WO2024257575A1 - Alkali cellulose material, viscose, and method for producing viscose - Google Patents
Alkali cellulose material, viscose, and method for producing viscose Download PDFInfo
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- WO2024257575A1 WO2024257575A1 PCT/JP2024/019027 JP2024019027W WO2024257575A1 WO 2024257575 A1 WO2024257575 A1 WO 2024257575A1 JP 2024019027 W JP2024019027 W JP 2024019027W WO 2024257575 A1 WO2024257575 A1 WO 2024257575A1
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- cellulose
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B1/00—Preparatory treatment of cellulose for making derivatives thereof, e.g. pre-treatment, pre-soaking, activation
- C08B1/08—Alkali cellulose
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B16/00—Regeneration of cellulose
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B9/00—Cellulose xanthate; Viscose
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/06—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/06—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
- D01F2/08—Composition of the spinning solution or the bath
- D01F2/18—Addition to the spinning solution of substances to influence ripening
Definitions
- the present invention relates to an alkali cellulose material that is an intermediate material for producing viscose, and in particular to an alkali cellulose material that uses regenerated cellulose as a raw material.
- cellulose products such as cellophane, rayon, and beads generates by-products such as scraps and non-standard products.
- by-products such as scraps and non-standard products.
- cellulose does not have thermoplasticity and does not dissolve in general-purpose solvents, using cellulose products as a raw material to prepare a cellulose solution such as viscose for reuse requires complicated work processes and high costs.
- viscose is prepared by first coarsely crushing the raw material dissolving pulp sheet and immersing it in a large amount of alkaline aqueous solution to turn it into alkaline cellulose (mercerization), squeezing it to remove excess alkaline aqueous solution, crushing it, reacting it with carbon disulfide to convert it into cellulose xanthate (sulfurization), and dissolving this in an alkaline aqueous solution.
- Non-Patent Document 1 describes a method for producing viscose from wood pulp by uniformly spraying a small amount of concentrated caustic soda solution onto the pulp to omit squeezing in order to reduce the amount of alkaline aqueous solution used (non-squeezing method).
- Patent Document 1 describes the preparation of alkali cellulose, which is made from recycled artificial cellulose-based raw materials, by immersing the raw materials in an alkaline aqueous solution and then squeezing the raw materials, which undergoes sulfurization and dissolution.
- Non-Patent Document 1 the viscose produced by the method described in Non-Patent Document 1 has the problem that a large amount of unreacted fibers remain, resulting in poor dispersion and dissolution.
- the present invention aims to solve the above problems, and its purpose is to provide an alkali cellulose material that uses regenerated cellulose as a raw material to obtain viscose with physical properties suitable for use as a raw material for forming various cellulose molded products.
- a mixed alkali cellulose material comprising any one of the alkali cellulose materials of aspects 1 to 5 and an alkali cellulose material for the same application produced from a cellulose material other than regenerated cellulose.
- a mixed sulfide of alkali cellulose material with carbon disulfide comprising the sulfide of alkali cellulose material of aspect 7 with carbon disulfide and a sulfide of alkali cellulose material for the same use produced from a cellulose material other than regenerated cellulose with carbon disulfide.
- a mixed viscose comprising the viscose of aspect 9 and a viscose produced from a cellulose material other than regenerated cellulose.
- a method for producing viscose comprising sulfurizing an alkali cellulose material with carbon disulfide, the alkali cellulose material comprising regenerated cellulose, an alkali, and water, the alkali cellulose material having a cellulose concentration of 27-40% by mass, preferably 29-38% by mass, and more preferably 30-36% by mass, and an alkali concentration of 8-20% by mass, preferably 9-18% by mass, and more preferably 10-16% by mass.
- Viscose according to aspect 9 or 12 having a cellulose concentration of 5% by mass or more, preferably 6 to 12% by mass, and more preferably 8 to 10% by mass.
- a mixed viscose according to aspect 10 having a regenerated cellulose content of 1 to 99% by mass, preferably 2 to 50% by mass, and more preferably 3 to 20% by mass, based on the cellulose component.
- the present invention provides an alkali cellulose material that uses regenerated cellulose as a raw material to obtain viscose with physical properties suitable for use as a raw material for molding various cellulose molded products.
- the present invention provides viscose with physical properties suitable for use as a raw material for molding various cellulose molded products, using this alkali cellulose material as an intermediate material.
- the present invention also provides a method for producing viscose with physical properties suitable for use as a raw material for molding various cellulose molded products, using regenerated cellulose as a raw material.
- FIG. 1 is a schematic diagram of a graph in which characteristic values of viscose for calculating the degree of clogging are plotted.
- the regenerated cellulose used as a raw material is mainly cellulose obtained by liquefying natural cellulose by the conventionally known viscose method or cuprammonium method, and then solidifying and molding it into a predetermined shape.
- Regenerated cellulose includes cellulose molded products, cellulose products produced by cutting cellulose molded products, and by-products produced when manufacturing cellulose molded products. They may be pulverized to improve reaction efficiency. Specific examples of regenerated cellulose include scraps, non-standard products, defective products, and waste cellulose products generated when manufacturing cellulose molded products such as cellophane, rayon, and beads. Furthermore, regenerated cellulose can be reused as a raw material instead of natural cellulose.
- the natural cellulose used as the raw material for viscose is not particularly limited, and examples thereof include pulp made from biomass such as wood, cotton, straw, bamboo, hemp, jute, and kenaf.
- the manufacturing method is also not particularly limited, and may be a mechanical method, a chemical method, or a method that combines the two. In terms of pulp quality, highly refined dissolving pulp, which is the main raw material for paper pulp, artificial fiber, cellophane, etc., is preferred.
- alkali cellulose material Regenerated cellulose is reacted with an aqueous alkali solution to convert the cellulose contained therein into alkali cellulose. This process is generally called mercerization.
- the alkali cellulose material may be in the form of a solution, a dispersion containing insoluble matter, or a solid. Mercerization causes the cellulose to swell, improving the reaction efficiency when sulfurizing the alkali cellulose.
- strong alkaline compounds such as sodium hydroxide, lithium hydroxide, and potassium hydroxide can be used.
- the mercerization process is generally carried out by immersing the cellulose material in a large amount of an aqueous alkaline solution, followed by squeezing to remove the excess aqueous alkaline solution.
- mercerization is carried out by adding to the regenerated cellulose in advance the minimum amount of concentrated aqueous alkaline solution necessary for sulfurizing and dissolving the regenerated cellulose.
- spraying or other means may be used to add it uniformly. Because an excessive amount of aqueous alkaline solution is not added, a dehydration process such as squeezing is unnecessary and is not carried out.
- the amount of alkaline aqueous solution added is adjusted according to the moisture content of the regenerated cellulose used as a raw material, but is adjusted so that the alkali concentration in the mixture of regenerated cellulose and alkaline aqueous solution is 8 to 20 mass%, preferably 9 to 18 mass%, and more preferably 10 to 16 mass%.
- the cellulose concentration in the mixture is adjusted to 27 to 40 mass%, preferably 29 to 38 mass%, and more preferably 30 to 36 mass%.
- the alkaline aqueous solution and the regenerated cellulose are mixed and stirred to proceed with mercerization.
- a stirring device suitable for mixing a small amount of alkaline aqueous solution with solid regenerated cellulose is selected.
- the stirring device has a stirring tank and preferably has a temperature control jacket around the stirring tank that can control the temperature. In order to precisely control the reaction temperature, it is preferable to use a device equipped with low-speed blades that homogenize the temperature of the mixture by stirring the entire inside of the stirring tank during the reaction in mercerization.
- the shape of the low-speed blades includes anchor blades, ribbon anchor blades, helical ribbon blades, gate blades, paddle blades, etc., and among these, anchor blades and ribbon anchor blades are more preferable.
- the stirring shaft may be made oblique, horizontal, or eccentric, and a baffle plate may be provided in the stirring tank or the stirring tank itself may be rotated.
- Mercerization of regenerated cellulose is carried out at temperatures between -20 and 50°C, preferably between 0 and 40°C, and more preferably between 10 and 30°C. If the temperature during mercerization is less than -20°C, labor and energy are required to maintain the liquid temperature at a low temperature, and if it exceeds 50°C, labor and time are required to cool it to a temperature suitable for sulfurization.
- the reaction time for mercerization is usually in the range of 0.5 to 120 hours, preferably 1 to 72 hours, and more preferably 2 to 48 hours.
- reaction time for mercerization is too short, penetration will be insufficient and the reaction will not progress to the center, resulting in an increase in undissolved matter, but if the reaction time is too long, the degree of polymerization will decrease.
- mercerization since this decrease in the degree of polymerization occurs due to oxidation with oxygen in the air, mercerization may be carried out under reduced pressure or by replacing the air with nitrogen gas, hydrogen gas, etc.
- the alkali cellulose material of the present invention can be used by mixing with an alkali cellulose material prepared by a conventional method from a cellulose material other than regenerated cellulose.
- the alkali cellulose material to be mixed with the alkali cellulose material of the present invention is preferably used for the purpose of producing viscose by sulfurization with carbon disulfide.
- Examples of cellulose materials other than regenerated cellulose include natural cellulose such as dissolving pulp.
- the content of regenerated cellulose in the mixed alkali cellulose material is 1 to 99% by mass, preferably 2 to 50% by mass, and more preferably 3 to 20% by mass, based on the cellulose component.
- the alkali cellulose material of the present invention is reacted with carbon disulfide and converted into cellulose xanthate. This process is generally called sulfurization. Sulfurization can be carried out by adding carbon disulfide to the alkali cellulose material after mercerization, and mixing and stirring the mixture. It is also possible to mix cellulose, an aqueous alkali solution, and carbon disulfide at once to carry out mercerization and sulfurization simultaneously.
