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US3034700A - Method of producing high vacuum - Google Patents

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US3034700A
US3034700A US14222A US1422260A US3034700A US 3034700 A US3034700 A US 3034700A US 14222 A US14222 A US 14222A US 1422260 A US1422260 A US 1422260A US 3034700 A US3034700 A US 3034700A
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pump
fluids
vapor
ring
polyphenyl
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Kenneth C D Hickman
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Rochester Institute of Technology
University of Rochester
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    • 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
    • C09K3/00Materials not provided for elsewhere
    • 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
    • C09K3/00Materials not provided for elsewhere
    • C09K3/10Materials in mouldable or extrudable form for sealing or packing joints or covers
    • 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

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  • Vacuum Pumps and Pump Oils articles by applicant here, appearing in the Journal of The Franklin Institute, vol. 221, Nos. 2 and 3, February and March, 1936, discuss the operation of such working fluids in the production of high vacuums.
  • An object of this invention is to supply organic pumping fluids capable of producing vacuums which, without a cooled trap, are 100 times better than have been obtainable with previous fluids under the same operating conditions.
  • Another object of the invention is to provide fluids which can be heated to and used at higher boiler pressures and/or higher temperatures than hitherto known in the art, so that greater thermodynamic efliciency may be secured and pumps can be constructed which operate against unusually high fore pressures.
  • FIG. 1 is a vertical sectional view of a single stage vertical glass vapor-actuated pump in which the working fluids herein disclosed and claimed may be used for the production of high vacuums;
  • FIG. 2 is a vertical sectional view of a three-stage fractionating pump in which such working fluids may be used for the production of high vacuums.
  • the pumping fluids which I have discovered belong to the class of the polyphenyl ethers and the polyphenoxy benzenes, and for convenience they are referred to herein as polyphenyl ethers.
  • the materials are usually named either as benzene derivatives or as ethers, according as to whether they have odd or even numbers of benzene rings, and have the typical construction:
  • Such materials may be prepared according to any of the known methods or obtained from various commercial sources.
  • the first type of polyphenyl is the meta-, and the second paralinked.
  • the metas are generally to be preferred because of their exceptional thermal and oxidative stability at high temperatures.
  • Advantages of mixed isomers are lowered melting points and commercial availability.
  • Mixtures of the compounds themselves but of molecular weight other than the isomeric forms are also contemplated.
  • a useful working fluid would be a 4-ring phenyl ether or mixture thereof, plus a S-ring phenyl ether or mixture thereof in a fractionating pump.
  • the 4-ring compounds would gather at the fore pressure and the 5-ring compounds at the fine pressure end of the pump.
  • the invention contemplates a single vapor-actuated pump or a train of such pumps in which one or more of such ring compounds from 3 to 7 are employed.
  • the 4-ring compounds either singly or as a mixture of isomers, exert a true vapor pressure of less than 10* mm. at elevated room temperature F.) and provide highly robust fluids to create vacuums comparable to those obtainable with previous pump fluids.
  • the 5-ring meta-ether of the general formula C H O which exerts a true vapor pressure of less than 10 mm. Hg at summer room temperature.
  • Very many isomers are possible and a synthesized mixture may be a mixture of such isomers which remain liquid when the individually pure compounds might be solid.
  • I include, however, within my invention all polyphenyl ethers and phenoxy benzenes in the range of 3 to 7 phenyl groups linked by 2 to 6 oxygen atoms and of molecular weights between 264 and 641 and mixtures thereof which remain liquid under the operating conditions of a vapor vacuum pump. Particularly useful are mixtures which remain permanently fluid at room temperature.
  • polyphenyl ether compounds and their mixtures have surprising characteristics as condensation pump fluids vis-a-vis conventional working fluids. They have lower vapor pressures and higher boiling points than pump fluids heretofore employed, and a very much higher resistance to thermal decomposition and oxidization.
  • Table #1 A comparison of these properties of the poly phenyl ethers and prior art working fluids is shown in Table #1, as follows:
  • B-ring 400 excellent-- 155-175 1Xl0 -1 l0' 1 10-"-1 (l0- 4-ring 433 do K 210-250 5X10 7Xl0 1X10- 2X10- 5-1ing 460 do 11 260-300 1Xl0- 5X10- 6-ring 460 ..-do R 320-305 l l0- 5Xl0- 7-ring 450 do 300-400 1Xl0- 1X10- Monsanto data Preliminary Report on the Polyphcnyl Ethers, Bulletin No. A.V. 5, May 1959. b Vapor Pressure of Phlegmatic Liquids, II. High Molecular Weight Esters and Silicone Oils. E. S. Perry and W. N. Weber.
  • the polyphenyl ethers are often prepared by interlinking halogen derivatives with elimination of halogen, and an essential step in purification of the finished ether so prepared is removal of the last trace of halogen. This may be accomplished in any of the well-known ways, such as treatment with sodium exthoxide in ethanol with subsequent washing in water and drying. Another required step in purification is to remove light ends and thermally labile or oxidizable material, which can be done by prolonged moderate heating under vacuum or bubbling an inert gas or dry air at temperatures below 200 C. through the ethers, preferably under vacuum.
  • the material after preliminary chemical and physical clean-up, to a slow distillation under high vacuum, rejecting the first 1% to 5%, or even and the last 1% to 5% of the distillate.
  • the 5-ring compound is obtained as a mixture of isomers in the fraction distilling between 210 and 230 C. at mm. absolute.
  • the rejected fractions are also superior pump fluids, judged by previous standards, and may be employed for less critical use, for instance in a fore or booster pump.
  • Part of the purification procedure may include treatment with an absorption grade alumina or activated charcoal or clessicated silica gel, either before or after distillation.
  • I may omit one or more steps in the purification proceduresuch, for instance, as the chemical pretreatment or the highly critical vacuum distillation. Also in those pumps that are fitted with means for rejecting fore vacuum distillate, I may increase the quantity of the primary charge and reduce the volume to normal by distilling a substantial fraction directly out of the pump. Whether, therefore, the polyphenyl ether fluids are conditioned for high vacuum use during manufacture or separately thereafter or in the pump itself, I regard the operating fluid so produced as coming within the scope of my invention.
  • a polyphenyl ether or mixture as herein disclosed in any suitable vapor-actuated pump such as a single stage glass vertical pump, a three stage glass fractionating pump, or a Langmuir inverted type of metal pump, either single compartment or fractionating.
  • the heat requirements of the polyphenyl ethers may be as much as 25% to 50% greater than required for conventional working fluids, such as Octoil.
  • conventional working fluids such as Octoil.
  • I have found that by modifying the pump so as to cool the diffuser behind the jet to catch backstreaming molecules, but drastically cutting the cooling in front of the jet, I can maintain a long column of forwardly moving pump fluid vapor, and the longer this column the less chance the molecules have of diffusing backstream.
  • the chimney of the inverted type Langmuir pump can be lengthened so that a long hot diffuser region can be accommodated below the jet, thereby diminishing greatly the heat requirements. This expedient improves the ultimate vacuum and at the same time conserves so much heat that a pump thus modified may require no more, or even less, heat than an unmodified pump would using conventional working fluids.
  • a shallow alembic 6 is connected with manifold 5 and boiler 1 by branched tube 7.
  • a second alembic 8, a side tube 9, and a closure 10 complete the structural part of the pump.
  • a filling of polyphenyl ethers is placed in the boiler 1 to a depth shown at 12 permitting sufficicnt reserve so that the alembics and side tubes may be filled with liquid without the heater becoming bare.
  • Lagging 13 conveniently formed by a pad of glass wool batting, is applied around the upper portion of the diffuser and optionally a glass fibre fabric sleeve 14 is placed in the diffuser.
  • the pump boiler may be lagged as at 15, and a small air blast is conveniently directed at the region 16 while the pump is in operation.
  • Example 1 Using the pump of FIGURE 1, charged with a purified amount of the 5-ring meta polyphenyl ether and attached to an ionization gauge of the type known as VG-l-A, a reading indicating a vacuum of 5 1()* millimeters was obtained on blank-off at an ambient temperature of 80 F.
  • Example 2 150 grams of a purified sample of the 5-ring polyphenyl ether isomers were placed in a 3-stage glass fractionating pump of the type shown in FIGURE 2, except that the connecting tubes between the boilers were lengthened and provided with means such as loops to prevent 1 back diffusion of the pump fluids during their forward travel.
  • a Bayard-Alpert gauge 21, selected because of its ability to make the lowest known pressure measure- 7-ring meta- E-ring metam-B is (m-ph enoxyphenoxy) -benzeue Gring meta- Bis[m- (m-phenoxyphenoxy, phenyl] ether 5-ring meta-para m-Bls[m- (-phenoxyphenoxy) -phenoxy] benzene Q- -Q O- Q Q Q Q ments, was sealed by a wide bore bent glass tube 22 to the closed low pressure end of the pump.
  • the pump was heavily insulated with glass wool batting to conserve heat, and auxiliary heating coils 23 and 24 were placed around the necks of the middle and high vacuum jets further to minimize loss of heat.
  • the glass pump was evacuated by an oil sealed mechanical fore pump and heated by an electric current at 95 volts delivering 225 watts.
  • a system is evacuated by means of a vapor actuated pump, the step of entraining gas in a stream of vapors of a working fluid, comprising a polyphenyl ether having at least three phenyl groups and two oxygen linkages, and at most seven phenyl groups and six oxygen linkages.
  • said working fluid essentially consists of a polyphenyl ether or mixtures thereof which boil between C. and 300 C. at .1 millimeter.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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  • Thermal Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polyethers (AREA)

Description

May 15, 1962 K. c. D. HICKMAN METHOD OF PRODUCING HIGH VACUUM 2 Sheets-Sheet 1 Filed March 11, 1960 May 15, 1962 K. c. D. HICKMAN METHOD OF PRODUCING HIGH VACUUM 2 Sheets-Sheet 2 Filed March 11, 1960 iii... 11:11 71 1!.
I N V EN TOR. Ker/22671 6, z, walrznvr 3,034,700 METHOD OF PRODUCING HIGH VACUUM Kenneth C. D. Hickman, Rochester, N.Y., assignor to Rochester Institute of Technology, Rochester, N.Y. Filed Mar. 11, 1960, Ser. No. 14,222 4 Claims. (Cl. 230-101) This invention pertains to improvements in materials and apparatus for the production of high Vacuums, and is concerned particularly with working fluids for use in vapor-actuated pumps variously known as diffusion pumps, condensation pumps, and .vapor booster pumps.
The original Gaede-Langmuir condensation pump employed mercury as a working fluid, and mercury remains in use today, Wider use, however, has been made of high boiling organic fluids introduced by Burch in 1927. US. Patents #l,857,506, 411,857,508, #2,l47,488, and #2,147,479 describe groups of, individual organic compounds, liquid at room temperature, which have special advantages as working fluids in vapor pumps and can produce very high vacuums without use of a specially cooled trap. Two of these fluids, 2-ethyl hexyl phthalate and 2-ethylhexyl sebacate, available as octoil and octoil S, have been in wide use for many years and are accepted as standards of performance. Vacuum Pumps and Pump Oils, articles by applicant here, appearing in the Journal of The Franklin Institute, vol. 221, Nos. 2 and 3, February and March, 1936, discuss the operation of such working fluids in the production of high vacuums. Other compounds, particularly certain silicone oils, equal the foregoing in ability to produce high vacuum and exceed them in thermal stability.
In the last few years, notably since the advent of high energy particle accelerators and other nuclear and atomic devices, still higher vacuums have become necessary and the vacuums produced by existing fluids, even when used with auxiliary refrigerated traps, have left much to be desired so that, in some cases, they have been discarded in favor of so-called ion and getter pumps which vaporize titanium and other reactive metals. Satisfactory though these new pumps are from the point of view of end use, they are expensive and relatively diflicult to operate. There is thus an acute need for liquid pump fluids useful in vapor-actuated pumps to attain a completely new order of high vacuum performance, with or without cooled traps.
An object of this invention is to supply organic pumping fluids capable of producing vacuums which, without a cooled trap, are 100 times better than have been obtainable with previous fluids under the same operating conditions.
Another object of the invention is to provide fluids which can be heated to and used at higher boiler pressures and/or higher temperatures than hitherto known in the art, so that greater thermodynamic efliciency may be secured and pumps can be constructed which operate against unusually high fore pressures.
