US20100243969A1 - Dielectric heat-transfer fluid - Google Patents

Dielectric heat-transfer fluid Download PDF

Info

Publication number
US20100243969A1
US20100243969A1 US12/748,891 US74889110A US2010243969A1 US 20100243969 A1 US20100243969 A1 US 20100243969A1 US 74889110 A US74889110 A US 74889110A US 2010243969 A1 US2010243969 A1 US 2010243969A1
Authority
US
United States
Prior art keywords
oil
less
high oleic
use according
fatty acids
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
Application number
US12/748,891
Other languages
English (en)
Inventor
Serge Rebouillat
Susan Knowlton
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to US12/748,891 priority Critical patent/US20100243969A1/en
Publication of US20100243969A1 publication Critical patent/US20100243969A1/en
Assigned to E. I. DU PONT DE NEMOURS AND COMPANY reassignment E. I. DU PONT DE NEMOURS AND COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KNOWLTON, SUSAN, REBOUILLAT, SERGE
Priority to US13/961,210 priority patent/US9185826B2/en
Priority to US14/926,399 priority patent/US9455066B2/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/20Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/08Materials not undergoing a change of physical state when used
    • C09K5/10Liquid materials
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B3/00Refining fats or fatty oils
    • C11B3/005Refining fats or fatty oils by wave energy or electric current, e.g. electrodialysis
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F27/00Details of transformers or inductances, in general
    • H01F27/08Cooling; Ventilating
    • H01F27/10Liquid cooling
    • H01F27/12Oil cooling
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K7/00Constructional details common to different types of electric apparatus
    • H05K7/20Modifications to facilitate cooling, ventilating, or heating
    • H05K7/20218Modifications to facilitate cooling, ventilating, or heating using a liquid coolant without phase change in electronic enclosures
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2861Coated or impregnated synthetic organic fiber fabric

