Esterification Method 1 Method 8196 27 to 2800 mg/l (as acetic acid) Reagent Solution

Similar documents
USEPA 1 FerroVer Method 2 Method to 3.00 mg/l Fe Powder Pillows or AccuVac Ampuls

Phosphorus, Reactive (Orthophosphate)

Cadmium Reduction Method Method to 30.0 mg/l NO 3 N (HR) Powder Pillows or AccuVac Ampuls

FerroVer Method 1 Method to 3.0, 1.0 to 30.0 and 10.0 to mg/l Fe Powder Pillows

Color, True and Apparent

Color, True and Apparent

Quaternary Ammonium Compounds DOC

LZV585 (B) The 1-cm path is aligned with the arrow on the adapter

Chlorine, Total. DPD Method 1 Method to 5.00 mg/l Cl 2 Test 'N Tube Vials. Test preparation. Instrument-specific information

Dimethylglyoxime Method Method to 6.0 mg/l Ni TNTplus 856

Scope and application: For testing residual corrosion inhibitors (oxygen scavengers) in boiler feed water or condensate

Nitrogen, Ammonia. Known Addition ISE Method 1 Method Minimum of 0.8 mg/l NH 3 N. Ammonia ISE. Test preparation. Instrument-specific table

DR/4000 PROCEDURE. CHLORINE, Free

Method 8155 NITROGEN, AMMONIA (0 to 0.50 mg/l NH 3 -N) For water, wastewater, seawater

Solids, Volatile Dissolved and Fixed Dissolved

Direct ISE Method Method to 1000 mg/l Na + Sodium ISE

USEPA Electrode Method Method 8156

Direct Measurement Method Method to 20.0 mg/l (or 0 to 200% saturation) O 2 Clark-type Amperometric Sensor

Total Aerobic Bacteria, Yeasts and Molds

Determining the Quantity of Iron in a Vitamin Tablet. Evaluation copy

Pocket Colorimeter II

An Introduction to Standards and Quality Control for the Laboratory Barbara Martin

Standard Operating Procedure for Total Kjeldahl Nitrogen (Lachat Method)

Hot water extractable acidity or alkalinity of paper (Reaffirmation of T 428 om-08) (No changes from Draft 1)

COMMON LABORATORY APPARATUS

Factors Affecting Enzyme Activity

EXPERIMENT 5. Molecular Absorption Spectroscopy: Determination of Iron With 1,10-Phenanthroline

Colorimetric Determination of Iron in Vitamin Tablets

Physical and Chemical Properties and Changes

In this experiment, we will use three properties to identify a liquid substance: solubility, density and boiling point..

Phosphorus, colorimetry, phosphomolybdate, automated-segmented flow

Apparatus error for each piece of equipment = 100 x margin of error quantity measured

Enzyme Pre-Lab. Using the Enzyme worksheet and Enzyme lab handout answer the Pre-Lab questions the pre-lab must be complete before beginning the lab.

METHOD 3510C SEPARATORY FUNNEL LIQUID-LIQUID EXTRACTION

5.0 EXPERIMENT ON DETERMINATION OF TOTAL HARDNESS

The Determination of an Equilibrium Constant

Hands-On Labs SM-1 Lab Manual

ISOLATION OF CAFFEINE FROM TEA

Catalase. ***You will be working with hot water, acids and bases in this laboratory*** ****Use Extreme Caution!!!****

Agarose Gel Electrophoresis with Food Color- Teacher Guide

Neutralizing an Acid and a Base

Creatine Kinase (CK) Enzymatic Assay Kit Manual Catalog #:

CONFIRMATION OF ZOLPIDEM BY LIQUID CHROMATOGRAPHY MASS SPECTROMETRY

Experiment 8 Synthesis of Aspirin

Rat Creatine Kinase MB isoenzyme,ck-mb ELISA Kit

# 12 Condensation Polymerization: Preparation of Two Types of Polyesters

OBJECTIVES: Visitors learn what an antioxidant is and how it behaves. They also learn how to test for the presence of vitamin C..

Colorimetric Determination of Iron in Vitamin Tablets

POLYDIMETHYLSILOXANE

Practical 1: Measure the molar volume of a gas

Experiment 2 Kinetics II Concentration-Time Relationships and Activation Energy

Experiment 12- Classification of Matter Experiment

STANDARDIZATION OF A SODIUM HYDROXIDE SOLUTION EXPERIMENT 14

6 H2O + 6 CO 2 (g) + energy

NITRIC OXIDE and NITROGEN DIOXIDE 6014

GCE Chemistry PSA14: A2 Physical Chemistry Determine an equilibrium contstant

Enzyme Action: Testing Catalase Activity

PREPARATION AND PROPERTIES OF A SOAP

Measurement and Calibration

Determination of the Mass Percentage of Copper in a Penny. Introduction

Phosphates (ortho- and total)

BRIEFING Plastic Packaging Systems for Pharmaceutical Use.

PECTINS. SYNONYMS INS No. 440 DEFINITION DESCRIPTION. FUNCTIONAL USES Gelling agent, thickener, stabilizer, emulsifier CHARACTERISTICS

XI. Methods of Analysis DETERMINATION OF POTASSIUM CARBONATE CALCULATIONS REAGENTS PROCEDURE

Back to School Promotion Offers - consumable (Aug 2014)

Experiment 13H THE REACTION OF RED FOOD COLOR WITH BLEACH 1

MOLECULAR WEIGHT BY BOILING POINT ELEVATION

Experiment 3: Extraction: Separation of an Acidic, a Basic and a Neutral Substance

HS 1003 Part 2 HS 1003 Heavy Metals Test

Calibration of Volumetric Glassware

TOTAL SULPHITE (SO 2 )

AN EXPERIMENT IN ALCHEMY: COPPER TO SILVER TO GOLD 2005, 2000, 1996 by David A. Katz. All rights reserved

Experiment 6 Coffee-cup Calorimetry

Odor (Threshold Odor, Consistent Series)

4.0 EXPERIMENT ON DETERMINATION OF CHLORIDES

1.4 This method is capable of measuring DO in the range of 0.20 to 20 mg/l.

OXIDATION-REDUCTION TITRATIONS-Permanganometry

Mixtures and Pure Substances

Measuring Protein Concentration through Absorption Spectrophotometry

The Molar Mass of a Gas

Assessment of Accuracy and Precision

SODIUM CARBOXYMETHYL CELLULOSE

Mouse Creatine Kinase MB isoenzyme (CKMB) ELISA

Synthesis of Fragrant Esters

Human Free Testosterone(F-TESTO) ELISA Kit

Carolina s Solution Preparation Manual

Where the exp subscripts refer to the experimental temperature and pressure acquired in the laboratory.

Standard Operating Procedure for the Determination of Total and Total Dissolved Solids CCAL 13A.2

MOISTURE (Karl Fischer, Buffered)

ph and Acidity in Wine and Fruit Juice

Phenolphthalein-NaOH Kinetics

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

18 Conductometric Titration

Enzyme Action: Testing Catalase Activity

CHEMICAL REACTIONS OF COPPER AND PERCENT YIELD KEY

(1) Hydrochloric acid reacts with sodium hypochlorite to form hypochlorous acid: NaOCl(aq) + HCl(aq) HOCl(aq) + NaCl(aq) hypochlorous acid

Reaction Stoichiometry and the Formation of a Metal Ion Complex

Tamsulosin Hydrochloride Capsules

EXPERIMENT 9 (Organic Chemistry II) Pahlavan - Cherif Synthesis of Aspirin - Esterification

Evaluation copy. Enzyme Action: Testing Catalase Activity (Method 1 O 2 Gas Sensor) Computer 2

Transcription:

Volatile Acids DOC316.53.01144 Esterification Method 1 Method 8196 27 to 2800 mg/l (as acetic acid) Reagent Solution Scope and application: For digestor sludges. 1 Adapted from The Analyst, 87, 949 (1962). Test preparation Instrument-specific information Table 1 shows all of the instruments that have the program for this test. The table also shows sample cell and orientation requirements for reagent addition tests, such as powder pillow or bulk reagent tests. To use the table, select an instrument, then read across to find the applicable information for this test. Table 1 Instrument-specific information Instrument Sample cell orientation Sample cell DR 6000 DR 3800 DR 2800 DR 2700 DR 1900 DR 5000 DR 3900 The fill line is to the right. 2495402 The fill line is toward the user. DR 900 The orientation mark is toward the user. 2401906 Before starting Install the instrument cap on the DR 900 cell holder before ZERO or READ is pushed. Review the Safety Data Sheets (MSDS/SDS) for the chemicals that are used. Use the recommended personal protective equipment. Dispose of reacted solutions according to local, state and federal regulations. Refer to the Safety Data Sheets for disposal information for unused reagents. Refer to the environmental, health and safety staff for your facility and/or local regulatory agencies for further disposal information. Items to collect Description Quantity Centrifuge 1 Centrifuge tubes and caps 2 Cylinder, 10-mL graduated 1 Ethylene Glycol Ferric Chloride-Sulfuric Acid Solution 3 ml 20 ml 1

Items to collect (continued) Description Funnel and filter paper Quantity varies Hot Plate 1 Hydroxylamine Hydrochloride Solution, 100-g/L 1 ml Pipet filler 1 Pipet, 2-mL 1 Pipet, Class A volumetric, 0.50-mL 1 1 Pipet, Class A volumetric, 10-mL 1 Sample cells (For information about sample cells, adapters or light shields, refer to Instrumentspecific information on page 1.) Sodium Hydroxide Standard Solution, 4.5 N Sulfuric Acid Standard Solution, 19.2 N 2 4 ml 0.4 ml Water bath and rack 1 Water, deionized 20.5 ml 1 A TenSette Pipet can be used in place of individual pipets in this procedure. Refer to Consumables and replacement items on page 5 for order information. Sample collection and storage Esterification method Collect samples in clean glass or plastic bottles. To preserve samples for later analysis, keep the samples at or below 6 C (43 F) for up to 24 hours. Let the sample temperature increase to room temperature before analysis. Start 1. Start program 770 Volatile Acids. For information about sample cells, adapters or light shields, refer to Instrumentspecific information on page 1. 2. Prepare the blank: Use a pipet to add 0.5 ml of deionized water to a sample cell. 3. Use a filter or a centrifuge to separate 10 ml of sample. 4. Prepare the sample: Use a pipet to add 0.5 ml of the filtrate or supernatant to a second sample cell. Note: Although the program name can be different between instruments, the program number does not change. 2 Volatile Acids, Esterification Method (2800 mg/l)

5. Add 1.5 ml of Ethylene Glycol to each sample cell. 6. Swirl to mix. 7. Add 0.2 ml of 19.2 N Sulfuric Acid to each sample cell. 8. Swirl to mix. 9. Put both cells into a boiling water bath. The sample cells can also be boiled in a 500-mL beaker. 10. Start the instrument timer. A 3-minute reaction time starts. 11. When the timer expires, use a cold water bath to cool the samples to 25 C (the cells will feel cold). 12. Add 0.5 ml of Hydroxylamine Hydrochloride Solution to each sample cell. 13. Swirl to mix. 14. Add 2.0 ml of 4.5 N Sodium Hydroxide Standard Solution to each cell. 15. Swirl to mix. 16. Add 10 ml of Ferric Chloride Sulfuric Acid Solution to each sample cell. 17. Swirl to mix. 18. Add 10 ml of deionized water to each sample cell. 19. Put the stopper on both cells. Invert both cells to mix. 20. Transfer 10 ml of the blank solution to a clean sample cell. Volatile Acids, Esterification Method (2800 mg/l) 3

21. Transfer 10 ml of the prepared sample solution to a clean sample cell. 22. Start the instrument timer. A second 3-minute reaction time starts. 23. When the timer expires, clean the blank sample cell. 24. Insert the blank into the cell holder. Set the instrument to zero during this reaction time. Zero Read 25. Push ZERO. The display shows 0 mg/l HOAC. 26. Clean the prepared sample cell. 27. Insert the prepared sample into the cell holder. 28. Push READ. Results show in mg/l HOAC. Accuracy check Standard additions method (sample spike) Use the standard additions method (for applicable instruments) to validate the test procedure, reagents and instrument and to find if there is an interference in the sample. Items to collect: Volatile Acid Voluette Ampule Standard, 62,500-mg/L as acetic acid Ampule breaker Pipet, TenSette, 0.1 1.0 ml and tips Mixing cylinders, 25-mL (3) 1. Use the test procedure to measure the concentration of the sample, then keep the (unspiked) sample in the instrument. 2. Go to the Standard Additions option in the instrument menu. 3. Select the values for standard concentration, sample volume and spike volumes. 4. Open the standard solution. 5. Prepare three spiked samples: use the TenSette pipet to add 0.1 ml, 0.2 ml and 0.3 ml of the standard solution, respectively, to three 25-mL portions of fresh sample. Mix well. 6. Use the test procedure to measure the concentration of each of the spiked samples. Start with the smallest sample spike. Measure each of the spiked samples in the instrument. 7. Select Graph to compare the expected results to the actual results. Note: If the actual results are significantly different from the expected results, make sure that the sample volumes and sample spikes are measured accurately. The sample volumes and 4 Volatile Acids, Esterification Method (2800 mg/l)

sample spikes that are used should agree with the selections in the standard additions menu. If the results are not within acceptable limits, the sample may contain an interference. Standard solution method Use the standard solution method to validate the test procedure, the reagents and the instrument. Items to collect: Volatile Acid Voluette Ampule Standard, 62,500-mg/L as acetic acid 500-mL volumetric flask, Class A 4-mL volumetric pipet, Class A and pipet filler safety bulb Deionized water 1. Prepare a 500 mg/l volatile acids standard solution as follows: a. Use a pipet to add 4.00 ml of 62,500-mg/L as acetic acid standard solution into the volumetric flask. b. Dilute to the mark with deionized water. Mix well. Prepare this solution daily. 2. Use the test procedure to measure the concentration of the prepared standard solution. 3. Compare the expected result to the actual result. Note: The factory calibration can be adjusted slightly with the standard adjust option so that the instrument shows the expected value of the standard solution. The adjusted calibration is then used for all test results. This adjustment can increase the test accuracy when there are slight variations in the reagents or instruments. Method performance The method performance data that follows was derived from laboratory tests that were measured on a spectrophotometer during ideal test conditions. Users can get different results under different test conditions. Program Standard Precision (95% confidence interval) Sensitivity Concentration change per 0.010 Abs change 770 1350 mg/l as acetic acid (HOAC) 1218 1482 mg/l as acetic acid (HOAC) 27 mg/l as acetic acid (HOAC) Summary of method The volatile acids test is designed specifically to determine volatile acids in digestor sludges. The method is based on esterification of the carboxylic acids present in the sample and subsequent determination of the esters by the ferric hydroxamate reaction. All volatile acids present are reported as their equivalent mg/l as acetic acid. The measurement wavelength is 495 nm for spectrophotometers or 520 nm for colorimeters. Consumables and replacement items Required reagents Description Quantity/test Unit Item no. Water, deionized varies 4 L 27256 Volatile Acid Reagent Set 1 90 tests 2244700 Includes: Ethylene Glycol 3 ml 1000 ml 203953 Ferric Chloride-Sulfuric Acid Solution 20 ml 1000 ml 204253 Hydroxylamine Hydrochloride Solution, 100-g/L 1 ml 100 ml 81842 Volatile Acids, Esterification Method (2800 mg/l) 5

Consumables and replacement items (continued) Description Quantity/test Unit Item no. Sodium Hydroxide Standard Solution, 4.5 N 4 ml 1000 ml 204053 Sulfuric Acid Standard Solution, 19.2 N 0.4 ml 1000 ml 203832 Required apparatus Description Quantity/test Unit Item no. Centrifuge, 115 VAC, 6 x 15 ml 1 each 2676500 Centrifuge tubes, 15-mL 2 10/pkg 2278739 Centrifuge tube caps 2 20/pkg 2585220 Cylinder, graduated, 10-mL 1 each 50838 Filter paper, folded, 12.5-cm 1 100/pkg 189457 Funnel, poly, 65-mm 1 each 108367 Hot plate, 7 inch x 7 inch, digital, 120 VAC 1 each 2881500 Hot Plate, 7-inch digital, 240 VAC 1 each 2881502 Pipet filler, safety bulb 1 each 1465100 Pipet, serological, 2-mL 1 each 53236 Pipet, volumetric, Class A, 0.5-mL 1 each 1451534 Pipet, volumetric, Class A, 10.00-mL 1 each 1451538 Cell holder assembly 1 each 4788000 Evaporating dish, 125 mm x 65 mm 1 each 2764700 Sample cells, 10-mL square, matched pair 2 2/pkg 2495402 Recommended standards and apparatus Description Unit Item no. Volatile Acids Standard Solution, 10-mL Voluette Ampule, 62,500-mg/L as HOAC 16/pkg 1427010 Ampule Breaker, 10-mL Voluette Ampules each 2196800 Optional reagents and apparatus Description Unit Item no. Mixing cylinder, graduated, 25-mL each 189640 Water bath and rack each 195555 Pipet, TenSette, 1.0 10.0 ml each 1970010 Pipet tips for TenSette Pipet, 1.0 10.0 ml 250/pkg 2199725 Pipet tips for TenSette Pipet, 1.0 10.0 ml 50/pkg 2199796 Pipet, TenSette, 0.1 1.0 ml each 1970001 Pipet tips for TenSette Pipet, 0.1 1.0 ml 50/pkg 2185696 Pipet tips for TenSette Pipet, 0.1 1.0 ml 1000/pkg 2185628 Flask, volumetric, Class A, 500-mL glass each 1457449 Finger cots 2/pkg 1464702 6 Volatile Acids, Esterification Method (2800 mg/l)

Volatile Acids, Esterification Method (2800 mg/l) 7

FOR TECHNICAL ASSISTANCE, PRICE INFORMATION AND ORDERING: In the U.S.A. Call toll-free 800-227-4224 Outside the U.S.A. Contact the HACH office or distributor serving you. On the Worldwide Web www.hach.com; E-mail techhelp@hach.com HACH COMPANY WORLD HEADQUARTERS Telephone: (970) 669-3050 FAX: (970) 669-2932 Hach Company/Hach Lange GmbH, 1989 2014. All rights reserved. 01/2014, Edition 9