Archive for July, 2008

Hexafluoro-2-propanol

Friday, July 18th, 2008

1,1,1,3,3,3-Hexafluoro-2-propanol

IUPAC name
1,1,1,3,3,3-Hexafluoro
-2-propanol

Other names
Hexafluoroisopropanol,
Hexafluoroisopropyl alcohol,
HFIP

Identifiers

CAS number

RTECS number
UB6450000

SMILES

 
C(F)(F)(F)C(O)C(F)(F)(F)

Properties

Molecular formula
C3H2F6O

Molar mass
168.05 g/mol

Appearance
Colorless liquid

Density
1.596 g/ml, liquid

Melting point

−3.3°C (269 K)

Boiling point

58.2°C (331 K)

Solubility in water
Miscible, 100 g/100 ml (25°C)

Solubility in other solvents
Miscible

Viscosity
1.65 cP at 20°C

Hazards

MSDS
External MSDS

Main hazards
Corrosive (C)

NFPA 704


0
3
0
 

R-phrases
R20/22, R34, R41

S-phrases
S26, S36/37/39, S45

Flash point
>373°C

Related compounds

Related organofluorides
Hexafluoro-2-propanone

Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

Hexafluoroisopropanol, commonly abbreviated HFIP is the organic compound with the formula (CF3)2CHOH. This fluorinated alcohol finds use as solvent for polymer systems. It appears as a colorless, volatile liquid that is characterized by a strong, pungent odor. As a solvent hexafluoro-2-propanol exhibits strong hydrogen bonding properties enabling it to dissolve substances that serve as hydrogen-bond acceptors, such as amides and ethers. Hexafluoro-2-propanol is also a polar compound, transparent to UV light with high density, low viscosity and low refractive index.

Contents

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Production

Hexafluoro-2-propanol is prepared from hexafluoropropylene via hexafluoroacetone, which is reduced by catalytic hydrogenation or by hydride reagents.

(CF3)2CO + H2 → (CF3)2CHOH

Uses

Hexafluoro-2-propanol is a specialty solvent in organic synthesis It has also found use in biochemistry to solubilize peptides. Industrially hexafluoro-2-propanol is used as an intermediate for pharmaceuticals (anesthetics) and agrochemicals or as a solvent and cleaner in electronics.

Safety

Hexafluoro-2-propanol is a corrosive and is therefore destructive to tissues of the mucous membranes, upper respiratory tract, skin and eyes, resulting in burns or ulceration. Overexposure by inhalation may result in spasm, inflammation, chemical pneumonitis and larynx, bronchi or pulmonary edema. In case of contact with eyes corneal and conjunctival ulceration or blindness may result. Hexafluoro-2-propanol is not considered carcinogenic, but the effects of a chronic exposure are unknown.

References

Notes

  1. ^ Günter Siegemund, Werner Schwertfeger, Andrew Feiring, Bruce Smart, Fred Behr, Herward Vogel, Blaine McKusick “Fluorine Compounds, Organic” Ullmann’s Encyclopedia of Industrial Chemistry, John Wiley & Sons, 2007.
  2. ^ Review: Bégué, J.-P.; Bonnet-Delpon, D.; Crousse, B. Fluorinated Alcohols: A New Medium for Selective and Clean Reaction. Synthesis, 2004,(1), pp. 18-29.
  3. ^ Review: Shuklov, Ivan A. ; Dubrovina, Natalia V.; Börner, Armin Fluorinated Alcohols as Solvents, Cosolvents and Additives in Homogeneous Catalysis , Synthesis 2007, pp. 2925-2943
  4. ^ Apffel, A.; Chakel, J.A.; Fischer, S.; Lichtenwalter, K.; Hancock, W.S., Analysis of oligonucleotides by HPLC-electrospray ionization mass spectrometry. Anal. Chem, 1997,(69), pp. 1320-1325.

Sources

  • Radlick, Phillip C (1982-02-02). “Methods of synthesizing hexafluoroisopropanol from impure mixtures and synthesis of a fluoromethyl ether therefrom”. United States Patent 4,314,087. Retrieved on 2006-10-18.
  • Cheminal, Bernard; H. Mathais and M. Thomarat (1987-03-03). “Process for the synthesis of 2,2,2-trifluoroethanol and 1,1,1,3,3,3-hexafluoroisopropanol”. United States Patent 4,647,706. Retrieved on 2006-10-18.
  • “Hexafluoroisopropanol datasheet”. DuPont. Retrieved on 2006-10-18.

Retrieved from “http://en.wikipedia.org/wiki/Hexafluoro-2-propanol
Categories: Organofluorides | Halogenated solvents | Alcohols

Organoarsenic compound

Friday, July 18th, 2008

An organoarsenic compound in organic chemistry is an organic compound containing a chemical bond between arsenic and carbon. Many organoarsenic compounds are produced industrially with uses as insecticide, herbicide and fungicide. The parent compound is arsine. The oldest known representative (1760) is the foul smelling cacodyl. Despite their toxicity, organoarsenic biomolecules are known for example the As betaine pendant arsenobetaine first identified in the Western rock lobster . In other biomolecules arsenicum is bound to carbohydrates collectively known as arsenosugars (found especially in seaweeds). The cause for the accumulation of arsenic in some marine organisms and the biochemistry forming the compounds is still unknown. Although arsenic and most of its compounds are toxic for humans one of the first synthetic antiobiotics was Salvarsan.

Contents

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Relevant compounds

Some relevant organoarsenic compound are listed in he table below:

Organoarsenic
R

Molar mass
CAS number
Properties

10,10′-oxybis-10H-Phenoxarsine


502.2318
58-36-6

Triphenylarsine
Phenyl

306.23
603-32-7
Melting point 58-61 °C

Phenyldichloroarsine
phenyl, chlorine

222.93
696-28-6

Arsenobetaine

64436-13-1

Representative organoarsenic compounds

Other uses

The compounds 1,2-Bis(dimethylarsino)benzene and triphenylarsine are used as a chelating ligand. Trimethylarsine is used in Chemical vapor deposition in microelectronics. Thorin is an indicator for several metals.

Arsphenamine, Neosalvarsan and Atoxyl have at one time been used as drugs. Roxarsone is a food additive for chickens, improving weight gain.

