US20040250334A1 - Max phase glove and condom formers - Google Patents
Max phase glove and condom formers Download PDFInfo
- Publication number
- US20040250334A1 US20040250334A1 US10/666,639 US66663903A US2004250334A1 US 20040250334 A1 US20040250334 A1 US 20040250334A1 US 66663903 A US66663903 A US 66663903A US 2004250334 A1 US2004250334 A1 US 2004250334A1
- Authority
- US
- United States
- Prior art keywords
- glove
- condom
- former
- latex
- synthetic polymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 229920001059 synthetic polymer Polymers 0.000 claims abstract description 26
- 229920000126 latex Polymers 0.000 claims abstract description 21
- 239000004816 latex Substances 0.000 claims abstract description 21
- 239000010936 titanium Chemical group 0.000 claims abstract description 12
- 239000010955 niobium Chemical group 0.000 claims abstract description 10
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000011651 chromium Chemical group 0.000 claims abstract description 8
- 239000000203 mixture Chemical group 0.000 claims abstract description 8
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 8
- 229910052732 germanium Inorganic materials 0.000 claims abstract description 7
- 229910052758 niobium Inorganic materials 0.000 claims abstract description 7
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 6
- 229910052733 gallium Inorganic materials 0.000 claims abstract description 6
- 229910052735 hafnium Inorganic materials 0.000 claims abstract description 6
- 229910052738 indium Inorganic materials 0.000 claims abstract description 6
- 229910052706 scandium Inorganic materials 0.000 claims abstract description 6
- 229910052715 tantalum Chemical group 0.000 claims abstract description 6
- 229910052718 tin Inorganic materials 0.000 claims abstract description 6
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 5
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 5
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000004411 aluminium Substances 0.000 claims abstract description 4
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052757 nitrogen Chemical group 0.000 claims abstract description 4
- 239000010703 silicon Substances 0.000 claims abstract description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical group [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 3
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims abstract description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 3
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical group [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims abstract description 3
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims abstract description 3
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical group [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims abstract description 3
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical group [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 claims abstract description 3
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical group [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims abstract description 3
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical group [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims abstract description 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical group [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000011248 coating agent Substances 0.000 claims description 7
- 238000000576 coating method Methods 0.000 claims description 7
- 238000007598 dipping method Methods 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 229920003008 liquid latex Polymers 0.000 claims description 5
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 229910052723 transition metal Inorganic materials 0.000 claims 1
- 150000003624 transition metals Chemical class 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 6
- 239000000463 material Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 239000000919 ceramic Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229910052745 lead Inorganic materials 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229910052573 porcelain Inorganic materials 0.000 description 3
- 230000035939 shock Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 2
- 229910009818 Ti3AlC2 Inorganic materials 0.000 description 2
- 229910009821 Ti3GeC2 Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 229910019829 Cr2AlC Inorganic materials 0.000 description 1
- 229910019855 Cr2GaN Inorganic materials 0.000 description 1
- 229910003842 Hf2InC Inorganic materials 0.000 description 1
- 229910003835 Hf2InN Inorganic materials 0.000 description 1
- 229910003836 Hf2SnC Inorganic materials 0.000 description 1
- 229910003837 Hf2SnN Inorganic materials 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- 229910015419 Mo2GaC Inorganic materials 0.000 description 1
- 229910019637 Nb2AlC Inorganic materials 0.000 description 1
- 229910019707 Nb2AsC Inorganic materials 0.000 description 1
- 229910019710 Nb2GaC Inorganic materials 0.000 description 1
- 229910019701 Nb2InC Inorganic materials 0.000 description 1
- 229910019698 Nb2SnC Inorganic materials 0.000 description 1
- 229910004447 Ta2AlC Inorganic materials 0.000 description 1
- 229910004477 Ta2GaC Inorganic materials 0.000 description 1
- 229910009594 Ti2AlN Inorganic materials 0.000 description 1
- 229910009600 Ti2CdC Inorganic materials 0.000 description 1
- 229910009930 Ti2GaC Inorganic materials 0.000 description 1
- 229910009925 Ti2GaN Inorganic materials 0.000 description 1
- 229910009926 Ti2GeC Inorganic materials 0.000 description 1
- 229910009927 Ti2InC Inorganic materials 0.000 description 1
- 229910009928 Ti2InN Inorganic materials 0.000 description 1
- 229910009966 Ti2PbC Inorganic materials 0.000 description 1
- 229910010013 Ti2SnC Inorganic materials 0.000 description 1
- 229910010014 Ti2TlC Inorganic materials 0.000 description 1
- 229910009846 Ti4AlN3 Inorganic materials 0.000 description 1
- 229910008196 Zr2InC Inorganic materials 0.000 description 1
- 229910008255 Zr2PbC Inorganic materials 0.000 description 1
- 229910008248 Zr2SnC Inorganic materials 0.000 description 1
- 229910008244 Zr2TlC Inorganic materials 0.000 description 1
- 229910008237 Zr2TlN Inorganic materials 0.000 description 1
- UGACIEPFGXRWCH-UHFFFAOYSA-N [Si].[Ti] Chemical compound [Si].[Ti] UGACIEPFGXRWCH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 239000011507 gypsum plaster Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000003562 lightweight material Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000007569 slipcasting Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A41—WEARING APPAREL
- A41D—OUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
- A41D19/00—Gloves
- A41D19/0055—Plastic or rubber gloves
Definitions
- the present invention relates to glove and condom formers used in the manufacture of natural latex or synthetic polymer gloves and condoms.
