The equipment used for preparation the extraction unit are shown in Figure 1. The pH of aqueous solution containing 10 μg L−1 of Cd (II) and 50 μg L−1 of Pb (II) was adjusted with HNO3 and NaOH (0.1 M). Then 2 mL of this solution was poured into the syringe. Afterward, 2 mg of NDNPG was added to the extraction unit and immersed in an ultrasonic bath for 60 s to disperse the NDNPG in the sample solution and increase the contact surface between the adsorbent and solution. After sonication, NDNPG was separated from sample solution easily by pressing the plunger, the sample solution from the syringe came out and NDNPG adsorbent remain in the syringe. In the next step, for removing interference, the sorbent was washed with distilled water. Then, …show more content…
For this method, 0.2 g hair was weighed and it was placed in to a beaker. Then, 2 mL of a mixture of HNO3 and H2O2 with a ratio of (2:1, v/v) was added in to beaker and it was placed at room temperature for 10 minutes. Next, the solution was heated on an electric hot plate up to precipitate obtained. The resulting precipitate was dissolved in 10 mL distilled water and the solution was filtered with a Whatman No. 42 filter paper.
Result and discussion
Synthesis of nitrogen doped nanoporous graphene
Nitrogen Doped Nanoporous Graphene (NDNPG) was produced by a chemical vapor deposition (CVD) method with using aniline (AN) and methane as nitrogen and carbon sources over Fe- Mo/MgO catalyst. The catalyst was placed in a quartz boat and then placed in a quartz tube. To grow NDNPG, methane as the carbon source with a flow rate of 50 ml min-1 passed through aniline (as nitrogen source) in gas washing bottle at 〖40〗^℃, and hydrogen, with a flow rate of 250 ml min-1 at 〖1000〗^℃ , was used as carrier gas, for 60 min. The catalyst was activated by hydrogen stream at the flow rate of 300 ml min-1 for 180 min. The furnace, under the nitrogen atmosphere, was cooled down to room temperature and a black product was formed after the end of the reaction.Fig. 3 SEM images of NPNDG at low (a) and high (b)
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Two-step purification method was used for removing such impurities. In the first step, 10 g of the pristine NDNPG sample was added to 150 ml of an 18% HCl solution and were mixed for 16 hours at ambient temperature. Then, the mixture was filtered and washed many times with distilled water to be neutralized. In second purification step, the resulting materials dissolved in 6 mol L-1 nitric acid for 3h at 〖70〗^℃. Then, the washing step was repeated with HNO3 solution. The resulting cake was dried at 〖80〗^℃, for 12
Ge doped fullerene has the highest low frequency values among all of these compounds, this compound has the largest force constants. Higher values of low frequencies obtained for doped fullerene interacting with glycine can be regarded as a higher protection from thermal decomposition of thus molecules. Zero-Point Vibrational Energy (ZPE) for fullerene doped Silicon (Si) interacting with glycine is greater than Germanium (Ge) doped fullerene - glycine molecules. These molecules show that the relative thermal stability of fullerene doped with Si is higher than C19Ge-glycine compound are listed in Table 3. The Infrared vibrational frequencies are computed to further provide the
In this lab, the oxidation of a secondary alcohol was performed and analyzed. An environmentally friendly reagent, sodium hypochlorite, was used to oxidize the alcohol, and an IR spectrum was obtained in order to identify the starting compound and final product. The starting compound could have been one of four alcohols, cyclopentanol, cyclohexanol, 3-heptanol, or 2-heptanol. Since these were the only four initial compounds, the ketone obtained at the end of the experiment could only be one of four products, cyclopentanone, cyclohexanone, 3-heptanone, or 2-heptanone. In order to retrieve one of these ketones, first 1.75g of unknown D was obtained.
The anion tests followed the cation tests. To test for the presence of the chloride (Cl-) anion, a small scoop of the unknown compound was mixed with 1 mL of water in a test tube to create a solution. Then, 1 mL of 6 M nitric acid (HNO3) and 1 mL of silver nitrate (Ag(NO3)2) solution were added to the test tube to see if a white precipitate formed. To test for the presence of the sulfate (SO42-) anion, a small scoop of the unknown compound was mixed with 1 mL of water in a test tube to create a solution. Then, 1 mL of 6 M hydrochloric acid (HCl) and 1 mL of barium chloride (BaCl2) solution were added to the test tube to see if a white precipitate formed.
