This action might not be possible to undo. Are you sure you want to continue?
through the process of diazotization. The process involves using nitrous acid, HNO2, to create the nitrosonium ion, N=O+. The nitrosonium ion is eventually turned into a diazonium salt by reacting it with an aromatic amine. Since the diazonium ion is a weak electrophile, it reacts with electron-rich, aromatic coupling agents to produce an azo dye. The products are mainly ortho and para due to the reaction being an electrophilic aromatic substitution.
In this experiment, p-nitroaniline was reacted with HCl and NaNO2 to produce the diazonium ion, which was then reacted with 2-naphthol to create the azo dye, Para Red. The diazo component, p-nitroaniline reacted with hydrochloric acid to produce a salt. The salt then reacts with the sodium nitrite. Losing water, after two proton transfers, produces the diazonium ion. Sodium 2-naphthoxide reacts with the diazonium ion to produce the azo dye.
Procedure Chemical p-nitroaniline 2-naphthol hydrochloric acid sodium nitrite sodium hydroxide sulfuric acid Part A: Dissolve 10 mmol of the phenol coupling component in 20 mL of 1 M NaOH in a 125 mL Erlenmeyer flask. Cool the solution in an ice/salt bath 0° C. Part B: Diazotization of an Aromatic Amine Wear gloves and work under the hood when performing this procedure. Dissolve 10 mmol of the assigned diazo component in 8 mL of 3 M HCl. Heat the solution gently. If necessary add up to 10 mL of water in order to dissolve the solid. After the solid has dissolved cool the solution to 0° C in an ice/salt bath with stirring. While stirring add 10mL of freshly prepared 1.0 M NaNO2. Adjust the rate of addition so that the temperature does not rise above 10° C. Test the solution with starch iodide paper. If the paper does not immediately turn blue-violet, add 1.0 M NaNO2 dropwise until the paper turns blueviolet. The diazonium salt must be used immediately. While stirring add the diazonium salt solution to the solution of the coupling component from Part A. Allow the solution to remain in the ice bath for 15 minutes until the crystallization is complete. Collect the diazo dye by vacuum filtration. Dry the crystals in a vacuum oven at 80 ° C before weighing. Part C: Direct Dyeing with the Azo Dye Suspend 0.5 g of the dye in 100 mL of hot water. Acidify the solution with a few drops of H2SO4. Obtain two pieces of special cloth containing strips of different fabrics. Submerge the cloth in the dye solution for 10 minutes. Remove the cloth, rinse with cold water and allow the fabric to air dry. If the fabric does not appear to pick up the dye it may be necessary to adjust the pH with dilute HCl or NaOH. To test for fade resistance wash one of the dyed pieces of cloth with detergent five times. Compare the colors of the fabrics after drying. Part D: Recording the UV-Visible Spectrum of the Dye. Dissolve 100 mg of the dye in 100mL of ethanol using a 100mL volumetric flask. Record the spectrum from 800-350 nm in 25 nm intervals. It may be necessary to dilute the dye solution to keep the spectrum on scale. Part E: Determining the pH Range of the Dye Transfer 1mL of the solution from part D to a 10mL volumetric flask using a volumetric pipette. Fill the flask to the mark with ethanol. Add two drops of the dye solution to 20 mL of deionized water in a small beaker. Swirl the solution to mix thoroughly. Divide the solution into 3 test tubes. Record the color of the solution and the pH using pHydrion paper for test tube #1. To test tube #2 add dropwise 0.1 M HCL, swirling well after each addition, until a color change occurs. Record the color and pH of test tube #2. To test tube #3, add 0.1 M NaOH dropwise, swirling well after each addition, until a color Amount 1.381 g 1.442 g 8 mL 10 mL 20 mL 5 mL
change occurs. Record the color and pH of test tube #3. Determine whether or not the dye prepared would be a good acid-base indicator. If so indicate the pH range of the indicator activity. Part F: Determining the Antibacterial Properties of Dye Obtain two Hinton Mueller agar plates, a broth culture of Staphylococcus aureus and Escherichia coli, 2 sterile swabs, a pair of forceps and a Petri dish containing sterile blank disks. Swab the first agar plate with Staphylococcus aureus and the second agar plate with Escherichia coli. Cover every square mm of the plate. Label the plates. Dissolve 30 mg of the dye in 10 mL of deionized water. Dip a sterile disk into the dye solution using a pair of forceps. Place three disk equally space on each plate. Incubate the plates for 48 hours. Measure the zone of inhibition around each disk. The larger the zone of inhibition the more effective the dye is at controlling bacterial growth. Dispose of all plates and broth as biohazard waste. Results Data Actual Yield 2.147 g Theoretical Yield 2.932 g Percent Yield 73.23%
