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Pre-heating time and exposure duration: Effects on post-irradiation properties of a thermo-viscous resin-composite

机译:预热时间和曝光持续时间:对热粘性树脂复合材料的照射后性能的影响

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Objective. To evaluate the effects of pre-heating time and exposure duration on the degree of conversion (DC), maximum rate of polymerization (RPmax), polymerization shrinkage strain (PS) and surface micro-hardness (VHN) of Viscalor.Methods. Viscalor syringes were pre-heated using a Caps Warmer (VOCO, Germany) in T3 mode (at 68 degrees C) for 30 s (T3-30s) and 3 min (T3-3min) and then the composite paste was extruded into appropriately sized molds. Light irradiation was applied at zero distance from the upper surface with a LED-LCU of mean irradiance 1200 mW/cm(2) for either 20 or 40 s. The real-time polymerization kinetics and DC at 5 min and 24h post-irradiation (DC5min and DC24h) were measured using ATR-FTIR (n = 3). PS was obtained with the bonded-disk technique (n = 3). Top and bottom Vickers micro-hardness (VHNtop and VHNbottom) were measured at 5 min post-irradiation and after 24 h dry storage (n = 5). Data were analysed using one-way ANOVA, two-way ANOVA, independent t-test and Tukey post hoc tests (p 0.05).Results. Polymerization kinetic curves of Viscalor from 0 to 15 min were similar for different pre-heating times and exposure durations. Pre-heated Viscalor (T3-30s and T3-3min) with 40 s exposure had greater VHNtop and VHNbottom than for Viscalor (no heat) (p 0.05). Exposure duration did not significantly affect DC, RPmax and PS (p 0.05). After 24 h storage, DC and VHN increased. Pre-heating did not increase the DC24h, relative to no pre-heating (p 0.05). Two-way ANOVA showed that there was no significant interaction between pre-heating time and exposure duration (p 0.05).Significance. Increasing irradiation time from 20 to 40s did not affect DC, RPmax or PS, but increased VHNtop. Composite pre-heating had no adverse effect through any premature polymerization. For Viscalor, 3 min pre-heating and 20 s irradiation were sufficient to provide adequate hardness, without increasing PS or compromising polymerization kinetics. (C) 2020 The Academy of Dental Materials. Published by Elsevier Inc. All rights reserved.
机译:客观的。为了评估预热时间和暴露持续时间对转化程度(DC)的影响,最大聚合速率(RPMAX),聚合收缩菌株(PS)和Viscalor的表面微硬度(VHN)。方法。使用T3模式(68℃)的盖子加热器(Voco,德国)预加热粘度胶剂注射器30s(T3-30s)和3分钟(T3-3min),然后将复合膏挤出到适当的大小模具。在20或40秒的情况下,从上表面施加光照照射以距上表面的零距离为1200mW / cm(2)的LED-LCU。使用ATR-FTIR(n = 3)测量实时聚合动力学和5分钟后照射后(DC5min和DC24H)。用键合磁盘技术(n = 3)获得PS。在5分钟后测量顶部和底部维氏微型硬度(VHNTOP和VHNBottom),在24小时干燥储存后(n = 5)。使用单向ANOVA,双向ANOVA,独立T检验和Tukey HOC测试进行分析数据(P <0.05)。对于不同预热时间和曝光持续时间,粘度粘剂的聚合动力学曲线与0至15分钟相似。具有40次暴露的预热粘性粘度(T3-30s和T3-3min)具有比粘度胶剂更大的VHNTOP和VHNBottom(无热量)(P <0.05)。暴露持续时间没有显着影响DC,RPMAX和PS(P> 0.05)。 24小时后,DC和VHN增加。预热不增加DC24H,相对于没有预热(P> 0.05)。双向ANOVA表明,预热时间和暴露持续时间之间没有显着的相互作用(P> 0.05)。景点。将20至40秒的辐射时间增加不影响DC,RPMAX或PS,而是增加了VHNTOP。复合预热通过任何过早聚合没有不利影响。对于粘度胶,3分钟预热和20秒的辐射足以提供足够的硬度,而不增加PS或妥协的聚合动力学。 (c)2020牙科材料学院。由elsevier Inc.出版的所有权利保留。

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