[go: up one dir, main page]

US20190256387A1 - Extract of plant powder, and water purifier - Google Patents

Extract of plant powder, and water purifier Download PDF

Info

Publication number
US20190256387A1
US20190256387A1 US16/333,440 US201716333440A US2019256387A1 US 20190256387 A1 US20190256387 A1 US 20190256387A1 US 201716333440 A US201716333440 A US 201716333440A US 2019256387 A1 US2019256387 A1 US 2019256387A1
Authority
US
United States
Prior art keywords
component
water
measurement
fractionated
ethanol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US16/333,440
Inventor
Takanori Fujita
Ryu Shimada
Masahiko Ito
Masato Hasegawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dexerials Corp
Original Assignee
Dexerials Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dexerials Corp filed Critical Dexerials Corp
Priority claimed from PCT/JP2017/032941 external-priority patent/WO2018051992A1/en
Assigned to DEXERIALS CORPORATION reassignment DEXERIALS CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: FUJITA, TAKANORI, HASEGAWA, MASATO, ITO, MASAHIKO, SHIMADA, Ryu
Publication of US20190256387A1 publication Critical patent/US20190256387A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D21/00—Separation of suspended solid particles from liquids by sedimentation
    • B01D21/01—Separation of suspended solid particles from liquids by sedimentation using flocculating agents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00—Treatment of water, waste water, or sewage
    • C02F1/28—Treatment of water, waste water, or sewage by sorption
    • C02F1/286—Treatment of water, waste water, or sewage by sorption using natural organic sorbents or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00—Treatment of water, waste water, or sewage
    • C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/5263—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using natural chemical compounds
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00—Treatment of water, waste water, or sewage
    • C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/5272—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using specific organic precipitants
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00—Treatment of water, waste water, or sewage
    • C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/54—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using organic material
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00—Treatment of water, waste water, or sewage
    • C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/54—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using organic material
    • C02F1/56—Macromolecular compounds
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00—Treatment of water, waste water, or sewage
    • C02F1/58—Treatment of water, waste water, or sewage by removing specified dissolved compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/716—Glucans
    • A61K31/722—Chitin, chitosan
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6921—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a particulate, a powder, an adsorbate, a bead or a sphere
    • A61K47/6927—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a particulate, a powder, an adsorbate, a bead or a sphere the form being a solid microparticle having no hollow or gas-filled cores
    • A61K47/6929—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a particulate, a powder, an adsorbate, a bead or a sphere the form being a solid microparticle having no hollow or gas-filled cores the form being a nanoparticle, e.g. an immuno-nanoparticle
    • A61K47/6931—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a particulate, a powder, an adsorbate, a bead or a sphere the form being a solid microparticle having no hollow or gas-filled cores the form being a nanoparticle, e.g. an immuno-nanoparticle the material constituting the nanoparticle being a polymer
    • A61K47/6939—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a particulate, a powder, an adsorbate, a bead or a sphere the form being a solid microparticle having no hollow or gas-filled cores the form being a nanoparticle, e.g. an immuno-nanoparticle the material constituting the nanoparticle being a polymer the polymer being a polysaccharide, e.g. starch, chitosan, chitin, cellulose or pectin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K49/00—Preparations for testing in vivo
    • A61K49/06—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations
    • A61K49/18—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes
    • A61K49/1818—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles
    • A61K49/1821—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles coated or functionalised microparticles or nanoparticles
    • A61K49/1824—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles coated or functionalised microparticles or nanoparticles coated or functionalised nanoparticles
    • A61K49/1827—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles coated or functionalised microparticles or nanoparticles coated or functionalised nanoparticles having a (super)(para)magnetic core, being a solid MRI-active material, e.g. magnetite, or composed of a plurality of MRI-active, organic agents, e.g. Gd-chelates, or nuclei, e.g. Eu3+, encapsulated or entrapped in the core of the coated or functionalised nanoparticle
    • A61K49/1851—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles coated or functionalised microparticles or nanoparticles coated or functionalised nanoparticles having a (super)(para)magnetic core, being a solid MRI-active material, e.g. magnetite, or composed of a plurality of MRI-active, organic agents, e.g. Gd-chelates, or nuclei, e.g. Eu3+, encapsulated or entrapped in the core of the coated or functionalised nanoparticle having a (super)(para)magnetic core coated or functionalised with an organic macromolecular compound, i.e. oligomeric, polymeric, dendrimeric organic molecule
    • A61K49/1863—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles coated or functionalised microparticles or nanoparticles coated or functionalised nanoparticles having a (super)(para)magnetic core, being a solid MRI-active material, e.g. magnetite, or composed of a plurality of MRI-active, organic agents, e.g. Gd-chelates, or nuclei, e.g. Eu3+, encapsulated or entrapped in the core of the coated or functionalised nanoparticle having a (super)(para)magnetic core coated or functionalised with an organic macromolecular compound, i.e. oligomeric, polymeric, dendrimeric organic molecule the organic macromolecular compound being a polysaccharide or derivative thereof, e.g. chitosan, chitin, cellulose, pectin, starch
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00—Treatment of water, waste water, or sewage
    • C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/5236—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00—Nature of the contaminant
    • C02F2101/10—Inorganic compounds
    • C02F2101/103—Arsenic compounds
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00—Nature of the contaminant
    • C02F2101/10—Inorganic compounds
    • C02F2101/12—Halogens or halogen-containing compounds
    • C02F2101/14—Fluorine or fluorine-containing compounds
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00—Nature of the contaminant
    • C02F2101/10—Inorganic compounds
    • C02F2101/20—Heavy metals or heavy metal compounds
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00—Nature of the contaminant
    • C02F2101/10—Inorganic compounds
    • C02F2101/20—Heavy metals or heavy metal compounds
    • C02F2101/203—Iron or iron compound
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00—Nature of the contaminant
    • C02F2101/10—Inorganic compounds
    • C02F2101/20—Heavy metals or heavy metal compounds
    • C02F2101/22—Chromium or chromium compounds, e.g. chromates

