Review Assignment Example | Topics and Well Written Essays - 500 words

Review - Assignment Example Most importantly, the application of secure data mechanisms such as the use virtual private networks in mobile has well been covered in the organization. Additionally, the use data encryption and decryption techniques to manage contents have effectively been applied in the organization. In general, the organization has an effective approach in management of content. As seen in the document information flow in the article has been very precise. The paper has began by outlining the research subject followed by a deep analysis of the necessity information security in an organization. The information content in the article is divided into two main segments, which are utilization of virtual private networks and a project. In the first section, it starts with an overview followed by history of VPNS, VPN technical aspects, PPTP, L2TP, IPsec, authentication and finally vulnerabilities. It is also essential to specify that the subject of vulnerabilities has addressed issues such as user threats and hardware and software threats. The second section is the project. The flow of information in the project begins with a background, materials, planning and finally implementation and testing. In essence, this a well organized flow of information in the paper. It is also vital to note that the paper contains an effective use of diagrams. This is as stipulated below. The first diagram illustrates a general application of virtual private networks in an organization using the site-to-site approach. It has been designed in a way that makes it easier for one to comprehend its ability to facilitate secure data transfer. The second diagram goes deep into the subject of VPNs by stipulating a three step tunneling approach from a client to server. There is also a diagram for secure data access in the organization. In general, the diagrams in the article have

Giant Pool of Money Essay Example for Free

Giant Pool of Money Essay The house prices were on the rise and many traditional home owners attempted their dreams of becoming a real estate tycoon. Although some buyers might have lived through the recessions in the 70’s, they never experienced it as a consumer and so only seeing housing prices go higher and higher, the idea of owning a home for the long run was embedded as a sure money maker. The last recession was more than 40 years ago and people don’t remember it because all of them were yet to be born or they were just too young. This is the case with all of the players in The Giant Pool of Money. Jim Finkel, Rachard the marine, Clarence Nathan, Adam Davidson, Ceyla Pazarbasioglu, Mike Francis, Mike Gardner, Glen Pizzolorusso, and Tonko Gast. I can’t blame any of them for falling in to Availability Bias because I too fell for it. Luckily, I bought a house that I could afford, unfortunately many of my neighbors did not. I was born in 1978 and this was my first opportunity of making a large investment for myself. Because I was bit weary, I asked a lot older mentors and family members if I should buy a home and not a single person said no. All of my friends had houses 2000sq ft or bigger houses for themselves! I couldn’t think of one reason why I shouldn’t buy a house and I’m sure many Americans felt the same and I was amazed how easy the entire process was! Like Richard the marine, I had the ability to lock in a 30 year fixed Veterans Administration loan but my lender opted for the interest only mortgage. Biases due to the irretrievability of instances also came in to play when asking, why throw money away when you can buy? It’s common knowledge to anyone that buying is always better than renting however, there are instances where renting can be more advantageous. People like Mike Garner that worked at mortgage banks were in a race to make the most deals against other lenders who were doing the exact same thing. Interesting enough, Mike stated that his boss hated the loans that they were dealing but he couldn’t do anything about it because â€Å"Other people are offering it†. His boss had been in the business for 25 years and everyone was making money. Glen Pizzolorusso, a sales manager like Mike Garner was making more money than he knew what to do with it so he did what everyone else did, buy houses! The second bias I’d like to look at is insensitivity to prior probability which is conveyed in the paragraph above. People tend to think of real estate investment as a solid investment like the people that had their piece in the pool of money and everyone involved. People are always going to resort to buying a real estate property versus renting if given the choice. It is perfectly reasonable to predict that house prices will rise in the future. I don’t think many people will ask themselves â€Å"how likely would this house devalue by threefold in next couple of years? † or much more modest â€Å"how likely would house prices fall next couple of years? † Prior availability of data available suggest that the chances are very slim. It seems like it was a perfect storm brewing with all the right elements that caused this bias. People with money to invest felt it was the right move since federal funds were at record low interest levels and there were significant growth in the housing sector. The bank workers such as Mike Francis simply satisfied the investors without knowing the outcome and with the initial success, the need of further investigating disappeared. One recommendation I have to prevent availability bias and insensitivity to prior probability, I would say is to carefully examine past history. We all know that last recession was in 1970’s but most people only know as the recession caused by the oil crisis but looking much more in depth, we all know that it was just more than oil crisis that resulted in the recession. Likewise, people are going to talk about the recession in 2000’s as greedy home owners trying to make money on houses that they couldn’t afford but we know that wasn’t the cause. There is more to the story then the headline and people need to investigate and look at all the possible outcomes. These two biases make it difficult to examine some of the outcomes and it’s everyone’s responsibility to look at all of the possible outcomes even if the chances are very small. We cannot point the finger at just one person in the story of Giant Pool of Money.

Water Mist Replacement for Halon Extinguishers

Water Mist Replacement for Halon Extinguishers CHAPTER ONE: 1.1: Introduction Choosing the best fire suppression technology is not an easy task. It even involves discussing risks and operations with insurance companies. The most relevant concern of a fire safety engineer is the protection of life which entails the safe evacuation of personnel. The starting point of a suppression system is a risk analysis to reduce the potential occurrence of a fire. This is followed by the control of the damage and the recovery effort or emergency response associated with the means of fire suppression adopted. The quality of installation, efficiency and maintenance of the suppression system adopted cannot be over-emphasised. The phase out of halons, due to environmental concerns, has lead to forceful development of new fire prevention strategies and technologies that are efficient, as well as environmentally friendly technologies. Fire protection halons were phased out of production in developing countries due to the quest to regulate the use of ozone depleting substances(ODS) as reflected in the Montreal Protocol,1987(London Amendment 1990, and Copenhagen amendment1992). Fire suppression agents have two (2) toxicological aspects to them: The toxicity of the agent The toxicity of combustion products of the agent. Several new fire suppression systems have been developed such as inert and halocarbon gaseous systems, water mist systems, gas and aerosol generators. Fire has been extinguished with water since ancient times. Water in the normal form is not a suitable suppression medium of all classes of fire. The efficiency of water in suppression is enhanced by its use of water in form of mists. Survey by Mawhinney and Richardson in 1996 showed that about 50 agencies worldwide are involved in the research and development of water fire mist and suppression systems. Water mist in fire suppression does not behave like true gaseous agents and is affected by fire size, the degree of obstruction, ceiling and the ventilation conditions of the compartment. To effectively suppress a fire, a water mist system must generate and deliver optimum sized droplets with an adequate. 1.2: Objectives and Structure of Dissertation This project aims at studying the water mist as a replacement for halons systems in the extinguishment of fires. This replacement is a direct consequence of the phase out of halons due to environmental issues and the need to find a drop-in replacement or a suitable alternative in areas where high level of fire safety is required and the cost of fatalities is too high. Chapter 2 2.1: Overview of Fire Suppression To suppress fires, the type of fire needs to be identified. The class of the fire to be extinguished also determines the type of extinguisher that can be used. There are six (6) types of fires: Class A FIRES: These involve flammable or combustible solids such as wood, rubber, fabric, paper and some plastics. Class B FIRES: These are fires involving flammable and combustible liquids or liquefiable solids such as oil, alcohol, petrol, paint and liquefiable waxes.[9] Class C FIRES: These are fires involving flammable gases such as natural gas, hydrogen, propane, butane.[9] Class D FIRES: These are fires involving combustible metals, such as sodium and potassium.[9] Class E FIRES: These are fires involving any of the materials found in Class A and B fires, but including electrical appliances, wiring, or other electrically energized objects in the vicinity of the fire, with a resultant electrical shock risk if a conductive agent is used to control the fire.