GB2060429A - Method of regenerating weak base ion exchange resins - Google Patents
Method of regenerating weak base ion exchange resins Download PDFInfo
- Publication number
- GB2060429A GB2060429A GB7935136A GB7935136A GB2060429A GB 2060429 A GB2060429 A GB 2060429A GB 7935136 A GB7935136 A GB 7935136A GB 7935136 A GB7935136 A GB 7935136A GB 2060429 A GB2060429 A GB 2060429A
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- resins
- regenerant
- weak base
- anion exchange
- resin
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- C—CHEMISTRY; METALLURGY
- C13—SUGAR INDUSTRY
- C13B—PRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
- C13B20/00—Purification of sugar juices
- C13B20/14—Purification of sugar juices using ion-exchange materials
- C13B20/146—Purification of sugar juices using ion-exchange materials using only anionic ion-exchange material
-
- 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
- B01J49/00—Regeneration or reactivation of ion-exchangers; Apparatus therefor
- B01J49/05—Regeneration or reactivation of ion-exchangers; Apparatus therefor of fixed beds
- B01J49/07—Regeneration or reactivation of ion-exchangers; Apparatus therefor of fixed beds containing anionic exchangers
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatment Of Water By Ion Exchange (AREA)
Abstract
After weak base ion exchange resins are regenerated, e.g with a solution of NaOH, Na2CO3 or aqueous ammonia, and washed with water or carbonic acid solution to remove a portion of the regenerant wastes, the resins are contacted with a solution of carbonic acid to remove the remaining regenerant wastes.
Description
SPECIFICATION
Method of regenerating weak base ion exchange resins
This invention relates to a method of treating weak base ion exchange resins. More particularly, the invention relates to a method of treating weak base ion exchange resins whereby the regenerated resins are washed with water to remove a portion of the regenerant wastes and then washed with a solution of carbonic acid to remove substantially all the remaining regenerant wastes.
Ion exchange processes generally involve a reversible chemical reaction between a solid ion exchanger and an aqueous solution whereby ions are interchanged between the exchanger and the solution. The most widely used exchangers are ion exchange resins which comprise, for the most part, insoluble organic polymer matrices having attached functional groups which provide mobile ions which may be exchanged for ions in the solution bearing the same charge. To impart increased stability to the resins, the matrices are usually prepared by addition copolymerization reactions which provide varying degrees of crosslinking. Depending upon the nature of the functional group, ion exchange resins are classified broadly as strong acid, weak acid, strong base and weak base.The acid exchange resins are further classified as cation exchangers while the base exchange resins are usually referred to as anion exchangers.
Strong acid cation exchange resins typically comprise sulfonated copolymerized styrenedivinylbenzene products cross-linked to varying degrees. Such resins are widely used in water conditioning, demineralization of sugar and corn syrups, chromatographic separations, and metal recovery.
Weak acid cation exchange resins are commonly prepared by reacting an unsaturated carboxylic acid, e.g., acrylic or methacrylic acid, with a cross-linking agent such as divinylbenzene or ethylene dimethacrylate. Functional groups may comprise phenoiic, phosphonous or carboxylic entities, combinations of these and others. Weak acid resins have found application in water conditioning, chromatographic separation, and metal recovery.
Strong base anion exchange resins generally are prepared by affixing quaternary ammonium groups to a polystyrene divinylbenzene matrix. Resins of this type are used principally in water conditioning.
Weak base anion exchange resins contain primary, secondary and tertiary amine groups or mixtures of such groups. Such resins are available in a variety of types including condensation products of amines with formaldehyde, alkyl dihalides, chloromethylated styrene-divinylbenzene, etc. Resins of this type are used principally in demineraiization of corn syrups and corn sugar.
Ion exchange resins may be used in batch or column type operations. The latter type of operation is most widely used in industrial operations. In this case, a column or a vertical cylinder is filled with the resin, and the resin is supported by a porous plate or other means which is permeable to the solution to be treated. The solution may be passed down through the resin (down-flow operation) or up through the resin (up-flow operation). Resin columns may also be operated using counter-current flow techniques whereby the feed solution is passed downwardly and the regenerate upwardly or vice versa.