Definitions

  • the present invention relates to a plant powder extract and a water-purifying agent containing the extract, both used for purification of water such as industrial wastewater.
  • waste liquids including environmentally hazardous substances such as metal ions and fluorine ions as inorganic ions have been generated in the processes for producing various products in plants.
  • the flocculating precipitation method there has been proposed a method of performing a step of adding a base to wastewater in which heavy metal ions are dissolved, to make the wastewater basic, insolubilize at least part of the heavy metal ions, and form a suspended solid matter, a step of adding an inorganic flocculant to the wastewater to make the suspended solid matter flocculate and settle, a step of adding a polymeric flocculant to the wastewater to turn the suspended solid matter to a macrofloc, and an adsorbing step of passing the wastewater through an adsorption layer containing a cation exchanger formed of a leafy vegetable such as mulukhiya and Japanese mustard spinach (see, e.g., PTL 1).
  • the present invention has an object to identify effective components in plant powders that contribute to water purification and provide a water-purifying agent that can exhibit an excellent water-purifying performance to wastewater efficiently even in a small amount and infallibly.
  • a fractionated component 1 (hereinafter, may also be referred to as component 1 in the present invention) of a water extract of a plant powder,
  • fractionated component 1 is a fractionated component having a fractionation molecular weight of 12,000 or greater
  • an ethanol-undissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in a Fourier transform infrared spectroscopy (FT-IR) measurement and exhibits a peak attributable to cellulose in a gas chromatography mass spectrometry (GC-MS) measurement, and
  • FT-IR Fourier transform infrared spectroscopy
  • GC-MS gas chromatography mass spectrometry
  • an ethanol-dissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in the FT-IR measurement and exhibits a peak attributable to a plant protein in the GC-MS measurement.
  • fractionated component 1 contains a substance having a weight average molecular weight (Mw) of 300,000 or greater by 50% or greater.
  • plant powder is a powder of Corchorus olitorius.
  • a fractionated component 2 (hereinafter, may also be referred to as component 2 in the present invention) of a water extract of a plant powder,
  • fractionated component 2 is a fractionated component having a fractionation molecular weight of less than 3,400,
  • an ethanol-dissolved component of the fractionated component 2 exhibits a peak attributable to an amide group in the FT-IR measurement.
  • fractionated component 2 contains a substance having a weight average molecular weight (Mw) of from 200 through 2,500 by 90% or greater.
  • fractionated component 2 is a water-soluble chitosan.
  • plant powder is a powder of Corchorus olitorius.
  • a water-purifying agent including:
  • a water-purifying agent including:
  • a water-purifying agent including:
  • a water-purifying agent including:
  • an extracted component which is formed of a fractionated component 1 having a fractionation molecular weight of 12,000 or greater, is contained in the plant powder in an amount of 0.5% by mass or greater,
  • an ethanol-undissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in a FT-IR measurement and exhibits a peak attributable to cellulose in a GC-MS measurement
  • an ethanol-dissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in the FT-IR measurement and exhibits a peak attributable to a plant protein in the GC-MS measurement.
  • fractionated component 1 contains a substance having a weight average molecular weight (Mw) of 300,000 or greater by 50% or greater.
  • plant powder is a powder of Corchorus olitorius.
  • a water-purifying agent including:
  • an extracted component which is formed of a fractionated component 2 having a fractionation molecular weight of less than 3,400, is contained in the plant powder in an amount of 0.05% by mass or greater,
  • an ethanol-dissolved component of the fractionated component 2 exhibits a peak attributable to an amide group in the FT-IR measurement.
  • fractionated component 2 contains a substance having a weight average molecular weight (Mw) of from 200 through 2,500 by 90% or greater.
  • fractionated component 2 is a water-soluble chitosan.
  • plant powder is a powder of Corchorus olitorius.
  • the water-purifying agent is the water-purifying agent according to any one of ⁇ 18> to ⁇ 23>.
  • polymeric flocculant is polyacrylamide
  • a wastewater treatment method including:
  • wastewater is wastewater including the inorganic unnecessary substance containing at least any one selected from the group consisting of nickel, fluorine, iron, copper, zinc, chromium, arsenic, cadmium, tin, and lead.
  • the present invention can provide a water-purifying agent that can exhibit an excellent water-purifying performance to wastewater efficiently even in a small amount and infallibly.
  • FIG. 1 is an image diagram illustrating a fractionated component 1 (may also be referred to as component 1) and a fractionated component 2 (may also be referred to as component 2), which are the subjects of the present invention among water extracts of a plant powder;
  • FIG. 2 is an image diagram illustrating a method for extracting the component 1 and the component 2;
  • FIG. 3 is a graph plotting a result of an experiment of a water-purifying effect of the component 1;
  • FIG. 4 plots a result of a microscopic IR measurement of the component 2
  • FIG. 5 is a graph plotting a result of an experiment of a water-purifying effect of the component 2;
  • FIG. 6A plots a result of a Fourier transform infrared spectroscopy (FT-IR) measurement of an ethanol-undissolved component (component A) of the component 1;
  • FT-IR Fourier transform infrared spectroscopy
  • FIG. 6B plots a result of a Fourier transform infrared spectroscopy (FT-IR) measurement of an ethanol-dissolved component (component B) of the component 1;
  • FT-IR Fourier transform infrared spectroscopy
  • FIG. 6C plots a result of a Fourier transform infrared spectroscopy (FT-IR) measurement of an ethanol-undissolved component (component G) of the component 2;
  • FT-IR Fourier transform infrared spectroscopy
  • FIG. 6D plots a result of a Fourier transform infrared spectroscopy (FT-IR) measurement of an ethanol-dissolved component (component H) of the component 2;
  • FT-IR Fourier transform infrared spectroscopy
  • FIG. 7A plots a result of a gas chromatography mass spectrometry (GC-MS) measurement of the ethanol-undissolved component (component A) of the component 1;
  • GC-MS gas chromatography mass spectrometry
  • FIG. 7B plots a result of a gas chromatography mass spectrometry (GC-MS) measurement of the ethanol-dissolved component (component B) of the component 1;
  • GC-MS gas chromatography mass spectrometry
  • FIG. 7C plots a result of a gas chromatography mass spectrometry (GC-MS) measurement of the ethanol-undissolved component (component G) of the component 2;
  • GC-MS gas chromatography mass spectrometry
  • FIG. 7D plots a result of a gas chromatography mass spectrometry (GC-MS) measurement of the ethanol-dissolved component (component H) of the component 2;
  • GC-MS gas chromatography mass spectrometry
  • FIG. 8A plots a result of a gel permeation chromatograph (GPC) measurement of the component 1;
  • FIG. 8B plots a result of a gel permeation chromatograph (GPC) measurement of the component 2;
  • FIG. 9 is a diagram indicating an identification number of “intermediate jute No. 3” that may be used in the present invention.
  • FIG. 10 is a diagram indicating an identification number of “intermediate kenaf” that may be used in the present invention.
  • extracted components which are formed of a fractionated component 1 (may also be referred to as component 1 in the present invention) having a fractionation molecular weight of 12,000 or greater and a fractionated component 2 (may also be referred to as component 2 in the present invention) having a fractionation molecular weight of less than 3,400 illustrated in FIG. 1 , each have an excellent water-purifying action.
  • the plant is not particularly limited and any plant that contains the component 1 and the component 2 in effective amounts respectively may be used.
  • Preferable examples of the plant include Corchorus olitorius and mulukhiya.
  • Corchorus olitorius for example, Corchorus olitorius produced in Nansha City of China, or “intermediate jute No. 4” under nationally identified hemp 2013, “intermediate jute No. 3” under varieties identification of registration No. 1209006 in Anhui province, “intermediate jute No. 1” under XPD005-2005, and “intermediate kenaf” under varieties identification of registration No. 1209001 in Anhui province, which are identification numbers in Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, can be suitably used.
  • the “intermediate jute No. 4”, the “intermediate jute No. 3”, and the “intermediate kenaf” are more preferable, and the “intermediate jute No. 4” is particularly preferable.
  • the identification number of the “intermediate jute No. 3” is indicated in FIG. 9 .
  • the identification number of the “intermediate kenaf” is indicated in FIG. 10 .
  • the “intermediate jute No. 4” has the following properties.
  • the fractionated component 1 can be extracted according to a method illustrated in FIG. 2 . Specifically, a dry plant is ground and subjected to extraction using ethyl acetate. Subsequently, the extraction residue is further subjected to extraction using distilled water, to obtain a supernatant. The supernatant is subjected to dialysis, to separate a component having a fractionation molecular weight of 12,000 or greater. In this way, the fractionated component 1 is obtained.
  • ethanol-undissolved component (denoted by component A in FIG. 1 ) of the fractionated component 1 was measured by a Fourier transform infrared spectroscopy (FT-IR) method. The result of the measurement is plotted in FIG. 6A .
  • This FT-IR measurement was performed with FTS-7000e/UMA600, VARIAN, and microscopic diamond cells.
  • FT-IR measurements of a component B, a component G, and a component H described below were also performed under the same conditions.
  • the component A exhibited peaks attributable to carboxylic acid in the FT-IR measurement. That is, the component A exhibited peaks near 1,700 (cm ⁇ 1 ) (ketone stretching) and near 1,600 (cm ⁇ 1 ) (amide stretching).
  • the component A was also measured by a gas chromatography mass spectrometry (GC-MS) method. The result of the measurement is plotted in FIG. 7A .
  • GC-MS gas chromatography mass spectrometry
  • This GC-MS measurement was performed with JMS-600H available from JEOL, using Ionization mode: EI+.
  • GC-MS measurements of the component B, the component G, and the component H described below were also performed under the same conditions.
  • the component A exhibited peaks attributable to cellulose in the GC-MS measurement.
  • Attributions of the peaks (A1) to (A20) in FIG. 7A are estimated to be as follows.
  • the component B exhibited peaks attributable to carboxylic acid in the FT-IR measurement. That is, the component B exhibited peaks near 1,700 (cm ⁇ 1 ) (ketone stretching) and near 1,600 (cm ⁇ 1 ) (amide stretching).
  • the component B was also measured by GC-MS. The result of the measurement is plotted in FIG. 7B .
  • the component B exhibited peaks attributable to a plant protein in the GC-MS measurement.
  • Attributions of the peaks (B1) to (B16) in FIG. 7B are estimated to be as follows.
  • the component 1 is considered to be formed of uronic acid or carboxylic acid that has a structure similar to galacturonic acid. Hence, the component 1 is considered to have inorganic ions adsorb thereto and exhibit an excellent effect in water purification.
  • the component 1 was also measured by gel permeation chromatograph (GPC). The result of the measurement is plotted in FIG. 8A .
  • GPC measurement was performed with GPC SYSTEM 21, Shodex, and TSKgel GMPW.
  • GPC measurement of the component 2 described below was also performed under the same conditions.
  • the component 1 contains a substance having a weight average molecular weight (Mw) of 300,000 or greater by 50% (area) or greater.
  • the component 1 was able to improve the water quality (reduction in the Ni ion concentration) in a smaller amount than the PAM.
  • the fractionated component 2 can be extracted according to the method illustrated in FIG. 2 . Specifically, a component having a fractionation molecular weight of less than 12,000, which was obtained by the dialysis described above, is further subjected to dialysis, to obtain a component having a fractionation molecular weight of less than 6,000, which is further subjected to dialysis, to obtain and separate a component having a fractionation molecular weight of less than 3,400. In this way, the fractionated component 2 is obtained.
  • the component G exhibits peaks attributable to an amide group in the FT-IR measurement. That is, the component G exhibits main peaks in a range of from 1,590 (cm ⁇ 1 ) through 1,630 (cm ⁇ 1 ) (amide stretching).
  • the component G was also measured by GC-MS. The result of the measurement is plotted in FIG. 7C .
  • the component G exhibits peaks of 1,8-diazacyclotetradecane-2,7-dione in the GC-MS measurement.
  • Attributions of the peaks (C1) to (C13) in FIG. 7C are estimated to be as follows.
  • the component H exhibits peaks attributable to an amide group in the FT-IR measurement. That is, the component H exhibits main peaks in a range of from 1,590 (cm ⁇ 1 ) through 1,630 (cm ⁇ 1 ) (amide stretching).
  • the component H was also measured by GC-MS. The result of the measurement is plotted in FIG. 7D .
  • the component H exhibits peaks of 1,8-diazacyclotetradecane-2,7-dione in the GC-MS measurement.
  • Attributions of the peaks (D1) to (D17) in FIG. 7C are estimated to be as follows.
  • the component 2 is considered to be a water-soluble chitosan.
  • Chitosans (chitins) extracted from, for example, crustacean are typically water-insoluble, but water-soluble chitosan is considered to be effective in adsorption of inorganic ions.
  • water solubility means solubility of 50% by mass of greater in water.
  • the component 2 was also measured by GPC. The result of the measurement is plotted in FIG. 8B .
  • the component 2 contains a substance having a weight average molecular weight (Mw) of from 200 through 2,500 by 90% (area) or greater.
  • FIG. 5 (i) plots the change of the Ni ion concentration when the extract formed of the component 2 was directly added in water containing Ni.
  • FIG. 5 (ii) and (iii) plot the changes of the Ni ion concentration when a commercially available ZETA ACE as a flocculant and chitosan were added in water containing Ni.
  • the component 2 achieved a result similar to the case of adding chitosan in the wastewater. Also from this result, the component 2 is considered to be a chitosan.
  • the water-purifying agent of the present invention contains a plant powder.
  • the plant powder contain the component 1 or the component 2, or both thereof, which is/are (Extract of plant powder) described above.
  • the water-purifying agent contain a plant powder that contains extracted component(s) formed of the component 1 or the component 2, or both thereof in predetermined effective amount(s).
  • the water-purifying agent of the present invention contains the component 1 or the component 2, or both thereof extracted by the production method described above.
  • the water-purifying agent of the present invention contain both of the component 1 and the component 2 extracted by the production method described above.
  • the component 1 and the component 2 both have a water-purifying function but have different mechanisms of the water-purifying function.
  • a water-purifying agent containing both of the component 1 and the component 2 is more preferable.
  • the water-purifying agent of the present invention contains a plant powder containing extracted component(s) formed of the component 1 or the component 2, or both thereof.
  • the component 1 is contained in the plant powder in an amount of 0.5% by mass or greater, more preferably in an amount of 0.7% by mass, and yet more preferably in an amount of 0.9% by mass as will be demonstrated by Examples.
  • the component 2 is contained in the plant powder in an amount of 0.05% by mass or greater, and more preferably in an amount of 0.07% by mass.
  • the component 1 and the component 2 were extracted from a dried product of Corchorus olitorius including all leaves, stalks, and roots.
  • Table 1 the result presented in Table 1 below was achieved as a result of one experiment example.
  • the numerals (1) to (5) in Table 1 correspond to the numerals (1) to (5) in FIG. 2 . That is, when the raw material of the plant powder is regarded as 100 parts by mass, the component 1 was extracted in an amount of 0.9 parts by mass, and the component 2 was extracted in an amount of 0.07 parts by mass (see the results of (2) and (5) in Table 1).
  • the yields of the component 1 and the component 2 vary depending on the plant powder, which is the raw material. Hence, it is preferable to appropriately adjust the contents of the component 1 and the component 2 to desired ranges respectively, by varying the ratio among leaves, stalks, and roots of the plant.
  • the water-purifying agent may contain additives such as a polymeric flocculant, a filler, a thickener, a colorant, and a thixotropy imparting agent as other additives.
  • additives such as a polymeric flocculant, a filler, a thickener, a colorant, and a thixotropy imparting agent as other additives.
  • the polymeric flocculant is not particularly limited so long as the polymeric flocculant exhibits an effect of removing the inorganic unnecessary substance in wastewater like the powder of the plant described above.
  • the polymeric flocculant include polyacrylamide (PAM), a salt obtained by partially hydrolyzing polyacrylamide, sodium alginate, sodium polyacrylate, and CMC sodium salt.
  • PAM polyacrylamide
  • polyacrylamide is preferable for use.
  • commercially available products FLOPAN AN 956, FLOPAN AN 995SH, FA 920SH, FO 4490, and AN 923 available from SNF Japan Co., Ltd.
  • the ratio of the component 1 in the water-purifying agent that also contains the other additives such as the polymeric flocculant be 0.5% by mass or greater relative to the total amount of the water-purifying agent.
  • the ratio of the component 2 be 0.05% by mass or greater relative to the total amount of the water-purifying agent.
  • a wastewater treatment method of the present invention is for removing the inorganic unnecessary substance in wastewater by feeding the water-purifying agent of the present invention described above to the wastewater.
  • the inorganic unnecessary substance examples include an inorganic unnecessary substance that contains at least any one selected from the group consisting of nickel, fluorine, iron, copper, zinc, chromium, arsenic, cadmium, and lead.
  • the wastewater treatment method of the present invention will be specifically described.
  • the water-purifying agent of the present invention after an insolubilizing step of adding a base to wastewater to make the wastewater basic, insolubilize at least part of the heavy metal ions, and form a suspended solid matter.
  • the water-purifying agent is fed to the wastewater to make the inorganic unnecessary substance flocculate and settle, and the settled, separated precipitate is removed. In this way, the wastewater is purified.
  • intermediate jute No. 4 which was Corchorus olitorius having an identification number 2013 in Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, was used.
  • a dried product (containing the component 1 in an amount of 0.56% by mass) of a plant including all leaves, stalks, and roots of the intermediate jute No. 4 (with a ratio of the leaves in the plant of 8% by mass) was used.
  • the intermediate jute No. 4 was dried and ground, and then separated through a sieve, in order to use a product with a size of 250 micrometers or less.
  • the component 1 being contained in an amount of 0.56% by mass in the dried product of the intermediate jute No. 4 used in the present Example was confirmed by performing the extracting operation described below.
  • ethyl acetate was added to the dried product of the intermediate jute No. 4, to obtain a 10% by mass solution, which was left to stand still at room temperature (23 degrees C.) for 8 hours, followed by filtration through a filter paper.
  • the residue was washed with ethyl acetate, and then further subjected to extraction using distilled water, to obtain a supernatant, which was subjected to dialysis to separate a component having a fractionation molecular weight of 12,000 or greater, to obtain the component 1.
  • the ratio of the component 1 relative to the dried product of the intermediate jute No. 4, which was the raw material was calculated.
  • the initial Ni ion concentration was 60 ppm.
  • the result of the nickel ion concentration when the water-purifying agent of the present invention was added is presented in Table 3 below. As presented in Table 3, reduction in the nickel ion concentration was confirmed. With a nickel ion concentration of 8 ppm or lower, it can be judged that the water-purifying agent is non-problematic in practical use.
  • Example 2 An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, the dried product of the intermediate jute No. 4 was changed to a dried product with a ratio of leaves of 10% by mass (containing the component 1 in an amount of 0.7% by mass). As presented in Table 3 below, reduction in the nickel ion concentration was confirmed in Example 2.
  • Example 3 An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, the dried product of the intermediate jute No. 4 was changed to a dried product with a ratio of leaves of 100% by mass (containing the component 1 in an amount of 7.0% by mass). As presented in Table 3 below, reduction in the nickel ion concentration was confirmed in Example 3.
  • Example 2 An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, the dried product of the intermediate jute No. 4 was changed to a dried product mainly containing stalks and roots but free of leaves (containing the component 1 in an amount of 0.1% by mass). As presented in Table 3 below, reduction in the nickel ion concentration was poor in Comparative Example 1.
  • Example 2 An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, the dried product of the intermediate jute No. 4 was changed to a dried product with a ratio of leaves of 3% by mass (containing the component 1 in an amount of 0.21% by mass). As presented in Table 3 below, a sufficient reduction in the nickel ion concentration was not achieved in Comparative Example 2.
  • Example 3 An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, the dried product of the intermediate jute No. 4 was changed to a dried product with a ratio of leaves of 5% by mass (containing the component 1 in an amount of 0.35% by mass). As presented in Table 3 below, a sufficient reduction in the nickel ion concentration was not achieved in Comparative Example 3.
  • Example 4 An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, an extract formed of the component 1, extracted from the dried product of the intermediate jute No. 4, was used instead of the dried product of the intermediate jute No. 4, and this extract was directly added in an amount of 50 ppm. As presented in Table 3 below, reduction in the nickel ion concentration was confirmed in Example 4.
  • Example 4 An experiment was performed in the same manner as in Example 4, except that unlike in Example 4, the extract formed of the component 1, extracted from the dried product of the intermediate jute No. 4, was added with the amount of addition changed to 5 ppm. As presented in Table 3 below, an excellent reduction in the nickel ion concentration that is the same as in Example 4 was confirmed with even such a small amount of addition.
  • Example 6 Although the nickel ion concentration reducing effect was better in Example 1, a good nickel ion concentration reducing effect, which was almost the same as in Example 1, was exhibited in Example 6.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Environmental & Geological Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Hydrology & Water Resources (AREA)
  • Engineering & Computer Science (AREA)
  • Water Supply & Treatment (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Separation Of Suspended Particles By Flocculating Agents (AREA)
  • Removal Of Specific Substances (AREA)
  • Peptides Or Proteins (AREA)
  • Water Treatment By Sorption (AREA)

Abstract

Provided are an extract, which is a fractionated component 1 of a water extract of a plant powder, wherein the fractionated component 1 is a fractionated component having a fractionation molecular weight of 12,000 or greater, wherein an ethanol-undissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in a Fourier transform infrared spectroscopy (FT-IR) measurement and exhibits a peak attributable to cellulose in a gas chromatography mass spectrometry (GC-MS) measurement, and wherein an ethanol-dissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in the FT-IR measurement and exhibits a peak attributable to a plant protein in the GC-MS measurement, and a water-purifying agent containing the extract.

Description

    TECHNICAL FIELD
  • The present invention relates to a plant powder extract and a water-purifying agent containing the extract, both used for purification of water such as industrial wastewater.
    • BACKGROUND ART
  • In recent years, large amounts of waste liquids including environmentally hazardous substances such as metal ions and fluorine ions as inorganic ions have been generated in the processes for producing various products in plants.
  • Meanwhile, regulations on effluence of such inorganic ions have been becoming gradually strict. In order to comply with the effluent control, an inorganic ion removing method that can effectively remove inorganic ions from wastewater including the inorganic ions and can be carried out as easily and inexpensively as possible is demanded.
  • Hitherto, as the method for removing impurity ions from, for example, wastewater from plants, for example, a flocculating precipitation method, an ion-exchange method, a method for adsorption to an adsorbent such as activated charcoal, an electrosorption method, and a magnetic adsorption method have been proposed.
  • For example, as the flocculating precipitation method, there has been proposed a method of performing a step of adding a base to wastewater in which heavy metal ions are dissolved, to make the wastewater basic, insolubilize at least part of the heavy metal ions, and form a suspended solid matter, a step of adding an inorganic flocculant to the wastewater to make the suspended solid matter flocculate and settle, a step of adding a polymeric flocculant to the wastewater to turn the suspended solid matter to a macrofloc, and an adsorbing step of passing the wastewater through an adsorption layer containing a cation exchanger formed of a leafy vegetable such as mulukhiya and Japanese mustard spinach (see, e.g., PTL 1).
  • There has also been proposed a flocculating method of flocculating and separating particles in a suspension by means of mixed use or combined use of a flocculant containing at least any one of mulukhiya, a dried product of mulukhiya, and an extract of mulukhiya with a polymeric flocculant (see, e.g., PTL 2).
  • There have also been proposed a water-purifying agent formed of a granulated substance containing a mixture of a plant powder and a polymeric flocculant, and a water-purifying method using the water-purifying agent (see, e.g., PTL 3).
  • However, although it hitherto has been known that plant powders can be used for water purification of wastewater, what contribute to water purification, or the specific contributing components have not been elucidated. Hence, there is a matter of study left in use of plant powders for water purification of wastewater.
    • CITATION LIST Patent Literature PTL 1: Japanese Patent Application Laid-Open (JP-A) No. 2011-194385 PTL 2: JP-A No. 11-114313 PTL 3: JP-A No. 2016-73898 SUMMARY OF INVENTION Technical Problem
  • The present invention has an object to identify effective components in plant powders that contribute to water purification and provide a water-purifying agent that can exhibit an excellent water-purifying performance to wastewater efficiently even in a small amount and infallibly.
    • Solution to Problem
  • Means for solving the above problems are as follows.
  • <1> An extract, being formed of:
  • a fractionated component 1 (hereinafter, may also be referred to as component 1 in the present invention) of a water extract of a plant powder,
  • wherein the fractionated component 1 is a fractionated component having a fractionation molecular weight of 12,000 or greater,
  • wherein an ethanol-undissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in a Fourier transform infrared spectroscopy (FT-IR) measurement and exhibits a peak attributable to cellulose in a gas chromatography mass spectrometry (GC-MS) measurement, and
  • wherein an ethanol-dissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in the FT-IR measurement and exhibits a peak attributable to a plant protein in the GC-MS measurement.
  • <2> The extract according to <1>,
  • wherein the ethanol-undissolved component and the ethanol-dissolved component of the fractionated component 1 exhibit the peaks near 1,700 (cm−1) and near 1,600 (cm−1) in the FT-IR measurement.
  • <3> The extract according to <1> or <2>,
  • wherein the fractionated component 1 contains a substance having a weight average molecular weight (Mw) of 300,000 or greater by 50% or greater.
  • <4> The extract according to any one of <1> to <3>,
  • wherein the plant powder is a powder of Corchorus olitorius.
  • <5> An extract, being formed of:
  • a fractionated component 2 (hereinafter, may also be referred to as component 2 in the present invention) of a water extract of a plant powder,
  • wherein the fractionated component 2 is a fractionated component having a fractionation molecular weight of less than 3,400,
  • wherein an ethanol-undissolved component of the fractionated component 2 exhibits a peak attributable to an amide group in a FT-IR measurement, and
  • wherein an ethanol-dissolved component of the fractionated component 2 exhibits a peak attributable to an amide group in the FT-IR measurement.
  • <6> The extract according to <5>,
  • wherein the ethanol-undissolved component and the ethanol-dissolved component of the fractionated component 2 exhibit main peaks in a range of from 1,590 (cm−1) through 1,630 (cm−1) in the FT-IR measurement.
  • <7> The extract according to <5> or <6>,
  • wherein the ethanol-undissolved component and the ethanol-dissolved component of the fractionated component 2 exhibit peaks of 1,8-diazacyclotetradecane-2,7-dione in a GC-MS measurement.
  • <8> The extract according to any one of <5> to <7>,
  • wherein the fractionated component 2 contains a substance having a weight average molecular weight (Mw) of from 200 through 2,500 by 90% or greater.
  • <9> The extract according to any one of <5> to <8>,
  • wherein the fractionated component 2 is a water-soluble chitosan.
  • <10> The extract according to any one of <5> to <9>,
  • wherein the plant powder is a powder of Corchorus olitorius.
  • <11> A water-purifying agent, including:
  • the extract according to any one of <1> to <4>.
  • <12> A water-purifying agent, including:
  • the water-purifying agent according to <11>; and
  • the extract according to any one of <5> to <10>.
  • <13> A water-purifying agent, including:
  • the extract according to any one of <5> to <10>.
  • <14> A water-purifying agent, including:
  • a plant powder,
  • wherein when the plant powder is subjected to water extraction, an extracted component, which is formed of a fractionated component 1 having a fractionation molecular weight of 12,000 or greater, is contained in the plant powder in an amount of 0.5% by mass or greater,
  • wherein an ethanol-undissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in a FT-IR measurement and exhibits a peak attributable to cellulose in a GC-MS measurement, and
  • wherein an ethanol-dissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in the FT-IR measurement and exhibits a peak attributable to a plant protein in the GC-MS measurement.
  • <15> The water-purifying agent according to <14>,
  • wherein the ethanol-undissolved component and the ethanol dissolved component of the fractionated component 1 exhibit the peaks near 1,700 (cm−1) and near 1,600 (cm−1) in the FT-IR measurement.
  • <16> The water-purifying agent according to <14> or <15>,
  • wherein the fractionated component 1 contains a substance having a weight average molecular weight (Mw) of 300,000 or greater by 50% or greater.
  • <17> The water-purifying agent according to any one of <14> to <16>,
  • wherein the plant powder is a powder of Corchorus olitorius.
  • <18> A water-purifying agent, including:
  • a plant powder,
  • wherein when the plant powder is subjected to water extraction, an extracted component, which is formed of a fractionated component 2 having a fractionation molecular weight of less than 3,400, is contained in the plant powder in an amount of 0.05% by mass or greater,
  • wherein an ethanol-undissolved component of the fractionated component 2 exhibits a peak attributable to an amide group in a FT-IR measurement, and
  • wherein an ethanol-dissolved component of the fractionated component 2 exhibits a peak attributable to an amide group in the FT-IR measurement.
  • <19> The water-purifying agent according to <18>,
  • wherein the ethanol-undissolved component and the ethanol-dissolved component of the fractionated component 2 exhibit main peaks in a range of from 1,590 (cm−1) through 1,630 (cm−1) in the FT-IR measurement.
  • <20> The water-purifying agent according to <18> or <19>,
  • wherein the ethanol-undissolved component and the ethanol-dissolved component of the fractionated component 2 exhibit peaks of 1,8-diazacyclotetradecane-2,7-dione in a GC-MS measurement.
  • <21> The water-purifying agent according to any one of <18> to <20>,
  • wherein the fractionated component 2 contains a substance having a weight average molecular weight (Mw) of from 200 through 2,500 by 90% or greater.
  • <22> The water-purifying agent according to any one of <18> to <21>,
  • wherein the fractionated component 2 is a water-soluble chitosan.
  • <23> The water-purifying agent according to any one of <18> to <22>,
  • wherein the plant powder is a powder of Corchorus olitorius.
  • <24> The water-purifying agent according to any one of <14> to <17>,
  • wherein the water-purifying agent is the water-purifying agent according to any one of <18> to <23>.
  • <25> The water-purifying agent according to any one of <11> to <24>, including:
  • a polymeric flocculant.
  • <26> The water-purifying agent according to <25>,
  • wherein the polymeric flocculant is polyacrylamide.
  • <27> A wastewater treatment method, including:
  • feeding the water-purifying agent according to any one of <11> to <26> to wastewater, to remove an inorganic unnecessary substance in the wastewater.
  • <28> The wastewater treatment method according to <27>,
  • wherein the wastewater is wastewater including the inorganic unnecessary substance containing at least any one selected from the group consisting of nickel, fluorine, iron, copper, zinc, chromium, arsenic, cadmium, tin, and lead.
    • Advantageous Effects of Invention
  • The present invention can provide a water-purifying agent that can exhibit an excellent water-purifying performance to wastewater efficiently even in a small amount and infallibly.
    • BRIEF DESCRIPTION OF DRAWINGS
  • FIG. 1 is an image diagram illustrating a fractionated component 1 (may also be referred to as component 1) and a fractionated component 2 (may also be referred to as component 2), which are the subjects of the present invention among water extracts of a plant powder;
  • FIG. 2 is an image diagram illustrating a method for extracting the component 1 and the component 2;
  • FIG. 3 is a graph plotting a result of an experiment of a water-purifying effect of the component 1;
  • FIG. 4 plots a result of a microscopic IR measurement of the component 2;
  • FIG. 5 is a graph plotting a result of an experiment of a water-purifying effect of the component 2;
  • FIG. 6A plots a result of a Fourier transform infrared spectroscopy (FT-IR) measurement of an ethanol-undissolved component (component A) of the component 1;
  • FIG. 6B plots a result of a Fourier transform infrared spectroscopy (FT-IR) measurement of an ethanol-dissolved component (component B) of the component 1;
  • FIG. 6C plots a result of a Fourier transform infrared spectroscopy (FT-IR) measurement of an ethanol-undissolved component (component G) of the component 2;
  • FIG. 6D plots a result of a Fourier transform infrared spectroscopy (FT-IR) measurement of an ethanol-dissolved component (component H) of the component 2;
  • FIG. 7A plots a result of a gas chromatography mass spectrometry (GC-MS) measurement of the ethanol-undissolved component (component A) of the component 1;
  • FIG. 7B plots a result of a gas chromatography mass spectrometry (GC-MS) measurement of the ethanol-dissolved component (component B) of the component 1;
  • FIG. 7C plots a result of a gas chromatography mass spectrometry (GC-MS) measurement of the ethanol-undissolved component (component G) of the component 2;
  • FIG. 7D plots a result of a gas chromatography mass spectrometry (GC-MS) measurement of the ethanol-dissolved component (component H) of the component 2;
  • FIG. 8A plots a result of a gel permeation chromatograph (GPC) measurement of the component 1;
  • FIG. 8B plots a result of a gel permeation chromatograph (GPC) measurement of the component 2;
  • FIG. 9 is a diagram indicating an identification number of “intermediate jute No. 3” that may be used in the present invention; and
  • FIG. 10 is a diagram indicating an identification number of “intermediate kenaf” that may be used in the present invention.
    •  DESCRIPTION OF EMBODIMENTS (Extract of Plant Powder)
  • As a result of earnest studies into the water-purifying function of a plant powder, the present inventors have found effective components of a plant powder that contribute to water purification.
  • It has been confirmed that among water extracts of the plant powder, extracted components, which are formed of a fractionated component 1 (may also be referred to as component 1 in the present invention) having a fractionation molecular weight of 12,000 or greater and a fractionated component 2 (may also be referred to as component 2 in the present invention) having a fractionation molecular weight of less than 3,400 illustrated in FIG. 1, each have an excellent water-purifying action.
  • Here, the plant is not particularly limited and any plant that contains the component 1 and the component 2 in effective amounts respectively may be used. Preferable examples of the plant include Corchorus olitorius and mulukhiya.
  • Particularly, as Corchorus olitorius, for example, Corchorus olitorius produced in Nansha City of China, or “intermediate jute No. 4” under nationally identified hemp 2013, “intermediate jute No. 3” under varieties identification of registration No. 1209006 in Anhui province, “intermediate jute No. 1” under XPD005-2005, and “intermediate kenaf” under varieties identification of registration No. 1209001 in Anhui province, which are identification numbers in Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, can be suitably used.
  • Above all, the “intermediate jute No. 4”, the “intermediate jute No. 3”, and the “intermediate kenaf” are more preferable, and the “intermediate jute No. 4” is particularly preferable.
  • The identification number of the “intermediate jute No. 3” is indicated in FIG. 9. The identification number of the “intermediate kenaf” is indicated in FIG. 10.
  • The “intermediate jute No. 4” has the following properties.
  • Agricultural product type: Jute
    • <Extract Formed of Fractionated Component 1> <<Method for Extracting Fractionated Component 1>>
  • The fractionated component 1 can be extracted according to a method illustrated in FIG. 2. Specifically, a dry plant is ground and subjected to extraction using ethyl acetate. Subsequently, the extraction residue is further subjected to extraction using distilled water, to obtain a supernatant. The supernatant is subjected to dialysis, to separate a component having a fractionation molecular weight of 12,000 or greater. In this way, the fractionated component 1 is obtained.
    • <<Result of Analysis of Fractionated Component 1>> <<<Result of Analysis of Component A>>
  • An ethanol-undissolved component (denoted by component A in FIG. 1) of the fractionated component 1 was measured by a Fourier transform infrared spectroscopy (FT-IR) method. The result of the measurement is plotted in FIG. 6A. This FT-IR measurement was performed with FTS-7000e/UMA600, VARIAN, and microscopic diamond cells. FT-IR measurements of a component B, a component G, and a component H described below were also performed under the same conditions.
  • As plotted in FIG. 6A, the component A exhibited peaks attributable to carboxylic acid in the FT-IR measurement. That is, the component A exhibited peaks near 1,700 (cm−1) (ketone stretching) and near 1,600 (cm−1) (amide stretching).
  • The component A was also measured by a gas chromatography mass spectrometry (GC-MS) method. The result of the measurement is plotted in FIG. 7A. This GC-MS measurement was performed with JMS-600H available from JEOL, using Ionization mode: EI+. GC-MS measurements of the component B, the component G, and the component H described below were also performed under the same conditions.
  • As plotted in FIG. 7A, the component A exhibited peaks attributable to cellulose in the GC-MS measurement.
  • Attributions of the peaks (A1) to (A20) in FIG. 7A are estimated to be as follows.
  • (A1): CO2
  • (A2): acetaldehyde
  • (A3) ◯: ethanol
  • (A4) ◯: acetyl formaldehyde
  • (A5) ◯: diacetyl
  • (A6) ◯: acetic acid
  • (A7) ◯: acetol
  • (A8) Δ: toluene
  • (A9) ◯: acetoxyacetic acid
  • (A10) ◯: 3-furaldehyde
  • (A11) ◯: pyruvic acid methyl ester
  • (A12) ◯: furfural (2-furaldehyde)
  • (A13) ◯: the compound below
  • Figure US20190256387A1-20190822-C00001
  • (A14) ◯: the compound below
  • Figure US20190256387A1-20190822-C00002
  • (A15) ◯: the compound below
  • Figure US20190256387A1-20190822-C00003
  • (A16) Δ: phenol
  • (A17) Δ: 4-pyridinol
  • (A18) Δ: cresol
  • (A19) Δ: indole
  • (A20): acetyl tributyl citrate
  • The symbol “◯” affixed to the above signs denotes a peak of a fragment attributable to cellulose.
  • The symbol “Δ” affixed to the above signs denotes a peak of a fragment attributable to gluten (plant protein).
    • <<<Result of Analysis of Component B>>
  • An ethanol-dissolved component (denoted by component B in FIG. 1) of the fractionated component 1 was measured by FT-IR. The result of the measurement is plotted in FIG. 6B.
  • As plotted in FIG. 6B, the component B exhibited peaks attributable to carboxylic acid in the FT-IR measurement. That is, the component B exhibited peaks near 1,700 (cm−1) (ketone stretching) and near 1,600 (cm−1) (amide stretching).
  • The component B was also measured by GC-MS. The result of the measurement is plotted in FIG. 7B.
  • As plotted in FIG. 7B, the component B exhibited peaks attributable to a plant protein in the GC-MS measurement.
  • Attributions of the peaks (B1) to (B16) in FIG. 7B are estimated to be as follows.
  • (B1): CO2
  • (B2): acetaldehyde
  • (B3) ◯: diacetyl
  • (B4) □: acetic acid
  • (B5) ◯: the compound below
  • Figure US20190256387A1-20190822-C00004
  • (B6) □: acetic anhydride
  • (B7) ◯: pyruvic acid methyl ester
  • (B8) ◯: furfural (2-furaldehyde)
  • (B9) ◯: the compound below
  • Figure US20190256387A1-20190822-C00005
  • (B10) ◯: the compound below
  • Figure US20190256387A1-20190822-C00006
  • (B11) Δ: phenol
  • (B12) Δ: cresol
  • (B13) ◯: the compound below
  • Figure US20190256387A1-20190822-C00007
  • (B14) Δ: indole
  • (B15): hydroquinone
  • (B16): oleamide
  • The symbol “◯” affixed to the above signs denotes a peak of a fragment attributable to cellulose.
  • The symbol “□” affixed to the above signs denotes a peak of a fragment attributable to cellulose acetate.
  • The symbol “Δ” affixed to the above signs denotes a peak of a fragment attributable to gluten (plant protein).
  • From the results of the FT-IR measurements and the GC-MS measurements of the component A and the component B, the component 1 is considered to be formed of uronic acid or carboxylic acid that has a structure similar to galacturonic acid. Hence, the component 1 is considered to have inorganic ions adsorb thereto and exhibit an excellent effect in water purification.
  • The component 1 was also measured by gel permeation chromatograph (GPC). The result of the measurement is plotted in FIG. 8A. This GPC measurement was performed with GPC SYSTEM 21, Shodex, and TSKgel GMPW. GPC measurement of the component 2 described below was also performed under the same conditions.
  • From the result of FIG. 8A, it can be seen that the component 1 contains a substance having a weight average molecular weight (Mw) of 300,000 or greater by 50% (area) or greater.
    • <<Water-Purifying Action of Fractionated Component 1>>
  • An experiment of a water-purifying action was performed using the extract formed of the component 1. The result is plotted in FIG. 3.
  • In FIG. 3, (i) plots the change of the Ni ion concentration when the extract formed of the component 1 was directly added in water containing NI. On the other hand, in FIG. 3, (ii) plots the change of the Ni ion concentration when a commercially available polymeric flocculant (polyacrylamide: PAM) was added as a water-purifying agent in water containing Ni.
  • From the result of FIG. 3, it was confirmed that the component 1 was able to improve the water quality (reduction in the Ni ion concentration) in a smaller amount than the PAM.
    • <Extract Formed of Fractionated Component 2> <<Method for Extracting Fractionated Component 2>>
  • The fractionated component 2 can be extracted according to the method illustrated in FIG. 2. Specifically, a component having a fractionation molecular weight of less than 12,000, which was obtained by the dialysis described above, is further subjected to dialysis, to obtain a component having a fractionation molecular weight of less than 6,000, which is further subjected to dialysis, to obtain and separate a component having a fractionation molecular weight of less than 3,400. In this way, the fractionated component 2 is obtained.
    • <<Result of Analysis of Fractionated Component 2>> <<<Result of Analysis of Component G>>
  • An ethanol-undissolved component (denoted by component G in FIG. 1) of the fractionated component 2 was measured by FT-IR. The result of the measurement is plotted in FIG. 6C.
  • As plotted in FIG. 6C, the component G exhibits peaks attributable to an amide group in the FT-IR measurement. That is, the component G exhibits main peaks in a range of from 1,590 (cm−1) through 1,630 (cm−1) (amide stretching).
  • The component G was also measured by GC-MS. The result of the measurement is plotted in FIG. 7C.
  • As plotted in FIG. 7C, the component G exhibits peaks of 1,8-diazacyclotetradecane-2,7-dione in the GC-MS measurement.
  • Attributions of the peaks (C1) to (C13) in FIG. 7C are estimated to be as follows.
  • (C1): CO2
  • (C2): acetone
  • (C3): acetol
  • (C4) Δ: toluene
  • (C5) x: pyrrole
  • (C6): cyclopentanone
  • (C7): the compound below
  • Figure US20190256387A1-20190822-C00008
  • (C8) Δ: cresol
  • (C9) x: 2-pyrrolidinone
  • (C10) x: indole
  • (C11): hydroquinone
  • (C12): acetyl tributyl citrate
  • (C13) x: 1,8-diazacyclotetradecane-2,7-dione
  • The symbol “x” affixed to the above signs denotes a peak of a fragment attributable to polysaccharide such as chitin and chitosan.
  • The symbol “Δ” affixed to the above signs denotes a peak of a fragment attributable to gluten (plant protein).
    • <<<Result of Analysis of Component H>>
  • An ethanol-dissolved component (denoted by component H in FIG. 1) of the fractionated component 2 was measured by FT-IR. The result of the measurement is plotted in FIG. 6D.
  • As plotted in FIG. 6D, the component H exhibits peaks attributable to an amide group in the FT-IR measurement. That is, the component H exhibits main peaks in a range of from 1,590 (cm−1) through 1,630 (cm−1) (amide stretching).
  • The component H was also measured by GC-MS. The result of the measurement is plotted in FIG. 7D.
  • As plotted in FIG. 7D, the component H exhibits peaks of 1,8-diazacyclotetradecane-2,7-dione in the GC-MS measurement.
  • Attributions of the peaks (D1) to (D17) in FIG. 7C are estimated to be as follows.
  • (D1): CO2
  • (D2): methyl ethyl ketone
  • (D3): acetic acid
  • (D4) ◯: acetol
  • (D5) Δ: toluene
  • (D6) x: pyrrole
  • (D7): styrene
  • (D8) x: 2-methyl-1H-pyrrole
  • (D9) x: the compound below
  • Figure US20190256387A1-20190822-C00009
  • (D10) Δ: phenol
  • (D11): p-methoxytoluene
  • (D12) Δ: cresol
  • (D13): p-ethylphenol
  • (D14) x: indole
  • (D15): hydroquinone
  • (D16): acetyl tributyl citrate
  • (D17) x: 1,8-diazacyclotetradecane-2,7-dione
  • The symbol “◯” affixed to the above sign denotes a peak of a fragment attributable to cellulose.
  • The symbol “x” affixed to the above signs denotes a peak of a fragment attributable to polysaccharide such as chitin and chitosan.
  • The symbol “Δ” affixed to the above signs denotes a peak of a fragment attributable to gluten (plant protein).
  • The result of a microscopic infrared spectroscopy (microscopic IR) measurement in which the extract formed of the component 2 was compared with chitosan is plotted in FIG. 4.
  • From the results of the FT-IR measurements and the GC-MS measurements of the component G and the component H and the result of FIG. 4, the component 2 is considered to be a water-soluble chitosan. Chitosans (chitins) extracted from, for example, crustacean are typically water-insoluble, but water-soluble chitosan is considered to be effective in adsorption of inorganic ions.
  • In the present invention, water solubility means solubility of 50% by mass of greater in water.
  • The component 2 was also measured by GPC. The result of the measurement is plotted in FIG. 8B.
  • From the result of FIG. 8, it can be seen that the component 2 contains a substance having a weight average molecular weight (Mw) of from 200 through 2,500 by 90% (area) or greater.
    • <<Water-Purifying Action of Fractionated Component 2>>
  • An experiment of a water-purifying action was performed using the extract formed of the component 2. The result is plotted in FIG. 5.
  • In FIG. 5, (i) plots the change of the Ni ion concentration when the extract formed of the component 2 was directly added in water containing Ni. On the other hand, in FIG. 5, (ii) and (iii) plot the changes of the Ni ion concentration when a commercially available ZETA ACE as a flocculant and chitosan were added in water containing Ni.
  • From the results of FIG. 5, addition of ZETA ACE in a higher amount led to greater suppression of floc growth and a poorer water quality level, whereas the component 2 succeeded in improving the water quality (reducing the Ni ion concentration) regardless of the amount of addition. The component 2 is considered to exhibit a water-purifying effect based on a mechanism that cannot be explained only by the flocculating effect exhibited by ZETA ACE, i.e., a mechanism different from a zeta potential.
  • Moreover, as plotted in FIG. 5, the component 2 achieved a result similar to the case of adding chitosan in the wastewater. Also from this result, the component 2 is considered to be a chitosan.
    • (Water-Purifying Agent)
  • The water-purifying agent of the present invention contains a plant powder.
  • As the first mode of the water-purifying agent of the present invention, it is preferable that the plant powder contain the component 1 or the component 2, or both thereof, which is/are (Extract of plant powder) described above.
  • This is because an effective water-purifying action can be exhibited efficiently even if the amount of addition is small.
  • As the second mode of the water-purifying agent of the present invention, it is preferable that the water-purifying agent contain a plant powder that contains extracted component(s) formed of the component 1 or the component 2, or both thereof in predetermined effective amount(s).
    • <First Mode>
  • The water-purifying agent of the present invention contains the component 1 or the component 2, or both thereof extracted by the production method described above.
  • Particularly, it is preferable that the water-purifying agent of the present invention contain both of the component 1 and the component 2 extracted by the production method described above. As plotted in FIG. 3 and FIG. 5, it is inferred that the component 1 and the component 2 both have a water-purifying function but have different mechanisms of the water-purifying function. Hence, containing both of the components makes it possible to express the water-purifying function by a plurality of approaches. Therefore, a water-purifying agent containing both of the component 1 and the component 2 is more preferable.
    • <Second Mode>
  • The water-purifying agent of the present invention contains a plant powder containing extracted component(s) formed of the component 1 or the component 2, or both thereof.
  • Here, the component 1 is contained in the plant powder in an amount of 0.5% by mass or greater, more preferably in an amount of 0.7% by mass, and yet more preferably in an amount of 0.9% by mass as will be demonstrated by Examples.
  • The component 2 is contained in the plant powder in an amount of 0.05% by mass or greater, and more preferably in an amount of 0.07% by mass.
  • According to the flowchart illustrated in FIG. 2, the component 1 and the component 2 were extracted from a dried product of Corchorus olitorius including all leaves, stalks, and roots. As the yield of each extracted component, the result presented in Table 1 below was achieved as a result of one experiment example. The numerals (1) to (5) in Table 1 correspond to the numerals (1) to (5) in FIG. 2. That is, when the raw material of the plant powder is regarded as 100 parts by mass, the component 1 was extracted in an amount of 0.9 parts by mass, and the component 2 was extracted in an amount of 0.07 parts by mass (see the results of (2) and (5) in Table 1).
  • Next, the component 1 and the component 2 were extracted from a dried product of Corchorus olitorius including only leaves. The results as the yields of the respective components are presented below (Table 2 below).
  • As can be seen from Table 1 below and Table 2 below, the yields of the component 1 and the component 2 vary depending on the plant powder, which is the raw material. Hence, it is preferable to appropriately adjust the contents of the component 1 and the component 2 to desired ranges respectively, by varying the ratio among leaves, stalks, and roots of the plant.
  • TABLE 1
    Yield of extracted component
    (relative to 100.00% of raw material
    (leaves, stalks, and
    Fractionation of molecular weight roots) indicated by (1) in FIG. 2)
    12,000~ 0.900% (indicated by (2) in FIG. 2)
     6,000~12,000 0.600% (indicated by (4) in FIG. 2)
    3,400~6,000 0.400% (indicated by (4) in FIG. 2)
    ~3,400   0.070% (indicated by (5) in FIG. 2)
  • TABLE 2
    Yield of extracted component
    (relative to 100.00% of raw
    material (only leaves)
    Fractionation of molecular weight indicated by (1) in FIG. 2)
    12,000~ 7.000% (indicated by (2) in FIG. 2)
    6,000~12,000 3.000% (indicated by (4) in FIG. 2)
    3,400~6,000 0.790% (indicated by (4) in FIG. 2)
    ~3,400   5.666% (indicated by (5) in FIG. 2)
    • <Other Additives>
  • In addition to the powder of the plant, the water-purifying agent may contain additives such as a polymeric flocculant, a filler, a thickener, a colorant, and a thixotropy imparting agent as other additives.
    • <<Polymeric Flocculant>>
  • The polymeric flocculant is not particularly limited so long as the polymeric flocculant exhibits an effect of removing the inorganic unnecessary substance in wastewater like the powder of the plant described above. Examples of the polymeric flocculant include polyacrylamide (PAM), a salt obtained by partially hydrolyzing polyacrylamide, sodium alginate, sodium polyacrylate, and CMC sodium salt. Among these polymeric flocculants, polyacrylamide is preferable for use. As the polyacrylamide, for example, commercially available products FLOPAN AN 956, FLOPAN AN 995SH, FA 920SH, FO 4490, and AN 923 (available from SNF Japan Co., Ltd.) can be used.
  • It is preferable that the ratio of the component 1 in the water-purifying agent that also contains the other additives such as the polymeric flocculant be 0.5% by mass or greater relative to the total amount of the water-purifying agent.
  • It is preferable that the ratio of the component 2 be 0.05% by mass or greater relative to the total amount of the water-purifying agent.
    • (Wastewater Treatment Method)
  • A wastewater treatment method of the present invention is for removing the inorganic unnecessary substance in wastewater by feeding the water-purifying agent of the present invention described above to the wastewater.
  • Examples of the inorganic unnecessary substance include an inorganic unnecessary substance that contains at least any one selected from the group consisting of nickel, fluorine, iron, copper, zinc, chromium, arsenic, cadmium, and lead.
  • The wastewater treatment method of the present invention will be specifically described.
  • For example, it is possible to add the water-purifying agent of the present invention after an insolubilizing step of adding a base to wastewater to make the wastewater basic, insolubilize at least part of the heavy metal ions, and form a suspended solid matter.
  • The water-purifying agent is fed to the wastewater to make the inorganic unnecessary substance flocculate and settle, and the settled, separated precipitate is removed. In this way, the wastewater is purified.
    • EXAMPLES
  • The present invention will be described below by way of Examples. The present invention should not be construed as being limited to these Examples.
    • Example 1
  • As the plant, “intermediate jute No. 4”, which was Corchorus olitorius having an identification number 2013 in Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, was used.
  • A dried product (containing the component 1 in an amount of 0.56% by mass) of a plant including all leaves, stalks, and roots of the intermediate jute No. 4 (with a ratio of the leaves in the plant of 8% by mass) was used.
  • The intermediate jute No. 4 was dried and ground, and then separated through a sieve, in order to use a product with a size of 250 micrometers or less.
  • The component 1 being contained in an amount of 0.56% by mass in the dried product of the intermediate jute No. 4 used in the present Example was confirmed by performing the extracting operation described below.
  • That is, ethyl acetate was added to the dried product of the intermediate jute No. 4, to obtain a 10% by mass solution, which was left to stand still at room temperature (23 degrees C.) for 8 hours, followed by filtration through a filter paper. The residue was washed with ethyl acetate, and then further subjected to extraction using distilled water, to obtain a supernatant, which was subjected to dialysis to separate a component having a fractionation molecular weight of 12,000 or greater, to obtain the component 1. Then, the ratio of the component 1 relative to the dried product of the intermediate jute No. 4, which was the raw material, was calculated.
  • To wastewater containing nickel, FeCl3 was added by 250 ppm as a primary flocculant, and then the water-purifying agent containing the dried product of Corchorus olitorius containing the component 1 in an amount of 0.56% by mass was added.
  • The initial Ni ion concentration was 60 ppm.
  • The result of the nickel ion concentration when the water-purifying agent of the present invention was added is presented in Table 3 below. As presented in Table 3, reduction in the nickel ion concentration was confirmed. With a nickel ion concentration of 8 ppm or lower, it can be judged that the water-purifying agent is non-problematic in practical use.
    • Example 2
  • An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, the dried product of the intermediate jute No. 4 was changed to a dried product with a ratio of leaves of 10% by mass (containing the component 1 in an amount of 0.7% by mass). As presented in Table 3 below, reduction in the nickel ion concentration was confirmed in Example 2.
    • Example 3
  • An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, the dried product of the intermediate jute No. 4 was changed to a dried product with a ratio of leaves of 100% by mass (containing the component 1 in an amount of 7.0% by mass). As presented in Table 3 below, reduction in the nickel ion concentration was confirmed in Example 3.
    • Comparative Example 1
  • An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, the dried product of the intermediate jute No. 4 was changed to a dried product mainly containing stalks and roots but free of leaves (containing the component 1 in an amount of 0.1% by mass). As presented in Table 3 below, reduction in the nickel ion concentration was poor in Comparative Example 1.
    • Comparative Example 2
  • An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, the dried product of the intermediate jute No. 4 was changed to a dried product with a ratio of leaves of 3% by mass (containing the component 1 in an amount of 0.21% by mass). As presented in Table 3 below, a sufficient reduction in the nickel ion concentration was not achieved in Comparative Example 2.
    • Comparative Example 3
  • An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, the dried product of the intermediate jute No. 4 was changed to a dried product with a ratio of leaves of 5% by mass (containing the component 1 in an amount of 0.35% by mass). As presented in Table 3 below, a sufficient reduction in the nickel ion concentration was not achieved in Comparative Example 3.
    • Example 4
  • An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, an extract formed of the component 1, extracted from the dried product of the intermediate jute No. 4, was used instead of the dried product of the intermediate jute No. 4, and this extract was directly added in an amount of 50 ppm. As presented in Table 3 below, reduction in the nickel ion concentration was confirmed in Example 4.
    • Example 5
  • An experiment was performed in the same manner as in Example 4, except that unlike in Example 4, the extract formed of the component 1, extracted from the dried product of the intermediate jute No. 4, was added with the amount of addition changed to 5 ppm. As presented in Table 3 below, an excellent reduction in the nickel ion concentration that is the same as in Example 4 was confirmed with even such a small amount of addition.
    • Example 6
  • An experiment was performed in the same manner as in Example 1, except that unlike in Example 1, as the kind of the plant, “intermediate jute No. 3”, which was Corchorus olitorius having an identification number in Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, i.e., varieties identification of registration No. 1209006 in Anhui province, was used instead of the intermediate jute No. 4.
  • Although the nickel ion concentration reducing effect was better in Example 1, a good nickel ion concentration reducing effect, which was almost the same as in Example 1, was exhibited in Example 6.
  • TABLE 3
    Amount of Content of Ni ion
    water-purifying component 1 in concentration after
    Part of plant agent added (ppm) plant (% by mass) treatment (ppm)
    Comp. Ex. 1 Other than leaves 50 0.1 35
    Comp. Ex. 2 3% by mass of leaves 50 0.21 15
    Comp. Ex. 3 5% by mass of leaves 50 0.35 10
    Ex. 1 8% by mass of leaves 50 0.56 6
    Ex. 2 10% by mass of leaves 50 0.7 5.6
    Ex. 3 100% by mass of leaves 50 7.0 5
    Ex. 4 Component 1 50 100 Lower than 5
    Ex. 5 Component 1 5 100 Lower than 5

Claims (17)

1. An extract, being formed of:
a fractionated component 1 of a water extract of a plant powder,
wherein the fractionated component 1 is a fractionated component having a fractionation molecular weight of 12,000 or greater,
wherein an ethanol-undissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in a Fourier transform infrared spectroscopy (FT-IR) measurement and exhibits a peak attributable to cellulose in a gas chromatography mass spectrometry (GC-MS) measurement, and
wherein an ethanol-dissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in the FT-IR measurement and exhibits a peak attributable to a plant protein in the GC-MS measurement.
2. An extract, being formed of:
a fractionated component 2 of a water extract of a plant powder,
wherein the fractionated component 2 is a fractionated component having a fractionation molecular weight of less than 3,400,
wherein an ethanol-undissolved component of the fractionated component 2 exhibits a peak attributable to an amide group in a FT-IR measurement, and
wherein an ethanol-dissolved component of the fractionated component 2 exhibits a peak attributable to an amide group in the FT-IR measurement.
3. The extract according to claim 2,
wherein the ethanol-undissolved component and the ethanol-dissolved component of the fractionated component 2 exhibit peaks of 1,8-diazacyclotetradecane-2,7-dione in a GC-MS measurement.
4. The extract according to claim 2,
wherein the fractionated component 2 is a water-soluble chitosan.
5. A water-purifying agent, comprising:
the extract according to claim 1.
6. A water-purifying agent, comprising:
a plant powder,
wherein when the plant powder is subjected to water extraction, an extracted component, which is formed of a fractionated component 1 having a fractionation molecular weight of 12,000 or greater, is contained in the plant powder in an amount of 0.5% by mass or greater,
wherein an ethanol-undissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in a FT-IR measurement and exhibits a peak attributable to cellulose in a GC-MS measurement, and
wherein an ethanol-dissolved component of the fractionated component 1 exhibits a peak attributable to carboxylic acid in the FT-IR measurement and exhibits a peak attributable to a plant protein in the GC-MS measurement.
7. A water-purifying agent, comprising:
a plant powder,
wherein when the plant powder is subjected to water extraction, an extracted component, which is formed of a fractionated component 2 having a fractionation molecular weight of less than 3,400, is contained in the plant powder in an amount of 0.05% by mass or greater,
wherein an ethanol-undissolved component of the fractionated component 2 exhibits a peak attributable to an amide group in a FT-IR measurement, and
wherein an ethanol-dissolved component of the fractionated component 2 exhibits a peak attributable to an amide group in the FT-IR measurement.
8. The water-purifying agent according to claim 7,
wherein the ethanol-undissolved component and the ethanol-dissolved component of the fractionated component 2 exhibit peaks of 1,8-diazacyclotetradecane-2,7-dione in a GC-MS measurement.
9. The water-purifying agent according to claim 7,
wherein the fractionated component 2 is a water-soluble chitosan.
10. (canceled)
11. The water-purifying agent according to claim 5, comprising:
a polymeric flocculant.
12. The water-purifying agent according to claim 11,
wherein the polymeric flocculant is polyacrylamide.
13. A wastewater treatment method, comprising:
feeding the water-purifying agent according to claim 5 to wastewater, to remove an inorganic unnecessary substance in the wastewater.
14. The wastewater treatment method according to claim 13,
wherein the wastewater is wastewater that comprises the inorganic unnecessary substance that comprises at least any one selected from the group consisting of nickel, fluorine, iron, copper, zinc, chromium, arsenic, cadmium, tin, and lead.
15. A water-purifying agent, comprising:
the extract according to claim 2.
16. A wastewater treatment method, comprising:
feeding the water-purifying agent according to claim 6 to wastewater, to remove an inorganic unnecessary substance in the wastewater.
17. A wastewater treatment method, comprising:
feeding the water-purifying agent according to claim 7 to wastewater, to remove an inorganic unnecessary substance in the wastewater.
US16/333,440 2016-09-16 2017-09-12 Extract of plant powder, and water purifier Abandoned US20190256387A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP2016181619 2016-09-16
JP2016-181619 2016-09-16
JP2017174021A JP7131894B2 (en) 2016-09-16 2017-09-11 Method for producing extract, extract, water purification agent, and wastewater treatment method
JP2017-174021 2017-09-11
PCT/JP2017/032941 WO2018051992A1 (en) 2016-09-16 2017-09-12 Extract of plant powder, and water purifier

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2017/032941 A-371-Of-International WO2018051992A1 (en) 2016-09-16 2017-09-12 Extract of plant powder, and water purifier

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US17/410,356 Division US11866354B2 (en) 2016-09-16 2021-08-24 Extract of plant powder, and water purifier
US18/177,182 Continuation US11952297B2 (en) 2016-09-16 2023-03-02 Extract of plant powder, and water purifier

Publications (1)

Publication Number Publication Date
US20190256387A1 true US20190256387A1 (en) 2019-08-22

Family

ID=61765750

Family Applications (2)

Application Number Title Priority Date Filing Date
US16/333,440 Abandoned US20190256387A1 (en) 2016-09-16 2017-09-12 Extract of plant powder, and water purifier
US17/410,356 Active 2037-12-03 US11866354B2 (en) 2016-09-16 2021-08-24 Extract of plant powder, and water purifier

Family Applications After (1)

Application Number Title Priority Date Filing Date
US17/410,356 Active 2037-12-03 US11866354B2 (en) 2016-09-16 2021-08-24 Extract of plant powder, and water purifier

Country Status (7)

Country Link
US (2) US20190256387A1 (en)
EP (1) EP3513857B1 (en)
JP (1) JP7131894B2 (en)
KR (1) KR102438091B1 (en)
BR (1) BR112019004936A2 (en)
RU (1) RU2019110785A (en)
TW (1) TWI734834B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11952297B2 (en) 2016-09-16 2024-04-09 Dexerials Corporation Extract of plant powder, and water purifier

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6722807B1 (en) * 2019-05-31 2020-07-15 デクセリアルズ株式会社 Water treatment agent and method for producing the same, and water treatment method
WO2022070745A1 (en) * 2020-10-01 2022-04-07 デクセリアルズ株式会社 Organic coagulant and method for producing same, and water-cleaning agent and method for producing same
JP2022059562A (en) * 2020-10-01 2022-04-13 デクセリアルズ株式会社 Organic coagulant and method for producing the same, and water-cleaning agent and method for producing the same

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0341014A (en) * 1989-07-07 1991-02-21 Ichimaru Pharcos Co Ltd Corchorus olitorius extract-containing cosmetic
JPH0769910A (en) * 1993-09-01 1995-03-14 Otsuka Pharmaceut Co Ltd Composition for improving lipid metabolism and suppressing increase of blood sugar level
JPH0770208A (en) * 1993-09-07 1995-03-14 Kyodo Nyugyo Kk Method for producing viscous polysaccharide of Moroheiya
EP0872490B1 (en) * 1997-04-16 2006-05-17 Sony Corporation High-molecular flocculant, method for producing the flocculant and water-treatment method employing the flocculant
JP3049279B2 (en) 1997-08-19 2000-06-05 工業技術院長 Chitosan, method for producing the same, and polymer flocculant
JP3876497B2 (en) * 1997-10-09 2007-01-31 ソニー株式会社 Flocculant and flocculation method using the same
JP2000140509A (en) 1998-11-16 2000-05-23 Kansai Kako Kk Novel flocculant and sludge treatment using the same
CA2507017A1 (en) 2003-05-07 2005-01-20 Research Institute For Production Development Chitin oligomer composition and/or chitosan oligomer composition, and process for producing the same
US20060216362A1 (en) 2003-05-19 2006-09-28 Tatsuji Enoki Remedy
JP2008126168A (en) 2006-11-22 2008-06-05 Fuji Eng Kk Coagulating sedimentation method of waste water
JP5640419B2 (en) 2010-03-24 2014-12-17 ソニー株式会社 Removal method of heavy metal ions in waste water
JP2011194385A (en) 2010-03-24 2011-10-06 Sony Corp Cation exchanger and method for removing heavy metal ion in wastewater
CN102583681B (en) * 2011-01-14 2014-07-02 索尼公司 Coagulant of plant origin, coagulant mixture, method of coagulation and method of preparing coagulant of plant origin
CN102247814A (en) 2011-05-17 2011-11-23 中国农业科学院麻类研究所 Biomass adsorbent for treatment of heavy metal wastewater and treatment method of heavy metal wastewater
GB201116050D0 (en) 2011-09-16 2011-11-02 Ntnu Technology Transfer As Ionic gel
CN102432692A (en) 2011-12-27 2012-05-02 西华师范大学 Boletus speciosus polysaccharide
JP2014008428A (en) 2012-06-28 2014-01-20 Sony Corp Coagulant mixture and coagulation method
US9617176B2 (en) 2013-05-29 2017-04-11 Aguas De Manizales S.A. E.S.P. Compositions for water treatment and methods of using thereof
CN103641936B (en) 2013-12-09 2016-03-23 吴彪 A kind of method adopting ultrafiltration and nanofiltration to prepare water-soluble chitosan oligosaccharide
JP6301802B2 (en) * 2014-10-03 2018-03-28 デクセリアルズ株式会社 Water purification agent and water purification method
CN104562632B (en) * 2015-01-12 2016-08-24 哈尔滨工业大学 A kind of microwave quickly modified Corchorus olitorius L. prepares method and the application of heavy metal ion exchange fiber
JP6695662B2 (en) 2015-02-12 2020-05-20 国立大学法人京都大学 Dispersion containing polysaccharide nanofibers, dispersion medium and monomer, and resin composition obtained from the dispersion

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11952297B2 (en) 2016-09-16 2024-04-09 Dexerials Corporation Extract of plant powder, and water purifier

Also Published As

Publication number Publication date
TW201813933A (en) 2018-04-16
EP3513857B1 (en) 2021-05-26
JP2018047454A (en) 2018-03-29
JP7131894B2 (en) 2022-09-06
US11866354B2 (en) 2024-01-09
TWI734834B (en) 2021-08-01
RU2019110785A (en) 2020-10-16
EP3513857A4 (en) 2020-06-03
EP3513857A1 (en) 2019-07-24
BR112019004936A2 (en) 2019-06-18
US20210380444A1 (en) 2021-12-09
KR102438091B1 (en) 2022-08-31
KR20190046992A (en) 2019-05-07

Similar Documents

Publication Publication Date Title
US11866354B2 (en) Extract of plant powder, and water purifier
Abdelhadi et al. Production of biochar from olive mill solid waste for heavy metal removal
Wang et al. Comparison of characteristics of twenty-one types of biochar and their ability to remove multi-heavy metals and methylene blue in solution
Mohanasrinivasan et al. Studies on heavy metal removal efficiency and antibacterial activity of chitosan prepared from shrimp shell waste
Sun et al. Adsorption properties of N-succinyl-chitosan and cross-linked N-succinyl-chitosan resin with Pb (II) as template ions
CN101880356B (en) Preparation method of grafting amphoteric chitosan flocculant
US20120024795A1 (en) Biosorbents for the extraction of metals
CN102626608A (en) Straw modified into amphiprotic adsorbent and preparation method thereof
Li et al. Removal of heavy metal Ions in aqueous solution by Exopolysaccharides from Athelia rolfsii
US11952297B2 (en) Extract of plant powder, and water purifier
Bhuvaneshwari et al. Comparative studies for chitosan yield and chelating ability of Aspergillus niger and Rhizopus oryzae
CN103599754B (en) A kind of biomass adsorbent and Synthesis and applications thereof processing lead waste water
Kong et al. Self-aggregation effect of the ternary system “Alga EPS-DOM-HMs” and the characterization of the self-adaptation metabolic response of microalgae
Tayel et al. The potentiality of cross-linked fungal chitosan to control water contamination through bioactive filtration
US20190359503A1 (en) Water purification dispersion, production method for water purification dispersion, and waste water treatment method
CN110698566B (en) A flocculant for capturing microalgae and its preparation method and application
CN112321657B (en) Extraction method of stevioside
Wang et al. Chemical modification of chitosan under high-intensity ultrasound and properties of chitosan derivatives
CN108530288A (en) A kind of more effect components separation of wood vinegar and complete utilization method
JP5046052B2 (en) Metal ion adsorbent and adsorption method using the same
CN1460648A (en) Double-machine flocculant
CN110204059A (en) A kind of heat-resisting sewage treatment reagent being unlikely to deteriorate
Alouiz et al. Elimination of olive mill wastewater polyphenols through an olive pomace-derived activated charcoal
JP2000084538A (en) How to remove heavy metal ions
CN101045697A (en) Clausena lansium stone extraction and preparation method thereof

Legal Events

Date Code Title Description
AS Assignment

Owner name: DEXERIALS CORPORATION, JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:FUJITA, TAKANORI;SHIMADA, RYU;ITO, MASAHIKO;AND OTHERS;SIGNING DATES FROM 20190308 TO 20190401;REEL/FRAME:048793/0014

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE AFTER FINAL ACTION FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION