Name

Lab Day

Laboratory Techniques

Procedure: Laboratory Burners. Essentially all single-barrel burners used in

chemical laboratories are Bunsen burners or some modification of that burner that was invented by the German chemist, Robert Bunsen (1811 – 1899) . One common burner used at Chemeketa C C is a modification of the Bunsen burner called a Tirrill burner (see below).

These burners make possible the complete combustion (nearly) of gaseous fuels by providing the proper ratio of fuel to air and the correct mixing of these gases in the barrel of the burner. Since this type of burner is used in many chemical experiments, it is important that you understand its operation and its adjustments in order to obtain the maximum efficiency.

A flame is produced by the chemical reaction of two gases, a fuel and oxygen (in the air). The temperature of a flame is dependent mainly on two factors: the nature of the fuel, and on the rate and completeness of mixing and burning of the gases.

Natural gas is composed largely of methane (CH4). Methane burns to form carbon dioxide and water in an unlimited supply of oxygen. The chemical equation for the reaction is:

CH4 + 2 O2 → CO2 + 2 H2O methane oxygen carbon dioxide water

If oxygen is limited, considerable amounts of free carbon is formed. The very small particles of carbon are heated to incandescence. This produces a luminous flame or the yellow carbon flame. The equation for this reaction is:

CH4 + O2 → C + 2 H2O

In cases when there is insufficient oxygen combining with methane, some of poisonous gas carbon monoxide is formed. This is another example of the incomplete combustion of methane. The reaction showing this formation of carbon monoxide is:

2 CH4 + 3 O2 → 2 CO + 4 H2O

First, let’s begin adjusting the gas supply and air inlet. These are both screw-type adjustments that do not allow for rapid adjustments.

Connect the burner with the laboratory supply of natural gas by using a piece of rubber tubing. A burner is usually lit with the air vents nearly closed. The vents are closed by turning the barrel of the burner in a clockwise direction. After the gas has been turned on and lit, the size and the quality of the flame is adjusted by admitting air and regulating the flow of gas. Air is admitted by rotating the barrel; gas is regulated with the needle valve. Insufficient air will cause a bright yellow, smoky flame; too much air will cause the flame to be noisy and blow itself out. A Bunsen burner flame that is best for most purposes is shown below; such a flame is said to be nonluminous. The hottest part of the flame is just above the bright blue cone.

Glassworking. Place any broken glass in the container provided. Some of the experiments that you will do will require construction of simple glass apparatus. In preparing for these experiments, you will need to become familiar with the various manipulations of glass tubing. Improper techniques may result in an apparatus that does not work well, or may result in nasty cuts.

(1) Cutting of glass tubes (or rods). Place on your lab bench desk top a piece of 6 mm glass tubing about 12 cm long. Make a deep

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scratch across the tube with one stroke using a triangular file. If the file is dull, several strokes may be required – all strokes should be in the same direction, do not saw the glass. Grasp the tube with both hands, turn the tube so that the scratch is away from you and your thumbs are opposite the scratch. Pull your arms back along side of your body and bend the tube outward. This, with a little practice will give a clean right angle break. Use the same procedure in cutting glass rods.

(2) Fire-polishing. The glass tubes and rods that you have just cut need to have the sharp edges smoothed. Hold the ends of the glass tubes in your burner. Rotate the tube slowly until the glass starts to melt and the sharp edges are smooth. Do not heat the tubes so much that the opening becomes constricted. Careful! This glass is hot!

(3) Bending Glass Tubing. Put a flame spreader on your burner and adjust the flame so that a sharply defined region of intense blue color is visible. Heat a piece of 6 mm glass tubing by rotating it in the flame until it begins to sag. When the glass tube feels flexible, remove the tube from the flame and bend it rapidly to 90º. Hold the bent tube at this angle until it hardens and then place it on an insulating surface (Ceramfab pad or wire gauze). Many poor bends are the result of uneven or excessive heating and failure to continue to rotate the tube in the flame. Practice making several bends of different angles and have the instructor check them. Some good and bad bands are shown below:

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good bends

not so good bends

(4) Construction of a glass spoon. As a final exercise in glass manipulating, try making a glass spoon by following the following steps. You will probably need a Fisher burner (the Bunsen burner’s big brother) to get the glass hot enough for the procedure.

