<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kiani, Daniyal</style></author><author><style face="normal" font="default" size="100%">Silva, Manoj</style></author><author><style face="normal" font="default" size="100%">Sheng, Yiying</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Experimental Insights into the Genesis and Growth of Struvite Particles on Low Solubility Dolomite Mineral Surfaces</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry CThe Journal of Physical Chemistry C</style></secondary-title><short-title><style face="normal" font="default" size="100%">J. Phys. Chem. C</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019/09/24</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.jpcc.9b05292</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><notes><style face="normal" font="default" size="100%">doi: 10.1021/acs.jpcc.9b05292</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Valter, Mikael</style></author><author><style face="normal" font="default" size="100%">Busch, Michael</style></author><author><style face="normal" font="default" size="100%">Wickman, Björn</style></author><author><style face="normal" font="default" size="100%">Grönbeck, Henrik</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Hellman, Anders</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrooxidation of Glycerol on Gold in Acidic Medium: A Combined Experimental and DFT Study</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title><short-title><style face="normal" font="default" size="100%">J. Phys. Chem. C</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2018/05/17</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.jpcc.8b02685</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">122</style></volume><pages><style face="normal" font="default" size="100%">10489 - 10494</style></pages><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">19</style></issue><notes><style face="normal" font="default" size="100%">doi: 10.1021/acs.jpcc.8b02685</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Navizaga, Criztel</style></author><author><style face="normal" font="default" size="100%">Lenzo, Courtney</style></author><author><style face="normal" font="default" size="100%">Zhang, Hanyu</style></author><author><style face="normal" font="default" size="100%">Brazienė, Zita</style></author><author><style face="normal" font="default" size="100%">Paltanavicius, Virgilijus</style></author><author><style face="normal" font="default" size="100%">Petrauskiene, Julija</style></author><author><style face="normal" font="default" size="100%">Mazeika, Romas</style></author><author><style face="normal" font="default" size="100%">Staugaitis, Gediminas</style></author><author><style face="normal" font="default" size="100%">Sviklas, Alfredas Martynas</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efficiency Evaluation of Dairy Wastewater Derived Zinc Micronutrient Containing Sustainable Fertilizers</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Sustainable Chemistry &amp; Engineering</style></secondary-title><short-title><style face="normal" font="default" size="100%">ACS Sustainable Chem. Eng.</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2017/08/07</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/acssuschemeng.7b00933</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">5</style></volume><pages><style face="normal" font="default" size="100%">6692 - 6699</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">8</style></issue><notes><style face="normal" font="default" size="100%">doi: 10.1021/acssuschemeng.7b00933</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Peng, Rui</style></author><author><style face="normal" font="default" size="100%">Shrestha, Khadga</style></author><author><style face="normal" font="default" size="100%">Mishra, Gautam</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Wu, Chia-Ming</style></author><author><style face="normal" font="default" size="100%">Koodali, Ranjit T.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efficient photocatalytic hydrogen evolution system by assembling earth abundant NixOy nanoclusters in cubic MCM-48 mesoporous materials.</style></title><secondary-title><style face="normal" font="default" size="100%">RSC Advances</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">MCM mesoporous material nickel oxide nanocluster photocatalytic hydrogen evolution</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2016</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">59169 - 59180</style></pages><isbn><style face="normal" font="default" size="100%">2046-2069</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">A cubic MCM-48 mesoporous material was employed as a support to encapsulate earth abundant NixOy species (NiO and Ni2O3).  The cubic MCM-48 mesoporous support provides an excellent platform to not only effectively disperse NiO and/or Ni2O3 species but also to limit their particle sizes.  The presence of Ni2O3 species at an optimal amt. seems to enhance the photocatalytic activity of Ni-MCM-48 materials in comparison to a Ni-MCM-48 mesoporous material having only NiO dispersed in it.  In addn., the presence of bulk NiO species also seems to be detrimental to the generation of solar hydrogen.  