[9] http://www.sqa.org.uk/e-learning/FirstLineO2CD/page_06.htm Class F FIRES: These fires involve cooking fats and oils, especially in industrial kitchens. The temperature of these fats and oil on fire is much greater than that of other flammable liquids. 2.2: Means of Fire Suppression The aim of fire suppression is to provide cooling, control the spread of the fire as well as extinguish the fire. The behaviour of a fire is charcterised by the fire triangle which has fuel, oxygen and heat as its three sides. Combustion process is represented by: Fuel + O2 HEAT H2O + CO2 †¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦.eqn2.1 The combustion process is an exothermic reaction, involving a fuel and oxygen. The ratio of fuel to air must be within the flammability limits of the fuel for combustion to occur. The Lower Flammability Limit (LFL) is the minimum concentration of fuel vapour in air, below which a flame cannot be supported in the presence of an ignition source. The Upper Flammability Level (UFL) is the maximum concentration of fuel vapour in air, above which a flame cannot be supported. Stoichiometric Mixture is the ratio of fuel in oxygen that requires minimal energy to support a flame. A branch of the triangle must be removed for the fire to be extinguished. Fires can either be smoldering or flaming combustion. Smoldering occurs when solids such as wood or plastics burn at or on the surface. It usually involves the release of toxic gases and can be difficult to extinguish. Flaming combustion is a gas phase phenomenon that involves the release of visible and infrared radiation. This type of fire generates much more heat. The extinguishing of a fire involves either chemical or physical mechanisms. Physical mechanism: Involves the removal of one side of the fire triangle. This can be done by either blanketing the fire (causing the fuel and air to be separated) or by removing the heat source using an agent with a high heat capacity/ latent heat of vaporization (this will cool the flame by absorbing the heat). Physical mechanism could be thermal or dilution. Thermal physical effect involves adding non-reactive gas to a fire plume leading to a reduction in the flame temperature. This is achieved by the distribution of the heat generated to a larger heat area. The heat capacity of the introduced agent determines the efficiency of the process. On the other hand, for dilution physical effect, the collision frequency of oxygen molecules with the fuel is lowered when the additional gas is introduced into the fuel-air mixture. This effect is quite minimal and negligible. Chemical mechanism: This is the use of an extinguishing agent or its degradation product to disrupt the chain reaction for sustaining combustion. This entails inhibition by halogen atoms. Most good suppressants apply both the physical and the chemical mechanisms. The type of hazard associated with an area determines the fire protection system that will be put in place. Halons have been used in a wide range of applications. Other alternatives include: Water Sprinkler Systems: This is a very common type of fixed protection that offers safe protection to limit structural damage. The cost of installing water sprinkler systems into existing structures is quite expensive. They are better at protecting structures than its contents [11]. The reliability of water sprinkler system has encouraged its wide use. Accidental discharge is uncommon with water sprinkler systems. Water sprinklers have a much slower response than other systems. They also cause a considerable secondary damage. They cannot be used on live electrical equipment and flammable liquids, but they are used widely in computer and control rooms as well as storage rooms in the USA. Detectors: This involves the use of high sensitive smoke detection. This is not exactly an active fire protection approach but it serves as an initiator to other fire protection systems [2]. Carbon dioxide: Carbon dioxide is widely used in gaseous based fire extinguishing systems. There are two types of carbon dioxide system depending on the manner by which they are stored. These are high pressure and low pressure carbon dioxide systems. It is a clean agent and has a good penetrating ability. This makes it safe for use on live electrical equipment. They are also used in unoccupied spaces such as computer and control rooms. Carbon dioxide causes very minimal direct or secondary damage and allows the installation being put back to immediate use after a fire. It is however toxic and cannot be used in total flooding situations. Carbon dioxide cannot also be used in situations where weight and space are important. High concentrations of carbon dioxide are required for extinguishment and as such they are bulky and heavy. They cannot be used in manned areas because they reduce the oxygen concentration to levels below life support and thus cannot be set in automatic mode. Carbon dioxide systems are generally fast acting and cost effective. Carbon dioxide has also found use in record storage, flammable liquid fires, chemical processing equipment, turbine generators, marine applications, computer rooms and shipboard machinery. Inert Gases: inert gases in use for fire suppression are majorly argon and nitrogen mixtures. These are electrically non-conductive fire suppressants. The mechanism behind their use is the lowering of the oxygen concentration of air to that below the lower flammability point (LFL). They are not liquefied gases and they are bulky because they are stored at high pressure. The concentration of inert gases released in the hazardous area is high because they have densities that are similar to that of air. Their response time is not very fast and so they are not efficient in situations where the rate of fire spread is high. Inert gases do not decompose thermally and thus they form no breakdown products [2]. Inert gases can cause an extreme decrease in the composition of oxygen in the body accompanied by an increase in the concentration of carbon dioxide leading to loss of consciousness or death and as such health and safety issues have to be considered in its use. Inert gases have found wi de acceptance because they pose no environmental problems. They are not ozone depleting substances neither do they contribute to global warming. They are employed in computer and control rooms, record storage, flammable liquid fires and shipboard machinery [2]. Halocarbon Gases: These are hydrofluorocarbons and perfluorocarbons with zero ozone depleting potentials. They are however greenhouse gases and are governed by the Kyoto protocol and hence its release counts towards the national emissions inventory of global warming gases. Halocarbons are electrically non-conductive, are clean agents and are not bulky in terms of space and weight. Foam Systems: Foam systems could be low, medium or high expansion systems. Foam systems are efficient for extinguishing liquid pool fires and large cable fires. In this case, the foam acts as a barrier between the fire and the supply of oxygen. The use of chemical dispersants to clean up after its use has limited the wide use of foam systems. Furthermore the use of smoke detectors for its activation limits its speed of response. They cannot be used to protect any substance that reacts violently with water. Foams systems are often used with water sprinklers. This increases the efficiency of the systems. Foam systems have found use in the extinguishment of flammable liquid fires, engine compartments and shipboard machinery. Dry Powder: Powders have very high response time for extinguishing fires but have no cooling effect. They thus become ineffective as soon as it settles [2]. They are limited in application to extinguishing flammable liquid fires as well as engine spaces. Fine Solid Particulates: This system is used in combination with halocarbon gases and inert gases [2]. They have the advantage of reduced wall and surface losses relative to water mist and particle size is easier to control[2]. They however pose problems to sensitive equipment and cannot be used for explosion suppression applications because they are generated at high temperatures. Fine solid particulates can only be used in unmanned areas because of the problems associated with inhalation of particulate substances. Water Mist: This employs the use of fine water sprays, usually less than 100 microns in diameter. Water mists can be used on flammable liquid fires, as well as electrical equipment. They are not as effective on small or slow burning fires. Water mist installations pose problems in their design and fabrication. Hybrid Systems: Hybrid systems combine one or more of the above fire protection system. A common example of this is the combination of water mist systems and carbon dioxide. There are two methods of applying fire extinguishing agents-Total Flooding and Local Application. Total Flooding: They are operated automatically and manually. It entails applying an extinguishing agent to an enclosed space to achieve a concentration of the extinguisher that is capable of putting out the fire. This method is the most common system of application Local Application: The agent is applied directly onto the fire plume or the affected enclosure. Portable fire extinguishers are the most common forms of this approach. This method is also known as streaming application. There is an increase in the need for the phasing out of halons and this has brought the search for the perfect or drop-in replacement. The department of trade and industry in 1995 listed checklists for the selection of alternatives to halons in critical uses situations as: Fire fighting effectiveness: This involves the speed of fire suppression, the post fire hold time, the ability of the alternative to permeate, the elimination of the risk of reignition, the suitability of the alternative to the fire hazard. Ease of Installation: Ease of maintenance, pipe work, and cost of installation, cost of refill, floor space and weight, system re-instate time, and availability of the extinguisher. Hazards to occupants: Toxicity, noise levels, pressurisation, inhalation, visibility, safety as regards electrical work, thermal