International Journal of Applied Glass Science最新文献

{"title":"Simulation and measurement of ultrathin glass residual stress","authors":"Lianjie Tong,&nbsp;Shimin Liu,&nbsp;Yaming Sun,&nbsp;Jianmin Gu,&nbsp;Shiqing Xu","doi":"10.1111/ijag.16612","DOIUrl":"10.1111/ijag.16612","url":null,"abstract":"<p>Accurate simulation and measurement of the residual stress are pressing needs in ultrathin glass (UTG) industrial stable production. Herein, the heat transfer in an annealing lehr and the residual stresses at different positions along the width of the UTG ribbon were simulated by the finite element method and measured via the Vickers indentation. The residual stresses at 400 and 600 mm to the edge were large, which caused serious production loss. Besides, we conducted molecular dynamics (MD) simulation to reveal the mechanism for residual stress formation. During UTG cooling, the cooling rate of the core is slower than that of the surface. Due to the influence of the relaxation process, the latter would hinder the former's R–O (where R is Na, Mg, Ca, Al, or Si) length contraction, implying that the surface would generate residual compressive stress. The temperature difference between them increases as the cooling rate grows, leading to the residual stress increase. Finally, based on revealing the formation principle of residual stress by MD, the edge electric heatings were set in zone B, and the residual stresses at 400 and 600 mm to the edge are reduced.</p>","PeriodicalId":13850,"journal":{"name":"International Journal of Applied Glass Science","volume":"14 2","pages":"279-287"},"PeriodicalIF":2.1,"publicationDate":"2022-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49315064","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Liquid fragility maximum in lithium borate glass-forming melts related to the local structure","authors":"Oliver L. G. Alderman,&nbsp;Chris J. Benmore,&nbsp;Bryce Reynolds,&nbsp;Brock Royle,&nbsp;Steve Feller,&nbsp;Rick J. K. Weber","doi":"10.1111/ijag.16611","DOIUrl":"10.1111/ijag.16611","url":null,"abstract":"<p>The structure of liquid lithium pyroborate, Li₄B₂O₅ (<i>J</i> = Li/B = 2), has been measured over a wide temperature range by high-energy X-ray diffraction, and compared to that of its glass and borate liquids of other compositions. The results indicate a gradual increase in tetrahedral boron fraction from 3(1)% to 6(1)% during cooling from <i>T</i> = 1271(15) to 721(8) K, consistent with the larger <i>N</i>₄ = 10(1)% found for the glass, and literature ¹¹B nuclear magnetic resonance measurements. van't Hoff analysis based on a simple boron isomerization reaction BØ₃O²^– ⇌ BØO₂^2– yields Δ<i>H</i> = 13(1) kJ mol^–1 and Δ<i>S</i> = 40(1) J mol^–1 K^–1 for the boron coordination change from 4 to 3, which are, respectively, smaller and larger than found for singly charged isomers for <i>J</i> ≤ 1. With these, we extend our model for <i>N</i>₄(<i>J</i>, <i>T</i>), nonbridging oxygen fraction <i>f</i>_nbr(<i>J</i>, <i>T</i>), configurational heat capacity <math>\u0000 <semantics>\u0000 <mrow>\u0000 <msubsup>\u0000 <mi>C</mi>\u0000 <mi>P</mi>\u0000 <mi>conf</mi>\u0000 </msubsup>\u0000 <mrow>\u0000 <mo>(</mo>\u0000 <mi>J</mi>\u0000 <mo>,</mo>\u0000 <mi>T</mi>\u0000 <mo>)</mo>\u0000 </mrow>\u0000 </mrow>\u0000 <annotation>$C_{rm{P}}^{{rm{conf}}}(J,T)$</annotation>\u0000 </semantics></math>, and entropy <i>S</i>^conf(<i>J</i>, <i>T</i>) contributions up to <i>J</i> = 3. A maximum is revealed in <math>\u0000 <semantics>\u0000 <mrow>\u0000 <msubsup>\u0000 <mi>C</mi>\u0000 <mi>P</mi>\u0000 <mi>conf</mi>\u0000 </msubsup>\u0000 <mrow>\u0000 <mo>(</mo>\u0000 <mi>J</mi>\u0000 <mo>,</mo>\u0000 <mi>T</mi>\u0000 <mo>=</mo>\u0000 <msub>\u0000 <mi>T</mi>\u0000 <mi>g</mi>\u0000 </msub>\u0000 <mo>)</mo>\u0000 </mrow>\u0000 </mrow>\u0000 <annotation>$C_{rm{P}}^{{rm{conf}}}(J,T = {T_{rm{g}}})$</annotation>\u0000 </semantics></math> at <i>J</i> = 1, and shown semi-quantitatively