- the cellulose concentration and the concentration of the alkali compound are diluted with carbon disulfide added after mercerization unless further adjustment is required.
- the amount of carbon disulfide added to the mixture is adjusted to 5-60% by mass, preferably 10-50% by mass, and more preferably 15-40% by mass, based on the mass of cellulose. If the amount of carbon disulfide added is less than 5% by mass, the reaction with the alkali cellulose will be insufficient, and if it exceeds 60% by mass, side reactions of carbon disulfide will increase or unreacted carbon disulfide will remain, which may reduce safety.
- the temperature of the mixture is made uniform by stirring the entire inside of the mixing vessel.
- the alkali cellulose is a solid, whereas carbon disulfide exists as a liquid or gas. Therefore, as in mercerization, it is preferable to use a mixing device equipped with a low-speed blade that rotates along the wall of the mixing vessel to homogenize the mixture and that has a temperature-regulating jacket.
- the sulfurization of alkali cellulose is carried out at a temperature of 0 to 50°C, preferably 5 to 40°C, and more preferably 10 to 30°C. If the temperature during sulfurization is below 0°C, it takes time and energy to maintain the liquid temperature low, and if it exceeds 50°C, the degree of polymerization of the cellulose is likely to decrease and the risk of fire increases.
- the sulfurization reaction time is set so that carbon disulfide is sufficiently permeated throughout the alkali cellulose, and is usually in the range of 30 minutes to 12 hours, preferably 1 to 9 hours, and more preferably 2 to 6 hours.
- the obtained sulfide is dissolved at a temperature of 0 to 40°C, preferably 5 to 35°C, and more preferably 10 to 30°C. If the temperature during dissolution is less than 0°C, labor and energy are required to maintain the liquid temperature at a low temperature, and if it exceeds 40°C, the solubility of the cellulose is likely to decrease.
- the dissolution time is set so that the clogging degree reaches the desired value and is completed, and although it depends on the stirring conditions, it is usually in the range of 2 minutes to 48 hours, preferably 4 minutes to 36 hours, and more preferably 5 minutes to 24 hours. In this case, dissolution can be achieved in a short time, especially when high-speed impellers are used in combination.
- the shape of the high-speed impeller can be a dispersion impeller, a turbine impeller, a propeller impeller, a paddle impeller, a rotor/stator, etc., and among these, a dispersion impeller is preferable.
- the carbon disulfide sulfide of the alkali cellulose material of the present invention can be used to produce viscose by dissolving it in an alkaline aqueous solution, or it can be mixed with the carbon disulfide sulfide of the alkali cellulose material prepared by a conventional method from a cellulose material other than regenerated cellulose.
- cellulose materials other than regenerated cellulose include natural cellulose, and in addition to pulp made from biomass such as wood, cotton, straw, bamboo, hemp, jute, and kenaf, waste paper, paper powder, etc. can also be used, with pulp made from wood being particularly preferred.
- the content of regenerated cellulose in the sulfide of the mixed alkali cellulose material produced by carbon disulfide is 1 to 99% by mass, preferably 2 to 50% by mass, and more preferably 3 to 20% by mass, based on the cellulose component.
- the viscose of the present invention obtained after completion of sulfurization and dissolution has the same physical properties as viscose, such as viscose, which is a raw material for forming various cellulose molded products.
- the viscose of the present invention has a clogging degree of 6,000 or less, preferably 4,000 or less, more preferably 2,000 or less. The smaller the clogging degree, the more excellent the solubility of the cellulose xanthate in the sulfide. The method for calculating the clogging degree is shown below.
- FIG. 1 is a schematic diagram of a graph on which the measured characteristic values of viscose are plotted.
- Clogging degree 100,000 x k
- the viscose of the present invention has a cellulose concentration of 5% by mass or more, preferably 6 to 12% by mass, and more preferably 8 to 10% by mass. Such a cellulose concentration is at the same level as that of viscose, which is a raw material for forming various cellulose molded products. If the cellulose concentration of the viscose is high, the viscosity will be too high, and if it is low, the strength of the cellulose molded product will be insufficient and the amount of chemicals such as acid used will increase, reducing economic efficiency. The method for measuring the cellulose concentration is shown below.
- the viscose is thinly spread on a pre-weighed glass plate using a Baker applicator (SA-201, manufactured by Tester Sangyo Co., Ltd.), the mass is measured, and the mass of the viscose is calculated.
- SA-201 manufactured by Tester Sangyo Co., Ltd.
- the plate is then left to stand in a constant temperature dryer at 70°C for 40 minutes, and each plate is immersed in a 10% by mass aqueous solution of ammonium chloride for 30 minutes to peel off the solidified viscose from the plate.
- the viscose of the present invention has an alkali concentration of 2% by mass or more, preferably 4 to 12% by mass, and more preferably 5 to 10% by mass. Such an alkali concentration is at the same level as that of viscose, which is a raw material for forming various cellulose molded products. If the alkali concentration of the viscose is high, the amount of acid required for neutralization increases, and if it is low, the solubility decreases.
- the viscose of the present invention easily solidifies when placed in a salt solution, a dilute acid such as sulfuric acid or hydrochloric acid, an organic solvent, or when heated, and can be regenerated with acid to obtain molded products such as cellophane, rayon, and beads. Furthermore, when a dilute acid is used for coagulation, coagulation and regeneration proceed simultaneously.
- a dilute acid such as sulfuric acid or hydrochloric acid, an organic solvent, or when heated
- the viscose of the present invention can be used in combination with viscose prepared by conventional methods from cellulose materials other than regenerated cellulose.
- cellulose materials other than regenerated cellulose include natural cellulose such as dissolving pulp.
- the content of regenerated cellulose in the mixed viscose is 1 to 99% by mass, preferably 2 to 50% by mass, and more preferably 3 to 20% by mass, based on the cellulose component.
- the present invention will be explained in more detail with reference to the following examples, but the present invention is not limited thereto.
- the unit "parts" in the examples is a unit based on mass.
- Example 1 As a regenerated cellulose sample, cellophane ("PT #300" (product name) manufactured by Rengo Co., Ltd.) was mechanically crushed, passed through a round net with a diameter of 1 mm ⁇ , and washed with water to remove any adhering softener (glycerin) to prepare a wet product (cellulose content: 43% by mass).
- PT #300 product name
- glycerin adhering softener
- viscosity The temperature of the viscose was adjusted to 20° C., and the viscosity was measured using a Brookfield viscometer (No. 5 rotor ⁇ 20 rpm).
- Example 2 Viscose was obtained in the same manner as in Example 1, except that 25% by mass of carbon disulfide per mass of cellulose was added to the alkali cellulose prepared in Example 1, and the resulting sulfide was dissolved for 10 minutes while stirring at 5,000 rpm at room temperature using a high-speed stirrer equipped with a dispersing blade ("Labo-Lusion" (trade name) manufactured by Primix Corporation).
- the obtained viscose contained 9.6% by mass of cellulose and 6.1% by mass of sodium hydroxide.
- the obtained alkali cellulose contained 22% by weight of cellulose and 16% by weight of sodium hydroxide.
- Viscose was obtained in the same manner as in Example 1, except that this alkali cellulose was used.
- the obtained viscose contained 8.2% by mass of cellulose and 6.1% by mass of sodium hydroxide.
- Non-Patent Document 1 which uses pulp as the raw material, filtering of viscose is more difficult than with the conventional method (the filtering time for 300 g of viscose is 177.4 seconds with the conventional method and 320 seconds with this method), which is considered to be due to the presence of hemicellulose and other contaminants in the raw pulp and the non-uniformity of the alkali cellulose.
- the raw material was replaced with regenerated cellulose, filtering was possible with this application, whereas filtering was not possible with the conventional method, and this is thought to be due to the low hemicellulose content in the raw material.
- Example 3 Mixing viscose produced from cellophane in Example 1 with industrial viscose Ten parts of the viscose in Example 1 were mixed with 90 parts of viscose manufactured by Rengo Co., Ltd. (prepared from dissolving pulp in a conventional manner) to prepare a mixed viscose (cellulose: 9.7% by mass, sodium hydroxide: 6.2% by mass).
- Example 4 Mixing the sulfurized cellophane of Example 1 with sulfurized pulp
- the sulfurized regenerated cellulose sample of Example 1 was mixed with a sulfide prepared from dissolving pulp by a conventional method so that the mass ratio of regenerated cellulose to native cellulose was 1:9, and the mixture was dissolved in an alkaline aqueous solution to prepare viscose (cellulose: 9.8% by mass, sodium hydroxide: 6.1% by mass).
- Example 5 The mercerized cellophane of Example 1 was mixed with the mercerized pulp.
- the mercerized regenerated cellulose sample of Example 1 was mixed with mercerized pulp prepared from dissolving pulp by a conventional method so that the mass ratio of regenerated cellulose to native cellulose was 1:9. 35% by mass of carbon disulfide was added per mass of cellulose, and the mixture was sulfurized for 4 hours.
- the mixture was then dissolved in an alkaline aqueous solution to prepare viscose (cellulose: 9.8% by mass, sodium hydroxide: 6.1% by mass).
- ⁇ Comparative Example 2> Mixing crushed cellophane with pulp The regenerated cellulose sample and dissolving pulp were mixed so that the mass ratio of regenerated cellulose to native cellulose was 1:9. The mixture was immersed in an 18% by mass aqueous sodium hydroxide solution at 50°C for 1.5 hours to perform mercerization, and then pressed to obtain alkali cellulose (cellulose: 26% by mass, sodium hydroxide: 16% by mass). Carbon disulfide was added to the alkali cellulose to a concentration of 35% by mass per cellulose mass, and sulfurization was performed for 4 hours. Aqueous sodium hydroxide solution was added to the obtained sulfide, and the mixture was dissolved while stirring at 20°C for 19 hours to prepare viscose (cellulose: 9.6% by mass, sodium hydroxide: 6.0% by mass).
