WO2016196260A1 - Cleaning solvent compositions and their use - Google Patents

Cleaning solvent compositions and their use Download PDF

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Publication number
WO2016196260A1
WO2016196260A1 PCT/US2016/034569 US2016034569W WO2016196260A1 WO 2016196260 A1 WO2016196260 A1 WO 2016196260A1 US 2016034569 W US2016034569 W US 2016034569W WO 2016196260 A1 WO2016196260 A1 WO 2016196260A1
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Prior art keywords
weight percent
composition
amount
present
phosphate ester
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PCT/US2016/034569
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French (fr)
Inventor
Wells Cunningham
Elizabeth P. NORWOOD
Venesia L. HURTUBISE
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Zynon Technologies, Llc
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Application filed by Zynon Technologies, Llc filed Critical Zynon Technologies, Llc
Priority to EP16804100.2A priority Critical patent/EP3303538B1/en
Priority to CN201680031019.XA priority patent/CN107636135A/en
Priority to US15/577,194 priority patent/US10883071B2/en
Priority to ES16804100T priority patent/ES2830200T3/en
Priority to PL16804100T priority patent/PL3303538T3/en
Publication of WO2016196260A1 publication Critical patent/WO2016196260A1/en

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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/50Solvents
    • C11D7/5004Organic solvents
    • C11D7/5018Halogenated solvents
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/24Organic compounds containing halogen
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/004Surface-active compounds containing F
    • C11D1/006Surface-active compounds containing fluorine and phosphorus
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/78Neutral esters of acids of phosphorus
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/825Mixtures of compounds all of which are non-ionic
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/201Monohydric alcohols linear
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/2017Monohydric alcohols branched
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/2034Monohydric alcohols aromatic
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2041Dihydric alcohols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2041Dihydric alcohols
    • C11D3/2044Dihydric alcohols linear
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2041Dihydric alcohols
    • C11D3/2048Dihydric alcohols branched
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2041Dihydric alcohols
    • C11D3/2058Dihydric alcohols aromatic
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2065Polyhydric alcohols

Definitions

  • the present invention concerns solvent-based cleaning compositions of the type used in industrial processes for cleaning a wide variety of items including metals and plastics in the metal-working, electronics and other industries.
  • Solvent based cleaning compositions are used in industrial processes for cleaning a wide variety of soiling substances and residues (below sometimes referred to as "soils” or “soiling substances”).
  • the electronics industry typically cleans fluxes, solder pastes, adhesives and coatings from a variety of devices before and after assembly of components.
  • Such devices may comprise one or more of a wide range of materials comprising metal, ceramic and synthetic polymer (plastic) substrates and components.
  • Metal working operations must remove lubricant oils and soaps, grinding media and greases from metal surfaces. Many of these soils are very difficult to strip from metal surfaces, especially with nonaqueous cleaners.
  • non-flammable blends of solvents that provide a cleaning solvent which can be used safely in aerosol packages, or as wiping fluids or in bulk cleaning tanks, for example, in vapor degreasing ("VDG") units.
  • these cleaning solvents comprise halogenated compounds that are either non-flammable themselves or can be rendered non-flammable in a mixture with other halogenated compounds.
  • Many solvent- based cleaning compositions rely heavily on the use of additives to target specific applications, that is, to remove specific soiling substances from various objects.
  • a widely used class of additives is phosphate esters, known for use as anionic surfactants.
  • U.S. Patent 5,856,286 to Nalewajek issued on January 5, 1999 discloses surfactants for use in drying and dry cleaning compositions, in particular, surfactants which may be used with halocarbons including hydrochlorofluorocarbons and hydrofluorocarbons and hydrofluoroethers.
  • the invention is premised on the discovery that placement of fluorine on the surfactant molecule is critical to surfactant solubility in the halogenated solvent compounds disclosed.
  • U.S. Patent 5,908,822 to Dishart issued on June 1 , 1999 discloses compositions and processes for drying substrates in which the drying and/or cleaning compositions contain surfactants which are primary or secondary amine salts of various perfluoro hydrogen and dihydrogen phosphates.
  • U.S. Patent 6,053,952 to Kaiser issued on April 25, 2000 discloses a method of dry cleaning using a highly fluorinated organic solvent which contains at least one hydrogen atom per molecule, for example, highly fluorinated hydrocarbons or highly fluorinated ethers.
  • these compounds are combined with dichloroethylene and a surfactant may be included in the composition.
  • surfactants may comprise organic al- kyl phosphate ester, dialkyl sodium succinate or isopropylamine alkyl benzene sulfonate. The use of phosphate ester salts in dry cleaning is disclosed.
  • U.S. Patent 8,637,443 to Basu et al. issued on January 28, 2014 discloses a dry cleaning method using a highly fluorinated organic solvent, such as hydrofluorcarbons (HFC) or hydrofluoroethers (HFE).
  • HFC hydrofluorcarbons
  • HFE hydrofluoroethers
  • TDE transdichloroethylene
  • surfactants including organic alkyl phosphate ester, dialkyl sodium succinates, isopropylamine alkyl benzene sulfonate is disclosed.
  • the latter may be used with other surfactant ingredients in Vertrel® MCA Plus.
  • the present invention concerns cleaning solvent compositions whose components exhibit good mutual solvency and highly efficient cleaning.
  • the cleaning solvent compositions of the present invention comprise one or more free acid forms of phosphate ester surfactants, one or more halogenated hydrocarbon solvents, and one or more alcohols.
