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	       <dc:title>The effect of temperatures and γ-ray irradiation on silica-based calix[4]arene-R14 adsorbent modified with surfactants for the adsorption of cesium from nuclear waste solution</dc:title>
	       <dc:creator>Chen, Zi; Wu, Yan; Wei, Yuezhou</dc:creator>
	       <dc:subject>37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; ABSORBED RADIATION DOSES; ADSORBENTS; ADSORPTION; CALIXARENES; CESIUM; CONCENTRATION RATIO; IRRADIATION; ISOTHERMS; NITRIC ACID; RADIATION EFFECTS; RADIOACTIVE WASTES; REDUCTION; SILICA; SILICON OXIDES; SURFACTANTS; TEMPERATURE DEPENDENCE</dc:subject>
	       <dc:subjectRelated></dc:subjectRelated>
	       <dc:description>1,3-[(2,4-Diethylheptylethoxy)oxy]-2,4-crown-6-Calix[4]arene(Calix[4] arene-R14), used as an extractant of Cs(I) from nitric acid, modified by dodecanol and dodecyl benzenesulfonic acid (DBS), was loaded into the pores of macroporous silica-based polymer support (SiO{sub 2}-P) particles. To evaluate the stability of the adsorbent, the adsorption data at different temperatures (298–323 K) and γ-ray absorbed doses (10–200 kGy) were analyzed by the Langmuir isotherm. The minimum adsorbed amount was calculated to be 0.121 mmol g{sup −1} at 323 K, approximately 23% reduction compared to 298 K. The maximum adsorbed amount of not-irradiated adsorbent with 0.156 mmol g{sup −1} decreased by 20% than that irradiated in 0.5 M HNO{sub 3}. The thermodynamic parameters have revealed that this adsorption reaction is an exothermic and spontaneous process. The reduction in 3 M HNO{sub 3} was about 45% by the comparison between the before- and after-irradiation. It was found that both the concentrations of HNO{sub 3} and DBS have significant influence on the degradation of the adsorbents. - Highlights: • The adsorbed amount of Cs(I) on the adsorbent decreases with increasing temperature. • The values of G° and H° are calculated from the plots of ln K{sub L} versus 1/T. • The adsorption ability of the irradiated adsorbent for Cs(I) decreases with increasing dose.</dc:description>
	       <dcq:publisher></dcq:publisher>
	       <dcq:publisherResearch></dcq:publisherResearch>
	       <dcq:publisherAvailability>Available from http://dx.doi.org/10.1016/j.radphyschem.2014.06.004</dcq:publisherAvailability>
	       <dcq:publisherSponsor></dcq:publisherSponsor>
	       <dcq:publisherCountry>United Kingdom</dcq:publisherCountry>
		   <dc:contributingOrganizations></dc:contributingOrganizations>
	       <dc:date>2014-10-15</dc:date>
	       <dc:language>English</dc:language>
	       <dc:type>Journal Article</dc:type>
	       <dcq:typeQualifier></dcq:typeQualifier>
	       <dc:relation>Journal Name: Radiation Physics and Chemistry (1993); Journal Volume: 103; Other Information: Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)</dc:relation>
	       <dc:coverage></dc:coverage>
	       <dc:format>Medium: X; Size: page(s) 222-226</dc:format>
	       <dc:doi>https://doi.org/10.1016/J.RADPHYSCHEM.2014.06.004</dc:doi>
	       <dc:identifier>PII: S0969-806X(14)00252-7</dc:identifier>
		   <dc:journalName>[]</dc:journalName>
		   <dc:journalIssue></dc:journalIssue>
		   <dc:journalVolume>103</dc:journalVolume>
	       <dc:identifierReport></dc:identifierReport>
	       <dcq:identifierDOEcontract></dcq:identifierDOEcontract>
	       <dc:identifierOther>Journal ID: ISSN 0969-806X; CODEN: RPCHDM; Other: PII: S0969-806X(14)00252-7; TRN: GB16R4933055177</dc:identifierOther>
	       <dc:source>INIS</dc:source>
	       <dc:rights></dc:rights>
	       <dc:dateEntry>2016-05-23</dc:dateEntry>
	       <dc:dateAdded></dc:dateAdded>
	       <dc:ostiId>22485193</dc:ostiId>
	       <dcq:identifier-purl></dcq:identifier-purl>
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