- the glove and condom formers are comprised of a chemical resistant, durable, and thermal shock resistant material referred to herein as a MAX phase.
- Latex and synthetic polymer examination and surgical gloves and condoms are produced using rigid molds sized and shaped to the dimensions of the finished product.
- formers are comprised of materials such as ceramic, porcelain, plastic, steel and/or aluminum.
- the former is dipped, usually fingers first in the case of a glove former, into a bath of liquid latex or synthetic polymer and admixed chemicals so that the latex or synthetic polymer adheres to the former.
- the glove or condom former is heated prior to dipping in the liquid latex or synthetic bath.
- the glove and condom former is pre-coated with a coagulant such as calcium nitrate which serves to gel the latex or synthetic polymer and facilitates removal of the latex or synthetic polymer glove or condom from the former.
- a coagulant such as calcium nitrate which serves to gel the latex or synthetic polymer and facilitates removal of the latex or synthetic polymer glove or condom from the former.
- the latex or synthetic polymer coating on the former is allowed to dry. Additional dippings in the latex or synthetic polymer bath, followed by drying of the additional coating may be required. Further, in some production methods, the coating is further treated by leaching and/or washing to remove residual chemicals prior to removal from the former.
- the glove or condom is typically released from the former by peeling the latex or synthetic polymer coating from the former, thereby inverting the glove or condom in the process.
- the outer layer from the former is the innermost layer of the glove or condom.
- the glove or condom is removed from the former in water.
- the gloves or condoms are then packaged for shipping. In some embodiments, the gloves or condoms are sterilized prior to or in conjunction with packaging.
- An object of the present invention is to provide a glove or condom former comprising a MAX phase.
- the MAX phase makes up the majority of the material used to produce the glove and condom formers.
- Another object of the present invention is to provide methods for producing latex or synthetic polymer gloves and condoms which comprises dipping a glove or condom former comprising a MAX phase into a liquid latex or synthetic polymer bath so that latex or synthetic polymer coats the former; allowing the latex or synthetic polymer coating to dry on the former; and releasing the formed latex or synthetic polymer glove or condom from the former.
- the present invention provides a new family of materials, referred to herein as MAX phases, for use in glove and condom formers.
- MAX phases provide a chemical resistant, durable, and thermal shock resistant material for glove and condom formers.
- MAX phase or “MAX phases” as used herein it is meant a material comprising M n+1 Ax n.
- M is selected from scandium (Sc), titanium (Ti), vanadium (V), chromium (Cr), zirconium (Zr), niobium (Nb), hafnium (Hf), and tantalum (Ta).
- M may comprise a single transitional metal selected from any of Sc, Ti, V, Cr, Zr, Nb, Hf and Ta.
- M may comprise a mixture of two or more transitional metals selected from any of Sc, Ti, V, Cr, Zr, Nb, Hf and Ta.
- A is an element selected from aluminium (Al), silicon (Si), gallium (Ga), germanium (Ge), tin (Sn), lead (Pb) and indium (In).
- A may comprise a single element selected from Al, Si, Ga, Ge, Sn, Pb and In.