  • a composition comprising from about 0.2 to about 15 weight percent of one or more free acid forms of phosphate ester surfactants selected from the group consisting of one or both of:
  • R is selected from the group consisting of one or more of ethoxylated hydrocarbons, alkylated hydrocarbons, fluorinated hydrocarbons, and ethoxylated and fluorinated hydrocarbons;
  • an alcohol selected from the group consisting of one or more of straight chain and branched alkyl alcohols, monohydric and polyhy- dric aromatic alcohols and monohydric and polyhydric heteroaromatic alcohols; and
  • R is one or more of
  • R' is one or more of H, CH 3 , an alkyl group and an aryl group
  • n is an integer from 2 to 20, for example, n is an integer from 2 to 5.
  • the alcohol is selected from the group consisting of one or more of methanol, ethanol, isopropanol and n-butanol.
  • the one or more halogenated hydrocarbon solvents are selected from the group consisting of one or more of perfluorocarbons ("PFCs”), chlorofluorocarbons (“CFCs”), hydrofluorocarbons (“HFCs”), hy- drofluoroethers (“HFEs”), hydrofluoroolefins (“HFOs”), partially brominated hydrocarbons, fully brominated hydrocarbons, partially chlorinated hydrocarbons and fully chlorinated hydrocarbons.
  • PFCs perfluorocarbons
  • CFCs chlorofluorocarbons
  • HFCs hydrofluorocarbons
  • HFEs hy- drofluoroethers
  • HFOs hydrofluoroolefins
  • composition comprising from about 0.2 to about 15 weight percent of one or more free acid forms of phosphate ester surfactants selected from the group consisting of:
  • R is selected from the group consisting of one or more of ethoxylated hydrocarbons, alkylated hydrocarbons, fluorinated hydrocarbons, and ethoxylated and fluorinated hydrocarbons;
  • R is one or more of
  • R' is one or more of H, CH 3 , an alkyl group and an aryl group
  • n is an integer from 2 to 20, for example, n is an integer from 2 to 5.
  • the halogenated hydrocarbon solvent is selected from the group consisting of one or more of perfluorocarbons (“PFCs”), chlorofluorocarbons (“CFCs”), hydrofluorocar- bons (“HFCs”), hydrofluoroethers (“HFEs”), hydrofluoroolefins (“HFOs”), partially brominated hydrocarbons, fully brominated hydrocarbons, partially chlorinated hydrocarbons and fully chlorinated hydrocarbons.
  • PFCs perfluorocarbons
  • CFCs chlorofluorocarbons
  • HFCs hydrofluorocar- bons
  • HFEs hydrofluoroethers
  • HFOs hydrofluoroolefins
  • compositions of the invention may include a non-halogenated hydrocarbon solvent.
  • TDE Trans-Dichloroethylene,.Chemical Abstracts Number
  • HFCs Hydrofluorocarbons such as HFC 43-1 Ome, sold under the trademark Vertrel® XF, CAS # 1384-95-42 and HFC365mfc CAS # 406-58-6. These materials are available from E.I. DuPont de Nemours and Co. of Wilmington, Delaware.
  • HFEs Hydrofluoroethers such as HFE 7100, CAS # 163702-08-7 and 163702-07-6.
  • NPB n-Propyl bromide, CAS # 106-94-5.
  • SION A blend of 96% trans-dichloroethylene and 4% methylperfluorohexene (HFX-1 10). This material has a boiling point of 121 °F (49.4°C) and is available from E.I. DuPont de Nemours and Co. of Wilmington, Delaware.
  • CMS CMS
  • HFC 43-1 Ome 2,3- dihydrodecafluoropentane
  • MCA trans-dichloroethylene, 38% 2,3- dihydrodecafluoropentane
  • SDG trans-dichloroethylene, 7% 2,3- dihydrodecafluoropentane (HFC 43- 10me); 10% hexafluorocyclopentane.
  • HFC 43- 10me 2,3- dihydrodecafluoropentane
  • Bp 109F This material has a boiling point of 109°F (42.8°C) and is available from E.I. DuPont de Nemours and Co. of Wilmington, Delaware.
  • Chlorofluorocarbons such as those sold under the trademark Solstice, for example, trans-chlorotrifluoromethyl propene CAS # 2730-43-0. This material has a boiling point of 68°F (20°C) and is available from Honeywell International of Morristown, New Jersey.
  • DBE dimethyl succinate, glutarate and adipate having a boiling point of >250°F (121 .1 °C) is available from Invista of Wichita, Kansas. [0021 ] Phosphate Esters
  • Capstone FS-66 A fluorinated alkyl substituted phosphate ester in free acid form, available from E.I. DuPont de Nemours and Co. of Wilmington, Delaware.
  • Rhodafac RS710 An ethoxylated alkyl substituted phosphate ester in free acid form, available from Solvay Rhodia which has a place of business in Houston, Texas.
  • No-Clean Lead-Free Solder Pastes available from Alpha Corporation of Altoona, Pennsylvania and Suwanee, Georgia under the designation Omnix 340, or from Nihon Almit Co. Ltd. of Tokyo, Japan under the designation SN62U. Additional fluxes and pastes as are used in the industry are: AIM Corporation 217 Gel Flux, NC Paste Flux (257), NC Flux Pen (280), M8 Paste, RMA258-15R and Loctite Corporation GC3 (Water Soluble), Loctite GC10 and Alpha Corporation OM340 and Indium Corporation 8.9HF1 and SMQ92-J (Leaded).
