Determination of Carbonyl Functional Groups in Bio-oils by Potentiometric Titration: The Faix Method

요약

Here we present a potentiometric titration technique for accurately quantifying carbonyl compounds in pyrolysis bio-oils.

초록

Carbonyl compounds present in bio-oils are known to be responsible for bio-oil property changes upon storage and during upgrading. Specifically, carbonyls cause an increase in viscosity (often referred to as 'aging') during storage of bio-oils. As such, carbonyl content has previously been used as a method of tracking bio-oil aging and condensation reactions with less variability than viscosity measurements. Additionally, carbonyls are also responsible for coke formation in bio-oil upgrading processes. Given the importance of carbonyls in bio-oils, accurate analytical methods for their quantification are very important for the bio-oil community. Potentiometric titration methods based on carbonyl oximation have long been used for the determination of carbonyl content in pyrolysis bio-oils. Here, we present a modification of the traditional carbonyl oximation procedures that results in less reaction time, smaller sample size, higher precision, and more accurate carbonyl determinations. While traditional carbonyl oximation methods occur at room temperature, the Faix method presented here occurs at an elevated temperature of 80 °C.

서문

While pyrolysis bio-oils are comprised of a large variety of compounds and chemical functional groups, quantification of carbonyl groups is especially important. Carbonyls are known to be responsible for the instability of bio-oil during both storage¹ and processing². The titration method presented here is a simple technique which can reliably quantify the total carbonyl content of bio-oils. Only aldehyde and ketone functional groups are quantified using this method; carboxylic acid and lactone groups are not quantified.

For analysis of bio-oils, quantification of carbonyl groups by titration has traditionally been accomplished using the method of Nicolaides³. This method has been commonly used in the bio-oil literature^4,5,6,7. This is a simple procedure where carbonyls are converted to the corresponding oxime (see Figure 1). The liberated HCl reacts with pyridine to force the equilibrium to completion. The conjugate acid of pyridine is titrated with a known amount of NaOH (base titrant). The number of equivalents of NaOH used is stoichiometrically equivalent to the moles of carbonyl present in the bio-oil.

The Nicolaides method, however, has several limitations. It can require reaction times in excess of 48 hours to reach completion. This severely limits sample throughput. It utilizes pyridine, which is toxic. Sample weights of 1 to 2 g are required. Sample weight used is dependent on the amount of hydroxylamine HCl present and the carbonyl content of the sample. If initial estimates of the sample weight used are incorrect, the titration has to be repeated.

Faix et al.⁸ developed a method that has been modified here to address the issues of the Nicolaides method. The reaction is carried out at 80 °C for 2 hours, thereby increasing sample throughput. Pyridine has been replaced with triethanolamine, which is a less toxic chemical. The sample size can be reduced to 100 to 150 mg. The triethanolamine consumes the liberated HCl, driving the reaction to completion and the unconsumed triethanolamine is titrated directly. A secondary titration of the hydroxylamine is unnecessary. Comparison of these titration methods has shown that the Nicolaides method significantly underestimates carbonyl content of bio-oils⁹.

The method described here has been modified from the original method⁸ to be more applicable to the analysis of pyrolysis bio-oils. This method was developed for the analysis of raw pyrolysis bio-oils, but it has been successfully applied to other types of biomass-derived oils, including hydrotreated bio-oils. Additionally, this method has been used to monitor changes in carbonyl content during both aging and upgrading.

프로토콜

Caution: Please review all relevant material safety data sheets (MSDS) before beginning. Ethanol is flammable. All applicable chemical handling procedures should be followed, as well as all applicable waste disposable and handling procedures.

1. Reagent Solutions

1. Prepare the hydroxylamine hydrochloride solution (Solution A): Add 7.7 g of hydroxylamine hydrochloride and 50 mL of deionized water to a 250 mL volumetric flask. When all solids have dissolved, dilute to mark with ethanol. This results in a 0.55 M hydroxylamine hydrochloride solution in 80% (v/v) ethanol.
2. Prepare the triethanolamine solution (Solution B): Add 17.4 mL of triethanolamine to a 250 mL volumetric flask. Add 10 mL of water, and then dilute up to the mark with ethanol. 95% ethanol can also be used if the addition of water is skipped. This results in a 0.48 M triethanolamine solution in 96 % (v/v) ethanol
3. Prepare the hydrochloric acid solution. Either purchase 0.1 N solution or prepare using 10 mL concentrated HCl and 1 L water.