to lead to a corresponding maximum in fragility contribution, akin to that observed in the total fragilities by temperature-modulated differential scanning calorimetry. Lithium is bound to 4.6(2) oxygen in the pyroborate liquid, with 2.7(1) bonds centered around 1.946(8) Å and 1.9(1) around 2.42(1) Å. In the glass, <i>n</i><sub>","PeriodicalId":13850,"journal":{"name":"International Journal of Applied Glass Science","volume":"14 1","pages":"52-68"},"PeriodicalIF":2.1,"publicationDate":"2022-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/ijag.16611","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43073883","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Effect of starting materials of nucleation agents on crystallization of CaO–Al2O3–SiO2 glass","authors":"Shingo Machida,&nbsp;Kei Maeda,&nbsp;Ken-ichi Katsumata,&nbsp;Atsuo Yasumor","doi":"10.1111/ijag.16609","DOIUrl":"10.1111/ijag.16609","url":null,"abstract":"<p>The effect of the starting materials of the nucleation agents for glass–ceramics (GCs) was explored. The number of hexagonal platy particles of metastable-CaAl₂Si₂O₈ in CaO–Al₂O₃–SiO₂ (CAS) GCs was increased by changing the sizes of molybdenum oxide (MoO₃) and carbon particles used as starting materials of the nucleation agents. X-ray diffraction patterns indicated that all of GC specimens display reflections attributed to metastable-CaAl₂Si₂O₈ solely. In addition, scanning electron microscopy (SEM) revealed that, compared with the CAS GC with precipitated hexagonal platy particles of metastable-CaAl₂Si₂O₈ (CAS GC-H) prepared using MoO₃ particles with a Brunauer–Emmett–Teller (BET) surface area of 3.5 m²/g and 10–50 μm carbon particles, CAS GC-Hs prepared using MoO₃ particles with a BET surface area of 1.2 m²/g or carbon fibers 10–50 μm in length and ∼5 μm in diameter resulted in approximately a twofold increase in the number of platy particles of metastable-CaAl₂Si₂O₈ and a decrease in the average particle size from 13 to 11 μm. The microstructures of the CAS GC-Hs are closer looks. In addition, no major differences in volume fractions estimated using the binarized SEM images are observed between those GC specimens. These results indicated that the starting materials of nucleation agents affect the crystallization of CAS GCs.</p>","PeriodicalId":13850,"journal":{"name":"International Journal of Applied Glass Science","volume":"14 1","pages":"88-96"},"PeriodicalIF":2.1,"publicationDate":"2022-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/ijag.16609","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45529844","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Assessment of rhenium as a surrogate for technetium in Hanford low activity waste borosilicate glasses: Speciation, solubility, and redox effects","authors":"Hao Gan,&nbsp;David A. McKeown,&nbsp;Xiaogang Xie,&nbsp;Ian L. Pegg","doi":"10.1111/ijag.16610","DOIUrl":"10.1111/ijag.16610","url":null,"abstract":"<p>Re is often used as a nonradioactive surrogate for Tc in borosilicate melts because both elements have similar valences, ionic radii, and coordination environments. Re solubility in high sodium borosilicate waste glasses is sensitive to melter redox conditions; at 1150°C the solubility is ∼4130 ppm under oxidizing atmospheres. Raman, X-ray absorption spectroscopy, and X-ray diffraction show that Re dissolved in waste glasses under oxidizing conditions is in perrhenate tetrahedra; under more reducing conditions, Re⁰ separates from the melt. From air to <math>\u0000 <semantics>\u0000 <msub>\u0000 <mi>P</mi>\u0000 <msub>\u0000 <mi>O</mi>\u0000 <mn>2</mn>\u0000 </msub>\u0000 </msub>\u0000 <annotation>$ {rm P}_{{rm O}_2} $</annotation>\u0000 </semantics></math>∼ 10⁻⁴ atm, both Re⁷⁺ and Tc⁷⁺ are dominant species in borosilicate melts. However, Tc and Re behaviors deviate between <math>\u0000 <semantics>\u0000 <msub>\u0000 <mi>P</mi>\u0000 <msub>\u0000 <mi>O</mi>\u0000 <mn>2</mn>\u0000 </msub>\u0000 </msub>\u0000 <annotation>$ {rm P}_{{rm O}_2} $</annotation>\u0000 </semantics></math>&lt; 10⁻⁴ atm and <math>\u0000 <semantics>\u0000 <msub>\u0000 <mi>P</mi>\u0000 <msub>\u0000 <mi>O</mi>\u0000 <mn>2</mn>\u0000 </msub>\u0000 </msub>\u0000 <annotation>$ {rm P}_{{rm O}_2} $</annotation>\u0000 </semantics></math>&gt; 10⁻⁸ atm, where Tc⁴⁺ becomes dominant, whereas Re⁷⁺ remains stable. Unlike Tc⁴⁺, Re⁴⁺ is not observed in borosilicate melts at 1150°C and associated glasses. Near <math>\u0000 <semantics>\u0000 <msub>\u0000 <mi>P</mi>\u0000 <msub>\u0000 <mi>O</mi>\u0000 <mn>2</mn>\u0000 </msub>\u0000 </msub>\u0000 <annotation>$ {rm P}_{{rm O}_2} $</annotation>\u0000 </semantics></math>= 10⁻⁸ atm, Tc⁴⁺ reduces to Tc⁰, whereas below <math>\u0000 <semantics>\u0000 <msub>\u0000 <mi>P</mi>\u0000 <msub>\u0000 <mi>O</mi>\u0000 <mn>2</mn>\u0000 </msub>\u0000 </msub>\u0000 <annotation>$ {rm P}_{{rm O}_2} $</annotation>\u0000 </semantics></math>= 10⁻⁸ atm, Re⁷⁺ reduces to Re⁰. Re is found to be a good surrogate for Tc under oxidizing conditions (<math>\u0000 <semantics>\u0000 <msub>\u0000 <mi>P</mi>\u0000 <msub>\u0000 <mi>O</mi>\u0000 <mn>2</mn>\u0000 </msub>\u0000 </msub>\u0000 <annota","PeriodicalId":13850,"journal":{"name":"International Journal of Applied Glass Science","volume":"14 1","pages":"97-112"},"PeriodicalIF":2.1,"publicationDate":"2022-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45062538","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Structure-terahertz property relationship in sodium borosilicate glasses","authors":"Nicholas J. Tostanoski,&nbsp;Doris Möncke,&nbsp;Randall Youngman,&nbsp;S. K. Sundaram","doi":"10.1111/ijag.16608","DOIUrl":"10.1111/ijag.16608","url":null,"abstract":"<p>We report, for the first time, an early evidence of structure-terahertz (THz) property relationship for two tie-lines within the sodium borosilicate glass system. The NaBSi series was chosen to study the effect of the substitution of silicon dioxide for boron oxide, whereas the BNaSi series studies the substitution of silicon dioxide for sodium oxide. Nuclear magnetic resonance, infrared absorption, and Raman spectroscopies were used to determine structural changes across both series. THz time-domain spectroscopy was used to record the refractive index over the measured bandwidth. Individual measurements at .502 THz were used as a frequency of focus for comparisons. The foundation for the proposed structure-THz property relationship is based on higher measurable THz refractive index changes correlated to a depolymerized glass network, <i>R</i> &gt; .5, a network consisting of SiO₄ tetrahedra and charge-deficient [BØ₄]⁻ tetrahedra-forming borosilicate danburite and reedmergnerite rings with mixed Si–O–B bridges, and the formation of nonbridging oxygen (nbO) atoms on silicate tetrahedra. A polymerized glass network, <i>R</i> &lt; .5, consists of homonuclear boroxol and silica rings within sodium borate and silicate subnetworks. Calculated and experimental fractions of tetrahedral borate and silicate tetrahedra with one nbO, optical basicity, density, and network connectivity data support the structure-THz property relationship.</p>","PeriodicalId":13850,"journal":{"name":"International Journal of Applied Glass Science","volume":"14 2","pages":"288-306"},"PeriodicalIF":2.1,"publicationDate":"2022-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45529729","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Unveiling the electronic structures and optical properties of alkaline-earth oxides–modified silicate glasses","authors":"Neng Li,&nbsp;Tian Kang,&nbsp;Zuhao Shi,&nbsp;Yuling Liu,&nbsp;Tengfei Deng","doi":"10.1111/ijag.16607","DOIUrl":"10.1111/ijag.16607","url":null,"abstract":"<p>The electronic structure, interatomic bonding, and optical properties of mixed alkaline-earth metal oxides MO (M = Mg, Ca) on amorphous silica glasses were calculated by combined ab initio molecular dynamics and the orthogonalized linear combination of atomic orbitals approaches. With the addition of alkaline-earth metal oxides, the original structural network model is destroyed, nonbridging oxygen is generated, and the covalent bonding is reduced, which reduces the total bond order density for silicate glass. The complex dielectric function plot shows that there are three distinct peaks in the imaginary part of the original silica glasses, and the last two peaks level off with the modification of alkaline earth oxides.