See also

  • Arsole, the arsenicum endant of pyrrole.
  • Chemistry of other elements bonded to carbon

CH

He

CLi
CBe

CB
CC
CN
CO
CF
Ne

CNa
CMg

CAl
CSi
CP
CS
CCl
Ar

CK
CCa
CSc
CTi
CV
CCr
CMn
CFe
CCo
CNi
CCu
CZn
CGa
CGe
CAs
CSe
CBr
Kr

CRb
CSr
CY
CZr
CNb
CMo
CTc
CRu
CRh
CPd
CAg
CCd
CIn
CSn
CSb
CTe
CI
Xe

CCs
CBa

CHf
CTa
CW
CRe
COs
CIr
CPt
CAu
CHg
CTl
CPb
CBi
CPo
CAt
Rn

Fr
Ra

Rf
Db
Sg
Bh
Hs
Mt
Ds
Rg
Uub
Uut
Uuq
Uup
Uuh
Uus
Uuo

La
CCe
Pr
Nd
Pm
Sm
Eu
Gd
Tb
Dy
Ho
Er
Tm
Yb
Lu

Ac
Th
Pa
CU
Np
Pu
Am
Cm
Bk
Cf
Es
Fm
Md
No
Lr

Chemical bonds to carbon

Core organic chemistry
many uses in chemistry.

Academic research, but no widespread use
Bond unknown / not assessed.

References

  1. ^ Arsenic Species in Marine Samples Kevin A. Francesconi, and John S. Edmonds CROATICA CHEMICA ACTA CCACAA 71 (2) 343–359 (1998) “organoarsenic” Article link
  2. ^ John S. Edmonds, Kevin A. Francesconi, Jack R. Cannon, Colin L. Raston, Brian W. Skelton and Allan H. White (1977). “Isolation, crystal structure and synthesis of arsenobetaine, the arsenical constituent of the western rock lobster panulirus longipes cygnus George”. Tetrahedron Letters 18 (18): 1543-1546. doi:10.1016/S0040-4039(01)93098-9. 
  3. ^ www.sigmaaldrich.com

Retrieved from “http://en.wikipedia.org/wiki/Organoarsenic_compound
Categories: Arsenic compounds | Organic compounds

Solubility chart

Friday, July 18th, 2008

A blue solubility chart refers to a chart with a list of ions and how, when mixed with other ions, they can become precipitates or remain aqueous. The following chart shows the solubilities of various compounds at a pressure of 1 atm and at room temperature (approx. 293.15 K). Any box that reads “soluble” results in an aqueous product, while “slightly soluble” and “insoluble” markings means that there is a precipitate that will form (usually, this is a solid). Boxes marked “other” can mean that many different states of products can result. For more detailed information of the exact solubility of the compounds, see solubility table.

 
Bromide
Br−

Carbonate
CO32−

Chloride
Cl−
Hydroxide
OH−
Nitrate
NO3−
Oxide
O2−
Phosphate
PO43−
Sulfate
SO42−
Dichromate
Cr2O72−

Aluminium
Al3+
S
X
S
I
S
I
I
S
I

Ammonium

NH4+

S
S
S
S
S
X
S
S
S

Calcium
Ca2+
S
I
S
I
S
sS
I
sS
I

Copper(II)
Cu2+
S
X
S
I
S
I
I
S
I

Iron(II)
Fe2+
S
I
S
I
S
I
I
S
I

Iron(III)
Fe3+
S
X
S
I
S
I
I
sS
I

Magnesium
Mg2+
S
I
S
I
S
I
I
S
I

Potassium
K+
S
S
S
S
S
S
S
S
S

Silver
Ag+
I
I
I
X
S
I
I
sS
I

Sodium
Na+
S
S
S
S
S
S
S
S
S

Zinc
Zn2+
S
I
S
I
S
I
I
S
I

Key:

S
soluble

I
insoluble

sS
slightly soluble

X
other

See also

  • Solubility
  • Solubility table

External links

  • Additional Ionic Combinations

Retrieved from “http://en.wikipedia.org/wiki/Solubility_chart
Categories: Solutions

Ochratoxin

Friday, July 18th, 2008


Chemical structure of Ochratoxin A

Ochratoxin A, B, and C are mycotoxins produced by some Aspergillus species and Penicillium species, like A. ochraceus or P. viridicatum, with ochratoxin A as the most prevalent and relevant fungal toxin of this group.

Ochratoxin A is known to occur in commodities like cereals, coffee, dried fruit and red wine. It is considered a human carcinogen and is of special interest as it can be accumulated in the meat of animals. Thus meat and meat products can be contaminated with this toxin. Exposure to ochratoxins through diet can have can acute toxicity to mammalian kidneys, and may be carcinogenic.

See also

  • Ochratoxin A

External links

  • Detailed information about mycotoxins
  • Extensive information about mycotoxins and animal feed

Retrieved from “http://en.wikipedia.org/wiki/Ochratoxin
Categories: Mycotoxins

Concentrate

Friday, July 18th, 2008

For other uses, see Concentration (disambiguation).
For the 1958 screenplay, see Concentrate (screenplay).

A concentrate is a form of substance which has had the majority of its base component (in the case of a liquid: the solvent) removed. Typically this will be the removal of water from a solution or suspension such as the removal of water from fruit juice. One benefit of producing a concentrate is that of a reduction in weight and volume for transportation as the concentrate can be re-constituted at the time of usage by the addition of the solvent.

Development

Concentrated juice was developed during World War II to provide nourishment for the armed forces.

Bronson Cushing Skinner, developer of the first palatable orange juice concentrate, was born June 26, 1889. After graduating in 1911 from Stevens Institute of Technology, Bronson Skinner managed the Skinner Machinery Company, founded by his father. In 1929 he sold the company to Food Machinery Corporation, although he continued to manage it. In 1935 he left FMC and founded Citrus Concentrates, Inc. to manufacture concentrated orange juice.

To develop his concentrate, Skinner boiled water out of juice under a partial vacuum at a temperature so low, the flavor and vitamin content were not damaged. He adapted evaporators for this purpose. He began selling his concentrate to Great Britain between 1936 and 1941. When the United States entered World War II, the War Food Administration sent him $1.5 million to build a plant to supply concentrate for the Allies. The plant operated until August 27, 1945, 13 days after Japan surrendered. Bronson Cushing Skinner died August 4, 1981. His Great Floridian plaque is located at the Minute Maid plant, 427 San Christopher Drive, Dunedin, Florida.

