Biodegradable resin processing method and biodegradable resin processing system

Abstract

To provide biodegradable resin treatment method and treatment system capable of generating methane efficiently without adding an additive other than biodegradable resin and water.SOLUTION: Biodegradable resin treatment method and treatment system include: a decomposition step for mixing a waste substance containing biodegradable resin 1 and water 2, hydrolyzing the mixture at a temperature of 120°C or higher in a sealed decomposition tank 11, and acquiring decomposition liquid 3 containing a decomposition product of the biodegradable resin 1; and a methane fermentation step for treating an organic waste substance 4 containing hardly degradable solid matter and the decomposition liquid 3 at a temperature of 30-60°C in a methane fermentation tank 21 under the presence of methanogen. In the methane fermentation step, the decomposition liquid 3 is added to the organic waste substance 4 so that an organic load in the methane fermentation tank 21 becomes 0.60-5.0 gCODCr / L / day.SELECTED DRAWING: Figure 1

Description

[Technical field]

[0001] The present invention relates to a method for treating a biodegradable resin and a system for treating a biodegradable resin. [Background technology]

[0002] Research and development into materials to replace conventional plastics has been actively conducted in recent years. Among these, biodegradable plastics, whose main component is polylactic acid (PLA) made from renewable resources, are environmentally friendly biomass plastics that can be decomposed by microorganisms. Biomass plastics are used as materials for shopping bags instead of conventional plastics that are difficult to decompose, and because they are highly safe for the human body, they are used as medical materials such as dissolving sutures.

[0003] In recent years, the demand for biofuels has been increasing due to the sudden rise in the price of petroleum resources, and efforts to convert biomass plastics such as polylactic acid made from renewable resources into methane-containing biogas through methane fermentation have once again attracted attention.

[0004] Patent Document 1 discloses a waste treatment system including a decomposition tank for heating resin-containing waste in the presence of an amine compound to hydrolyze it into monomers, and a methane fermentation section for methane fermenting the monomers obtained in the decomposition tank and organic waste containing difficult-to-decompose solids in a fermentation tank to which the monomers and organic waste containing difficult-to-decompose solids are supplied. This method can produce methane without going through a mixed gas mainly containing hydrogen and carbon monoxide, as compared to chemical recycling, which regenerates waste plastics into gases that can be used as chemical raw materials or fuels. In addition, by supplying monomers to a fermentation tank in which methane fermentation of organic waste containing difficult-to-decompose solids is being performed, both methane fermentation of the organic waste containing difficult-to-decompose solids and methane fermentation of the monomers can be achieved in the fermentation tank, enabling efficient methane fermentation.

[0005] Patent Document 2 discloses a method for producing methane gas, which includes a step of decomposing a polylactic acid resin in a decomposition liquid containing a biodegradable enzyme, calcium carbonate, ethanol, and water, and then subjecting the decomposition liquid to methane fermentation. It is described that this method increases the amount of gas generated by about 1.5 times compared to when ethanol is not added. It is also described that the amount of gas generated increases by about 1.3 times compared to when ethanol and calcium carbonate are not added, making this an efficient method for producing methane gas. [Prior art documents] [Patent documents]

[0006] [Patent Document 1] JP 2022-170390 A [Patent Document 2] Patent No. 5696971 Summary of the Invention [Problem to be solved by the invention]

[0007] However, in the waste treatment systems described in Patent Documents 1 and 2, additives such as amine compounds, ethanol, and calcium carbonate are added to the decomposition tank. Therefore, when the decomposition liquid generated in the decomposition tank is added to the fermentation tank, there is a risk that these additives will adversely affect the methanogens in the fermentation tank, reducing the efficiency of methane production.

[0008] An object of the present invention is to provide a method and system for treating biodegradable resin that can produce methane with high efficiency without adding any additives other than the biodegradable resin and water or water vapor. [Means for solving the problem]

[0009] The characteristic configuration of the method for treating biodegradable resin of the present invention is as follows: a decomposition step of mixing waste containing a biodegradable resin with water and hydrolyzing the mixture at a temperature of 120°C or higher in a sealed decomposition tank to obtain a decomposition liquid containing a decomposition product of the biodegradable resin; a methane fermentation step of treating the organic waste containing the hardly decomposable solid content and the decomposition liquid in a methane fermentation tank in which methane bacteria are present at a temperature of 30°C to 60°C, In the methane fermentation step, the decomposition liquid is added to the organic waste so that the organic load in the methane fermentation tank is 0.60 g CODCr / L / day or more and 5.0 g CODCr / L / day or less. The characteristic configuration of the method for treating biodegradable resin of the present invention is as follows: a decomposition step of mixing waste containing a biodegradable resin with water vapor and hydrolyzing the mixture at a temperature of 120° C. or higher in a sealed decomposition tank to obtain a decomposition liquid containing a decomposition product of the biodegradable resin; a methane fermentation step of treating the organic waste containing the hardly decomposable solid content and the decomposition liquid in a methane fermentation tank in which methane bacteria are present at a temperature of 30°C to 60°C, In the methane fermentation step, the decomposition liquid is added to the organic waste so that the organic load in the methane fermentation tank is 0.60 g CODCr / L / day or more and 5.0 g CODCr / L / day or less. The characteristic configuration of the biodegradable resin processing system of the present invention is as follows: a decomposition device for mixing waste containing a biodegradable resin with water and hydrolyzing the mixture in a sealed decomposition tank at a temperature of 120°C or higher to obtain a decomposition liquid containing a decomposition product of the biodegradable resin; a methane fermentation apparatus for treating organic waste containing a hardly decomposable solid content and the decomposition liquid in a methane fermentation tank in which methane bacteria are present at a temperature of 20°C or higher and 60°C or lower; The decomposition liquid is added to the organic waste so that the organic load in the methane fermentation tank is 0.60 g CODCr / L / day or more and 5.0 g CODCr / L / day or less. The characteristic configuration of the biodegradable resin processing system of the present invention is as follows: a decomposition device for mixing waste containing a biodegradable resin with steam and hydrolyzing the mixture at a temperature of 120°C or higher in a sealed decomposition tank to obtain a decomposition liquid containing a decomposition product of the biodegradable resin; a methane fermentation apparatus for treating organic waste containing a hardly decomposable solid content and the decomposition liquid in a methane fermentation tank in which methane bacteria are present at a temperature of 20°C or higher and 60°C or lower; The decomposition liquid is added to the organic waste so that the organic load in the methane fermentation tank is 0.60 g CODCr / L / day or more and 5.0 g CODCr / L / day or less.

[0010] In methane fermentation of organic waste containing difficult-to-decompose solids, such as sewage sludge, the difficult-to-decompose solids are solubilized to convert them into organic matter such as amino acids, sugars, and long-chain fatty acids. These organic matter are then decomposed by anaerobic bacteria into organic compounds such as organic acids and alcohols, and methane is produced from these organic compounds. Here, since the solubilization of the non-degradable solids proceeds slowly, methane fermentation of organic waste containing non-degradable solids is difficult. Therefore, when only organic waste containing non-degradable solids is subjected to methane fermentation in a fermenter, the volume load on the fermenter cannot be increased, resulting in a low volume load and ineffective use of the fermenter. However, according to this characteristic configuration, a mixture containing a biodegradable resin and water or steam can be hydrolyzed to produce a decomposition liquid containing a decomposition product of the biodegradable resin. This decomposition liquid is more likely to undergo methane fermentation than organic waste containing a non-degradable solid content. Therefore, by supplying the decomposition liquid to a methane fermentation tank in which methane fermentation of organic waste containing a non-degradable solid content is being performed, it is possible to achieve both methane fermentation of organic waste containing a non-degradable solid content (production of methane through a solubilization stage of the non-degradable solid content and an acid fermentation stage of the organic matter) and methane fermentation of the decomposition product of the biodegradable resin in the decomposition liquid (production of methane through an acid fermentation stage when the decomposition product is an organic matter, and production of methane based on the organic acid when the decomposition product is an organic acid) in the fermentation tank in which methane bacteria are present. Therefore, methane can be produced more efficiently from the organic waste and the decomposition product in the decomposition liquid than when only organic waste is subjected to methane fermentation. Furthermore, according to this characteristic configuration, since there is no need to add additives other than the biodegradable resin and water or water vapor, methane fermentation is not inhibited by additives and methane can be produced with high efficiency. Furthermore, according to this characteristic configuration, by setting the organic load of the decomposition liquid within the above range, a decrease in pH in the fermentation tank is prevented, and there is no adverse effect on methane fermentation, which is preferable.