- A may comprise a mixture of two or more elements selected from any of Al, Si, Ga, Ge, Sn, Pb and In.
- X as used in this chemical formula, is carbon and/or nitrogen.
- n as used in this chemical formula, is 1, 2 or 3.
- the MAX phase makes up the majority, meaning more than 50%, of the material used to produce the glove and condom formers.
- An exemplary MAX phase compound useful in the present invention is Ti 3 SiC 2 Additional exemplary MAX phases which have been synthesized and found to exhibit similar characteristics are Ti 3 GeC 2 and Ti 3 AlC 2 .
- MAX phases such as Ti 3 SiC 2 , Ti 3 GeC 2 , and Ti 3 AlC 2 are also referred to herein as “312” compounds for the number of atoms of each element in the compound, respectively. In these MAX phases, n is equal to 2.
- MAX phases may also comprise a “211” formula wherein n is equal to 1, or a “413” formula wherein n is equal to 3.
- An exemplary MAX phase with a 413 formula is Ti 4 AlN 3 .
- Exemplary MAX phases with a 211 formula are shown in the following Table 1.
- Carbides are generally known to be hard or brittle and not suitable for use in the manufacture of machine parts.
- MAX phases such as titanium silicon carbide (Ti 3 SiC 2 ) and other exemplified 312, 413 and 212 compounds described herein results in a soft, machinable, strong and lightweight material almost as machinable as graphite.
- single-phase samples and composites of the MAX phase Ti 3 SiC 2 were characterized for thermal stability and oxidation-resistance. Sample bars of Ti 3 SiC 2 were quenched from 1,400° C. in water and found to have a slightly increased strength after quenching.
- MAX phases such as Ti 3 SiC 2 have properties of both metals and ceramics. Like a metal, they are machinable, thermally and electrically conductive, resistant to thermal shock, and plastic at elevated temperatures. Like a ceramic, they are refractory (i.e., have a decomposition temperature of greater than 2,000° C.), oxidation-resistant, stiff and lightweight (roughly 4.5 grams per cubic centimeter). Further, their thermal expansion is relatively low, more like a ceramic than a metal.
- a MAX phase of the present invention is slip cast and sintered into a glove or condom former by dispersing the MAX phase ceramic powder in water along with a binder and viscosity modifying agent.
- the dispersion preferably ranges from about 25% to 85% solids.
- the binder and viscosity modifier are preferably cellulose based materials.
- the resulting dispersion or slurry is referred to as the slip.
- This slip is poured into a plaster of paris mold and allowed set for at least 10 to 15 minutes, more preferably up to 60 minutes, before the excess slip is drained.
- the glove or condom former is removed from the mold and allowed to air dry. After drying, the former is sintered by heating in an oven at temperatures ranging from about 1300° C. to about 1600° C.
- MAX phase samples of Ti3SiC2 exhibited excellent corrosion resistance in both acids and alkalis.
- glove and condom formers of the present invention comprising a MAX phase are expected to exhibit substantially increased durability and a phase are expected to exhibit substantially increased durability and a chemical resistance as compared to current commercially available formers.
- the MAX phase glove and condom formers of the present invention are useful in the production of latex and synthetic polymer gloves and condoms.
- Latex and synthetic polymer gloves and/or condoms can be produced in accordance with well known procedures by dipping the glove or condom former of the present invention comprising a MAX phase into a liquid latex or synthetic polymer bath so that latex or synthetic polymer coats the former. The latex or synthetic polymer coating is then allowed to dry on the former and the resulting glove or condom is released from the former.
- the enhanced durability of MAX phase condom and glove formers results in a reduction in the frequency with which the formers used in this proceed must be replaced while maintaining the quality of the glove or condom produced.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Orthopedics, Nursing, And Contraception (AREA)
Abstract
Glove or condom formers of Mn+1AXn, wherein M is scandium, titanium, vanadium, chromium, zirconium, niobium, hafnium, and tantalum or a mixture thereof, A is aluminium (Al), silicon (Si), gallium (Ga), germanium (Ge), tin (Sn), lead (Pb) or indium (In) or a mixture thereof, X is carbon or nitrogen, and n is 1, 2 or 3, are provided. Methods for producing latex and synthetic polymer gloves and condoms with these formers are also provided.
Description
- This patent application claims the benefit of priority from U.S. Provisional Application Ser. No. 60/478,903, filed Jun. 13, 2003, which is herein incorporated by reference in its entirety.
- The present invention relates to glove and condom formers used in the manufacture of natural latex or synthetic polymer gloves and condoms. In this invention, the glove and condom formers are comprised of a chemical resistant, durable, and thermal shock resistant material referred to herein as a MAX phase.
- Latex and synthetic polymer examination and surgical gloves and condoms are produced using rigid molds sized and shaped to the dimensions of the finished product. Typically, such formers are comprised of materials such as ceramic, porcelain, plastic, steel and/or aluminum. The former is dipped, usually fingers first in the case of a glove former, into a bath of liquid latex or synthetic polymer and admixed chemicals so that the latex or synthetic polymer adheres to the former.
- In some production methods, the glove or condom former is heated prior to dipping in the liquid latex or synthetic bath.
- Further, in some production methods, the glove and condom former is pre-coated with a coagulant such as calcium nitrate which serves to gel the latex or synthetic polymer and facilitates removal of the latex or synthetic polymer glove or condom from the former.
- After dipping the former in the latex or synthetic polymer bath, the latex or synthetic polymer coating on the former is allowed to dry. Additional dippings in the latex or synthetic polymer bath, followed by drying of the additional coating may be required. Further, in some production methods, the coating is further treated by leaching and/or washing to remove residual chemicals prior to removal from the former.
- The glove or condom is typically released from the former by peeling the latex or synthetic polymer coating from the former, thereby inverting the glove or condom in the process. Thus, in the finished articles, the outer layer from the former is the innermost layer of the glove or condom. In some embodiments, the glove or condom is removed from the former in water.
- The gloves or condoms are then packaged for shipping. In some embodiments, the gloves or condoms are sterilized prior to or in conjunction with packaging.
- After repeated use involving dipping of the formers into the latex or synthetic polymer and admixed chemical baths, the ceramic, porcelain, plastic, steel or aluminum formers begin to degrade. Quality of the gloves or condoms diminishes until a replacement former is needed. For example, in accelerated aging studies with concentrated hot potassium hydroxide, a former comprised of porcelain requires replacement due to degrading after only two weeks.
- Thus, there is a need for glove and condom formers comprised of more durable materials that will increase the length of use and reduce the frequency with which the formers must be replaced while maintaining the quality of the glove or condom produced.
- An object of the present invention is to provide a glove or condom former comprising a MAX phase. By “MAX phase” or “MAX phases” as used herein it is meant a material comprising Mn+1 Axn(n=1,2,3) wherein M is selected from Sc, Ti, V, Cr, Zr, Nb, Hf and Ta or a mixture thereof; wherein A is selected from Al, Si, Ga, Ge, Sn, Pb and In or a mixture thereof, and wherein X is carbon and/or nitrogen. In a preferred embodiment of the present invention, the MAX phase makes up the majority of the material used to produce the glove and condom formers.
- Another object of the present invention is to provide methods for producing latex or synthetic polymer gloves and condoms which comprises dipping a glove or condom former comprising a MAX phase into a liquid latex or synthetic polymer bath so that latex or synthetic polymer coats the former; allowing the latex or synthetic polymer coating to dry on the former; and releasing the formed latex or synthetic polymer glove or condom from the former.
- The present invention provides a new family of materials, referred to herein as MAX phases, for use in glove and condom formers. As demonstrated herein, MAX phases provide a chemical resistant, durable, and thermal shock resistant material for glove and condom formers.
- By “MAX phase” or “MAX phases” as used herein it is meant a material comprising Mn+1 Axn.
- M, as used in this chemical formula, is selected from scandium (Sc), titanium (Ti), vanadium (V), chromium (Cr), zirconium (Zr), niobium (Nb), hafnium (Hf), and tantalum (Ta). M may comprise a single transitional metal selected from any of Sc, Ti, V, Cr, Zr, Nb, Hf and Ta. Alternatively, M may comprise a mixture of two or more transitional metals selected from any of Sc, Ti, V, Cr, Zr, Nb, Hf and Ta.
- A, as used in this chemical formula, is an element selected from aluminium (Al), silicon (Si), gallium (Ga), germanium (Ge), tin (Sn), lead (Pb) and indium (In). A may comprise a single element selected from Al, Si, Ga, Ge, Sn, Pb and In. Alternatively, A may comprise a mixture of two or more elements selected from any of Al, Si, Ga, Ge, Sn, Pb and In.