Other

Concentrate can also be the residue valuable metal from which most of the waste rock has been removed. The residue metal becomes the raw material for smelting.


 This chemistry article is a stub. You can help Wikipedia by expanding it.

Retrieved from “http://en.wikipedia.org/wiki/Concentrate
Categories: Solutions | Chemical compounds | Chemistry stubs

Cytochalasin E

Friday, July 18th, 2008

Cytochalasin E, a member of the Cytochalasin group, is an inhibitor of actin polymerization in blood platelets. It inhibits angiogenesis and tumor growth. Unlike cytochalasin A and cytochalasin B, it does not inhibit glucose transport.

Because of its antiangiogenic effect, Cytochalasin E is mentioned as a potential drug for age-related macular degeneration, a kind of blindness caused by an abnormal proliferation of blood vessels in the eye.

References

  1. ^ eyesight.org

External links


 This biochemistry article is a stub. You can help Wikipedia by expanding it.

Retrieved from “http://en.wikipedia.org/wiki/Cytochalasin_E
Categories: Biochemistry stubs | Toxicology | Mycology | Mycotoxins

Benzalkonium chloride

Friday, July 18th, 2008

Benzalkonium chloride

Molar mass
(mixture)

CAS number

EINECS number
264-151-6

Properties

Density
0.98

Solubility in water
very soluble

Hazards

EU classification
C, N

NFPA 704


0
1
0
 

R-phrases
R21/22, R34, R50

S-phrases
S36/37/39, S45, S61

Flash point
250 °C

RTECS number
BO3150000

Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

Benzalkonium chloride, also known as alkyldimethylbenzylammonium chloride and ADBAC, is a mixture of alkylbenzyldimethylammonium chlorides of various even-numbered alkyl chain lengths. This product is a nitrogenous cationic surface-acting agent belonging to the quaternary ammonium group. It has three main categories of use; as a biocide, a cationic surfactant and phase transfer agent in the chemical industry.

Contents

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Properties

Benzalkonium chloride is readily soluble in ethanol, and acetone. Although dissolution in water is slow, aqueous solutions are easier to handle and are preferred. Solutions should be neutral to slightly alkaline, with colour ranging from clear to a pale yellow. Solutions foam profusely when shaken, have a bitter taste and a faint almond-like odour which is only detectable in concentrated solutions.

Availability

Standard concentrates are manufactured as 50% and 80% w/w solutions, and sold under trade names such as BC50, BC80, BAC50, BAC80, etc. The 50% solution is purely aqueous, while more concentrated solutions require incorporation of rheology modifiers (alcohols, polyethylene glycols, etc.) to prevent increases in viscosity or gel formation under low temperature conditions.

Applications

Applications are extremely wide ranging, from disinfectant formulations to microbial corrosion inhibition in the oilfield sector. It has been considered one of the safest synthetic biocides known and has a long history of efficacious use. It is currently used in human pharmaceuticals such as leave-on skin antiseptics, hygienic towelettes, and wet wipes. Ethanol-free benzalkonium solutions are often used for skin disinfection prior to withdrawing blood for blood alcohol content tests. Its use as a preservative in cosmetics such as eye and nasal drops attests to its general safety; however, there have been reports of allergy associated with continuous, long-term use in sensitive users, especially on mucous membranes.

Biological activity

The greatest biocidal activity is associated with the C12-C14 alkyl derivatives. The mechanism of bactericidal/microbicidal action is thought to be due to disruption of intermolecular interactions. This can cause dissociation of cellular membrane bilayers, which compromises cellular permeability controls and induces leakage of cellular contents. Other biomolecular complexes within the bacterial cell can also undergo dissociation. Enzymes, which finely control a plethora of respiratory and metabolic cellular activities, are particularly susceptible to deactivation. Critical intermolecular interactions and tertiary structures in such highly specific biochemical systems can be readily disrupted by cationic surfactants.

Benzalkonium chloride solutions are rapidly acting biocidal agents with a moderately long duration of action. They are active against bacteria and some viruses, fungi, and protozoa. Bacterial spores are considered to be resistant. Solutions are bacteriostatic or bactericidal according to their concentration. Gram-positive bacteria are generally more susceptible than Gram-negative. Activity is not greatly affected by pH, but increases substantially at higher temperatures and prolonged exposure times.

Newer formulations using benzalkonium blended with various quaternary ammonium derivatives can be used to extend the biocidal spectrum and enhance the efficacy of benzalkonium based disinfection products. This technique has been used to improve virucidal activity of quaternary ammonium-based formulations to healthcare infection hazards such as hepatitis, HIV, etc. Quaternary ammonium formulations are now the disinfectants of choice for hospitals. This is on account of user and patient safety even on contact with treated surfaces and the absence of harmful fumes. Benzalkonium solutions for hospital use tend to be neutral to alkaline, non-corrosive on metal surfaces, non-staining and safe to use on all washable surfaces.

The use of appropriate supporting excipients can also greatly improve efficacy and detergency, and prevent deactivation under use conditions. Formulation requires great care as Benzalkonium solutions can be readily inactivated in the presence of organic and inorganic contamination. Solutions are incompatible with soaps, and must not be mixed with anionic surfactants. Hard water salts can also reduce biocidal activity. As with any disinfectant, it is recommended that surfaces are free from visible dirt and interfering materials for maximal disinfection performance by quaternary ammonium products.

Although hazardous levels are not likely to be reached under normal use conditions, it is important to remember that benzalkonium and other detergents can pose a hazard to marine organisms. Quaternary ammonium disinfectants are effective at very low ppm levels, so it is important avoid excess in use. Responsible care ensures that we do not disrupt the fragile marine ecosystems that sustain us.

Safety

Please help improve this article or section by expanding it.
Further information might be found on the talk page or at requests for expansion. (February 2007)

Benzalkonium chloride is an allergen

Some products have been reformulated in light of this research, but it is still widely used in eyewashes, hand and face washes, mouthwashes, spermicidal creams, and in various other cleaners, sanitizers, and disinfectants. Manufacturers of over-the-counter artificial tears and eye washes became concerned about chemical sensitivity from long-term daily use and have in some products substituted EDTA as a preservative. Some have added “for sensitive eyes” to labeling. There has also been concern that long-term use of benzalkonium as a preservative in nose sprays may cause swelling of mucosa and lead to Rhinitis medicamentosa. Some manufacturers have put 3-day limits on safe use of such nose sprays.