- ⁇ Comparative Example 3> The mercerized cellophane of Comparative Example 1 was mixed with the mercerized pulp.
- the mercerized regenerated cellulose sample of Comparative Example 1 was mixed with mercerized pulp prepared from dissolving pulp by a conventional method in a mass ratio of regenerated cellulose to native cellulose of 1:9. After sulfurization, the mixture was dissolved in an alkaline aqueous solution to prepare viscose (cellulose: 9.6 mass%, sodium hydroxide: 6.0 mass%).
- Examples 3, 4 and 5 have good solubility.
- Comparative Examples 2 and 3 which were subjected to conventional soaking and squeezing, have poor solubility.
- Example 5 has lower solubility than Examples 3 and 4. This is thought to be because cellophane, which has a small surface area, is less reactive in the sulfurization reaction than pulp, and the sulfurization proceeds unevenly. By sulfurizing cellophane and pulp separately, the reaction becomes uniform, which is expected to be more favorable in terms of solubility.
- the conditions for obtaining alkali cellulose by mercerizing regenerated cellulose have been optimized, and it has been found that viscose suitable for producing molded bodies can be obtained by mixing it with viscose from wood pulp at that stage or in a sulfurized state, or by mixing it with industrial viscose in the form of viscose that has been sulfurized and dissolved in an alkaline aqueous solution. This reduces the need for dedicated production equipment, allows the effective use of existing equipment, and is also advantageous in terms of energy costs.
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Abstract
Description
本発明は、ビスコースを製造するための中間材料であるアルカリセルロース材料に関し、特に、原料として再生セルロースを用いるアルカリセルロース材料に関する。 The present invention relates to an alkali cellulose material that is an intermediate material for producing viscose, and in particular to an alkali cellulose material that uses regenerated cellulose as a raw material.
セロファン、レーヨン及びビーズ等のセルロース製品を製造する際には端材及び規格外品などの副産物が発生する。一方、セルロースは熱可塑性を有さず、汎用の溶媒に溶解しないために、原料としてセルロース製品を使用し、ビスコース等のセルロース溶液を調製して再利用するには、煩雑な作業工程及び高いコストが必要になる。 The production of cellulose products such as cellophane, rayon, and beads generates by-products such as scraps and non-standard products. However, since cellulose does not have thermoplasticity and does not dissolve in general-purpose solvents, using cellulose products as a raw material to prepare a cellulose solution such as viscose for reuse requires complicated work processes and high costs.
通常、ビスコースは、まず原料の溶解パルプシートを粗粉砕しながら多量のアルカリ水溶液に浸漬してアルカリセルロースとし(マーセル化)、圧搾して余分なアルカリ水溶液を除去後に粉砕し、二硫化炭素と反応させてセルロースザンテートに変換して(硫化)、これをアルカリ水溶液に溶解することで調製される。 Typically, viscose is prepared by first coarsely crushing the raw material dissolving pulp sheet and immersing it in a large amount of alkaline aqueous solution to turn it into alkaline cellulose (mercerization), squeezing it to remove excess alkaline aqueous solution, crushing it, reacting it with carbon disulfide to convert it into cellulose xanthate (sulfurization), and dissolving this in an alkaline aqueous solution.
非特許文献1には、木材パルプを原料に、アルカリ水溶液の使用量を削減する目的で圧搾を省略するため、少量の濃厚苛性ソーダ溶液を均一に噴霧してビスコースを製造する方法(無圧搾法)が記載されている。 Non-Patent Document 1 describes a method for producing viscose from wood pulp by uniformly spraying a small amount of concentrated caustic soda solution onto the pulp to omit squeezing in order to reduce the amount of alkaline aqueous solution used (non-squeezing method).
特許文献1には、再生利用人工セルロース系原材料を原料に、アルカリ水溶液に浸漬し、続けて圧搾する工程により、硫化及び溶解を行うアルカリセルロースを調製することが記載されている。 Patent Document 1 describes the preparation of alkali cellulose, which is made from recycled artificial cellulose-based raw materials, by immersing the raw materials in an alkaline aqueous solution and then squeezing the raw materials, which undergoes sulfurization and dissolution.
しかしながら、非特許文献1の方法で製造されたビスコースは、未反応繊維が多く残存しており、分散溶解状態に劣るという問題がある。 However, the viscose produced by the method described in Non-Patent Document 1 has the problem that a large amount of unreacted fibers remain, resulting in poor dispersion and dissolution.
また、特許文献1のアルカリセルロースは、硫化及び溶解した場合に、セルロースの溶解性が低いために、未溶解分を多く含むビスコースが生成する。そうしたビスコースでは濾過性が悪化する上に、強度物性の低い成形体しか得られず、実用性に劣るという問題がある。 In addition, when the alkali cellulose of Patent Document 1 is sulfurized and dissolved, cellulose has low solubility, so viscose containing a large amount of undissolved matter is produced. Such viscose has problems such as poor filterability and only molded bodies with low strength properties can be obtained, making it less practical.
本発明は前記課題を解決するものであり、その目的とするところは、原料として再生セルロースを用いて、各種セルロース成形物の成形原料として使用するのに適した物性のビスコースを得ることができる、アルカリセルロース材料を提供することにある。 The present invention aims to solve the above problems, and its purpose is to provide an alkali cellulose material that uses regenerated cellulose as a raw material to obtain viscose with physical properties suitable for use as a raw material for forming various cellulose molded products.
本発明は以下の態様を提供する。
[態様1]二硫化炭素で硫化することでビスコースを製造するために使用する、再生セルロース、アルカリ及び水を含むアルカリセルロース材料であって、27~40質量%、好ましくは29~38質量%、より好ましくは30~36質量%のセルロース濃度及び8~20質量%、好ましくは9~18質量%、より好ましくは10~16質量%のアルカリ濃度を有する、アルカリセルロース材料。
The present invention provides the following aspects.
[Aspect 1] An alkali cellulose material containing regenerated cellulose, an alkali, and water, which is used to produce viscose by sulfurization with carbon disulfide, the alkali cellulose material having a cellulose concentration of 27 to 40% by mass, preferably 29 to 38% by mass, and more preferably 30 to 36% by mass, and an alkali concentration of 8 to 20% by mass, preferably 9 to 18% by mass, and more preferably 10 to 16% by mass.
[態様2]セルロース成分は天然セルロースを含まない、態様1のアルカリセルロース材料。 [Aspect 2] An alkali cellulose material according to aspect 1, in which the cellulose component does not contain natural cellulose.
[態様3]セルロース成分は再生セルロースから成る、態様1または2のアルカリセルロース材料。 [Aspect 3] An alkali cellulose material according to aspect 1 or 2, wherein the cellulose component is made of regenerated cellulose.
[態様4]前記ビスコースは5質量%以上、好ましくは6~12質量%、より好ましくは8~10質量%のセルロース濃度を有する、態様1~3のいずれかのアルカリセルロース材料。 [Aspect 4] The alkali cellulose material of any one of aspects 1 to 3, wherein the viscose has a cellulose concentration of 5% by mass or more, preferably 6 to 12% by mass, and more preferably 8 to 10% by mass.
[態様5]前記ビスコースは6,000以下、好ましくは4,000以下、より好ましくは2,000以下の目詰まり度を有する、態様1~4のいずれかのアルカリセルロース材料。 [Aspect 5] The alkali cellulose material of any one of aspects 1 to 4, wherein the viscose has a clogging degree of 6,000 or less, preferably 4,000 or less, and more preferably 2,000 or less.
[態様6]態様1~5のいずれかのアルカリセルロース材料と、再生セルロース以外のセルロース材料から製造された同じ用途のアルカリセルロース材料とを含む、混合アルカリセルロース材料。 [Aspect 6] A mixed alkali cellulose material comprising any one of the alkali cellulose materials of aspects 1 to 5 and an alkali cellulose material for the same application produced from a cellulose material other than regenerated cellulose.
[態様7]再生セルロース、アルカリ及び水を含み、27~40質量%、好ましくは29~38質量%、より好ましくは30~36質量%のセルロース濃度及び8~20質量%、好ましくは9~18質量%、より好ましくは10~16質量%のアルカリ濃度を有するアルカリセルロース材料の二硫化炭素による硫化物。 [Aspect 7] A sulfide of an alkali cellulose material containing regenerated cellulose, an alkali, and water, the sulfide having a cellulose concentration of 27-40% by mass, preferably 29-38% by mass, and more preferably 30-36% by mass, and an alkali concentration of 8-20% by mass, preferably 9-18% by mass, and more preferably 10-16% by mass, with carbon disulfide.
[態様8]態様7のアルカリセルロース材料の二硫化炭素による硫化物と、再生セルロース以外のセルロース材料から製造された同じ用途のアルカリセルロース材料の二硫化炭素による硫化物とを含む、混合された、アルカリセルロース材料の二硫化炭素による硫化物。 [Aspect 8] A mixed sulfide of alkali cellulose material with carbon disulfide, comprising the sulfide of alkali cellulose material of aspect 7 with carbon disulfide and a sulfide of alkali cellulose material for the same use produced from a cellulose material other than regenerated cellulose with carbon disulfide.
