scholarly journals Formation of Defects in Solid-Liquid Reaction-Diffusion Bonding of Copper Using a Tin Film Interlayer

2017 ◽  
Vol 6 (5) ◽  
pp. 188-194
Author(s):  
Shinji FUKUMOTO ◽  
Toshinari KIZAWA ◽  
Michiya MATSUSHIMA ◽  
Hiroaki HOKAZONO ◽  
Kozo FUJIMOTO
Keyword(s):  
Diffusion Bonding ◽  
Reaction Diffusion ◽  
Tin Film ◽  
Liquid Reaction ◽  
Solid Liquid

Reaction–diffusion bonding of CVD SiC using CrAl thin coating layer

2021 ◽  
Author(s):  
Hyeon-Geun Lee ◽  
Daejong Kim ◽  
Weon-Ju Kim ◽  
Ji Yeon Park
Keyword(s):  
Diffusion Bonding ◽  
Coating Layer ◽  
Reaction Diffusion ◽  
Thin Coating

Nickel-tin solid-liquid inter-diffusion bonding

2014 ◽  
Vol 15 (1) ◽  
pp. 143-147 ◽  
Author(s):  
Chen-Chiang Yu ◽  
Pei-Chen Su ◽  
Seoung Jai Bai ◽  
Tung-Han Chuang
Keyword(s):  
Diffusion Bonding ◽  
Solid Liquid

scholarly journals Superplastic Forming and Reaction Diffusion Bonding Process of Hollow Structural Component for Mg-Gd-Y-Zn-Zr Rare Earth Magnesium Alloy

Metals ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 152
Author(s):  
Peng Peng ◽  
Shaosong Jiang ◽  
Zhonghuan Qin ◽  
Zhen Lu
Keyword(s):  
Mechanical Properties ◽  
Diffusion Bonding ◽  
Structural Component ◽  
Bonding Temperature ◽  
Reaction Diffusion ◽  
Superplastic Forming ◽  
Tensile Tests ◽  
Interface Roughness ◽  
Size Growth ◽  
Cu Interlayer

This work fabricated a double hollow structural component of Mg-8.3Gd-2.9Y-0.8Zn-0.2Zr alloy by superplastic forming (SPF) and reaction-diffusion bonding (RDB). The superplastic characteristic and mechanical properties of Mg-8.3Gd-2.9Y-0.8Zn-0.2Zr alloy sheets at 250–450 °C were studied. Tensile tests showed that the maximum elongation of tensile specimens was about 1276.3% at 400 °C under a strain rate of 1 × 10−3 s−1. Besides, the effect of bonding temperature and interface roughness on microstructure and mechanical properties of the reaction diffusion-bonded joints with a Cu interlayer was investigated. With the increase of temperature, the diffusion coefficient of Cu increases, and the diffusion transition region becomes wider, leading to tightening bonding of the joint. However, the bonding quality of the joint will deteriorate due to grain size growth at higher temperatures. Shear tests showed that the highest strength of the joints was 152 MPa (joint efficiency = 98.7%), which was performed at 460 °C.

scholarly journals Improved Understanding of the Sulfidization Mechanism in Amine Flotation of Smithsonite: An XPS, AFM and UV–Vis DRS Study

Minerals ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 370 ◽  
Author(s):  
Ruizeng Liu ◽  
Bin Pei ◽  
Zhicheng Liu ◽  
Yunwei Wang ◽  
Jialei Li ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
High Reactivity ◽  
Phase Imaging ◽  
Solid Product ◽  
Force Microscopy ◽  
Atomic Force ◽  
Liquid Reaction ◽  
Solid Liquid ◽  
Heterogeneous Solid

