The present invention relates to noise suppression structures and, more particularly, to methods of making noise suppression structures for aircraft ducts and plenums.
Many aircraft are powered by jet engines. In most instances, jet engines include one or more gas-powered turbine engines, auxiliary power units (APUs), and/or environmental control systems (ECSs), which can generate both thrust to propel the aircraft and electrical energy to power systems installed in the aircraft. Although aircraft engines are generally safe, reliable, and efficient, the engines do exhibit certain drawbacks. For example, the turbine engines, as well as other components that make up the engine, can be sources of unwanted noise, especially during aircraft take-off and landing operations. Moreover, APUs and ECSs can be sources of unwanted ramp noise. Thus, various governmental rules and regulations aimed at mitigating such noise sources have been enacted.
To address, and at least somewhat alleviate, the unwanted noise emanating from aircraft noise sources, and to thereby comply with the above-noted rules and regulations, various types of noise reduction treatments have been developed. For example, one type of noise reduction treatment that has been developed for use in aircraft ducts is a noise suppression panel. In many instances, noise suppression panels are flat or contoured, and include a honeycomb structure disposed between a backing plate and a face plate. Other noise suppression materials and structure may also be disposed between the backing plate and face plate. The noise suppression panels are typically placed on the interior surface of engine or APU inlet and/or outlet plenums, as necessary, to reduce noise emanations.
Although the above-described noise suppression panels do exhibit fairly good noise suppression characteristics, the panels also exhibit certain drawbacks. For example, the honeycomb structure can be costly to manufacture, and difficult to conform to contoured surfaces. The honeycomb structure can also be difficult to bond to the backing plate and/or face plate. Moreover, the honeycomb structure used in these panels is typically uniform in size and shape, which can result in the noise suppression panel being highly effective over only a relatively narrow frequency range.
The present invention provides methods of making a noise suppression panel that can be readily bonded to backing and/or face plates, and is effective over a relatively wide frequency range.
In one embodiment, and by way of example only, a method of forming a foam includes pressurizing a foaming agent and a foamable material in a closed vessel. The foaming agent and the foamable material are then decompressed, whereby a foam having a plurality of cells is formed.
Other independent features and advantages of the preferred noise suppression panel manufacturing methods will become apparent from the following detailed description, taken in conjunction with the accompanying drawings which illustrate, by way of example, the principles of the invention.
Before proceeding with the detailed description, it is to be appreciated that the described embodiment is not limited to use in conjunction with a particular type of engine, or in a particular type of vehicle. Thus, although the present embodiment is, for convenience of explanation, described as being implemented in an aircraft environment, it will be appreciated that it can be implemented in various other types of vehicles, and in various other systems and environments.
Turning now to the description, and with reference first to
The face plate 104 is constructed of any one of numerous types of materials such as, for example, aluminum, and carbon composites. In a particular preferred embodiment, however, the face plate 104 is constructed of BMI, and is perforated to a desired percent open area (POA) value. As is generally known, relatively low POA values (e.g., ˜5%) provide acoustic resistance, whereas relatively high POA values (e.g., ˜30%) provide acoustic transparency. In a particular preferred embodiment, the face plate 104 is perforated to a POA value greater than about 30% to ensure the face plate 104 is acoustically transparent to any incident sound. Similar to the back plate 102, and as will be described further below, the face plate 104 is also preferably bonded to the foam bulk absorber 106 during manufacture of the panel 100.
The foam bulk absorber 106 is disposed between the back plate 102 and face plate 104 and, as was mentioned above, is preferably directly bonded to each plate 102, 104 during manufacture of the panel 100. The foam bulk absorber 106, following fabrication, is preferably open cell foam. Thus, it is preferably constructed of a foamable material. Some non-limiting examples of these materials include various thermoset materials, such as bismaleimide (BMI) or phenolic, various ceramic powder compounds, such as alumina or zirconia, and various metal powder compounds, such as 316L stainless steel, or carbonyl iron and nickel compounds. The thermoset materials are preferably used for relatively low temperature applications (e.g., 200-400° F.), and the ceramic or metal powder compounds are preferably used for relatively high temperature applications (e.g., 1200-1500° F.). Moreover, when the ceramic or metal powder compounds are used, a binder may additionally be included. Non-limiting examples of such binders include agar gels, polystyrene, or other polymer/wax combinations.