1. Using about a 20 cm piece of 6 mm tubing, fire-polish one end normally, for the other end fire-polish until it completely seals shut.

2. Remove from the flame and blow a small bubble.3. Direct a tiny flame on one side of the bubble. Heat and

then remove from flame. 4. Suck in gently, forming spoon5. Cut off the handle at a handy length and seal shut the

opposite end from the bubble you made in step 2.

(5) Inserting glass tubing into a rubber stopper. Lubricate the hole in the rubber stopper with glycerol (also called glycerine), Grasp the fire-polished tubing about 1 cm from the end to be inserted. Holding the lubricated stopper in the other hand, start the tubing into the hole by gently twisting it, and gradually work it all the way through the stopper. Do not grip the tubing much more than 1 cm from the stopper since gripping a greater distances will break the tubing and poke your hand. The end of the tube should stick-out a couple of mm from the stopper so that any liquids passing through the tubing do not touch the rubber. Wipe the excess glycerol off with a paper towel.

Evaporation. Prepare a water bath by filling a 400 mL beaker about half full of water and placing the beaker on a hot plate. Turn the hot plate on high until the water boils, then turn the heat down keeping the water boiling at all times. You may have to add additional water to the beaker during the evaporation process. Cover the bottom of a standard test tube with a small amount of sodium chloride. Add distilled water until the test tube is about ¼ full and stir with a glass rod until the salt dissolves. Pour the sodium chloride solution into an evaporating dish and place the dish on top of the 400 mL beaker with the boiling water in it. If you have a small evaporating dish, you may have to use a smaller beaker so the dish fits without falling into the beaker. Heat the evaporating dish until all of the water has evaporated from the sodium chloride solution, leaving the sodium chloride as a residue. Flush the sodium chloride residue down the sink.

Filtration. Separating suspended solids from liquids is accomplished by the use of filters. Insoluble solids called residues or precipitates form during the course of some chemical reactions. In lab, these residues are separated from solutions by filtering them out on a paper filter. The liquid that passes through the paper is called the

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filtrate. Fill a regular test tube about ½ full of lead(II) nitrate solution. Fill a second test tube about ¼ full of potassium chromate solution. Pour the first test tube contents into a 100 or 150 mL beaker. Slowly pour the second test tube contents into the beaker and observe the results. The yellow precipitate (residue) that forms is lead(II) chromate. Fold a circle of filter paper in half, then fold it in half again. Open the paper into a cone. Place the cone of filter paper into a funnel, wet the paper with distilled water to allow the paper to cling to the funnel and remain opened. Clamp the funnel and filter paper cone to a ring stand or support it with a iron ring (or just hold it). Place a small beaker beneath the funnel to catch the filtrate. Stir the yellow lead(II) chromate solution and pour it into the filter paper cone. Do not over-fill the filter paper cone. After you have filtered all the yellow solution, compare the residue (on the filter paper) with a sample of solid lead(II) chromate that you will find on the lab supply cart. Lead(II) chromate is toxic and should not be flushed down the sink. Use your forceps to remove the filter paper with the yellow residue on it from your funnel and place the paper and all in a waste jar on the lab supply cart. The rest of the yellow residue can be washed down the sink.

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Name

Date

Report for Experiment

Laboratory Burners and Glassworking

Articles Instructor’s Check

Straight tubes (2)

Right-angle bends (2)

Spoon (1)

Questions & Problems

1. Why is it necessary to turn off the gas with the gas cock rather that with the value on the burner?

2. Why is air mixed with gas in the barrel of the burner before the gas is burned?

3. How would you adjust a burner with:

(a) has a yellow and smoky flame?

(b) is noisy with a tendency to blow itself out?

4. Why are glass tubes and rods always fire-polished after cutting?

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5. Explain how to insert glass tubing into a rubber stopper.

6. What is the name of the lubricant used for inserting glass tubing in a rubber stopper?

Evaporation

7. What is the name of the residue remaining after evaporation?

Filtration

8. what is the name and color of the precipitate recovered by filtration?

name

color

9. Why is the filter paper with the precipitate on it collected in a jar instead of thrown into the trash?

10. What is the main substance in the filtrate?

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