- X, as used in this chemical formula, is carbon and/or nitrogen.
- n, as used in this chemical formula, is 1, 2 or 3.
- In a preferred embodiment of the present invention, the MAX phase makes up the majority, meaning more than 50%, of the material used to produce the glove and condom formers.
- An exemplary MAX phase compound useful in the present invention is Ti3SiC2 Additional exemplary MAX phases which have been synthesized and found to exhibit similar characteristics are Ti3GeC2 and Ti3AlC2. MAX phases such as Ti3SiC2, Ti3GeC2, and Ti3AlC2 are also referred to herein as “312” compounds for the number of atoms of each element in the compound, respectively. In these MAX phases, n is equal to 2.
- MAX phases may also comprise a “211” formula wherein n is equal to 1, or a “413” formula wherein n is equal to 3. An exemplary MAX phase with a 413 formula is Ti4AlN3. Exemplary MAX phases with a 211 formula are shown in the following Table 1.
TABLE 1 “211” COMPOUNDS Ti2AlC Ti2AlN Hf2PbC Cr2GaC V2AsC Ti2InN Nb2AlC (Nb, Ti)2AlC Ti2AlN1/2 C1/4 Nb2GaC Nb2AsC Zr2InN Ti2GeC Cr2AlC Zr2SC Mo2GaC Ti2CdC Hf2InN Zr2SnC Ta2AlC Ti2SC Ta2GaC Sc2InC Hf2SnN Hf2SnC V2AlC Nb2SC Ti2GaN Ti2InC Ti2TlC Ti2SnC V2PC Hf2SC Cr2GaN Zr2InC Zr2TlC Nb2SnC Nb2PC Ti2GaC V2GaN Nb2InC IIf2TlC Zr2PbC Ti2PbC V2GaC V2GeC Hf2InC Zr2TlN - Carbides are generally known to be hard or brittle and not suitable for use in the manufacture of machine parts. However, synthesis of MAX phases such as titanium silicon carbide (Ti3SiC2) and other exemplified 312, 413 and 212 compounds described herein results in a soft, machinable, strong and lightweight material almost as machinable as graphite. Further, single-phase samples and composites of the MAX phase Ti3SiC2 were characterized for thermal stability and oxidation-resistance. Sample bars of Ti3SiC2 were quenched from 1,400° C. in water and found to have a slightly increased strength after quenching.
- Accordingly, MAX phases such as Ti3SiC2 have properties of both metals and ceramics. Like a metal, they are machinable, thermally and electrically conductive, resistant to thermal shock, and plastic at elevated temperatures. Like a ceramic, they are refractory (i.e., have a decomposition temperature of greater than 2,000° C.), oxidation-resistant, stiff and lightweight (roughly 4.5 grams per cubic centimeter). Further, their thermal expansion is relatively low, more like a ceramic than a metal.
- Various methods well known to those skilled in the art can be used for producing formers from the MAX Phases of the present invention. Exemplary methods include, but are not limited to slip casting and sintering and gel casting.
- In one embodiment, a MAX phase of the present invention is slip cast and sintered into a glove or condom former by dispersing the MAX phase ceramic powder in water along with a binder and viscosity modifying agent. The dispersion preferably ranges from about 25% to 85% solids. The binder and viscosity modifier are preferably cellulose based materials. The resulting dispersion or slurry is referred to as the slip. This slip is poured into a plaster of paris mold and allowed set for at least 10 to 15 minutes, more preferably up to 60 minutes, before the excess slip is drained. Once set, the glove or condom former is removed from the mold and allowed to air dry. After drying, the former is sintered by heating in an oven at temperatures ranging from about 1300° C. to about 1600° C.
- MAX phase samples of Ti3SiC2 exhibited excellent corrosion resistance in both acids and alkalis. Thus, glove and condom formers of the present invention comprising a MAX phase are expected to exhibit substantially increased durability and a phase are expected to exhibit substantially increased durability and a chemical resistance as compared to current commercially available formers.