[態様9]再生セルロース、アルカリ及び水を含み、27~40質量%、好ましくは29~38質量%、より好ましくは30~36質量%のセルロース濃度及び8~20質量%、好ましくは9~18質量%、より好ましくは10~16質量%のアルカリ濃度を有するアルカリセルロース材料の二硫化炭素による硫化物を含む、ビスコース。 [Aspect 9] Viscose containing regenerated cellulose, alkali and water, and containing a sulfide of an alkali cellulose material with carbon disulfide having a cellulose concentration of 27-40% by mass, preferably 29-38% by mass, more preferably 30-36% by mass, and an alkali concentration of 8-20% by mass, preferably 9-18% by mass, more preferably 10-16% by mass.
[態様10]態様9のビスコースと、再生セルロース以外のセルロース材料から製造されたビスコースとを含む、混合ビスコース。 [Aspect 10] A mixed viscose comprising the viscose of aspect 9 and a viscose produced from a cellulose material other than regenerated cellulose.
[態様11]再生セルロース、アルカリ及び水を含み、27~40質量%、好ましくは29~38質量%、より好ましくは30~36質量%のセルロース濃度及び8~20質量%、好ましくは9~18質量%、より好ましくは10~16質量%のアルカリ濃度を有するアルカリセルロース材料を、二硫化炭素で硫化することを含む、ビスコースの製造方法。 [Aspect 11] A method for producing viscose, comprising sulfurizing an alkali cellulose material with carbon disulfide, the alkali cellulose material comprising regenerated cellulose, an alkali, and water, the alkali cellulose material having a cellulose concentration of 27-40% by mass, preferably 29-38% by mass, and more preferably 30-36% by mass, and an alkali concentration of 8-20% by mass, preferably 9-18% by mass, and more preferably 10-16% by mass.
[態様12]6,000以下、好ましくは4,000以下、より好ましくは2,000以下の目詰まり度を有する、態様9のビスコース。 [Aspect 12] The viscose of aspect 9, having a clogging degree of 6,000 or less, preferably 4,000 or less, more preferably 2,000 or less.
[態様13]5質量%以上、好ましくは6~12質量%、より好ましくは8~10質量%のセルロース濃度を有する、態様9又は12のビスコース。 [Aspect 13] Viscose according to aspect 9 or 12, having a cellulose concentration of 5% by mass or more, preferably 6 to 12% by mass, and more preferably 8 to 10% by mass.
[態様14]2質量%以上、好ましくは4~12質量%、より好ましくは5~10質量%のアルカリ濃度を有する、態様9、12又は13のビスコース。 [Aspect 14] Viscose according to aspect 9, 12 or 13, having an alkali concentration of 2% by mass or more, preferably 4 to 12% by mass, and more preferably 5 to 10% by mass.
[態様15]セルロース成分を基準にして1~99質量%、好ましくは2~50質量%、より好ましくは3~20質量%の再生セルロースの含有量を有する、態様10の混合ビスコース。 [Aspect 15] A mixed viscose according to aspect 10, having a regenerated cellulose content of 1 to 99% by mass, preferably 2 to 50% by mass, and more preferably 3 to 20% by mass, based on the cellulose component.
本発明によれば、原料として再生セルロースを用いて、各種セルロース成形物の成形原料として使用するのに適した物性のビスコースを得ることができる、アルカリセルロース材料が提供される。本発明によれば、このアルカリセルロース材料を中間材料として使用した、各種セルロース成形物の成形原料として使用するのに適した物性のビスコースが提供される。また、本発明によれば、原料として再生セルロースを用いて、各種セルロース成形物の成形原料として使用するのに適した物性のビスコースの製造方法が提供される。 The present invention provides an alkali cellulose material that uses regenerated cellulose as a raw material to obtain viscose with physical properties suitable for use as a raw material for molding various cellulose molded products. The present invention provides viscose with physical properties suitable for use as a raw material for molding various cellulose molded products, using this alkali cellulose material as an intermediate material. The present invention also provides a method for producing viscose with physical properties suitable for use as a raw material for molding various cellulose molded products, using regenerated cellulose as a raw material.
以下、本発明の実施形態について詳細に説明するが、本発明の範囲はここで説明する実施形態に限定されるものではなく、本発明の趣旨を逸脱しない範囲で種々の変更ができる。また、特定のパラメータについて、複数の上限値及び下限値が記載されている場合、これらの上限値及び下限値の内、任意の上限値と下限値とを組合せて好適な数値範囲とすることができる。 The following describes in detail an embodiment of the present invention, but the scope of the present invention is not limited to the embodiment described here, and various modifications can be made without departing from the spirit of the present invention. Furthermore, when multiple upper and lower limit values are listed for a particular parameter, any of these upper and lower limit values can be combined to create a suitable numerical range.
<再生セルロース>
原料として使用する再生セルロースは、主に天然セルロースを従来公知のビスコース法や銅アンモニア法により液化した後に、所定の形状に凝固して成形したセルロースをいう。再生セルロースには、セルロース成形物、セルロース成形物を裁断等して製造されたセルロース製品、セルロース成形物を製造する際の副産物等が含まれる。それらは、反応効率を向上させるため、粉砕されていてもよい。再生セルロースの具体例としては、セロファン、レーヨン及びビーズ等のセルロース成形物を製品化する際に発生する端材、規格外品、不良品、及びセルロース製品の廃棄物等が挙げられる。さらに、天然セルロースの代わりに、再生セルロースを原料として再利用することもできる。
<Regenerated cellulose>
The regenerated cellulose used as a raw material is mainly cellulose obtained by liquefying natural cellulose by the conventionally known viscose method or cuprammonium method, and then solidifying and molding it into a predetermined shape. Regenerated cellulose includes cellulose molded products, cellulose products produced by cutting cellulose molded products, and by-products produced when manufacturing cellulose molded products. They may be pulverized to improve reaction efficiency. Specific examples of regenerated cellulose include scraps, non-standard products, defective products, and waste cellulose products generated when manufacturing cellulose molded products such as cellophane, rayon, and beads. Furthermore, regenerated cellulose can be reused as a raw material instead of natural cellulose.
<天然セルロース>
ビスコースの原料に用いられる天然セルロースとしては、特に限定されず、例えば、木材、木綿、わら、竹、麻、ジュート、ケナフ等のバイオマスを原料とするパルプが挙げられる。また、その製造方法も特に限定されず、機械的方法、化学的方法、あるいはその中間で二つを組み合せた方法でもよい。パルプの品位としては、製紙用パルプの他に、人造繊維、セロファンなどの主原料となる、精製度合いの高い溶解パルプが好ましい。
<Natural cellulose>
The natural cellulose used as the raw material for viscose is not particularly limited, and examples thereof include pulp made from biomass such as wood, cotton, straw, bamboo, hemp, jute, and kenaf. The manufacturing method is also not particularly limited, and may be a mechanical method, a chemical method, or a method that combines the two. In terms of pulp quality, highly refined dissolving pulp, which is the main raw material for paper pulp, artificial fiber, cellophane, etc., is preferred.
<アルカリセルロース材料>
再生セルロースは、アルカリ水溶液に接触させて反応させ、これに含まれるセルロースをアルカリセルロースに変換する。この工程は、一般にマーセル化と呼ばれる。再生セルロース、アルカリ及び水を含む、マーセル化後の混合物を、アルカリセルロース材料という。アルカリセルロース材料の性状は、溶液、不溶物を含む分散物、又は固形物であってよい。マーセル化によってセルロースは膨潤し、アルカリセルロースを硫化する際の反応効率が向上する。アルカリとしては、水酸化ナトリウム、水酸化リチウム、水酸化カリウム等の強アルカリ化合物を使用することができる。
<Alkaline Cellulose Material>
Regenerated cellulose is reacted with an aqueous alkali solution to convert the cellulose contained therein into alkali cellulose. This process is generally called mercerization. The mixture after mercerization, which contains regenerated cellulose, alkali, and water, is called alkali cellulose material. The alkali cellulose material may be in the form of a solution, a dispersion containing insoluble matter, or a solid. Mercerization causes the cellulose to swell, improving the reaction efficiency when sulfurizing the alkali cellulose. As the alkali, strong alkaline compounds such as sodium hydroxide, lithium hydroxide, and potassium hydroxide can be used.
マーセル化工程は、一般に、セルロース材料を多量のアルカリ水溶液に浸漬して行われ、続けて圧搾することで過剰なアルカリ水溶液が除去される。これに対し、本発明では、予め再生セルロースの硫化及び溶解に必要な最低限の量の濃厚アルカリ水溶液を、再生セルロースに添加してマーセル化を行う。再生セルロースの状態によっては、均一に添加するために噴霧などの手段を用いても良い。アルカリ水溶液を過剰に添加しないため、圧搾等の脱水行程は不要であり、行わない。 The mercerization process is generally carried out by immersing the cellulose material in a large amount of an aqueous alkaline solution, followed by squeezing to remove the excess aqueous alkaline solution. In contrast, in the present invention, mercerization is carried out by adding to the regenerated cellulose in advance the minimum amount of concentrated aqueous alkaline solution necessary for sulfurizing and dissolving the regenerated cellulose. Depending on the state of the regenerated cellulose, spraying or other means may be used to add it uniformly. Because an excessive amount of aqueous alkaline solution is not added, a dehydration process such as squeezing is unnecessary and is not carried out.
再生セルロースは、アルカリ水溶液に浸漬した場合に、水分を多く吸着して強く膨潤する。そのため、圧搾等の通常行われる脱水手段では、セルロース濃度を適切な水準に上昇させることが困難である。 When regenerated cellulose is immersed in an alkaline aqueous solution, it absorbs a large amount of water and swells significantly. For this reason, it is difficult to increase the cellulose concentration to an appropriate level using the usual dehydration methods such as squeezing.