[0011] A further characteristic feature of the method for treating a biodegradable resin of the present invention is that in the decomposition step, 0.30 parts by mass or more and 20 parts by mass or less of water or water vapor is mixed with 1.0 part by mass of the biodegradable resin. A further characteristic feature of the biodegradable resin treatment system of the present invention is that 0.30 parts by mass or more and 20 parts by mass or less of water or water vapor is mixed with respect to 1.0 part by mass of the biodegradable resin in the decomposition tank.

[0012] When organic waste or decomposition liquid containing a large amount of water is added to a methane fermentation tank containing methane bacteria, the ratio of methane bacteria in the methane fermentation tank decreases, methane fermentation becomes difficult to proceed, and there is a risk of reducing the amount of digested sludge generated in the methane fermentation tank. In such a case, it is necessary to carry out an operation to reduce the moisture before and after putting the organic waste or decomposition liquid into the methane fermentation tank, which makes the treatment process complicated. According to this characteristic configuration, by using a decomposition liquid obtained by mixing an appropriate amount of water with a biodegradable resin in the decomposition process in the methane fermentation process, methane fermentation can be carried out efficiently without concentrating the decomposition liquid.

[0013] A further characteristic feature of the method for treating biodegradable resin of the present invention is that at least the portion of the decomposition tank that comes into contact with the decomposition liquid is made of austenitic stainless steel. A further characteristic feature of the biodegradable resin processing system of the present invention is that at least the portion of the decomposition tank that comes into contact with the decomposition liquid is made of austenitic stainless steel.

[0014] According to this characteristic configuration, by using acid-resistant austenitic stainless steel as the material for the parts in contact with the decomposition liquid in the decomposition tank, it is possible to prevent the acid derived from the biodegradable resin generated in the decomposition step from corroding the austenitic stainless steel in the decomposition tank, and as a result, it is possible to prevent impurities derived from the decomposition tank from being mixed into the fermentation tank.

[0015] A further characteristic feature of the method for treating a biodegradable resin of the present invention is that the hydrolysis temperature in the decomposition step is 120°C or higher and 170°C or lower. A further characteristic feature of the biodegradable resin processing system of the present invention is that the temperature of hydrolysis in the decomposition tank is 120°C or higher and 170°C or lower.

[0016] According to this characteristic configuration, it is possible to further prevent the acid derived from the biodegradable resin generated in the decomposition step from corroding the austenitic stainless steel of the decomposition tank, thereby preventing impurities from being mixed into the fermentation tank.

[0017] A further characteristic feature of the method for treating a biodegradable resin of the present invention is that the biodegradable resin contains at least one of polybutylene succinate and polyhydroxyalkanoate. A further characteristic feature of the biodegradable resin treatment system of the present invention is that the biodegradable resin contains at least one of polybutylene succinate and polyhydroxyalkanoate.

[0018] According to this characteristic configuration, by using the above-mentioned biodegradable resin, the decomposition products contain acid, making acid fermentation unnecessary, and methane fermentation using the decomposition products can be efficiently carried out.

[0019] A further characteristic feature of the method for treating a biodegradable resin of the present invention is that the biodegradable resin mixed in the decomposition step contains 0.1 part by mass or more of polylactic acid per 1.0 part by mass of a biodegradable resin other than polylactic acid. A further characteristic feature of the biodegradable resin processing system of the present invention is that the biodegradable resin mixed in the decomposition tank contains 0.1 part by mass or more of polylactic acid per 1.0 part by mass of a biodegradable resin other than polylactic acid.

[0020] According to this characteristic configuration, in the decomposition process, the biodegradable resin in the decomposition tank contains a predetermined amount of polylactic acid in addition to biodegradable resins other than polylactic acid, so that the hydrolysis of the biodegradable resins other than polylactic acid can be accelerated, and as a result, the decomposition of the waste can be accelerated. [Brief description of the drawings]

[0021] [Figure 1] FIG. 1 is a schematic diagram of a method for treating a biodegradable resin according to an embodiment of the present invention. [Diagram 2] FIG. 1 is a block flow diagram of a method for treating a biodegradable resin according to an embodiment of the present invention. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0022] The present invention relates to a method for treating biodegradable resin, which includes a decomposition step S101 in which waste material containing a biodegradable resin 1 is mixed with water 2 and hydrolyzed in a decomposition tank 11 at a temperature of 120°C or higher under a pressure of 198 kPa or higher to obtain a decomposition liquid 3 containing a decomposition product of the biodegradable resin, and a methane fermentation step S102 in which organic waste material 4 containing a hardly decomposable solid content and the decomposition liquid 3 are treated at a predetermined temperature in a methane fermentation tank 21 in which methanogens are present. <Biodegradable resin> The biodegradable resin 1 may be any resin having biodegradability, such as chemically synthesized resins, microbial resins, and resins using natural products. Specific examples include aliphatic polyesters, polyvinyl alcohol (PVA), celluloses, and starches. Examples of aliphatic polyesters include polylactic acid (PLA) resin derivatives, polybutylene succinate (PBS) resin derivatives, polycaprolactone (PCL), polyhydroxybutyrate (PHB) and its derivatives, polyethylene adipate (PEA), polyethylene terephthalate succinate (PETS), polyhydroxyalkanoate (PHA), polyglycolic acid (PGA), polytetramethylene adipate, and condensates of diol and dicarboxylic acid. Examples of polyhydroxyalkanoates include polyhydroxypropionic acid, polyhydroxyvaleric acid, poly-4-hydroxybutanoic acid, PHBH (poly(3-hydroxybutyrate-co-3-hydroxyhexanoate)), PHBV (poly(3-hydroxybutyrate-co-3-hydroxyvaleric acid)), 3HB4HB (poly(3-hydroxybutyrate-co-4-hydroxybutyrate)), and PHBP (poly(3-hydroxybutyrate-co-3-hydroxypropionic acid)). Examples of celluloses include methyl cellulose, ethyl cellulose, and acetyl cellulose. These may be used alone, as a copolymer, or in combination of two or more kinds.Examples of components that form the copolymer include polyhydric alcohols such as ethylene glycol, propylene glycol, butanediol, octanediol, dodecanediol, neopentyl glycol, glycerin, pentaerythritol, sorbitan, bisphenol A, and polyethylene glycol; dicarboxylic acids such as succinic acid, adipic acid, sebacic acid, glutaric acid, decanedicarboxylic acid, cyclohexanedicarboxylic acid, terephthalic acid, isophthalic acid, and anthracenedicarboxylic acid; hydroxycarboxylic acids such as glycolic acid, L-lactic acid, D-lactic acid, hydroxypropionic acid, hydroxybutyric acid, hydroxyvaleric acid, hydroxycaproic acid, mandelic acid, and hydroxybenzoic acid; and lactones such as glycolide, caprolactone, butyrolactone, valerolactone, propylolactone, and undecalactone.

[0023] In this embodiment, polybutylene succinate and polyhydroxyalkanoate are used as the biodegradable resin 1. With this configuration, since the decomposition products of these contain acid, acid fermentation is not necessary, and methane fermentation using the decomposition products can proceed efficiently.

[0024] The biodegradable resin 1 may be a mixture of the above-mentioned biodegradable resin, a general-purpose chemical resin, and additives, such as plasticizers, heat stabilizers, light stabilizers, antioxidants, UV absorbers, flame retardants, colorants, pigments, fillers, inorganic fillers, release agents, antistatic agents, fragrances, lubricants, foaming agents, antibacterial and antifungal agents, and nucleating agents.

[0025] The biodegradable resin 1 preferably contains a decomposition accelerator, and preferably contains 0.10 to 20 parts by weight, for example 1.0 to 20 parts by weight, of the decomposition accelerator relative to 100 parts by weight of the biodegradable resin. If too little decomposition promoter is used, it may be difficult to promote the decomposition of the biodegradable resin, and if more than necessary is used, there is a risk that decomposition of the biodegradable resin will begin during the preparation stage of the resin composition or when it is used as a molded article.

[0026] Here, the molded body of the biodegradable resin 1 may be a molded body molded by a known molding method. Known molding methods include injection molding, extrusion molding, sheet molding, vacuum molding, air pressure molding, compression molding, cast molding, etc. The layer structure of the obtained molded body is not limited to a single layer structure but may be a multilayer structure, and the layers constituting the multilayer may be a blend of two or more resins or a mixture with an additive. The multilayer molded body may be molded by co-extrusion molding or co-injection molding using an extruder or injector in a number corresponding to the number of resins, or a film or the like may be attached to the single layer molded body or multilayer molded body in a post-process using an adhesive, thermocompression bonding, extrusion coating, etc.

[0027] The decomposition accelerator preferably releases an acid by hydrolysis, and the acid released is preferably one that has a pH (25°C) of 4.0 or less, particularly 3.0 or less in an aqueous solution or dispersion at a concentration of 0.0050 g / ml, and a polymer that is easily hydrolyzed to release an acid when mixed with water is preferably used. Specific examples include oxalic acid, maleic acid, maleic anhydride, glycolic acid, etc., of which oxalic acid and glycolic acid are preferred. Examples of such decomposition accelerators include polyoxalate, polyethylene maleate, polyglycolic acid, etc. Preferred decomposition accelerators are polyethylene oxalate and polyglycolic acid. These may be copolymers, used alone, or in combination of two or more. Examples of components that form copolymers include polyhydric alcohols such as ethylene glycol, propylene glycol, butanediol, octanediol, dodecanediol, neopentyl glycol, glycerin, pentaerythritol, sorbitan, bisphenol A, and polyethylene glycol; dicarboxylic acids such as succinic acid, adipic acid, sebacic acid, glutaric acid, decanedicarboxylic acid, cyclohexanedicarboxylic acid, terephthalic acid, isophthalic acid, and anthracenedicarboxylic acid; hydroxycarboxylic acids such as glycolic acid, L-lactic acid, D-lactic acid, hydroxypropionic acid, hydroxybutyric acid, hydroxyvaleric acid, hydroxycaproic acid, mandelic acid, and hydroxybenzoic acid; and lactones such as glycolide, caprolactone, butyrolactone, valerolactone, propylolactone, and undecalactone.

[0028] In addition, the above-mentioned decomposition accelerator is preferably one whose glass transition point (Tg) is lower than the deactivation temperature of the enzyme used to decompose the biodegradable resin. By using such an accelerator with a low glass transition point, it is possible to more rapidly promote the decomposition of the biodegradable resin by the enzyme. The glass transition temperature can be measured, for example, using a DSC6220 (differential scanning calorimetry) manufactured by Seiko Instruments Inc.

[0029] The substances contained in the biodegradable resin 1 other than the biodegradable resin are not particularly limited as long as they do not adversely affect methane fermentation. <Water> The water 2 contained in the blend may be tap water, ion-exchanged water, well water, distilled water, ultrapure water, etc. Water 2 may contain impurities as long as they do not interfere with the decomposition reaction of the biodegradable resin and the methane fermentation reaction. Water 2 may be liquid or steam. <Disassembly process> The method for treating a biodegradable resin of the present invention includes a decomposition step S101 in which a mixture containing the above-mentioned biodegradable resin 1 and water 2 is hydrolyzed at a predetermined temperature in a sealed decomposition tank 11 to obtain a decomposition liquid 3 containing a decomposition product of the biodegradable resin 1.

[0030] In the decomposition step S101, when hydrolysis is performed at a predetermined temperature in a sealed decomposition tank 11 using the above-mentioned biodegradable resin 1 and water 2, the water 2 may be supplied as steam and mixed with the biodegradable resin 1 in the decomposition tank 11 for hydrolysis, or the water may be present in the decomposition tank 11 and heated to turn it into steam, which is then mixed with the biodegradable resin 1 for hydrolysis.

[0031] The decomposition products of the biodegradable resin 1 include oligomers and / or monomers that are the basis of the biodegradable resin, which is a polymer, as well as molecules formed by decomposition of decomposition accelerators, general-purpose chemical resins, additives, etc.

[0032] When the biodegradable resin 1 contains a resin that takes longer to hydrolyze than polylactic acid, the time required for hydrolysis can be shortened by including polylactic acid in addition to the resin. That is, in this case, the biodegradable resin 1 contains polylactic acid and a biodegradable resin other than polylactic acid. For example, the biodegradable resin 1 contains polylactic acid and polybutylene succinate, or polylactic acid and polyhydroxyacetic acid. In addition, the biodegradable resin 1 preferably contains 0.1 parts by mass or more of polylactic acid relative to 1.0 parts by mass of the biodegradable resin other than polylactic acid, and if the content of polylactic acid is less than 0.1 parts by mass, the rate of hydrolysis of the biodegradable resin other than polylactic acid becomes relatively slow. In addition, there is no particular upper limit on the content of polylactic acid relative to 1.0 parts by mass of the biodegradable resin other than polylactic acid, but it is preferable to contain 2.0 parts by mass or less of polylactic acid, more preferably 1.5 parts by mass or less of polylactic acid, and even more preferably 1.0 parts by mass or less of polylactic acid.

[0033] As shown in Fig. 1, the decomposition apparatus 10 includes a decomposition tank 11. The decomposition tank 11 includes an inlet section (not shown) into which the biodegradable resin 1 is introduced, an inlet section (not shown) into which water 2 flows in, a temperature control section (not shown) for controlling the temperature inside the decomposition tank 11, and a pressure adjustment section (not shown) for controlling the pressure inside the decomposition tank 11. The pressure inside the decomposition tank 11 is not particularly limited as long as the hydrolysis reaction of the biodegradable resin 1 proceeds, but is preferably 800 kPa or less.

[0034] In the decomposition tank 11, when the biodegradable resin 1 is polylactic acid (PLA) or its derivatives, a decomposition liquid 3 containing lactic acid, a decomposition promoter, etc. is generated by hydrolysis. When the biodegradable resin 1 is polybutylene succinate (PBS) or its derivatives, a decomposition liquid 3 containing succinic acid, 1,4-butanediol, a decomposition promoter, etc. is generated. When the biodegradable resin 1 is polyhydroxybutyrate (PHB) or its derivatives, a decomposition liquid 3 containing 3-hydroxybutyric acid, a decomposition promoter, etc. is generated.

[0035] The material of the decomposition tank 11 is not particularly limited as long as it can promote hydrolysis of the biodegradable resin 1, but it is preferable to use a material with excellent acid resistance such as PTFE, austenitic stainless steel with high acid resistance, etc. Examples of such austenitic stainless steel include SUS316 and SUS316L. In particular, when austenitic stainless steel is used as the material for decomposition tank 11, austenitic stainless steel containing 1.0% to 4.0% molybdenum is more preferable because it has particularly high acid resistance. Examples of such austenitic stainless steel include SUS316 and SUS316L. Furthermore, when austenitic stainless steel is used as the material for decomposition tank 11, it is preferable that the material contains 8.0% or more of nickel. By adopting such a configuration, the corrosion resistance of decomposition tank 11 can be improved. In selecting the decomposition tank 11, it is not necessary that the entire decomposition tank 11 is made of PTFE, austenitic stainless steel containing 1.0% or more of molybdenum, or the like. It is sufficient that at least the material of the part of the decomposition tank 11 that comes into contact with the decomposition liquid is made of PTFE, austenitic stainless steel containing 1.0% or more and 4.0% or less of molybdenum, or the like.

[0036] The biodegradable resin 1 includes those that generate acid by hydrolysis, such as polylactic acid. In addition, the decomposition promoter contained in the biodegradable resin 1 may contain acid, and acid derived from the decomposition promoter may flow into the decomposition liquid in the decomposition step S101. With the above configuration, the material of the decomposition tank 11 is less likely to corrode when the biodegradable resin 1 is decomposed in the decomposition tank 11. As a result, it is possible to suppress impurities from being mixed into the decomposition liquid, and to make it less likely to adversely affect methane fermentation.

[0037] When the biodegradable resin 1 and the water 2 are mixed, the ratio of the biodegradable resin 1 to the water 2 is not particularly limited as long as the decomposition reaction of the biodegradable resin 1 proceeds, but it is preferable that the water content is 0.30 parts by mass or more and 20 parts by mass or less, and more preferably 1.0 parts by mass or more and 15 parts by mass or less, per 1.0 part by mass of the biodegradable resin. If the water content is less than 0.30 parts by mass per 1.0 part by mass of the biodegradable resin, the decomposition reaction of the biodegradable resin 1 may not proceed sufficiently. If the water content is more than 20 parts by mass per 1.0 part by mass of the biodegradable resin, the proportion of the biodegradable resin 1 decreases, and the amount of the biodegradable resin that undergoes methane fermentation in the methane fermentation process described below decreases, and as a result, the amount of methane obtained may also decrease.