  • Standard Procedure A stencil was made with 3-mm holes, a 3-mm pitch (edge-to-edge distance between holes) and a 0.075 mm thickness. Flux or solder paste were stencil printed onto 7.62 x 15.24 mm (3 inch x 6 inch) steel panels creating a test array of 3-mm diameter by 0.075 mm high dots of paste. The paste dots were then re- flowed by placing the steel plates in a 350°C oven for 4 minutes or by passing through an Aminstrument T-962A benchtop reflow oven set to achieve 350°C maximum for 2 minutes.
  • Cleaning trials were conducted in standard 2-sump vapor degreasers or in bench top simulation using beakers of boiling cleaning solvent blend after which the cleaned dots were rinsed in an ambient rinse solution that did not contain phosphate esters.
  • the following examples report the results of cleaning trials conducted pursuant to this Standard Procedure.
  • Example 1 Chlorofluorocarbon based solvents used to clean "No-clean" Solder Pastes as the soiling substance.
  • No-clean Solder Pastes contain organic binders or rosins in which are dispersed the solder and the surface activating components which help bond the solder to a substrate.
  • the results of Example 1 show that especially in lead free, "no clean" systems, the binders can often be removed with existing cleaning formulations but the activators will be left behind leaving a characteristic white residue on the part. Addition of an alcohol to the cleaning composition (trial 5) is seen to help start removal of the ionic white residues but does not adequately clean the part.
  • Trials 6 and 7 dramatically illustrate that the synergy of combining CFC, methanol and a phosphate ester acid successfully removes flux residue.
  • Trials 9 and 1 1 of Example 2 show that excellent results were obtained without the use of alcohol as a co-solvent for the halogenated solvent component.
  • Trials 13 and 15 show that addition of a phosphate ester acid to a cleaning composition containing alcohol and a halogenated hydrocarbon content will complete the cleaning process as well as achieve significant metal brightening.
  • Example 3 HFCs / TDE with alcohol and phosphate ester used to clean No-Clean Solder Pastes as the soiling substance.
  • Trials 16 and 17 of Example 3 show that SDG and Vertrel® SFR are close in cleaning capabilities. Both have high transdichloroethylene (“TDE”) content that removes organic soils readily. (SDG is 83% TDE and Vertrel® SFR is 67% TDE. However, Trial 16 left behind significant dull gray ionic residues.)
  • TDE transdichloroethylene
  • the addition of alcohol to the Vertrel® SFR (Trial 17) somewhat improves the removal of ionic residues but still left some residue.
  • the addition to Vertrel® SFR of the free acid phosphate ester (Trial 18) enabled attainment of a fully cleaned and brightened part.
  • Example 4 HFEs / TDE with alcohol and with phosphate ester used to clean No-Clean Solder Pastes as the soiling substance.
  • Trial 21 of Example 4 shows that the same satisfactory results of Trial 18 of Example 3 are obtained with hydrofluoroethers as the base component of a free acid phosphate ester.
  • the results of Trials 19 and 20 using hydrofluoroethers are comparable to those of Trials 16 and 17 of Example 3.
  • Example 5 "NPB” (n-propylbromide) with alcohol and free acid phosphate ester used to clean No-Clean Solder Pastes as the soiling substance.
  • Trial 24 of Example 5 shows that the same results as obtained in Trial 21 of Example 4 are obtained using brominated solvents as the base component.
  • Example 6 Hydrofluorocarbon organic solvent with alcohol and free acid phosphate ester used to clean No-Clean Solder Pastes as the soiling substance.
  • Trial 27 of Example 6 illustrates the successful use of an organic solvent instead of TDE (Trans-Dichloroethylene) used in earlier fluorinated systems to remove or soften the rosin portion of the flux.
  • Trial 27 also shows that the addition of alcohol and free acid phosphate ester provided a composition which successfully fully removed no-clean fluxes.
  • the alcohol is included in the halogenated
  • Phosphate Ester Surfactant (Acid Form) about 2 to about 4 an ethoxylated alkyl-substituted phosphate
  • the composition of Trial 21 was selected from this example.
  • Halogenated Hydrocarbon Solvent about 94 to about 98 a blend of from about 51 to about 56 weight
  • methoxy-nonafluorobutane eth- oxy-nonafluorobutane, 2-trifluoromethyl-3- ethoxydodecofluorohexane and 3-ethoxy- 1 ,1 ,1 ,2, 3,4,4,5,6,6, 6-dodecafluoro-2- trifluoromethyl-hexane, about 42 to about
  • the alcohol is included in the halogenated
  • Phosphate Ester Surfactant (Acid Form) about 2 to about 4 an ethoxylated alkyl-substituted phosphate
  • the composition of Trial 24 was selected from this example.

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Abstract

A cleaning solvent composition comprises from about 0.2 to 15 weight percent of mono- or di-phosphate ester in free acid form, and from about 85 to 99.8 weight percent of one or more halogenated hydrocarbon solvents. Other cleaning solvent compositions further comprise one or more alcohols. For example, such alcohol-containing compositions may comprise from about 0.2 to 15 weight percent of mono- or di-phosphate ester in free acid form, from about 2 to about 25 weight percent of one or more alcohols, and from about 25 to about 97.8 weight percent of one or more halogenated hydrocarbon solvents.

Description

CLEANING SOLVENT COMPOSITIONS AND THEIR USE
BACKGROUND OF THE INVENTION
CROSS-REFERENCE TO RELATED APPLICATION
[0001 ] This application claims priority of provisional patent application Serial No. 62/168,306 filed on May 29, 2015 in the name of Wells Cunningham et al. and entitled "Cleaning Solvent Compositions and Their Use ".
Field of the Invention
[0002] The present invention concerns solvent-based cleaning compositions of the type used in industrial processes for cleaning a wide variety of items including metals and plastics in the metal-working, electronics and other industries.
Description of Related Art
[0003] Solvent based cleaning compositions are used in industrial processes for cleaning a wide variety of soiling substances and residues (below sometimes referred to as "soils" or "soiling substances"). The electronics industry typically cleans fluxes, solder pastes, adhesives and coatings from a variety of devices before and after assembly of components. Such devices may comprise one or more of a wide range of materials comprising metal, ceramic and synthetic polymer (plastic) substrates and components. Metal working operations must remove lubricant oils and soaps, grinding media and greases from metal surfaces. Many of these soils are very difficult to strip from metal surfaces, especially with nonaqueous cleaners.
[0004] Of special interest are non-flammable blends of solvents that provide a cleaning solvent which can be used safely in aerosol packages, or as wiping fluids or in bulk cleaning tanks, for example, in vapor degreasing ("VDG") units. Typically, these cleaning solvents comprise halogenated compounds that are either non-flammable themselves or can be rendered non-flammable in a mixture with other halogenated compounds. Many solvent- based cleaning compositions rely heavily on the use of additives to target specific applications, that is, to remove specific soiling substances from various objects. A widely used class of additives is phosphate esters, known for use as anionic surfactants. For example, see Phosphate Esters, a technical brochure published by Lakeland Laboratories Limited of Manchester, England (Lakeland Phos. Esters (4), 3/00). [0005] U.S. Patent 4,724,096 to Figiel et al. issued on February 9, 1988 discloses the use trichlorotrifluoroethane with butanol and aryl- ethoxylated phosphate ester acid form for drying formulations.
[0006] U.S. Patent 5,856,286 to Nalewajek issued on January 5, 1999 discloses surfactants for use in drying and dry cleaning compositions, in particular, surfactants which may be used with halocarbons including hydrochlorofluorocarbons and hydrofluorocarbons and hydrofluoroethers. As noted at column 1 , line 54 et seq., the invention is premised on the discovery that placement of fluorine on the surfactant molecule is critical to surfactant solubility in the halogenated solvent compounds disclosed.
[0007] U.S. Patent 5,908,822 to Dishart issued on June 1 , 1999 discloses compositions and processes for drying substrates in which the drying and/or cleaning compositions contain surfactants which are primary or secondary amine salts of various perfluoro hydrogen and dihydrogen phosphates.
[0008] U.S. Patent 6,053,952 to Kaiser issued on April 25, 2000 discloses a method of dry cleaning using a highly fluorinated organic solvent which contains at least one hydrogen atom per molecule, for example, highly fluorinated hydrocarbons or highly fluorinated ethers. In one embodiment, these compounds are combined with dichloroethylene and a surfactant may be included in the composition. These surfactants may comprise organic al- kyl phosphate ester, dialkyl sodium succinate or isopropylamine alkyl benzene sulfonate. The use of phosphate ester salts in dry cleaning is disclosed.
[0009] U.S. Patent 8,637,443 to Basu et al. issued on January 28, 2014 discloses a dry cleaning method using a highly fluorinated organic solvent, such as hydrofluorcarbons (HFC) or hydrofluoroethers (HFE). For example, the combination of a fluorinated solvent containing at least one hydrogen atom with transdichloroethylene ("TDE") and a blend of surfactants including organic alkyl phosphate ester, dialkyl sodium succinates, isopropylamine alkyl benzene sulfonate is disclosed. The latter may be used with other surfactant ingredients in Vertrel® MCA Plus.
SUMMARY OF THE INVENTION
[0010] Generally, the present invention concerns cleaning solvent compositions whose components exhibit good mutual solvency and highly efficient cleaning. In one aspect, the cleaning solvent compositions of the present invention comprise one or more free acid forms of phosphate ester surfactants, one or more halogenated hydrocarbon solvents, and one or more alcohols. [001 1 ] Specifically, in accordance with the present invention there is provided a composition comprising from about 0.2 to about 15 weight percent of one or more free acid forms of phosphate ester surfactants selected from the group consisting of one or both of:
Figure imgf000004_0001
wherein R is selected from the group consisting of one or more of ethoxylated hydrocarbons, alkylated hydrocarbons, fluorinated hydrocarbons, and ethoxylated and fluorinated hydrocarbons;
from about 2 to about 25 weight percent of an alcohol selected from the group consisting of one or more of straight chain and branched alkyl alcohols, monohydric and polyhy- dric aromatic alcohols and monohydric and polyhydric heteroaromatic alcohols; and
from about 25 to about 97.8 weight percent of one or more halogenated hydrocarbon solvents.
[0012 Another aspect of the present invention provides that R is one or more of
Figure imgf000004_0002
R' is one or more of H, CH3, an alkyl group and an aryl group; and
n is an integer from 2 to 20, for example, n is an integer from 2 to 5.
[0013] In another aspect of the present invention the alcohol is selected from the group consisting of one or more of methanol, ethanol, isopropanol and n-butanol.
[0014] Another aspect of the present invention provides that the one or more halogenated hydrocarbon solvents are selected from the group consisting of one or more of perfluorocarbons ("PFCs"), chlorofluorocarbons ("CFCs"), hydrofluorocarbons ("HFCs"), hy- drofluoroethers ("HFEs"), hydrofluoroolefins ("HFOs"), partially brominated hydrocarbons, fully brominated hydrocarbons, partially chlorinated hydrocarbons and fully chlorinated hydrocarbons.
[0015] Another aspect of the present invention provides a composition comprising from about 0.2 to about 15 weight percent of one or more free acid forms of phosphate ester surfactants selected from the group consisting of:
Figure imgf000004_0003
wherein R is selected from the group consisting of one or more of ethoxylated hydrocarbons, alkylated hydrocarbons, fluorinated hydrocarbons, and ethoxylated and fluorinated hydrocarbons; and
from about 85 to about 97.8 weight percent of a halogenated hydrocarbon solvent.
[0016] Yet another aspect of the present invention provides that in the two- component (phosphate ester and halogenated hydrocarbon composition), R is one or more of
Figure imgf000005_0001
R' is one or more of H, CH3, an alkyl group and an aryl group; and
n is an integer from 2 to 20, for example, n is an integer from 2 to 5.
[0017] Another aspect of the present invention provides that in the two-component composition, the halogenated hydrocarbon solvent is selected from the group consisting of one or more of perfluorocarbons ("PFCs"), chlorofluorocarbons ("CFCs"), hydrofluorocar- bons ("HFCs"), hydrofluoroethers ("HFEs"), hydrofluoroolefins ("HFOs"), partially brominated hydrocarbons, fully brominated hydrocarbons, partially chlorinated hydrocarbons and fully chlorinated hydrocarbons.
[0018] Other aspects of the present invention will be apparent from the following description. For example, the compositions of the invention may include a non-halogenated hydrocarbon solvent.
DETAILED DESCRIPTION OF THE INVENTION AND SPECIFIC EMBODIMENTS THEREOF
[0019] The following abbreviations, trademarks and trade names have the following meanings, whether used in the singular or plural form.
[0020] Solvent Formulations
"TDE". Trans-Dichloroethylene,.Chemical Abstracts Number ("CAS #") 156-60-5. "HFCs". Hydrofluorocarbons such as HFC 43-1 Ome, sold under the trademark Vertrel® XF, CAS # 1384-95-42 and HFC365mfc CAS # 406-58-6. These materials are available from E.I. DuPont de Nemours and Co. of Wilmington, Delaware.
"HFEs". Hydrofluoroethers such as HFE 7100, CAS # 163702-08-7 and 163702-07-6. "NPB". n-Propyl bromide, CAS # 106-94-5.
"Vertrel® SFR". A blend of 67% trans-dichloroethylene, 18% 2,3- dihydrodecafluoropentane (HFC 43-1 Ome); 12% heptafluorocyclopentane; 3% methanol. This material has a boiling point of 106°F (41 .1 °C) and is available from E.I. DuPont de Nemours and Co. of Wilmington, Delaware.
"SION". A blend of 96% trans-dichloroethylene and 4% methylperfluorohexene (HFX-1 10). This material has a boiling point of 121 °F (49.4°C) and is available from E.I. DuPont de Nemours and Co. of Wilmington, Delaware.
"CMS". A blend of 41 .5% trans-dichloroethylene, 18% HFC 365mfc, 37% 2,3- dihydrodecafluoropentane (HFC 43-1 Ome), 3.5% methanol. This material has a boiling point of 97°F (36.1 °C) and is available from MicroCare Corporation of New Britain, Connecticut, an affiliated company of the assignee of this application.
"MCA". A blend of 62% trans-dichloroethylene, 38% 2,3- dihydrodecafluoropentane (HFC 43-1 Ome). This material has a boiling point of 102°F (38.9°C) and is available from E.I. DuPont de Nemours and Co. of Wilmington, Delaware.
"SDG". A blend of 83% trans-dichloroethylene, 7% 2,3- dihydrodecafluoropentane (HFC 43- 10me); 10% hexafluorocyclopentane. Bp 109F. This material has a boiling point of 109°F (42.8°C) and is available from E.I. DuPont de Nemours and Co. of Wilmington, Delaware.
"Vertrel® XP". A blend of 96.75% 2,3-dihydrodecafluoropentane (HFC 43-1 Ome), 3.25% isopropanol. This material has a boiling point of 126°F (52.2°C) and is available from E.I. DuPont de Nemours and Co. of Wilmington, Delaware.
"CFCs". Chlorofluorocarbons such as those sold under the trademark Solstice, for example, trans-chlorotrifluoromethyl propene CAS # 2730-43-0. This material has a boiling point of 68°F (20°C) and is available from Honeywell International of Morristown, New Jersey.
"DBE". A blend of dimethyl succinate, glutarate and adipate having a boiling point of >250°F (121 .1 °C) is available from Invista of Wichita, Kansas. [0021 ] Phosphate Esters
"Capstone FS-66". A fluorinated alkyl substituted phosphate ester in free acid form, available from E.I. DuPont de Nemours and Co. of Wilmington, Delaware.
"Rhodafac RS710". An ethoxylated alkyl substituted phosphate ester in free acid form, available from Solvay Rhodia which has a place of business in Houston, Texas.
[0022] Soiling Substances
"No-Clean Lead-Free Solder Pastes" available from Alpha Corporation of Altoona, Pennsylvania and Suwanee, Georgia under the designation Omnix 340, or from Nihon Almit Co. Ltd. of Tokyo, Japan under the designation SN62U. Additional fluxes and pastes as are used in the industry are: AIM Corporation 217 Gel Flux, NC Paste Flux (257), NC Flux Pen (280), M8 Paste, RMA258-15R and Loctite Corporation GC3 (Water Soluble), Loctite GC10 and Alpha Corporation OM340 and Indium Corporation 8.9HF1 and SMQ92-J (Leaded).
[0023] Standard Procedure. A stencil was made with 3-mm holes, a 3-mm pitch (edge-to-edge distance between holes) and a 0.075 mm thickness. Flux or solder paste were stencil printed onto 7.62 x 15.24 mm (3 inch x 6 inch) steel panels creating a test array of 3-mm diameter by 0.075 mm high dots of paste. The paste dots were then re- flowed by placing the steel plates in a 350°C oven for 4 minutes or by passing through an Aminstrument T-962A benchtop reflow oven set to achieve 350°C maximum for 2 minutes. Cleaning trials were conducted in standard 2-sump vapor degreasers or in bench top simulation using beakers of boiling cleaning solvent blend after which the cleaned dots were rinsed in an ambient rinse solution that did not contain phosphate esters. The following examples report the results of cleaning trials conducted pursuant to this Standard Procedure.
[0024] In the following Examples 1 -6, the types of components ("Component Type") of each Cleaning Formulation tested is indicated by abbreviations in parentheses. The abbreviations are: "HHC" = halogenated hydrocarbon solvents; "NHH" = non- halogenated hydrocarbon solvents; "ALC" = alcohol; APE" = free acid phosphate ester; and "HFE" = hydrofluoroether solvents. Unless otherwise stated, all references herein to the percentage of a component in a composition are percent by weight of the total weight of the composition.
[0025] Example 1. Chlorofluorocarbon based solvents used to clean "No-clean" Solder Pastes as the soiling substance.
Figure imgf000007_0001
Figure imgf000008_0001
[0026] No-clean Solder Pastes contain organic binders or rosins in which are dispersed the solder and the surface activating components which help bond the solder to a substrate. The results of Example 1 show that especially in lead free, "no clean" systems, the binders can often be removed with existing cleaning formulations but the activators will be left behind leaving a characteristic white residue on the part. Addition of an alcohol to the cleaning composition (trial 5) is seen to help start removal of the ionic white residues but does not adequately clean the part. Trials 6 and 7 dramatically illustrate that the synergy of combining CFC, methanol and a phosphate ester acid successfully removes flux residue. Trials 3 and 4 show the importance of an alcohol component because substituting the strong organic solvent DBE for the methanol did not provide the desired results. [0027] Example 2. HFC / TDE blends used to clean Rosin Metal Activating ("RMA") Solder Pastes as the soiling substance.
Figure imgf000009_0001
[0028] The results of Trials 9 and 1 1 of Example 2 show that excellent results were obtained without the use of alcohol as a co-solvent for the halogenated solvent component. Trials 13 and 15 show that addition of a phosphate ester acid to a cleaning composition containing alcohol and a halogenated hydrocarbon content will complete the cleaning process as well as achieve significant metal brightening.
[0029] Example 3. HFCs / TDE with alcohol and phosphate ester used to clean No-Clean Solder Pastes as the soiling substance.
Figure imgf000009_0002
Figure imgf000010_0001
[0030] Trials 16 and 17 of Example 3 show that SDG and Vertrel® SFR are close in cleaning capabilities. Both have high transdichloroethylene ("TDE") content that removes organic soils readily. (SDG is 83% TDE and Vertrel® SFR is 67% TDE. However, Trial 16 left behind significant dull gray ionic residues.) The addition of alcohol to the Vertrel® SFR (Trial 17) somewhat improves the removal of ionic residues but still left some residue. However, the addition to Vertrel® SFR of the free acid phosphate ester (Trial 18) enabled attainment of a fully cleaned and brightened part.
[0031 ] Example 4. HFEs / TDE with alcohol and with phosphate ester used to clean No-Clean Solder Pastes as the soiling substance.
Figure imgf000011_0001
[0032] Trial 21 of Example 4 shows that the same satisfactory results of Trial 18 of Example 3 are obtained with hydrofluoroethers as the base component of a free acid phosphate ester. The results of Trials 19 and 20 using hydrofluoroethers are comparable to those of Trials 16 and 17 of Example 3.
[0033] Example 5. "NPB" (n-propylbromide) with alcohol and free acid phosphate ester used to clean No-Clean Solder Pastes as the soiling substance.
Figure imgf000012_0001
[0034] Trial 24 of Example 5 shows that the same results as obtained in Trial 21 of Example 4 are obtained using brominated solvents as the base component.
[0035] Example 6. "HFC" (hydrofluorocarbon organic solvent with alcohol and free acid phosphate ester used to clean No-Clean Solder Pastes as the soiling substance.
Figure imgf000013_0001
[0036] Trial 27 of Example 6 illustrates the successful use of an organic solvent instead of TDE (Trans-Dichloroethylene) used in earlier fluorinated systems to remove or soften the rosin portion of the flux. Trial 27 also shows that the addition of alcohol and free acid phosphate ester provided a composition which successfully fully removed no-clean fluxes.
[0037] The following examples A-H each describe a range of ingredients and quantities of various cleaning solvent compositions in accordance with aspects of the present invention. Specific compositions used in some of the Trials described above were selected from these examples, the compositions of which are defined in the indicated claims. Example A
The composition of Trial 6 was selected from this example.
Figure imgf000014_0001
Example C
The composition of Trials 13 and 18 was selected from this example.
Figure imgf000015_0001
Weight Percent of the
Ingredient Composition
Alcohol
The alcohol is included in the halogenated
hydrocarbon solvent blend.
Phosphate Ester Surfactant (Acid Form) about 2 to about 4 an ethoxylated alkyl-substituted phosphate
ester
Example E
The composition of Trial 21 was selected from this example.
Weight Percent of the
Ingredient Composition
Halogenated Hydrocarbon Solvent about 94 to about 98 a blend of from about 51 to about 56 weight
percent hydrofluoroether selected from one
or more of methoxy-nonafluorobutane, eth- oxy-nonafluorobutane, 2-trifluoromethyl-3- ethoxydodecofluorohexane and 3-ethoxy- 1 ,1 ,1 ,2, 3,4,4,5,6,6, 6-dodecafluoro-2- trifluoromethyl-hexane, about 42 to about
48 weight percent trans-dichloroethylene
and about 2 to about 4 weight percent eth- anol
Alcohol
The alcohol is included in the halogenated
hydrocarbon solvent blend.
Phosphate Ester Surfactant (Acid Form) about 2 to about 4 an ethoxylated alkyl-substituted phosphate
ester Example F
The composition of Trial 24 was selected from this example.
Figure imgf000017_0001
Example H
[0038] One or more of methanol, ethanol, isopropanol and n-butanol is substituted for the alcohol component of Examples A-G.
[0039] While the invention has been described in detail with reference to specific embodiments, it will be appreciated that numerous variations may be made to the described embodiment, which variations nonetheless lie within the scope of the present invention.

Claims

THE CLAIMS What is claimed is:
1 . A composition comprising from about 0.
2 to about 15 weight percent of one or more free acid forms of phosphate ester surfactants selected from the group consisting of one or both of:
Figure imgf000018_0001
wherein R is selected from the group consisting of one or more of ethoxylated hydrocarbons, alkylated hydrocarbons, fluorinated hydrocarbons, and ethoxylated and fluorinated hydrocarbons;
from about 2 to about 25 weight percent of an alcohol selected from the group consisting of one or more of straight chain and branched alkyl alcohols, monohydric and polyhy- dric aromatic alcohols and monohydric and polyhydric heteroaromatic alcohols; and
from about 25 to about 97.8 weight percent of one or more halogenated hydrocarbon solvents.
The composition of claim 1 wherein R is one or more of
Figure imgf000018_0003
Figure imgf000018_0002
R is one or more of H, CH3, an alkyl group and an aryl group; and
n is an integer from 2 to 20.
3. The composition of claim 2 wherein n is an integer from 2 to 5.
3A. The composition of claim 1 or claim 2 wherein the alcohol is selected from the group consisting of one or more of methanol, ethanol, isopropanol and n-butanol.
4. The composition of claim 1 or claim 2 wherein the one or more halogenated hydrocarbon solvents are selected from the group consisting of one or more of perfluorocar- bons ("PFCs"), chlorofluorocarbons ("CFCs"), hydrofluorocarbons ("HFCs"), hydrofluoro- ethers ("HFEs"), hydrofluoroolefins ("HFOs"), partially brominated hydrocarbons, fully bro- minated hydrocarbons, partially chlorinated hydrocarbons and fully chlorinated hydrocarbons.
5. The composition of claim 1 or claim 2 wherein:
the halogenated hydrocarbon solvent comprises one or both of trans- chlorodifluormethyl propene and cis-chlorodifluoromethyl propene and is present in the amount of from about 50 to about 96 weight percent of the composition;
the alcohol comprises one or more of straight and branched chain alkyl alcohols, aromatic and heteroaromatic alcohols, all having from 1 -20 carbon atoms and is present in the amount of from about 2 to about 15 weight percent of the composition; and
the phosphate ester surfactant comprises one or more of alkoxylated alkyl and aryl substituted phosphate esters, alkoxylated phosphate esters, fluorinated alkyl and aromatic phosphate esters, and alkyl and aromatic substituted phosphate esters, and is present in the amount of from about 0.2 to about 15 weight percent of the composition.
6. The composition of claim 1 or claim 2 wherein:
the halogenated hydrocarbon solvent comprises trans-chlorodifluoromethyl propene and is present in the amount of from about 92 to about 96 weight percent of the composition; the alcohol comprises methanol and is present in the amount of from about 2 to about 4 weight percent of the composition; and
the phosphate ester surfactant comprises a fluorinated alkyl-substituted phosphate ester and is present in the amount of from about 2 to about 4 weight percent of the composition.
