JoVE Science Education
Environmental Science
A subscription to JoVE is required to view this content.  Sign in or start your free trial.
JoVE Science Education Environmental Science
Determination Of NOx in Automobile Exhaust Using UV-VIS Spectroscopy
  • 00:00Overview
  • 01:08Principles of NOx Quantification in Automobile Exhausts
  • 02:41Preparation of Nitrite Stock Solution and Indicator Solutions
  • 04:10Preparation of Calibration Standards and Creation of a Standard Curve
  • 05:23Automobile Exhaust Sample Measurement
  • 07:38Applications
  • 09:32Summary

Determinación de NOx en los gases de escape de los automóviles mediante espectroscopia UV-VIS

English

Share

Overview

Fuente: Laboratorios de Margaret obrero y Kimberly Frye – Universidad de Depaul

En la troposfera, ozono se forma naturalmente cuando la luz del sol divide el dióxido de nitrógeno (NO2):

NO2 + luz solar → NO + O

Oh + O2 → O3

Ozono (O3) puede pasar al reaccionar con el óxido nítrico (NO) para formar dióxido de nitrógeno (NO2) y oxígeno:

NO + O3 → NO2 + O2

El resultado no hay ganancia neta de ozono (O3). Sin embargo, con la producción antropogénica de ozono formando precursores (NO, NO2y compuestos orgánicos volátiles) a través de la combustión de combustibles fósiles, se han encontrado niveles elevados de ozono en la troposfera. Escape del vehículo de motor es una fuente significativa de estos precursores de formación de ozono: NO, NO2y compuestos orgánicos volátiles (COV). Por ejemplo, fuentes móviles constituyen casi el 60% de las emisiones de NO + NO2 .

En las altas temperaturas encontradas la cámara de combustión de un automóvil, nitrógeno y oxígeno del aire reaccionan para formar óxido nítrico (NO) y dióxido de nitrógeno (NO2):

N2.g + O2 (g)→ 2 NO(g)

2 NO(g) + O2.g→ 2 NO2.g

El óxido nítrico (NO) emitido en los gases de escape del coche poco a poco se oxida a dióxido de nitrógeno (NO2) en el aire ambiente. Esta mezcla de NO y NO2 se refiere a menudo como NOx. Cuando NOx reacciona con compuestos orgánicos volátiles en la atmósfera en presencia de luz solar, formas de ozono troposférico, como se ve en este habían simplificado de reacción química:

NOx + COV + luz solar → oh3 + otros productos

Esta mezcla nociva de la contaminación atmosférica, que puede incluir aldehídos, peroxyacetyl nitratos, ozono, compuestos orgánicos volátiles y NOx, se llama smog fotoquímico. El ozono es el mayor componente del smog fotoquímico. Esta contaminación se encuentra en todas las ciudades modernas, pero se encuentra sobre todo en ciudades con climas soleados, calientes, seco y gran cantidad de vehículos de motor. El color amarillo-marrón de smog en el aire es debido en parte al dióxido de nitrógeno presente, ya que este gas absorbe luz visible cerca de 400 nm (figura 1).

A corto plazo que no2 exposición (30 minutos a 1 día) conduce a efectos respiratorios adversos en personas sanas y el aumento de los síntomas respiratorios en las personas con asma. NOx reacciona con el amoníaco y otros compuestos a las partículas de la forma. Estas pequeñas partículas pueden penetrar en los pulmones y causar problemas respiratorios, incluyendo bronquitis y el enfisema. Personas que pasan mucho tiempo en la carretera o que viven cerca de un camino de experiencia exposición considerablemente mayor a2.

Debido al impacto que tiene sobre la salud humana y el medio ambiente, la Agencia de protección ambiental de Estados Unidos (EPA) ha clasificado NO2 como un contaminante criterio y ha establecido el estándar primario a 100 ppb (percentil 98 de las concentraciones máximas diarias 1-h, un promedio de más de 3 años) y 53 ppb (media anual). Teniendo en cuenta que en carretera vehículos representan aproximadamente 1/3 de ninguna emisión dex en los Estados Unidos, las emisiones de automóviles se regulan por lo tanto a través de la ley de aire limpio. La EPA establece normas de emisión que fabricantes de automóviles deben seguir cuando se producen los coches. En la actualidad, normas de emisiones Tier 2 establece que los fabricantes no deben tener media flotax las emisiones de no más de 0,07 g/milla.

