WO2000053832A1 - Constructions biodegradables en acetate de cellulose et filtre pour tabac - Google Patents
Constructions biodegradables en acetate de cellulose et filtre pour tabac Download PDFInfo
- Publication number
- WO2000053832A1 WO2000053832A1 PCT/JP2000/001477 JP0001477W WO0053832A1 WO 2000053832 A1 WO2000053832 A1 WO 2000053832A1 JP 0001477 W JP0001477 W JP 0001477W WO 0053832 A1 WO0053832 A1 WO 0053832A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cellulose acetate
- biodegradation
- structure according
- tobacco
- fiber
- Prior art date
Links
- 229920002301 cellulose acetate Polymers 0.000 title claims abstract description 245
- 241000208125 Nicotiana Species 0.000 title claims description 93
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- 238000001782 photodegradation Methods 0.000 claims description 7
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Classifications
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- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24D—CIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
- A24D3/00—Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
- A24D3/06—Use of materials for tobacco smoke filters
- A24D3/067—Use of materials for tobacco smoke filters characterised by functional properties
- A24D3/068—Biodegradable or disintegrable
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B3/00—Preparation of cellulose esters of organic acids
- C08B3/06—Cellulose acetate, e.g. mono-acetate, di-acetate or tri-acetate
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24D—CIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
- A24D3/00—Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
- A24D3/06—Use of materials for tobacco smoke filters
- A24D3/08—Use of materials for tobacco smoke filters of organic materials as carrier or major constituent
- A24D3/10—Use of materials for tobacco smoke filters of organic materials as carrier or major constituent of cellulose or cellulose derivatives
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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
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
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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
- D01F2/24—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives
- D01F2/28—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives from organic cellulose esters or ethers, e.g. cellulose acetate
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/425—Cellulose series
- D04H1/4258—Regenerated cellulose series
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2967—Synthetic resin or polymer
Definitions
- the present invention relates to a cellulose acetate structure having excellent biodegradability, and a tobacco filter.
- Cellulose acetate is used in various structures, for example, as a fiber for tobacco filter materials and woven fabrics for clothing, as a film, and in other injection molding and It is widely used as a structure (molded product) obtained by extrusion or the like.
- a typical example of a cellulose acetate structure is a fiber.
- tobacco finalizers are mostly composed of cellulose acetate fibers.
- Such cellulose acetate fibers are currently manufactured as follows. First, the flakes of cellulose acetate as a raw material are dissolved in a solvent such as acetone to prepare a cellulose acetate spinning stock solution. This spinning stock solution is supplied to a spinning nozzle device and spun by a dry spinning method in which the spinning solution is discharged into a high-temperature atmosphere to obtain a cellulose acetate fiber. Instead of the dry spinning method, a wet spinning method can be used.
- Cellulose acetate fibers used in particular as tobacco filter materials, facilitate the manufacture of tobacco filters.
- the total fineness is set appropriately and finished as a fiber tow.
- the tobacco filter is opened after the cellulose acetate fiber tow is opened by a tobacco filter plug winding device, and a plasticizer is impregnated. It is formed into a rod shape on a roll of paper and cut into a specified length.
- Senorelose acetate is obtained by subjecting senorelose to estenolate acetate and is essentially a biodegradable substance. However, in practice, this cellulose acetate is not always biodegradable.
- a tobacco filter made of cellulose acetate fiber even if buried in the soil, still retains its original shape in one or two years, and the tobacco filter is completely removed. It takes a very long time to be biodegraded.
- Tobacco filters are incorporated into tobacco products, distributed to consumers, smoked, and ultimately discarded as cigarette butts. Some are directly discarded as production residues from tobacco filter manufacturing plants. The waste from these tobacco filters is collected as garbage and is sometimes landfilled for disposal. In addition, cigarette butts are sometimes left in the natural environment without being collected as garbage. This situation applies not only to tobacco finoletors but also to cellulose acetate structures in general.
- the acetyl group of the cellulose acetate is cleaved by an extracellular enzyme released from the microorganism, resulting in a decrease in the DS of the cellulose acetate. Thereafter, the cellulose acetate with reduced DS is easily enzymatically degraded by cellulase widely existing in the environment, and finally undergoes microbial metabolism, resulting in carbon dioxide and water. To be utilized.
- the rate-limiting step of the biodegradation rate is thought to be due to the initial cleavage of the acetyl group.
- the same can be said for plastic materials in general, not only for cellulose acetate, but the biodegradation rate of structures consisting of these plastic forces also depends on the surface area of those structures. It is said to be. In other words, for the same material, the biodegradation rate increases as the contact area per unit weight with the microbial environment increases. In other words, increasing the surface area of the plastic structure increases the chance of contact with the degrading bacteria.
- Japanese Patent Application Laid-Open No. 9-9901 describes a technique of adding an oxide having an acid dissociation constant larger than that of acetic acid to cellulose acetate.
- this method is applied to the current manufacturing process of cellulose acetate fiber, etc., acid compounds will be converted to cellulose acetate.
- the acetyl group of the cellulose acetate undergoes a chemical hydrolysis reaction due to the effect of the acid compound.
- the chemical hydrolysis of the acetyl group of cellulose acetate in the presence of this acid compound produces acetic acid as the DS of cellulose acetate decreases.