A disinfectant containing benzalkonium chloride and the related compound didecyl-dimethyl ammonium chloride (DDAC) has been identified as the most probable cause of birth defects and fertility problems in caged mice.

References

  1. ^ a b c Record of Quaternary ammonium compounds, benzyl-C8–18-alkyldimethyl, chlorides in the European chemical Substances Information System ESIS
  2. ^ US EPA: Reregistration Eligibility Decision for Alkyl Dimethyl Benzyl Ammonium Chloride (ADBAC)
  3. ^ quatchem.co.uk
  4. ^ Park HJ, Kang HA, Lee JY, Kim HO (2000). “Allergic contact dermatitis from benzalkonium chloride in an antifungal solution”. Contact Derm. 42 (5): 306–7. PMID 10789868. 
  5. ^ Liu H, Routley I, Teichmann KD (2001). “Toxic endothelial cell destruction from intraocular benzalkonium chloride”. J Cataract Refract Surg 27 (11): 1746–50. doi:10.1016/S0886-3350(01)01067-7. PMID 11709246. 
  6. ^ Chiambaretta F, Pouliquen P, Rigal D (1997). “” (in French). J Fr Ophtalmol 20 (1): 8–16. PMID 9099278. 
  7. ^ Wong DA, Watson AB (2001). “Allergic contact dermatitis due to benzalkonium chloride in plaster of Paris”. Australas. J. Dermatol. 42 (1): 33–5. doi:10.1046/j.1440-0960.2001.00469.x. PMID 11233718. 
  8. ^ Kanerva L, Jolanki R, Estlander T (2000). “Occupational allergic contact dermatitis from benzalkonium chloride”. Contact Derm. 42 (6): 357–8. PMID 10871106. 
  9. ^ Oiso N, Fukai K, Ishii M (2005). “Irritant contact dermatitis from benzalkonium chloride in shampoo”. Contact Derm. 52 (1): 54. doi:10.1111/j.0105-1873.2005.0483j.x. PMID 15701139. 
  10. ^ Basketter DA, Marriott M, Gilmour NJ, White IR (2004). “Strong irritants masquerading as skin allergens: the case of benzalkonium chloride”. Contact Derm. 50 (4): 213–7. doi:10.1111/j.0105-1873.2004.00331.x. PMID 15186375. 
  11. ^ Graf P (2001). “Benzalkonium chloride as a preservative in nasal solutions: re-examining the data”. Respir Med 95 (9): 728–33. doi:10.1053/rmed.2001.1127. PMID 11575893. 
  12. ^ Marple B, Roland P, Benninger M (2004). “Safety review of benzalkonium chloride used as a preservative in intranasal solutions: an overview of conflicting data and opinions”. Otolaryngol Head Neck Surg 130 (1): 131–41. doi:10.1016/j.otohns.2003.07.005. PMID 14726922. 
  13. ^ Nature magazine: Lab disinfectant harms mouse fertility

Further reading

  • Bernstein IL: Is the use of benzalkonium chloride as a preservative for nasal formulations a safety concern? J Allergy Clin Immunol 2000 Jan; 105(1 Pt 1): 39-44.
  • Graf P: Adverse effects of benzalkonium chloride on the nasal mucosa: allergic rhinitis and rhinitis medicamentosa. Clin Ther 1999 Oct; 21(10): 1749-55.
  • Graf P, Hallen H, Juto JE: Benzalkonium chloride in a decongestant nasal spray aggravates rhinitis medicamentosa in healthy volunteers. Clin Exp Allergy 1995 May; 25(5): 395-400.

External links

  • Nasal Saline Sprays - The Additives May Be the Problem
  • Use of benzalkonium in ocular preparations and eye drops, cytotoxic, allergenic and other consequences of benzalkonium use
  • Chemical Database

References

Retrieved from “http://en.wikipedia.org/wiki/Benzalkonium_chloride
Categories: Chlorides | Quaternary ammonium compounds | Surfactants | Antiseptics | DisinfectantsHidden categories: Articles to be expanded since February 2007 | All articles to be expanded

Magnesium

Friday, July 18th, 2008

12
sodium ← magnesium → aluminium

Be

Mg

Ca

Periodic table - Extended periodic table

General

Name, symbol, number
magnesium, Mg, 12

Chemical series
alkaline earth metals

Group, period, block
2, 3, s

Appearance
silvery white solid at room temp

Standard atomic weight
24.3050(6) g·mol−1

Electron configuration
3s2

Electrons per shell
2, 8, 2

Physical properties

Phase
solid

Density (near r.t.)
1.738 g·cm−3

Liquid density at m.p.
1.584 g·cm−3

Melting point
923 K
(650 °C, 1202 °F)

Boiling point
1363 K
(1091 °C, 1994 °F)

Heat of fusion
8.48 kJ·mol−1

Heat of vaporization
128 kJ·mol−1

Specific heat capacity
(25 °C) 24.869 J·mol−1·K−1

Vapor pressure

P/Pa
1
10
100
1 k
10 k
100 k

at T/K
701
773
861
971
1132
1361

Atomic properties

Crystal structure
hexagonal

Oxidation states
2, 1
(strongly basic oxide)

Electronegativity
1.31 (Pauling scale)

Ionization energies
(more)
1st: 737.7 kJ·mol−1

2nd: 1450.7 kJ·mol−1

3rd: 7732.7 kJ·mol−1

Atomic radius
150 pm

Atomic radius (calc.)
145 pm

Covalent radius
130 pm

Van der Waals radius
173 pm

Miscellaneous

Magnetic ordering
paramagnetic

Electrical resistivity
(20 °C) 43.9 nΩ·m

Thermal conductivity
(300 K) 156 W·m−1·K−1

Thermal expansion
(25 °C) 24.8 µm·m−1·K−1

Speed of sound (thin rod)
(r.t.) (annealed)
4940 m·s−1

Young’s modulus
45 GPa

Shear modulus
17 GPa

Bulk modulus
45 GPa

Poisson ratio
0.29

Mohs hardness
2.5

Brinell hardness
260 MPa

CAS registry number
7439-95-4

Selected isotopes

Main article: Isotopes of magnesium

iso
NA
half-life
DM
DE (MeV)
DP

24Mg
78.99%
24Mg is stable with 12 neutrons

25Mg
10%
25Mg is stable with 13 neutrons

26Mg
11.01%
26Mg is stable with 14 neutrons

References

This box: view • talk • edit

Magnesium (pronounced /mægˈniːziəm/) is a chemical element with the symbol Mg, the atomic number 12, and an atomic mass of 24.31. Magnesium is the ninth most abundant element in the universe by mass. Magnesium ions are essential to all living cells, and is the 11th most abundant element by mass in the human body. The free element (metal) is not found in nature. Once produced from magnesium salts, this alkaline earth metal is now mainly obtained by electrolysis of brine and is used as an alloying agent to make aluminium-magnesium alloys, sometimes called “magnalium” or “magnelium”.

Contents

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Notable characteristics

Elemental magnesium is a fairly strong, silvery-white, light-weight metal (two thirds the density of aluminium). It tarnishes slightly when exposed to air, although unlike the alkaline metals, storage in an oxygen-free environment is unnecessary because magnesium is protected by a thin layer of oxide which is fairly impermeable and hard to remove. Like its lower periodic table group neighbor calcium, magnesium reacts with water at room temperature, though it reacts much more slowly than calcium. When it is submerged in water, hydrogen bubbles will almost unnoticeably begin to form on the surface of the metal, though if powdered it will react much more rapidly. Magnesium also reacts with hydrochloric acid (HCl) and produces heat and hydrogen when added to it. The magnesium will begin to bubble and become too hot to touch comfortably. The reaction will occur faster with higher temperatures (see precautions).

Magnesium is a highly flammable metal, but while it is easy to ignite when powdered or shaved into thin strips, it is difficult to ignite in mass or bulk. Once ignited, it is difficult to extinguish, being able to burn in both nitrogen (forming magnesium nitride), and carbon dioxide (forming magnesium oxide and carbon). On burning in air, magnesium produces a brilliant white light. Thus magnesium powder (flash powder) was used as a source of illumination in the early days of photography. Later, magnesium ribbon was used in electrically ignited flash bulbs. Magnesium powder is used in the manufacture of fireworks and marine flares where a brilliant white light is required.

Magnesium compounds are typically white crystals. Most are soluble in water, providing the sour-tasting magnesium ion Mg2+. Small amounts of dissolved magnesium ion contributes to the tartness and taste of natural waters. Magnesium ion in large amounts is an ionic laxative, and magnesium sulfate (Epsom salts) is sometimes used for this purpose. So-called “milk of magnesia” is a water suspension of one of the few insoluble magnesium compounds, magnesium hydroxide. The undissolved particles give rise to its appearance and name. Milk of magnesia is a mild base commonly used as an antacid.

Applications

As the metal

Magnesium is the third most commonly used structural metal, following steel and aluminium.

Magnesium compounds, primarily magnesium oxide, are used mainly as refractory material in furnace linings for producing iron, steel, nonferrous metals, glass and cement. Magnesium oxide and other compounds also are used in agricultural, chemical and construction industries. As a metal, this element’s principal use is as an alloying additive to aluminium with these aluminium-magnesium alloys being used mainly for beverage cans.

Magnesium, in its purest form, can be compared with aluminium, and is strong and light, so it is used in several high volume part manufacturing applications, including automotive and truck components. Specialty, high-grade car wheels of magnesium alloy are called “mag wheels”. In 1957 a Corvette SS, designed for racing, was constructed with magnesium body panels. Porsche’s all-out quest to decrease the weight of their racecars led to the use of magnesium frames in the famous 917/053 which won Le Mans in 1971, and still holds the absolute distance record. The 917/30 Can-Am car also featured a magnesium spaceframe, helping it to make the most of its prodigious 1100-1500hp. Volkswagen has used magnesium in its engine components for many years. For a long time, Porsche used magnesium alloy for its engine blocks due to the weight advantage. There is renewed interest in magnesium engine blocks, as featured in the 2006 BMW 325i and 330i models. The BMW engine uses an aluminium alloy insert for the cylinder walls and cooling jackets surrounded by a high temperature magnesium alloy AJ62A. The application of magnesium AE44 alloy in the 2006 Corvette Z06 engine cradle has advanced the technology of designing robust automotive parts in magnesium. Both of these alloys are recent developments in high temperature low creep magnesium alloys. The general strategy for such alloys is to form intermetallic precipitates at the grain boundaries, for example by adding mischmetal or calcium. New alloy development and lower costs, which are becoming competitive to aluminium, will further the number of automotive applications.


Products made of magnesium: firestarter and shavings, sharpener, magnesium ribbon

The second application field of magnesium is electronic devices. Due to low weight, good mechanical and electrical properties, magnesium is widely used for manufacturing of mobile phones, laptop computers, cameras, and other electronic components. Magnesium is even used to make some higher end yo-yos, such as the Duncan Freehand Mg.

Historically, magnesium was one of the main aerospace construction metals and was used for German military aircraft as early as World War I and extensively for German aircraft in World War II. The Germans coined the name ‘Elektron’ for magnesium alloy which is still used today. Due to perceived hazards with magnesium parts in the event of fire, the application of magnesium in the commercial aerospace industry was generally restricted to engine related components. Currently the use of magnesium alloys in aerospace is increasing, mostly driven by the increasing importance of fuel economy and the need to reduce weight. The development and testing of new magnesium alloys notably Elektron 21 which has successfully undergone extensive aerospace testing for suitability in both engine, internal and airframe components. European Community runs three R&D magnesium projects in Aerospace priority of Six Framework Program.


Magnesium firestarter (in left hand), used with a pocket knife and flint to create sparks which ignite the shavings

  • Incendiary use: Magnesium is flammable, burning at a temperature of approximately 2500 K (2200 °C, 4000 °F), and the autoignition temperature of magnesium is approximately 744 K (473 °C, 883 °F) in air. The extremely high temperature at which magnesium burns makes it a handy tool for starting emergency fires during outdoor recreation. Other related uses include flashlight photography, flares, pyrotechnics, fireworks sparklers, and incendiary bombs.

Other uses include:

  • Removal of sulfur from iron and steel.
  • Production of titanium
  • Photoengraved plates in the printing industry.
  • Combined in alloys, this metal is essential for airplane and missile construction.
  • When used as an alloying agent, this metal improves the mechanical, fabrication and welding characteristics of aluminium.
  • Additive agent for conventional propellants and used in producing nodular graphite in cast iron.
  • Reducing agent for the production of pure uranium and other metals from their salts.
  • Magnesium turnings or ribbon are used to prepare Grignard reagents, which are useful in organic synthesis
  • Easily reacting with water, it can serve as a desiccant

In magnesium compounds

  • The magnesium ion is necessary for all life (see magnesium in biological systems), so magnesium salts are an additive for foods, fertilizers (Mg is a component of chlorophyll), and culture media.
  • Magnesium hydroxide is used in milk of magnesia, its chloride, oxide, gluconate and citrate used as oral magnesium supplements, and its sulfate (Epsom salts) for various purposes in medicine, and elsewhere (see the article for more). Oral magnesium supplements have been claimed to be therapeutic for some individuals who suffer from Restless Leg Syndrome (RLS).
  • Magnesium borate, magnesium salicylate and magnesium sulfate are used as antiseptics.
  • Magnesium bromide is used as a mild sedative (this action is due to the bromide, not the magnesium).
  • Dead-burned magnesite is used for refractory purposes such as brick and liners in furnaces and converters.
  • Magnesium carbonate (MgCO3) powder is also used by athletes, such as gymnasts and weightlifters, to improve the grip on objects – the apparatus or lifting bar.
  • Magnesium stearate is a slightly flammable white powder with lubricative properties. In pharmaceutical technology it is used in the manufacturing of tablets, to prevent the tablets from sticking to the equipment during the tablet compression process (i.e., when the tablet’s substance is pressed into tablet form).
  • Magnesium sulfite is used in the manufacture of paper (sulfite process).
  • Magnesium phosphate is used to fireproof wood for construction.
  • Magnesium hexafluorosilicate is used in mothproofing of textiles.

History

The name originates from the Greek word for a district in Thessaly called Magnesia. It is related to magnetite and manganese, which also originated from this area, and required differentiation as separate substances. See manganese for this history.

Magnesium is the seventh most abundant element in the earth’s crust by mass and eighth by molarity. It is found in large deposits of magnesite, dolomite, and other minerals, and in mineral waters, where magnesium ion is soluble. In 1618 a farmer at Epsom in England attempted to give his cows water from a well. They refused to drink because of the water’s bitter taste. However the farmer noticed that the water seemed to heal scratches and rashes. The fame of Epsom salts spread. Eventually they were recognized to be hydrated magnesium sulfate, MgSO4.

The metal itself was first produced in England by Sir Humphry Davy in 1808 using electrolysis of a mixture of magnesia and HgO. A. A. B. Bussy prepared it in coherent form in 1831. Davy’s first suggestion for a name was magnium, but the name magnesium is now used.

Sources

Although magnesium is found in over 60 minerals, only dolomite, magnesite, brucite, carnallite, talc, and olivine are of commercial importance.

In the United States this metal is principally obtained by electrolysis of fused magnesium chloride from brines, wells, and sea water:

cathode: Mg2+ + 2 e- → Mg
anode: 2 Cl- → Cl2 (gas) + 2 e-


Vapor-deposited magnesium crystals from the Pidgeon process

The United States has traditionally been the major world supplier of this metal, supplying 45% of world production even as recently as 1995. Today, the US market share is at 7%, with a single domestic producer left, US Magnesium, a company born from now-defunct Magcorp. As of 2005 China has taken over as the dominant supplier, pegged at 60% world market share, which increased from 4% in 1995. Unlike the above described electrolytic process, China is almost completely reliant on a different method of obtaining the metal from its ores, the silicothermic Pidgeon process (the reduction of the oxide at high temperatures with silicon).

Magnesium from sea water

The Mg2+ cation is the second most abundant cation in seawater (occurring at about 12% of the mass of sodium there), which makes seawater and sea-salt an attractive commercial source of Mg. To extract the magnesium, calcium carbonate is added to sea water to form magnesium carbonate precipitate.

MgCl2 + CaCO3 → MgCO3 + CaCl2

Magnesium carbonate is insoluble in water so it can be filtered out, and reacted with hydrochloric acid to obtain concentrated magnesium chloride.

MgCO3 + 2HCl → MgCl2 + CO2 + H2O

From magnesium chloride, electrolysis produces magnesium.

See also: Category:Magnesium minerals

Biological role

Main article: Magnesium in biology

Magnesium ions are essential to the basic nucleic acid chemistry of life, and thus are essential to all cells of all known living organisms. Plants have an additional use for magnesium in that chlorophylls are magnesium-centered porphyrins. Many enzymes require the presence of magnesium ions for their catalytic action, especially enzymes utilizing ATP, or those which use other nucleotides to synthesize DNA and RNA. Magnesium deficiency in plants causes late-season yellowing between leaf veins, especially in older leaves, and can be corrected by applying epsom salts (which is rapidly leached), or else crushed dolomitic limestone to the soil.


Food sources of magnesium

Magnesium is a vital component of a healthy human diet and deficiency has been implicated in a number of human diseases. Magnesium is readily available in many common foods, but according to the Community Nutrition Research Group (CNRG), only 32% of Americans met the RDA-DRI for magnesium.

Isotopes

Magnesium has three stable isotopes: 24Mg, 25Mg, 26Mg. All are present in significant amounts (see table of isotopes above). About 79% of Mg is 24Mg. The isotope 28Mg is radioactive and in the 1950s to 1970s was made commercially by several nuclear power plants for use in scientific experiments. This isotope has a relatively short half-life (21 hours) and so its use was limited by shipping times.

26Mg has found application in isotopic geology, similar to that of aluminium. 26Mg is a radiogenic daughter product of 26Al, which has a half-life of 717,000 years. Large enrichments of stable 26Mg have been observed in the Ca-Al-rich inclusions of some carbonaceous chondrite meteorites. The anomalous abundance of 26Mg is attributed to the decay of its parent 26Al in the inclusions. Therefore, the meteorite must have formed in the solar nebula before the 26Al had decayed. Hence, these fragments are among the oldest objects in the solar system and have preserved information about its early history.

It is conventional to plot 26Mg/24Mg against an Al/Mg ratio. In an isochron dating plot, the Al/Mg ratio plotted is27Al/24Mg. The slope of the isochron has no age significance, but indicates the initial 26Al/27Al ratio in the sample at the time when the systems were separated from a common reservoir.

Precautions


The magnesium-bodied Honda RA302 of Jo Schlesser crashes and burns during the 1968 French Grand Prix. Schlesser was killed

Magnesium metal and alloys are highly flammable in their pure form when molten, as a powder, or in ribbon form. Burning or molten magnesium metal reacts violently with water. Magnesium powder is an explosive hazard. One should wear safety glasses while working with magnesium, and if burning it, these should include a heavy U.V. filter, similar to welding eye protection. The bright white light (including ultraviolet) produced by burning magnesium can permanently damage the retinas of the eyes, similar to welding arc burns.

Water should not be used to extinguish magnesium fires, because it can produce hydrogen which will feed the fire, according to the reaction:

Mg (s) + 2 H2O (g) → Mg(OH)2 (s) + H2 (g)
or in words:
Magnesium (solid) + steam → Magnesium hydroxide (solid) + Hydrogen (gas)

Carbon dioxide fire extinguishers should not be used either, because magnesium can burn in carbon dioxide (forming magnesium oxide, MgO, and carbon). A Class D dry chemical fire extinguisher should be used if available, or else the fire should be covered with sand or magnesium foundry flux. An easy way to put out small metal fires is to place a polyethylene bag filled with dry sand on top of the fire. The heat of the fire will melt the bag and the sand will flow out onto the fire.

See also

  • Magnesium minerals
  • Magnesium compounds

References

  1. ^ a b . “Abundance and form of the most abundant elements in Earth’s continental crust” (PDF). Retrieved on 2008-02-15.
  2. ^ Alan A. Luo and Bob R. Powell (2001). “Tensile and Compressive Creep of Magnesium-Aluminum-Calcium Based Alloys” (PDF). Materials & Processes Laboratory, General Motors Research & Development Center. Retrieved on 2007-08-21.
  3. ^ Vardi, Nathan (February 22, 2007). “Man With Many Enemies”. Forbes.com. Retrieved on 2006-06-26.
  4. ^ http://www.ars.usda.gov/is/AR/archive/may04/energy0504.htm?pf=1 Last paragraph
  5. ^ Magnesium
  6. ^ Kontani M, Hara A, Ohta S, Ikeda T (2005). “Hypermagnesemia induced by massive cathartic ingestion in an elderly woman without pre-existing renal dysfunction”. Intern. Med. 44 (5): 448–52. doi:10.2169/internalmedicine.44.448. PMID 15942092. 
  7. ^ “Science Safety: Chapter 8″. Government of Manitoba. Retrieved on 2007-08-21.
  8. ^ “Chemistry : Periodic Table : magnesium : chemical reaction data”. webelements.com. Retrieved on 2006-06-26.
  9. ^ “Demo Lab: Reaction Of Magnesium Metal With Carbon Dioxide”. Retrieved on 2006-06-26.

External links

Wikimedia Commons has media related to:
Magnesium

Look up magnesium in
Wiktionary, the free dictionary.

  • WebElements.com – Magnesium
  • Online Resource for industry professionals - Magnesium.com
  • The Magnesium Website – Includes full text papers and textbook chapters by leading magnesium authorities Mildred Seelig, Jean Durlach, Burton M. Altura and Bella T. Altura. Links to over 300 articles discussing magnesium and magnesium deficiency.
  • Magnesium in Health - Mg12.info

v • d • e

Periodic table

H
 
He

Li
Be
 
B
C
N
O
F
Ne

Na
Mg
 
Al
Si
P
S
Cl
Ar

K
Ca
 
Sc
Ti
V
Cr
Mn
Fe
Co
Ni
Cu
Zn
Ga
Ge
As
Se
Br
Kr

Rb
Sr
 
Y
Zr
Nb
Mo
Tc
Ru
Rh
Pd
Ag
Cd
In
Sn
Sb
Te
I
Xe

Cs
Ba
La
Ce
Pr
Nd
Pm
Sm
Eu
Gd
Tb
Dy
Ho
Er
Tm
Yb
Lu
Hf
Ta
W
Re
Os
Ir
Pt
Au
Hg
Tl
Pb
Bi
Po
At
Rn

Fr
Ra
Ac
Th
Pa
U
Np
Pu
Am
Cm
Bk
Cf
Es
Fm
Md
No
Lr
Rf
Db
Sg
Bh
Hs
Mt
Ds
Rg
Uub
Uut
Uuq
Uup
Uuh
Uus
Uuo

 

Alkali metals
Alkaline earth metals
Lanthanides
Actinides
Transition elements
Other metals
Metalloids
Other nonmetals
Halogens
Noble gases

Retrieved from “http://en.wikipedia.org/wiki/Magnesium
Categories: Chemical elements | Alkaline earth metals | Dietary minerals | Food additives | Pyrotechnic fuels | Magnesium | DesiccantsHidden categories: All articles with unsourced statements | Articles with unsourced statements since February 2008

Gear oil

Friday, July 18th, 2008

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Please help improve this article by adding citations to reliable sources. Unverifiable material may be challenged and removed.

Gear oil is a motor oil made specifically for transmissions, transfer cases, and differentials in automobiles, trucks, and other machinery. It is of a higher viscosity to better protect the gears and usually is associated with a strong sulfur smell. The high viscosity ensures transfer of lubricant throughout the gear train. This is necessary since the devices needing this heavy oil do not have pumps for transferring the oil with only a portion of the lowermost gears bathed in an oil sump. This heavy oil can create viscous drag leading to inefficiencies in vehicle operation. Some modern automatic transaxles (integrated transmission and differential) do not use a heavy oil at all but lubricate with the lower viscosity hydraulic fluid, which is available at pressure within the automatic transmission.

Most lubricants for manual gearboxes and differentials are hypoid gear oils. These contain extreme pressure (EP) additives and antiwear additives to cope with the sliding action of hypoid bevel gears.

API ratings

Gear oils are classified by the American Petroleum Institute using GL ratings. For example, most modern gearboxes require a GL4 oil, and separate differentials (where fitted) require a GL5 oil. It is important that purchasers check the oil against the vehicle manufacturer’s specification to ensure it does not contain any aggressive chemicals that may attack gear components, such as the phosphor bronze used in many Japanese boxes.

API viscosity ratings for gear oils are not directly comparable with those for motor oil, and they are thinner than the figures suggest. For example, many modern gearboxes use a 75W90 gear oil, which is actually of equivalent viscosity to a 10W40 motor oil. Multigrade gear oils are becoming more common; while gear oil does not reach the temperatures of motor oil, it does warm up appreciably as the car is driven, due mostly to shear friction (with a small amount of heat conduction through the bellhousing from the engine block).

Fully synthetic gear oils are also used in many vehicles, and have a greater resistance to shear breakdown than mineral oils. They can improve the shifting performance of “difficult” gearboxes, where the excessive slipperiness of some mineral oils can impede synchromesh action.

API classification subdivides all transmission oils into 6 classes:

  • API GL-1, oils for light conditions. They consist of base oils without additives. Sometimes they contain small amounts of antioxidizing additives, corrosion inhibitors, depresants and antifoam additives. API GL-1 oils are designed for spiral-bevel, worm gears and manual transmissions without synchronizers in trucks and farming machines.
  • API GL-2, oils for moderate conditions. They contain antiwear additives and are designed for worm gears. Recommended for proper lubrication of tractor and farming machine transmissions.
  • API GL-3, oils for moderate conditions. Contain up to 2.7% antiwear additives. Designed for lubricating bevel and other gears of truck transmissions. Not recommended for hypoid gears.
  • API GL-4, oils for various conditions - light to heavy. They contain up to 4.0% effective antiscuffing additives. Designed for bevel and hypoid gears which have small displacement of axes, the gearboxes of trucks, and axle units. Recommended for non-synchronized gearboxes of US trucks, tractors and buses and for main and other gears of all vehicles. These oils are basic for synchronized gearboxes, especially in Europe.
  • API GL-5, oils for severe conditions. They contain up to 6.5% effective antiscuffing additives. The general application of oils in this class are for hypoid gears having significant displacement of axes. They are recommended as universal oils to all other units of mechanical transmission (except gearboxes). Oils in this class, which have special approval of vehicle manufacturers, can be used in synchronized manual gearboxes only. API GL-5 oils can be used in limited slip differentials if they correspond to the requirements of specification MIL-L-2105D or ZF TE-ML-05. In this case the designation of class will be another, for example API GL-5+ or API GL-5 LS.
  • API GL-6, oils for very heavy conditions (high speeds of sliding and significant shock loadings). They contain up to 10% high performance antiscuffing additives. They are designed for hypoid gears with significant displacement of axes. Class API GL-6 is not applied any more as it is considered that class API GL-5 well enough meets the most severe requirements.

Retrieved from “http://en.wikipedia.org/wiki/Gear_oil
Categories: Lubricants | Gears | Oils | Automotive chemicalsHidden categories: Articles lacking sources from April 2008 | All articles lacking sources

Motorcycle oil

Friday, July 18th, 2008


Yamahas own-brand of motorcyle engine oil

This article needs additional citations for verification.
Please help improve this article by adding reliable references. Unsourced material may be challenged and removed. (December 2007)

Motorcycle Oils are a range of lubricants, including engine oils, which are specifically developed for the unique needs of motorcycles. They may also be used in quad-bikes.

Contents

//

Motorcycle Engine Oil

The vast majority of modern motorcycles use the same oil to lubricate the engine, transmission, and (with the exception of bikes with dry clutches, such as Ducatis) the clutch. Normal, “car-derived” motor oils are designed just for engines, but was historically suitable in motorcycles. However, some of the latest American Petroleum Institute, or API specifications are completely unsuitable for motorcycles with wet clutches. Representative organisations of motorcycle manufactures, particularly Japanese Automotive Standards Organization, or JASO, work with lubricants manufacturers to create “motorcycle-specific” standards for oils, and the relevant oil companies then develop and test oils which are specifically made for motorcycles.

Transmission lubrication

Motorcycle transmissions, just like all gear-based automotive transmissions can quickly degrade a multi-viscosity, or multi-grade engine oil. Conventional car and truck transmission oils have specific EP, and other specialised anti-wear additives, but these EP additives are not suitable for the combined application of lubricating the engine and transmission with the same oil, as is the norm in motorcycles.

Multi-viscosity car-based engine oils contain viscosity increaser chemicals known as VIs that keep the oil from becoming too thin at high temperatures. The VIs are large chemicals that can be sheared between the cogs of a motorcycle transmission. A motorcycle transmission can degrade a 10W40 oil into a 10W30 oil in around a thousand miles.

Single weight oils do not have VIs and aren’t susceptible to degradation in the transmission. However, single weight oils do not work well in cold starts. The best solution is to use a synthetic oil. Synthetic oil can have a high viscosity range with minimal VIs.

Clutch lubrication


Energy Conserving (EC) oil can cause wet clutches to slip.

With the exception of most Ducatis, most motorcycles have a “wet clutch”. In a wet clutch, the clutch plates are immersed in oil. Some oils make the friction plates in the clutch slippery so that the clutch doesn’t engage properly when shifting gears, or the clutch slips when the engine exceeds a certain torque. Some oils contain friction reducing chemicals. These oils are unsuitable for motorcycles. All 5W20 and 10W30 non-motorcycle engine oils have these friction reducers. Oils with an operating weight of 40 or greater are not required to have friction reducers. These oils are unlikely to cause clutch slippage.

A properly specified motorcycle oil will still allow for the appropriate lubrication and cooling of a motorcycle clutch, whilst maintaining 100% of the drive to be transmitted by the clutch, even under arduous operating conditions.

Cooling properties

Some motorcycles are air cooled, and rely soley on the oil to carry heat away from the engine. Synthetic oils are much better than conventional oils at cooling.

Some popular major producers of motor oil

  • American Refining Group, Inc.
  • Castrol
  • Fuchs Silkolene
  • Mobil
  • Motul
  • Pentosin
  • Royal Dutch Shell

WikiHow - Change your own oil

  • WikiHow - the WikiHow Guide on how to change your Motorcycle Engine Oil & Filter

References

1. All about Oil
2. The Motor Oil Bible eBook
3. Motorcycle Consumer News

Retrieved from “http://en.wikipedia.org/wiki/Motorcycle_oil
Categories: Motorcycling | Petroleum products | Lubricants | Motor oils | Automotive chemicalsHidden categories: Articles needing additional references from December 2007 | All articles with unsourced statements | Articles with unsourced statements since May 2008 | Articles with unsourced statements since April 2008 | Articles with unsourced statements since December 2007