アルカリ水溶液の添加量は、原料として用いる再生セルロースの水分に応じて調節されるが、再生セルロース及びアルカリ水溶液を混合した混合物中のアルカリ濃度として8~20質量%、好ましくは9~18質量%、より好ましくは10~16質量%となるように調節する。また、前記混合物中のセルロース濃度は27~40質量%、好ましくは29~38質量%、より好ましくは30~36質量%となるように調節する。前記混合物中のアルカリ濃度及びセルロース濃度を前記範囲に調節することで、得られるビスコースの物性がセルロース成形物の成形原料として適切なものになる。 The amount of alkaline aqueous solution added is adjusted according to the moisture content of the regenerated cellulose used as a raw material, but is adjusted so that the alkali concentration in the mixture of regenerated cellulose and alkaline aqueous solution is 8 to 20 mass%, preferably 9 to 18 mass%, and more preferably 10 to 16 mass%. The cellulose concentration in the mixture is adjusted to 27 to 40 mass%, preferably 29 to 38 mass%, and more preferably 30 to 36 mass%. By adjusting the alkali concentration and cellulose concentration in the mixture to within the above ranges, the physical properties of the resulting viscose become suitable as a raw material for molding cellulose products.
次いで、アルカリ水溶液と再生セルロースとを混合及び撹拌してマーセル化を進める。このときの混合及び撹拌には、固体の再生セルロースに少量のアルカリ水溶液を混合するのに適した撹拌装置が選ばれる。撹拌装置は撹拌槽を有し、撹拌槽の周囲に温度調節することが可能な温度調節ジャケットを有するものが望ましい。反応温度を精度よく調節するため、マーセル化において、反応中は撹拌槽内全体をかき混ぜることで、前記混合物の温度を均一化する低速翼を備えるものを使用することが好ましい。低速翼の形状としては、アンカー翼、リボンアンカー翼、ヘリカルリボン翼、ゲート翼、パドル翼などがあるが、中でもアンカー翼やリボンアンカー翼がより好ましい。さらに、撹拌効率を向上させるため、撹拌軸を斜めや水平にしたり、偏心させたりする他、撹拌槽に邪魔板を設けたり、撹拌槽自体を回転させたりしても良い。 Then, the alkaline aqueous solution and the regenerated cellulose are mixed and stirred to proceed with mercerization. For mixing and stirring at this time, a stirring device suitable for mixing a small amount of alkaline aqueous solution with solid regenerated cellulose is selected. The stirring device has a stirring tank and preferably has a temperature control jacket around the stirring tank that can control the temperature. In order to precisely control the reaction temperature, it is preferable to use a device equipped with low-speed blades that homogenize the temperature of the mixture by stirring the entire inside of the stirring tank during the reaction in mercerization. The shape of the low-speed blades includes anchor blades, ribbon anchor blades, helical ribbon blades, gate blades, paddle blades, etc., and among these, anchor blades and ribbon anchor blades are more preferable. Furthermore, in order to improve the stirring efficiency, the stirring shaft may be made oblique, horizontal, or eccentric, and a baffle plate may be provided in the stirring tank or the stirring tank itself may be rotated.
再生セルロースのマーセル化は、-20~50℃、好ましくは0~40℃、より好ましくは10~30℃の温度にて行う。マーセル化時の温度が-20℃未満であると液温を低温に維持するために手間及びエネルギーを要し、50℃を超えると硫化に適した温度に冷却するために、手間及び時間を要することになる。マーセル化の反応時間は、通常0.5~120時間、好ましくは1~72時間、より好ましくは2~48時間の範囲である。マーセル化の反応時間は、短すぎると浸透が不十分となって反応が中心部まで進まずに未溶解分が増加するが、長すぎると重合度低下が生じる。また、この重合度低下は空気中の酸素で酸化することによって起こるため、減圧下、あるいは窒素ガス、水素ガスなどで空気を置換してマーセル化を行っても良い。 Mercerization of regenerated cellulose is carried out at temperatures between -20 and 50°C, preferably between 0 and 40°C, and more preferably between 10 and 30°C. If the temperature during mercerization is less than -20°C, labor and energy are required to maintain the liquid temperature at a low temperature, and if it exceeds 50°C, labor and time are required to cool it to a temperature suitable for sulfurization. The reaction time for mercerization is usually in the range of 0.5 to 120 hours, preferably 1 to 72 hours, and more preferably 2 to 48 hours. If the reaction time for mercerization is too short, penetration will be insufficient and the reaction will not progress to the center, resulting in an increase in undissolved matter, but if the reaction time is too long, the degree of polymerization will decrease. In addition, since this decrease in the degree of polymerization occurs due to oxidation with oxygen in the air, mercerization may be carried out under reduced pressure or by replacing the air with nitrogen gas, hydrogen gas, etc.
本発明のアルカリセルロース材料は、常法で再生セルロース以外のセルロース材料から調製したアルカリセルロース材料と混合して使用することができる。本発明のアルカリセルロース材料と混合される前記アルカリセルロース材料は、好ましくは、二硫化炭素で硫化することでビスコースを製造する目的にて使用するものである。再生セルロース以外のセルロース材料としては、溶解パルプ等の天然セルロースが挙げられる。 The alkali cellulose material of the present invention can be used by mixing with an alkali cellulose material prepared by a conventional method from a cellulose material other than regenerated cellulose. The alkali cellulose material to be mixed with the alkali cellulose material of the present invention is preferably used for the purpose of producing viscose by sulfurization with carbon disulfide. Examples of cellulose materials other than regenerated cellulose include natural cellulose such as dissolving pulp.
その場合、混合されたアルカリセルロース材料中の再生セルロースの含有量は、セルロース成分を基準にして1~99質量%、好ましくは2~50質量%、より好ましくは3~20質量%である。前記再生セルロースの含有量をできるだけ多くすることで、再生セルロースのリサイクル率を向上させ、環境負荷の低減効果を高めることができる。 In this case, the content of regenerated cellulose in the mixed alkali cellulose material is 1 to 99% by mass, preferably 2 to 50% by mass, and more preferably 3 to 20% by mass, based on the cellulose component. By increasing the content of the regenerated cellulose as much as possible, the recycling rate of the regenerated cellulose can be improved, and the effect of reducing the environmental load can be enhanced.
本発明のアルカリセルロース材料は、二硫化炭素に接触させて反応させ、セルロースザンテートに変換する。この工程は、一般に硫化と呼ばれる。硫化は、マーセル化後のアルカリセルロース材料に、二硫化炭素を加えて混合及び撹拌することで行うことができる。また、セルロースとアルカリ水溶液と二硫化炭素を一度に混合して、マーセル化と硫化を同時に行うこともできる。 The alkali cellulose material of the present invention is reacted with carbon disulfide and converted into cellulose xanthate. This process is generally called sulfurization. Sulfurization can be carried out by adding carbon disulfide to the alkali cellulose material after mercerization, and mixing and stirring the mixture. It is also possible to mix cellulose, an aqueous alkali solution, and carbon disulfide at once to carry out mercerization and sulfurization simultaneously.
再生セルロースとアルカリ水溶液と二硫化炭素とを含む混合物について、セルロース濃度及びアルカリ化合物の濃度は、新たに調整する必要のない限り、マーセル化の後に添加される二硫化炭素で希釈された値となる。前記混合物における二硫化炭素添加量は、セルロースの質量に対して5~60質量%、好ましくは10~50質量%、より好ましくは15~40質量%に調節する。二硫化炭素添加量が5質量%未満であるとアルカリセルロースとの反応が不十分となり、60質量%を超えると二硫化炭素の副反応が増加したり、未反応の二硫化炭素が残存したりして安全性が低下するおそれがある。 For a mixture containing regenerated cellulose, an aqueous alkali solution, and carbon disulfide, the cellulose concentration and the concentration of the alkali compound are diluted with carbon disulfide added after mercerization unless further adjustment is required. The amount of carbon disulfide added to the mixture is adjusted to 5-60% by mass, preferably 10-50% by mass, and more preferably 15-40% by mass, based on the mass of cellulose. If the amount of carbon disulfide added is less than 5% by mass, the reaction with the alkali cellulose will be insufficient, and if it exceeds 60% by mass, side reactions of carbon disulfide will increase or unreacted carbon disulfide will remain, which may reduce safety.
硫化の間は、撹拌槽内全体をかき混ぜることで混合物の温度を均一化する。硫化においては、アルカリセルロースは固体であるのに対し、二硫化炭素は液体又は気体で存在するために、撹拌装置としては、マーセル化と同様に、撹拌槽の壁面に沿って回転することで混合物を均一化する低速翼を備え、温度調節ジャケットを有するものを使用することが好ましい。 During sulfurization, the temperature of the mixture is made uniform by stirring the entire inside of the mixing vessel. In sulfurization, the alkali cellulose is a solid, whereas carbon disulfide exists as a liquid or gas. Therefore, as in mercerization, it is preferable to use a mixing device equipped with a low-speed blade that rotates along the wall of the mixing vessel to homogenize the mixture and that has a temperature-regulating jacket.
アルカリセルロースの硫化は、0~50℃、好ましくは5~40℃、より好ましくは10~30℃の温度にて行う。硫化時の温度が0℃未満であると液温を低温に維持するために手間及びエネルギーを要し、50℃を超えるとセルロースの重合度が低下し易くなり、発火などの危険性も増大する。硫化の反応時間は、アルカリセルロース全体に二硫化炭素が十分に浸透する様に設定され、通常30分~12時間、好ましくは1~9時間、より好ましくは2~6時間の範囲である。 The sulfurization of alkali cellulose is carried out at a temperature of 0 to 50°C, preferably 5 to 40°C, and more preferably 10 to 30°C. If the temperature during sulfurization is below 0°C, it takes time and energy to maintain the liquid temperature low, and if it exceeds 50°C, the degree of polymerization of the cellulose is likely to decrease and the risk of fire increases. The sulfurization reaction time is set so that carbon disulfide is sufficiently permeated throughout the alkali cellulose, and is usually in the range of 30 minutes to 12 hours, preferably 1 to 9 hours, and more preferably 2 to 6 hours.
