"CO2" redirects here. For other uses, see CO2 (disambiguation).
Carbon dioxide
Names
Other names
Carbonic acid gas
Carbonic anhydride
Carbonic oxide
Carbon oxide
Carbon(IV) oxide
Dry ice (solid phase)
Identifiers
CAS Number
124-38-9Y
3D model (JSmol)
Interactive image
Interactive image
3DMet
B01131
Beilstein Reference
1900390
ChEBI
CHEBI:16526Y
ChEMBL
ChEMBL1231871N
ChemSpider
274Y
ECHA InfoCard
100.004.271
EC Number
204-696-9
E number
E290 (preservatives)
Gmelin Reference
989
KEGG
D00004Y
MeSH
Carbon+dioxide
PubChem CID
280
RTECS number
FF6400000
UNII
142M471B3JY
UN number
1013 (gas), 1845 (solid)
InChI
InChI=1S/CO2/c2-1-3Y
Key: CURLTUGMZLYLDI-UHFFFAOYSA-NY
InChI=1/CO2/c2-1-3
Key: CURLTUGMZLYLDI-UHFFFAOYAO
SMILES
O=C=O
C(=O)=O
Properties
Chemical formula
CO2
Molar mass
44.01 g·mol−1
Appearance
Colorless gas
Odor
Low concentrations: none
High concentrations: sharp; acidic[1]
Density
1562 kg/m3(solid at 1 atm and −78.5 °C)
1101 kg/m3(liquid at saturation −37°C)
1.977 kg/m3(gas at 1 atm and 0 °C)
Melting point
−56.6 °C; −69.8 °F; 216.6 K (Triple point at 5.1 atm)
Sublimation conditions
−78.5 °C; −109.2 °F; 194.7 K (1 atm)
Solubility in water
1.45 g/L at 25 °C (77 °F), 100 kPa
Vapor pressure
5.73 MPa (20 °C)
Acidity (pKa)
6.35, 10.33
Magnetic susceptibility (χ)
−20.5·10−6 cm3/mol
Refractive index (nD)
1.00045
Viscosity
0.07 cP at −78.5 °C
Dipole moment
0 D
Structure
Crystal structure
trigonal
Molecular shape
linear
Thermochemistry
Heat capacity (C)
37.135 J/K mol
Std molar entropy (So298)
214 J·mol−1·K−1
Std enthalpy of formation (ΔfHo298)
−393.5 kJ·mol−1
Pharmacology
ATC code
V03AN02 (WHO)
Hazards
Safety data sheet
See: data page Sigma-Aldrich
NFPA 704
[4][5]
Lethal dose or concentration (LD, LC):
LCLo (lowest published)
90,000 ppm (human, 5 min)[3]
US health exposure limits (NIOSH):
PEL (Permissible)
TWA 5000 ppm (9000 mg/m3)[2]
REL (Recommended)
TWA 5000 ppm (9000 mg/m3) ST 30,000 ppm (54,000 mg/m3)[2]
IDLH (Immediate danger)
40,000 ppm[2]
Related compounds
Other anions
Carbon disulfide
Carbon diselenide
Carbon ditelluride
Other cations
Silicon dioxide
Germanium dioxide
Tin dioxide
Lead dioxide
Related carbon oxides
Carbon monoxide
Carbon suboxide
Dicarbon monoxide
Carbon trioxide
Related compounds
Carbonic acid
Carbonyl sulfide
Supplementary data page
Structure and properties
Refractive index (n), Dielectric constant (εr), etc.
Thermodynamic data
Phase behaviour solid–liquid–gas
Spectral data
UV, IR, NMR, MS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Nverify (what is YN ?)
Infobox references
Carbon dioxide (chemical formula CO2) is a colorless gas with a density about 60% higher than that of dry air. Carbon dioxide consists of a carbon atom covalently double bonded to two oxygen atoms. It occurs naturally in Earth's atmosphere as a trace gas. The current concentration is about 0.04% (410 ppm) by volume, having risen from pre-industrial levels of 280 ppm. Natural sources include volcanoes, hot springs and geysers, and it is freed from carbonate rocks by dissolution in water and acids. Because carbon dioxide is soluble in water, it occurs naturally in groundwater, rivers and lakes, ice caps, glaciers and seawater. It is present in deposits of petroleum and natural gas. Carbon dioxide is odorless at normally encountered concentrations. However, at high concentrations, it has a sharp and acidic odor.[1]
As the source of available carbon in the carbon cycle, atmospheric carbon dioxide is the primary carbon source for life on Earth and its concentration in Earth's pre-industrial atmosphere since late in the Precambrian has been regulated by photosynthetic organisms and geological phenomena. Plants, algae and cyanobacteria use light energy to photosynthesize carbohydrate from carbon dioxide and water, with oxygen produced as a waste product.[6]
CO2 is produced by all aerobic organisms when they metabolize carbohydrates and lipids to produce energy by respiration.[7] It is returned to water via the gills of fish and to the air via the lungs of air-breathing land animals, including humans. Carbon dioxide is produced during the processes of decay of organic materials and the fermentation of sugars in bread, beer and wine making. It is produced by combustion of wood and other organic materials and fossil fuels such as coal, peat, petroleum and natural gas. It is an unwanted byproduct in many large scale oxidation processes, for example, in the production of acrylic acid (over 5 million tons/year).[8][9][10][11]
It is a versatile industrial material, used, for example, as an inert gas in welding and fire extinguishers, as a pressurizing gas in air guns and oil recovery, as a chemical feedstock and as a supercritical fluid solvent in decaffeination of coffee[12] and supercritical drying. It is added to drinking water and carbonated beverages including beer and sparkling wine to add effervescence. The frozen solid form of CO2, known as dry ice is used as a refrigerant and as an abrasive in dry-ice blasting.
Carbon dioxide is the most significant long-lived greenhouse gas in Earth's atmosphere. Since the Industrial Revolution anthropogenic emissions – primarily from use of fossil fuels and deforestation – have rapidly increased its concentration in the atmosphere, leading to global warming. Carbon dioxide also causes ocean acidification because it dissolves in water to form carbonic acid.[13]
Contents
1Background
2Chemical and physical properties
2.1Structure and bonding
2.2In aqueous solution
2.3Chemical reactions of CO2
2.4Physical properties
3Isolation and production
4Applications
4.1Precursor to chemicals
4.2Foods
4.2.1Beverages
4.2.2Wine making
4.2.3Stunning animals
4.3Inert gas
4.4Fire extinguisher
4.5Supercritical CO2 as solvent
4.6Agricultural and biological applications
4.7Medical and pharmacological uses
4.8Oil recovery
4.9Bio transformation into fuel
4.10Refrigerant
4.11Coal bed methane recovery
4.12Minor uses
5In Earth's atmosphere
6In the oceans
7Biological role
7.1Photosynthesis and carbon fixation
7.2Toxicity
7.2.1Below 1%
7.2.2Ventilation
7.3Human physiology
7.3.1Content
7.3.2Transport in the blood
7.3.3Regulation of respiration
8See also
9References
10Further reading
11External links
Background
Crystal structure of dry ice
Carbon dioxide was the first gas to be described as a discrete substance. In about 1640,[14] the Flemish chemist Jan Baptist van Helmont observed that when he burned charcoal in a closed vessel, the mass of the resulting ash was much less than that of the original charcoal. His interpretation was that the rest of the charcoal had been transmuted into an invisible substance he termed a "gas" or "wild spirit" (spiritus sylvestris).[15]
The properties of carbon dioxide were further studied in the 1750s by the Scottish physician Joseph Black. He found that limestone (calcium carbonate) could be heated or treated with acids to yield a gas he called "fixed air." He observed that the fixed air was denser than air and supported neither flame nor animal life. Black also found that when bubbled through limewater (a saturated aqueous solution of calcium hydroxide), it would precipitate calcium carbonate. He used this phenomenon to illustrate that carbon dioxide is produced by animal respiration and microbial fermentation. In 1772, English chemist Joseph Priestley published a paper entitled Impregnating Water with Fixed Air in which he described a process of dripping sulfuric acid (or oil of vitriol as Priestley knew it) on chalk in order to produce carbon dioxide, and forcing the gas to dissolve by agitating a bowl of water in contact with the gas.[16]
Carbon dioxide was first liquefied (at elevated pressures) in 1823 by Humphry Davy and Michael Faraday.[17] The earliest description of solid carbon dioxide was given by Adrien-Jean-Pierre Thilorier, who in 1835 opened a pressurized container of liquid carbon dioxide, only to find that the cooling produced by the rapid evaporation of the liquid yielded a "snow" of solid CO2.[18][19]
Chemical and physical properties
Stretching and bending oscillations of the CO2 carbon dioxide molecule. Upper left: symmetric stretching. Upper right: antisymmetric stretching. Lower line: degenerate pair of bending modes.
Structure and bonding
See also: Molecular orbital diagram § Carbon dioxide
The carbon dioxide molecule is linear and centrosymmetric. The carbon–oxygen bond length is 116.3 pm, noticeably shorter than the bond length of a C–O single bond and even shorter than most other C–O multiply-bonded functional groups.[20] Since it is centrosymmetric, the molecule has no electrical dipole. Consequently, only two vibrational bands are observed in the IR spectrum – an antisymmetric stretching mode at 2349 cm−1 and a degenerate pair of bending modes at 667 cm−1. There is also a symmetric stretching mode at 1388 cm−1 which is only observed in the Raman spectrum.[21]
In aqueous solution
See also: Carbonic acid
Carbon dioxide is soluble in water, in which it reversibly forms H 2CO 3 (carbonic acid), which is a weak acid since its ionization in water is incomplete.
CO 2 + H 2O ⇌ H 2CO 3
The hydration equilibrium constant of carbonic acid is Kh=[H2CO3][CO2(aq)]=1.70×10−3displaystyle K_mathrm h =frac rm [H_2CO_3]rm [CO_2(aq)]=1.70times 10^-3 (at 25 °C). Hence, the majority of the carbon dioxide is not converted into carbonic acid, but remains as CO2 molecules, not affecting the pH.
The relative concentrations of CO 2, H 2CO 3, and the deprotonated forms HCO− 3 (bicarbonate) and CO2− 3(carbonate) depend on the pH. As shown in a Bjerrum plot, in neutral or slightly alkaline water (pH > 6.5), the bicarbonate form predominates (>50%) becoming the most prevalent (>95%) at the pH of seawater. In very alkaline water (pH > 10.4), the predominant (>50%) form is carbonate. The oceans, being mildly alkaline with typical pH = 8.2–8.5, contain about 120 mg of bicarbonate per liter.
