USPatent applicationPatented

Tri-blend resin of PBI, PAEK, and PEI

Granted 8 Dec 2009 · 1 office action

Life of the application

8 dated events
⤢ drag to zoom2008201020122014201620182020202220242026ProsecutionOwnershipTerm & fees
ProsecutionOwnershipTerm & feeshover for detail · click to open

Abstract

A polymer blend comprises PBI, PAEK, and PEI. A method of making the foregoing blend comprises the steps of intimately blending PBI, PAEK, and PEI by dissolving PBI, PAEK, and PEI in a strong acid or melt blending PBI, PAEK, and PEI.

Description

5 parts
›FIELD OF THE INVENTION

An engineered plastic is a blend of PBI, PAEK, and PEI.

›BACKGROUND OF THE INVENTION

Polybenzimidazoles (PBI), polyaryleneketones, also referred to as polyaryletherketones, (PAEK), and polyetherimides (PEI) are known. See: Billmeyer, F. W., Textbook of Polymer Science, 3 rd Edition, John Wiley & Sons, New York City, N.Y. (1984).

In U.S. Pat. No. 4,912,176, a sintered molded article is made from a homogenous blend of PBI and PAEK. The homogenous blend is formed by dry blending the constituent particulates in a high speed mixer. U.S. Pat. No. 4,912,176, column 7, lines 38-54.

In U.S. Pat. No. 4,973,630, a miscible composition is made from PBI and PEI. The miscible composition is prepared by first dissolving the constituents in a mutual polar solvent, such polar solvents being: e.g., N,N-dimethylformamide, N,N-dimethylacetamide (DMAc), or N-methylpyrrolidone (NMP). U.S. Pat. No. 4,973,630, column 8, lines 18-24.

While each of the foregoing blends has good attributes, there continues to be a need to find new methods of making engineered plastics and new engineered plastics that have still better properties.

›SUMMARY OF THE INVENTION

A polymer blend comprises PBI, PAEK, and PEI. A method of making the foregoing blend comprises the steps of intimately blending PBI, PAEK, and PEI by dissolving PBI, PAEK, and PEI in a strong acid or melt blending PBI, PAEK, and PEI.

›DESCRIPTION OF THE INVENTION

Polybenzimidazole (PBI) refers to a polymer having a high thermal stability and excellent resistance to oxidative or hydrolytic degradation. One embodiment of PBI may be represented by a polymer having the following repeat units:

where Ar 1 represents a tetravalent aromatic moiety, e.g.,

where R may represent, for example, —O—, —SO 2 —, CH 2 x , and x being a positive integer,

where Ar 2 represents a divalent aromatic moiety, e.g.,

where R 1 represents, for example, —O—, CH 2 x , —Si(CH 3 ) 2 —O—Si(CH 3 ) 2 —, and x being a positive integer. PBI is commercially available from PBI Performance Products, Inc. of Charlotte, N.C.

Polyaryleneketone, also referred to as polyaryletherketone, (PAEK) refers to a polymer having good chemical resistance and moderate compressive strength but poorer mechanical properties at elevated temperatures when compared to PBI. One embodiment of PAEK may be represented a polymer having the following repeat units:

where X, Y, and N are positive integers. There are several variants Of PAEK. Examples of the variants include, but are not limited to:

PAEKs are commercially available under the tradename VICTREX® from Victrex plc of Lancashire, UK.

Polyetherimide (PEI) refers to a polymer having high heat resistance, high strength-to-weight ratio, high modulus, excellent non-flammability characteristics, processability on conventional molding equipment, low smoke evolution, high dielectric strength, a stable dielectric constant and dissipation factor over a wide range of temperatures and frequencies, and good chemical resistance except to, for example, chlorinated solvents, ethylene glycol, and N,N-dimethylformamide. One embodiment of PEI may be represented a polymer having the following repeat units:

where n is a positive integer. One class of PEI is commercially available under the tradename ULTEM® from General Electric Plastics of Pittsfield, Mass.

The tri-blend composition comprises PBI, PAEK, and PEI. In one embodiment, the minimum amount of each component may be 10% by weight. In another embodiment, the maximum amount of any one component may be 85%. In another embodiment, the maximum amount of any one component may be 75%.

The tri-blend's components, PBI, PAEK, and PEI, are intimately blended and then harvested. Intimately blending is a process where the components are mixed. Harvesting refers to the process for recovering the intimately mixed tri-blend for use. Each is discussed in greater detail below.

