Abstract: A liquid-liquid extraction process of ketones, alcohols, aldehydes, alkyl esters of carboxylic acids, carboxylic acids, ethers, amines and heterocyclic compounds, from their aqueous solutions, comprising the addition under stirring to said aqueous solutions of a fluorinated extracting liquid selected from A) hydrofluoropolyethers, B) hydrofluorocarbons, C) hydrofluoroethers, or mixtures thereof, with formation of an aqueous phase and of an organic phase; the separation of the organic phase from the aqueous phase; the fractional distillation of the organic phase to separate the polar organic substance from the extractant.

Abstract: Perfluoropolyethers having structural formula R1O—(CF2O)n—(CF2CF2O)mR2??(I) wherein: R1 is —CH3 or —C2H5; R2 is equal to R1 or —CF2H n is integer from 1 to 100; m is an integer from 1 to 100 or, when R2 is —CF2H, in can also be 0; the oxyfluoro-alkylene units —(CF2CF2O)— and —(CF2O)— are statistically distributed along the polymer chain.

Abstract: A process for preparing peroxidic perfluoropolyethers having a peroxidic content (PO) higher than 1.2 of formula A-CF2O(CF2CF2O)m(CF2O)n—(CF2CF2OO)ml(CF2OO)nlCF2—B??(I) wherein A, B, equal to or different from each other are Cl—, F—, C1CF2—, COF—, —OCOF, —CF3, m, ml, n, nl are integers such that the (m+ml)/(n+nl) ratio is between 0.9 and 5 and the m/n ratio is between 0.8 and 3, the number average molecular weight is in the range 35,000-45,000, by tetrafluoroethylene (TFE) photooxidation in the presence of UV light, at a temperature from ?80° C. to ?40° C., in the presence of a mixture of solvents formed of HFC-227 (heptafluoropropane) and a solvent selected from HFC-125 (pentafluoroethane) and FC-218 (perfluoropropane).

Abstract: A process for preparing peroxidic perfluoropolyethers having a perioxidic content (PO) lower than or equal to 1.2 of formula A-CF2O(CF2CF2O)m(CF2O)n—(CF2CF2OO)m1(CF2OO)n1CF2—B??(I) Wherein A, B equal to or different from each other are —C1, —F, —F2CC1, —COF, —OCOF, —CF3, m, m1, n, n1 are integers such that the (m+m1)/(n+n1) ratio is between 0.6 and 1.3 and the m/n ration is between 0.5 and 1.2; the number average molecular weight is in the range 35,000-45,000, by tetrafluoroethylene (TFE) photooxidation in the presence of UV light, at a temperature from ?80° C. to ?40° C., in the presence of a mixture of solvents formed of HFC-227 (hepta-fluoropropane) and a solvent selected between HFC-125 (pentafluoroethane) and FC-218 (perfluoropropane).

Abstract: Perfluoropolyethers having structural formula R1O—(CF2O)n—(CF2CF2O)mR2??(I) wherein: R1 is —CH3 or —C2H5; R2 is equal to R1 or —CF2H n is 0 or an integer from 1 to 100; m is an integer from 1 to 100 or, when R2 is —CF2H, m can also be 0; the oxyfluoro-alkylene units —(CF2CF2O)— and —(CF2O)— are statistically distributed along the polymer chain.

Abstract: Perfluoropolyethers having structural formula R1O—(CF2O)n—(CF2CF2O)mR2??(I) wherein: R1 is —CH3 or —C2H5; R2 is equal to R1 or —CF2H n is 0 or an integer from 1 to 100; m is an integer from 1 to 100 or, when R2 is —CF2H, m can also be 0; the oxyfluoroalkylene units —(CF2CF2O)— and —(CF2O)— are statistically distributed along the polymer chain.

Abstract: Peroxidic perfluoropolyethers having formula: X1—O(CF2O)n1(CF2CF2O)m1(CF2(CF2)zCF2O)p1(O)h—X2??(I) wherein: X1 and X2, equal to or different from each other, are chain end groups selected among —CF2COF, —COF, —SO2F; n1, m1, p1 and h are integers such that the number average molecular weight is in the range 700-100,000; z=1 or 2; with the proviso that: the m1/n1 ratio is between 0.2 and 10; the p1/(n1+m1) ratio is lower than 0.05; the h/(n1+m1+p1) ratio is such that the PO content, defined as grams of active oxygen/100 g of compound, is in the range 0.8-4.5, preferably 1.4-3.8; the perfluorooxyalkylene units being statistically distributed along the polymeric chain.

Abstract: Peroxidic perfluoropolyethers having formula: X1—O(CF2O)n1(CF2CF2O)m1(CF2(CF2)zCF2O)p1(O)h—X2 ??(I) wherein: X1 and X2, equal to or different from each other, are chain end groups selected between —CF2COF and —COF; n1, m1, p1 and h are integers such that the number average molecular weight is in the range 700-100,000; z=1 or 2; with the proviso that: the m1/n1 ratio is between 0.2 and 10; the p1/(n1+m1) ratio is lower than 0.05; the h/(n1+m1+p1) ratio is such that the PO content, defined as grams of active oxygen/100 g of compound, is in the range 0.8-4.5, preferably 1.4-3.8; the perfluorooxyalkylene units being statistically distributed along the polymeric chain.