decomposition products [2]. Discharge effect on equipment: water damage, clean up, corrosion, thermal shock. Environmental acceptability: Ozone depletion potential, atmospheric lifetime, and global warming potential. Discharge damage: This entails clean up of the agent after use, water damage, thermal shock and corrosion. Esso Australia, while looking for alternatives to halons on their installations considered the following issues [14]: Effectiveness at extinguishing fires Environmental effects (a zero ozone depleting and global warming potential) of the agent before use and after thermal decomposition. Toxicity level and a safety margin between its No Observed Adverse Effects Level (NOAEL value) and the extinguishing concentration required Third party approval from regulatory bodies and safety partners such as International Maritime Organisation (IMO), NFPA, and EPA or Underwriters laboratory Organisations. Level of engineering required to modify an existing halon protected installations. Availability as regards to installation and maintenance at a reasonable cost. 2.2: Health and Safety Issues Considering the health and safety in the UK, there is no specific regulation as regards choice of fire extinguishing systems. Otherwise fire risks and risk from the use of extinguishment can be categorised under risks at work. The Management of Health and Safety at Work Regulations 1992 stipulates all risks at work are to be assessed and prevented where ever it is reasonably practicable, controlled. In cases where fire extinguishing systems contain toxic substances then the Control of Substances Hazardous to Health Regulations 1988 (COSHH regs) will also apply. The basis of the two regulations is the prevention rather than control of the risk. 2.3: Environmental regulations The International Maritime Organisation (IMO) has prohibited the use of new halon systems from 1994, but accepts the use of existing ones. The EU has banned its use onboard vessels by the end of 2003. The following are regulations that are put in place to phase out the use of halons. The Montreal protocol on Substances that Deplete the Ozone layer- the Montreal protocol, signed by 25 countries on the 16th of September, 1987 is an international treaty for the control of the production and use of ozone depleting substances. It involves the restriction and eventual prohibition of the production, distribution and use of Ozone Depleting Substances. A copy of this document is attached in Appendix 1. The EC regulations: This European legislation was put in place to further tighten the restriction on the ban of ozone depleting substances. EC Regulation 3093/94 came into force on the 23rd of December 1994. EC Regulation 3093/94 is directly binding in all EU Member States and does not require any national implementing legislation. The new Regulation EC 2037/2000 came into force on 1 October 2000, replacing the Regulation 3093/94. The enforcement requires the use of bodies such as the HM Customs and Excise concerning import of controlled substances. The Department of the Environment proposes to implement these arrangements through enforcement regulations made under both the Environmental Protection Act 1990 s.140 and the European Communities Act 1972.(EC REGULATION) The new requirements are applicable to the production, distribution, use and recovery, and control of hazardous substances. The regulations also require the recovery of used controlled substances from certain equipment, s uch as fire protection systems, for disposal or recycling, during servicing and maintenance procedures of equipment. A copy of the regulation is attached to Appendix 2. The Victorian Environment Protection Legislation for the Control of Ozone Depleting substances (Victorian Government Gazette No.S57, 1990) this piece of legislation depicts the Australian governments compliance, reliance and advocacy to the implementation of the Montreal protocol on the phasing out of halon use [14]. Environmental Protection agency: Under the Clean Air Amendment, the United States Environmental Protection agency, EPA analysed various substances that could substitute fire extinguishing agents that destroy the ozone layer. These substances also have low global warming potential and low Atmospheric lifetime. The SNAP program (Significant New Alternatives Policy) is used by the EPA to replace the use of halons with environmentally friendly systems in the United States. The Clean Air Act was signed into law in 1990. With this Act, the US banned the production and import of new halons 1211, 1301 and 2402 from the 1st of January 1994 in compliance with the Montreal Protocol. The US government also imposed excise tax on halons through specialized training and proper recycling and disposal. Chapter Three: Halon Systems Halon is the generic name for bromine contained halogenated hydrocarbons. Halons systems were first installed in the late 1960s and early 1970s. In the gaseous form, halons are excellent fire extinguishers. Halons are mostly employed in situations where fire safety standards are high. Halons are identified by a four digit number. The numbering system is assigned by the number of carbon, number of fluorine, chlorine and bromine atoms respectively. Halon 1301, containing carbon, fluorine and bromine is used in total flooding applications while halon 1211, containing carbon, fluorine, chlorine and bromine is used as hand held portable extinguishers. The two common halon types described are effective in extinguishing classes A, B and C fires. These halons are preferred because they exhibited: high efficiency in suffocating combustion, availability in volume at reasonable cost, high storage stability, low electrical conductivity, as well as acceptable toxic properties. 3.1: Characteristics of Halons Halons interfere with the chemical reactions which take place during a fire. The properties of halons allow for its use in most situations and thus most of its applications are linked to particular characteristics. These principal applications include: Clean fire fighting agent: Halons leave no residue after use. This eliminates secondary damages and keeping loss caused by the fire to a minimum [12]. Electrically non-conductive: This property makes it suitable for safe application on fires involving electrical equipment. It will prevent exposure of fire fighters to electric shock. Low toxicity: This property makes halons acceptable and in most cases halon flooding systems are set in automatic mode by default. They can also be used to extinguish fires while people are present in the protected room. Halon flooding systems do not displace so much oxygen which can lead to suffocation[12] Rapid response: Halons are effective for rapid knockdown of flames. This property is mostly essential for class B fires involving liquid and liquefiable solids. Low concentration requirement: This means low quantity or amount of halons are required for extinguishment. It minimizes weight and space allowance [12]. Gaseous state: This allows for good penetration and effective extinguishment in confined spaces. Boiling point: The boiling point of about -4 allows it to be discharged (in the case of hand-held extinguishers) as a liquid for a while before it vaporises. This is a key requirement in some manual fire fighting applications.[12] Low heat of vaporisation: Halons will not condense to form water or ice in halon flooding systems. The most important advantage of halons is in its cost effectiveness. Halon fixed systems are the most cost effective of all extinguishing systems. 3.2: Extinguishing Mechanisms of Halons Halons extinguish fires both chemically and physically. Chemically they interfere with the chemical reactions that take place during the fire. This characterises halons as inhibitors. Radicals released during combustion to keep the fire burning are suppressed chemically by halons. This reaction is anti-catalytic. When halons are heated during combustion, they produce free radicals which compete with those produced by the original combustion process [2]. Halon 1301 produces bromine radicals which react with hydrogen free radicals to produce hydrogen bromide. The hydrogen bromide then reacts with hydroxyl radical to form water and bromide. The bromide released reacts with the combustion fire again and the whole cycle is repeated. The hydrogen and hydroxyl free radicals produced by combustion are greatly reduced in concentration by combining with the halogen free radicals produced by halons [3]. Where RH is the combustible fuel, XBr is a halon agent RH + O2 ENERGY OH + R †¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦.eqn3.1 XBr ENERGY Br + X†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.2 RH + Br HBr + R†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.3 HBr + OH H2O + Br†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.4 RH ENERGY R + H†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.5 H + Br HBr†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.6 The combination of bromine and hydroxyl radical is also an ozone destructive reaction: HOBr UV Br + OH†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦..eqn3.7 OH + O3 HO2 + O2..eqn3.8 Br + O3 BrO + O2†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.9 BrO + HO2 HOBr + O2 †¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦..eqn3.10 3.3: HALONS AND THE OZONE 3.3.1: The ozone layer The earth is enclosed by the atmosphere. This atmosphere is made up of a mixture of numerous gases in varying proportions. The atmosphere is further subdivided into three regions depending on temperature. These regions are: Mesosphere, Stratosphere and Troposphere. The word ozone is from a Greek word, ozein, for to smell. It is an allotropic form of oxygen having three atoms in each molecule. It is a pale blue, highly poisonous gas with a strong odour. [10] In its thickest part in the stratosphere, it is only a trace gas.. Ozone is highest in concentration, about 97%, in the stratosphere (15-60 kilometers above the Earths surface) where it absorbs the ultraviolet radiation from the sun. Ozone is also highly concentrated at the Earths surface in and around cities. The buildup of ozone on the earths surface in and around cities is a result of industrial activities and is toxic to organisms living at the Earths surface. Table 3.1 shows the percentage volume composition of the constituents of atmospheric air *variable gases http://www.physicalgeography.net/fundamentals/7a.html Ozone is very reactive and a stronger oxidising agent than oxygen. It is used in purifying water, sterilising air, and bleaching certain foods. Ozone is formed when an electric spark is passed through oxygen. Ozone is prepared commercially by passing cold, dry oxygen through a silent electrical discharge [7]. Ozone formed in the atmosphere is from nitrogen oxides and organic gases emitted by automobiles and industrial sources [7]. This is achieved by short wavelength ultraviolet. This is actually a health hazard, and it may cause crop damage in some regions. Ultraviolet wavelengths less than 200 nanometer reacts with oxygen molecules to make ozone. O2 UV O + O†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.11 O + O2 O3 + Heat†¦Ã¢â‚¬ ¦.eqn3.12 The heat released here is absorbed by the atmosphere and results in a rise in temperature of the atmosphere. The structure of ozone has 3 oxygen atoms, but steric hindrance prevents it from forming a triangular structure, with each O atom forming the expected 2 bonds. Instead each atom of oxygen forms only 1 bond, with the remaining negative charge being spread throughout the molecule.