Adsorption Chromatography Separating Ferrocene and Acetylferrocene by Adsorption Chromatography Dry Pack Method Leah Monroe February 27‚ 2003 Organic Chemistry Lab II Experiment performed on February 18 and 20‚ 2003 Abstract: Adsorption column chromatography is one way to separate compounds out of a mixture. In this technique‚ a solid stationary phase called the adsorbent is packed in a glass column and an eluent‚ which is the mobile phase‚ moves slowly through the packed column. In this
Premium Chromatography
First‚ the amount of total protein removed by the Affinity Chromatography is difficult to quantify because there appears to be an error in the analysis data for 65% cut precipitate. The protein from the previous purification step limits the amount of protein that can be recovered by the subsequent purification step. In this case‚ the total protein recovered by 65% cut was 159 mg‚ but Affinity Chromatography recovered 350 mg of protein. Purification steps cannot gain protein unless
Premium Metabolism Enzyme Glucose
purifying LDH (fold purification). As we can see looking at the Total Protein column on Table 3‚ the most effective step with regard to the percent of remaining protein removed was affinity chromatography because it was able to remove 98.6% of the remaining proteins. In comparison to 81.93% removed during the 65% ammonium sulfate precipitation and 81.3% during the size exclusion. This means that the affinity chromatography removed a big percentage of contaminating proteins. However‚ removing this huge
Premium Water Revenue Balance sheet
INTRODUCTION Plant pigments consist of four main chemicals. These are Chlorophylls‚ The carotenoids‚ Anthocyanin and Betacaine. The aims of this experiment is to separate the plant pigment into different colours using solvents and column chromatography. The hypothesis of this experiment is that this plant pigment from spinach will contain the chlorophyll pigment or may contain the others too. Chlorophyll: Chlorophyll a is the main component of the plant pigments. This is used for the most
Premium Color Green Light
distillation‚ the difference of boiling points between the substances must be more than 40 to 50 degrees C. A fractional distillation column is needed in a fractional distillation. The column in a fractional distillation column provides a temperature gradient where the temperature is lower at the top of the column and the temperature is greater at the bottom at the column. In the first step‚ the unknown solution was added to a round bottom flask with a stir bar. The reason the stir bar was needed‚ was
Premium Water Temperature Thermodynamics
Abstract: An electrophilic aromatic substitution reaction was performed on bromobenzene with nitric acid producing both 2-bromonitrobenzene and 4-bromonitrobenzene. Products of the reaction were purified through multiple recrystallizations and column chromatography creating multiple crops of a yellow powder. The percent yield of products was determined to be 51%. The melting point of Crop 1 was found to be 110-115 °C‚ and Crop 2 was found to be 37-90 °C indicating impurity in both crops. TLC analysis
Premium Electrophilic aromatic substitution Aromaticity Organic reaction
you? So there is science behind this. The colors of the soda is made of pigments. The fruit color will make the color of the soda brighter. Column Chromatography is a new technical method to separate the chemical inside the mixture. I can use this method to separate the dyes of the grape soda. The chemical mixtures in the grape soda will pour through the column and at the bottom the mixture will come out and separately.That
Premium Chemistry Color Chlorine
Date: Lab Section: Selected Known Compounds Name Structural Formula Literature Melting Point Acetanilide C8H9NO 114.3°C Fluorene C13H10 116.5°C Experimental Data Sample Composition 1. 100% Acetanilide 2. 10% Acetanilide 3. 25% Acetanilide 4. 50% Acetanilide Fluorene 5. 75% Acetanilide 6. 90% Acetanilide 7. 100% Fluorene Melting Range 108-116°C 108-112°C 105-112°C 102-109°C 105-112°C 109-115°C 108-114.5°C Graph of Data Discussion of Results The purpose
Premium Melting point Chemistry
molecules in the mixture being passed through the column is strong. Hence‚ the retention time of polar molecules is shorter because they pass through the column faster. Reversed phase HPLC is the most commonly used form of HPLC which separate solutes based on non-polar differences. In this experiment‚ reverse phase chromatography was used. The more polar antioxidant is expected to elute first due to the weak attraction to the non-polar column. Figure 2 below shows the structures of the two antioxidants
Premium Immune system Nutrition Bacteria
HPLC Theory: System Suitability Parameters High performance liquid chromatography is defined as a separation of mixtures of compounds due to differences in their distribution equilibrium between two phases‚ the stationary phase packed inside columns and the mobile phase‚ delivered through the columns by high pressure pumps. Components whose distribution into the stationary phase is higher‚ are retained longer‚ and get separated from those with lower distribution into the stationary phase. The
Premium Chromatography High performance liquid chromatography Analytical chemistry