Negative Additive Manufacturing of Complex Shaped Boron Carbides

Summary

A method called negative additive manufacturing is used to produce near fully dense complex shaped boron carbide parts of various length scales. This technique is possible via the formulation of a novel suspension involving resorcinol-formaldehyde as a unique gelling agent that leaves behind a homogenous carbon sintering aid after pyrolysis.

Abstract

Boron carbide (B₄C) is one of the hardest materials in existence. However, this attractive property also limits its machineability into complex shapes for high wear, high hardness, and lightweight material applications such as armors. To overcome this challenge, negative additive manufacturing (AM) is employed to produce complex geometries of boron carbides at various length scales. Negative AM first involves gelcasting a suspension into a 3D-printed plastic mold. The mold is then dissolved away, leaving behind a green body as a negative copy. Resorcinol-formaldehyde (RF) is used as a novel gelling agent because unlike traditional hydrogels, there is little to no shrinkage, which allows for extremely complex molds to be used. Furthermore, this gelling agent can be pyrolyzed to leave behind ~50 wt% carbon, which is a highly effective sintering aid for B₄C. Due to this highly homogenous distribution of in situ carbon within the B₄C matrix, less than 2% porosity can be achieved after sintering. This protocol highlights in detail the methodology for creating near fully dense boron carbide parts with highly complex geometries.

Introduction

Boron carbide (B₄C), with a Vickers hardness of about 38 GPa, is known as the third hardest commercially available material, behind diamond (~115 GPa) and cubic boron nitride (~48 GPa). This particular property, along with a low density (2.52 g/cm³), makes it attractive for defense applications such as armors¹. B₄C also has a high melting point, superior wear resistance, and high neutron absorption cross section^2,3,4. However, utilization of these favorable mechanical properties typically requires B₄C to be sintered to a high density. Hot pressing is a conventional method for sintering B₄C to full densification. This technique is often limited to simple geometries with limited curvature and fairly uniform thickness. Expensive and labor-intensive machining with polycrystalline diamond tooling or laser cutting is required to introduce finer or more complex features.

Alternatively, colloidal forming techniques with pressure-less sintering can produce near-full density parts that require minimal to no machining. Due to a lack of external pressure during consolidation, sintering aids are normally added to the ceramic medium to increase the effectiveness of pressureless sintering. Carbon is commonly used as a sintering aid for B₄C^5,6,7.Various carbon sources, such as nanoparticle powders or carbonized organics from pyrolysis, can be used. Homogeneous distribution of the carbon sintering aid along grain boundaries is an important factor for obtaining uniform sintering of B₄C. Therefore, carbon concentration and B₄C particle size are also important and interrelated factors for sintering parts to high density⁸.

One of the most promising colloidal forming techniques for obtaining complex shaped ceramic parts is gelcasting. This technique involves casting a ceramic suspension with an organic monomer into a mold which polymerizes in situ to act as a gel^9,10,11. The gel serves as a binder to form a green body in the shape of the mold that is strong enough to be handled without breakage in subsequent processing steps. Previously impossible 3D mold geometries can now be produced through low-cost polymer-based additive manufacturing (AM) techniques such as stereolithography (SLA) and fused deposition modeling (FDM)¹². The recent availability of 3D printers has opened new possibilities for designing ceramics with highly complex geometries.

Negative additive manufacturing is a technique that combines gelcasting with sacrificial 3D-printed molds. The complexity of the ceramic part is directly related to the complexity of the mold design. Mold designs can now be incredibly sophisticated with the advent of high resolution plastic 3D printers. For example, 3D scanning tools can be used to capture an individual's contours and be incorporated into molds. By using negative AM, lightweight ceramic armors tailored to the individual's body size and shape can be created. Such design customizations can provide lighter weight armors with enhanced mobility for users.