2. Bio-oil Sampling and Handling

1. Make sure the oil sample is at room temperature prior to withdrawing a sample. Thoroughly homogenize (mix by shaking vigorously for at least 1 minute, and visually inspect the sample to ensure it is homogenous. Some bio-oils may require longer shaking times) bio-oil to obtain a representative sample.
2. For the bio-oil sample, use 100 to 150 mg of bio-oil.
3. Minimize exposure to oxygen and heat to prevent sample degradation prior to analysis.

3. Analytical Procedure

1. Standardization of the Base Solution
   1. Dry Na₂CO₃ primary standard in an oven at 105 °C overnight to ensure a dry sample. Allow the Na₂CO₃ to cool to room temperature before weighing.
   2. Weigh 100 to 150 mg of sodium carbonate to a titration vessel, record the actual weight, add a stir bar and add enough water to cover the pH electrode bulb and junction.
   3. Transfer the sample to a titration vessel, washing the reaction vial several times separately with ethanol and water in proportions to make a final 80% solution of ethanol/water. Titrate with the acid solution using an automatic titrator to the endpoint. Record the endpoint. The endpoint is defined as the inflection point on the titration curve.
   4. Repeat the process twice to obtain three points.
   5. Use the average value as the normality of the acid solution.
2. Preparation of Titration Blanks
   1. For Blank A: add 0.5 mL dimethyl sulfoxide (DMSO) to a 5 mL vial with a spin vane.
   2. Add 2 mL hydroxylamine hydrochloride solution (solution A).
   3. Add 2 mL triethanolamine solution (solution B).
   4. Cap tightly, place in preheated (80 °C) heater block or water bath and stir for 2 hours.
   5. Titrate with acid solution using an automatic titrator to the endpoint, and record endpoint.
   6. For Blank B: If mineral acid is suspected to be present in sample, add 0.5 mL DMSO to 5 mL vial with a spin vane.
   7. Add 2 mL triethanolamine solution (solution B).
   8. Cap tightly and stir at 80 °C for 2 hours.
   9. Transfer the sample to a titration vessel, washing the reaction vial several times separately with ethanol and water in proportions to make a final 80% solution of ethanol/water. Titrate with the acid solution using an automatic titrator to the endpoint. Record the endpoint.
   10. Repeat process three times to obtain three points.
3. Validation of the Method Using a Known Carbonyl
   1. Weigh ~ 100 mg of 4-(benzyloxy)benzaldehyde (4-BBA) to a 5 mL vial, record the actual weight, add a spin vane.
   2. Add 0.5 mL DMSO.
   3. Dissolve the sample in 2 mL hydroxylamine hydrochloride solution (solution A).
   4. Add 2 mL triethanolamine solution (solution B).
   5. Close lid tightly and stir at 80 °C for 2 hours.
   6. Transfer the sample to a titration vessel, washing the reaction vial several times separately with ethanol and water in proportions to make a final 80% solution of ethanol/water. Titrate with the acid solution using an automatic titrator to the endpoint. Record the endpoint.
   7. Repeat the process three times, to obtain three points.
4. Analysis of Bio-oil Using the Method
   1. Weigh close to 100 mg of the bio-oil to 5 mL vial, record the actual weight and add a spin vane.
   2. Add 0.5 mL DMSO.
   3. Dissolve the sample in 2 mL hydroxylamine hydrochloride solution (solution A).
   4. Add 2 mL triethanolamine solution (solution B).
   5. Close lid tightly and stir at 80 °C for 2 hours.
   6. Transfer the sample to a titration vessel, washing the reaction vial several times separately with ethanol and water in proportions to make a final 80% solution of ethanol/water. Titrate with the acid solution using an automatic titrator to the endpoint. Record the endpoint.
   7. Repeat the process three times, to obtain three points.
   8. Blank C: If mineral acid is suspected to be present in sample, weigh close to 100 mg of the bio-oil into a 5 mL vial, record the weight and add a spin vane.
   9. Add 0.5 mL DMSO.
   10. Add 2 mL triethanolamine solution (solution B).
   11. Cap tightly and stir at 80 °C for 2 hours.
   12. Transfer the sample to a titration vessel, washing the reaction vial several times separately with ethanol and water in proportions to make a final 80% solution of ethanol/water. Titrate with the acid solution using an automatic titrator to the endpoint. Record the endpoint.
   13. Repeat process three times to obtain three points.

