CHEMICAL PRECIPITATION: WATER SOFTENING



Similar documents
ENE 806, Project Report 3 CHEMICAL PRECIPITATION: WATER SOFTENING. Grégoire Seyrig Wenqian Shan

Water Softening for Hardness Removal. Hardness in Water. Methods of Removing Hardness 5/1/15. WTRG18 Water Softening and Hardness

Hardness - Multivalent metal ions which will form precipitates with soaps. e.g. Ca 2+ + (soap) Ca(soap) 2 (s)

5.0 EXPERIMENT ON DETERMINATION OF TOTAL HARDNESS

Hardness ions also interfere with many chemical processes such as chemical compounding and aqueous cleaners.

DRINKING WATER - LAB EXPERIMENTS. Coagulation and flocculation LAB EXPERIMENTS. Jartest

Additional Lecture: TITRATION BASICS

Determination of the Amount of Acid Neutralized by an Antacid Tablet Using Back Titration

Hydrochemistry. Deacidification. Junianti Roslinda Sihombing. Practical Date : Monday, Report Delivery : Monday,

Estimation of Hardness of Water by EDTA Method

Complexometric Titration Analysis of Ca 2+ and Mg 2+ in seawater

Complexometric Titrations

Experiment 16-Acids, Bases and ph

HEXAVALENT CHROMIUM REMOVAL FROM INDUSTRIAL WATSEWATER BY CHEMICAL PRECIPITATION METHOD

Factors Affecting Precipitation of Calcium Carbonate

CHEMICAL DETERMINATION OF EVERYDAY HOUSEHOLD CHEMICALS

Organic Chemistry Lab Experiment 4 Preparation and Properties of Soap

Calcium Analysis by EDTA Titration

ph: Measurement and Uses

Tutorial 4 SOLUTION STOICHIOMETRY. Solution stoichiometry calculations involve chemical reactions taking place in solution.

Syllabus OC18 Use litmus or a universal indicator to test a variety of solutions, and classify these as acidic, basic or neutral

To determine the equivalence points of two titrations from plots of ph versus ml of titrant added.

ph Alkalinity of Water

The role of CO 2 in pool water

1. Read P , P & P ; P. 375 # 1-11 & P. 389 # 1,7,9,12,15; P. 436 #1, 7, 8, 11

Using Magnesium Hydroxide

Properties of Acids and Bases

Hardness Comparisons

WATER CHEMISTRY AND POOL WATER BALANCE

CHM1 Review for Exam 12

ION EXCHANGE FOR DUMMIES. An introduction

APPENDIX B: EXERCISES

Phosphate Recovery from Municipal Wastewater through Crystallization of Calcium Phosphate

Separation by Solvent Extraction

Non-polar hydrocarbon chain

4.0 EXPERIMENT ON DETERMINATION OF CHLORIDES

Chem101: General Chemistry Lecture 9 Acids and Bases

Chapter 17. The best buffer choice for ph 7 is NaH 2 PO 4 /Na 2 HPO 4. 19)

EXPERIMENT 12 A SOLUBILITY PRODUCT CONSTANT

Experiment 8 - Double Displacement Reactions

ph Measurements of Common Substances

QUESTION (2012:3) (a) (i) Complete the table below showing the conjugate acids and bases. CO 3 H 2 O OH HCN CN -

Swimming Pool and Spa Water Chemical Adjustments

EXPERIMENT 10 Chemistry 110. Solutions Part 2 ACIDS, BASES, AND ELECTROLYTES

Standard Methods for the Examination of Water and Wastewater

Determining the Identity of an Unknown Weak Acid

Determination of calcium by Standardized EDTA Solution

Potentiometric determination. Application Bulletin 125/3 e. Branch General analytical laboratories; water analysis; beverages

Balancing Chemical Equations

Chemistry at Work. How Chemistry is used in the Water Service

Acid-Base Titrations. Setup for a Typical Titration. Titration 1

Experiment 3 Limiting Reactants

NUTRIENT REMOVAL FROM SECONDARY EFFLUENT BY ALUM FLOCCULATION AND LIME PRECIPITATION*

Total Suspended Solids Total Dissolved Solids Hardness

Determination of Ascorbic Acid in Vitamin C Tablets by Redox and Acid/Base Titrations

Ascorbic Acid Titration of Vitamin C Tablets This lab will be completed individually! Make sure you come prepared!

