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SpanishDetermining Hydroxyl Value for Polyols Compliant with JIS K 1557-6
April 7, 2025
Download This ApplicationIntroduction
Polyurethanes have excellent tensile strength, abrasion and oil resistance, and are found in numerous consumer products, including paints, adhesives, sponges, fibers, leathers and car upholstery. These polymers are manufactured by the polymerization reaction (polyaddition) of a polyol, which has hydroxyl groups, with an isocyanate (Figure 1). Since the number of reactive hydroxyl groups in a polyol that is polymerized in the presence of isocyanate directly influences the number of urethane linkages, it considerably impacts the physical properties of the polyurethane product. Traditionally, the hydroxyl value* has been used to determine the number of hydroxyl groups, and measuring and controlling this value ensures proper production of polyurethane.
The JIS K 1557-1 standard specifies an indirect method for determining the hydroxyl value for polyols, based on titration of residual reagents that were not consumed in the titration reaction for acetylation or phthalation of hydroxyl groups of polyols (hereafter referred to as the standard method). However, this wet-chemistry method requires several reagents for titration and is time consuming. Recently, Fourier transform near-infrared (FT-NIR) spectroscopy has been used to determine the hydroxyl value for various materials based on JIS K 1557-6, allowing rapid measurements to be performed. Although it is necessary to determine the hydroxyl value using the standard method in advance, by creating a calibration curve that shows the correlation between the hydroxyl values obtained by the standard method and the FT-NIR method, the value for a small amount of sample can be easily determined in a short time, and unlike the standard method, no reagents other than the sample need to be prepared. In this application note, we describe a measurement example compliant with JIS K 1557-6 for analyzing a variety of hydroxyl values using the JASCO FT-IR spectrometer and a multivariate statistical analysis technique, the partial least squares (PLS) model.
*The number of milligrams of potassium hydroxide (KOH) required to neutralize one gram of the sample is called the hydroxyl value.
Experimental
Sample
Polyoxypropylene glycol (hydroxyl value: 27.3 mg KOH/g to 563 mg KOH/g)
Table 1 Hydroxyl value for each sample per hydroxyl value
| Sample | Hydroxyl value [mg/KOH g] | Sample | Hydroxyl value [mg/KOH g] | Sample | Hydroxyl value [mg/KOH g] |
| A-1 | 563 | B-1 | 273 | C-1 | 109 |
| A-2 | 553 | B-2 | 278 | C-2 | 113 |
| A-3 | 556 | B-3 | 275 | C-3 | 111 |
| Sample | Hydroxyl value [mg/KOH g] | Sample | Hydroxyl value [mg/KOH g] | Sample | Hydroxyl value [mg/KOH g] |
| D-1 | 55.6 | E-1 | 34.4 | F-1 | 26.6 |
| D-2 | 56.7 | E-2 | 36.0 | F-2 | 28.0 |
| D-4 | 56.3 | E-3 | 35.0 | F-3 | 27.3 |
System
Instrument: FT/IR-6X FT-IR spectrometer
Accessory: Air-cooled Peltier-element holder (customized-ordered) and sampling test tubes
Program: PLS-4X PLS Quantitative analysis program
Parameters
Resolution: 8 cm-1 Accumulations: 16 (approx. 10 sec)
Beam splitter: Broadband KBr Detector: InGaAs
The near-infrared spectrum of polyols is affected by the sample temperature at the time of measurement. To reduce this dependence, the sample was heated to 70°C in an incubator before measurement, and then transferred to the test tube using a Pasteur pipette. The sample was allowed to stabilize for two minutes in the Peltier holder, while maintaining a temperature of 70°C, and the sample spectrum was then measured. The Peltier holder allows the temperature of multiple tubes to be stabilized while waiting for the next measurement to
Keywords
Hydroxyl value, polyol, polyurethane, near-infrared spectroscopy, multivariate statistical analysis, PLS model, JIS K 1557-6
Results
Near IR spectrum
Figure 4 shows the NIR spectra for the sample and the calculation ranges used for creating a PLS calibration curve. The combination band at 4348 cm-1 to 5000 cm-1 associated with R-OH functional groups, and the band at 6666 cm-1 to 7246 cm-1 associated with the first R-OH overtone, as described in JIS K 1557-6, were used for the calculation.
PLS calibration curve
Each sample was measured two times and a PLS calibration curve was created (Figure 5). The calibration curve yielded a high correlation coefficient of 0.9999. The PLS method could capture the changes in the broad absorption band in the near-infrared region, indicating that a calibration curve can be created to accurately quantify the hydroxyl value for polyols.
Near IR spectrum
Figure 4 shows the NIR spectra for the sample and the calculation ranges used for creating a PLS calibration curve. The combination band at 4348 cm-1 to 5000 cm-1 associated with R-OH functional groups, and the band at 6666 cm-1 to 7246 cm-1 associated with the first R-OH overtone, as described in JIS K 1557-6, were used for the calculation.
Table 2 Cross-validation results (percentage error = absolute error / true value x 100)
| Sample | True Value | Quantitation Value | TPercentage Error (%) |
| A-2 (1st measurement) | 553 | 554.5 | 0.27 |
| A-2 (2nd measurement) | 553 | 556.6 | 0.65 |
| B-1 (1st measurement) | 273 | 270.8 | 0.81 |
| B-1 (2nd measurement) | 273 | 274.3 | 0.48 |
| D-2 (1st measurement) | 56.7 | 56.0 | 1.23 |
| D-2 (2nd measurement) | 56.7 | 56.2 | 0.88 |
Conclusion
It was shown that the hydroxyl value for polyols could be accurately determined using a combination of near-infrared spectroscopy and multivariate analysis (PLS). The measurements could be performed for small sample volumes in a short time, in accordance with JIS K 1557-6. This is a powerful approach to quality control, quality testing and production process control environments for pharmaceuticals and food products, and not only for polymers.
References
Applicative Solution Lab Division S. Norimoto
Determining Hydroxyl Value for Polyols Compliant with JIS K 1557-6
Introduction
Polyurethanes have excellent tensile strength, abrasion and oil resistance, and are found in numerous consumer products, including paints, adhesives, sponges, fibers, leathers and car upholstery. These polymers are manufactured by the polymerization reaction (polyaddition) of a polyol, which has hydroxyl groups, with an isocyanate (Figure 1). Since the number of reactive hydroxyl groups in a polyol that is polymerized in the presence of isocyanate directly influences the number of urethane linkages, it considerably impacts the physical properties of the polyurethane product. Traditionally, the hydroxyl value* has been used to determine the number of hydroxyl groups, and measuring and controlling this value ensures proper production of polyurethane.
The JIS K 1557-1 standard specifies an indirect method for determining the hydroxyl value for polyols, based on titration of residual reagents that were not consumed in the titration reaction for acetylation or phthalation of hydroxyl groups of polyols (hereafter referred to as the standard method). However, this wet-chemistry method requires several reagents for titration and is time consuming. Recently, Fourier transform near-infrared (FT-NIR) spectroscopy has been used to determine the hydroxyl value for various materials based on JIS K 1557-6, allowing rapid measurements to be performed. Although it is necessary to determine the hydroxyl value using the standard method in advance, by creating a calibration curve that shows the correlation between the hydroxyl values obtained by the standard method and the FT-NIR method, the value for a small amount of sample can be easily determined in a short time, and unlike the standard method, no reagents other than the sample need to be prepared. In this application note, we describe a measurement example compliant with JIS K 1557-6 for analyzing a variety of hydroxyl values using the JASCO FT-IR spectrometer and a multivariate statistical analysis technique, the partial least squares (PLS) model.
*The number of milligrams of potassium hydroxide (KOH) required to neutralize one gram of the sample is called the hydroxyl value.
Experimental
Sample
Polyoxypropylene glycol (hydroxyl value: 27.3 mg KOH/g to 563 mg KOH/g)
Table 1 Hydroxyl value for each sample per hydroxyl value
| Sample | Hydroxyl value [mg/KOH g] | Sample | Hydroxyl value [mg/KOH g] | Sample | Hydroxyl value [mg/KOH g] |
| A-1 | 563 | B-1 | 273 | C-1 | 109 |
| A-2 | 553 | B-2 | 278 | C-2 | 113 |
| A-3 | 556 | B-3 | 275 | C-3 | 111 |
| Sample | Hydroxyl value [mg/KOH g] | Sample | Hydroxyl value [mg/KOH g] | Sample | Hydroxyl value [mg/KOH g] |
| D-1 | 55.6 | E-1 | 34.4 | F-1 | 26.6 |
| D-2 | 56.7 | E-2 | 36.0 | F-2 | 28.0 |
| D-4 | 56.3 | E-3 | 35.0 | F-3 | 27.3 |
System
Instrument: FT/IR-6X FT-IR spectrometer
Accessory: Air-cooled Peltier-element holder (customized-ordered) and sampling test tubes
Program: PLS-4X PLS Quantitative analysis program
Parameters
Resolution: 8 cm-1 Accumulations: 16 (approx. 10 sec)
Beam splitter: Broadband KBr Detector: InGaAs
The near-infrared spectrum of polyols is affected by the sample temperature at the time of measurement. To reduce this dependence, the sample was heated to 70°C in an incubator before measurement, and then transferred to the test tube using a Pasteur pipette. The sample was allowed to stabilize for two minutes in the Peltier holder, while maintaining a temperature of 70°C, and the sample spectrum was then measured. The Peltier holder allows the temperature of multiple tubes to be stabilized while waiting for the next measurement to
Results
Near IR spectrum
Figure 4 shows the NIR spectra for the sample and the calculation ranges used for creating a PLS calibration curve. The combination band at 4348 cm-1 to 5000 cm-1 associated with R-OH functional groups, and the band at 6666 cm-1 to 7246 cm-1 associated with the first R-OH overtone, as described in JIS K 1557-6, were used for the calculation.
PLS calibration curve
Each sample was measured two times and a PLS calibration curve was created (Figure 5). The calibration curve yielded a high correlation coefficient of 0.9999. The PLS method could capture the changes in the broad absorption band in the near-infrared region, indicating that a calibration curve can be created to accurately quantify the hydroxyl value for polyols.
Near IR spectrum
Figure 4 shows the NIR spectra for the sample and the calculation ranges used for creating a PLS calibration curve. The combination band at 4348 cm-1 to 5000 cm-1 associated with R-OH functional groups, and the band at 6666 cm-1 to 7246 cm-1 associated with the first R-OH overtone, as described in JIS K 1557-6, were used for the calculation.
Table 2 Cross-validation results (percentage error = absolute error / true value x 100)
| Sample | True Value | Quantitation Value | TPercentage Error (%) |
| A-2 (1st measurement) | 553 | 554.5 | 0.27 |
| A-2 (2nd measurement) | 553 | 556.6 | 0.65 |
| B-1 (1st measurement) | 273 | 270.8 | 0.81 |
| B-1 (2nd measurement) | 273 | 274.3 | 0.48 |
| D-2 (1st measurement) | 56.7 | 56.0 | 1.23 |
| D-2 (2nd measurement) | 56.7 | 56.2 | 0.88 |
Conclusion
It was shown that the hydroxyl value for polyols could be accurately determined using a combination of near-infrared spectroscopy and multivariate analysis (PLS). The measurements could be performed for small sample volumes in a short time, in accordance with JIS K 1557-6. This is a powerful approach to quality control, quality testing and production process control environments for pharmaceuticals and food products, and not only for polymers.
Keywords
Hydroxyl value, polyol, polyurethane, near-infrared spectroscopy, multivariate statistical analysis, PLS model, JIS K 1557-6
References
Applicative Solution Lab Division S. Norimoto