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    PAE Synthesis Lab Report

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    2.2 Materials and Methods: Polyamino-ether was obtained from the collaborator Dr. Kaushal Rege lab in Arizona state University. All other chemicals were obtained from Sigma-Aldrich (St. Louis, MO). 2.2.1 Synthesis of the bioreducible modified-PAE: The obtained PAE polymer was synthesized by reacting neomycin with glycidyl ether at molar ratio of 1:2 as reported in detail by Rege et al. previously[14]. The modified bioreducible PAE(mPAE) was synthesized by a simple one step reaction with Traut’s

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    Ultrasound treatment was done according to method by [21] with some modifications. Ultrasonic probe (JY92-IIN, Ningbo Scientz Biotechnology Co. Ltd, Ningbo, China) was used, with maximum power 1000Watt, frequency 25 kHz and probe diameter of 13mm. Pectin solutions were treated at 60% duty cycles, sonication times was fixed at 20 minutes, sonication power (200 and 400 watts). Effect of acidity on sonication was determined at pH 2, 4 and 6, by adjusting solution pH using acetic acid. Native pectin

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    have been much different due to incorrect temperature measurement. Another source of error could have been from accidental pipetting of some borax crystals while retrieving 5mL of the solution. This is especially apparent in our two last titrations at 35*C and 30*C. At these temperatures, most of the solution which remained on top of the borax crystals were already

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    Paper 1 This article is going to help establish if combination therapy is a good choice for this patient. The reason that combination therapy should be considered for this patient is because the HGBA1C is at 9%; this is in the range where there is a great about of controversy as to the best treatment for the patient. 9% is right on the boarder to needing a second agent right off the bat, but research and data are limited on best practice for this situation. Controlling hyperglycemia in type

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    with a detection limit of 0.12 mg/L. The interferences from chlorine may be reduced by the addition of oxalic acid, sodium cyclamate, or thioacetamide (Sweetin et al. 1996). APHA Method 4500-CLO2-B, iodometric titration analysis, measures the concentration of chlorine dioxide in water by titration with iodide, which is reduced to form iodine. Iodine is then measured colorimetrically when a blue color forms from the production of a starch-iodine complex. The detection limit for this method is 20 µg/L

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    Clenbuterol

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    As a stimulant, Clenbuterol is actually harsh on cardiac tissue and the cardio-vascular system, although there is some evidence that Clenbuterol promotes cardiac recovery and muscle growth in patients with chronic heart-failure using high dosage. Nonetheless, the peak Clenbuterol dosage used in the study is considered extreme and is not to be attempted by anyone due to its high-risk nature. Also, Myocardial Ischemia is a reported risk of Clenbuterol usage, a condition whereby there is insufficient

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    Discussion This audit provides an insight into the prevalence of hypoglycemia in subacute setting with the aim of identifying precipitant factors and implementing prevention strategies. From this audit we found that there were 10% of patient with type 2 diabetes has moderate hypoglycemia episode whilst in the subacute hospital. This number is smaller than expected from previous audit done in Kingston center, estimating 20-30 cases of hypoglycemia per month. The team hypothesis that if hypoglycemia

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    In this experimental investigation, various brands and types of orange juices, with each trial using 25.0±0.6mL, mixed with 10 drops of Oxalic acid, were titrated with a standardized 0.0037Μ Iodine (I2) solution to oxidize the Ascorbic Acid, causing a colour change in the new solution due to the new blue-black starch-I2 complex that was created. The type of orange juice that was experimented with in this experimental report was the President’s Choice: Frozen from Concentrate orange juice whereas

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    Subjects performed an experiment to investigate the effects of fluid ingestion on kidney function, in which they measured with the kidney output. Before beginning the experiment, each subject was to take a sample collection and that was Sample 1. Once returned to class, the subjects recorded the time of urination and began to do the investigation. In order to begin the investigation, subjects drank one of the four fluids, and measured the effect it had on the urine output. The four fluids were bottled

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    Hemagglutination is defined as the aggregation of red blood cells in the presence of hemagglutinin virus particles (Woytek, 2017). Some of the benefits of using a hemagglutination assay includes its rapidity and ease of titration of a large number of samples. In this lab, the purpose of this experiment was to conduct a HA assay to obtain a titer for a virus stock and the Influenza A virus harvested. Our hypothesis was that hemagglutination of the Influenza A virus compared

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