Definitions

  • the present invention relates to the field of dielectric heat-transfer fluids, in particular dielectric fluid made from vegetable oils for use in, e.g. liquid filled transformers.
  • Electrical transformers typically have windings of conducting wire which must be separated by a dielectric (i.e. non-conducting) material.
  • a dielectric i.e. non-conducting
  • the heat-transfer medium must act as a dielectric as well.
  • cellulosic and/or aramid paper or board is used as the dielectric material.
  • the cellulosic/aramid material is wrapped around the conducting wire, and used to separate the windings dielectrically, and may also be used as a structural support for the windings or other elements such as the cores.
  • the fluid heat-transfer medium is typically an oil, which may be, for example mineral oil or a sufficiently robust vegetable oil.
  • the dielectric material and heat-transfer fluid are subjected to significant electromagnetic fields and significant variations of temperature and power surges and breakdowns. Over time, the relatively extreme conditions can lead to failure of the dielectric material and deterioration of the heat-transfer fluid. Deterioration leads to power loss due to dielectric loss, and may eventually lead to discharges and catastrophic failure of the transformer causing major pollution and/or fires.
  • the dielectric and heat-transfer fluid can furthermore be directly and indirectly degraded by oxygen migration and water formation or ingression in the transformer.
  • the invention provides a use of a soy oil as a heat-transfer dielectric fluid in a device to generate, store, convert and/or distribute electrical energy, wherein the soy oil is one in which at least 70%, preferably at least 75% of the fatty acids are C 14 to C 22 mono-unsaturated, and less than 16%, preferably less than 7%, more preferably less than 6% of the fatty acids are polyunsaturated.
  • the invention provides a device to generate, store, convert and/or distribute electrical energy and/or optical signals, comprising:
  • a conducting material (a) a conducting material; (b) a dielectric material; and (c) a heat-transfer dielectric fluid, which is a soy oil in which at least 70%, preferably at least 75% of the fatty acids are C 14 to C 22 mono-unsaturated, and less than 16%, preferably less than 7%, more preferably less than 6% of the fatty acids are polyunsaturated.
  • the invention provides a method for preconditioning a heat-transfer dielectric fluid which is a vegetable triacylglycerol, comprising the step:
  • the invention provides a dielectric material comprising an organic fibrous structure (woven or non-woven) impregnated, with at least 1 wt % of a vegetable triacylglycerol, preferably a soy oil, in which at least 70%, preferably at least 75% of the fatty acids are C 14 to C 22 mono-unsaturated, and less than 16%, preferably less than 7%, more preferably less than 6% of the fatty acids are polyunsaturated.
  • a vegetable triacylglycerol preferably a soy oil
  • the invention provides a use of a vegetable oil as a heat-transfer dielectric fluid in a device to generate, store, convert and/or distribute electrical energy, wherein the vegetable oil is a triacylglycerol having at least one hydroxy fatty acid.
  • the invention provides a blended high oleic oil with an improved Df value at a constant temperature comprising:
  • the invention provides a blended high oleic oil with an improved Df value at a constant temperature comprising:
  • FIG. 1 shows the dielectric loss factor (Df) vs temperature for comparative fluids C1 (FR3) and C2 (Biotemp) and a fluid for use according to the invention, E1 (one of the oils of the invention, VGO-B1),
  • the squares ⁇ and triangles ⁇ show the loss factor for comparative fluid C1 (FR3) (measured at two different times), the crosses X show the loss factor for comparative fluid C2 (Biotemp), the diamonds ⁇ show the loss factor for a soybean oil for use according to the invention E1 (VGO-B1), and the filled circles ⁇ show the loss factor for mineral oil, which is included as a reference.
  • FIG. 2 shows the thermo-gravimetric pattern and heat flux generated before (dotted lines) and after (solid lines) a pharmaceutical grade of Ricinoleic oil is exposed to the electromagnetic microwave treatment of Example 8.
  • FIG. 3 shows the thermo-gravimetric pattern and heat flux generated before (dotted lines) and after (solid lines) a commercial grade of High Oleic Sunflower oil, the comparative fluid C2, is exposed to the electromagnetic microwave treatment of Example 8.
  • FIG. 4 shows the thermo-gravimetric pattern and heat flux generated before (solid lines) and after (dotted lines) a commercial grade of normal soybean oil, the comparative fluid C1, was exposed to the electromagnetic microwave treatment of Example 8.
  • FIG. 5 shows the thermo-gravimetric pattern and heat flux generated before (solid lines) and after (dotted lines) the fluid for the use of the invention, E1, was exposed to the electromagnetic microwave treatment of Example 8.
  • FIG. 6 shows the thermal behaviour of untreated Kraft paper (solid line), Kraft paper imbibed with the fluid for use according to the invention (dotted lines) and Kraft paper imbibed with the fluid for use according to the invention and pre-treated with microwaves according to Example 8 (dash-dot lines).
  • FIG. 7A shows the Df value measured vs temperature for soy oils for use according to the invention, E2, such as “HOSO”; designated by squares and high oleic soy oil having 70%, oleic acid and 16% polyunsaturates (designated by triangles), compared to soy oils having 21% oleic acid and 61% polyunsaturates (“Cm”; designated by X's), 65% oleic acid and 20% polyunsaturates (designated by diamonds).
  • FIG. 7B shows the DF value measured vs temperature for soy oils for use according to the invention.
  • the crosses designate the results for E4, having 74.36% oleic (74%);
  • the X's designate the results for the commodity soy oil (Cm) having 21′)/0 oleic acid and 61% polyunsaturates.
  • the triangles designate the results for a soy oil blend having 70% oleic and 16% polyunsaturates.
  • the diamonds designate the results for a soy oil blend having 65% oleic and 20% polyunsaturates.
  • FIG. 8 shows the variation of Df vs oleic acid content for blended soy oils at two different temperatures (upper line: 130° C.; lower line: 90° C.).
  • FIG. 9 shows the dielectric loss factor (Df) vs temperature for comparative fluids C1 (FR3) and C2 (Biotemp) and two oils for use according to the invention, E2 (E1, VGO-B1) and E4 (E1, VGO-B2).
  • FIG. 10 depicts fragment PHP19340A.
  • FIG. 11 depicts fragment PHP17752A.
  • FIG. 12 depicts plasmid PHP19340.
  • FIG. 13 depicts plasmid PHP17752.
  • SEQ ID NO: 1 sets forth the nucleotide sequence of plasmid PHP19340A.
  • SEQ ID NO: 2 sets forth the nucleotide sequence of plasmid PHP17752A.
  • SEQ ID NO: 3 sets forth the nucleotide sequence of plasmid PHP19340.
  • SEQ ID NO: 4 sets forth the nucleotide sequence of plasmid PHP17752.
  • dielectric loss factor dielectric loss value
  • Df value dielectric loss value
  • Df dielectric dissipation loss
  • E1 is directed to all the high oleic soy oils of the invention and includes the range of the fatty acid compositions shown in Table 1 and includes without limitation the following oils: VGO-B1, VGO-B2, HOSO, the 70% oleic soybean oil shown in Table 6, E2, and E4.
  • Fatty acid contents of oils may be determined using gas chromatography with flame ionization detection, or reverse-phase liquid chromatography with fluorescence detection. Percentages quoted relate to relative percent expressed as %, i.e. the area under the peak of one specific fatty acid divided by the sum of the peak areas of all fatty acid in a particular sample, unless stated otherwise.
  • Tocopherol content of oils is determined using an HPLC method.
  • the soy oil for use according to the invention has at least 80% content of monounsaturated C 14 to C 22 fatty acids, particularly preferably at least 82%, preferably at least 84% content of monounsaturated C 14 to C 22 fatty acids, or at or about 85% content of monounsaturated C 14 to C 22 fatty acids.
  • the soy oil for use according to the invention has less than 4% of polyunsaturated fatty acids.
  • the soy oil for use according to the invention has at least 80% content of monounsaturated C 14 to C 22 fatty acids, and less than 4% of polyunsaturated fatty acids.
  • the monounsaturated fatty acids are C 18 monounsaturated fatty acids. Most preferably, they are oleic acid.
  • the polyunsaturated fatty acids are C 18 fatty acids having two or three double bonds, for example C18:2 and/or C18:3.
  • C18:2 is less than or equal to 5%.
  • the soy oil has a C18:1 content of greater than about 75% of the fatty acid moieties, and a combined C18:2 and C18:3 content of less than 7%, more preferably less than 6% of the fatty acid.
  • the soy oil has a saturated fatty acid content of less than at or about 12%, more preferably less than at or about 10%. Higher saturated fatty acid content leads to an undesirable higher pour point, and diminished dynamic heat transfer ability.
  • the soy oil has the following fatty acid content: at or about 6% C16:0, 3% C18:0, 86% C18:1, 2% C18:2 and 0-2% C18:3.
  • the soy oil has the following fatty acid content: at or about 6% C16:0, 4% C18:0, 79% C18:1, 4% C18:2, 2% C18:3.
  • soy oil has the following fatty acid content: at or about (see table below):
  • the soy oil preferably has a water content of less than at or about 300 ppm.
  • the soy oil additionally comprises tocopherol antioxidants.
  • the tocopherols are present at a concentration of at least 85 mg/100 g of oil, more preferably at least 100 mg/100 g of oil, as measured by a known HPLC method.
  • the tocopherol may be selected from naturally occurring tocopherols, in particular alpha-, beta- and gamma- and delta-tocopherols, and mixtures of these.
  • the soy oil has a tocopherol content as measured by a known HPLC method of at or about 160 mg/100 g oil, and has the following fatty acid content: at or about 6% C16:0, 3% C18:0, 86% C18:1, 2% C18:2 and 2% C18:3.
