Fire Remediation Services Kyle

Fire Remediation Services , termed a bonfire Play media The ignition and extinguishing of a pile of wood shavings Play media The fire maps show the locations of actively burning fires around the world on a monthly basis, based on observations from the Moderate Resolution Imaging Spectroradiometer (MODIS) on NASA’s Terra satellite. The colors are based on a count of the number (not size) of fires observed within a 1,000-square-kilometer area. Fire Damage Cleaning show the high end of the count—as many as 100 fires in a 1,000-square-kilometer area per day. Yellow pixels show as many as 10 fires, orange shows as many as 5 fires, and red areas as few as 1 fire per day.

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Fire is the rapid oxidation of a material in the exothermic chemical process of combustion, releasing heat, light, and various reaction products.[1] Slower oxidative processes like rusting or digestion are not included by this definition.

Fire is hot because the conversion of the weak double bond in molecular oxygen, O2, to the stronger bonds in the combustion products carbon dioxide and water releases energy (418 kJ per 32 g of O2); the bond energies of the fuel play only a minor role here.[2] At a certain point in the combustion reaction, called the ignition point, flames are produced. The flame is the visible portion of the fire. Flames consist primarily of carbon dioxide, water vapor, oxygen and nitrogen. If hot enough, the gases may become ionized to produce plasma.[3] Depending on the substances alight, and any impurities outside, the color of the flame and that’s why they use best fire damage assessment services will be different.

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Fire in its most common form can result in conflagration, which has the potential to cause physical damage through burning. Fire is an important process that affects ecological systems around the globe. The positive effects of fire include stimulating growth and maintaining various ecological systems.

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The negative effects of fire include hazard to life and property, atmospheric pollution, and water contamination.[4] If fire removes protective vegetation, heavy rainfall may lead to an increase in soil erosion by water.[5] Also, when vegetation is burned, the nitrogen it contains is released into the atmosphere, unlike elements such as potassium and phosphorus which remain in the ash and are quickly recycled into the soil.

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Fire has been used by humans in rituals, in agriculture for clearing land, for cooking, generating heat and light, for signaling, propulsion purposes, smelting, forging, incineration of waste, cremation, and as a weapon or mode of destruction.

Main article: Combustion The fire tetrahedron

Once ignited, a chain reaction must take place whereby fires can sustain their own heat by the further release of heat energy in the process of combustion and may propagate, provided there is a continuous supply of an oxidizer and fuel.

Fire can be extinguished by removing any one of the elements of the fire tetrahedron. Consider a natural gas flame, such as from a stovetop burner. The fire can be extinguished by any of the following:

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In contrast, fire is intensified by increasing the overall rate of combustion. Methods to do this include balancing the input of fuel and oxidizer to stoichiometric proportions, increasing fuel and oxidizer input in this balanced mix, increasing the ambient temperature so the fire’s own heat is better able to sustain combustion, or providing a catalyst; a non-reactant medium in which the fuel and oxidizer can more readily react.

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Fire Damage Cleaning Cost Smoke Smoke from a bee smoker, used in beekeeping. An internationally recognizable "No Smoking" sign.

Smoke is a collection of airborne solid and liquid particulates and gases[1] emitted when a material undergoes combustion or pyrolysis, together with the quantity of air that is entrained or otherwise mixed into the mass. It is commonly an unwanted by-product of fires (including stoves, candles, oil lamps, and fireplaces), but may also be used for pest control (fumigation), communication (smoke signals), defensive and offensive capabilities in the military (smoke-screen), cooking, or smoking (tobacco, cannabis, etc.). Smoke is used in rituals where incense, sage, or resin is burned to produce a smell for spiritual purposes. Smoke is sometimes used as a flavoring agent, and preservative for various foodstuffs. Smoke is also a component of internal combustion engine exhaust gas, particularly diesel exhaust.

Smoke inhalation is the primary cause of death in victims of indoor fires. The smoke kills by a combination of thermal damage, poisoning and pulmonary irritation caused by carbon monoxide, hydrogen cyanide and other combustion products.

Smoke is an aerosol (or mist) of solid particles and liquid droplets that are close to the ideal range of sizes for Mie scattering of visible light.[2] This effect has been likened to three-dimensional textured privacy glass[citation needed] — a smoke cloud does not obstruct an image, but thoroughly scrambles it.

The composition of smoke depends on the nature of the burning fuel and the conditions of combustion.