4. Calculations

1. Standardization of the Base Solution
   1. Calculate the concentration of the acid solution (mol/L) using the following equation. The weight of the dry sodium carbonate in grams is w₁, the purity is written as a fraction (i.e., 99% is 0.99), and the endpoint is in mL.
         
2. Validation of the Method Using a Known Carbonyl
   1. Calculate the concentration of 4BBA (mol/L) in the sample using the following equation. The weight of the 4BBA in grams is w₂, the 4BBA purity is written as a fraction (i.e., 99% is 0.99), the concentration of the acid solution (mol/L) is [acid], the triethanolamine/hydroxylamine•HCl blank endpoint is EP_BA (the average value of three blanks, in mL), and the endpoint is EP (in mL).
         
3. Analysis of Bio-oil
   1. Calculate the concentration of carbonyls in bio-oils [CO] (mmol/g-bio oil) using the following equation. The weight of the bio-oil in grams is w₃, the concentration of the acid solution (mol/L) is [acid], the triethanolamine/hydroxylamine•HCl blank endpoint is EP_BA (the average value of three blanks in mL), and the endpoint is EP (in mL).
         
4. Acid Correction
   NOTE: The presence of mineral acids or organic acids with pKa < 2 can cause artificially low carbonyl values due to the reaction of the acid with triethanolamine.
   1. If this is suspected, perform the blanks detailed in sections 3.2.6 and 3.4.8. The weight of bio-oil in the sample in grams is w₃, EP is the endpoint of the sample and EP_BA is the triethanolamine/hydroxylamine blank. EP_BB is the endpoint of Blank B, EP_BC is endpoint of Blank C and the weight (g) of oil used in Blank C is w_BC:
         
      For bio-oil samples that contain mostly acetic acid, this is an unnecessary step.

결과

A typical titration curve consists of a single endpoint, as shown in Figure 2. Typical titrations for both a raw bio-oil sample, and a blank titration, are shown. As the endpoint lies at the inflection point in the titration curve; the endpoint can be easily identified by plotting the first derivative of the titration curve (shown on the right axis, dpH/dV, in Figure 2). Many automatic titration systems have software that calculates the derivative of the ...

토론

Representative titration curves are shown in Figure 2. A blank titration, as well as a titration for a pyrolysis oil sample, are shown. Furthermore, the first derivative of the titration curve (dpH/dV) is shown, which allows for easy recognition of the titration endpoint. The inset table on Figure 2 shows triplicate data for both pyrolysis oil and blank titrations, with average values and standard deviations. The endpoint values shown (in mL) are used in Section 4 to calculate the total ...

자료

Name	Company	Catalog Number	Comments
Analytical balance			accurate to 0.1 mg
dry block heater with magnetic stirrer, or hot water bath with magnetic stirrer
Automatic titrator			We used a Metrohm Titrando 809 automatic titrator, though other equivalent systems are acceptable
Deionized water
Ethanol (reagent grade)			CAS # 64-17-5
Hydroxylamine hydrochloride			CAS # 5470-11-1
Triethanolamine			CAS #102-71-6
Hydrochloric acid (37%)			CAS # 7647-01-0
Sodium Carbonate (primary standard)	SigmaAldrich	223484
4-(benzyloxy)benzaldehyde			CAS # 4397-53-9
Dimethyl sulfoxide			CAS # 67-68-5
5 mL glass Reacti-vials with solid lid and teflon spinvane	Thermoscientific	TS-13223
200 mL volumetric flask
Volumetric or mechanical pipettes