[0038] The temperature of the hydrolysis reaction in the decomposition step S101 is preferably 110° C. or higher, and more preferably 120° C. or higher. The upper limit of the temperature of the hydrolysis reaction is preferably 170° C. or lower, and more preferably 150° C. or lower. If the temperature is lower than 110° C., the hydrolysis reaction of the biodegradable resin 1 may not proceed. If the temperature exceeds 160° C., the stainless steel may become susceptible to corrosion.

[0039] Furthermore, when austenitic stainless steel containing 1.0% to 4.0% molybdenum is used as the material for the decomposition tank 11, the temperature of the hydrolysis reaction in the decomposition step S101 is preferably 120° C. to 150° C. By adopting such a configuration, the corrosion rate of the austenitic stainless steel can be made to be corrosion resistant (0.050 to 1.0 mm / year) or completely corrosion resistant (0.050 mm / year or less) as described in the Chemical Industry Handbook (2nd edition), and impurities can be prevented from being mixed into the decomposition liquid.

[0040] Furthermore, when using an austenitic stainless steel containing 1.0% to 4.0% molybdenum, it is more preferable that the temperature of the hydrolysis reaction in the decomposition step S101 be 120°C or higher and 150°C or lower, since this makes it possible to make the corrosion rate of the austenitic stainless steel completely corrosion-resistant (0.050 mm / year or lower) and further suppresses the mixing of impurities into the decomposition liquid.

[0041] In addition, when the biodegradable resin 1 contains a decomposition accelerator, the temperature can be set in consideration of the temperature conditions under which the decomposition accelerator exerts its action. In that case, for example, the following can be used as the standard: (glass transition temperature of the decomposition accelerator-5.0°C) < decomposition temperature < upper limit of the temperature exhibiting enzyme activity. For example, when polyethylene oxalate is used as the decomposition accelerator, decomposition can be promoted under a temperature condition of, for example, 37°C, and when polyglycolic acid is used as the decomposition accelerator, decomposition can be promoted by setting the temperature at, for example, 45°C. In addition, the time for decomposing a biodegradable resin (2.0 cm x 2.0 cm, thickness 100 μm) in the decomposition liquid is preferably 1 to 10 days. More preferably, it is 1 to 7 days. Even more preferably, it is within 4 days. In addition, there are no particular limitations on the stirring conditions of the decomposition liquid, as long as the decomposition liquid is stirred uniformly.

[0042] It is considered that the above-mentioned process can achieve a high decomposition rate of the biodegradable resin 1, suppress the formation of aggregated precipitates during the decomposition of the biodegradable resin 1, and efficiently produce oligomers and / or monomers. The obtained oligomers can be decomposed into monomers. The oligomers referred to here are polymers in which monomers are bonded, such as dimers, trimers, and tetramers. The oligomers and / or monomers may have straight chains or side chains. The oligomers and / or monomers may react with additives such as neutralizers, buffer solutions, medium components, and nutrients, and take the form of a reaction product between the oligomers and / or monomers and the additives.

[0043] The biodegradable resin 1 may be a molded product of the biodegradable resin. In this case, it may contain general-purpose chemical resins, additives, decomposition accelerators, resins blended when molding the biodegradable resin 1, adhesives, films, etc. contained in the biodegradable resin 1. In addition, when the molded product of the biodegradable resin 1 is a container such as a plate or cup, a straw, a bag, a package, etc. whose main component is the biodegradable resin 1, it may be organic waste such as food and drink or waste with moisture attached to the surface of these.

[0044] The decomposition liquid 3 may contain substances other than the biodegradable resin 1, and such substances can be removed before being put into the methane fermentation tank 21, or the substances can be removed while methane fermentation is progressing in the methane fermentation tank 21, or the substances can be removed from the treated liquid after the fermentation process. <Methane fermentation process> The method for treating biodegradable resins of the present invention further includes a methane fermentation step S102 in which organic waste 4 containing difficult-to-decompose solids and the decomposition liquid 3 obtained in the decomposition step S101 are treated at a predetermined temperature in a methane fermentation tank 21 in which methanogens are present.

[0045] 1, the methane fermentation apparatus 20 includes a methane fermentation tank 21. The methane fermentation tank 21 includes an addition unit (not shown) that adds the decomposition liquid 3 obtained in the decomposition step S101 to the methane fermentation tank 21, an organic waste supply unit (not shown) that supplies organic waste 4 containing a hard-to-decompose solid content to the methane fermentation tank 21, and a temperature adjustment unit (not shown) that can adjust and keep the temperature inside the methane fermentation tank 21 warm. The methane fermentation tank 21 may also include a pressure adjustment unit (not shown) that adjusts the pressure inside the methane fermentation tank 21, a methane bacteria supply unit (not shown) that supplies methane bacteria into the methane fermentation tank 21, and an agitation unit (not shown) that mixes and agitates the decomposition liquid 3 and the organic waste 4 in the methane fermentation tank 21.

[0046] The organic waste 4 containing a hard-to-decompose solid content means waste containing one or more types of solid organic matter. In this embodiment, the organic waste is sewage sludge.

[0047] The method of subjecting the decomposition liquid 3 obtained in the decomposition step S101 to the methane fermentation step S102 may be a mode in which methane bacteria (including culture solution if cultured) are directly added to the decomposition liquid 3 via a methane bacteria supply unit, or a mode in which methane bacteria are first cultured in a methane fermentation tank or the like and a part of the decomposition liquid 3 is added via an addition unit. In addition to the batch system, a fed-batch system in which the decomposition liquid 3 or a culture solution of methane bacteria is appropriately added as necessary, or a continuous system in which the decomposition liquid 3 is continuously supplied may be used.

[0048] The decomposition liquid 3 is preferably added to the organic waste 4 in the methane fermentation tank 21 so that the organic load in the methane fermentation tank 21 is 0.60 gCODCr / L / day or more and 5.0 gCODCr / L / day or less. By adding the decomposition liquid within this range to the methane fermentation tank 21, the pH in the methane fermentation tank 21 can be appropriately maintained. As a result, the methanation reaction can proceed with high efficiency.

[0049] CODCr is an index showing the amount of organic matter in water, and is the amount of oxygen when potassium dichromate oxidizes a target oxidizable substance. In this embodiment, the organic load substantially corresponds to the oligomers and / or monomers that are the base of the biodegradable resin, which is a polymer, among the decomposition products of the biodegradable resin 1, and is more precisely calculated by the following formula (1).

[0050] Organic load = Decomposition liquid input amount (mL / L / day) x lactic acid concentration (%) x 1.06 (gCODCr / g lactic acid)...Equation (1) The specific gravity of the decomposition liquid was set to 1.0.

[0051] The methane fermentation apparatus 20 includes a methane fermentation tank 21, in which the organic waste 4 (sewage sludge in this embodiment) and the decomposition product of the biodegradable resin 1 are fermented to produce methane. Specifically, when the subject of methane fermentation is sewage sludge, the organic matter obtained by solubilizing the hard-to-decompose solids is fermented with acid, and methane is produced from the organic acid thus obtained. On the other hand, when the subject of methane fermentation is lactic acid, succinic acid, or 3-hydroxybutyric acid, methane is produced from the lactic acid, succinic acid, or 3-hydroxybutyric acid. That is, according to the methane fermentation apparatus 20, methane fermentation of sewage sludge and methane fermentation of lactic acid, succinic acid, or 3-hydroxybutyric acid can be carried out in parallel.

[0052] Here, since sewage sludge contains a hard-to-decompose solid content, in order to obtain methane by methane fermentation of the sewage sludge, it is necessary to go through a stage of solubilization of the hard-to-decompose solid content, which has a slow progress rate. Therefore, when methane fermentation of only sewage sludge is performed in the methane fermentation tank 21, the volume load on the methane fermentation tank 21 is low. On the other hand, in the methane fermentation of the decomposition liquid 3 obtained by hydrolysis in the decomposition device 10, the stage of solubilization of the hard-to-decompose solid content is not required, regardless of whether the decomposition liquid 3 is an organic matter or an organic acid. Therefore, in the methane fermentation device 20 of this embodiment, the decomposition liquid 3 is supplied to the methane fermentation tank 21 in which the methane fermentation of sewage sludge is performed in a state where the volume load on the methane fermentation tank 21 is low, so that the methane fermentation of the sewage sludge and the methane fermentation of the decomposition product of the biodegradable resin 1 can be compatible as described above.

[0053] In this way, methane can be efficiently produced from sewage sludge and monomers by effectively utilizing the methane fermentation apparatus 20, which has a low volume load on the methane fermentation tank 21 when only sewage sludge is fermented. Furthermore, when the decomposition product is an organic acid, not only solubilization but also acid fermentation is unnecessary, compared to methane fermentation of only sewage sludge, and methane can be produced more efficiently.

[0054] In this embodiment, when the decomposition liquid is added to the sewage sludge (organic waste 4) in the methane fermentation tank 21, methane fermentation is performed under conditions where the volume load in the methane fermentation tank 21 is 0.60 g CODCr / L / day or more and 5.0 g CODCr / L / day or less.

[0055] In the methane fermentation step S102 in which the decomposition liquid 3 is subjected to methane fermentation, the method of methane fermentation is not particularly limited and may be a wet method or a dry method. Those skilled in the art can appropriately set the conditions, etc. using their general knowledge.

[0056] Methanogens are archaea that synthesize methane under anaerobic conditions, and are not particularly limited as long as they are used in the art for methane fermentation. For example, facultative anaerobes include hydrocarbon decomposition bacteria such as those of the genus Clostridium, Bacillus, and Staphylococcus, fiber decomposition bacteria such as Plecridium spumarum and Caduceus cellosaehydrogenicus, protein decomposition bacteria such as those of the genus Clostridium, Proteus, Bacterium, and Bacillus, and Clostridium kluberii. Examples of essential anaerobic bacteria include fat-decomposing bacteria such as Methanococcus, Methanobacterium, and Methanosarcina. One or more types of these methane fermentation bacteria can be used, and as methane fermentation continues, one or more of these methane fermentation bacteria act depending on the environment to progress the reaction.

[0057] In the above methane fermentation step S102, the fermentation liquid may contain other organic substances for carrying out methane fermentation, such as food processing residues or food waste, as well as nutrients for supporting the growth and activity of methanogens. In order to increase the efficiency of methane fermentation of the organic substances, pretreatment such as acid decomposition, alkali decomposition, thermal decomposition, steam decomposition, enzymatic decomposition, decomposition by microorganisms other than methane bacteria, etc. may be carried out before methane fermentation, and a combination of these pretreatments may also be carried out.

[0058] Methane fermentation can be carried out while stirring appropriately with a stirring unit as necessary. The temperature of methane fermentation is not particularly limited, and a temperature suitable for fermentation can be appropriately set by a person skilled in the art, and can be, for example, 20 to 80°C, preferably 35 to 50°C, for example, 37°C. In this case, it is preferable to carry out fermentation by using a thermostatic chamber to maintain an appropriate temperature.

[0059] Furthermore, the treatment time for acid decomposition treatment (acid fermentation) and methane fermentation can be appropriately set by a person skilled in the art depending on the amount of decomposed biodegradable resin, the amount of decomposition liquid, the type of methane bacteria used, and the fermentation temperature; however, it can be, for example, about 1 to 30 days, preferably 1 to 20 days, and more preferably 1 to 10 days.

[0060] When methane fermentation is performed, it is possible to simultaneously use other organic biodegradation methods such as hydrogen fermentation, ethanol fermentation, lactic acid fermentation, and acetone-butanol fermentation. For example, when hydrogen fermentation is used in combination, it is possible to take the form of two-stage hydrogen and methane fermentation, and hydrogen and methane can be efficiently recovered by subjecting the organic acids generated by hydrogen fermentation, such as acetic acid, butyric acid, propionic acid, and lactic acid, to methane fermentation.

[0061] The methane gas produced often contains various impurities, and can be purified as necessary. Gas purification methods include desulfurization and denitrification, and these processes can be carried out using a gas purification tank or the like, allowing high-purity methane gas to be obtained.

[0062] <Biodegradable resin treatment system> The biodegradable resin treatment system A of the present invention includes the above-mentioned decomposition apparatus 10 and methane fermentation apparatus 20. The decomposition apparatus 10 has a decomposition tank 11, in which waste material containing a biodegradable resin 1 and water 2 are added and mixed. The decomposition tank 11 is sealed, and the contents are hydrolyzed at a decomposition temperature of 120°C or higher to obtain a decomposition liquid 3 containing a decomposition product of the biodegradable resin 1.

[0063] The methane fermentation apparatus 20 has a methane fermentation tank 21, in which methane bacteria are present, and treats organic waste 4 containing hard-to-decompose solids and decomposition liquid 3 at a temperature of 30° C. to 60° C. At this time, the decomposition liquid 3 is added to the organic waste 4 so that the organic load in the methane fermentation tank 21 is 0.60 g CODCr / L / day to 5.0 g CODCr / L / day.

[0064] In the biodegradable resin treatment system A of the present invention, it is preferable to mix 0.30 parts by mass or more and 20 parts by mass or less of water 2 with respect to 1.0 part by mass of biodegradable resin in the decomposition tank 11 .

[0065] By configuring it in this manner, methane fermentation can be performed using a decomposition liquid obtained by mixing an appropriate amount of water with the biodegradable resin, so that methane fermentation can proceed efficiently without the need to concentrate the decomposition liquid.

[0066] In the decomposition device 10, the hydrolysis temperature is preferably 120° C. or higher and 170° C. or lower. This configuration can further prevent the acid derived from the biodegradable resin from corroding the austenitic stainless steel in the decomposition tank. As a result, it is possible to prevent impurities from being mixed into the fermentation tank.

[0067] The recovered methane gas can be reused for power generation, fuel production, and polymer synthesis. When hydrogen fermentation, ethanol fermentation, lactic acid fermentation, acetone-butanol fermentation, etc. are used in combination, it is possible to obtain the respective fermentation products at the same time, and these can also be reused. The obtained methane gas can be recovered by normal methods and reused according to the purpose. For example, when using it for power generation, it can be stored in a gas holder, or it can be directly input into a fuel cell or gas generator. In addition, the residue and wastewater generated in the fermentation process can be reused by converting them into fertilizer and animal feed.

[0068] Examples of the present invention will be described below, but the present invention is not limited to these.

[0069] <Hydrolysis treatment of polylactic acid> (Test Example 1) 1.0 g of polylactic acid pellets (Mitsui Chemicals, LACEA H-100J) and 19 g of water were placed in a PTFE sample digestion container (HU-25, San-Ai Science Co., Ltd.), and the container was closed with a lid to create a tight seal. Then, hydrolysis was performed at 120°C for 48 hours. The concentration of the resulting aqueous lactic acid solution was measured using high performance liquid chromatography.

[0070] (Test Example 2) The test and measurements were carried out under the same conditions as in Test Example 1, except that the hydrolysis temperature was set to 130°C.

[0071] (Test Example 3) The test and measurements were carried out under the same conditions as in Test Example 1, except that the hydrolysis temperature was set to 100°C.

[0072] (Test Example 4) The test and measurements were carried out under the same conditions as in Test Example 1, except that the hydrolysis temperature was set to 110°C.

[0073] The results of Test Examples 1-4 are shown in Table 1. In Test Examples 1 and 2, the lactic acid concentration of the decomposition liquid was 6.3%, while in Test Examples 3 and 4, the lactic acid concentration of the decomposition liquid was 0.0%. From these results, it is understood that the hydrolysis of polylactic acid proceeds in Test Examples 1 and 2, but does not proceed in Test Examples 3 and 4. Therefore, in order to hydrolyze polylactic acid, the temperature needs to be 120° C. or higher.

[0074] [Table 1]

[0075] <Relationship between organic load of digested liquid and methane production> Example 1 A mixture was obtained by placing 4.0 g of polylactic acid pellets (LACEA H-100J, manufactured by Mitsui Chemicals, Inc.) and 16 g of water in a PTFE sample decomposition container (HU-25, manufactured by San-Ai Scientific Co., Ltd.).The container was then sealed with a lid and hydrolysis treatment was carried out at 140°C for 48 hours to obtain a decomposition liquid with a lactic acid concentration of 24.1%.