- the acetyl group released from senorelose acetate is released as acetic acid. Therefore, according to this method, the cellulose acetate structure gives a strong acetic acid odor due to the effect of liberated acetic acid. Acetic acid odor is not a desirable factor in products, for example, in a tobacco finale, the acetic acid odor significantly degrades tobacco taste.
- Japanese Patent Publication No. 7-500385 discloses a method of adding a water-soluble compound and a bacterium-decomposable organic compound to cellulose acetate.
- added water-soluble compounds and organic compounds capable of decomposing bacterium are eluted with water in the natural environment, and then escape from cellulose acetate through bacterial decomposition.
- the cellulose acetate structure is destroyed, and the surface area of the structure is increased.
- the biodegradation rate of cellulose acetate is increased.
- the present invention essentially increases the interaction between cellulose acetate and the cellulose acetate-degrading bacterium, and thus the natural environment of the cellulose acetate.
- the purpose is to provide a means for further improving the biodegradability of the biomass.
- the present invention provides a cellulose acetate structure excellent in biodegradability and quality deterioration, in particular, generation of acetic acid odor is suppressed, and a tobacco filter using the same. aimed to.
- Another object of the present invention is to provide a biodegradable cellulose acetate structure that can be manufactured without greatly changing the current manufacturing method.
- the present inventors have conducted intensive studies to solve the above-mentioned problems, and as a result, by including a predetermined compound in cellulose acetate, particularly when producing cellulose acetate in the form of fibers, the present invention has been developed. It has been found that the biodegradability of cellulose acetate is significantly improved by adding a predetermined compound to a spinning dope and spinning the fiber using the spinning dope.
- the present invention at least the surface area Promotes biodegradation of at least one compound selected from the group consisting of oxyacid salts of phosphorus, esters of oxyacids of phosphorus, and salts of carbonic acid and its salts
- the present invention provides a cellulose acetate structure comprising a biodegradable cellulose acetate composition in which an agent is contained in cellulose acetate.
- Cellulose acetate preferably has a DS value of 2.0 and a DS value of 2.6.
- the biodegradation promoter preferably has a solubility in water at room temperature of 2 g / dm 3 or less.
- Such biodegradation promoters include cellulose phosphate, phosphate start, diphosphoric acid phosphate, calcium tertiary phosphate and calcium hydroxide phosphate. You can choose from several groups.
- the biodegradable cellulose acetate composition may further contain a dispersant for dispersing the fine particles in the composition. I like it.
- the biodegradable cellulose acetate composition further contains a photodegradation accelerator.
- the cellulose acetate structure of the present invention may be in the form of a fiber or a non-woven fabric composed of short fibers having a length of 1 to 10 Omm.
- a tobacco finoletor comprising the cell-mouth-acetate structure of the present invention in the form of fiber or non-woven fabric.
- Figure 1 shows the phosphoric acid contained in cellulose acetate. This is a daraf showing the results of leaching water elution.
- the present invention relates to a cellulose acetate structure and a tobacco filter made from a biodegradable cellulose acetate composition in which cellulose acetate contains a predetermined biodegradation promoter. .
- the cellulose acetate used in the present invention may be a cellulose acetate, and its DS value is not particularly limited.
- cellulose diacetate having a DS of 2.0 to 2.6, cellulose triacetate having a DS of 2.6 or more can be used.
- Cellulose acetate of DS 2.0 or less which is a region with good biodegradability, can also be used.
- senolerose diacetate having a DS of 2.0 to 2.6 is preferably used.
- the biodegradation promoter contained in cellulose acetate may be a salt of linoleic acid, an ester or salt of linoleic acid, or carbonic acid and a salt thereof. At least one compound selected from the group consisting of:
- Oxy acids are also called oxo acids or oxy acids, and are acids in which hydrogen that can be dissociated as a proton is bonded to an oxygen atom, and condensates thereof, if appropriate. included. More specifically, the oxygen acids of phosphorus include orthophosphoric acid (herein, orthophosphoric acid may be simply referred to as phosphoric acid), pi. Includes oral, metallic, and polyphosphoric acids. Oxygen acids other than these include phosphorous acid and hypophosphorous acid. Further, the ester of oxyacid of phosphorus is a compound in which at least one hydroxy group is esterified, and po ( ⁇
- the salt includes a hydrogen salt, and also includes a double salt such as phosphoric acid phosphate.
- biodegradation promoter compound in which a hydrate exists includes the hydrate, and the number of the bound water is not limited.
- biodegradation promoters be safe, supplied in large quantities and at acceptable prices.
- a spinning method of discharging a cellulose acetate solution (a stock solution for spinning) from a spun nodose fiber is used.
- the biodegradation accelerator used in the present invention is a solvent for dissolving cellulose acetate (for example, acetate, methylene chloride). / Methanol mixed solvent) or a compound that can be pulverized to such an extent that it does not affect the physical properties of the fiber during the spinning process, even if it is soluble or insoluble in the solvent. are preferred.
- the biodegradation accelerator used in the present invention is at room temperature (2 ° C.).
- C) for water 2 Preferably, it has a solubility of g / dm 3 or less.
- the solubility in water is as low as this, and the elution of water from the cellulose acetate structure is suppressed.