A typical cycle for the operation of an ion exchange column is as follows:
1. Exhaustion Step - The solution being treated is passed through the column in order to remove ions by exchanging them for an equivalent amount of similarly charged ions on the resin until the resin is essentially exhausted of the latter ions.
2. Regeneration Step - A solution containing the necessary ion to recharge the resin is passed through the column.
3. Rinse Step - Water is passed through the column to remove regenerant waste products and excess regenerant. Regenerant waste products are materials which are chemicaily or physically adsorbed on the resin during the exhaustion step.
Certain optional steps may also be carried out. For example, when the solution being treated is of significant economic importance, a rinse step may be included before regeneration to preclude mixing of the solution being treated and the regenerant. Also, there may be included a backwash prior to
regeneration whereby, the upward flow of water removes insoluble contaminants and the resin bed is loosened.
Weak base resins have found wide application in deionization of corn syrups, including high fructose corn syrups, for the purpose of removing salts and weakly acidic colored bodies. Other types of resins are also used for purification or refining such syrups.
Since ion exchange resins, including weak base resins, contain a finite number of ion exchange sites, the exchange capacity of the resin eventually becomes effectively exhausted. The length of time for this to occur is dependent upon the amount of ionic material removed from the solution and the flow rate of the solution through the resin. The economics of ion exchange refining make it desirable that the resins be reused.
When weak base anion exchange resins are utilized to refine or purify corn syrups and the ion exchange capacity is effectively exhausted, the typical regeneration cycle is:
1 ) The ion exchange column is "sweetened off" by displacement of the syrup from the resin with water.
2) Water is passed upwardly through the column to backwash the resin and thereby remove insoluble debris which was filtered out of the corn syrup and also to reclassify the resin in the column so as to minimize pressure drop and channelling.
3) The resin is regenerated to the weak free base form bypassing downwardly therethrough, for instance, a solution at suitable concentration of NaOH, Na2CO3, ammonia or the like to regenerate the ion exchange capacity of the resin. The regenerant solution may be passed through the bed until typically about one bed volume of regenerant is in contact with the resin.
4) The regenerant is displaced from the column by slow addition of rinse water which additionally removes a considerable portion of the regenerant waste products. This rinse is referred to in the art as the "slow rinse step" since the rate at which water is introduced into the column approximately equals the rate at which the regenerant was introduced into the column. If the rate the regenerant is passed through the resin column is too rapid, the contact period necessary for satisfactory regeneration to take place may be too short.
5) More water is passed through the column to remove the remaining regenerant and waste products. This is generally referred to in the art as the "fast rinse step" since the rate at which water is passed through the resin bed is typically about three times faster than that utilized in the slow rinse step. The fast rinse is continued until the resin is essentially free of regenerant solution as determined by measuring the pH or conductivity of the column effluent.
After several regeneration cycles the weak base anion exchange resins require more rinse water to achieve the same degree of ion exchange capacity. S.B. Applebaum, Demineralization by Ion
Exchange, pp. 146-147, Academic Press, New York (1968) attributed this need for more water to oxidative attack by the water which causes the formation of weak acid groups on the resin which combine with sodium or like ions thereby hindering theremoval of regenerant waste products by rinse water. One proposed solution to this problem was the utilization of a solution containing relatively small amounts of ammonia for regeneration. However, this approach suffers from the disadvantage that, when dealing with large amounts of regenerant, the ammonia present interferes with the operation of biological waste treatment facilities.Another solution was to use heated water for rinsing, however, this requires energy expenditures and has the tendency to cause physical deterioration of the resin.
According to the present invention there is provided a process for regenerating exhausted weak base anion exchange resins comprising contacting the resins with a regenerant solution under conditions whereby the anion exchange capacity of the resins is substantially restored and regenerant waste products are produced, washing the resins with water or carbonic acid to remove a portion of the regenerant waste products and then washing with a solution of carbonic acid to remove additional amounts of regenerant waste products.
Utilization of carbonic acid (a water solution of carbon dioxide) during the fast rinse for removal of regenerant waste products from a weak base anion exchange resin provides a number of distinct advantages over the utilization of water or "decationized water" (water treated with a strong acid cation exchange resin in hydrogen ion form). First, the period of time for the fast rinse step may be reduced by about one-third that normally required at the same flow rate of the rinse, thus the resin is available for use more quickly than would otherwise be the case.
