\"In this work the synthesis of non radioactive and radioactive nanoparticles (NPs) through radiolytic and wet chemistry was studied. Non radioactive NPs of rhenium, iridium, and rhodium were synthesized from aqueous solutions containing the metal salt precursors by gamma irradiation. The solutions were irradiated to generate reducing species that led to the nucleation and growth of the nanoparticles. Amorphous rhenium oxide nanoparticles with average sizes ranging from 10 nm to 55 nm were obtained. Metallic iridium and rhodium nanoparticles were produced in polyvinyl-pyrrolidone (PVP) having narrow particle size distributions and average particle sizes from 2 nm to 6 nm. The stability of the NPs in PVP was explained based on the interaction of the metal with both of the functional groups, C-N and C=O, of the PVP. Iridium NPs supported on carbon nanotubes were also synthesized by gamma irradiation. The NPs were finely distributed on the surface of the nanotubes. The nanoparticle yield was found to increase with the radiation dose and the precursor concentration.
The synthesis of radioactive NPs, specifically lanthanum phosphate containing ²²³Ra and ²²⁵Ra isotopes, was carried out in aqueous media using a precipitation method. The NPs crystallized in rhabdophane structure with a mean particle size of 3.4 nm and 6.3 nm for core and core-2 shells respectively. The ability of LaPO₄ NPs to retain the isotopes within their structure was investigated. It was found that core NPs retained up to 88% of the activity over a period of 35 days. It was also found that the addition of two LaPO₄ shells to the core NPs increases the retention ability up to 99.99%. This fact suggests that LaPO₄ NPs are potential carriers of radium isotopes for targeted alpha therapy.\"--Abstract, page iv.
","abstract_html":"<p>"In this work the synthesis of non radioactive and radioactive nanoparticles (NPs) through radiolytic and wet chemistry was studied. Non radioactive NPs of rhenium, iridium, and rhodium were synthesized from aqueous solutions containing the metal salt precursors by gamma irradiation. The solutions were irradiated to generate reducing species that led to the nucleation and growth of the nanoparticles. Amorphous rhenium oxide nanoparticles with average sizes ranging from 10 nm to 55 nm were obtained. Metallic iridium and rhodium nanoparticles were produced in polyvinyl-pyrrolidone (PVP) having narrow particle size distributions and average particle sizes from 2 nm to 6 nm. The stability of the NPs in PVP was explained based on the interaction of the metal with both of the functional groups, C-N and C=O, of the PVP. Iridium NPs supported on carbon nanotubes were also synthesized by gamma irradiation. The NPs were finely distributed on the surface of the nanotubes. The nanoparticle yield was found to increase with the radiation dose and the precursor concentration.</p> <p>The synthesis of radioactive NPs, specifically lanthanum phosphate containing ²²³Ra and ²²⁵Ra isotopes, was carried out in aqueous media using a precipitation method. The NPs crystallized in rhabdophane structure with a mean particle size of 3.4 nm and 6.3 nm for core and core-2 shells respectively. The ability of LaPO₄ NPs to retain the isotopes within their structure was investigated. It was found that core NPs retained up to 88% of the activity over a period of 35 days. It was also found that the addition of two LaPO₄ shells to the core NPs increases the retention ability up to 99.99%. This fact suggests that LaPO₄ NPs are potential carriers of radium isotopes for targeted alpha therapy."--Abstract, page iv.</p>","abstract_has_math":false,"creators":["Rojas Marin, Jessika Viviana"],"institution":"Missouri University of Science and Technology","degree_name":"Ph. D. in Nuclear Engineering","degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2016,"date_issued":"2016-02-10T08:00:00Z","date_published":"2016-02-10T08:00:00Z","updated_at":"2026-07-24T03:19:54Z","subjects":["Metallic Nanoparticles","Radiation Induced Chemistry","Targeted Alpha Therapy","Nuclear Engineering"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://scholarsmine.mst.edu/doctoral_dissertations/2285","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Rojas Marin, Jessika Viviana"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.available","label":"Dc Date Available","values":["2016-02-10T08:00:00Z"]},{"key":"dc:type","label":"Dc Type","values":["Dissertation - Open Access"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph. D. in Nuclear Engineering"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["Missouri University of Science and Technology"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Metallic Nanoparticles","Radiation Induced Chemistry","Targeted Alpha Therapy","Nuclear Engineering"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://scholarsmine.mst.edu/doctoral_dissertations/2285"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["\"In this work the synthesis of non radioactive and radioactive nanoparticles (NPs) through radiolytic and wet chemistry was studied. Non radioactive NPs of rhenium, iridium, and rhodium were synthesized from aqueous solutions containing the metal salt precursors by gamma irradiation. The solutions were irradiated to generate reducing species that led to the nucleation and growth of the nanoparticles. Amorphous rhenium oxide nanoparticles with average sizes ranging from 10 nm to 55 nm were obtained. Metallic iridium and rhodium nanoparticles were produced in polyvinyl-pyrrolidone (PVP) having narrow particle size distributions and average particle sizes from 2 nm to 6 nm. The stability of the NPs in PVP was explained based on the interaction of the metal with both of the functional groups, C-N and C=O, of the PVP. Iridium NPs supported on carbon nanotubes were also synthesized by gamma irradiation. The NPs were finely distributed on the surface of the nanotubes. The nanoparticle yield was found to increase with the radiation dose and the precursor concentration.
The synthesis of radioactive NPs, specifically lanthanum phosphate containing ²²³Ra and ²²⁵Ra isotopes, was carried out in aqueous media using a precipitation method. The NPs crystallized in rhabdophane structure with a mean particle size of 3.4 nm and 6.3 nm for core and core-2 shells respectively. The ability of LaPO₄ NPs to retain the isotopes within their structure was investigated. It was found that core NPs retained up to 88% of the activity over a period of 35 days. It was also found that the addition of two LaPO₄ shells to the core NPs increases the retention ability up to 99.99%. This fact suggests that LaPO₄ NPs are potential carriers of radium isotopes for targeted alpha therapy.\"--Abstract, page iv.
"]},{"key":"dc:title","label":"Title","values":["Synthesis of radioactive and nonradioactive nanostructures through radiolytic and wet chemistry"]}]}],"canonical_facts":{"dc:creator":["Rojas Marin, Jessika Viviana"],"dc:date.available":["2016-02-10T08:00:00Z"],"dc:description.abstract":["\"In this work the synthesis of non radioactive and radioactive nanoparticles (NPs) through radiolytic and wet chemistry was studied. Non radioactive NPs of rhenium, iridium, and rhodium were synthesized from aqueous solutions containing the metal salt precursors by gamma irradiation. The solutions were irradiated to generate reducing species that led to the nucleation and growth of the nanoparticles. Amorphous rhenium oxide nanoparticles with average sizes ranging from 10 nm to 55 nm were obtained. Metallic iridium and rhodium nanoparticles were produced in polyvinyl-pyrrolidone (PVP) having narrow particle size distributions and average particle sizes from 2 nm to 6 nm. The stability of the NPs in PVP was explained based on the interaction of the metal with both of the functional groups, C-N and C=O, of the PVP. Iridium NPs supported on carbon nanotubes were also synthesized by gamma irradiation. The NPs were finely distributed on the surface of the nanotubes. The nanoparticle yield was found to increase with the radiation dose and the precursor concentration.
The synthesis of radioactive NPs, specifically lanthanum phosphate containing ²²³Ra and ²²⁵Ra isotopes, was carried out in aqueous media using a precipitation method. The NPs crystallized in rhabdophane structure with a mean particle size of 3.4 nm and 6.3 nm for core and core-2 shells respectively. The ability of LaPO₄ NPs to retain the isotopes within their structure was investigated. It was found that core NPs retained up to 88% of the activity over a period of 35 days. It was also found that the addition of two LaPO₄ shells to the core NPs increases the retention ability up to 99.99%. This fact suggests that LaPO₄ NPs are potential carriers of radium isotopes for targeted alpha therapy.\"--Abstract, page iv.
"],"dc:identifier":["https://scholarsmine.mst.edu/doctoral_dissertations/2285"],"dc:subject":["Metallic Nanoparticles","Radiation Induced Chemistry","Targeted Alpha Therapy","Nuclear Engineering"],"dc:title":["Synthesis of radioactive and nonradioactive nanostructures through radiolytic and wet chemistry"],"dc:type":["Dissertation - Open Access"],"thesis:degree_name":["Ph. D. in Nuclear Engineering"],"thesis:institution_name":["Missouri University of Science and Technology"]},"updated_at":"2026-07-24T03:19:54Z"}