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Altering the optical, physical, and TL Dosimetric properties of MgSO4:Dy2O3:B2O3 transparent glass ceramic system: Evaluating the impact of roughness control and ZnO inclusion 改变 MgSO4:Dy2O3:B2O3 透明玻璃陶瓷系统的光学、物理和 TL 剂量特性:评估粗糙度控制和氧化锌加入的影响
Q1 Physics and Astronomy Pub Date : 2024-06-01 DOI: 10.1016/j.nocx.2024.100212
Hayder Salah Naeem , Iskandar Shahrim Mustafa , N.N. Yusof , Muna E. Raypah , Hammam Abdurabu Thabit , M.H.A. Mhareb , Thair Hussein Khazaalah , Nabasu Seth Ezra , Munirah Jamil , G.I. Efenji , Muhammad Fadhirul Izwan bin Abdul Malik

This research examines the influence of surface roughness and the incorporation of ZnO (0.05–0.20 mol%) on the magnesium sulfate: dysprosium oxide: boron oxide (0.1 < x < 0.5) glass ceramic system for dosimeter applications. The parent glasses were prepared using the melt-quenching technique, with all samples melted at 1350 °C, except for B, which was melted at 700 °C. The crystallization, roughness, and optical properties were further determined using X-ray Diffraction (XRD), Atomic Force Microscopy (AFM), and UV–Visible Spectrophotometry, respectively. The glass ceramics were exposed to 2.97 mGy of X-ray radiation ten cycles to assess specific dosimetric capabilities. Among the doped samples, MgSO4:Dy2O3-(0.2B2O3:0.05ZnO) exhibited the most promising performance as a dosimeter. Notably, the Thermoluminescence Dosimetry (TLD) readings of the pre- and post-polished 0.2MDB were 1041.96 nC and 1278.84 nC, respectively, with roughness values of 1.83 nm and 54.7 nm. Similarly, the TLD readings of the pre- and post-polished 0.05MDBZ were 1888.33 nC and 3262.63 nC, respectively, with roughness values of 17.3 nm and 19.8 nm. This work highlights that surface roughness significantly enhances trapping efficiency, underscoring the importance of dosimeter polishing as a beneficial step in enhancing their performance.

本研究探讨了表面粗糙度和氧化锌(0.05-0.20 摩尔%)的加入对用于剂量计的硫酸镁:氧化镝:氧化硼(0.1 < x < 0.5)玻璃陶瓷系统的影响。母玻璃采用熔融淬火技术制备,除 B 样品在 700 °C 下熔化外,其他样品均在 1350 °C 下熔化。分别使用 X 射线衍射 (XRD)、原子力显微镜 (AFM) 和紫外-可见分光光度法进一步测定了结晶、粗糙度和光学特性。对玻璃陶瓷进行了十次 2.97 mGy 的 X 射线照射,以评估其特定的剂量测定能力。在掺杂样品中,MgSO4:Dy2O3-(0.2B2O3:0.05ZnO)作为剂量计的性能最有前途。值得注意的是,抛光前和抛光后的 0.2MDB 的热释光剂量计(TLD)读数分别为 1041.96 nC 和 1278.84 nC,粗糙度值分别为 1.83 nm 和 54.7 nm。同样,抛光前和抛光后的 0.05MDBZ 的 TLD 读数分别为 1888.33 nC 和 3262.63 nC,粗糙度值分别为 17.3 nm 和 19.8 nm。这项研究表明,表面粗糙度可显著提高捕获效率,从而强调了剂量计抛光作为提高其性能的一个有利步骤的重要性。
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引用次数: 0
Amorphous Sb2Te3 nanowires: Synthesis, characterization and size-dependent phase transition behavior 非晶 Sb2Te3 纳米线:合成、表征和尺寸依赖性相变行为
Q1 Physics and Astronomy Pub Date : 2024-01-13 DOI: 10.1016/j.nocx.2024.100206
Chandrasiri A. Ihalawela, Mayur Sundararajan, Gang Chen

Understanding the phase transition behavior of phase-change (PC) material with respect to the scaling effect is essential for the application of PC materials. Among all the PC materials, SbTe binary plays a significant role in the well-known Ge-Sb-Te system. Here we have used an unconventional and cost-effective method to fabricate a wide range of prototypical Sb2Te3 amorphous nanowires (18–220 nm in diameter) using templated electrodeposition. Compositional, morphological, and structural characterization of the amorphous nanowires were performed, and the crystallization temperature of in-template nanowires was measured using a four-probe resistivity meter. We report that the crystallization temperature of amorphous Sb2Te3 nanowires can be tuned with respect to the diameter of the nanowires and a significant increase was observed for the nanowires with diameters ≤35 nm. Our study sheds light on the size-dependent phase transition behavior of PC NWs with implications for further advancement of the PC memory technology.

了解相变(PC)材料在缩放效应方面的相变行为对于 PC 材料的应用至关重要。在所有 PC 材料中,SbTe 二元在著名的 Ge-Sb-Te 系统中发挥着重要作用。在这里,我们采用了一种非常规的、具有成本效益的方法,利用模板化电沉积制造出了多种 Sb2Te3 非晶纳米线原型(直径为 18-220 nm)。我们对非晶纳米线的成分、形态和结构进行了表征,并使用四探针电阻率仪测量了模板内纳米线的结晶温度。我们发现非晶 Sb2Te3 纳米线的结晶温度可随纳米线直径的变化而调整,直径≤35 nm 的纳米线的结晶温度显著升高。我们的研究揭示了 PC 纳米线随尺寸变化的相变行为,对进一步推动 PC 存储技术的发展具有重要意义。
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引用次数: 0
Compositional effects on the chemical durabilities of aluminophosphate glasses: A review 成分对铝磷酸盐玻璃化学耐久性的影响:综述
Q1 Physics and Astronomy Pub Date : 2023-12-23 DOI: 10.1016/j.nocx.2023.100205
Saehwa Chong, Brian J. Riley

Phosphate glasses have a range of applications including as hosts for immobilizing radioactive wastes. Studies have shown that addition of iron and/or aluminum oxides can drastically improve the chemical durability of phosphate glasses where the accurate measurement of chemical durability is one of the most important factors for determining the long-term viability of a given waste form. However, due to inconsistencies with the experimental methods used to generate chemical durability data, comparing and interpreting such data is a tedious task. These variables include the temperature of the test, the specimen form (e.g., coupon, particles), the pressure of the test (e.g., atmospheric pressure, elevated pressure in an autoclave), the exposure time, the exposure medium, and how the loss is documented (e.g., total mass lost, normalized elemental release). This review paper summarizes a large collection of chemical durability tests on aluminophosphate glasses in various studies. In addition, the effects of different oxides on the properties of phosphate glasses are summarized.

磷酸盐玻璃有多种用途,包括作为固定放射性废料的宿主。研究表明,添加铁和/或铝氧化物可大幅提高磷酸盐玻璃的化学耐久性,而准确测量化学耐久性是确定特定废物形式长期可行性的最重要因素之一。然而,由于生成化学耐久性数据的实验方法不一致,比较和解释这些数据是一项繁琐的工作。这些变量包括测试温度、试样形式(如试样板、颗粒)、测试压力(如大气压、高压灭菌器中的高压)、暴露时间、暴露介质以及记录损失的方式(如总质量损失、归一化元素释放)。本综述文件总结了各种研究中对磷酸铝玻璃进行的大量化学耐久性测试。此外,还总结了不同氧化物对磷酸盐玻璃特性的影响。
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引用次数: 0
Nanostructured sol-gel bioactive glass 60S: In vitro study of bioactivity and antibacterial properties in combination with vancomycin 纳米结构溶胶-凝胶生物活性玻璃60S:与万古霉素联用生物活性及抗菌性能的体外研究
Q1 Physics and Astronomy Pub Date : 2023-09-09 DOI: 10.1016/j.nocx.2023.100200
Andrii Kusyak , Vadym Poniatovskyi , Olena Oranska , Dominika Marcin Behunova , Inna Melnyk , Vitalii Dubok , Volodymyr Chornyi , Olexander Bur'yanov , Petro Gorbyk

Nanostructured samples of bioactive glass 60S (BG 60S) with a composition (mol %) of 60% SiO2, 36% CaO, 4% P2O5 were synthesized by the sol-gel method in this research. The bioactivity of the synthesized material was evaluated by in vitro assays. The dynamics of the formation of hydroxyapatite (HA), contributing to the formation of effective bonds with bones and soft tissues during immersion in a simulated body fluid (SBF Kokubo), was evaluated using FTIR, XRD, and SEM-EDX. Changes of the specific surface values, particle size and zeta potential for soaked samples in SBF were also investigated. Determination of the antibacterial activity of BG 60S/vancomycin composites was carried out on test cultures of gram-positive microorganisms being one of the most frequent etiological factors of infectious complications in injuries – Staphylococcus aureus. The effectiveness of the release of the antibiotic was confirmed by determining the zone of inhibition of the test culture using the modified Kirby–Bauer disk diffusion method. It is shown that BG 60S/vancomycin composites are characterized by the preservation of antibacterial properties of vancomycin with its prolonged release, and osteoconductive properties, which are inherent in bioactive sol-gel glass and are promising for practical use in the surgical treatment of bone diseases. Based on the foundings, it is possible to suggest a positive effect of the joint application of BG 60S and vancomycin as part of composites with an effective combination of the functions of bone tissue restoration, treatment and prevention of postoperative infectious complications.

本研究采用溶胶-凝胶法合成了组成(mol%)为60%SiO2、36%CaO、4%P2O5的生物活性玻璃60S(BG 60S)纳米结构样品。通过体外试验评价了合成材料的生物活性。使用FTIR、XRD和SEM-EDX评估了羟基磷灰石(HA)的形成动力学,羟基磷灰石有助于在浸泡在模拟体液(SBF-Kokubo)中期间与骨骼和软组织形成有效结合。研究了SBF中浸泡样品的比表面积、粒径和ζ电位的变化。BG 60S/万古霉素复合物的抗菌活性测定是在革兰氏阳性微生物的测试培养物上进行的,革兰氏阳性微生物是损伤感染并发症最常见的病因之一——金黄色葡萄球菌。通过使用改良的Kirby–Bauer圆盘扩散法确定试验培养物的抑制区,证实了抗生素释放的有效性。研究表明,BG 60S/万古霉素复合材料具有保留万古霉素的抗菌性能及其缓释性和骨传导性能的特点,这是生物活性溶胶凝胶玻璃所固有的,有望在骨病的外科治疗中得到实际应用。基于这些基础,有可能表明BG 60S和万古霉素作为复合材料的一部分联合应用具有骨组织修复、治疗和预防术后感染性并发症的有效组合的积极效果。
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引用次数: 0
Durability evaluation of glasses to immobilize Fukushima (1F) secondary waste using ASTM C1220 (MCC-1) testing 使用ASTM C1220(MCC-1)测试固定福岛(1F)二次废物的玻璃的耐久性评估
Q1 Physics and Astronomy Pub Date : 2023-09-01 DOI: 10.1016/j.nocx.2023.100197
Benjamin Parruzot , Joelle T. Reiser , Xiaonan Lu , Jarrod V. Crum , Richard A. Reyes , Kevin G. Finucane , Keith S. Witwer , Sadaaki Abeta , Masahiro Yoshioka , John D. Vienna

Following the 2011 accident at the Fukushima Daiichi Nuclear Power Plant (1F), contaminated water was treated to remove radionuclides. The water treatment processes generated ∼4500 m3 of secondary wastes including sludges and spent media. Vitrification using GeoMelt® In-Container Vitrification (ICV)™ is a technology being considered for treatment of these wastes. ICV is well suited due to its ability to process a broad range of wastes at high temperatures without the need to pour glass which results in high waste loading and high chemical durability. The objective of this study was to formulate glasses suitable for ICV processing of 1F secondary wastes with high chemical durability. Thirty-six glasses were formulated for different 1F secondary waste blends with loadings ranging from 60 to 92 wt%. Materials Characterization Center durability test number 1 (MCC-1 – ASTM C1220) responses were measured for the glasses in deionized water at 90 °C for 7 to 365 days. Their MCC-1 responses were equal or below those for well-characterized reference waste glasses from US, Japan, and France demonstrating their high durability. The 1F glass MCC-1 data were combined with literature data from US, French, and Japanese high-level waste glasses and a model was fitted to MCC-1 durability response as a function of glass composition. Component effects on MCC-1 responses were discussed in context of glass alteration theory.

2011年福岛第一核电站(1F)发生事故后,对受污染的水进行了处理以去除放射性核素。水处理过程产生了约4500立方米的二次废物,包括污泥和废介质。使用GeoMelt®容器内玻璃化(ICV)™进行玻璃化是一种被考虑用于处理这些废物的技术。ICV非常适合,因为它能够在高温下处理各种废物,而不需要倒玻璃,这导致高废物负荷和高化学耐久性。本研究的目的是制备适合ICV处理具有高化学耐久性的1F二次废物的玻璃。为不同的1F二级废物混合物配制了36个玻璃杯,其装载量从60%到92%不等。材料表征中心耐久性试验编号1 (mc -1 - ASTM C1220)对玻璃在90°C去离子水中放置7至365天的反应进行了测量。他们的mc1反应等于或低于来自美国、日本和法国的具有良好特征的参考废弃玻璃,表明其高耐用性。将1F玻璃的mc1数据与美国、法国和日本高放废弃玻璃的文献数据相结合,并拟合了mc1耐久性响应模型,该模型是玻璃成分的函数。在玻璃蚀变理论的背景下讨论了组分对mc1响应的影响。
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引用次数: 0
Impact of solution pH (5–9) and dissolution products on in vitro behaviour of the bioactive glass S53P4 溶液pH(5-9)和溶解产物对生物活性玻璃S53P4体外行为的影响
Q1 Physics and Astronomy Pub Date : 2023-09-01 DOI: 10.1016/j.nocx.2023.100199
Minna Siekkinen, Markus Engblom, Leena Hupa

The impact of dissolution products on the reaction behaviour of bioactive glasses was explored. Bioactive glass S53P4 particles were immersed in solutions with initial pH of 5–9. After 24 and 72 h, the solution extracts were used for testing unreacted particles. The pH, ion concentrations, and glass surfaces were analysed as functions of immersion time. More Ca, Na, and P dissolved at lower pH (5) than at higher pH (7.4 or 9). The dissolution changed from an incongruent to an apparent congruent with increasing pH. Dissolution products in extracts changed the reaction layer structure on glass particles and led to lower ion release at pH 7.4 and 9. Dissolution increased almost linearly with time in acidic solutions. Silica-rich layer and calcium phosphate were identified on the particles after immersion in all solutions except at pH 9. Local ion concentration variations affected dissolution, leading to nonuniform ion release rates.

探讨了溶解产物对生物活性玻璃反应行为的影响。生物活性玻璃S53P4颗粒浸泡在初始pH为5-9的溶液中。24和72 h后,溶液提取物用于检测未反应颗粒。分析了pH值、离子浓度和玻璃表面随浸泡时间的变化。较低pH(5)下Ca、Na和P的溶解量大于较高pH(7.4或9)下Ca、Na和P的溶解量。随着pH的增加,Ca、Na和P的溶解量由不一致变为明显一致。在酸性溶液中,溶解度几乎随时间线性增加。除pH为9外,在所有溶液中浸泡后,颗粒表面均有富硅层和磷酸钙。局部离子浓度变化影响溶解,导致离子释放速率不均匀。
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引用次数: 1
Short range order structrures of lithium oxy-thiosilicophosphate glasses 氧-硫代硅酸锂玻璃的短程有序结构
Q1 Physics and Astronomy Pub Date : 2023-09-01 DOI: 10.1016/j.nocx.2023.100198
Guantai Hu, Victor M. Torres III, Steve W. Martin

In this work, the compositional series of sulfide and mixed oxysulfide (MOS) glasses 0.56Li2S + 0.44[(0.33-x)PS5/2 + xPO5/2 + 0.67SiS2] was prepared, where 0 ≤ x ≤ 0.33, and their short range order (SRO) structures and their thermal properties have been investigated. Powder x-ray diffraction (XRD) confirmed that the MOS glasses were free from crystallization, with only very minor diffraction peaks in the x = 0 glass being observed. Fourier transform infrared (FT-IR), Raman, and 29Si and 31P magic angle spinning (MAS) NMR spectroscopies were used to identify the SRO structures present in these glasses. These spectra revealed oxygen migration from P to Si during synthesis. Although oxygen was introduced in the form of phosphorus oxide, the majority of the oxygen in these glasses ends up being bonded to silicon, thereby creating sulfur-rich SROs centered by phosphorus and MOS SROs centered by silicon. It was further found that the P-S SRO species were predominantly charged non-bridging sulfurs (NBS). The Si SRO species were comprised of neutral bridging oxygens (BOs) and charged non-bridging oxygens (NBOs) and neutral bridging sulfurs (BS) and charged non-bridging sulfurs with the neutral BO and BS species being larger in fraction than the NBO and NBS. These results suggest that the preponderance of the mobile Li+ cations in these glasses are located near the more negatively charged P centers and not near the more neutrally charged Si centers. The average negative charge of the P SRO structures was found to be ∼ − 3.0 with ∼97% of the phosphorous species in the P0 SRO while the average negative charge of the Si SRO structures was found to be −2.3. Consistent with the creation of the large numbers of NBS on the P and more BOs and BSs on the Si, these values are more negative and more positive, respectively, than the compositionally expected average value of −2.55. Differential scanning calorimetry (DSC) measurements of their glass transition (Tg) and crystallization (Tc) temperatures showed that the Tgs of these glasses are higher than 300 °C and their working ranges, ΔT ≡ Tc – Tg, are ∼100 °C.

在0≤x≤0.33的条件下,制备了0.56Li2S + 0.44[(0.33-x)PS5/2 + xPO5/2 + 0.67SiS2]组成系列的硫化物和混合氧化硫化物(MOS)玻璃,并对其短距离有序(SRO)结构和热性能进行了研究。粉末x射线衍射(XRD)证实了MOS玻璃没有结晶,在x = 0玻璃中只观察到非常小的衍射峰。傅里叶变换红外光谱(FT-IR)、拉曼光谱(Raman)和29Si和31P魔角旋转(MAS)核磁共振光谱(NMR)对这些玻璃中的SRO结构进行了鉴定。这些光谱揭示了氧在合成过程中从P向Si的迁移。虽然氧以氧化磷的形式引入,但这些玻璃中的大部分氧最终与硅结合,从而产生以磷为中心的富硫sro和以硅为中心的MOS sro。进一步发现,P-S SRO主要是带电的非桥接硫(NBS)。Si SRO主要由中性桥接氧(BOs)和带电非桥接氧(NBOs)、中性桥接硫(BS)和带电非桥接硫组成,其中BO和BS的比例大于NBO和NBS。这些结果表明,在这些玻璃中,Li+阳离子的优势位于带负电荷的P中心附近,而不在带中性电荷的Si中心附近。P SRO结构的平均负电荷为~ - 3.0,其中P SRO中有~ 97%的磷,而Si SRO结构的平均负电荷为−2.3。与P上大量的NBS和Si上更多的BOs和BSs的产生相一致,这些值分别比组成预期的平均值- 2.55更负和更正。差示扫描量热法(DSC)对它们的玻璃化转变(Tg)和结晶(Tc)温度的测量表明,这些玻璃的Tgs高于300℃,其工作范围ΔT≡Tc - Tg为~ 100℃。
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引用次数: 0
Ultrafast third-order nonlinear optical response of charge coupled gold nanoparticle-Ge24Se76 heterostructure 电荷耦合金纳米粒子- ge24se76异质结构的超快三阶非线性光学响应
Q1 Physics and Astronomy Pub Date : 2023-09-01 DOI: 10.1016/j.nocx.2023.100196
Vinod Kumar , Rituraj Sharma , Abhishek Bhatt , I. Csarnovics , Petr Nemec , H. Jain , K.V. Adarsh

The donor-acceptor interaction of a charge-coupled heterostructure encompassing a metal and an amorphous semiconductor subjected to a laser field has many potential applications in the realm of nonlinear optics. In this work, we fabricate an electron donor gold nanoparticle (AuNP) and acceptor amorphous Ge24Se76 heterostructure on a quartz substrate using a sequential thermal evaporation technique. In this charge coupled heterostructure, we demonstrate the ultrafast third-order nonlinear absorptive and refractive response, and their sign reversal compared to pristine Ge24Se76. Enhanced optical nonlinearity in these heterostructures of varying plasmonic wavelengths is due to charge transfer, verified by the Raman spectroscopy. Further, the ultrafast transient absorption measurements support the thesis of charge transfer in the AuNP/Ge24Se76 heterostructure. These findings open up exciting opportunities for developing novel device technologies with far-reaching applications in nonlinear optics.

由金属和非晶半导体组成的电荷耦合异质结构在激光场作用下的施主-受主相互作用在非线性光学领域有许多潜在的应用。在这项工作中,我们利用顺序热蒸发技术在石英衬底上制备了电子供体金纳米颗粒(AuNP)和受体非晶Ge24Se76异质结构。在这种电荷耦合异质结构中,我们证明了超快的三阶非线性吸收和折射响应,以及它们与原始Ge24Se76相比的符号反转。在这些异质结构中,不同等离子体波长的光学非线性增强是由于电荷转移,拉曼光谱证实了这一点。此外,超快瞬态吸收测量支持了AuNP/Ge24Se76异质结构中电荷转移的理论。这些发现为开发在非线性光学中具有深远应用的新型器件技术开辟了令人兴奋的机会。
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引用次数: 0
An overview on the effect of dissolved water on the viscosity of soda lime silicate melts 综述了溶解水对钠钙硅酸盐熔体粘度的影响
Q1 Physics and Astronomy Pub Date : 2023-09-01 DOI: 10.1016/j.nocx.2023.100195
J. Deubener , H. Behrens , R. Müller

In this review article, the impact of dissolved water on the viscous properties of soda lime silicate melts is addressed against the background of the upcoming switch from natural gas to hydrogen combustion. This change will lead to an increase in the total water content of the glasses by up to 0.4 mol%. In order to better define possible influences of water speciation, water-rich glasses were synthesised under increasing pressure up to the kbar range. It is shown that a distinction must be made between the influence of dissolved OH-groups and H2O-molecules in order to accurately reflect the dependence of isokom temperatures on water content. In addition, an increase of one order of magnitude in the tolerance to higher deformation rates was observed for the range of expected increased water contents during isothermal deformation processes, which is based on the time-temperature superposition principle, i.e. congruent flow curves were determined under isokomal conditions.

在这篇综述文章中,在即将从天然气燃烧转向氢燃烧的背景下,讨论了溶解水对钠钙硅酸盐熔体粘性特性的影响。这种变化将导致玻璃杯的总含水量增加0.4 mol%。为了更好地确定水形成的可能影响,在升高至kbar范围的压力下合成了富水玻璃。结果表明,必须区分溶解的oh -基团和h2o -分子的影响,以便准确地反映isoom温度对含水量的依赖。此外,在等温变形过程中,基于时间-温度叠加原理,即在等温条件下确定了一致的流动曲线,在期望增加的含水量范围内,对更高变形速率的容忍度增加了一个数量级。
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引用次数: 1
Ultrafast third-order nonlinear optical response of charge coupled gold nanoparticle-Ge24Se76 heterostructure 电荷耦合金纳米粒子- ge24se76异质结构的超快三阶非线性光学响应
Q1 Physics and Astronomy Pub Date : 2023-07-06 DOI: 10.1016/j.nocx.2023.100196
Vinod Kumar, Rituraj Sharma, Abhishek Bhatt, I. Csarnovics, P. Němec, H. Jain, K. V. Adarsh
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引用次数: 0
期刊
Journal of Non-Crystalline Solids: X
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