Salon Marie-Christine Brochier, Abdelmouleh Makki, Boufi Sami, Belgacem Mohamed Naceur, Gandini Alessandro
LGP2, Ecole Française de Papeterie et des Industries Graphiques (INPG), BP 65, Domaine Universitaire, St. Martin d'Hères, France.
J Colloid Interface Sci. 2005 Sep 1;289(1):249-61. doi: 10.1016/j.jcis.2005.03.070.
The hydrolysis of three alkoxysilane coupling agents, gamma-methacryloxypropyltrimethoxysilane (MPS), gamma-aminopropyltriethoxysilane (APS), and gamma-diethylenetriaminopropyltrimethoxysilane (TAS), was carried out in an ethanol/water (80/20) solution and followed by 1H, 13C, and 29Si NMR spectroscopy, which showed that its rate increased in the order MPS < APS < TAS. The formation of the silanol groups was followed by their self-condensation to generate oligomeric structure. APS and MPS only gave soluble products, whereas colloidal particles precipitated in the medium when TAS was hydrolyzed. Pristine and hydrolyzed MPS were then adsorbed onto a cellulose substrate and thereafter a thermal treatment at 110-120 degrees C under reduced pressure was applied to the modified fibers to create permanent bonding of the coupling agent at their surface.
在乙醇/水(80/20)溶液中对三种烷氧基硅烷偶联剂,即γ-甲基丙烯酰氧基丙基三甲氧基硅烷(MPS)、γ-氨丙基三乙氧基硅烷(APS)和γ-二乙烯三胺丙基三甲氧基硅烷(TAS)进行水解,随后通过1H、13C和29Si核磁共振光谱进行监测,结果表明水解速率按MPS < APS < TAS的顺序增加。硅醇基团形成后会发生自缩合以生成低聚结构。APS和MPS仅产生可溶产物,而TAS水解时会在介质中沉淀出胶体颗粒。然后将原始的和水解后的MPS吸附到纤维素基材上,之后对改性纤维在110 - 120℃下减压进行热处理,以使偶联剂在其表面形成永久键合。