A-520E Macroporous Strong Base Anion Exchange Resin (For the selective removal of nitrate)

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ION EXCHANGE RESINS A52E Macroporous Strong Base Anion Exchange Resin (For the selective removal of nitrate) Technical Data PRODUCT DESCRIPTION Purolite A52E is a macroporous strong base anion resin which is specially designed for the removal of nitrates from water for potable processes. The macroporous matrix and special ion exchange group functionality imparts ideal nitrate selectivity to Purolite A52E making this resin particularly suitable for nitrate removal even when moderate to high concentrations of sulphate are present. Hence this resin gives superior performance in nitrate removal applications when compared with standard exchange resins. A requirement of the nitrate removal process is to produce potable water meeting the quality standard defined by the European Economic Community in the Directive No. 8/778 of July 198. This directive limits the nitrates to a maximum admissable concentration (M.A.C.) of 5 mg NO 3 /l. The U.S.A. drinking water regulations limit nitrates to 45 mg NO 3 /l. Typical Physical & Chemical Characteristics Polymer Matrix Structure Macroporous StyreneDivinylbenzene Physical Form and Appearance Opaque Cream Spherical Beads Whole Bead Count 95% min. Functional Groups Quaternary Ammonium Ionic Form, as shipped Cl Shipping Weight (approx.) 68 g/l (42.5 lb/ft 3 ) Screen Size Range: U.S. Standard Screen 16 5 mesh, wet Particle Size Range +12 mm <5%, 3 mm <1% Moisture Retention, Cl form 5 56% Reversible Swelling Cl SO 4 /NO 3 negligible Total Exchange Capacity, Cl form, wet, volumetric.9 meq/ml min. dry, weight 2.8 meq/g min. Operating Temperature, Cl Form 1ºC (212ºF) max. ph Range, Stability 14 ph Range, operating 4.5 8.5 Page 1 of 8

Standard Operating Conditions Nitrate Removal Operation Rate Solution Minutes Amount Service 8 32 BV/h Influent water per design per design 1 4 gpm/ft 3 to be treated Backwash Refer to Fig. 2 Influent water 5 2 1.5 4 BV 1 2ºC 1 25 gal/ft 3 (5 68ºF) Regeneration 2 5 BV/h 3 1% NaCl 2 6 9 25 g/l.25.6 gpm/ft 3 7.8 15.6 lb/ft 3 Rinse, (slow) 2 5 BV/h Influent water 2 6 2 5 BV.25.6 gpm/ft 3 15 4 gal/ft 3 Rinse, (fast) 8 32 BV/h Influent water 1 4 gpm/ft 3 Backwash Expansion 5% to 75% Design Rising Space 1% "Gallons" refer to U.S. Gallon = 3.785 litres REGENEN Sodium chloride is generally preferred for regeneration for reasons of cost and efficiency. When available sea water can be used quite effectively. The use of softened water for make up of regenerant and rinse is often recommended to avoid the precipitation of calcium carbonate in and around the Purolite A52E (or any other resin used in this application). Although the precipitation is not particularly detrimental in the short term, the long term effects may include increased resin attrition and leakage of nitrates. PRECONDITIONING PROCEDURE Purolite A52E is processed to insure that it meets the requirements for use in the treatment of potable water. On installation it is recommended that the resin be regenerated with two bed volumes of 6% NaCl followed by a rinse of four bed volumes of potable water, prior to use. HYDRAULIC CHARACTERISTICS The pressure drop or headloss across a properly classified bed of ion exchange resin depends on the particle size distribution, bed depth, and void volume of the exchange material as well as on the viscosity (and hence on the temperature) of the influent solution. Factors affecting any of these parameters, for example the presence of particulate matter filtered out by the bed, abnormal compressability of the resin, or the incomplete classification of the bed will have an adverse effect and result in an increased headloss. Depending on the quality of the influent water, the application and the design of the plant, service flow rates may vary from 1 4 bed volumes/hour (1 5 gpm/ft 3 ). Typical pressure drop data is given in Fig. 1. Page 2 of 8

Fig. 1 PRESSURE DROP CHARACTERISTICS Fig. 2 BACKWASH EXPANSION PRESSURE DROP, kg/cm 2 /m of bed depth 1.1.8.6.4.2 SERVICE FLOW RATE, U.S. gpm/ft 2 4 8 12 16 5 C (41 F) 1 C (5 F) 2 C (68 F) 3 C (85 F) 1 2 3 4 SERVICE FLOW RATE, m/h 4 3 2 1 PRESSURE DROP, psi/ft of bed depth BED EXPANSION, Percent 1 8 6 4 2 FLOW RATE, U.S. gpm/ft 2.8 1.6 2.4 3.2 4. 5 C (41 F) 1 C (5 F) 2 C (68 F) 35 C (95 F) 5 C (12 F) 2 4 6 8 1 BACKWASH FLOW RATE, m/h During upflow backwash, the resin bed should be expanded in volume by between 5 and 7%. This operation will free it from any particulate matter, clear the bed of bubbles and voids, and reclassify the resin particles, ensuring minimum resistance to flow. Bed expansion increases with flow rate and decreases with temperature, as shown in Fig. 2. Care should be taken to avoid over expansion of the bed. Conversion of Units 1 m/h (cubic meters per square meter per hour) =.341 gpm/ft 2 =.49 U.S. gpm/ft 2 1 kg/cm 2 /m (kilograms per square cm = 4.33 psi/ft per meter of bed) = 1.3 atmos/m = 1 ft H 2 O/ft The high selectivity of Purolite A52E for nitrate over sulphate ensures that any necessary reduction in nitrate levels can be achieved even in the presence of high influent sulphate concentration. Hence it so offers the advantage over standard strong base resins that its exchange capacity for nitrates is less affected by a high influent OPERATING PERFORMANCE concentration of sulphate. For this reason, although Purolite A52E has a lower total exchange capacity than standard strong base anion resin, its use can produce advantageously higher throughputs for the following reasons. Page 3 of 8

Both standard gel type or macroporous strong base resins are quite capable of effective nitrate removal where sulphate to total anion ratios are low. However, on account of the high selectivity for sulphate in dilute solutions which follows the order, HCO 3 < Cl < NO 3 < SO 4 = selective displacement of nitrate by sulphate results in the effective nitrate removal capacity being reduced by sulphate loading. Apart from the obvious disadvantage of the reduction of treated water obtained on cycling, the exchange of both nitrate and sulphate by chloride will result in a less palatable and sometimes less acceptable water than the influent supply, in that the treated water may be more corrosive and the limits for chloride concentration may be exceeded. PUROLITE A52E, COCURRENT REGENEN BASE OPERATING CAPACITY, NO 3 eq/l Fig. 3 OPERATING CAPACITY VS. 1. 2.8 15.6 25 g NaCl/l (15 lb/ft 3 ) 1.4 125 g NaCl/l (8 lb/ft 3 ) 5.2.2.4.6.8 1. OPERATING CAPACITY, NO 3 Kgr/ft 3 NITRATE LEAKAGE, % OF INFLUENT Fig. 4 NITRATE LEAKAGE VS. 5 4 3 125 g NaCl/l (8 lb/ft 3 ) 2 25 g NaCl/l (15 lb/ft 3 ) 1.2.4.6.8 1. Fig. 3 and Fig. 4 give the operating capacity and nitrate leakage respectively which may be obtained using cocurrent regeneration at the given regeneration levels. Values obtained from Fig. 3 are expressed in terms of nitrate throughput, corrected for nitrate leakage, and hence may not be used directly to determine the throughput of water. All ion concentration values are either on a ppm or a meq/l basis for ratio determination. or cyclic output (U.S. gal) = Calculation for throughtput of treated water cyclic output (liters) = Vx OC x 1 3 L l n V f x OC k x 1 3.58 (L p l np ) where V = resin volume (liters) OC = operating capacity (eq/l) L = nitrate load (meq/l) l n = nitrate leakage (meq/l) where V f = resin volume (ft 3 ) OC k = operating capacity (kgr/ft 3 ) L p = nitrate load (ppm as CaCO 3 ) np = nitrate leakage (ppm as CaCO 3 ) Page 4 of 8

Similarly Fig. 5 and Fig. 6 give the values for countercurrent regeneration. It should be noted that in this case the nitrate leakage is lower for a given regeneration level. Hence the possibility to blend treated with untreated water on a 5% basis is a useful option which can make countercurrent regeneration attractive. On the other hand the choice of cocurrent regeneration can result in the production of higher volumes of treated water of satisfactory quality for direct use. The higher leakage (l n, l np, in the equations above) so reduces the load on the ion exchange bed that for a given operating capacity greater throughputs per cycle are obtained. This latter effect can influence the throughput more than differences in basic operating capacity. It therefore follows that both capacity and leakage for alternative modes of regeneration should be evaluated before recommending specific design conditions. PUROLITE A52E, COCURRENT REGENEN Fig. 5 OPERATING CAPACITY Fig. 6 NITRATE LEAKAGE BASE OPERATING CAPACITY, NO 3 eq/l VS. 1. 2.8 15.6 18 g NaCl/l (11.5 lb/ft 3 ) 1.4 125 g NaCl/l (8 lb/ft 3 ) 5.2.2.4.6.8 1. OPERATING CAPACITY, NO 3 Kgr/ft 3 NITRATE LEAKAGE, % OF INFLUENT 5 4 3 2 1 VS. 125 g NaCl/l (8 lb/ft 3 ) 18 g NaCl/l (11.5 lb/ft 3 ).2.4.6.8 1. Presupposing that the objective of the nitrate removal treatment is to obtain potable water of a quality which meets the World Health Organization (WHO) limit, where the nitrate/(nitrate + sulphate) ratio is higher than.6, a nitrate selective resin is not necessary. A standard strong base resin can give higher throughputs as a result of its higher total capacity. It will be seen that up to the ratio of.6 the curves in Figs. 3 6 are continuous to show where Purolite A52E is the recommended resin. The discontinuous curves are given so that comparisons may be made with alternative resins. Where lower leakages than the WHO limit are required, for example in the processing of certain foods, Purolite A52E will often give a superior performance to the standard resins even where nitrate/(nitrate + sulphate) ratios are higher than.6. One particular advantage here is that there is no slug of highly concentrated nitrate at breakthrough as is found with standard resins, hence the possibility to excessively contaminate the food product by overrunning the bed is avoided. Page 5 of 8

How to use Figs. 3 through 6. EXAMPLE OF CALCULATION It is assumed that it is required to treat a well water of the following analysis to produce a nitrate concentration of less than 5 mg/l. WATER ANALYSIS Anions ppm meq/l ppm as CaCO 3 Cations ppm meq/l Nitrate 93 1.5(L) 76(L p ) Calcium 9 4.5 Sulphate 98 2. 1 Magnesium 18 1.5 Chloride 71 2. 1 Sodium 3 1.3 [HCO 3 * 122 2. 1] Potassium 8.2 Total Anions 7.5 Total Cations 7.5 Equivalent Mineral Acidity (EMA) 5.5 Nitrate NO 3 76 Nitrate + Sulphate = = NO 3 + SO = 4 76 + 1 =.43 *Note: Unless concentration of bicarbonates is well above average it does not affect the performance to a significant extent. A regeneration level of 125 g NaCl/l has first been chosen, using cocurrent regeneration. To calculate the cyclic throughput from the equations given above; From Fig. 3, Base Capacity at.43 for NO 3 NO 3 + SO 4 = =.36 eq/l.43 NO From Fig. 4, Leakage at 3 = 23% = NO 3 + SO 4 Hence for each litre of resin, throughput = (.36/1.15) x 1 3 liters = 313 liters And for each cubic foot of resin, = [7.9/(.58 x 57.7)] x 1 3 = 236 U.S. gal. Depending upon the throughput requirement the resin volume is chosen so as to operate within the flow rate stipulations given in the standard operating conditions above. A design factor of.9 is also recommended as is customary. Hence throughput/liter of resin for design purposes will be 313 x.9 = 281.7 liters (2124 U.S. gal/ft 3 ). In this example the leakage is 17.3 ppm as CaCO 3 (21.4 ppm as NO 3 ), hence the useful option to blend treated water with raw water on a 5% basis could be applied. It would be of no advantage to move to countercurrent regeneration in this case. Reference to Fig. 5 will show that the basic capacity curve is very similar. However the throughput will be lower, because the reduced leakage increases the ion exchange load for a given throughput. When on the other hand nitrate concentrations or ratios are higher, it may be advantageous to operate countercurrent rather than increase the regeneration level while operating cocurrent. In this way a suitable blend may be obtained with lower regenerant costs (and costs of disposal). Page 6 of 8

NOTES Page 7 of 8

ION EXCHANGE RESINS WORLDWIDE OFFICES USA: www.puroliteusa.com International: www.purolite.com U.S.A. The Purolite Company 15 Monument Road Bala Cynwyd, PA 194 Phone: (1) 6166899 Toll Free: 834315 Telefax: (1) 616688139 Email: sales@puroliteusa.com TEXAS The Purolite Company 17 West Loop South Suite 74 Houston, TX 7727 Toll Free: 85626488 Telefax: (1) 713627789 CANADA The Purolite Company 625 Wabanaki Drive Unit #2 Kitchener, Ontario N2C 2G3 Toll Free: 8461 15 or (1) 5198966674 Telefax: (1) 5198966679 UNITED KINGDOM Purolite International Limited Kershaw House Great West Road Junction with Lampton Road Hounslow, TW5 OBU Sales Phone: (44) 181 574454 Telefax: (44) 1815727726 European Marketing Phone: (44) 1815771222 Telefax (44) 1815771136 GERMANY Purolite Deutschland GmbH Harkort Strasse 25 488 Ratingen Phone: (49) 2124633 Telefax: (49) 212443663 FRANCE Purolite International SARL 34 Avenue Matignon 758 Paris Phone: (33) 142564563 Telex: 648856 Telefax: (33) 145633826 SPAIN Purolite Iberica S.A. Parc Tecnologic del Valles Centre Empreses Noves Tecnologies 829 Cerdanyola del Valles (Barcelona) Phone: (34) 3582266 Telefax: (34) 3582268 EGYPT Purolite International Middle East Cairo Liaison Office 12 Obour Gardens Fifth Floor, App. No. 55 Salah Salem Street Nasr City, Cairo Phone: (2) 2421477 Telefax: (2) 2421478 ITALY Purolite International S.r.l. Viale Coni Zugna 29 2144 Milan Phone: (39) 24818145 Telefax: (39) 24812359 ROMANIA Purolite Romania International Business Center Modern Bdul Carol I No. 3436 5th Floor Bucharest, Sector 2 Phone: (4) 125553/528 Telefax: (4) 1255999 POLAND Head Office Radus Spolka z o.o. ul Przebendowskich 33 81543 Gdynia Phone/Fax (48) 586248118 GLIWICE Radus Spolka z o.o. ul Górnych Walów 25 441 Gliwice Phone: (48) 32315931 Telefax: (48) 32315931 SLASK Radus Spolka z o.o. ul 3 Maja 3/33 326 Oswiecim Phone: (48) 3342563 Telefax: (48) 3342563 CZECH & SLOVAK REPUBLICS Purolite International Nad Mazankou 17 182 Prague 8 Phone: (42) 2688186 Telefax: (42) 2688186 RUSSIA Head Office Purolite International 1th Floor 36 Lyusinovskaya Street Moscow Phone: (7) 95564812 Telefax: (7) 955648121 ST. PETERSBURG Purolite International Limited 12 Building A Tambovskaya St. St. Petersburg 1927 Russian Federation Phone: (7) 812327853 Telefax: (7) 812327979 KAZAKHSTAN Purolite RH Limited Office 25 24 Dostyk AV. Almaty 4851 Phone: (7) 3272641234 Telefax: (7) 3272641234 SINGAPORE Purolite International (Singapore) PTE Limited 324 The Concourse 3 Beach Road, 199555 Phone: (65) 297889 2971453 Telefax: (65) 2971986 CHINA Head office Purolite (China) Company, Ltd. Chengguan Town Deqing County Zhejiang Province 3132 Phone: (86) 572842298 Telefax: (86) 5728423954 TAIWAN Purolite International 16F2, No. 191 Fuhsing N. Road,Taipei Phone: (886) 2546778 Telefax: (886) 2546769 MEXICO Purolite International, S.A. De C.V. World Trade Center Montecito 38, Piso 33,Oficina19 Mexico D.F. 381 Phone: (52) 548894 Telefax: (52) 548896 UKRAINE Purolite International Limited 2 Korolenko Street. Dnepropetrovsk 327 Phone: (38) 5623265 5623266 Telefax: (38) 5623267 KOREA Purolite International (Korea) LLC Dae Yeon Bldg., Suite 43 9433 Daechidong Kangnamgu, Seoul Phone: (82) 23453762/763 Telefax: (82) 23453764 All suggestions and recommendations given above concerning the use of Purolite products are based on tests and data believed to be reliable. However, as Purolite cannot control the use of its products by others, no guarantee is either expressed or implied by any such suggestion or recommendation by Purolite nor is any information contained in this leaflet to be construed as a recommendation to infringe any patent currently valid. A52E/1299/SOP