Structural color of metallic glass through picosecond laser

The alteration in surface color of metallic glasses(MGs)holds great significance in the context of microstructuredesign and commercial utility.It is essential to accurately describe the structures that are formed during the laser and colorseparation processes in order to develop practical laser coloring applications.Due to the high oxidation sensitivity of Labasedmetallic glass,it can broaden the color range but make it more complex.Structure coloring by laser processing on thesurface of La-based metallic glass can be conducted after thermoplastic forming.It is particularly important to clarify therole of structure and composition in the surface coloring process.The aim is to study the relationship between amorphoussurface structural color,surface geometry,and oxide formation by laser processing in metallic glasses.The findings revealedthat the periodic structure primarily determines the surface color at laser energy densities below 1.0 J/mm^(2).In contrast,thesurface color predominantly depends on the proportion of oxides that are formed when energy densities exceed 1.0 J/mm^(2).Consequently,this study provides a novel concept for the fundamental investigation of laser coloring and establishes a newavenue for practical application.

NMR Study on Structural Characteristics of Rare Earth Doped Boro-Alumino-Silicate Glasses

The structural characteristics of Re2O3 doped B2O3-Al2O3-SiO2 glasses and factors such as the component and heat-treating conditions affecting the glass structure were investigated by magic angle spin nuclear magnetic resonance （MAS NMR） spectroscopy and differential thermal analysis （DTA）. It is found that, in B2O3-Al2O3-SiO2 glass, the boron （4）, and Al（5）, Al（6） changes to Al（4）. On the other hand, compared with Ba^2＋ , RE^3＋ can accumulate the boron network because of its higher field strength, which results in a large network structure. With the increase of samarium oxide, the silicate coordination Qa（3T） will have predominance gradually. Heat-treatment has little effect on the boron and aluminum coordination sites in the glass structure.

Influence of Al_(2)O_(3)/SiO_(2) Ratio on the Structure and Properties of Na^(+)/K^(+)Ion Exchange Na_(2)O-MgO-Al_(2)O_(3)-SiO_(2) Glasses

In this work,the structure,viscosity and ion-exchange process of Na_(2)O-MgO-Al_(2)O_(3)-SiO_(2) glasses with different Al_(2)O_(3)/SiO_(2) molar ratios were investigated.The results showed that,with increasing Al_(2)O_(3)/SiO_(2) ratio,the simple structural units Q_(1) and Q_(2) transformed into highly aggregated structural units Q_(3) and Q_(4),indicating the increase of polymerization degree of glass network.Meanwhile,the coefficient of thermal expansion decreased from 9.23×10^(-6)℃^(-1) to 8.88×10^(-6)℃^(-1).The characteristic temperatures such as melting,forming,softening and glass transition temperatures increased with the increase of Al_(2)O_(3)/SiO_(2) ratio,while the glasses working temperature range became narrow.The increasing Al_(2)O_(3)/SiO_(2) ratio and prolonging ion-exchange time enhanced the surface compressive stress(CS)and depth of stress layer(DOL).However,the increase of ion exchange temperature increased the DOL and decreased the CS affected by stress relaxation.There was a good linear relationship between stress relaxation and surface compressive stress.Chemical strengthening significantly improved the hardness of glasses,which reached the maximum value of(622.1±10)MPa for sample with Al_(2)O_(3)/SiO_(2) ratio of 0.27 after heat treated at 410℃for 2 h.

Effect of Fe_(2)O_(3)on the Structure,Physical Properties and Crystallization of CaO-Al_(2)O_(3)-SiO_(2)Glass

The calcium aluminosilicate-based glasses(CaO-Al_(2)O_(3)-SiO_(2),CAS)with different Fe_(2)O_(3)content(0.10wt%,0.50wt%,0.90wt%,and 1.30wt%)were prepared by traditional melt-quenching method.The glass network structure,thermal and mechanical properties,and crystallization behavior changes were investigated by nuclear magnetic resonance spectrometer,Fourier-transform infrared spectro-photometer,X-ray diffractometer,differential scanning calorimetry and field emission scanning electron microscope measurements.The change of Q^(n)in glass structures reveals the glass network connectivity decreases due to the increasing content of Fe_(2)O_(3)addition,resulting in the increasing of non-bridging number in glass structure.The glass densities slightly rise from 2.644 to 2.681 g/cm^(3),while Vickers’s hardness increases at first,from 6.469 to 6.901 GPa,then slightly drops to 6.745 GPa,with Fe_(2)O_(3)content increase.There is almost no thermal expansion coefficient change from different Fe_(2)O_(3)content.The glass transmittance in visible range gradually decreases with higher Fe_(2)O_(3)content,resulting from the strong absorption of Fe^(2+)and Fe^(3+)ions.The calculated activation energy from thermal analysis results first decreases from 282.70 to 231.18 kJ/mol,and then increases to 244.02 kJ/mol,with the Fe_(2)O_(3)content increasing from 0.10wt%to 1.30wt%.Meanwhile,the maximum Avrami constant of 2.33 means the CAS glasses exhibit two-dimensional crystallization.All of the CAS glass-ceramics samples contain main crystal phase of anorthite,the microstructure appears lamellar and columnar crystals.

Influence of Ultra Fine Glass Powder on the Properties and Microstructure of Mortars

This study focuses on the effect of ultrafine waste glass powder on cement strength,gas permeability and pore structure.Varying contents were considered,with particle sizes ranging from 2 to 20μm.Moreover,alkali activation was considered to ameliorate the reactivity and cementitious properties,which were assessed by using scanning electron microscopy(SEM),energy-dispersive X-ray spectroscopy(EDS),and specific surface area pore size distribution analysis.According to the results,without the addition of alkali activators,the performance of glass powder mortar decreases as the amount of glass powder increases,affecting various aspects such as strength and resistance to gas permeability.Only 5%glass powder mortar demonstrated a compressive strength at 60 days higher than that of the control group.However,adding alkali activator(CaO)during hydration ameliorated the hydration environment,increased the alkalinity of the composite system,activated the reactivity of glass powder,and enhanced the interaction of glass powder and pozzolanic reaction.In general,compared to ordinary cement mortar,alkali-activated glass powder mortar produces more hydration products,showcases elevated density,and exhibits improved gas resistance.Furthermore,alkali-activated glass powder mortar demonstrates an improvement in performance across various aspects as the content increases.At a substitution rate of 15%,the glass powder mortar reaches its optimal levels of strength and resistance to gas permeability,with a compressive strength increase ranging from 28.4%to 34%,and a gas permeation rate reduction between 51.8%and 66.7%.

Effect of melt cooling rate on glass transition kinetics and structural relaxation of Vit1 metallic glass

The thin ribbons and the bulk cylindrical rods with diameters of 2 mm and 10 mm of the Vit1 metallic glass(MG)were prepared by the single roller melt spinning method and the copper mold injection casting method,respectively.The cooling rates of the samples during melt solidification were evaluated.The glass transition behaviors of three groups of MG samples with different solidification cooling rates were studied by differential scanning calorimetry(DSC)at different heating rates.The effects of melt cooling rate on the glass transition kinetic parameters such as apparent activation energy(E)and fragility parameter(m)of the Vit1 MG were studied using the Kissinger and the Vogel-Fulcher-Tammann(VFT)equations.Additionally,the structural relaxation enthalpy(ΔHrel)of three groups of MG samples was quantitatively analyzed by DSC through multi-step temperature rise and fall measurements.Results show that the melt cooling rate(R)has a significant effect on the glass transition kinetics and the structural relaxation of the Vit1 MG.As R decreases in the order of magnitude,the glass transition temperature(Tg),E,m,andΔHrel of the Vit1 MG gradually decreases.Furthermore,in the range of the experimental cooling rates,E,m,andΔHrel all have an approximately linear relationship with lgR.

Synthesis and structural characterization of macroporous bioactive glass

Porous sol-gel glass of CaO-SiO2-P2O5 system with macropores larger than 100 μm was prepared by adding stearic acid as pore former when the sintering was carried out at 700 ℃ for 3h.The sol-gel porous glass shows an amorphous structure. The diameter of the pore created by pore former varies from 100 to 300 μm, and macroporous glass has a narrow and small pore size distribution in mesoporous scale. The porosity and pore size of macroporous bioactive glass can be controlled.