  • the soy oil has a tocopherol content as measured by a known HPLC method of at or about 160 mg/100 g oil, and has the following fatty acid content: at or about 6% C16:0, 4% C18:0, 79% C18:1, 4% C18:2, 2% C18:3.
  • the tocopherol is preferably tocopherol which is present in the soy oil or in any other vegetable oil as derived from the plant source or in natural plant extracts, NPE (i.e. as opposed to synthesized tocopherol that is added).
  • the soy oil may additionally comprise additives known in the art, which comprise generally less than 5 wt % of the dielectric heat-transfer fluid, for example: bactericides, metal chelators, corrosion inhibitors, antioxidants, heat-stabiliser, viscosity adjusters, pour point depressants, including natural plant extract promoting those functionalities etc.
  • additives known in the art comprise generally less than 5 wt % of the dielectric heat-transfer fluid, for example: bactericides, metal chelators, corrosion inhibitors, antioxidants, heat-stabiliser, viscosity adjusters, pour point depressants, including natural plant extract promoting those functionalities etc.
  • soy oil for use according to the invention can be blended with other fluids used for dielectric heat-transfer fluids, such as other vegetable oils, mineral oil, etc.
  • the oil is derived from soybeans prepared by recombinant manipulation to give increased expression of the activity of the gene encoding oleoyl 12-desaturase.
  • Glycine max there are two genes encoding oleoyl 12-desaturase activity, one of which (GmFad 2-1) is expressed only in the developing seed (Heppard et al. (1996) Plant Physiol. 110:311-319). The expression of this gene increases during the period of oil deposition, starting around 19 days after flowering, and its gene product is responsible for the synthesis of the polyunsaturated fatty acids found in soybean oil. GmFad 2-1 is described in detail by Okuley, J. et al. (1994) Plant Cell 6:147-158 and in WO94/11516. It is available from the ATCC in the form of plasmid pSF2-169K (ATCC accession number 69092).
  • the other gene (GmFad 2-2) is expressed in the seed, leaf, root and stem of the soy plant at a constant level and is the “housekeeping” 12-desaturase gene.
  • the Fad 2-2 gene product is responsible for the synthesis of polyunsaturated fatty acids for cell membranes.
  • GmFad 2-1 was placed under the control of a strong, seed-specific promoter derived from the ⁇ ′-subunit of the soybean ( Glycine max ) beta-conglycinin gene.
  • This promoter allows high level, seed specific expression of the trait gene. It spans the 606 by upstream of the start codon of the ⁇ ′ subunit of the Glycine max ⁇ -conglycinin storage protein.
  • the ⁇ -conglycinin promoter sequence represents an allele of the published ⁇ -conglycinin gene (Doyle et al., (1986) J. Biol. Chem. 261:9228-9238) having differences at 27 nucleotide positions.
  • the GmFad 2-1 open reading frame (ORF) was in a sense orientation with respect to the promoter so as to produce a gene silencing of the sense GmFad 2-1 cDNA and the endogenous GmFad 2-1 gene.
  • This phenomenon known as “sense suppression” is an effective method for deliberately turning off genes in plants and is described in U.S. Pat. No. 5,034,323.
  • the ⁇ -glucuronidase gene (GUS) from E. coli was used.
  • the cassette used consisted of the three modules; the Cauliflower Mosaic Virus 35S promoter, the ⁇ -glucuronidase gene (GUS) from E. coli and a 0.77 kb DNA fragment containing the gene terminator from the nopaline synthase (NOS) gene of the Ti-plasmid of Agrobacterium tumefaciens .
  • the 35S promoter is a 1.4 kb promoter region from CaMV for constitutive gene expression in most plant tissues (Odell et al.
  • the GUS cassette was cloned into the GmFad 2-1/pGEM-9z ( ⁇ ) construct and was designated pBS43.
  • Plasmid pBS43 was transformed into meristems of the elite soybean line A2396, by the method of particle bombardment (Christou et al., (1990) Trends Biotechnol. 8:145-151). Fertile plants were regenerated using methods well known in the art.
  • R4 plants Fourth generation segregant lines (R4 plants), generated from the original transformant, were allowed to grow to maturity.
  • R4 seeds which contained only the silencing Locus A (e.g., G94-1) did not contain any detectable GmFad 2-1 mRNA (when measured by Northern blotting) in samples recovered 20 days after flowering.
  • GmFad 2-2 mRNA although reduced somewhat compared with controls, was not suppressed.
  • the GmFad 2-1 sense construct had the desired effect of preventing the expression of the GmFad 2-1 gene and thus increasing the oleic acid content of the seed.
  • All plants homozygous for the GmFad 2-1 silencing locus had an identical Southern blot profile over a number of generations. This indicates that the insert was stable and at the same position in the genome over at least four generations.
  • the soy oil is extracted from the plant source using known methods of extraction.
  • Preferred methods of extractions are those that avoid steps that result in destruction of the natural tocopherol content. For example, it is preferred to avoid heating the oil to above 200° C. for prolonged periods, for example during deodorization steps which can be reduced or eliminated. In some instances it might be preferred to avoid hydrogenation.
  • soybean oil is produced using a series of steps which accomplish the extraction and purification of an edible oil product from the oil bearing seed.
  • the oils of the invention are not limited to food-grade oils. Soybean oils and soybean by-products are produced using the generalized steps shown in the diagram below.
  • Soybean seeds are cleaned, tempered, dehulled, and flaked which increases the efficiency of oil extraction.
  • Oil extraction is usually accomplished by solvent (hexane) extraction but can also be achieved by a combination of physical pressure and/or solvent extraction.
  • the resulting oil is called crude oil.
  • the crude oil may be degummed by hydrating phospholipids and other polar and neutral lipid complexes which facilitate their separation from the nonhydrating, triglyceride fraction (soybean oil).
  • the resulting lecithin gums may be further processed to make commercially important lecithin products used in a variety of food and industrial products as emulsification and release (antisticking) agents.
  • Degummed oil may be further refined for the removal of impurities; primarily free fatty acids, pigments, and residual gums. Refining is accomplished by the addition of caustic which reacts with free fatty acid to form soap and hydrates phosphatides and proteins in the crude oil. Water is used to wash out traces of soap formed during refining. The soapstock by-product may be used directly in animal feeds or acidulated to recover the free fatty acids. Color is removed through adsorption with a bleaching earth, powdered activated carbon and/or synthetic neutral resin. Which removes most of the chlorophyll and carotenoid compounds. Deodorization which is principally steam distillation under vacuum, is the last step and is designed to remove compounds which impart odor or flavor to the oil. A more detailed reference to soybean seed processing, soybean oil production and by-product utilization can be found in Erickson, 1995, Practical Handbook of Soybean Processing and Utilization, The American Oil Chemists' Society and United Soybean Board.
  • a second aspect of the invention provides a device to generate, store, convert and/or distribute electrical energy with or without optical signals therewith, comprising:
  • a conducting material (a) a conducting material; (b) a dielectric material; and (c) a heat-transfer dielectric fluid, which is a soy oil in which at least 70%, preferably at least 75% of the fatty acids are C 14 to C 22 mono-unsaturated, and less than 16%, preferably less than 7%, more preferably less than 6% of the fatty acids are polyunsaturated.
  • the heat-transfer dielectric fluid used in the device of the invention may be any of the preferred oils for use in the invention described herein and any mixtures thereof.
  • the device is a transformer.
  • the transformer will have conducting material in the form of coils or windings of conducting wire and connections (e.g. copper, aluminium, iron, steel, silver, etc.).
  • the conducting material is wound around and covered in the dielectric material, which is typically chosen from woven or non-woven fibrous material, films and laminates, such as paper, board and/or multidimensional structures.
  • the paper or board may be cellulosic or it may be, for example, composed of aramid fibres, preferably m-aramid fibres, polyimides, polyphenylsulfones, polyamides, polyesters (e.g.
  • PET PET
  • polyethylene polyethylene
  • the conducting material and the dielectric material are placed in a receptacle and the dielectric heat-transfer fluid is added to submerse or partially submerse the components.
  • the dielectric material e.g. paper or board
  • the dielectric material is impregnated with the dielectric heat-transfer fluid by absorption (“imbibing”) at various stages of its processing.
  • the dielectric heat-transfer fluid may be used for example in a generator, a capacitor, an inverter or electric motor, a switch and cables.
  • a third aspect of the invention is a method for preconditioning a heat-transfer dielectric fluid which is a vegetable triacylglycerol, comprising the step:
  • the electromagnetic field may be applied continuously or in series of constant and/or variable pulse and relaxation sequences; repeating the exposure as often as needed.
  • the beneficial effect of the pre-treatment extends to all triacylglycerol dielectric heat-transfer fluids and mixtures thereof, and is not limited to the fluid used in the use according to the invention.
  • the electromagnetic field is applied in the form of microwaves.
  • the electromagnetic field is applied at sufficient power and for a sufficient period of time to treat the vegetable triacylglycerol to at least at or about 100° C., preferably at least at or about 120° C., but not higher than at or about 170° C., more preferably not higher than at or about 160° C. It is particularly preferred to heat the vegetable triacylglycerol to at or about 140° C.
