CA1042572A - Purification of water for boiler - Google Patents
Purification of water for boilerInfo
- Publication number
- CA1042572A CA1042572A CA269,027A CA269027A CA1042572A CA 1042572 A CA1042572 A CA 1042572A CA 269027 A CA269027 A CA 269027A CA 1042572 A CA1042572 A CA 1042572A
- Authority
- CA
- Canada
- Prior art keywords
- resin
- water
- ozone
- organic molecules
- raw water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/72—Treatment of water, waste water, or sewage by oxidation
- C02F1/78—Treatment of water, waste water, or sewage by oxidation with ozone
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J41/00—Anion exchange; Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
- B01J41/04—Processes using organic exchangers
- B01J41/05—Processes using organic exchangers in the strongly basic form
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/42—Treatment of water, waste water, or sewage by ion-exchange
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/42—Treatment of water, waste water, or sewage by ion-exchange
- C02F2001/422—Treatment of water, waste water, or sewage by ion-exchange using anionic exchangers
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/02—Non-contaminated water, e.g. for industrial water supply
- C02F2103/023—Water in cooling circuits
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatment Of Water By Oxidation Or Reduction (AREA)
Abstract
PURIFICATION OF WATER FOR BOILER"
ABSTRACT OF THE DISCLOSURE
Ozone is dispersed in river water to be purified and used in a high pressure boiler. The ozone selec-tively degrades large organic molecules, dissolved in the water, which ordinarily will irreversibly foul the strongly basic anion attracting resin used to adsorb silicious con-taminants from the water. The degraded molecules are re-duced in resin-fouling capability and are removed from the resin during regeneration.
ABSTRACT OF THE DISCLOSURE
Ozone is dispersed in river water to be purified and used in a high pressure boiler. The ozone selec-tively degrades large organic molecules, dissolved in the water, which ordinarily will irreversibly foul the strongly basic anion attracting resin used to adsorb silicious con-taminants from the water. The degraded molecules are re-duced in resin-fouling capability and are removed from the resin during regeneration.
Description
104;~S72 B~CKGROUND OF T~IE INVENTION
This invention relates to a process for purifying raw water, containing dissolved organic molecules of high molecular weight and silicious contaminants, to render it suitable for use as boiler feed.
In purifying raw water, such as river or lake water, special consideration must be given to the removal of ~-silica in its various forms. Usually the silica is dissolved to some extent and is present in the water as silicic acids.
When the untreated raw water is introduced into a boiler, the silicic acids tend to be converted to silica, which forms a solid deposit on the boiler surfaces. This deposit detriment-ally interferes with heat transfer within the boiler.
In modern high pressure boilers, which operate at elevated water temperatures, silica and its related compounds (collectively termed 'silicious contaminants') pose a further problem. Several silicious contaminants are volatile at the temperatures at which high pressure boilers operate and can be carried in the evolving steam, to be deposited in solid form ~- -on equipment and pipes through which the steam passes.
It is a well-established feature of boiler operat-ing art that silicious contaminants in boiler feed water may be conveniently removed by contacting the water with a strongly -~ -basic anion-attracting exchange resin. The silicious contamin-ants are adsorbed by the resin.
Before the raw water is contacted with resin, such water is usually treated to remove most of the minerals ("softening") and insoluble organic materials ("clarifying").
This pre-treatment is done by contacting the raw water with certain chemicals, commonly one or more of: lime, alum, carbon, sodium aluminate, and clay. The treatment is done before the .. , . : .. .. , : , ..... .. . .
.. .. . . . . . . . .
, : . . . . .
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water contacts the resin, as the minerals and organic sub-stances themselves tend to be adsorbed onto the resin with the consequence that the resin will rapidly foul and will need regeneration. Regeneration usually involves contacting the resin with a base, such as sodium hydroxide.
A further step in the pre-treatment is con- - -tacting the raw water with chlorine to kill obnoxious bacteria.
The combination of traditional pre-treatment and contact with resin has been effective in purifying most -types of water used as boiler feed. However, a problem arises when the raw water, besides containing silicious contaminants, also contains significant quantities of large dissolved or-ganic molecules, which is the case when the water originates from regions where drainage areas are swampy. These organic molecules are thought to be humic acid or analogues thereof.
In any event, the organic molecules are substantially unaffected by the conventional pre-treatment process; instead, they are adsorbed by the resin and foul it. When the resin is regen-erated, these organic molecules are only partly removed by the first regeneration and less completely with subsequent regenerations, with the resin rapidly being rendered useless.
A probable reason for the organic molecules' affinity for the resin is that such resins are manufactured with a high pore volume at the surface to encourage ion exchange; it is believed that this porous structure offers sites where the large organic molecules can adhere to the resin.
Two known methods have been heretofore available for removing the offending water-soluble organic molecules.
The first method involves contacting the raw water with adsorbant activated charcoal. However, this method is 1()4ZS7;~
impractical for large flows. The second method involves con-tacting the raw water with a weakLy-basic anion attracting resin. This resin extracts substantially all organic molecules from the water, after which silicious contaminants may be removed in the usual way with a strongly basic resin. The guard resin may be periodically regenerated, but its use is characterized by: high capital cost, frequent regeneration, and frequent testing to monitor the effectiveness of the guard resin.
S~RY OF THE INVENTION
In accordance with the present invention, raw water containing silicious contaminants and high molecular weight water-soluble organic molecules, the latter usually having a molecular weight of 6,000 or greater, is contacted - -with ozone, before the water is contacted with the strongly-basic anion attracting resin. The ozone is dispersed in the water in sufficient quantity as to degrade larger organic molecules, with the result that the resin may satisfactorily be regenerated in conventional manner, as by contacting it with sodium hydroxide. Preferably the ozone is provided in an amount less than 2 parts per million by weight/per part per million by weight carbon present in the water as total organic carbon.
The invention is characterized by several advantages. Firstly, it appears that the ozone is selective in degrading the large organic molecules without significantly attacking the degradation products - thus the invention can be ~ ~ -practised without a high consumption of ozone. Secondly, the ozonized organic molecules are significantly less intense in their resin-fouling properties, thereby making it possible to use the resins longer before regeneration is needed. Thirdly, , :
~, , .: . . .. ~ . ~ :
1~)4Z~i7Z
because ozone is a powerful oxidizing agent, the need for chlo-rine pre-treatment is reduced or eliminated, thereb~ simpli-fying the water treatment operations. Finally, the process is relativeIy simple and inexpensive and does not require careful monitoring.
DESCRIPTION OF THE DRAWINGS
In the drawings~
Figure 1 is a block diagram illustrating the sequence of steps for a preferred form of the invention; and Figure 2 is a diagrammatic illustration of the invention as practised on the pilot run.
DESCRIPTION OF THE PREFERRED EMBODIMENT
The pilot circuit A shown in Figure 2 had been fed raw water taken from the Atha~asca River in Alberta. The drainage area for this river is characterized by large areas of swamp (known locally as "muskeg") and the water was con-taminated with appreciable quantities of mildly acidic organic material - it contained 10 - 30 ppm as total organic carbon (TOC~. It was found that, without ozonation, the strongly ; 20 basic resin would foul and become inoperative with 12 hours ~`
of operation. The resin was considered exhausted when a ~ sudden rise was noted of the conductivity of the emerging q water in conjunction with a drop in pH. The resin was re-,= generated once and operated satisfactorily, however within ~i 25 12 hours it was exhausted and, when contacted with regener-~'' ating base, was ineffective for ion exchange.
The invention was then practised as follows.
~; A laboratory plate-type ozonator 1 (Grace* model, LG-2-Ll, ", capacity 100 grams ozone per day) was used to disperse ozone into a contact column 2 having a diameter of 7 cm. and height i ~ ~
,- of 200 cm. The ozone produced by the ozonator 1 was introduced .... .
, s .
......
, "
:. .
~::
,. . . ~ ~ ;:
... . . .. .
~04;257;:
into column 2 through a porous glass diffuser 3 placed at the raw water intake 4. Excess ozone was removed from the column
This invention relates to a process for purifying raw water, containing dissolved organic molecules of high molecular weight and silicious contaminants, to render it suitable for use as boiler feed.
In purifying raw water, such as river or lake water, special consideration must be given to the removal of ~-silica in its various forms. Usually the silica is dissolved to some extent and is present in the water as silicic acids.
When the untreated raw water is introduced into a boiler, the silicic acids tend to be converted to silica, which forms a solid deposit on the boiler surfaces. This deposit detriment-ally interferes with heat transfer within the boiler.
In modern high pressure boilers, which operate at elevated water temperatures, silica and its related compounds (collectively termed 'silicious contaminants') pose a further problem. Several silicious contaminants are volatile at the temperatures at which high pressure boilers operate and can be carried in the evolving steam, to be deposited in solid form ~- -on equipment and pipes through which the steam passes.
It is a well-established feature of boiler operat-ing art that silicious contaminants in boiler feed water may be conveniently removed by contacting the water with a strongly -~ -basic anion-attracting exchange resin. The silicious contamin-ants are adsorbed by the resin.
Before the raw water is contacted with resin, such water is usually treated to remove most of the minerals ("softening") and insoluble organic materials ("clarifying").
This pre-treatment is done by contacting the raw water with certain chemicals, commonly one or more of: lime, alum, carbon, sodium aluminate, and clay. The treatment is done before the .. , . : .. .. , : , ..... .. . .
.. .. . . . . . . . .
, : . . . . .
ZS7;~
water contacts the resin, as the minerals and organic sub-stances themselves tend to be adsorbed onto the resin with the consequence that the resin will rapidly foul and will need regeneration. Regeneration usually involves contacting the resin with a base, such as sodium hydroxide.
A further step in the pre-treatment is con- - -tacting the raw water with chlorine to kill obnoxious bacteria.
The combination of traditional pre-treatment and contact with resin has been effective in purifying most -types of water used as boiler feed. However, a problem arises when the raw water, besides containing silicious contaminants, also contains significant quantities of large dissolved or-ganic molecules, which is the case when the water originates from regions where drainage areas are swampy. These organic molecules are thought to be humic acid or analogues thereof.
In any event, the organic molecules are substantially unaffected by the conventional pre-treatment process; instead, they are adsorbed by the resin and foul it. When the resin is regen-erated, these organic molecules are only partly removed by the first regeneration and less completely with subsequent regenerations, with the resin rapidly being rendered useless.
A probable reason for the organic molecules' affinity for the resin is that such resins are manufactured with a high pore volume at the surface to encourage ion exchange; it is believed that this porous structure offers sites where the large organic molecules can adhere to the resin.
Two known methods have been heretofore available for removing the offending water-soluble organic molecules.
The first method involves contacting the raw water with adsorbant activated charcoal. However, this method is 1()4ZS7;~
impractical for large flows. The second method involves con-tacting the raw water with a weakLy-basic anion attracting resin. This resin extracts substantially all organic molecules from the water, after which silicious contaminants may be removed in the usual way with a strongly basic resin. The guard resin may be periodically regenerated, but its use is characterized by: high capital cost, frequent regeneration, and frequent testing to monitor the effectiveness of the guard resin.
S~RY OF THE INVENTION
In accordance with the present invention, raw water containing silicious contaminants and high molecular weight water-soluble organic molecules, the latter usually having a molecular weight of 6,000 or greater, is contacted - -with ozone, before the water is contacted with the strongly-basic anion attracting resin. The ozone is dispersed in the water in sufficient quantity as to degrade larger organic molecules, with the result that the resin may satisfactorily be regenerated in conventional manner, as by contacting it with sodium hydroxide. Preferably the ozone is provided in an amount less than 2 parts per million by weight/per part per million by weight carbon present in the water as total organic carbon.
The invention is characterized by several advantages. Firstly, it appears that the ozone is selective in degrading the large organic molecules without significantly attacking the degradation products - thus the invention can be ~ ~ -practised without a high consumption of ozone. Secondly, the ozonized organic molecules are significantly less intense in their resin-fouling properties, thereby making it possible to use the resins longer before regeneration is needed. Thirdly, , :
~, , .: . . .. ~ . ~ :
1~)4Z~i7Z
because ozone is a powerful oxidizing agent, the need for chlo-rine pre-treatment is reduced or eliminated, thereb~ simpli-fying the water treatment operations. Finally, the process is relativeIy simple and inexpensive and does not require careful monitoring.
DESCRIPTION OF THE DRAWINGS
In the drawings~
Figure 1 is a block diagram illustrating the sequence of steps for a preferred form of the invention; and Figure 2 is a diagrammatic illustration of the invention as practised on the pilot run.
DESCRIPTION OF THE PREFERRED EMBODIMENT
The pilot circuit A shown in Figure 2 had been fed raw water taken from the Atha~asca River in Alberta. The drainage area for this river is characterized by large areas of swamp (known locally as "muskeg") and the water was con-taminated with appreciable quantities of mildly acidic organic material - it contained 10 - 30 ppm as total organic carbon (TOC~. It was found that, without ozonation, the strongly ; 20 basic resin would foul and become inoperative with 12 hours ~`
of operation. The resin was considered exhausted when a ~ sudden rise was noted of the conductivity of the emerging q water in conjunction with a drop in pH. The resin was re-,= generated once and operated satisfactorily, however within ~i 25 12 hours it was exhausted and, when contacted with regener-~'' ating base, was ineffective for ion exchange.
The invention was then practised as follows.
~; A laboratory plate-type ozonator 1 (Grace* model, LG-2-Ll, ", capacity 100 grams ozone per day) was used to disperse ozone into a contact column 2 having a diameter of 7 cm. and height i ~ ~
,- of 200 cm. The ozone produced by the ozonator 1 was introduced .... .
, s .
......
, "
:. .
~::
,. . . ~ ~ ;:
... . . .. .
~04;257;:
into column 2 through a porous glass diffuser 3 placed at the raw water intake 4. Excess ozone was removed from the column
2 through an overhead line 5 and decomposed in a tube furnace 6 packed with quartz chips and maintained at 1000C.
The ozonated water was then passed through the conventional water treatment circuit A comprising a weak acid cation- ~
attracting resin column 7, a strong acid cation-attracting -resin column 8 and the strong base anion-attracting resin column 9. Athabasca River water, which had been held in a storage tank, was fed to the column 2 at the same rate as had been the case before the ozonator circuit B had been in-stalled, i.e. 200 cm3/minute. This water contained 30 ppm TOC. The test was carried out for a period of 6 days, with the strongly-basic resin being regenerated daily without noticeable decrease in its efficiency.
A particular advantage of the invention is that only enough ozone has to be added to the feed water to -~
degrade the large molecules, without the need for organic molecules to be oxidized all the way to carbon dioxide. This was demonstrated by analysis. On treating raw water with from five to six ppm ozone the total organic carbon tTOC) was reduced from fifteen ppm to fourteen ppm. Analysis of duplicate samples by the ultraviolet technique (UV) at 255nm, ~
however, showed that UV absorption in the ozone treated water ~-., . -was only about half the level of the untreated water. Since small molecules ab~orb less than larger molecules the diminished UV absorbance after ozone treatment is an indication of degration of the humic and fulvic acids. On the other hand the only slight diminution in TOC reveals that very little of the organic material was vapourized to carbon dioxide.
The selectivity whereby ozone pre~erentially degrades the ~04~57Z
larger organic molecules ensures that the invention is highly efficient in the uSe of ozone.
The ozonated water was then passed through the conventional water treatment circuit A comprising a weak acid cation- ~
attracting resin column 7, a strong acid cation-attracting -resin column 8 and the strong base anion-attracting resin column 9. Athabasca River water, which had been held in a storage tank, was fed to the column 2 at the same rate as had been the case before the ozonator circuit B had been in-stalled, i.e. 200 cm3/minute. This water contained 30 ppm TOC. The test was carried out for a period of 6 days, with the strongly-basic resin being regenerated daily without noticeable decrease in its efficiency.
A particular advantage of the invention is that only enough ozone has to be added to the feed water to -~
degrade the large molecules, without the need for organic molecules to be oxidized all the way to carbon dioxide. This was demonstrated by analysis. On treating raw water with from five to six ppm ozone the total organic carbon tTOC) was reduced from fifteen ppm to fourteen ppm. Analysis of duplicate samples by the ultraviolet technique (UV) at 255nm, ~
however, showed that UV absorption in the ozone treated water ~-., . -was only about half the level of the untreated water. Since small molecules ab~orb less than larger molecules the diminished UV absorbance after ozone treatment is an indication of degration of the humic and fulvic acids. On the other hand the only slight diminution in TOC reveals that very little of the organic material was vapourized to carbon dioxide.
The selectivity whereby ozone pre~erentially degrades the ~04~57Z
larger organic molecules ensures that the invention is highly efficient in the uSe of ozone.
Claims (5)
1. In the process in which raw water containing silicious contaminants and dissolved organic molecules is treated with strongly basic anion-attracting exchange resin to remove substantially all said silicious contaminants to prepare said water for use as boiler feed, said resin being subjected to periodic regeneration when its ion exchange capacity is reduced by use, the improvement which comprises:
dispersing ozone in said raw water, before the water is contacted with the strongly basic resin, said ozone being added in sufficient quantity as to degrade organic molecules whereby the resulting degraded organic molecules after adsorption on said strongly basic resin may be removed by regeneration with a strong base.
dispersing ozone in said raw water, before the water is contacted with the strongly basic resin, said ozone being added in sufficient quantity as to degrade organic molecules whereby the resulting degraded organic molecules after adsorption on said strongly basic resin may be removed by regeneration with a strong base.
2. Process according to claim 1 comprising:
contacting, used, ineffective resin, previously contacted by ozonated water, with a regenerating solution of strongly basic,water soluble substance, thereby converting said resin to an effective reusable condition.
contacting, used, ineffective resin, previously contacted by ozonated water, with a regenerating solution of strongly basic,water soluble substance, thereby converting said resin to an effective reusable condition.
3. Process according to claim 2 comprising:
contacting the resin with purified water to wash out residual amounts of said strongly basic water soluble substance to prepare said resin for further use in removal of silicious contaminants from raw water.
contacting the resin with purified water to wash out residual amounts of said strongly basic water soluble substance to prepare said resin for further use in removal of silicious contaminants from raw water.
4. Process according to claims 1, 2, or 3 wherein:
the quantity of ozone used is not more than 2 parts per million by weight for every part per million by weight of carbon present in said raw water as total organic carbon.
the quantity of ozone used is not more than 2 parts per million by weight for every part per million by weight of carbon present in said raw water as total organic carbon.
5. Process according to claims 1,2, or 3 wherein:
said raw water contains dissolved organic molecules of molecular weight in excess of 6,000.
said raw water contains dissolved organic molecules of molecular weight in excess of 6,000.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA269,027A CA1042572A (en) | 1976-12-31 | 1976-12-31 | Purification of water for boiler |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA269,027A CA1042572A (en) | 1976-12-31 | 1976-12-31 | Purification of water for boiler |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1042572A true CA1042572A (en) | 1978-11-14 |
Family
ID=4107638
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA269,027A Expired CA1042572A (en) | 1976-12-31 | 1976-12-31 | Purification of water for boiler |
Country Status (1)
Country | Link |
---|---|
CA (1) | CA1042572A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0604360A1 (en) * | 1992-12-14 | 1994-06-29 | Christ AG | Process for the controlled removal of insoluble or slightly soluble substances from a system wherein ozonized water is circulating |
-
1976
- 1976-12-31 CA CA269,027A patent/CA1042572A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0604360A1 (en) * | 1992-12-14 | 1994-06-29 | Christ AG | Process for the controlled removal of insoluble or slightly soluble substances from a system wherein ozonized water is circulating |
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