Fabricantes de una manera de cumplir con esta norma es mediante el uso de convertidores catalíticos en sus coches. Este dispositivo se coloca entre el motor y el tubo de escape. La corriente de escape pasa por el convertidor catalítico y se expone a un catalizador. Un catalizador de reducción de platino y el rodio se usa para reducir la concentración dex NO en el escape. Cuando una molécula de2 NO o NO en los gases de escape en contacto con el catalizador, el átomo del nitrógeno se agarró de la molécula y mantuvieron por el catalizador. El oxígeno se libera y forma O2. El átomo del nitrógeno en el catalizador se une con otro átomo de nitrógeno en el catalizador a forma N2.

Convertidores catalíticos han reducido grandemente las emisiones de NOx de escape coche – hasta 80% de reducción, cuando se realiza correctamente. Sin embargo, sólo funcionan cuando han alcanzado una temperatura bastante alta. Por lo tanto, al realizar un arranque en frío de un vehículo, del convertidor catalítico está quitando prácticamente no NOx. No es hasta el convertidor catalítico alcanza mayores temperaturas que elimina eficazmente el NOx de la corriente de escape. Convertidores catalíticos no funcionan en los coches de pasajeros diesel debido a las magras condiciones bajo las cuales operan. Además, el sulfuro en combustible diesel también desactiva el catalizador. NOx en motores diesel se reducen principalmente a través de la válvula de recirculación (EGR) de gas de escape que enfría la temperatura de los gases de combustión. Como resultado, los coches diesel emiten generalmente más NOx que los coches de gasolina.

Figure 1
Figura 1. Coloración característica de smog en California en la nube beige banco detrás del puente Golden Gate. La coloración marrón es debido al NOx en el smog fotoquímico.

Principles

Procedure

1. preparación de solución madre de nitrito (NO2–) Pesa 1,500 g NaNO2 y agregar a un matraz aforado de 1 L. Diluir hasta la marca usando el nanopure agua. (Compruebe el agua destilada del grifo – puede contener suficiente nitrito para interferir con las mediciones). Esto no produce una 1.000 μg solución2–/ml. Para hacer un 5.0 μg2–/ml solución, no tomar 1 mL de los 1.000 μg2 -/mL solució…

Results

Table 2 provides an example of proper results. Using the absorbance measurements of the standard solutions, a plot of Absorbance vs. Concentration of NO2can be made (Figure 4). Then, the best fit line of the data can be determined. Using the best-fit line of the standard curve, the concentration of NO2 in each unknown solution (µg/mL) can be calculated. This value can be converted to the concentration of NO2 in the exhaust gaseous sample using the following equation:

Equation 1

Based on the balanced equation of NO2 in H2O seen previously, a 2 mol NO2/1 mol NO2 ratio is expected. In empirical experiments, it has been found to be nearer a 1.39:1 ratio. The volume of solution used was 25 mL. The volume of the gas sample was 35 mL.

The concentration of NO2 calculated actually represents all of the NOX in the exhaust sample (Table 3). The equation for conversion between ppmV and µg/L depends on the temperature and pressure at which the samples were collected. The conversion equation is:

Equation 2

Where R = universal gas constant = 0.08206 atm·L/mol·K, P = atmospheric pressure in atm, T = temperature in K, and MW = molecular weight of NOx (as NO2) = 46.01 g/mol. Therefore,

Equation 3

It’s important to input T in K and P in atm.

Sample Absorbance
0.2 µg NO2/mL standard 0.22
0.4 µg NO2/mL standard 0.43
0.6 µg NO2/mL standard 0.60
0.8 µg NO2/mL standard 0.79
1.0 µg NO2/mL standard 1.05
Diesel Car Exhaust (upon startup) 1.03
Diesel Car Exhaust (after running 10 min) 1.03
Gasoline Car Exhaust (upon startup) 0.10
Gasoline Car Exhaust (after running 10 min) 0.04

Table 2. Data table with representative results of absorption.