Fires with high availability of oxygen burn at a high temperature and with small amount of smoke produced; the particles are mostly composed of ash, or with large temperature differences, of condensed aerosol of water. High temperature also leads to production of nitrogen oxides.[3] Sulfur content yields sulfur dioxide, or in case of incomplete combustion, hydrogen sulfide.[4] Carbon and hydrogen are almost completely oxidized to carbon dioxide and water.[5] Fires burning with lack of oxygen produce a significantly wider palette of compounds, many of them toxic.[5]Partial oxidation of carbon produces carbon monoxide, nitrogen-containing materials can yield hydrogen cyanide, ammonia, and nitrogen oxides.[6]Hydrogen gas can be produced instead of water.[6] Content of halogens such as chlorine (e.g. in polyvinyl chloride or brominated flame retardants) may lead to production of e.g. hydrogen chloride, phosgene, dioxin, and chloromethane, bromomethane and other halocarbons.[6][7]Hydrogen fluoride can be formed from fluorocarbons, whether fluoropolymers subjected to fire or halocarbon fire suppression agents. Phosphorus and antimony oxides and their reaction products can be formed from some fire retardant additives, increasing smoke toxicity and corrosivity.[7]Pyrolysis of polychlorinated biphenyls (PCB), e.g. from burning older transformer oil, and to lower degree also of other chlorine-containing materials, can produce 2,3,7,8-tetrachlorodibenzodioxin, a potent carcinogen, and other polychlorinated dibenzodioxins.[7] Pyrolysis of fluoropolymers, e.g. teflon, in presence of oxygen yields carbonyl fluoride (which hydrolyzes readily to HF and CO2); other compounds may be formed as well, e.g. carbon tetrafluoride, hexafluoropropylene, and highly toxic perfluoroisobutene (PFIB).[8]

Emission of soot in the fumes of a large diesel truck, without particle filters.

Pyrolysis of burning material, especially incomplete combustion or smoldering without adequate oxygen supply, also results in production of a large amount of hydrocarbons, both aliphatic (methane, ethane, ethylene, acetylene) and aromatic (benzene and its derivates, polycyclic aromatic hydrocarbons; e.g. benzo[a]pyrene, studied as a carcinogen, or retene), terpenes.[9]Heterocyclic compounds may be also present.[10] Heavier hydrocarbons may condense as tar; smoke with significant tar content is yellow to brown.[11] Presence of such smoke, soot, and/or brown oily deposits during a fire indicates a possible hazardous situation, as the atmosphere may be saturated with combustible pyrolysis products with concentration above the upper flammability limit, and sudden inrush of air can cause flashover or backdraft.[12]

Presence of sulfur can lead to formation of e.g. hydrogen sulfide, carbonyl sulfide, sulfur dioxide, carbon disulfide, and thiols; especially thiols tend to get adsorbed on surfaces and produce a lingering odor even long after the fire. Partial oxidation of the released hydrocarbons yields in a wide palette of other compounds: aldehydes (e.g. formaldehyde, acrolein, and furfural), ketones, alcohols (often aromatic, e.g. phenol, guaiacol, syringol, catechol, and cresols), carboxylic acids (formic acid, acetic acid, etc.).

The visible particulate matter in such smokes is most commonly composed of carbon (soot). Other particulates may be composed of drops of condensed tar, or solid particles of ash. The presence of metals in the fuel yields particles of metal oxides. Particles of inorganic salts may also be formed, e.g. ammonium sulfate, ammonium nitrate, or sodium chloride. Inorganic salts present on the surface of the soot particles may make them hydrophilic. Many organic compounds, typically the aromatic hydrocarbons, may be also adsorbed on the surface of the solid particles. Metal oxides can be present when metal-containing fuels are burned, e.g. solid rocket fuels containing aluminium. Depleted uranium projectiles after impacting the target ignite, producing particles of uranium oxides. Magnetic particles, spherules of magnetite-like ferrous ferric oxide, are present in coal smoke; their increase in deposits after 1860 marks the beginning of the Industrial Revolution.[13] (Magnetic iron oxide nanoparticles can be also produced in the smoke from meteorites burning in the atmosphere.)[14] Magnetic remanence, recorded in the iron oxide particles, indicates the strength of Earth's magnetic field when they were cooled beyond their Curie temperature; this can be used to distinguish magnetic particles of terrestrial and meteoric origin.[15]Fly ash is composed mainly of silica and calcium oxide. Cenospheres are present in smoke from liquid hydrocarbon fuels. Minute metal particles produced by abrasion can be present in engine smokes. Amorphous silica particles are present in smokes from burning silicones; small proportion of silicon nitride particles can be formed in fires with insufficient oxygen. The silica particles have about 10 nm size, clumped to 70-100 nm aggregates and further agglomerated to chains.[8] Radioactive particles may be present due to traces of uranium, thorium, or other radionuclides in the fuel; hot particles can be present in case of fires during nuclear accidents (e.g. Chernobyl disaster) or nuclear war.

Smoke particulates, like other aerosols, are categorized into three modes based on particle size:

Most of the smoke material is primarily in coarse particles. Those undergo rapid dry precipitation, and the smoke damage in more distant areas outside of the room where the fire occurs is therefore primarily mediated by the smaller particles.[16]

Aerosol of particles beyond visible size is an early indicator of materials in a preignition stage of a fire.[8]

Burning of hydrogen-rich fuel produces water; this results in smoke containing droplets of water vapor. In absence of other color sources (nitrogen oxides, particulates...), such smoke is white and cloud-like.

Smoke emissions may contain characteristic trace elements. Vanadium is present in emissions from oil fired power plants and refineries; oil plants also emit some nickel. Coal combustion produces emissions containing aluminium, arsenic, chromium, cobalt, copper, iron, mercury, selenium, and uranium.

Traces of vanadium in high-temperature combustion products form droplets of molten vanadates. These attack the passivation layers on metals and cause high temperature corrosion, which is a concern especially for internal combustion engines. Molten sulfate and lead particulates also have such effect.

Some components of smoke are characteristic of the combustion source. Guaiacol and its derivatives are products of pyrolysis of lignin and are characteristic of wood smoke; other markers are syringol and derivates, and other methoxy phenols. Retene, a product of pyrolysis of conifer trees, is an indicator of forest fires. Levoglucosan is a pyrolysis product of cellulose. Hardwood vs softwood smokes differ in the ratio of guaiacols/syringols. Markers for vehicle exhaust include polycyclic aromatic hydrocarbons, hopanes, steranes, and specific nitroarenes (e.g. 1-nitropyrene). The ratio of hopanes and steranes to elemental carbon can be used to distinguish between emissions of gasoline and diesel engines.[17]

Many compounds can be associated with particulates; whether by being adsorbed on their surfaces, or by being dissolved in liquid droplets. Hydrogen chloride is well absorbed in the soot particles.[16]

Inert particulate matter can be disturbed and entrained into the smoke. Of particular concern are particles of asbestos.

Deposited hot particles of radioactive fallout and bioaccumulated radioisotopes can be reintroduced into the atmosphere by wildfires and forest fires; this is a concern in e.g. the Zone of alienation containing contaminants from the Chernobyl disaster.

Polymers are a significant source of smoke. Aromatic side groups, e.g. in polystyrene, enhance generation of smoke. Aromatic groups integrated in the polymer backbone produce less smoke, likely due to significant charring. Aliphatic polymers tend to generate the least smoke, and are non-self-extinguishing. However presence of additives can significantly increase smoke formation. Phosphorus-based and halogen-based flame retardants decrease production of smoke. Higher degree of cross-linking between the polymer chains has such effect too.[18]

Smoke from a wildfire Smoke rising up from the smoldering remains of a recently extingished mountain fire in South Africa.

The naked eye detects particle sizes greater than 7 µm (micrometres). Visible particles emitted from a fire are referred to as smoke. Invisible particles are generally referred to as gas or fumes. This is best illustrated when toasting bread in a toaster. As the bread heats up, the products of combustion increase in size. The fumes initially produced are invisible but become visible if the toast is burnt.

An ionization chamber type smoke detector is technically a product of combustion detector, not a smoke detector. Ionization chamber type smoke detectors detect particles of combustion that are invisible to the naked eye. This explains why they may frequently false alarm from the fumes emitted from the red-hot heating elements of a toaster, before the presence of visible smoke, yet they may fail to activate in the early, low-heat smoldering stage of a fire.

Smoke from a typical house fire contains hundreds of different chemicals and fumes. As a result, the damage caused by the smoke can often exceed that caused by the actual heat of the fire. In addition to the physical damage caused by the smoke of a fire – which manifests itself in the form of stains – is the often even harder to eliminate problem of a smoky odor. Just as there are contractors that specialize in rebuilding/repairing homes that have been damaged by fire and smoke, fabric restoration companies specialize in restoring fabrics that have been damaged in a fire.

Smoke from oxygen-deprived fires contains a significant concentration of compounds that are flammable. A cloud of smoke, in contact with atmospheric oxygen, therefore has the potential of being ignited – either by another open flame in the area, or by its own temperature. This leads to effects like backdraft and flashover. Smoke inhalation is also a danger of smoke that can cause serious injury and death.

Woman of Nigeria processing fish without considering the health risk

Many compounds of smoke from fires are highly toxic and/or irritating. The most dangerous is carbon monoxide leading to carbon monoxide poisoning, sometimes with the additive effects of hydrogen cyanide and phosgene. Smoke inhalation can therefore quickly lead to incapacitation and loss of consciousness. Sulfur oxides, hydrogen chloride and hydrogen fluoride in contact with moisture form sulfuric, hydrochloric and hydrofluoric acid, which are corrosive to both lungs and materials. When asleep the nose does not sense smoke nor does the brain, but the body will wake up if the lungs become enveloped in smoke and the brain will be stimulated and the person will be awoken. This does not work if the person is incapacitated or under the influence of drugs and/or alcohol.

Cigarette smoke is a major modifiable risk factor for lung disease, heart disease, and many cancers. Smoke can also be a component of ambient air pollution due to the burning of coal in power plants, forest fires or other sources, although the concentration of pollutants in ambient air is typically much less than that in cigarette smoke. One day of exposure to PM2.5 at a concentration of 880 μg/m3, such as occurs in Beijing, China, is the equivalent of smoking one or two cigarettes in terms of particulate inhalation by weight.[19][20] The analysis is complicated, however, by the fact that the organic compounds present in various ambient particulates may have a higher carcinogenicity than the compounds in cigarette smoke particulates.[21] Secondhand tobacco smoke is the combination of both sidestream and mainstream smoke emissions from a burning tobacco product. These emissions contain more than 50 carcinogenic chemicals. According to the Surgeon General's latest report on the subject, "Short exposures to secondhand [tobacco] smoke can cause blood platelets to become stickier, damage the lining of blood vessels, decrease coronary flow velocity reserves, and reduce heart variability, potentially increasing the risk of a heart attack".[22] The American Cancer Society lists "heart disease, lung infections, increased asthma attacks, middle ear infections, and low birth weight" as ramifications of smoker's emission.[23]

Reduced visibility due to wildfire smoke in Sheremetyevo airport (Moscow, Russia) 7 August 2010.

Smoke can obscure visibility, impeding occupant exiting from fire areas. In fact, the poor visibility due to the smoke that was in the Worcester Cold Storage Warehouse fire in Worcester, Massachusetts was the exact reason why the trapped rescue firefighters couldn't evacuate the building in time. Because of the striking similarity that each floor shared, the dense smoke caused the firefighters to become disoriented.[24]

Smoke contains a wide variety of chemicals, many of them aggressive in nature. Examples are hydrochloric acid and hydrobromic acid, produced from halogen-containing plastics and fire retardants, hydrofluoric acid released by pyrolysis of fluorocarbon fire suppression agents, sulfuric acid from burning of sulfur-containing materials, nitric acid from high-temperature fires where nitrous oxide gets formed, phosphoric acid and antimony compounds from P and Sb based fire retardants, and many others. Such corrosion is not significant for structural materials, but delicate structures, especially microelectronics, are strongly affected. Corrosion of circuit board traces, penetration of aggressive chemicals through the casings of parts, and other effects can cause an immediate or gradual deterioration of parameters or even premature (and often delayed, as the corrosion can progress over long time) failure of equipment subjected to smoke. Many smoke components are also electrically conductive; deposition of a conductive layer on the circuits can cause crosstalks and other deteriorations of the operating parameters or even cause short circuits and total failures. Electrical contacts can be affected by corrosion of surfaces, and by deposition of soot and other conductive particles or nonconductive layers on or across the contacts. Deposited particles may adversely affect the performance of optoelectronics by absorbing or scattering the light beams.

Corrosivity of smoke produced by materials is characterized by the corrosion index (CI), defined as material loss rate (angstrom/minute) per amount of material gasified products (grams) per volume of air (m3). It is measured by exposing strips of metal to flow of combustion products in a test tunnel. Polymers containing halogen and hydrogen (polyvinyl chloride, polyolefins with halogenated additives, etc.) have the highest CI as the corrosive acids are formed directly with water produced by the combustion, polymers containing halogen only (e.g. polytetrafluoroethylene) have lower CI as the formation of acid is limited to reactions with airborne humidity, and halogen-free materials (polyolefins, wood) have the lowest CI.[16] However, some halogen-free materials can also release significant amount of corrosive products.[25]

Smoke damage to electronic equipment can be significantly more extensive than the fire itself. Cable fires are of special concern; low smoke zero halogen materials are preferable for cable insulation.

When smoke comes into contact with the surface of any substance or structure, the chemicals contained in it are transferred to it. The corrosive properties of the chemicals cause the substance or structure to decompose at a rapid rate. Certain materials or structures absorb these chemicals, which is why clothing, unsealed surfaces, potable water, piping, wood, etc., are replaced in most cases of structural fires.

As early as the 15th century Leonardo da Vinci commented at length on the difficulty of assessing smoke, and distinguished between black smoke (carbonized particles) and white 'smoke' which is not a smoke at all but merely a suspension of harmless water particulates.[26]

Smoke from heating appliances is commonly measured in one of the following ways:

In-line capture. A smoke sample is simply sucked through a filter which is weighed before and after the test and the mass of smoke found. This is the simplest and probably the most accurate method, but can only be used where the smoke concentration is slight, as the filter can quickly become blocked.[27]

The ASTM smoke pump is a simple and widely used method of in-line capture where a measured volume of smoke is pulled through a filter paper and the dark spot so formed is compared with a standard.

Filter/dilution tunnel. A smoke sample is drawn through a tube where it is diluted with air, the resulting smoke/air mixture is then pulled through a filter and weighed. This is the internationally recognized method of measuring smoke from combustion.[28]

Electrostatic precipitation. The smoke is passed through an array of metal tubes which contain suspended wires. A (huge) electrical potential is applied across the tubes and wires so that the smoke particles become charged and are attracted to the sides of the tubes. This method can over-read by capturing harmless condensates, or under-read due to the insulating effect of the smoke. However, it is the necessary method for assessing volumes of smoke too great to be forced through a filter, i.e., from bituminous coal.

Ringelmann scale. A measure of smoke color. Invented by Professor Maximilian Ringelmann in Paris in 1888, it is essentially a card with squares of black, white and shades of gray which is held up and the comparative grayness of the smoke judged. Highly dependent on light conditions and the skill of the observer it allocates a grayness number from 0 (white) to 5 (black) which has only a passing relationship to the actual quantity of smoke. Nonetheless, the simplicity of the Ringelmann scale means that it has been adopted as a standard in many countries.

Cossar scale. The change of atmospheric smoke particulate concentration resulting from the presence of Barry Cossar. The ratio of smoke to air exiting Barry Cossar is measured and compared against that in the surrounding atmosphere. This dynamic scale ranges from zero to seven; reported measurements typically average very near seven.[citation needed]

Optical scattering. A light beam is passed through the smoke. A light detector is situated at an angle to the light source, typically at 90°, so that it receives only light reflected from passing particles. A measurement is made of the light received which will be higher as the concentration of smoke particles becomes higher.

Optical obscuration. A light beam is passed through the smoke and a detector opposite measures the light. The more smoke particles are present between the two, the less light will be measured.

Combined optical methods. There are various proprietary optical smoke measurement devices such as the 'nephelometer' or the 'aethalometer' which use several different optical methods, including more than one wavelength of light, inside a single instrument and apply an algorithm to give a good estimate of smoke. It has been claimed that these devices can differentiate types of smoke and so their probable source can be inferred, though this is disputed.[29]

Inference from carbon monoxide. Smoke is incompletely burned fuel, carbon monoxide is incompletely burned carbon, therefore it has long been assumed that measurement of CO in flue gas (a cheap, simple and very accurate procedure) will provide a good indication of the levels of smoke. Indeed, several jurisdictions use CO measurement as the basis of smoke control. However it is far from clear how accurate the correspondence is.

Throughout recorded history, humans have used the smoke of medicinal plants to cure illness. A sculpture from Persepolis shows Darius the Great (522–486 BC), the king of Persia, with two censers in front of him for burning Peganum harmala and/or sandalwood Santalum album, which was believed to protect the king from evil and disease. More than 300 plant species in 5 continents are used in smoke form for different diseases. As a method of drug administration, smoking is important as it is a simple, inexpensive, but very effective method of extracting particles containing active agents. More importantly, generating smoke reduces the particle size to a microscopic scale thereby increasing the absorption of its active chemical principles.[30]

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Clean Up Australia Limited is a not-for-profit Australian environmental conservation organisation founded by Australian Ian Kiernan, and co-founder Kim McKay, in 1989. It works to foster relationships between the community, business and government to address the environmental issues of waste, water and climate change. Since its inception, Clean Up Australia has grown to include other projects and campaigns including Business Clean Up Day, Schools Clean Up Day, Clean Up the Alps, Clean Up the Kimberley and Clean Up the World. The organisation is behind Clean Up Australia Day, as well as other environmental projects and campaigns.[2][3]

Clean Up Australia Day is held on the first Sunday of March every year, and encourages people to clean up their local areas. Any person can register a place they plan to clean up on the Clean Up Australia website, and others can join them there. Activities on the day include removing large items such as car bodies from water ways and the collection of general waste lying around.

Clean Up Australia Day was first held in January 1989.[3] The idea was born out of an Australian Bicentenary event, "Clean-Up Lake Macquarie" which was instigated in 1987 by Ivan Welsh as Mayor of Lake Macquarie.[4] Then followed the local "Clean Up Sydney Harbour" event in 1989 with more than 40,000 volunteers who collected some 5,000 tonnes of rubbish. The 1990 Clean Up Australia Day event was launched by the then Prime Minister, Bob Hawke over the initial opposition of the then state Premier, Nick Greiner.[5] Greiner later reversed his position and offered his support for the event.[6]

"The Rubbish Report" is produced each year from data collected by surveying participants. As of 1990, 94% of rubbish was from packaging.[7] By 1993, the campaign was focusing more strongly on sorting the rubbish collected into recycleables,[8] and Kiernan was using Clean Up Australia Day to advocate for changes to legislation surrounding reduction of packaging and returning packaging to companies.[9] In 1994, over 8,000 sites were cleaned up as part of the day.[10] In 2008, Kiernan put a focus on bottled water, advocating for the expansion of container deposit refunds in Australia.[11] In 2012, sponsorship cutbacks and a drop in private donations caused the organisation to let go all of its paid staff.[12]

Clean Up the World was established in 1994 after Ian Kiernan and Kim McKay approached the United Nations Environment Programme, with an idea to take his Clean Up concept global.[13][14]

Clean Up the World is an international campaign that encourages communities to clean up, fix up and conserve their environment through the Clean Up the World Membership program.

A Clean Up the World weekend is held on the third weekend of September each year and, by 2007, the event attracted more than 35 million people from over 120 countries to volunteer.[14]

Business Clean Up Day[15] provides Australian businesses with an opportunity to contribute to waste reduction and the improvement of the environment.

Businesses register their commitment to implement at least one enivironment-friendly initiative in their workplace, giving them an opportunity to work as a team and make a difference to their local environment.

Schools Clean Up Day[16] is designed to allow students to participate in Clean Up Australia as part of a school activity.

Clean Up the Kimberley[17] is a series of community action-based projects focussed on the Kimberley region of Western Australia. The primary objectives of this initiative are to clean up rubbish hot spots, increase awareness of the scale and impact of rubbish in the region, change tourist and local community behaviour and improve local recycling and waste management infrastructure.

Clean Up the Alps[18] is a project aimed at protecting the Alpine region of Victoria. It is run in conjunction with Parks Victoria, Conservation Volunteers Australia and local communities as part of the Victorian Government’s ‘The Alps: A fresh start – a healthy future’ program. The project culminates in the Clean Up the Alps weekend, held annually in November.

  1. ^ Date of incorporation.

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The Accord on Fire and Building Safety in Bangladesh (the Accord) was signed on 15 May 2013. It is a five-year independent, legally binding agreement between global brands and retailers and trade unions designed to build a safe and healthy Bangladeshi Ready Made Garment (RMG) Industry. The agreement was created in the immediate aftermath of the Rana Plaza building collapse that led to the death of more than 1100 people and injured more than 2000. In June 2013, an implementation plan was agreed leading to the incorporation of the Bangladesh Accord Foundation in the Netherlands in October 2013.

The agreement consists of six key components:

  1. A five-year legally binding agreement between brands and trade unions to ensure a safe working environment in the Bangladeshi RMG industry
  2. An independent inspection program supported by brands in which workers and trade unions are involved
  3. Public disclosure of all factories, inspection reports and corrective action plans (CAP)
  4. A commitment by signatory brands to ensure sufficient funds are available for remediation and to maintain sourcing relationships
  5. Democratically elected health and safety committees in all factories to identify and act on health and safety risks
  6. Worker empowerment through an extensive training program, complaints mechanism and right to refuse unsafe work.

The accord was sponsored and created by the IndustriALL Global Union and the UNI Global Union in alliance with leading NGOs, the Clean Clothes Campaign and the Workers Rights Consortium. It is an expanded version of an earlier 2-year accord that had been signed only by PVH and Tchibo.[1]

Following the 2013 Savar building collapse on 24 April 2013 that resulted in over 1,100 deaths, there was wide global interest by both the consuming public and clothing retailers in establishing enforceable standards for fire and building safety in Bangladesh. The German government sponsored a meeting of retailers and NGOs at the beginning of May, and the meeting set a deadline of midnight of 16 May 2013 to sign up to the agreement.[1] Numerous companies had signed up by the deadline, covering over 1,000 Bangladeshi garment factories.[2]

In addition to schemes of building inspection and enforcement of fire and safety standards the accord requires that contracts by international retailers with Bangladesh manufacturers provide for compensation adequate to maintain safe buildings. Retailers agree to continue to support the Bangladesh textile industry despite possible higher costs. It is estimated that the total cost may be $1 billion, about $500,000 per factory.[3] Close co-operation with the International Labour Organization and the government of Bangladesh is required. A steering committee which governs the accord is established as are dispute resolution procedures such as arbitration. The accord calls for development of an Implementation Plan over 45 days.[4]

Since 29 October 2013, the Accord has been signed by over 200 apparel brands, retailers and importers from over 20 countries in Europe, North America, Asia and Australia; two global trade unions; and eight Bangladesh trade unions and four NGO witnesses.[5][6] Some of the notable companies are listed below. For a complete list see the Bangladesh Accord website.[7]

Most North American retailers did not sign the accord. Companies like Gap Inc. and Walmart cited liability concerns. According to spokespersons for the retail industry, American courts, which allow class actions, contingent fees, and do not require losing plaintiffs to pay legal fees, might permit liability claims against retailers in the event of another disaster which might result in substantial enforceable judgments, in contrast to European courts which generally do not allow class actions, forbid contingent fees, and require losing plaintiffs to pay winning defendants' legal fees and costs. However, as John C. Coffee, professor of corporate law at Columbia Law School, pointed out, Kiobel v. Royal Dutch Petroleum Co. might apply thus foreclosing suits by Bangladesh workers under the Alien Tort Claims Act, but this seems unlikely.[3] It is more likely that liability would be based on contract law.

On 10 July 2013, a group of 17 major North American retailers calling themselves the Alliance for Bangladesh Worker Safety announced the Bangladesh Worker Safety Initiative. The Initiative drew criticism from labour groups who complained that it was less stringent than the Accord and lacked legally binding commitments to pay for improvements.[8]

In two years, the Accord have inspected more than 1500 factories for fire, electrical and structural safety. Many safety issues were identified at each inspected factory. Accord said, fixing all these hazards is a huge work for the RMG industry, but safety remediation work in those factories is underway. There has been especially good progress on electrical remediation which is positive as most factory fires are caused by electrical hazards.[9] The Government of Bangladesh has said that the Accord will not be extended at the end of its five year term.[10]

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Flood Restoration Company   (Redirected from Water damage restoration) Interior of part of a damaged home in New Orleans after Hurricane Katrina. A smaller and more minor water spot caused by rain water leaking through a roof.

Water damage describes a large number of possible losses caused by water intruding where it will enable attack of a material or system by destructive processes such as rotting of wood, growth, rusting of steel, de-laminating of materials such as plywood, and many others.

The damage may be imperceptibly slow and minor such as water spots that could eventually mar a surface, or it may be instantaneous and catastrophic such as flooding. However fast it occurs, water damage is a major contributor to loss of property.

An insurance policy may or may not cover the costs associated with water damage and the process of water damage restoration. While a common cause of residential water damage is often the failure of a sump pump, many homeowner's insurance policies do not cover the associated costs without an addendum which adds to the monthly premium of the policy. Often the verbiage of this addendum is similar to "Sewer and Drain Coverage".

Those individuals who are affected by wide scale flooding may have the ability to apply for government and FEMA grants through the Individual Assistance program.[1] On a larger level, businesses, cities, and communities can apply to the FEMA Public Assistance program for funds to assist after a large flood. For example, the city of Fond du Lac Wisconsin received $1.2 million FEMA grant after flooding in June 2008. The program allows the city to purchase the water damaged properties, demolish the structures, and turn the properties into public green space.[2]

Water damage can originate by different sources such as a broken dishwasher hose, a washing machine overflow, a dishwasher leakage, broken/leaking pipes, and clogged toilets. According to the Environmental Protection Agency, 13.7% of all water used in the home today can be attributed to plumbing leaks.[3] On average that is approximately 10,000 gallons of water per year wasted by leaks for each US home. A tiny, 1/8-inch crack in a pipe can release up to 250 gallons of water a day.[4] According to Claims Magazine in August 2000, broken water pipes ranked second to hurricanes in terms of both the number of homes damaged and the amount of claims (on average $50,000 per insurance claim[citation needed]) costs in the US.[5] Experts suggest that homeowners inspect and replace worn pipe fittings and hose connections to all household appliances that use water at least once a year. This includes washing machines, dishwashers, kitchen sinks and bathroom lavatories, refrigerator icemakers, water softeners and humidifiers. A few US companies offer whole-house leak protection systems utilizing flow-based technologies. A number of insurance companies offer policy holders reduced rates for installing a whole-house leak protection system.

