Method for Nitrite determination on Low-Range Samples

Similar documents
Method for Chloride Determination by Ferric Thiocyanate, Version 2.0

Standard Operating Procedure for the Analysis of Nitrate/Nitrite and Nitrite in Fresh Waters CCAL 31B.1

Method for Ammonia Determination by Salicylate, Version 2.2

Method for Nitrate Determination by Cadmium Reduction, Version 2.3

Nitrate plus Nitrite and Nitrite in Seawater by Segmented Flow Analysis (SFA)

DETERMINATION OF NITRATE AND NITRITE BY ZONE FLUIDICS

Standard Operating Procedure for the Analysis of Silica in Fresh Waters CCAL 32A.2

Chloride by Flow Injection Analysis (FIA)

Hexavalent Chromium by Flow Injection Analysis (FIA)

Hach Company TNTplus 835/836 Nitrate Method Spectrophotometric Measurement of Nitrate in Water and Wastewater

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

Standard Operating Procedure for the Analysis of Dissolved Inorganic Carbon CCAL 21A.1

Hach Method Spectrophotometric Measurement of Free Chlorine (Cl 2 ) in Finished Drinking Water

Cadmium Reduction Method Method 8171 MR (0.1 to 10.0 mg/l NO 3

Cadmium Reduction Method Method to 10.0 mg/l NO 3 N (MR, spectrophotometers) 0.2 to 5.0 mg/l NO 3 N (MR, colorimeters)

Method for Ammonia Determination by Salicylate in Water and TKN Samples, Version 2.0 PRINCIPLE SUMMARY COMPLIANCE

Functional Genomics Research Stream. Lecture: February 17, 2009 Masses, Volumes, Solutions & Dilutions

Hach Method Total Organic Carbon in Finished Drinking Water by Catalyzed Ozone Hydroxyl Radical Oxidation Infrared Analysis

Anion and Cation analysis with Professional IC - automatic dilution and sample preparation with SPM

Bromide by Flow Injection Analysis (FIA)

Standard Operating Procedure for the Analysis of Fresh Water Samples for Orthophosphorus CCAL 34B.2

EnAlgae SOP sheet: Silicate - SFA. 1. Purpose This procedure is to analyse seawater and freshwater for silicate, SiO2.

Cadmium Reduction Method Method to 0.50 mg/l NO 3 N (LR) Powder Pillows

Determination of Orthophosphate Ion

Alkalinity, USEPA by Flow Injection Analysis (FIA)

ASCORBIC ACID METHOD FOR PHOSPHORUS DETERMINATION

Determination of Orthophosphate Ion

MEASUREMENT: PART II

Total Kjeldahl Nitrogen by Gas Diffusion and Flow Injection Analysis (FIA)

DR/4000 PROCEDURE NITRATE. Using Powder Pillows

Standard Operating Procedure for the Analysis of Chloride, Bromide and Sulfate in Fresh Waters by Ion Chromatography CCAL 50B.2

DR/4000 PROCEDURE NITRATE. 2. The display will show:

hydrideicp Hydride Generation System

DETERMINATION OF NITRATE IN 2M KCl SOIL EXTRACTS BY FLOW INJECTION ANALYSIS NITRATE REDUCTASE

Tetraphenylborate Method Method to 7.0 mg/l K Powder Pillows

Soil Cation Analysis Using High-Performance Capillary Zone Electrophoresis Last Modified: October 20, 2006

DETERMINATION OF NITRATE IN BRACKISH WATERS BY FLOW INJECTION ANALYSIS NITRATE REDUCTASE

Procedure for the Determination of Permanganate Oxidizable Carbon

Solubility Product Constants

Using FIMS to Determine Mercury Content in Sewage Sludge, Sediment and Soil Samples

USGS District Laboratory, Troy, NY Dissolved Inorganic Carbon Analysis Standard Operating Procedure

Method to 0.50 mg/l NH 3 N Powder Pillows

Standard Methods for the Examination of Water and Wastewater

Oxygen Demand, Chemical

Scope and application: For water, wastewater and seawater. Distillation is required for wastewater and seawater.

Method to 0.50 mg/l NH 3 N Powder Pillows

Determination of an Equilibrium Constant

Hach Company TNTplus TM Phosphorus Spectrophotometric Measurement of Phosphorus in Water and Wastewater

Supplementary information 1. INSTRUCTIONS FOR STUDENTS

Continuous Flow Analysis Methods David Davey University of South Australia. 21 February

Exercise 2-4. Titration of a Buffer Solution EXERCISE OBJECTIVES

Direct Determination of Aluminium in Milk by Graphite Furnace Atomic Absorption Spectrometry

Nutrient Analysis, Nitrate, Nitrite, Silicate, Phosphate and Ammonium

in Lab-on-Valve System

Revision: 11 (MBAS) ALLOWAY METHOD OUTLINE. Standard Laboratory Method:

Oxygen Demand, Chemical

The analysis of organic acid content of additives, premix, feed, and water.

Cadmium Reduction Method (Using Powder Pillows or AccuVac Ampuls)

Dimethylphenol Method Method to mg/l NO 3 N or 1.00 to mg/l NO

DR/4000 PROCEDURE. IRON, Total

Automating Wet Chemical Analysis. William Lipps Market Specialist for Water Analyzer Products December 11, 2008

Exercise 2-2. Titration of a Strong Acid EXERCISE OBJECTIVES

METHOD DETERMINATION OF SULFATE BY AUTOMATED COLORIMETRY. Edited by James W. O'Dell Inorganic Chemistry Branch Chemistry Research Division

ALLOWAY METHOD OUTLINE

N-NITROSODIETHANOLAMINE (NDELA) IN COSMETICS

EXPERIMENT 7. Determination of Sodium by Flame Atomic-Emission Spectroscopy

Sulfate by Flow Injection Analysis (FIA)

USGS Troy WSC Laboratory Inductively Coupled Plasma- NH4Cl Soil Extracts SOP 425 Jordan Road Rev. No. 2.0 Troy, NY Date: 03/16/2012 Page 1 of 7

PREPARATION FOR CHEMISTRY LAB: FLUORIDE IN WATER

Spectrophotometric Determination of Ferrocyanide in Effluents

Nitrogen, Total Inorganic

Multiphase Oscillatory Flow Strategy for in Situ Measurement and Screening of Partition Coefficients

Experiment#1 Beer s Law: Absorption Spectroscopy of Cobalt(II)

Phosphorus, Total. USEPA 1 PhosVer 3 with Acid Persulfate Digestion Method Method to 3.50 mg/l PO. Test preparation

REVIEW OF LAB TECHNIQUES

Ohio EPA Total (Extracellular and Intracellular) Microcystins - ADDA by ELISA Analytical Methodology Ohio EPA DES Version 2.

Determinations by Atomic Absorption Spectroscopy and Inductively Coupled Plasma-Atomic Emission

1. Preliminary qualitative analysis of unknown substances (liquid or solid).

Instrument Sample cell orientation Sample cell DR 6000 DR 3800 DR 2800 DR 2700 DR 1900 DR 5000 DR The fill line is to the right.

Automating Wet Chemical Analysis

Instrument Sample cell orientation Sample cell DR 6000 DR 3800 DR 2800 DR 2700 DR 1900 DR 5000 DR The fill line is to the right.

Method for estimation of iodine in urine

Standard Operating Procedure VUSP N

Standard Operating Procedure VUSP M

Technical Procedure for Concentration Determination of Methamphetamine in Liquids via HPLC

FerroZine Method 1 Method to 100 µg/l Fe (10-cm cell) Reagent Solution. Instrument Adapter Sample cell DR 6000 LZV

Calibrating Thermo Exactive with the Direct Analysis in Real Time (DART) Ambient Ionization Source (Protocol Adapted from US FDA FCC)

Laboratory Measurements and Procedures

Chromotropic Acid Method Method to 30.0 mg/l NO 3 N (HR) Test N Tube Vials

Nitric Oxide Synthase Ultrasensitive Colorimetric Assay

Experiment. Quantification of Ascorbic acid by Fluorescence Spectroscopy1

Micro Volume QuEChERS kit

Sodium Chloride - Analytical Standard

Dimethylglyoxime Method Method to 6.0 mg/l Ni TNTplus 856

METHOD DETERMINATION OF TOTAL CYANIDE BY SEMI-AUTOMATED COLORIMETRY

425 Jordan Road SOP. No. 8 Rev. No. 1.3 Troy, NY Date: 03/14/2012 Page 1 of 10

Direct Determination of Cadmium and Lead in honey by Electrothermal Atomization Atomic Absorption Spectrometry with Zeeman Effect Correction

Microcystin-LR ELISA Kit

QuickZyme Total Protein Assay (to be used with acid hydrolyzates)

UNIVERSITY OF MINNESOTA DULUTH DEPARTMENT OF CHEMICAL ENGINEERING ChE CONTINUOUS BINARY DISTILLATION

Transcription:

Method for Nitrite determination on Low-Range Samples

1. PRINCIPLE This method is designed for the determination of nitrite in soil, water and other forms of samples. The sample is prepared offline if necessary and then introduced to the FIAlab analyzer. Nitrite ions react with sulfanilamide and couple to N- (1-Naphthyl) ethylenediamine dihydrochloride to form a magenta colored azo dye.. 2. SUMMARY This method is designed for the determination of nitrite in high range samples of various matrices. The method is capable of detecting nitrite in the range of 0.002-2.5mg N / L. 3. SAFETY The toxicity or carcinogenicity of all reagents used in this method must be taken into account and therefore each chemical listed below should be handled accordingly. Each laboratory is responsible for maintaining compliance with OSHA regulations regarding the safe handling of the chemicals specified in this method. Material Safety Data Sheets (MSDS) should be made available to all personnel using the method. All waste materials should be disposed of in a responsible manner, in accordance with federal, state and other local regulations. The following chemicals have the potential to be highly toxic or highly hazardous, for detailed explanations consult the MSDS: - Phosphoric Acid

4. EQUIPMENT AND SUPPLIES Balance: - Analytical, with a 0.01 g resolution Glassware: - Class A volumetric flasks of at least 50 ml - Pipettes and appropriate beakers - Tinted glass storage containers Flow injection analysis apparatus: - FIAlab-2500 flow injection analyzer - Tungsten-halogen light source, Ocean Optics HL-2000-LL or corresponding - SMA-Z absorbance flow cell with 100 mm light path - Spectrophotometer, Ocean Optics USB4000-VIS/NIR, USB4000-UV/VIS, or corresponding - Fiber Optic Cables (2) Autosampler (for high sample loads): - Cetac ASX-260/520 or AIM-3200/3300 5. REAGENTS AND STANDARDS 5.1 List of chemicals - Deionized water, (H 2 O) [CAS - 7732-18-5]. - Sulfanilamide, (H 2 NC 6 H 4 SO 2 NH 2 ) [CAS - 63-74-1]. Sigma-Aldrich P/N S- 9251 or corresponding. - 85% Phosphoric acid, (H 3 PO 4 ) [CAS - 7664-38-2]. Sigma-Aldrich P/N 79606 or corresponding. - N-1-Naphthylethylene diamine dihydrochloride, (C 10 H 7 NHCH 2 CH 2 NH 2 2HCl) [CAS - 1465-25-4]. Sigma-Aldrich P/N 222488 or corresponding.

5.2 Preparation of reagents Carrier: Matrix match carrier to samples. Salt solution to seawater samples, extraction solution for soil samples, etc. Reagent 1: Sulfanilamide Solution (1L) - Mix 100ml of 85% phosphoric acid into 800ml of deionized water. - Dissolve 40g of sulfanilamide and 1.0g N-1-Naphthylethylene diamine dihydrochloride to this solution. - Add deionized water to a total volume of 1L. - Mix well and store in a dark glass bottle. Reagent 2: Unnecessary. Block R2 port on LOV with plug tubing Note: Use of high quality laboratory glass bottles is important. Reagent 1 should be prepared every four weeks 5.3 Preparation of standards - Dilute the 1000 mg/l N-(NO 2 ) stock solution with deionized water to the desired range of nitrite standards. 6. SAMPLE COLLECTION AND PRETREATMENT This protocol only covers the analysis process. Sample collection and pretreatment depends on the type of sample and will have to be determined separately.

7. INSTRUMENT SETUP LOW-RANGE Flow injection analysis apparatus parameters: - Peristaltic pump tubing: Tygon, 1.02mm/0.04in ID (white/black), FIAlab P/N 270300 - Sample injection loop: 140µL - 12.0in/30cm of Teflon capillary tubing with 0.03 in/0.75 mm ID, FIAlab P/N 270040 - Reaction coil 1: 50µL - 4.0in/10cm of Teflon capillary tubing with 0.03 in/0.75 mm ID, FIAlab P/N 270040 - Reaction coil 2: 750µL - 65.0in/165cm of Teflon capillary tubing with 0.03 in/0.75 mm ID, FIAlab P/N 270040 - SMA-Z flow cell: light path -100mm - Flow rate: 60% pump speed (approx. 2.0 ml/min flow rate per pump channel) - Bridge: 40µL 3.5in/9cm of Teflon capillary tubing with 0.03 in/0.75 mm ID, FIAlab P/N 270040 Recommended spectrometer parameters: Primary wavelength: 540nm Second wavelength: 580nm Third wavelength: 595nm Fourth wavelength: 600nm Reference wavelength: 650nm Fig. 1- Flow schematic for low-range nitrite determination on a FIAlab-2500

FIA-LOV Valve Flow Cell light path 100mm Mixing Coil 2 Sample Loop 140uL -12 /30cm of 0.03 /0.75mm ID Teflon tubing Mixing Coil 1 Pump Fig. 2- Pictorial representation of low-range nitrite setup on a FIAlab-2500

The program script using an autosampler is shown below. For manual sample introduction see the FIAlab-2500 software manual. 'Nitrate/Nitrite Assay 'FIA Template For FIAlab-2500 System Global Logon ' logon to all components Sample Description ' load sample description file Injection Valve Sample Load Optimize_FIAlab2500 'Set Wavelengths Hardware Settings Wavelength 1 (nm) 540 Hardware Settings Wavelength 2 (nm) 580 Hardware Settings Wavelength 3 (nm) 595 Hardware Settings Wavelength 4 (nm) 600 Reference Wavelength1 650 'Set delay time, start pump to prime lines Valve Delay 5000 ' sample inject (msec) Peristaltic Pump Clockwise(%) 60 Injection Valve Sample Load Delay (sec) 40 Hardware Settings Optimize Integration 'Put autosampler in first sample (usually a blank) Next Sample Delay (sec) 35 LoopStart (#) 5000 'Inject sample, load next sample 'Autosampler wash Analyte New Sample Next Sample Injection Valve Sample Inject Delay (sec) 3 'Perform reference scan and start absorbance scans Spectrometer Reference Scan Spectrometer Absorbance Scanning Delay (sec) 30 Spectrometer Stop Scanning 'Refresh plots and update concentrations Refresh Plot 'Method clean up (at end of run) If sampleid < 0 Then autosampler Wash ' Save Data Date-Time.dat End If Loop End

8. PERFORMANCE METRICS Fig. 3 Example plot and calibration data for low-range nitrite at 600nm Lower limit of detection: Upper limit of detection: Sample throughput: Startup: Shutdown: 0.002mg/L 1.4*10-7 moln/l 2.5mg/L 1.8*10-4 moln/l 100 samples/hr 5 minutes 5 minutes