WO2008110587A1 - An electrolytic cip-cleaning process for removing impurities from the inner surface of a metallic container - Google Patents
An electrolytic cip-cleaning process for removing impurities from the inner surface of a metallic container Download PDFInfo
- Publication number
- WO2008110587A1 WO2008110587A1 PCT/EP2008/052971 EP2008052971W WO2008110587A1 WO 2008110587 A1 WO2008110587 A1 WO 2008110587A1 EP 2008052971 W EP2008052971 W EP 2008052971W WO 2008110587 A1 WO2008110587 A1 WO 2008110587A1
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- WO
- WIPO (PCT)
- Prior art keywords
- electrode
- electrolyte solution
- contact area
- process according
- cathode
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 60
- 239000012535 impurity Substances 0.000 title claims abstract description 15
- 238000004140 cleaning Methods 0.000 title abstract description 21
- 239000008151 electrolyte solution Substances 0.000 claims description 42
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 9
- 239000003599 detergent Substances 0.000 claims description 5
- 235000011118 potassium hydroxide Nutrition 0.000 claims description 5
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 claims description 5
- 229910052939 potassium sulfate Inorganic materials 0.000 claims description 5
- 235000011121 sodium hydroxide Nutrition 0.000 claims description 5
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 5
- 239000008139 complexing agent Substances 0.000 claims description 4
- 239000001120 potassium sulphate Substances 0.000 claims description 4
- 235000011151 potassium sulphates Nutrition 0.000 claims description 4
- 235000011152 sodium sulphate Nutrition 0.000 claims description 4
- 239000000243 solution Substances 0.000 claims description 4
- 230000001427 coherent effect Effects 0.000 claims description 3
- 244000005700 microbiome Species 0.000 abstract description 6
- 238000012258 culturing Methods 0.000 abstract description 4
- 238000003860 storage Methods 0.000 abstract description 4
- 235000013365 dairy product Nutrition 0.000 abstract description 2
- 239000002207 metabolite Substances 0.000 abstract description 2
- 102000004169 proteins and genes Human genes 0.000 description 9
- 108090000623 proteins and genes Proteins 0.000 description 9
- 239000010935 stainless steel Substances 0.000 description 8
- 229910001220 stainless steel Inorganic materials 0.000 description 8
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 6
- 239000012620 biological material Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 229940079593 drug Drugs 0.000 description 4
- -1 proteins Chemical class 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 102000004877 Insulin Human genes 0.000 description 3
- 108090001061 Insulin Proteins 0.000 description 3
- XOJVVFBFDXDTEG-UHFFFAOYSA-N Norphytane Natural products CC(C)CCCC(C)CCCC(C)CCCC(C)C XOJVVFBFDXDTEG-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 229940125396 insulin Drugs 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002161 passivation Methods 0.000 description 3
- 238000004611 spectroscopical analysis Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 108020004414 DNA Proteins 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 108090001030 Lipoproteins Proteins 0.000 description 2
- 102000004895 Lipoproteins Human genes 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229910001882 dioxygen Inorganic materials 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 150000002632 lipids Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 229920001184 polypeptide Polymers 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- 108090000765 processed proteins & peptides Proteins 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 150000003431 steroids Chemical class 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical class [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 102000014171 Milk Proteins Human genes 0.000 description 1
- 108010011756 Milk Proteins Proteins 0.000 description 1
- 239000007832 Na2SO4 Substances 0.000 description 1
- 241000219289 Silene Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000004833 X-ray photoelectron spectroscopy Methods 0.000 description 1
- FRYDSOYOHWGSMD-UHFFFAOYSA-N [C].O Chemical class [C].O FRYDSOYOHWGSMD-UHFFFAOYSA-N 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000012864 cross contamination Methods 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000002163 immunogen Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002605 large molecules Chemical class 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D83/00—Containers or packages with special means for dispensing contents
- B65D83/76—Containers or packages with special means for dispensing contents for dispensing fluent contents by means of a piston
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F1/00—Electrolytic cleaning, degreasing, pickling or descaling
Definitions
- the invention relates to a novel electrolytic process for removing impurities from the inner surface of a metallic container.
- the process is particularly useful for cleaning process reactors used for culturing microorganisms, and storage tanks used for storing metabolites formed in the process reactor, as well as containers for dairy products.
- biological materials e.g. proteins
- metal surfaces e.g. stainless steel surfaces
- a monolayer of high molecular weight compounds or biological materials, e.g. proteins can be extremely difficult to completely remove without costly, energy demanding and time-consuming cleaning processes, which further may cause environmental problems.
- Residues of proteins that are partly degraded are potentially immunogenic. Residues of proteins may act as nuclei (seeds) for denaturation of proteins during a subsequent manufacturing campaign. To avoid cross-contamination when tanks are used to produce different proteins and protein products, it is essential that the inner surface of the container is clean at a nano-scale level.