[7] Ozone is very unstable. It is decomposed either by collision with monoatomic oxygen or by ultraviolet radiation on it. The decomposition causes ozone to form oxygen molecules. Heat is also released to the atmosphere by this reaction O + O3 O2 + O2†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦.eqn3.13 O3 UV O2 + O + Heat†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦.eqn3.14 Ozone is decomposed in the stratosphere to prevent highly energetic ultraviolet radiation from reaching the surface of the earth. 3.3.2: Halons and ozone depletion The ozone layer is mainly depleted by compounds containing chlorine and bromine. Halogens are a chemical family containing fluorine, chlorine, bromine and iodine; any carbon compound containing them is known as a halocarbon. While all halogens have the ability to catalyze ozone breakdown, they have an unequal impact on the ozone layer. The quantity of halons released into the atmosphere is small relative to the number of gases present in the atmosphere. Yet they are more active in destroying the ozone or disrupting the ozone balance for two reasons: Ozone is in a constant state of imbalance, as it is destroyed and produced by natural processes. This process is controlled by solar input that does not undergo significant fluctuations. The stability of halons makes it transportable from the troposphere to the stratosphere where halogens are made active and broken down very fast, destroying ozone in the stratosphere. . The impact is described as depletion potential of the halocarbon. The OZONE DEPLETING POTENTIAL (ODP) is a simple measure of its ability to destroy stratospheric ozone. The ODP of compounds are calculated with reference to the ODP of CFC-11, which is defined to be 1. Thus ODP is a relative measure. A compound withan ODP of 0.2 is, roughly speaking, one-fifth as bad as CFC-11. The ODP of a compound x is expressed mathematically as the ratio of the total amount of ozone destroyed by a fixed amount of compound x to the amount of ozone destroyed by the same mass of CFC-11[8]: Global loss of Ozone due to x ODP(x) == †¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦..eqn3.15[8] Global loss of ozone due to CFC-11. The above expression depicts that the ODP of CFC-11 is 1.0 by definition. The uncertainties experienced in evaluating the global loss of ozone due to a compound are eliminated here since the mathematical expression is a ratio. Evaluating the ODP of a compound is affected by the following: The quantity of chlorine or bromine atoms in a molecule. The nature of the halogen, as bromine is a more ozone- destructive catalyst than chlorine. Atmospheric lifetime of the substance: The atmospheric lifetime of the halon is the time it takes for the global amount of the gas to decay to 36.8% of its original concentration after initial emission. Compounds with low atmospheric lifetimes have lower ODP because it is destroyed in the troposphere. Molecular mass of the substance: This is because ODP is evaluated by comparing equal masses and not number of moles. Table3.2 gives time-dependent and steady-state ODPs for some halocarbon in wide use. Compound Formula Ozone Depletion Potential 10yr 30yr 100yr Steady State CFC-113 CF2ClFCl2 0.56 0.62 0.78 1.10 Carbon tetrachloride CCl4 1.25 1.22 1.14 1.08 Methyl Chloroform CH3CCl3 0.75 0.32 0.15 0.12 HCFC-22 CHF2Cl 0.17 0.12 0.07 0.05 Halon-1301 CF3Br 10.4 Water Mist Replacement for Halon Extinguishers Water Mist Replacement for Halon Extinguishers CHAPTER ONE: 1.1: Introduction Choosing the best fire suppression technology is not an easy task. It even involves discussing risks and operations with insurance companies. The most relevant concern of a fire safety engineer is the protection of life which entails the safe evacuation of personnel. The starting point of a suppression system is a risk analysis to reduce the potential occurrence of a fire. This is followed by the control of the damage and the recovery effort or emergency response associated with the means of fire suppression adopted. The quality of installation, efficiency and maintenance of the suppression system adopted cannot be over-emphasised. The phase out of halons, due to environmental concerns, has lead to forceful development of new fire prevention strategies and technologies that are efficient, as well as environmentally friendly technologies. Fire protection halons were phased out of production in developing countries due to the quest to regulate the use of ozone depleting substances(ODS) as reflected in the Montreal Protocol,1987(London Amendment 1990, and Copenhagen amendment1992). Fire suppression agents have two (2) toxicological aspects to them: The toxicity of the agent The toxicity of combustion products of the agent. Several new fire suppression systems have been developed such as inert and halocarbon gaseous systems, water mist systems, gas and aerosol generators. Fire has been extinguished with water since ancient times. Water in the normal form is not a suitable suppression medium of all classes of fire. The efficiency of water in suppression is enhanced by its use of water in form of mists. Survey by Mawhinney and Richardson in 1996 showed that about 50 agencies worldwide are involved in the research and development of water fire mist and suppression systems. Water mist in fire suppression does not behave like true gaseous agents and is affected by fire size, the degree of obstruction, ceiling and the ventilation conditions of the compartment. To effectively suppress a fire, a water mist system must generate and deliver optimum sized droplets with an adequate. 1.2: Objectives and Structure of Dissertation This project aims at studying the water mist as a replacement for halons systems in the extinguishment of fires. This replacement is a direct consequence of the phase out of halons due to environmental issues and the need to find a drop-in replacement or a suitable alternative in areas where high level of fire safety is required and the cost of fatalities is too high. Chapter 2 2.1: Overview of Fire Suppression To suppress fires, the type of fire needs to be identified. The class of the fire to be extinguished also determines the type of extinguisher that can be used. There are six (6) types of fires: Class A FIRES: These involve flammable or combustible solids such as wood, rubber, fabric, paper and some plastics. Class B FIRES: These are fires involving flammable and combustible liquids or liquefiable solids such as oil, alcohol, petrol, paint and liquefiable waxes.[9] Class C FIRES: These are fires involving flammable gases such as natural gas, hydrogen, propane, butane.[9] Class D FIRES: These are fires involving combustible metals, such as sodium and potassium.[9] Class E FIRES: These are fires involving any of the materials found in Class A and B fires, but including electrical appliances, wiring, or other electrically energized objects in the vicinity of the fire, with a resultant electrical shock risk if a conductive agent is used to control the fire.[9] http://www.sqa.org.uk/e-learning/FirstLineO2CD/page_06.htm Class F FIRES: These fires involve cooking fats and oils, especially in industrial kitchens. The temperature of these fats and oil on fire is much greater than that of other flammable liquids. 