Page 8 - дисертація Головчук
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                  its cavities between the particles are filled with air, which intensively oxidizes the

                  melt drops inside the PW and at their ends during the spraying of coating.

                         By  phase  analysis  it  was  established  that  the  matrix  phase  of  the  coating

                  structure made of 50Cr6Mn2MoSi PW was martensite with a small amount of Fe 3O 4

                  iron oxide while the coating of 250Cr21WVMnSi PW showed  residual austenite

                  with a small amount of martensite, (Cr 2O 3 + Fe 3O 4) chromium and iron oxides. The

                  rapid crystallization of drops on the steel base provided the formation of a large

                  amount of residual austenite in the coating structure. The matrix phase of the coating

                  made of 50CrNi25MnSi PW was martensite, which contained nanosize inclusions

                  of complex-alloyed FeCrB boride and a small amount of Fe 3O 4 iron oxide. In this

                  case, the rapid crystallization of drops led to the formation of a large number of

                  boride crystallization centers, which, due to the lack of time, managed to grow only

                  to nanosizes.

                         The porosity of the coatings of all alloying systems increases with the lamellae

                  thickness in their structure, due to the use of PW of larger diameter. This pattern is

                  caused  by  an  increase  of  the  drop  size  that  formed  the  coating.  Drops  of  larger

                  diameter during the impact on the surface are sprayed much more intensely, which

                  leads to the formation of microcavities between the lamellae.

                         It was found that the average microhardness of coatings (martensitic class and

                  boride-containing       martensitic      one)     made      of     50Cr6Mn2MoSi          PW

                  and 50CrNi25MnSi PW increases with lamellae thickness in their structure, which

                  was especially evident when PW of larger diameter were used. This was explained

                  by the evaporation and burnout of alloying elements from drops, especially carbon,

                  during their spraying. As the diameter of the drops increased, the amount of burned

                  out carbon decreased. And the higher carbon content in the martensitic matrix phase

                  of the coatings caused the increase in microhardness.

                         At  the  same  time,  the  larger  diameter  of 250Cr21WVMnSi  PW  coatings

                  (austenite of carbide class) were used, the opposite tendency of lamellar thickness

                  influence on microhardness was revealed. This results from phase composition of

                  these  coatings,  in  particular,  the  presence  of  a  significant  amount  of  residual
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