CA2353499A1 - Method for activating water and use of activated water of this type - Google Patents
Method for activating water and use of activated water of this type Download PDFInfo
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- CA2353499A1 CA2353499A1 CA002353499A CA2353499A CA2353499A1 CA 2353499 A1 CA2353499 A1 CA 2353499A1 CA 002353499 A CA002353499 A CA 002353499A CA 2353499 A CA2353499 A CA 2353499A CA 2353499 A1 CA2353499 A1 CA 2353499A1
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- water
- oxygen
- activated
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 95
- 238000000034 method Methods 0.000 title claims description 29
- 230000003213 activating effect Effects 0.000 title 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims abstract description 21
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000001301 oxygen Substances 0.000 claims abstract description 19
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 19
- 238000005516 engineering process Methods 0.000 claims abstract description 11
- 238000001311 chemical methods and process Methods 0.000 claims abstract description 5
- 238000004140 cleaning Methods 0.000 claims abstract description 5
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- 241000196324 Embryophyta Species 0.000 claims description 15
- 230000012010 growth Effects 0.000 claims description 11
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- 239000000203 mixture Substances 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 5
- 239000013589 supplement Substances 0.000 claims description 5
- 238000009736 wetting Methods 0.000 claims description 5
- 230000036642 wellbeing Effects 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 3
- 238000010422 painting Methods 0.000 claims description 3
- -1 phthalocyanines Chemical class 0.000 claims description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 3
- 239000007921 spray Substances 0.000 claims description 3
- MHIITNFQDPFSES-UHFFFAOYSA-N 25,26,27,28-tetrazahexacyclo[16.6.1.13,6.18,11.113,16.019,24]octacosa-1(25),2,4,6,8(27),9,11,13,15,17,19,21,23-tridecaene Chemical class N1C(C=C2C3=CC=CC=C3C(C=C3NC(=C4)C=C3)=N2)=CC=C1C=C1C=CC4=N1 MHIITNFQDPFSES-UHFFFAOYSA-N 0.000 claims description 2
- ZGXJTSGNIOSYLO-UHFFFAOYSA-N 88755TAZ87 Chemical compound NCC(=O)CCC(O)=O ZGXJTSGNIOSYLO-UHFFFAOYSA-N 0.000 claims description 2
- 241001465754 Metazoa Species 0.000 claims description 2
- 229960002749 aminolevulinic acid Drugs 0.000 claims description 2
- 150000004035 chlorins Chemical class 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- VVOLVFOSOPJKED-UHFFFAOYSA-N copper phthalocyanine Chemical group [Cu].N=1C2=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC=1C1=CC=CC=C12 VVOLVFOSOPJKED-UHFFFAOYSA-N 0.000 claims description 2
- 230000036541 health Effects 0.000 claims description 2
- 239000000976 ink Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000000178 monomer Substances 0.000 claims description 2
- 150000004032 porphyrins Chemical class 0.000 claims description 2
- 229930187593 rose bengal Natural products 0.000 claims description 2
- AZJPTIGZZTZIDR-UHFFFAOYSA-L rose bengal Chemical compound [K+].[K+].[O-]C(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 AZJPTIGZZTZIDR-UHFFFAOYSA-L 0.000 claims description 2
- 229940081623 rose bengal Drugs 0.000 claims description 2
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 claims description 2
- YNHJECZULSZAQK-UHFFFAOYSA-N tetraphenylporphyrin Chemical class C1=CC(C(=C2C=CC(N2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3N2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 YNHJECZULSZAQK-UHFFFAOYSA-N 0.000 claims description 2
- 239000002966 varnish Substances 0.000 claims description 2
- 239000000080 wetting agent Substances 0.000 claims description 2
- 239000007789 gas Substances 0.000 claims 1
- 230000004913 activation Effects 0.000 description 10
- 241000894006 Bacteria Species 0.000 description 8
- 244000046052 Phaseolus vulgaris Species 0.000 description 8
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- 208000015181 infectious disease Diseases 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000002560 therapeutic procedure Methods 0.000 description 6
- 229910002651 NO3 Inorganic materials 0.000 description 5
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 5
- 239000003440 toxic substance Substances 0.000 description 4
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 239000004202 carbamide Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000008635 plant growth Effects 0.000 description 3
- 231100000614 poison Toxicity 0.000 description 3
- 241000222122 Candida albicans Species 0.000 description 2
- 208000009889 Herpes Simplex Diseases 0.000 description 2
- 229940095731 candida albicans Drugs 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000003651 drinking water Substances 0.000 description 2
- 235000020188 drinking water Nutrition 0.000 description 2
- 230000002538 fungal effect Effects 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- 206010007134 Candida infections Diseases 0.000 description 1
- 208000010201 Exanthema Diseases 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- 241000605159 Nitrobacter Species 0.000 description 1
- 241000605122 Nitrosomonas Species 0.000 description 1
- 208000007027 Oral Candidiasis Diseases 0.000 description 1
- 241000269799 Perca fluviatilis Species 0.000 description 1
- 208000003251 Pruritus Diseases 0.000 description 1
- 244000088415 Raphanus sativus Species 0.000 description 1
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 1
- 206010037888 Rash pustular Diseases 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 241000950638 Symphysodon discus Species 0.000 description 1
- 241000287411 Turdidae Species 0.000 description 1
- 240000004922 Vigna radiata Species 0.000 description 1
- 235000010721 Vigna radiata var radiata Nutrition 0.000 description 1
- 235000011469 Vigna radiata var sublobata Nutrition 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 210000001015 abdomen Anatomy 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 201000003984 candidiasis Diseases 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 238000011443 conventional therapy Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
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- 238000010586 diagram Methods 0.000 description 1
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- 230000005670 electromagnetic radiation Effects 0.000 description 1
- 201000005884 exanthem Diseases 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000037311 normal skin Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 208000035824 paresthesia Diseases 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
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- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 208000029561 pustule Diseases 0.000 description 1
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- 238000012360 testing method Methods 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
Classifications
-
- 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
- C02F1/72—Treatment of water, waste water, or sewage by oxidation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- C02F1/30—Treatment of water, waste water, or sewage by irradiation
- C02F1/32—Treatment of water, waste water, or sewage by irradiation with ultraviolet light
-
- 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
- C02F1/68—Treatment of water, waste water, or sewage by addition of specified substances, e.g. trace elements, for ameliorating potable water
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/02—Non-contaminated water, e.g. for industrial water supply
- C02F2103/026—Treating water for medical or cosmetic purposes
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2305/00—Use of specific compounds during water treatment
- C02F2305/02—Specific form of oxidant
- C02F2305/023—Reactive oxygen species, singlet oxygen, OH radical
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Engineering & Computer Science (AREA)
- Hydrology & Water Resources (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Physical Water Treatments (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
Abstract
According to the invention, activated water is produced by producing singlet oxygen in a gaseous medium containing oxygen or in the water itself and bringing the singlet-oxygen into contact with the water. Water which has been activated in this way can be advantageously used in the fields of medicine, chemical process engineering, food technology, agriculture, printing, paint technology and/or cleaning technology.
Description
Method for activatioa of water aad usage of water activated is such a maaaer The present invention relates to a method for activation of water and also usage of activated water. Activated water and a method for the production thereof are required in the spheres of medicine, chemical process engineering, food chemistry, agriculture, printing and in further spheres of technology.
The object of the present invention is thereby to indicate a method for activation of water and to make available usages of water activated in such a manner.
This object is achieved by the method according to claim 1 and also the usages according to claim 19. Advantageous developments of the method according to the invention and the usages according to the invention are given in the dependent claims.
According to the method according to the invention water is activated by producing singlet oxygen and bringing this into contact with the water.
Oxygen occurs in its basic state as a triplet molecule 02 and can be converted into the excited singlet state by supplying energy. This excited singlet oxygen is particularly reactive and is itself already used in medicine and chemical process engineering. Relative to this excited singlet oxygen, water molecules for their part act as quenchers so that the excitation energy of the singlet oxygen passes non-radiatively into the water. Activated water is produced.
This activation is revealed in a change in the structure of the water, which structure is formed by hydrogen bonds.
The production of activated water can thereby be effected such that singlet oxygen is produced either in a gaseous, oxygen-containing medium and this now singlet oxygen-containing medium is introduced into the water or by the singlet oxygen being produced directly in the water. For this purpose oxygen must be dissolved in the water or oxygen must be introduced.
The object of the present invention is thereby to indicate a method for activation of water and to make available usages of water activated in such a manner.
This object is achieved by the method according to claim 1 and also the usages according to claim 19. Advantageous developments of the method according to the invention and the usages according to the invention are given in the dependent claims.
According to the method according to the invention water is activated by producing singlet oxygen and bringing this into contact with the water.
Oxygen occurs in its basic state as a triplet molecule 02 and can be converted into the excited singlet state by supplying energy. This excited singlet oxygen is particularly reactive and is itself already used in medicine and chemical process engineering. Relative to this excited singlet oxygen, water molecules for their part act as quenchers so that the excitation energy of the singlet oxygen passes non-radiatively into the water. Activated water is produced.
This activation is revealed in a change in the structure of the water, which structure is formed by hydrogen bonds.
The production of activated water can thereby be effected such that singlet oxygen is produced either in a gaseous, oxygen-containing medium and this now singlet oxygen-containing medium is introduced into the water or by the singlet oxygen being produced directly in the water. For this purpose oxygen must be dissolved in the water or oxygen must be introduced.
Water can be activated in a particularly effective manner if a gaseous oxygen-containing medium, for example air, which already contains singlet oxygen is mixed with the water to be activated by an atomiser. On the other hand, normal untreated air can also be mixed with the water to be activated and be atomised and the thus produced aerosol can be brought into contact with an illuminated photosensitiser in order to produce singlet oxygen.
The production of singlet oxygen is effected in the above described methods by means of a photosensitiser which is introduced into the gaseous, oxygen-containing medium, into the water or into the water-air mixture and irradiated with light. There is thereby meant by the term "light" an electromagnetic radiation from the ultraviolet range to the infrared range.
The photosensitiser can be attached to a formed piece. It is advantageous if the formed piece and the photosensitiser are water-insoluble materials so that the singlet oxygen can be produced within the water directly in contact with the water to be activated.
It is favourable for a high production rate of singlet oxygen if the formed piece contains a polymer matrix and is for example porous or has a rough surface since in this way the contact surface between the formed piece and the dissolved oxygen or the surrounding water is enlarged. For improved introduction of the exciting light, the matrix of the formed piece can be transparent. For example, the formed piece can be made of polytetrafluoroethylene (PTFE). Water-insoluble porphyrins, phthalocyanines, chlorins, tetraphenylporphyrins, benzoporphyrin derivatives, purpurins, pheophorbides, and the metal complexes thereof, especially copper (II) phthalocyanine, rose bengal or 5-amino-levulinic acid are suitable as photosensitiser.
The irradiation of the formed piece can be effected by an artificial light source or also directly by means of daylight, i.e. the sun. The formed piece can thereby contain the light source as an integral element.
The production of singlet oxygen is effected in the above described methods by means of a photosensitiser which is introduced into the gaseous, oxygen-containing medium, into the water or into the water-air mixture and irradiated with light. There is thereby meant by the term "light" an electromagnetic radiation from the ultraviolet range to the infrared range.
The photosensitiser can be attached to a formed piece. It is advantageous if the formed piece and the photosensitiser are water-insoluble materials so that the singlet oxygen can be produced within the water directly in contact with the water to be activated.
It is favourable for a high production rate of singlet oxygen if the formed piece contains a polymer matrix and is for example porous or has a rough surface since in this way the contact surface between the formed piece and the dissolved oxygen or the surrounding water is enlarged. For improved introduction of the exciting light, the matrix of the formed piece can be transparent. For example, the formed piece can be made of polytetrafluoroethylene (PTFE). Water-insoluble porphyrins, phthalocyanines, chlorins, tetraphenylporphyrins, benzoporphyrin derivatives, purpurins, pheophorbides, and the metal complexes thereof, especially copper (II) phthalocyanine, rose bengal or 5-amino-levulinic acid are suitable as photosensitiser.
The irradiation of the formed piece can be effected by an artificial light source or also directly by means of daylight, i.e. the sun. The formed piece can thereby contain the light source as an integral element.
By using a polymer or polymerised monomer matrix, photosensitisers can also be used which are not able to be coated on the surface of the formed piece but - instead are attached by the polymer matrix.
The activated water can now be used surprisingly in medicine, chemical process engineering, food technology, agriculture, printing, painting technology and also in cleaning technology.
On the one hand the activated water is suitable as a wetting agent as it improves the wetting properties of surfaces. Consequently it is suitable as a supplement or as a solvent itself for coating materials, such as for example printing inks, paints, varnish in printing and painting technology.
The advantageous wetting properties can also be used for improved wetting of plants with sprays in agriculture or also for improved contact of cleaning agents with the objects to be cleaned, activated water being used as a supplement to or as a solvent of sprays, pouring water or also cleaning liquids.
Furthermore an improvement was shown in the living and growth conditions of fish and of other aquatic organisms by means of improving the water quality when using activated water. This was established for example in coloured perch (scalar and discus fish). Plant growth is also improved by watering with activated water.
Further advantageous application areas of activated water are in wetting, watering, air humidification, in water sterilisation, in therapy of illnesses and also in increasing the health and/or the wellbeing of humans, animals and also plants. Thus illnesses which are for example virally or bacterially induced and also fungal attacks can be treated and cured with activated water. Activated water is particularly suitable for the treatment of infections with herpes simplex or the fungal yeast candida albicans.
The activated water can now be used surprisingly in medicine, chemical process engineering, food technology, agriculture, printing, painting technology and also in cleaning technology.
On the one hand the activated water is suitable as a wetting agent as it improves the wetting properties of surfaces. Consequently it is suitable as a supplement or as a solvent itself for coating materials, such as for example printing inks, paints, varnish in printing and painting technology.
The advantageous wetting properties can also be used for improved wetting of plants with sprays in agriculture or also for improved contact of cleaning agents with the objects to be cleaned, activated water being used as a supplement to or as a solvent of sprays, pouring water or also cleaning liquids.
Furthermore an improvement was shown in the living and growth conditions of fish and of other aquatic organisms by means of improving the water quality when using activated water. This was established for example in coloured perch (scalar and discus fish). Plant growth is also improved by watering with activated water.
Further advantageous application areas of activated water are in wetting, watering, air humidification, in water sterilisation, in therapy of illnesses and also in increasing the health and/or the wellbeing of humans, animals and also plants. Thus illnesses which are for example virally or bacterially induced and also fungal attacks can be treated and cured with activated water. Activated water is particularly suitable for the treatment of infections with herpes simplex or the fungal yeast candida albicans.
' Activated water can be used as a therapeutic measure and to increase the wellbeing and the constitution of living beings. By means of for example air humidification with activated water in the case of therapeutic treatment of a - patient, for example by means of chemotherapy, the wellbeing and the constitution of the patient is improved.
A few application examples of activated water are described subsequently.
There are shown:
Fig. 1 infrared spectra of varying length of activated water;
Fig. 2 the lengths of beans which were watered with normal or activated water;
Fig. 3 bean plants with varying waterings;
Fig. 4 the weight of seedlings of different plant sorts which have been watered with normal or activated water;
Fig. 5 the course of a method for degradation of toxic substances;
Fig.6 the toxic substance concentration after a degradation method according to Fig. 5, and Fig. 7 the bacterial growth in normal and activated water.
Fig. 1 shows the infrared spectra of water after half an hour, one and a half or two and a half hours activation according to the method according to the invention.
The activation of water is shown clearly in a change of the structure of the water formed by hydrogen bonds, which is represented in a characteristic displacement of the vibration bands as in Fig. 1. It can be detected immediately that the peak position is displaced with increasing activation from approximately 1.91 ~,m via 1.92 ~.m up to 1.94 ~,m. Furthermore, further shoulders and side bands appear for example at approximately 1.99 ~,m or 2.045 ~.m by means of activation.
Example 1 A patient was treated in whom a herpes simplex infection by the virus HSV 1 was detected. This attack led to a completely white area of attack, the size of one's palm, on the right abdomen surface, with blisters filled with liquid.
The patient complained of pain. The cause of the infection was unknown. It had already lasted for over seven years, various conventional traditional therapies having remained unsuccessful.
A first therapy was carned out with 0.25 1 of activated water to drink daily and also daily washing of the infected place with activated water. After three days, a clear reddening of the afflicted place was shown, formation of blisters no longer being able to be detected. The patient was free of pain. After four weeks a complete normal skin appearance occurred and the patient has remained to date completely complaint-free.
Example 2 A thrush fungal infection of the skin on the head caused by candida albicans was detected in one patient. There was shown an itchy reddened rash with white flaky places. An infection by skin-body contact during sport was suspected to be the cause as the patient is an active wrestler. Infections of this type occur frequently, for example due to inadequate disinfection of floor mats, as is known in the sphere of martial arts. The infection had already lasted six months, various conventional therapies remained without success.
There occurred a first therapy with 0.25 1 of activated water for drinking daily and also daily washing of the infected place with activated water: After just three days a clear decrease in the redness of the skin and drying of the - pustules was shown. The tingling sensation disappeared. After seven days the skin on the head was completely normal.
- The patient was reinfected twice after this therapy, the therapy here with activated water also leading respectively within one week to a complete healing of the infections.
Example 3 In a further example, beans were watered with normal and with activated water. In otherwise identical growth conditions and with an identical period of growth it can be detected in Fig. 2 that the beans which were watered with activated water have a greater tip length and also the average plant size is increased after the same period of growth. Two plants watered with normal water (plant 7 and plant 8) died in the course of the experiment but in the case of plants watered with activated water there were no losses.
Example 4 Fig. 3 shows the results of a series of tests with bean plants. The first and third bean plant in the row from the left were watered in a conventional manner while the second and the fourth bean plant in the row from the left were watered with activated water. It is shown clearly that the plant growth of the second and fourth plant is significantly greater than that of the first and third plant. As a result a great improvement was produced in plant growth of bean plants by means of watering with activated water.
Example 5 300 ml of drinking water were brought into contact with a formed piece. The formed piece was coated with copper phthalocyanine and provided with an integral light source. For five minutes air was then made to flow around the formed piece and it was irradiated.
In microscopic examination of the drinking water treated thus live bacteria were no longer found but merely a large number of destroyed bacteria.
Example 6 In a further example, the growth behaviour of various plant seedlings was determined over the growth period as an increase in weight. Plant seedlings were thereby compared which were either watered with normal water or with activated water. From the results in Fig. 4, it can be immediately detected that the radish seedlings or the mung bean seedlings, when watered with activated water, have a distinctly increased growth in comparison to the corresponding seedlings which were only watered with normal water.
Example 7 In a further example, two otherwise identical water basins were mixed with organic impurities (urea) and bacterial strains (nitrosomonas, nitrobacter).
These bacterial strains are commonly used for the biological degradation of toxic substances. In the one basin, the water was not treated further while in the other basin the water was activated in situ. The degradation of the toxic substances is thereby effected according to the method illustrated in Fig. 5 (nitrification). First of all decomposition products are thereby produced, by decomposing inter alia proteins via peptides into amino acids. In further degradation stages, ammonium, nitrite and nitrate are produced. Bacteria are thereby involved in all of the degradation steps. The number and the productivity of these bacteria determines essentially the rate of the degradation processes and thus has a great effect on the quantity of nutrient made available per unit of time for use by the plants.
In Fig. 6 the degradation of urea into a nitrate which is available for plants is illustrated according to the diagram according to Fig. S.
The initial high increase in ammonium in the basin with water activation can be clearly detected. This is verified by the higher productivity of the bacteria in the activated water which are responsible for the conversion of urea into ammonium.
After a short while, the nitrate content then also increases in this basin to a clearly higher level than in the reference basin with non-activated water in which very soon stagnation of the nitrate content occurs.
The activity of the bacteria which convert ammonium into nitrate then increases in the basin with activated water to such an extent that the ammonium production cannot keep up. As a result, the ammonium concentration sinks again in the basin with activated water.
Example 8 In order to directly demonstrate the accelerated bacterial growth in the activated water, the integral diffuse dispersion of light on the bacteria was measured in a further example. The results of the corresponding transmission measurements are illustrated in Fig. 7. It can be observed here that the transmission values are in direct ratio to the bacterial concentration. The reference values which were obtained in a bacterial culture with non-activated water are constantly smaller than the transmission values of the culture in which activated water is used. These measured values indicate a clearly higher bacterial count in the basin with water activation.
Consequently the total result is that, by using activated water, the density of bacteria can be increased significantly. A disinfectant effect of activated water, in which the bacterial density should be smaller relative to the usage of normal water could not be observed in the singlet oxygen production for activation of water according to the method according to the invention.
A few application examples of activated water are described subsequently.
There are shown:
Fig. 1 infrared spectra of varying length of activated water;
Fig. 2 the lengths of beans which were watered with normal or activated water;
Fig. 3 bean plants with varying waterings;
Fig. 4 the weight of seedlings of different plant sorts which have been watered with normal or activated water;
Fig. 5 the course of a method for degradation of toxic substances;
Fig.6 the toxic substance concentration after a degradation method according to Fig. 5, and Fig. 7 the bacterial growth in normal and activated water.
Fig. 1 shows the infrared spectra of water after half an hour, one and a half or two and a half hours activation according to the method according to the invention.
The activation of water is shown clearly in a change of the structure of the water formed by hydrogen bonds, which is represented in a characteristic displacement of the vibration bands as in Fig. 1. It can be detected immediately that the peak position is displaced with increasing activation from approximately 1.91 ~,m via 1.92 ~.m up to 1.94 ~,m. Furthermore, further shoulders and side bands appear for example at approximately 1.99 ~,m or 2.045 ~.m by means of activation.
Example 1 A patient was treated in whom a herpes simplex infection by the virus HSV 1 was detected. This attack led to a completely white area of attack, the size of one's palm, on the right abdomen surface, with blisters filled with liquid.
The patient complained of pain. The cause of the infection was unknown. It had already lasted for over seven years, various conventional traditional therapies having remained unsuccessful.
A first therapy was carned out with 0.25 1 of activated water to drink daily and also daily washing of the infected place with activated water. After three days, a clear reddening of the afflicted place was shown, formation of blisters no longer being able to be detected. The patient was free of pain. After four weeks a complete normal skin appearance occurred and the patient has remained to date completely complaint-free.
Example 2 A thrush fungal infection of the skin on the head caused by candida albicans was detected in one patient. There was shown an itchy reddened rash with white flaky places. An infection by skin-body contact during sport was suspected to be the cause as the patient is an active wrestler. Infections of this type occur frequently, for example due to inadequate disinfection of floor mats, as is known in the sphere of martial arts. The infection had already lasted six months, various conventional therapies remained without success.
There occurred a first therapy with 0.25 1 of activated water for drinking daily and also daily washing of the infected place with activated water: After just three days a clear decrease in the redness of the skin and drying of the - pustules was shown. The tingling sensation disappeared. After seven days the skin on the head was completely normal.
- The patient was reinfected twice after this therapy, the therapy here with activated water also leading respectively within one week to a complete healing of the infections.
Example 3 In a further example, beans were watered with normal and with activated water. In otherwise identical growth conditions and with an identical period of growth it can be detected in Fig. 2 that the beans which were watered with activated water have a greater tip length and also the average plant size is increased after the same period of growth. Two plants watered with normal water (plant 7 and plant 8) died in the course of the experiment but in the case of plants watered with activated water there were no losses.
Example 4 Fig. 3 shows the results of a series of tests with bean plants. The first and third bean plant in the row from the left were watered in a conventional manner while the second and the fourth bean plant in the row from the left were watered with activated water. It is shown clearly that the plant growth of the second and fourth plant is significantly greater than that of the first and third plant. As a result a great improvement was produced in plant growth of bean plants by means of watering with activated water.
Example 5 300 ml of drinking water were brought into contact with a formed piece. The formed piece was coated with copper phthalocyanine and provided with an integral light source. For five minutes air was then made to flow around the formed piece and it was irradiated.
In microscopic examination of the drinking water treated thus live bacteria were no longer found but merely a large number of destroyed bacteria.
Example 6 In a further example, the growth behaviour of various plant seedlings was determined over the growth period as an increase in weight. Plant seedlings were thereby compared which were either watered with normal water or with activated water. From the results in Fig. 4, it can be immediately detected that the radish seedlings or the mung bean seedlings, when watered with activated water, have a distinctly increased growth in comparison to the corresponding seedlings which were only watered with normal water.
Example 7 In a further example, two otherwise identical water basins were mixed with organic impurities (urea) and bacterial strains (nitrosomonas, nitrobacter).
These bacterial strains are commonly used for the biological degradation of toxic substances. In the one basin, the water was not treated further while in the other basin the water was activated in situ. The degradation of the toxic substances is thereby effected according to the method illustrated in Fig. 5 (nitrification). First of all decomposition products are thereby produced, by decomposing inter alia proteins via peptides into amino acids. In further degradation stages, ammonium, nitrite and nitrate are produced. Bacteria are thereby involved in all of the degradation steps. The number and the productivity of these bacteria determines essentially the rate of the degradation processes and thus has a great effect on the quantity of nutrient made available per unit of time for use by the plants.
In Fig. 6 the degradation of urea into a nitrate which is available for plants is illustrated according to the diagram according to Fig. S.
The initial high increase in ammonium in the basin with water activation can be clearly detected. This is verified by the higher productivity of the bacteria in the activated water which are responsible for the conversion of urea into ammonium.
After a short while, the nitrate content then also increases in this basin to a clearly higher level than in the reference basin with non-activated water in which very soon stagnation of the nitrate content occurs.
The activity of the bacteria which convert ammonium into nitrate then increases in the basin with activated water to such an extent that the ammonium production cannot keep up. As a result, the ammonium concentration sinks again in the basin with activated water.
Example 8 In order to directly demonstrate the accelerated bacterial growth in the activated water, the integral diffuse dispersion of light on the bacteria was measured in a further example. The results of the corresponding transmission measurements are illustrated in Fig. 7. It can be observed here that the transmission values are in direct ratio to the bacterial concentration. The reference values which were obtained in a bacterial culture with non-activated water are constantly smaller than the transmission values of the culture in which activated water is used. These measured values indicate a clearly higher bacterial count in the basin with water activation.
Consequently the total result is that, by using activated water, the density of bacteria can be increased significantly. A disinfectant effect of activated water, in which the bacterial density should be smaller relative to the usage of normal water could not be observed in the singlet oxygen production for activation of water according to the method according to the invention.
Claims (23)
1. Usage of water which has been activated by producing singlet oxygen and by bringing it into contact with the water for the purpose of wetting, watering, increasing the growth, the health and wellbeing of living organisms.
2. Usage according to claim 1 for increasing the growth of animals, humans and/or plants.
3. Usage according to claim 1 in medicine, chemical process engineering, food technology, agriculture, printing, painting technology and/or cleaning technology .
4. Usage of activated water according to the preceding claim as a supplement to or in aqueously dissolved coating materials such as printing inks, paints, varnishes or the like.
5. Usage of activated water according to one of the two preceding claims as a supplement to, in or as aqueous cleaning liquid or wetting agents.
6. Usage of activated water according to claim 1 or 2 as a supplement to, in or as pouring water or as sprays.
7. Usage according to one of the preceding claims, characterised in that singlet oxygen was produced in a gaseous, oxygen-containing medium and the gaseous, oxygen-containing medium was introduced into the water.
8. Usage according to one of the preceding claims, characterised in that the singlet oxygen, possibly in a gaseous, oxygen-containing medium, was produced and a mixture of the singlet oxygen or the gaseous, oxygen-containing medium and of the water to be activated was produced, possibly by means of an atomiser.
9. Method according to one of the preceding claims, characterised in that oxygen was dissolved in the water or was present already dissolved and the oxygen was converted into singlet oxygen.
10. Method according to one of the preceding claims, characterised in that a mixture of droplets of the water to be activated and of a gaseous, oxygen-containing medium was produced, possibly by means of an atomiser, and this mixture was brought into contact with an illuminated photosensitiser.
11. Method according to claim 9 or 10, characterised in that, in order to produce the singlet oxygen, a photosensitiser was introduced into the gaseous, oxygen-containing medium or the mixture of water to be activated and gaseous, oxygen-containing medium and was irradiated with light.
12. Method according to one of the claims 9 to 10, characterised in that a formed piece which contains a water-insoluble photosensitiser was introduced into the water or into the mixture of water and of the gaseous, oxygen-containing medium and was irradiated with light.
13. Method according to the preceding claim, characterised in that the formed piece contains a polymer matrix.
14. Method according to claim 13, characterised in that the matrix is transparent.
15. Method according to at least one of the claims 12 to 14, characterised in that the formed piece is porous and/or has a rough surface.
16. Method according to at least one of the claims 12 to 15, characterised in that the formed piece contains a polymer or a monomer.
17. Method according to the preceding claim, characterised in that the formed piece contains PTFE.
18. Method according to the preceding claim, characterised in that the formed piece contains the light source.
19. Method according to at least one of the claims 12 to 17, characterised in that the formed piece was subject to a flow by an oxygen-containing gas during irradiation.
20. Method according to at least one of the claims 12 to 19, characterised in that the photosensitiser is located on the surface of the formed piece.
21. Method according to at least one of the claims 10 to 20, characterised in that the photosensitiser is selected from water-insoluble porphyrins, phthalocyanines, chlorins, tetraphenylporphyrins, benzoporphyrin derivatives, purpurins, pheophorbides and the metal complexes thereof.
22. Method according to at least one of the claims 10 to 21, characterised in that the photosensitiser is copper (II) phthalocyanine, rose bengal or 5-amino-levulinic acid.
23. Method according to at least one of the claims 10 to 22, characterised in that irradiation was effected by the sun and/or by an artificial light source.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19855881.3 | 1998-12-03 | ||
DE19855881A DE19855881A1 (en) | 1998-12-03 | 1998-12-03 | Process for activating water and using such activated water |
PCT/EP1999/009488 WO2000032520A1 (en) | 1998-12-03 | 1999-12-03 | Method for activating water and use of activated water of this type |
Publications (1)
Publication Number | Publication Date |
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CA2353499A1 true CA2353499A1 (en) | 2000-06-08 |
Family
ID=7889906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002353499A Abandoned CA2353499A1 (en) | 1998-12-03 | 1999-12-03 | Method for activating water and use of activated water of this type |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP1144313A1 (en) |
JP (1) | JP2002531249A (en) |
BR (1) | BR9915885A (en) |
CA (1) | CA2353499A1 (en) |
DE (1) | DE19855881A1 (en) |
IL (1) | IL143413A0 (en) |
NO (1) | NO20012667L (en) |
WO (1) | WO2000032520A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9011700B2 (en) | 2007-11-26 | 2015-04-21 | Eng3 Corporation | Systems, devices, and methods for directly energizing water molecule composition |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
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DE19910561A1 (en) * | 1999-03-10 | 2000-09-14 | Schaffer Moshe | Use of porphyrin derivatives in aquariums |
DE10064064A1 (en) * | 2000-12-21 | 2002-07-18 | Fraunhofer Ges Forschung | Process for accelerating biocatalytic and / or hormonal processes and its use |
AT412084B (en) * | 2001-05-18 | 2004-09-27 | Christian Hubacek | DEVICE FOR CHANGING MOLECULAR STRUCTURES IN LIQUIDS |
IL150914A (en) * | 2002-07-25 | 2014-04-30 | Zamir Tribelsky | Method for hydro-optronic photochemical treatment of liquids |
DE102008020755A1 (en) * | 2008-04-18 | 2009-10-22 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Use of photosensitizer for cleaning air, water or contaminated surfaces and in filters, where the photosensitizer is covalently linked and/or linked over physical interaction to surface and activated by visible light to form singlet oxygen |
DE102015112400B4 (en) | 2015-07-29 | 2018-07-19 | Herbert Waldmann Gmbh & Co Kg | Method and device for sterilizing liquids by means of photosensitizers |
US20190047882A1 (en) * | 2016-03-04 | 2019-02-14 | Tomokazu KANDA | Coating liquid preparing device and coating device |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
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US4008136A (en) * | 1974-08-09 | 1977-02-15 | Temple University | Process for the treatment of waste water by heterogeneous photosensitized oxidation |
JPS55115484A (en) * | 1979-02-28 | 1980-09-05 | Asahi Chem Ind Co Ltd | Heterogeneous sensitizer for photosensitized oxidation |
CH658771A5 (en) * | 1984-05-28 | 1986-12-15 | Ciba Geigy Ag | AZAPHTHALOCYANINE AND THEIR USE AS PHOTOACTIVATORS. |
US4983670A (en) * | 1988-12-20 | 1991-01-08 | Allied-Signal Inc. | Cellulose acetate bound photosensitizer for producing singlet oxygen |
FR2642308A1 (en) * | 1989-02-02 | 1990-08-03 | Sitbon Georges | Medical treatment using a volcanic colloidal inorganic solution having strong oxidase activity |
GB9114290D0 (en) * | 1991-07-02 | 1991-08-21 | Courtaulds Plc | Polymer compositions |
US5635059A (en) * | 1994-10-20 | 1997-06-03 | Aqua-Ion Systems, Inc. | Method and apparatus for water treatment and purification using gas ion plasma source and disinfectant metal ion complexes |
US5679661A (en) * | 1995-07-25 | 1997-10-21 | The Procter & Gamble Company | Low hue photodisinfectants |
NO304735B1 (en) * | 1996-02-07 | 1999-02-08 | Singlet Oxygen Technologies As | Apparatus for providing a singlet oxygen-activated oxygen-containing gas stream |
DE19606081A1 (en) * | 1996-02-19 | 1997-08-21 | Schaffer Moshe Dr Med | Composition for combating bacteria, algae, yeast and fungi in water |
JPH09249811A (en) * | 1996-03-18 | 1997-09-22 | Toyo Ink Mfg Co Ltd | Curable resin composition, varnish and printing ink using the same |
-
1998
- 1998-12-03 DE DE19855881A patent/DE19855881A1/en not_active Withdrawn
-
1999
- 1999-12-03 CA CA002353499A patent/CA2353499A1/en not_active Abandoned
- 1999-12-03 IL IL14341399A patent/IL143413A0/en unknown
- 1999-12-03 BR BR9915885-0A patent/BR9915885A/en not_active IP Right Cessation
- 1999-12-03 WO PCT/EP1999/009488 patent/WO2000032520A1/en not_active Application Discontinuation
- 1999-12-03 JP JP2000585167A patent/JP2002531249A/en active Pending
- 1999-12-03 EP EP99958163A patent/EP1144313A1/en not_active Ceased
-
2001
- 2001-05-30 NO NO20012667A patent/NO20012667L/en not_active Application Discontinuation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9011700B2 (en) | 2007-11-26 | 2015-04-21 | Eng3 Corporation | Systems, devices, and methods for directly energizing water molecule composition |
Also Published As
Publication number | Publication date |
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EP1144313A1 (en) | 2001-10-17 |
JP2002531249A (en) | 2002-09-24 |
NO20012667D0 (en) | 2001-05-30 |
WO2000032520A1 (en) | 2000-06-08 |
DE19855881A1 (en) | 2000-06-08 |
IL143413A0 (en) | 2002-04-21 |
WO2000032520A9 (en) | 2000-11-30 |
NO20012667L (en) | 2001-08-02 |
BR9915885A (en) | 2001-08-21 |
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