With reference now to
The integrated noise suppression panel 100 described above is manufactured by first subjecting a foaming agent and a foamable material to pressure in a closed vessel. The foaming agent and amount used may vary, depending on the desired characteristics of the final bulk absorber material, the foamable material used, operating conditions, and equipment capabilities. Some non-limiting examples of foaming agents that may be used include CO2, N2, water, sodium bicarbonate and acid, or various other high-temperature agents. No matter the particular combination of foaming agent and foamable material selected, following pressurization the foaming agent and foamable material are allowed to undergo a relatively rapid decompression. As a result of the rapid decompression, and when certain other conditions are satisfied, which are described in more detail below, a plurality of open cells are formed in the foamable material, and the open cell foam bulk absorber 106 is formed. Depending on the particular process used, the foam bulk absorber 106 may be bonded to the back plate 102 and the face plate 104 either during or after the manufacturing process.
Various equipment arrangements and specific processes may be used to implement the general manufacturing process described above. Two exemplary equipment arrangements and the specific processes are disclosed herein. The first equipment arrangement is preferably used for relatively small-scale projects, such as for process development. Conversely, the second arrangement is preferably used for large-scale projects, such as for factory production.
Turning first to
A foaming agent 308 is also placed in the mold cavity 304. However, how and when the foaming agent 308 is placed in the mold cavity 304 may depend upon the type of foaming agent 308 used. For example, if the foaming agent 308 is a chemical agent, such as sodium bicarbonate and acid, the foaming agent is preferably dispersed within the foamable material charge 306. Conversely, if the foaming agent 308 is a physical foaming agent, such as CO2 or N2 gas, then the foamable material charge 306 is first sealed in the mold cavity 304 with the piston 310. Thereafter, the mold cavity 304 is pressurized through a channel 318 with the CO2 or N2 gas, which saturates the foamable material charge 306. It will be appreciated that when physical foaming agents are used, it is preferable that the foamable material charge 306 be in a granular or powdered form to reduce the diffusion time that may be needed for the physical foaming agent 308 to dissolve uniformly throughout the foamable material charge 306.
A particularly convenient form of a physical foaming agent 308 is solid CO2. In such an embodiment, a predetermined amount of solid CO2 is added to the mold cavity 304, which is then sealed with the piston 310. The solid CO2 sublimes to a gas, which, depending on the amount of the solid CO2 relative to the size of, and the temperature in, the mold cavity 304, generates a pressure. It will be appreciated that the generated pressure can be relatively high, e.g. greater than 6000 psi. This method of generating a relatively high pressure is very convenient since pressures significantly higher than those obtainable with gas cylinders (e.g. 829 psi for CO2 at 20° C.) can be obtained without the use of separate pressurization equipment.
Once the charge of foamable material 306, preferably in powder form, and the foaming agent 308 are placed in sealed the mold cavity 304, the machine 300 is then subject to a predetermined temperature change over a predetermined time period, which will vary depending on the type of the foamable material charge 306. In particular, the temperature-time relation is preferably selected to accommodate both the need to allow the foaming agent 308 to diffuse into the foamable material 306, and for the foamable material 306 to obtain sufficient mechanical properties, either through reaction, if the material is a thermoset, or by temperature reduction, if the material is a thermoplastic. In one particular exemplary embodiment, in which the foamable material 306 is powdered bismaleimide (BMI) and the foaming agent 308 is CO2, the machine 300 is raised to 165° C. from room temperature over approximately a 30-minute period. During this time the CO2 sublimes, pressurizing the mold cavity 304 to a pressure between about 800 and 2000 psi, and diffuses into the powdered BMI prior to its melting. The powdered BMI, now saturated with gas, is maintained at 165° C. for about 30 minutes to achieve sufficient mechanical properties, due to partial cure, so that the foam will not collapse upon pressure release.