7. The composition of claim 1 or claim 2 wherein:
the halogenated hydrocarbon solvent comprises a blend of from about 66 to about 68 weight percent of trans-dichloroethylene, about 17 to about 19 weight percent of 2,3- dihydrodecafluoropentane, about 1 1 to about 13 weight percent of heptafluorocyclopentane and about 1 to about 4 weight percent of an alcohol selected from one or more of straight and branched chain alkyl alcohols, aromatic and heteroaromatic alcohols, all having from 1 - 20 carbon atoms and is present in the amount of from about 2 to about 15 weight percent of the composition, the blend being present in the amount of from about 96 to about 98 weight percent of the composition; and the phosphate ester surfactant comprises an ethoxylated alkyl-substituted phosphate ester and is present in the amount of from about 2 to about 4 weight percent of the composition.
7A. The composition of claim 7 wherein the alcohol comprises methanol.
8. The composition of claim 1 or claim 2 wherein:
the halogenated hydrocarbon solvent comprises a blend of about 40 to about 44 weight percent of trans-dichloroethylene, about 17 to about 19 weight percent of the hydro- fluorocarbon pentafluorobutane, from about 36 to about 38 weight percent dihydrode- cafluoropentane and from about 3 to about 4 weight percent methanol, the blend being present in the amount of from about 96 to about 98 weight percent of the composition; and the phosphate ester surfactant comprises an ethoxylated alkyl-substituted phosphate ester and is present in the amount of from about 2 to about 4 weight percent of the composition.
9. The composition of claim 8 wherein the pentafluorobutane comprises 1 ,1 ,1 ,3,3-pentafluorobutane.
10. The composition of claim 1 or claim 2 wherein:
the halogenated hydrocarbon solvent comprises a blend of from about 51 to about 56 weight percent of a hydrofluoroether comprising one or more of methoxy-nonafluorobutane, ethoxy-nonafluorobutane, 2-trifluoromethyl-3-ethoxydodecofluorohexane and 3-ethoxy- 1 ,1 ,1 ,2,3,4,4,5, 6,6, 6-dodecafluoro-2-trifluoromethyl-hexane, about 42 to about 48 weight percent trans-dichloroethylene and about 2 to about 4 weight percent ethanol, the blend being present in the amount of from about 94 to about 98 weight percent of the composition; and the phosphate ester surfactant comprises an ethoxylated alkyl-substituted phosphate ester and is present in the amount of from about 2 to about 4 weight percent of the composition.
1 1 The composition of claim 1 or claim 2 wherein:
the halogenated hydrocarbon solvent comprises n-propyl bromide and is present in the amount of from about 70 to about 97 weight percent of the composition;
the alcohol comprises isopropanol and is present in the amount of from about 4 to about 25 weight percent of the composition; and the phosphate ester surfactant comprises an ethoxylated alkyl-substituted phosphate ester and is present in the amount of from about 0.4 to about 0.5 weight percent of the composition.
12. The composition of claim 1 or claim 2 wherein:
the halogenated hydrocarbon solvent comprises one or more hydrofluorocarbons and is present in the amount of from about 48 to about 54 weight percent of the composition; dipropylene glycol monomethyl ether present in the amount of from about 36 to about 44 weight percent of the composition;
the alcohol comprises benzyl alcohol and is present in the amount of from about 4 to about 6 weight percent of the composition; and
the phosphate ester surfactant comprises a fluorinated alkyl-substituted phosphate ester and is present in the amount of from about 2 to about 4 weight percent of the composition.
13 A composition comprising from about 0.2 to about 15 weight percent of one or more free acid forms of phosphate ester surfactants selected from the group consisting of:
Figure imgf000021_0001
wherein R is selected from the group consisting of one or more of ethoxylated hydrocarbons, alkylated hydrocarbons, fluorinated hydrocarbons, and ethoxylated and fluorinated hydrocarbons; and
from about 85 to about 97.8 weight percent of a halogenated hydrocarbon solvent.
14. The composition of claim 13 wherein R is one or more of
Figure imgf000021_0002
R is one or more of H, CH3, an alkyl group and an aryl group; and
n is an integer from 2 to 20.
15. The composition of claim 13 wherein n is an integer from 2 to 5.
16. The composition of claim 13 wherein the halogenated hydrocarbon solvent is selected from the group consisting of one or more of perfluorocarbons ("PFCs"), chloro- fluorocarbons ("CFCs"), hydrofluorocarbons ("HFCs"), hydrofluoroethers ("HFEs"), hydro- fluoroolefins ("HFOs"), partially brominated hydrocarbons, fully brominated hydrocarbons, partially chlorinated hydrocarbons and fully chlorinated hydrocarbons.
17. The composition of claim 13 or claim 14 wherein:
the halogenated hydrocarbon solvent comprises a blend of from about 94 to about 98 weight percent of trans-dichloroethylene and from about 2 to about 6 weight percent of methylperfluorohexene, the blend being present in the amount of from about 95 to about 99 weight percent of the composition; and
the phosphate ester surfactant comprises an ethoxylated alkyl-substituted phosphate ester and is present in the amount of from about 1 to about 5 weight percent of the composition.
18. The composition of claim 13 or claim 14 wherein:
the halogenated hydrocarbon solvent comprises a blend of from about 80 to about 86 weight percent trans-dichloroethylene, from about 5 to about 9 weight percent 2,3- dihydrodecafluoropentane and from about 8 to about 12 weight percent hexafluorocyclopen- tane, the blend being present in the amount of from about 94 to about 99 weight percent of the composition; and
the phosphate ester surfactant comprises an ethoxylated alkyl-substituted phosphate ester and is present in the amount of from about 1 to about 6 weight percent of the composition.
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