In commerical practice, it is necessary that a column of regenerated form resin be available to replace a column of resin in the system when it becomes exhausted. As the number of regeneration cycles increases, the rinse time required also increases. When the time required to regenerate and rinse the resin exceeds the time in which a column of resin is exhausted, the resin is discarded and replaced.
Therefore, when carbonic acid is utilized in the fast rinse step, the operating life of the resin is extended because the resin can be regenerated a greater number of times before discarding than when water is utilized in the fast rinse step, due to the shorter time required with the carbonic acid rinse. Thus, a second advantage is that the accumulated total amount of product refined perft3 of resin is increased by use of the process of the instant invention. Furthermore, an economic saving of water is achieved because the time required for the fast rinse is reduced.
The concentration of the carbonic acid solution utilized may vary over a relatively wide range. Low concentrations of carbonic acid will not remove regenerant waste products as speedily as do more highly concentrated solutions. It is preferred that water saturated with CO2 at ambient temperature and pressure be utilized. While super-saturated solutions can probably be utilized, no improvement is foreseen by such utilization.
The carbonic acid may be formed by simply bubbling CO2 into a water-filled holding tank and then transferring the solution upwardly or downwardly through the column of resin to remove regenerant waste products or, the CO2 may be introduced by suitable valve means into the rinse water being fed to the column.
The preferred regenerants utilized in this invention are solutions of NaOH, Na2CO3 and aqueous
NH3. The concentration and amounts of solution may vary widely but, for economic reasons, the least amount of solution which regenerates the resin to the desired degree is preferred. When sodium or similar ionic species are contained in the regenerant, the weak-acid groups on the resin are converted to sodium salts which, during water rinsing, are only slowly released or removed by hydrolysis. In the refining of corn syrups with ion exchange resins, it has sometimes been observed that after about 200 cycles of use, water rinsing to remove regenerant waste products takes such an inordinately long period that the resin is not ready for use when required. When this occurs, in certain instances, the resin is discarded even though the resin still has some exchange capacity.
Figure 1 illustrates the amount of CO2 which may typically be required to achieve a fast rinse effluent pH of about 9 versus the number of regeneration cycles the weak base resin was subjected to.
Predictably, the amount of CO2 necessary to achieve an effluent pH*of 9 increased proportionally with the number of regeneration cycles. A solution of Na2CO3 was utilized during regeneration and the substrates refined were high fructose corn syrup and 94 DE corn syrup.
While it is contemplated that a variety of weak base resins may be utilized in the present process, the preferred types are those which contain primary, secondary and tertiary amine groups or mixtures of such groups. Exemplary of such resins are those marketed by Diamond Shamrock Chemical Company and Rohrn and Haas Company under the trade names of DuoliteB ES-561 and Amberlite) IRA-93, respectively.
In order to more clearly describe the nature of the present invention, specific Examples will hereinafter be described. It should be understood, however, that this is done solely by way of example and is intended neither to delineate the scope of the invention nor limit the ambit of the appended claims. In the Examples and through the specification, percentages refer to per cent by weight unless otherwise specified.
EXAMPLE 1
This Example illustrates the utilization of a solution of carbonic acid to fast rinse a regenerated weak base anion exchange resin on a laboratory scale.
The resin utilized in this Example had 631 cycles of use in commercially refining a high fructose corn syrup. Two 50 ml samples of the exhausted weak base anion exchange resin (Duolite(!) ES--561 ) were placed in a column (2.5 cm diam x 30 cm high) and 63 ml of a 6 per cent solution of Na2CO3 was passed through each of the columns, followed by a slow rinse utilizing 63 ml of deionized water at a rate of 2 ml/min.
The columns were then fast rinsed at a rate equivalent to 0.5 to 1.0 GPM/ft3 of resin as follows:
Control Column: fast rinsed with "decationized water" at pH 3.
Test Column: fast rinsed with "decationized water" at pH 3 which had been saturated with CO2 at ambient temperature and pressure.
The pH values of the effluent solutions exiting the two columns at specified rinse volumes are shown in Figure 2.
