CHAPTER 3
METHODOLOGY
3.1 Chemical and Reagents
All chemicals, reagent and solvent that will be used in the preparation and characterization of silver nanoparticles will be purchased from various and legal standard suppliers. The reagents and chemical that will be used in this study are hydrochloric acid, sodium hydroxide, acetone, and ethanol.
3.2 Apparatus
Hot plate, spatula, glass rod, bottle sample, beaker (50 mL and 100 mL), measuring cylinder, volumetric flask (50 mL and 100 mL), pipette, thermometer, glass petri dishes, Erlenmeyer flask, and other appropriate glass wares.
3.3 Instrumentation and Characterization Techniques
There are several spectroscopic and analytical methods that are used throughout this research. The chitosan
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The removal flesh, dirt and any possible tissue at the leaf oyster will be done at UMT laboratory. Wash the shell of the leaf oyster with tap water and dried the shell under the sunlight for 1 or two days. After the sample is completely dry, grind the sample with ball mill mixer with 400 rpm speed for 15 minutes. Sieved the grinded sample to obtain uniform powder using 455-micron meter sieve.
3.4.2 Shell Demineralization
According to Abdulkarim et. al 2013, the sample demineralization will be carried out in dilute hydrochloric acid (HCl) solution. The sample will be treated with 0.68 M of HCl at ambient temperature for 6 hours. Wash the solid obtain with distilled water until relatively neutral. Dry and weight the demineralization sample.
3.4.3 Shell Deproteinization
After the demineralization process, the sample will be soaked in 0.62 M sodium hydroxide (NaOH) solution at ambient temperature for 16 hours (Abdulkarim et. al 2013). Al Sagheer et, al. (2003) state that the absence of the proteins are indicated by the absence of colour of the medium. Next, wash the resulting solution to neutrality. Finally, wash the sample with hot ethanol and boil in the acetone to remove impurities. Dry and weight the purified
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The chemical structure of chitin as shown in figure 4.1 below: Figure 4.1 : chitin
The chitin obtain will further react for deacetylation process to get chitosan. The extraction of chitosan from chitin is significant to proceed the synthesis of silver nanoparticles using green synthesis method. The chemical structure of chitosan are shown in figure 4.2 below: Figure 4.2 : Chitosan 4.2 Synthesis of Silver Nanoparticles
The deionized water will change colour into yellowish colour. The colour will become dark yellowish as the time passes. The characterization of silver nanoparticles using Ultraviolet-Visible (UV-Vis) will show the absorption band in range 400 nm to 500 nm. Scanning Electron Microscopy (SEM) will be used to insight the particles morphology and size. The morphology of the silver nanoparticles need to be spherical and without aggregation The X-Ray Diffraction (XRD) analysis for silver nanoparticles will be observed under 5000 magnification and 10 000
Cadet Eric Wiggins Date: 18 September 2014 Course Name: Chem 100 Instructor: Captain Zuniga Section: M3A Identification of a Copper Mineral Intro Minerals are elements or compounds that are created in the Earth by geological processes. The method of isolating metals in a compound mineral is normally conducted through two processes.
The chemical elements are divided into two broad groups, the metals and the non-metals. In this experiment, you will examine some members of the metal group and identify similarities and differences in their physical and chemical properties. Metals are the elements that are found in the left of the periodic table with high electrical and thermal conductivity. Metals lose electrons to create positive ion charges. Metals have a unique shine, are prone to forming, have a high tendency to form cations, and combine with oxygen to give mostly basic oxides.
We then weighed a filter paper which we will use later in the experiment. We then collected the crystallized acetylsalicylic acid by vacuum filtration in a Buchner funnel and washed the product with a little ice-cold water. We then pre-weighed a clean, empty watch glass and labelled it with our initials and the date, we did this do we could easily identify that it was ours when we go to weigh it with the crystals on. We
Phytochemistry Phytochemical studies of Cissus quadrangularis have shown the presence of various versatile constituents such as flavanoids, triterpenoids, Vitamin C, stilbene derivatives and many others, e.g. resveratrol, piceatannol, pallidol perthenocissin and phytosterols. Out of which ascorbic acid, triterpene, β-sitosterol, ketosteroid, two asymmetrical tetracyclic triterpenoids and calcium were identified as major constituents of this plant. Cissus quadrangularis have high contents of anabolic steroidal substances, ascorbic acid, carotene, and calcium.8,9,10 The plant contains ascorbic acid 479 mg and carotene 267 mg per 100 g freshly prepared paste in addition to calcium oxalate. The stem of the plant contains two asymmetric tetracyclic
Use the wash bottle with deionised water to transfer all the oxalic acid crystals from the glass beaker to the funnel. 11. Rinse out all the oxalic acid crystals with the wash bottle from the funnel in the volumetric flask. 12. Add deionized water to the volumetric flask to the 250ml mark on the volumetric flask.
Step 2: Mix both test tubes , shake gently and time the reaction. Step 3: The same step as procedure 1, and step 3 which is to record the observed color step 4: use the palette/color chart to help you identify the observations you make. Safety precautions: Pull your hair back Safety eye goggles Closed toe
1- 800 mL of raw water was transferred to six beakers using a measuring cylinder and a marker was used to assign different numbers to each beaker. 2- To make sure the pH was varied during the first part of the experiment, the pH in each beaker was adjusted. Using Hydrochloric Acid and Sodium Hydroxide, the pH of the six beakers was adjusted as follows: pH 3, pH 4, pH 5, pH 6, pH 7, and pH 8. However, the pH does not need to be exact.
Starch solution is then placed into the test tube at a quantity of 5 mL. 5 drops of Lugol’s Iodine solution is added to the test tube. If the color changes, then it is known that starches are present in the solution. Proteins are next tested. In order to do this, 5 mL of gelatin solution is added to the test tube. 10 drops of Biuret’s reagent are added to test for protein.
Wash the solid with 10 mL of acetone. Decant the liquid. 14. Evaporate the remaining acetone. 15.
A typical Ag-In phase diagram is shown in Figure-1, where seven equilibrium phases exist, out of which two are intermetallic phases i.e. Ag2In and AgIn2 also known as φ and γ phases, respectively [9]. The silver solid solution of Ag-In has solubility of indium up to 21 wt. % with a wide temperature range. Contrarily, the indium rich solid solution has lower solubility of silver i.e. ~1.0 wt. % of silver.
Pat McGurrin October 24, 2015 Period #1 Honors Biology Mr. Dinunzio Murder and Meal Lab Analysis Procedure: 1.) Gather all materials: Safety goggles, 250ml beaker, water, hot-plate, test-tubes, paper bag tear, stomach contents, pipette, Biruet solution, Benedict’s solution, and Iodine solution. 2.) Put on safety glasses.
can be a hazard to the students. Equipment and Materials the following equipment’s were required in the experiment: Equipment Reason for Choosing it 50 cm³ of HCL of varying concentrations I chose 50cm³ as a starting point, The different concentrations will be : 1.5, 1 and 2 M 0.06g of magnesium I chose 0.06 grams and it will have a length of 3 centimeters. Magnesium ribbon is an efficient way to check the rate of reaction. Pipette I am using a pipette to measure out the quantities for collecting the acid. I could have use a beaker or measuring cylinder to measure the volumes of acid and water, but chose a pipette because it's more accurate.
VIII. Methods and materials : hemoglobin types determined by cellulose acetate and citrate agar electrophoresis methods based on different electrical charges when place the sample in electrophoresis, when electrical current is passed through the hemoglobin blood sample, causes separation of hemoglobin type at different rates and form bands .(14)(15) materials 1. Tris-EDTA Boric Acid buffer (TEB), pH 8.4.
Step 10: Prepare chromatography strips by measuring and cutting 13mm x 130mm rectangular
If impure, preform recrystallization procedure to remove the impurities. Then calculate Percent Recovered on crystals formed, and preform melting point procedure. 2. You find that a solid substance you are trying to purify is very soluble in ethanol, but not very soluble in water. You decide that you are going to try to recrystallize it from a solvent pair, consisting of ethanol and water.