CARBON MONOXIDE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
CARBON MONOXIDE CARBONE (OXYDE DE) (French) CARBONIC OXIDE CARBONIO (OSSIDO DI) (Italian) CARBON MONOXIDE, REFRIGERATED LIQUID (CRYOGENIC LIQUID) CARBON OXIDE (CO) EXHAUST GAS FLUE GAS KOHLENMONOXID (German) KOHLENOXYD (German) KOOLMONOXYDE (Dutch) MONOXIDE OXYDE DE CARBONE (French) WEGLA TLENEK (Polish) CARBON MONOXIDE, CRYOGENIC LIQUID
IDENTIFIERS
1016-Carbon monoxide, compressed 1016-Carbon monoxide 9202-Carbon monoxide, refrigerated liquid (cryogenic liquid)
SYNONYM REFERENCE
- AAR, 2000; NIOSH, 2001; RTECS, 2001
USES/FORMS/SOURCES
Carbon monoxide is used in chemical manufacturing to produce methanol and phosgene and in plastic synthesis. It also plays a role in organic synthesis, especially in the oxo reaction and the Fischer-Tropsch processes for petroleum-type products (Budavari, 2000; CGA, 1999; HSDB , 2001; OHM/TADS , 2001). Carbon monoxide is used in metallurgy in the Mond process to recover high-purity nickel from crude ore and for reducing oxides and special steels. It is used to obtain highly pure powdered metals and to form particular metal catalysts used to synthesize hydrocarbons or organic oxygenating compounds. It is also used in the manufacture of white zinc pigments (Budavari, 2000; CGA, 1999). It is used in the manufacturing process for acids, esters, and hydroxy acids (acetic and propionic acids and their methyl esters), and glycolic acid (CGA, 1999).
SUMMARY Natural sources of carbon monoxide in the environment include oxidation of atmospheric methane, release from the ocean (originating from deep-sea organisms), volcanoes, grass and forest fires, marsh gases, and electrical storms (Harbison, 1998). These processes account for approximately 90 percent of atmospheric CO (HSDB , 2001). Incompletely combusted organic fuels will form carbon monoxide (Baselt, 2000). Automobile exhaust accounts for over half of manmade carbon monoxide. Industrial processes, space and water heaters, furnaces, and solid waste disposal procedures are also contributing sources (Harbison, 1998).
SOURCES OF EXPOSURE
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- SOURCES: Odorless, colorless gas produced by the incomplete combustion of any carbon containing substance. Common sources include household fires, home furnaces, stoves and water heaters, and vehicle exhaust. Another potential source is methylene chloride (often used as a paint stripper or degreaser) that is absorbed through inhalation, ingestion, or dermal contact and is subsequently metabolized by the liver to carbon monoxide.
- PHARMACOLOGY: Binds to hemoglobin with an affinity approximately 250 times greater than that of oxygen.
- TOXICOLOGY: Impairs oxygen delivery, producing cellular hypoxia and ischemia.
- EPIDEMIOLOGY: Common poisoning; one of the leading toxicologic causes of death.
MILD TO MODERATE TOXICITY: Headache, nausea, dizziness, vomiting, weakness, and confusion are often reported, with headache being the most common. SEVERE TOXICITY: Coma, syncope, seizures, cardiac dysrhythmias, myocardial ischemia, and death result from more severe poisonings and reflect damage to the organ systems (brain and heart) with the highest oxygen demand. Delayed neurocognitive effects, which include dementia, amnestic syndromes, psychosis, parkinsonism, chorea, apraxia, neuropathies, difficulty concentrating, and personality changes, can occur from 2 to 40 days following the initial exposure. Unfortunately, there are no good predictive markers for who will develop neurocognitive sequelae, including the initial carboxyhemoglobin level or the severity of the initial poisoning.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
TOXIC; may be fatal if inhaled or absorbed through skin. Contact with gas or liquefied gas may cause burns, severe injury and/or frostbite. Fire will produce irritating, corrosive and/or toxic gases. Runoff from fire control may cause pollution.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004)
TOXIC; Extremely Hazardous. Inhalation extremely dangerous; may be fatal. Contact with gas or liquefied gas may cause burns, severe injury and/or frostbite. Odorless, will not be detected by sense of smell.
ACUTE CLINICAL EFFECTS
PHARMACOLOGY: Binds to hemoglobin with an affinity approximately 250 times greater than that of oxygen. TOXICOLOGY: Impairs oxygen delivery, producing cellular hypoxia and ischemia. EPIDEMIOLOGY: Common poisoning; one of the leading toxicologic causes of death. MILD TO MODERATE TOXICITY: Headache, nausea, dizziness, vomiting, weakness, and confusion are often reported, with headache being the most common. SEVERE TOXICITY: Coma, syncope, seizures, cardiac dysrhythmias, myocardial ischemia, and death result from more severe poisonings and reflect damage to the organ systems (brain and heart) with the highest oxygen demand. Delayed neurocognitive effects, which include dementia, amnestic syndromes, psychosis, parkinsonism, chorea, apraxia, neuropathies, difficulty concentrating, and personality changes, can occur from 2 to 40 days following the initial exposure. Unfortunately, there are no good predictive markers for who will develop neurocognitive sequelae, including the initial carboxyhemoglobin level or the severity of the initial poisoning.
METABOLIC ACIDOSIS: According to a retrospective review of cases that occurred from 1996 to 2007, 5 pediatric patients out of 30 (16.7%) developed severe metabolic acidosis after CO exposure (Cho et al, 2008).
TACHYCARDIA: Clinical effects of CO poisoning include tachycardia, hypotension, peripheral vasodilation, cyanosis, shock, and cardiac arrest (Vacchiano & Torino, 2001; Thompson & Henry, 1983). Tachycardia is a compensatory mechanism for cellular hypoxia (Ernst & Zibrak, 1998). MYOCARDIAL ISCHEMIA: Chest pain, dyspnea, diaphoresis, syncope, or palpitations may occur (Allred et al, 1989; Kleinman et al, 1989; Atkins & Baker, 1985). MYOCARDIAL INFARCTION: Myocardial infarction in the absence of fixed coronary artery obstruction has been reported (Marius-Nunez, 1990). ELECTROCARDIOGRAM ABNORMAL: Electrocardiographic changes include ST-segment depression or elevation, T-wave abnormalities, atrial fibrillation, and intraventricular conduction block (Satran et al, 2005; Hayes & Hall, 1964). HYPOTENSIVE EPISODE: Hypotension may develop with severe poisoning (Chamberland et al, 2004; Meert et al, 1998; Tritapepe et al, 1998). MYOCARDITIS: Abnormal left ventricular wall motion has been reported in 3 of 5 cases studied. Papillary muscle dysfunction can also be found (Corya et al, 1976). CARDIOGENIC SHOCK: Two patients (a 29-year-old woman and her 8-year-old daughter) had a prolonged exposure to sublethal levels of CO (longer than 24 hours; carboxyhemoglobin levels of 20.4% and 22.6%), and acute cardiac failure developed despite evidence of neurologic recovery in both patients. The authors suggested that massive binding of the toxin to myocardial myoglobin and mitochondrial cytochrome chain enzymes might explain their protracted cardiac failure. It was suggested that stunned myocytes contributed to ventricular insufficiency, but that metabolic viability remained, which may explain the normal ECG findings and cardiac enzyme levels (Yanir et al, 2002).
BULLOUS ERUPTION: Skin changes may include bullae, vesicles, areas of edema, and erythematous patches (Myers et al, 1985a). An association between skin changes and poisoning severity has been suggested. FROSTBITE: Rapid release of compressed gas may cause frostbite (NFPA, 1991).
NAUSEA and VOMITING: Nausea and vomiting are common (Uyanik et al, 2011; Henz & Maeder, 2005; Swank et al, 2004). Symptoms may mimic acute gastroenteritis (Sternbach & Varon, 1991; Gasman et al, 1990).
RENAL FAILURE SYNDROME: Oliguric and nonoliguric acute renal failure have been reported (Bessoudo & Gray, 1978; Leavell et al, 1969; Jackson et al, 1959), sometimes associated with rhabdomyolysis (Kade et al, 2012; Vossberg & Skolnick, 1999; Florkowski et al, 1992).
DEAFNESS: Transient sensorineural hearing loss has been reported following acute poisoning (Baker & Lilly, 1977; Garland & Pearce, 1967). BAER ABNORMALITIES: Abnormal brainstem auditory evoked response (BAER) potentials have been described in patients with carbon monoxide (CO) poisoning (Choi, 1985). VISUAL FIELD DEFICITS: Paracentral scotomata, homonymous hemianopia, tunnel vision, temporary blindness, and permanent blindness are known sequelae (Dempsey et al, 1976) Uraneck et al, 1993).
HYPOXEMIA: Carbon monoxide (CO) combines with hemoglobin to form carboxyhemoglobin. This results in a decreased oxygen carrying capacity and a shift to the left of the oxygen-dissociation curve (reducing the unloading of oxygen to the tissues). THROMBOCYTOPENIC PURPURA: Thrombocytopenic purpura has been reported in association with CO exposure (Stonesifer et al, 1980). HEMOLYTIC ANEMIA: Hemolytic anemia has been reported following acute exposure (Nagy et al, 1979; Leavell et al, 1969). LEUKOCYTOSIS: Following acute exposure leukocytosis has been reported (Vossberg & Skolnick, 1999).
RHABDOMYOLYSIS has been reported following carbon monoxide poisoning (Kade et al, 2012; Jang & Park, 2010; Vacchiano & Torino, 2001; Florkowski et al, 1992). COMPARTMENT SYNDROME: Compartment syndrome may also occur, but it appears to be uncommon (Herman et al, 1988; Slevin, 1979; Finley et al, 1977; Jackson et al, 1959) Shapiro, 1989).
CENTRAL NERVOUS SYSTEM FINDING: Symptoms and signs of acute poisoning may include headache, dizziness, disorientation, abnormal reflexes, difficult concentration, memory loss, fainting, cerebral edema, coma, seizures, and death (Uyanik et al, 2011; Anon, 2005; Henz & Maeder, 2005) Turner & Clark, 1999. POST-INTERVAL SYNDROME (SEVERE DELAYED NEUROTOXICITY): Severe residual or delayed neurologic effects ("interval" form of CO poisoning) may occur after acute CO poisoning. Demyelination in the CNS and other effects may occur 48 to 72 hours after exposure. The patient should be observed carefully for CNS and other hypoxic effects. The most commonly involved regions of the brain are the globus pallidus and the deep white matter. SIGNS/SYMPTOMS: Delayed effects may include mental deterioration, irritability, aggressive behavior, apathy, disorientation, hypokinesia, akinetic mutism, distractibility, confusion, severe loss of memory, loss of consciousness, coma, gait disturbances, fecal and urinary incontinence, speech disturbance, tremor, bizarre behavior, visual loss, movement disorders, paresis, chorea, peripheral neuropathy, Tourette syndrome, and parkinsonian syndrome (Kondo et al, 2007; Aslan et al, 2004 ; Choi, 2002).
LOSS OF CONSCIOUSNESS: Eighty-three healthy men and women exposed to CO from heating stoves or gas-operated hot water heaters were studied. CO exposure ranged between 20 minutes and 480 minutes (average 52.5 minutes). The most common complaint was loss of consciousness (n=52; 62.7%), followed by palpitations (n=33; 39.8%), headache (n=27; 32.5%), confusion (n=20; 24.1%), dizziness (n=18; 21.7%), dyspnea (n=12; 14.5%), and weakness and fatigue (n=11; 13.3%) (Aslan et al, 2006).
HYPERVENTILATION: Hyperventilation and dyspnea may occur. In a series of children with carbon monoxide (CO) poisoning (many from smoke inhalation), tachypnea was common (Meert et al, 1998). Tachypnea is a compensatory mechanism for cellular hypoxia (Ernst & Zibrak, 1998). RESPIRATORY FAILURE: In a series of children with CO poisoning (many from smoke inhalation), bradypnea and apnea were common (Meert et al, 1998). ACUTE LUNG INJURY: Severe CO intoxication may be associated with an increase in alveolar-epithelial permeability and increased cardiac output with resultant pulmonary edema (Ernst & Zibrak, 1998)Sawa, 1981; (Fein et al, 1980; Ogawa et al, 1974). PULMONARY ASPIRATION: Aspiration pneumonia and respiratory alkalosis have been reported (Hart et al, 1988; Skorodin et al, 1986).
CHRONIC CLINICAL EFFECTS
- The effects of chronic exposure to low levels of CO are undefined (Rosenman, 1984). There has been disagreement as to whether chronic CO poisoning and acute poisoning are separate entities (Zorn & Kruger, 1960). A slight excess of deaths from cardiovascular disease has been reported in persons exposed to motor vehicle exhaust, which contains many other components in addition to CO (Stern, 1981). Chronic CO exposure can aggravate angina pectoris in persons with coronary artery disease (CAD) (Goldsmith & Aronow, 1975).
- A study of Holland tunnel workers exposed to 70 ppm CO for an average of 13 years found no obvious effects (Stevers et al, 1942). Chronic CO exposure at an airborne concentration of 30 to 60 mg/m3 (27 to 55 ppm) was associated with mild effects on the blood, nervous, and respiratory systems (Szollosi, 1970). Chronic low-level exposures did not increase the risk of atherosclerosis and did not produce abnormalities in cardiac rhythm (Weir & Fabiano, 1982; Prerovska & Drdkova, 1971; Prerovska & Drdkova, 1967) .
- NO SAFE LEVEL has been established for chronic exposure in persons with advanced CAD (Stewart, 1976). Employees of the Triborough Bridge and Tunnel Authority in New York City, who were exposed to an average of 63 ppm and a maximum of 217 ppm, were at increased risk for small airway disease and decreased pulmonary function (Ayres et al, 1973). Foundry workers had angina related to CO exposure and smoking, but ECG abnormalities were not related to CO levels (Hernberg, 1976).
- An increased rate of death from COPD was found in a cohort of Norwegian aluminum smelter workers who had been exposed to pot emissions 20 to 39 years previously; CO was one of the most prevalent exposures (Ronneberg, 1995a; Ronneberg, 1995b). These deaths could not be attributed to CO alone because of mixed exposure to coal tar pitch volatiles, fluorides, and sulfur dioxide (Ronneberg, 1995a).
- No association was found between CO exposure and ischemic heart disease death in a cohort of workers in a Norwegian aluminum smelter; CO was one of the most prevalent exposures (Ronneberg, 1995a; Ronneberg, 1995b). Other epidemiological studies have been carried out in groups of workers chronically exposed to CO (Fechter, 1980; Aleksieva, 1975; Zorn, 1975; Cabal, 1972; Lightfoot, 1972). The epidemiology of CO exposure and its possible association with cardiovascular disease has been reviewed (Zenz, 1994).
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. In case of contact with liquefied gas, thaw frosted parts with lukewarm water. In case of burns, immediately cool affected skin for as long as possible with cold water. Do not remove clothing if adhering to skin. Keep victim warm and quiet. Keep victim under observation. Effects of contact or inhalation may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004)
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. In case of contact with liquefied gas, thaw frosted parts with lukewarm water. Keep victim warm and quiet. Keep victim under observation. Effects of contact or inhalation may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.
FIRST AID EYE EXPOSURE: If eye tissue is frozen, seek medical attention immediately; if tissue is not frozen, immediately and thoroughly flush the eyes with large amounts of water for at least 15 minutes, occasionally lifting the lower and upper eyelids. If irritation, pain, swelling, lacrimation, or photophobia persist, get medical attention as soon as possible. DERMAL EXPOSURE: If frostbite has occurred, seek medical attention immediately; do NOT rub the affected areas or flush them with water. In order to prevent further tissue damage, do NOT attempt to remove frozen clothing from frostbitten areas. If frostbite has NOT occurred, immediately and thoroughly wash contaminated skin with soap and water. INHALATION EXPOSURE: If a person breathes large amounts of this chemical, move the exposed person to fresh air at once. If breathing has stopped, perform artificial respiration. Keep the affected person warm and at rest. Get medical attention as soon as possible. TARGET ORGANS: Cardiovascular system, lungs, blood, and central nervous system (National Institute for Occupational Safety and Health, 2007).
GENERAL INHALATION EXPOSURE INHALATION: Move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with an inhaled beta2-adrenergic agonist. Consider systemic corticosteroids in patients with significant bronchospasm. ACUTE LUNG INJURY: Maintain ventilation and oxygenation and evaluate with frequent arterial blood gases and/or pulse oximetry monitoring. Early use of PEEP and mechanical ventilation may be needed.
DERMAL EXPOSURE DECONTAMINATION: Remove contaminated clothing and jewelry and place them in plastic bags. Wash exposed areas with soap and water for 10 to 15 minutes with gentle sponging to avoid skin breakdown. A physician may need to examine the area if irritation or pain persists (Burgess et al, 1999). If frostbite has occurred, DO NOT rub the affected areas, DO NOT flush the affected areas with water, and DO NOT attempt to remove clothing. PREHOSPITAL Rewarming of a localized area should only be considered if the risk of refreezing is unlikely. Avoid rubbing the frozen area which may cause further damage to the area (Grieve et al, 2011; Hallam et al, 2010).
REWARMING Do not institute rewarming unless complete rewarming can be assured; refreezing thawed tissue increases tissue damage. Place affected area in a water bath with a temperature of 40 to 42 degrees Celsius for 15 to 30 minutes until thawing is complete. The bath should be large enough to permit complete immersion of the injured part, avoiding contact with the sides of the bath. A whirlpool bath would be ideal. Some authors suggest a mild antibacterial (ie, chlorhexidine, hexachlorophene or povidone-iodine) be added to the bath water. Tissues should be thoroughly rewarmed and pliable; the skin will appear a red-purple color (Grieve et al, 2011; Hallam et al, 2010; Murphy et al, 2000). Correct systemic hypothermia which can cause cold diuresis due to suppression of antidiuretic hormone; consider IV fluids (Grieve et al, 2011). Rewarming may be associated with increasing acute pain, requiring narcotic analgesics. For severe frostbite, clinical trials have shown that pentoxifylline, a phosphodiesterase inhibitor, can enhance tissue viability by increasing blood flow and reducing platelet activity (Hallam et al, 2010).
WOUND CARE Digits should be separated by sterile absorbent cotton; no constrictive dressings should be used. Protective dressings should be changed twice per day. Perform twice daily hydrotherapy for 30 to 45 minutes in warm water at 40 degrees Celsius. This helps debride devitalized tissue and maintain range of motion. Keep the area warm and dry between treatments (Hallam et al, 2010; Murphy et al, 2000). The injured extremities should be elevated and should not be allowed to bear weight. In patients at risk for infection of necrotic tissue, prophylactic antibiotics and tetanus toxoid have been recommended by some authors (Hallam et al, 2010; Murphy et al, 2000). Non-tense clear blisters should be left intact due to the risk of infection; tense or hemorrhagic blisters may be carefully aspirated in a setting where aseptic technique is provided (Hallam et al, 2010). Further surgical debridement should be delayed until mummification demarcation has occurred (60 to 90 days). Spontaneous amputation may occur. Analgesics may be required during the rewarming phase; however, patients with severe pain should be evaluated for vasospasm. IMAGING: Arteriography and noninvasive vascular techniques (e.g., plain radiography, laser Doppler studies, digital plethysmography, infrared thermography, isotope scanning), have been useful in evaluating the extent of vasospasm after thawing and assessing whether debridement is needed (Hallam et al, 2010). In cases of severe frostbite, Technetium 99 (triple phase scanning) and MRI angiography have been shown to be the most useful to assess injury and determine the extent or need for surgical debridement (Hallam et al, 2010). TOPICAL THERAPY: Topical aloe vera may decrease tissue destruction and should be applied every 6 hours (Murphy et al, 2000). IBUPROFEN THERAPY: Ibuprofen, a thromboxane inhibitor, may help limit inflammatory damage and reduce tissue loss (Grieve et al, 2011; Murphy et al, 2000). DOSE: 400 mg orally every 12 hours is recommended (Hallam et al, 2010). THROMBOLYTIC THERAPY: Thrombolysis (intra-arterial or intravenous thrombolytic agents) may be beneficial in those patients at risk to lose a digit or a limb, if done within the first 24 hours of exposure. The use of tissue plasminogen activator (t-PA) to clear microvascular thromboses can restore arterial blood flow, but should be accompanied by close monitoring including angiography or technetium scanning to evaluate the injury and to evaluate the effects of t-PA administration. Potential risk of the procedure includes significant tissue edema that can lead to a rise in interstitial pressures resulting in compartment syndrome (Grieve et al, 2011). CONTROVERSIAL: Adjunct pharmacological agents (ie, heparin, vasodilators, prostacyclins, prostaglandin synthetase inhibitors, dextran) are controversial and not routinely recommended. The role of hyperbaric oxygen therapy, sympathectomy remains unclear (Grieve et al, 2011). CHRONIC PAIN: Vasomotor dysfunction can produce chronic pain. Amitriptyline has been used in some patients; some patients may need a referral for pain management. Inability to tolerate the cold (in the affected area) has been observed following a single episode of frostbite (Hallam et al, 2010). MORBIDITIES: Frostbite can produce localized osteoporosis and possible bone loss following a severe case. These events may take a year or more to develop. Children may be at greater risk to develop more severe events (ie, early arthritis) (Hallam et al, 2010).
EYE EXPOSURE DECONTAMINATION: Remove contact lenses and irrigate exposed eyes with copious amounts of room temperature 0.9% saline or water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia persist after 15 minutes of irrigation, the patient should be seen in a healthcare facility. If contact with escaping gas has caused frostbite of the eye, DO NOT flush with water; early ophthalmologic consultation should be obtained.
ORAL EXPOSURE
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
A carbon monoxide (CO) concentration of 5000 parts per million (ppm) in air is lethal to humans after 5 minutes of exposure (RTECS , 2001). LCLo - (INHL) MAN: 4000 ppm for 30M (RTECS , 2001).
MAXIMUM TOLERATED EXPOSURE
A person with carboxyhemoglobin (blood saturation) above 65% to 70% will die if not treated with oxygen (Bingham et al, 2001). It has been noted that carboxyhemoglobin levels over 60% usually result in death (Hathaway et al, 1996).
LD50 values for animals can vary greatly. However, in most studies, carboxyhemoglobin (carbon monoxide bound to hemoglobin molecules) reaches a 60% level before a majority of animals die. Most die at COHb levels between 65% and 75% (Bingham et al, 2001).
- Carcinogenicity Ratings for CAS630-08-0 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Carbon monoxide EPA (U.S. Environmental Protection Agency, 2011): Not Listed IARC (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004): Not Listed NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed ; Listed as: Carbon monoxide MAK (DFG, 2002): Not Listed NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed
TOXICITY AND RISK ASSESSMENT VALUES
- EPA Risk Assessment Values for CAS630-08-0 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS630-08-0 (American Conference of Governmental Industrial Hygienists, 2010):
Editor's Note: The listed values are recommendations or guidelines developed by ACGIH(R) to assist in the control of health hazards. They should only be used, interpreted and applied by individuals trained in industrial hygiene. Before applying these values, it is imperative to read the introduction to each section in the current TLVs(R) and BEI(R) Book and become familiar with the constraints and limitations to their use. Always consult the Documentation of the TLVs(R) and BEIs(R) before applying these recommendations and guidelines.
- AIHA WEEL Values for CAS630-08-0 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS630-08-0 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS630-08-0 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS630-08-0 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS630-08-0 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS630-08-0 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS630-08-0 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS630-08-0 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS630-08-0 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS630-08-0 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS630-08-0 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1016 (49 CFR 172.101, 2005):
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 9202 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1016 (ICAO, 2002):
- ICAO International Shipping Name for UN9202 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS630-08-0 (NFPA, 2002):
-HANDLING AND STORAGE
SUMMARY
Awareness of the sources of carbon monoxide (CO) exposure can decrease the risk of morbidity and mortality from CO poisoning in both residential and occupational settings (Bingham et al, 2001). Recommendations for the prevention of CO intoxication include the continuous maintenance of combustion appliances and vehicle exhaust systems, using CO detectors with minimum sensitivity and alarm characteristic standards in indoor areas, and maintaining adequate ventilation in areas of CO production and potential exposure (Bingham et al, 2001; CGA, 1999). When exposure levels of CO gas are greater than or equal to 1500 parts per million (ppm), or in situations where exposure levels are undetermined, a supplied air respirator or self-contained breathing apparatus should be worn with a full-face mask operated in continuous-flow mode (Bingham et al, 2001; CHRIS , 2001).
HANDLING
- When working with CO, implement the "buddy system": Ensure that at least 2 people who are knowledgeable about safe CO handling procedures are stationed in the operating area (CGA, 1999).
- For trailer loading and unloading, pressure transfer or pump transfer liquid CO (CGA, 1999).
For pressure filling, raise the liquid storage container pressure to 10 to 25 pounds per square inch (psi) (69 kilopascals (kPa) to 172 kPa, differential) above the vessel being filled. Take specific system requirements into consideration (CGA, 1999). For pump filling, cool the pump first so that it will prime (CGA, 1999).
