Patent Application
20110241236
This invention concerns a method of forming granules from a nanopowder, and particularly but not exclusively a ceramic nanopowder, and also a method of manufacturing a component.
Several nanomaterials have been shown to yield desirable properties suitable for various applications. For example, nano grain sized alumina has been made in its unusual transparent form. Nano zirconia has been shown to have higher hydrothermal stability and fracture toughness than conventional zirconia ceramics. However, mass manufacturing of nanoceramic components is still a big challenge.
Die pressing is the preferred component manufacturing route. Unagglomerated ceramic nanopowders are though cohesive and have poor flowability and thus poor die filling characteristics. One way to overcome this problem is to granulate them. However, nanopowders have a tendency to form hard agglomerates during granulation, resulting in nanocomponents which may have undesirable material properties.
As the granule density increases, the primary particles (nanopowders) are closely packed within the granules. As the inter-particle distance reduces, the agglomerates thus formed are hard, i.e. they resist deformation when pressure is applied, and which leads to excessive grain growth during the sintering stage and hence the favourable nanostructure is lost. Low density granules are generally soft and hence crush down into fine particles yielding a homogeneous nanostructure when consolidated. However the latter suffer from poor flow and fill characteristics.
According to a first aspect of the present invention there is provided a method of forming granules, the method comprising forming a suspension of a nanopowder, adding to the suspension an additive, drying the suspension so as to form granules, and removing at least a substantial part of the additive from the granules to form flaws in the granules.
A concentrated suspension of nanoparticles may be produced, and the concentrated suspension may be produced by a method according to the applicant's patent application PCT/GB06/002081.
The additive may be a foaming agent or a pore former. The additive may have a boiling point or sublimation temperature of below 100° C. The additive may be a fluid or solid.
The additive may be any of freon, octylphenoxypolyethoyethanol such as Triton X available from National Diagnostics Inc of Atlanta USA, ammonium C6-10 alcohol ethoxysulfate such as Alpha foamer available from Stepan Canada Inc of Ontario Canada, or camphene.
The additive may be added to the suspension directly, or may be added in solution.
The suspension may be dried so as to form generally spherical granules, and may be dried using a spraying device. The suspension may be dried using spray freeze drying or spray drying.
As an alternative, the granules may be formed by fluidising or using a shear granulator.
Removing of the additive may include heating of the granules and/or subjecting the granules to reduced pressure. The heating may include microwave heating.
At least some of the additive may be removed in a controlled manner such that flaws are provided in the granules by removal of the additive.
At least some of the additive may be removed rapidly so as to produce cracks or other formations in the granules to provide flaws.
Additional additives may be added to the suspension, which additives may act as binders, plasticisers, or lubricants.
The nanopowder may be a ceramic powder, may be a zirconia powder, and may be yttria stabilised zirconia including up to 10 mol % yttria. The nanopowder may have a particle size of substantially 20 nm.
The suspension may be aqueous or non-aqueous.
According to a second aspect of the invention there is provided a method of manufacturing a component, the method including forming granules by a method according to any of the preceding thirteen paragraphs, locating the granules in a die press, and pressing the granules such that the granules break down to powder during pressing to form a green compact.
The green compact may be subsequently fired.
An embodiment of the present invention will now be described by way of example only and with reference to the accompanying drawings, in which:
An yttria stabilised nano zirconia powder containing 3 mol % yttria with a particle size of substantially 20 nm, was formed into a 60 wt % solids concentrated suspension by a method according to the applicant's patent application no. PCT/GB06/002081. Freon was added directly to the suspension as an additive and thoroughly mixed in.
The suspension was granulated by spray freeze drying which involves spraying the suspension into a cryogent, and then driving off the liquid at low temperature under vacuum. The freon was then removed by a 70° C. heat treatment for one hour. The voids left by the vacated freon provide meso, micro and macro flaws or structural defects in the granules.
The granules were then located into a die press and pressed to form a green compact. Pressing of the granules causes the granules to be crushed and break into their primary particles. The green compact can subsequently be fired.
The granules thus produced have excellent flowability as measured using a Hall flowmeter as illustrated in the graph of
The granules made by the above method are weaker than would be the case without the freon additive, and the fracture surface as shown in FIG. 2 of a pressed green compact made by the method shows a uniform microstructure which can thus be sintered into a dense nanograined ceramic. This contrasts with
The invention therefore provides a method of forming soft deformable nano granules which have excellent flowability, and also have high crushability. This means the granules can be broken down to their primary particles during pressing to provide the advantages as provided by nanoparticles outlined above.
It is to be realised that a wide range of modifications relative to the above described example can be made without departing from the scope of the invention. For example, different additives may be used, and potential examples include octylphenoxypolyethoyethanol such as Triton X available from National Diagnostics Inc of Atlanta USA, ammonium C6-10 alcohol ethoxysulfate such as Alpha foamer available from Stepan Canada Inc of Ontario Canada, or camphene. The additive will generally be a foaming agent or pore former, and it is advantageous if the additive has a boiling point of below 100° C. or is a sublimable solid which sublimes at a temperature of below 100° C. The additive can be added directly to the suspension or may be added as part of a solution.
The granules could be formed by spray drying, fluidising or using a shear granulator. The additive may be removed using heat and/or subjecting to reduced pressure. The heating may include microwave heating. The additive can be removed slowly and in a controlled manner to produce voids where the additive had been located, the voids providing flaws in the granules. Alternatively, the additive can be removed rapidly so as to produce cracks or other formations to provide flaws.
Additional additives may be added to the suspension to act as binders, plasticisers or lubricants. Different nanopowders could be used, which could be a different zirconia or other ceramics, or other materials, including for instance pharmaceuticals. The suspension may be aqueous or non-aqueous.
Whilst endeavouring in the foregoing specification to draw attention to those features of the invention believed to be of particular importance it should be understood that the Applicant claims protection in respect of any patentable feature or combination of features hereinbefore referred to and/or shown in the drawings whether or not particular emphasis has been placed thereon.
| Number | Date | Country | Kind |
|---|---|---|---|
| 0818851.8 | Oct 2008 | GB | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/GB2009/002463 | 10/14/2009 | WO | 00 | 6/13/2011 |