Theoretical Yield 1.381 g p-nitroaniline mol 138.124 g 293.277 g azo dye mol = 2.932 g azo dye
Percent Yield % Yield = (Actual/Theoretical) x 100 2.147 g 2.932 g x 100 = 73.23%
Direct Dyeing with the Azo Dye Fabric Spun Diacetate Bleached Cotton Spun Polyamide Spun Polyester Spun Polyacrylic Worsted Wool Acid - Unwashed yellow pink yellow pink pink red Acid - Washed bright yellow white yellow pink pink light yellow Base - Unwashed bright yellow white yellow pink pink light yellow Base - Washed yellow purple yellow purple purple dark yellow
Determination of the pH Range of the Dye pH Range Test Initial Solution 0.1M HCl 0.1M NaOH Color pale orange pale orange purple pH 6 1 10
UV-visible Spectrum Absorbance nm Absorbance 800 0.003 775 0.004 750 0.003 725 0.003 700 0.003 675 0.004 650 0.005 625 0.006 600 0.007 nm Absorbance 575 0.011 550 0.034 525 0.295 500 0.692 475 0.706 450 0.529 425 0.661 400 1.533 375 2.188 350 1.891
Discussion Para Red is an example of an azo dye and was the first azo dye used. The vivid colors of azo dyes are due to the delocalization of electrons in the aromatic rings and the nitrogen-nitrogen double bond (the azo bond). Several types of fabric were tested for colorfastness of the azo dye before and after being washed. Spun diacetate is a cellulose fabric that has been modified to remove many OH-groups found on the surface of the threads. Cotton is natural cellulose found in plant material. Nylon is a synthetic material made of many linked amide groups, somewhat similar in structure to wool or silk. Polyester (Dacron) is a synthetic material made from many linked ester groups. Acrylic (Orlon) is another synthetic fabric made from many acrylonitrile (CH2=CHCN) units linked together. After dyeing all previous fabrics mentioned with the azo dye, only the spun polyamide remained colorfast when dyed with both acidic and basic solution. The spun polyester and polyacrylic remained colorfast when dyed in the acidic solution, and the remaining fabrics remained colorfast in neither acidic nor basic solution. The visisble spectrum absorbance of the azo dye was tested using spectroscopy. When a compound absorbs a portion of the visible spectrum, it appears colored. If no visible light is absorbed, the compound appears colorless or white. The apparent color of the compound is due to the portion of
the visible spectrum that is not absorbed. Different azo dyes absorb light of different wavelengths due to their different structures. For example, more highly conjugated systems will absorb light with longer wavelengths (lower frequency, lower energy). Also, having an electron-donating and an electronwithdrawing group para to each other on an aromatic ring increases both the wavelength of absorption and the intensity of the absorption. However, Para Red has two electron-withdrawing groups para to each other on the aromatic ring, meaning it should absorb shorter wavelengths of light (higher frequency, higher energy). When tested, Para Red absorbed violet light, around 400 nm-1. This azo dye can act as an acid-base indicator because the structures of its acid and conjugate base forms absorbed light at different wavelengths. The conjugate base form was a purple/violet color, while the acid form was pale organge. However, the neutral solution was also pale orange. This means, as an indicator, Para Red would show no color change when added to an acidic solution. The azo dye would not be the most desirable indicator, but can partially function as one. The anti-bacterial properties of the dye were tested using agar dishes and two bacteria. Staphylococcus aureus and Escherichia coli were swabbed on the dish and the dye was place on the dish in several spots. The azo dye was shown to be ineffective at preventing the growth of the bacteria on the plate.
This action might not be possible to undo. Are you sure you want to continue?