Figure 4
Figure 4. A standard curve plot of Absorbance vs. Concentration of NO2.

Vehicle NOx Concentration (ppm)
Diesel Car (upon startup) 500
Diesel Car (after running 10 minutes) 500
Gasoline Car (upon startup) 48
Gasoline Car (after running 10 minutes) 21

Table 3. NOx concentration (ppm) per vehicle.

Applications and Summary

The measurement of nitrite using the modified Saltzman reaction is very common and useful in many different fields. As described, the method can be used to measure NOx concentrations in air samples – car exhaust, laboratory rooms, air quality of cities, etc. In addition, this method can be used to monitor NOx in cigarette smoke. The procedure would be very similar to this experiment, except instead of drawing car exhaust into the syringe, cigarette smoke would be drawn in. There is often a higher concentration of NOx in cigarette smoke than coming out of the tailpipe of automobiles, which tends to be surprising to many. Typical values for NOx in cigarette smoke range from 500-800 ppm.

This method can also be used to test the levels of nitrate produced in the presence of nitrification bacteria. Nitrification bacteria are found in soil and water and play an important role in the nitrogen cycle – oxidizing ammonia to nitrite and then nitrate. The nitrate in the sample is first converted to nitrite by the enzyme nitrate reductase. Then the nitrite is measured using the modified Saltzman reaction. Lastly, this method can be used to determine the concentration of nitrates and nitrites in food products. Nitrites and nitrates are added to food mainly to preserve meats and meat products. A typical value for nitrite in cured meats is approximately 125 µg/mL.

Transcript

A mixture of nitric oxide and nitrogen dioxide is generally referred to as NOx. As a by-product found in automobile exhaust, NOx can be harmful to the environment, forming damaging tropospheric ozone.

At high temperatures in the combustion chamber of an engine, nitrogen and oxygen from the air can react to form nitric oxide and nitrogen dioxide. In the presence of sunlight, NOx reacts with volatile organic compounds in the atmosphere to form ozone and other products. Tropospheric ozone is a health risk, potentially causing lung and eye irritation amongst other complaints, and it is a major component of photochemical smog.

This video will illustrate the principles behind NOx and tropospheric ozone production, how to fabricate indicator solutions, and how to measure and quantify NOx production from automobile exhausts.

On-road automobiles account for approximately one-third of NOx emissions in the US, and emissions are strictly regulated through the Clean Air Act. Catalytic converters, located between a car’s engine and tailpipe, can reduce NOx concentration in the exhaust significantly, but these require high temperatures to function, so will only reduce NOx after an automobile has been running long enough to warm the converter.

Because of this difference in the ability of catalytic converters to remove NOx at different temperatures, NOx emissions are typically read upon vehicle start up, and after running for 10 min. This gives a quantification of the NOx emission produced by the automobile, and also an indication of the ability of the catalytic converter to remove the NOx.

When NOx is added to a solution containing sulfanilic acid and naphthyl-ethylenediamine, the resultant reaction forms a pink colored azo dye molecule. The intensity of this pink is directly proportional to the concentration of NOx in the solution, and can be measured using a UV-VIS spectrophotometer to give a quantification of the amount of NOx when plotted against standards in a calibration curve.

Now that we are familiar with the process of NOx formation, let’s look at how NOx production by automobiles can be quantified in an experimental setting.

To begin the experiment, detection solutions that will react with the NOx should be prepared. To prepare the nitrite stock solution, first weigh out 1.5 g of sodium nitrite and add it to a 1-L volumetric flask. Add nitrite-free water to the 1 L mark on the flask. This produces a stock solution of 1,000 μg nitrite per mL. Label this stock solution appropriately. To make a working solution of 5 μg nitrite per milliliter, take a fresh flask and add 1 mL of the stock solution. Dilute to 200 mL.

To prepare the NOx indicator solution, first weigh out 5 g of anhydrous sulfanilic acid, and add to a 1-L volumetric flask. To the same flask, add 500 mL of nitrite free water, then 140 mL of glacial acetic. Swirl the solution, until the sulfanilic acid dissolves.

Next, weigh out 20 mg of naphthyl-ethylenediamine and add it to the flask. Finally, fill the flask to the 1-L line with nitrite free water. Transfer the solution to a dark bottle to prevent photodecomposition, stopper tightly, and label appropriately.

To generate a standard curve, calibration standards need to be created. First, put 1 mL of the 5.0-μg nitrite stock solution into a 25-mL volumetric flask and dilute with the NOx indicator solution to the calibration mark. This makes a 0.2 μg NO2-/mL standard solution.

Next, prepare 0.4, 0.6, 0.8, and 1 μg NO2-/mL standard solutions by adding 2, 3, 4, and 5 mL nitrite solutions to separate 25-mL flasks, and fill each to the mark with NOx indicator solution.

Using a UV-VIS spectrophotometer, set the instrument to read absorbance. Next, set the wavelength to 550 nanometers. Add the NOx indicator solution to a clean spectrophotometer sample cell, and use this to zero the spectrophotometer. Finally, measure the absorbance of the five standard solutions, and record the values.

To begin the readings, start the diesel-powered automobile. Take a 60 mL gas-tight syringe and insert it a few inches into the tail pipe, taking care to avoid burns or inhaling fumes. Draw in and expel the exhaust twice to condition the syringe.

Next, draw 25 mL of the NOx indicator solution into the syringe. Expel any air from the syringe without spilling the indicator solution. Finally, draw 35 mL of exhaust into the syringe, pulling the plunger to the 60 mL mark, then withdraw and cap the syringe.

Shake the solution in the syringe by hand for 2 min. Cover the syringe with aluminum foil. Finally, measure the air temperature at the sample tail pipe. Repeat the sampling process with a gasoline powered automobile, and any other model or design of automobile desired.

Repeat the experiment after the vehicles have been running for at least 10 min. Once all the samples have been collected, wait 45 min to allow color to develop. Finally, expel the gas from the syringes, and place the sample indicator solutions into individual cuvettes. Measure the absorbance using the spectrophotometer set at 550 nm, and record the values.

Using the absorbance measurements of the standard solutions, make a plot of absorbance versus concentration of nitrite. Determine the best-fit line of the data. Using this best-fit line, calculate the concentration of nitrite in each test solution. This value can then be converted to nitrogen dioxide in the exhaust.

The concentration of nitrogen dioxide calculated actually represents all of the NOx in the exhaust sample. The ppmV, or parts per million by volume to μg/L conversion is dependent on the temperature and pressure at which the samples were collected.

Automobiles are not the only source of NOx. Monitoring its production is important in a wide range of fields.

Cigarette smoke often contains a higher concentration of NOx than emitted from automobile engines. Typical values for NOx in cigarette smoke range from 500-800 ppm, compared to 21-48 ppm for emissions from a gasoline car, or around 500 ppm for a diesel vehicle. This can result in a variety of personal health issues, including bronchitis, irritation of the nose and throat, respiratory infections, or blocking of oxygen transfer in the bloodstream. NOx levels in cigarette smoke can also be quantified using the methods shown in this video.

Nitrifying bacteria are found in soil and water, and play an important role in the nitrogen cycle, oxidizing ammonia to nitrite and then nitrate. As with exhaust fumes and cigarette smoke, the NOx levels in soil can also be examined and quantified colorimetrically.

Nitrates and nitrites can also be found in measureable amounts in food products. For cured foods, nitrates and nitrites may be added as a preservative, most commonly in meats and meat products. These have antimicrobial as well as color-fixing and preservation actions, and a significant indirect beneficial effect on flavor. However, too high of nitrite content can lead to medical complications including infant methemoglobinemia, or cause shortened shelf life of products due to effects like nitrite burn. Nitrite contents in cured foods therefore should be monitored closely, and this can be carried out using a modified version of the colorimetric test.

You’ve just watched JoVE’s introduction to the determination of NOx. You should now understand how NOx is formed in automobile engines, how to formulate NOx indicator solutions, and how to measure and quantify NOx from vehicle exhaust fumes.

Thanks for watching!

Tags

Cite This
JoVE Science Education Database. JoVE Science Education. Determination Of NOx in Automobile Exhaust Using UV-VIS Spectroscopy. JoVE, Cambridge, MA, (2023).