Sulfidization is required in the amine flotation of smithsonite; however, the sulfidization mechanism of smithsonite is still not fully understood. In this work, X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM) and UV–vis diffuse reflectance spectroscopy (UV–vis DRS) were used to characterize sulfidized and unsulfidized smithsonite. The XPS and UV–vis DRS analyses showed that smithsonite sulfidization is a transformation of ZnCO3 to ZnS on the smithsonite surfaces. However, this transformation is localized, resulting in the coexistence of ZnCO3 and ZnS or in the formation of ZnS island structures on the sulfidized smithsonite surfaces. AFM height imaging showed that sulfidization can substantially change the surface morphology of smithsonite; in addition, AFM phase imaging demonstrated that sulfidization occurs locally on the smithsonite surfaces. Based on our findings, it can be concluded that smithsonite sulfidization is clearly a heterogeneous solid–liquid reaction in which the solid product attaches at the surfaces of unreacted smithsonite. Smithsonite sulfidization involves heterogeneous nucleation and growth of ZnS nuclei. Moreover, the ZnS might nucleate and grow preferentially in the regions with high reactivity, which might account for the formation of ZnS island structures. In addition, sphalerite-structured ZnS is more likely to be the sulfidization product of smithsonite under flotation-relevantconditions, as also demonstrated by the results of our UV–vis DRS analyses. The results of this study can provide deeper insights into the sulfidization mechanism of smithsonite.

scholarly journals Solid-Liquid Reaction in the Si3N4-AlN-Y2O3 System under 1 MPa of Nitrogen

1996 ◽  
Vol 79 (6) ◽  
pp. 1717-1719 ◽  
Author(s):  
Zhen-Kun Huang ◽  
Tseng-Ying Tien
Keyword(s):  
Liquid Reaction ◽  
Solid Liquid

Solid-Liquid Reaction Synthesis and Characterization of Bioinorganic Complexes of Nicotinic Acid with Antimony(III) and Bismuth(III) Ion

2011 ◽  
Vol 282-283 ◽  
pp. 267-270 ◽  
Author(s):  
Guo Qing Zhong ◽  
Mei Gu ◽  
Yan Zhang
Keyword(s):  
Crystal Structure ◽  
Nicotinic Acid ◽  
Room Temperature ◽  
Synthesis And Characterization ◽  
Reaction Synthesis ◽  
Monoclinic System ◽  
Triclinic System ◽  
Liquid Reaction ◽  
Solid Liquid

Bioinorganic complexes of nicotinic acid with trivalent antimony and bismuth are synthesized by solid-liquid reaction at room temperature. The formula of the complexes is Sb(C5H4NCOOH)2Cl3•H2O and Bi(C5H4NCOOH)2Cl3•H2O respectively. The crystal structure of the complex of nicotinic acid and Sb(III) belongs to triclinic system and that of nicotinic acid and Bi(III) belongs to monoclinic system. Thermal analysis can indicate the complex formation between antimony or bismuth ion and nicotinic acid.

Low-temperature synthesis and sintering of γ-Y2Si2O7

2006 ◽  
Vol 21 (6) ◽  
pp. 1443-1450 ◽  
Author(s):  
Ziqi Sun ◽  
Yanchun Zhou ◽  
Meishuan Li
Keyword(s):  
Single Phase ◽  
Synthesis Temperature ◽  
Densification Rate ◽  
Calcination Time ◽  
Low Temperature Synthesis ◽  
Temperature Synthesis ◽  
Liquid Reaction ◽  
The Stability ◽  
Yttrium Disilicate ◽  
Solid Liquid

In this article, a novel pressureless solid-liquid reaction method is presented for preparation of yttrium disilicate (γ-Y2Si2O7). Single-phase γ-Y2Si2O7 powder was synthesized by calcination of SiO2 and Y2O3 powders with the addition of LiYO2 at 1400 °C for 4 h. The addition of LiYO2 significantly decreased the synthesis temperature, shortened the calcination time, and enhanced the stability of γ-Y2Si2O7. The sintering of these powders in air and O2 was studied by means of thermal mechanical analyzer. It is shown that the γ-Y2Si2O7 sintered in oxygen had a faster densification rate and a higher density than that sintered in air. Furthermore, single-phase γ-Y2Si2O7 with a density of 4.0 g/cm3 (99% of the theoretical density) was obtained by pressureless sintering at 1400 °C for 2 h in oxygen. Microstructures of the sintered samples are studied by scanning electron microscope.

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