Being diprotic, carbonic acid has two acid dissociation constants, the first one for the dissociation into the bicarbonate (also called hydrogen carbonate) ion (HCO3−):
H2CO3 ⇌ HCO3− + H+
Ka1 = 6999250000000000000♠2.5×10−4 mol/L; pKa1 = 3.6 at 25 °C.[20]
This is the true first acid dissociation constant, defined as Ka1=[HCO3−][H+][H2CO3]displaystyle K_a1=frac rm [HCO_3^-][H^+]rm [H_2CO_3], where the denominator includes only covalently bound H2CO3 and does not include hydrated CO2(aq). The much smaller and often-quoted value near 6993416000000000000♠4.16×10−7 is an apparent value calculated on the (incorrect) assumption that all dissolved CO2 is present as carbonic acid, so that Ka1(apparent)=[HCO3−][H+][H2CO3]+[CO2(aq)]displaystyle K_mathrm a1 rm (apparent)=frac rm [HCO_3^-][H^+]rm [H_2CO_3]+[CO_2(aq)]. Since most of the dissolved CO2 remains as CO2 molecules, Ka1(apparent) has a much larger denominator and a much smaller value than the true Ka1.[22]
The bicarbonate ion is an amphoteric species that can act as an acid or as a base, depending on pH of the solution. At high pH, it dissociates significantly into the carbonate ion (CO32−):
In organisms carbonic acid production is catalysed by the enzyme, carbonic anhydrase.
Chemical reactions of CO2
CO2 is a weak electrophile. Its reaction with basic water illustrates this property, in which case hydroxide is the nucleophile. Other nucleophiles react as well. For example, carbanions as provided by Grignard reagents and organolithium compounds react with CO2 to give carboxylates:
MR + CO2 → RCO2M
where M = Li or MgBr and R = alkyl or aryl.
In metal carbon dioxide complexes, CO2 serves as a ligand, which can facilitate the conversion of CO2 to other chemicals.[23]
The reduction of CO2 to CO is ordinarily a difficult and slow reaction:
CO2 + 2 e− + 2H+ → CO + H2O
Photoautotrophs (i.e. plants and cyanobacteria) use the energy contained in sunlight to photosynthesize simple sugars from CO2 absorbed from the air and water:
n CO2 + nH 2O → (CH 2O) n + nO 2
The redox potential for this reaction near pH 7 is about −0.53 V versus the standard hydrogen electrode. The nickel-containing enzyme carbon monoxide dehydrogenase catalyses this process.[24]
Physical properties
Further information: Carbon dioxide data
Pellets of "dry ice", a common form of solid carbon dioxide
Carbon dioxide is colorless. At low concentrations the gas is odorless; however, at sufficiently-high concentrations, it has a sharp, acidic odor.[1] At standard temperature and pressure, the density of carbon dioxide is around 1.98 kg/m3, about 1.67 times that of air.
Carbon dioxide has no liquid state at pressures below 5.1 standard atmospheres (520 kPa). At 1 atmosphere (near mean sea level pressure), the gas deposits directly to a solid at temperatures below −78.5 °C (−109.3 °F; 194.7 K) and the solid sublimes directly to a gas above −78.5 °C. In its solid state, carbon dioxide is commonly called dry ice.
Pressure–temperature phase diagram of carbon dioxide
Liquid carbon dioxide forms only at pressures above 5.1 atm; the triple point of carbon dioxide is about 5.1 bar (517 kPa) at 217 K (see phase diagram). The critical point is 7.38 MPa at 31.1 °C.[25][26] Another form of solid carbon dioxide observed at high pressure is an amorphous glass-like solid.[27] This form of glass, called carbonia, is produced by supercooling heated CO2 at extreme pressure (40–48 GPa or about 400,000 atmospheres) in a diamond anvil. This discovery confirmed the theory that carbon dioxide could exist in a glass state similar to other members of its elemental family, like silicon (silica glass) and germanium dioxide. Unlike silica and germania glasses, however, carbonia glass is not stable at normal pressures and reverts to gas when pressure is released.
At temperatures and pressures above the critical point, carbon dioxide behaves as a supercritical fluid known as supercritical carbon dioxide. In this state it is starting (as of 2018) to be used for power generation.
Isolation and production
Carbon dioxide can be obtained by distillation from air, but the method is inefficient. Industrially, carbon dioxide is predominantly an unrecovered waste product, produced by several methods which may be practiced at various scales.[28]
The combustion of all carbon-based fuels, such as methane (natural gas), petroleum distillates (gasoline, diesel, kerosene, propane), coal, wood and generic organic matter produces carbon dioxide and, except in the case of pure carbon, water. As an example, the chemical reaction between methane and oxygen:
CH 4+ 2 O 2→ CO 2+ 2 H 2O
It is produced by thermal decomposition of limestone, CaCO 3 by heating (calcining) at about 850 °C (1,560 °F), in the manufacture of quicklime (calcium oxide, CaO), a compound that has many industrial uses:
CaCO 3→ CaO + CO 2
Iron is reduced from its oxides with coke in a blast furnace, producing pig iron and carbon dioxide:[29]
Carbon dioxide is a byproduct of the industrial production of hydrogen by steam reforming and the water gas shift reaction in ammonia production. These processes begin with the reaction of water and natural gas (mainly methane).[30] This is a major source of food-grade carbon dioxide for use in carbonation of beer and soft drinks, and is also used for stunning animals such as poultry. In the summer of 2018 a shortage of carbon dioxide for these purposes arose in Europe due to the temporary shut-down of several ammonia plants for maintenance.[31]
Acids liberate CO2 from most metal carbonates. Consequently, it may be obtained directly from natural carbon dioxide springs, where it is produced by the action of acidified water on limestone or dolomite. The reaction between hydrochloric acid and calcium carbonate (limestone or chalk) is shown below:
CaCO 3+ 2 HCl → CaCl 2+ H 2CO 3
The carbonic acid (H 2CO 3) then decomposes to water and CO2:
H 2CO 3→ CO 2+ H 2O
Such reactions are accompanied by foaming or bubbling, or both, as the gas is released. They have widespread uses in industry because they can be used to neutralize waste acid streams.
Carbon dioxide is a by-product of the fermentation of sugar in the brewing of beer, whisky and other alcoholic beverages and in the production of bioethanol. Yeast metabolizes sugar to produce CO2 and ethanol, also known as alcohol, as follows:
C 6H 12O 6 → 2 CO 2+ 2 C 2H 5OH
All aerobic organisms produce CO2 when they oxidize carbohydrates, fatty acids, and proteins. The large number of reactions involved are exceedingly complex and not described easily. Refer to (cellular respiration, anaerobic respiration and photosynthesis). The equation for the respiration of glucose and other monosaccharides is:
C 6H 12O 6 + 6 O 2 → 6 CO 2 + 6 H 2O
Anaerobic organisms decompose organic material producing methane and carbon dioxide together with traces of other compounds.[32] Regardless of the type of organic material, the production of gases follows well defined kinetic pattern. Carbon dioxide comprises about 40–45% of the gas that emanates from decomposition in landfills (termed "landfill gas"). Most of the remaining 50–55% is methane.[33]
Applications
Carbon dioxide is used by the food industry, the oil industry, and the chemical industry.[28] The compound has varied commercial uses but one of its greatest use as a chemical is in the production of carbonated beverages; it provides the sparkle in carbonated beverages such as soda water, beer and sparkling wine.
Precursor to chemicals
In the chemical industry, carbon dioxide is mainly consumed as an ingredient in the production of urea, with a smaller fraction being used to produce methanol and a range of other products,[34] such as metal carbonates and bicarbonates.[citation needed] Some carboxylic acid derivatives such as sodium salicylate are prepared using CO2 by the Kolbe-Schmitt reaction.[35]
In addition to conventional processes using CO2 for chemical production, electrochemical methods are also being explored at a research level. In particular, the use of renewable energy for production of fuels from CO2 (such as methanol) is attractive as this could result in fuels that could be easily transported and used within conventional combustion technologies but have no net CO2 emissions.[36]
Foods
Carbon dioxide bubbles in a soft drink.
Carbon dioxide is a food additive used as a propellant and acidity regulator in the food industry. It is approved for usage in the EU[37] (listed as E number E290), US[38] and Australia and New Zealand[39] (listed by its INS number 290).
A candy called Pop Rocks is pressurized with carbon dioxide gas[40] at about 4 x 106 Pa (40 bar, 580 psi). When placed in the mouth, it dissolves (just like other hard candy) and releases the gas bubbles with an audible pop.
Leavening agents cause dough to rise by producing carbon dioxide.[41]Baker's yeast produces carbon dioxide by fermentation of sugars within the dough, while chemical leaveners such as baking powder and baking soda release carbon dioxide when heated or if exposed to acids.
Beverages
Carbon dioxide is used to produce carbonated soft drinks and soda water. Traditionally, the carbonation of beer and sparkling wine came about through natural fermentation, but many manufacturers carbonate these drinks with carbon dioxide recovered from the fermentation process. In the case of bottled and kegged beer, the most common method used is carbonation with recycled carbon dioxide. With the exception of British Real Ale, draught beer is usually transferred from kegs in a cold room or cellar to dispensing taps on the bar using pressurized carbon dioxide, sometimes mixed with nitrogen.
Wine making
Dry ice used to preserve grapes after harvest.
Carbon dioxide in the form of dry ice is often used during the cold soak phase in wine making to cool clusters of grapes quickly after picking to help prevent spontaneous fermentation by wild yeast. The main advantage of using dry ice over water ice is that it cools the grapes without adding any additional water that might decrease the sugar concentration in the grape must, and thus the alcohol concentration in the finished wine. Carbon dioxide is also used to create a hypoxic environment for carbonic maceration, the process used to produce Beaujolais wine.
Carbon dioxide is sometimes used to top up wine bottles or other storage vessels such as barrels to prevent oxidation, though it has the problem that it can dissolve into the wine, making a previously still wine slightly fizzy. For this reason, other gases such as nitrogen or argon are preferred for this process by professional wine makers.
Stunning animals
Carbon dioxide is often used to "stun" animals before slaughter.[42] "Stunning" may be a misnomer, as the animals are not knocked out immediately and may suffer distress.[43][44]
Inert gas
It is one of the most commonly used compressed gases for pneumatic (pressurized gas) systems in portable pressure tools. Carbon dioxide is also used as an atmosphere for welding, although in the welding arc, it reacts to oxidize most metals. Use in the automotive industry is common despite significant evidence that welds made in carbon dioxide are more brittle than those made in more inert atmospheres. It is used as a welding gas primarily because it is much less expensive than more inert gases such as argon or helium.[citation needed] When used for MIG welding, CO2 use is sometimes referred to as MAG welding, for Metal Active Gas, as CO2 can react at these high temperatures. It tends to produce a hotter puddle than truly inert atmospheres, improving the flow characteristics. Although, this may be due to atmospheric reactions occurring at the puddle site. This is usually the opposite of the desired effect when welding, as it tends to embrittle the site, but may not be a problem for general mild steel welding, where ultimate ductility is not a major concern.
