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Query: UMLS:C0432222 (SEM)
 47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The purpose of this in vitro study was to determine the shear bond strength [SBS] of Syntac to dentin; to determine the quantitative microleakage (ML) of Class V preparations in dentin restored with the Syntac system; and to study resin penetration into the dentin tubules by SEM. The occlusal surfaces of 30 extracted human mandibular permanent first and second molars were ground wet on 600-grit SiC to expose the superficial dentin. The teeth were embedded in brass tooth cups with cold cure acrylic resin. The Syntac Primer and the Syntac Adhesive were applied to the demarcated bonding sites as recommended by the manufacturer. Radiopaque Heliomolar was transferred to the opening in a split teflon mold in three increments, each compressed firmly and cured for 40 seconds. Fifteen of the test specimens were disassembled 60 seconds after cure [A], and the remainder 15 min after cure and the latter specimens stored in saline at 37 degrees C for 24 hours [B]. A shear load was applied at a crosshead speed of 0.5 mm/min, the SBS calculated and expressed in MPa. The data were analyzed by a two-sample t-test. Class V cavities were prepared on the facial surfaces of 15 human premolars and restored. The ML was determined quantitatively by a spectrophotometric dye recovery method and expressed as microgram dye/restoration. The mean +/- SD of the SBS in MPa were: A: 10.14 +/- 2.80; B: 15.90 +/- 2.13 and the ML 2.57 +/- 0.97 microgram dye/restoration. The SBS recorded after 24 hours storage was significantly greater than after 1 minute (P < 0.0001). The bonding resin penetrated deeply into the dentin tubules.
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PMID:Evaluation of the Syntac bonding system. 832 56

The present paper mainly reports a new method to synthesize long afterglow photoluminescent material BaAl2O4:Eu2+, Dy3+. Al(NO3)3.9H2O, Ba(NO3)2, urea, RE(NO3) 3(RE==Eu, Dy) were employed as raw materials, the admixture of H2O/n-butanol and H2O/n-butanol/SBS were used as medium, then BaAl2O4:Eu2+, Dy3+ phosphor was achieved by calcining the precursor, which was synthesized by hydrothermal method, at 130 degrees C under reduction atmosphere. The TEM and SEM were used to analyse the morphology and BaAl2O4:Eu2+, Dy3+ synthesized by annealing at 1300 degrees C are all nanorods. The excitation and emission spectra of the phosphor indicated that all of them are broad band, and the main emission peak is around 498 nm, which is due to 5d-->4f transition of Eu2+. The state-solid synthesis of the long afterglow phosphor BaAl2O4:Eu2+, Dy3+ generally requires a high calcination temperature, so the products are easily agglomerated, and in this paper the hydrothermal solvothermal synthesis was used, so the synthesized products calcined at 130 degrees degrees C still present well-dispersed rod structure, need not milling, and display well luminescence performance. The authors compared the two different conditions of experiment, and found that under the condition without surfactant the authors can still get well-dispersed rod structure of BaAl2O4:Eu2+, Dy3+. The method is hopeful to be used in synthesizing other alkali-earth aluminate and silicate and other luminescent materials.
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PMID:[Synthesis and properties of nanorod-long afterglow BaAl2O4:Eu2+, Dy3+ phosphor]. 2030 73