Structural evolution study of additions of Sb_2S_3 and CdS into GeS_2 chalcogenide glass by Raman spectroscopy

The structures of pseudo-binary GeS2-Sb2S3, GeS2-CdS, Sb2S3-CdS, and pseudo-ternary GeS2-Sb2S3-CdS chalco- genide systems are systematically investigated by Raman spectroscopy. It is shown that a small number of [S3Ge-GeS3] structural units （SUs） and -S-S-/S8 groups exist simultaneously in GeS2 glass which has a three-dimensional continuous network backbone consisting of cross-linked corner-sharing and edge-sharing [GeS4] tetrahedra. When Sb2S3 is added into GeS2 glass, the network backbone becomes interconnected [GeS4] tetrahedra and [SbS3] pyramids. Moreover, Ge atoms in [S3Ge-GeS3] SUs tend to capture S atoms from Sb2S3, leading to the formation of [S2Sb-SbS2] SUs. When CdS is added into GeS2 glass, [Cd4GeS6] polyhedra are formed, resulting in a strong crystallization tendency. In addition, Ge atoms in [S3Ge-GeS3] SUs tend to capture S atoms from CdS, resulting in the dissolution of Ge-Ge bond. Co-melting of Sb2S3 or CdS with GeS2 reduces the viscosity of the melt and improves the homogeneity of the glass. The GeS2 glass can only dissolve up to 10-mol% CdS without crystallization. In comparison, GeS2-SbzS3 glasses can dissolve up to 20-mo1% CdS, implying that Sb2S3 could delay the construction of [Cd4GeS6] polyhedron and increase the dissolving amount of CdS in the glass.

STRUCTURAL REARRANGEMENT AND PROPERTIES OF QUENCHED TITANATE GLASSES REHEATED AT T_g

The structural rearrangement of quenched titanate glasses reheated at T-g was investigated by ESR and IR spectroscopies. Front the ESR observations it is suggested that the structure was readjusted and became more compact after the heat-treatment. A removal of residual vacancies is related to the diffusion of oxygen ions. The combination of more oxygen with titanium ions to form titanium-oxygen polyhedra and the transformation of boron-oxygen groups are confirmed front IR spectra. Some physical properties are improved after heating.

Structural Change of SiO_(2) Glass Under High Pressure - a Molecular Dynamics Study

Pressure-induced structural transition in SiOa glass at 300 K.has been investigated by molecular dynamics simulation,The compression of SiO_(2) glass appears to be accommodated by three processes occuring in our calcul&tion.Below 10 GPa,the Si-Ot O-O and Si-Si bond dist&nces decrease with compression.Also in this pressure,region the O-Si-O angle is always peaked at about 109°.Above 10 GPa,the Si-O bond distance increase quickly with compression and the O-Si-O angle deviates from 109°.At about 46 GPa,the structural information shows that the coordination number of Si becones six.Then,the structural behavior of SiO_(2) glass becomes normal with further compression.

Structural origin for composition-dependent nearest atomic distance in Cu–Zr metallic glass

We systematically investigate the structures of Cu–Zr metallic glass(MG) by varying the Cu concentration in classic molecular-dynamics simulation. From the pair distribution functions(PDFs), it is found that the nearest atomic distance between Zr atom and Zr atom increases significantly after adding Cu, which is related to the composition-dependent coordination behavior between Cu atom and Zr atom in the nearest neighbors. The portion of PDF related to the nearest connection is decomposed into the contributions from quadrilateral structure, pentagonal structure, hexagonal structure,and heptagonal bipyramid structure. Although the population of denser structures, i.e. 5-, 6-, and 7-number sharing ones,increases with Cu addition increasing, the connection distances between the central atoms in all these bipyramids increase for Zr–Zr pairs, leading to the expansion of Zr–Zr nearest atomic distance. These results unveil the effect of the interplay between chemical interaction and geometric packing on the atomic-level structure in Cu–Zr metallic glasses.

Morphological and Structural Investigations on Iron Borosilicate Glasses

Borosilicate glasses and glass ceramics in the system 30Na2O-2Al2O3-25SiO2-xFe2O3(43-x)B2O3 (x = 0 - 20 mol%) have been prepared and studied by distinguished techniques. X-ray diffraction (XRD), transmission electron microscope (TEM), electron diffraction pattern (EDP) and SEM experiments are applied to explore the induced structural changes. Nanometer-sized species of polycrystalline structure are formed particularly in low Fe2O3 containing glasses. The size of the crystallites is found to depend on Fe2O3 concentrations. It is ranged from 10 to 33 nanometers. Structurally, these materials are suggested to contain different components, crystalline component and an interfacial component which situated between the crystallized domains. Presence of these components affects the atomic arrangement without short- or long-range order. An intermediate range ordered structure is dominant in glass ceramics of Fe2O3 2O3 concentration, since more disordered structure of lower size is present. These structural changes are found to be connected with the role of Fe2O3 and Na2O in glasses. Na2O is the strong glass modifier in the studied composition region, while Fe2O3 is consumed also as a modifier in composition of 2O3 is mainly dominant in the composition region of higher iron oxide concentration (8 - 20 mol%).

Relationship of glass forming ability and local structural properties of liquid Cu-Zr alloys

Molecular dynamics(MD) simulations were performed to investigate the glass forming ability(GFA) and microscopic structural properties of liquid Cu-Zr alloys.Based on the analysis of composition dependences of the reduced glass transition temperatures and the excess volume,we found that the Cu-Zr glasses have the largest GFA at Cu65Zr35 composition.To get more detailed information of local structure,we calculated the pair correlation functions,partial pair correlation functions,the excess entropy,chemical order parameter,coordination number,and Voronoi index of Cu-Zr liquids.We found that there exists an obvious and close relationship among the GFA,the excess entropy calculated using the total pair correlation functions,chemical order parameters,and some Cu centered cluster with Voronoi index <0,2,8,1> and Zr centered cluster with Voronoi index <0,3,6,4>,which all have nonlinear dependences on Cu/Zr concentration and have extreme values at liquid Cu65Zr35 composition.

Structural, Morphology and Some Optical Properties of Chalcogenide Ga_80-xSe_xTe₂₀(Where x = 10%, 15% and 20%) Glassy Material

Ga80-xSexTe20 amorphous system was prepared by conventional technique. Structural, morphology and optical properties have been investigated. X-ray diffraction (XRD) patterns reveal the non-crystalline nature of the prepared sample. Differential thermal analysis (DTA) traces indicate the presence glass transition temperature Tg?for all samples below 500°C. Addition Tg values increases by increasing Se content. Energy dispersive X-ray spectroscopy (EDX) data shows good agreement with actual composition. Moreover, surface characterization was achieved by scanning electron microscope (SEM). The patterns confirmed the non-crystalline nature. In order to analyze the data, the cohesive energy C.E was calculated by all three composition optical properties that have been investigated in the wavelength range 500 - 2500 nm. Reflectivity R and transmitivity T spectrum were used to estimate the band gap energy using UV-Visible absorption spectrum. It is worthy mention that the optical band gap follows the Tg and cohesive energy behavior, where it increases by increasing Se content.

Structural Changes by Thermal Treatment up to Glass Obtention of P₂O₅-Na₂O-CaO-SiO₂Compounds with Bioglass Composition Types

P2O5-Na2O-CaO-SiO2 compounds are the base of certain glass types. Glasses are solids obtained by fast cooling of melted mix of certain compounds. Different compositions give origin to many products with a variety of applications such as: bottles, coatings, windows, tools for chemical industry, laboratory equipment, optics, as bioceramics, etc. The aim of this work was to analyze structural changes of different composition in the P2O5-Na2O-CaO-SiO2 systems thermally treated up to 1250?C, that is to say, before glass formation, by X ray diffraction. Intermediate and final developed phases up to 1100?C thermal treatment in samples were generated as a function of Na2O/CaO (1 and 1.62) and P2O5/Na2O ratios (0, 0.2 and 0.245). High-and low-combeites, calcium and sodium-calcium silicate were found at the highest studied temperature.

Structural and Magnetic Properties of MnO-P_2O_5-PbO Glasses

The xMnO(100-x)[2P2O5.PbO] glasses were prepared with MnO concentration being in the range of 0≤x≤50 mole fraction and were investigated by EPR spectroscopy and magneticsusceptibility measurements. Octahedral symmetric sites tetragonally distorted were detected for x≤5 mole fraction MnO. Only Mn2+ ions were identified in these glasses, involved in dipoledipole interactions

Structural Characterization of Novel Cerium Phosphate Glass Ionomer Cements (GICs) Doped with GaCl (Phthalocyanine)

Cerium Pyrophosphate glass is prepared and investigated by different structural techniques. Resin modified glass ionomer cements (RGICs) of pyro cerium phosphate (40CeO2-60P2Os) composition doped with different concentrations from GaCl Phthalocyanine (C32H16ClGaN8) have been also prepared and studied for the first time. Different techniques have been applied to shed?light on the structural changes induced upon addition of GaCl-Phthalocyanine. The corresponding changes in material structure are widely approved by results of 31P magic angle spinning nuclear magnetic resonance (MAS-NMR), X-Ray diffraction and FTIR spectroscopy. The network structure of both base glass and GIC free from C32H16ClGaN8 is confirmed to be amorphous. Doping even with little concentration from GaCl-Phthalocyanine leads to changing the network structure from amorphous to a highly crystalline one. Formulation of GaCl-Phthalocyanine with water soluble acid leads to monocrystalline structure due to monoclinic lattice structure of Phthalocyanine. Carbonated hydroxyl cerium and gallium phosphate structural phases are evidenced to be formed upon GaCl-Phthalocyanine addition. Presence of such bioactive phases can support that the prepared GICs of considerable C32H16ClGaN8 concentration (1 and 1.5 mol%) can be applied as biocompatible materials used in biodental applications. The morphologies of some selected samples were characterized by SEM. The micrographs have revealed that formulating of cerium phosphate powder of the amorphous glass with polymeric acid successfully led to the formation of CePO4-H2O nanofibrous bundles. But formulation with GIC containing GaCl-Phthalocyanine can simply form co-aligned and elongated nanofibers (15 - 40 nm thick and up to ca. 1.2 m long). The formed nanofibers are mainly consisted of hydrated and carbonated CePO4 and GaPO4 nanocrystals. The hardness of the cemented material increases with increasing GaCl-Phthalocyanine concentrations.

Structural Glass Fiber Reinforced Concrete for Slabs on Ground

This paper aims to contribute to the classification and specification of glass fiber reinforced concrete (GFRC) and to deal with the question if structural glass fiber reinforced concrete as a special kind of glass fiber reinforced concrete is suited for use in load-bearing members. Despite excellent material properties, the use of glass fibers in a concrete matrix is carried out so far only in non- structural elements or as a modification for the prevention of shrinkage cracks. The aim of re- search at the University of Applied Sciences in Leipzig is the use of alkali-resistant macro glass fibers as concrete reinforcement in structural elements as an alternative to steel fiber reinforcement. Slabs on ground, as an example for structural members, provide a sensible application for the new material because they can be casted as load bearing and non-load bearing and are mostly made of steel fiber reinforced concrete. In the future, structural glass fiber reinforced concrete shall provide a simple and visually appealing alternative to conventional steel bar or steel fiber reinforced concrete. The glass fibers can also be used in combination with conventional reinforcing bars or mat reinforcements. Initial investigations have announced some potential.

Molecular dynamics simulation of relationship between local structure and dynamics during glass transition of Mg_7Zn_3 alloy

The rapid solidification process of Mg7Zn3 alloy was simulated by the molecular dynamics method. The relationship between the local structure and the dynamics during the liquid-glass transition was deeply investigated. It was found that the Mg-centered FK polyhedron and the Zn-centered icosahedron play a critical role in the formation of Mg7Zn3 metallic glass. The self-diffusion coefficients of Mg and Zn atoms deviate from the Arrhenius law near the melting temperature and then satisfy the power law. According to the time correlation functions of mean-square displacement, incoherent intermediate scattering function and non-Gaussian parameter, it was found that the β-relaxation in Mg7Zn3 supercooled liquid becomes more and more evident with decreasing temperature, and the α-relaxation time rapidly increases in the VFT law. Moreover, the smaller Zn atom has a faster relaxation behavior than the Mg atom. Some local atomic structures with short-range order have lower mobility, and they play a critical role in the appearance of cage effect in theβ-relaxation regime. The dynamics deviates from the Arrhenius law just at the temperature as the number of local atomic structures begins to rapidly increase. The dynamic glass transition temperature （Tc） is close to the glass transition point in structure （TgStr）.