Abstract

An investigation was carried out to determine the effects of room-temperature aging on the structure and composition of NaY zelite synthesis gels prepared from colloidal silica. Alkaline solutions containing varying amounts of sodium aluminate were added to a colloidal silica sol to produce gels of composition 4 Na 2O, x Al 2O 3, 10 SiO 2, 180 H 2O ( x = 0.0 –1.5). Each of the gels was homogenized and then allowed to age at room temperature. Changes in the composition and structure of the solid and liquid phases of zeolite synthesis gels were followed as a function of time using elemental analysis; n.m.r., i.r. and Raman spectroscopies; and X-ray diffraction. Initial mixing of the colloidal silica, caustic, and aluminate has no noticeable chemical or structural effects beyond gelation via flocculation of the silica particles and adsorption of AI and Na onto the surface of the particles. The colloidal silica dissolves during aging as a consequence of successive cleavage of siloxane bonds. Adsorption of AI reduces the rate of silica dissolution. The slow dissolution of the silica releases monomeric silicate anions that rapidly react with aluminate anions to form an aluminosilicate precipitate, estimated to have a Si Ai ratio of 1. Once the dissolved aluminum is depleted from the liquid phase, the remaining colloidal silica dissolves away, leaving only an amorphous aluminosilicate in the solid phase, which can then rearrange through interaction with the silicates anions in solution. As discussed in a companion study, the aluminosilicate precipitate formed during aging serves as the precursor for nuclei which induce the cyrstallization of NaY zeolite.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.