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        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/787" />
        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/786" />
        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/785" />
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    <dc:date>2026-03-27T08:27:40Z</dc:date>
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    <title>Visible light responsive heterostructured α- Bi2O3/ZnO doped β-Bi2O3 photocatalyst for remediation of organic pollutants,</title>
    <link>http://localhost:8080/xmlui/handle/123456789/787</link>
    <description>Title: Visible light responsive heterostructured α- Bi2O3/ZnO doped β-Bi2O3 photocatalyst for remediation of organic pollutants,
Authors: Kaur, G; Sharma, S; Bansal, P
Abstract: Novel visible-light active α-Bi2&#xD;
O3&#xD;
/ZnO doped β-Bi2&#xD;
O3&#xD;
 (ZB) photocatalyst was synthesized at different temperatures 400°C (ZB4), 500°C (ZB5), and 600°C (ZB6) by modified sol–gel method. The structural, morphological, compositional, and optical properties of synthesized photocatalyst were&#xD;
characterized using X-ray powder diffraction, field emission scanning electron microscopy, energy&#xD;
dispersive X-rays spectroscopy, Fourier transform infrared spectroscopy, and UV-vis spectroscopy.&#xD;
With an increase in calcination temperature, the bandgap of the prepared photocatalyst increases,&#xD;
and metastable β-phase Bi2&#xD;
O3&#xD;
 changes to α-phase. The photocatalytic activity was evaluated using&#xD;
Alizarin Red S (ARS) as a model organic compound. The rate of degradation was estimated from&#xD;
residual concentration spectrophotometrically. The results revealed that with an increase in calcination temperature, the photocatalytic activity of synthesized ZB photocatalyst decreases. Maximum&#xD;
decolorization efficiency (88%) was shown by the photocatalyst prepared at 400°C which is 29%&#xD;
and 37% higher than that of photocatalyst prepared at 500°C and 600°C, respectively</description>
    <dc:date>2020-01-01T00:00:00Z</dc:date>
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  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/786">
    <title>Synthesis, characterization and visible‐light‐induced photocatalytic activity of powdered semiconductor oxides of bismuth and zinc toward degradation of Alizarin Red S,</title>
    <link>http://localhost:8080/xmlui/handle/123456789/786</link>
    <description>Title: Synthesis, characterization and visible‐light‐induced photocatalytic activity of powdered semiconductor oxides of bismuth and zinc toward degradation of Alizarin Red S,
Authors: Sharma, S; Kaur, G; Bansal, P et al.
Abstract: Semiconductor oxides of bismuth and zinc have been synthesized using modified sol-gel method and sol-combustion method, respectively. The synthesized catalysts were characterized by X-ray powder diffraction (XRD), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), and UV-vis spectroscopy. The photocatalytic activity of Bi2 O3 and ZnO was evaluated for the degradation of Alizarin Red S (ARS), as a model pollutant, at 20 mg/L level in water under visible light irradiation. The percentage of photocatalytic degradation was determined using UV-vis spectrophotometer. The photocatalytic results revealed that Bi2 O3 and ZnO could effectively degrade 73% and 53% of ARS, respectively, within 13 hr under visible light illumination, indicating that synthesized Bi2 O3 is a better photocatalyst than ZnO. Photodegradation of ARS with Bi2 O3 and ZnO is remarkably influenced by change in pH of the dye solution, and pH 8 was found to be the most favorable for maximum removal of ARS in case of both Bi2 O3 (75%) and ZnO (58%) photocatalyst. PRACTITIONER POINTS: Photocatalytic degradation of ARS dye depends on pH of the solution. Calcination temperature influences the crystallite size of prepared semiconductor oxides of bismuth and zinc. Bi2 O3 shows better photocatalytic degradation efficiency than ZnO under visible light illumination.</description>
    <dc:date>2020-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/785">
    <title>Reactions of MoCl5 and MoO2Cl2 with 4-Phenylimidazole- 2-thiol and 2-Thiazoline-2-thiol</title>
    <link>http://localhost:8080/xmlui/handle/123456789/785</link>
    <description>Title: Reactions of MoCl5 and MoO2Cl2 with 4-Phenylimidazole- 2-thiol and 2-Thiazoline-2-thiol
Authors: Rani, D; Singh, G; Sharma, S
Abstract: Reactions of MoCl5/MoO2Cl2 with 4-phenylimidazole-2-thiol/2-thiazoline-2-thiol in CH3CNsolvent in 1:1/1:2 molar ratios have been carried out at room temperature. Products obtained MoCl3(C9H7N2S)(CH3CN), [1];MoCl2(C9H7N2S)(CH3CN), [2]; Mo2OCl4(C9H8N2S)2, [3] and Mo4O2Cl12(C9H7N2S)4, [4]; MoO2Cl3(C3H5NS2)2, [5] and Mo2O4Cl3(C3H5NS2)2, [6] have been analyzed and characterizedby elemental analysis, FTIR, 1H NMR and LC-MS techniques. Compounds being moisture and air sensitive, these have been prepared in inert atmosphere using vacuum line and liquid nitrogen cooled traps. Fragments obtained in LC-MS spectra support the formulae derived.</description>
    <dc:date>2020-01-01T00:00:00Z</dc:date>
  </item>
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