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Probing the chemistry, structure, an...

Lockwood, Glenn K.

Probing the chemistry, structure, and dynamics of the water-silica interface.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Probing the chemistry, structure, and dynamics of the water-silica interface.
作者:	Lockwood, Glenn K.
面頁冊數:	219 p.
附註:	Source: Dissertation Abstracts International, Volume: 74-08(E), Section: B.
附註:	Adviser: Stephen H. Garofalini.
Contained By:	Dissertation Abstracts International74-08B(E).
標題:	Engineering, Materials Science.
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3558691
ISBN:	9781303032042

Probing the chemistry, structure, and dynamics of the water-silica interface.
Lockwood, Glenn K.

Probing the chemistry, structure, and dynamics of the water-silica interface. - 219 p.

Source: Dissertation Abstracts International, Volume: 74-08(E), Section: B.

Thesis (Ph.D.)--Rutgers The State University of New Jersey - New Brunswick, 2013.

Despite its natural abundance and wide-ranging technological relevance, much remains unknown or unclear about water-silica interfaces. Computer simulation stands to bridge the gaps of knowledge left by experiment, and a recently developed Dissociative Water Potential has enabled the simulation of large amorphous silica surfaces in contact with water without having to impose a model of surface chemistry a priori. Earlier work with this model has revealed the existence of several protonated surface sites such as SiOH2 + and Si-(OH+)-Si that have yet to be extensively characterized. However, both experiment and quantum mechanical simulation have provided an increasing body of evidence that suggests these sites exist, and these sites may play key roles in some of the unexplained phenomena observed in water-silica systems.

ISBN: 9781303032042Subjects--Topical Terms:

226940
Engineering, Materials Science.

Probing the chemistry, structure, and dynamics of the water-silica interface.
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245 1 0 $a Probing the chemistry, structure, and dynamics of the water-silica interface.
300 $a 219 p.
500 $a Source: Dissertation Abstracts International, Volume: 74-08(E), Section: B.
500 $a Adviser: Stephen H. Garofalini.
502 $a Thesis (Ph.D.)--Rutgers The State University of New Jersey - New Brunswick, 2013.
520 $a Despite its natural abundance and wide-ranging technological relevance, much remains unknown or unclear about water-silica interfaces. Computer simulation stands to bridge the gaps of knowledge left by experiment, and a recently developed Dissociative Water Potential has enabled the simulation of large amorphous silica surfaces in contact with water without having to impose a model of surface chemistry a priori. Earlier work with this model has revealed the existence of several protonated surface sites such as SiOH2 + and Si-(OH+)-Si that have yet to be extensively characterized. However, both experiment and quantum mechanical simulation have provided an increasing body of evidence that suggests these sites exist, and these sites may play key roles in some of the unexplained phenomena observed in water-silica systems.
520 $a To this end, this Dissociative Water Potential has been applied to develop a comprehensive picture of the chemistry, structure, and dynamics of the water-silica interface that is unbiased by any expectation of what sites should form. The bridging OH site, Si-(OH+)-Si, does form and is characterized as a highly acidic site that occurs predominantly on strained Si-O-Si bridges near the interface. Similarly, the transient formation of SiOH2 + is observed, and this site is found to be more acidic than Si-(OH +)-Si. In addition to H3O+ that forms near the interface, all of these sites readily deprotonate and are expected to play a role in the enhanced proton conductivity experimentally observed in hydrated mesoporous silica.
520 $a The reactions between water and silica are particularly relevant to the engineering of nuclear waste forms, and the role of water-silica interactions are also explored within the context of the degradation of silica-based waste forms exposed to radiation. Despite the significant simulation effort employed in glassy waste form research, no molecular models of radiation damage in silica include the effects of moisture. This deficiency is addressed, and water is found to play a significant role in accelerating the degradation of amorphous silica under irradiation. Water inhibits healing of the network and promotes the formation of voids into which more water can penetrate, giving way to new damage accumulation mechanisms not seen in any past simulations.
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650 4 $a Chemistry, Inorganic. $3 197298
650 4 $a Physics, Molecular. $3 227726
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710 2 $a Rutgers The State University of New Jersey - New Brunswick. $b Materials Science and Engineering. $3 660271
773 0 $t Dissertation Abstracts International $g 74-08B(E).
790 $a 0190
791 $a Ph.D.
792 $a 2013
793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3558691

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