  • the vegetable triacylglycerol is exposed to the electromagnetic field as a neat fluid (i.e. in a suitable receptacle), and then used as desired.
  • the vegetable triacylglycerol is first applied to an absorbent dielectric material, such as paper (e.g. cellulosic or aramid), and then the imbibed paper is subjected to the electromagnetic field including in-line processing treatment.
  • an absorbent dielectric material such as paper (e.g. cellulosic or aramid)
  • in-line processing treatment will be preferably performed in a way that maximize the exposure of the oil to the electromagnetic field such as reducing gradients, mainly temperature and/or electromagnetic radiation flux, within the bulk of the material treated. Falling film transfer equipment and/or droplet chambers are suitable.
  • a fourth aspect of the invention is a dielectric material comprising an organic fibrous structure (e.g. woven tissues or textiles or non-woven) impregnated with at least 1 wt % of a vegetable triacylglycerol, preferably a soy oil, in which at least 70%, preferably at least 75% of the fatty acids are C 14 to C 22 mono-unsaturated, and less than 16%, preferably less than 7%, more preferably less than 6% of the fatty acids are polyunsaturated.
  • a vegetable triacylglycerol preferably a soy oil
  • the vegetable triacylglycerol used for impregnation may be any of the fluids for use according to the invention described herein.
  • the organic fibrous structure is a non-woven made of cellulosic or aramid fibres, polyimides, polyphenylsulfones, polyamides, polyesters (e.g. PET) and polyethylene and combination therewith in various forms composites, laminates and tailored morphologically tailored surfaces and/or multidimensional structures and hybrids/mixtures thereof.
  • the vegetable triacylglycerol is preferably present at about 1 wt %-10 wt %, more preferably 10 wt % to about 50 wt %, even more preferably at or about 20 wt % to 40 wt %.
  • the invention provides a use of a vegetable oil as a heat-transfer dielectric fluid in a device to generate, store, convert and/or distribute electrical energy, wherein the vegetable oil is a triacylglycerol having at least one hydroxy fatty acid.
  • the hydroxyl fatty acid is cis-12-hydroxyoctadec-9-enoic acid, preferably having the D configuration at the chiral carbon.
  • all of the fatty acids in the triacylglycerol are D-cis-12-hydroxyoctadec-9-enoic acid (Castor oil or ricinoleic acid) and this triacylglycerol is mixed in varying proportions with a triacylglycerol in which at least 70%, preferably at least 75% of the fatty acids are C 14 to C 22 mono-unsaturated, and less than 16%, preferably less than 7%, more preferably less than 6% of the fatty acids are polyunsaturated.
  • the castor oil represents from 5 to 15% of the triacylglycerol.
  • high oleic soybean refers to soybean seeds that have an oleic acid content of at least 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, 69%, 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, and 95%.
  • Preferred high oleic soybean oil starting materials are disclosed in World Patent Publication WO94/11516, the disclosure of which is hereby incorporated by reference.
  • high oleic oil refers to an oil having an oleic acid content of at least 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, and 95%.
  • Useful examples of contents of polyunsaturated of the oil for the use of the present invention are less than 16%, 15%, 14%, 13%, 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%.
  • the invention provides a blended high oleic oil with an improved Df value at a constant temperature comprising:
  • percent volume for the oils a) and b) of the blended oil of the invention are 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, 69%, 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%
  • the invention provides a blended high oleic oil with an improved Df value at a constant temperature comprising:
  • percent volume for the oils a), b) and c) of the blended oil of the invention are 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, 69%, 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%
  • the oil b) that is a mono-alkyl ester of oleic acid can be any C 1 -C 12 alkyl ester of oleic acid. Particularly preferred are C 1 -C 8 alkyl esters, more preferably C 1 -C 6 alkyl esters, such as methyl, ethyl, propyl, butyl, pentyl and hexyl esters, both straight and branched.
  • Df dielectric dissipation loss
  • the dielectric dissipation loss, Df represents the tendency of the fluid in an alternating electromagnetic field to depart from the ideal of a pure dielectric medium in which no energy dissipation losses would occur.
  • the dielectric loss typically increases with the presence of impurities in the fluid, especially charged impurities, with increase in water content, with free acids and with molecular breakdown of the fluid into smaller species.
  • the stability of the dielectric loss versus temperature within a representative temperature range is an insurance of a durable fluid composition exhibiting good performance over prolonged period of time (i.e. good aging behaviour).
  • the measurement of Df is made using ASTM D924, and is based on the superheterodyne principle.
  • the soy oil or blended oil for use according to the invention preferably shows a Df of less than at or about 1.2 ⁇ 10 ⁇ 3 when measured at 23° C., preferably less than at or about 5.4 ⁇ 10 ⁇ 3 when measured at 70° C., preferably less than 9.1 ⁇ 10 ⁇ 3 when measured at 90° C., preferably less than at or about 1.21 ⁇ 10 ⁇ 2 when measured at 100° C., preferably less than at or about 1.95 ⁇ 10 ⁇ 2 when measured at 120° C., preferably less than at or about 2.32 ⁇ 10 ⁇ 2 when measured at 130° C., and preferably, it shows a Df of less than at or about 2.32 ⁇ 10 ⁇ 2 over a temperature range of at or about 23-130° C.
  • the soy oil or blended oil for use according to the invention preferably shows a Df of less than at or about 2.5 ⁇ 10 ⁇ 4 when measured at 23° C., preferably less than at or about 2.5 ⁇ 10 ⁇ 3 , more preferably less than at or about 1.5 ⁇ 10 ⁇ 3 when measured at 70° C., preferably less than at or about 5 ⁇ 10 ⁇ 3 , more preferably less than at or about 3 ⁇ 10 ⁇ 3 when measured at 90° C., preferably less than at or about 7 ⁇ 10 ⁇ 3 , more preferably less than at or about 4 ⁇ 10 ⁇ 3 when measured at 100° C., preferably less than at or about 2 ⁇ 10 ⁇ 2 , more preferably less than at or about 7 ⁇ 10 ⁇ 3 when measured at 120° C., and preferably less than at or about 2 ⁇ 10 ⁇ 2 , more preferably less than at or about 1 ⁇ 10 ⁇ 2 when measured at 130° C.
  • it shows a Df of less than at or about 2 ⁇ 10 ⁇ 2 , more preferably
  • a blended oil may be used.
  • Such blends are made by blending a high oleic soy oil having an oleic acid content of at least 70%, preferably at least 75% with another oil, preferably a vegetable oil.
  • the quantity of high oleic soy oil to be added to another oil may be determined by titration: the high oleic soy oil may be added until the blended oil has a Df of less than at or about 1.2 ⁇ 10 ⁇ 3 when measured at 23° C., preferably less than at or about 5.4 ⁇ 10 ⁇ 3 when measured at 70° C., preferably less than 9.1 ⁇ 10 ⁇ 3 when measured at 90° C., preferably less than at or about 1.21 ⁇ 10 ⁇ 2 when measured at 100° C., preferably less than at or about 1.95 ⁇ 10 ⁇ 2 when measured at 120° C., preferably less than at or about 2.32 ⁇ 10 ⁇ 2 when measured at 130° C., and preferably, it shows a Df of less than at or about 2.32 ⁇ 10 ⁇ 2 over a temperature range of at or about 23-130° C.
  • the high oleic soy oil that is used for blending preferably has a polyunsaturated content of less than at or about 16%, more preferably less than at or about 7%.
  • a blended oil may be used.
  • Such blends are made by blending a high oleic soy oil having an oleic acid content of at least 70%, preferably at least 75% with another oil, preferably a vegetable oil.
  • the quantity of high oleic soy oil to be added to another oil may be determined by titration: the high oleic soy oil may be added until the blended oil has a Df of less than at or about 2.5 ⁇ 10 ⁇ 4 when measured at 23° C., preferably less than at or about 2.5 ⁇ 10 ⁇ 3 , more preferably less than at or about 1.5 ⁇ 10 ⁇ 3 when measured at 70° C., preferably less than at or about 5 ⁇ 10 ⁇ 3 , more preferably less than at or about 3 ⁇ 10 ⁇ 3 when measured at 90° C., preferably less than at or about 7 ⁇ 10 ⁇ 3 , more preferably less than at or about 4 ⁇ 10 ⁇ 3 when measured at 100° C., preferably less than at or about 2 ⁇ 10 ⁇ 2 , more preferably less than at or about 7 ⁇ 10 ⁇ 3 when measured at 120° C., and preferably less than at or about 2 ⁇ 10 ⁇ 2 , more preferably less than at or about 1 ⁇ 10 ⁇ 2 when measured at 130° C.
  • the blended oil shows a Df of less than at or about 0.02, more preferably less than at or about 1 ⁇ 10 ⁇ 2 over a temperature range of at or about 23-130° C.
  • the high oleic soy oil that is used for blending preferably has a polyunsaturated content of less than at or about 16%, more preferably less than at or about 7%.
  • a dynamic (natural or forced) heat transfer takes place in most electrical equipment cooled and electrically insulated with oils.
  • the heating of a liquid filled transformer must be controlled, in large proportion by the coolant and dielectric fluid, taking into account fairly large temperature variations, between the internal hotspots and the external temperature extremes, in winter and in summer. Under good controlled conditions the transformer can be in operation for more than 30 years; but can also be quickly damaged with relatively small deviations, sometime less than 10° C., from the ideal operating temperature defined for each category of transformers and the energy transformation load for which they have been designed.
  • At least four important properties of the oil vary with temperature, each of them at various degrees leading to reversible or irreversible property changes in the dielectric heat-transfer fluid (oil). These properties are the density, the thermal conductivity, the dynamic viscosity (all three of which decrease with increasing temperature) and the specific heat (which increases with increasing temperature).