- Thus, the MAX phase glove and condom formers of the present invention are useful in the production of latex and synthetic polymer gloves and condoms. Latex and synthetic polymer gloves and/or condoms can be produced in accordance with well known procedures by dipping the glove or condom former of the present invention comprising a MAX phase into a liquid latex or synthetic polymer bath so that latex or synthetic polymer coats the former. The latex or synthetic polymer coating is then allowed to dry on the former and the resulting glove or condom is released from the former. The enhanced durability of MAX phase condom and glove formers results in a reduction in the frequency with which the formers used in this proceed must be replaced while maintaining the quality of the glove or condom produced.
- It is understood that various changes and modifications to the embodiments described herein will be apparent to those skilled in the art upon reading this disclosure. Such changes and modifications can be made without departing from the spirit and scope of the present invention and its advantages over the prior art. It is, therefore, intended that such changes and modifications be included within the scope of the following claims.
Claims (3)
1. A glove or condom former comprising Mn+1AXn,
wherein M is a transition metal selected from scandium, titanium, vanadium, chromium, zirconium, niobium, hafnium, and tantalum, or a mixture thereof;
wherein A is an element selected from aluminium, silicon, gallium, germanium, tin, lead and indium, or a mixture thereof;
wherein X is carbon or nitrogen; and
n is 1, 2 or 3.
2. The glove or condom former of claim 1 where M is titanium, A is selected from silicon, germanium or aluminium, X is carbon and n is 2.
3. A method for producing a latex or synthetic polymer glove or condom comprising:
(a) dipping the glove or condom former of claim 1 in a liquid latex or synthetic polymer bath;
(b) allowing the latex or synthetic polymer coating to dry on the former; and
(c) releasing the formed latex or synthetic polymer glove or condom from the former.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/666,639 US20040250334A1 (en) | 2003-06-13 | 2003-09-19 | Max phase glove and condom formers |
PCT/US2004/018528 WO2004112641A2 (en) | 2003-06-13 | 2004-06-10 | Max phase glove and condom formers |
US11/435,052 US20060202389A1 (en) | 2003-06-13 | 2006-05-16 | MAX phase glove and condom formers |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US47890303P | 2003-06-13 | 2003-06-13 | |
US10/666,639 US20040250334A1 (en) | 2003-06-13 | 2003-09-19 | Max phase glove and condom formers |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/435,052 Continuation US20060202389A1 (en) | 2003-06-13 | 2006-05-16 | MAX phase glove and condom formers |
Publications (1)
Publication Number | Publication Date |
---|---|
US20040250334A1 true US20040250334A1 (en) | 2004-12-16 |
Family
ID=33514293
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/666,639 Abandoned US20040250334A1 (en) | 2003-06-13 | 2003-09-19 | Max phase glove and condom formers |
US11/435,052 Abandoned US20060202389A1 (en) | 2003-06-13 | 2006-05-16 | MAX phase glove and condom formers |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/435,052 Abandoned US20060202389A1 (en) | 2003-06-13 | 2006-05-16 | MAX phase glove and condom formers |
Country Status (2)
Country | Link |
---|---|
US (2) | US20040250334A1 (en) |
WO (1) | WO2004112641A2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050049136A1 (en) * | 2001-12-18 | 2005-03-03 | Gromelski Stanley J | Carbide and nitride ternary ceramic glove and condom formers |
US20170304109A1 (en) * | 2016-04-25 | 2017-10-26 | Gamal Ragheb | Birth Control Assembly |
CN111943205A (en) * | 2020-08-28 | 2020-11-17 | 郑州轻工业大学 | Method for preparing MAX phase by adopting melt displacement reaction, prepared MAX phase and application |
US10964302B2 (en) | 2014-01-14 | 2021-03-30 | Raytheon Technologies Corporation | Vibration damping material for high temperature use |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8056571B2 (en) | 2006-02-13 | 2011-11-15 | Propel Mobility | Axilla area force receiver apparatus |