The apparent quantum yield (AQY) of the most active material, Ni-MCM-48-2.5% was estd. to be 5.35%.  This was over 250 times higher than a bulk, NiO (AQY = 0.02%) under identical exptl. conditions.  This study indicates that MCM-48 can be used as an effective support to disperse NixOy species. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">64</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2016:982565(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mazeika, Romas</style></author><author><style face="normal" font="default" size="100%">Staugaitis, Gediminas</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Engineered Pelletized Organo-Mineral Fertilizers (OMF) from Poultry Manure, Diammonium Phosphate and Potassium Chloride.</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Sustainable Chemistry &amp; Engineering</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">pelletized organomineral fertilizer poultry manure diammonium phosphate potassium chloride</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2016</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">4</style></volume><pages><style face="normal" font="default" size="100%">2279 - 2285</style></pages><isbn><style face="normal" font="default" size="100%">2168-0485</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">In this work, we engineered a pilot scale process for the prodn. of granulated org.- and organo-mineral fertilizers (OGF and OMF) from poultry manure.  We investigated the effects of moisture content in the manure, energy consumption during the three main stages of the process and the possibility to obtain nutrient balanced fertilizers using conventional straw drying and granulation equipment, common on the farms.  Poultry manure was dried and shredded to no less than 90% of dry mass at 95 °C.  Granulation was performed via extrusion with and without mineral additives, such as diammonium phosphate (DAP) and potassium chloride (KCl).  This process was used to achieve 4-3-3 OGF, as well as tunable NPK content (4-4-2, 4-3-6 and 4-4-9) OMF.  Energy consumption as the manure dried was about 100 kWh/t of product.  This limiting step of the process suggests that the max. achievable drying of sub 10% water currently commonly used is not necessarily economically optimal.  DAP was used to increase water-sol. phosphate concn. and was limited to 6% of the total amt. by the emission of ammonia during the granulation process.  Addnl., the presence of hygroscopic KCl in combination with DAP resulted in significant moisture absorption and loss of the granulized pellet structural integrity after 72 h at 30 °C and 80% RH.  Significant increases in yields of rapeseed and potato crops were obsd. with the 2 t/ha application of OGF or DAP/KCl enhanced OMF.  The engineered process will provide for sustainable prodn. of nutrient balanced organo-mineral fertilizers on the manure prodn. sites using conventional equipment already used for straw processing. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2016:403621(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Seal, Mark</style></author><author><style face="normal" font="default" size="100%">Singh, Nirala</style></author><author><style face="normal" font="default" size="100%">McFarland, Eric W.</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrochemically Deposited Sb and In Doped Tin Sulfide (SnS) Photoelectrodes.</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Physical Chemistry C</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antimony indium doping tin sulfide photoelectrode hydrogen wastewater oxidn</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">119</style></volume><pages><style face="normal" font="default" size="100%">6471 - 6480</style></pages><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Semiconducting tin sulfide (SnS) was deposited electrochem. from electrolytes contg. Sn and S precursors and conditions optimized to maximize its performance as a photoelectrode.  Films composed of primarily orthorhombic SnS were electrodeposited on titanium substrates from electrolyte contg. 20 mM SnSO4 and 100 mM Na2S2O3 at pH 2.5.  For deposition a cathodic pulse of -1.25 V vs Ag/AgCl was applied for 2.75 s followed by a 0.25 s pulse of +0.25 V vs Ag/AgCl repeated for 30-45 min.  The films were annealed in argon at 300 °C for 3 h.  The addn. of SbCl3 (&lt;5%) to the electrolyte gave rise to doping of the SnS film with Sb which resulted in an increase in the photocurrent as well as a switch from p- to n-type semiconducting behavior in an acidified Na2S2O3 electrolyte.  Incorporation of p-type In into the films from addn. of In(NO3)3 had a smaller effect on the measured photocurrent, and at higher precursor concn. (&gt;5%) the dopants resulted in the formation of secondary phases of Sb and In oxides with redn. in the measured photocurrent.  This doped SnS material could potentially be used in systems for the photoelectrochem. prodn. of hydrogen and oxidn. of org. wastewater.  D. functional theory calcns. supported the exptl. obsd. cond. increase for photoelectrons as an Sb dopant induced curvature of the valence band.  These calcns. also provided an explanation to the previous exptl. work where Sb doping was used to decrease the resistivity of SnS films.  The combination of an automated electrodeposition of an earth abundant metal sulfide with the theor. calcns. to guide the synthesis is an exemplar of how to improve the efficiency of SnS-based solar energy conversion materials. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">12</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2015:427097(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hellman, Anders</style></author><author><style face="normal" font="default" size="100%">Iandolo, Beniamino</style></author><author><style face="normal" font="default" size="100%">Wickman, Bjoern</style></author><author><style face="normal" font="default" size="100%">Groenbeck, Henrik</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electro-oxidation of water on hematite: Effects of surface termination and oxygen vacancies investigated by first-principles.</style></title><secondary-title><style face="normal" font="default" size="100%">Surface Science</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">OER hydroxyl oxygen terminated hematite Electrooxidn water DFT</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year></dates><publisher><style face="normal" font="default" size="100%">Elsevier B.V.</style></publisher><volume><style face="normal" font="default" size="100%">640</style></volume><pages><style face="normal" font="default" size="100%">45 - 49</style></pages><isbn><style face="normal" font="default" size="100%">0039-6028</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The oxygen evolution reaction on hydroxyl- and oxygen-terminated hematite was investigated using first-principle calcns. within a theor. electrochem. framework.  Both pristine hematite and hematite contg. oxygen vacancies were considered.  The onset potential was detd. to be 1.79 V and 2.09 V vs. the reversible hydrogen electrode (RHE) for the pristine hydroxyl- and oxygen-terminated hematite, resp.  The presence of oxygen vacancies in the hematite surface resulted in pronounced shifts of the onset potential to 3.09 V and 1.83 V, resp.  Electrochem. oxidn. measurements conducted on thin-film hematite anodes, resulted in a measured onset potential of 1.66 V vs.  RHE.  Furthermore, the threshold potential between the hydroxyl- and oxygen-terminated hematite was detd. as a function of pH.  The results indicate that electrochem. water oxidn. on hematite occurs on the oxygen-terminated hematite, contg. oxygen vacancies. [on SciFinder(R)]</style></abstract><notes><style face="normal" font="default" size="100%">CAPLUS AN 2015:594301(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yi, Wentao</style></author><author><style face="normal" font="default" size="100%">Yan, Chunyan</style></author><author><style face="normal" font="default" size="100%">Hamdy, Mohamed S.</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Mul, Guido.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of bismuth addition and photodeposition of platinum on (surface) composition, morphology and visible light photocatalytic activity of sol-gel derived TiO2.</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Catalysis, B: Environmental</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">bismuth contg titania platinum nanoparticle visible light photocatalyst</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><publisher><style face="normal" font="default" size="100%">Elsevier B.V.</style></publisher><volume><style face="normal" font="default" size="100%">154-155</style></volume><pages><style face="normal" font="default" size="100%">153 - 160</style></pages><isbn><style face="normal" font="default" size="100%">0926-3373</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Several remarkable observations regarding structure, (surface) compn. and visible light induced photocatalytic activity of Bi-promoted anatase photocatalysts are reported.  First, XPS characterization data show that compns. of mixed Bi-Ti-oxide phases obtained by hydrothermal treatment at 180° C of aq. solns. of ethanol, titanium n-butoxide, and bismuth nitrate, are surface enriched with a specific fraction of metallic-like bismuth.  Second, the formation of highly dispersed nanoparticles of platinum on these composites by photodeposition is accompanied by significant morphol. changes.  Third, the platinum functionalized, bismuth-promoted Anatase composites exhibit extraordinary photocatalytic activity in the photocatalytic degrdn. of org. compds. (Acid orange 7 and salicylic acid, resp.) upon illumination at 447 nm, higher than obsd. for P25 upon UV illumination in similar reactor configuration.  An optimized Pt-Bi-Ti-O composite consists of 1 wt% Pt and 5 wt% Bi.  The high activity of the composite is discussed on the basis of the cryst. morphol. and surface compn. [on SciFinder(R)]</style></abstract><notes><style face="normal" font="default" size="100%">CAPLUS AN 2014:517386(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kas, Recep</style></author><author><style face="normal" font="default" size="100%">Kortlever, Ruud</style></author><author><style face="normal" font="default" size="100%">Milbrat, Alexander</style></author><author><style face="normal" font="default" size="100%">Koper, Marc T. M.</style></author><author><style face="normal" font="default" size="100%">Mul, Guido</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrochemical CO2 reduction on Cu2O-derived copper nanoparticles: controlling the catalytic selectivity of hydrocarbons.</style></title><secondary-title><style face="normal" font="default" size="100%">Physical Chemistry Chemical Physics</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">electrochem carbon dioxide redn cuprous oxide copper nanoparticle catalysis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><publisher><style face="normal" font="default" size="100%">Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">12194 - 12201</style></pages><isbn><style face="normal" font="default" size="100%">1463-9076</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The catalytic activity and hydrocarbon selectivity in electrochem. carbon dioxide (CO2) redn. on cuprous oxide (Cu2O) derived copper nanoparticles is discussed.  Cuprous oxide films with [100], [110] and [111] orientation and variable thickness were electrodeposited by redn. of copper(II) lactate on com. available copper plates.  After initiation of the electrochem. CO2 redn. by these oxide structures, the selectivity of the process largely depends on the parent Cu2O film thickness, rather than on the initial crystal orientation.  Starting with thin Cu2O films, besides CO and hydrogen, selective formation of ethylene is obsd. with very high ethylene-to-methane ratios (∼8 to 12).  In addn. to these products, thicker Cu2O films yield a remarkably large amt. of ethane.  Long term faradaic efficiency anal. of hydrocarbons shows no sign of deactivation of the electrodes after 5 h of continuous expt.  Online mass spectroscopy studies combined with x-ray diffraction data suggest the redn. of the Cu2O films in the presence of CO2, generating a nanoparticulate Cu morphol., prior to the prodn. of hydrogen, CO, and hydrocarbons.  Optimizing coverage, no. d. and size of the copper nanoparticles, as well as local surface pH, may allow highly selective formation of the industrially important product ethylene. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">24</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2014:886640(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amornpitoksuk, Pongsaton</style></author><author><style face="normal" font="default" size="100%">Intarasuwan, Khanitta</style></author><author><style face="normal" font="default" size="100%">Suwanboon, Sumetha</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of phosphate salts (Na3PO4, Na2HPO4, and NaH2PO4) on Ag3PO4 morphology for photocatalytic dye degradation under visible light and toxicity of the degraded dye products.</style></title><secondary-title><style face="normal" font="default" size="100%">Industrial &amp; Engineering Chemistry Research</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">phosphate salt silver phosphate morphol photocatalytic dye degrdn</style></keyword><keyword><style  face="normal" font="default" size="100%">visible light toxicity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">52</style></volume><pages><style face="normal" font="default" size="100%">17369 - 17375</style></pages><isbn><style face="normal" font="default" size="100%">0888-5885</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Ag3PO4 was synthesized by the pptn. method using three different types of phosphate salts (Na3PO4, Na2HPO4, and NaH2PO4) as a pptg. agent.  Hydrolysis of each phosphate salt gave a specific pH that affected the purity and morphol. of the prepd. Ag3PO4.  The Ag3PO4 prepd. from Na2HPO4 showed the best photocatalytic activity induced by visible light to degrade methylene blue dye.  During the photocatalytic process, Ag3PO4 decompd. and produced metallic Ag, and this evidence was confirmed by the X-ray diffraction technique and XPS.  The photocatalytic efficiency decreased with the no. of recycles used.  This Ag3PO4 photocatalyst also degraded another cationic dye, rhodamine B, but did not degrade reactive orange, an anionic dye.  The degraded products produced by the photocatalysis had lower toxicities than the untreated dyes using Chlorella vulgaris as a bioindicator. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">49</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2013:1789489(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Monick, Martha M.</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Powers, Linda S.</style></author><author><style face="normal" font="default" size="100%">Borcherding, Jennifer A.</style></author><author><style face="normal" font="default" size="100%">Caraballo, Juan C.</style></author><author><style face="normal" font="default" size="100%">Mudunkotuwa, Imali</style></author><author><style face="normal" font="default" size="100%">Peate, David W.</style></author><author><style face="normal" font="default" size="100%">Walters, Katherine</style></author><author><style face="normal" font="default" size="100%">Thompson, Jay M.</style></author><author><style face="normal" font="default" size="100%">Grassian, Vicki H.</style></author><author><style face="normal" font="default" size="100%">Gudmundsson, Gunnar</style></author><author><style face="normal" font="default" size="100%">Comellas, Alejandro P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of Eyjafjallajokull volcanic ash on innate immune system responses and bacterial growth in vitro</style></title><secondary-title><style face="normal" font="default" size="100%">Environmental health perspectives</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><volume><style face="normal" font="default" size="100%">121</style></volume><pages><style face="normal" font="default" size="100%">691 - 8</style></pages><isbn><style face="normal" font="default" size="100%">1552-9924</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">BACKGROUND:  On 20 March 2010, the Icelandic volcano Eyjafjallajokull erupted for the first time in 190 years.  Despite many epidemiological reports showing effects of volcanic ash on the respiratory system, there are limited data evaluating cellular mechanisms involved in the response to ash.  Epidemiological studies have observed an increase in respiratory infections in subjects and populations exposed to volcanic eruptions.  METHODS:  We physicochemically characterized volcanic ash, finding various sizes of particles, as well as the presence of several transition metals, including iron.  We examined the effect of Eyjafjallajokull ash on primary rat alveolar epithelial cells and human airway epithelial cells (20-100 μg/cm(2)), primary rat and human alveolar macrophages (5-20 μg/cm(2)), and Pseudomonas aeruginosa (PAO1) growth (3 μg/104 bacteria).  RESULTS:  Volcanic ash had minimal effect on alveolar and airway epithelial cell integrity.  In alveolar macrophages, volcanic ash disrupted pathogen-killing and inflammatory responses.  In in vitro bacterial growth models, volcanic ash increased bacterial replication and decreased bacterial killing by antimicrobial peptides.  CONCLUSIONS:  These results provide potential biological plausibility for epidemiological data that show an association between air pollution exposure and the development of respiratory infections.  These data suggest that volcanic ash exposure, while not seriously compromising lung cell function, may be able to impair innate immunity responses in exposed individuals.[on SciFinder (R)]</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><notes><style face="normal" font="default" size="100%">MEDLINE AN 2013450089(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, N.I.H., EXTRAMURAL); (RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.))</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amornpitoksuk, Pongsaton</style></author><author><style face="normal" font="default" size="100%">Suwanboon, Sumetha</style></author><author><style face="normal" font="default" size="100%">Muensit, Nantakan</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced photocatalytic activities of Ag/ZnO powders modified by diblock copolymer.</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Materials Research (Durnten-Zurich, Switzerland)</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">photocatalysis Ag ZnO powder modified diblock copolymer</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><publisher><style face="normal" font="default" size="100%">Trans Tech Publications Ltd.</style></publisher><volume><style face="normal" font="default" size="100%">770</style></volume><pages><style face="normal" font="default" size="100%">34 - 37</style></pages><isbn><style face="normal" font="default" size="100%">1662-8985</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Ag/ZnO powders were synthesized through a pptn. method, using poly(ethylene oxide)-block-poly(propylene oxide) as stabilizer.  X-ray diffraction patterns of all prepd. powders showed a mixed phase of Ag and ZnO.  The existence of metallic Ag on the surface of all prepd. ZnO powders was confirmed by XPS.  Their photocatalytic activities were investigated through the degrdn. of a methylene blue soln. under blacklight illumination.  The Ag/ZnO prepd. from the Zn2+ soln. contg. 7 mol% of Ag+ had the highest photocatalytic activity and this also showed better photocatalytic activity than a com. ZnO powder. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">Applied Physics and Material Applications</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2014:266267(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mahoney, Luther</style></author><author><style face="normal" font="default" size="100%">Wu, Chia-Ming</style></author><author><style face="normal" font="default" size="100%">Kibombo, Harrison S.</style></author><author><style face="normal" font="default" size="100%">Thiruppathi, Eagappanath</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Rasalingam, Shivatharsiny</style></author><author><style face="normal" font="default" size="100%">Koodali, Ranjit T.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Exploration of the role of anions in the synthesis of Cr containing mesoporous materials at room temperature.</style></title><secondary-title><style face="normal" font="default" size="100%">Microporous and Mesoporous Materials</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">anion chromium mesoporous material room temp</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><publisher><style face="normal" font="default" size="100%">Elsevier Inc.</style></publisher><volume><style face="normal" font="default" size="100%">170</style></volume><pages><style face="normal" font="default" size="100%">211 - 225</style></pages><isbn><style face="normal" font="default" size="100%">1387-1811</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Chromium contg. mesoporous silica materials were synthesized via a modified Stoeber synthesis at room temp.  The chromium ion loading and the effect of counterion in the synthesis were studied.  The mesoporous materials were extensively characterized by powder XRD, N2 physisorption, Atomic Absorption Spectroscopy (AAS), FTIR Spectroscopy (FTIR), Diffuse Reflectance Spectroscopy (DRS UV-visible), hydrogen Temp.-Programmed Redn. (H2-TPR), XPS, and TEM studies.  A transition from Ia3̅d cubic phase to p6mm hexagonal or wormhole phases was noted as more amts. of chromium were incorporated into the siliceous materials.  Chromium species present in the silica matrix include monochromate, polychromate, and chromium oxide (Cr2O3) clusters. [on SciFinder(R)]</style></abstract><notes><style face="normal" font="default" size="100%">CAPLUS AN 2013:185238(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Hatch, Courtney</style></author><author><style face="normal" font="default" size="100%">Orlando, Roberto.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electronic Properties and Reactivity of Simulated Fe3+ and Cr3+ Substituted α-Al2O3 (0001) Surface.</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Physical Chemistry C</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">carbon monoxide adsorption iron chromium substituted alumina surface</style></keyword><keyword><style  face="normal" font="default" size="100%">electronic property reactivity iron chromium substituted alumina surface</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2012///</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">116</style></volume><pages><style face="normal" font="default" size="100%">18847 - 18856</style></pages><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Metal oxide-based minerals naturally contain transition metal impurities isomorphically substituted into the structure that can alter the structural and electronic properties as well as the reactivity of these metal oxides.  Natural α-Al2O3 (corundum) can contain up to 9.17% (wt./wt.) Fe2O3 and 1.81% (wt./wt.) of Cr2O3.  Here the authors report on changes in the structural and electronic properties of undoped and doped α-Al2O3 (0001) surfaces using periodic d. functional theory (DFT) methods with spin unrestricted B3LYP functional and a local at. basis set.  Both structural and electronic properties are altered upon doping.  Implications for doping effects on photochem. processes are discussed.  As metal oxides are major components of the environment, including atm. mineral aerosol, DFT was also used to study the effect of transition metal impurities on gas/surface interactions of a model acidic atm. gas mol., CO.  The theor. results indicated that the presence of Fe3+ and Cr3+ impurities substituted on the outer layer of natural corundum surfaces reduces the propensity toward CO adsorption relative to the undoped surface.  However, CO-surface interactions resemble that of bulk α-Al2O3 when the impurity is substituted below the 1st surface layer.  The presence and location of the mineral dopant significantly altered the structural and electronic properties and gas/surface interactions studied here. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">35</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2012:1152034(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Parayil, Sreenivasan Koliyat</style></author><author><style face="normal" font="default" size="100%">Kibombo, Harrison S.</style></author><author><style face="normal" font="default" size="100%">Wu, Chia-Ming</style></author><author><style face="normal" font="default" size="100%">Peng, Rui</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Koodali, Ranjit T.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced photocatalytic water splitting activity of carbon-modified TiO2 composite materials synthesized by a green synthetic approach.</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Hydrogen Energy</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">carbon titanium oxide composite photocatalytic water splitting hydrothermal method</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2012///</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Elsevier Ltd.</style></publisher><volume><style face="normal" font="default" size="100%">37</style></volume><pages><style face="normal" font="default" size="100%">8257 - 8267</style></pages><isbn><style face="normal" font="default" size="100%">0360-3199</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">We report a green and facile approach for the prepn. of carbon-modified (C-modified) TiO2 composite materials by hydrothermal synthesis followed by pyrolytic treatment.  The resultant materials were characterized by powder X-ray diffraction (XRD), nitrogen physisorption studies, Raman spectroscopy, XPS, diffuse reflectance spectroscopy (DRS), photoluminescence (PL) spectroscopy, and transmission electron microscopy (TEM).  The photocatalytic performances of these materials were evaluated by calcg. the amt. of hydrogen evolved from the decompn. of water under solar simulated irradn. conditions.  An improvement was achieved from no H2 evolution at all with the bare TiO2, to an evolution of 0.21 mL g-1 h-1 from a composite material modified with an optimum carbon loading of 3.62%.  These results suggested that the interaction of carbon with predominantly rutile form of TiO2 can promote shallow trapping of photogenerated electrons in the oxygen vacancies.  This phenomenon consequently enhances the photocatalytic activity by minimizing charge carrier recombination, a characteristic demonstrated by fluorescence quenching of the TiO2 emission. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">10</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2012:405985(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Runge, M. B.</style></author><author><style face="normal" font="default" size="100%">Dadsetan, M.</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, J.</style></author><author><style face="normal" font="default" size="100%">Yaszemski, M. J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrically conductive surface modifications of three-dimensional polypropylene fumarate scaffolds</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of biological regulators and homeostatic agents</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2011///</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">25</style></volume><pages><style face="normal" font="default" size="100%">S15-23</style></pages><isbn><style face="normal" font="default" size="100%">0393-974X</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Polypropylene fumarate (PPF) scaffolds fabricated by rapid prototyping were surface modified by solution deposition of electrically conductive polypyrrole coatings with or without hydroxyapatite.  Scaffolds were electrically conductive with resistivity as low as 2Ω.  Scaffold characterization by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy and thermo gravimetric analysis shows both polypyrrole and hydroxyapatite are present.  Cell viability, attachment, proliferation, and differentiation were analyzed using human fetal osteoblast cells.  These studies show that surface modification using hydroxyapatite improved cell attachment and proliferation of osteoblasts onto the PPF scaffolds.  Alkaline phosphatase activity as a marker for osteogenic differentiation of cell to mature osteoblasts was analyzed.  Our data reveal that osteoblasts maintained their phenotype on PPF scaffolds with and without coatings.  Thus, these scaffolds could be appropriate candidates for our future in vivo studies.[on SciFinder (R)]</style></abstract><issue><style face="normal" font="default" size="100%">2 Suppl</style></issue><notes><style face="normal" font="default" size="100%">MEDLINE AN 2012053473(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, N.I.H., EXTRAMURAL); (RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.))</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Petruskevicius, Raimondas</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Kezys, Darius</style></author><author><style face="normal" font="default" size="100%">Mikolajunas, Marius</style></author><author><style face="normal" font="default" size="100%">Grigaliunas, Viktoras</style></author><author><style face="normal" font="default" size="100%">Virzonis, Darius.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">E-beam lithography of computer generated holograms using fully vectorial 3D beam propagation method.</style></title><secondary-title><style face="normal" font="default" size="100%">Microelectronic Engineering</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">electron beam lithog computer generated holograms fully vectorial 3D</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2010///</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Elsevier B.V.</style></publisher><volume><style face="normal" font="default" size="100%">87</style></volume><pages><style face="normal" font="default" size="100%">2332 - 2337</style></pages><isbn><style face="normal" font="default" size="100%">0167-9317</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">A fully vectorial 3D beam propagation method (BPM) has been applied to obtain a required pattern of computer generated hologram (CGH) with a variable profile of four phase levels.  The computer reconstruction of the CGH image having one and two focal spots was performed by application of the fully vectorial 3D BPM method.  After transferring the CGH by EBL technique an adequate phase profile was obtained.  Inter-level parameter method was developed to obtain the estd. an electron beam dose required for the even topog. patterning.  Using this method, an EBL exposure dose detd. to achieve the required relief amplitude of 1.29 μm was 43 μC/cm2.  The manufd. holograms showed that the overall proposed prodn. process, from the 3D BPM computer simulation to e-beam lithog., can be used to obtain good quality product with reasonable time and computational resources. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">11</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2010:985606(Journal)</style></notes></record></records></xml>