The experiments were conducted using homogenous anion exchange membranes (AEM) and cation exchange membranes (CEM) supplied by Permionics Membranes Pvt. Ltd. (Vadodara, India). The membrane size was 200 mm × 120 mm. The laboratory ED unit was fabricated using transparent acrylic plate purchased from Sushil enterprises (Saharanpur, India). The titanium electrodes (anode and cathode) were procured from Titanium Tantlum Pvt. Ltd., Chennai. The direct current was supplied by a power supply operating at 0-16 volt. Sulfuric acid, glucose, xylose and phenolphthalein were obtained from HiMedia Laboratories (Mumbai, India) and used without any further purification. Ultrapure Type 1 was used throughout the experiments.
4.2 Lignocellulosic Hydrolysate Preparation
The Kansas grass hydrolysate liquor was prepared in the Biochemical Engineering Laboratory, Indian Institute of Technology Roorkee, Roorkee in a laboratory scale vertical pretreatment reactor operated at conditions of 100°C, an approximate 30 minutes
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The synthetic hydrolysate solutions were also prepared from different concentration of sulfuric acid and distilled water to conduct the initial set of experiments for optimization.
4.3 Experimental Procedure
All the experiments were conducted in a laboratory scale parallel planar electrodialyser using one cell pair of electrodialysis stack as shown in figure 1 and figure 2. The cell unit is composed of one anode and one cathode as well as membranes one anion exchange membrane (A) and two cation exchange membrane (C) along with spacers (S). The center of the cell has an opening of 36 cm2, which represents the effective area of etectrodialyser cell. The membranes are arranged to facilitate unidirectional ion flow under an applied
The goal of this experiment is to find out what is the identity of the unknown hydrate? To answer this question first, we should know what a hydrate, and how to identify a hydrate using the law of constant proportions. A hydrate is a pure substance because it contains water molecules embedded in its crystal structure that does not vary. By heating the unknown hydrate, we can calculate the mass of the hydrated, and the percentage of water in the hydrate.
Organic Chemistry Laboratory Manual, 7th Edition, Eiley, New York, pp 96-99 Dehydration Notes
An enzyme can not be considered a reactant because, like catalysts, the enzyme is never used up in the reaction and is reused again in another chemical reaction. In this lab, the source of hydrogen peroxidase was the potato solution. The substrate that the hydrogen peroxidase acts upon is the hydrogen peroxide.
Tn 4351 was originally isolated from bacteroides fragilis [30] . The transposon was successfully introduced into Cytophaga succinicans, Flavobacterium meningosepticum, Flexibacter canadiansis, Flexibacter strain SFI and Sporocytophaga myxococcoides by conjugation [25]. Tn 4351carries two antibiotic resistance gene. One of the codes for resistance to erythromycin and clindamycin which is expressed in bactroides but not in E.Coli. The other gene codes for resistance in tetracycline and is expressed in aerobically grpwn E. coli, but not in anaerobically grpwn E. coli or in bacteroides.
LABORATORY REPORT Activity: Enzyme Activity Name: Natalie Banc Instructor: Elizabeth Kraske Date: 09.26.2016 Predictions 1. Sucrase will have the greatest activity at pH 6 2. Sucrase will have the greatest activity at 50 °C (122 °F) 3.
Introduction: In this lab, of water in a hydrate, or a substance whose crystalline structure is bound to water molecules by weak bonds, is determined by heating up a small sample of it. By heating, the water of hydration, or bound water, is removed, leaving only what is called an anhydrous compound. Based on the percent water in the hydrate, it can be classified as one of three types: BaCl2O ⋅ 2H20, with a percent water of about 14.57%, CuSO4
Aim: To find out the relationship between the greater concentration of sodium thiosulfate when mixed with hydrochloric acid and the time it takes for the reaction (the time it takes for the solution to turn cloudy) to take place and to show the effect on the rate of reaction when the concentration of one of the reactants change. Introduction: The theory of this experiment is that sodium thiosulfate and hydrochloric acid reach together to produce sulfur as one of its products. Sulfur is a yellow precipitate so, the solution will turn to yellow color while the reaction is occurring and it will continue until it will slowly turn completely opaque. The reaction of the experiment happens with this formula: “Na2 S2 O3 + HCL =
Acids are proton donors in chemical reactions which increase the number of hydrogen ions in a solution while bases are proton acceptors in reactions which reduce the number of hydrogen ions in a solution. Therefore, an acidic solution has more hydrogen ions than a basic solution; and basic solution has more hydroxide ions than an acidic solution. Acid substances taste sour. They have a pH lower than 7 and turns blue litmus paper into red. Meanwhile, bases are slippery and taste bitter.
Practical I: Acid-base equilibrium & pH of solutions Aims/Objectives: 1. To determine the pH range where the indicator changes colour. 2. To identify the suitable indicators for different titrations. 3.
Chemistry IA Background information: Introduction: Electrolysis it’s a chemical process that when you pass an electric current into a solution or a liquid that contains ions to separate substances back to their original form. The main components that are required for electrolysis to take a place are: Electrolyte: it’s a substance that when dissolved in water it ionize and then it will contain free moving ions and without these moving ions the process of electrolysis won’t take place. Direct current (DC): This current provides the energy needed to discharge the ions in the electrolyte Electrodes: it’s an object that conducts electricity and it’s used in electrolysis as a bridge between the solution and power supply. A great example
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.
One of the possible systematic error that may occur in this experiment is that the hydrated (II) ammonium sulfate is contaminated as the iron (II) salt was left uncovered. The iron (II) salt was prepared by the lab assistant and the salt was left at the table uncovered for students to scoop the desired amount of salt they want. The iron (II) salt might be contaminated by dust particles and even saliva. This would cause the standard iron (II) solution to have less iron (II) salt in it and this means that less potassium permanganate solution is needed to titrate the iron (II) solution. This is a systematic error because the iron (II) solution used throughout the experiment.
Introduction The goal of the experiment is to examine how the rate of reaction between Hydrochloric acid and Sodium thiosulphate is affected by altering the concentrations. The concentration of Sodium thiosulfate will be altered by adding deionised water and decreasing the amount of Sodium thiosulphate. Once the Sodium thiosulphate has been tested several times. The effect of concentration on the rate of reaction can be examined in this experiment.
This experiment is to investigate the relationship between solute concentration and the movement of water through semipermeable membrane by the process of osmosis. The purpose of this The Visking tubing apparatus establishes the osmosis procedure. The Visking tubing is a semipermeable membrane filled up with concentrated sucrose solution. The surface of the semipermeable membrane symbolizes the visking tubes and the mixture demonstrates the cytoplasm. If the Visking tube is absorbed in water, after a period of time, it will be have water inside water, this is because the water molecules can pass through the tubing, while the larger sugar molecules cannot diffuse out from the tubing because the size of sugar molecules do not allow it to go through the tubing.
Abstract — This experiment was conducted to familiarize the students with the procedures regarding distillation—to be more precise, the separation of ethanol from an alcoholic beverage—using a distillation set-up consisting of boiling chips, a Bunsen burner, a condenser, a thermometer and several other materials. In the end, it was discovered that one may actually separate a homogeneous mixture, given that the components of said mixture differ in volatility and that they utilize a complete distillation set-up and follow laboratory safety rules and regulations. Keywords — Matter, homogeneous and hetereogeneous mixtures, distillation, volatility, boiling point I. INTRODUCTION There are typically two categories of matter, these are pure substances