  • the density change be less than at or about 5%, the conductivity change be less than at or about 3%, the heat capacity change be less than at or about 10%.
  • the viscosity change is by far the most substantial, since it can reach 50% for the same range of temperature.
  • Soybean embryogenic suspension cultures are transformed by the method of particle gun bombardment using procedures known in the art (Klein et al. (1987) Nature (London) 327:70 73; U.S. Pat. No. 4,945,050; Hazel et al. (1998) Plant Cell. Rep. 17:765 772; Samoylov et al. (1998) In Vitro Cell Dev. Biol. Plant 34:8 13).
  • particle gun bombardment procedures it is possible to use purified 1) entire plasmid DNA or, 2) DNA fragments containing only the recombinant DNA expression cassette(s) of interest.
  • Stock tissue for transformation experiments are obtained by initiation from soybean immature seeds. Secondary embryos are excised from explants after 6 to 8 weeks on culture initiation medium.
  • the initiation medium is an agar solidified modified MS (Murashige and Skoog (1962) Physiol. Plant. 15:473 497) medium supplemented with vitamins, 2, 4-D and glucose. Secondary embryos are placed in flasks in liquid culture maintenance medium and maintained for 7-9 days on a gyratory shaker at 26+/ ⁇ 2° C. under ⁇ 80 ⁇ Em-2s-1 light intensity.
  • the culture maintenance medium is a modified MS medium supplemented with vitamins, 2, 4-D, sucrose and asparagine.
  • clumps of tissue Prior to bombardment, clumps of tissue are removed from the flasks and moved to an empty 60 ⁇ 15 mm petri dish for bombardment. Tissue is dried by blotting on Whatman #2 filter paper. Approximately 100-200 mg of tissue corresponding to 10-20 clumps (1-5 mm in size each) are used per plate of bombarded tissue.
  • tissue from each bombarded plate is divided and placed into two flasks of liquid culture maintenance medium per plate of bombarded tissue. Seven days post bombardment, the liquid medium in each flask is replaced with fresh culture maintenance medium supplemented with 100 ng/ml selective agent (selection medium).
  • selective agent used can be a sulfonylurea (SU) compound with the chemical name, 2 chloro N ((4 methoxy 6 methyl 1,3,5 triazine 2 yl)aminocarbonyl)benzenesulfonamide (common names: DPX-W4189 and chlorsulfuron).
  • SU sulfonylurea
  • Chlorsulfuron is the active ingredient in the DuPont sulfonylurea herbicide, GLEAN®.
  • the selection medium containing SU is replaced every week for 6-8 weeks. After the 6-8 week selection period, islands of green, transformed tissue are observed growing from untransformed, necrotic embryogenic clusters. These putative transgenic events are isolated and kept in media with SU at 100 ng/ml for another 2-6 weeks with media changes every 1-2 weeks to generate new, clonally propagated, transformed embryogenic suspension cultures. Embryos spend a total of around 8-12 weeks in contact with SU. Suspension cultures are subcultured and maintained as clusters of immature embryos and also regenerated into whole plants by maturation and germination of individual somatic embryos.
  • a Soybean ( Glycine max ) event was produced by particle co-bombardment as described in Example 1 with fragments PHP19340A ( FIG. 10 ; SEQ ID NO: 1) and PHP17752A ( FIG. 11 ; SEQ ID NO: 2). These fragments were obtained by Asc I digestion from a source plasmid. Fragment PHP19340A was obtained from plasmid PHP19340 ( FIG. 12 ; SEQ ID NO: 3) and fragment PHP17752A was obtained from plasmid PHP17752 ( FIG. 13 ; SEQ ID NO: 4). The PHP19340A fragment contains a cassette with a 597 by fragment of the soybean microsomal omega-6 desaturase gene 1 (gm-fad2-1) (Heppard et al., 1996, Plant Physiol. 110: 311-319).
  • the presence of the gm-fad2-1 fragment in the expression cassette acts to suppress expression of the endogenous omega-6 desaturases, resulting in an increased level of oleic acid and decreased levels of palmitic, linoleic, and linolenic acid levels.
  • Upstream of the gm-fad2-1 fragment is the promoter region from the Kunitz trypsin inhibitor gene 3 (KTi3) (Jofuku and Goldberg, 1989, Plant Cell 1: 1079-1093; Jofuku et al., 1989, Plant Cell 1: 427-435) regulating expression of the transcript.
  • KTi3 Kunitz trypsin inhibitor gene 3
  • the KTi3 promoter is highly active in soy embryos and 1000-fold less active in leaf tissue (Jofuku and Goldberg, 1989, Plant Cell 1: 1079-1093).
  • the 3′ untranslated region of the KTi3 gene (KTi3 terminator) (Jofuku and Goldberg, 1989, Plant Cell 1: 1079-1093) terminates expression from this cassette.
  • the PHP17752A fragment contains a cassette with a modified version of the soybean acetolactate synthase gene (gm-hra) encoding the GM-HRA protein with two amino acid residues modified from the endogenous enzyme and five additional amino acids at the N-terminal region of the protein derived from the translation of the soybean acetolactate synthase gene 5′ untranslated region (Falco and Li, 2003, US Patent Application: 2003/0226166).
  • the gm-hra gene encodes a form of acetolactate synthase, which is tolerant to the sulfonylurea class of herbicides.
  • the GM-HRA protein is comprised of 656 amino acids and has a molecular weight of approximately 71 kDa.
  • the expression of the gm-hra gene is controlled by the 5′ promoter region of the S-adenosyl-L-methionine synthetase (SAMS) gene from soybean (Falco and Li, 2003, US Patent Application: 2003/0226166).
  • This 5′ region consists of a constitutive promoter and an intron that interrupts the SAMS 5′ untranslated region (Falco and Li, 2003).
  • the terminator for the gm-hra gene is the endogenous soybean acetolactate synthase terminator (als terminator) (Falco and Li, 2003, US Patent Application: 2003/0226166).
  • transgenic plants from event DP-305423-1 were obtained by microprojectile bombardment as described in Example 1. Embryogenic tissue samples were taken for molecular analysis to confirm the presence of the gm-fad2-1 and gm-hra transgenes by Southern analysis. Plants were regenerated from tissue derived from each unique event and transferred to the greenhouse for seed production.
  • Genomic DNA was extracted from frozen soybean leaf tissue of individual plants of the T4 and T5 generations of DP 305423 1 and of control (variety: Jack) using a standard Urea Extraction Buffer method. Genomic DNA was quantified on a spectrofluorometer using Pico Green® reagent (Molecular Probes, Invitrogen). Approximately 4 ⁇ g of DNA per sample was digested with Hind III or Nco I. For positive control samples, approximately 3 pg (2 genome copy equivalents) of plasmid PHP19340 or PHP17752 was added to control soybean genomic DNA prior to digestion. Negative control samples consisted of unmodified soybean genomic DNA (variety: Jack). DNA fragments were separated by size using agarose gel electrophoresis.
  • the separated DNA fragments were depurinated, denatured, neutralized in situ, and transferred to a nylon membrane in 20 ⁇ SSC buffer using the method as described for TURBOBLOTTERTM Rapid Downward Transfer System (Schleicher & Schuell). Following transfer to the membrane, the DNA was bound to the membrane by UV crosslinking.
  • DNA probes for gm-fad2-1 and gm-hra were labelled with digoxigenin (DIG) by PCR using the PCR DIG Probe Synthesis Kit (Roche).
  • the tubes were prepared for derivatization by wrapping the threaded portions with PTFE sealant tape. Derivatization was performed as follows: The tubes were vortex mixed and 1 mL of derivatization acid stock (prepared by adding 5 mL acetyl chloride (Fluka 00990; Sigma Aldrich St Louis Mo., USA) to 50 ml ice-cold anhydrous methanol) was added. The tubes were capped tightly, re-vortex and incubated at 80° C. in a heat block for 1 hr. The tubes were cooled to room temp and 1 mL of aqueous 1M NaCl was added followed 0.5 mL heptane.
  • derivatization acid stock prepared by adding 5 mL acetyl chloride (Fluka 00990; Sigma Aldrich St Louis Mo., USA) to 50 ml ice-cold anhydrous methanol
  • the tubes were capped tightly, re-vortex and incubated at 80°
  • the initial oven temperature was 160° C. for 4 min and the oven temperature was then ramped to 220° C. at 2 C/min and was then held at the final temperature for 10 min (total run time 44 min).
  • Detection was by flame ionization and a NuChek Prep 461 Standard (1:100 dilution in heptane; NuChek Prep; Elysian Minn., USA) was used to identify peaks, by co-chromatography. All peaks with an area >0.01% were included in the analysis.
  • Tocopherol contents were measured according to AOCS Official Method Ce 8-89 on an Agilent 1100 HPLC system fitted with a 250 ⁇ 4 mm Lycoshere Si 60 (5 um) analytical column and a G1321A fluorescence detector. Oil stocks, as described above, without internal standard were used for this analysis. Quantitative standards dissolved in heptane, were prepared with authentic ⁇ (alpha), ⁇ (beta), ⁇ (gamma) and ⁇ (delta) tocopherol standards (Supelco, Bellefonte Pa., USA).
  • Standard concentrations were confirmed by UV-spectroscopy using the following wavelengths and extinction coefficients [ ⁇ (alpha), OD292, 0.0076; ⁇ (beta) OD296, 0.0089; ⁇ (gamma) OD298, 0.0091; ⁇ (delta) OD298, 0.0087].
  • Free fatty acid contents of the oils were performed by titration using a Mettler-Toledo DL22 F&B titrator (Mettler-Toledo, Columbus Ohio, USA) according to the manufacturers protocol M345 (Acid Number of edible oils).
  • Peroxide values of the oils were performed by iodometric titration using a Mettler-Toledo DL22 F&B titrator (Mettler-Toledo, Columbus Ohio, USA) according to the manufacturers protocol M346 (Peroxide value in edible oils and fats).
  • p-Anisidine values were determined on oils according to AOCS official method Cd 18-90.
  • the oxidative stability index was measured on 5.0+/ ⁇ 0.2 g samples of pure oil samples (with or without additives) according to AOCS official method Cd 12b-92, using an OSI-24 Oxidative Stability Instrument. Instrument control and data analysis were performed using OSI Program v8.18 and Instacal 5.33 software (Omnion, Inc, Rockland Mass., USA).
