Light, precious gold-titanium based alloy containing, by mass, at least 750% of gold, characterized in that said alloy has the following composition formula:

Ti.sub.aAu.sub.bM.sub.cT.sub.d

where a, b, c, d are atomic proportions such that:

a+b+c+d=1,

0.45≦a≦0.55; 0.41≦b≦0.495; 0.025≦c≦0.13; 0.001≦d≦0.025,

where M represents one or more elements taken from among a first group including Nb, V, Pd, Pt, Fe,
and where T represents a maximum of two elements taken from among a second group including Nb, V, Pd, Pt, Fe, Mo, Ta, W, Co, Ni, Ru, Rh, Ir, Cr, Mn, Cu, Zn, Ag, Al, B, Si, Ge, Sn, Sb, In, with the exception of said metals M comprised in said alloy.

Component for timepiece or for jewellery made from such a light, precious gold-titanium based alloy.

A two-phase metallic alloy comprising precipitates of Ag possessing a volume-averaged diameter of less than about 500 nm dispersed in a matrix selected from the group consisting of Ni, Fe, combinations of Ni with Cu and combinations of Fe with Cu.

A two-phase metallic alloy comprising precipitates of Ag possessing a volume-averaged diameter of less than about 500 nm dispersed in a matrix selected from the group consisting of Ni, Fe, combinations of Ni with Cu and combinations of Fe with Cu.

The present invention relates to a HEA foam prepared by selective dissolution of a second phase within a two-phase separating alloy comprising the HEA and a manufacturing method thereof. The manufacturing method of the HEA foam of the present invention has the effect of preparing a novel HEA foam, which was not available in the past, by leaving only a first phase after manufacturing a two-phase separating alloy comprising a first phase by HEA, wherein at least 3 metal elements act as a common solvent.

Furthermore, the HEA foam of the present invention has a structure, wherein pores are distributed inside the HEA, in which at least 3 metal elements act as a common solvent. By adding a functional characteristic of low heat conductivity, etc., to the existing high strength characteristic of HEA, the HEA foam of the present invention can exhibit a complex effect by the combination of the two particular effects, thereby being capable of exhibiting excellent physical characteristics.

The present invention relates to a HEA foam prepared by selective dissolution of a second phase within a two-phase separating alloy comprising the HEA and a manufacturing method thereof. The manufacturing method of the HEA foam of the present invention has the effect of preparing a novel HEA foam, which was not available in the past, by leaving only a first phase after manufacturing a two-phase separating alloy comprising a first phase by HEA, wherein at least 3 metal elements act as a common solvent.

Furthermore, the HEA foam of the present invention has a structure, wherein pores are distributed inside the HEA, in which at least 3 metal elements act as a common solvent. By adding a functional characteristic of low heat conductivity, etc., to the existing high strength characteristic of HEA, the HEA foam of the present invention can exhibit a complex effect by the combination of the two particular effects, thereby being capable of exhibiting excellent physical characteristics.

A method for manufacturing a pressure measuring cell, which has a ceramic platform and a ceramic measuring membrane, wherein the measuring membrane is joined with the platform pressure tightly by an active hard solder, or braze, wherein the method includes: providing the platform, the measuring membrane and the active hard solder, or braze, positioning the active hard solder, or braze, between the platform and the measuring membrane; melting the active hard solder, or braze, by irradiating the active hard solder, or braze, by a laser, wherein the irradiating of the active hard solder, or braze, occurs through the measuring membrane; and letting the active hard solder, or braze, solidify by cooling.

A method for manufacturing a pressure measuring cell, which has a ceramic platform and a ceramic measuring membrane, wherein the measuring membrane is joined with the platform pressure tightly by an active hard solder, or braze, wherein the method includes: providing the platform, the measuring membrane and the active hard solder, or braze, positioning the active hard solder, or braze, between the platform and the measuring membrane; melting the active hard solder, or braze, by irradiating the active hard solder, or braze, by a laser, wherein the irradiating of the active hard solder, or braze, occurs through the measuring membrane; and letting the active hard solder, or braze, solidify by cooling.

A permanent magnet of an embodiment includes: a composition represented by a composition formula: R(Fe.sub.pM.sub.qCu.sub.rCo.sub.1-p-q-r).sub.z, where R is at least one element selected from rare-earth elements, M is at least one element selected from Zr, Ti, and Hf, and relations of 0.3≦p≦0.4, 0.01≦q≦0.05, 0.01≦r≦0.1, and 7≦z≦8.5 (atomic ratio) are satisfied; and a structure including a cell phase having a Th.sub.2Zn.sub.17 crystal phase, and a cell wall phase existing to surround the cell phase. An average magnetization of the cell wall phase is 0.2 T or less.

A permanent magnet of an embodiment includes: a composition represented by a composition formula: R(Fe.sub.pM.sub.qCu.sub.rCo.sub.1-p-q-r).sub.z, where R is at least one element selected from rare-earth elements, M is at least one element selected from Zr, Ti, and Hf, and relations of 0.3≦p≦0.4, 0.01≦q≦0.05, 0.01≦r≦0.1, and 7≦z≦8.5 (atomic ratio) are satisfied; and a structure including a cell phase having a Th.sub.2Zn.sub.17 crystal phase, and a cell wall phase existing to surround the cell phase. An average magnetization of the cell wall phase is 0.2 T or less.

The present invention provides an R-T-B based permanent magnet, comprising: a main phase which is composed of the structure of R.sub.2T.sub.14B (R is at least one element selected from Y, La, Ce, Pr, Nd, Sm, Eu and Gd, and T is one or more transition metal elements having Fe or a combination of Fe and Co as necessary); and a grain boundary phase which is composed of Ce.sub.xM.sub.1-x (M is at least one element selected from Mg, Al, Si, Ti, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Y, Zr, Nb, Mo, Ag, In, Sn, La, Pr, Nd, Sm, Eu, Gd, Hf, Ta, W and Bi, and x is within the range of 0.20≦x≦0.55), and the cross-sectional ratio Atre of the grain boundary phase to the whole magnet structure is within the range of 0.03<Atre<0.07.