US2883343A - Method and apparatus for blending lubricating oil stocks - Google Patents
Method and apparatus for blending lubricating oil stocks Download PDFInfo
- Publication number
- US2883343A US2883343A US453871A US45387154A US2883343A US 2883343 A US2883343 A US 2883343A US 453871 A US453871 A US 453871A US 45387154 A US45387154 A US 45387154A US 2883343 A US2883343 A US 2883343A
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- Prior art keywords
- additive
- mixing zone
- rate
- sample
- lubricating oil
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- 238000002156 mixing Methods 0.000 title claims description 71
- 239000010687 lubricating oil Substances 0.000 title claims description 34
- 238000000034 method Methods 0.000 title description 13
- 239000000654 additive Substances 0.000 claims description 112
- 230000000996 additive effect Effects 0.000 claims description 98
- 239000000523 sample Substances 0.000 claims description 33
- 230000005855 radiation Effects 0.000 claims description 25
- 238000010521 absorption reaction Methods 0.000 claims description 17
- 239000000463 material Substances 0.000 claims description 17
- 230000000694 effects Effects 0.000 claims description 5
- 238000004804 winding Methods 0.000 claims description 5
- 239000011872 intimate mixture Substances 0.000 claims description 3
- 238000004353 relayed correlation spectroscopy Methods 0.000 claims 2
- 239000003921 oil Substances 0.000 description 28
- 239000000203 mixture Substances 0.000 description 23
- 230000001050 lubricating effect Effects 0.000 description 6
- 230000001276 controlling effect Effects 0.000 description 5
- 229910052596 spinel Inorganic materials 0.000 description 4
- 239000011029 spinel Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- -1 primarytsaturated aliphatic alcohols Chemical class 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 229910052594 sapphire Inorganic materials 0.000 description 3
- 239000010980 sapphire Substances 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 238000009924 canning Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000001235 sensitizing effect Effects 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 229920001567 vinyl ester resin Polymers 0.000 description 2
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 235000002198 Annona diversifolia Nutrition 0.000 description 1
- 101100174178 Dictyostelium discoideum forJ gene Proteins 0.000 description 1
- 241000282842 Lama glama Species 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/35—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light
- G01N21/3577—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light for analysing liquids, e.g. polluted water
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F33/00—Other mixers; Mixing plants; Combinations of mixers
- B01F33/80—Mixing plants; Combinations of mixers
- B01F33/84—Mixing plants with mixing receptacles receiving material dispensed from several component receptacles, e.g. paint tins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F35/00—Accessories for mixers; Auxiliary operations or auxiliary devices; Parts or details of general application
- B01F35/20—Measuring; Control or regulation
- B01F35/21—Measuring
- B01F35/2132—Concentration, pH, pOH, p(ION) or oxygen-demand
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F35/00—Accessories for mixers; Auxiliary operations or auxiliary devices; Parts or details of general application
- B01F35/80—Forming a predetermined ratio of the substances to be mixed
- B01F35/83—Forming a predetermined ratio of the substances to be mixed by controlling the ratio of two or more flows, e.g. using flow sensing or flow controlling devices
- B01F35/833—Flow control by valves, e.g. opening intermittently
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F35/00—Accessories for mixers; Auxiliary operations or auxiliary devices; Parts or details of general application
- B01F35/80—Forming a predetermined ratio of the substances to be mixed
- B01F35/88—Forming a predetermined ratio of the substances to be mixed by feeding the materials batchwise
- B01F35/883—Forming a predetermined ratio of the substances to be mixed by feeding the materials batchwise using flow rate controls for feeding the substances
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/0318—Processes
- Y10T137/0324—With control of flow by a condition or characteristic of a fluid
- Y10T137/0329—Mixing of plural fluids of diverse characteristics or conditions
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/0318—Processes
- Y10T137/0324—With control of flow by a condition or characteristic of a fluid
- Y10T137/0329—Mixing of plural fluids of diverse characteristics or conditions
- Y10T137/034—Controlled by conductivity of mixture
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/2496—Self-proportioning or correlating systems
- Y10T137/2499—Mixture condition maintaining or sensing
- Y10T137/2509—By optical or chemical property
Definitions
- This invention relates-*to a method of and apparatus for analyzing a lubricating oil stock' containing an additive. In another aspect, it relates to a method of and apparatus forJ controlling the blending of additives with lubricating oilfstocks:
- additives of various types lare commonly added to improve the properties of the oil, forl example, to ⁇ improve the viscosity index of the lubricating oil stock.
- synthetic oil-soluble polymerized esters of-the acrylic acid or the vinyl ester seriesfeither aloneA or copolymerized with monohydric primarytsaturated aliphatic alcohols are of particular value.
- the cost oftheseandother additives is'rathei ⁇ high. Consequently, in" order to secure economical operation, it is quitevimportant that the concentration of additive in the oil be carefully controlledsoas-to securethe requisite improvementin lubricating oil properties Without wasting the valuabley additives.
- the beam? output isf representative of the additive concentration in the lubricating oil stock.
- the analyzer output can' be used, in. ainovel manner, to control either acontinuous-or batch blending'operation'to provide high-- quality vadditive;containing.lubricatingoil'stocks with maxmumi economy in theuse ofV additive:
- Figure 1 isaow diagram of av continuous-blending operation conducted in accordance with the invention.
- Figure 2 is allow diagram of a batch blending operation conducted in accordance with the inventiongand Figure ⁇ 3 ⁇ is a graph illustrating4 the manner of sensitizing anfinfraredV analyzer and analyzing for the presence of a particular additive.-
- a source 10 of :aA lubricating oil stock A and a source 11:v of anfoil stock B Intypical blending operations for producinghigh quality lubricating oils, two or more suchstocks-of varying 'viscosity are blended, together with additives, tofform ai superior oil.
- stock A can be a-No. ⁇ 20 oil
- stock B can be aNo. 50 oil' which can eitherlbe blended together or with additional amounts of other stocks, such as No. 10 and No. 250 oil.
- the blending system also includes a storage vessel 12 for an additive A and a storage vessel 13 for an additive B.
- 4additive A is a detergent material, such as an alkyl aryl sulfonate, which does not have a-radiation absorption band in the 5.5 to 6.1 micron region.
- additive A- can be a mixture (X) of barium phenyl sulde, calcium sulfonate, zinc alkyl dithiophosphate, and a plasticizer, such as methyl Carbitol. This compound acts as'a ⁇ combined detergent and oxidation inhibitor.
- Additive Bis a polymer of a compound having" the formula llama in which R is a monovalent hydrocarbon radical containing more than four carbon atoms or an. ether derivative of said hydrocarbon radical, either alone or copolymerized with monohydric saturated primary aliphatic alcohols containing from 5 to 18 carbon atoms per molecule.
- R is a monovalent hydrocarbon radical containing more than four carbon atoms or an. ether derivative of said hydrocarbon radical, either alone or copolymerized with monohydric saturated primary aliphatic alcohols containing from 5 to 18 carbon atoms per molecule.
- Additive B is added to the oil. in the proportion of 2 to 8 percent by weight, usually 5 to, 6 percent and additive ⁇ A can be added, in amounts of 0.1 to 12.0 percent.
- a typical quality oil blend has the following composition Volume, Viscosity Viscosity ⁇ Component Percent; (SUS at Index Oil Stock A, 10H 1 80 39-40 99-105. 5 Oil Stock B, 50H 1 20 115-118 97-98 Additive A (Mixture X)3 2 8.5 Additive' B (Polymcrized ester of acrylic acid compound)4 2 5.0
- the sources10, 11, 12 and 13 are connected by valved hoses or other conduits 10a to 13a, respectively, to a blending machine having Valved conduits 10b to 13b, respectively, whichlead to a common outlet conduit 14.
- the jtmction between the pipes 10b and 13b and conduit 14 can be regarded as a mixing zone or vessel where they actual blending takes place.
- the admixed materials are: fed through a homogenizer 15,which produces an intimate mixture of the oil stocks and additives, and a pipe 16 to a canning machine 17.
- the homogenizer 15 and pipe 16 can be considered part of the mixing vessel or zone for the purposes of withdrawing a sample of material to be analyzed.
- valves in conduits b and 13b are connected to and controlled by a set 10c to 13e of rate of ow controllers, respectively, which meter the various streams fed to the mixing zone.
- the controller 13C has a settable element 18 by which the amount of additive B owing to the mixing zone can be adjusted.
- the described system provides a very convenient and effective means for providing desired blends of lubricating oils.
- the hoses 10a and 11a can be readily connected to or disconnected from oil stock sources 10, 11 and other oil sources can be applied to the mixing device as desired to select various particular oil stocks for any desired blending operation.
- different additive materials can be chosen for diiferent blends.
- a sample of the blend is withdrawn from a portion of the mixing zone, such as pipe 16, and the amount of additive B therein is determined by an infrared analyzer 19.
- an orifice 20 is provided in pipe 16 and a sample is withdrawn at the upstream side of the oriiice through a sample line 21 whence it passes through a sample cell 19a of the analyzer and, thence, returns to the downstream side of the orifice 20 through a sample line 22.
- the blended oil stock is traversed by twin beams of infrared radiation from a source 19b which are reflected by mirrors in two paths to the cell 19t ⁇ and 19d which are provided with windows, formed, for example, from calcium uoride, which are substantially transparent to the radiation used.
- a radiation detector 19j such as a bolometer
- the other beam passes through a sapphire filter 19g to a second detector or bolometer 19h.
- the analyzer is sensitized, in the manner hereinafter explained in detail, so that it produces rotation of a shaft 191' in an amount proportional to the quantity of additive B in the lubricating oil blend.
- the analyzer can be of the type disclosed in Hutchins Patent 2,579,825 with the inclusion of the particular lters here described.
- the shaft 191' is coupled to an indicator 24 which produces a continuous indication of the amount of additive B in the lubricating oil blend, and also to a disk 25 carrying a movable contact element 25a.
- This element cooperates with a pair of fixed contact points 25b and 25C which are connected, respectively, to solenoid windings 26 and 27.
- the contact element 25a is connected through the operating winding and a normally closed contact set of a time delay relay 28 to one terminal of a battery 29, the other terminal of which is grounded and thereby connected to both solenoid coils 26 and 27.
- the solenoids 26 and 27 are provided, respectively, with pawl members 26a and 27a coacting with the teeth of a ratchet wheel 30.
- the ratchet wheel 30, in turn, is connected to the settable element 18 of controller 13C.
- the analyzer 19 continuously determines the amount of additive B in the lubricating oil blend and this is shown by indicator 24. If the concentration of additive B falls below a predetermined value, shaft 191' rotates and closes a circuit between contacts 25a, 25C. This causes a momentary actuation of solenoid 26 and a resultant stepwise clockwise movement of ratchet wheel 30. Thereupon, settable element 18 is moved to increase the amount of additive B admixed with the blend. After this stepwise movement of ratchet wheel 30, the circuit to solenoid 26 is broken by the opening of the contacts of relay 28. After the time delay period of this relay elapses, its contacts again close and, if the desired proportion of additive is now present in the blend, the circuit between contacts 25a, 25o is broken and no further action takes place. However,
- Relay 28 operates in the same manner as previously described to disable the control system for a predetermined interval until the etect of the rst stepwise adjustment is manifested at the analyzer 19.
- control action is effected independently of the color of the oil stream.
- the analyzer 19 is sensitized to the particular additive which is to be controlled.
- the aforementioned polymerized esters of the acrylic acid or vinyl ester series have a strong absorption band at the 5.5 to 6.1 micron region of the spectrum, as indicated by the line 35 of the graph, Figure 3.
- one of the twin beams of infrared radiation passes through a spinel filter 19e having a thickness of 4 millimeters, the absorption characteristics of which in the region of interest are indicated by line 36, Figure 3.
- the other radiation beam passes through the sapphire filter 19g, which can have a thickness of 1 millimeter.
- the absorption characteristics of this material are indicated by line 37, Figure 3, in the wave length region of interest.
- the spinel and sapphire filters are equally transparent so that the reading of the instrument is not aiected thereby. Consequently, the output of the instrument is a direct measure of the amount of additive B present in the blend. From this, it will be understood that the instrument can be sensitized to other additive materials having one or more strong infrared absorption bands by proper choice of lter media to the end that the additive in question produces a different absorption eiect in one beam than in the other beam.
- a standard sample of lubricating oil a sample of acetone can be used, or other materials with low transmission in the 5.5 to 6.1 micron band can be used.
- FIG. 2 we have shown a batch type blending system incorporating storage vessels 40, 41, 42 and 43 for oil stock A, oil stock B, additive A, and additive B, respectively. Material is fed from these storage units to a mixing vessel 44 through the respective pumps 40a to 43a and valved lines 40b to 43b.
- An infrared analyzer 45 of the type described in connection with Figure 1 has a sample cell 45a, and a sample from the vessel 44 is continuously withdrawn through a sample line 45b, passed through the cell 45a by a pump 45e, and returned to the mixing vessel by a sample line 45d.
- the analyzer 45 therefore, indicates the proportion of additive B present in the mixing vessel 44.
- v"lille lblended oil product is removed fromthe vessel 44 A,hy-al valved conduit 47, which can be considered as forming apart ofthe mixing zone, and transferred to a .canning machine 48.
- An infrared analyzer 49 has a sample cell 49a ⁇ to which a sample is admitted from the line 49b .on Athe. upstream side of an Anlagen 47a in the conduit 47, the material returning rto the downstream side of the sau 47a through a sample line 49e.
- the .analyzer 49 indicates the proportion of additive B in lthe .conduit 4.7, and Ithe output of the analyzer is fed to a recorder 50 which provides a continuous record of the finished production.
- the output of analyzer 45 appears as a ,rotation of a shaft 51 .to which is -xed -a .cam 52.
- a rack v53 which is geared to 5a pinion ,'54 which, -in.turn, is connected by a shaft 55 to a settable element 56 of a rate of How-controller 57.
- T he controller .'57 is operatively connected -to a valve 58 in the conduit 4312,., and it is. arranged to meter additive B into thevmixing vessel -44' ata rate determined by the :position ⁇ of settable element 56.
- cam 5-2 Asthe Aconcentra-tionof additive B increases toward a predetermined value, cam 5-2 ⁇ rotates lin a clockwise direction responsive to the action of analyzer 45. As this concentration approaches the desired value, a curved face SZb of the cam engages rack 53 with the result that pinion 54 and settable element 56 are actuated so as to gradually decrease the rate of tlow of additive B to the mixing vessel. Thus, the addition of the additive proceeds at a slower rate than the initial rate.
- additive B is metered into the blend at a rapid rate during the initial stages of its addition. As the desired concentration of additive B is approached, the additive proceeds more and more slowly, and stops when the predetermined value is attained.
- a source of oil stock A a source of oil stock B
- a storage vessel containing an additive A a storage vessel containing an additive B which has an infrared absorption band within the 5.5 to 6.1 micron region
- means defining a mixing zone valved conduits connecting said sources and the storage vessel for additive A, respectively, to said mixing zone, rate of flow controllers operatively connected to the respective valves to maintain preset rates of ow through the conduits controlled thereby, a line connecting said storage vessel for additive B to said mixing zone, a valve in said line, a rate of iiow controller operatively connected to "said valve to maintain a preset rate of flow of additive B tolsaid mixing zone, said controller having a settable yele- 6 ment arranged to vary the rate of flow of said additive B, said mixing zone incorporating a homogenizer to secure an intimate mixture of said cil stocks and said additives, an
- a pair of xed contacts spaced from said contact member whereby rotation of said shaft a predetermined amount in one direction closes a circuit between one fixed contact and said movable contact member while rotation of the ⁇ shaft a predetermined amount Vin 'the opposite direction closes a circuit between said movable Contact member and the other fixed contact, an adjusting member connected to 4said settable element, a solenoid arranged to effect stepwise movement of said adjusting member in one direction, a second solenoid arranged to effect stepwise movement of said adjusting member in the other direction, said solenoids being connected to circuit, respectively, with said iixed contacts, ⁇ a current source, a time delay ⁇ relay having an operating winding and a set of normally closed contacts, and means ⁇ for completing both solenoid ,circuits through said movable contact member the operating winding and contacts of said relay, and said current source.
- the method of preparing a lubricating oil stock which comprises adding a material containing carboxylic groups as an additive to a lubricating oil stock, intermixing said additive and said stock, passing a beam of infrared radiation through a sample of the intermixed material, producing an electrical output representative of the portion of radiation in the wave length of range of 5.5 to 6.1 microns passing through said sample, said output being proportional to the amount of said additive in said stock, and regulating the relative amounts of additive and stock fed to the admixing step in accordance with said output so as to maintain a ixed concentration of additive in said stock.
- the method of blending an additive into a lubricating oil stock which comprises introducing a stream of lubricating oil stock and a stream of lubricating oil additives into a mixing zone, continuously withdrawing a sample of the additive-lubricating oil mixture from the mixing zone, passing a beam of infrared radiation through the vwithdrawn sample, producing an output representative of the intensity of said beam after it has passed through said sample, and regulating the rate of flow of one of said streams to the mixing zone in accordance with said output to maintain said -output at a constant predetermined value.
- the method of blending an additive into a lubrieating oil stock which comprises introducing a plurality of streams of diierent lubricating oil stocks and a stream of lubricating oil additive into a mixing zone, continuously withdrawing a sample of the additive-lubricating oil mixture from the mixing zone, passing a beam of infrared radiation through the withdrawn sample, producing an output representative of the intensity of said beam after it has passed through said sample, and regulating the rate of ow of said additive stream to the mixing zone in accordance with said output to maintain said output at -a constant predetermined value.
- the method of continuously blending an additive into a lubricating oil which comprises passing a stream of an oil stock A, a stream of an oil stock B, a stream of an additive A and a stream of an -additive B into a mixing zone, said additive B having an infrared absorption band within the 5.5 to 6.1 micron region, maintaining a conw stant rate of flow of said oil stock A, oil stock B, and said additive A into the mixing zone, homogenizing the mixture of oil stocks and additive within the mixing zone, continuously withdrawing a sample of homogenized material from the mixing zone, passing a beam of infrared radiation through the withdrawn sample, ltering the radiation to provide an output substantially representative of energy within said 5.5 to 6.1 micron region and substantially unaffected by radiation outside said region, and controlling the rate of ow of said additive B into the mixing zone in accordance with said output to maintain said output and thus the concentration of additive B at a constant predetermined value.
- a method of batch blending a lubricating stock which comprises feeding predetermined amounts of a lubricating oil stock A, a lubricating oil stock B, and an additive A to a mixing zone, agitating the mixture in the mixing zone, withdrawing a sample of material from the mixing zone, passing a beam of infrared radiation through the sample, filtering the radiation so as to produce an output sensitive to radiation within the 5.5 to 6.1 micron region and substantially insensitive to radiation outside said region, adding an additive B having an infrared absorption band within the 5.5 to 6.1 micron region to the mixing tank, controlling the rate of ow of said additive B in accordance with said output to cause said additive B to ow into the mixing tank until said output reaches a predetermined value, and thereupon terminating the flow of said additive B to the mixing tank.
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Description
April 21, 1959 J. A.V FAVRE ET AL 2,883,343 METHOD AND APPARATUS FOR BLENDING LUBRICATING om sTocKs Filed sept. 2, 1954 v 2 Sheets-Sheet 1 ASSEN April 2l, 1959 J. AFAVRE ET AL 2,883,343
METHOD AND APPARATUS FOR BLENDING LUBRICATING on. sTooKs Eiled sept. 2, 1954 2 sheets-sheet 2 kuub.
: SSR,
United States Patent O lVIETHOD AND APPARATUS FR BLENDING LUBRICATING GIL STCKS John. A. Favre, James P. Butler, and Bill'Mitacek, Bartlesville, Okla., assignors-to Phillips Petroleum Company, acorporation of Delaware Application September 2, 1954, Serial No. 453,871
7 Claims. (Cl. 252-56) This invention relates-*to a method of and apparatus for analyzing a lubricating oil stock' containing an additive. In another aspect, it relates to a method of and apparatus forJ controlling the blending of additives with lubricating oilfstocks:
In theproduction `of lubricating-oil stocksof superior quality, additives of various types lare commonly added to improve the properties of the oil, forl example, to `improve the viscosity index of the lubricating oil stock. Of these additives, synthetic oil-soluble polymerized esters of-the acrylic acid or the vinyl ester seriesfeither aloneA or copolymerized with monohydric primarytsaturated aliphatic alcohols are of particular value. However, the cost oftheseandother additives is'rathei` high. Consequently, in" order to secure economical operation, it is quitevimportant that the concentration of additive in the oil be carefully controlledsoas-to securethe requisite improvementin lubricating oil properties Without wasting the valuabley additives.
In accordance with this invention, the amount `of additive is= accurately determined' and controlled by passing a beamofl infrared radiation through the stock and producingan outputfrepresentative off beam intensity after it` has passed: through the sample. Where the additive has a definite characteristic absorption band,` the beam? output isf representative of the additive concentration in the lubricating oil stock. Inl` particular, inthe case of the specific polymerizedesters'mentioned above, there is a strong absorption band inthe wavelength` regionfof 5.5 to 6.1l
microns; Accordingly,tby` sensitizing the.r analyzer to this wavelength. band, the additivee concentration` isv quickly and' accurately determined.
Further'. inV accordancexwith4 the invention, the analyzer output can' be used, in. ainovel manner, to control either acontinuous-or batch blending'operation'to provide high-- quality vadditive;containing.lubricatingoil'stocks with maxmumi economy in theuse ofV additive:
Accordingly,.it isA anxobjectl of, the` invention to provide an improved method of and apparatus for analyzing a lubricating. oilfstock containingan additive. by virtue of the radiation-absorption characteristics of. such. additive.
Itis. a` further'objectto provide an. improved method of and apparatus for controlling an operation where one` or more lubricating oil stocks are blended with one or more additives either' on a batch or continuous basis.
Various: other4 objects, advantages and features. of the invention` will become apparent from. the following detailed description, takenV inv conjunction: with the accompanying drawings, in which:
Figure 1 isaow diagram of av continuous-blending operation conducted in accordance with the invention;
Figure 2 is allow diagram of a batch blending operation conducted in accordance with the inventiongand Figure` 3 `is a graph illustrating4 the manner of sensitizing anfinfraredV analyzer and analyzing for the presence of a particular additive.-
Referring now to Figure l, we nave shown a source 10 of :aA lubricating oil stock A and a source 11:v of anfoil stock B. Intypical blending operations for producinghigh quality lubricating oils, two or more suchstocks-of varying 'viscosity are blended, together with additives, tofform ai superior oil. For example, stock A can be a-No.` 20 oil and stock B can be aNo. 50 oil' which can eitherlbe blended together or with additional amounts of other stocks, such as No. 10 and No. 250 oil.
The blending system also includesa storage vessel 12 for an additive A and a storage vessel 13 for an additive B. In a preferred embodiment of the invention, 4additive A is a detergent material, such as an alkyl aryl sulfonate, which does not have a-radiation absorption band in the 5.5 to 6.1 micron region. Alternatively, additive A- can be a mixture (X) of barium phenyl sulde, calcium sulfonate, zinc alkyl dithiophosphate, and a plasticizer, such as methyl Carbitol. This compound acts as'a` combined detergent and oxidation inhibitor.
Additive Bis a polymer of a compound having" the formula llama in which R is a monovalent hydrocarbon radical containing more than four carbon atoms or an. ether derivative of said hydrocarbon radical, either alone or copolymerized with monohydric saturated primary aliphatic alcohols containing from 5 to 18 carbon atoms per molecule. Such additives are described in detail in Patent. 2,091,627.
They have molecular weights ranging from 2,000 to 100,-V
000 andnormally contain less than 30 carbon atoms `in the aforementioned hydrocarbon groups and radicals. We havediscovered that such additiveshave a strong infrared absorption band in the 5.5 to 6.1 micron-region which, it is our belief, can be attributed tothe carbonyl group.
Other additives, in many cases, have definite and strongl absorption bands at other regions of the spectrum.
Additive B is added to the oil. in the proportion of 2 to 8 percent by weight, usually 5 to, 6 percent and additive` A can be added, in amounts of 0.1 to 12.0 percent.
A typical quality oil blend has the following composition Volume, Viscosity Viscosity` Component Percent; (SUS at Index Oil Stock A, 10H 1 80 39-40 99-105. 5 Oil Stock B, 50H 1 20 115-118 97-98 Additive A (Mixture X)3 2 8.5 Additive' B (Polymcrized ester of acrylic acid compound)4 2 5.0
l Of total hydrocarbons. 2 Of total blend.
a Paranox 114.
The sources10, 11, 12 and 13 are connected by valved hoses or other conduits 10a to 13a, respectively, to a blending machine having Valved conduits 10b to 13b, respectively, whichlead to a common outlet conduit 14.
` The jtmction between the pipes 10b and 13b and conduit 14 can be regarded as a mixing zone or vessel where they actual blending takes place. The admixed materials are: fed through a homogenizer 15,which produces an intimate mixture of the oil stocks and additives, and a pipe 16 to a canning machine 17. In a broad sense, the homogenizer 15 and pipe 16 can be considered part of the mixing vessel or zone for the purposes of withdrawing a sample of material to be analyzed.
The valves in conduits b and 13b are connected to and controlled by a set 10c to 13e of rate of ow controllers, respectively, which meter the various streams fed to the mixing zone. The controller 13C has a settable element 18 by which the amount of additive B owing to the mixing zone can be adjusted.
It will be appreciated that the described system provides a very convenient and effective means for providing desired blends of lubricating oils. Thus, the hoses 10a and 11a can be readily connected to or disconnected from oil stock sources 10, 11 and other oil sources can be applied to the mixing device as desired to select various particular oil stocks for any desired blending operation. Similarly, different additive materials can be chosen for diiferent blends.
In accordance with the invention, a sample of the blend is withdrawn from a portion of the mixing zone, such as pipe 16, and the amount of additive B therein is determined by an infrared analyzer 19. To this end, an orifice 20 is provided in pipe 16 and a sample is withdrawn at the upstream side of the oriiice through a sample line 21 whence it passes through a sample cell 19a of the analyzer and, thence, returns to the downstream side of the orifice 20 through a sample line 22.
In the cell 19a, the blended oil stock is traversed by twin beams of infrared radiation from a source 19b which are reflected by mirrors in two paths to the cell 19t` and 19d which are provided with windows, formed, for example, from calcium uoride, which are substantially transparent to the radiation used. One beam passes through a spinel filter 19e to a radiation detector 19j, such as a bolometer, and the other beam passes through a sapphire filter 19g to a second detector or bolometer 19h. The analyzer is sensitized, in the manner hereinafter explained in detail, so that it produces rotation of a shaft 191' in an amount proportional to the quantity of additive B in the lubricating oil blend. Preferably and advantageously, the analyzer can be of the type disclosed in Hutchins Patent 2,579,825 with the inclusion of the particular lters here described.
The shaft 191' is coupled to an indicator 24 which produces a continuous indication of the amount of additive B in the lubricating oil blend, and also to a disk 25 carrying a movable contact element 25a. This element cooperates with a pair of fixed contact points 25b and 25C which are connected, respectively, to solenoid windings 26 and 27. The contact element 25a is connected through the operating winding and a normally closed contact set of a time delay relay 28 to one terminal of a battery 29, the other terminal of which is grounded and thereby connected to both solenoid coils 26 and 27.
The solenoids 26 and 27 are provided, respectively, with pawl members 26a and 27a coacting with the teeth of a ratchet wheel 30. The ratchet wheel 30, in turn, is connected to the settable element 18 of controller 13C.
In the operation of the system, therefore, the analyzer 19 continuously determines the amount of additive B in the lubricating oil blend and this is shown by indicator 24. If the concentration of additive B falls below a predetermined value, shaft 191' rotates and closes a circuit between contacts 25a, 25C. This causes a momentary actuation of solenoid 26 and a resultant stepwise clockwise movement of ratchet wheel 30. Thereupon, settable element 18 is moved to increase the amount of additive B admixed with the blend. After this stepwise movement of ratchet wheel 30, the circuit to solenoid 26 is broken by the opening of the contacts of relay 28. After the time delay period of this relay elapses, its contacts again close and, if the desired proportion of additive is now present in the blend, the circuit between contacts 25a, 25o is broken and no further action takes place. However,
if the additive concentration is still too small, contacts a, 25e remain closed and a further stepwise actuation of the ratchet Wheel occurs at the expiration of the delay period of relay 28. This delay period is so chosen that the eiect of adjusting the flow rate of additive B has time to manifest itself at the analyzer 19 before a further correction is made. This prevents hunting or overshooting the control system and improves the economy of operation.
Conversely, if the additive concentration becomes too high, shaft 19i rotates disk 25 so as to close contacts 25a, 2511. This results in a momentary energization of solenoid 27 and a stepwise counterclockwise movement of ratchet wheel 30 to effect a downward adjustment of the rate of ow of additive B. Relay 28 operates in the same manner as previously described to disable the control system for a predetermined interval until the etect of the rst stepwise adjustment is manifested at the analyzer 19.
It will be evident, therefore, that we have provided an eflicient rapid acting control system for providing a predetermined amount of additive in `a lubricating oil blend which does away with the loss of time heretofore required for analysis of the lubricating oil stock and additive cony tent. Further, due to the use of infrared radiation, the
control action is effected independently of the color of the oil stream.
As previously noted, the analyzer 19 is sensitized to the particular additive which is to be controlled. The aforementioned polymerized esters of the acrylic acid or vinyl ester series have a strong absorption band at the 5.5 to 6.1 micron region of the spectrum, as indicated by the line 35 of the graph, Figure 3.