FR2901721B1 (en) * | 2006-05-30 | 2008-08-22 | Commissariat Energie Atomique | MAX PHASE POWDERS AND PROCESS FOR PRODUCING SAID POWDERS |
US11572298B2 (en) * | 2018-05-11 | 2023-02-07 | Entegris, Inc. | Molds that include a ceramic material surface, and related methods for making and using the molds |
WO2020010783A1 (en) | 2018-07-10 | 2020-01-16 | 中国科学院宁波材料技术与工程研究所 | Max phase material, preparation method therefor, and application thereof |
CN108922705B (en) * | 2018-08-15 | 2020-03-10 | 中国科学院宁波材料技术与工程研究所 | Ternary layered MAX phase material with A bit as magnetic element, and preparation method and application thereof |
CN110394449A (en) * | 2019-08-27 | 2019-11-01 | 西安交通大学 | A kind of quaternary MAX phase enhances nickel-base high-temperature Oxidation Resistance Composites and its synthetic method |
CN111389316B (en) * | 2020-04-07 | 2021-07-06 | 青岛科技大学 | Sea urchin-like microsphere and preparation method thereof |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1635576A (en) * | 1927-01-12 | 1927-07-12 | John R Gammeter | Method of making dipped rubber articles |
US3852826A (en) * | 1974-01-18 | 1974-12-10 | Int Corp | Surgical gloves |
US5018532A (en) * | 1988-06-27 | 1991-05-28 | Etheredge Iii Robert W | Novel phosphorescent condoms |
US5116551A (en) * | 1987-05-07 | 1992-05-26 | Davidson Roderick I | Method and apparatus for producing an article by microwave heating |
US5194204A (en) * | 1989-02-01 | 1993-03-16 | Hoechst Ceramtec Aktiengesellschaft | Process for producing a silicized silicon carbide dipping former |
US5451365A (en) * | 1993-05-24 | 1995-09-19 | Drexel University | Methods for densifying and strengthening ceramic-ceramic composites by transient plastic phase processing |
US5609922A (en) * | 1994-12-05 | 1997-03-11 | Mcdonald; Robert R. | Method of manufacturing molds, dies or forming tools having a cavity formed by thermal spraying |
US5882561A (en) * | 1996-11-22 | 1999-03-16 | Drexel University | Process for making a dense ceramic workpiece |
US5942455A (en) * | 1995-11-14 | 1999-08-24 | Drexel University | Synthesis of 312 phases and composites thereof |
US6013322A (en) * | 1997-01-10 | 2000-01-11 | Drexel University | Surface treatment of 312 ternary ceramic materials and products thereof |
US6231969B1 (en) * | 1997-08-11 | 2001-05-15 | Drexel University | Corrosion, oxidation and/or wear-resistant coatings |
US6345394B1 (en) * | 2000-06-29 | 2002-02-12 | Zeon Corporation | Rubber glove and process for producing same |
US6461989B1 (en) * | 1999-12-22 | 2002-10-08 | Drexel University | Process for forming 312 phase materials and process for sintering the same |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003051791A1 (en) * | 2001-12-18 | 2003-06-26 | Ansell Healthcare Products, Inc. | Carbide and nitride ternary ceramic glove and condom formers |
-
2003
- 2003-09-19 US US10/666,639 patent/US20040250334A1/en not_active Abandoned
-
2004
- 2004-06-10 WO PCT/US2004/018528 patent/WO2004112641A2/en active Application Filing
-
2006
- 2006-05-16 US US11/435,052 patent/US20060202389A1/en not_active Abandoned
Patent Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1635576A (en) * | 1927-01-12 | 1927-07-12 | John R Gammeter | Method of making dipped rubber articles |
US3852826A (en) * | 1974-01-18 | 1974-12-10 | Int Corp | Surgical gloves |
US5116551A (en) * | 1987-05-07 | 1992-05-26 | Davidson Roderick I | Method and apparatus for producing an article by microwave heating |
US5018532A (en) * | 1988-06-27 | 1991-05-28 | Etheredge Iii Robert W | Novel phosphorescent condoms |
US5194204A (en) * | 1989-02-01 | 1993-03-16 | Hoechst Ceramtec Aktiengesellschaft | Process for producing a silicized silicon carbide dipping former |
US5451365A (en) * | 1993-05-24 | 1995-09-19 | Drexel University | Methods for densifying and strengthening ceramic-ceramic composites by transient plastic phase processing |
US5609922A (en) * | 1994-12-05 | 1997-03-11 | Mcdonald; Robert R. | Method of manufacturing molds, dies or forming tools having a cavity formed by thermal spraying |
US5942455A (en) * | 1995-11-14 | 1999-08-24 | Drexel University | Synthesis of 312 phases and composites thereof |
US5882561A (en) * | 1996-11-22 | 1999-03-16 | Drexel University | Process for making a dense ceramic workpiece |
US6013322A (en) * | 1997-01-10 | 2000-01-11 | Drexel University | Surface treatment of 312 ternary ceramic materials and products thereof |
US6231969B1 (en) * | 1997-08-11 | 2001-05-15 | Drexel University | Corrosion, oxidation and/or wear-resistant coatings |
US6497922B2 (en) * | 1997-08-11 | 2002-12-24 | Drexel University | Method of applying corrosion, oxidation and/or wear-resistant coatings |
US6461989B1 (en) * | 1999-12-22 | 2002-10-08 | Drexel University | Process for forming 312 phase materials and process for sintering the same |
US6345394B1 (en) * | 2000-06-29 | 2002-02-12 | Zeon Corporation | Rubber glove and process for producing same |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050049136A1 (en) * | 2001-12-18 | 2005-03-03 | Gromelski Stanley J | Carbide and nitride ternary ceramic glove and condom formers |
US7157393B2 (en) * | 2001-12-18 | 2007-01-02 | Arsell Healthcare Products Llc | Carbide and nitride ternary ceramic glove and condom formers |
US20070021290A1 (en) * | 2001-12-18 | 2007-01-25 | Gromelski Stanley J | Carbide and nitride ternary ceramic glove and condom formers |
US7235505B2 (en) | 2001-12-18 | 2007-06-26 | Ansell Healthcare Products Llc | Carbide and nitride ternary ceramic glove and condom formers |
US10964302B2 (en) | 2014-01-14 | 2021-03-30 | Raytheon Technologies Corporation | Vibration damping material for high temperature use |
US20170304109A1 (en) * | 2016-04-25 | 2017-10-26 | Gamal Ragheb | Birth Control Assembly |
US10159597B2 (en) * | 2016-04-25 | 2018-12-25 | Gamal Ragheb | Birth control assembly |
CN111943205A (en) * | 2020-08-28 | 2020-11-17 | 郑州轻工业大学 | Method for preparing MAX phase by adopting melt displacement reaction, prepared MAX phase and application |
Also Published As
Publication number | Publication date |
---|---|
US20060202389A1 (en) | 2006-09-14 |
WO2004112641A2 (en) | 2004-12-29 |
WO2004112641A3 (en) | 2005-10-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20060202389A1 (en) | MAX phase glove and condom formers | |
US7235505B2 (en) | Carbide and nitride ternary ceramic glove and condom formers | |
KR0127871B1 (en) | Silicon nitride-based siuters | |
JPH09170016A (en) | Production of high-temperature-stable object made of in706 type iron/nickel super alloy | |
WO2020190229A1 (en) | Nickel-based bulk metallic glass alloys containing high amount of refractory metal and boron | |
DK160973B (en) | Method for the manufacture of a compact from an iron alloy | |
JPH0624726A (en) | Zirconia/molybdenum disilicide composition and its production | |
JPH0633112A (en) | Production of porous mold material | |
JP4243437B2 (en) | Method for producing metal-ceramic composite material having a pore-less surface | |
JPH11255523A (en) | Mold for forming glass mold and its production | |
JPS5891074A (en) | Manufacture of silicon nitride sintered body | |
JPH08217530A (en) | Aluminous sintered compact and its production | |
JP4167318B2 (en) | Method for producing metal-ceramic composite material | |
WO2003097264A2 (en) | Transition metal and transition metal oxide glove and condom formers and coatings therefor | |
JPH0142915B2 (en) | ||
KR960004397B1 (en) | Treatment for reinforcing surface of silicon nitride | |
JPS63230571A (en) | Manufacture of sic-tic normal pressure sintered body | |
JPH05221723A (en) | Si-sic composite material | |
JP2002212690A (en) | Method for producing metal-ceramics composite material having thickness part | |
JP2003089840A (en) | METAL/Al2O3 COMPOSITE MATERIAL AND ITS MANUFACTURING METHOD | |
JP2001262249A (en) | Method for producing metal-ceramics composite material | |
JPS63399B2 (en) | ||
JP2001261443A (en) | Heat-treated molybdenum-disilicide-based sintered body material and its production process | |
JPH06144932A (en) | Production of silicon nitride-based sintered compact | |
JPH08319513A (en) | Treatment of iron-chrome-nickel-aluminum type ferritic alloy |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: DREXEL UNIVERSITY, PENNSYLVANIA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:EL-RAGHY, TAMER;BARSOUM, MICHEL W.;REEL/FRAME:015258/0337 Effective date: 20040412 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |