2008
DOI: 10.1590/s0100-46702008000100009
|View full text |Cite
|
Sign up to set email alerts
|

Reação de precipitação de Ag na liga Cu-8%Al-6%Ag

Abstract: A reação de precipitação de prata na liga Cu-8%Al-6%Ag foi estudada usando medidas de variação da microdureza com a temperatura e o tempo de envelhecimento, difratometria de raios X (DRX), calorimetria exploratória diferencial (DSC), microscopia eletrônica de varredura (MEV). Os resultados obtidos indicaram que o mecanismo da reação de precipitação da prata é um processo controlado pela difusão da prata e a velocidade desta reação atinge um máximo em torno de 500°C.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
1
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 7 publications
0
1
0
Order By: Relevance
“…Widefield autofluorescence imaging, which is often used in most inherited retinal disease clinics, may detect presymptomatic retinitis pigmentosa and often demonstrates character-istic findings in carriers of X-linked disease, such as retinitis pigmentosa, choroideremia, or ocular albinism. 4 In some of these cases, retinal images can be so characteristic that they alone are often sufficient to diagnose carrier status, and hence, the familial inheritance pattern. Other examples include autosomal dominant disease, such as Sorsby fundus dystrophy, where latephase indocyanine green angiography may illustrate characteristic changes 5 or Stargardt-like disease where quantitative autofluorescence imaging may detect increased lipofuscin accumulation in absence of any other retinal changes.…”
mentioning
confidence: 99%
“…Widefield autofluorescence imaging, which is often used in most inherited retinal disease clinics, may detect presymptomatic retinitis pigmentosa and often demonstrates character-istic findings in carriers of X-linked disease, such as retinitis pigmentosa, choroideremia, or ocular albinism. 4 In some of these cases, retinal images can be so characteristic that they alone are often sufficient to diagnose carrier status, and hence, the familial inheritance pattern. Other examples include autosomal dominant disease, such as Sorsby fundus dystrophy, where latephase indocyanine green angiography may illustrate characteristic changes 5 or Stargardt-like disease where quantitative autofluorescence imaging may detect increased lipofuscin accumulation in absence of any other retinal changes.…”
mentioning
confidence: 99%