[0076] Next, 2.0 L of high-temperature anaerobic digestion sludge collected from a general sewage treatment plant was placed into a 3.0 L jar fermenter (NBC-3000, manufactured by Mitsuwa Frontech Co., Ltd.), and the headspace was purged for 5 minutes with a nitrogen flow rate of 1.0 L / min. After that, the lid was closed and the tank was heated to 55°C to construct a lab-scale methane fermentation tank.

[0077] The methane fermentation tank was operated under these conditions for one month, and after confirming that the methane generation rate had stabilized at 0.90 L / L / day, the concentrated sludge was added at 100 mL / day, and a decomposition liquid with a lactic acid concentration of 24.1% was added so that the organic load was 4.3 g CODCr / L / day. The excess sludge was withdrawn so that the digested sludge volume in the digestion tank was maintained at 2.0 L. The methane fermentation tank was operated for one month, and the methane generation rate and the average pH value of the digested sludge in the methane fermentation tank were measured for the last five days. A compact pH meter (LAQUAtwin pH-11B, manufactured by Horiba, Ltd.) was used as the pH measuring device. The results are shown in Table 2.

[0078] Example 2 Methane fermentation was carried out under the same conditions as in Example 1, except that a decomposition liquid with a lactic acid concentration of 24.1% was added so that the organic load was 2.0 g CODCr / L / day. The results are shown in Table 2.

[0079] Example 3 Methane fermentation was carried out under the same conditions as in Example 1, except that a decomposition liquid with a lactic acid concentration of 24.1% was added so that the organic load was 0.60 g CODCr / L / day. The results are shown in Table 2.

[0080] Example 4 Methane fermentation was carried out under the same conditions as in Example 1, except that a decomposition liquid with a lactic acid concentration of 24.1% was added so that the organic load was 0.30 g CODCr / L / day. The results are shown in Table 2.

[0081] Comparative Example 1 Methane fermentation was carried out under the same conditions as in Example 1, except that a decomposition liquid with a lactic acid concentration of 24.1% was added so that the organic load was 5.1 g CODCr / L / day. The results are shown in Table 2.

[0082] (Reference example 1) As a reference example, methane fermentation was carried out under the same conditions as in Example 1, except that the organic load was set to 0.0 g CODCr / L / day, i.e., only digested sludge was used without adding the decomposition liquid. The results are shown in Table 2.

[0083] [Table 2] From the above results, when the organic load exceeded 5.0 gCODCr / L / day, the amount of methane generated decreased, falling below the amount generated before the digestion liquid was added. This is thought to be because the organic matter decomposition activity of the bacteria in the digested sludge decreased as the pH decreased.

[0084] It is also clear that in order to increase the amount of methane generated to 1.5 times or more the amount generated in Reference Example 1 in which only sewage sludge was added, the decomposition liquid should be added at an organic load of 0.60 g CODCr / L / day or more.

[0085] <Relationship between the ratio of digested liquid to water and the evaporation residue of digested sludge> Example 5 In the same manner as in Example 1, a decomposition liquid with a lactic acid concentration of 24.1% was obtained.

[0086] Next, 2.0 L of high-temperature anaerobic digestion sludge collected from a general sewage treatment plant was placed into a 3.0 L jar fermenter (NBC-3000, manufactured by Mitsuwa Frontech Co., Ltd.), and the headspace inside the jar fermenter was purged with nitrogen at a flow rate of 1.0 L / min for 5 minutes.The lid was then closed and the vessel was heated to 55°C to construct a lab-scale methane fermentation tank.

[0087] In order to ensure that the retention time in the methane fermentation tank was 20 days, 100 mL of concentrated sludge from the same sewage treatment plant was added to the tank, and 100 mL of excess sludge was withdrawn. The methane fermentation tank was operated under these conditions for one month, and after confirming that the evaporation residue ratio of the digested sludge in the methane fermentation tank was stable at 4.0% and that the methane generation rate was stable at 0.90 L / L / day, 100 mL of concentrated sludge was added to the methane fermentation tank, and the amount of decomposition liquid with a lactic acid concentration of 24.1% was adjusted so that the organic load was 0.60 gCODCr / L / day. The withdrawal of excess sludge was adjusted so that the digested sludge volume in the digestion tank was maintained at 2.0 L. The methane fermentation tank was operated for one month, and the evaporation residue ratio of the digested sludge was measured. The results are shown in Table 3.

[0088] Example 6 Hydrolysis was performed under the conditions of adding 0.50 g of polylactic acid pellets (manufactured by Mitsui Chemicals, Inc., LACEA H-100J) and 19.5 g of water to a PTFE sample decomposition container (manufactured by San-Ai Science Co., Ltd., HU-25), i.e., mixing 39 parts by mass of water for 1.0 part by mass of polylactic acid (biodegradable resin), to obtain a decomposition liquid with a lactic acid concentration of 3.1%. Thereafter, methane fermentation was performed under the same conditions as in Example 5, except that the decomposition liquid with a lactic acid concentration of 3.1% was added to the methane fermentation tank by adjusting the amount of the decomposition liquid input so that the organic load in the methane fermentation tank was 0.60 g CODCr / L / day. The results are shown in Table 3.

[0089] Example 7 Hydrolysis was performed under the conditions of adding 1.0 g of polylactic acid pellets (manufactured by Mitsui Chemicals, Inc., LACEA H-100J) and 19 g of water to a PTFE sample decomposition container (manufactured by San-Ai Science Co., Ltd., HU-25), i.e., mixing 19 parts by mass of water for 1.0 part by mass of polylactic acid (biodegradable resin), to obtain a decomposition liquid with a lactic acid concentration of 5.8%. Thereafter, hydrolysis and methane fermentation were performed under the same conditions as in Example 5, except that the decomposition liquid with a lactic acid concentration of 5.8% was added to the methane fermentation tank by adjusting the amount of the decomposition liquid input so that the organic load in the methane fermentation tank was 0.60 g CODCr / L / day. The results are shown in Table 3.

[0090] Example 8 Hydrolysis was performed under the conditions of adding 2.0 g of polylactic acid pellets (manufactured by Mitsui Chemicals, Inc., LACEA H-100J) and 18 g of water to a PTFE sample decomposition container (manufactured by San-Ai Science Co., Ltd., HU-25), i.e., mixing 9.0 parts by mass of water for 1.0 part by mass of polylactic acid (biodegradable resin), to obtain a decomposition liquid with a lactic acid concentration of 11.9%. Thereafter, hydrolysis and methane fermentation were performed under the same conditions as in Example 5, except that the decomposition liquid with a lactic acid concentration of 11.9% was added to the methane fermentation tank by adjusting the amount of the decomposition liquid input so that the organic load in the methane fermentation tank was 0.60 g CODCr / L / day. The results are shown in Table 3.

[0091] Example 9 Hydrolysis was performed under the conditions of adding 10 g of polylactic acid pellets (manufactured by Mitsui Chemicals, Inc., LACEA H-100J) and 10 g of water to a PTFE sample decomposition container (manufactured by San-Ai Science Co., Ltd., HU-25), i.e., mixing 1.0 part by mass of water for 1.0 part by mass of polylactic acid (biodegradable resin), to obtain a decomposition liquid with a lactic acid concentration of 60.5%. Thereafter, hydrolysis and methane fermentation were performed under the same conditions as in Example 5, except that the decomposition liquid with a lactic acid concentration of 60.5% was added to the methane fermentation tank by adjusting the amount of the decomposition liquid input so that the organic load in the methane fermentation tank was 0.60 g CODCr / L / day. The results are shown in Table 3.

[0092] Example 10 Hydrolysis was performed under the conditions of adding 15 g of polylactic acid pellets (manufactured by Mitsui Chemicals, Inc., LACEA H-100J) and 5.0 g of water to a PTFE sample decomposition container (manufactured by San-Ai Science Co., Ltd., HU-25), i.e., mixing 0.30 parts by mass of water for 1.0 parts by mass of polylactic acid (biodegradable resin), to obtain a decomposition liquid with a lactic acid concentration of 92.3%. Thereafter, hydrolysis and methane fermentation were performed under the same conditions as in Example 5, except that the decomposition liquid with a lactic acid concentration of 92.3% was added to the methane fermentation tank by adjusting the amount of the decomposition liquid input so that the organic load in the methane fermentation tank was 0.60 g CODCr / L / day. The results are shown in Table 3.

[0093] (Reference example 1) For comparison, as a reference example, methane fermentation was carried out under the same conditions as in Example 5, except that the organic load was set to 0.0 g CODCr / L / day, i.e., only digested sludge was used without adding the decomposition liquid. The results are shown in Table 3.

[0094] [Table 3] It has been found that if the amount of water is 0.30 to 20 parts by mass per 1.0 part by mass of biodegradable resin, the concentration of the digested sludge will not decrease even if the decomposition liquid is added to the methane fermentation tank without being concentrated, i.e., the progress of methane fermentation will not be hindered.

[0095] In Example 6, the ratio of the evaporation residue in the digested sludge was 3.5%, which was lower than in other Examples. Since continued operation may reduce the amount of methanogens in the digested sludge, this is not suitable for long-term operation, but it shows that for short-term operation, this condition allows for highly efficient methane production without adding any additives other than biodegradable resin and water.

[0096] <<Measurement of corrosion rate>> Example 11 20 mL of the decomposition solution with a lactic acid concentration of 24.1% obtained in Example 1 was added to a PTFE sample decomposition container (HU-25, manufactured by San-Ai Scientific Co., Ltd.). Next, a SUS304 test piece with a length of 20 mm, width of 15 mm, and thickness of 2.5 mm was immersed, the lid was closed so as to be in a sealed state, and heat treatment was performed at 120°C for 30 days. After 30 days, the corrosion rate (mm / year) was calculated from the weight loss of the test piece. The results are shown in Table 4.

[0097] Example 12 Except for the fact that the material of the test piece was SUS316, the corrosion rate (mm / year) was calculated under the same conditions as in Example 11. The results are shown in Table 4.

[0098] (Example 13) Except for the fact that the material of the test piece was SUS316L, the corrosion rate (mm / year) was calculated under the same conditions as in Example 11. The results are shown in Table 4.

[0099] Example 14 The corrosion rate (mm / year) was calculated under the same conditions as in Example 11, except that the material of the test piece was SUS316 and the temperature was 140° C. The results are shown in Table 4.

[0100] Example 15 The corrosion rate (mm / year) was calculated under the same conditions as in Example 11, except that the material of the test piece was SUS316 and the temperature was 160° C. The results are shown in Table 4.

[0101] [Table 4] The above results show that regardless of which stainless steel is used, it will be classified as completely corrosion-resistant (0.050 mm / year or less) or corrosion-resistant (0.050 mm / year or more and 0.10 mm / year or less) as described in the Chemical Engineering Handbook (2nd edition), and therefore there will be no problems with corrosion resistance if these stainless steels are used as the material for the decomposition tank.

[0102] It is also clear that SUS316 and SUS316L, which are austenitic stainless steels containing 1.0% or more of molybdenum, have better corrosion resistance than SUS304.

[0103] Furthermore, if the treatment temperature for SUS316 is 150°C or less, the corrosion rate of the stainless steel is 0.050 mm / year or less, and it is classified as completely corrosion resistant.

[0104] These results show that using SUS304, SUS316 or SUS316L as the materials for the decomposition tank and hydrolyzing the biodegradable resin at a temperature between 120°C and 170°C reduces corrosion of the decomposition tank and prevents impurities from the decomposition tank from being mixed into the decomposition liquid.

[0105] Furthermore, when SUS316 or SUS316L is used as the material for the digestion tank, if the hydrolysis temperature is set to 120°C or higher and 150°C or lower, the corrosion rate of the stainless steel is 0.050 mm / year or less and it is classified as completely corrosion-resistant. This means that hydrolysis can be carried out at a high temperature, which is preferable in terms of the efficiency of methane fermentation.

[0106] <Relationship between types of biodegradable resins and methane production> Example 16 Hydrolysis and methane fermentation of polybutylene succinate were carried out under the same conditions as in Example 2, except that 4.0 g of polylactic acid was replaced with 4.0 g of polybutylene succinate pellets (Showa Polymer Co., Ltd., Bionolle #1001), and the amount of methane generated over the final 5 days was measured. The results are shown in Table 5.

[0107] (Example 17) Hydrolysis and methane fermentation of polyhydroxybutyric acid were carried out under the same conditions as in Example 2, except that 4.0 g of polylactic acid was replaced with 4.0 g of polyhydroxybutyric acid powder (Biosoft 915, manufactured by Sumitomo Pharma Food & Chemical Co., Ltd.), and the amount of methane generated over the final 5 days was measured. The results are shown in Table 5.

[0108] [Table 5] From the above results, it is clear that methane can be produced by methane fermentation even when the decomposition liquid of biodegradable resins such as polybutylene succinate or polyhydroxybutyrate is subjected to methane fermentation.

[0109] (Example 18) 2g of polylactic acid pellets (Mitsui Chemicals, LACEA H-100J), 2g of polyhydroxybutyric acid powder (Sumitomo Pharma Food & Chemicals, Biosoft 915), and 10g of water were placed in a PTFE sample decomposition container (San-Ai Science, HU-25), the lid was closed to seal the container, and hydrolysis treatment was performed at 160°C for 5 or 10 hours. The dissolved residue was separated using a metal mesh with a mesh size of 106 μm, and the weight was measured after drying at 40°C for 16 hours. The results are shown in Table 6.

[0110] (Example 19) The weight of the residue after drying was measured under the same conditions as in Example 18, except that the amount of polylactic acid pellets added was 1 g and the amount of polyhydroxybutyric acid powder added was 3 g. The results are shown in Table 6.

[0111] (Example 20) The weight of the residue after drying was measured under the same conditions as in Example 18, except that the amount of polylactic acid pellets added was 0.5 g and the amount of polyhydroxybutyric acid powder added was 3.5 g. The results are shown in Table 6.

[0112] Example 21 The weight of the residue after drying was measured under the same conditions as in Example 18, except that the amount of polylactic acid pellets added was 0.2 g and the amount of polyhydroxybutyric acid powder added was 3.8 g. The results are shown in Table 6.

[0113] Example 22 The weight of the residue after drying was measured under the same conditions as in Example 18, except that no polyhydroxybutyric acid powder was added and 2 g of polybutylene succinate was added. The results are shown in Table 6.

[0114] (Example 23) The weight of the residue after drying was measured under the same conditions as in Example 18, except that 1 g of polyhydroxybutyric acid powder and 1 g of polybutylene succinate were added. The results are shown in Table 6.

[0115] Example 24 The weight of the residue after drying was measured under the same conditions as in Example 18, except that the treatment temperature was 140° C. The results are shown in Table 6.

[0116] (Example 25) The weight of the residue after drying was measured under the same conditions as in Example 18, except that no polyhydroxybutyric acid powder was added, 2 g of polybutylene succinate was added, and the treatment temperature was 140° C. The results are shown in Table 6.

[0117] (Example 26) Synthesis of biodegradable resin PHBH and decomposition of PHBH A medium (pH 7.0) was prepared by adding 5 g of meat extract, 5 g of peptone, 2 g of yeast extract, 0.5 g of KH2PO4, 1.5 g of K2HPO4, 0.1 g of MgSO4·7H2O, and water to a total volume of 1 liter, and Aeromonas hydrophila OL-338 strain was added to this medium and cultured with shaking at 30°C for 48 hours. After the culture was completed, the culture broth was centrifuged to collect the bacterial cells.

[0118] Next, 25.4 g of β-hydroxycaproic acid, 1.5 g of KH2PO4, 1.5 g of K2HPO4, 0.25 g of MgSO4·7H2O, 0.5 g of Tween85, and water were added to prepare a medium (pH 7.0) to make a total volume of 1 liter, and the entire amount of the above-mentioned bacteria was added to this medium and cultured with shaking at 30°C for 24 hours. After the culture was completed, the bacteria were washed with distilled water and methanol, and dried under reduced pressure to obtain dried bacteria. The dried bacteria were extracted with chloroform at 50°C for 2 hours. After the bacteria were removed, 10 times the amount of methanol was added to the chloroform extract, and poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (biodegradable resin PHBH) with a ratio of 3-hydroxybutyrate:3-hydroxyhexanoate = 51:49 was precipitated and collected. Decomposition of biodegradable resin PHBH The weight of the residue after drying was measured under the same conditions as in Example 18, except that no polyhydroxybutyric acid powder was added and 2 g of PHBH was added. The results are shown in Table 6.

[0119] Fermentation of PHBH solution The CODcr of the resulting PHBH solution was measured, and 30 ml of high-temperature anaerobic digestion sludge and the PHBH solution were added to a 50 ml vial (Maruemu Co., Ltd.) so that the amount of COD was 0.05 g COD. The gas phase was purged with nitrogen, the lid was closed, and the mixture was shake-cultured at 55°C and 50 rpm for 20 days, and the amount of biogas generated was measured. The amount of biogas generated was 34 ml. This is almost the same amount of biogas as when 0.05 g COD of PLA solution was added and the mixture was shake-cultured for 20 days in the same manner as above, generating 35 ml of biogas.

[0120] Example 27 <Hydrolysis by water vapor> 4g of water was placed in a PTFE sample decomposition container (HU-25, San-Ai Scientific Co., Ltd.), and then 8g of 1 / 8-inch PTFE balls were placed in the container. 2g of polylactic acid pellets (LACEA H-100J, Mitsui Chemicals, Inc.) and 2g of PBS pellets (Bionolle, Showa Polymer Co., Ltd.) were placed on top of the balls. The container was then closed with a lid to create an airtight seal, and hydrolysis treatment was carried out at 160°C for 5 or 10 hours. The remaining residue was separated using a metal mesh with 106μm openings, and the weight was measured after drying at 40°C for 16 hours. The results are shown in Table 6.

[0121] Example 17 In Example 2, 4.0 g of polyhydroxybutyric acid powder (Biosoft 915, manufactured by Sumitomo Pharma Food & Chemical Co., Ltd.) was used instead of 4.0 g of polylactic acid, and hydrolysis of polyhydroxybutyric acid was carried out under the same conditions as in Example 2, and the degree of decomposition was confirmed after 5 hours and 10 hours.

[0122] Example 16 In Example 2, 4.0 g of polylactic acid was replaced with 4.0 g of polybutylene succinate pellets (Showa Polymer Co., Ltd., Bionolle #1001). Hydrolysis of polybutylene succinate was carried out under the same conditions as in Example 2, and the degree of decomposition was confirmed after 5 hours and 10 hours.

[0123] From the above comparative test, it was confirmed that the addition of PLA caused hydrolysis to proceed more rapidly.

[0124] [Table 6] In Examples 17 and 16 in Table 6, it was confirmed that after 10 hours of decomposition treatment, 50% or more of the resin input was not decomposed, but after 48 hours of decomposition treatment, all of the resin was dissolved.

[0125] In Table 6, for the degree of decomposition after 5 hours of treatment and after 10 hours of treatment, if the value of (weight of residue) ÷ 4g of input amount is less than 10%, it is marked with a 〇, if it is 10% or more but less than 50%, it is marked with a △, and if it is 50% or more, it is marked with an ×.

[0126] Although the embodiments and examples of the present disclosure have been described above, it is intended from the outset that the configurations of the above-described embodiments and examples may be appropriately combined or modified in various ways.

[0127] The embodiments and examples disclosed herein are illustrative in all respects and should not be considered as limiting. The scope of the present invention is indicated by the claims, not by the embodiments and examples described above, and is intended to include the meaning equivalent to the claims and all modifications within the scope. [Industrial Applicability]

[0128] INDUSTRIAL APPLICABILITY The present invention can be used for a method and a system for treating biodegradable resin. [Explanation of symbols]

[0129] 1 Biodegradable resin 2 water 3 Decomposition liquid 4. Organic waste 10 Decomposition equipment 11 Decomposition tank 20 Methane fermentation equipment 21 Methane fermentation tank A Biodegradable resin processing system S101 Decomposition process S102 Methane fermentation process

Claims

1. a decomposition step of mixing waste containing a biodegradable resin with water and hydrolyzing the mixture at a temperature of 120° C. or higher in a sealed decomposition tank to obtain a decomposition liquid containing a decomposition product of the biodegradable resin; a methane fermentation step of treating the organic waste containing the hardly decomposable solid content and the decomposition liquid in a methane fermentation tank in which methane bacteria are present at a temperature of 30° C. or higher and 60° C. or lower, In the methane fermentation step, the decomposition liquid is added to the organic waste so that the organic load in the methane fermentation tank is 0.60 g CODCr / L / day or more and 5.0 g CODCr / L / day or less.

2. a decomposition step of mixing waste containing a biodegradable resin with water vapor and hydrolyzing the mixture at a temperature of 120° C. or higher in a sealed decomposition tank to obtain a decomposition liquid containing a decomposition product of the biodegradable resin; a methane fermentation step of treating the organic waste containing the hardly decomposable solid content and the decomposition liquid in a methane fermentation tank in which methane bacteria are present at a temperature of 30° C. or higher and 60° C. or lower, In the methane fermentation step, the decomposition liquid is added to the organic waste so that the organic load in the methane fermentation tank is 0.60 g CODCr / L / day or more and 5.0 g CODCr / L / day or less.

3. The method for treating a biodegradable resin according to claim 1 or 2, wherein in the decomposition step, 0.30 parts by mass or more and 20 parts by mass or less of water or water vapor is mixed with 1.0 part by mass of the biodegradable resin.

4. 3. The method for treating a biodegradable resin according to claim 1, wherein at least a portion of the decomposition tank that comes into contact with the decomposition liquid is made of austenitic stainless steel.

5. The method for treating a biodegradable resin according to claim 4, wherein the hydrolysis temperature in the decomposition step is 120°C or higher and 170°C or lower.

6. 3. The method for treating a biodegradable resin according to claim 1, wherein the biodegradable resin contains at least one of polybutylene succinate and polyhydroxyalkanoate.

7. 7. The method for treating a biodegradable resin according to claim 6, wherein the biodegradable resin mixed in the decomposition step contains 0.1 part by mass or more of polylactic acid per 1.0 part by mass of a biodegradable resin other than polylactic acid.

8. a decomposition device for mixing waste containing a biodegradable resin with water and hydrolyzing the mixture in a sealed decomposition tank at a temperature of 120° C. or higher to obtain a decomposition liquid containing a decomposition product of the biodegradable resin; a methane fermentation apparatus for treating organic waste containing a hardly decomposable solid content and the decomposition liquid in a methane fermentation tank in which methane bacteria are present at a temperature of 20° C. or higher and 60° C. or lower, A biodegradable resin treatment system, in which the decomposition liquid is added to the organic waste so that the organic load in the methane fermentation tank is 0.60 g COD Cr / L / day or more and 5.0 g COD Cr / L / day or less.

9. a decomposition device for mixing waste containing a biodegradable resin with steam and hydrolyzing the mixture at a temperature of 120° C. or higher in a sealed decomposition tank to obtain a decomposition liquid containing a decomposition product of the biodegradable resin; a methane fermentation apparatus for treating organic waste containing a hardly decomposable solid content and the decomposition liquid in a methane fermentation tank in which methane bacteria are present at a temperature of 20° C. or higher and 60° C. or lower, A biodegradable resin treatment system, in which the decomposition liquid is added to the organic waste so that the organic load in the methane fermentation tank is 0.60 g COD Cr / L / day or more and 5.0 g COD Cr / L / day or less.

10. The system for treating a biodegradable resin according to claim 8 or 9, wherein 0.30 parts by mass or more and 20 parts by mass or less of water or water vapor is mixed in the decomposition tank with respect to 1.0 part by mass of the biodegradable resin.

11. 10. The system for treating a biodegradable resin according to claim 8, wherein at least a portion of the decomposition tank that comes into contact with the decomposition liquid is made of austenitic stainless steel.

12. The system for treating a biodegradable resin according to claim 11, wherein the temperature of hydrolysis in the decomposition tank is 120°C or higher and 170°C or lower.

13. The biodegradable resin treatment system according to claim 8 or 9, wherein the biodegradable resin includes at least one of polybutylene succinate and polyhydroxyalkanoate.

14. 14. The system for treating a biodegradable resin according to claim 13, wherein the biodegradable resin mixed in the decomposition tank contains 0.1 part by mass or more of polylactic acid per 1.0 part by mass of a biodegradable resin other than polylactic acid.

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