2.2: Means of Fire Suppression The aim of fire suppression is to provide cooling, control the spread of the fire as well as extinguish the fire. The behaviour of a fire is charcterised by the fire triangle which has fuel, oxygen and heat as its three sides. Combustion process is represented by: Fuel + O2 HEAT H2O + CO2 †¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦.eqn2.1 The combustion process is an exothermic reaction, involving a fuel and oxygen. The ratio of fuel to air must be within the flammability limits of the fuel for combustion to occur. The Lower Flammability Limit (LFL) is the minimum concentration of fuel vapour in air, below which a flame cannot be supported in the presence of an ignition source. The Upper Flammability Level (UFL) is the maximum concentration of fuel vapour in air, above which a flame cannot be supported. Stoichiometric Mixture is the ratio of fuel in oxygen that requires minimal energy to support a flame. A branch of the triangle must be removed for the fire to be extinguished. Fires can either be smoldering or flaming combustion. Smoldering occurs when solids such as wood or plastics burn at or on the surface. It usually involves the release of toxic gases and can be difficult to extinguish. Flaming combustion is a gas phase phenomenon that involves the release of visible and infrared radiation. This type of fire generates much more heat. The extinguishing of a fire involves either chemical or physical mechanisms. Physical mechanism: Involves the removal of one side of the fire triangle. This can be done by either blanketing the fire (causing the fuel and air to be separated) or by removing the heat source using an agent with a high heat capacity/ latent heat of vaporization (this will cool the flame by absorbing the heat). Physical mechanism could be thermal or dilution. Thermal physical effect involves adding non-reactive gas to a fire plume leading to a reduction in the flame temperature. This is achieved by the distribution of the heat generated to a larger heat area. The heat capacity of the introduced agent determines the efficiency of the process. On the other hand, for dilution physical effect, the collision frequency of oxygen molecules with the fuel is lowered when the additional gas is introduced into the fuel-air mixture. This effect is quite minimal and negligible. Chemical mechanism: This is the use of an extinguishing agent or its degradation product to disrupt the chain reaction for sustaining combustion. This entails inhibition by halogen atoms. Most good suppressants apply both the physical and the chemical mechanisms. The type of hazard associated with an area determines the fire protection system that will be put in place. Halons have been used in a wide range of applications. Other alternatives include: Water Sprinkler Systems: This is a very common type of fixed protection that offers safe protection to limit structural damage. The cost of installing water sprinkler systems into existing structures is quite expensive. They are better at protecting structures than its contents [11]. The reliability of water sprinkler system has encouraged its wide use. Accidental discharge is uncommon with water sprinkler systems. Water sprinklers have a much slower response than other systems. They also cause a considerable secondary damage. They cannot be used on live electrical equipment and flammable liquids, but they are used widely in computer and control rooms as well as storage rooms in the USA. Detectors: This involves the use of high sensitive smoke detection. This is not exactly an active fire protection approach but it serves as an initiator to other fire protection systems [2]. Carbon dioxide: Carbon dioxide is widely used in gaseous based fire extinguishing systems. There are two types of carbon dioxide system depending on the manner by which they are stored. These are high pressure and low pressure carbon dioxide systems. It is a clean agent and has a good penetrating ability. This makes it safe for use on live electrical equipment. They are also used in unoccupied spaces such as computer and control rooms. Carbon dioxide causes very minimal direct or secondary damage and allows the installation being put back to immediate use after a fire. It is however toxic and cannot be used in total flooding situations. Carbon dioxide cannot also be used in situations where weight and space are important. High concentrations of carbon dioxide are required for extinguishment and as such they are bulky and heavy. They cannot be used in manned areas because they reduce the oxygen concentration to levels below life support and thus cannot be set in automatic mode. Carbon dioxide systems are generally fast acting and cost effective. Carbon dioxide has also found use in record storage, flammable liquid fires, chemical processing equipment, turbine generators, marine applications, computer rooms and shipboard machinery. Inert Gases: inert gases in use for fire suppression are majorly argon and nitrogen mixtures. These are electrically non-conductive fire suppressants. The mechanism behind their use is the lowering of the oxygen concentration of air to that below the lower flammability point (LFL). They are not liquefied gases and they are bulky because they are stored at high pressure. The concentration of inert gases released in the hazardous area is high because they have densities that are similar to that of air. Their response time is not very fast and so they are not efficient in situations where the rate of fire spread is high. Inert gases do not decompose thermally and thus they form no breakdown products [2]. Inert gases can cause an extreme decrease in the composition of oxygen in the body accompanied by an increase in the concentration of carbon dioxide leading to loss of consciousness or death and as such health and safety issues have to be considered in its use. Inert gases have found wi de acceptance because they pose no environmental problems. They are not ozone depleting substances neither do they contribute to global warming. They are employed in computer and control rooms, record storage, flammable liquid fires and shipboard machinery [2]. Halocarbon Gases: These are hydrofluorocarbons and perfluorocarbons with zero ozone depleting potentials. They are however greenhouse gases and are governed by the Kyoto protocol and hence its release counts towards the national emissions inventory of global warming gases. Halocarbons are electrically non-conductive, are clean agents and are not bulky in terms of space and weight. Foam Systems: Foam systems could be low, medium or high expansion systems. Foam systems are efficient for extinguishing liquid pool fires and large cable fires. In this case, the foam acts as a barrier between the fire and the supply of oxygen. The use of chemical dispersants to clean up after its use has limited the wide use of foam systems. Furthermore the use of smoke detectors for its activation limits its speed of response. They cannot be used to protect any substance that reacts violently with water. Foams systems are often used with water sprinklers. This increases the efficiency of the systems. Foam systems have found use in the extinguishment of flammable liquid fires, engine compartments and shipboard machinery. Dry Powder: Powders have very high response time for extinguishing fires but have no cooling effect. They thus become ineffective as soon as it settles [2]. They are limited in application to extinguishing flammable liquid fires as well as engine spaces. Fine Solid Particulates: This system is used in combination with halocarbon gases and inert gases [2]. They have the advantage of reduced wall and surface losses relative to water mist and particle size is easier to control[2]. They however pose problems to sensitive equipment and cannot be used for explosion suppression applications because they are generated at high temperatures. Fine solid particulates can only be used in unmanned areas because of the problems associated with inhalation of particulate substances. Water Mist: This employs the use of fine water sprays, usually less than 100 microns in diameter. Water mists can be used on flammable liquid fires, as well as electrical equipment. They are not as effective on small or slow burning fires. Water mist installations pose problems in their design and fabrication. Hybrid Systems: Hybrid systems combine one or more of the above fire protection system. A common example of this is the combination of water mist systems and carbon dioxide. There are two methods of applying fire extinguishing agents-Total Flooding and Local Application. Total Flooding: They are operated automatically and manually. It entails applying an extinguishing agent to an enclosed space to achieve a concentration of the extinguisher that is capable of putting out the fire. This method is the most common system of application Local Application: The agent is applied directly onto the fire plume or the affected enclosure. Portable fire extinguishers are the most common forms of this approach. This method is also known as streaming application. There is an increase in the need for the phasing out of halons and this has brought the search for the perfect or drop-in replacement. The department of trade and industry in 1995 listed checklists for the selection of alternatives to halons in critical uses situations as: Fire fighting effectiveness: This involves the speed of fire suppression, the post fire hold time, the ability of the alternative to permeate, the elimination of the risk of reignition, the suitability of the alternative to the fire hazard. Ease of Installation: Ease of maintenance, pipe work, and cost of installation, cost of refill, floor space and weight, system re-instate time, and availability of the extinguisher. Hazards to occupants: Toxicity, noise levels, pressurisation, inhalation, visibility, safety as regards electrical work, thermal decomposition products [2]. Discharge effect on equipment: water damage, clean up, corrosion, thermal shock. Environmental acceptability: Ozone depletion potential, atmospheric lifetime, and global warming potential. Discharge damage: This entails clean up of the agent after use, water damage, thermal shock and corrosion. Esso Australia, while looking for alternatives to halons on their installations considered the following issues [14]: Effectiveness at extinguishing fires Environmental effects (a zero ozone depleting and global warming potential) of the agent before use and after thermal decomposition. Toxicity level and a safety margin between its No Observed Adverse Effects Level (NOAEL value) and the extinguishing concentration required Third party approval from regulatory bodies and safety partners such as International Maritime Organisation (IMO), NFPA, and EPA or Underwriters laboratory Organisations. Level of engineering required to modify an existing halon protected installations. Availability as regards to installation and maintenance at a reasonable cost. 2.2: Health and Safety Issues Considering the health and safety in the UK, there is no specific regulation as regards choice of fire extinguishing systems. Otherwise fire risks and risk from the use of extinguishment can be categorised under risks at work. The Management of Health and Safety at Work Regulations 1992 stipulates all risks at work are to be assessed and prevented where ever it is reasonably practicable, controlled. In cases where