Abstract: A rotary tool accessory in one embodiment includes a base, a circular wall extending upwardly from the base about a central axis, the circular wall including an inner face, an outer face and a circular rim, a first cutting group including a first inwardly extending tooth extending from a location directly above the circular wall to a location closer to the central axis than the inner face, a first outwardly extending tooth extending from a location directly above the circular wall to a location farther from the central axis than the outer face, and a first gullet extending downwardly from the rim toward the base, a second cutting group including a second inwardly extending tooth, a second outwardly extending tooth, and a second gullet, and a toothless expanse of the rim extending between the first cutting group and the second cutting group.

Abstract: Various 13C and 14C carbon labeled compounds Rf—bCF(U)y(T)z??Formula 1A or Rf—bCF2bCF(U)y(T)z??Formula 1B wherein Rf is a linear or branched perfluoroalkyl radical Z(CmF2m)—, m is 1, 3 to 20, or a mixture thereof; Z is F when m is 1, and Z is F, Cl, or H when m is 3 to 20 or a mixture thereof; b is 13 or 14; y is 1, and z is 0 or 1; and when y and z are each 1, U is F, and T is selected from the group consisting of monovalent radicals —X wherein X is I or Br, —CH2—CH2—X, —CH?CH2, —CH2—CH2—OH, —CH2—COOH, —CH2OH, —bCH2OH, —COOH, —bCOOH, —O—CF(CF3)—C(O)F, —O—CF(CF3)—X, —SO2Y wherein Y is H, F or Cl, and —SO3H; and when y is 1, and z is 0, U is selected from the group consisting of divalent radicals ?CH—COOH, ?CH—CH2—OH, and =0, are disclosed, and a process for their preparation which selectively introduces 13C and 14C carbon labels into a fluoroalkyl chain.

Abstract: Perfluoropolyether alkyl alcohol comprising a perfluoropolyether segment and one or more alcohol segments wherein the alcohol segment has a general formula, —CH2(CqH2q)OH, wherein CqH2q represents a divalent linear or branched alkyl radical where q is an integer from 1 to about 10, such that the hydroxy group is insulated from fluorine atoms, are disclosed. Also disclosed herein are processes to produce these perfluoropolyether alkyl alcohols by reaction of perfluoropolyether primary or secondary bromides or iodides either an alkene or alkenol followed by further reaction to produce the alcohol.

Abstract: Perfluoropolyether alkyl alcohol comprising a perfluoropolyether segment and one or more alcohol segments wherein the alcohol segment has a general formula, —CH2(CqH2q)OH, wherein CqH2q represents a divalent linear or branched alkyl radical where q is an integer from 1 to about 10, such that the hydroxy group is insulated from fluorine atoms, are disclosed. Also disclosed herein are processes to produce these perfluoropolyether alkyl alcohols by reaction of perfluoropolyether primary or secondary bromides or iodides either an alkene or alkenol followed by further reaction to produce the alcohol.

Abstract: A method of lubricating a sootblower comprising use of an oil or grease that is thermally stable at temperatures of at least 160° C. Sootblower components which can be lubricated include lance support bearings, gears, chains, seals, and shaft bearings. The oil or grease can be an ester, silicone, or halogenated oil or grease including perfluoropolyether or perfluoroalkyl ether, a fluorosilicone, a polytrifluorochloroethylene, derivatized perfluoropolyethers, such as fluoroether triazines, and mixtures of two or more thereof.

Abstract: A process to prepare substituted aryl pnictogen derivatives comprising contacting a fluoropolyether or fluoroalkyl primary bromide or iodide, with a pnictogen derivative such as triaryl phosphine, triaryl arsine, or triaryl stibine or triaryl phosphine oxide, triaryl arsine oxide or triaryl stibine oxide, to produce the corresponding fluoropolyether- or fluoroalkyl- substituted aryl phosphine oxide, aryl arsine oxide or aryl stibine oxide; and optionally, contacting the oxide product with a reducing agent to form the corresponding substituted aryl phosphine, arsine or stibine.

Abstract: A process to prepare substituted aryl pnictogen derivatives comprising contacting a fluoropolyether or fluoroalkyl primary bromide or iodide, with a pnictogen derivative such as triaryl phosphine, triaryl arsine, or triaryl stibine or triaryl phosphine oxide, triaryl arsine oxide or triaryl stibine oxide, to produce the corresponding fluoropolyether- or fluoroalkyl-substituted aryl phosphine oxide, aryl arsine oxide or aryl stibine oxide; and optionally, contacting the oxide product with a reducing agent to form the corresponding substituted aryl phosphine, arsine or stibine.

Abstract: A composition is disclosed which comprises an aryl perfluoropolyether, optionally a halogenated oil, and further optionally a thickening agent. The composition can be used as a lubricant itself or as an additive to an oil or grease lubricant and can withstand temperatures higher than 300° C. without decomposition. The halogenated oil can be a perfluoropolyether, a fluorosilicone, a polytrifluorochloroethylene, or combinations of two or more thereof. The thickening agent can be finely divided silica, boron nitride, clay, soap, poly(tetrafluoroethylene), clay, talc, silica, titanium dioxide, polydimethylsiloxane, polyurea, polyurethane, or combinations of two or more thereof.

Abstract: Substituted aryl pnictogen derivative compositions having the structure of [Rf1—(CtR(u+v))]mE(O)n(CtR1(u+v+1))(3-m) wherein E is phosphorous, arsenic or antimony; Rf1 is a fluoropolyether chain; CtR(u+v) and CtR1(u+v+1) represent aryl groups, n is 0 or 1 and m is greater than about 0.5 to about 3. Such compositions have utility as additives for high temperature lubricants.

Abstract: A process to prepare substituted aryl pnictogen derivatives comprising contacting a fluoropolyether or fluoroalkyl primary bromide or iodide, with a pnictogen derivative such as triaryl phosphine, triaryl arsine, or triaryl stibine or triaryl phosphine oxide, triaryl arsine oxide or triaryl stibine oxide, to produce the corresponding fluoropolyether- or fluoroalkyl-substituted aryl phosphine oxide, aryl arsine oxide or aryl stibine oxide; and optionally, contacting the oxide product with a reducing agent to form the corresponding substituted aryl phosphine, arsine or stibine.

Abstract: Perfluoropolyether alkyl alcohol comprising a perfluoropolyether segment and one or more alcohol segments wherein the alcohol segment has a general formula, —CH2(CqH2q)OH , wherein CqH2q represents a divalent linear or branched alkyl radical where q is an integer from 1 to about 10, such that the hydroxy group is insulated from fluorine atoms, are disclosed. Also disclosed herein are processes to produce these perfluoropolyether alkyl alcohols by reaction of perfluoropolyether primary or secondary bromides or iodides either an alkene or alkenol followed by further reaction to produce the alcohol.

Abstract: Various 13C and 14C carbon labeled compounds Rf—bCF(U)y(T)z??Formula 1A or Rf—bCF2bCF(U)y(T)z??Formula 1B wherein Rf is a linear or branched perfluoroalkyl radical Z(CmF2m)—, m is 1, 3 to 20, or a mixture thereof; Z is F when m is 1, and Z is F, Cl, or H when m is 3 to 20 or a mixture thereof; b is 13 or 14; y is 1, and z is 0 or 1; and when y and z are each 1, U is F, and T is selected from the group consisting of monovalent radicals —X wherein X is I or Br, —CH2—CH2—X, —CH?CH2, —CH2—CH2—OH, —CH2—COOH, —CH2OH, —bCH2OH, —COOH, —bCOOH, —O—CF(CF3)—C(O)F, —O—CF(CF3)—X, —SO2Y wherein Y is H, F or Cl, and —SO3H; and when y is 1, and z is 0, U is selected from the group consisting of divalent radicals ?CH—COOH, ?CH—CH2—OH, and ?O, are disclosed, and a process for their preparation which selectively introduces 13C and 14C carbon labels into a fluoroalkyl chain.