- US 7,090,753 Bl discloses an electrolytic cell which can produce charged water having excellent performance of improving surface cleaning or treatment.
- KR 1082761 A discloses a method for grinding the inner walls of a drug tank in order to maintain the degree of purity of stored drugs by minimizing the gush of metal components from the inner walls of the drug tank.
- the inner wall is i.a. grinded by an electrolytic solution, and subsequently an oxide membrane is formed by reacting the surface with 20% nitric acid solution. It is stated that the use of high purity detergents can be reduced and that the cleaning time can be shortened.
- the present invention provides an electrolytic process for removing impurities, e.g. contaminants and residues, in particular impurities consisting of biological materials, from the inner surface of a metallic container (5), said process comprising the step of
- C ⁇ P clean in place
- Figure 1 illustrates a process reactor (reaction vessel) (5) having a wall (1) used as the anode, and having arranged therein a ratable tubular member (2) for facilitating flow of the electrolyte solution (3) provided via a pump (not shown).
- the tubular member is also used as the cathode (as shown) or can have a cathode arranged therein (alternative embodiment).
- the contact area (4) is moved across a substantial part of the inner surface.
- Figure 2 illustrates a process reactor (reaction vessel) (5) having a wall (1) used as the anode, and having arranged therein a ratable member (2) for facilitating flow of the electrolyte solution (3) provided via a pump (not shown).
- the tubular member is moved close to the inner wall and has a slit which allows the electrolyte solution to exit the tubular member.
- the tubular member is also used as the cathode (as shown) or can have a cathode arranged therein (alternative embodiment).
- the elongated contact area (4) is moved across a substantial part of the inner surface.
- Figure 3 illustrates various embodiments of the cross-section of the tubular member illustrated in Figure 2.
- FIGs 4 and 5 illustrate the arrangement of a ratable spraying device within a process reactor.
- the spraying device second electrode; cathode in Figure 4 and anode in Figure 5
- the inner wall of the container first electrode; anode in Figure 4 and cathode in Figure 5
- the spraying device provides several streams (3') collectively representing the electrolyte solution (3)
- the "contact area” (4) is a collection of a number of individual contact areas (4').
- the present invention provides an electrolytic process of removing impurities from the inner surface of containers, i.e. containers having an inner surface of a metallic material, such as stainless steel, titanium, tantalum or niobium.
- containers having an inner surface of a metallic material such as stainless steel, titanium, tantalum or niobium.
- Containers of stainless steel are of particular importance.
- Containers for which the present process is particularly relevant are reactors for culturing microorganisms and cells and for storing, handling, processing and purifying biological material, e.g. microorganisms, cells, polypeptides, proteins, DNA, RNA, lipoproteins, lipids (steroids, terpenes, waxes and fatty acids), high-molecular carbonhydrates and the like.
- biological material e.g. microorganisms, cells, polypeptides, proteins, DNA, RNA, lipoproteins, lipids (steroids, terpenes, waxes and fatty acids), high-molecular carbonhydrates and the like.
- the term “container” encompasses process reactors, tubes, pipes, storage tanks, etc.
- Containers for handling diary products are also highly relevant.
- the process of the invention is particularly relevant for industrial scale equipment; hence the container preferably has a volume of at least 10 L, such as at least 100 L, or even at least 1,000 L.
- the invention resides in the finding that electrolytic cleaning of the inner surface of a metallic surface of a container can be obtained by application of a high current density by means of an electrical circuit comprising (a) the wall of the container as a first electrode (1), (b) a second electrode (2), and (c) an electrolyte solution (3) forming electrical connection between said first electrode and said second electrode, wherein the connection between the first electrode and the electrolyte solution defines a contact area (4).
- Means are included which facilitate that the contact area can be moved across at least a substantial part of the metallic inner surface of the container, while a predetermined current density is simultaneously applied at said contact area (4), i.e. the electrolytic process is effectuated over a substantial part of the inner surface.
- the current density is in the range 1-60 A/dm 2 , e.g. in the range of 1-30 A/dm 2 , such as 3-20 A/dm 2 .
- the contact area at any time of the process only represents a fraction of the total area to be treated.
- the ratio between (i) the total area of the part of the inner surface which the contact area is moved across and (ii) the contact area is at least 10: 1, such as at least 20: 1, or even at least 50: 1.
- contact area in question may be the sum of a number of individual contact areas, e.g. as illustrated in Figures 4 and 5.
- the surface chemistry gets very alkaline at the cathode and in that way acts as the builder chemistry in conventional cleaning chemistry.
- the rational behind the invention is that the high cathodic current density applied to the metallic surface, e.g. a stainless steel surface, will result in the formation of hydrogen bubbles at the inner surface of the container, and that any material which adheres to the surface thereby will be removed under the influence of the formed hydrogen and hydroxyl ions. Furthermore, the electrochemical interaction with the immobilized organic impurities at the surface will be destroyed thereby leaving the surface cleaned upon molecular or nano- scale. This is illustrated in Example 2.
- the process according to the invention cleans the inner surface using only electricity and an electrolyte solution.
- the electrolyte solution needs in principle only to contain very dilute amounts of non-toxic chemicals, such as alkali-metal hydroxides, such as NaOH and KOH, or a neutral salt, such as Na 2 SO 4 or K 2 SO 4 , in purified water.
- the electrolyte solution is preferably a solution of one or more components selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium sulphate and potassium sulphate.
- the ionic strength of the electrolyte solution is typically in the range 0.05-2.0 N, such as 0.1- 1.0 N.
- the electrolyte solution may in some interesting embodiment additionally comprise one or more complexing agent, such as one or more selected from gluconates, EDTA, and hydroxyl carboxylic acid (e.g. citric acid).
- one or more complexing agent such as one or more selected from gluconates, EDTA, and hydroxyl carboxylic acid (e.g. citric acid).
- the electrolyte solution is preferably essentially free of detergents.
- the contact time should preferably be sufficiently long so as to allow for an efficient removal of the impurities.
- the movement of the second electrode relative to the inner surface of the container will determine the period at which an incremental area of the inner surface is exposed to the applied current.
- the movement of the contact area is such that the contact time of the contact area is at least 1 second.
- the equipment used for facilitating the movement of the contact area across the inner surface may include motors, e.g. stepper motors, as well as robots. Further, the movement may - although not particularly preferred - be effected manually.
- the electrical circuit comprises the first electrode, the second electrode and the electrolyte solution.
- the first electrode is the cathode and the second electrode is the anode.
- hydrogen gas is formed at the inner surface of the container.
- the first electrode is the anode and the second electrode is the cathode.
- oxygen gas is formed at the inner surface of the container.
- That constellation makes it also possible - in a special embodiment - to passivate the stainless steel surface as a post treatment after the electrolytic CIP-cleaning, where the first electrode is used as a cathode.
- the first electrode act as the anode and that makes it possible to form a passivating layer consisting of oxides, i.e a treatment very similarly to the passivation in nitric acid.
- the Pourbaix-diagram in figure 6 indicates the possible area for passivation.
- the anodic current density which is necessary to render the process effective is typically at least 1 A/dm 2 corresponding to a potential (SHE) between +400 mV and +1500 mV.
- the current density is typically in the range 1-60 A/dm 2 , e.g. in the range of 1-30 A/dm 2 .
- the second electrode is a tubular member facilitating a flow of the electrolyte solution.
- the tubular member may be designed as a low pressure spray nozzle to ensure a coherent beam of the electrolyte, which form a linear contact area with some extent.
- the electrode is placed in the water beam formed by a spray nozzle. This embodiment corresponds to the one illustrated in Figure 1.
- the electrolyte solution is fed to the gap between the first electrode and the second electrode by means of a tubular member having a slit.
- This embodiment corresponds to the one illustrated in Figure 2.
- the residence time of the electrolyte solution may be increased by arranging a porous structure in the before-mentioned gap.
- the electrolytic process is carried out within a jet beam between the area to be cleaned (the first electrode; a cathode) and a cleaning nozzle.
- An anode is inserted into the tank in appropriate distance allowing a non-interrupted and coherent beam of electrolyte to connect to the anode and cathode (tank wall).
- the beam is moved to cover the whole area of the tank.
- the flow of the electrolyte solution is preferably predominantly laminar.
- the electrolyte solution which forms electrical communication between said first electrode and said second electrode is held in a porous structure, e.g. in a sponge or a brush.
- a porous structure may be moved across the inner surface my mechanical means, e.g. by a motor/motors or a robot.
- the process according to invention comprising the step of:
- an electrical circuit comprising (a) the wall of the container as the anode (1), (b) a cathode (2), and (c) an electrolyte solution (3) of one or more components selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium sulphate and potassium sulphate, optionally further comprising a complexing agent, said electrolyte solution forming electrical connection between said anode and said cathode, the connection between the first electrode and the electrolyte solution defining a contact area (4); and
- the cleanness of the surfaces treated according to the process according to the present invention can be verified via XPS (X-ray photon Spectroscopy), e.g. as described in the Examples section.
- the process according to the invention can suitably be used for cleaning process reactors being contaminated with a variety of organic constituent, e.g. proteins, milk, etc., and the use is therefore not restricted to the drug industry.
- organic constituent e.g. proteins, milk, etc.
- XPS is a versatile technique for analyzing the top ⁇ 10 nm of a surface, providing information on the elements present at the surface and the chemical state they are in.
- Table 1 shows the XPS measurement of a pristine surface of stainless steel type 316.
- the surface is seen to consist of oxides of mainly chromium and less amounts of iron oxide.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Mechanical Engineering (AREA)
- Cleaning By Liquid Or Steam (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
Abstract
The invention relates to a novel electrolytic process for removing impurities from the inner surface of a metallic container. The process is particularly useful for cleaning process reactors used for culturing microorganisms, and storage tanks used for storing metabolites formed in the process reactor, as well as containers for dairy products.
Description
AN ELECTROLYTIC CIP-CLEANING PROCESS FOR REMOVING IMPURITIES FROM THE INNER SURFACE OF A METALLIC CONTAINER
FIELD OF THE INVENTION
The invention relates to a novel electrolytic process for removing impurities from the inner surface of a metallic container. The process is particularly useful for cleaning process reactors used for culturing microorganisms, and storage tanks used for storing metabolites formed in the process reactor, as well as containers for dairy products.
BACKGROUND OF THE INVENTION
For industrial scale processes, e.g. for culturing microorganisms and cells and for handling, processing and purifying biological materials, e.g. microorganisms, cells, polypeptides, proteins, DNA, RNA, lipoproteins, lipids (steroids, terpenes, waxes and fatty acids), high- molecular carbon hydrates and the like, it has proven to be particularly difficult to completely remove all traces of material on nano-scale from the inner surface of the container(s) which have been involved in such processes.
It turns out that biological materials, e.g. proteins, strongly adhere to metal surfaces, e.g. stainless steel surfaces, and that a monolayer of high molecular weight compounds or biological materials, e.g. proteins, can be extremely difficult to completely remove without costly, energy demanding and time-consuming cleaning processes, which further may cause environmental problems.
Residues of proteins that are partly degraded are potentially immunogenic. Residues of proteins may act as nuclei (seeds) for denaturation of proteins during a subsequent manufacturing campaign. To avoid cross-contamination when tanks are used to produce different proteins and protein products, it is essential that the inner surface of the container is clean at a nano-scale level.
US 7,090,753 Bl discloses an electrolytic cell which can produce charged water having excellent performance of improving surface cleaning or treatment.
KR 1082761 A discloses a method for grinding the inner walls of a drug tank in order to maintain the degree of purity of stored drugs by minimizing the gush of metal components from the inner walls of the drug tank. In the process, the inner wall is i.a. grinded by an electrolytic solution, and subsequently an oxide membrane is formed by reacting the surface
with 20% nitric acid solution. It is stated that the use of high purity detergents can be reduced and that the cleaning time can be shortened.
However, there is still a need for cost- and time efficient processes for cleaning the surface of containers of the above-mentioned type on a nano-scale, in particular such methods which due to their simplicity are environmentally acceptable.
BRIEF DESCRIPTION OF THE INVENTION
The present invention provides an electrolytic process for removing impurities, e.g. contaminants and residues, in particular impurities consisting of biological materials, from the inner surface of a metallic container (5), said process comprising the step of
a) establishing an electrical circuit comprising (a) the wall of the container as a first electrode (1), (b) a second electrode (2), and (c) an electrolyte solution (3) forming electrical connection between said first electrode and said second electrode, the connection between the first electrode and the electrolyte solution defining a contact area (4); and
b) facilitating that said contact area (4) is moved across at least a substantial part of said inner surface so as to allow said electrolyte solution (3) to contact said inner surface to be depleted of the impurities, and simultaneously applying a predetermined current density at said contact area (4).
The process has to the best of the inventors' knowledge never been used before for "clean in place" (CΙP)-cleaning of the inner surface of containers (e.g. production or storage tanks or pipes for medical production).
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 illustrates a process reactor (reaction vessel) (5) having a wall (1) used as the anode, and having arranged therein a ratable tubular member (2) for facilitating flow of the electrolyte solution (3) provided via a pump (not shown). The tubular member is also used as the cathode (as shown) or can have a cathode arranged therein (alternative embodiment). Upon rotation and up-and-down movement of the tubular member, the contact area (4) is moved across a substantial part of the inner surface.
Figure 2 illustrates a process reactor (reaction vessel) (5) having a wall (1) used as the anode, and having arranged therein a ratable member (2) for facilitating flow of the electrolyte solution (3) provided via a pump (not shown). The tubular member is moved close to the inner wall and has a slit which allows the electrolyte solution to exit the tubular member. The tubular member is also used as the cathode (as shown) or can have a cathode arranged therein (alternative embodiment). Upon rotation of the tubular member around the axis (show with a dashed line), the elongated contact area (4) is moved across a substantial part of the inner surface.
Figure 3 illustrates various embodiments of the cross-section of the tubular member illustrated in Figure 2.
Figures 4 and 5 illustrate the arrangement of a ratable spraying device within a process reactor. After having served to establish electrical connection between the spraying device (second electrode; cathode in Figure 4 and anode in Figure 5) and the inner wall of the container (first electrode; anode in Figure 4 and cathode in Figure 5), the electrolyte solution is collected in the lower part of the container and is pumped back through the ratable spraying device via the pump. It is noted that the spraying device provides several streams (3') collectively representing the electrolyte solution (3), and that the "contact area" (4) is a collection of a number of individual contact areas (4').
DETAILED DESCRIPTION OF THE INVENTION
As mentioned above, the present invention provides an electrolytic process of removing impurities from the inner surface of containers, i.e. containers having an inner surface of a metallic material, such as stainless steel, titanium, tantalum or niobium. Containers of stainless steel are of particular importance.
Containers for which the present process is particularly relevant are reactors for culturing microorganisms and cells and for storing, handling, processing and purifying biological material, e.g. microorganisms, cells, polypeptides, proteins, DNA, RNA, lipoproteins, lipids (steroids, terpenes, waxes and fatty acids), high-molecular carbonhydrates and the like. Hence, in the present context, the term "container" encompasses process reactors, tubes, pipes, storage tanks, etc. Containers for handling diary products are also highly relevant.
It is understood that the process of the invention is particularly relevant for industrial scale equipment; hence the container preferably has a volume of at least 10 L, such as at least 100 L, or even at least 1,000 L.
The invention resides in the finding that electrolytic cleaning of the inner surface of a metallic surface of a container can be obtained by application of a high current density by means of an electrical circuit comprising (a) the wall of the container as a first electrode (1), (b) a second electrode (2), and (c) an electrolyte solution (3) forming electrical connection between said first electrode and said second electrode, wherein the connection between the first electrode and the electrolyte solution defines a contact area (4). Means are included which facilitate that the contact area can be moved across at least a substantial part of the metallic inner surface of the container, while a predetermined current density is simultaneously applied at said contact area (4), i.e. the electrolytic process is effectuated over a substantial part of the inner surface.
In the most typically embodiments, the current density is in the range 1-60 A/dm2, e.g. in the range of 1-30 A/dm2, such as 3-20 A/dm2.
It should be understood that the contact area at any time of the process only represents a fraction of the total area to be treated. Hence, preferably, the ratio between (i) the total area of the part of the inner surface which the contact area is moved across and (ii) the contact area is at least 10: 1, such as at least 20: 1, or even at least 50: 1.
It should be understood that the contact area in question may be the sum of a number of individual contact areas, e.g. as illustrated in Figures 4 and 5.
Upon application of a high current density between the first electrode and the second electrode (one of which being the anode and the other being the cathode) having an aqueous electrolyte solution there between, hydrogen gas will be formed at the cathode and oxygen gas will be formed at the anode.
The chemical reactions involved are:
Anode reaction: 2H2O → O2 + 4H+ + 4e'
Cathode reaction: 2H2O + 2e~ → H2 + 2OH"
Under the real cleaning process, the surface chemistry gets very alkaline at the cathode and in that way acts as the builder chemistry in conventional cleaning chemistry.
The rational behind the invention is that the high cathodic current density applied to the metallic surface, e.g. a stainless steel surface, will result in the formation of hydrogen
bubbles at the inner surface of the container, and that any material which adheres to the surface thereby will be removed under the influence of the formed hydrogen and hydroxyl ions. Furthermore, the electrochemical interaction with the immobilized organic impurities at the surface will be destroyed thereby leaving the surface cleaned upon molecular or nano- scale. This is illustrated in Example 2.
The process according to the invention cleans the inner surface using only electricity and an electrolyte solution. The electrolyte solution needs in principle only to contain very dilute amounts of non-toxic chemicals, such as alkali-metal hydroxides, such as NaOH and KOH, or a neutral salt, such as Na2SO4 or K2SO4, in purified water. For environmental reasons, and for reasons of disposal, the electrolyte solution is preferably a solution of one or more components selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium sulphate and potassium sulphate.
The ionic strength of the electrolyte solution is typically in the range 0.05-2.0 N, such as 0.1- 1.0 N.
Moreover, the electrolyte solution may in some interesting embodiment additionally comprise one or more complexing agent, such as one or more selected from gluconates, EDTA, and hydroxyl carboxylic acid (e.g. citric acid).
On the other hand, and contrary to conventional methods for cleaning process reactors which utilizes various types of detergents, the electrolyte solution is preferably essentially free of detergents.
Apart from the requirement of a sufficient current density, the contact time should preferably be sufficiently long so as to allow for an efficient removal of the impurities. The movement of the second electrode relative to the inner surface of the container will determine the period at which an incremental area of the inner surface is exposed to the applied current. Hence, typically, the movement of the contact area is such that the contact time of the contact area is at least 1 second.
The equipment used for facilitating the movement of the contact area across the inner surface (or at least a part thereof), may include motors, e.g. stepper motors, as well as robots. Further, the movement may - although not particularly preferred - be effected manually.
The electrical circuit comprises the first electrode, the second electrode and the electrolyte solution.
In one embodiment, the first electrode is the cathode and the second electrode is the anode. In this embodiment, hydrogen gas is formed at the inner surface of the container.
In another embodiment, the first electrode is the anode and the second electrode is the cathode. In this embodiment, oxygen gas is formed at the inner surface of the container.
That constellation makes it also possible - in a special embodiment - to passivate the stainless steel surface as a post treatment after the electrolytic CIP-cleaning, where the first electrode is used as a cathode.
Under the passivation process, the first electrode act as the anode and that makes it possible to form a passivating layer consisting of oxides, i.e a treatment very similarly to the passivation in nitric acid. The Pourbaix-diagram in figure 6 indicates the possible area for passivation.
The anodic current density which is necessary to render the process effective is typically at least 1 A/dm2 corresponding to a potential (SHE) between +400 mV and +1500 mV. For
practical reasons, the current density is typically in the range 1-60 A/dm2, e.g. in the range of 1-30 A/dm2.
In one particularly interesting embodiment, the second electrode is a tubular member facilitating a flow of the electrolyte solution. The tubular member may be designed as a low pressure spray nozzle to ensure a coherent beam of the electrolyte, which form a linear contact area with some extent. Alternatively, the electrode is placed in the water beam formed by a spray nozzle. This embodiment corresponds to the one illustrated in Figure 1.
In another interesting embodiment, the electrolyte solution is fed to the gap between the first electrode and the second electrode by means of a tubular member having a slit. This embodiment corresponds to the one illustrated in Figure 2. In this embodiment the residence time of the electrolyte solution may be increased by arranging a porous structure in the before-mentioned gap.
In a further variant, the electrolytic process is carried out within a jet beam between the area to be cleaned (the first electrode; a cathode) and a cleaning nozzle. An anode is inserted into the tank in appropriate distance allowing a non-interrupted and coherent beam of electrolyte to connect to the anode and cathode (tank wall). The beam is moved to cover the whole area of the tank. Within this embodiment, the flow of the electrolyte solution is preferably predominantly laminar.
In an alternative embodiment, the electrolyte solution which forms electrical communication between said first electrode and said second electrode is held in a porous structure, e.g. in a sponge or a brush. Such a porous structure may be moved across the inner surface my mechanical means, e.g. by a motor/motors or a robot.
In one particularly preferred embodiment, the process according to invention comprising the step of:
a) establishing an electrical circuit comprising (a) the wall of the container as the anode (1), (b) a cathode (2), and (c) an electrolyte solution (3) of one or more components selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium sulphate and potassium sulphate, optionally further comprising a complexing agent, said electrolyte solution forming electrical connection between said anode and said cathode, the connection between the first electrode and the electrolyte solution defining a contact area (4); and
b) facilitating that said contact area (4) is moved across at least a substantial part of said inner surface so as to allow said electrolyte solution (3) to contact said inner surface to be
depleted of the impurities, and simultaneously applying a current density in the range 1-60 A/dm2,
wherein the ratio between (i) the total area of the part of the inner surface which the contact area is moved across and (ii) the contact area is at least 50: 1, and
wherein the movement of the contact area is such that the contact time of the contact area is at least 1 second.
The cleanness of the surfaces treated according to the process according to the present invention can be verified via XPS (X-ray photon Spectroscopy), e.g. as described in the Examples section.
The process of removing impurities as defined herein is believed to reduce the cleaning cycle of the equipment significantly; as compared to conventional CIP cleaning and will "re-set" the surface. This is illustrated by the results presented in the examples section which shows that X-ray photon spectroscopy measurements of a pristine stainless steel surface and a stainless steel surface treated in accordance with the process of the invention appear to be essentially the same.
The process according to the invention can suitably be used for cleaning process reactors being contaminated with a variety of organic constituent, e.g. proteins, milk, etc., and the use is therefore not restricted to the drug industry.
EXAMPLES
XPS (X-ray photon Spectroscopy)
XPS is a versatile technique for analyzing the top ~10 nm of a surface, providing information on the elements present at the surface and the chemical state they are in.
Example 1
Table 1 shows the XPS measurement of a pristine surface of stainless steel type 316. The surface is seen to consist of oxides of mainly chromium and less amounts of iron oxide.
Table 1
XPS average values of the reference surface. All results are in atomic %
Example 2
In Table 2, below, the elemental compositions of surfaces after immersion in insulin solution and additional various cleaning processes are given. The presence of nitrogen and sulfur along with the increased carbon signal show that insulin is still present at the surface after cleaning by water immersion, water spray and conventional CIP detergent (CIP 100 supplied by Steris, UK), while a surface that is practically identical to the pristine surface is obtained after conducting the process in accordance with the present invention.
Table 2
XPS average values of surface after immersion in insulin and additional cleaning processes. All results are in atomic %
Claims
1. An electrolytic process for removing impurities from the inner surface of a metallic container (5), said process comprising the step of:
a) establishing an electrical circuit comprising (a) the wall of the container as a first electrode (1), (b) a second electrode (2), and (c) an electrolyte solution (3) forming electrical connection between said first electrode and said second electrode, the connection between the first electrode and the electrolyte solution defining a contact area (4); and
b) facilitating that said contact area (4) is moved across at least a substantial part of said inner surface so as to allow said electrolyte solution (3) to contact said inner surface to be depleted of the impurities, and simultaneously applying a predetermined current density at said contact area (4).
2. The process according to claim 1, wherein the current density is in the range 1-60 A/dm2.
3. The process according to any one of the preceding claims, wherein the ratio between (i) the total area of the part of the inner surface which the contact area is moved across and (ii) the contact area is at least 10: 1.
4. The process according to any one of the preceding claims, wherein the electrolyte solution is a solution of one or more components selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium sulphate and potassium sulphate.
5. The process according to any one of the preceding claims, wherein the electrolyte solution additionally comprises one or more complexing agent.
6. The process according to any one of the preceding claims, wherein the electrolyte solution is essentially free of detergents.
7. The process according to any one of the preceding claims, wherein the movement of the contact area is such that the contact time of the contact area is at least 1 second.
8. The process according to any one of the preceding claims, wherein the first electrode is the cathode and the second electrode is the anode.
9. The process according to any one of the claims 1-7, wherein the first electrode is the anode and the second electrode is the cathode.
10. The process according to any one of the preceding claims, wherein the second electrode is a tubular member facilitating a flow of the electrolyte solution.
11. The process according to claim 10, wherein the flow of the electrolyte solution is predominantly laminar and coherent.
12. The process according to any one of the claims 10-11, wherein the electrolyte solution is fed to the gap between the first electrode and the second electrode by means of a tubular member having a slit.
13. The process according to any one of the preceding claims, wherein the electrolyte solution which forms electrical connection between said first electrode and said second electrode is held in a porous structure.
14. The process according to claim 1 comprising the step of:
a) establishing an electrical circuit comprising (a) the wall of the container as the anode (1), (b) a cathode (2), and (c) an electrolyte solution (3) of one or more components selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium sulphate and potassium sulphate, optionally further comprising a complexing agent, said electrolyte solution forming electrical connection between said anode and said cathode, the connection between the first electrode and the electrolyte solution defining a contact area (4); and
b) facilitating that said contact area (4) is moved across at least a substantial part of said inner surface so as to allow said electrolyte solution (3) to contact said inner surface to be depleted of the impurities, and simultaneously applying a current density in the range 1-60 A/dm2,
wherein the ratio between (i) the total area of the part of the inner surface which the contact area is moved across and (ii) the contact area is at least 50: 1, and
wherein the movement of the contact area is such that the contact time of the contact area is at least 1 second.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08717715A EP2126160A1 (en) | 2007-03-13 | 2008-03-13 | An electrolytic cip-cleaning process for removing impurities from the inner surface of a metallic container |
| US13/109,518 US20120018298A1 (en) | 2007-03-13 | 2011-05-17 | Electrolytic CIP-Cleaning Process for Removing Impurities from the Inner Surface of a Metallic Container |
| US13/778,940 US20130299520A1 (en) | 2007-03-13 | 2013-02-27 | Electrolytic cip-cleaning process for removing impurities from the inner surface of a metallic container |
| US14/223,177 US20140203044A1 (en) | 2007-03-13 | 2014-03-24 | Electrolytic CIP-Cleaning Process for Removing Impurities from the Inner Surface of a Metallic Container |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07104036 | 2007-03-13 | ||
| EP07104036.4 | 2007-03-13 |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US12529639 A-371-Of-International | 2008-03-13 | ||
| US72890510A Continuation | 2007-03-13 | 2010-03-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2008110587A1 true WO2008110587A1 (en) | 2008-09-18 |
Family
ID=38319776
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2008/052971 WO2008110587A1 (en) | 2007-03-13 | 2008-03-13 | An electrolytic cip-cleaning process for removing impurities from the inner surface of a metallic container |
Country Status (3)
| Country | Link |
|---|---|
| US (3) | US20120018298A1 (en) |
| EP (1) | EP2126160A1 (en) |
| WO (1) | WO2008110587A1 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2518790A1 (en) * | 2014-09-08 | 2014-11-05 | Universidad De Granada | Procedure and device for cleaning metal surfaces using a direct current |
| EP2840170A1 (en) * | 2013-08-20 | 2015-02-25 | Thermos L.L.C. | Metal container washing apparatus |
| TWI630290B (en) * | 2016-07-26 | 2018-07-21 | Crown Manufacturing Corporation | Cleaning device for metal container |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008110587A1 (en) * | 2007-03-13 | 2008-09-18 | Novo Nordisk A/S | An electrolytic cip-cleaning process for removing impurities from the inner surface of a metallic container |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4661220A (en) * | 1984-07-04 | 1987-04-28 | Ab Asea-Atom | Method for local cleaning of surfaces on a nuclear reactor which are coated with oxides or other corrosion products, in connection with inspection |
| EP0246557A1 (en) * | 1986-05-21 | 1987-11-25 | Poligrat Gmbh | Internal surfaces of a gas bottle, and process for their manufacture |
| GB2295483A (en) * | 1994-11-24 | 1996-05-29 | Alfred Richard Solly | An electrolytic method for removing surface radioactivity from nuclear reactor cooling circuit ducting and associated components |
| GB2319259A (en) * | 1996-11-15 | 1998-05-20 | Babcock Rosyth Defence Limited | reducing radionucleide contamination of a metallic component |
| JP2004052089A (en) * | 2002-07-24 | 2004-02-19 | Kao Corp | Cleaning method for steel sheet for plating |
| WO2004061165A1 (en) * | 2003-01-06 | 2004-07-22 | Auckland Uniservices Limited | Electrochemical process and apparatus |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2365807T3 (en) * | 2001-05-16 | 2011-10-11 | ELI LILLY & COMPANY | MEDICATION INJECTOR DEVICE WITH MOTOR ASSEMBLY THAT FACILITATES REARME. |
| US8195328B2 (en) * | 2003-09-19 | 2012-06-05 | Vesta Medical, Llc | Combination disposal and dispensing apparatus and method |
| US7660724B2 (en) * | 2003-09-19 | 2010-02-09 | Vesta Medical, Llc | Waste sorting system utilizing removable liners |
| WO2008110587A1 (en) * | 2007-03-13 | 2008-09-18 | Novo Nordisk A/S | An electrolytic cip-cleaning process for removing impurities from the inner surface of a metallic container |
| EP2125083B1 (en) * | 2007-03-21 | 2013-08-21 | Novo Nordisk A/S | A medical delivery system having container recognition and container for use with the medical delivery system |
| CA2753138C (en) * | 2009-02-27 | 2017-11-14 | Lifescan, Inc. | Medical module for drug delivery pen |
| US8636702B2 (en) * | 2009-08-21 | 2014-01-28 | Beckton Dickinson France, S.A.S. | Magnifying collapsed plunger rod |
| US8632519B2 (en) * | 2009-08-21 | 2014-01-21 | Becton Dickinson France, S.A.S. | Syringe having a collapsible plunger rod |
-
2008
- 2008-03-13 WO PCT/EP2008/052971 patent/WO2008110587A1/en active Application Filing
- 2008-03-13 EP EP08717715A patent/EP2126160A1/en not_active Withdrawn
-
2011
- 2011-05-17 US US13/109,518 patent/US20120018298A1/en not_active Abandoned
-
2013
- 2013-02-27 US US13/778,940 patent/US20130299520A1/en not_active Abandoned
-
2014
- 2014-03-24 US US14/223,177 patent/US20140203044A1/en not_active Abandoned
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4661220A (en) * | 1984-07-04 | 1987-04-28 | Ab Asea-Atom | Method for local cleaning of surfaces on a nuclear reactor which are coated with oxides or other corrosion products, in connection with inspection |
| EP0246557A1 (en) * | 1986-05-21 | 1987-11-25 | Poligrat Gmbh | Internal surfaces of a gas bottle, and process for their manufacture |
| GB2295483A (en) * | 1994-11-24 | 1996-05-29 | Alfred Richard Solly | An electrolytic method for removing surface radioactivity from nuclear reactor cooling circuit ducting and associated components |
| GB2319259A (en) * | 1996-11-15 | 1998-05-20 | Babcock Rosyth Defence Limited | reducing radionucleide contamination of a metallic component |
| JP2004052089A (en) * | 2002-07-24 | 2004-02-19 | Kao Corp | Cleaning method for steel sheet for plating |
| WO2004061165A1 (en) * | 2003-01-06 | 2004-07-22 | Auckland Uniservices Limited | Electrochemical process and apparatus |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2840170A1 (en) * | 2013-08-20 | 2015-02-25 | Thermos L.L.C. | Metal container washing apparatus |
| CN104419943A (en) * | 2013-08-20 | 2015-03-18 | 膳魔师(中国)家庭制品有限公司 | Metal container washing apparatus |
| TWI507572B (en) * | 2013-08-20 | 2015-11-11 | Crown Mfg Corp | Wash the metal container cleaning device |
| US9669435B2 (en) | 2013-08-20 | 2017-06-06 | Thermos L.L.C. | Metal container washing apparatus |
| CN104419943B (en) * | 2013-08-20 | 2018-07-27 | 膳魔师(中国)家庭制品有限公司 | Clean the cleaning device of canister |
| ES2518790A1 (en) * | 2014-09-08 | 2014-11-05 | Universidad De Granada | Procedure and device for cleaning metal surfaces using a direct current |
| TWI630290B (en) * | 2016-07-26 | 2018-07-21 | Crown Manufacturing Corporation | Cleaning device for metal container |
Also Published As
| Publication number | Publication date |
|---|---|
| US20130299520A1 (en) | 2013-11-14 |
| US20120018298A1 (en) | 2012-01-26 |
| US20140203044A1 (en) | 2014-07-24 |
| EP2126160A1 (en) | 2009-12-02 |
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