- When transferring CO liquid to or from a trailer, only authorized personnel may be present in the loading/unloading area. Check to see that hose connections are compatible with CO (CGA, 1999).
- Do not handle containers of CO that are broken, unless wearing suitable personal protective clothing and equipment (AAR, 2000).
- Nonsparking tools and equipment must be used when working with CO. This is especially important when opening and closing containers of CO (Sittig, 1991).
STORAGE
CO cylinders should be grounded. Ensure that check valves exist on the cylinders so that foreign materials do not backflow into them (CGA, 1999). Metal containers of CO of 5 gallons or more should be grounded and bonded. Drums containing CO must be equipped with self-closing valves, pressure vacuum bungs, and flame arresters (Sittig, 1991). Store pressurized CO gas in steel cylinders for shipping. Ship the cryogenic liquid in portable tanks. On trucks, railcars, or barges, ship in refrigerated tanks (NFPA, 1997). Steel and aluminum are acceptable metals for use in storage containers for dry, sulfur-free CO at pressures up to 2000 pounds per square inch gauge (psig). Iron and nickel containers may react with CO at high pressures to produce small quantities of carbonyls (CGA, 1999). The maximum pressure authorized for CO cylinders is 1000 psig at 70 degrees F (6900 kPa at 21.1 degrees C). If the CO gas is dry and sulfur-free, cylinders may be charged to 5/6 of service pressure, never to exceed 2000 psig at 70 degrees F (13,790 kPa at 21.1 degrees C) (CGA, 1999). Storage cylinders for liquid CO should be properly insulated as to maintain liquid temperature without pressure rise or venting. All systems for storing and transporting CO should meet ASME (American Society of Mechanical Engineers) standards and comply with all local and state regulations where applicable (CGA, 1999).
- ROOM/CABINET RECOMMENDATIONS
Keep all ignition sources and hot surfaces out of areas where CO is stored (CGA, 1999). Areas in which CO is stored should be equipped with CO detectors for the protection of personnel (CGA, 1999). Storage temperatures (CHRIS , 2001): Store CO in a cool, dry, well-ventilated location (NFPA, 1997; Sittig, 1991). Store CO in well-ventilated, safe areas. Keep containers away from sunlight (ITI, 1995).
Keep cylinders containing CO gas separate from cylinders containing oxygen or flammable or highly oxidizing substances, such as chlorine or chlorine dioxide (CGA, 1999; Sittig, 1991). Separate from alkali metals (HSDB , 2001).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004)
Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible. Always wear thermal protective clothing when handling refrigerated/cryogenic liquids.
EYE/FACE PROTECTION
- Safety glasses should be worn when working with carbon monoxide (CO) (CHRIS , 2001).
RESPIRATORY PROTECTION
- Refer to "Recommendations for respirator selection" in the NIOSH Pocket Guide to Chemical Hazards on TOMES Plus(R) for respirator information.
- Exposure to CO at levels above 350 parts per million (ppm) requires the use of a supplied air respirator or self-contained breathing apparatus (SCBA). Levels of exposure above 875 ppm require the use of a supplied air respirator or SCBA operated in continuous-flow mode. When CO levels are undetermined or are known to exceed 1500 ppm, a supplied air respirator or SCBA with a full-face mask operated in continuous-flow mode with an auxiliary SCBA should be used (Bingham et al, 2001).
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 630-08-0.
-PHYSICAL HAZARDS
FIRE HAZARD
Editor's Note: Information from more than one emergency response guide is associated with this material. POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004) Flammable; may be ignited by heat, sparks or flames. May form explosive mixtures with air. Those substances designated with a "P" may polymerize explosively when heated or involved in a fire. Vapors from liquefied gas are initially heavier than air and spread along ground. Vapors may travel to source of ignition and flash back. Some of these materials may react violently with water. Cylinders exposed to fire may vent and release toxic and flammable gas through pressure relief devices. Containers may explode when heated. Ruptured cylinders may rocket. Runoff may create fire or explosion hazard.
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004) EXTREMELY FLAMMABLE. May be ignited by heat, sparks or flames. Flame may be invisible. Containers may explode when heated. Vapor explosion and poison hazard indoors, outdoors or in sewers. Vapors from liquefied gas are initially heavier than air and spread along ground. Vapors may travel to source of ignition and flash back. Runoff may create fire or explosion hazard.
Carbon monoxide is very flammable. It burns in air with a flame ranging in appearance from almost colorless to bright blue (Budavari, 2000; CHRIS , 2001). Carbon monoxide poisoning is the most frequent cause of immediate fire deaths. Any fire victim should be evaluated for carbon monoxide poisoning (HSDB , 2001).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS630-08-0 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
Water spray, fog or alcohol-resistant foam. FOR CHLOROSILANES, DO NOT USE WATER; use AFFF alcohol-resistant medium expansion foam. Move containers from fire area if you can do it without risk. Damaged cylinders should be handled only by specialists.
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004)
- TANK FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Cool containers with flooding quantities of water until well after fire is out. Do not direct water at source of leak or safety devices; icing may occur. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire.
- TANK FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004)
Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Cool containers with flooding quantities of water until well after fire is out. Do not direct water at source of leak or safety devices; icing may occur. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire.
- NFPA Extinguishing Methods for CAS630-08-0 (NFPA, 2002):
- Before extinguishing a fire, stop the flow of gas (AAR, 2000; Lewis, 2000; NFPA, 1997).
- If containers of carbon monoxide are exposed to heat or fire, use water spray to keep them cool (NFPA, 1997).
- Do not apply water directly onto liquid carbon monoxide or its container (Bowen, 1995).
- Avoid using carbon dioxide, vapor sealing foams, or firefighting foams as extinguishing agents for carbon monoxide fires (Bowen, 1995).
Asphyxiation may result from carbon dioxide production in a fire (CHRIS , 2001). Carbon monoxide posioning is the most frequent cause of immediate fire deaths. Any fire victim should be evaluated for CO poisoning (HSDB , 2001).
EXPLOSION HAZARD
- Carbon monoxide is a severe explosion hazard when exposed to heat or flame (Lewis, 2000).
- When involved in a fire, cylinders of carbon monoxide may rupture violently and rocket (AAR, 2000).
- Refer to the REACTIVITY HAZARD section for information on explosive/violent reactions.
DUST/VAPOR HAZARD
- Carbon monoxide is a chemical asphyxiant gas (ACGIH, 1986; (Bingham et al, 2001).
- Carbon monoxide inhaled in various amounts can cause headache, mental dullness, dizziness, weakness, nausea, vomiting, loss of muscular control, increased then decreased respiratory and pulse rates, collapse, unconsciousness, or death (Budavari, 2000).
REACTIVITY HAZARD
- Carbon monoxide decomposes into carbon and carbon dioxide between 400 and 700 degrees C (at lower temperatures when in contact with catalytic surfaces). Above 800 degrees C the equilibrium reaction favors carbon monoxide formation. Hopcalite, a mixture of the oxides of manganese and copper, catalyzes the decomposition at room temperature, as does palladium on silica gel (Budavari, 2000).
- Carbon monoxide forms a violent or explosive reaction on contact with bromine trifluoride, bromine pentafluoride, chlorine dioxide, and peroxodisulfuryl difluoride (Lewis, 2000). It is also incompatible with strong oxidizers, chlorine triflouride and lithium (HSDB , 2001).
- Mixtures of liquid carbon monoxide and liquid oxygen are explosive. Carbon monoxide reacts with sodium or potassium to form explosive products sensitive to shock, heat, or contact with water (Lewis, 2000).
- Carbon monoxide with copper powder + copper(II) perchlorate + water forms an explosive complex. Combinations of liquid carbon monoxide and liquid dinitrogen oxide form rocket propellants (Lewis, 2000).
- An explosive reaction may occur when carbon monoxide comes in contact with iron(III) oxide between 0 and 150 degrees C (Lewis, 2000).
- When charging carbon monoxide into a mixture of fluorine and oxygen during preparation of bis(fluoroformyl) peroxide, an explosion can result (Urben, 1999).
- Explosive complexes form when preparing copper(I) perchlorate under an atmosphere of carbon monoxide (Urben, 1999).
- Potassium and carbon monoxide react quickly to form carbonyl potassium, which is explosive (Urben, 1999).
- Blast hazards are possible when dinitrogen oxide and liquid carbon monoxide, a propellant combination, are used (Urben, 1999).
- Carbon monoxide and sodium form sodium benzene hexoxide, which explodes at 90 degrees C (Urben, 1999).
- May form extremely explosive mixture with air (Pohanish & Greene, 1997).
- Carbon monoxide ignites on warming with iodine heptafluoride. It ignites on contact with cesium oxide + water (Lewis, 2000).
- Carbon monoxide forms an exothermic reaction with CIF3; (Li + H2O); NF3; OF2; (K + O2); Ag2O; and (Na + NH3) (Lewis, 2000).
EVACUATION PROCEDURES
- Initial Isolation and Protective Action Distances (ERG, 2004)
Data presented from the Emergency Response Guidebook Table of Initial Isolation and Protective Action Distances are for use when a spill has occurred and there is no fire. If there is a fire, or if a fire is involved, evacuation information presented under FIRE - PUBLIC SAFETY EVACUATION DISTANCES should be used. Generally, a small spill is one that involves a single, small package such as a drum containing up to approximately 200 liters, a small cylinder, or a small leak from a large package. A large spill is one that involves a spill from a large package, or multiple spills from many small packages. Suggested distances to protect from vapors of toxic-by-inhalation and/or water-reactive materials during the first 30 minutes following the spill. DOT ID No. 1016 - Carbon monoxide SMALL SPILLS LARGE SPILLS
DOT ID No. 1016 - Carbon monoxide, compressed SMALL SPILLS LARGE SPILLS
DOT ID No. 9202 - Carbon monoxide, refrigerated liquid (cryogenic liquid) SMALL SPILLS LARGE SPILLS
- SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
Increase, in the downwind direction, as necessary, the isolation distance of at least 100 to 200 meters (330 to 660 feet) in all directions.
- SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004)
Increase, in the downwind direction, as necessary, the isolation distance of at least 100 meters (330 feet) in all directions.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
If tank, rail car or tank truck is involved in a fire, ISOLATE for 1600 meters (1 mile) in all directions; also, consider initial evacuation for 1600 meters (1 mile) in all directions.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004)
If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions.
- PUBLIC SAFETY MEASURES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004)
CALL Emergency Response Telephone Number on Shipping Paper first. If Shipping Paper not available or no answer, refer to appropriate telephone number: MEXICO: SETIQ: 01-800-00-214-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5559-1588; For calls originating elsewhere, call: 011-52-555-559-1588.
CENACOM: 01-800-00-413-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5550-1496, 5550-1552, 5550-1485, or 5550-4885; For calls originating elsewhere, call: 011-52-555-550-1496, or 011-52-555-550-1552; 011-52-555-550-1485, or 011-52-555-550-4885.
ARGENTINA: CIQUIME: 0-800-222-2933 in the Republic of Argentina; For calls originating elsewhere, call: +54-11-4613-1100.
BRAZIL: PRÓ-QUÍMICA: 0-800-118270 (Toll-free in Brazil); For calls originating elsewhere, call: +55-11-232-1144 (Collect calls are accepted).
COLUMBIA: CISPROQUIM: 01-800-091-6012 in Colombia; For calls originating in Bogotá, Colombia, call: 288-6012; For calls originating elsewhere, call: 011-57-1-288-6012.
CANADA: UNITED STATES:
For additional details see the section entitled "WHO TO CALL FOR ASSISTANCE" under the ERG Instructions. As an immediate precautionary measure, isolate spill or leak area for at least 100 meters (330 feet) in all directions. Keep unauthorized personnel away. Stay upwind. Many gases are heavier than air and will spread along ground and collect in low or confined areas (sewers, basements, tanks). Keep out of low areas. Ventilate closed spaces before entering.
- PUBLIC SAFETY MEASURES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004)
CALL Emergency Response Telephone Number on Shipping Paper first. If Shipping Paper not available or no answer, refer to appropriate telephone number: MEXICO: SETIQ: 01-800-00-214-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5559-1588; For calls originating elsewhere, call: 011-52-555-559-1588.
CENACOM: 01-800-00-413-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5550-1496, 5550-1552, 5550-1485, or 5550-4885; For calls originating elsewhere, call: 011-52-555-550-1496, or 011-52-555-550-1552; 011-52-555-550-1485, or 011-52-555-550-4885.
ARGENTINA: CIQUIME: 0-800-222-2933 in the Republic of Argentina; For calls originating elsewhere, call: +54-11-4613-1100.
BRAZIL: PRÓ-QUÍMICA: 0-800-118270 (Toll-free in Brazil); For calls originating elsewhere, call: +55-11-232-1144 (Collect calls are accepted).
COLUMBIA: CISPROQUIM: 01-800-091-6012 in Colombia; For calls originating in Bogotá, Colombia, call: 288-6012; For calls originating elsewhere, call: 011-57-1-288-6012.
CANADA: UNITED STATES:
For additional details see the section entitled "WHO TO CALL FOR ASSISTANCE" under the ERG Instructions. As an immediate precautionary measure, isolate spill or leak area for at least 100 meters (330 feet) in all directions. Keep unauthorized personnel away. Stay upwind. Many gases are heavier than air and will spread along ground and collect in low or confined areas (sewers, basements, tanks). Keep out of low areas. Ventilate closed spaces before entering.
- Consider evacuating a one-third mile radius if fire cannot be controlled or containers of carbon monoxide are exposed directly to flame (AAR, 2000).
- If carbon monoxide is leaking, but not on fire, make evacuation decisions dependant upon the amount of the substance released, location, and weather conditions (AAR, 2000).
- AIHA ERPG Values for CAS630-08-0 (AIHA, 2006):
Listed as Carbon Monoxide ERPG-1 (units = ppm): 200 ERPG-2 (units = ppm): 350 ERPG-3 (units = ppm): 500 Under Ballot, Review, or Consideration: No Definitions: ERPG-1: The ERPG-1 is the maximum airborne concentration below which it is believed nearly all individuals could be exposed for up to one hour without experiencing more than mild, transient adverse health effects or perceiving a clearly defined objectionable odor. ERPG-2: The ERPG-2 is the maximum airborne concentration below which it is believed nearly all individuals could be exposed for up to one hour without experiencing or developing irreversible or other serious health effects or symptoms that could impair an individual's ability to take protective action. ERPG-3: The ERPG-3 is the maximum airborne concentration below which it is believed nearly all individuals could be exposed for up to one hour without experiencing or developing life-threatening health effects.
- DOE TEEL Values for CAS630-08-0 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS630-08-0 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; United States Environmental Protection Agency Office of Pollution Prevention and Toxics, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 62 FR 58840, 1997; 65 FR 14186, 2000; 65 FR 39264, 2000; 65 FR 77866, 2000; 66 FR 21940, 2001; 67 FR 7164, 2002; 68 FR 42710, 2003; 69 FR 54144, 2004):
Listed as: Carbon monoxide Final Value: AEGL-1 10 min exposure: ppm: Not recommended because susceptible persons may experience more serious effects (equivalent to AEGL-2) at concentrations that do not yet cause AEGL-1 effects in the general population mg/m3: Not recommended because susceptible persons may experience more serious effects (equivalent to AEGL-2) at concentrations that do not yet cause AEGL-1 effects in the general population
30 min exposure: 1 hr exposure: 4 hr exposure: 8 hr exposure:
Definitions: AEGL-1 is the airborne concentration of a substance above which it is predicted that the general population, including susceptible individuals, could experience notable discomfort, irritation, or certain asymptomatic non-sensory effects. However, the effects are not disabling, are transient, and are reversible upon cessation of exposure.
Listed as: Carbon monoxide Final Value: AEGL-2 10 min exposure: ppm: 420 ppm mg/m3: 480 mg/m(3)
30 min exposure: ppm: 150 ppm mg/m3: 170 mg/m(3)
1 hr exposure: ppm: 83 ppm mg/m3: 95 mg/m(3)
4 hr exposure: ppm: 33 ppm mg/m3: 38 mg/m(3)
8 hr exposure: ppm: 27 ppm mg/m3: 31 mg/m(3)
Definitions: AEGL-2 is the airborne concentration of a substance above which it is predicted that the general population, including susceptible individuals, could experience irreversible or other serious, long-lasting adverse health effects or an impaired ability to escape.
Listed as: Carbon monoxide Final Value: AEGL-3 10 min exposure: ppm: 1700 ppm mg/m3: 1900 mg/m(3)
30 min exposure: ppm: 600 ppm mg/m3: 690 mg/m(3)
1 hr exposure: ppm: 330 ppm mg/m3: 380 mg/m(3)
4 hr exposure: ppm: 150 ppm mg/m3: 170 mg/m(3)
8 hr exposure: ppm: 130 ppm mg/m3: 150 mg/m(3)
Definitions: AEGL-3 is the airborne concentration of a substance above which it is predicted that the general population, including susceptible individuals, could experience life-threatening health effects or death.
- NIOSH IDLH Values for CAS630-08-0 (National Institute for Occupational Safety and Health, 2007):
IDLH: 1200 ppm Note(s): Not Listed
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004) ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). All equipment used when handling the product must be grounded. Fully encapsulating, vapor protective clothing should be worn for spills and leaks with no fire. Do not touch or walk through spilled material. Stop leak if you can do it without risk. Do not direct water at spill or source of leak. Use water spray to reduce vapors or divert vapor cloud drift. Avoid allowing water runoff to contact spilled material. FOR CHLOROSILANES, use AFFF alcohol-resistant medium expansion foam to reduce vapors. If possible, turn leaking containers so that gas escapes rather than liquid. Prevent entry into waterways, sewers, basements or confined areas. Isolate area until gas has dispersed.
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004) ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). All equipment used when handling the product must be grounded. Fully encapsulating, vapor protective clothing should be worn for spills and leaks with no fire. Do not touch or walk through spilled material. Stop leak if you can do it without risk. Use water spray to reduce vapors or divert vapor cloud drift. Avoid allowing water runoff to contact spilled material. Do not direct water at spill or source of leak. If possible, turn leaking containers so that gas escapes rather than liquid. Prevent entry into waterways, sewers, basements or confined areas. Isolate area until gas has dispersed.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 119 (ERG, 2004) Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 168 (ERG, 2004) Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible. Always wear thermal protective clothing when handling refrigerated/cryogenic liquids.
Use water spray to cool and disperse vapors and protect personnel. Consider isolation or evacuation with cryogenic liquid releases (NFPA, 1997).
For carbon monoxide gas leaks, use forced ventilation to keep gas concentrations below the explosive range. Move the container to an open area and allow gas to bleed off into the atmosphere (ITI, 1995). Combustion of oxygenated fuels results in less carbon monoxide output from automobiles. Air was monitored at 62 sites in eleven states from 1986 through 1992. Carbon monoxide levels decreased more in areas where oxygenated fuel was used than where it was not (1.2 ppm vs. 0.6 ppm decrease). Results were similar for mean daily concentrations (2.8 ppm vs. 1.4 ppm decrease) (Mannino & Etsel, 1996). Waste management activities associated with material disposition are unique to individual situations. Proper waste characterization and decisions regarding waste management should be coordinated with the appropriate local, state, or federal authorities to ensure compliance with all applicable rules and regulations.
For in situ cleanup, sponge out with air (OHM/TADS , 2001). GAS INCINERATION: Pipe carbon monoxide gas into an incinerator or into a pit where it can burn away (ITI, 1995; OHM/TADS , 2001). LIQUID INCINERATION: Atomize carbon monoxide liquid into an incinerator. To improve incineration, mix the liquid with a more flammable solvent (ITI, 1995; OHM/TADS , 2001). SOLID INCINERATION: For solid material, enfold pieces in paper or other flammable material and incinerate. Alternatively, dissolve the solid in a flammable solvent and spray into a fire chamber (ITI, 1995; OHM/TADS , 2001). "At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices." (HSDB , 2001)
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- Natural sources produce about 90 percent of atmospheric carbon monoxide. Such sources include atmospheric oxidation of methane, forest fires, terpene oxidation, and the ocean (where microorganisms produce carbon monoxide). Human activity is responsible for about 10 percent of CO production (HSDB , 2001).
- Motor vehicles account for about 55 to 60 percent of global man-made emissions of carbon monoxide (Harbison, 1998; ILO , 1998).
- Carbon monoxide is an ingredient of gaseous fuels (producer gas, water gas) which have been largely replaced by natural gas. It occurs primarily as a product of incomplete combustion of most carbonaceous materials, especially in internal combustion engine exhaust. High concentrations are frequently encountered in blast furnace operations in the steel industry. Other major carbon monoxide sources include: space heaters, improperly adjusted oil or gas burners, and fires in buildings. Tobacco smokers are the most heavily exposed, non-industrial segment of the population (ACGIH, 1991).
ENVIRONMENTAL FATE AND KINETICS
BIODEGRADATION
- The photosynthetic bacterium Rhodospirillum rubrum was used to convert carbon monoxide (CO) and water to carbon dioxide and hydrogen by the gas shift reaction. The yield of hydrogen from CO and water was 0.87 mol/mol, or 87 percent of a theoretical yield (Klasson et al, 1993).
ENVIRONMENTAL TOXICITY
- AQUATIC TOXICITY (FRESHWATER) (OHM/TADS , 2001)
LCLo - (WATER) VARIOUS FISH: 1.2 ppm LCLo - (WATER) MINNOW & SUNFISH: 1.5 ppm for 1-6H LCLo - (WATER) MINNOW: 47.5 ppm for 0.75-5H LCLo - (WATER) SUNFISH: 47.5 ppm for 0.5H LCLo - (WATER) ORANGE-SPOTTED SUNFISH: 75 ppm for 1H LCLo - (WATER) MINNOW & SUNFISH: 146 ppm for 10M-4H LCLo - (WATER) STRAW-COLORED MINNOW: 1160 ppm for 1H LCLo - (WATER) BLUNT-NOSED MINNOW: 1160 ppm for 115M LCLo - (WATER) GREEN SUNFISH: 1160 ppm for 5H LCLo - (WATER) ORANGE-SPOTTED SUNFISH: 1160 ppm for 340M LCLo - (WATER) BLACKBULLHEAD: 11, 31, and 4 ppm for 10H
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Carbon monoxide is an extremely poisonous, odorless, colorless, tasteless gas (Budavari, 2000).
- Carbon monoxide is also found as a colorless cryogenic liquid, which exists at -192 degrees C (-313 degrees F) (AAR, 2000; CGA, 1999).
VAPOR PRESSURE
- >760 mmHg (at 20 degrees C; 68 degrees F) (NFPA, 1997)
- 40 mmHg (at -210 degrees C) (OHM/TADS , 2001)
SPECIFIC GRAVITY
- STANDARD TEMPERATURE AND PRESSURE
- OTHER TEMPERATURE AND/OR PRESSURE
- TEMPERATURE AND/OR PRESSURE NOT LISTED
DENSITY
- NORMAL TEMPERATURE AND PRESSURE
(25 degrees C; 77 degrees F and 760 mmHg) VAPOR: 0.967 (Bingham et al, 2001; OHM/TADS , 2001)
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
-205 degrees C (Budavari, 2000; OHM/TADS , 2001) -207 degrees C (Bingham et al, 2001) -213 degrees C (Lewis, 2000)
BOILING POINT
- -191.5 degrees C (Budavari, 2000; CHRIS , 2001)
- -190 degrees C (condensation point) (Bingham et al, 2001; Lewis, 2000)
- -312.7 degrees F (-191.5 degrees C; 81.7 Kelvin) (at 1 atm) (CHRIS , 2001)
FLASH POINT
- Not Applicable (NIOSH , 2001)
AUTOIGNITION TEMPERATURE
- 700 degrees C (Budavari, 2000)
- 609 degrees C; 1128 degrees F (Lewis, 2000; OHM/TADS , 2001)
EXPLOSIVE LIMITS
12.5 percent (Lewis, 2000; OHM/TADS , 2001) 12 percent (Budavari, 2000; CHRIS , 2001; Lewis, 1997)
74.2 percent (Lewis, 2000; OHM/TADS , 2001) 75 percent (Budavari, 2000; CHRIS , 2001; Lewis, 1997)
SOLUBILITY
3.3/100 mL (at 0 degrees C) (Budavari, 2000) 2.3/100 mL (at 20 degrees C) (Budavari, 2000) Carbon monoxide is slightly soluble in water (ITI, 1995)
Carbon monoxide is appreciably soluble in some organic solvents, such as ethyl acetate, chloroform, and acetic acid (Budavari, 2000; ITI, 1995). Carbon monoxide's solubility in methanol and ethanol is about seven times greater than its solubility in water (Budavari, 2000). Carbon monoxide is soluble in acetic acid, methanol, and ethanol (Lewis, 2000).
Carbon monoxide is freely absorbed by a concentrated solution of cuprous chloride in hydrogen chloride or in ammonium hydroxide (Budavari, 2000). Carbon monoxide is readily soluble in hydrochloric acid or concentrated, ammonical solution of cuprous chloride (ITI, 1995).
OTHER/PHYSICAL
- DECOMPOSITION TEMPERATURE
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