Binder Removal from Powder Injection Molded 316L Stainless Steel
Muhammad Rafi Raza,
This study reports the results of preparation of 316L stainless steel polymer based injection molded feed stock, rheology of feed stock and injection molding. The plastic binder was extracted from molded samples. The binder extraction was carried out in two steps: by solvent and thermal techniques. The results showed that feed stock prepared was suitable for injection molding and this was confirmed by rheology data measured by using capillary rheometer. The test samples were injection molded without physical defects. Paraffin Wax (major binder) was extracted by using solvent extraction for 300 min. The thermal debinding was performed four different heating rates rage 1-7°C min-1. The SEM results showed that the PW was completely extracted from the test samples after 300 min.
Received: October 22, 2010;
Accepted: November 01, 2010;
Published: April 18, 2011
Complex shaped high performance and more précised metal or ceramic components
can be produced economically with conventional injection machine and this process
is known as Powder injection molding (PIM) (German, 1990;
German and Bose, 1997). Powder injection molding consists
of four sub sequential steps mixing, injection molding, debinding and sintering
(Zlatkov et al., 2008; Jamaludin
et al., 2007). The PIM process starts with the mixing of powder and
binder. The final mixture is known as feed stock. Feed stock is very important
step in PIM process any deficiency in feedstock can not be recovered latter
(Supati et al., 2000). The role of binder systems
like transporter, which is helpful for the homogeneous distribution of metal
powder into the desired shaped. These systems also hold the particles in the
beginning of sintering process (German and Bose, 1997).
Due to this reason binder system has key role for the success of injection molding
process. Binder played important role to achieve the shape and strength of the
product. Several binder systems are available but the formulation depends upon
the metal powder size, shape and size (Quan et al.,
2008). The binder system has low viscosity, small molecular weight, surfactant
inexpensive and environment friendly (German, 2007).
Zaky et al. (2009) investigated different binder systems and found
that the binder system contained 62wt.% of paraffin wax is an excellent one.
They also concluded that solvent immersion is suitable technique to remove the
major binder. They removed the major binder completely heating at 40°C for
5 h. Feed stock is than converted into granules followed by injection molding.
After the injection molding the green product is debinded. Finally the sintering
is done to obtain optimum properties.
A large number of researchers investigated the different aspects of 316L stainless
steel. German (2007) suggested that the powder should
have size less than 20 μm, tap density less than 50% of theoretical density,
spherical in shape and free from agglomeration. Quan et
al. (2008) and Barriere et al. (2003) suggested
that for better deformation resistance vacuum environment is more beneficial
than gas (N2) atmosphere. They also conclude that particle size,
shape, solid loading, heating rate and atmosphere also affect the deformation
defects. (Quan et al., 2008). Nylund
et al. (1995) found that sintered density is more important to achieve
excellent mechanical properties and good corrosion resistance. Various techniques
are employed to improve the density. Loh et al. (2001)
used TiC with 316L stainless steel to improve the mechanical properties. The
also found that sintering temperature and heating rate also effect the mechanical
properties. The packing density also increased by using different size powders
(German, 1992; German and Bulgeeim,
1992). Huang and Hsu (2009) also studied the effects
of back bone polymer (LDPE and HDPE) on dimensional changes and mechanical properties
of MIM 316L components. Ji et al. (2001) suggested
that the factor such as sintering temperature, sintering time, heating rate
and atmosphere affect the sinter density. They got maximum 96% of sinter density.
Becker et al. (2000) adopted the PM route and
achieve the 98% sintered density of water atomized 316L stainless steel. According
to them the liquid phase is responsible for high density. Omar
(1999) obtained the 96% sintered density of PIM 316L stainless steel using
PEG and PMMA binder system under argon atmosphere, while Jamaludin
et al. (2008) obtained 99% sintered density by using same system
except the sintering atmosphere (Vacuum) between temperature range 1340-1400
with heating rate 10C/min and dwell time 4 h.
Yimin et al. (1999) studied the effect of solid
loading on MIM gas atomized 17-4 Stainless steel on density and mechanical properties.
