Abstract: Provided herein are copolymers that comprise copolymerized residues of a perfluorotrivinyltriazine monomer of Formula 1. Preferred Rf groups include, without limitation, —(CF2)n— (n=1-6); —(CF2)m—[OCF(CF3)CF2]p— (m=1-4, p=1-4); and —[(CF(CF3)—O)x—(CF2)k]— (x=1-3, k=1-5). Preferred comonomers for copolymerization with the perfluorotrivinyltriazine monomer (1) include, without limitation, tetrafluoroethylene (TFE); vinylidene fluoride (VF2); hexafluoropropylene (HFP); vinyl fluoride (VF); EVE; PSEPVE; perfluoro-(long chain vinyl ethers); E; P; PFBE; PEVE; EVE-OH; EVE-P; PDD; and the cure-site monomers BTFB, ITFB, 8-CNVE, 8-SAVE, and the like. Also provided are methods of synthesizing the copolymers and articles comprising the copolymers.

Abstract: The present invention provides 1,3,3,3-tetrafluoropropene (HFO-1234ze) copolymers comprising 1,3,3,3-tetrafluoropropene and one or more comonomers selected from the group consisting of vinyl fluoride (VF), vinylidene fluoride (VF2), tetrafluoroethylene (TFE), chlorotrifluoroethylene (CTFE), hexafluoropropylene (HFP), and perfluoro(alkyl vinyl ether) (PAVE), wherein said alkyl contains 1 to 5 carbon atoms, the copolymers being a fluoroplastic or a fluoroelastomer, depending upon monomer content.

Abstract: Provided herein are copolymers that comprise copolymerized residues of a perfluorotrivinyltriazine monomer of Formula 1. Preferred Rf groups include, without limitation, —(CF2)n— (n=1-6); —(CF2)m—[OCF(CF3)CF2]p— (m=1-4, p=1-4); and —[(CF(CF3)—O)x—(CF2)k]— (x=1-3, k=1-5). Preferred comonomers for copolymerization with the perfluorotrivinyltriazine monomer (1) include, without limitation, tetrafluoroethylene (TFE); vinylidene fluoride (VF2); hexafluoropropylene (HFP); vinyl fluoride (VF); EVE; PSEPVE; perfluoro-(long chain vinyl ethers); E; P; PFBE; PEVE; EVE-OH; EVE-P; PDD; and the cure-site monomers BTFB, ITFB, 8-CNVE, 8-SAVE, and the like. Also provided are methods of synthesizing the copolymers and articles comprising the copolymers.

Abstract: An automatic vehicle parking assistance correcting system with instant environmental detection for detecting at least one surrounding vehicle and immediately correcting a driving vehicle includes a vehicle sensor, a plurality of distance sensors and an electronic control unit. The vehicle sensor detects a vehicle parameter data of the driving vehicle and outputs the vehicle parameter data. The distance sensors detect the surrounding vehicle located around the driving vehicle and output a plurality of distance values between the driving vehicle and the surrounding vehicle. The electronic control unit receives the distance values and the vehicle parameter data to generate a parking space data, and calculates the distance values, the parking space data and the vehicle parameter data to generate an initial parking trajectory according to a trajectory planning algorithm.

Abstract: The present invention provides 1,3,3,3-tetrafluoropropene (HFO-1234ze) copolymers comprising 1,3,3,3-tetrafluoropropene and one or more comonomers selected from the group consisting of vinyl fluoride (VF), vinylidene fluoride (VF2), tetrafluoroethylene (TFE), chlorotrifluoroethylene (CTFE), hexafluoropropylene (HFP), and perfluoro(alkyl vinyl ether) (PAVE), wherein said alkyl contains 1 to 5 carbon atoms, the copolymers being a fluoroplastic or a fluoroelastomer, depending upon monomer content.

Abstract: The process is provided for forming the reaction product comprising the homologue mixture of I(CF2)nI, wherein n is 3 to 7, which may contain at least one of the contaminants ICF2I and I(CF2)2I, by the steps comprising (a) reacting iodine with hexafluoropropylene oxide at a temperature of 150° C. to 210° C. in a reactor, the amount of said hexafluoro-propylene oxide being a portion of the total amount of hexafluoropropylene oxide to be reacted with said iodine, thereby forming a reaction product containing gaseous perfluoroacetyl fluoride as a reaction by-product, (b) cooling said reaction product to become liquid except for said gaseous perfluoroacetyl fluoride, (c) venting said perfluoroacetyl fluoride from said reactor, and (d) repeating said steps (a), (b), and (c) until said total amount of said HFPO is reacted with said iodine.

Abstract: Compositions comprising fluoroelastomers having copolymerized units of a cyano-containing cure site monomer are cured (i.e. crosslinked) with a fluoropolymer having pendant sulfonyl azide groups. The latter fluoropolymer comprises copolymerized units of a fluoroalkanesulfonyl azide of formula CF2?CF—(O)p—Rf—(CH2)n—SO2N3, wherein p=0 or 1; n=0-4; and Rf is a C1-C16 perfluoroalkyl or perfluoroalkoxy group. The crosslinks are tetrazole rings formed by the reaction of the pendant sulfonyl azide groups on the fluoropolymer with pendant cyano groups on the fluoroelastomer.

Abstract: The present invention is the process comprising forming a stable mixture comprising I(CF2)nI, wherein n is at least 3 and at least one of I(CF2)nI, wherein n is 1 or 2, as a contaminant in said mixture and heating said mixture to a temperature of at least 220° C. to reduce the amount of said contaminant to be no greater than 1% when said contaminant is ICF2I (n=1) and no greater than 0.1% when said contaminant is ICF2CF2I (n=2).

Abstract: Compositions comprising fluoroelastomers having copolymerized units of a cyano-containing cure site monomer are cured (i.e. crosslinked) with a fluoropolymer having pendant sulfonyl azide groups. The latter fluoropolymer comprises copolymerized units of a fluoroalkanesulfonyl azide of formula CF2?CF—(O)p—Rf—(CH2)n—SO2N3, wherein p=0 or 1; n=0-4; and Rf is a C1-C16 perfluoroalkyl or perfluoroalkoxy group. The crosslinks are tetrazole rings formed by the reaction of the pendant sulfonyl azide groups on the fluoropolymer with pendant cyano groups on the fluoroelastomer.

Abstract: The process is provided for forming the reaction product comprising the homologue mixture of I(CF2)nI, wherein n is 3 to 7, which may contain at least one of the contaminants ICF2I and I(CF2)2I, by the steps comprising (a) reacting iodine with hexafluoropropylene oxide at a temperature of 150° C. to 210° C. in a reactor, the amount of said hexafluoro-propylene oxide being a portion of the total amount of hexafluoropropylene oxide to be reacted with said iodine, thereby forming a reaction product containing gaseous perfluoroacetyl fluoride as a reaction by-product, (b) cooling said reaction product to become liquid except for said gaseous perfluoroacetyl fluoride, (c) venting said perfluoroacetyl fluoride from said reactor, and (d) repeating said steps (a), (b), and (c) until said total amount of said HFPO is reacted with said iodine.

Abstract: The present invention is the process comprising forming a stable mixture comprising I(CF2)nI, wherein n is at least 3 and at least one of I(CF2)nI, wherein n is 1 or 2, as a contaminant in said mixture and heating said mixture to a temperature of at least 220° C. to reduce the amount of said contaminant to be no greater than 1% when said contaminant is ICF2I (n=1) and no greater than 0.1% when said contaminant is ICF2CF2I (n=2).

Abstract: Compositions comprising fluoroelastomers having copolymerized units of a cyano-containing cure site monomer are cured (i.e. crosslinked) with certain aromatic diazide curatives. The crosslinks are tetrazole rings formed by the reaction of the aromatic diazide with pendant cyano groups on the fluoroelastomer.

Abstract: This invention pertains to fluoroelastomers comprising copolymerized units of vinylidene fluoride, at least one other fluoroolefin and a cure site monomer having a secondary cyano group, as well as cured fluoroelastomer compositions made therefrom. It has been surprisingly discovered that fluoroelastomers that contain a cure site monomer having a secondary cyano group contain much less gel than do similar fluoroelastomers that employ a cure site monomer having a primary cyano group. Furthermore cured (i.e. crosslinked) fluoroelastomer compositions that contain a fluoroelastomer having secondary cyano groups have a better (i.e. lower) compression set than do similar cured fluoroelastomer compositions that contain a fluoroelastomer having primary cyano groups.

Abstract: Disclosed herein is a crosslinked fluoropolymer network formed by the free radical initiated crosslinking of a diacrylate fluoropolymer. The diacrylate copolymer is of formula CH2?CR?COO—(CH2)n—R—(CH2)n—OOCR??CH2, wherein R is selected from the group consisting of i) an oligomer comprising copolymerized units of vinylidene fluoride and perfluoro(methyl vinyl ether), ii) an oligomer comprising copolymerized units of vinylidene fluoride and hexafluoropropylene, iii) an oligomer comprising copolymerized units of tetrafluoroethylene and perfluoro(methyl vinyl ether), and iv) an oligomer comprising copolymerized units of tetrafluoroethylene and a hydrocarbon olefin, R? is H or —CH3, n is 1-4 and wherein said oligomer has a number average molecular weight of 1000 to 25,000 daltons. The source of the free radicals may be a photoinitiator or an organic peroxide.

Abstract: Disclosed herein is a telechelic diacrylate fluoropolymer and a process for manufacture of the fluoropolymer. The diacrylate copolymer is of formula CH2?CR?COO—(CH2)n—R—(CH2)n—OOCCR??CH2, wherein R is selected from the group consisting of i) an oligomer comprising copolymerized units of vinylidene fluoride and perfluoro(methyl vinyl ether), ii) an oligomer comprising copolymerized units of vinylidene fluoride and hexafluoropropylene, iii) an oligomer comprising copolymerized units of tetrafluoroethylene and perfluoro(methyl vinyl ether), and iv) an oligomer comprising copolymerized units of tetrafluoroethylene and a hydrocarbon olefin, R? is H or—CH3, n is 1-4 and wherein said oligomer has a number average molecular weight of 1000 to 25,000 daltons.

Abstract: This invention relates to curable fluoroelastomer compositions comprising a) fluoroelastomers having either nitrile, alkyne or azide cure sites and b) fluorinated curatives containing diazide, dinitrile or dialkyne groups for reacting with cure sites on the fluoroelastomer. Fluoroelastomers having azide cure sites form crosslinks with curatives having dinitrile or dialkyne groups. Fluoroelastomers having nitrile or alkyne cure sites form crosslinks with curatives having diazide groups.

Abstract: A process for manufacturing a polyfluroalkanoyl phosphorodichloridate comprising reacting a polyfluoroalkanol having the general formula Rf—CH2—OH, wherein Rf is a linear or branched C1-C8 perfluoroalkyl group optionally interrupted by O, with at least 4 moles of POCl3 per mole of Rf—CH2—OH in the presence of 0.1 to 0.2 moles of LiCl catalyst per mole of Rf—CH2—OH at a temperature between 95° C. and 110° C. to form a phosphorodichloridate of the general formula Rf—CH2—O—P(O)Cl2.

Abstract: A process for manufacturing a polyfluroalkanoyl phosphorodichloridate comprising reacting a polyfluoroalkanol having the general formula Rf—CH2—OH, wherein Rf is a linear or branched C1-C8 perfluoroalkyl group optionally interrupted by O, with at least 4 moles of POCl3 per mole of Rf—CH2—OH in the presence of 0.1 to 0.2 moles of LiCl catalyst per mole of Rf—CH2—OH at a temperature between 95° C. and 110° C. to form a phosphorodichloridate of the general formula Rf—CH2—O—P(O)Cl2.

Abstract: Disclosed herein is a telechelic diacrylate fluoropolymer and a process for manufacture of the fluoropolymer. The diacrylate copolymer is of formula CH2?CR?COO—(CH2)n—R—(CH2)n—OOCCR??CH2, wherein R is selected from the group consisting of i) an oligomer comprising copolymerized units of vinylidene fluoride and perfluoro(methyl vinyl ether), ii) an oligomer comprising copolymerized units of vinylidene fluoride and hexafluoropropylene, iii) an oligomer comprising copolymerized units of tetrafluoroethylene and perfluoro(methyl vinyl ether), and iv) an oligomer comprising copolymerized units of tetrafluoroethylene and a hydrocarbon olefin, R? is H or —CH3, n is 1-4 and wherein said oligomer has a number average molecular weight of 1000 to 25,000 daltons.