Abstract: Electrolytic compositions comprising a perfluoropolyether additive of formula (I): wherein: d, e, f are integers; a, b, c can be zero or integers; being a+b+c+d+e+f such that the number average molecular weight ranges from 500 to 5×105; T are end groups —CF2X (X?F,CF3, Cl), —C3F7, —CF(CF3)COO?(1/n)Mn+, —CF2COO?(1/n) Mn+, —CF2C(O(1/n)Mn+)2CF3; Mn? is a cation having valence n=1-4.

Abstract: A process to obtain perfluoropolyethers comprising: a) synthesis of the peroxidic perfluoropolyether by one of the following reactions: a1) TFE photooxidation, in the presence of UV light, at low temperature, in solvents selected between perfluorocarbons and (mono)hydrofluorocarbons, of general formula: CyF(2y+2?x)Hx ??(II) wherein y is an integer from 2 to 4; x is an integer equal to 0 or 1; in the presence of fluorine diluted with an inert gas; or a2) TFE oxidation using as radical initiator fluorine or hypofluorites of formula RfOF (III) (Rf pefluoroalkyl radical from 1 to 3 carbon atoms), operating from ?40° C. to ?100° C. at a pressure comprised between 0 and 12 bar, in an inert solvent under the reaction conditions; b) thermal treatment of the product obtained in a) at a temperature from 150° C. to 250° C.

Abstract: Use as heat exchange or hydraulic liquids in circuits or equipments subjected to ionizing radiations and/or irradiation with neutrons, of fluorinated liquids selected from the group formed by: A) (per)fluoropolyethers, B) (per)fluorocarbons, C) hydrofluoroethers, appearing liquid under room conditions (25° C., 1 atm).

Abstract: A process for preparing perfluoropolyoxyalkylenes having —OCF2H, —OCF2CF2H and —OCF(CF3)H end groups and a number average molecular weight from 120 to 3,000, by decarboxylation of the corresponding perfluoropolyoxyalkylenes having —OCF2COOH, —OCF2CF2COOH, —OCF(CF3)COOH end groups, in the presence of catalytic amounts of salts formed by perfluoropolyoxyalkylenes having end groups selected from —OCF2COOZ, —OCF2CF2COOZ and —OCF(CF3)COOZ, wherein Z is a monovalent cation of the group Ia or Ib or Z is —NR4+ wherein R is hydrogen or a C1-C4 alkyl, using ratios between Z and the —COOH equivalents of the perfluoropolyoxyalkylenes to be decarboxylated from 0.01 to 0.08, at a temperature between 120° C. and 180° C., in the presence of water, at pH <5 and at a pressure comprised between 2 and 80 atmospheres.

Abstract: Linear perfluoropolyethers of formula:

Abstract: Perfluoropolyethers obtained by oxidation of perfluorodioxoles of formula (I) 1

Abstract: A process for preparing perfluoropolyoxyalkylenes having —OCF2H, —OCF2CF2H and —OCF(CF3)H end groups and a number average molecular weight from 120 to 3,000, by decarboxylation of the corresponding perfluoropolyoxyalkylenes having —OCF2COOH, —OCF2CF2COOH, —OCF(CF3)COOH end groups, in the presence of catalytic amounts of salts formed by perfluoropolyoxyalkylenes having end groups selected from —OCF2COOZ, —OCF2CF2COOZ and —OCF(CF3)COOZ, wherein Z is a monovalent cation of the group Ia or Ib or Z is —NR4+ wherein R is hydrogen or a C1-C4 alkyl, using ratios between Z and the —COOH equivalents of the perfluoropolyoxyalkylenes to be decarboxylated from 0.01 to 0.08, at a temperature between 120° C. and 180° C., in the presence of water, at pH <5 and at a pressure comprised between 2 and 80 atmospheres.

Abstract: A liquid-liquid extraction process of ketones, alcohols, aldehydes, alkyl esters of carboxylic acids, carboxylic acids, ethers, amines and heterocyclic compounds, from their aqueous solutions, comprising the addition under stirring to said aqueous solutions of a fluorinated extracting liquid selected from

Abstract: Use as heat exchange or hydraulic liquids in circuits or equipments subjected to ionizing radiations and/or irradiation with neutrons, of fluorinated liquids selected from the group formed by:

Abstract: Perfluoropolyethers having structural formula

Abstract: Electrolytic compositions comprising a perfluoropolyether additive of formula (I): 1

Abstract: Perfluoropolyether lubricants containing sulphonylfluoride groups pending along the perfluoropolyether chain and having the following formula: wherein: T are end groups selected from —CF2X (X═F,CF3Cl), —C3F7, —COF, —CF(CF3)COF, —CF2COF, —CF2COCF3; d,e,f,h are integers; a,b,c can be zero or integers; said units are statistically distributed along the chain, being a+b+c+d+e+f+h such that the number average molecular weight ranges from 500 to 5×105, preferably from 1,000 to 50,000.