4.1 Stoichiometry. 3 Basic Steps. 4. Stoichiometry. Stoichiometry. Butane Lighter 2C 4 H O 2 10H 2 O + 8CO 2

ATOMS. Multiple Choice Questions

Return to Lab Menu. Acids and Bases in Your House

Ion Exchange Design Hand calculation. Brian Windsor (Purolite International Ltd)

Molarity of Ions in Solution

Precipitation Titration: Determination of Chloride by the Mohr Method by Dr. Deniz Korkmaz

EXPERIMENT 20: Determination of ph of Common Substances

Equilibrium Constants The following equilibrium constants will be useful for some of the problems.

Titrations. Acid-Base Indicators and Titration Curves. Shapes of Titration Curves. A titration curve is a graphical history of a titration

Copyright 2009 by Pearson Education, Inc. Upper Saddle River, New Jersey All rights reserved.

Corrosivity of Water Supplies

Chemistry Unit Test Review

Chemistry 52. Reacts with active metals to produce hydrogen gas. Have a slippery, soapy feeling. React with carbonates to produce CO 2

Solubility of Salts - Ksp. Ksp Solubility

Preparation of frequently used solutions

Chemical Reactions in Water Ron Robertson

Feasibility study of crystallization process for water softening in a pellet reactor

Removal of Sulfate from Waste Water by Activated Carbon. Mohammed Sadeq Salman Computer Centre/ University of Baghdad

Topic 8 Acids and bases 6 hours

9. Analysis of an Acid-Base Titration Curve: The Gran Plot

D. LAB 4. ACID-BASE TITRATIONS, ALKALINITY, AND BUFFER CAPACITY

OXIDATION-REDUCTION TITRATIONS-Permanganometry

Stoichiometry Limiting Reagent Laboratory. Chemistry 118 Laboratory University of Massachusetts, Boston

ION EXCHANGE RESINS INTRODUCTION

Name period Unit 9: acid/base equilibrium

Chemistry 132 NT. Solubility Equilibria. The most difficult thing to understand is the income tax. Solubility and Complex-ion Equilibria

Chapter 16: Tests for ions and gases

DETERMINATION OF PHOSPHORIC ACID CONTENT IN SOFT DRINKS

Lab 25. Acid-Base Titration and Neutralization Reactions: What Is the Concentration of Acetic Acid in Each Sample of Vinegar?

Iron and Manganese BACTERIA AND IRON AND MANGANESE

Practical Lesson No 4 TITRATIONS

Chemistry 106 Fall 2007 Exam 3 1. Which one of the following salts will form a neutral solution on dissolving in water?

2. DECOMPOSITION REACTION ( A couple have a heated argument and break up )

Formulas, Equations and Moles

Determination of the amount of sodium carbonate and sodium hydroxide in a mixture by titration.

An acid is a substance that produces H + (H 3 O + ) Ions in aqueous solution. A base is a substance that produces OH - ions in aqueous solution.

GROUP II ELEMENTS. Beryllium to Barium

Q.1 Classify the following according to Lewis theory and Brønsted-Lowry theory.

Experiment 1 Chemical Reactions and Net Ionic Equations


Acid/base Definitions. Acid/Base Definitions. Acid / Base Chemistry. Acid/Base Definitions. Identifying Acids and Bases

Acid Base Titrations

6 Reactions in Aqueous Solutions

ACIDS, BASES AND SALTS

Transcription:

CHEMICAL PRECIPITATION: WATER SOFTENING Submitted to: Dr. Hashsham Research Complex Engineering Department of Civil and Environmental Engineering Michigan State University East Lansing, MI 4884 Authors Dipa Dey Amanda Herzog Vidya Srinivasan ENE 806 May, 007 i

Acknowledgement We are grateful to Dr. Syed A. Hashsham for his invaluable guidance and support during the course of this project. We would also like to thank Mr. Joseph Nguyen for his assistance and cooperation. May, 007 Dipa Dey Amanda Herzog Vidya Srinivasan ii

CONTENTS Caption Title page Acknowledgement Contents List of Figures and Tables Page No. i ii iii iv Abstract 1 Introduction Chemistry of Hardness Removal Process 3 Objective 5 Methods and Materials 5 Results and discussion 6 Conclusions 8 References 9 Appendix -1 10 RAW DATA 10 Appendix- 11 Sample Calculation to Determine the Lime Dosage 11 Appendix-3 13 Water Softening and alkalinity Protocol 13 Appendix-4 16 Pictures 16 iii

LIST OF FIGURES AND TABLES Caption Figure 1: Variation of hardness, alkalinity and ph for varying lime dosages (run1) Figure : Variation of hardness, alkalinity and ph for varying lime dosages (run) Page No. 6 7 Figure3: Comparison of replicate runs 8 Setup and Samples with lime dosages 16 Floc. Formation 16 Filtration Setup 16 Samples After Filtration 16 Before Titration 16 Mid-Titration 16 End of Titration 16 Table 1: : Run1 for varying lime dosages 10 Table: Run for varying lime dosages 10 iv

ABSTRACT Hard water can cause many problems including scaling and excessive soap consumption. In the United States, hard water is mostly found in the mid western and western states. It ranges between 10-50 mg/l as CaCO 3 or beyond 50 mg/l as CaCO 3 for very hard waters. The acceptable water hardness range is between 60-10 mg/l as CaCO 3. A water softening experiment was conducted in replicate to observe the changes in parameters such as total hardness, calcium hardness, magnesium hardness, alkalinity and ph with varying dosages of lime. A lime dosage range of 30-180% of the stoichiometric amount was chosen for the experiments. The sample used was groundwater from an East Lansing well which had a total hardness of 33 mg/l as CaCO 3. Results indicated that an increase in lime dosage upto 90% caused a decrease in total hardness, alkalinity, magnesium hardness and calcium hardness concentrations. However, for a lime dosage beyond 10%, the total hardness, alkalinity, and calcium hardness concentrations increased while magnesium hardness concentration decreased to lower values. The ph continually increased for a lime dosage between 30% and 180%. 1

INTRODUCTION Hard water is the most common water quality problem reported by consumers throughout the United States. More than 60 percent of the Earth s water is ground water and hard water is found in more than 85% of the country. The water travels through rocks and soil picking up minerals including calcium and magnesium, ions which produce hard water. (Water Review, Consumer report, 1990). Hard water interferes with almost every cleaning task from laundering and dishwashing to bathing and personal grooming (IANR, Water Quality 1996). Clothes laundered in hard water may look dingy and feel harsh and scratchy. Dealing with hard water problems in the home can be a nuisance. In addition, hard water affects the amount of soap and detergent necessary for cleaning. Soap used in hard water combines with the minerals to form a sticky soap curd. Some synthetic detergents are less effective in hard water because the active ingredient is partially inactivated by hardness, even though it stays dissolved. Bathing with soap in hard water leaves a film of sticky soap curd on the skin. The film may prevent removal of dirt and bacteria. Soap curd interferes with the return of skin to its normal, slightly acid condition, and may lead to irritation. Soap curd on hair may make it dull, lifeless and difficult to manage. Hard water also contributes to inefficient and costly operation of water treatment equipment. Heated hard water forms a scale of calcium and magnesium minerals that can contribute to the inefficient operation or failure of water treatment equipment. Pipes can become clogged with scale which reduces water flow and ultimately results in pipe replacement. Hard water is not a health hazard. In fact, the National Research Council (National Academy of Sciences) states that drinking hard water generally contributes to the total calcium and magnesium needs in humans. Water utilities struggling with source water that contains high amounts of calcium and/or magnesium often turn to lime softening to remove hardness. Raising treatment ph above 9.6 converts soluble calcium bicarbonate hardness to insoluble calcium carbonate. An increase in ph beyond 10.6 converts soluble magnesium bicarbonate to insoluble magnesium hydroxide. Aggressive magnesium removal often requires a treatment ph of 11 or higher, a process known as excess lime softening (Jones, C; et.al. 005).

Chemistry of Hardness Removal Process During precipitation softening, calcium is removed form water in the form of CaCO 3 precipitate and magnesium is removed as Mg(OH) precipitate (Frederick W. Pontius). The carbonic acid concentration present and the ph play an important role in the precipitation of these two solids. Carbonate hardness can be removed by the addition of hydroxide ions and raising the ph by which the bicarbonate ions are converted to carbonate form having a ph above 10. Due to the increase in carbonate concentration, precipitates of calcium carbonate is formed. The remaining calcium, i.e. non carbonate hardness, cannot be removed by simple adjustment of ph. Therefore, soda ash (sodium carbonate) must be externally added to precipitate this remaining calcium. Magnesium is removed due to the precipitation of magnesium hydroxide. In the lime soda ash process, lime is added to raise the ph while sodium carbonate is added to provide a source of carbonate ion. H CO3 + Ca( OH ) CaCO3 + H O (1) Eq.(1) is the neutralization reaction between CO carbonic acid and lime. This equation does not result any net change in water hardness. This also suggest that for each mg/l of carbonic acid expressed as CaCO 3 present, 1mg/L of lime expressed as CaCO 3 will be required for neutralization by knowing the stoichiometric ratios. + Ca + HCO3 + Ca( OH ) CaCO3 ( s) + H O () Eq.() presents the removal of calcium carbonate hardness. It also shows that for each molecule of calcium bicarbonate present, two carbonate ions can be formed by increasing the ph. This also suggest that for each mg/l of calcium bicarbonate present, 1mg/L of lime expressed as CaCO 3 will be required for its removal by knowing the stoichiometric ratios between them. Ca + SO4 + Cl + NaCO 3 CaCO 3 + Na + SO4 + Cl (3) Eq.(3) reflects the removal of calcium noncarbonated hardness. The stoichiometric coefficient suggest that for each mg/l of calcium noncarbonate hardness present, 1mg/L of sodium carbonate expressed as CaCO 3 will be required for its removal. 3

+ Mg + HCO3 + Ca( OH ) CaCO3 + Mg( OH ) ( s) + H O (4) Eq. (4) is similar to eq.(). If the magnesium bicarbonate and lime are expressed as CaCO 3, then the stoichiometric ratios suggest that for each mg/l of magnesium bicarbonate hardness present, mg/l of lime expressed as CaCO 3 will be needed for its removal. Mg + SO4 + Cl + Ca( OH ) 3 Mg( OH ) ( s) + Ca + SO4 + Cl (5) Eq. (5) represents the removal of magnesium noncarbonate hardness. If the magnesium noncarbonate hardness and lime are expressed as CaCO 3, stoichiometric ratios suggest that for each mg/l of magnesium noncarbonate hardness present, 1 mg/l of lime expressed as CaCO 3 will be needed for its removal. Here no net change in the hardness level resulted as for each magnesium ion removed calcium ion is added. Thus to complete the hardness removal process, sodium carbonate required to be added to precipitate the calcium as presented in the equation below. Ca + SO4 + Cl + NaCO 3 CaCO 3 ( s) + Na + SO4 + Cl (6) 4

OBJECTIVE The objective of the water softening experiment was to determine the effects of varying lime dosages on parameters such as total hardness, calcium hardness, magnesium hardness, alkalinity and ph. METHODS and MATERIALS Very hard ground water was obtained from a well located in East Lansing provided by Joseph Nguyen. Initial sample characteristics such as ph, alkalinity, and total hardness are provided in Appendix. A lime, Ca(OH), stock solution of 10mg/mL was prepared for dosing the sample with 30, 60, 90, 10, 150 and 180 percent of the stoichiometric amount of lime. The jar test was executed with the conventional apparatus with six -liter beakers (Appendix-) mixing the groundwater with the various amounts of lime for 0 min at 30 rpm. The samples were then filtered through 0.45µm filter and then titrated for total hardness, calcium hardness, and alkalinity. In addition ph and magnesium hardness were noted down. This experiment was done in replicate to compare results and determine the degree of experimental error. Detailed protocols for this experiment, including titrations and calculations, are available in the appendix. 5

RESULTS and DISSCUSSION Run 1: Water Softening Replicate 1: Variation of Hardness, Alkalinity and ph for varying Lime dosages 350 13 Concentartion, mg/l as CaCO 3 300 50 00 150 100 50 ph Total Hardness Alkalinity Magnesium Hardness Calcium Hardness 1 11 10 9 8 ph 0 7 0 0 40 60 80 100 10 140 160 180 Lime dose, % Stoichiometric Amount Figure 1: Variation of Hardness, Alkalinity and ph for varying Lime dosages (Run1) Replicate runs for the water softening experiment evaluated parameters such as alkalinity, hardness and ph in response to varying lime dosages from 30% to 180% of the stoichiometric amount. In Run 1, the total hardness reached a minimum value of approximately 160 mg/l as CaCO 3 for a lime dosage of 90% (fig.1). The calcium hardness first decreased in concentration to a minimum of 35mg/L as CaCO 3 for a lime dosage of 90% and then after that continued to increase in concentration with an increase of lime dosage. This increase in calcium hardness was observed due to the addition of excess lime and the absence of alkalinity caused by carbonates. The plateau between 60% and 90% of lime is due to the presence of extra alkalinity. Any excess lime added in this region converts bicarbonates to carbonates and those carbonates combine with the free calcium ions to form precipitates. Magnesium hardness concentration decreased with the increasing dosage of lime. Alkalinity decreased to a minimum at approximately 90% of lime and increased thereafter. This is due to the addition of lime and the precipitation of species, which consumes alkalinity that causes the initial decrease. At lime dosages higher than 10%, alkalinity increases due to an addition of excess lime. For every addition of lime, free 6

OH - ions are released, therefore an increase in OH - ions is responsible for an increase in ph. Run : Water Softening Replicate : Variation of Hardness, Alkalinity and ph for various Lime dosages 400 13 Concentration, mg/l as CaCO 3 300 00 100 ph Total Hardness Alkalinity Magnesium Hardness Calcium Hardness 1 11 10 9 8 ph 0 7 0 0 40 60 80 100 10 140 160 180 Lime dose, % Stoichiometric Amount Figure : Variation of Hardness, Alkalinity and ph for varying Lime dosages (Run) In Run, the total hardness reaches a minimum value of approximately 160 mg/l as CaCO 3 for a lime dosage of 10% (fig.). The calcium hardness concentration first decreases to a minimum of 35 mg/l as CaCO 3 for a lime dosage of 60% and then starts to increase above a lime dosage of 90%. This result was due to the addition of excess lime and the absence of alkalinity caused by carbonates. The plateau between 60% and 90% of lime was because of the presence of extra alkalinity. Any excess lime added in this region converts bicarbonates to carbonates and combine with the free calcium ions to form precipitates. Magnesium hardness decreases with an increase in lime dosage and reaches a concentration of 30mg/L as CaCO 3, for a lime dosage of 180%. This concentration indicates an approximate solubility limit of magnesium ions. In addition alkalinity decreased to a minimum around 90% of lime but increases thereafter. The trends observed in Run1 and Run were in good correlation with each other. 7

400 350 Comparative Study of Replicate Runs : Water Softening y = 1.0797x R = 0.8977 300 50 Run 00 150 100 Magnesium Hardness, mg/l as CaCO 3 Alkalinity, mg/l as CaCO 3 Total Hardness, mg/l as CaCO 3 50 Calcium Hardness, mg/l as CaCO 3 Linear Trendline 0 0 100 00 300 400 Run 1 Figure 3: Comparison of Replicate Runs This plot is a comparative study of the data obtained from run 1 and run. The data from each run have an R correlation of 0.90 for the parameters of this study. Hence, the experiment is reproducible and the trends observed for each parameter in response to varying lime dosages are in agreement with the expected trends. CONCLUSIONS This experiment yielded the following conclusions: Calcium hardness concentrations decreased with an increase in lime dosage but concentrations increased at dosages higher than 90%. Magnesium hardness decrease with an increase in lime dosage, especially when calcium hardness was increased (dosage higher than 90%) Alkalinity decreased to a minimum value of approximately 135 mg/l as CaCO 3 at a lime dosage of 90% and increased thereafter due to the addition of excess lime. ph increased with an increase in lime dosage due to the generation of free OH - ions. The replicate runs conducted were in correlation with each other, thereby demonstrating reproducibility. 8

REFERENCES 1. IANR, Water Resources management, Water Quality, 1996.. Jones, C; Corriagn,T; Graham, D.B; McMullen, L.D, 005. Reduced Lime Feed: Effects on Operational Costs and water Quality. 3. Syed Hashsham. Chemical Precipitation: Water Softening. Lab Report, 1993 4. Water Quality and Treatment: A Handbook of Community Water Supplies. American Water Works Association. Fourth edition, 1990 5. Water Review, Consumer Report, Vol.5,No.1. 1990. A publication of the water quality research council 6. Water Treatment Principles and Design. MWH. Second edition, 005 9

APPENDIX 1 RAW DATA Table1: Run 1 Lime dose (%) Ca hardness (Titrant Volume) Total hardness (Titrant Volume) Alkalinity (Titrant volume) Ca Hardness Total Hardness Alkalinity Mg Hardness 0 5 8.3 31.1 00 33 311 13 7.7 30 3.1 6.7 4 14 68 40 144 8.4 60 1.1 4. 15 44 168 150 14 9.3 90 0.9 3.7 13.5 36 148 135 11 11 10 1.7 4.1 13 68 164 130 96 11 150 3.7 4.6 15 148 184 150 36 1 180 5.8 6.3.5 3 5 5 0 1 ph Table: Run Lime dose (%) Ca hardness (Titrant Volume) Total hardness (Titrant Volume) Alkalinity (Titrant volume) Ca Hardness Total Hardness Alkalinity Mg Hardness 0 5 8.3 31.1 00 33 311 13 7.7 30.9 6.8 3.6 116 7 36 156 8.4 60 0.9 4.4 14.4 36 176 144 140 10 90 0.9 4.4 13.5 36 176 135 140 10 10 1.6 4.1 13.7 64 164 137 100 11 150 3.7 5. 14.9 148 08 149 60 1 180 8.5 9. 1.4 340 368 14 8 1 ph 10

APPENDIX Sample Calculation to Determine the Lime Dosage Sample: Ground water ph= 7.7 Ca + = 00 mg/l Mg + = 13 mg/l Temperature= 0 0 C Alkalinity= 311 mg/l Total Hardness= 33 mg/l Carbonate Hardness= Alkalinity = 311 mg/l CaCO 3 Non Carbonate hardness = Total hardness- Alkalinity = 1 mg/l CaCO 3 From the above values we know that it is an excess lime soda ash process 0 00 33 Ca + Mg + Other Cations Other Anions HCO 3 0 311 Step1: Assume ph=7, so all alkalinity is in the bicarbonate form 61 1 1 a) [HCO 3 ]=311 ( ) ( ) ( ) = 6. x 10-3 mol/l 50 1000 61 14.8435-3404.71 /93 0.03786 (93) b) K 1 =10 K 1 = 4.6 x 10-7 6.498-909.39/93-0.0379(93) K = 10 K = 3.97 x 10-11 1 c) α 1 = 7 7 1 10 / K + 1+ K /1 10 = 1 10 = 0.81 7 1 / 4.6 10 7 1 + 1+ 3.97 10 11 /1 10 7 11

d) C T = 6. 10 3 3 0.81 = 7.679 10 mol/l e) [HCO 3 * ]= 7.679 x 10-3 -6. x 10-3 = 1.477 x 10-3 mol/l [HCO 3 * ]= 1.477 x 10-3 mol/l x 6 g/mol = 0.0915 g/l= 91.5 mg/l [HCO 3 * ]= 147.7 mg/l CaCO 3 147.7 0 00 33 Ca + Mg + Other Cations H CO 3 = 147.7 HCO 3 - Other Anions 147.7 0 311 Step: Total Hardness= 33 mg/l Ca + Carbonate Hardness = 00 mg/l Ca + Non Carbonate Hardness = 0 mg/l Mg + Carbonate Hardness = 311-00 = 111 mg/l Mg + Non Carbonate Hardness= 33-311= 1 mg/l Step3: Lime Dosage: 147.7 + 00 +(111) +1= 590.7 mg/l as CaCO 3 590.7 X (37/50) = 437.118 mg/l as Ca(OH) Soda Ash dose: =0+1=1 mg/l as CaCO 3 53 Soda ash dose = 1 =.6 mg/l as Na CO 3 50 1

APPENDIX 3 - Water Softening and alkalinity Protocol Water Softening Protocol TRIAL RUN: 1. Prepare a Lime stock of 10 mg/ml. Prepare 0.1 M EDTA stock 3. Using ground water samples measure Total hardness, Calcium hardness, Magnesium hardness, Alkalinity, ph and Temperature a. Total hardness, Calcium hardness and Alkalinity protocols attached at the end of this document. 4. Determine the appropriate water softening process: a. i.e. East Lansing well water= excess lime soda-ash 5. Calculate and add lime dosage for 100% stoichiometric amount to a liter of ground water a. Use AWWA equations for dosage calculation. Conduct flocculation for 0 min at 30 RPM 3. Filter the entire sample through 0.45 ul filter (smooth side of filter facing down in the funnel) 4. Collect supernatant and measure Alkalinity, Calcium and Total hardness and ph 5. Calculate Magnesium hardness RUN 1 & : 1. Calculate and add lime dosage for 30, 60, 90, 10, 150, and 180% of the stoichiometric amount to a liter of ground water. a. Use AWWA equations for dosage calculation. Conduct flocculation for 0 min at 30 RPM 3. Filter the entire sample through 0.45 ul filter (smooth side down in the funnel) 4. Collect supernatant and measure Alkalinity, Calcium and Total hardness and ph 5. Calculate Magnesium hardness 6. Repeat experiment to determine degree of experimental error 13

ALKALINITY PROTOCOL: 1. Use ph 7.0 buffer and adjust the ph meter to 7.0. Use ph 4.0 buffer and adjust the ph meter to 4.0.. Titrate 100 ml of sample with 0.0 N HSO4 to obtain ph 4.5 by vigorously stirring towards the end of the titration step. This is done in order to break the surface and to obtain rapid equilibrium between CO in solution and CO in the atmosphere. 3. Total Alkalinity is measured as CaCO3 in mg/l= (ml of titrant) X 10 To prepare 0.0N HSO4, Use the following formula: Nf*Vf=Ni*Vi Where: Nf: Final normality desired Vf: Final total volume Ni: Initial normality Vi: Initial volume TOTAL HARDNESS: 1. Take 5mL of sample and add 5 ml of DI water. Add 1 ml of hardness buffer and measure ph Ideal ph for reaction is above 10 3. Add a scoop of Erichrome Black T indicator The solution will turn pink 4. Titrate 0.1M EDTA until a permanent blue color appears This is when Ca ++ and Mg ++ ions complex w/ EDTA 5. Total Hardness= Volume of titrant*1*(1000/vol. of sample) 14

Ca ++ HARDNESS: 1. Take 5mL of sample and add 5mL of DI water. Add ml 8N NaOH solution and measure ph ph ideally above 10, usually 1 or 13 3. Add a scoop of Erichrome Blue Black R indicator The solution will turn pink 4. Titrate 0.01 N EDTA until a permanent blue color appears 5. Calcium Hardness=Volume of titrant*1*(1000/vol. of sample) Total Hardness= Ca ++ Hardness + Mg ++ Hardness Carbonate Hardness=Alkalinity Non-carbonate Hardness=Total Hardness Alkalinity 15

APPENDIX 4 - Pictures Setup & Samples with Lime Dosage Filtration Setup Before Titration Floc. Formation Samples After Filtration Mid-Titration End of Titration 16