Other and further objects of the invention will be ap parent from the following description and claim which set forth the best mode contemplated of carrying out the invention. Other embodiments of the invention may be used without departing from the scope of the present invention a set forth in the appended claims.
In the drawings, of which there are two sheets:
FIG. 1 is a vertical sectional view of a single stage vertical glass vapor-actuated pump in which the working fluids herein disclosed and claimed may be used for the production of high vacuums; and
FIG. 2 is a vertical sectional view of a three-stage fractionating pump in which such working fluids may be used for the production of high vacuums.
dfifldfifld Patented May 15, 1962 The pumping fluids which I have discovered belong to the class of the polyphenyl ethers and the polyphenoxy benzenes, and for convenience they are referred to herein as polyphenyl ethers. The materials are usually named either as benzene derivatives or as ethers, according as to whether they have odd or even numbers of benzene rings, and have the typical construction:
Such materials may be prepared according to any of the known methods or obtained from various commercial sources.
The first type of polyphenyl is the meta-, and the second paralinked. For the highest vacuums, the metas are generally to be preferred because of their exceptional thermal and oxidative stability at high temperatures. Mixturm of metaand paracome next, although paraand orthotypes and internal and physical mixtures of meta-, and orthoare useful and are within the scope of this invention. Advantages of mixed isomers are lowered melting points and commercial availability. Mixtures of the compounds themselves but of molecular weight other than the isomeric forms are also contemplated. Thus a useful working fluid would be a 4-ring phenyl ether or mixture thereof, plus a S-ring phenyl ether or mixture thereof in a fractionating pump. The 4-ring compounds would gather at the fore pressure and the 5-ring compounds at the fine pressure end of the pump. The invention contemplates a single vapor-actuated pump or a train of such pumps in which one or more of such ring compounds from 3 to 7 are employed.
The 3-ring ethers with N=1 in Equation #1 provide excellent fillings for those booster pumps which are designed to operate against backing pressures of .2-20 millimeters to produce intermediate vacuums in the range of 1 millimeter to 1 micron.
Their high melting points, 141 C. for the metacompound, 203 C. for the ortho-, and 171 C. for the para-, make it desirable to use mixtures of two or all three isomers to avoid solidification in parts of the pump.
The 4-ring compounds, either singly or as a mixture of isomers, exert a true vapor pressure of less than 10* mm. at elevated room temperature F.) and provide highly robust fluids to create vacuums comparable to those obtainable with previous pump fluids. i have found particularly useful the 5-ring meta-ether of the general formula C H O which exerts a true vapor pressure of less than 10 mm. Hg at summer room temperature. Very many isomers are possible and a synthesized mixture may be a mixture of such isomers which remain liquid when the individually pure compounds might be solid. I include, however, within my invention all polyphenyl ethers and phenoxy benzenes in the range of 3 to 7 phenyl groups linked by 2 to 6 oxygen atoms and of molecular weights between 264 and 641 and mixtures thereof which remain liquid under the operating conditions of a vapor vacuum pump. Particularly useful are mixtures which remain permanently fluid at room temperature.
These polyphenyl ether compounds and their mixtures have surprising characteristics as condensation pump fluids vis-a-vis conventional working fluids. They have lower vapor pressures and higher boiling points than pump fluids heretofore employed, and a very much higher resistance to thermal decomposition and oxidization. A comparison of these properties of the poly phenyl ethers and prior art working fluids is shown in Table #1, as follows:
TABLE #1 Lowest Decom- Measured position Resistance Boiling Extrapolated Lowest diffusion Blank-oh Pres- Temperao Point 1mm. Vapor Pressure l-stage, mm. Hg sure in Glass ture C. Oxidation Hg C. 25 GJmm. Hg Pump 3-stago Fractionating, mm. Hg
2-ethyl hexyl sebacate 272 good b 218 b 2X10 7X10- Silicone 704 304 excellent... v 250 1.7 1X10- Hydrocarbon pump 338 poor s 5 l0- 5 10- Phenyl Ethers:
B-ring 400 excellent-- 155-175 1Xl0 -1 l0' 1 10-"-1 (l0- 4-ring 433 do K 210-250 5X10 7Xl0 1X10- 2X10- 5-1ing 460 do 11 260-300 1Xl0- 5X10- 6-ring 460 ..-do R 320-305 l l0- 5Xl0- 7-ring 450 do 300-400 1Xl0- 1X10- Monsanto data Preliminary Report on the Polyphcnyl Ethers, Bulletin No. A.V. 5, May 1959. b Vapor Pressure of Phlegmatic Liquids, II. High Molecular Weight Esters and Silicone Oils. E. S. Perry and W. N. Weber.
