Chapter 3: Methodology 3.0 Preparation of Polyaniline 1 0.2 M Aniline hydrochloride was oxidized with 0.25M ammonium peroxydisulfate in an aqueous medium. Firstly, the Aniline hydrochloride was dissolved in distilled water in a volumetric flask to obtain 50mL of the solution. The same step was repeated with Ammonium peroxydisulfate. Both solutions were stored for 1 hour at room temperature and then mixed in a beaker, stirred and left to polymerize. A day later, the PANI precipitate was collected on a filter and washed with three portions of 100mL of 0.2M HCl, and then with the same amount of acetone. The Polyaniline hydrochloride was dried in air and then in a vacuum at 60 degrees Celcius. These reaction and processing conditions are the standard …show more content…
The mentioned ratio of the two materials were collected in a quartz crucible. Next, de-ionized water was added into the quartz crucible containing the nickel nitrate and urea. The de-ionized water was poured until it made up 50% of the portion of the solution After that, the entire solution was placed in an oven for about 1 hour. This was done to age the mixture and the temperature was maintained at 80oC. The solution was then taken out of the oven to be put in a pre-heated muffle furnace which was maintained at 650oC. This was done for the calcination of the solution. After 2 hours, the quartz crucible was removed from the furnace to be cooled down to ambient temperature. The mixture of nickel nitrate, urea and de-ionized water was grinded for four hours after being removed. Preparation of Nickel Oxide
The purpose of the lab is to acquire the percent composition of zinc and copper. The procedure included obtaining a post 1983 penny and washing it with soap and water. Using a triangular file, we made an X on the penny. Then, we cleaned the top and bottom of the penny with steel wool until it was shiny. We rinsed the penny in acetone and dried it with paper towel.
While the solution dissolved, 50 mL of distilled water was added to a 150 mL beaker and heated on the hot plate. When the solution started to boil 2.65 grams of Na2SiO3*5H2O was added to the beaker with a stir bar and heated to a gentle boil. When both solutions began to boil, the sodium silicate solution was slowly added to the sodium aluminate. The solution was kept at 900C for 60 minutes and stirred with stir bar. After 60 minutes, the zeolite solution was cooled for 5 minutes and for the magnetized zeolite , 0.78 grams of FeCl3 and 0.39 grams of FeSO4*7H2O was added to the flask and stirred until the iron parts dissolved.
Discussion 1. Zn0 (s)+ Cu2+S6+O42-(aq) →Cu0(s) + Zn2+S6+O42-(aq) Zn0(s) → Zn2+(aq) + 2e- Cu2+(aq) + 2e- → Cu0(s) Zn0(s) + Cu2+(aq) → Zn2+(aq) + Cu0(s) Oxidant (oxidizing agent) is the element which reduces in experiment.
The difference in this chemical and physical properties will aid in their separation. Processes like solubility, gravitational filtration and recrystallization will be used to separate the substances present in Panacetin. The melting and boiling point of the substances will help in concluding on which of these compounds will be presented at the end of experiment. Procedure and observation The Panacetin content was weighed approximately 3.0493g and transferred to the Erlenmeyer flask; 75ml of dichloromethane (CH¬2CL2) was added to the content. The dichloromethane (CH2Cl2) dissolved the sucrose, leaving the active unknown agent and aspirin behind.
How to cook the perfect Boston butt in the oven Pork is the most popularly consumed meat in America and there is no surprise as to why. I mean, who doesn’t love slow cooked, delicious, BBQ? Whether you prefer sliced, chopped, or pulled pork; a Boston butt is the absolute best cut of meat for the job. It is tender, juicy, deliciousness just waiting to be topped with a well-balanced sauce or stuffed into a potato. But how often do you truly have the time to hunt down the best BBQ or venture to your favorite BBQ restaurant?
Prepare the standard solution of FeSCN2+ pipetting 18 mL of 0.200 M Fe(NO3)3 in a 20 * 150 mm test tube labeled five. Pipet 2 mL 0.0020 M KSCN into the test tube and stir. 6. Prepare a blank. Fill the plastic cuvette ¾ full with distilled H2O. Properly clean the cuvette and handle only by the top ribbed edge while wearing gloves.