また、得られた硫化物の溶解は、0~40℃、好ましくは5~35℃、より好ましくは10~30℃の温度にて行う。溶解時の温度が0℃未満であると液温を低温に維持するために手間及びエネルギーを要し、40℃を超えるとセルロースの溶解性が低下し易くなる。溶解の時間は、目詰まり度が所望する値に到達、完結する様に設定され、撹拌等の条件にもよるが、通常2分~48時間、好ましくは4分~36時間、より好ましくは5分~24時間の範囲である。このとき、特に高速翼を併用すると短時間で溶解することができる。高速翼の形状としては、ディスパ翼、タービン翼、プロペラ翼、パドル翼、ローター・ステーターなどがあるが、中でもディスパ翼が好ましい。 The obtained sulfide is dissolved at a temperature of 0 to 40°C, preferably 5 to 35°C, and more preferably 10 to 30°C. If the temperature during dissolution is less than 0°C, labor and energy are required to maintain the liquid temperature at a low temperature, and if it exceeds 40°C, the solubility of the cellulose is likely to decrease. The dissolution time is set so that the clogging degree reaches the desired value and is completed, and although it depends on the stirring conditions, it is usually in the range of 2 minutes to 48 hours, preferably 4 minutes to 36 hours, and more preferably 5 minutes to 24 hours. In this case, dissolution can be achieved in a short time, especially when high-speed impellers are used in combination. The shape of the high-speed impeller can be a dispersion impeller, a turbine impeller, a propeller impeller, a paddle impeller, a rotor/stator, etc., and among these, a dispersion impeller is preferable.
本発明のアルカリセルロース材料の二硫化炭素による硫化物は、アルカリ水溶液に溶解することでビスコースを製造するために使用したり、常法で再生セルロース以外のセルロース材料から調製したアルカリセルロース材料の二硫化炭素による硫化物と混合して使用したりすることができる。再生セルロース以外のセルロース材料としては天然セルロースが挙げられ、木材、木綿、わら、竹、麻、ジュート、ケナフ等のバイオマスを原料とするパルプに加え、古紙や紙粉等を使用することもできるが、中でも木材から製造したパルプが好ましい。 The carbon disulfide sulfide of the alkali cellulose material of the present invention can be used to produce viscose by dissolving it in an alkaline aqueous solution, or it can be mixed with the carbon disulfide sulfide of the alkali cellulose material prepared by a conventional method from a cellulose material other than regenerated cellulose. Examples of cellulose materials other than regenerated cellulose include natural cellulose, and in addition to pulp made from biomass such as wood, cotton, straw, bamboo, hemp, jute, and kenaf, waste paper, paper powder, etc. can also be used, with pulp made from wood being particularly preferred.
その場合、混合された、アルカリセルロース材料の二硫化炭素による硫化物中の再生セルロースの含有量は、セルロース成分を基準にして1~99質量%、好ましくは2~50質量%、より好ましくは3~20質量%である。前記再生セルロースの含有量をできるだけ多くすることで、再生セルロースのリサイクル率を向上させ、環境負荷の低減効果を高めることができる。 In this case, the content of regenerated cellulose in the sulfide of the mixed alkali cellulose material produced by carbon disulfide is 1 to 99% by mass, preferably 2 to 50% by mass, and more preferably 3 to 20% by mass, based on the cellulose component. By increasing the content of the regenerated cellulose as much as possible, the recycling rate of the regenerated cellulose can be improved, and the effect of reducing the environmental load can be enhanced.
<ビスコース>
硫化及び溶解の終了後に得られる本発明のビスコースは、各種セルロース成形物の成形原料であるビスコース等のビスコースと同等の物性を有している。本発明のビスコースは、6,000以下、好ましくは4,000以下、より好ましくは2,000以下の目詰まり度を示す。かかる目詰まり度は小さい値のものほど、硫化物中のセルロースザンテートが溶解性に優れたものであることを意味している。目詰まり度の計算方法を以下に示す。
<Viscose>
The viscose of the present invention obtained after completion of sulfurization and dissolution has the same physical properties as viscose, such as viscose, which is a raw material for forming various cellulose molded products. The viscose of the present invention has a clogging degree of 6,000 or less, preferably 4,000 or less, more preferably 2,000 or less. The smaller the clogging degree, the more excellent the solubility of the cellulose xanthate in the sulfide. The method for calculating the clogging degree is shown below.
(目詰まり度)
ビスコースについて、綿布5枚重ねのろ布を用いて、23℃で0.04MPaの圧力をかけて加圧ろ過を行い、経時的にろ液の質量V(g)を測定する。一定時間経過後に、ろ過時間t(分)とろ過速度の逆数t/Vをプロットし、得られた直線の傾き(k/2)から、下記式に基づき、目詰まり度を算出する。図1は、ビスコースの測定された特性値がプロットされたグラフの模式図である。
目詰まり度=100,000×k
(Clogging degree)
Viscose is filtered at 23°C under a pressure of 0.04 MPa using a filter cloth made of five layers of cotton, and the mass V (g) of the filtrate is measured over time. After a certain time has passed, the filtration time t (min) and the reciprocal of the filtration rate t/V are plotted, and the degree of clogging is calculated from the slope (k/2) of the resulting line based on the following formula: Figure 1 is a schematic diagram of a graph on which the measured characteristic values of viscose are plotted.
Clogging degree = 100,000 x k
本発明のビスコースは、5質量%以上、好ましくは6~12質量%、より好ましくは8~10質量%のセルロース濃度を有する。かかるセルロース濃度は各種セルロース成形物の成形原料であるビスコース等のビスコースと同等の水準である。ビスコースのセルロース濃度が高いと粘度が高くなりすぎ、低いとセルロース成形物の強度が不十分なものとなり、酸等の薬品の使用量なども増加するために経済性も低下する。セルロース濃度の測定方法を以下に示す。 The viscose of the present invention has a cellulose concentration of 5% by mass or more, preferably 6 to 12% by mass, and more preferably 8 to 10% by mass. Such a cellulose concentration is at the same level as that of viscose, which is a raw material for forming various cellulose molded products. If the cellulose concentration of the viscose is high, the viscosity will be too high, and if it is low, the strength of the cellulose molded product will be insufficient and the amount of chemicals such as acid used will increase, reducing economic efficiency. The method for measuring the cellulose concentration is shown below.
(セルロース濃度)
ビスコースを、予め秤量したガラス板上にベーカー式アプリケーター(テスター産業(株)製、SA-201)を使って薄く広げてから質量を測定し、ビスコースの質量を計算する。その後、70℃の定温乾燥機内に40分間静置し、ガラス板毎、10質量%塩化アンモニウム水溶液に30分間浸漬して、凝固したビスコースをガラス板から剥離する。それを蒸留水で水洗後、105℃の熱風乾燥機で乾燥して質量を測定し、次式からビスコースのセルロース濃度を算出する。
セルロース濃度={乾燥後の質量/(ビスコースの質量)}×100
(Cellulose concentration)
The viscose is thinly spread on a pre-weighed glass plate using a Baker applicator (SA-201, manufactured by Tester Sangyo Co., Ltd.), the mass is measured, and the mass of the viscose is calculated. The plate is then left to stand in a constant temperature dryer at 70°C for 40 minutes, and each plate is immersed in a 10% by mass aqueous solution of ammonium chloride for 30 minutes to peel off the solidified viscose from the plate. The plate is washed with distilled water and then dried in a hot air dryer at 105°C, the mass is measured, and the cellulose concentration of the viscose is calculated using the following formula:
Cellulose concentration={mass after drying/(mass of viscose)}×100
本発明のビスコースは、2質量%以上、好ましくは4~12質量%、より好ましくは5~10質量%のアルカリ濃度を有する。かかるアルカリ濃度は各種セルロース成形物の成形原料であるビスコース等のビスコースと同等の水準である。ビスコースのアルカリ濃度が高いと中和に必要な酸の量が増加し、低いと溶解性が低下する。 The viscose of the present invention has an alkali concentration of 2% by mass or more, preferably 4 to 12% by mass, and more preferably 5 to 10% by mass. Such an alkali concentration is at the same level as that of viscose, which is a raw material for forming various cellulose molded products. If the alkali concentration of the viscose is high, the amount of acid required for neutralization increases, and if it is low, the solubility decreases.
本発明のビスコースは、塩溶液、硫酸や塩酸等の希酸、有機溶媒等に投入したり、加熱したりすると容易に凝固し、酸で再生することによりセロファン、レーヨン及びビーズ等の成形物を得ることができる。また、凝固に希酸を使用した場合は、凝固と再生が同時に進行する。 The viscose of the present invention easily solidifies when placed in a salt solution, a dilute acid such as sulfuric acid or hydrochloric acid, an organic solvent, or when heated, and can be regenerated with acid to obtain molded products such as cellophane, rayon, and beads. Furthermore, when a dilute acid is used for coagulation, coagulation and regeneration proceed simultaneously.
本発明のビスコースは、常法で再生セルロース以外のセルロース材料から調製したビスコースと混合して使用することができる。再生セルロース以外のセルロース材料としては、溶解パルプ等の天然セルロースが挙げられる。 The viscose of the present invention can be used in combination with viscose prepared by conventional methods from cellulose materials other than regenerated cellulose. Examples of cellulose materials other than regenerated cellulose include natural cellulose such as dissolving pulp.