Intimately blending is a process where the components are mixed. In one embodiment, intimately blending may be accomplished by blending solutions of the components. When blending solutions, a common solvent for each component may be used. One group of common solvents may be strong acids. Strong acids may be selected from the group of sulfuric acid, methane sulfonic acid, trifluoromethane sulfonic acid, trifluoroacetic acid, dichloroacetic acid, and combinations thereof. In one embodiment, sulfuric acid is preferred. In another embodiment, intimately blending may be accomplished by melt blending. When melt blending, the components may be intimately blended in an extruder. Prior to blending in the extruder, the components may be dry blended in, for example, a tumbler or a high shear mixer.

Harvesting is the process for recovering the intimately blended tri-blend for use. In one embodiment, when the tri-blend is made by the solution process, the tri-blend may be recovered by: precipitating out the tri-blend in a non-solvent, for example water or methanol, filtering the tri-blend from the common solvent, washing the tri-blend, neutralizing any residual solvent in the tri-blend, washing the neutralized tri-blend, and drying the tri-blend. This harvesting may include all of the foregoing steps or any combination of those steps as needed. In another embodiment, when the tri-blend is made by the melt blend process, the tri-blend may be ground to the appropriate particulate size.

The foregoing tri-blends may be used, for example, in the manufacture of semiconductor devices including microchips, flat panel displays, and the like. In the manufacture of such apparatus, materials may be vapor deposited upon a substrate. During the vapor deposition, the substrates are held by jigs, fixtures, and/or molds. These jigs, fixtures, and/or molds must be inert to the vapor deposition environment, so to prevent contamination arising from the off-gassing, or the like, of the materials from which the jigs, fixtures, and molds are made. Likewise, other components of the vapor deposition chamber may also be made from the blends discussed herein. Furthermore, these blends may be used in like components of semiconductor etching, ashing, wafer transportation, and as hard-disc media cassettes where support components may function as a seal, insulator, holding or transportation device which must endure exposure to the harsh process environment. Further application for the blends discussed herein can be found in various industrial, chemical, and petrochemical processes where the temperature resistance, chemical resistance, strength and modulus of this material enables production in harsher environments or extends the life cycle of parts used in these processes.

›EXAMPLES

The foregoing description of the invention is further illustrated by way of the following, non-limiting examples.

Raw materials: The following materials were used: PBI—PBI 100 (Tg—434° C.) from PBI Performance Products; PAEK—VICTREX® PEEK 150 PF (Tg—145° C.) from Victrex plc; and PEI—ULTEM® 100 (Tg—218° C.) from GE Plastics.

Stock solutions: Stock solutions were prepared as follows: PBI—100 g of PBI and 900 g of 96% H 2 SO 4 were added to a 1000 ml three-necked flask equipped with a mechanical stirrer (4 blades) and nitrogen inlet/outlet. The mixture was stirred for 16 hours (h) at 60° C. and cooled to room temperature to produce a 10% PBI stock solution. PAEK—100 g of PEEK and 900 g of 96% H 2 SO 4 were added to a 1000 ml three-necked flask equipped with a mechanical stirrer (4 blades) and nitrogen inlet/outlet. The mixture was stirred for 16 h at room temperature to produce a 10% PAEK stock solution. PEI—100 g of PEI and 900 g of 96% H 2 SO 4 is added to a 1000 ml three-necked flask equipped with a mechanical stirrer (4 blades) and nitrogen inlet/outlet. The mixture was stirred for 0.5 h at room temperature to produce a 10% PEI stock solution.

Solution blends: Solution blends of the PBI/PAEK/PEI were prepared as follows: PEI incrementally added—Solution blends, where PEI is incrementally added, sufficient solution of 10% PEI stock solution is added and stirred for 1.5 h at room temperature, poured into one liter of fast stirring water in a Waring blender, filtered to collect the tri-blend. The tri-blend is washed with water, neutralized with ammonium hydroxide, filtered, washed again with water, and then dried for overnight under vacuum at 120° C. PAEK incrementally added—Solution blends, where PAEK is incrementally added, sufficient solution of 10% PAEK stock solution is added and stirred for 1.5 h at room temperature, poured into one liter of fast stirring water in a Waring blender, filtered to collect the tri-blend. The tri-blend is washed with water, neutralized with ammonium hydroxide, filtered, washed again with water, and then dried for overnight under vacuum at 120° C.

Melt blends: Melt blends of the PBI/PAEK/PEI were prepared as follows: Components were weighted, pre-dry-mixed, and fed through a Brabender extruder with an ¾ inch (in) diameter barrel 18 in long with three heating zones at 50-100 rpm. 100 g of the blend were extruded under the following conditions:

Testing: Samples were tested for glass transition temperature (Tg) and for thermal stability by TGA. Tg was measured using a differential scanning calorimeter (TA Instruments DSC 2020 Modulated DSC), samples were continuously flushed with nitrogen. Tgs were measured for both scanning the first heating, cooling, and then scanning the second heating with a heating rate of 10° C./min. The rate of cooling the sample between the two heating was 10° C./min. TGA measurements were made using a TGA/SDTA 857e Mettler Toledo instrument with a heating rate of 10° C./min under nitrogen.

Test results are as follows:

The present invention may be embodied in other forms without departing from the spirit and the essential attributes thereof, and, accordingly, reference should be made to the appended claims, rather than to the foregoing specification, as indicated the scope of the invention.

›Tables in the description — 2
PBI/PAEK/PEI1 ST ZONE (° C.)2 ND ZONE (° C.)3 RD ZONE (° C.)
50/50/0310370400
45/45/10300370390
37.5/37.5/25290360380
25/25/50300360380
12.5/12.5/75280350370
50/0/50290370400
45/10/45280370390
37.5/25/37.5280370390
25/50/25285370390
12.5/75/12.5280370390
PBI/PAEK/PEITg1Tg2TGATd10
Prepared by Solution Method
50/50/0*154415
50/50/0151426547555
45/45/10157405535539
37.5/37.5/25175399512498
25/25/50193429424489
12.5/12.5/75197430324438
50/0/50199431459599
45/10/45162382471529
37.5/25/37.5182395483512
25/50/25154381524520
12.5/75/12.5168426535552
Prepared by Melt Method
50/50/0*154415
50/50/0148411547555
45/45/10169410535539
37.5/37.5/25171419512498
25/25/50190404424489
12.5/12.5/75202409324438
Comparison of Solution and Melt Methods
SolutionMelt
PBI/PAEK/PEITGATd10TGATd10
50/50/0547555565581
45/45/10535539541558
37.5/37.5/25512498532548
25/25/50424489526541
12.5/12.5/75324438524539
50/0/50459599521543
45/10/45471529524544
37.5/25/37.5483512529543
25/50/25524520535549
12.5/75/12.5535552547562
*Commercially available CELAZOLE TU-60 from PBI Performance Products
Tg1 = first glass transition temperature (° C.)
Tg2 = second glass transition temperature (° C.)
TGA = degradation temperature at onset (° C.)
Td10 = temperature at 10% weight loss (° C.)

Claims as granted

5 claims

Log in to read the claims of this application.

Log in to unlock

Classifications

9 codes
IPC · International Patent Classification
Section C — Chemistry; metallurgy
  • C08L79/06
  • C08L77/06
  • C08L79/08
USPC · US Patent Classification
525/435525/425525/432525/931525/420525/436

Claim changes

Soon
Coming soonHow the claims changed between publication and grant

See which claims were amended, added or cancelled during examination, with every added and removed word marked.

AmendedAddedCancelledUnchanged

The published claims of this application are not paired with the granted ones in what we hold.

File wrapper

⤢ drag to zoomJan 2007Jul 2007Jan 2008Jul 2008Jan 2009Jul 2009Jan 2010USPTOApplicantNon-final rejectionResponse after non-finalNotice of allowance
USPTOApplicanthover for detail · click to open
Pendency
2.8 y
1,036 days filing → grant
Office actions
1
non-final + final
Responses
1
no RCE
Interviews
1
examiner interview summaries
Examiner
Ana L Woodward
art unit 1796 · TC 1700
Citations: 5 back · 0 forward

See the full prosecution history — every USPTO and applicant action on this file, in order.

Log in to unlock

Documents

Log in to open the documents of this file: the application as filed, every office action and response, the notice of allowance.

Log in to unlock

Chain of title

⤢ drag to zoom2008201020122014201620182020202220242026Owner 1
Titlehover for detail · click to open

See the full assignment history — every owner this patent has passed through, with recordation dates and reel/frame numbers.

Log in to unlock