CA3001284A1 - Composition for the degradation of plastic - Google Patents
Composition for the degradation of plastic Download PDFInfo
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- CA3001284A1 CA3001284A1 CA3001284A CA3001284A CA3001284A1 CA 3001284 A1 CA3001284 A1 CA 3001284A1 CA 3001284 A CA3001284 A CA 3001284A CA 3001284 A CA3001284 A CA 3001284A CA 3001284 A1 CA3001284 A1 CA 3001284A1
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- plastic
- molecular weight
- composition
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- heptane
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0033—Additives activating the degradation of the macromolecular compound
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J11/00—Recovery or working-up of waste materials
- C08J11/04—Recovery or working-up of waste materials of polymers
- C08J11/10—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation
- C08J11/105—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with enzymes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J11/00—Recovery or working-up of waste materials
- C08J11/04—Recovery or working-up of waste materials of polymers
- C08J11/10—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation
- C08J11/16—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with inorganic material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J11/00—Recovery or working-up of waste materials
- C08J11/04—Recovery or working-up of waste materials of polymers
- C08J11/10—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation
- C08J11/18—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material
- C08J11/22—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material by treatment with organic oxygen-containing compounds
- C08J11/24—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material by treatment with organic oxygen-containing compounds containing hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/02—Halogenated hydrocarbons
- C08K5/03—Halogenated hydrocarbons aromatic, e.g. C6H5-CH2-Cl
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0055—Oxidoreductases (1.) acting on diphenols and related substances as donors (1.10)
- C12N9/0057—Oxidoreductases (1.) acting on diphenols and related substances as donors (1.10) with oxygen as acceptor (1.10.3)
- C12N9/0059—Catechol oxidase (1.10.3.1), i.e. tyrosinase
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/62—Plastics recycling; Rubber recycling
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Sustainable Development (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
A composition for the degradation of plastic in the form of an additive used during the manufacturing of plastic. The composition being comprised of a predetermined amount of heptane, cellulose, methyl rhenium trioxide, butylated hydroxytoluene, and polyphenol oxidase. The additive can be selectively programmed to cause the plastic to begin disintegrating at a predetermined time
Description
I. TITLE: "COMPOSITION FOR THE DEGRADATION OF
PLASTIC"
II. TECHNICAL FIELD
1. Field of the Invention.
[001] The present invention relates to a composition and, more particularly, to a composition for the degradation of plastic.
III. BACKGROUND ART
PLASTIC"
II. TECHNICAL FIELD
1. Field of the Invention.
[001] The present invention relates to a composition and, more particularly, to a composition for the degradation of plastic.
III. BACKGROUND ART
[002] Most plastics include polluting substances that are not biodegradable.
Several formulations for environmentally-friendly compositions have been created in the past. None of them, however, use an undercover additive derived from the plastic targeted for degradation, hidden in a chemical cloak synthesized via the same plastic targeted for degradation's polymer structure itself, which is partially dissolved to create a cover for a Nano-programmed chemical addition on the inside. When activated this additive first decomposes the current polymer links between monomers and subsequently supplant them for weaker links susceptible to degradation through water, oxidation and/or anaerobic/aerobic biodegradation. In addition, none of them include a polymerization process that opens the time window for Nano programmable matter to catalyze the needed reaction to reassign the links structure on the plastics, including oil-derived high density plastics, without compromising its thermo stability, thermo plasticity, physical, mechanical, chemical stability and quality overall standards.
Several formulations for environmentally-friendly compositions have been created in the past. None of them, however, use an undercover additive derived from the plastic targeted for degradation, hidden in a chemical cloak synthesized via the same plastic targeted for degradation's polymer structure itself, which is partially dissolved to create a cover for a Nano-programmed chemical addition on the inside. When activated this additive first decomposes the current polymer links between monomers and subsequently supplant them for weaker links susceptible to degradation through water, oxidation and/or anaerobic/aerobic biodegradation. In addition, none of them include a polymerization process that opens the time window for Nano programmable matter to catalyze the needed reaction to reassign the links structure on the plastics, including oil-derived high density plastics, without compromising its thermo stability, thermo plasticity, physical, mechanical, chemical stability and quality overall standards.
3 PCT/US2015/020204 [003] Other patents describing the closest subject matter provide for a number of more or less complicated features that fail to solve the problem in an efficient and economical way. None of these patents suggest the novel features of the present invention.
IV. SUMMARY OF THE INVENTION
IV. SUMMARY OF THE INVENTION
[004] It is one of the main objects of the present invention to provide a composition for the formation of plastics susceptible to degradation.
[005] It is another object of this invention to provide a composition for an additive which adds the degradable variable to oil-derived high density plastics and the set of plastics in general with a melting point under 500 C.
[006] It is another object of this invention to provide a composition that uses Nano additives, which are very small and inexpensive yet, can alter a huge amount of polymer.
[007] It is another object of this invention to provide a composition for a chemical structure that works as a cloak for undercover Nano additives to catalyze a homogeneous blend between those and the plastic targeted for degradation.
[008] It is another object of this invention to provide a composition that is made of a 100% homogeneous blend that leaves no carbon footprint.
[009] It is another object of this invention to provide a composition to program the degradation time with an inverse factor additive/plastic's mass, whose variation changes the plastic targeted for degradation's obsolescence time-ratio.
[010] It is still another object of the present invention to provide a composition that stabilizes a blend between a large molecule, such as a polymer, and a small one, such as the present additive, while retaining the original molecular structure, quality, thermo plasticity, and other physical, thermic, and mechanical characteristics.
[011] It is yet another object of this invention to provide such a composition that is inexpensive to produce.
[012] Further objects of the invention will be brought out in the following part of the specification, wherein detailed description is for the purpose of fully disclosing the invention without placing limitations thereon.
V. DETAILED DESCRIPTION OF THE PREFERRED
EMBODIMENT
V. DETAILED DESCRIPTION OF THE PREFERRED
EMBODIMENT
[013] In its basic format, the present invention comprises the following substances: heptane, cellulose, methyl rhenium trioxide, butylated hydroxytoluene, and polyphenol oxidase.
To properly make the composition, a portion of sample plastic must be partially desynthesized using heptane. The resulting mix is then combined at 75% of the sample plastic's melting temperature with a precise measure of cellulose, methyl rhenium trioxide, butylated hydroxytoluene, and polyphenol oxidase. The resulting composition is then added as an additive to a predetermined plastic production demand. The resulting plastic, homogenized with the additive subject of the present invention, has weaker links susceptible to oxidation, water degradation, and biodegradation. The types of plastics that can be treated with the present composition are those with a melting temperature below 500 C.
The present invention also works on oil-derived high density polymers.
The heptane used in the present invention partially breaks the polymer's structure while retaining the physical characteristics of the original plastic taken for sample in the additive composite. The present invention then uses cellulose, methyl rhenium trioxide, butylated hydroxytoluene, and polyphenol oxidase to replace those broken links for weaker links that are more susceptible to environmental-degrading elements.
Every molecule in the plastic is homogenized with the additive. The other ingredients also act to reduce the potency of the heptane so that the plastic degrades over time and not all of a sudden, as heptane has the potential of doing. The additive can be programmed to disintegrate the plastic at a predetermined time. The obsolescence time is addressed stoichiometrically, and depends on the plastic's density. Each type of plastic has a different obsolescence time, yet relating the density of the plastic with the inverse factor additive/plastic's mass, the obsolescence time can be controlled. A higher factor for a shorter time and a lower factor for a longer time.
The following discloses the ratios required to make the additive composition subject of the present invention:
The additive's obsolescence time programmability is given by the following composition:
The percentages are related to molecular weight (g/mol), * SP= Sample plastic. Different types of plastic will require a different amount of heptane in the first step.
* CA, CB, CC and CD= Compound A, B, C and D
* BA= Additive subject of the present invention * PD = Amount of actual production demand of the plastic that was sampled (1): SP <100%> + Heptane Volumetric in solution approach until solute (SP) partially dissolves into the solvent (Heptane) = CA
This means that heptane is added to 100% of the sample plastic until the sample plastic partially dissolves into the Heptane.
(2): CA <100%> + Cellulose <100%> = CB
This means that cellulose is added to CA until the molecular weight of the quantity of cellulose being added equals the molecular weight of CA.
(3): CB <100%> + Methyl rhenium trioxide <50%> = CC
This means that methyl rhenium trioxide is added to CB until the molecular weight of the quantity of methyl rhenium trioxide being added equals half the molecular weight of CB.
(4): CC <100%> + Butylated hydroxytoluene <15%> = CD
This means that butylated hydroxytoluene is added to CC until the molecular weight of the quantity of butylated hydroxytoluene being added equals 15% of the molecular weight of CB.
(5): CD <100%> + Polyphenol oxidase <75%> = BA
This means that polyphenol oxidase is added to CD until the molecular weight of the quantity of polyphenol oxidase being added equals 75% of the molecular weight of CD.
(6): BA <0.1%> + PD <100%> = Final commercial-production plastic SP = clients' needs. (0.1% is equivalent to an inverse factor (additive/plastic's mass) of 1.
BA equals the final additive. Once BA is created, 0.1% of the molecular weight of the amount of plastic desired to be produced is added in the form of the additive (BA).
The above molecular weight percentages disclose the most effective amount known to the applicant. However, each molecular weight percentage can still work in a +/- 5% range, albeit not as effectively. To illustrate, the percentage of the molecular weight in cellulose added can be within the range of 90% and 100% and still function. Similarly, the percentage of methyl rhenium trioxide can be in the range of 45%-55% and function. The percentage of butylated hydroxytoluene can be within the range of 10%-20% and still function and the percentage of polyphenol oxidase can be within the range of 70% - 80% and still function. The amount of additive to be added to the amount of plastic sought to be produced can range between 0.09% and 1%.
To properly make the composition, a portion of sample plastic must be partially desynthesized using heptane. The resulting mix is then combined at 75% of the sample plastic's melting temperature with a precise measure of cellulose, methyl rhenium trioxide, butylated hydroxytoluene, and polyphenol oxidase. The resulting composition is then added as an additive to a predetermined plastic production demand. The resulting plastic, homogenized with the additive subject of the present invention, has weaker links susceptible to oxidation, water degradation, and biodegradation. The types of plastics that can be treated with the present composition are those with a melting temperature below 500 C.
The present invention also works on oil-derived high density polymers.
The heptane used in the present invention partially breaks the polymer's structure while retaining the physical characteristics of the original plastic taken for sample in the additive composite. The present invention then uses cellulose, methyl rhenium trioxide, butylated hydroxytoluene, and polyphenol oxidase to replace those broken links for weaker links that are more susceptible to environmental-degrading elements.
Every molecule in the plastic is homogenized with the additive. The other ingredients also act to reduce the potency of the heptane so that the plastic degrades over time and not all of a sudden, as heptane has the potential of doing. The additive can be programmed to disintegrate the plastic at a predetermined time. The obsolescence time is addressed stoichiometrically, and depends on the plastic's density. Each type of plastic has a different obsolescence time, yet relating the density of the plastic with the inverse factor additive/plastic's mass, the obsolescence time can be controlled. A higher factor for a shorter time and a lower factor for a longer time.
The following discloses the ratios required to make the additive composition subject of the present invention:
The additive's obsolescence time programmability is given by the following composition:
The percentages are related to molecular weight (g/mol), * SP= Sample plastic. Different types of plastic will require a different amount of heptane in the first step.
* CA, CB, CC and CD= Compound A, B, C and D
* BA= Additive subject of the present invention * PD = Amount of actual production demand of the plastic that was sampled (1): SP <100%> + Heptane Volumetric in solution approach until solute (SP) partially dissolves into the solvent (Heptane) = CA
This means that heptane is added to 100% of the sample plastic until the sample plastic partially dissolves into the Heptane.
(2): CA <100%> + Cellulose <100%> = CB
This means that cellulose is added to CA until the molecular weight of the quantity of cellulose being added equals the molecular weight of CA.
(3): CB <100%> + Methyl rhenium trioxide <50%> = CC
This means that methyl rhenium trioxide is added to CB until the molecular weight of the quantity of methyl rhenium trioxide being added equals half the molecular weight of CB.
(4): CC <100%> + Butylated hydroxytoluene <15%> = CD
This means that butylated hydroxytoluene is added to CC until the molecular weight of the quantity of butylated hydroxytoluene being added equals 15% of the molecular weight of CB.
(5): CD <100%> + Polyphenol oxidase <75%> = BA
This means that polyphenol oxidase is added to CD until the molecular weight of the quantity of polyphenol oxidase being added equals 75% of the molecular weight of CD.
(6): BA <0.1%> + PD <100%> = Final commercial-production plastic SP = clients' needs. (0.1% is equivalent to an inverse factor (additive/plastic's mass) of 1.
BA equals the final additive. Once BA is created, 0.1% of the molecular weight of the amount of plastic desired to be produced is added in the form of the additive (BA).
The above molecular weight percentages disclose the most effective amount known to the applicant. However, each molecular weight percentage can still work in a +/- 5% range, albeit not as effectively. To illustrate, the percentage of the molecular weight in cellulose added can be within the range of 90% and 100% and still function. Similarly, the percentage of methyl rhenium trioxide can be in the range of 45%-55% and function. The percentage of butylated hydroxytoluene can be within the range of 10%-20% and still function and the percentage of polyphenol oxidase can be within the range of 70% - 80% and still function. The amount of additive to be added to the amount of plastic sought to be produced can range between 0.09% and 1%.
[014] The foregoing description conveys the best understanding of the objectives and advantages of the present invention. Different embodiments may be made of the inventive concept of this invention. It is to be understood that all matter disclosed herein is to be interpreted merely as illustrative, and not in a limiting sense.
VI. INDUSTRIAL APPLICABILITY
VI. INDUSTRIAL APPLICABILITY
[015] It is apparent from the previous paragraphs that a new and non-obvious composition for the degradation of plastic is useful and desirable because it provides for an additive that degrades plastic. By using the composition subject of the present invention, there will be less pollution in the environment from plastic while retaining the original molecular structure, quality, thermo plasticity, and other physical, thermic, and mechanical characteristics. In addition, the additive composition will have no carbon footprint. Thus, the industrial applicability is readily established in that the present invention has financial and practical advantages over the prior arts.
Claims (2)
What is claimed is:
1. A composition for degrading plastic, comprising:
A) a predetermined amount of plastic dissolved into a predetermined amount of heptane until said plastic partially solvents in said heptane;
B) from 90% to 100% of the molecular weight of the previous solute of cellulose;
C) from 45% to 55% of the molecular weight of the previous combination of methyl rhenium trioxide;
D) from 10% to 20% of the molecular weight of the previous combination of butylated hydroxytoluene; and E) from 70% to 80% of the molecular weight of the previous combination of polyphenol oxidase.
A) a predetermined amount of plastic dissolved into a predetermined amount of heptane until said plastic partially solvents in said heptane;
B) from 90% to 100% of the molecular weight of the previous solute of cellulose;
C) from 45% to 55% of the molecular weight of the previous combination of methyl rhenium trioxide;
D) from 10% to 20% of the molecular weight of the previous combination of butylated hydroxytoluene; and E) from 70% to 80% of the molecular weight of the previous combination of polyphenol oxidase.
2. A composition for degrading plastic, consisting essentially of:
A) a predetermined amount of plastic dissolved into a predetermined amount of heptane until said plastic solvents in said heptane;
B) from 90% to 100% of the molecular weight of the previous solute of cellulose;
C) from 45% to 55% of the molecular weight of the previous combination of methyl rhenium trioxide;
D) from 10% to 20% of the molecular weight of the previous combination of butylated hydroxytoluene; and E) from 70%
to 80% of the molecular weight of the previous combination of polyphenol oxidase.
A) a predetermined amount of plastic dissolved into a predetermined amount of heptane until said plastic solvents in said heptane;
B) from 90% to 100% of the molecular weight of the previous solute of cellulose;
C) from 45% to 55% of the molecular weight of the previous combination of methyl rhenium trioxide;
D) from 10% to 20% of the molecular weight of the previous combination of butylated hydroxytoluene; and E) from 70%
to 80% of the molecular weight of the previous combination of polyphenol oxidase.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US2015/020204 WO2016144363A1 (en) | 2015-03-12 | 2015-03-12 | Composition for the degradation of plastic |
Publications (1)
Publication Number | Publication Date |
---|---|
CA3001284A1 true CA3001284A1 (en) | 2016-09-15 |
Family
ID=56878630
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA3001284A Abandoned CA3001284A1 (en) | 2015-03-12 | 2015-03-12 | Composition for the degradation of plastic |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP3268424A4 (en) |
JP (1) | JP2018511309A (en) |
CN (1) | CN107406620A (en) |
BR (1) | BR112017018857A2 (en) |
CA (1) | CA3001284A1 (en) |
MX (1) | MX2017011690A (en) |
WO (1) | WO2016144363A1 (en) |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5212219A (en) * | 1987-05-21 | 1993-05-18 | Epron Industries Limited | Degradable plastics |
JP3423094B2 (en) * | 1995-01-19 | 2003-07-07 | 三井化学株式会社 | Biodegradable polymer composition |
US6482872B2 (en) * | 1999-04-01 | 2002-11-19 | Programmable Materials, Inc. | Process for manufacturing a biodegradable polymeric composition |
JP4233345B2 (en) * | 2002-02-21 | 2009-03-04 | 花王株式会社 | Biodegradable film manufacturing method and biodegradable film |
KR20040086377A (en) * | 2002-02-21 | 2004-10-08 | 카오카부시키가이샤 | Biodegradable film |
ITMI20041627A1 (en) * | 2004-08-06 | 2004-11-06 | Lachifarma S R L Lab Chimi Co | PROCESS FOR THE RECOVERY OF THYROSOL HYDROXYTYROSOL AND OTHER PHENOLIC COMPONENTS FROM VEGETATION WATERS AND METHOD OF CATALYTIC OXIDATION OF THYROXIS TO HYDROXYSIROSOL |
JP4869842B2 (en) * | 2006-09-05 | 2012-02-08 | ヤマハリビングテック株式会社 | Resin product manufacturing method and resin product repair method |
JP2009233166A (en) * | 2008-03-27 | 2009-10-15 | Terumo Corp | Bioabsorbable material and device using the same to be placed in the living body |
US20100203129A1 (en) * | 2009-01-26 | 2010-08-12 | Egalet A/S | Controlled release formulations with continuous efficacy |
KR101105292B1 (en) * | 2009-06-05 | 2012-01-17 | 주식회사 리젠 바이오텍 | Biodegradable polymeric microparticles and their preparation method |
MX2013011827A (en) * | 2011-04-29 | 2014-01-08 | Novozymes Inc | Methods for enhancing the degradation or conversion of cellulosic material. |
US10342897B2 (en) * | 2012-05-17 | 2019-07-09 | Cartiheal (2009) Ltd | Biomatrix hydrogels and methods of use thereof |
CN102671718B (en) * | 2012-06-11 | 2015-06-17 | 淄博东大弘方化工有限公司 | Supermacroporous strong base anion exchange resin with quaternary amine group and preparation process thereof |
BR112015025767A2 (en) * | 2013-04-11 | 2017-10-17 | B G Negev Tech Ltd | composition and method for decomposing polyethylene |
US9181412B2 (en) * | 2014-01-20 | 2015-11-10 | Bioplast, Llc | Composition for the degradation of plastic |
-
2015
- 2015-03-12 CN CN201580077717.9A patent/CN107406620A/en active Pending
- 2015-03-12 EP EP15884882.0A patent/EP3268424A4/en not_active Withdrawn
- 2015-03-12 JP JP2017547575A patent/JP2018511309A/en active Pending
- 2015-03-12 CA CA3001284A patent/CA3001284A1/en not_active Abandoned
- 2015-03-12 BR BR112017018857A patent/BR112017018857A2/en not_active Application Discontinuation
- 2015-03-12 WO PCT/US2015/020204 patent/WO2016144363A1/en active Application Filing
- 2015-03-12 MX MX2017011690A patent/MX2017011690A/en unknown
Also Published As
Publication number | Publication date |
---|---|
CN107406620A (en) | 2017-11-28 |
BR112017018857A2 (en) | 2018-04-24 |
WO2016144363A1 (en) | 2016-09-15 |
EP3268424A1 (en) | 2018-01-17 |
JP2018511309A (en) | 2018-04-26 |
MX2017011690A (en) | 2018-02-09 |
EP3268424A4 (en) | 2018-07-18 |
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