“…So far, various aminosilanes including aminomethyl- (C1), 273 2-aminoethyl- (C2), 273 3-aminopropyl- (APS), 120,125,126,134,273–287 4-aminobutyl- (C4), 273 5-aminoamyl- (C5), 273 N -methylaminopropyl- (MAPS), 274 N -butylaminopropyl- (NBAPS), 288,289 3-amino-3-methylbutyl- (AMBS), 127 tert -butylaminopropyl- (TBAPS), 127 N -cyclohexylaminopropyl- (CHAPS), 127 N -phenylaminopropyl- (PHAPS), 288 N , N -dimethylaminopropyl- (DMAPS), 274 3-(2-aminoethylamino)propyl- (DI), 134,287,290–292 3-(2-aminopropylamino)propylsilane ( l -propyl), 134 N , N ′-bis(3-trimethoxysilpropyl)urea (UREA), 275 3-[2-(2-aminoethylamino)ethylamino]propyl- (TRI), 114,120,128,129,287,293–295 3-(2-aminoethylamino)methylsilane (CH 2 DETA), 296 bis(2-aminoethyl)amine (B-ethyl), 134,296 bis(2-aminopropyl)amine (B-propyl), 134 and TREN, 121,134,260 have been tested for their ability to capture CO 2 from ultradilute concentrations of gas mixtures. In general, primary amines have higher amine efficiencies than secondary and tertiary amines due to the entropy effect, 274,288 which has led to the widespread use of APS for capturing CO 2 under ultradilute conditions.…”