Skip to content

JASCO JASCO

  • News
  • Events
  • E-Store
  • My Account
  • Contact Us
  • Worldwide
Search
Click to view menu
MENUMENU
  • Products
    • Chromatography
      • HPLC
      • RHPLC
      • UHPLC
      • LC-MS
      • Preparative LC
      • Analytical SFC
      • Semi-Preparative SFC
      • Hybrid SFC
      • Fuel Analysis by SFC-FID
      • Preparative SFC
      • Supercritical Fluid Extraction
      • Chromatography Software
    • Molecular Spectroscopy
      • Circular Dichroism
      • High-Throughput CD
      • Vibrational CD
      • Circularly Polarized Luminescence (CPL)
      • Polarimeters
      • FTIR Spectrometers
      • FTIR Microscopy
      • FTIR Portable
      • Raman Microscopy
      • Palmtop Raman Spectrometer
      • Probe Raman
      • UV-Visible/NIR Spectrophotometers
      • UV-Visible/NIR Microscopy
      • Fluorescence Spectrophotometers
      • Film Thickness
      • Spectra Manager™ Suite
    • Refurbished
      • Refurbished HPLC Systems
      • HPLC Switching Valves
      • FTIR Accessories
  • Service
    • Service and Support Plans
    • Service Request Form
  • Applications
  • KnowledgeBase
  • Learning Center
    • Best Practice
      • Circular Dichroism Tips & Tricks for Biological Samples
      • CD Scale Calibration with ACS
      • Fluorescence Tips & Tricks
      • Raman Spectroscopy Tips & Tricks
    • Training Videos
      • ChromNAV
      • SF-NAV
      • Circular Dichroism
      • UV-Visible/NIR
      • Fluorescence
    • Training Seminars
      • Training Registration Form
    • Webinars
    • eBooks
    • Theory
      • Theory of Molecular Spectroscopy
      • Chromatography
  • About Us
    • President’s Message
    • Contact
    • History
    • Careers
  • News
  • Events
  • Worldwide
  • Shop
  • My Account
  • Contact Us

Home / Applications / Quantitative Determination of Low-Concentration Hexavalent Chromium by Diphenylcarbazide Method

  • Industry

  • Technique

Quantitative Determination of Low-Concentration Hexavalent Chromium by Diphenylcarbazide Method

By Spectroscopy Team

PDF IconDownload This Application

November 26, 2024

Introduction

Hexavalent chromium (Cr(VI)) is a form of metallic chromium. Cr(VI) compounds are widely used in industrial processes including stainless steel production, leather tanning, and textile manufacturing. While Cr(VI) compounds have many practical uses, they can be harmful to the human body. In fact, these compounds are known to cause cancer. In addition, they target the respiratory system, kidneys, liver, skin and eyes.

Therefore, international standards have been set for chromium. For example, the EPA (U.S. Environmental Protection Agency) has a drinking water standard of 0.1 milligrams per liter (mg/L) or 100 parts per billion (ppb) for total chromium. This includes all forms of chromium, including Cr(VI). The most widely used method for quantitative analysis of Cr(VI) is the diphenycarbazide absorption method using a UV-visible spectrophotometer.

This application note describes the use of a JASCO V-730 spectrophotometer to determine the detection and quantitation limits for chromium. The spectrophotometer was equipped with a vacuum sipper and a 50-mm path flow cell, which enables efficient operation without time-consuming manual cell cleaning, and can be used for samples with low absorbance. A calibration curve was created using a color reaction kit from a commercial reagent manufacturer for simple quantitative determinations.

Experimental

Sample
Standards:  0, 0.01, 0.02, 0.04, 0.05, 0.06, 0.08, and 1 mg/L K2CrO4 aqueous solutions
Test solutions:  0.005 and 0.01 mg/L K2CrO4 aqueous solutions
Reaction reagent:  LR-Cr6+ color kit for Cr(VI)
(KYORITSU CHEMICAL-CHECK Lab., Corp.)

UV-Visible spectrophotometer equipped with a vacuum sipper

System
Instrument:  V-730 UV-Visible spectrophotometer
Accessory:  NQF-929 Vacuum sipper with long-path flow cell
Software:  VWQM-978 Spectrum quantitative measurement program

Conditions
Measurement range:  700 – 400 nm  Data interval:  0.1 nm
Bandwidth:  1.0 nm  Response:  0.96 sec
Scan speed:  200 nm/min  Path length:  50 mm

Keywords

Water testing, hexavalent chromium, chromium, color reaction, vacuum sipper, long-path flow cell

Results

Creating a calibration curve

Fig. 1 Spectrum of Cr(IV)

A calibration curve was obtained using standards with the following concentrations of Cr(VI): 0, 0.01, 0.02, 0.04, 0.05, 0.06, 0.08, and 1 mg/L. The standard solutions turned pink after adding the reaction reagent, except the 0 mg/L solution. Each standard was measured three times. The spectra of the standards showed a peak at 542 nm, with a sloped baseline (Fig. 1). The baseline slope was most likely due to residues in the reaction reagent, which did not dissolve even after the reaction was completed. Therefore, the baseline was drawn between the absorbance values at 450 and 650 nm. The calibration curve showed a high degree of linearity with a coefficient of determination (R2) of 0.999 (Fig. 2). The limits of detection and quantitation were 0.0014 and 0.0048 mg/L, respectively, as determined based on 3σ and 10σ, where σ is a standard deviation of 10 measurements of the 0 mg/L standard solution.

Testing the calibration curve

Fig. 2 Calibration curve

Solutions were prepared with Cr(VI) concentrations of 0.005 and 0.01 mg/L to test the obtained calibration curve. Each test solution was measured five times, and the concentrations were determined using the calibration curve (Table 1). The determined concentrations matched the prepared concentrations, validating the accuracy of the curve. In addition, the coefficient of variation (CV) for the five measurements was less than 10%, indicating the high precision of the system.

 

No.
Test Solutions / mg•L-1
0.005 mg•L-1
0.01 mg•L-1
1
0.0051
0.0095
2
0.0042
0.0107
3
0.0046
0.0094
4
0.0048
0.0099
5
0.0052
0.0100
Ave.
0.0048
0.0099
CV
8.42%
5.20%

Conclusion

The long-path flow cell enabled low-absorbance measurements. The measurement accuracy at low absorbance was validated by the high linearity and the accuracy of the calibration curve.

The vacuum sipper significantly reduced the time for cell cleaning to six times less than that for the standard cell holder*.

This system can potentially be applied to the screening of a large number of samples with low absorbance.

*Based on the cell cleaning time required using a vacuum sipper or a standard cell holder. With a vacuum sipper, cell cleaning was performed by flushing with ultrapure water and blowing air through the flow, both of which were achieved simply by pushing the lever on the sipper. With a standard cell holder, the cell was washed five times with ultrapure water, followed by flushing with ethanol and acetone (two times each), and then blowing with N2 gas. These process were performed manually.

 

Note: The measurements described above can also be performed using the V-750/760/770/780.

References

National Institute of Environmental Health Sciences: “Hexavalent Chromium” <https://www.niehs.nih.gov/health/topics/agents/hex-chromium/index.cfm>, (accessed 2023.04.05)

International Agency for Research on Cancer: “List of Classifications” <https://monographs.iarc.who.int/list-of-classifications>, (accessed 2023.04.05)

U.S. Department of Labor: “Hexavalent Chromium” <https://www.osha.gov/hexavalent-chromium>, (accessed 2023.04.05)

U.S. Environmental Protection Agency: “Chromium in Drinking Water” <https://www.epa.gov/sdwa/chromium-drinking-water>, (accessed 2023.04.05)

Applicative Solution Lab Division  A. Yamane

 

 

This document has been prepared based on information available at the time of publication and is subject to revision without notice. Although the contents are checked with the utmost care, we do not guarantee their accuracy or completeness. JASCO Corporation assumes no responsibility or liability for any loss or damage incurred as a result of the use of any information contained in this document. Copyright and other intellectual property rights in this document remain the property of JASCO Corporation. Please do not attempt to copy, modify, redistribute, or sell etc. in whole or in part without prior written permission.

About the Author

JASCO Application Note

Quantitative Determination of Low-Concentration Hexavalent Chromium by Diphenylcarbazide Method

Introduction

Hexavalent chromium (Cr(VI)) is a form of metallic chromium. Cr(VI) compounds are widely used in industrial processes including stainless steel production, leather tanning, and textile manufacturing. While Cr(VI) compounds have many practical uses, they can be harmful to the human body. In fact, these compounds are known to cause cancer. In addition, they target the respiratory system, kidneys, liver, skin and eyes.

Therefore, international standards have been set for chromium. For example, the EPA (U.S. Environmental Protection Agency) has a drinking water standard of 0.1 milligrams per liter (mg/L) or 100 parts per billion (ppb) for total chromium. This includes all forms of chromium, including Cr(VI). The most widely used method for quantitative analysis of Cr(VI) is the diphenycarbazide absorption method using a UV-visible spectrophotometer.

This application note describes the use of a JASCO V-730 spectrophotometer to determine the detection and quantitation limits for chromium. The spectrophotometer was equipped with a vacuum sipper and a 50-mm path flow cell, which enables efficient operation without time-consuming manual cell cleaning, and can be used for samples with low absorbance. A calibration curve was created using a color reaction kit from a commercial reagent manufacturer for simple quantitative determinations.

Experimental

Sample
Standards:  0, 0.01, 0.02, 0.04, 0.05, 0.06, 0.08, and 1 mg/L K2CrO4 aqueous solutions
Test solutions:  0.005 and 0.01 mg/L K2CrO4 aqueous solutions
Reaction reagent:  LR-Cr6+ color kit for Cr(VI)
(KYORITSU CHEMICAL-CHECK Lab., Corp.)

UV-Visible spectrophotometer equipped with a vacuum sipper

System
Instrument:  V-730 UV-Visible spectrophotometer
Accessory:  NQF-929 Vacuum sipper with long-path flow cell
Software:  VWQM-978 Spectrum quantitative measurement program

Conditions
Measurement range:  700 – 400 nm  Data interval:  0.1 nm
Bandwidth:  1.0 nm  Response:  0.96 sec
Scan speed:  200 nm/min  Path length:  50 mm

Results

Creating a calibration curve

Fig. 1 Spectrum of Cr(IV)

A calibration curve was obtained using standards with the following concentrations of Cr(VI): 0, 0.01, 0.02, 0.04, 0.05, 0.06, 0.08, and 1 mg/L. The standard solutions turned pink after adding the reaction reagent, except the 0 mg/L solution. Each standard was measured three times. The spectra of the standards showed a peak at 542 nm, with a sloped baseline (Fig. 1). The baseline slope was most likely due to residues in the reaction reagent, which did not dissolve even after the reaction was completed. Therefore, the baseline was drawn between the absorbance values at 450 and 650 nm. The calibration curve showed a high degree of linearity with a coefficient of determination (R2) of 0.999 (Fig. 2). The limits of detection and quantitation were 0.0014 and 0.0048 mg/L, respectively, as determined based on 3σ and 10σ, where σ is a standard deviation of 10 measurements of the 0 mg/L standard solution.

Testing the calibration curve

Fig. 2 Calibration curve

Solutions were prepared with Cr(VI) concentrations of 0.005 and 0.01 mg/L to test the obtained calibration curve. Each test solution was measured five times, and the concentrations were determined using the calibration curve (Table 1). The determined concentrations matched the prepared concentrations, validating the accuracy of the curve. In addition, the coefficient of variation (CV) for the five measurements was less than 10%, indicating the high precision of the system.

 

No.
Test Solutions / mg•L-1
0.005 mg•L-1
0.01 mg•L-1
1
0.0051
0.0095
2
0.0042
0.0107
3
0.0046
0.0094
4
0.0048
0.0099
5
0.0052
0.0100
Ave.
0.0048
0.0099
CV
8.42%
5.20%

Conclusion

The long-path flow cell enabled low-absorbance measurements. The measurement accuracy at low absorbance was validated by the high linearity and the accuracy of the calibration curve.

The vacuum sipper significantly reduced the time for cell cleaning to six times less than that for the standard cell holder*.

This system can potentially be applied to the screening of a large number of samples with low absorbance.

*Based on the cell cleaning time required using a vacuum sipper or a standard cell holder. With a vacuum sipper, cell cleaning was performed by flushing with ultrapure water and blowing air through the flow, both of which were achieved simply by pushing the lever on the sipper. With a standard cell holder, the cell was washed five times with ultrapure water, followed by flushing with ethanol and acetone (two times each), and then blowing with N2 gas. These process were performed manually.

 

Note: The measurements described above can also be performed using the V-750/760/770/780.

Keywords

Water testing, hexavalent chromium, chromium, color reaction, vacuum sipper, long-path flow cell

References

National Institute of Environmental Health Sciences: “Hexavalent Chromium” <https://www.niehs.nih.gov/health/topics/agents/hex-chromium/index.cfm>, (accessed 2023.04.05)

International Agency for Research on Cancer: “List of Classifications” <https://monographs.iarc.who.int/list-of-classifications>, (accessed 2023.04.05)

U.S. Department of Labor: “Hexavalent Chromium” <https://www.osha.gov/hexavalent-chromium>, (accessed 2023.04.05)

U.S. Environmental Protection Agency: “Chromium in Drinking Water” <https://www.epa.gov/sdwa/chromium-drinking-water>, (accessed 2023.04.05)

Applicative Solution Lab Division  A. Yamane

 

 

This document has been prepared based on information available at the time of publication and is subject to revision without notice. Although the contents are checked with the utmost care, we do not guarantee their accuracy or completeness. JASCO Corporation assumes no responsibility or liability for any loss or damage incurred as a result of the use of any information contained in this document. Copyright and other intellectual property rights in this document remain the property of JASCO Corporation. Please do not attempt to copy, modify, redistribute, or sell etc. in whole or in part without prior written permission.
28600 Mary’s Court, Easton, MD 21601 USA • (800) 333-5272 • Fax: (410) 822-7526 • jascoinc.com/applications

Close

Designed in Tokyo. TRUSTED globally.

View our support plans

Connect with JASCO

  • Facebook
  • Twitter
  • LinkedIn
  • JASCO Sales
  • 800-333-5272

Receive the latest promotions and special offers

  • This field is for validation purposes and should be left unchanged.
  • Careers
  • Press Kit
  • JASCO Privacy Policy
  • Sitemap
  • Environmental Policy

© , JASCO. All Rights Reserved.