It is used in many consumer products that require pressurized gas because it is inexpensive and nonflammable, and because it undergoes a phase transition from gas to liquid at room temperature at an attainable pressure of approximately 60 bar (870 psi, 59 atm), allowing far more carbon dioxide to fit in a given container than otherwise would. Life jackets often contain canisters of pressured carbon dioxide for quick inflation. Aluminium capsules of CO2 are also sold as supplies of compressed gas for air guns, paintball markers/guns, inflating bicycle tires, and for making carbonated water. Rapid vaporization of liquid carbon dioxide is used for blasting in coal mines.[citation needed] High concentrations of carbon dioxide can also be used to kill pests. Liquid carbon dioxide is used in supercritical drying of some food products and technological materials, in the preparation of specimens for scanning electron microscopy[citation needed] and in the decaffeination of coffee beans.
Fire extinguisher
Use of a CO2 fire extinguisher.
Carbon dioxide can be used to extinguish flames by flooding the environment around the flame with the gas. It does not itself react to extinguish the flame, but starves the flame of oxygen by displacing it. Some fire extinguishers, especially those designed for electrical fires, contain liquid carbon dioxide under pressure. Carbon dioxide extinguishers work well on small flammable liquid and electrical fires, but not on ordinary combustible fires, because although it excludes oxygen, it does not cool the burning substances significantly and when the carbon dioxide disperses they are free to catch fire upon exposure to atmospheric oxygen. Their desirability in electrical fire stems from the fact that, unlike water or other chemical based methods, Carbon dioxide will not cause short circuits, leading to even more damage to equipment. Because it is a gas, it is also easy to dispense large amounts of the gas automatically in IT infrastructure rooms, where the fire itself might be hard to reach with more immediate methods because it is behind rack doors and inside of cases. Carbon dioxide has also been widely used as an extinguishing agent in fixed fire protection systems for local application of specific hazards and total flooding of a protected space.[45]International Maritime Organization standards also recognize carbon dioxide systems for fire protection of ship holds and engine rooms. Carbon dioxide based fire protection systems have been linked to several deaths, because it can cause suffocation in sufficiently high concentrations. A review of CO2 systems identified 51 incidents between 1975 and the date of the report (2000), causing 72 deaths and 145 injuries.[46]
Supercritical CO2 as solvent
See also: Supercritical carbon dioxide
Liquid carbon dioxide is a good solvent for many lipophilic organic compounds and is used to remove caffeine from coffee. Carbon dioxide has attracted attention in the pharmaceutical and other chemical processing industries as a less toxic alternative to more traditional solvents such as organochlorides. It is used by some dry cleaners for this reason (see green chemistry). It is used in the preparation of some aerogels because of the properties of supercritical carbon dioxide.
Agricultural and biological applications
Plants require carbon dioxide to conduct photosynthesis. The atmospheres of greenhouses may (if of large size, must) be enriched with additional CO2 to sustain and increase the rate of plant growth.[47][48] At very high concentrations (100 times atmospheric concentration, or greater), carbon dioxide can be toxic to animal life, so raising the concentration to 10,000 ppm (1%) or higher for several hours will eliminate pests such as whiteflies and spider mites in a greenhouse.[49]
It has been proposed that CO2 from power generation be bubbled into ponds to stimulate growth of algae that could then be converted into biodiesel fuel.[50]
Medical and pharmacological uses
In medicine, up to 5% carbon dioxide (130 times atmospheric concentration) is added to oxygen for stimulation of breathing after apnea and to stabilize the O 2/CO 2 balance in blood.
Carbon dioxide can be mixed with up to 50% oxygen, forming an inhalable gas; this is known as Carbogen and has a variety of medical and research uses.
Oil recovery
Carbon dioxide is used in enhanced oil recovery where it is injected into or adjacent to producing oil wells, usually under supercritical conditions, when it becomes miscible with the oil. This approach can increase original oil recovery by reducing residual oil saturation by between 7% to 23% additional to primary extraction.[51] It acts as both a pressurizing agent and, when dissolved into the underground crude oil, significantly reduces its viscosity, and changing surface chemistry enabling the oil to flow more rapidly through the reservoir to the removal well.[52] In mature oil fields, extensive pipe networks are used to carry the carbon dioxide to the injection points.
Bio transformation into fuel
Main article: Carbon capture and utilization
A strain of the cyanobacterium Synechococcus elongatus has been genetically engineered to produce the fuels isobutyraldehyde and isobutanol from CO2 using photosynthesis.[53]
Refrigerant
Comparison of phase diagrams of carbon dioxide (red) and water (blue) as a log-lin chart with phase transitions points at 1 atmosphere
Liquid and solid carbon dioxide are important refrigerants, especially in the food industry, where they are employed during the transportation and storage of ice cream and other frozen foods. Solid carbon dioxide is called "dry ice" and is used for small shipments where refrigeration equipment is not practical. Solid carbon dioxide is always below −78.5 °C at regular atmospheric pressure, regardless of the air temperature.
Liquid carbon dioxide (industry nomenclature R744 or R-744) was used as a refrigerant prior to the discovery of R-12 and may enjoy a renaissance due to the fact that R134a contributes to climate change more than CO2 does. Its physical properties are highly favorable for cooling, refrigeration, and heating purposes, having a high volumetric cooling capacity. Due to the need to operate at pressures of up to 130 bar (1880 psi), CO2 systems require highly resistant components that have already been developed for mass production in many sectors. In automobile air conditioning, in more than 90% of all driving conditions for latitudes higher than 50°, R744 operates more efficiently than systems using R134a. Its environmental advantages (GWP of 1, non-ozone depleting, non-toxic, non-flammable) could make it the future working fluid to replace current HFCs in cars, supermarkets, and heat pump water heaters, among others. Coca-Cola has fielded CO2-based beverage coolers and the U.S. Army is interested in CO2 refrigeration and heating technology.[54][55]
The global automobile industry is expected to decide on the next-generation refrigerant in car air conditioning. CO2 is one discussed option.(see Sustainable automotive air conditioning)
Coal bed methane recovery
In enhanced coal bed methane recovery, carbon dioxide would be pumped into the coal seam to displace methane, as opposed to current methods which primarily rely on the removal of water (to reduce pressure) to make the coal seam release its trapped methane.[56]
Minor uses
A carbon dioxide laser.
Carbon dioxide is the lasing medium in a carbon dioxide laser, which is one of the earliest type of lasers.
Carbon dioxide can be used as a means of controlling the pH of swimming pools,[57] by continuously adding gas to the water, thus keeping the pH from rising. Among the advantages of this is the avoidance of handling (more hazardous) acids. Similarly, it is also used in the maintaining reef aquaria, where it is commonly used in calcium reactors to temporarily lower the pH of water being passed over calcium carbonate in order to allow the calcium carbonate to dissolve into the water more freely where it is used by some corals to build their skeleton.
Used as the primary coolant in the British advanced gas-cooled reactor for nuclear power generation.
Carbon dioxide induction is commonly used for the euthanasia of laboratory research animals. Methods to administer CO2 include placing animals directly into a closed, prefilled chamber containing CO2, or exposure to a gradually increasing concentration of CO2. In 2013, the American Veterinary Medical Association issued new guidelines for carbon dioxide induction, stating that a displacement rate of 10% to 30% of the gas chamber volume per minute is optimal for the humane euthanization of small rodents.[58] However, there is opposition to the practice of using carbon dioxide for this, on the grounds that it is cruel.[44]
Carbon dioxide is also used in several related cleaning and surface preparation techniques.
In Earth's atmosphere
Main articles: Carbon dioxide in Earth's atmosphere and Carbon cycle
The Keeling Curve of atmospheric CO2 concentrations measured at Mauna Loa Observatory
Carbon dioxide in Earth's atmosphere is a trace gas, currently (mid 2018) having a global average concentration of 409 parts per million by volume[59][60][61] (or 622 parts per million by mass). Atmospheric concentrations of carbon dioxide fluctuate slightly with the seasons, falling during the Northern Hemisphere spring and summer as plants consume the gas and rising during northern autumn and winter as plants go dormant or die and decay. Concentrations also vary on a regional basis, most strongly near the ground with much smaller variations aloft. In urban areas concentrations are generally higher[62] and indoors they can reach 10 times background levels.
Yearly increase of atmospheric CO2: In the 1960s, the average annual increase was 37% of the 2000–2007 average.[63]
The concentration of carbon dioxide has risen due to human activities.[64] Combustion of fossil fuels and deforestation have caused the atmospheric concentration of carbon dioxide to increase by about 43% since the beginning of the age of industrialization.[65] Most carbon dioxide from human activities is released from burning coal and other fossil fuels. Other human activities, including deforestation, biomass burning, and cement production also produce carbon dioxide. Human activities emit about 29 billion tons of carbon dioxide per year, while volcanoes emit between 0.2 and 0.3 billion tons.[66][67] Human activities have caused CO2 to increase above levels not seen in hundreds of thousands of years. Currently, about half of the carbon dioxide released from the burning of fossil fuels remains in the atmosphere and is not absorbed by vegetation and the oceans.[68][69][70][71]
Carbon dioxide is a greenhouse gas, absorbing and emitting infrared radiation at its two infrared-active vibrational frequencies (see the section "Structure and bonding" above). This causes carbon dioxide to warm the surface and lower atmosphere while cooling the upper atmosphere.[72][73] Increases in atmospheric concentrations of CO2 and other long-lived greenhouse gases such as methane, nitrous oxide and ozone have correspondingly strengthened their absorption and emission of infrared radiation, causing the rise in average global temperature since the mid-20th century. Carbon dioxide is of greatest concern because it exerts a larger overall warming influence than all of these other gases combined and because it has a long atmospheric lifetime (hundreds to thousands of years).
CO2 in Earth's atmosphere if half of global-warming emissions are not absorbed.[68][69][70][71] (NASA computer simulation).
Not only do increasing carbon dioxide concentrations lead to increases in global surface temperature, but increasing global temperatures also cause increasing concentrations of carbon dioxide. This produces a positive feedback for changes induced by other processes such as orbital cycles.[74] Five hundred million years ago the carbon dioxide concentration was 20 times greater than today, decreasing to 4–5 times during the Jurassic period and then slowly declining with a particularly swift reduction occurring 49 million years ago.[75][76]
Local concentrations of carbon dioxide can reach high values near strong sources, especially those that are isolated by surrounding terrain. At the Bossoleto hot spring near Rapolano Terme in Tuscany, Italy, situated in a bowl-shaped depression about 100 m (330 ft) in diameter, concentrations of CO2 rise to above 75% overnight, sufficient to kill insects and small animals. After sunrise the gas is dispersed by convection.[77] High concentrations of CO2 produced by disturbance of deep lake water saturated with CO2 are thought to have caused 37 fatalities at Lake Monoun, Cameroon in 1984 and 1700 casualties at Lake Nyos, Cameroon in 1986.[78]
In the oceans
Main article: Carbon cycle
Pterapod shell dissolved in seawater adjusted to an ocean chemistry projected for the year 2100.