その場合、混合された、ビスコース中の再生セルロースの含有量は、セルロース成分を基準にして1~99質量%、好ましくは2~50質量%、より好ましくは3~20質量%である。前記再生セルロースの含有量をできるだけ多くすることで、再生セルロースのリサイクル率を向上させ、環境負荷の低減効果を高めることができる。 In this case, the content of regenerated cellulose in the mixed viscose is 1 to 99% by mass, preferably 2 to 50% by mass, and more preferably 3 to 20% by mass, based on the cellulose component. By increasing the content of the regenerated cellulose as much as possible, the recycling rate of the regenerated cellulose can be improved, and the effect of reducing the environmental load can be enhanced.
以下の実施例により本発明を更に具体的に説明するが、本発明はこれらに限定されない。実施例中の単位「部」は質量を基準にする単位である。 The present invention will be explained in more detail with reference to the following examples, but the present invention is not limited thereto. The unit "parts" in the examples is a unit based on mass.
<実施例1>
再生セルロース試料として、セロファン(レンゴー(株)製「PT #300」(商品名))を機械粉砕して直径1mmΦの丸網を通過させ、水洗して付着している柔軟剤(グリセリン)を除去した湿潤品(セルロース分:43質量%)を調製した。
Example 1
As a regenerated cellulose sample, cellophane ("PT #300" (product name) manufactured by Rengo Co., Ltd.) was mechanically crushed, passed through a round net with a diameter of 1 mmΦ, and washed with water to remove any adhering softener (glycerin) to prepare a wet product (cellulose content: 43% by mass).
再生セルロース試料100部及び40質量%水酸化ナトリウム水溶液36部を撹拌装置の撹拌槽に投入して、パドル翼を備えた低速撹拌機(新東科学(株)製、スリーワンモーター BL-600)を用いて混合した。この混合物を撹拌しながら、約20℃の室温でマーセル化を行ってアルカリセルロースを得た。得られたアルカリセルロースは、セルロース32質量%及び水酸化ナトリウム11質量%を含むものである。 100 parts of the regenerated cellulose sample and 36 parts of 40% by weight aqueous sodium hydroxide solution were placed in the mixing tank of the mixing device and mixed using a low-speed mixer equipped with a paddle blade (Three-One Motor BL-600, manufactured by Shinto Scientific Co., Ltd.). While stirring, this mixture was mercerized at room temperature of approximately 20°C to obtain alkali cellulose. The obtained alkali cellulose contains 32% by weight of cellulose and 11% by weight of sodium hydroxide.
このアルカリセルロースに、セルロース質量当たり35質量%の二硫化炭素を加えて、前記低速撹拌機を用いて30rpmで撹拌しながら4時間硫化を行った。得られた硫化物に水酸化ナトリウム水溶液を加え、室温にて19時間600rpmで撹拌しながら溶解して、ビスコースを得た。得られたビスコースは、セルロース9.8質量%、水酸化ナトリウム6.0質量%を含むものである。 To this alkali cellulose, 35% by mass of carbon disulfide per mass of cellulose was added, and sulfurization was carried out for 4 hours while stirring at 30 rpm using the low-speed stirrer. Aqueous sodium hydroxide solution was added to the obtained sulfide, and it was dissolved while stirring at 600 rpm at room temperature for 19 hours to obtain viscose. The obtained viscose contains 9.8% by mass of cellulose and 6.0% by mass of sodium hydroxide.
硫化及び溶解の終了後に得られたビスコースについて、粘度及び目詰まり度を測定した。セルロースの溶解性は目詰まり度に基づき評価した。結果を表1に示す。 The viscosity and clogging degree of the viscose obtained after sulfurization and dissolution were measured. The solubility of cellulose was evaluated based on the clogging degree. The results are shown in Table 1.
(粘度)
ビスコースを20℃に調温し、B型粘度計(No.5ローター×20rpm)を使用して粘度を測定した。
(viscosity)
The temperature of the viscose was adjusted to 20° C., and the viscosity was measured using a Brookfield viscometer (No. 5 rotor×20 rpm).
(溶解性)
溶解性の評価基準は以下の通りにした。
(Solubility)
The evaluation criteria for solubility were as follows:
A(優)目詰まり度:2,000以下
B(良)目詰まり度:6,000以下
C(劣)目詰まり度:6,000を超える
A (Excellent) Clogging level: 2,000 or less B (Good) Clogging level: 6,000 or less C (Poor) Clogging level: Over 6,000
<実施例2>
実施例1にて調製したアルカリセルロースに、セルロース質量当たり25質量%の二硫化炭素を加えて得られた硫化物を、ディスパ翼を備えた高速撹拌機(プライミクス(株)製「ラボ・リューション」(商品名))を用いて室温にて5,000rpmで撹拌しながら10分間溶解を行った以外は同様にして、ビスコースを得た。得られたビスコースはセルロース9.6質量%、水酸化ナトリウム6.1質量%を含むものである。
Example 2
Viscose was obtained in the same manner as in Example 1, except that 25% by mass of carbon disulfide per mass of cellulose was added to the alkali cellulose prepared in Example 1, and the resulting sulfide was dissolved for 10 minutes while stirring at 5,000 rpm at room temperature using a high-speed stirrer equipped with a dispersing blade ("Labo-Lusion" (trade name) manufactured by Primix Corporation). The obtained viscose contained 9.6% by mass of cellulose and 6.1% by mass of sodium hydroxide.
<比較例1>
実施例1にて調製した再生セルロース試料100部を18質量%水酸化ナトリウム水溶液1000部に50℃にて1.5時間浸漬することでマーセル化を行い、遠心機HF110F型(商品名、(株)コクサン製)を用いて3,000rpmで溶液の排出が止まるまで脱水して、アルカリセルロースを得た。得られたアルカリセルロースは、セルロース22質量%及び水酸化ナトリウム16質量%を含むものである。
<Comparative Example 1>
100 parts of the regenerated cellulose sample prepared in Example 1 was immersed in 1000 parts of 18% by weight aqueous sodium hydroxide solution at 50°C for 1.5 hours to perform mercerization, and the sample was dehydrated at 3,000 rpm using a centrifuge HF110F (trade name, manufactured by Kokusan Co., Ltd.) until the discharge of the solution stopped, to obtain an alkali cellulose. The obtained alkali cellulose contained 22% by weight of cellulose and 16% by weight of sodium hydroxide.
このアルカリセルロースを使用した以外は実施例1と同様にして、ビスコースを得た。得られたビスコースは、セルロース8.2質量%、水酸化ナトリウム6.1質量%を含むものである。 Viscose was obtained in the same manner as in Example 1, except that this alkali cellulose was used. The obtained viscose contained 8.2% by mass of cellulose and 6.1% by mass of sodium hydroxide.
得られたビスコースについて、実施例1と同様にして、粘度及び目詰まり度を測定した。セルロースの溶解性は目詰まり度に基づき評価した。結果を表1に示す。 The viscosity and clogging degree of the obtained viscose were measured in the same manner as in Example 1. The solubility of cellulose was evaluated based on the clogging degree. The results are shown in Table 1.
比較例1のように、一般的なビスコースの製造方法に従って再生セルロースであるセロファンを溶解しようとした場合、溶解性が低くなる。その原因は、セロファンがアルカリ水溶液に著しく膨潤して、十分に脱水されず、アルカリセルロースのセルロース濃度が低くなった(25質量%以下)ことにある。つまり、アルカリセルロースの脱水が不十分な場合、硫化時に副反応が多くなり、セルロースザンテートへの変換率が低下して、溶解性が低下したと考えられる。 When trying to dissolve cellophane, a regenerated cellulose, according to a typical viscose manufacturing method, as in Comparative Example 1, the solubility is low. The reason for this is that cellophane swells significantly in the alkaline aqueous solution and is not sufficiently dehydrated, resulting in a low cellulose concentration in the alkali cellulose (25% by mass or less). In other words, it is believed that when the alkali cellulose is not sufficiently dehydrated, there are more side reactions during sulfurization, the conversion rate to cellulose xanthate decreases, and the solubility decreases.
実施例1及び2では、二硫化炭素の添加量と溶解時の撹拌状況に違いはあるが、再生セルロースを多量のアルカリ水溶液に浸漬及び脱水する代わりに、少量で必要最低限の濃厚アルカリ水溶液を再生セルロースに添加して均一に混合することで、32質量%とセルロース濃度の高いアルカリセルロースを調製することができた。その結果、セルロースの溶解性に優れたビスコースを得ることができた。 In Examples 1 and 2, although there were differences in the amount of carbon disulfide added and the stirring conditions during dissolution, instead of soaking the regenerated cellulose in a large amount of alkaline aqueous solution and dehydrating it, a small amount of the minimum necessary concentrated alkaline aqueous solution was added to the regenerated cellulose and mixed uniformly, making it possible to prepare alkaline cellulose with a high cellulose concentration of 32% by mass. As a result, a viscose with excellent cellulose solubility was obtained.
なお、パルプを原料に用いた非特許文献1では、常法に対してビスコースの濾過が困難化(ビスコース300gの濾過時間が、常法では177.4秒に対し、本法では320秒)しており、原料パルプ中のヘミセルロース等の混入やアルカリセルロースの不均一性が原因と考察されている。しかし、原料を再生セルロースに置き換えたところ、常法では濾過できなかったものの、本願では濾過が可能となっており、原料中のヘミセルロースの含有量が少ないことなどが原因と考えられる。 In addition, in Non-Patent Document 1, which uses pulp as the raw material, filtering of viscose is more difficult than with the conventional method (the filtering time for 300 g of viscose is 177.4 seconds with the conventional method and 320 seconds with this method), which is considered to be due to the presence of hemicellulose and other contaminants in the raw pulp and the non-uniformity of the alkali cellulose. However, when the raw material was replaced with regenerated cellulose, filtering was possible with this application, whereas filtering was not possible with the conventional method, and this is thought to be due to the low hemicellulose content in the raw material.