As far as insurance coverage is concerned, most damage caused by bad weather is considered flood damage and normally is not covered under homeowners insurance. Coverage for bad weather would usually require flood insurance.

Category 1 Water - Refers to a source of water that does not pose substantial threat to humans and classified as "clean water". Examples are broken water supply lines, tub or sink overflows or appliance malfunctions that involves water supply lines.

Category 2 Water - Refers to a source of water that contains a significant degree of chemical, biological or physical contaminants and causes discomfort or sickness when consumed or even exposed to. Known as "grey water". This type carries micro organisms and nutrients of micro organisms. Examples are toilet bowls with urine (no feces), sump pump failures, seepage due to hydrostatic failure and water discharge from dishwashers or washing machines.

Category 3 Water - Known as "black water" and is grossly unsanitary. This water contains unsanitary agents, harmful bacteria and fungi, causing severe discomfort or sickness. Type 3 category are contaminated water sources that affects the indoor environment. This category includes water sources from sewage, seawater, rising water from rivers or streams, ground surface water or standing water. Category 2 Water or Grey Water that is not promptly removed from the structure and or have remained stagnant may be re classified as Category 3 Water. Toilet back flows that originates from beyond the toilet trap is considered black water contamination regardless of visible content or color.[6]

Class of water damage is determined by the probable rate of evaporation based on the type of materials affected, or wet, in the room or space that was flooded. Determining the class of water damage is an important first step, and will determine the amount and type of equipment utilized to dry-down the structure.[7]

Class 1 - Slow Rate of Evaporation. Affects only a portion of a room. Materials have a low permeance/porosity. Minimum moisture is absorbed by the materials.

Class 2 - Fast Rate of Evaporation. Water affects the entire room of carpet and cushion. May have wicked up the walls, but not more than 24 inches.

Class 3 - Fastest Rate of Evaporation. Water generally comes from overhead, affecting the entire area; walls, ceilings, insulation, carpet, cushion, etc.

Class 4 - Specialty Drying Situations. Involves materials with a very low permeance/porosity, such as hardwood floors, concrete, crawlspaces, plaster, etc. Drying generally requires very low specific humidity to accomplish drying.

Different removal methods and measures are used depending on the category of water. Due to the destructive nature of water, chosen restoration methods also depend heavily on the amount of water, and on the amount of time the water has remained stagnant. For example, as long as carpet has not been wet for longer than 48 hours, and the water involved was not sewage based, a carpet can usually be saved; however, if the water has soaked for longer, then the carpet is probably irreparable and will have to be replaced.[8] Water damage restoration can be performed by property management teams, building maintenance personnel, or by the homeowners themselves; however, contacting a certified professional water damage restoration specialist is often regarded as the safest way to restore water damaged property.

While there are currently no government regulations in the United States dictating procedures, two certifying bodies, the Institute of Inspection Cleaning and Restoration Certification (IICRC) and the RIA, do recommend standards of care. The IICRC-recommended standard is IICRC S500.[9]

Fire and Water Restoration companies are regulated by the appropriate state's Department of Consumer Affairs - usually the state contractors license board. In California, all Fire and Water Restoration companies must register with the California Contractors State License Board.[10] Presently, the California Contractors State License Board has no specific classification for "water and fire damage restoration."

Water damage restoration is often prefaced by a loss assessment and evaluation of affected materials. The damaged area is inspected with water sensing equipment such as probes and other infrared tools in order to determine the source of the damage and possible extent of area affected. Restoration services would then be rendered to the residence in order to dry the structure, sanitize any affected or cross contaminated areas, and deodorize all affected areas and materials. After the labor is completed, water damage equipment including air movers, air scrubbers, dehumidifiers, wood floor drying systems, and sub floor drying equipment is left in the residence. Industry standards state that drying vendors should return at regular time intervals, preferably every twenty-four hours, to monitor the equipment, temperature, humidity, and moisture content of the affected walls and contents.[6]

See also: Mold prevention

Slight discolorations on the walls and ceiling may go unnoticed for a long time as they gradually spread and get more severe. Even if they are noticed, they often are ignored because it is thought that some discoloration will occur as a part of normal wear and tear in a home. Molds spread throughout the living space leading to serious health consequences. Symptoms caused by mold allergy are watery, itchy eyes, a chronic cough, headaches or migraines, difficulty breathing, rashes, tiredness, sinus problems, nasal blockage and frequent sneezing.[citation needed]

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