Referring now to
It will be appreciated that in some instances the piston 310 may be further moved within the mold cavity 304 following pressurization, to thereby further pressurize the charge of foamable material 306 and foaming agent 308. Such an instance is depicted in
As shown in
The rapid decompression described above allows the pressurized charge of foamable material 306 and foaming agent 308 to decompress, and undergo a rapid expansion in the fixed volume of the mold cavity 304. As was previously described, a plurality of open cells having a distribution of sizes about a mean size are formed in the foamable material 306 during this rapid decompression, thereby forming the open cell foam bulk absorber 106. If, as was previously mentioned, the back plate 102 and the face plate 104 are positioned at opposite ends of the mold cavity 304, an “uncured” noise suppression panel 100 is formed between the plates 102, 104. Thereafter, as represented in
In one particular exemplary embodiment of the above-described process, a 27-g charge of powdered BMI and 0.5 g of a powdered carbon fiber reinforcement material was mixed to form the charge of foamable material 306. The foamable material 306 and an 8.7 g charge of solid CO2, which was used as the foaming agent 308, were placed in the mold cavity 304. The piston 310 was positioned such that the mold cavity volume was approximately 92 cubic centimeters. The mold cavity 304 was then heated from room temperature to 165° C. over a period of about 29 minutes, during which time the CO2 pressurized the mold cavity 304 to about 1050 psi. The foamable material 306 was then cured for an additional 30 minutes at 165° C. Thereafter, the mold cavity 304 was vented rapidly by releasing the hydraulic cylinder, forming the foam bulk absorber 106. The temperature of the depressurized foam bulk absorber 106 was then raised to 200° C. for 1 hour to complete the cure cycle. The mold 302 was then allowed to cool back to room temperature and the foam bulk absorber 106 was removed.
The machine 300 depicted in
A photomicrograph of a foam bulk absorber 106 produced by the above-described machine 300 and process is depicted in
The machine 300 shown in
The depicted device is a compression mold 500 that includes a base plate 502 (
Once the foamable material 306 (306 not shown in 7A) and foaming agent are disposed within the mold cavity 508, the release plate 506 is then placed over the top plate 504. A toggle clamp 518, which is held in place by a hydraulic press 520, holds the release plate 506 in place. A plurality of threaded shoulder bolts 522 extend through the release plate 506 and are threaded into threaded shoulder bolt openings 524 formed in the top plate 504. The shoulder bolts 522 limit the upward travel of the release plate 506. Thereafter, the heaters 510 are energized and the foamable material 306 and foaming agent 308 are heated, and the mold cavity 508 thus is pressurized. In the depicted embodiment, a plurality of o-rings 525 surround the through-holes 516 in the top plate 504, and substantially prevent pressure loss due to leakage. In an alternative embodiment, a gaseous blowing agent may be charged through a high-pressure line to the mold 500 prior to melting of the foamable material 306.
By analogy to embodiment depicted in
An integrated noise suppression panel made in accordance with the processes disclosed herein includes a foam bulk absorber having an open cell structure with cells having a distribution of sizes about a mean size, and a density gradient between the back plate and face plate. As such, the foam bulk absorber described herein provides broadband absorption, as compared to presently known materials.
While the invention has been described with reference to a preferred embodiment, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt to a particular situation or material to the teachings of the invention without departing from the essential scope thereof. Therefore, it is intended that the invention not be limited to the particular embodiment disclosed as the best mode contemplated for carrying out this invention, but that the invention will include all embodiments falling within the scope of the appended claims.