<実施例3>
実施例1のセロファンから製造したビスコースを工業用ビスコースと混合
実施例1のビスコース10部をレンゴー(株)製ビスコース(常法で溶解パルプから調製したもの)90部と混合して、混合ビスコース(セルロース:9.7質量%、水酸化ナトリウム:6.2質量%)を調製した。
Example 3
Mixing viscose produced from cellophane in Example 1 with industrial viscose Ten parts of the viscose in Example 1 were mixed with 90 parts of viscose manufactured by Rengo Co., Ltd. (prepared from dissolving pulp in a conventional manner) to prepare a mixed viscose (cellulose: 9.7% by mass, sodium hydroxide: 6.2% by mass).
得られたビスコースについて、実施例1と同様にして、粘度及び目詰まり度を測定した。セルロースの溶解性は目詰まり度に基づき評価した。結果を表2に示す。 The viscosity and clogging degree of the obtained viscose were measured in the same manner as in Example 1. The solubility of cellulose was evaluated based on the clogging degree. The results are shown in Table 2.
<実施例4>
実施例1の硫化後のセロファンを硫化したパルプと混合
実施例1の硫化した再生セルロース試料を、常法で溶解パルプから調製した硫化物と、再生セルロースと天然セルロースの質量比が1:9となるように混合し、アルカリ水溶液に溶解して、ビスコース(セルロース:9.8質量%、水酸化ナトリウム:6.1質量%)を調製した。
Example 4
Mixing the sulfurized cellophane of Example 1 with sulfurized pulp The sulfurized regenerated cellulose sample of Example 1 was mixed with a sulfide prepared from dissolving pulp by a conventional method so that the mass ratio of regenerated cellulose to native cellulose was 1:9, and the mixture was dissolved in an alkaline aqueous solution to prepare viscose (cellulose: 9.8% by mass, sodium hydroxide: 6.1% by mass).
得られたビスコースについて、実施例1と同様にして、粘度及び目詰まり度を測定した。セルロースの溶解性は目詰まり度に基づき評価した。結果を表2に示す。 The viscosity and clogging degree of the obtained viscose were measured in the same manner as in Example 1. The solubility of cellulose was evaluated based on the clogging degree. The results are shown in Table 2.
<実施例5>
実施例1のマーセル化後のセロファンをマーセル化したパルプと混合
実施例1のマーセル化した再生セルロース試料を、常法で溶解パルプから調製したマーセル化パルプと、再生セルロースと天然セルロースの質量比が1:9となるように混合し、セルロース質量当たり35質量%の二硫化炭素を添加して4時間硫化後にアルカリ水溶液に溶解して、ビスコース(セルロース:9.8質量%、水酸化ナトリウム:6.1質量%)を調製した。
Example 5
The mercerized cellophane of Example 1 was mixed with the mercerized pulp. The mercerized regenerated cellulose sample of Example 1 was mixed with mercerized pulp prepared from dissolving pulp by a conventional method so that the mass ratio of regenerated cellulose to native cellulose was 1:9. 35% by mass of carbon disulfide was added per mass of cellulose, and the mixture was sulfurized for 4 hours. The mixture was then dissolved in an alkaline aqueous solution to prepare viscose (cellulose: 9.8% by mass, sodium hydroxide: 6.1% by mass).
得られたビスコースについて、実施例1と同様にして、粘度及び目詰まり度を測定した。セルロースの溶解性は目詰まり度に基づき評価した。結果を表2に示す。 The viscosity and clogging degree of the obtained viscose were measured in the same manner as in Example 1. The solubility of cellulose was evaluated based on the clogging degree. The results are shown in Table 2.
<比較例2>
粉砕したセロファンをパルプと混合
再生セルロース試料と溶解パルプを、再生セルロースと天然セルロースとの質量比が1:9となるように混合した。この混合物を18質量%水酸化ナトリウム水溶液に50℃にて1.5時間浸漬することでマーセル化を行い、圧搾してアルカリセルロースを得た(セルロース:26質量%、水酸化ナトリウム:16質量%)。アルカリセルロースに、セルロース質量当たり35質量%となるように二硫化炭素を加えて4時間硫化を行った。得られた硫化物に水酸化ナトリウム水溶液を加え、20℃で19時間撹拌しながら溶解し、ビスコース(セルロース:9.6質量%、水酸化ナトリウム:6.0質量%)を調製した。
<Comparative Example 2>
Mixing crushed cellophane with pulp The regenerated cellulose sample and dissolving pulp were mixed so that the mass ratio of regenerated cellulose to native cellulose was 1:9. The mixture was immersed in an 18% by mass aqueous sodium hydroxide solution at 50°C for 1.5 hours to perform mercerization, and then pressed to obtain alkali cellulose (cellulose: 26% by mass, sodium hydroxide: 16% by mass). Carbon disulfide was added to the alkali cellulose to a concentration of 35% by mass per cellulose mass, and sulfurization was performed for 4 hours. Aqueous sodium hydroxide solution was added to the obtained sulfide, and the mixture was dissolved while stirring at 20°C for 19 hours to prepare viscose (cellulose: 9.6% by mass, sodium hydroxide: 6.0% by mass).
得られたビスコースについて、実施例1と同様にして、粘度及び目詰まり度を測定した。セルロースの溶解性は目詰まり度に基づき評価した。結果を表2に示す。 The viscosity and clogging degree of the obtained viscose were measured in the same manner as in Example 1. The solubility of cellulose was evaluated based on the clogging degree. The results are shown in Table 2.
<比較例3>
比較例1のマーセル化後のセロファンをマーセル化したパルプと混合
比較例1のマーセル化した再生セルロース試料を、常法で溶解パルプから調製したマーセル化パルプと、再生セルロースと天然セルロースの質量が1:9となるように混合し、硫化後にアルカリ水溶液に溶解して、ビスコース(セルロース:9.6質量%、水酸化ナトリウム:6.0質量%)を調製した。
<Comparative Example 3>
The mercerized cellophane of Comparative Example 1 was mixed with the mercerized pulp. The mercerized regenerated cellulose sample of Comparative Example 1 was mixed with mercerized pulp prepared from dissolving pulp by a conventional method in a mass ratio of regenerated cellulose to native cellulose of 1:9. After sulfurization, the mixture was dissolved in an alkaline aqueous solution to prepare viscose (cellulose: 9.6 mass%, sodium hydroxide: 6.0 mass%).
得られたビスコースについて、実施例1と同様にして、粘度及び目詰まり度を測定した。セルロースの溶解性は目詰まり度に基づき評価した。結果を表2に示す。 The viscosity and clogging degree of the obtained viscose were measured in the same manner as in Example 1. The solubility of cellulose was evaluated based on the clogging degree. The results are shown in Table 2.
実施例3、4及び5は溶解性が良好である。これに対し、常法の浸漬及び圧搾を行った比較例2及び3は溶解性が悪化している。また、実施例5は、実施例3及び4より溶解性が低くなっている。その原因は、硫化反応において表面積が少ないセロファンはパルプに比べて反応性が低く、硫化が不均一に進行したためと考えられる。セロファンとパルプは別々に硫化することで反応が均一になり、溶解性の点ではより好ましいと予想される。 Examples 3, 4 and 5 have good solubility. In contrast, Comparative Examples 2 and 3, which were subjected to conventional soaking and squeezing, have poor solubility. Also, Example 5 has lower solubility than Examples 3 and 4. This is thought to be because cellophane, which has a small surface area, is less reactive in the sulfurization reaction than pulp, and the sulfurization proceeds unevenly. By sulfurizing cellophane and pulp separately, the reaction becomes uniform, which is expected to be more favorable in terms of solubility.
本発明において、再生セルロースをマーセル化してアルカリセルロースを得る条件が最適化されたため、その段階あるいは硫化した状態で木材パルプからのそれと混合したり、硫化してアルカリ水溶液に溶解したビスコースの状態で工業用ビスコースと混合したりしても、成形体の製造に適したビスコースが得られることが分かった。それにより、専用の製造設備を用意する必要が少なくなり、既存の設備を有効利用できる上に、エネルギーコストの面でも有利となる。 In the present invention, the conditions for obtaining alkali cellulose by mercerizing regenerated cellulose have been optimized, and it has been found that viscose suitable for producing molded bodies can be obtained by mixing it with viscose from wood pulp at that stage or in a sulfurized state, or by mixing it with industrial viscose in the form of viscose that has been sulfurized and dissolved in an alkaline aqueous solution. This reduces the need for dedicated production equipment, allows the effective use of existing equipment, and is also advantageous in terms of energy costs.
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| JPS5346234B2 (en) * | 1975-09-29 | 1978-12-12 | ||
| JPS6234053B2 (en) * | 1978-01-17 | 1987-07-24 | Hoechst Ag | |
| JPH08239504A (en) * | 1994-12-13 | 1996-09-17 | Hoechst Ag | Reutilizing method for dyed cellulose material waste |
| JP2018505973A (en) * | 2015-02-06 | 2018-03-01 | レンツィング アクチェンゲゼルシャフト | Reuse of artificial cellulosic fibers |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5346234B2 (en) * | 1975-09-29 | 1978-12-12 | ||
| JPS6234053B2 (en) * | 1978-01-17 | 1987-07-24 | Hoechst Ag | |
| JPH08239504A (en) * | 1994-12-13 | 1996-09-17 | Hoechst Ag | Reutilizing method for dyed cellulose material waste |
| JP2018505973A (en) * | 2015-02-06 | 2018-03-01 | レンツィング アクチェンゲゼルシャフト | Reuse of artificial cellulosic fibers |
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