Journal American Chemical Society 71 3726 (1949).
s A New Silicone Diffusion Pump Fluid: A. R. Huntress, A. L. Smith, B. D. Power and N. '1. M. Dennis, Symposium on on Vacuum Technology, 1958, p. 104-111. Pergamon Press, New York.
The polyphenyl ethers are often prepared by interlinking halogen derivatives with elimination of halogen, and an essential step in purification of the finished ether so prepared is removal of the last trace of halogen. This may be accomplished in any of the well-known ways, such as treatment with sodium exthoxide in ethanol with subsequent washing in water and drying. Another required step in purification is to remove light ends and thermally labile or oxidizable material, which can be done by prolonged moderate heating under vacuum or bubbling an inert gas or dry air at temperatures below 200 C. through the ethers, preferably under vacuum. For highly critical use I subject the material, after preliminary chemical and physical clean-up, to a slow distillation under high vacuum, rejecting the first 1% to 5%, or even and the last 1% to 5% of the distillate. By way of example, only the 5-ring compound is obtained as a mixture of isomers in the fraction distilling between 210 and 230 C. at mm. absolute. The rejected fractions are also superior pump fluids, judged by previous standards, and may be employed for less critical use, for instance in a fore or booster pump. Part of the purification procedure may include treatment with an absorption grade alumina or activated charcoal or clessicated silica gel, either before or after distillation.
Where the manufacturer of polyphenyl others has prepared a particularly pure batch of such ethers, I may omit one or more steps in the purification proceduresuch, for instance, as the chemical pretreatment or the highly critical vacuum distillation. Also in those pumps that are fitted with means for rejecting fore vacuum distillate, I may increase the quantity of the primary charge and reduce the volume to normal by distilling a substantial fraction directly out of the pump. Whether, therefore, the polyphenyl ether fluids are conditioned for high vacuum use during manufacture or separately thereafter or in the pump itself, I regard the operating fluid so produced as coming within the scope of my invention.
By fractional distillation a specific polyphenyl ether can be obtained with a purity exceeding 80%, with the balance isomers and/or inert compounds. For most applications a mixture of the isomers of a 3, 4, 5, 6 or 7-ring polyphenyl compound will be satisfactory, but such mixtures need not be limited to the isomers of any specific ring compound; that is, a mixture of two or more of the ring compounds within the group indicated will be satisfactory.
Because the fluids boil at such high temperatures, it is feasible to use simple air cooling of the pump diffuser and to keep certain parts of the pump hotter than usual. This greater variation in temperature throughout the pump has the doubly advantageous effect of rejecting any self-generated impurities and also impurities acquired vents, etc., remaining in the pump from a poor attempt at cleaning.
To produce high vacuum in accordance with my invention, I place a polyphenyl ether or mixture as herein disclosed in any suitable vapor-actuated pump, such as a single stage glass vertical pump, a three stage glass fractionating pump, or a Langmuir inverted type of metal pump, either single compartment or fractionating.
Where a polyphenyl working fluid embodying the invention is merely substituted for the old in a conventional pump, the heat requirements of the polyphenyl ethers may be as much as 25% to 50% greater than required for conventional working fluids, such as Octoil. However, I have found that by modifying the pump so as to cool the diffuser behind the jet to catch backstreaming molecules, but drastically cutting the cooling in front of the jet, I can maintain a long column of forwardly moving pump fluid vapor, and the longer this column the less chance the molecules have of diffusing backstream. The chimney of the inverted type Langmuir pump can be lengthened so that a long hot diffuser region can be accommodated below the jet, thereby diminishing greatly the heat requirements. This expedient improves the ultimate vacuum and at the same time conserves so much heat that a pump thus modified may require no more, or even less, heat than an unmodified pump would using conventional working fluids.
