CONTENTS
Chapter 1 Introduction 1
1.1 Background 1
1.2 Objectives 2
1.3 Scope of Project 2
1.4 Structure of Report 2
Chapter 2 Literature Review 4
2.1 Introduction 4
2.2 Chemistry of Chlorine as a Disinfectant 4
2.3 Alternative Disinfectants 7
2.3.1 Chloramines 7
2.3.2 Chlorine dioxide 7
2.3.3 Ozone 8
2.4 DBP Precursors 8
2.4.1 Natural Organic Matter (NOM) 8
2.4.2 Soluble Microbial Products (SMPs) 9
2.4.3 Bromide & Iodide 9
2.4.4 Dissolved Organic Nitrogen (DON) 10
2.5 Classification of Disinfection Byproducts (DBPs) 10
2.5.1 Trihalomethanes (THMs) 10
2.5.2 Haloacetic Acids (HAAs) 10
2.5.3 Trihaloacetaldehydes (THAlds) 10
2.5.4 Halopropanones (HPNs) 10
2.5.5 N-DBPs: 10
2.5.6 Total Organic Halogen (TOX) 11
2.6 Kinetics of DBP formation 11
2.7
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At similar concentrations of chlorine and bromine, bromine incorporation into THMs and HAAs is preferred over chlorine incorporation. This is because HOBr is 20 times stronger oxidant than HOCl so reacts faster with NOM shifting the distribution of THMs and HAAs to more brominated species. Ratio of applied chlorine to bromine plays an important role in the speciation of THMs and HAAs (Uyak & Toroz, 2007). Increase in bromide ion concentration first results in the formation of mixed choro-bromo species to fully brominated ones (Hua et al., 2006). It has been reported that brominated DBPs so formed are more carcinogenic as compared to the chlorinated ones (Uyak & Toroz, 2007). Water and wastewater treatment processes remove organic carbon but bromide ion is quite resistant to be removed by these and hence ultimately ratio of bromide ion to total organic carbon (TOC) increases. This increases the fraction of brominated DBPs (Roccaro et al., …show more content…
Also humic acids results in the production of more TOX, THMs, HAAs and haloacetonitriles as compared to the fulvic fraction of the same source (Ates et al., 2007). UV absorbance can also be correlated with DBP formation as activated aromatic structures like phenolics and aromatic amines substituted with nucleophilic groups serve as primary sites attacked by chlorine as well as other disinfectants. UV absorbance technique is practically easy to implement as only a small amount of sample without any intense sample preparation can be used for characterising DOM (Ates et al.,
Insecticides are found in urban streams. Herbicides used in agricultural production are found in water from rural watersheds. Furthermore Bartram states that pesticides and herbicides used in agriculture frequently lead to the contamination of surface water and groundwater. According to Harrison pesticides in water aquifers are not easily degraded and persist in the aquifers due to reduced microbial activity, lower
The hypothesis was supported by the employed methods. Introduction: This experiment was performed to show how bromination of alkenes reacts, and to be able to successfully synthesize meso-stilbene dibromide. The reaction of bromine with alkenes is an addition reaction where the nucleophilic double bond attacks the electrophilic bromine
However, there are many unknown compounds present in water, which could pose health risks if not removed. Identification of unknown compounds is based on comparison of the mass spectra of the peaks in the sample with mass libraries or interpretation of the fragmentation. The identification of water contaminations is interesting and similar to the Unknown White Compound lab by making comparisons to other compounds to help identify the
Did you know some byproducts of of chloramine are way more toxic than chlorines? A byproduct is a secondary or incidental product formed from the first. In the article it states that “ Chloramines are widely used in the U.S, and water providers in the East Bay and San Francisco already rely on the source. Another reason to why Chloramines are dangerous because it is toxic to aquatic life, including the mosquito fish, the mosquito fishes are put into our ponds to control the mosquito populations.
As the name implies, the bromination mechanism in an electrophilic aromatic substitution reaction that replaces an atom on the ring with a bromine atom. The addition of the bromine is driven by the presence of a Lewis acid catalyst and a bromine atom. In most bromination mechanisms, liquid bromine is the preferred reagent to complete the reaction. However, due to potential safety concerns, the aromatic ring was brominated by using a compound of hydrobromic acid and potassium bromate in an acetic acid solution (see Figure 2 for the bromine formation).1 Liquid bromine is known for generating hazardous fumes, so this solution is significantly safer for bromine production. This formation of bromine is crucial for the bromination reaction to
The goal of the experiment is to synthesize a bromohexane compound from 1-hexene and HBr(aq) under reflux conditions and use the silver nitrate and sodium iodide tests to determine if the product is a primary or secondary hydrocarbon. The heterogeneous reaction mixture contains 1-hexene, 48% HBr(aq), and tetrabutylammonium bromide and was heated to under reflux conditions. Heating under reflux means that the reaction mixture is heated at its boiling point so that the reaction can proceed at a faster rate. The attached reflux condenser allows volatile substances to return to the reaction flask so that no material is lost. Since alkenes are immiscible with concentrated HBr, tetrabutylammonium bromide is used as a phase-transfer catalyst.
Based on the result from the bromine test conducted, the clear appearance of the 4-methylcyclonexene demonstrated that the bromine had all been used up, and there is an unsaturated compound present. Infrared spectroscopy was another method of identifying an alkene. Figures 1 and 2 show the IR spectra for the reactant (4-methylcyclohexanol) and the product (4-methylcyclohexene), respectively; each were compared and analyzed. The IR spectrum for 4-methylcyclohexanol revealed a broad peak at 3328 cm-1, signifying an OH group and therefore an alcohol. In contrast, the IR spectrum for 4-methylcyclohexene no longer showed that broad band, but instead displayed a sharp peak at 1651 cm-1, representing a double bond and therefore an alkene.
According to the data in my experiment, lemon oil cleaned better than Clorox in both the girls bathroom and on the elementary handrail. But my results were still somewhat inconclusive. In the case of the girls bathroom the results weren’t too messy, there was 23.6% bacteria on the surface before I cleaned it, and after I cleaned it with Clorox the amount of bacteria was reduced by 20% to 3.6%. However, after I cleaned it with lemon oil it was reduced to only .9% bacteria which is 2.7% less bacteria than when I cleaned it with Clorox.
Tetrachloroethylene is a clear, nonflammable liquid, and is a commonly used solvent that has been in commercial use since the early 1900s. It can be found in water repellant, paint remover, printing ink, glue, sealant, polish, and can also be used to make other chemicals. Although it has been detected in small amounts in the air and in some sources of drinking water, the most common source of exposure is in the industries that use this chemical. Such industries are the dry-cleaning business, where it is used as a solvent, and businesses that degrease and clean metals, or need to dissolve greases and oils from fabrics. Because Tetrachloroethylene is a chlorinated hydrocarbon, it is a central nervous system depressant, and can easily enter the body through respiratory or dermal exposure, allowing this to be taken into the body dangerously easy.
Danio rerio (also known by the common name “zebrafish” due to its conspicuous striped appearance) can be seen in the aquarium section of just about any local pet store, and it has become equally as ubiquitous in scientific research. Biologist George Streisinger is generally credited as the pioneer for D. rerio use as a model organism (Tucker). Streisinger, inspired by his home aquarium hobby, began experimenting with these diminutive fish as early as the 1970s, though his initial work gained little attention, and was at the time was not received without skepticism (Tucker). Specifically, what merit was there in studying a pet store novelty when other animals with an established history as model organisms, such as mice and fruit flies, were already widely available?
Chem 51 LB Experiment 3 Report Scaffold: Bromination of Trans-Cinnamic Acid 1. The goal of this experiment was to perform a halogenation reaction through the addition of two bromides from pyridinium tribromide. This was accomplished by reacting trans-cinnamic acid with pyridinium tribromide. After the reaction took place, melting point analysis was conducted to find out the stereochemistry of the product, which could either be syn-addition, anti-addition, or syn + anti-addition. 2.
The next part of the experiment, alkyl halide classification tests, will be used to determine the degree of substitution of the alkyl halide that was formed during the reaction. For this experiment specifically, this allows for the verification of the formation of a primary bromoalkane from the primary alcohol. The success of the experiment will be determined by a percent yield, analysis of the infrared spectroscopy reading, and the results of the alkyl
Experiment TWO: Bleach Oxidation of Isoborneol Reaction (15 pts) –accurate drawing with ChemDraw Procedure Isoborneol (1.32 g, 8.5 mmol), NaOCL (1 mL, 7.6 mmol), and acetic acid (1.7 mL) was vigorously stirred in a flask. The solution was then heated to 50°C. NaOCl (15 mL) was added dropwise to the solution over a 10 minute time period. Parafilm was then used to seal the flask, while being stirred and heated (50°C).
Contamination in Puerto Rican Beaches As everyone knows, Puerto Rico is a tropical beauty with ravishing coastlines, enchanting flora and unique creatures. Locals are fortunate enough to call this divine paradise, “home”. Having accessibility to all these wonders, it comes as no surprise that a large percentage of Puerto Ricans luxuriate in the beaches and wildlife the island has to offer. The heart of the Caribbean and the ultimate tropical utopia, Puerto Rico is an Eden worthy of protection, care and nourishment, yet the case seems to be the opposite.
Bromination is a type of electrophilic aromatic substitution reaction where one hydrogen atom of benzene or benzene derivative is replaced by bromine due to an electrophilic attack on the benzene ring. The purpose of this experiment is to undergo bromination reaction of acetanilide and aniline to form 4-bromoacetanilide and 2,4,6-tribromoaniline respectively. Since -NHCOCH3 of acetanilide and -NH2 of aniline are electron donating groups, they are ortho/para directors due to resonance stabilized structure. Even though the electron donating groups activate the benzene ring, their reactivities are different and result in the formation of different products during bromination.