Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/TATB> ?p ?o }
- TATB abstract "TATB, triaminotrinitrobenzene or 2,4,6-triamino-1,3,5- trinitrobenzene is an aromatic explosive, based on the basic six-carbon benzene ring structure with three nitro functional groups (NO2) and three amine (NH2) groups attached, alternating around the ring.TATB is a powerful explosive (somewhat less powerful than RDX, but more than TNT), but it is extremely insensitive to shock, vibration, fire, or impact. Because it is so difficult to detonate by accident, even under severe conditions, it has become preferred for applications where extreme safety is required, such as the explosives used in nuclear weapons, where accidental detonation during an airplane crash or rocket misfiring would present extreme dangers. All British nuclear warheads, except those where weight is a factor, are believed to use TATB-based explosives for main explosive charges. According to David Albright, South Africa's nuclear weapons used TATB to increase their safety.TATB is normally used as the explosive ingredient in plastic bonded explosive compositions, such as PBX-9502, LX-17-0, and PBX-9503 (with 15% HMX). These formulations are described as Insensitive High Explosives or IHE in nuclear weapons literature.Though it could theoretically be mixed with other explosive compounds in castable mixtures or other use forms, the applications for such forms would be unclear since they would largely undo the insensitivity of pure TATB.TATB's chemical structure is somewhat similar to the powerful experimental insensitive high explosive FOX-7.".
- TATB iupacName "1,3,5-triamino-2,4,6-trinitrobenzene".
- TATB thumbnail Triaminotrinitrobenzene.png?width=300.
- TATB wikiPageID "2455122".
- TATB wikiPageLength "5656".
- TATB wikiPageOutDegree "44".
- TATB wikiPageRevisionID "670400673".
- TATB wikiPageWikiLink 1,1,1-trimethylhydrazinium_iodide.
- TATB wikiPageWikiLink 1,3,5-Trichlorobenzene.
- TATB wikiPageWikiLink 1,3,5-trichloro-2,4,6-trinitrobenzene.
- TATB wikiPageWikiLink 1,3,5-trichlorobenzene.
- TATB wikiPageWikiLink 2,4,6-Trinitroaniline.
- TATB wikiPageWikiLink Amination.
- TATB wikiPageWikiLink Amine.
- TATB wikiPageWikiLink Ammonium_chloride.
- TATB wikiPageWikiLink Aromaticity.
- TATB wikiPageWikiLink Benzene.
- TATB wikiPageWikiLink Casting_(metalworking).
- TATB wikiPageWikiLink Category:Anilines.
- TATB wikiPageWikiLink Category:Explosive_chemicals.
- TATB wikiPageWikiLink Category:Nitrobenzenes.
- TATB wikiPageWikiLink David_Albright.
- TATB wikiPageWikiLink Detonation.
- TATB wikiPageWikiLink Dunnite.
- TATB wikiPageWikiLink Explosive_D.
- TATB wikiPageWikiLink Explosives_safety.
- TATB wikiPageWikiLink FOX-7.
- TATB wikiPageWikiLink Fire.
- TATB wikiPageWikiLink Gram.
- TATB wikiPageWikiLink HMX.
- TATB wikiPageWikiLink Impact_(mechanics).
- TATB wikiPageWikiLink Insensitive_High_Explosives.
- TATB wikiPageWikiLink Insensitive_munition.
- TATB wikiPageWikiLink Methyl_iodide.
- TATB wikiPageWikiLink Metre_per_second.
- TATB wikiPageWikiLink Nitration.
- TATB wikiPageWikiLink Nitro_compound.
- TATB wikiPageWikiLink Nitro_functional_group.
- TATB wikiPageWikiLink Nuclear_warhead.
- TATB wikiPageWikiLink Nuclear_weapon.
- TATB wikiPageWikiLink Phloroglucinol.
- TATB wikiPageWikiLink Picramide.
- TATB wikiPageWikiLink Plastic_bonded_explosive.
- TATB wikiPageWikiLink Polymer-bonded_explosive.
- TATB wikiPageWikiLink RDX.
- TATB wikiPageWikiLink RE_factor.
- TATB wikiPageWikiLink Relative_effectiveness_factor.
- TATB wikiPageWikiLink Rhombohedral.
- TATB wikiPageWikiLink Shock_(mechanics).
- TATB wikiPageWikiLink South_Africa_and_weapons_of_mass_destruction.
- TATB wikiPageWikiLink Substitution_reaction.
- TATB wikiPageWikiLink Transamination.
- TATB wikiPageWikiLink Trigonal_crystal_system.
- TATB wikiPageWikiLink Trinitrotoluene.
- TATB wikiPageWikiLink UDMH.
- TATB wikiPageWikiLink Unsymmetrical_dimethylhydrazine.
- TATB wikiPageWikiLink Vibration.
- TATB wikiPageWikiLink Vicarious_nucleophilic_substitution.
- TATB wikiPageWikiLinkText "1,3,5-triamino-2,4,6-trinitrobenzene".
- TATB wikiPageWikiLinkText "TATB".
- TATB hasPhotoCollection TATB.
- TATB imagefile "TATB-3D-vdW.png".
- TATB imagefile "Triaminotrinitrobenzene.png".
- TATB imagesize "150".
- TATB iupacname "135".
- TATB verifiedfields "changed".
- TATB verifiedrevid "470476118".
- TATB wikiPageUsesTemplate Template:Chembox.
- TATB wikiPageUsesTemplate Template:Fact.
- TATB wikiPageUsesTemplate Template:Reflist.
- TATB subject Category:Anilines.
- TATB subject Category:Explosive_chemicals.
- TATB subject Category:Nitrobenzenes.
- TATB type Article.
- TATB type ChemicalCompound.
- TATB type ChemicalSubstance.
- TATB type Article.
- TATB type Chemical.
- TATB type Enamine.
- TATB type ChemicalObject.
- TATB type Thing.
- TATB type Q11173.
- TATB comment "TATB, triaminotrinitrobenzene or 2,4,6-triamino-1,3,5- trinitrobenzene is an aromatic explosive, based on the basic six-carbon benzene ring structure with three nitro functional groups (NO2) and three amine (NH2) groups attached, alternating around the ring.TATB is a powerful explosive (somewhat less powerful than RDX, but more than TNT), but it is extremely insensitive to shock, vibration, fire, or impact.".
- TATB label "TATB".
- TATB sameAs TATB.
- TATB sameAs Triaminotrinitrobenzol.
- TATB sameAs Triaminotrinitrobenceno.
- TATB sameAs تیایتیبی.
- TATB sameAs Triamminotrinitrobenzene.
- TATB sameAs トリアミノトリニトロベンゼン.
- TATB sameAs Triaminotrinitrobenzeen.
- TATB sameAs m.07f98h.
- TATB sameAs Триаминотринитробензол.
- TATB sameAs TATB.
- TATB sameAs TATB.
- TATB sameAs TATB.
- TATB sameAs Q420723.
- TATB sameAs Q420723.
- TATB wasDerivedFrom TATB?oldid=670400673.
- TATB depiction Triaminotrinitrobenzene.png.