As indicated in Figure 2, the pH of the effluent exiting from the column rinsed with CO2 saturated water dropped dramatically in a very short period whereas the pH of the effluent exiting the control column rinsed with "decationized water" dropped only slowly and never reached a pH of below about 10 during the period of the test. Figure 2 also shows that when the pH of the effluent rinse water reaches about 5, the pH of the effluent remained relatively constant even when "decationized water" was used for further rinsing.
The amount of sodium in the effluents exiting the columns were plotted against the volumes of rinse water shown in Figure 3. As shown by the curves in this figure, a much greater amount of sodium was contained in the effluent from the column fast rinsed with CO2 saturated water.
EXAMPLE II
This Example illustrates the regeneration of weak base anion exchange resins that have been utilized to refine corn syrup in commercial practice.
After 699 cycles of use in refining an enzymatically produced high fructose corn syrup, two columns, each containing about 50 cubic feet of weak base anion exchange resin (DuoliteB ES-56 1), were regenerated with a sufficient amount of a solution of Na2CO3 to provide 4.5 pounds Na2CO3 per cubic foot of resin. The resin column was then slow rinsed with about 400 gal. "decationized water" at a rate of 13 GPM.
The control resin column was then fast rinsed with "decationized water" at a pH of 3 and the other column was rinsed with "decationized water" at pH 3 saturated with CO2 at ambient temperature and pressure. Both fast rinses were conducted at an average flow rate of about 43 gallons per minute.
The pH values of the effluent solutions exiting the two columns are shown in Figure 4.
EXAMPLE III
This Example illustrates the regeneration of weak base anion exchange resins that have been utilized to refine a carbon treated 94 DE corn syrup over a number of cycles.
The parameters within which this Example were performed are set forth in Table I below together with the results obtained.
TABLE I
Fast Rinse
With Saturated Fast Rinse
CO2 Solution With Water
Columns
1 2 3 4 5 6
Average Number of Regeneration Cycles
Completed During the Comparative Test 216 122 333 216 122 333
Lbs. of Na2CO3 per cubic ft of
resin utilized for regeneration 5.0 5.0 5.0 5.0 5.0 5.0 Slow rinse volume (gal/ft3 resin) 10 10 10 10 10 10
Average fast rinse volume (gal/ft3 resin) 93 70 88 381 180 451
Average fast rinse flow rate (GPM/ft3 resin) 0.6 0.6 0.6 0.6 0.6 0.6
Average period (min.) to achievepH 10.0 153 115 145 630 297 746
EXAMPLE IV
This Example illustrates that by following the regeneration process of the present invention, the amount of acid necessary to lower the pH of the refined high fructose corn syrup after refining is substantially reduced.
Generally, after refining a high fructose corn syrup, the pH thereof is reduced to about 4.5 since this is the pH at which the stability of the syrup against color formation is the greatest
Two coiumns of exhausted weak base anion exchange resin (Duolite() ES-56 1) were regenerated and slow rinsed with "decationized water". One column was fast rinsed with a saturated water solution of CO2 at pH 3 and the other fast rinsed with "decationized water" also at pH 3. High fructose corn syrup was passed through each of the columns at the same flow rate and the pH's of the effluents of the high fructose corn syrups exiting the columns were determined and are shown in Figure 5. Because of the relatively low pH values of the high fructose corn syrup exiting the column which was fast rinsed with a saturated water solution of CO2, less acid was required to lower the pH of the same to the desired level than the corn syrup exiting the column which was fast rinsed with "decationized water".
Claims (9)
1. A process for regenerating exhausted weak base anion exchange resins comprising contacting the resins with a regenerant solution under conditions whereby the anion exchange capacity of the resins is substantially restored and regenerant waste products are produced, washing the resins with water or carbonic acid to remove a portion of the regenerant waste products and then washing with a solution of carbonic acid to remove additional amounts of regenerant waste products.
2. A process for regenerating exhausted weak base anion exchange resins as defined in claim 1, wherein the regenerant is a solution of NaOH, Na2CO3 or aqueous NH3.
3. A process for regenerating exhausted weak base anion exchange resins as defined in claim 1, wherein the regenerant solution comprises a source of Na ions.
4. A process for regenerating exhausted weak base anion exchange resins as defined in any one of the preceding claims, wherein the carbonic acid is formed by saturating water with CO2 at ambient temperature and pressure.
5. A process for regenerating exhausted weak base anion exchange resins as defined in any one of the preceding claims, wherein the resins contain primary, secondary or tertiary amine groups or mixture thereof.
6. A process for regenerating exhausted weak base anion exchange resins as defined in claim 5, wherein the resin has been utilized to refine corn syrups.
7. A process for regenerating exhausted weak base anion exchange resin as defined in claim 5 or 6, wherein said resin disposed in a column is washed by passing water upwardly through the column to remove insoluble debris and to reclassify the resin; regenerant solution is passed downwardly through the column to restore the anion exchange capacity of the resin and regenerant waste products are formed, an amount of water about equal to the volume of the regenerant solution is passed downwardly through the column to remove the regenerant and a portion of the regenerant waste products, and then a solution of carbonic acid is rapidly passed through the column to remove additional amounts of regenerant waste products.
8. A process for regenerating exhausted weak base anion exchange resins as defined in claim 6 or 7, wherein resins which have been regenerated after more than about 200 cycles of use are contacted with a sufficient amount of a solution of carbonic acid to lower the pH of the resins to below about 9.
9. A process for regenerating exhausted weak base anion exchange resins according to claim 1, substantially as hereinbefore described with reference to the Examples.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7935136A GB2060429A (en) | 1979-10-10 | 1979-10-10 | Method of regenerating weak base ion exchange resins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7935136A GB2060429A (en) | 1979-10-10 | 1979-10-10 | Method of regenerating weak base ion exchange resins |
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GB2060429A true GB2060429A (en) | 1981-05-07 |
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GB7935136A Withdrawn GB2060429A (en) | 1979-10-10 | 1979-10-10 | Method of regenerating weak base ion exchange resins |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0106466A2 (en) * | 1982-09-02 | 1984-04-25 | Rohm And Haas Company | Removal of sulfonic resin extractables from aqueous sugar solutions using acrylic anion exchange resin |
EP0308521A1 (en) * | 1987-09-19 | 1989-03-29 | Kernforschungszentrum Karlsruhe Gmbh | Process to separate unwanted organic materials and inorganic anions from sugar solutions |
EP0425322A2 (en) * | 1989-10-23 | 1991-05-02 | Rar - Refinarias De Acucar Reunidas, S.A. | Process for decolourisation and decalcification of sugar solutions |
EP2137101A1 (en) * | 2007-03-19 | 2009-12-30 | Easymining Sweden AB | Phosphorus recovery |
-
1979
- 1979-10-10 GB GB7935136A patent/GB2060429A/en not_active Withdrawn
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0106466A2 (en) * | 1982-09-02 | 1984-04-25 | Rohm And Haas Company | Removal of sulfonic resin extractables from aqueous sugar solutions using acrylic anion exchange resin |
EP0106466A3 (en) * | 1982-09-02 | 1986-02-05 | Rohm And Haas Company | Removal of sulfonic resin extractables from aqueous sugar solutions using acrylic anion exchange resin |
EP0308521A1 (en) * | 1987-09-19 | 1989-03-29 | Kernforschungszentrum Karlsruhe Gmbh | Process to separate unwanted organic materials and inorganic anions from sugar solutions |
EP0425322A2 (en) * | 1989-10-23 | 1991-05-02 | Rar - Refinarias De Acucar Reunidas, S.A. | Process for decolourisation and decalcification of sugar solutions |
EP0425322A3 (en) * | 1989-10-23 | 1991-10-09 | Rar - Refinarias De Acucar Reunidas, S.A. | Process for decolourisation and decalcification of sugar solutions |
EP2137101A1 (en) * | 2007-03-19 | 2009-12-30 | Easymining Sweden AB | Phosphorus recovery |
EP2137101A4 (en) * | 2007-03-19 | 2013-06-12 | Easymining Sweden Ab | Phosphorus recovery |
US8518359B2 (en) | 2007-03-19 | 2013-08-27 | Easymining Sweden Ab | Phosphorus recovery |
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