</p>","PeriodicalId":13850,"journal":{"name":"International Journal of Applied Glass Science","volume":"14 2","pages":"216-228"},"PeriodicalIF":2.1,"publicationDate":"2022-08-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43547804","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Effect of high pressure in barium disilicate glass investigated by DTA and Raman spectroscopy","authors":"Leonardo Evaristo,&nbsp;Rafael Silveira,&nbsp;Matheus Tissot,&nbsp;Gisele Hippler,&nbsp;Benjamin Moulton,&nbsp;Silvio Buchner","doi":"10.1111/ijag.16606","DOIUrl":"10.1111/ijag.16606","url":null,"abstract":"<p>This work aimed to explore the effect of high pressures at room temperature on the vibrational modes and the thermal properties and stability of barium disilicate glass (BaO-2SiO₂) (BS2). The BS2 was prepared through the conventional melting route at atmospheric pressure. After being submitted to different pressure values (2.5 GPa, 4.0 GPa, and 7.7 GPa) and room temperature, the samples were characterized ex situ by Raman spectroscopy and differential thermal analysis. With this, it is possible to see that the pressure modifies the Raman vibrational modes of the glass, in the region associated with the Si-O-Si symmetrical bending modes. The Si-O symmetrical stretching vibrational modes (Qⁿ) remain unchanged, however there are changes on values of glass transition and decrease crystallization temperature, as well as the parameters of thermal stability of the glass.</p>","PeriodicalId":13850,"journal":{"name":"International Journal of Applied Glass Science","volume":"14 2","pages":"240-246"},"PeriodicalIF":2.1,"publicationDate":"2022-08-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48069660","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Structural characterization of the near-surface region of soda–lime–silica glass by X-ray photoelectron spectroscopy","authors":"Barsheek Roy,&nbsp;Felix Baier,&nbsp;Andreas Rosin,&nbsp;Thorsten Gerdes,&nbsp;Stefan Schafföner","doi":"10.1111/ijag.16604","DOIUrl":"10.1111/ijag.16604","url":null,"abstract":"<p>The structural chemistry of the near-surface region of soda–lime–silica (SLS) glass is described in terms of silicate network connectivity using X-ray photoelectron spectroscopy (XPS). A thorough investigation of O1s and Si2p spectral lines by sequential XPS measurements, accompanied by Ar⁺ sputtering, revealed the variation of concentration of bridging oxygen, non-bridging oxygen (NBO), and hydrous species (SiOH/H₂O) as a function of depth from the glass surface. The O_total/Si atomic ratio was calculated to vary in the range of 2.90–3.74 throughout the depth of sputtering for a total duration of 110 min, while considering each of the aforementioned oxygen speciations in the curve-fitted spectra of O1s orbital. The glass surface up to a depth of 1–3 nm had the highest O_total/Si ratio of 3.74, which was representative for a mechanically weak structure with Q⁰ and Q¹ species, marked by the respective linkages of four and three NBOs per silica tetrahedral unit. This dictates the vital contribution of the hydrous species associated with silanol groups to the near-surface structure of SLS glass.</p>","PeriodicalId":13850,"journal":{"name":"International Journal of Applied Glass Science","volume":"14 2","pages":"229-239"},"PeriodicalIF":2.1,"publicationDate":"2022-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/ijag.16604","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41410589","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Red glass in Kunckel's Ars Vitraria Experimentalis: The importance of temperature","authors":"Márcia Vilarigues,&nbsp;Andreia Ruivo,&nbsp;Thijs Hagendijk,&nbsp;Mario Bandiera,&nbsp;Mathilda Coutinho,&nbsp;Luis C. Alves,&nbsp;Sven Dupré","doi":"10.1111/ijag.16605","DOIUrl":"10.1111/ijag.16605","url":null,"abstract":"<p>The role of the melting conditions and furnaces used to the obtained final colors has always been a question raised when investigating formulations and recipes of historical glasses. The focus of the present work is the reproduction of three recipes of red enamel glass of the manuscript by Neri, <i>L'arte vetraria</i> (1612) following the translation and comments by Kunckel's in <i>Ars Vitraria Experimentalis</i> (1679). The reproductions include the production of each individual compound of the selected recipes following instructions, and the final glass production in electric and wood-fire furnaces to assess the effect of different melting conditions. A multianalytical approach was used to fully characterize the produced samples allowing the study of the enamel chemical composition, color, crystals formations, and thermal properties. The results indicate that no significant color differences may be attributed to the melting conditions. However, it revealed that the samples produced in the electric furnace at 1200°C present a high crystallinity degree and the formation of white crystals at room temperature in a short period of time. The formation of crystals on glass is critical, and historically, to avoid it, these recipes must have been made at temperatures between 1050 and 1100°C.</p>","PeriodicalId":13850,"journal":{"name":"International Journal of Applied Glass Science","volume":"14 2","pages":"201-215"},"PeriodicalIF":2.1,"publicationDate":"2022-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44407484","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"High-temperature near-IR spectral properties and thermal radiation conductivity of (un)colored silicate glass melts","authors":"Anne Jans Faber,&nbsp;Mathi Rongen,&nbsp;Domingos De Sousa Meneses","doi":"10.1111/ijag.16603","DOIUrl":"10.1111/ijag.16603","url":null,"abstract":"<p>Using an emittance technique with a fast CO₂ laser heating of glass samples, the high-temperature absorption spectra in the near-infrared region of ultrapure and colored (Co-, Cu-, Mn-, and Ni-doped) glasses are measured. The effects of higher glass temperatures on these absorption spectra are explained in the framework of the ligand field theory. Thus, the temperature-dependent absorption bands of the previous transition metal ions are assigned to electronic transitions among the ligand field energy levels of these ions. In particular, spectral shifts, spectral broadening, and changes in absorption strength are ascribed to changes in the structural symmetry of the ionic sites in the glass matrix and to changes of the ligand field strength at increasing temperatures.</p><p>Besides, the temperature-dependent Rosseland mean absorptions of the sulfate fined soda lime silicate glass melts, colored with the previous transition metal ions, are derived from the absorption spectra. Combining all the data, semiempirical correlations are derived, which predict the Rosseland thermal radiation properties as a function of glass temperature and of glass redox chemistry. The latter property involves the temperature-dependent concentration of the specific valency of the coloring ions, determined independently, e.g. by a Gibbs minimization redox calculation tool.</p>","PeriodicalId":13850,"journal":{"name":"International Journal of Applied Glass Science","volume":"14 2","pages":"189-200"},"PeriodicalIF":2.1,"publicationDate":"2022-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44458665","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}