Because of the high thermal stability, it is practical in the case of a single stage vertical glass pump or any combination of stages to surround the upper or exit portion of the diffuser or receiving jet with heavy thermal lagging. In the case of an upwardly directed jet, means for catching rejected distillate and impurities are provided at the top of the pump, and I may employ any retention means, such for instance as a glass fibre fabric, for lining the inside of the diffuser walls to provide both thermal lagging and liquid hold-up. Such a pump is illustrated in FIGURE 1, where a glass boiler 1 is provided with heater element 2 formed of a resistance wire, in the well-known manner. A jet 3 cooperates with diffuser 4 fastened to the usual glass manifold 5 connected with the closed system to be evacuated. A shallow alembic 6 is connected with manifold 5 and boiler 1 by branched tube 7. A second alembic 8, a side tube 9, and a closure 10 complete the structural part of the pump. A filling of polyphenyl ethers is placed in the boiler 1 to a depth shown at 12 permitting sufficicnt reserve so that the alembics and side tubes may be filled with liquid without the heater becoming bare. Lagging 13, conveniently formed by a pad of glass wool batting, is applied around the upper portion of the diffuser and optionally a glass fibre fabric sleeve 14 is placed in the diffuser. The pump boiler may be lagged as at 15, and a small air blast is conveniently directed at the region 16 while the pump is in operation.
Example 1 Using the pump of FIGURE 1, charged with a purified amount of the 5-ring meta polyphenyl ether and attached to an ionization gauge of the type known as VG-l-A, a reading indicating a vacuum of 5 1()* millimeters was obtained on blank-off at an ambient temperature of 80 F.
Example 2 150 grams of a purified sample of the 5-ring polyphenyl ether isomers were placed in a 3-stage glass fractionating pump of the type shown in FIGURE 2, except that the connecting tubes between the boilers were lengthened and provided with means such as loops to prevent 1 back diffusion of the pump fluids during their forward travel. A Bayard-Alpert gauge 21, selected because of its ability to make the lowest known pressure measure- 7-ring meta- E-ring metam-B is (m-ph enoxyphenoxy) -benzeue Gring meta- Bis[m- (m-phenoxyphenoxy, phenyl] ether 5-ring meta-para m-Bls[m- (-phenoxyphenoxy) -phenoxy] benzene Q- -Q O- Q Q Q Q ments, was sealed by a wide bore bent glass tube 22 to the closed low pressure end of the pump. The pump was heavily insulated with glass wool batting to conserve heat, and auxiliary heating coils 23 and 24 were placed around the necks of the middle and high vacuum jets further to minimize loss of heat. The glass pump was evacuated by an oil sealed mechanical fore pump and heated by an electric current at 95 volts delivering 225 watts.
After one hour the fore pressure measured 11 microns by hot wire gauge and the fine pressure 5 X10 mm. Hg by the Bayard-Alpert gauge. The pressure fell successively to 1.4 1O in the next hour and to 1.7 l0- in four hours. Next day a pressure of 6X 10- mm. was recorded and maintained continuously. The temperature of the low pressure end of the glass pump was 100 F. and the ambient temperature of the laboratory at the test bench was 80 F. No trapping or refrigeration of any kind was used other than the bent glass tube 22 which remained slightly above ambient temperature. The low pressure end of the pump was then torched with a gas flame until its temperature was 200 -F.i5. The Bayard-Alpert gauge registered a rise of pressure to 5X10' mm. which shortly relapsed to 5 1O- with pump manifold at 100 F.
In a re-test, air was admitted to the pump to atmospheric pressure for 5 minutes while the pump was hot (but with the heating current oif), after which fore vacuum and heating were again restored. Gauge readings fell to 3 10- mm. in 35 minutes, 5X10- in 75 minutes, and 1X10 in two hours. Later a limiting reading of 5 10- was recorded. These pressures are 100 times lower than have ever been recorded in a condensation pump under similar circumstances, and there is reason to believe that the actual pressures obtained were lower, since the Bayard-Alpert gauge, like other ionization gauges, is beset by secondary effects such as X-rays at these very low pressures.
Other specific examples of working fluids embodying the invention are:
Ming meta- Bis (m-phenoxyphenyl) ether When the high boiling polyphenyl ethers are contaminated with organic liquids of greatly inferior thermal stability or are used in admixture with pump oils of much lower stability, the impurities or admixed oils become decomposed with liberation of gas which spoils the vacuum. In a similar manner, metals which contain zinc, lead or tin, metallic salts and halogenated solvents all can cause decomposition if exposed to the polyphenyl ethers at their normal temperatures of operation in the pump. Failure to reach the vacuum described according to this invention can be due to any of the forms of contamination above mentioned.
While I have described preferred embodiments of my invention, it is understood that these are capable of modification, and I therefore do not Wish to be limited to the precise details set forth but desire to avail myself of such changes and alterations as fall Within the purview of the following claims.
I claim:
1. In a method wherein a system is evacuated by means of a vapor actuated pump, the step of entraining gas in a stream of vapors of a working fluid, comprising a polyphenyl ether having at least three phenyl groups and two oxygen linkages, and at most seven phenyl groups and six oxygen linkages.
2. That method according to claim 1 wherein said working fluid essentially consists of a mixture of such polyphenyl ethers.
3. In a method wherein a system is evacuated by means of a vapor actuated pump, the step of entraining gas in a stream of vapors of a working fluid wherein said working fluid contains a polyphenyl ether having a molecular weight in the range of 264 to 641 inclusive.
4. That method according to claim 2 wherein said working fluid essentially consists of a polyphenyl ether or mixtures thereof which boil between C. and 300 C. at .1 millimeter.
References Cited in the file of this patent UNITED STATES PATENTS Shepardson Sept. 6, 1960

Claims (1)

1. IN A METHOD WHEREIN A SYSTEM IS EVACUATED BY MEANS OF A VAPOR ACTUATED PUMP, THE STEP OF ENTRAINING GAS IN A STREAM OF VAPOR OF A WORKING FLUID, COMPRISING A POLYPHENYL ETHER HAVING AT LEAST THREE PHENYL GROUPS AND TWO OXYGEN LINKAGES, AND AT MOST SEVEN PHENYL GROUPS AND SIX OXYGEN LINKAGE.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3173873A (en) * 1962-01-23 1965-03-16 Monsanto Res Corp Functional fluid compositions
US3221058A (en) * 1965-11-30 Aromatic polyethers
US3228910A (en) * 1960-09-22 1966-01-11 Du Pont Process for preparing solid poly-1, 4-phenylene ethers
US3355094A (en) * 1963-07-02 1967-11-28 Ceskoslovenska Akademie Ved Diffusion vacuum pump
US3391195A (en) * 1963-12-04 1968-07-02 Monsanto Res Corp Fluorinated polyphenyl ethers
US3923424A (en) * 1974-11-11 1975-12-02 Alvin E Buggele Self-cleansing diffusion pump
US5059002A (en) * 1989-12-21 1991-10-22 Minnesota Mining And Manufacturing Company Second harmonic generation with achiral, straight-chain carbamic acid derivatives

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2951629A (en) * 1958-07-21 1960-09-06 Dow Corning Silicate diffusion pump fluids

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2951629A (en) * 1958-07-21 1960-09-06 Dow Corning Silicate diffusion pump fluids

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3221058A (en) * 1965-11-30 Aromatic polyethers
US3228910A (en) * 1960-09-22 1966-01-11 Du Pont Process for preparing solid poly-1, 4-phenylene ethers
US3173873A (en) * 1962-01-23 1965-03-16 Monsanto Res Corp Functional fluid compositions
US3355094A (en) * 1963-07-02 1967-11-28 Ceskoslovenska Akademie Ved Diffusion vacuum pump
US3391195A (en) * 1963-12-04 1968-07-02 Monsanto Res Corp Fluorinated polyphenyl ethers
US3923424A (en) * 1974-11-11 1975-12-02 Alvin E Buggele Self-cleansing diffusion pump
US5059002A (en) * 1989-12-21 1991-10-22 Minnesota Mining And Manufacturing Company Second harmonic generation with achiral, straight-chain carbamic acid derivatives

Also Published As

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DE1250049B (en) 1967-09-14
GB924784A (en) 1963-05-01

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