CA2157916C - Method of cleaning and maintaining potable water distribution pipe systems - Google Patents
Method of cleaning and maintaining potable water distribution pipe systems Download PDFInfo
- Publication number
- CA2157916C CA2157916C CA002157916A CA2157916A CA2157916C CA 2157916 C CA2157916 C CA 2157916C CA 002157916 A CA002157916 A CA 002157916A CA 2157916 A CA2157916 A CA 2157916A CA 2157916 C CA2157916 C CA 2157916C
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- scale
- acid
- pipe
- cleaning solution
- water
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Links
- 238000004140 cleaning Methods 0.000 title claims abstract description 46
- 238000009826 distribution Methods 0.000 title claims abstract description 30
- 238000000034 method Methods 0.000 title claims abstract description 28
- 239000003651 drinking water Substances 0.000 title claims abstract description 15
- 235000012206 bottled water Nutrition 0.000 title claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 51
- 239000013049 sediment Substances 0.000 claims abstract description 27
- 230000002378 acidificating effect Effects 0.000 claims abstract description 14
- 238000011010 flushing procedure Methods 0.000 claims abstract description 6
- 239000002253 acid Substances 0.000 claims description 29
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 15
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 14
- 239000000344 soap Substances 0.000 claims description 10
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 9
- 239000011707 mineral Substances 0.000 claims description 9
- 150000007524 organic acids Chemical class 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 8
- 229910021529 ammonia Inorganic materials 0.000 claims description 8
- 235000005985 organic acids Nutrition 0.000 claims description 7
- 239000002028 Biomass Substances 0.000 claims description 5
- 241000295146 Gallionellaceae Species 0.000 claims description 5
- 239000003112 inhibitor Substances 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 4
- 230000000149 penetrating effect Effects 0.000 claims description 4
- 239000002738 chelating agent Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 150000007522 mineralic acids Chemical class 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 2
- 239000008235 industrial water Substances 0.000 claims description 2
- 238000007789 sealing Methods 0.000 claims description 2
- 235000020188 drinking water Nutrition 0.000 claims 1
- 238000005086 pumping Methods 0.000 claims 1
- 239000000243 solution Substances 0.000 description 48
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 11
- 150000007513 acids Chemical class 0.000 description 7
- 238000005260 corrosion Methods 0.000 description 7
- 230000007797 corrosion Effects 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 229960004275 glycolic acid Drugs 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- -1 hydrochloric Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-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
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000009533 lab test Methods 0.000 description 3
- 238000004062 sedimentation Methods 0.000 description 3
- 239000005711 Benzoic acid Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 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 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 229940048842 sodium xylenesulfonate Drugs 0.000 description 2
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- ZZXDRXVIRVJQBT-UHFFFAOYSA-M Xylenesulfonate Chemical compound CC1=CC=CC(S([O-])(=O)=O)=C1C ZZXDRXVIRVJQBT-UHFFFAOYSA-M 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical group 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 229940071104 xylenesulfonate Drugs 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B08—CLEANING
- B08B—CLEANING IN GENERAL; PREVENTION OF FOULING IN GENERAL
- B08B9/00—Cleaning hollow articles by methods or apparatus specially adapted thereto
- B08B9/02—Cleaning pipes or tubes or systems of pipes or tubes
- B08B9/027—Cleaning the internal surfaces; Removal of blockages
- B08B9/032—Cleaning the internal surfaces; Removal of blockages by the mechanical action of a moving fluid, e.g. by flushing
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/02—Inorganic compounds
- C11D7/04—Water-soluble compounds
- C11D7/08—Acids
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/265—Carboxylic acids or salts thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/32—Organic compounds containing nitrogen
- C11D7/3218—Alkanolamines or alkanolimines
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G1/00—Cleaning or pickling metallic material with solutions or molten salts
- C23G1/02—Cleaning or pickling metallic material with solutions or molten salts with acid solutions
-
- E—FIXED CONSTRUCTIONS
- E03—WATER SUPPLY; SEWERAGE
- E03B—INSTALLATIONS OR METHODS FOR OBTAINING, COLLECTING, OR DISTRIBUTING WATER
- E03B7/00—Water main or service pipe systems
- E03B7/006—Arrangements or methods for cleaning or refurbishing water conduits
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/14—Hard surfaces
- C11D2111/20—Industrial or commercial equipment, e.g. reactors, tubes or engines
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Mechanical Engineering (AREA)
- Hydrology & Water Resources (AREA)
- Inorganic Chemistry (AREA)
- Public Health (AREA)
- Water Supply & Treatment (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Emergency Medicine (AREA)
- Cleaning In General (AREA)
- Cleaning By Liquid Or Steam (AREA)
- Detergent Compositions (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
- Processing Of Solid Wastes (AREA)
Abstract
A method of cleaning and maintaining potable water distribution system which have reduced flow due to an increase of water scale deposits, sediment, and the like on the inside surface of the pipe is disclosed. An aqueous acidic cleaning solution (12) is introduced and circulated through the pipe (25) to be treated for a sufficient time to dissolve and loosen the scale and sediment, and the spent solution containing dissolved or suspended scale and sediment is flushed from the pipe (25) to provide a cleaned pipe with improved water flow.
It is also desirable to flush the water distribution pipe system with high pressure water after the treatment to remove loosened scale and sediment that was not removed during the circulation and flushing of the treating solution (12).
It is also desirable to flush the water distribution pipe system with high pressure water after the treatment to remove loosened scale and sediment that was not removed during the circulation and flushing of the treating solution (12).