Carbon dioxide dissolves in the ocean to form carbonic acid (H2CO3), bicarbonate (HCO3−) and carbonate (CO32−). There is about fifty times as much carbon dissolved in the oceans as exists in the atmosphere. The oceans act as an enormous carbon sink, and have taken up about a third of CO2 emitted by human activity.[79]
As the concentration of carbon dioxide increases in the atmosphere, the increased uptake of carbon dioxide into the oceans is causing a measurable decrease in the pH of the oceans, which is referred to as ocean acidification. This reduction in pH affects biological systems in the oceans, primarily oceanic calcifying organisms. These effects span the food chain from autotrophs to heterotrophs and include organisms such as coccolithophores, corals, foraminifera, echinoderms, crustaceans and mollusks. Under normal conditions, calcium carbonate is stable in surface waters since the carbonate ion is at supersaturating concentrations. However, as ocean pH falls, so does the concentration of this ion, and when carbonate becomes undersaturated, structures made of calcium carbonate are vulnerable to dissolution.[80] Corals,[81][82][83] coccolithophore algae,[84][85][86][87] coralline algae,[88] foraminifera,[89]shellfish[90] and pteropods[91] experience reduced calcification or enhanced dissolution when exposed to elevated CO 2.
Gas solubility decreases as the temperature of water increases (except when both pressure exceeds 300 bar and temperature exceeds 393 K, only found near deep geothermal vents)[92] and therefore the rate of uptake from the atmosphere decreases as ocean temperatures rise.
Most of the CO2 taken up by the ocean, which is about 30% of the total released into the atmosphere,[93] forms carbonic acid in equilibrium with bicarbonate. Some of these chemical species are consumed by photosynthetic organisms that remove carbon from the cycle. Increased CO2 in the atmosphere has led to decreasing alkalinity of seawater, and there is concern that this may adversely affect organisms living in the water. In particular, with decreasing alkalinity, the availability of carbonates for forming shells decreases,[94] although there's evidence of increased shell production by certain species under increased CO2 content.[95]
NOAA states in their May 2008 "State of the science fact sheet for ocean acidification" that:
"The oceans have absorbed about 50% of the carbon dioxide (CO2) released from the burning of fossil fuels, resulting in chemical reactions that lower ocean pH. This has caused an increase in hydrogen ion (acidity) of about 30% since the start of the industrial age through a process known as "ocean acidification." A growing number of studies have demonstrated adverse impacts on marine organisms, including:
The rate at which reef-building corals produce their skeletons decreases, while production of numerous varieties of jellyfish increases.
The ability of marine algae and free-swimming zooplankton to maintain protective shells is reduced.
The survival of larval marine species, including commercial fish and shellfish, is reduced."
Also, the Intergovernmental Panel on Climate Change (IPCC) writes in their Climate Change 2007: Synthesis Report:[96]
"The uptake of anthropogenic carbon since 1750 has led to the ocean becoming more acidic with an average decrease in pH of 0.1 units. Increasing atmospheric CO2 concentrations lead to further acidification ... While the effects of observed ocean acidification on the marine biosphere are as yet undocumented, the progressive acidification of oceans is expected to have negative impacts on marine shell-forming organisms (e.g. corals) and their dependent species."
Some marine calcifying organisms (including coral reefs) have been singled out by major research agencies, including NOAA, OSPAR commission, NANOOS and the IPCC, because their most current research shows that ocean acidification should be expected to impact them negatively.[97]
Carbon dioxide is also introduced into the oceans through hydrothermal vents. The Champagne hydrothermal vent, found at the Northwest Eifuku volcano in the Marianas Trench, produces almost pure liquid carbon dioxide, one of only two known sites in the world as of 2004, the other being in the Okinawa Trough.[98] The finding of a submarine lake of liquid carbon dioxide in the Okinawa Trough was reported in 2006.[99]
Biological role
Carbon dioxide is an end product of cellular respiration in organisms that obtain energy by breaking down sugars, fats and amino acids with oxygen as part of their metabolism. This includes all plants, algae and animals and aerobic fungi and bacteria. In vertebrates, the carbon dioxide travels in the blood from the body's tissues to the skin (e.g., amphibians) or the gills (e.g., fish), from where it dissolves in the water, or to the lungs from where it is exhaled. During active photosynthesis, plants can absorb more carbon dioxide from the atmosphere than they release in respiration.
Photosynthesis and carbon fixation
Overview of photosynthesis and respiration. Carbon dioxide (at right), together with water, form oxygen and organic compounds (at left) by photosynthesis, which can be respired to water and (CO2).
Overview of the Calvin cycle and carbon fixation
Carbon fixation is a biochemical process by which atmospheric carbon dioxide is incorporated by plants, algae and (cyanobacteria) into energy-rich organic molecules such as glucose, thus creating their own food by photosynthesis. Photosynthesis uses carbon dioxide and water to produce sugars from which other organic compounds can be constructed, and oxygen is produced as a by-product.
Ribulose-1,5-bisphosphate carboxylase oxygenase, commonly abbreviated to RuBisCO, is the enzyme involved in the first major step of carbon fixation, the production of two molecules of 3-phosphoglycerate from CO2 and ribulose bisphosphate, as shown in the diagram at left.
RuBisCO is thought to be the single most abundant protein on Earth.[100]
Phototrophs use the products of their photosynthesis as internal food sources and as raw material for the biosynthesis of more complex organic molecules, such as polysaccharides, nucleic acids and proteins. These are used for their own growth, and also as the basis of the food chains and webs that feed other organisms, including animals such as ourselves. Some important phototrophs, the coccolithophores synthesise hard calcium carbonate scales.[101] A globally significant species of coccolithophore is Emiliania huxleyi whose calcite scales have formed the basis of many sedimentary rocks such as limestone, where what was previously atmospheric carbon can remain fixed for geological timescales.
Plants can grow as much as 50 percent faster in concentrations of 1,000 ppm CO2 when compared with ambient conditions, though this assumes no change in climate and no limitation on other nutrients.[102] Elevated CO2 levels cause increased growth reflected in the harvestable yield of crops, with wheat, rice and soybean all showing increases in yield of 12–14% under elevated CO2 in FACE experiments.[103][104]
Increased atmospheric CO2 concentrations result in fewer stomata developing on plants[105] which leads to reduced water usage and increased water-use efficiency.[106] Studies using FACE have shown that CO2 enrichment leads to decreased concentrations of micronutrients in crop plants.[107] This may have knock-on effects on other parts of ecosystems as herbivores will need to eat more food to gain the same amount of protein.[108]
The concentration of secondary metabolites such as phenylpropanoids and flavonoids can also be altered in plants exposed to high concentrations of CO2.[109][110]
Plants also emit CO2 during respiration, and so the majority of plants and algae, which use C3 photosynthesis, are only net absorbers during the day. Though a growing forest will absorb many tons of CO2 each year, a mature forest will produce as much CO2 from respiration and decomposition of dead specimens (e.g., fallen branches) as is used in photosynthesis in growing plants.[111] Contrary to the long-standing view that they are carbon neutral, mature forests can continue to accumulate carbon[112] and remain valuable carbon sinks, helping to maintain the carbon balance of Earth's atmosphere. Additionally, and crucially to life on earth, photosynthesis by phytoplankton consumes dissolved CO2 in the upper ocean and thereby promotes the absorption of CO2 from the atmosphere.[113]
Toxicity
See also: Carbon dioxide poisoning
Main symptoms of carbon dioxide toxicity, by increasing volume percent in air.[114]
Carbon dioxide content in fresh air (averaged between sea-level and 10 kPa level, i.e., about 30 km (19 mi) altitude) varies between 0.036% (360 ppm) and 0.041% (410 ppm), depending on the location.[115][clarification needed]
CO2 is an asphyxiant gas and not classified as toxic or harmful in accordance with Globally Harmonized System of Classification and Labelling of Chemicals standards of United Nations Economic Commission for Europe by using the OECD Guidelines for the Testing of Chemicals. In concentrations up to 1% (10,000 ppm), it will make some people feel drowsy and give the lungs a stuffy feeling.[114] Concentrations of 7% to 10% (70,000 to 100,000 ppm) may cause suffocation, even in the presence of sufficient oxygen, manifesting as dizziness, headache, visual and hearing dysfunction, and unconsciousness within a few minutes to an hour.[116] The physiological effects of acute carbon dioxide exposure are grouped together under the term hypercapnia, a subset of asphyxiation.
Because it is heavier than air, in locations where the gas seeps from the ground (due to sub-surface volcanic or geothermal activity) in relatively high concentrations, without the dispersing effects of wind, it can collect in sheltered/pocketed locations below average ground level, causing animals located therein to be suffocated. Carrion feeders attracted to the carcasses are then also killed. Children have been killed in the same way near the city of Goma by CO2 emissions from the nearby volcano Mt. Nyiragongo.[117] The Swahili term for this phenomenon is 'mazuku'.
Rising levels of CO2 threatened the Apollo 13 astronauts who had to adapt cartridges from the command module to supply the carbon dioxide scrubber in the lunar module, which they used as a lifeboat.
Adaptation to increased concentrations of CO2 occurs in humans, including modified breathing and kidney bicarbonate production, in order to balance the effects of blood acidification (acidosis). Several studies suggested that 2.0 percent inspired concentrations could be used for closed air spaces (e.g. a submarine) since the adaptation is physiological and reversible, as decrement in performance or in normal physical activity does not happen at this level of exposure for five days.[118][119] Yet, other studies show a decrease in cognitive function even at much lower levels.[120][121] Also, with ongoing respiratory acidosis, adaptation or compensatory mechanisms will be unable to reverse such condition.
Below 1%
There are few studies of the health effects of long-term continuous CO2 exposure on humans and animals at levels below 1%. Occupational CO2 exposure limits have been set in the United States at 0.5% (5000 ppm) for an eight-hour period.[122] At this CO2 concentration, International Space Station crew experienced headaches, lethargy, mental slowness, emotional irritation, and sleep disruption.[123] Studies in animals at 0.5% CO2 have demonstrated kidney calcification and bone loss after eight weeks of exposure.[124] A study of humans exposed in 2.5 hour sessions demonstrated significant effects on cognitive abilities at concentrations as low as 0.1% (1000ppm) CO2 likely due to CO2 induced increases in cerebral blood flow.[120] Another study observed a decline in basic activity level and information usage at 1000 ppm, when compared to 500 ppm.[121]
Ventilation
Poor ventilation is one of the main causes of excessive CO2 concentrations in closed spaces. Carbon dioxide differential above outdoor concentrations at steady state conditions (when the occupancy and ventilation system operation are sufficiently long that CO2 concentration has stabilized) are sometimes used to estimate ventilation rates per person.[citation needed] Higher CO2 concentrations are associated with occupant health, comfort and performance degradation.[citation needed]ASHRAE Standard 62.1–2007 ventilation rates may result in indoor concentrations up to 2,100 ppm above ambient outdoor conditions. Thus if the outdoor concentration is 400 ppm, indoor concentrations may reach 2,500 ppm with ventilation rates that meet this industry consensus standard. Concentrations in poorly ventilated spaces can be found even higher than this (range of 3,000 or 4,000).
Miners, who are particularly vulnerable to gas exposure due to an insufficient ventilation, referred to mixtures of carbon dioxide and nitrogen as "blackdamp," "choke damp" or "stythe." Before more effective technologies were developed, miners would frequently monitor for dangerous levels of blackdamp and other gases in mine shafts by bringing a caged canary with them as they worked. The canary is more sensitive to asphyxiant gases than humans, and as it became unconscious would stop singing and fall off its perch. The Davy lamp could also detect high levels of blackdamp (which sinks, and collects near the floor) by burning less brightly, while methane, another suffocating gas and explosion risk, would make the lamp burn more brightly.
Human physiology
Content
Reference ranges or averages for partial pressures of carbon dioxide (abbreviated pCO2)
kPa
mmHg
Venous blood carbon dioxide
5.5–6.8
41–51[125]
Alveolar pulmonary gas pressures
4.8
36
Arterial blood carbon dioxide
4.7–6.0
35–45[125]
The body produces approximately 2.3 pounds (1.0 kg) of carbon dioxide per day per person,[126] containing 0.63 pounds (290 g) of carbon. In humans, this carbon dioxide is carried through the venous system and is breathed out through the lungs, resulting in lower concentrations in the arteries. The carbon dioxide content of the blood is often given as the partial pressure, which is the pressure which carbon dioxide would have had if it alone occupied the volume.[127] In humans, the blood carbon dioxide contents is shown in the adjacent table:
Transport in the blood
CO2 is carried in blood in three different ways. (The exact percentages vary depending whether it is arterial or venous blood).
Most of it (about 70% to 80%) is converted to bicarbonate ions HCO− 3 by the enzyme carbonic anhydrase in the red blood cells,[128] by the reaction CO2 + H 2O → H 2CO 3 → H+ + HCO− 3.
5–10% is dissolved in the plasma[128]
5–10% is bound to hemoglobin as carbamino compounds[128]
Hemoglobin, the main oxygen-carrying molecule in red blood cells, carries both oxygen and carbon dioxide. However, the CO2 bound to hemoglobin does not bind to the same site as oxygen. Instead, it combines with the N-terminal groups on the four globin chains. However, because of allosteric effects on the hemoglobin molecule, the binding of CO2 decreases the amount of oxygen that is bound for a given partial pressure of oxygen. This is known as the Haldane Effect, and is important in the transport of carbon dioxide from the tissues to the lungs. Conversely, a rise in the partial pressure of CO2 or a lower pH will cause offloading of oxygen from hemoglobin, which is known as the Bohr effect.
Regulation of respiration
Carbon dioxide is one of the mediators of local autoregulation of blood supply. If its concentration is high, the capillaries expand to allow a greater blood flow to that tissue.
Bicarbonate ions are crucial for regulating blood pH. A person's breathing rate influences the level of CO2 in their blood. Breathing that is too slow or shallow causes respiratory acidosis, while breathing that is too rapid leads to hyperventilation, which can cause respiratory alkalosis.
Although the body requires oxygen for metabolism, low oxygen levels normally do not stimulate breathing. Rather, breathing is stimulated by higher carbon dioxide levels. As a result, breathing low-pressure air or a gas mixture with no oxygen at all (such as pure nitrogen) can lead to loss of consciousness without ever experiencing air hunger. This is especially perilous for high-altitude fighter pilots. It is also why flight attendants instruct passengers, in case of loss of cabin pressure, to apply the oxygen mask to themselves first before helping others; otherwise, one risks losing consciousness.[128]
The respiratory centers try to maintain an arterial CO2 pressure of 40 mm Hg. With intentional hyperventilation, the CO2 content of arterial blood may be lowered to 10–20 mm Hg (the oxygen content of the blood is little affected), and the respiratory drive is diminished. This is why one can hold one's breath longer after hyperventilating than without hyperventilating. This carries the risk that unconsciousness may result before the need to breathe becomes overwhelming, which is why hyperventilation is particularly dangerous before free diving.
See also
Chemistry portal
Arterial blood gas
Bosch reaction
Bottled gas
Carbon dioxide sensor
Carbon sequestration
Cave of Dogs
EcoCute – as refrigerants
Emission standards
Indoor air quality
Kaya identity
Lake Kivu
List of least carbon efficient power stations
List of countries by carbon dioxide emissions
Meromictic lake
pCO2
Gilbert Plass (early work on CO2 and climate change)
Sabatier reaction
NASA's Orbiting Carbon Observatory 2 and Greenhouse Gases Observing Satellite
^Lénárd-István Csepei (2011). Kinetic studies of propane oxidation on Mo and V based mixed oxide catalysts(PDF) (PHD thesis). Technical University of Berlin.
^Hävecker, M.; Wrabetz, S.; Kröhnert, J.; Csepei, L.-I.; Naumann d’Alnoncourt, R.; Kolen’ko, Y.V.; Girgsdies, F.; Schlögl, R.; Trunschke, A. (2012). "Surface chemistry of phase-pure M1 MoVTeNb oxide during operation in selective oxidation of propane to acrylic acid" (PDF). Journal of Catalysis. 285: 48–60. doi:10.1016/j.jcat.2011.09.012. hdl:11858/00-001M-0000-0012-1BEB-F.
^Naumann d’Alnoncourt, Raoul; Csepei, Lénárd-István; Hävecker, Michael; Girgsdies, Frank; Schuster, Manfred E.; Schlögl, Robert; Trunschke, Annette (2014). "The reaction network in propane oxidation over phase-pure MoVTeNb M1 oxide catalysts" (PDF). Journal of Catalysis. 311: 369–385. doi:10.1016/j.jcat.2013.12.008. hdl:11858/00-001M-0000-0014-F434-5.
^G.N. Sapkale, S.M. Patil, U.S. Surwase and P.K. Bhatbhage. "Supercritical Fluid Extraction" (PDF). Sadguru Publications.CS1 maint: Uses authors parameter (link)
^Ocean Acidification: A National Strategy to Meet the Challenges of a Changing Ocean. Washington, DC: National Academies Press. 2010-04-22. doi:10.17226/12904. ISBN 978-0-309-15359-1.
^DavidFraser Harris (September 1910). "The Pioneer in the Hygiene of Ventilation". The Lancet. 176 (4542): 906–908. doi:10.1016/S0140-6736(00)52420-9.
^Almqvist, Ebbe (2003). History of industrial gases. Springer. ISBN 978-0306472770. p. 93
^Priestley, Joseph; Hey, Wm (1772). "Observations on Different Kinds of Air". Philosophical Transactions. 62: 147–264. doi:10.1098/rstl.1772.0021.
^Davy, Humphry (1823). "On the Application of Liquids Formed by the Condensation of Gases as Mechanical Agents". Philosophical Transactions. 113: 199–205. doi:10.1098/rstl.1823.0020. JSTOR 107649.
^"Solidification of carbonic acid". The London and Edinburgh Philosophical Magazine. 8 (48): 446–447. 1836. doi:10.1080/14786443608648911.
^ abGreenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 0-08-037941-9.
^Atkins P. and de Paula J. Physical Chemistry (8th ed., W.H. Freeman 2006) pp. 461, 464 ISBN 0716787598
^Jolly, William L., Modern Inorganic Chemistry (McGraw-Hill 1984), p. 196 ISBN 0-07-032760-2
^M. Aresta (Ed.) "Carbon Dioxide as a Chemical Feedstock" 2010, Wiley-VCH: Weinheim. ISBN 978-3527324750
^Finn, Colin; Schnittger, Sorcha; Yellowlees, Lesley J.; Love, Jason B. (2012). "Molecular approaches to the electrochemical reduction of carbon dioxide". Chemical Communications. 48 (10): 1392–1399. doi:10.1039/c1cc15393e. PMID 22116300.
^"Phase change data for Carbon dioxide". National Institute of Standards and Technology. Retrieved 2008-01-21.
^Kudryavtseva I.V., Kamotskii V.I., Rykov S.V., Rykov V.A., "Calculation Carbon Dioxide Line of Phase Equilibrium", Processes and equipment for food production, Number 4(18), 2013
^ abPierantozzi, Ronald (2001). "Carbon Dioxide". Kirk-Othmer Encyclopedia of Chemical Technology. Kirk-Othmer Encyclopedia of Chemical Technology. Wiley. doi:10.1002/0471238961.0301180216090518.a01.pub2. ISBN 978-0471238966.
^ Strassburger, Julius (1969). Blast Furnace Theory and Practice. New York: American Institute of Mining, Metallurgical, and Petroleum Engineers. ISBN 978-0677104201.
^Susan Topham "Carbon Dioxide" in Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a05_165
^"CO2 shortage: Food industry calls for government action". BBC. Jun 21, 2018.
^"Collecting and using biogas from landfills". U.S. Energy Information Administration. January 11, 2017. Retrieved 2015-11-22.
^"Facts About Landfill Gas" (PDF). U.S. Environmental Protection Agency. January 2000.
^"IPCC Special Report on Carbon dioxide Capture and Storage" (PDF).
^R.T. Morrison and R.N. Boyd (1983). Organic Chemistry (4th ed.). Allyn and Bacon. pp. 976–977. ISBN 978-0205058389.
^Badwal, Sukhvinder P. S.; Giddey, Sarbjit S.; Munnings, Christopher; Bhatt, Anand I.; Hollenkamp, Anthony F. (24 September 2014). "Emerging electrochemical energy conversion and storage technologies (open access)". Frontiers in Chemistry. 2: 79. Bibcode:2014FrCh....2...79B. doi:10.3389/fchem.2014.00079. PMC 4174133. PMID 25309898.
^UK Food Standards Agency: "Current EU approved additives and their E Numbers". Retrieved 2011-10-27.
^US Food and Drug Administration: "Food Additive Status List". Retrieved 2015-06-13.
^Australia New Zealand Food Standards Code"Standard 1.2.4 – Labelling of ingredients". Retrieved 2011-10-27.
^Futurific Leading Indicators Magazine Volume 1. CRAES LLC. ISBN 978-0984767014.
^Vijay, G. Padma (2015-09-25). Indian Breads: A Comprehensive Guide to Traditional and Innovative Indian Breads. Westland. ISBN 978-9385724466.
^Andy Coghlan (Feb 3, 2018). "A more humane way of slaughtering chickens might get EU approval". New Scientist.
^"What is CO2 stunning?". RSPCA.
^ abArchie Campbell (Mar 10, 2018). "Humane execution and the fear of the tumbril". New Scientist.
^National Fire Protection Association Code 12
^Carbon Dioxide as a Fire Suppressant: Examining the Risks, US EPA. 2000.
^Whiting, David; Roll, Michael; Vickerman, Larry (August 2010). "Plant Growth Factors: Photosynthesis, Respiration, and Transpiration". CMG GardenNotes. Colorado Master Gardener Program. Archived from the original on 2014-09-02. Retrieved 2011-10-10.
^Waggoner, Paul E. (February 1994). "Carbon dioxide". How Much Land Can Ten Billion People Spare for Nature?. Retrieved 2011-10-10.
^Stafford, Ned (7 February 2007). "Future crops: The other greenhouse effect". Nature. 448 (7153): 526–528. Bibcode:2007Natur.448..526S. doi:10.1038/448526a. PMID 17671477.
^Clayton, Mark (2006-01-11). "Algae – like a breath mint for smokestacks". The Christian Science Monitor. Retrieved 2007-10-11.
^"Appendix A: CO2 for use in enhanced oil recovery (EOR)". Accelerating the uptake of CCS: industrial use of captured carbon dioxide. Global CCS Institute. 20 Dec 2011. Retrieved 2017-01-02.
^Austell, J Michael (2005). "CO2 for Enhanced Oil Recovery Needs – Enhanced Fiscal Incentives". Exploration & Production: The Oil & Gas Review. Archived from the original on 2012-02-07. Retrieved 2007-09-28.
^Atsum, Shota; Higashide, Wendy; Liauo, James C. (November 2009). "Direct photosynthetic recycling of carbon dioxide to isobutyraldehyde". Nature Biotechnology. 27 (12): 1177–1180. doi:10.1038/nbt.1586. PMID 19915552.
^"The Coca-Cola Company Announces Adoption of HFC-Free Insulation in Refrigeration Units to Combat Global Warming". The Coca-Cola Company. 2006-06-05. Retrieved 2007-10-11.
^"Modine reinforces its CO2 research efforts". R744.com. 2007-06-28. Archived from the original on 2008-02-10.
^"Enhanced coal bed methane recovery". ETH Zurich. 31 August 2006. Archived from the original on 6 July 2011.
^TCE, the Chemical Engineer. Institution of Chemical Engineers. 1990.
^"2013 AVMA Guidelines for the Euthanasia of Animals" (PDF). Retrieved 2014-01-14.
^National Oceanic & Atmospheric Administration (NOAA) – Earth System Research Laboratory (ESRL), Trends in Carbon Dioxide: Globally averaged marine surface monthly mean data Values given are dry air mole fractions expressed in parts per million (ppm). For an ideal gas mixture this is equivalent to parts per million by volume (ppmv).
^Pashley, Alex (10 March 2016). "CO2 levels make largest recorded annual leap, Noaa data shows". The Guardian. Retrieved 2016-03-14.
^"Record annual increase of carbon dioxide observed at Mauna Loa for 2015". NOAA. 9 March 2016. Retrieved 2016-03-14.
^George, K.; Ziska, L.H.; Bunce, J.A.; Quebedeaux, B. (2007). "Elevated atmospheric CO2 concentration and temperature across an urban–rural transect". Atmospheric Environment. 41 (35): 7654–7665. Bibcode:2007AtmEn..41.7654G. doi:10.1016/j.atmosenv.2007.08.018.
^Tans, Pieter (3 May 2008) "Annual CO2 mole fraction increase (ppm)" for 1959–2007. National Oceanic and Atmospheric Administration Earth System Research Laboratory, Global Monitoring Division (additional details.)
^Li, Anthony HF. "Hopes of Limiting Global Warming? China and the Paris Agreement on Climate Change." China Perspectives 1 (2016): 49.
^"After two large annual gains, rate of atmospheric CO2 increase returns to average". NOAA News Online, Story 2412. 2005-03-31.
^"Global Warming Frequently Asked Questions". Climate.gov. NOAA. Archived from the original on 11 January 2017.
^Gerlach, T.M. (4 June 1991). "Present-day CO2 emissions from volcanoes". Eos, Transactions, American Geophysical Union. 72 (23): 249, 254–255. Bibcode:1991EOSTr..72..249.. doi:10.1029/90EO10192.
^ abBuis, Alan; Ramsayer, Kate; Rasmussen, Carol (12 November 2015). "A breathing planet, off balance". NASA. Retrieved 2015-11-13.
^ abStaff (12 November 2015). "Audio (66:01) – NASA News Conference – Carbon & Climate Telecon". NASA. Retrieved 2015-11-12.
^ abSt. Fleur, Nicholas (10 November 2015). "Atmospheric Greenhouse Gas Levels Hit Record, Report Says". The New York Times. Retrieved 2015-11-11.
^ abRitter, Karl (9 November 2015). "UK: In 1st, global temps average could be 1 degree C higher". Associated Press. Retrieved 2015-11-11.
^UCAR (2012). "Carbon Dioxide Absorbs and Re-emits Infrared Radiation". UCAR Center for Science Education. Retrieved 2017-09-09.
^dana1981 (July 2015). "How do we know more CO2 is causing warming?". Skeptical Science. Retrieved 2017-09-09.
^Genthon, G.; Barnola, J.M.; Raynaud, D.; Lorius, C.; Jouzel, J.; Barkov, N.I.; Korotkevich, Y.S.; Kotlyakov, V.M. (1987). "Vostok ice core: climatic response to CO2 and orbital forcing changes over the last climatic cycle". Nature. 329 (6138): 414–418. Bibcode:1987Natur.329..414G. doi:10.1038/329414a0.
^"Climate and CO2 in the Atmosphere". Retrieved 2007-10-10.
^Berner, Robert A.; Kothavala, Zavareth (2001). "GEOCARB III: A revised model of atmospheric CO2 over Phanerozoic Time" (PDF). American Journal of Science. 301 (2): 182–204. Bibcode:2001AmJS..301..182B. CiteSeerX 10.1.1.393.582. doi:10.2475/ajs.301.2.182. Retrieved 2008-02-15.
^van Gardingen, P.R.; Grace, J.; Jeffree, C.E.; Byari, S.H.; Miglietta, F.; Raschi, A.; Bettarini, I. (1997). "Long-term effects of enhanced CO2 concentrations on leaf gas exchange: research opportunities using CO2 springs". In Raschi, A.; Miglietta, F.; Tognetti, R.; van Gardingen, P.R. Plant responses to elevated CO2: Evidence from natural springs. Cambridge: Cambridge University Press. pp. 69–86. ISBN 978-0521582032.
^Martini, M. (1997). "CO2 emissions in volcanic areas: case histories and hazards". In Raschi, A.; Miglietta, F.; Tognetti, R.; van Gardingen, P.R. Plant responses to elevated CO2: Evidence from natural springs. Cambridge: Cambridge University Press. pp. 69–86. ISBN 978-0521582032.
^Doney, Scott C.; Levine, Naomi M. (2006-11-29). "How Long Can the Ocean Slow Global Warming?". Oceanus. Retrieved 2007-11-21.
^Nienhuis, S.; Palmer, A.; Harley, C. (2010). "Elevated CO2 affects shell dissolution rate but not calcification rate in a marine snail". Proceedings of the Royal Society B: Biological Sciences. 277 (1693): 2553–2558. doi:10.1098/rspb.2010.0206. PMC 2894921. PMID 20392726.
^ Gattuso, J.-P.; Frankignoulle, M.; Bourge, I.; Romaine, S. & Buddemeier, R. W. (1998). "Effect of calcium carbonate saturation of seawater on coral calcification". Global and Planetary Change. 18 (1–2): 37–46. Bibcode:1998GPC....18...37G. doi:10.1016/S0921-8181(98)00035-6.
^ Gattuso, J.-P.; Allemand, D.; Frankignoulle, M (1999). "Photosynthesis and calcification at cellular, organismal and community levels in coral reefs: a review on interactions and control by carbonate chemistry". American Zoologist. 39: 160–183. doi:10.1093/icb/39.1.160.
^ Langdon, C; Atkinson, M. J. (2005). "Effect of elevated pCO2 on photosynthesis and calcification of corals and interactions with seasonal change in temperature/irradiance and nutrient enrichment". Journal of Geophysical Research. 110 (C09S07): C09S07. Bibcode:2005JGRC..110.9S07L. doi:10.1029/2004JC002576.
^ Riebesell, Ulf; Zondervan, Ingrid; Rost, Björn; Tortell, Philippe D.; Zeebe, Richard E. & François M.M. Morel (2000). "Reduced calcification of marine plankton in response to increased atmospheric CO 2". Nature. 407 (6802): 364–367. Bibcode:2000Natur.407..364R. doi:10.1038/35030078. PMID 11014189.
^ Zondervan, I.; Zeebe, R.E.; Rost, B.; Rieblesell, U. (2001). "Decreasing marine biogenic calcification: a negative feedback on rising atmospheric CO2". Global Biogeochemical Cycles. 15 (2): 507–516. Bibcode:2001GBioC..15..507Z. doi:10.1029/2000GB001321.
^Zondervan, I.; Rost, B.; Rieblesell, U. (2002). "Effect of CO2 concentration on the PIC/POC ratio in the coccolithophore Emiliania huxleyi grown under light limiting conditions and different day lengths" (PDF). Journal of Experimental Marine Biology and Ecology. 272 (1): 55–70. doi:10.1016/S0022-0981(02)00037-0.
^Delille, B.; Harlay, J.; Zondervan, I.; Jacquet, S.; Chou, L.; Wollast, R.; Bellerby, R.G.J.; Frankignoulle, M.; Borges, A.V.; Riebesell, U.; Gattuso, J.-P. (2005). "Response of primary production and calcification to changes of pCO2 during experimental blooms of the coccolithophorid Emiliania huxleyi". Global Biogeochemical Cycles. 19 (2): GB2023. Bibcode:2005GBioC..19.2023D. doi:10.1029/2004GB002318.
^Kuffner, I.B.; Andersson, A.J.; Jokiel, P.L.; Rodgers, K.S.; Mackenzie, F.T. (2007). "Decreased abundance of crustose coralline algae due to ocean acidification". Nature Geoscience. 1 (2): 114–117. Bibcode:2008NatGe...1..114K. doi:10.1038/ngeo100.
^ Phillips, Graham; Chris Branagan (2007-09-13). "Ocean Acidification – The BIG global warming story". ABC TV Science: Catalyst. Australian Broadcasting Corporation. Retrieved 2007-09-18.
^ Gazeau, F.; Quiblier, C.; Jansen, J.M.; Gattuso, J.-P.; Middelburg, J.J. & Heip, C.H.R. (2007). "Impact of elevated CO 2 on shellfish calcification". Geophysical Research Letters. 34 (7): L07603. Bibcode:2007GeoRL..34.7603G. CiteSeerX 10.1.1.326.1630. doi:10.1029/2006GL028554.
^ Comeau, C.; Gorsky, G.; Jeffree, R.; Teyssié, J.-L.; Gattuso, J.-P. (2009). "Impact of ocean acidification on a key Arctic pelagic mollusc (Limacina helicina)". Biogeosciences. 6 (9): 1877–1882. doi:10.5194/bg-6-1877-2009.
^Duana, Zhenhao; Rui Sun (2003). "An improved model calculating CO2 solubility in pure water and aqueous NaCl solutions from 273 to 533 K and from 0 to 2000 bar". Chemical Geology. 193 (3–4): 257–271. Bibcode:2003ChGeo.193..257D. doi:10.1016/S0009-2541(02)00263-2.
^Cai, W.-J.; Chen, L.; Chen, B.; Gao, Z.; et al. (2010). "Decrease in the CO2 Uptake Capacity in an Ice-Free Arctic Ocean Basin". Science. 329 (5991): 556&ndash, 559. Bibcode:2010Sci...329..556C. doi:10.1126/science.1189338. PMID 20651119.
