3. Experimental Procedure 3.1. Sample preparation Bis-GMA should be made photo-polymerizable by combining with camphoroquinone (CQ) and dimethylamine ethyl methacrylate (DMAEMA). The chemical characteristics of the materials used for preparing the polymer are presented in table 1. The procedure for composing the materials is as follows: 1. All materials left in the room temperature for 2 hours before using. 2. Bis-GMA was heated to 50°C to reduce viscosity and mix with the photo-initiators. 3. 0.4 mol% CQ and 0.8 mol% DMAEMA were added to Bis-GMA and blended completely by a spatula. 4. The mixture stored in a dark container prior to prepare the molds. Some molds of a translucent polymer with 5 mm diameter and 11 mm height were prepared. The internal walls of the molds were lubricated carefully to avoid sticking the polymer after polymerization. Then the photo-polymerized Bis-GMA was injected into the mold and cured with 400 W/m2 LED light for 60 seconds from each side (i.e. top, bottom and surrounding). After that, all samples were ejected from the mold. The top and bottom surfaces of the specimens were grounded by a sand paper to smooth it and to make the …show more content…
The surface of the disks and the test sample were chosen as the master surface and the slave surface, respectively. The contact direction was then defined from the surface of disks toward the specimen due to the fact that only the master surface can penetrate into the slave one. The finite sliding was selected for the sliding formulation. Moreover, tangential friction was defined between the polymer sample and the compression disks. Since the compression disks are stainless steel, the value of friction coefficient was selected according to the previously defined value for the friction between stainless steel and polymers [24, 25] which is equal to
After 28 minutes, the mixture stopped boiling, and approximately 4.5 ml of bromobenzene was added drop by drop in the mixture, and color of the mixture was turned light brown orange. Then, the phenylmagnesium bromide was cooled in ice bath for a few minutes, and 10 ml of anhydrous diethyl ether was added in the mixture by using the syringe. After that, approximately 2.3 ml of methyl benzoate was added to the reaction, and it was added slowly slowly because the reaction was exothermic which needed to be cool in order to maintain a gentle reflux. Once all the methyl benzoate solution was added, the heating mantle was removed from the reaction flask and was cooled to the room temperature. During the reaction, a milky white salt began to precipitate, and the reaction flask was swirled for ten minutes until most of the reaction became visibly subdivided.
Purpose: The main goal of this lab experiment is to synthesize acetylsalicylic acid through using different processes such as crystallization and filtration. Additionally, determining the purity of the synthesize product alongside with a commercial ASA provided in the lab, through using one of the melting point apparatus or conducting a USP test are also the objectives of this experiment. Results Discussion: As discussed in the lab manual, there are certain instructions which apply to proper measurement to provide accurate values throughout the experiments. For example, the transferring of 10 ml of ASA solution to a vial tube by volumetric pipette was necessary to acquire consistent results for our salicylic acid content.
#24 was assigned. During the first week of the experiment, the Grignard reagent was prepared from an alkyl bromide and magnesium. During the hydrolysis,
In the talk, “Adventures in Organic Chemistry – Over Three Decades of Synthetic Organic Chemistry” presented by Dr. Chris Condeiu, he tried to relate the industry of organic chemistry to a students’ perspective. Three major points were drawn out through the talk. The first was the perspective of how capitalism drives the industry and the mechanism of doxycycline was formed. With an overview of his talk, the expectation was that a deeper understanding of how pharmaceutical drugs’ mechanisms are formed; instead, an insight of how the pharmaceutical industry can make one prosperous or just benefit the industry as a whole. Starting with the point about how capitalism governs the pharmaceutical industry, this relates to society in general.
Abstract During this experiment we will produce Isopentyl Acetate via the fisher mechanisms. The alcohol group is converted into an ester giving off a banana scent. This reaction does not favor the products therefore we must add an excessive amoinut of Acetic Acid to shift the equilibrium to favor the products. Our results showed a successful reaction by comparing our boiling results and infrared results to the textbook data on Isopentyl Acetate. Introduction Isopentyl Acetate is an ester that is commonly referred to as banana oil, this is due to the similarity in odor of bananas.
The powder on the filter paper could've fell and this caused it to have a smaller percent purity, percent yield and also cause a lower absorbance and concentration of pure ASA. Another error would be not using a properly dried sample for the pure ASA in part C when making the crystals, this could have cause tye percent yield error. This would make a lower melting point. To prevent this from occurring next time there could be a dry sample that is completely dry and this would not alter the mass of the sample and this would make the solution have a more
Some types include Dry Friction; which resists the motion of two solid surfaces. Fluid Friction; which
Water is used for the pigment to merge and set with plaster, than becoming a part of the
1. INTRODUCTION One of the actual problems in the manufacturing engineering is related to the assembly of the sheet metals, thin-walled tubes or profiles. These tasks could be performed using Friction Drilling technology, which enable to simplify assembly process and to improve reliability of the joint. Friction drilling is also called Thermal Drilling, Flow Drilling, Form Drilling, or Friction Stir Drilling.
Lance Feig CH 128L Experiment Report Purpose The purpose of this lab was to synthesize methyl benzoate from benzoic acid and methanol through Fischer esterification. The identity of the product was verified through IR, GC, and 1H-NMR analysis, where the experimental readings were compared to known readings of methyl benzoate. Furthermore, a percent yield of the product was calculated.
Usually though, for the reactive products, plastic or laminated tubes are used, a detailed report of which is in the next chapter. (Morris,
A. INTRODUCTION DESCRIPTION Metronidazole is 1-(2-hydroxyethyl)-2-methyl-5-nitroimidazole B.P. It appears as a white to brownish cream crystalline substance with melting point 159-162C. Solubility in water at 20C is 1g/100mL; in ethyl alcohol, 0.5g/100mL; in chloroform, 0.4g/100mL; slightly soluble in ether and soluble in dilute acids. When reconstituted as Metronidazole IV for Infusion, it has a pH of between 4.8 and 5.2. B. Composition Each ml contains metronidazole B.P. 5mg, anhydrous citric acid B.P. 0.4mg, sodium phosphate B.P. 1.5mg and sodium chloride B.P. 7.4mg.
INTRODUCTION I have chosen to produce a report on the compound Methanol. In this report I will discuss the industrial synthesis, main uses, demand, origins, availability, cost and environmental impact of methanol. Methanol is also widely known as methyl alcohol or wood alcohol. The chemical formula for methanol is CH3OH. Methanol is a light, colourless and flammable liquid that isn’t fit for human consumption due to its highly toxicnature.
Materials All the chemicals used for synthesis purposes were of AR grade, purchased from Sigma Aldrich chemicals, and for spectral analysis spectral grade solvents were used. Double distilled water was used for preparing solutions. The test strains, Escherichia coli (E. coli) gram-negative, Staphylococcus aureus (S. aureus) gram-positive bacteria and Pseudomonas aeruginosa (P. aeruginosa) were purchased from IMTECH, Chandigarh, India. Yeast extract, tryptophan and bacterial-grade agar–agar were purchased from Hi-media Laboratories, Mumbai, India.
EXPERIMENTAL SECTION General remarks. All of the reagents and solvents were commercially available and purchased from Fluka, Merck, and Aldrich chemical companies. Transmission electron microscopy (TEM) analyse was performed using a TEM microscope Philips CM 120 KV Netherland. X-ray diffraction (XRD) patterns were obtained on Inel French, EQUINOX 3000 model X-ray diffractometer using Cu-K radiation. Scanning electron/electron backscatter diffraction microscopy (SEM)/(EBSD) has been performed using an SU3500 microscope with scanning range from 0 to 20 keV. Electron dispersive X-ray spectroscopy (EDX) measurements were made with an IXRF model 550i attached to SEM.