- Such degradation promoters include cellulose phosphate, starch phosphate, calcium phosphate dibasic, calcium phosphate tertiary, calcium phosphate phosphate, or a mixture thereof. Especially preferred is a mixture.
- the biodegradation rate of cell-acetate can be designed depending on the amount of the biodegradation promoter added.
- the amount of the biodegradation promoter added can be arbitrarily set depending on the target biodegradation rate. For example, when a rapid biodegradation is desired, a large amount of a decomposition accelerator may be added. However, considering the production stability of the cellulose acetate structure, particularly the fiber, the biodegradation accelerator is added at a ratio of 0.01 to 10% by weight based on the cellulose acetate. This is preferred, and it is more preferred to add it in a proportion of 0.01 to 3% by weight.
- the dispersed state of the biodegradation accelerator has an effect of accelerating the biodegradation rate.
- the effect of the biodegradation accelerator in the cellulose acetate fiber in a more dispersed state is better. Was found to be more pronounced. Therefore, it is more preferable to use a suitable dispersant in combination.
- a carboxylic acid polymer can be used as such a dispersant.
- the particle size of the biodegradation promoter insoluble in the cellulose acetate solvent greatly contributes to the effect of promoting the biodegradation rate, and when compared with the same amount, the particle size is smaller. It was also found that the promoting effect was more remarkable in those. Accordingly, the biodegradation promoter preferably has a smaller particle size. It was found that the biodegradation promoter insoluble in the cell-acetate solvent preferably had an average particle size of 1.0 m or less.
- the present inventor has added a photodegradation accelerator such as titanium oxide for a high photoactive catalyst together with the biodegradation accelerator of the present invention, whereby the biodegradation accelerator of the present invention can be obtained. It was found that, together with the acceleration of the biodegradation rate, the degradability of the cellulose acetate structure could be further enhanced. In this case, the remarkable destruction of the cellulose acetate structure which can be achieved by the biodegradation accelerator of the present invention makes it easier for the photodegradation accelerator, such as titanium oxide for a high photoactive catalyst, to exhibit the promoting effect.
- a photodegradation accelerator such as titanium oxide for a high photoactive catalyst
- the destruction of the cellulose acetate structure produced by a photodegradation accelerator such as titanium oxide for a highly photoactive catalyst causes the biodegradation rate of the biodegradation accelerator of the present invention. Promote the promotion effect even more. In this way, the disappearance of the cellulose acetate structure in the decomposition process can be synergistically accelerated.
- a tobacco finolator made of cellulose acetate fiber containing both the biodegradation accelerator of the present invention and a photodegradation accelerator such as titanium oxide for a highly photoactive catalyst is used.
- Titanium oxide as a photodegradation promoter is preferably an anatase-type titanium oxide having a particle size of 0.1 / m or less, and is preferably 0.1 to 1 to cellulose acetate. It is preferable to add at a ratio of 0% by weight, and it is more preferable to add at a ratio of 0.01 to 3% by weight.
- the cellulose acetate composition of the present invention can be formed into various structures by a usual method except that the biodegradation accelerator and other additives of the present invention are contained, the cellulose acetate composition is usually used. There is no need to change the method of manufacturing the cellulosic acetate structure.
- the cellulose acetate structure of the present invention can be prepared by adding a biodegradation accelerator of the present invention to a solution of cellulose acetate, methylene chloride, or the like. It can be molded by a conventional method after melt-mixing a biodegradation accelerator, etc., with thermoformable cellulose acetate containing a plasticizer, etc. You can do it.
- Cellulose acetate fibers used in tobacco finale letters can be produced, for example, as follows. First, a solution (spinning stock solution) containing cellulose acetate and the additive of the present invention is prepared.
- the solvent may be a single solvent such as methylene chloride or acetone, or methylene chloride and methanol. It is possible to use a mixed solvent such as
- the concentration of cellulose acetate is generally between 15 and 35% by weight, preferably
- This spinning dope additives such as a biodegradation accelerator are contained in the proportions described above.
- This spinning stock solution is prepared by dissolving or dispersing additives such as a biodegradation accelerator in a cellulose acetate solvent, and a cellulose acetate solvent in a cellulose acetate solvent. It can be prepared by mixing with a dissolved solution or by directly adding an additive such as a biodegradation accelerator to a solution of cellulose acetate.
- a dry spinning method in which the cellulose acetate spinning stock solution containing the additive such as the biodegradation accelerator of the present invention thus obtained is supplied to a spinning nozzle device and discharged into a high-temperature atmosphere. By spinning, cellulose acetate fibers can be obtained. In addition, wet spinning may be performed instead of dry spinning. Further, in spinning, as described above, the uniformly dispersed spinning dope may be directly spun into a fibrous form. However, the cellulose acetate spinning dope containing the additive of the present invention may be used. And a cellulose acetate spinning stock solution to which these additives are not added, so that cellulose acetate containing at least the additive of the present invention appears on the fiber surface.
- a composite spinning method such as a fiber side-by-side type or a sheath-core type can also be used.
- other additives can be used in combination as long as the properties are not impaired.
- emulsifier, solubilization to improve the uniformity of spinning dope or to adjust viscosity Agents, viscosity modifiers and the like may be used in combination.
- each cellulose acetate fiber constituting the tobacco filter plug of the present invention contains the additive of the present invention at least in its surface region. .
- the cellulose acetate fiber of the present invention thus obtained can be manufactured as a tobacco filter by a conventional method.
- the manufacturing method and the filter structure there is no particular limitation on the manufacturing method and the filter structure, and for example, it can be manufactured as follows.
- the above cellulose acetate fiber is formed into a tow, which is opened by a tobacco filter plug winding device, and a plasticizer (for example, triacetylglycerin) is added. After the attachment, it is formed into a fiber rod shape and cut to the required length to form a filter plug. In addition, the total fineness of the fiber bundle is appropriately set in order to facilitate the preparation of the filter plug.
- a plasticizer for example, triacetylglycerin
- a tobacco filter in which cellulose acetate fiber tow is hardened with a plasticizer the cellulose acetate fibers are more firmly bonded by fusion bonding, and as a result, in natural environments. Tobacco filters that have been discarded tend to maintain a stable mouth shape for a long time.
- a tobacco filter made of non-woven sheets can be easily locked by a large amount of water (rain, seawater, river water, lake water, etc.) when dumped into the natural environment. Do The shape collapses and spreads out on the ground in a sheet-like manner.
- the contact area of the material with the microbial environment that affects the biodegradation rate is increased, and as a result, the decomposition rate of the tobacco filter is further accelerated. Therefore, the decomposition rate of the tobacco filter can be further increased in combination with the promotion of the biodegradation rate of the cellulose acetate of the present invention.
- the nonwoven cloth sheet used in this case has excellent water dispersibility. Such a nonwoven fabric sheet having excellent water dispersibility can be obtained, for example, by the method described in Japanese Patent Application Laid-Open No. 9-94949.
- the method of this is to mold the defibrated fibers in ⁇ E blanking, resulting 4 0-1 0 0 weight partially saponified poly bicycloalkyl two Le Al co Lumpur web 0 /. And poly vinyl acetate 0 to
- the tobacco filter is usually wrapped in finoletor paper with a cellulose acetate towel or cellulose acetate fiber towel. Finished in a shape wrapped.
- the cellulose acetate fiber of the present invention may be used alone to produce a filter, or the cellulose acetate fiber of the present invention may be used as one constituent material and other constituent materials may be used. Final letters can also be manufactured by using them together.
- Such other constituent materials include natural or semi-synthetic materials (eg, pulp, linter, cotton, hemp, viscose rayon, copper ammonia rayon).
- Biodegradable polymers of microbial production system such as cyano alkanoate, and ordinary synthetic materials (for example, polyolefin such as polypropylene, polyethylene terephthalate, etc.) (Polyester, Polyamide), biodegradable synthetic materials (eg, polylactic acid, polylactic acid, polybutylene succinate, polyvinylinoleate) Call), a photodegradable material or the like can be used in the form of fiber or nonwoven fabric. In that case, it is preferable to use a material that is particularly excellent in biodegradability. In addition, although not fiber, starch foam can be used as a material with excellent biodegradability.
- the shape of the cellulose acetate fiber may be either staple or filament, but the cellulose acetate fiber constituting the tobacco filter of the present invention may be used.
- a fiber tow shape is preferable, and the total fineness of the tow can be arbitrarily set.
- a bundle of 0.5 to 15 denier fibers is bundled into a bundle of 30000 to 500000, and a crimp of 10 to 50 is applied to a length of 25 mm. (In bundle form?) Is preferred.
- the cross-sectional shape of each fiber is not particularly limited, such as a round shape and a square shape, but from the viewpoint of the filtration performance as a tobacco filter, a multi-lobed cross-sectional shape is preferred.
- the cellulose acetate fibers may be in the form of fibrils. When in the form of fibrinole, it can be used in combination with the other constituent materials mentioned above, or with the cellulose acetate fibers of the present invention in the form of ordinary fibers. I like it.
- the plastic it is preferable to use a water-soluble adhesive instead of the adhesive.
- a plasticizer When a plasticizer is used, the cellulose acetate fibers are strongly bonded to each other by fusion bonding, and as a result, the tobacco filter discarded in the natural environment is stable for a long time. It tends to maintain the shape of the mouth.
- a water-soluble adhesive when a water-soluble adhesive is used, the point of adhesion between cellulose acetate fibers may be damaged by a large amount of water (rain, seawater, river water, It is easily dissociated by lake water. As a result, the tobacco filter can easily collapse the rod shape.
- Cellulose acetate fiber whose rod shape has collapsed is spread in the natural environment, for example, on the ground surface, and the area of contact with the microbial environment of the material that affects the biodegradation rate increases.
- the degradability of tobacco filters is further enhanced. Therefore, in combination with the promotion of the biodegradability of the cellulose acetate of the present invention, the degradability of the tobacco finoletter can be further enhanced.
- a water-soluble adhesive a water-soluble adhesive described in Japanese Patent Application Laid-Open No. Hei 8-18773 / Japanese Patent Application Laid-Open No. Hei 9-26673 is preferred. Can be illustrated.
- water-soluble adhesives include various water-soluble polymers, for example, polyvinyl alcohol, polyvinyl pyrrolidone, polyvinyl ether, and vinyl monomers (for example, vinyl acetate, vinyl polyether, etc.).
- a copolymerizable monomer having a resin, a vinyloxyalkyl ether, or a styrene) and a canolepoxyl group, a snolefonic acid group, or a salt thereof for example, (meth) acrylic acid, ⁇ , jS monoethylenically unsaturated carboxylic acid such as leic acid, maleic acid, crotonic acid, etc.
- ethylene Vinyl-based water-soluble polymers such as copolymers with ⁇ , ⁇ -ethylenically unsaturated sulfonates or salts thereof such as sulfonates, etc .
- Polyalkylene oxide, water-soluble polyester, water-soluble polyamide, etc. are included.
- the filter paper having excellent water dispersibility as the filter paper.
- the filter web is made of cellulose, such as pulp, and this cellulose is a material having extremely excellent biodegradability. Therefore, in the natural environment, the filter paper disposed on the outer peripheral surface of the tobacco filter disappears relatively quickly (about 1 to 6 months). And, depending on the environment in which they are located, may remain in their original form for more than a year.
- a filter paper with excellent water dispersibility as the filter paper. I like it.
- the tobacco filter dumped in the natural environment is easily disposed on the outer surface by a large amount of water (rain, seawater, river water, lake water, etc.).
- the web can be dispersed and detached, so that cellulose acetate fibers can be spread directly on the surface of the ground, for example, and the area of contact of the material with the microbial environment that affects the rate of biodegradation As a result, the decomposition rate of the tobacco filter is further enhanced.
- Japanese Patent Application Laid-Open No. Hei 9-47271 / Japanese Patent Application Laid-Open No. Heisei 91-47272 discloses a filter roll having such excellent water dispersibility.
- An example is a router web.
- These filter webs are made of a water-dispersible base material including water-soluble paper or hydrolyzed paper.
- water-soluble paper or water-disintegrated paper papermaking fibers (water dispersibility) that have been given water dispersibility by a technology that is known per se to reduce the beating and reduce the mutual contact between fibers and the bonding between fibers
- a water-soluble paper or a water-disintegrated paper obtained by mixing a fibrous force with a fibrous force, such as lboximetyl cellulose cellulose salt or fibrous canoleboxyl cellulose cellulose salt is preferred.
- a water-dispersible base material obtained by mixing a water-dispersible fiber and fibrous carboxymethyl cellulose or fibrous phenolic cellulose is also preferable.
- water-dispersible fibers include wood pulp fibers such as softwood kraft pulp, hardwood kraft pulp, and dissolved pulp, and non-wood-based fibers such as Z or kenaf pulp, flax pulp, and linter. Plant fiber can be used.
- Cellulose acetate fibers containing the additive according to the present invention as a cellulose acetate structure and a tobacco filter material have the following features.
- the addition of the additive to the cellulose acetate structure according to the present invention is carried out simply and without any change in a conventional cellulose acetate structure manufacturing process. be able to.
- the cellulose acetate structure of the present invention can be produced by melt-mixing the additive with thermoformable cellulose acetate mixed with a plasticizer or the like. .
- the spinning process since it is pulverized to such an extent that fiber properties are not affected, it does not make it difficult to produce cellulose acetate fibers.
- the method for producing cellulose acetate fiber according to the present invention only requires a step of adding an additive to the spinning dope, and otherwise requires no change to the existing process. Can be applied immediately.
- the additive to the cellulose acetate structure and the cellulose acetate fiber according to the present invention may be added to the cellulose acetate structure and the cellulose acetate fiber.
- its acidity or basicity is a low value without any problem, and it reacts with cellulose acetate in any manner.
- it can be stably present in cellulose acetate structures and cellulose acetate fibers. Therefore, the cellulose acetate structure and cellulose acetate fiber are free from the deterioration of quality (especially, odor of acetic acid) caused by the use of the additive, and No equivalent to normal cellulose acetate structure and cellulose acetate fiber Present quality.
- the cellulose acetate structure and the cellulose acetate fiber according to the present invention and the tobacco filter comprising the cellulose acetate fiber can be used in a natural environment. When discarded, they exhibit remarkable biodegradability due to the effect of promoting the biodegradation of the contained additives.
- the additive according to the present invention selects its solubility in water from predetermined ones, the additive is used in the natural environment and in the cellulose acetate structure and in the natural environment. Cell mouth-Long-term stay in cellulose acetate structure and cellulose acetate fiber without easily detaching (leaching out of water) from acetate fiber be able to. In other words, the additive can always exert the effect of promoting the biodegradation rate of the additive in the natural environment at any time and place.
- calcium tertiary phosphate was added at a ratio of 5% by weight based on the cell opening acetate, and the mixture was stirred to be uniform.
- the obtained cellulose acetate solution was cast on a glass plate and dried to obtain a cellulose acetate phenol having a thickness of about 10.
- cellulose phosphate was added at a ratio of 5% by weight based on cellulose acetate, and the mixture was stirred to make it uniform.
- the obtained cellulose acetate solution was cast on a glass plate and dried to obtain a cellulose acetate finolem having a thickness of about 100 ⁇ .
- polyphosphoric acid was added at a ratio of 5% by weight with respect to cellulose acetate, and the mixture was stirred to make it uniform.
- the obtained cellulose acetate solution is cast on a glass plate, dried, and dried to give a cellulose acetate solution having a thickness of about 100 / zm. I got Nonolem.
- the cell containing the biodegradation accelerator according to the present invention is 2 A
- the cellulose acetate composition does not generate acetic acid odor (deterioration in quality) due to the use of the biodegradation accelerator.
- the biodegradation accelerator according to the present invention does not chemically react with cellulose acetate during the production process of the cellulose acetate composition or at the product stage without any chemical reaction. It is stably present in the cellulose acetate composition and therefore has a quality equivalent to that of a normal cellulose acetate composition without additives.
- the water elution behavior of the additives from the cellulose acetate films obtained in Examples 1 to 3 was evaluated.
- a circular piece (5 cm in diameter) of the prepared film was immersed in ion-exchanged water for 10 days, and then the additive eluted into the water from the cellulose acetate film was measured. I went there.
- the water elution amount of the additive was calculated from the film weight (dry weight) before and after immersion in water, and the water elution rate was calculated based on the ratio to the initial addition amount. Table 2 shows the results. Table 2: Evaluation results of water elution amount of additives from cellulose acetate film
- the cellulose acetate composition of the present invention It can be seen that the various additives do not elute in water. This result indicates that in the natural environment, the additive does not easily release (elution from water) from the cellulose acetate composition, but remains in the cellulose acetate composition for a long period of time. It means that you can do it. That is, the biodegradation promoter of the present invention can always exert the effect of promoting the biodegradation rate of the additive in the natural environment at any time and place.
- Cellulose acetate (DS: 2.5) is dissolved in acetonitrile so as to have a concentration of 28% by weight of 0 / ⁇ , and 0.5% by weight of the cellulose acetate is added to the cellulose acetate.
- titanium oxide weight-average particle size: 0.2 Zm
- calcium diphosphate weight average particle diameter 0.46 ⁇ m
- the undiluted spinning solution was filtered and spun by dry spinning using a conventional filter tow spinning apparatus.
- a predetermined amount of the produced cellulose acetate filament was bundled and crimped to obtain a cellulose acetate fiber tow.
- the cellulose acetate fiber was finished to have a Y-shaped fiber cross-section, a denier of single yarn of 3 denier, and a total denier of 360,000 denier.
- a tobacco filter was produced as follows. That is, the cellulose acetate fiber tow is opened with a conventional tobacco finoleta plug winding device, and a plasticizer (triacetyl lyserine) is added to the cellulose. After being impregnated at 6.% by weight with respect to the acetate fiber tow, it is wrapped in filter paper and formed into a rod shape to obtain a predetermined length. It was cut to make a filter plug.
- a plasticizer triacetyl lyserine
- a solid additive such as calcium phosphate dibasic used in this example can be contained in the cellulose acetate fiber.
- the tobacco filters obtained in Examples 4 to 5 and Comparative Examples 3 to 4 were evaluated for acetic acid concentration and acetic acid odor level.
- acetic acid concentration pack a tobacco finoletor (finoleter length 25 mm) in an odor bag immediately after preparation, leave it in a 50 ° C constant temperature room, and leave it for two weeks.
- Acetic acid concentration in gas by gas detector tube method The measurement was performed by measuring At the same time, the acetic acid odor level of the tobacco filter was evaluated by a sensory test method. Table 5 shows the results.
- the cellulose acetate fiber according to the present invention does not generate acetic acid odor (deterioration in quality) due to the use of the additive.
- the additive according to the present invention does not chemically react with cellulose acetate during the production process of the cellulose acetate fiber and at the product stage without causing any chemical reaction with cellulose acetate. It is stably present in acetate fibers and therefore has the same quality as ordinary cellulose acetate fibers without additives.
- Example 4 Using the tobacco filter obtained in Example 4, the water elution behavior of the additive from the cellulose acetate fiber was evaluated.
- the evaluation test method is as follows. The tobacco filter (filter length: 25 mm; no paper roll) is immersed in water (using ion-exchanged water), and the tobacco filter is used. The content of calcium diphosphate in the cellulose acetate fiber formed was measured over time. The content of calcium phosphate 2 was calculated in the same manner as in Example 4. The results are shown in Figure 1.
- the acceleration of the biodegradation rate of the tobacco filter was achieved. Furthermore, it can be seen that the biodegradation rate of the tobacco filter depends on the particle size of the additive. In other words, it can be seen that when the biodegradation is to be carried out quickly, the particle size of the additive should be smaller.
- Cellulose acetate (DS 2.5) concentration 28 weight 0 /. And dissolved in acetone so as to obtain a titanium oxide for a high photoactive catalyst (weight average particle diameter: 0.02 / im) at a ratio of 1% by weight to the cellulose acetate. Was added and stirred to disperse uniformly. To this dispersion solution, calcium diphosphate (weight average particle diameter: 1.20 / Zm) was added at a ratio of 1% by weight to cellulose acetate, and the mixture was stirred until it was uniformly dispersed. To obtain a spinning dope. Cellulose acetate fiber tow and tobacco filter were produced in the same manner as in Example 4 using this spinning stock solution.
- Example 5 The overall degradability of the tobacco filters obtained in Example 5, Example 6, Comparative Example 3 and Comparative Example 5 in the natural environment was evaluated (biodegradation, photolysis, shape collapse, etc.). From several factors). The evaluation was conducted by placing the prepared tobacco filter (filter length 25 mm; no paper roll) on outdoor soil, and after 6 months, the tobacco filter The measurement was performed by measuring the change in appearance and the rate of volume reduction. The volume reduction rate was calculated from the volume of the tobacco filter before and after installation on outdoor soil. Table 7 shows the results of external observation and the volume reduction rate. Table 7: Evaluation results of decomposability of tobacco filters
- a cellulose acetate structure excellent in biodegradability and suppressed in quality deterioration (in particular, generation of acetic acid odor) and a tobacco finale using the same are provided.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Textile Engineering (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biodiversity & Conservation Biology (AREA)
- Manufacturing & Machinery (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Cigarettes, Filters, And Manufacturing Of Filters (AREA)
- Biological Depolymerization Polymers (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Filtering Materials (AREA)
- Nonwoven Fabrics (AREA)
- Artificial Filaments (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2001-7011062A KR100460598B1 (ko) | 1999-03-11 | 2000-03-10 | 생분해성 셀룰로오스아세테이트 구조물 및 담배필터 |
CA002365014A CA2365014C (en) | 1999-03-11 | 2000-03-10 | Biodegradable cellulose acetate constructions and tobacco filter |
EP00908007A EP1167589B1 (en) | 1999-03-11 | 2000-03-10 | Biodegradable cellulose acetate constructions and tobacco filter |
DE60036202T DE60036202T2 (de) | 1999-03-11 | 2000-03-10 | Bioabbaubare gegenstände aus celluloseacetat und tabakrauchfilter |
AU29419/00A AU2941900A (en) | 1999-03-11 | 2000-03-10 | Biodegradable cellulose acetate constructions and tobacco filter |
DK00908007T DK1167589T3 (da) | 1999-03-11 | 2000-03-10 | Bionedbrydelige artikler af celluloseacetat samt filter for tobaksrög |
JP2000603451A JP3583721B2 (ja) | 1999-03-11 | 2000-03-10 | 生分解性セルロースアセテート構造物、およびたばこフィルター |
US09/941,839 US6739344B2 (en) | 1999-03-11 | 2001-08-30 | Biodegradable cellulose acetate structure and tobacco filter |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6523599 | 1999-03-11 | ||
JP11/65235 | 1999-03-11 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/941,839 Continuation US6739344B2 (en) | 1999-03-11 | 2001-08-30 | Biodegradable cellulose acetate structure and tobacco filter |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000053832A1 true WO2000053832A1 (fr) | 2000-09-14 |
Family
ID=13281063
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2000/001477 WO2000053832A1 (fr) | 1999-03-11 | 2000-03-10 | Constructions biodegradables en acetate de cellulose et filtre pour tabac |
Country Status (16)
Country | Link |
---|---|
US (1) | US6739344B2 (ja) |
EP (1) | EP1167589B1 (ja) |
JP (1) | JP3583721B2 (ja) |
KR (1) | KR100460598B1 (ja) |
CN (1) | CN1195908C (ja) |
AT (1) | ATE371757T1 (ja) |
AU (1) | AU2941900A (ja) |
CA (1) | CA2365014C (ja) |
DE (1) | DE60036202T2 (ja) |
DK (1) | DK1167589T3 (ja) |
ES (1) | ES2291193T3 (ja) |
PT (1) | PT1167589E (ja) |
RU (1) | RU2219200C2 (ja) |
TR (1) | TR200102793T2 (ja) |
TW (1) | TWI274556B (ja) |
WO (1) | WO2000053832A1 (ja) |
Cited By (6)
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JP2012505271A (ja) * | 2008-10-14 | 2012-03-01 | ローディア アセトウ ゲーエムベーハー | 生分解性プラスチックとその使用 |
US8324374B2 (en) | 2007-07-03 | 2012-12-04 | Taiyu Kensetsu Kabushiki Kaisha | Process for production of monosaccharide and process for production of ethanol both utilizing cellulose-based substance |
JP2013507949A (ja) * | 2009-10-23 | 2013-03-07 | イノヴィア フィルムズ リミテッド | 生分解性たばこフィルタートウおよびその製造方法 |
JP2013523122A (ja) * | 2010-03-30 | 2013-06-17 | セラニーズ アセテート,エルエルシー | 環境に分解性を有するたばこフィルター |
JP2021121209A (ja) * | 2012-10-10 | 2021-08-26 | アール・ジエイ・レイノルズ・タバコ・カンパニー | 喫煙物品のフィルター要素のためのフィルター材料、ならびに関連システムおよび方法 |
EP4212189A1 (en) | 2022-01-17 | 2023-07-19 | V. Mane Fils | Volatile substance device, uses and methods relating to same |
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KR20240103718A (ko) | 2022-12-27 | 2024-07-04 | 주식회사 케이티앤지 | 가수분해효소를 포함하는 캡슐을 함유하는 흡연물품용 필터 및 이를 포함하는 흡연물품 |
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EP0632970A2 (de) * | 1993-07-09 | 1995-01-11 | Rhone-Poulenc Rhodia Aktiengesellschaft | Aus Celluloseacetat geformte Gebilde, deren Verwendung zur Herstellung von Filtertow,Verwendung des Filtertows zur Herstellung eines Tabakrauchfilterelements sowie Filtertow und Tabakrauchfilterelement |
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-
2000
- 2000-03-10 PT PT00908007T patent/PT1167589E/pt unknown
- 2000-03-10 CA CA002365014A patent/CA2365014C/en not_active Expired - Fee Related
- 2000-03-10 KR KR10-2001-7011062A patent/KR100460598B1/ko not_active IP Right Cessation
- 2000-03-10 AT AT00908007T patent/ATE371757T1/de active
- 2000-03-10 TR TR2001/02793T patent/TR200102793T2/xx unknown
- 2000-03-10 WO PCT/JP2000/001477 patent/WO2000053832A1/ja active IP Right Grant
- 2000-03-10 ES ES00908007T patent/ES2291193T3/es not_active Expired - Lifetime
- 2000-03-10 DE DE60036202T patent/DE60036202T2/de not_active Expired - Lifetime
- 2000-03-10 AU AU29419/00A patent/AU2941900A/en not_active Abandoned
- 2000-03-10 EP EP00908007A patent/EP1167589B1/en not_active Expired - Lifetime
- 2000-03-10 JP JP2000603451A patent/JP3583721B2/ja not_active Expired - Fee Related
- 2000-03-10 DK DK00908007T patent/DK1167589T3/da active
- 2000-03-10 CN CNB008048150A patent/CN1195908C/zh not_active Expired - Fee Related
- 2000-03-10 RU RU2001127532/04A patent/RU2219200C2/ru not_active IP Right Cessation
- 2000-03-10 TW TW089104398A patent/TWI274556B/zh not_active IP Right Cessation
-
2001
- 2001-08-30 US US09/941,839 patent/US6739344B2/en not_active Expired - Fee Related
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JPS63105655A (ja) * | 1986-10-24 | 1988-05-10 | Ajinomoto Co Inc | 畜肉加工品の製造方法 |
WO1993024685A1 (en) * | 1992-05-27 | 1993-12-09 | Eastman Chemical Company | Environmentally non-persistant cellulose ester fibers |
EP0597478A1 (en) * | 1992-11-13 | 1994-05-18 | Daicel Chemical Industries, Ltd. | Biodegradable cellulose ester composition and article produced from the same |
EP0632970A2 (de) * | 1993-07-09 | 1995-01-11 | Rhone-Poulenc Rhodia Aktiengesellschaft | Aus Celluloseacetat geformte Gebilde, deren Verwendung zur Herstellung von Filtertow,Verwendung des Filtertows zur Herstellung eines Tabakrauchfilterelements sowie Filtertow und Tabakrauchfilterelement |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8324374B2 (en) | 2007-07-03 | 2012-12-04 | Taiyu Kensetsu Kabushiki Kaisha | Process for production of monosaccharide and process for production of ethanol both utilizing cellulose-based substance |
JP2012505271A (ja) * | 2008-10-14 | 2012-03-01 | ローディア アセトウ ゲーエムベーハー | 生分解性プラスチックとその使用 |
JP2013507949A (ja) * | 2009-10-23 | 2013-03-07 | イノヴィア フィルムズ リミテッド | 生分解性たばこフィルタートウおよびその製造方法 |
JP2013523122A (ja) * | 2010-03-30 | 2013-06-17 | セラニーズ アセテート,エルエルシー | 環境に分解性を有するたばこフィルター |
JP2021121209A (ja) * | 2012-10-10 | 2021-08-26 | アール・ジエイ・レイノルズ・タバコ・カンパニー | 喫煙物品のフィルター要素のためのフィルター材料、ならびに関連システムおよび方法 |
JP7228622B2 (ja) | 2012-10-10 | 2023-02-24 | アール・ジエイ・レイノルズ・タバコ・カンパニー | 喫煙物品のフィルター要素のためのフィルター材料、ならびに関連システムおよび方法 |
EP4212189A1 (en) | 2022-01-17 | 2023-07-19 | V. Mane Fils | Volatile substance device, uses and methods relating to same |
WO2023135211A1 (en) | 2022-01-17 | 2023-07-20 | V. Mane Fils | Volatile substance device, uses and methods relating to same |
Also Published As
Publication number | Publication date |
---|---|
TR200102793T2 (tr) | 2002-05-21 |
CA2365014A1 (en) | 2000-09-14 |
JP3583721B2 (ja) | 2004-11-04 |
PT1167589E (pt) | 2007-11-16 |
US20020096300A1 (en) | 2002-07-25 |
ES2291193T3 (es) | 2008-03-01 |
AU2941900A (en) | 2000-09-28 |
DK1167589T3 (da) | 2007-10-29 |
DE60036202D1 (de) | 2007-10-11 |
CA2365014C (en) | 2009-07-14 |
EP1167589B1 (en) | 2007-08-29 |
TWI274556B (en) | 2007-03-01 |
KR100460598B1 (ko) | 2004-12-08 |
US6739344B2 (en) | 2004-05-25 |
ATE371757T1 (de) | 2007-09-15 |
CN1343267A (zh) | 2002-04-03 |
EP1167589A1 (en) | 2002-01-02 |
DE60036202T2 (de) | 2008-05-21 |
KR20010102450A (ko) | 2001-11-15 |
EP1167589A4 (en) | 2004-11-03 |
RU2219200C2 (ru) | 2003-12-20 |
CN1195908C (zh) | 2005-04-06 |
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