The study concludes that 68Vol% is the best solid loading with binder 65%PW,
30% EVA and 5%SA.
During the present study two formulation of the feed stock with solid loading 60 and 65vol.% were prepared using paraffin wax based binder system (PW 70vol%, PP 25vol% and SA5vol%). The feed stock was characterized by TGA and Rheometer. The injection molded samples were debinded and analyzed by using SEM/FESEM.
MATERIALS AND METHODS
Materials: The metal powder used in this study was stainless steel 316L
(PF-10R) water atomized supplied by PICIFIC SOWA Japan. The mean particle size
D50 is 5-7μm. The chemical composition and morphology of the
powder is given in Table 1 and Fig. 1a,
respectively. To make the easy flow of metal powder into mold cavity, polymeric
based binder system was used. In the current research work a paraffin wax (PW)
based system was prepared. The ingredients with paraffin wax (PW) were Polypropylene
(PP) and Stearic Acid (SA). The composition of the binder system was PW 70vol%,
PP 25vol% and SA 5vol%, minor components of the binder system acts as surface
active agent. The binder system was thermally characterized by using TGA (Perkin
Elmer).Testing was done under nitrogen atmosphere with heating rate of 20°C
min-1. The flow behavior was studied by using capillary rheometer
CFT 500D with die 1x10mm at different loads and temperatures.
Feed stock preparation: Two formulations F1 and F2 were prepared with
solid loading 60 and 65vol%, respectively.
|| Chemical composition of 316L Stainless Steel
The stainless steel powder was mixed with binder using Z-blade mixer at temperature
165°C for 90 min at speed 60 rpm. After mixing, the paste was converted
into granules. The characterization of the feed stock was done by using TGA
and capillary rheometer.
Molding: The tensile specimens were molded by using 100KSA vertical injection molding machine. The samples were molded at temperature 164°C and pressure 4.5 bar. The molding time varies from 0.3-0.5 min.
Physical examination: In powder injection molding the common molding
defects are cracks, powder-binder separation, short shots, sink mark, internal
voids etc. these defects may be due to the bad material or improper molding
conditions (Nanjo et al., 1993). In molded samples
no defects were observed.
Debinding: The debinding process is most appropriate for removal of binder from Powder injection molded green parts. It consists of (1) solvent extraction and (2) thermal debinding.
Solvent extraction process the soluble component of the binder removed from
the molded parts (Johnson, 1988, Wiech,
1980, German, 1990). Different organic solvents such
as n-hexane, n-heptane and iso-octane were at different temperature ranging
from 30-60°C (Fu et al., 2005).
During the present study solvent extraction process was followed by thermal
debinding process. Solvent extraction process was carried out by immersing test
samples in n-heptane at 60°C. To study the effect of time on loss of PW
the test specimens were heated upto 5 h. The debinding ratio was measured (Zaky,
2004; Omar et al., 2003). Finally, the results
were verified by using SEM.
During thermal debinding process test specimens were heated at 450°C for 1 h with four different heating rates (1°C/min, 3°C/min, 5°C/ min and 7°C/ min) to optimize the suitable debinding rate.
Sintering: The test specimens will be sintered under vacuum to observe the effect of different heating and cooling rate on density, mechanical properties and corrosion as well.
RESULTS AND DISCUSSION
Material characterization: Scanning electron micrograph of Stainless
steel 316L showing in Fig.1a. while the particle size analysis
is shown in Fig.1b. From Fig. 1a it is
clear that powder particles have round shape and particle size between 4-7 μm.
TGA analysis of binder and feed stock: TGA analysis of binder and feedstock was done. The data given in Fig. 2 indicate that no residue was left after the decomposition of binder. The decomposition of binder started about 250°C. From the graph shown in Fig. 2, it is clear that after the decomposition of feedstock F1 about 91wt. % residue left. This amount of residue is same as SS powder calculated in feedstock.
Rheology of binder and feed stock: The rheological behavior of both
feeds tocks were studied at different temperature ranging from 100 to 160°C.
The results are shown in Fig. 3. From graphs it is clear that
shear rate and viscosity showed slightly Pseudo plastic behavior. The viscosity
of both formulation of feeds stock is lower than 20Pa.S, because the presence
of Paraffin wax having viscosity less than 10Pa.S (Zaky
et al., 2009).
|| SEM micrograph of 316L stainless steel at 3KX
||Particle size distribution of 316 L Stainless steel
||Comparison of TGA scan for PW, PP, SA, binder, and 60vol%
||Viscosity of feedstock F1 as a function of shear rate at different
temperatures raging 100 to 160°C
||Viscosity of feedstock F2 as a function of shear rate at different
temperatures raging 100 to 160°C
||Comparison of masses of green parts for both formulations
F1 and F1 after molding
||Weight percentage of Paraffin Wax removed with respect to
debinding time for 60% vol (F1) and 65% vol (F2) solid loading
||SEM micrograph of molded sample of F1 showing the well dispersion
of powder (surface view)
||SEM micrograph of molded sample of F1 showing the well dispersion
of powder (fracture view)
||SEM micrograph of F1 showing the top of as molded part after
leaching for 300 min
||SEM micrograph of F1 surface showing the fracture view of
as molded part after 300 min leaching
||SEM micrograph of F2 showing the surface of molded part
||SEM micrograph of F2 showing the fracture view of molded part
||SEM micrograph of F2 showing the top of as molded part for
300 min leaching
For successful metal injection molding the shear rate ranges between 102-105
S-1. The maximum suitable viscosity for feedstock is 103 Pa s at molding temperature
(Shah and Nunn, 1987; Mutsuddy,
1983; Jorge, 2008). Fu et al.
(2005) suggested that at high temperature low viscosity is suitable for
injection molding. For ceramic injection molding the shear rate between 100
and 1000 S-1 and viscosity should be less than 1000Pa.s. From the results,it
is clear that the feed stocks for both formulation is suitable for injection
Visual examination: The visual examination was carried out, no defects were observed on the samples. The mass and dimensions of all samples were measured. In both formulations the molded samples have almost same masses and dimensions Fig. 4.
Leached samples: From results obtained by debinding ratio are given in Fig. 5. It is clear that for both formulations the major binder PW was completely removed. From the results it is clear that 300 min is the suitable time to remove the major binder from the samples. After the solvent extraction process no swelling or cracks were observed on surfaces of the test samples. The results were also verified by SEM analysis as well.
Thermal debinding: The samples from both formulations were thermally debinded with heating rate 1°C, 3°C, 5°C and 7°C. There was no swelling or cracks on the surface of the debinded samples. The debinded samples have brown colour. The only one sample from formulation 65% vol heated with rate 1°C having dark brown colour.
Binder removal by leaching: Figure 6 shows SEM micrographs
for metal and binder (60 vol% solid loading) before and solvent extraction.
Fig. 6 (a-b) shows the surface and fracture
micrographs magnification 1KX respectively. It is clear that the powder is well
distributed in binder system. Fig. 6 (c-d)
showed the surface and fracture view of the solvent debinding after 300 min.
from both micrographs it is clear that there are pores initiate from surface
to the core of the sample. These pores are helpful for thermal debinding process
to remove the gasses from the test samples to avoide the cracks on the samples.
From these pores are indications that PW is completely removed from the molded
Figure 7 represents the surface and fracture view of the
65% vol solid loading. From Fig. 7a and b
it is clear that there is no aggloromation of powder in binder. Figure
7b and c showed the pores on the surface and fracture
surface of the test samples which indicate that PW dissolved in n- heptane.
From the measurement it is clear that Paraffin Wax entirely removed after 300
From the above research work, we can conclude following:
||For solvent extraction suitable temperature is 60 and time is 300 min
||For both solid loading 60% vol and 65% vol solid loading the shear rate
showed pseudo plastic behavior
||For both solid loading the viscosity is less than 20 which is suitable
for Powder injection molding
||Both formulations are suitable for Injection molding
||The debinding heating rate 1°C is not suit able for solid loading
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