Other common ceramic AM techniques such as direct ink write (DIW), selective laser sintering (SLS), and binder jetting (BJ) are also effective in producing complex shaped ceramic parts. However, most of these techniques are only useful for producing fine porous structures and are not efficient when scaling up to large parts, such as armor applications^{13,14,15,16,17}. Moreover, most of these techniques are not feasible for high volume production due to high expenses. Therefore, negative AM is a preferred and relatively inexpensive route for industrial-level production of large-scale parts.

The B₄C suspensions used for gelcasting must be low in viscosity and contain a gelling agent and sintering aid. Resorcinol and formaldehyde are chosen for their ability to undergo polycondensation reactions to form a resorcinol-formaldehyde (RF) network, which helps to bind the B₄C particles together. Traditional hydrogels used for gelcasting are limited to molds with hollow cores due to the high inward shrinkage experienced during the drying process¹⁸. Since RF is commonly used as an aerogel, there is little to no shrinkage, which permits the use of more intricately shaped molds. Another advantage of using RF is that the gelation rate can be controlled by altering the pH of the suspension (Figure 3). Additionally, suspensions containing either resorcinol or formaldehyde can be prepared in advanced and stored separately until they are ready for casting. Most importantly, the RF gel can be pyrolyzed to leave behind 50 wt% carbon¹⁹. This highly homogenous distribution of carbon can aid the densification of B₄C to near-full densities during sintering. 15 wt% of RF relative to boron carbide is used in the formulation of the suspension to provide 7.5 wt% of carbon after pyrolysis of the cast parts.

The overall goal of this work is to combine traditional gelcasting techniques with inexpensive 3D printing capabilities and a unique gelling agent to obtain near-full density boron carbide parts with highly complex geometries. In addition to ceramics, negative AM can be applied to other material fields to create entirely new geometries of multi-material systems. The methodology described here expands on the work presented in Lu et al.⁸ and aims to provide a more detailed protocol for reproducing those results.

Protocol

CAUTION: Please consult with the safety data sheets (SDS) of all materials, and wear proper protective equipment (PPE) when handling materials before casting and curing. Resorcinol and polyethylene imine are known to be toxic. Formaldehyde is both toxic and carcinogenic²⁰. Preparation of ceramic suspensions should be done in chemical fume hoods or other properly ventilated work environments.

1. Negative Additive Manufacturing

1. Preparation of a 120 mL two-part suspension
   NOTE: A two-part suspension will be prepared to help prolong the shelf life of the suspensions before casting. One suspension (R-mix) will contain the resorcinol component, and the other (F-mix) will contain the formaldehyde component. Both suspensions will be mixed together to form a final suspension that will initiate the gelation process.
   1. To create the R-mix, begin by dissolving 0.88 g of polyethylene imine (PEI) in 25.00 g of water using a planetary mixer.
   2. To create a separate F-mix, dissolve 0.88 g of polyethylene imine (PEI) in 16.83 g of water using a planetary mixer.
      NOTE: Using a planetary mixer at 2000 rpm for at least several minutes will provide sufficient shearing forces to help dissolve the viscous PEI, resorcinol, and formaldehyde, and to suspend the boron carbide particles. PEI serves as the dispersing agent for the B₄C particles
   3. Dissolve 12.60 g of resorcinol powder into the R-mix. The solution should turn from a cloudy-white to a clear transparent solution after complete dissolution of the powder from mixing.
   4. Add 17.03 g of formaldehyde solution to the F-mix and ensure complete mixing.
   5. Incrementally add 5.25 g (12 increments until reaching 63.00 g) of boron carbide powder (1500F) into both the R-mix and F-mix separately.
   6. Add 6.50 g of acetic acid to the R-mix and F-mix and ensure complete mixing in each.
      NOTE: At this point, the two-part suspensions will have 42 vol% of B₄C and are ready to be combined for casting or stored for future use (if adequately sealed). Beware that if the suspensions sit for ~1 h or more, particle settling will occur. Ensure that the particles are resuspended by applying thorough agitation before using the suspensions. Also, three different commercial batches of boron carbides, 1250F, 1500F, and 3000F (named according to their approximate sieved mesh sizes), were originally tested. Each batch has a different particle size distribution, and the 1500F B₄C batch was found to achieve the highest sintering density, as reported in Lu et al.⁸. Acetic acid can also be added before the B₄C solids loading step as well, but adding at the end offers better ease of handling by limiting acetic acid odors.
2. Preparation of the 3D printed molds for casting
   1. Prepare the mold design in a computer-aided design (CAD) software program.
   2. Print the molds using a Fused Deposition Modeling (FDM) 3D printer with acrylonitrile butadiene styrene (ABS) filaments.
      NOTE: Acetone vapors can be used to smooth out the mold texture if desired²¹. The suggested nozzle and bed temperatures are 240 °C and 110 °C, respectively. Parameters such as layer thickness (0.2 mm), extrusion speed, and cooling rate are chosen to optimize the quality of the part with minimum deformations. This requires some trial and error with each unique printer system. A wall thickness of at least 1 mm is advised. The minimum feature size is 0.5 mm; however, it is suggested not to go below 1 mm. Molds from Lu et al.⁸ are available for download online in supporting material.
3. Combination of the two-part suspension to prepare for casting
   1. Before combining, thoroughly agitate (by using a vortex or planetary mixer) the R-mix with the F-mix suspensions individually to ensure the B₄C particles are well-suspended.
   2. Combine the R-mix and F-mix to obtain the final suspension.
      NOTE: The pH of the combined suspension should be 2.8, which will provide about 30 minutes of working time to de-air and cast the final suspension before gelation starts occurring. The onset of gelation can be observed from the sharp increase in viscosity of the suspension.
   3. Before casting, mix and apply vacuum (20-200 torr or 2.7-27 kPa) to the final suspension mixture for about 10 minutes to remove air bubbles without boiling the water. This can be accomplished by using a stirring plate at 200-300 rpm with a vacuum jar.
4. Gelcasting
   1. Immediately pour the de-aired suspension into the 3D-printed molds.
   2. Place the molds inside a sealed glass container to prevent moisture loss during the curing process.
   3. Place the sealed container with the molds into a 60-80 °C oven to initiate the curing process.
   4. Allow the casts to cure for at least 8 hours for parts that are several centimeters in length scale or possibly longer for larger molds.
5. Dissolution of the molds to obtain green bodies
   1. Remove the sealed container with the molds from the oven and allow it to cool to room temperature.
   2. Add enough acetone into the container until the mold is fully submersed. The amount will vary depending on the size and volume of the mold used (generally ~100 mL of acetone for a mold that is 50 cm³ in dimension).
      NOTE: This process may take up to 2-4 days depending on the volume of plastic that needs to be dissolved away. Minimal agitation of the acetone bath or heating it slightly to 40 °C may help speed up the process. Execute caution when heating acetone bath, as it is a flammable chemical and may become explosive when combined with air in certain composition ranges.
   3. Extract the free green body from the acetone bath after the ABS plastic is dissolved away.
      NOTE: After the RF is cured, the mold can be dissolved away to obtain a solid green body shaped as a negative copy of the inner mold geometry. This green body should be strong enough to survive gentle and careful handling in the subsequent post-processing steps without breaking.
   4. Place the green bodies in an oven at 80 °C to ensure complete drying and removal of all moisture.
      NOTE: Drying time varies depending on the volume of the green body. Leaving the part to dry overnight (> 8 hours) is sufficient for green body sizes less than 1000 cm³. There is no harm in over-drying.

2. Carbonization

1. After drying, place each green body in a 2-inch quartz tube lined with graphite foil and put them into a furnace with flowing gas [250 standard cubic centimeters of air (SCCM) consisting of 4 wt% H₂(g) and 96 wt% Ar(g) to create a reducing atmosphere during the pyrolysis treatment].
2. Heat the green bodies inside the furnace at 5 °C/min until 1050 °C and hold for 3 hours.
   NOTE: The gel-cast green bodies will have 15 wt% of RF relative to the B₄C and will provide about 7.5 wt% in carbon after the pyrolysis process. This process removes much of the resorcinol-formaldehyde residue and will severely contaminate the furnace if no trap is used.
3. Ensure that the green bodies come out uniformly darker in color, indicating the presence of carbon from the pyrolysis treatment.

3. Sintering

NOTE: After sintering, the surface roughness of the samples will improve slightly compared to the surface roughness of the molds used. This is a consequence of the 57-58 vol% shrinkage of the samples from sintering.

1. Place the carbonized parts in a graphite furnace with vacuum backfilled flowing helium gas (420 SCCM) for sintering. Apply 280 SCCM to the front and pyrometer windows and 140 SCCM directly into the sample chamber with an inlet pressure of ~170 kPa.
2. Heat up the furnace to 2290 °C (20 K/min to 2000 °C then 3 K/min to 2290 °C) and hold for 1 hour to achieve optimal densification of the parts.
   NOTE: Archimedes density is a common and quick technique to measure the density of the sintered boron carbide parts. Archimedes density kits can be added onto analytical balance scales to measure the density of samples or manually determined²². Boron carbide with 7.5 wt% in carbon will have a theoretical maximum density (TMD) of 2.49 g/cm³. Parts sintered at 2290 °C from this methodology will result in 2.43 ± 0.01 g/cm³ which is 97.6 ± 0.4% TMD.

Results

Following the outlined procedure (Figure 1), complex shaped boron carbide parts with carbon (B₄C/C) can be sintered up to 97.6 ± 0.4% of theoretical max density with a Vicker's hardness of 23.0 ± 1.8 GPa⁸. Several possible examples of sintered B₄C/C parts are demonstrated (Figure 2). These examples show the fine textural features that can be copied by the gelcasting technique. This is...

Discussion

The methodology of negative additive manufacturing described in the protocol allows complex shaped boron carbide parts to be produced at nearly full density after sintering at an optimal temperature of 2290 °C. The first several steps related to preparation and casting are the most critical for generating a high-quality cast with minimal defects. If the viscosity of the suspension is too high, poor mixing will occur. The porosity of the sintered part is also affected since increased viscosity hinders air bubble remo...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Boron carbide powder 1250F	Tetrabor Ceramics	Lot 211M419	>96% purity
Boron carbide powder 1500F	Tetrabor Ceramics	Lot 209M102/9	>96% purity
Boron carbide powder 3000F	Tetrabor Ceramics	Lot 111m53/9	>96% purity
Polyethylene Imine (PEI)	Sigma Aldrich	MKBP3417V	Averaged MW ~25,000 by L.S.
Resorcinol	Sigma Aldrich	MKBG6751V	BioXtra, ≥99%
Formaldehyde	Fisher Scientific	F79-1	37% by weight; Stabilized with 10-15% Methanol
Acetic Acid	Sigma Aldrich	SKU 695092	Glacial ≥99.7%
Acetone	Sigma Aldrich	SKU 179124	ACS Reagent Grade ≥99.5%
Water	LLNL In-house (Milli-Q)
Planetary Mixer	Thinky	AR-250	Fits 150mL and 300mL Thinky containers
Acrylonitrile butadiene styrene (ABS) plastic filament	eSUN		Natural color
Taz 6 (3D printer)	Lulzbot		FDM 3D printer
4%H2/96%Ar gas	Air Gas	UHP	4% Hydrogen, balanced Argon
Helium gas	Air Gas	UHP	Helium
Heating oven	Neytech	Vulcan 9493308	Oven for 80 °C curing
Quartz tube furnace	Applied Test Systems, Inc.	LEA 05-000075	Furnace for 1050 °C carbonization
Graphite furnace	Thermal Technology LLC		Sintering furnace
Scanning Electron Microscope (SEM)	Jeol	JSM-7401F
pH meter	Thermo Scientific	Orion 4 Star	calibrated with buffer standards
Rheometer	TA Instrument	AR2000ex	For measurement of viscosity
X-ray Diffractometer (XRD)	Bruker	AX D8 Advanced
Analytical balance	Mettler Toledo	XS104
Bruker EVA			XRD Analysis Software