  • the loss factor (Df) was measured using ASTM D924 for the dielectric heat-transfer fluids shown in Table 2, at different temperatures. Loss factor was plotted VS temperature.
  • FIG. 1 The results are shown in FIG. 1 , wherein the squares ⁇ and triangles ⁇ show the loss factor for comparative fluid C1 (measured at two different times), the crosses X show the loss factor for comparative fluid C2, the diamonds ⁇ show the loss factor for a soybean oil for use according to the invention E1, and the filled circles ⁇ show the loss factor for mineral oil, which is included as a reference.
  • soybean oil for use according to the invention (E1)) shows a low dielectric loss factor that stays relatively consistent with increase in temperature, whereas the other vegetable oils (C1 and C2) show significant increases in loss factor as the temperature is increased.
  • the dielectric breakdown voltage is an essential parameter to compare fluids used for dielectric insulation and/or heat exchange in the presence of electrical and magnetic fields. It is also a relevant indication of the arcing transmission characteristics of the fluid.
  • the dielectric breakdown voltage measured according to ASTM D877, characterises the dielectric performance limit of the fluid, which is a bulk property giving indirect access to the ultimate voltage under which the dielectric can be used and its ability to sustain eventual voltage pulses.
  • the soy oil for use according to the invention (E1) has a breakdown voltage at 23° C. within the range of 57 to 66 kV.
  • the two comparative fluids C1 and C2 have breakdown voltages in the range of 47 to 65 kV at 25° C., i.e. significantly broader and lower.
  • the fluid for use according to the invention (E1) is clearly superior, exhibiting better consistency versus arcing transmission as well.
  • the fluid for the use according to the invention (E1) as well as the two comparative fluids (C1 and C2) of a mass of 2.6 g were exposed to a commercial microwave treatment of one minute at a maximum power of 900 W. Such conditions were selected to yield a fluid temperature inferior to 200° C. and preferably lower than 160° C. in order to maintain the molecular integrity of the essential components of the fluid.
  • FIG. 2 shows the thermo-gravimetric pattern and heat flux generated before (dotted lines) and after (solid lines) a pharmaceutical grade of Ricinoleic oil is exposed to the electromagnetic microwave treatment of Example 8.
  • the heat flux signal definition and their relative strength clearly show a beneficial preconditioning of the oil by the electromagnetic microwave treatment process and method therewith, as is shown for example by the sharpness of the peaks, the start and the onset temperatures after the pre-treatment.
  • FIG. 3 shows the thermo-gravimetric pattern and heat flux generated before (dotted lines) and after (solid lines) a commercial grade of High Oleic Sunflower oil, the comparative fluid C2, is exposed to the electromagnetic microwave treatment of Example 8.
  • the heat flux signal definition and their relative strength clearly show a beneficial preconditioning of the oil by the electromagnetic microwave treatment process and method therewith, as is shown by the sharpness of the peaks after the pre-treatment.
  • FIG. 4 shows the thermo-gravimetric pattern and heat flux generated before (solid lines) and after (dotted lines) a commercial grade of normal soybean oil, the comparative fluid C1, was exposed to the electromagnetic microwave treatment of Example 8.
  • the heat flux signal definition and their relative strength clearly show a beneficial preconditioning of the oil by the electromagnetic microwave treatment process and method therewith, as is shown by the sharpness of the peaks after the pre-treatment.
  • FIG. 5 shows the thermo-gravimetric pattern and heat flux generated before (solid lines) and after (dotted lines) the fluid for the use of the invention, E1, was exposed to the electromagnetic microwave treatment of Example 8.
  • the heat flux signal definition and their relative strength clearly show a beneficial preconditioning of the oil by the electromagnetic microwave treatment process and method therewith, as is shown by the sharpness of the peaks after the pre-treatment.
  • the beneficial effect of the pre-treatment extends to all triacylglycerol dielectric heat-transfer fluids and mixtures thereof, and is not limited to the fluid used in the use according to the invention.
  • transformer insulation Kraft paper from Weidmann AG, Rapperswill, Switzerland, was impregnated at room temperature, via a naturally occurring imbibing process, with an amount equivalent to 30 wt % of the fluid for use according to the invention.
  • the initial specific weight of the paper was 95 g/m 2 .
  • FIG. 6 shows the thermal behaviour of untreated Kraft paper (solid line), Kraft paper imbibed with the fluid for use according to the invention (dotted lines) and Kraft paper imbibed with the fluid for use according to the invention and pre-treated with microwaves according to Example 8 (dash-dot lines).
  • the imbibing of the Kraft paper with the fluid for use according to the invention results in an enhancement of the thermal resistance of the paper by 20-40° C.
  • the microwave pre-treatment results in a further enhancement by 10° C.
  • the impregnation can be done during the manufacture of the paper or after.
  • the microwave treatment can be repeated as many times as needed and can be performed by exposing said fluid to a constant and uniformly distributed electromagnetic field applied continuously or in series of constant and/or variable pulse and relaxation sequences; repeating the exposure sequence as often as needed.
  • the imbibing oil can be any oil mixtures of the invention.
  • An oil of the invention mixed with 20% of a commodity linseed oil has surprisingly shown good sealing properties that are especially valuable in sealed electrical devices of the invention, especially transformers, which tend to micro-leak with time, especially for those used for relatively long period of time, such as 20 to 30 years.
  • the sealing nature of the oil of the blends of the invention is especially appreciated.
  • Naturally occurring or synthesised epoxidized vegetable oil have also been found as exhibiting similar sealing effect of the insulating paper as well as at sealing interfaces.
  • the paper treatment with the oil of the invention and/or mixtures thereof has valuable effect on the viscoelastic behaviour of the paper and its mechanical resistance to puncture and tearing, for example; leading to enhance paper endurance appreciated to extend the life of the electrical device, such as liquid filled transformers.
  • An oil for use according to the invention was subjected to the same heat aging, and no change in dynamic viscosity was observed.
  • This kind property makes the oil particularly useful as a dielectric heat-transfer fluid.
  • a given amount of a low linoleic soy oil (LL) having the fatty acid composition (“FAC”) profile given in Table 6 was blended with an oil for the use of the invention, E4, of the profile given in Table 6 to produce blended oils corresponding to 70% and 65% oleic acid oil mixtures of the FAC profile given in Table 6.
  • a commodity soy oil sample (Cm) of the FAC profile given in Table 6 served as a representative of a lower oleic oil content sample.
  • FIGS. 7A and 7B show the variation of Df as a function of temperature for the oils and blended oils listed in Table 6.
  • FIG. 7A shows oils of the invention comprising 78% oleic acid (E2,) compared to commodity oil and a 65% oleic acid blend and a 70% oleic acid blend.
  • FIG. 7B shows oils of the invention comprising a 74% oleic acid content (E4) compared to commodity oil and a 65% oleic acid blend and a 70% oleic acid blend.
  • the triangles designate the results for a soy oil blend having 70% oleic and 16% polyunsaturates in FIGS. 7A and 7B .
  • the diamonds designate the results for a soy oil blend having 65% oleic and 20% polyunsaturates in FIGS. 7A and 7B .
  • oils for use according to the invention E1 show superior behaviour over the other oils, in that the Df is lower and stays lower over the entire temperature range of 23-130° C. Furthermore, the oils of the invention E1, such as for example the 70% oleic acid blend, the oil E2 and oil E4 show less increase in Df with temperature.
  • the commodity soy oil Cm without antioxidants and other additives responds similarly to the commercial soy oil C1 containing traditional additives for the transformer applications.
  • FIG. 8 shows the variation of Df as a function of the oleic content in percent, at two temperatures (130° C., upper line, and 90° C., lower line). It can be seen from FIG. 8 that at both temperatures the Df drops as the oleic acid content increases, with a sharp decrease from at or about 65% oleic acid to at or about 70% oleic acid.
  • the oil used for this experiment was oil E2 as an example for one of the oils of the invention.
  • the Df was measured at various temperatures according to Example 6. The results are listed in Table 8. The results clearly show that oils E2 and E4, which are soy oils for use according to the invention, show significantly lower Df's over the temperature range of 23-130° C., and show less increase in Df at high temperatures than the comparative oils.
  • the high oleic sunflower Df data are locally just in between E4 and C1, close to C1 indicating a significant variation of the high oleic sunflower Df values within the 23 to 130 C temperature range.
  • the high oleic sunflower without antioxidants and other additives responds similarly to the commercial high oleic sunflower C2 containing traditional additives for the transformer applications.
  • FIG. 9 shows in graphic form the dielectric loss factor (Df) VS temperature for comparative fluids C1 and C2 and for oils E2 and E4, wherein the squares ⁇ show the loss factor for comparative fluid C1, the open triangles ⁇ show the loss factor for comparative fluid C2, the diamonds ⁇ show the loss factor for a soybean oil for use according to the invention E2 and E4, lower line E2, upper line E4.
  • Df dielectric loss factor

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Thermal Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Combustion & Propulsion (AREA)
  • Materials Engineering (AREA)
  • Power Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Electrochemistry (AREA)
  • Microbiology (AREA)
  • Wood Science & Technology (AREA)
  • Fats And Perfumes (AREA)
  • Organic Insulating Materials (AREA)
  • Edible Oils And Fats (AREA)
  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
  • Insulating Of Coils (AREA)
  • Lubricants (AREA)
US12/748,891 2009-03-27 2010-03-29 Dielectric heat-transfer fluid Abandoned US20100243969A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US12/748,891 US20100243969A1 (en) 2009-03-27 2010-03-29 Dielectric heat-transfer fluid
US13/961,210 US9185826B2 (en) 2009-03-27 2013-08-07 Dielectric heat-transfer fluid
US14/926,399 US9455066B2 (en) 2009-03-27 2015-10-29 Dielectric heat-transfer fluid

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16407409P 2009-03-27 2009-03-27
US12/748,891 US20100243969A1 (en) 2009-03-27 2010-03-29 Dielectric heat-transfer fluid

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US13/961,210 Continuation US9185826B2 (en) 2009-03-27 2013-08-07 Dielectric heat-transfer fluid

Publications (1)

Publication Number Publication Date
US20100243969A1 true US20100243969A1 (en) 2010-09-30

Family

ID=42235436

Family Applications (3)

Application Number Title Priority Date Filing Date
US12/748,891 Abandoned US20100243969A1 (en) 2009-03-27 2010-03-29 Dielectric heat-transfer fluid
US13/961,210 Active 2030-05-06 US9185826B2 (en) 2009-03-27 2013-08-07 Dielectric heat-transfer fluid
US14/926,399 Active US9455066B2 (en) 2009-03-27 2015-10-29 Dielectric heat-transfer fluid

Family Applications After (2)

Application Number Title Priority Date Filing Date
US13/961,210 Active 2030-05-06 US9185826B2 (en) 2009-03-27 2013-08-07 Dielectric heat-transfer fluid
US14/926,399 Active US9455066B2 (en) 2009-03-27 2015-10-29 Dielectric heat-transfer fluid

Country Status (9)

Country Link
US (3) US20100243969A1 (zh)
EP (2) EP3093324A1 (zh)
JP (2) JP6090834B2 (zh)
KR (1) KR20110138260A (zh)
CN (1) CN102365343B (zh)
AU (1) AU2010229686B2 (zh)
BR (1) BRPI1006424B8 (zh)
CA (1) CA2754291C (zh)
WO (1) WO2010111698A2 (zh)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012061647A2 (en) 2010-11-03 2012-05-10 Solazyme, Inc. Microbial oils with lowered pour points, dielectric fluids produced therefrom, and related methods
WO2013003268A1 (en) * 2011-06-27 2013-01-03 Dow Global Technologies Llc Genetically-engineered microbial oil dielectric fluid
US20130225023A1 (en) * 2011-09-23 2013-08-29 E I Du Pont De Nemours And Company Dielectric Fluids Comprising Polyol Esters
WO2013134603A1 (en) * 2012-03-09 2013-09-12 Davis Bob Lee Haloalkene complexes
US9121490B2 (en) * 2011-05-12 2015-09-01 Audi Ag Method for operating a motor vehicle with a hybrid drive
WO2018067669A1 (en) * 2016-10-04 2018-04-12 Cargill, Incorporated Ultra refined vegetable oil and its use in personal care and cosmetic applications

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008151149A2 (en) 2007-06-01 2008-12-11 Solazyme, Inc. Production of oil in microorganisms
RU2542374C2 (ru) 2008-04-09 2015-02-20 Солазим, Инк. Способ химической модификации липидов микроводорослей, способ получения мыла и мыло, включающее соли жирных кислот омыленных липидов микроводорослей
US20100303989A1 (en) 2008-10-14 2010-12-02 Solazyme, Inc. Microalgal Flour
ES2583639T3 (es) 2008-11-28 2016-09-21 Terravia Holdings, Inc. Producción de aceites específicos en microorganismos heterótrofos
JP5996527B2 (ja) 2010-05-28 2016-09-21 テラヴィア ホールディングス, インコーポレイテッド 用途に応じた油を含む食品成分
EP2659492B1 (en) 2010-12-30 2014-12-17 Union Carbide Chemicals & Plastics Technology LLC Method of removing impurities from natural ester oil, manufacture of oil-based dielectric fluids
JP6071904B2 (ja) 2011-02-02 2017-02-01 テラヴィア ホールディングス, インコーポレイテッド 組み換え油産生微生物から生成される用途に応じた油
BR112013028621A2 (pt) 2011-05-06 2016-11-29 Solazyme Inc "microalgas oleaginosas recombinantes, método para produzir biomassa de microalga ou um produto produzido da biomassa, e método para produzir uma composição lipídica de microalga".
EP2758969B1 (en) * 2011-09-23 2015-11-04 E. I. du Pont de Nemours and Company Dielectric fluids comprising polyol esters, methods for preparing mixtures of polyol esters, and electrical apparatuses comprising polyol ester dielectric fluids
WO2013052956A2 (en) 2011-10-07 2013-04-11 E. I. Du Pont De Nemours And Company Liquid compositions used as insulating and heat transfer means, electrical devices containing said compositions and preparation methods for such compositions
SG11201406711TA (en) 2012-04-18 2014-11-27 Solazyme Inc Tailored oils
US9719114B2 (en) 2012-04-18 2017-08-01 Terravia Holdings, Inc. Tailored oils
JP2014063876A (ja) * 2012-09-21 2014-04-10 Aichi Electric Co Ltd 油入電気機器
CA2887040C (en) * 2012-10-18 2020-10-13 Dow Global Technologies Llc Triglyceride based, low viscosity, high flash point dielectric fluids
KR102133739B1 (ko) * 2012-10-18 2020-07-15 다우 글로벌 테크놀로지스 엘엘씨 비-올레산 트리글리세리드 기재의 저점도 고인화점 유전 유체
CA2887006C (en) * 2012-10-18 2020-10-06 Dow Global Technologies Llc Oleic and medium chain length triglyceride based, low viscosity, high flash point dielectric fluids
CN104798143A (zh) * 2012-11-13 2015-07-22 纳幕尔杜邦公司 可用作介电流体组合物的共混的油组合物及其制备方法
WO2014100649A1 (en) * 2012-12-20 2014-06-26 Cargill, Incorporated Enzymatically-degummed oil and uses thereof
US10098371B2 (en) 2013-01-28 2018-10-16 Solazyme Roquette Nutritionals, LLC Microalgal flour
US9249252B2 (en) 2013-04-26 2016-02-02 Solazyme, Inc. Low polyunsaturated fatty acid oils and uses thereof
FR3009619B1 (fr) 2013-08-07 2017-12-29 Roquette Freres Compositions de biomasse de microalgues riches en proteines de qualite sensorielle optimisee
WO2015051319A2 (en) 2013-10-04 2015-04-09 Solazyme, Inc. Tailored oils
US9394550B2 (en) 2014-03-28 2016-07-19 Terravia Holdings, Inc. Lauric ester compositions
CN106574255A (zh) 2014-07-10 2017-04-19 泰拉瑞亚控股公司 酮脂酰acp合酶基因及其用途
ES1135742Y (es) * 2015-01-14 2015-04-27 Coprecitec Sl Bomba eléctrica
BR112019018200B1 (pt) 2017-03-03 2024-02-20 Pioneer Hi-Bred International, Inc Método para medir a quantidade de um sucrosil-oligossacarídeo,método para medir estaquiose, método para processar sementes de soja geneticamente modificadas
JP6991653B2 (ja) * 2017-09-15 2022-02-03 日清オイリオグループ株式会社 油脂組成物
WO2021138403A1 (en) * 2019-12-30 2021-07-08 Calyxt, Inc. High oleic acid soybean oil

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4945050A (en) * 1984-11-13 1990-07-31 Cornell Research Foundation, Inc. Method for transporting substances into living cells and tissues and apparatus therefor
US5981781A (en) * 1996-04-26 1999-11-09 E. I. Du Pont De Nemours And Company Soybean oil having high oxidative stability
US20020049145A1 (en) * 1998-05-11 2002-04-25 Cannon Glenn S. Vegetable-based transformer oil and transmission line fluid
US20030226160A1 (en) * 1997-11-18 2003-12-04 Pioneer Hi-Bred International, Inc. Compositions and methods for locating preferred integration sites within the genome of a plant
US20040089855A1 (en) * 1996-06-18 2004-05-13 Abb Technology Ag High oleic acid oil compositions and methods of making and electrical insulation fluids and devices comprising the same
US20050072964A1 (en) * 2003-10-02 2005-04-07 Rapp Kevin J. Additive for dielectric fluid
US6905638B2 (en) * 1995-12-21 2005-06-14 Cooper Industries, Inc. Vegetable oil based dielectric fluid and methods of using same
US20060226166A1 (en) * 2005-04-06 2006-10-12 Mark Hartelius Product dispenser

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4627192B1 (en) * 1984-11-16 1995-10-17 Sigco Res Inc Sunflower products and methods for their production
US5034323A (en) 1989-03-30 1991-07-23 Dna Plant Technology Corporation Genetic engineering of novel plant phenotypes
FR2688146B1 (fr) * 1992-03-05 1994-05-20 Charles Frei Procede et dispositif de purification d'un liquide electriquement non conducteur.
WO1994011516A1 (en) 1992-11-17 1994-05-26 E.I. Du Pont De Nemours And Company Genes for microsomal delta-12 fatty acid desaturases and related enzymes from plants
DE69726427T2 (de) * 1996-06-18 2004-09-09 Abb Inc. Triglyceridzusammensetzung
US7217858B2 (en) 1998-12-21 2007-05-15 E. I. Du Pont De Nemours And Company S-adenosyl-L-methionine synthetase promoter and its use in expression of transgenic genes in plants
US6534454B1 (en) * 2000-06-28 2003-03-18 Renewable Lubricants, Inc. Biodegradable vegetable oil compositions
FR2839067B1 (fr) * 2002-04-25 2006-04-07 Aldivia Nouveau procede d'elimination des peroxydes et de leurs derives d'oxydation presents dans les composes insatures, seuls ou en melange
US7759507B2 (en) * 2003-09-05 2010-07-20 Abbott Laboratories Lipid system and methods of use
WO2006052906A2 (en) * 2004-11-08 2006-05-18 Neopharm, Inc. Synthesis of cardiolipin analogues and uses thereof
BRPI0618409C1 (pt) * 2005-10-11 2011-12-20 Biolectric Pty Ltd fluido dielétricos à base de óleo contendo ácido monoinsaturado de baixa viscosidade, processo para suas produções, transformador e modificador de viscosidade
ES2423480T3 (es) * 2007-03-16 2013-09-20 Alberto Sánchez De Lema Equipo eléctrico aislado con un fluido dieléctrico biodegradable

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4945050A (en) * 1984-11-13 1990-07-31 Cornell Research Foundation, Inc. Method for transporting substances into living cells and tissues and apparatus therefor
US6905638B2 (en) * 1995-12-21 2005-06-14 Cooper Industries, Inc. Vegetable oil based dielectric fluid and methods of using same
US5981781A (en) * 1996-04-26 1999-11-09 E. I. Du Pont De Nemours And Company Soybean oil having high oxidative stability
US20040089855A1 (en) * 1996-06-18 2004-05-13 Abb Technology Ag High oleic acid oil compositions and methods of making and electrical insulation fluids and devices comprising the same
US7048875B2 (en) * 1996-06-18 2006-05-23 Abb Technology Ag High oleic acid oil compositions and methods of making and electrical insulation fluids and devices comprising the same
US20030226160A1 (en) * 1997-11-18 2003-12-04 Pioneer Hi-Bred International, Inc. Compositions and methods for locating preferred integration sites within the genome of a plant
US20020049145A1 (en) * 1998-05-11 2002-04-25 Cannon Glenn S. Vegetable-based transformer oil and transmission line fluid
US20050072964A1 (en) * 2003-10-02 2005-04-07 Rapp Kevin J. Additive for dielectric fluid
US20060226166A1 (en) * 2005-04-06 2006-10-12 Mark Hartelius Product dispenser

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012061647A2 (en) 2010-11-03 2012-05-10 Solazyme, Inc. Microbial oils with lowered pour points, dielectric fluids produced therefrom, and related methods
EP3521408A1 (en) 2010-11-03 2019-08-07 Corbion Biotech, Inc. Genetically-engineered chlorella or prototheca microbe and oil produced therefrom
US9121490B2 (en) * 2011-05-12 2015-09-01 Audi Ag Method for operating a motor vehicle with a hybrid drive
WO2013003268A1 (en) * 2011-06-27 2013-01-03 Dow Global Technologies Llc Genetically-engineered microbial oil dielectric fluid
KR20140045437A (ko) * 2011-06-27 2014-04-16 다우 글로벌 테크놀로지스 엘엘씨 유전자-조작 미생물 오일 유전성 유체
CN103781887A (zh) * 2011-06-27 2014-05-07 陶氏环球技术有限责任公司 基因工程化微生物油的介电流体
US9362980B2 (en) 2011-06-27 2016-06-07 Dow Global Technologies Llc Genetically-engineered microbial oil dielectric fluid
KR101971135B1 (ko) * 2011-06-27 2019-04-22 다우 글로벌 테크놀로지스 엘엘씨 유전자-조작 미생물 오일 유전성 유체
US20130225023A1 (en) * 2011-09-23 2013-08-29 E I Du Pont De Nemours And Company Dielectric Fluids Comprising Polyol Esters
US9028727B2 (en) * 2011-09-23 2015-05-12 E I Du Pont De Nemours And Company Dielectric fluids comprising polyol esters
WO2013134603A1 (en) * 2012-03-09 2013-09-12 Davis Bob Lee Haloalkene complexes
WO2018067669A1 (en) * 2016-10-04 2018-04-12 Cargill, Incorporated Ultra refined vegetable oil and its use in personal care and cosmetic applications

Also Published As

Publication number Publication date
BRPI1006424B8 (pt) 2022-12-06
AU2010229686B2 (en) 2015-09-03
CA2754291C (en) 2016-10-11
EP2411481B1 (en) 2016-08-03
JP6121459B2 (ja) 2017-04-26
CN102365343A (zh) 2012-02-29
JP6090834B2 (ja) 2017-03-08
BRPI1006424B1 (pt) 2020-10-20
US20160049219A1 (en) 2016-02-18
CN102365343B (zh) 2016-08-03
AU2010229686A1 (en) 2011-09-08
CA2754291A1 (en) 2010-09-30
KR20110138260A (ko) 2011-12-26
WO2010111698A3 (en) 2010-11-18
JP2015118942A (ja) 2015-06-25
US9455066B2 (en) 2016-09-27
BRPI1006424A2 (pt) 2017-04-25
US9185826B2 (en) 2015-11-10
EP3093324A1 (en) 2016-11-16
US20140036447A1 (en) 2014-02-06
EP2411481A2 (en) 2012-02-01
WO2010111698A2 (en) 2010-09-30
JP2012522337A (ja) 2012-09-20

Similar Documents

Publication Publication Date Title
US9455066B2 (en) Dielectric heat-transfer fluid
Konda et al. Metabolic engineering of soybean seeds for enhanced vitamin E tocochromanol content and effects on oil antioxidant properties in polyunsaturated fatty acid-rich germplasm
TWI575538B (zh) 基因工程化微生物油的介電質流體
CN101300644A (zh) 低粘度植物油基介电流体
CN102782051A (zh) 用于电气元件的藻类油基介电流体
JP7326312B2 (ja) 安定度を高めた天然生物由来油を含む誘電流体
EP2920287A1 (en) Blended oil compositions useful as dielectric fluid compositions and methods of preparing same
CN107680712B (zh) 一种天然酯绝缘油用复配抗氧化剂及其应用
US20140131642A1 (en) Blended oil compositions useful as dielectric fluid compsotions and methods of preparing same
AU2015227411A1 (en) Dielectric heat-transfer fluid
EP2128874B1 (en) Electrical equipment insulated with a biodegradable dielectric fluid
EP2128873B1 (en) Biodegradable dielectric fluid
US20140131634A1 (en) Blended oil compositions useful as dielectric fluid compositions and methods of preparing same
US20140131637A1 (en) Blended oil compositions useful as dielectric fluid compositions and methods of preparing same
US20140131638A1 (en) Blended oil compositions useful as dielectric fluid compositions and methods of preparing same
US20140131635A1 (en) Blended oil compositions useful as dielectric fluid compositions and methods of preparing same
Diaby et al. Physicochemical properties of refined and unrefined oils of gingerbread plum (Neocarya macrophylla) kernels from Guinea and Niger
EP2920794A1 (en) Blended oil compositions useful as dielectric fluid compositions and methods of preparing same
JPWO2019183214A5 (zh)
US20140131640A1 (en) Blended oil compositions useful as dielectric fluid compositions and methods of preparing same
US20140131641A1 (en) Blended oil compositions useful as dielectric fluid compositions and methods of preparing same
US20140135522A1 (en) Blended oil compositions useful as dielectric fluid compositions and methods of preparing same
US20140131636A1 (en) Blended oil compositions useful as dielectric fluid compositions and methods of preparing same

Legal Events

Date Code Title Description
AS Assignment

Owner name: E. I. DU PONT DE NEMOURS AND COMPANY, DELAWARE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:REBOUILLAT, SERGE;KNOWLTON, SUSAN;REEL/FRAME:025367/0219

Effective date: 20100427

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION