also conducted. The 4 products were kept for 3 days at 150 ° C: - with sodium oxalate, sodium chloride and sodium carbonate: the materials are burned with strong caramel smells, - with citric acid: the color remains light yellow . Citric acid is therefore preferred because it limits compatibility problems with other compounds. Indeed, the molecular weight has been identified in the context of the present invention as a preponderant element to obtain a good mixture of polymers, algae and other compounds. Moreover, it is preferable to favor an activating agent which can also be a heat stabilizer, such as citric acid.
    权利要求:
    Claims (21)
    [1" id="c-fr-0001]
    1) A process for preparing an algae powder, in particular for the manufacture of a plastic product, comprising the successive steps of: - growing and / or harvesting a biomass of algae, - reduction of minus 10% of the intrinsic protein content of the algae, in mass relative to the protein mass of the harvested biomass, - drying, - reduction to powder or granules.
    [0002]
    2) Process for the preparation of an algae powder according to claim 1, characterized in that the reduction step is a reduction step of at least 40%, preferably at least 70%, more preferably at least 75% of the intrinsic protein content of the algae, in mass relative to the mass of proteins of the biomass harvested.
    [0003]
    3) Process for the preparation of an algae powder according to claim 1 or claim 2, characterized in that the reduction of the amount of intrinsic protein of the algae harvested comprises: - the enzymatic hydrolysis of the intrinsic proteins by mixing of the algal biomass harvested, preferably ground, and one or more proteases, and then - the separation of a hydrolyzate enriched in peptides and / or amino acids and a residue of algae.
    [0004]
    4) Process for the preparation of an algae powder according to claim 3, characterized in that the enzymatic hydrolysis of the proteins is carried out using one or more proteases, in particular one or more endopeptidases, and or exopeptidases, of bacterial or fungal origin, such as one or more enzymes obtained from Bacillus licheniformis, Bacillus subtilis, Bacillus amyloliquefaciens or Aspergillus oryzae, preferentially from Bacillus licheniformis.
    [0005]
    5) A method for preparing an algae powder according to one of claims 1 to 4, characterized in that it further comprises a step of: - depigmentation of algae with or without treatment with a chemical agent, following the step of harvesting a biomass of algae and prior to the reduction of the intrinsic amount of protein from the algae harvested.
    [0006]
    6) A method for preparing an algae powder according to one of claims 1 to 5, characterized in that it further comprises, directly after the step of reducing the amount of intrinsic protein algae: - a step of destructuring the cell walls of the algae, by mixing the algae residue and a polysaccharide solubilizing agent, such as a chelating agent or an inorganic acid, preferably chosen from citric acid, citric acid monohydrate, sodium oxalate, hydrochloric acid, sodium carbonate, more preferably citric acid, heating the mixture at a temperature between 80 and 100 °, preferably 90 ° C, for 1 to 4 hours, preferably 2 hours, then cooling and concentration of the algae residue, it being understood that said step does not involve any elimination or separation of the organic and inorganic components.
    [0007]
    7) A process for preparing an algae powder according to claim 6, characterized in that said step of destructuring the cell walls of the algae comprises the successive steps of: - obtaining a pulp of the algal biomass, - mixture of said grinding and water to obtain a paste, - adding a solubilizing agent, in particular citric acid, up to a pH of between 2.5 and 3.5, preferably 3, - heating the mixture to a temperature between 80 and 100 °, preferably 90 ° C., for 1 to 4 hours, preferably 2 hours, - cooling at a temperature of less than or equal to 45 ° C., - concentration under vacuum at a temperature of between 45 and 50 ° C., - adjustment ph of the residue obtained at a pH between 7 and 8, preferably 7.7 with a base such as sodium hydroxide.
    [0008]
    8) A method for preparing an algae powder according to one of claims 6 to 7, characterized in that it further comprises, after the step of reducing the amount of intrinsic protein algae and, when the method comprises a step of destructuring the cell walls of the algae, directly after the latter, a step of obtaining a paste comprising the steps of: - precipitation with alcohol, - alcohol and precipitate separation, - drying the precipitate.
    [0009]
    9) Process according to claim 8, characterized in that the method further comprises, immediately before the step of obtaining a paste, a step of adding starch to the algae residue comprising the steps of mixture of a starch dispersion and the previously ground algae residue, heating of the mixture at a temperature of between 80 and 100 ° C. for 1 to 3 hours, cooling to a temperature of between 45 and 50 ° C.
    [0010]
    10) Method according to one of the preceding claims, characterized in that the method comprises a step of algae cultivation in conditions favoring starch biosynthesis, said culture comprising the installation in the basin of a biomass of algae and the culture for four to six weeks, preferably four weeks, in a seawater culture medium without fertilizer, especially without nitrogen inputs.
    [0011]
    11) Method according to one of the preceding claims, characterized in that the algae are microalgae or macroalgae, preferably green algae (chlorophycées) or brown (pheophycées) ((red (rhodophycées)), more preferably algae of the genus Ulva or the family sargassaceae.
    [0012]
    12) Algae powder obtained by a process according to one of claims 1 to 11.
    [0013]
    13) Powder of algae according to claim 12, characterized in that it contains less than 5% protein, mass of protein relative to the total mass of the powder.
    [0014]
    14) A bioplastic composition, especially for the manufacture of a plastic product, comprising an algae powder obtained by means of a process according to one of claims 1 to 11.
    [0015]
    15) Composition according to claim 14, characterized in that it comprises at least one other component such as a plasticizer compound, a natural polymer, a stabilizer, an antioxidant, an anti-ultraviolet, a dye, a filler, water or a preservative.
    [0016]
    16) Composition according to claim 15, characterized in that it comprises between 10 and 60%, by weight, preferably between 15 and 55%, by weight, of a powder of algae obtained using a method according to one of claims 1 to 10 and between 90 and 40% of at least one other component.
    [0017]
    17) A method of manufacturing a plastic product, characterized in that it comprises a method for preparing an algae powder as described in one of claims 1 to 11.
    [0018]
    18) A method of manufacturing a plastic product according to claim 17, characterized in that it comprises, in addition, a step of preparing a composition according to one of claims 14 to 16 and a step of extrusion of said granular composition.
    [0019]
    19) A method of manufacturing a plastic product according to claim 18, characterized in that it comprises a step of shaping the product by injection molding, extrusion blow molding or extrusion flat die, said bioplastic composition.
    [0020]
    20) Plastic product obtained from a process according to one of claims 17 to 19.
    [0021]
    21) Product according to claim 20, characterized in that said product is a food film, a non-food film, a molded article, thermoformed products, packaging such as multi-layer or sheets.
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    同族专利:
    公开号 | 公开日
    WO2017046356A1|2017-03-23|
    FR3041351B1|2020-01-24|
    US10870733B2|2020-12-22|
    US20180258231A1|2018-09-13|
    CN108350178A|2018-07-31|
    EP3359587A1|2018-08-15|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US5779960A|1993-01-29|1998-07-14|International Technology Management Associates, Inc.|Algal plastics|
    WO2010125490A2|2009-04-28|2010-11-04|Kimberly-Clark Worldwide, Inc.|Algae-blended compositions for thermoplastic articles|
    WO2012114045A1|2011-02-25|2012-08-30|Arjo Wiggins Fine Papers Limited|Methods for preparing paper pulp and for manufacturing paper from seaweed powder|
    WO2014128411A1|2013-02-20|2014-08-28|Algopack|Method for producing a brown macroalgae powder and method for producing rigid objects from said powder|
    FR3012817A1|2013-11-07|2015-05-08|Super Film Ambalaj San Tic A S|COMPOSITION BASED ON POLYMERS FOR THE PRODUCTION OF PLASTIC PRODUCTS DEGRADABLE IN THE ENVIRONMENT AND PLASTIC PRODUCTS OBTAINED|
    SG179157A1|2009-09-15|2012-05-30|Sapphire Energy Inc|A system for transformation of the chloroplast genome of scenedesmus sp. and dunaliella sp.|
    CN104144984A|2011-08-24|2014-11-12|阿尔吉斯有限责任公司|Macrophyte-based bioplastic|MA40103B1|2017-03-08|2018-11-30|Mustapha Benmoussa|A process for preparing a coating to improve the efficiency and quality of fertilizers|
    FR3066917A1|2017-06-06|2018-12-07|Lessonia|PASTE AND COATING OF ALGAE WITH CONTROLLED HEAVY METAL CONTENT|
    CN107573544A|2017-07-31|2018-01-12|浦江县昂宝生物技术有限公司|The preparation method of edible packing membrane based on sargassan|
    US10485253B2|2017-08-21|2019-11-26|Mustapha Benmoussa|Method of microalgal biomass processing for high-value chemicals production, the resulting composition of butyrogenic algal slowly fermenting dietary fiber, and a way to improve colon health using a slowly fermenting butyrogenic algal dietary fiber|
    FR3106411B1|2020-01-20|2022-01-21|Pixminds|Computer peripheral comprising an element made from algae.|
    法律状态:
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    2017-10-13| TP| Transmission of property|Owner name: ERANOVA, FR Effective date: 20170908 |
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    优先权:
    申请号 | 申请日 | 专利标题
    FR1558743A|FR3041351B1|2015-09-17|2015-09-17|PROCESS FOR THE PREPARATION OF A REDUCED PROTEIN CONTENT OF ALGAE AND A BIOPLASTIC COMPOSITION FORMULATED FROM SUCH A POWDER|
    FR1558743|2015-09-17|FR1558743A| FR3041351B1|2015-09-17|2015-09-17|PROCESS FOR THE PREPARATION OF A REDUCED PROTEIN CONTENT OF ALGAE AND A BIOPLASTIC COMPOSITION FORMULATED FROM SUCH A POWDER|
    EP16775503.2A| EP3359587A1|2015-09-17|2016-09-16|Method for preparing an algae powder with reduced protein content and bioplastic composition formulated from such a powder|
    CN201680063939.XA| CN108350178A|2015-09-17|2016-09-16|The biological plastics composition for preparing the method for the algae powder of protein content reduction and being prepared with the powder|
    PCT/EP2016/072020| WO2017046356A1|2015-09-17|2016-09-16|Method for preparing an algae powder with reduced protein content and bioplastic composition formulated from such a powder|
    US15/760,901| US10870733B2|2015-09-17|2016-09-16|Process for preparing an algal powder containing a reduced content of proteins, and bioplastic composition formulated from such a powder|
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