fire extinguishing systems contain toxic substances then the Control of Substances Hazardous to Health Regulations 1988 (COSHH regs) will also apply. The basis of the two regulations is the prevention rather than control of the risk. 2.3: Environmental regulations The International Maritime Organisation (IMO) has prohibited the use of new halon systems from 1994, but accepts the use of existing ones. The EU has banned its use onboard vessels by the end of 2003. The following are regulations that are put in place to phase out the use of halons. The Montreal protocol on Substances that Deplete the Ozone layer- the Montreal protocol, signed by 25 countries on the 16th of September, 1987 is an international treaty for the control of the production and use of ozone depleting substances. It involves the restriction and eventual prohibition of the production, distribution and use of Ozone Depleting Substances. A copy of this document is attached in Appendix 1. The EC regulations: This European legislation was put in place to further tighten the restriction on the ban of ozone depleting substances. EC Regulation 3093/94 came into force on the 23rd of December 1994. EC Regulation 3093/94 is directly binding in all EU Member States and does not require any national implementing legislation. The new Regulation EC 2037/2000 came into force on 1 October 2000, replacing the Regulation 3093/94. The enforcement requires the use of bodies such as the HM Customs and Excise concerning import of controlled substances. The Department of the Environment proposes to implement these arrangements through enforcement regulations made under both the Environmental Protection Act 1990 s.140 and the European Communities Act 1972.(EC REGULATION) The new requirements are applicable to the production, distribution, use and recovery, and control of hazardous substances. The regulations also require the recovery of used controlled substances from certain equipment, s uch as fire protection systems, for disposal or recycling, during servicing and maintenance procedures of equipment. A copy of the regulation is attached to Appendix 2. The Victorian Environment Protection Legislation for the Control of Ozone Depleting substances (Victorian Government Gazette No.S57, 1990) this piece of legislation depicts the Australian governments compliance, reliance and advocacy to the implementation of the Montreal protocol on the phasing out of halon use [14]. Environmental Protection agency: Under the Clean Air Amendment, the United States Environmental Protection agency, EPA analysed various substances that could substitute fire extinguishing agents that destroy the ozone layer. These substances also have low global warming potential and low Atmospheric lifetime. The SNAP program (Significant New Alternatives Policy) is used by the EPA to replace the use of halons with environmentally friendly systems in the United States. The Clean Air Act was signed into law in 1990. With this Act, the US banned the production and import of new halons 1211, 1301 and 2402 from the 1st of January 1994 in compliance with the Montreal Protocol. The US government also imposed excise tax on halons through specialized training and proper recycling and disposal. Chapter Three: Halon Systems Halon is the generic name for bromine contained halogenated hydrocarbons. Halons systems were first installed in the late 1960s and early 1970s. In the gaseous form, halons are excellent fire extinguishers. Halons are mostly employed in situations where fire safety standards are high. Halons are identified by a four digit number. The numbering system is assigned by the number of carbon, number of fluorine, chlorine and bromine atoms respectively. Halon 1301, containing carbon, fluorine and bromine is used in total flooding applications while halon 1211, containing carbon, fluorine, chlorine and bromine is used as hand held portable extinguishers. The two common halon types described are effective in extinguishing classes A, B and C fires. These halons are preferred because they exhibited: high efficiency in suffocating combustion, availability in volume at reasonable cost, high storage stability, low electrical conductivity, as well as acceptable toxic properties. 3.1: Characteristics of Halons Halons interfere with the chemical reactions which take place during a fire. The properties of halons allow for its use in most situations and thus most of its applications are linked to particular characteristics. These principal applications include: Clean fire fighting agent: Halons leave no residue after use. This eliminates secondary damages and keeping loss caused by the fire to a minimum [12]. Electrically non-conductive: This property makes it suitable for safe application on fires involving electrical equipment. It will prevent exposure of fire fighters to electric shock. Low toxicity: This property makes halons acceptable and in most cases halon flooding systems are set in automatic mode by default. They can also be used to extinguish fires while people are present in the protected room. Halon flooding systems do not displace so much oxygen which can lead to suffocation[12] Rapid response: Halons are effective for rapid knockdown of flames. This property is mostly essential for class B fires involving liquid and liquefiable solids. Low concentration requirement: This means low quantity or amount of halons are required for extinguishment. It minimizes weight and space allowance [12]. Gaseous state: This allows for good penetration and effective extinguishment in confined spaces. Boiling point: The boiling point of about -4 allows it to be discharged (in the case of hand-held extinguishers) as a liquid for a while before it vaporises. This is a key requirement in some manual fire fighting applications.[12] Low heat of vaporisation: Halons will not condense to form water or ice in halon flooding systems. The most important advantage of halons is in its cost effectiveness. Halon fixed systems are the most cost effective of all extinguishing systems. 3.2: Extinguishing Mechanisms of Halons Halons extinguish fires both chemically and physically. Chemically they interfere with the chemical reactions that take place during the fire. This characterises halons as inhibitors. Radicals released during combustion to keep the fire burning are suppressed chemically by halons. This reaction is anti-catalytic. When halons are heated during combustion, they produce free radicals which compete with those produced by the original combustion process [2]. Halon 1301 produces bromine radicals which react with hydrogen free radicals to produce hydrogen bromide. The hydrogen bromide then reacts with hydroxyl radical to form water and bromide. The bromide released reacts with the combustion fire again and the whole cycle is repeated. The hydrogen and hydroxyl free radicals produced by combustion are greatly reduced in concentration by combining with the halogen free radicals produced by halons [3]. Where RH is the combustible fuel, XBr is a halon agent RH + O2 ENERGY OH + R †¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦.eqn3.1 XBr ENERGY Br + X†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.2 RH + Br HBr + R†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.3 HBr + OH H2O + Br†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.4 RH ENERGY R + H†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.5 H + Br HBr†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.6 The combination of bromine and hydroxyl radical is also an ozone destructive reaction: HOBr UV Br + OH†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦..eqn3.7 OH + O3 HO2 + O2..eqn3.8 Br + O3 BrO + O2†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.9 BrO + HO2 HOBr + O2 †¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦..eqn3.10 3.3: HALONS AND THE OZONE 3.3.1: The ozone layer The earth is enclosed by the atmosphere. This atmosphere is made up of a mixture of numerous gases in varying proportions. The atmosphere is further subdivided into three regions depending on temperature. These regions are: Mesosphere, Stratosphere and Troposphere. The word ozone is from a Greek word, ozein, for to smell. It is an allotropic form of oxygen having three atoms in each molecule. It is a pale blue, highly poisonous gas with a strong odour. [10] In its thickest part in the stratosphere, it is only a trace gas.. Ozone is highest in concentration, about 97%, in the stratosphere (15-60 kilometers above the Earths surface) where it absorbs the ultraviolet radiation from the sun. Ozone is also highly concentrated at the Earths surface in and around cities. The buildup of ozone on the earths surface in and around cities is a result of industrial activities and is toxic to organisms living at the Earths surface. Table 3.1 shows the percentage volume composition of the constituents of atmospheric air *variable gases http://www.physicalgeography.net/fundamentals/7a.html Ozone is very reactive and a stronger oxidising agent than oxygen. It is used in purifying water, sterilising air, and bleaching certain foods. Ozone is formed when an electric spark is passed through oxygen. Ozone is prepared commercially by passing cold, dry oxygen through a silent electrical discharge [7]. Ozone formed in the atmosphere is from nitrogen oxides and organic gases emitted by automobiles and industrial sources [7]. This is achieved by short wavelength ultraviolet. This is actually a health hazard, and it may cause crop damage in some regions. Ultraviolet wavelengths less than 200 nanometer reacts with oxygen molecules to make ozone. O2 UV O + O†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦eqn3.11 O + O2 O3 + Heat†¦Ã¢â‚¬ ¦.eqn3.12 The heat released here is absorbed by the atmosphere and results in a rise in temperature of the atmosphere. The structure of ozone has 3 oxygen atoms, but steric hindrance prevents it from forming a triangular structure, with each O atom forming the expected 2 bonds. Instead each atom of oxygen forms only 1 bond, with the remaining negative charge being spread throughout the molecule.[7] Ozone is very unstable. It is decomposed either by collision with monoatomic oxygen or by ultraviolet radiation on it. The decomposition causes ozone to form oxygen molecules. Heat is also released to the atmosphere by this reaction O + O3 O2 + O2†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦.eqn3.13 O3 UV O2 + O + Heat†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦.eqn3.14 Ozone is decomposed in the stratosphere to prevent highly energetic ultraviolet radiation from reaching the surface of the earth. 3.3.2: Halons and ozone depletion The ozone layer is mainly depleted by compounds containing chlorine and bromine. Halogens are a chemical family containing fluorine, chlorine, bromine and iodine; any carbon compound containing them is known as a halocarbon. While all halogens have the ability to catalyze ozone breakdown, they have an unequal impact on the ozone layer. The quantity of halons released into the atmosphere is small relative to the number of gases present in the atmosphere. Yet they are more active in destroying the ozone or disrupting the ozone balance for two reasons: Ozone is in a constant state of imbalance, as it is destroyed and produced by natural processes. This process is controlled by solar input that does not undergo significant fluctuations. The stability of halons makes it transportable from the troposphere to the stratosphere where halogens are made active and broken down very fast, destroying ozone in the stratosphere. . The impact is described as depletion potential of the halocarbon. The OZONE DEPLETING POTENTIAL (ODP) is a simple measure of its ability to destroy stratospheric ozone. The ODP of compounds are calculated with reference to the ODP of CFC-11, which is defined to be 1. Thus ODP is a relative measure. A compound withan ODP of 0.2 is, roughly speaking, one-fifth as bad as CFC-11. The ODP of a compound x is expressed mathematically as the ratio of the total amount of ozone destroyed by a fixed amount of compound x to the amount of ozone destroyed by the same mass of CFC-11[8]: Global loss of Ozone due to x ODP(x) == †¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦..eqn3.15[8] Global loss of ozone due to CFC-11. The above expression depicts that the ODP of CFC-11 is 1.0 by definition. The uncertainties experienced in evaluating the global loss of ozone due to a compound are eliminated here since the mathematical expression is a ratio. Evaluating the ODP of a compound is affected by the following: The quantity of chlorine or bromine atoms in a molecule. The nature of the halogen, as bromine is a more ozone- destructive catalyst than chlorine. Atmospheric lifetime of the substance: The atmospheric lifetime of the halon is the time it takes for the global amount of the gas to decay to 36.8% of its original concentration after initial emission. Compounds with low atmospheric lifetimes have lower ODP because it is destroyed in the troposphere. Molecular mass of the substance: This is because ODP is evaluated by comparing equal masses and not number of moles. Table3.2 gives time-dependent and steady-state ODPs for some halocarbon in wide use. Compound Formula Ozone Depletion Potential 10yr 30yr 100yr Steady State CFC-113 CF2ClFCl2 0.56 0.62 0.78 1.10 Carbon tetrachloride CCl4 1.25 1.22 1.14 1.08 Methyl Chloroform CH3CCl3 0.75 0.32 0.15 0.12 HCFC-22 CHF2Cl 0.17 0.12 0.07 0.05 Halon-1301 CF3Br 10.4

The Movie Amarcord Essay -- essays research papers fc

The movie Amarcord was directed by Federico Fellini and shot in 1974. The setting of the story is a small town in Italy during the time period of the 1930’s. In my research, I discovered that Mr. Fellini based most of his movies on his life experiences. The town depicted in this movie is Rimini, his home town. He was a well known director who was not afraid to express his characters’ emotions and actions in bizarre or unorthodox ways. The scene I watched opens with a young man, Titta, stopping by a tobacco store to purchase a cigarette. The shopkeeper is a robust, very well-endowed older women. When he walks in, the fat woman is all alone. Titta is skinny and immature and wants to prove his strength by claiming he can lift the fat woman off the ground. The fat woman closes the door for privacy and lets Titta try. He is so determined that Titta accomplishes this feat by lifting her more than once. Titta is sweating a great deal and breathing so heavy after this that he has to sit down to get his breath. As Titta struggles to lift her, the fat woman has a look of ecstasy on her face as if she was engaged in sexual activity. The next thing that happens is the fat woman opens her sweater and whips out her breasts. Titta is inexperienced and does not know how to handle the situation. He’s not sure what he’s supposed to do. The fat woman tells him to suck her breasts. Titta tries to please her, but again b ecause he is inexperienced. He struggles to give her sexual satisfaction by continuing to suck and ask if he is doing it right. The fat woman becomes frustrated because she has not reached her sexual peak and rebuffs Titta. The next thing you know she gives him a cigarette and tells him to leave. Titta is too tired and weak to open the door, so the fat woman says she’ll do it and opens it easily. The director used the camera angles to illustrate the emotions of the two characters. The camera focused on the fat woman’s big girth when Titta first walked into the shop and again when he was trying to lift her. There were several close-up shots of the woman’s face depicting sexual arousal as he was trying to lift her and again as he was sucking on her breasts. The close-up shots of Titta’s face were also well done because they showed him sweating and making these strange facial expressions because she was too heavy. You could tell from the close-up shots of his fac... ... the director, Federico Fellini, did a brilliant job in creating this movie. The varying camera angles and lighting techniques helped to make the film seem true to life. In my opinion, the movie did not have a specific plot. I believe it was more of an attempt to look at life through a young man’s fantasies. The movie received several awards including an Academy Award in 1975 for Best Foreign Language Film, New York Film Critics Circle Awards for Best Director and Best Film (1974), and Best Foreign Language Film (1974) from National Board of Review. If you like farcical comedy, then you would enjoy this movie. I would recommend it for adults of all ages. Bibliography Amarcord. Dir. Federico Fellini. Screenplay Federico Fellini and Tonino Guerra. Perf. Magali Noel and Bruno Zanin. S.C. Produzzioni S.R.L – P.E.C.F. 1974 Giannetti, Louis and Scott Eyman. Flash-back: A Brief History of Film. 4th ed. New Jersey: Prentice-Hall, Inc, 2001. Internet Movie Database Inc. Amarcord IMDb. 2002. Juggling Information Service. Amarcord – Juggling. 2000. . . FILM APPRECIATION SECOND PAPER

American Alligator Primary Habitats

Alligator mississippiensis is in the family Crocodylidae. This family has existed since the upper Triassic period, but the modern family members appear in the fossil record as little as 80 million years ago. There are three subfamilies, Alligatorinae, Crocodylinae, and Gavaialinae. Some people also include a fourth subfamily, Tomistominae, which contains a single species, the False Gharial. Alligatorinae includes the American and Chinese alligators and the caimans. Crocodylinae includes the crocodiles. Gavaialinae contains the gharials (or gavials). The alligators are unusually tolerant of cold and have been found frozen in ice at the most northern parts of their ranges (Beck). All of the family Crocodylidae is endangered. However, the American alligator has undergone a dramatic population resurgence because of human protection. Restrictions are still in place on capturing alligators from the wild (Beck). Studies have shown that using hormones such as norethindrone can be used to feminize alligator embryos at the male producing temperature (Lance, 79). This could lead to a way to help alligators increase in numbers of both sexes as well as help other members of the family Crocodylidae. Alligators are important ecologically and are dependent on the spatial and temporal patterns of water fluctuations. Patterns of courtship, mating, nesting, and habitat use are all dependent on marsh water levels. Alligators are a great study organism to study the adaptations and responses to the seasonal changes to the hydrological conditions in the everglades. Alligators seem to be able to adjust the height of the nest egg cavity based on the spring water levels, which historically indicated the water levels later in the nesting season. Water levels also determine the availability of food therefore affecting the patterns of growth and survival. Alligators are most abundant in central sloughs, which is probably due to recommendations regarding managing hydrological conditions for alligators focused on maintaining alligators in central slough habitats (Mazzotti, 485). The American alligator is one of the keystone species in the Florida everglades and other marsh systems. It is the only large, abundant, widespread nonmarine carnivore left in the southeastern United States (Mazzotti, 485). They are spread as far west as reserves in Texas, and their northern boundary is in South Carolina. The interesting thing about alligators is the temperature determination of sex. At 29? C all females will be produced. At 32? C all males are produced. Temperatures in-between will produce mixed sets of young. The lower the temperature the less yolk there is for the young, there fore the young turns out smaller and female (Allsteadt, 76). It would be the opposite for warmer temperatures. The female alligator chooses the nest site, which in turn determines the sex of the young. The sex of the young is determined in the first two-thirds of incubation. During the final third of incubation the quality of the young is determined. Snout length, carcass lean dry and lipid mass, and yolk sac lean dry and lipid mass are determined by the final third of the incubation period (Congdon, 497). These characteristics could affect the vitality of the young in competition after they hatch. In South Carolina growth rates of alligators were thought to be slower, but it seems that alligators reach sexual maturity at a later age and larger body size than alligators elsewhere. It is assumed that the delayed breeding of alligators in South Carolina may be related more to social dominance than to growth rates. It is essential that age and size relations need to be understood better if alligators are to be managed effectively (Wilkinson, 397). All alligators, caimans, gavials, and crocodiles are carnivorous. In the wild, each depends upon a somewhat different selection of prey from its local fauna. For captive specimens, diet should vary with the size of the animal and the availability of prey. Small captives will do well on small animals (e. g.. goldfish, insects, or mice. ) As the reptile grows, its diet should change from mice to rats to rabbits, chickens, and other suitable larger prey. It's prudent to supplement meals with added calcium. Reptiles are susceptible to a variety of cutaneous and deep mycotic infections, however relatively few cases are reported in the American alligator. A juvenile alligator in Texas was captured that was covered with a fungus-like material, which was a dermetophillic fungus (Foreyt, 530). This could indicate that alligators are becoming more susceptible to cutaneous infections. Since alligator's sex is determined by temperature there is a problem with primarily one sex being born. This causes a major problem since you have to have both male and female to produce young in alligators. Many surveys of juveniles and adults show a male-biased ratio, although a female-biased ratio exists in Louisiana. From a study of 25 nests with 778 hatchlings a ratio of 1 male to every 3. 8 females was determined (Rhodes, 640). However since sex ratios vary temporally and spatially, long tern studies in representative habitats would be required for adequate ratios. Hypoxic incubated alligator eggs temp to hatch later and produce smaller young. Their hematocrit was significantly higher after hatching. Alligators exposed to 20% Oxygen maintained oxygen consumption relative to their normoxic siblings despite their lower mass (Warburton, 44). Obviously being in hypoxic conditions wouldn't be life threatening to a certain point, but in future competition being smaller than the rest of the alligators is not a good quality. Humans as usual are a threat to any type of wildlife including alligators. Thirty farms in Florida's swampland are currently raising an estimated 100,000 alligators. They sold nearly 26,000 adult skins in 1995. The price for skins has increased 67% since 1993, and 30 % from 1995 to 1996 (Good). With skins being worth more each year, $150. 00 in 1996, more people may decide to take a risk in capturing alligators from the wild to sell skins. This could be detrimental to the wild population of alligators. However in 1998 trappers reported a decline in the demand for alligator skins resulting in a decrease in the price for skins. This helps slow programs where alligators that frighten people are killed (Falling, 6). If skins become popular again programs like these would hurt the population. This program has flaws because most alligators are relatively calm. The psychological orientation of alligators is interesting. It appears that alligators tend to regard humans as animals larger than themselves and thus will not generally attack a human without provocation. However, they will certainly look after their interests, and a small number of accidents have occurred when their predatory or protective instincts were inadvertently triggered. Crocodilians will attack in self-defense, to obtain food, and to protect their young up to two years after birth. Indeed, the outstanding parental care they afford is unique among herps and (along with certain anatomical features) illustrates the close alliance of this family to birds and, ultimately, dinosaurs (Beck).

Big Problems Of Child Labor Young People Essays

Big Problems Of Child Labor Young People Essays Big Problems Of Child Labor Young People Essay Big Problems Of Child Labor Young People Essay Child labour is one of the biggest jobs around the universe because it puts kids in danger. It is fundamentally utilizing that under elderly kids in any signifier coercing them to work which maltreatment, injuries or violet them. This maltreatment may be physical, mental or sexual denying the kids of their rights of basic instruction. This job is increasing in many states that are because of poorness and other issues, but poorness is the most ground for doing child labour. ( 1 2 3 Help Me. Internet resources. ) There are many different causes of bad kid labour around the universe. Parents are one of the causes for child labour particularly illiterate parents. Some parents are non able to work so they force their kids to work alternatively of them. Hence, kids are more easy employed because they get less money paid than grownups and they are easier to acquire abused. Other cause that is the seedbed of child labour and the biggest cause for child labour is Poverty. In some hapless states, the authorities does nt assist hapless households by supplying instruction, wellness attention or happen for them work to acquire money. So, in this instance parents are forced to direct their kids to work and acquire money to their parents. Ignorance for the rights of kid to be educated and non to be abused, so there are some parents that are rich but they spend their money on imbibing, purchasing drugsaˆÂ ¦ they force their kids to work. Otherwise, the kids can be beaten or can be abused by their pa rents so kids are forced to go forth the place. And when they leave place besides they are forced to work because they lost the protection and they need to acquire me to last entirely in this difficult life. ( Child Labour . OVC Support. Internet resources. ) Most societies expect kids to make signifier of work. So, kids are expected to play a portion in household work from an early age. This will take to harmful effects of child labour including low wage. Employers think that mistreating kids is easier than grownups, so kids are frequently paid much less for work done than grownups. Long hours, some kids are expected to work inordinate hours that will ensue by physical injury. Besides, one of the effects of child labour is losing instruction and taking their rights. Working kids will take for physical injury in many ways, because of long hours of working the organic structure of the kid can non keep difficult work as adult male therefore they will endure from physical injuries. Besides, Children working in mills that contain large machines may do the kids to cut their custodies or hurt themselves. Children that work in the street are besides at hazard of physical force from constabulary officers. Besides, they may confront in the street aliens or stealers that would steal their money. Children that work in street may acquire ill because of the bad conditions and they do nt hold money to purchase apparels. Besides, kids that work in mills that contain toxic gases may take for bad diseases for kids. kids that work in any topographic point but particularly in mills and street may be abused sexually. Physical, sexual or emotional maltreatment can go forth terrible impact on the kid for old ages. It can do several jobs in the in the physical and emotional development of the kid. Some other common psychological consequence of kid maltreatment is behavior job attending job, or drug maltreatment. These all psychological maltreatment for kid will take to be a bad individual in future when he/she grows up. They will do bad things because when they were kids their rights were taken from them and they were abused. Therefore, they will ache other people abuse them, bargain, taking drugs, hapless relationship with the opposite s ex, and do bad things that with done for them when they were kids. ( Buzzle. Internet resources. ) Exploitative kid labour is a immense job impacting the universe today. Some people think it impossible to stop exploitatory kid labour. There are possible solutions, though. One measure towards eliminating child labour is making international Torahs that states can follow in order to halt kid labour. Governments can play a cardinal function in extinguishing child labour by go throughing Torahs that ban child labour under a certain age. But in some states these Torahs are nt enforced. So, authorities must work more to implement these Torahs so that it can do a positive impact on diminishing child labour. Sometimes, child labour is caused because parents do non hold steady occupations or adequate income. Therefore, authoritiess must back up these hapless states in order to diminish the figure of kids working in streets. Children need to larn and compose. Besides, authoritiess must do instruction free and mandatory up until the minimal legal age for employment. Hence, authoritiess of al l states must take rough step against kid trafficking. Replacing child worker by grownup workers is a solution for child labour. ( library.thinkquest.org/03oct/ /globalsolutions.htm ) Child labour is a complex job that requires comprehensive, many-sided solution. The most of import solution is to give kids their right to be educated, protected, and to inquire existent kid labour what they think the best solution would be, since it is they who would really be affected. Child labour is a abhorrent job that must be faced to salvage the hereafter of those kids. ( library.thinkquest.org/03oct/ /globalsolutions.htm ) Mentions 1 2 3 Help Me. Internet resources. 23 January 2010. lt ; www.123helpme.com gt ; Child Labour . OVC Support. Internet resources. 23 January 2010. lt ; hypertext transfer protocol: //www.ovcsupport.net/sw3424.asp gt ; Buzzle. Internet resources. 23 January 2010. lt ; www.buzzle.com/ /the psychological_effect of _child abuse.hmtl gt ; lt ; library.thinkquest.org/03oct/ /globalsolutions.htm gt ; lt ; library.thinkquest.org/03oct/ /globalsolutions.htm gt ;