^Garrison, Tom (2004). Oceanography: An Invitation to Marine Science. Thomson Brooks. p. 125. ISBN 978-0534408879.
^"PMEL Ocean Acidification Home Page". Pmel.noaa.gov. Retrieved 2014-01-14.
^Lupton, J.; Lilley, M.; Butterfield, D.; Evans, L.; Embley, R.; Olson, E.; Proskurowski, G.; Resing, J.; Roe, K.; Greene, R.; Lebon, G. (2004). "Liquid Carbon Dioxide Venting at the Champagne Hydrothermal Site, NW Eifuku Volcano, Mariana Arc". American Geophysical Union. Fall. Meeting (abstract #V43F–08): V43F–08. Bibcode:2004AGUFM.V43F..08L.
^Fumio Inagaki (2006). "Microbial community in a sediment-hosted CO2 lake of the southern Okinawa Trough hydrothermal system". PNAS. 103 (38): 14164–14169. Bibcode:2006PNAS..10314164I. doi:10.1073/pnas.0606083103. PMC 1599929. PMID 16959888. Videos can be downloaded at Supporting Information.
^Dhingra A, Portis AR, Daniell H (2004). "Enhanced translation of a chloroplast-expressed RbcS gene restores small subunit levels and photosynthesis in nuclear RbcS antisense plants". Proc. Natl. Acad. Sci. U.S.A. 101 (16): 6315–6320. Bibcode:2004PNAS..101.6315D. doi:10.1073/pnas.0400981101. PMC 395966. PMID 15067115. (Rubisco) is the most prevalent enzyme on this planet, accounting for 30–50% of total soluble protein in the chloroplast;
^G., Falkowski, Paul; H., Knoll, Andrew; (2006.01.), Symposium (2007-01-01). Evolution of primary producers in the sea. Elsevier, Academic Press. ISBN 978-0123705181. OCLC 845654016.
^Blom, T.J.; W.A. Straver; F.J. Ingratta; Shalin Khosla; Wayne Brown (December 2002). "Carbon Dioxide In Greenhouses". Retrieved 2007-06-12.
^Ainsworth, Elizabeth A. (2008). "Rice production in a changing climate: a meta-analysis of responses to elevated carbon dioxide and elevated ozone concentration" (PDF). Global Change Biology. 14 (7): 1642–1650. Bibcode:2008GCBio..14.1642A. doi:10.1111/j.1365-2486.2008.01594.x. Archived from the original (PDF) on 2011-07-19.
^F. Woodward; C. Kelly (1995). "The influence of CO2 concentration on stomatal density". New Phytologist. 131 (3): 311–327. doi:10.1111/j.1469-8137.1995.tb03067.x.
^Drake, Bert G.; Gonzalez-Meler, Miquel A.; Long, Steve P. (1997). "More efficient plants: A consequence of rising atmospheric CO2?". Annual Review of Plant Physiology and Plant Molecular Biology. 48 (1): 609–639. doi:10.1146/annurev.arplant.48.1.609. PMID 15012276.
^Loladze, I (2002). "Rising atmospheric CO2 and human nutrition: toward globally imbalanced plant stoichiometry?". Trends in Ecology & Evolution. 17 (10): 457–461. doi:10.1016/S0169-5347(02)02587-9.
^Carlos E. Coviella; John T. Trumble (1999). "Effects of Elevated Atmospheric Carbon Dioxide on Insect-Plant Interactions". Conservation Biology. 13 (4): 700–712. doi:10.1046/j.1523-1739.1999.98267.x. JSTOR 2641685.
^Davey, M.P.; Harmens, H.; Ashenden, T.W.; Edwards, R.; Baxter, R. (2007). "Species-specific effects of elevated CO2 on resource allocation in Plantago maritima and Armeria maritima". Biochemical Systematics and Ecology. 35 (3): 121–129. doi:10.1016/j.bse.2006.09.004.
^Davey, M.; Bryant, D.N.; Cummins, I.; Ashenden, T.W.; Gates, P.; Baxter, R.; Edwards, R. (2004). "Effects of elevated CO2 on the vasculature and phenolic secondary metabolism of Plantago maritima". Phytochemistry. 65 (15): 2197–2204. doi:10.1016/j.phytochem.2004.06.016. PMID 15587703.
^"Global Environment Division Greenhouse Gas Assessment Handbook – A Practical Guidance Document for the Assessment of Project-level Greenhouse Gas Emissions". World Bank. Archived from the original on 2016-06-03. Retrieved 2007-11-10.
^Falkowski P, Scholes RJ, Boyle E, Canadell J, Canfield D, Elser J, Gruber N, Hibbard K, Högberg P, Linder S, Mackenzie FT, Moore B 3rd, Pedersen T, Rosenthal Y, Seitzinger S, Smetacek V, Steffen W (2000). "The global carbon cycle: a test of our knowledge of earth as a system". Science. 290 (5490): 291–296. Bibcode:2000Sci...290..291F. doi:10.1126/science.290.5490.291. PMID 11030643.
^ abFriedman, Daniel. Toxicity of Carbon Dioxide Gas Exposure, CO2 Poisoning Symptoms, Carbon Dioxide Exposure Limits, and Links to Toxic Gas Testing Procedures. InspectAPedia
^"CarbonTracker CT2011_oi (Graphical map of CO2)". esrl.noaa.gov.
^"Carbon Dioxide as a Fire Suppressant: Examining the Risks". U.S. Environmental Protection Agency:.
^Volcano Under the City. PBS.org (1 November 2005).
^Glatte Jr H. A.; Motsay G.J.; Welch B.E. (1967). "Carbon Dioxide Tolerance Studies". Brooks AFB, TX School of Aerospace Medicine Technical Report. SAM-TR-67-77. Retrieved 2008-05-02.
^Lambertsen, C.J. (1971). "Carbon Dioxide Tolerance and Toxicity". Environmental Biomedical Stress Data Center, Institute for Environmental Medicine, University of Pennsylvania Medical Center. IFEM. Report No. 2-71. Retrieved 2008-05-02.
^ abSatish U.; Mendell M.J.; Shekhar K.; Hotchi T.; Sullivan D.; Streufert S.; Fisk W.J. (2012). "Is CO2 an Indoor Pollutant? Direct Effects of Low-to-Moderate CO2 Concentrations on Human Decision-Making Performance" (PDF). Environmental Health Perspectives. 120 (12): 1671–1677. doi:10.1289/ehp.1104789. PMC 3548274. PMID 23008272. Archived from the original (PDF) on 5 March 2016. Retrieved 11 December 2014.
^ abJoseph G. Allen; Piers MacNaughton; Usha Satish; Suresh Santanam; Jose Vallarino; John D. Spengler (2016). "Associations of Cognitive Function Scores with Carbon Dioxide, Ventilation, and Volatile Organic Compound Exposures in Office Workers: A Controlled Exposure Study of Green and Conventional Office Environments". Environmental Health Perspectives. 124 (6): 805–812. doi:10.1289/ehp.1510037. PMC 4892924. PMID 26502459. Archived from the original on 23 January 2016.
^"Exposure Limits for Carbon Dioxide Gas – CO2 Limits". InspectAPedia.com.
^Law J.; Watkins S.; Alexander, D. (2010). "In-Flight Carbon Dioxide Exposures and Related Symptoms: Associations, Susceptibility and Operational Implications" (PDF). NASA Technical Report. TP–2010–216126. Archived from the original (PDF) on 27 June 2011. Retrieved 2014-08-26.
^Schaefer, K.E. (1979). "Effect of Prolonged Exposure to 0.5% CO2 on Kidney Calcification and Ultrastructure of Lungs". Undersea Biomed Res. S6: 155–161. PMID 505623. Retrieved 2014-10-19.
Seppänen, O.A.; Fisk, W.J.; Mendell, M.J. (December 1999). "Association of Ventilation Rates and CO2 Concentrations with Health and Other Responses in Commercial and Institutional Buildings" (PDF). Indoor Air. 9 (4): 226–252. doi:10.1111/j.1600-0668.1999.00003.x. Archived from the original (PDF) on 27 December 2016.
Shendell, D.G.; Prill, R.; Fisk, W.J.; Apte, M.G.; Blake, D.; Faulkner, D. (October 2004). "Associations between classroom CO2 concentrations and student attendance in Washington and Idaho" (PDF). Indoor Air. 14 (5): 333–341. doi:10.1111/j.1600-0668.2004.00251.x. PMID 15330793. Archived from the original (PDF) on 27 December 2016.
Soentgen, Jens (February 2014). "Hot air: The science and politics of CO2". Global Environment. 7 (1): 134–171. doi:10.3197/197337314X13927191904925.
Good plant design and operation for onshore carbon capture installations and onshore pipelines: a recommended practice guidance document. Global CCS Institute. Energy Institute and Global Carbon Capture and Storage Institute. 1 Sep 2010. This new title is an essential guide for engineers, managers, procurement specialists and designers working on global carbon capture and storage projects.
External links
Wikimedia Commons has media related to Carbon dioxide.
Library resources about Carbon dioxide
Resources in your library
Resources in other libraries
International Chemical Safety Card 0021
Carbon dioxide MSDS by Amerigas in the SDSdata.org database.
CDC – NIOSH Pocket Guide to Chemical Hazards – Carbon Dioxide
CO2 Carbon Dioxide Properties, Uses, Applications
Dry Ice information
Trends in Atmospheric Carbon Dioxide (NOAA)
"A War Gas That Saves Lives". Popular Science, June 1942, pp. 53–57.
The on-line catalogue of CO2 natural emissions in Italy
Reactions, Thermochemistry, Uses, and Function of Carbon Dioxide
Carbon Dioxide – Part One and Carbon Dioxide – Part Two at The Periodic Table of Videos (University of Nottingham)
v
t
e
Oxides
Mixed oxidation states
Antimony tetroxide (Sb2O4)
Cobalt(II,III) oxide (Co3O4)
Europium(II,III) oxide (Eu3O4)
Iron(II,III) oxide (Fe3O4)
Lead(II,IV) oxide (Pb3O4)
Manganese(II,III) oxide (Mn3O4)
Silver(I,III) oxide (Ag2O2)
Triuranium octoxide (U3O8)
Carbon suboxide (C3O2)
Mellitic anhydride (C12O9)
Praseodymium(III,IV) oxide (Pr6O11)
Terbium(III,IV) oxide (Tb4O7)
+1 oxidation state
Copper(I) oxide (Cu2O)
Dicarbon monoxide (C2O)
Dichlorine monoxide (Cl2O)
Gallium(I) oxide (Ga2O)
Lithium oxide (Li2O)
Potassium oxide (K2O)
Rubidium oxide (Rb2O)
Silver oxide (Ag2O)
Thallium(I) oxide (Tl2O)
Sodium oxide (Na2O)
Water (hydrogen oxide) (H2O)
+2 oxidation state
Aluminium(II) oxide (AlO)
Barium oxide (BaO)
Beryllium oxide (BeO)
Cadmium oxide (CdO)
Calcium oxide (CaO)
Carbon monoxide (CO)
Chromium(II) oxide (CrO)
Cobalt(II) oxide (CoO)
Copper(II) oxide (CuO)
Europium(II) oxide (EuO)
Germanium monoxide (GeO))
Iron(II) oxide (FeO)
Lead(II) oxide (PbO)
Magnesium oxide (MgO)
Manganese(II) oxide (MnO)
Mercury(II) oxide (HgO)
Nickel(II) oxide (NiO)
Nitric oxide (NO)
Palladium(II) oxide (PdO)
Silicon monoxide (SiO)
Strontium oxide (SrO)
Sulfur monoxide (SO)
Disulfur dioxide (S2O2)
Thorium monoxide (ThO)
Tin(II) oxide (SnO)
Titanium(II) oxide (TiO)
Vanadium(II) oxide (VO)
Zinc oxide (ZnO)
+3 oxidation state
Aluminium oxide (Al2O3)
Antimony trioxide (Sb2O3)
Arsenic trioxide (As2O3)
Bismuth(III) oxide (Bi2O3)
Boron trioxide (B2O3)
Cerium(III) oxide (Ce2O3)
Dibromine trioxide (Br2O3)
Chromium(III) oxide (Cr2O3)
Dinitrogen trioxide (N2O3)
Dysprosium(III) oxide (Dy2O3)
Erbium(III) oxide (Er2O3)
Europium(III) oxide (Eu2O3)
Gadolinium(III) oxide (Gd2O3)
Gallium(III) oxide (Ga2O3)
Holmium(III) oxide (Ho2O3)
Indium(III) oxide (In2O3)
Iron(III) oxide (Fe2O3)
Lanthanum oxide (La2O3)
Lutetium(III) oxide (Lu2O3)
Manganese(III) oxide (Mn2O3)
Neodymium(III) oxide (Nd2O3)
Nickel(III) oxide (Ni2O3)
Phosphorus trioxide (P4O6)
Praseodymium(III) oxide (Pr2O3)
Promethium(III) oxide (Pm2O3)
Rhodium(III) oxide (Rh2O3)
Samarium(III) oxide (Sm2O3)
Scandium oxide (Sc2O3)
Terbium(III) oxide (Tb2O3)
Thallium(III) oxide (Tl2O3)
Thulium(III) oxide (Tm2O3)
Titanium(III) oxide (Ti2O3)
Tungsten(III) oxide (W2O3)
Vanadium(III) oxide (V2O3)
Ytterbium(III) oxide (Yb2O3)
Yttrium(III) oxide (Y2O3)
+4 oxidation state
Americium dioxide (AmO2)
Carbon dioxide (CO2)
Carbon trioxide (CO3)
Cerium(IV) oxide (CeO2)
Chlorine dioxide (ClO2)
Chromium(IV) oxide (CrO2)
Dinitrogen tetroxide (N2O4)
Germanium dioxide (GeO2)
Hafnium(IV) oxide (HfO2)
Lead dioxide (PbO2)
Manganese dioxide (MnO2)
Neptunium(IV) oxide (NpO2)
Nitrogen dioxide (NO2)
Osmium dioxide (OsO2)
Plutonium(IV) oxide (PuO2)
Praseodymium(IV) oxide (PrO2)
Protactinium(IV) oxide (PaO2)
Rhodium(IV) oxide (RhO2)
Ruthenium(IV) oxide (RuO2)
Selenium dioxide (SeO2)
Silicon dioxide (SiO2)
Sulfur dioxide (SO2)
Tellurium dioxide (TeO2)
Terbium(IV) oxide (TbO2)
Thorium dioxide (ThO2)
Tin dioxide (SnO2)
Titanium dioxide (TiO2)
Tungsten(IV) oxide (WO2)
Uranium dioxide (UO2)
Vanadium(IV) oxide (VO2)
Zirconium dioxide (ZrO2)
+5 oxidation state
Antimony pentoxide (Sb2O5)
Arsenic pentoxide (As2O5)
Dinitrogen pentoxide (N2O5)
Niobium pentoxide (Nb2O5)
Phosphorus pentoxide (P2O5)
Protactinium(V) oxide (Pa2O5)
Tantalum pentoxide (Ta2O5)
Vanadium(V) oxide (V2O5)
+6 oxidation state
Chromium trioxide (CrO3)
Molybdenum trioxide (MoO3)
Rhenium trioxide (ReO3)
Selenium trioxide (SeO3)
Sulfur trioxide (SO3)
Tellurium trioxide (TeO3)
Tungsten trioxide (WO3)
Uranium trioxide (UO3)
Xenon trioxide (XeO3)
Iridium trioxide (IrO3)
+7 oxidation state
Dichlorine heptoxide (Cl2O7)
Manganese heptoxide (Mn2O7)
Rhenium(VII) oxide (Re2O7)
Technetium(VII) oxide (Tc2O7)
+8 oxidation state
Osmium tetroxide (OsO4)
Ruthenium tetroxide (RuO4)
Xenon tetroxide (XeO4)
Iridium tetroxide (IrO4)
Hassium tetroxide (HsO4)
Related
Oxocarbon
Suboxide
Oxyanion
Ozonide
Peroxide
Superoxide
Oxides are sorted by oxidation state. Category:Oxides
v
t
e
Oxocarbons
Common oxides
CO
CO 2
Exotic oxides
CO 3
CO 4
CO 5
CO 6
C 2O
C 2O 2
C 2O 3
C 2O 4
C 2O 4
C 3O
C 3O 2
C 3O 3
C 3O 6
C 4O 2
C 4O 4
C 4O 6
C 5O 2
C 5O 5
C 6O 6
C 6O 6
C 8O 8
C 9O 9
C 10O 8
C 10O 10
C 12O 6
C 12O 9
C 12O 12
Polymers
Graphite oxide
C3O2
CO
CO2
Compounds derived from oxides
Metal carbonyls
Carbonic acid
Bicarbonates
Carbonates
Dicarbonates
Tricarbonates
v
t
e
Inorganic compounds of carbon and related ions
Compounds
CBr4
CCl4
CF
CF4
CI4
CO
CO2
CO3
COS
CS
CS2
CSe2
C3O2
C3S2
SiC
Carbon ions
Carbides [:C≡C:]2–, [::C::]4–, [:C=C=C:]4–
Cyanides [:C≡N:]–
Cyanates [:O-C≡N:]–
Thiocyanates [:S-C≡N:]–
Fulminates [:C≡N-O:]–
Thiofulminates [:C≡N-S:]–
Oxides and related
Oxides
Metal carbonyls
Carbonic acid
Bicarbonates
Carbonates
v
t
e
Global warming and climate change
Temperatures
Brightness temperature
Effective temperature
Geologic record
Hiatus
Historical climatology
Instrumental record
Paleoclimatology
Paleotempestology
Proxy data
Record of the past 1,000 years
Satellite measurements
Causes
Anthropogenic(caused by human activity)
Attribution of recent climate change
Aviation
Biofuel
Black carbon
Carbon dioxide
Deforestation
Earth's energy budget
Earth's radiation balance
Ecocide
Fossil fuel
Global dimming
Global warming potential
Greenhouse effect
(Infrared window)
Greenhouse gases
(Halocarbons)
Land use, land-use change, and forestry
Radiative forcing
Tropospheric ozone
Urban heat island
Natural
Albedo
Bond events
Climate oscillations
Climate sensitivity
Cloud forcing
Cosmic rays
Feedbacks
Glaciation
Global cooling
Milankovitch cycles
Ocean variability
AMO
ENSO
IOD
PDO
Orbital forcing
Solar variation
Volcanism
Models
Global climate model
History
History of climate change science
Atmospheric thermodynamics
Svante Arrhenius
James Hansen
Charles David Keeling
Opinion and climate change
General
Environmental ethics
Media coverage of climate change
Public opinion on climate change
(Popular culture)
Scientific opinion on climate change
Scientists who disagree with the mainstream assessment
Climate change denial
Global warming conspiracy theory
By country & region
Africa
Arctic
Argentina
Australia
Bangladesh
Belgium
Canada
China
Europe
European Union
Finland
Grenada
Japan
Luxembourg
New Zealand
Norway
Russia
Scotland
South Korea
Sweden
Tuvalu
United Kingdom
United States
Politics
Clean Power Plan
Climate change denial
(Manufactured controversy)
Intergovernmental Panel on Climate Change (IPCC)
March for Science
People's Climate March
United Nations Framework Convention on Climate Change (UNFCCC / FCCC)
Global climate regime
Potential effects and issues
General
Abrupt climate change
Anoxic event
Arctic dipole anomaly
Arctic haze
Arctic methane emissions
Climate change and agriculture
Climate change and ecosystems
Climate change and gender
Climate change and poverty
Drought
Economics of global warming
Effects on plant biodiversity
Effects on health
Effects on humans
Effects on marine mammals
Environmental migrant
Extinction risk from global warming
Fisheries and climate change
Forest dieback
Industry and society
Iris hypothesis
Megadrought
Ocean acidification
Ozone depletion
Physical impacts
Polar stratospheric cloud
Regime shift
Retreat of glaciers since 1850
Runaway climate change
Sea level rise
Season creep
Shutdown of thermohaline circulation
By country
Australia
South Asia
India
Nepal
United States
Mitigation
Kyoto Protocol
Clean Development Mechanism
Joint Implementation
Bali Road Map
2009 United Nations Climate Change Conference
Governmental
European Climate Change Programme
G8 Climate Change Roundtable
United Kingdom Climate Change Programme
Paris Agreement
United States withdrawal
Regional climate change initiatives in the United States
List of climate change initiatives
Emissions reduction
Carbon credit
Carbon-neutral fuel
Carbon offset
Carbon tax
Emissions trading
Fossil fuel phase-out
Carbon-free energy
Carbon capture and storage
Efficient energy use
Low-carbon economy
Nuclear power
Renewable energy
Personal
Individual action on climate change
Simple living
Other
Carbon dioxide removal
Carbon sink
Climate action
Climate Action Plan
Climate change mitigation scenarios
Climate engineering
Individual and political action on climate change
Reducing emissions from deforestation and forest degradation
up vote 0 down vote favorite My code workes perfectly for other queries, but for one query I am infinitely getting the same tweet. I can't understand what the problem is. API call: query='Allergic asthma OR Nonallergic asthma OR Occupational asthma OR EIB OR Exercise-induced bronchoconstriction OR Nocturnal asthma OR Cough-variant asthma' new_tweets = api.search(q=searchQuery, count=100, since_id=since_id, lang='en',tweet_mode='extended') if not new_tweets: print("No more tweets found") break for tweet in new_tweets: if True: print(jsonpickle.encode(tweet._json, unpicklable=False)) my_file = open('searchTweets.txt','a') my_file.write(jsonpickle.encode(tweet._json, unpicklable=False)+'n') my_file.close() else: continue Output in file: https://pastebin.com/JmRCsTeE These are the JSONs of the same Tweet. Other queries that work: Breast cancer OR Prostate cancer OR Colon cancer OR Lung cancer Type 2 dia