In the round-bottom flask (100 mL), we placed p-aminobenzoic acid (1.2 g) and ethanol (12 mL). We swirled the mixture until the solid dissolved completely. We used Pasteur pipet to add concentrated sulfuric acid (1.0 mL) to the flask. We added boiling stone and assembled the reflux. Then, we did reflux for 75 minutes.
Observations: 1. The first step had to be repeated due to not following proper instructions. I did not grease the screw, so as I was shaking the mixture, solids were forming around the screwpart of the separatory funnel. 2. When adding 5.0 mL of NaOH to the unknown mixture and shaking it for about 30 seconds, layers had formed.
Introduction The purpose of this lab is to use control variables to help identify different macromolecules. Biological systems are made up of these four major macromolecules: carbohydrates, lipids, proteins and nucleic acids. Carbohydrates are sugar molecules (monosaccharides, disaccharides, and polysaccharides) which make them the most abundant macromolecule on the earth. Lipids (oils and fats, phospholipids and steroids) are insoluble in water and perform many functions such as energy source, essential nutrients, hormones and insulators (Lehman, 1955).
INTRODUCTION A gas chromatograph (GC) can be utilized to analyze the contents of a sample quantitatively or in certain circumstances also qualitatively. In the case of preparative chromatography, a pure compound can be extracted from a mixture. The principle of gas chromatography can be explained as following: A micro syringe is used to inject a known volume of vaporous or liquid analyte into the head or entrance of a column whereby a stream of an inert gas acts a carrier (mobile phase). The column acts as a separator of individual or chemically similar components.
Properties of Substances Express Lab 1)The purpose of this lab was to compare the physical properties of different types of solids and how the properties of solids are determined by their intermolecular forces and their intramolecular bonds. Then we were to classify each type of solid as either ionic, metallic, non-polar molecular, polar molecular, or network. Paraffin wax classified as a non-polar molecular, Silicon dioxide was classifies as a network, Sodium chloride was classified as ionic, Sucrose was classified as polar molecular and Tin was classified as metallic. (2)The intermolecular forces that are present in Paraffin wax are dispersion forces, because it is non-polar and carries a negative charge. Followed by Sucrose that has
Also, although this likely served no contribution in disheveling the results, using a stirrer of the same material to ensure the separate testing of each substance will be as uniform as
Immediately 10 μL of double distilled water was added with a micropipette; this way our concentration of the treatment was the intended concentration.
Experiment #7: Column Chromatography of Food Dye Arianne Jan D. Tuozo Mr. Carlos Edward B. Santos October 12, 2015 Abstract Column chromatography is the separation of mixture’s components through a column. Before proceeding with the column chromatography itself, a proper solvent system must be chosen among the different solvents. The green colored food dye is the mixture whose components are separated.
Properties of Ionic and Covalent Substances Lab Report Introduction The purpose of this lab was to determine which of the following substances: wax, sugar, and salt, are an ionic compound and which are a covalent compound. In order to accurately digest the experiments results, definitions of each relating factor were researched, leading to the following information: ionic compounds are positive and negatively charged ions that experience attraction to each other and pull together in a cluster of ionic bonds; they are the strongest compound, are separated in high temperatures, and can be separated by polar water molecules. A covalent compound is formed when two or more nonmetal atoms share valence electrons; covalent compounds are also categorized into two sections: polar covalent and nonpolar covalent. Furthermore, polar covalent compounds dissolve in water, while nonpolar covalent compounds do not.
Biochemical tests are the tests used for the identification of bacterial species based on the differences in the biochemical activities of different bacteria. Bacterial physiology differs from one species to the other. These differences in carbohydrate metabolism, protein metabolism, fat metabolism, production of certain enzymes and ability to utilize a particular compound help them to be identified by the biochemical tests. Gram’s stain was originally devised by histologist Hans Christian Gram in 1884. Gram-positive bacteria stain purple, while Gram-negative bacteria stain pink when subjected to Gram staining.
Materials Required: 1. Pellets of Sodium Hydroxide (NaOH) 2. Phenolphthalein solution (1%) 3. Potassium acid phthalate (KHC8H4O4) 4. Graduated cylinder - 10 mL 5.
Abstract The unknown concentration of benzoic acid used when titrated with standardized 0.1031M NaOH and the solubility was calculated at two different temperatures (20◦C and 30◦C). With the aid of the Van’t Hoff equation, the enthalpy of solution of benzoic acid at those temperatures was determined as 10.82 KJ. This compares well with the value of 10.27KJ found in the literature.