Description
HETHOD OF CLEANING AND IrIAINTAINING POTABLE WATER
DIBTRIHUTION PIPE BYSTEMS
It is well known that hardness and suspended solids in water sources vary widely in composition depending on the source and will result in scale deposition and sedimentation on surfaces wherever water is used. Scale deposition and sedimentation is particularly troublesome in water distribution pipe systems which service the residential and commercial customers of municipalities, private water companies and the lils:e along with industrial process water distribution pipe systems as found in the mining, petroleum, agriculture and the like industries. In these system:, the formation of scale and sediment can reduce the water flow through the pipe system which will limit the capacity of the pipe to service the requirements of the customers or to provide the _ required water necessary for an industrial process, irrigation, etc. For instance, in municipal systems an increase in the fire risk would be obvious if the fire hydrant did not supply sufficient water to extinguish the fire due to scale and sediment deposits in the feed pipe 7:ine. At some point, the water distribution pipe would have to be replaced due to these restrictions at a high cost and with prolonged interruption of service.
Additionally, scale and sedimentation will increase the possibility of corrosion in the water distribution pipe along with promoting the growth of organisms. The organisms also can be a health hazard, promoting corrosion and biomass which binds scale and sediment together and to the surfaces of the system.
Corrosion will eventually lead to the leakage of the systeau and the necessity to replace the leaking sectia~n.
Strong acids have been used to clean water wells, however, submersible pumps are removed prior to treatment to prevent corrosion by the acids employed.
Also, organic acids, mixtures of mineral acids and organic acids or inhibited acid compositions have been found to clean water wells without the necessity of removing the pumps or other equipment. These methods ~1~ ~9~_~
DIBTRIHUTION PIPE BYSTEMS
It is well known that hardness and suspended solids in water sources vary widely in composition depending on the source and will result in scale deposition and sedimentation on surfaces wherever water is used. Scale deposition and sedimentation is particularly troublesome in water distribution pipe systems which service the residential and commercial customers of municipalities, private water companies and the lils:e along with industrial process water distribution pipe systems as found in the mining, petroleum, agriculture and the like industries. In these system:, the formation of scale and sediment can reduce the water flow through the pipe system which will limit the capacity of the pipe to service the requirements of the customers or to provide the _ required water necessary for an industrial process, irrigation, etc. For instance, in municipal systems an increase in the fire risk would be obvious if the fire hydrant did not supply sufficient water to extinguish the fire due to scale and sediment deposits in the feed pipe 7:ine. At some point, the water distribution pipe would have to be replaced due to these restrictions at a high cost and with prolonged interruption of service.
Additionally, scale and sedimentation will increase the possibility of corrosion in the water distribution pipe along with promoting the growth of organisms. The organisms also can be a health hazard, promoting corrosion and biomass which binds scale and sediment together and to the surfaces of the system.
Corrosion will eventually lead to the leakage of the systeau and the necessity to replace the leaking sectia~n.
Strong acids have been used to clean water wells, however, submersible pumps are removed prior to treatment to prevent corrosion by the acids employed.
Also, organic acids, mixtures of mineral acids and organic acids or inhibited acid compositions have been found to clean water wells without the necessity of removing the pumps or other equipment. These methods ~1~ ~9~_~
for cleaning w<~ter wells have involved static and surging treatment.
A proper cleaning and maintenance program for water distribution systems will prevent decreased water flow capacity, corrosion and the necessity to replace the system or portions thereof. A simple and effective method for cleaning and maintaining these systems is needed.
ES-A-533818 discloses a method for eliminating lime incrust.ations from domestic water supply installations which represents the prior art as referred to in the preamble to Claim 1.
US-A-4025359 discloses an inhibited acid composition fo:r cleaning water systems which has a reduced tendency to attack galvanized pipe or steel pipe.
WO-A-92/20629 discloses soap compositions of carboxylic acids and amines useful in removal and prevention of scale containing calcium or magnesium carbonate, oxide or hydroxide.
FR-A-2602571 discloses a method and apparatus for cleaning a con~~uit of a potable water distribution network in which pulsE~s of fluid under pressure, such as water, are passed through the conduit.
In accordance with the present invention, a method of cleaning a potable water distribution pipe system of scale comprising providing a reservoir for containing an aqueous cleaning solution for the removal of the scale, sealing off a section of pipe in the system for circulation of the cleaning solution therethrough, circulating the cleaning solution from the reservoir through the pipe section and returning the solution to the reservoir for the removal of the scale, characterised in that the aque~~us cleaning solution is adapted to remove scale associated with sulfate-reducing and iron bacteria consisting pr~_marily of iron oxide, biomass and sediment from inside surfaces of the pipe section, in that the section of pipe is an underground section of a A(~E~:DE~ SHEET
X21 g 7 9 1 ~6 -3a-distribution pipe system and in that the circulating cleaning solution is monitored and the cleaning solution circulated for a sufficient period of time until the scale and sediment i.s observed to be dissolved, loosened and/or suspended in t:he circulating cleaning solution.
This invention is directed to a method of cleaning and maintaining water distribution systems. Water systems having interior scale and sediment deposits are cleaned by introducing and - circulating an effective amount of an aqueous treatment solution for a sufficient period of time which results in the solution, loosening and suspension of the undesired scale and sediment. Thereafter, the spent treating solution containing the dissolved or suspended scale and sediment is flushed from the water distribution system to pro~ride a clean system with improved water flow and operation. Additionally, further flushing with high pressure water will also remove additional scale that had been loosened by the treating solution.
The cleaning solution may be acidic, neutral or basic. In th~~ most preferred form, in potable water pipe systems, mineral acids or organic acids, and mixtures thereof, are employed as acidic treatment solutions. The acidic treatment solution may contain .,..
-w WO 94/21865 ~ ~~ PCT/US94/03065 furthsar additives such as inhibitors, chelating agents, penetrating and/or dispersing agents to assist in the removed of scale and sediment and to minimize any adver::e effects on the pipes, valves, or other system surfaces due to the acids employed.
This invention provides a simple, low cost and effective method of removing water scale and sediment from water distribution systems in order to maintain proper water flow, operation and to prevent corrosion of the system which would require the high cost a.nd inconvenience of replacement.
Other advantages and objectives of this invention will be further understood with reference to the following detailed description and drawings.
DETAILED DESCRIPTION OF THE INVENTION
Among the acidic treatment solutions found to be useful in practicing the method of this invention are aqueous solutions of mineral acids such as hydrochloric, nitric, phosphoric, polyphosphoric, hydrofluoric, boric, sulfuric, sulfurous, and the like.
Aqueous solutions of mono-, di- and polybasic organic acids have also been found to be useful and include formic, acetic, propionic, citric, glycolic, lactic, tartaric, polyacrylic, succinic, p-toluenesulfonic, and the like. The useful treatment solutions may also be aqueous mixtures of the above mineral and organic acids.
21579 1a Alkaline, acid, or neutral cleaning solutions may also beg employed, as indicated above, depending upon the t:~pe of scale that needs to be removed.
Sequestering or chelating agents such as ECTA
(ethylenediamine tetraacetic acid), NTA
(nitrilotria~cetic acid), and derivatives, i.e., basic alkali saltsc, and the like have also been found to be useful in th,e treatment solution in certain cases.
Th.e acidic treatment solution may also contain acid inhibitors which substantially reduce the acidic act~Lon on metal surfaces of the water distribution system, particularly valves, fire hydrants, etc., and these various inhibitors for acids have been well documented in the patent art. Typical, but not necessarily all inclusive, examples of acid inhibitors a:re disclosed in the following U.S. Patents:
2,758,970; 2,807,585; 2,941,949; 3,077,454; 3,607,781;
3,668,137; 3,885,913; 4,089,795; 4,199,469; 4,310,435;
A proper cleaning and maintenance program for water distribution systems will prevent decreased water flow capacity, corrosion and the necessity to replace the system or portions thereof. A simple and effective method for cleaning and maintaining these systems is needed.
ES-A-533818 discloses a method for eliminating lime incrust.ations from domestic water supply installations which represents the prior art as referred to in the preamble to Claim 1.
US-A-4025359 discloses an inhibited acid composition fo:r cleaning water systems which has a reduced tendency to attack galvanized pipe or steel pipe.
WO-A-92/20629 discloses soap compositions of carboxylic acids and amines useful in removal and prevention of scale containing calcium or magnesium carbonate, oxide or hydroxide.
FR-A-2602571 discloses a method and apparatus for cleaning a con~~uit of a potable water distribution network in which pulsE~s of fluid under pressure, such as water, are passed through the conduit.
In accordance with the present invention, a method of cleaning a potable water distribution pipe system of scale comprising providing a reservoir for containing an aqueous cleaning solution for the removal of the scale, sealing off a section of pipe in the system for circulation of the cleaning solution therethrough, circulating the cleaning solution from the reservoir through the pipe section and returning the solution to the reservoir for the removal of the scale, characterised in that the aque~~us cleaning solution is adapted to remove scale associated with sulfate-reducing and iron bacteria consisting pr~_marily of iron oxide, biomass and sediment from inside surfaces of the pipe section, in that the section of pipe is an underground section of a A(~E~:DE~ SHEET
X21 g 7 9 1 ~6 -3a-distribution pipe system and in that the circulating cleaning solution is monitored and the cleaning solution circulated for a sufficient period of time until the scale and sediment i.s observed to be dissolved, loosened and/or suspended in t:he circulating cleaning solution.
This invention is directed to a method of cleaning and maintaining water distribution systems. Water systems having interior scale and sediment deposits are cleaned by introducing and - circulating an effective amount of an aqueous treatment solution for a sufficient period of time which results in the solution, loosening and suspension of the undesired scale and sediment. Thereafter, the spent treating solution containing the dissolved or suspended scale and sediment is flushed from the water distribution system to pro~ride a clean system with improved water flow and operation. Additionally, further flushing with high pressure water will also remove additional scale that had been loosened by the treating solution.
The cleaning solution may be acidic, neutral or basic. In th~~ most preferred form, in potable water pipe systems, mineral acids or organic acids, and mixtures thereof, are employed as acidic treatment solutions. The acidic treatment solution may contain .,..
-w WO 94/21865 ~ ~~ PCT/US94/03065 furthsar additives such as inhibitors, chelating agents, penetrating and/or dispersing agents to assist in the removed of scale and sediment and to minimize any adver::e effects on the pipes, valves, or other system surfaces due to the acids employed.
This invention provides a simple, low cost and effective method of removing water scale and sediment from water distribution systems in order to maintain proper water flow, operation and to prevent corrosion of the system which would require the high cost a.nd inconvenience of replacement.
Other advantages and objectives of this invention will be further understood with reference to the following detailed description and drawings.
DETAILED DESCRIPTION OF THE INVENTION
Among the acidic treatment solutions found to be useful in practicing the method of this invention are aqueous solutions of mineral acids such as hydrochloric, nitric, phosphoric, polyphosphoric, hydrofluoric, boric, sulfuric, sulfurous, and the like.
Aqueous solutions of mono-, di- and polybasic organic acids have also been found to be useful and include formic, acetic, propionic, citric, glycolic, lactic, tartaric, polyacrylic, succinic, p-toluenesulfonic, and the like. The useful treatment solutions may also be aqueous mixtures of the above mineral and organic acids.
21579 1a Alkaline, acid, or neutral cleaning solutions may also beg employed, as indicated above, depending upon the t:~pe of scale that needs to be removed.
Sequestering or chelating agents such as ECTA
(ethylenediamine tetraacetic acid), NTA
(nitrilotria~cetic acid), and derivatives, i.e., basic alkali saltsc, and the like have also been found to be useful in th,e treatment solution in certain cases.
Th.e acidic treatment solution may also contain acid inhibitors which substantially reduce the acidic act~Lon on metal surfaces of the water distribution system, particularly valves, fire hydrants, etc., and these various inhibitors for acids have been well documented in the patent art. Typical, but not necessarily all inclusive, examples of acid inhibitors a:re disclosed in the following U.S. Patents:
2,758,970; 2,807,585; 2,941,949; 3,077,454; 3,607,781;
3,668,137; 3,885,913; 4,089,795; 4,199,469; 4,310,435;
4,541,945; 4,554,090 4,587,030; 4,614,600; 4,637,899;
4,670,186; 4,780,150 and 4,851,149.
The treatment solution may also contain dispersing, penetrating or emulsifying agents to assist in the removal of the scale and sediment. These surface active agents may be anionic, cationic, nonionic or amphoteric as defined in the art.
Compounds such as alkyl ether sulfates, alkyl or aryl sulfates, al.kanolamines, ethoxylated alkanolamides, b , ~, WO 94/21865 ~ ~. a~ PCT/LJS94/03065 amine oxides, ammonium and alkali soaps, betaines, hydrot.ropes such as sodium aryl sulfonates; ethoxylated and propoxylated fatty alcohols and sugars, ethoxylated and poopoxylated alkylphenols, sulfonates, phosphate esters, quarternaries, sulfosuccinates, and mixtures thereof, have been found to be useful in admixture with the acid treating solution.
DRAWINGS AND OPERATING ERAMPLES
Fig. 1 is a schematic of a laboratory test system illustrating the method of this invention.
Fig. 2 is a diagram of a field system for cleaning a potable water distribution system.
With reference to Fig. 1, a laboratory test system is shown to evaluate the removal of scale and sediment by acidic treating solutions from a test pipe sample taken from a water distribution system. This system includes a 15 gallon acidic treating solution reservoir 5, submersible acidic treat;n~ ~~~"+;.", circul~3tion pump 6 rated at 1200 gallons per hour, 1"
inlet transfer line 7, drain valve 8, heavy rubber diaphragm seals 9 for the ends of the test pipe specimen 10, 1" outlet transfer line 11 and the treating solution 12. The test pipe specimen 10 is mounted at about a 30 degree angle so that the test solution will contact essentially the entire inner pipe surface' to be treated.
A laboratory test, for example, was run on a four foot section of 6" diameter pipe which had been 5 ~ PCT/US94/03065 removed from a potable water distribution system that had been used for over 40 years. The scale on the inside: of the pipe consisted of nodules of up to 1 to 1 i inc:hes in height covering 100% of the inside pipe surface which had substantially reduced the opening inside the pipe for water to flow. Analysis of the scale indicated it consisted of primarily iron with some calcium, magnesium and manganese in the form oxides, hydroxides and carbonates along with fine mineral acid insoluble solids and some "biomass". This is typical scale associated with sulfate-reducing and iron bacteria along with the associated corrosion.
About 10 gallons of a 12.5% aqueous inhibited hydroc:hloric/glycolic acid solution containing a penetrating agent was placed in the reservoir 5 and circulated through the test pipe 10 for a period of 24 hours. After 2 hours of circulation, particles of the scale were breaking loose and could be heard in the outlet transfer line 11 and observed entering the reservoir 5. The color of the treating solution also became increasingly darker with circulation time.
After 24 hours the circulation was stopped and the system was drained of the treating solution. The diaphragms 9 were removed and the inside of the test pipe was observed to be about 80% cleaned of scale and sediment solids.
On treating the test pipe with a second identical treating solution for a period of 21.5 hours, WO 94/Z1865 ~ '~ ~ ~, PCT/US94/03065 _g_ about 80% of the interior surface of the test pipe was obser~;red to still be covered over with a scale and/or sediment that was a soft and paste-like semi-solid which contained some grit and could be easily removed with a probe. The remaining scale nodules had been substantially reduced in size since the end of the first treatment. It was concluded that the second treatiaent would probably not be necessary if a high pressure water flush was employed to remove the insoluble soft sediment which had coated the remaining scale nodules after the first treatment.
With reference to Fig. 2, a field equipment and system diagram is shown which may be employed in the cleaning of a potable water pipe distribution system. Two 500 gallon treating solution reservoir tanks 20 and 21 along with a 100 gallon per minute circulation pump 22 and sight glass 23 are mounted on a flat: bed truck (not shown) . In this example, a 2~
inlet pipe 24 is secured to a 650 foot section of 6"
water distribution pipe 25 after the main shut off valve 26. The fire hydrant 27 and fire hose 28 were employed for the acidic treating solution return to tanks 20 and 21.
The section of pipe 25 to be treated was isolated by closing off the two water main shut-off valves 26 and 29 along with all service line valves, typically 30 and 31. With valves 32 and 33 closed, 1000 gallons of acidic treating solution was prepared WO 94/21865 ~ ~ PCT/US94/03065 _g-in tanks 20 and 21. With the coupling 34 open, the treating solution w:a allowed to enter the system by opening valves 33 and 35 and turning on the circulation pump 22. The pH of the water- coming from the open coupling was then monitored until a decrease was noted which indicated the acid treating solution had displaced the water in the section to be treated. The circulation pump 22 was turned off and the coupling 34 connecaed. Valves 36 and 37 were then closed and valve l0 32 opened for circulation. The circulation pump 22 was then started again for the treatment period. Valve 37 was c:Losed to allow for scale solids to accumulate in tank :?0 while the treating solution could overflow at 38 to tank 21 which reduces the chances of plugging during treatment.
The treating solution was then circulated in the system of Fig. 2 for a period of 5 hours.
Observation of the treating solution through the sight glass 23 showed an increasingly darker discoloration with time. At the end of the treatment period, the circulation pump 22 was turned off, and valves 33 and 35 were closed. The main shut-off valve 26 was slowly opened and fresh water allowed to enter the system until the treating solution was displaced as noted when the tanks 20 and 21 were full. Valve 32 was then closed. The fire hose 28 was then disconnected from the fire hydrant 27 and the main shut-off valve 26 opened full to allow high pressure flushing of the WO 94/21865 PCTIUS94I03(~~
-lo-treated water main 25. As the flush water emerged from the fire hydrant 27 it was dark in color with cons~iderahle scale and sediment solids. Flushing continued until the flush water was clean of solids for a period of time prior to putting the treated section of the water distribution system back into service.
The flow rate through the fire hydrant 27 prior to treatment had been determined by a Pitot Gauge to be 588 gallons per minute. After treatment, the flow rate was determined to be 790 gallons per minute.
This was an increase of 34.5%.
Also, improved mechanical operations of the hydrants and valves of the system were achieved. The flow of cleaning solution may also be reversed in the system to further improve cleaning efficiency. The above cleaning solutions met the requirements of the National Sanitation Foundation (NSF International, Ann Arbo~~, Michigan), Standard 60 for potable water dist~_-ibution systems.
Other examples of cleaning solutions may be employed as follows:
PrebJ~end Ingredients % by wt 31% Flydrochloric acid in water 87.14 +/- 2%
70% G:lycolic acid in water 5.27 +/- 0.3%
40% fiodium xylene sulfonate in water 2.06 +/- 0.2%
Triet:hanolamine and diethanolamine 2.96 +/- 0.2%
mi~,aure (85%/15%) Water 2.57 +/- 0.2%
In a preferred form of the invention, the above: preblended cleaning solution is used in an amount of ax~out 12.5% by weight with water in the field for WO 94/21865 ~ PCT/US94/03065 cleansing an underground potable water distribution pipe system. However, more generally, the solution may be emplo!,red in amounts of from about 5 to about 50% by weighi: with water in the field, depending upon such variables as the amount of scale, pipe volume to be cleanE:d, circulation time and other factors. The amounia of anhydrous chemicals in a broader range of ingredients are about 1% to 27% HC1, 0.1% to 4%
glycol_ic acid, 0.04% to 1% sodium xylene sulfonate and a b o a t 0 . 1 % t o 2 . 5 % o f t h a triethanolamine/diethanolomine mixture (hereinafter referred to as "TEA").
It should be understood that the above chemical ingredients may be blended in the field for cleaning the underground potable pipes, for example, hydrochloric acid may be added to a concentrate of the glycolic acid, sodium xylene sulfonate and TEA. In the potable water distribution systems, an underground section of the pipe to be cleaned is sealed off from the rest of the system. As illustrated above in Fig.
2, the cleaning solution is then introduced from a tank into the pipe section and, if water is in that section of pine, it is removed upon the introduction of the cleaning solution. After the cleaning solution has been introduced into the pipe section, circulation of the cleaning solution through the underground pipe is initiated for a sufficient period of time for solubilization, loosening and/or suspension of the scale and sediments.
In thE~ above preblends, a soap having a 1:1 stoichiometri<: equivalent of the acid (HC1 and glycolic acid) and TEA base is formed with an excess of the acid.
This composition has been found to work effectively in the field for the: removal of scale associated with sulfate-reducing and iron bacteria consisting primarily of iron oxide, biomas:~ and sediment. These 1:1 soaps have also been described in co-pending Canadian Application Serial No.
2,103,141. These soaps may be more generally categorized as soaps of mineral and/or organic acids and a base such as an amine and ammonia. Further examples of these soaps include 1:1 soaps of TEA and glycolic acid (also known as hydroxyacetic acid); TEA and acetic acid; TEA and citric acid; TEA and benzoic acid; hydrochloric acid and ammonia;
sulfuric acid and ammonia; nitric acid and ammonia; TEA and hydrochloric acid; TEA and sulfuric acid; TEA and nitric acid; ammonia and glycolic acid; ammonia and benzoic acid;
and ammonia a.nd p-toluenesulfonic acid. Accordingly, it will be understood that other cleaning solutions of the acidic type employing 1:1 soaps may be employed to effectively solubilize, loosen and/or suspend the scale and 21.~'~~~~
sediment from the potable pipe in accordance with the principles of this invention.
In view of the above detailed description, other method variations to clean domestic and industrial water distribution systems, like houses, hotels, plants, offices, etc., will be apparent to a person of ordinary skill in the ~:rt. The method is especially advantageous in cleaning underground potable water distribution systems having scale associated with sulfate-reducing and iron bacteria consisting primarily of iron oxide, biomass and sediment.
4,670,186; 4,780,150 and 4,851,149.
The treatment solution may also contain dispersing, penetrating or emulsifying agents to assist in the removal of the scale and sediment. These surface active agents may be anionic, cationic, nonionic or amphoteric as defined in the art.
Compounds such as alkyl ether sulfates, alkyl or aryl sulfates, al.kanolamines, ethoxylated alkanolamides, b , ~, WO 94/21865 ~ ~. a~ PCT/LJS94/03065 amine oxides, ammonium and alkali soaps, betaines, hydrot.ropes such as sodium aryl sulfonates; ethoxylated and propoxylated fatty alcohols and sugars, ethoxylated and poopoxylated alkylphenols, sulfonates, phosphate esters, quarternaries, sulfosuccinates, and mixtures thereof, have been found to be useful in admixture with the acid treating solution.
DRAWINGS AND OPERATING ERAMPLES
Fig. 1 is a schematic of a laboratory test system illustrating the method of this invention.
Fig. 2 is a diagram of a field system for cleaning a potable water distribution system.
With reference to Fig. 1, a laboratory test system is shown to evaluate the removal of scale and sediment by acidic treating solutions from a test pipe sample taken from a water distribution system. This system includes a 15 gallon acidic treating solution reservoir 5, submersible acidic treat;n~ ~~~"+;.", circul~3tion pump 6 rated at 1200 gallons per hour, 1"
inlet transfer line 7, drain valve 8, heavy rubber diaphragm seals 9 for the ends of the test pipe specimen 10, 1" outlet transfer line 11 and the treating solution 12. The test pipe specimen 10 is mounted at about a 30 degree angle so that the test solution will contact essentially the entire inner pipe surface' to be treated.
A laboratory test, for example, was run on a four foot section of 6" diameter pipe which had been 5 ~ PCT/US94/03065 removed from a potable water distribution system that had been used for over 40 years. The scale on the inside: of the pipe consisted of nodules of up to 1 to 1 i inc:hes in height covering 100% of the inside pipe surface which had substantially reduced the opening inside the pipe for water to flow. Analysis of the scale indicated it consisted of primarily iron with some calcium, magnesium and manganese in the form oxides, hydroxides and carbonates along with fine mineral acid insoluble solids and some "biomass". This is typical scale associated with sulfate-reducing and iron bacteria along with the associated corrosion.
About 10 gallons of a 12.5% aqueous inhibited hydroc:hloric/glycolic acid solution containing a penetrating agent was placed in the reservoir 5 and circulated through the test pipe 10 for a period of 24 hours. After 2 hours of circulation, particles of the scale were breaking loose and could be heard in the outlet transfer line 11 and observed entering the reservoir 5. The color of the treating solution also became increasingly darker with circulation time.
After 24 hours the circulation was stopped and the system was drained of the treating solution. The diaphragms 9 were removed and the inside of the test pipe was observed to be about 80% cleaned of scale and sediment solids.
On treating the test pipe with a second identical treating solution for a period of 21.5 hours, WO 94/Z1865 ~ '~ ~ ~, PCT/US94/03065 _g_ about 80% of the interior surface of the test pipe was obser~;red to still be covered over with a scale and/or sediment that was a soft and paste-like semi-solid which contained some grit and could be easily removed with a probe. The remaining scale nodules had been substantially reduced in size since the end of the first treatment. It was concluded that the second treatiaent would probably not be necessary if a high pressure water flush was employed to remove the insoluble soft sediment which had coated the remaining scale nodules after the first treatment.
With reference to Fig. 2, a field equipment and system diagram is shown which may be employed in the cleaning of a potable water pipe distribution system. Two 500 gallon treating solution reservoir tanks 20 and 21 along with a 100 gallon per minute circulation pump 22 and sight glass 23 are mounted on a flat: bed truck (not shown) . In this example, a 2~
inlet pipe 24 is secured to a 650 foot section of 6"
water distribution pipe 25 after the main shut off valve 26. The fire hydrant 27 and fire hose 28 were employed for the acidic treating solution return to tanks 20 and 21.
The section of pipe 25 to be treated was isolated by closing off the two water main shut-off valves 26 and 29 along with all service line valves, typically 30 and 31. With valves 32 and 33 closed, 1000 gallons of acidic treating solution was prepared WO 94/21865 ~ ~ PCT/US94/03065 _g-in tanks 20 and 21. With the coupling 34 open, the treating solution w:a allowed to enter the system by opening valves 33 and 35 and turning on the circulation pump 22. The pH of the water- coming from the open coupling was then monitored until a decrease was noted which indicated the acid treating solution had displaced the water in the section to be treated. The circulation pump 22 was turned off and the coupling 34 connecaed. Valves 36 and 37 were then closed and valve l0 32 opened for circulation. The circulation pump 22 was then started again for the treatment period. Valve 37 was c:Losed to allow for scale solids to accumulate in tank :?0 while the treating solution could overflow at 38 to tank 21 which reduces the chances of plugging during treatment.
The treating solution was then circulated in the system of Fig. 2 for a period of 5 hours.
Observation of the treating solution through the sight glass 23 showed an increasingly darker discoloration with time. At the end of the treatment period, the circulation pump 22 was turned off, and valves 33 and 35 were closed. The main shut-off valve 26 was slowly opened and fresh water allowed to enter the system until the treating solution was displaced as noted when the tanks 20 and 21 were full. Valve 32 was then closed. The fire hose 28 was then disconnected from the fire hydrant 27 and the main shut-off valve 26 opened full to allow high pressure flushing of the WO 94/21865 PCTIUS94I03(~~
-lo-treated water main 25. As the flush water emerged from the fire hydrant 27 it was dark in color with cons~iderahle scale and sediment solids. Flushing continued until the flush water was clean of solids for a period of time prior to putting the treated section of the water distribution system back into service.
The flow rate through the fire hydrant 27 prior to treatment had been determined by a Pitot Gauge to be 588 gallons per minute. After treatment, the flow rate was determined to be 790 gallons per minute.
This was an increase of 34.5%.
Also, improved mechanical operations of the hydrants and valves of the system were achieved. The flow of cleaning solution may also be reversed in the system to further improve cleaning efficiency. The above cleaning solutions met the requirements of the National Sanitation Foundation (NSF International, Ann Arbo~~, Michigan), Standard 60 for potable water dist~_-ibution systems.
Other examples of cleaning solutions may be employed as follows:
PrebJ~end Ingredients % by wt 31% Flydrochloric acid in water 87.14 +/- 2%
70% G:lycolic acid in water 5.27 +/- 0.3%
40% fiodium xylene sulfonate in water 2.06 +/- 0.2%
Triet:hanolamine and diethanolamine 2.96 +/- 0.2%
mi~,aure (85%/15%) Water 2.57 +/- 0.2%
In a preferred form of the invention, the above: preblended cleaning solution is used in an amount of ax~out 12.5% by weight with water in the field for WO 94/21865 ~ PCT/US94/03065 cleansing an underground potable water distribution pipe system. However, more generally, the solution may be emplo!,red in amounts of from about 5 to about 50% by weighi: with water in the field, depending upon such variables as the amount of scale, pipe volume to be cleanE:d, circulation time and other factors. The amounia of anhydrous chemicals in a broader range of ingredients are about 1% to 27% HC1, 0.1% to 4%
glycol_ic acid, 0.04% to 1% sodium xylene sulfonate and a b o a t 0 . 1 % t o 2 . 5 % o f t h a triethanolamine/diethanolomine mixture (hereinafter referred to as "TEA").
It should be understood that the above chemical ingredients may be blended in the field for cleaning the underground potable pipes, for example, hydrochloric acid may be added to a concentrate of the glycolic acid, sodium xylene sulfonate and TEA. In the potable water distribution systems, an underground section of the pipe to be cleaned is sealed off from the rest of the system. As illustrated above in Fig.
2, the cleaning solution is then introduced from a tank into the pipe section and, if water is in that section of pine, it is removed upon the introduction of the cleaning solution. After the cleaning solution has been introduced into the pipe section, circulation of the cleaning solution through the underground pipe is initiated for a sufficient period of time for solubilization, loosening and/or suspension of the scale and sediments.
In thE~ above preblends, a soap having a 1:1 stoichiometri<: equivalent of the acid (HC1 and glycolic acid) and TEA base is formed with an excess of the acid.
This composition has been found to work effectively in the field for the: removal of scale associated with sulfate-reducing and iron bacteria consisting primarily of iron oxide, biomas:~ and sediment. These 1:1 soaps have also been described in co-pending Canadian Application Serial No.
2,103,141. These soaps may be more generally categorized as soaps of mineral and/or organic acids and a base such as an amine and ammonia. Further examples of these soaps include 1:1 soaps of TEA and glycolic acid (also known as hydroxyacetic acid); TEA and acetic acid; TEA and citric acid; TEA and benzoic acid; hydrochloric acid and ammonia;
sulfuric acid and ammonia; nitric acid and ammonia; TEA and hydrochloric acid; TEA and sulfuric acid; TEA and nitric acid; ammonia and glycolic acid; ammonia and benzoic acid;
and ammonia a.nd p-toluenesulfonic acid. Accordingly, it will be understood that other cleaning solutions of the acidic type employing 1:1 soaps may be employed to effectively solubilize, loosen and/or suspend the scale and 21.~'~~~~
sediment from the potable pipe in accordance with the principles of this invention.
In view of the above detailed description, other method variations to clean domestic and industrial water distribution systems, like houses, hotels, plants, offices, etc., will be apparent to a person of ordinary skill in the ~:rt. The method is especially advantageous in cleaning underground potable water distribution systems having scale associated with sulfate-reducing and iron bacteria consisting primarily of iron oxide, biomass and sediment.
Claims (14)
1. A method of cleaning a water distribution pipe system of scale comprising providing a reservoir (20,21) for containing an aqueous cleaning solution for the removal of the scale, circulating the cleaning solution from the reservoir (20,21) through a section (25) of pipe in the system and returning the solution to the reservoir (20,21) for the removal of the scale, characterised in that the aqueous cleaning solution is suitable for removal of scale associated with sulfate-reducing and iron bacteria consisting primarily of iron oxide, biomass and sediment from inside surfaces of the water distribution system, in that the section of pipe (25) is a section of a distribution pipe system and in that the method includes sealing off the section (25) for circulation of cleaning solution therethrough.
2. A method as claimed in claim 1 wherein the pipe section (25) is sealed between two fire hydrants (27) and the cleaning solution is circulated by connecting one of the fire hydrants (27) to the reservoir (20,21) for pumping the cleaning solution therethrough.
3. A method as claimed in either claim 1 or claim 2 comprising flushing the system with clean water after the removal of the spent cleaning solution.
4. A method as claimed in any preceding claim comprising flushing the system with high pressure water for the removal of any spent cleaning solution, scale and/or sediment.
5. A method as claimed in any preceding claim wherein the aqueous treatment solution is acidic.
6. A method as claimed in claim 5 wherein the acid solution contains further additives selected from the group consisting of acid inhibitors, chelating agents, surfactants, penetrating agents and dispensing agents, and mixtures thereof to assist in the removal of scale and sediment.
7. A method as claimed in either claim 5 or claim 6 wherein the acid is selected from the group consisting of mineral and organic acids and mixtures thereof.
8. A method as claimed in claim 7 wherein the mineral acid is selected from the group consisting of hydrochloric, nitric, phosphoric, polyphosphoric, hydrofluoric, boric, sulfuric, and sulfurous and mixtures thereof.
9. A method as claimed in either claim 7 or claim 8 wherein the organic acid is selected from the group consisting of formic, acetic, propionic, citric, glycolic, lactic, tartaric, polyacrylic, succinic, p-toluenesulfonic, and mixtures thereof.
10. A method as claimed in any preceding claim wherein the cleaning solution is a mixture of hydrochloric acid, glycolic acid, an alkanolamine and a surfactant.
11. A method as claimed in any preceding claim wherein the cleaning solution contains a soap having a 1:1 stoichiometric equivalent of an acid and a base wherein the acid is selected from the group consisting of a mineral acid and an organic acid and the base is selected from a group consisting of an amine and ammonia, where an effective amount of free acid is present in the solution to react with the scale.
12. A method as claimed in any preceding claim wherein the reservoir is truck mounted for makeup, storage and disposal of cleaning solution.
13. A method as claimed in any preceding claim wherein the pipe distribution system is a domestic or industrial water system.