The nitronium ion mixture was slowly added to the concentrated sulfuric acid methyl benzoate mixture to prevent vigorous reaction that if present could lead to unwanted dinitro by-products. The mixture after settling and heating to room temperature was poured over ice in order to rapidly cool the sample inducing formation of the crystals. The water was allowed to melt before it was vacuum filtered to neutralize the acid that might be remaining
Abstract In this experiment, the reaction kinetics of the hydrolysis of t-butyl chloride, (CH3)3CCl, was studied. The experiment was to determine the rate constant of the reaction, as well as the effects of solvent composition on the rate of reaction. A 50/50 V/V isopropanol/water solvent mixture was prepared and 1cm3 of (CH3)3CCl was added. At specific instances, aliquots of the reaction mixture were withdrawn and quenched with acetone.
Put the beaker with the water and the metal on the wire gauze of the ring stand that has the bunsen burner under it. Fill the graduated cylinder with enough water to about fill the calorimeter and record the amount of water and the temperature of the water that is in the graduated cylinder. When the water starts to boil in the beaker, use the thermometer to record the temperature of the water. Pour the water from the graduated cylinder into the calorimeter. Use the crucible tongs to take the metal out of the beaker and place the metal into the calorimeter and close the
The product obtained was (2S, 3R)-2, 3-dibromo-3-phenylpropanoic acid and (2R, 3S)-2, 3-dibromo-3-phenylpropanoic acid, which are enantiomers. This was determined through melting point analysis. The melting point range for the product was 198 to 202 degrees Celsius, which is a lot close to the given melting point of the anti-addition product, 202-204 degrees Celsius. The given melting point range was 93.5-95 degrees Celsius. Furthermore, the syn-addition product is unlikely and difficult to produce due to stereochemistry selectivity.
Weighed 1 gram of NaC2H3O2 and mixed it with ionized water. Boiled 12 mL of 1.0M Acetic Acid added into a beaker containing the sodium carbonate on a hot plate until all the liquid is evaporated
First, two grams on an unknown white compound were given. The possible compounds the known could be were CaCO3, KNO3, NH4Cl, CaCl2, K2SO4, (NH4)2SO2, Ca(NO3)2, NaC2H2O2, K2CO3, MgCl2, Na2CO3, 0.1 M AgNO3, MgSO4, NaCl, 0.2 M BaCl2, KCl, NaSO4, Mg(s), HCl, HNO3, NaOH, HC2H3O2, H2SO4, and KOH. The solubility test required using a scale to measure .575 of our unknown white compound. The unknown compound was measured in a 100 mL beaker.
Paragraph 1 The objective of the experiment is to test; how will water temperature affect the rate of reaction of an alka-seltzer tablet? The dependent variable of the experiment is the dissolving time. When an alka-seltzer tablet starts to fizz it begins to dissolve, due to the citric acid and sodium bicarbonate the tablet contains (Clark, “Why does Alka-Seltzer fizz?).
Stoichiometry of a Double Displacement Reaction The objective of this lab is to find the percent yield of a product of a double displacement reaction. Procedure: Refer to handout entitled “Stoichiometry of a Double Displacement Reaction” Materials: Refer to handout entitled “Stoichiometry of a Double Displacement Reaction” Data & Observations: Data Table Calculated Molar Mass of CuSO4•5H2O 249.677 g Calculated Molar Mass of CuO 79.545 g Starting mass of CuSO4•5H2O 2.050 g Mass of 100-ml beaker and filter paper 52.600 g Mass of 100-ml beaker, filter paper, and CuO precipitate 53.450 g Calculations:
Weight a clean, dry, porcelain evaporating dish on the electric balance and record this mass on an appropriate data table. If the crucible needs to be washed before use, then heat the crucible in the Bunsen burner flame for a few minutes and remove any residual water. Then allow it to cool before continuing. Fill the crucible about 1 gram with the hydrated salt and reweight. Assemble the ring stand, ring, clay triangle, and Bunsen burner