ArturoJones
Materials
- Sep 22, 2006
- 4
I am currently involved in an effort to develop new molds for bladder molded tubular products and I am looking for some advice on tooling and process design. I have experience and a reasonable understanding (I think) of autoclave molding, film infusion, as well as the liquid molding technologies however the bladder molding is new to me.
We have done some preliminary development work using molds which were given to us and so far the results have been wanting. We are following what I would believe to be a typical bladder molding process: roll-wrapping pre-preg on to silicon bladders, extracting the mandrel, placing the pre-form in the mold, mold goes in the heated press, bladder is pressure cycled and then left pressurized at 90psi. The parts have the right outer shape and are well compacted, that is to say there are no issues with fibre bridging, however porosity is prevalent in the parts.
It seems to me that strategies for eliminating porosity are based (in the most general sense) on two philosophies: a) Use vacuum to remove all the air from the laminate before the resin flows (vacuum infusion / semi-preg approaches) b) Keep the resin (as opposed to the fibre bed) pressure high, particularly when near gelation (autoclave / RTM approach). Our current moldset has no provision for applying vacuum to the part. Secondly, the molds have very large flash cavities which offer essentially no restriction to resin flow. It seems that because of this, increasing the bladder pressure just bleeds more resin from the part without actually generating any resin pressure.
With that preamble out of the way, here are my specific questions:
1) Is vacuum necessarily applied to the mold cavity in successful bladder molding operations?
2) What measures are usually taken in order to restrict resin flow, and hence to facilitate higher resin pressures during processing? It would seem to me that smaller flash cavities and / or restrictions between the part and the cavity would help. Is this on the right track?
3) How critical, if at all, is the timing of pressure application? Is there any advantage to applying the pressure stepwise, or perhaps waiting until the resin viscosity has started to climb before applying the full process pressure?
4) Our bladder pressure of 90 psi was rather arbitrarily inspired by autoclave cure cycle recipes. Are there significant advantages to be gained by going to higher pressures?
Obviously any other process advice would be welcome as well. Thanks in advance.
We have done some preliminary development work using molds which were given to us and so far the results have been wanting. We are following what I would believe to be a typical bladder molding process: roll-wrapping pre-preg on to silicon bladders, extracting the mandrel, placing the pre-form in the mold, mold goes in the heated press, bladder is pressure cycled and then left pressurized at 90psi. The parts have the right outer shape and are well compacted, that is to say there are no issues with fibre bridging, however porosity is prevalent in the parts.
It seems to me that strategies for eliminating porosity are based (in the most general sense) on two philosophies: a) Use vacuum to remove all the air from the laminate before the resin flows (vacuum infusion / semi-preg approaches) b) Keep the resin (as opposed to the fibre bed) pressure high, particularly when near gelation (autoclave / RTM approach). Our current moldset has no provision for applying vacuum to the part. Secondly, the molds have very large flash cavities which offer essentially no restriction to resin flow. It seems that because of this, increasing the bladder pressure just bleeds more resin from the part without actually generating any resin pressure.
With that preamble out of the way, here are my specific questions:
1) Is vacuum necessarily applied to the mold cavity in successful bladder molding operations?
2) What measures are usually taken in order to restrict resin flow, and hence to facilitate higher resin pressures during processing? It would seem to me that smaller flash cavities and / or restrictions between the part and the cavity would help. Is this on the right track?
3) How critical, if at all, is the timing of pressure application? Is there any advantage to applying the pressure stepwise, or perhaps waiting until the resin viscosity has started to climb before applying the full process pressure?
4) Our bladder pressure of 90 psi was rather arbitrarily inspired by autoclave cure cycle recipes. Are there significant advantages to be gained by going to higher pressures?
Obviously any other process advice would be welcome as well. Thanks in advance.