14. A method as claimed in any preceding claim wherein the aqueous treatment solution meets the requirements of the US National Sanitation Foundation Standard 60 for drinking water treatment chemicals for use in potable water distribution systems.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US209,953 | 1993-03-17 | ||
US036,188 | 1993-03-23 | ||
US08/036,188 US5360488A (en) | 1993-03-23 | 1993-03-23 | Method of cleaning and maintaining water distribution pipe systems |
US20995394A | 1994-03-17 | 1994-03-17 | |
PCT/US1994/003065 WO1994021865A1 (en) | 1993-03-23 | 1994-03-22 | Method of cleaning and maintaining potable water distribution pipe systems |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2157916A1 CA2157916A1 (en) | 1994-09-29 |
CA2157916C true CA2157916C (en) | 2000-01-25 |
Family
ID=26712917
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002157916A Expired - Fee Related CA2157916C (en) | 1993-03-23 | 1994-03-22 | Method of cleaning and maintaining potable water distribution pipe systems |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP0690944B1 (en) |
JP (1) | JP3597193B2 (en) |
AT (1) | ATE170583T1 (en) |
AU (1) | AU673426B2 (en) |
BR (1) | BR9406139A (en) |
CA (1) | CA2157916C (en) |
DE (1) | DE69413017T2 (en) |
WO (1) | WO1994021865A1 (en) |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0766765A1 (en) * | 1994-06-20 | 1997-04-09 | H.E.R.C. Products Incorporated | Method of cleaning and maintaining potable water distribution pipe systems with a heated cleaning solution |
US5755155A (en) * | 1997-02-28 | 1998-05-26 | Tetra Laval Holdings & Finance S.A. | Aseptic process interface group |
JPH11141713A (en) * | 1997-09-05 | 1999-05-28 | Tetra Laval Holdings & Finance Sa | Sterile valve assembly |
JP2002052322A (en) * | 2000-08-10 | 2002-02-19 | Kurita Water Ind Ltd | Washing method |
JP4283098B2 (en) * | 2003-12-04 | 2009-06-24 | 花王株式会社 | Metal component processing solution |
JP5200326B2 (en) * | 2006-03-30 | 2013-06-05 | 栗田工業株式会社 | Scale cleaner and scale removal method |
WO2016068525A1 (en) * | 2014-10-27 | 2016-05-06 | 이기원 | Method for removing scale |
RU2594426C1 (en) * | 2015-02-26 | 2016-08-20 | Акционерное общество "Научно-исследовательский и проектный институт по переработке газа" (АО "НИПИгазпереработка") | Method for cleaning inner surface of process equipment and pipelines (versions) |
CA2969174A1 (en) | 2017-06-02 | 2018-12-02 | Fluid Energy Group Ltd. | Novel modified acid compositions as alternatives to conventional acids in the oil and gas industry |
DE202019003089U1 (en) * | 2019-07-24 | 2020-10-27 | Josef Schallameier | Decalcification of pressurized pipes of any length |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3667487A (en) * | 1970-12-11 | 1972-06-06 | Richardson Chem Cleaning Servi | Integrated chemical cleaning apparatus |
US4025359A (en) * | 1974-04-01 | 1977-05-24 | Connelly Jr George F | Inhibited acid composition for cleaning water systems |
EP0027980B1 (en) * | 1979-10-24 | 1984-01-25 | Georg Fischer Aktiengesellschaft | Method and apparatus for rinsing, cleaning, disinfecting and coating a conduit on the interior, especially a water conduit in a new construction |
DE3244443C2 (en) * | 1982-12-01 | 1986-11-06 | Späne, Rainer, 7888 Rheinfelden | Process for removing iron, calcium and manganese-containing ocher deposits and / or sintering from facilities operated for water supply |
DE3583586D1 (en) * | 1984-11-30 | 1991-08-29 | Feldmann Chemie Gmbh | USE OF MIXTURE OF ORGANIC AND / OR INORGANIC ACIDS AND / OR ACID SALTS FOR THE REMOVAL OF IRON AND MANGANIZED DEPOSITS AND CONSTRUCTIONS. |
FR2602571B1 (en) * | 1986-08-06 | 1989-02-03 | Assainissement Rationnel Pompa | METHOD FOR CLEANING A PIPELINE, PARTICULARLY OF A DRINKING WATER DISTRIBUTION NETWORK AND SYSTEM FOR CARRYING OUT SAID METHOD |
DE3631459A1 (en) * | 1986-09-16 | 1988-03-24 | Wegener Paul | METHOD FOR CLEANING THE INTERIOR OF BRANCHED PIPELINES AND / OR AGGREGATES AND DEVICE FOR CARRYING OUT THIS METHOD |
DE3731441A1 (en) * | 1987-08-13 | 1989-02-23 | Imhof Elisabeth | Process and device for cleaning, corrosion removal, descaling if appropriate, and sealing of building water installations |
DE3828229A1 (en) * | 1988-08-19 | 1990-02-22 | Feldmann Chemie Gmbh | Means for cleaning, disinfection and maintaining drinking water plants and beverage industry plants |
DE4015201A1 (en) * | 1990-05-11 | 1991-11-14 | Heimo Wessollek | CLEANER FOR DRINKING WATER SYSTEMS |
DE4015202A1 (en) * | 1990-05-11 | 1991-11-14 | Heimo Wessollek | CLEANER FOR DRINKING WATER SYSTEMS |
US5322635A (en) * | 1991-05-16 | 1994-06-21 | H.E.R.C. Incorporated | Soap compositions of carboxylic acids and amines useful in removal and prevention of scale |
DE4125315C2 (en) * | 1991-07-31 | 1995-09-28 | Oertzen Arndt H Gmbh & Co | Device for cleaning pipelines |
-
1994
- 1994-03-22 EP EP94912283A patent/EP0690944B1/en not_active Expired - Lifetime
- 1994-03-22 BR BR9406139A patent/BR9406139A/en not_active IP Right Cessation
- 1994-03-22 AU AU64903/94A patent/AU673426B2/en not_active Ceased
- 1994-03-22 WO PCT/US1994/003065 patent/WO1994021865A1/en active IP Right Grant
- 1994-03-22 JP JP52131394A patent/JP3597193B2/en not_active Expired - Fee Related
- 1994-03-22 DE DE69413017T patent/DE69413017T2/en not_active Expired - Fee Related
- 1994-03-22 AT AT94912283T patent/ATE170583T1/en active
- 1994-03-22 CA CA002157916A patent/CA2157916C/en not_active Expired - Fee Related
Also Published As
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ATE170583T1 (en) | 1998-09-15 |
DE69413017D1 (en) | 1998-10-08 |
DE69413017T2 (en) | 1999-01-28 |
CA2157916A1 (en) | 1994-09-29 |
WO1994021865A1 (en) | 1994-09-29 |
JPH08509908A (en) | 1996-10-22 |
AU6490394A (en) | 1994-10-11 |
EP0690944A1 (en) | 1996-01-10 |
BR9406139A (en) | 1996-01-30 |
EP0690944B1 (en) | 1998-09-02 |
AU673426B2 (en) | 1996-11-07 |
JP3597193B2 (en) | 2004-12-02 |
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