It will be noted that one of the twin beams of infrared radiation passes through a spinel filter 19e having a thickness of 4 millimeters, the absorption characteristics of which in the region of interest are indicated by line 36, Figure 3. The other radiation beam passes through the sapphire filter 19g, which can have a thickness of 1 millimeter. The absorption characteristics of this material are indicated by line 37, Figure 3, in the wave length region of interest. Thus, in the 5.5 to 6.1 micron region, there is a difference in the eiect of the additive upon the two beams so that, when the intensity of these beams is electrically compared by the analyzer to produce a resultant output, this output varies in accordance with the concentration of the additive in the system.
At other regions of the spectrum where strong absorption bands are present due to the components of the oil stocks and additive A, the spinel and sapphire filters are equally transparent so that the reading of the instrument is not aiected thereby. Consequently, the output of the instrument is a direct measure of the amount of additive B present in the blend. From this, it will be understood that the instrument can be sensitized to other additive materials having one or more strong infrared absorption bands by proper choice of lter media to the end that the additive in question produces a different absorption eiect in one beam than in the other beam.
Instead of spinel, a standard sample of lubricating oil, a sample of acetone can be used, or other materials with low transmission in the 5.5 to 6.1 micron band can be used.
Referring now to Figure 2, we have shown a batch type blending system incorporating storage vessels 40, 41, 42 and 43 for oil stock A, oil stock B, additive A, and additive B, respectively. Material is fed from these storage units to a mixing vessel 44 through the respective pumps 40a to 43a and valved lines 40b to 43b.
An infrared analyzer 45 of the type described in connection with Figure 1 has a sample cell 45a, and a sample from the vessel 44 is continuously withdrawn through a sample line 45b, passed through the cell 45a by a pump 45e, and returned to the mixing vessel by a sample line 45d. The analyzer 45, therefore, indicates the proportion of additive B present in the mixing vessel 44.
v"lille lblended oil product is removed fromthe vessel 44 A,hy-al valved conduit 47, which can be considered as forming apart ofthe mixing zone, and transferred to a .canning machine 48. An infrared analyzer 49 has a sample cell 49a`to which a sample is admitted from the line 49b .on Athe. upstream side of an orice 47a in the conduit 47, the material returning rto the downstream side of the orice 47a through a sample line 49e. As a result, the .analyzer 49 indicates the proportion of additive B in lthe .conduit 4.7, and Ithe output of the analyzer is fed to a recorder 50 which provides a continuous record of the finished production.
The output of analyzer 45 appears as a ,rotation of a shaft 51 .to which is -xed -a .cam 52. Cooperating with the face of cam 52 is a rack v53 which is geared to 5a pinion ,'54 which, -in.turn, is connected by a shaft 55 to a settable element 56 of a rate of How-controller 57. T he controller .'57 is operatively connected -to a valve 58 in the conduit 4312,., and it is. arranged to meter additive B into thevmixing vessel -44' ata rate determined by the :position `of settable element 56.
In operation, the 4ingredients of the blend, with the exception of additive B, are charged to the mixing vessel 44 in proper amounts to make the desired blend. Thereupon,
*addition of yadditive -B -is started. At Ethis time, rack 53 rests 'upon a `tiat portion SZafof the cam 52 and, in. this position, settable `element -56 controls unit 57 `so as to maintain valve v58 Iin a -fully open position, thereby Yperv-mitting -a maximum -rateof ow of additive B finto -the mixing vessel.
Asthe Aconcentra-tionof additive B increases toward a predetermined value, cam 5-2 `rotates lin a clockwise direction responsive to the action of analyzer 45. As this concentration approaches the desired value, a curved face SZb of the cam engages rack 53 with the result that pinion 54 and settable element 56 are actuated so as to gradually decrease the rate of tlow of additive B to the mixing vessel. Thus, the addition of the additive proceeds at a slower rate than the initial rate.
As the concentration of additive B reaches the desired value, the continued clockwise rotation of cam 52 causes a at part 52C of the cam to engage rack 53, thereby moving pinion 54 and settable element 56 so as to stop the ow of additive into the mixing vessel 44.
As a result, additive B is metered into the blend at a rapid rate during the initial stages of its addition. As the desired concentration of additive B is approached, the additive proceeds more and more slowly, and stops when the predetermined value is attained.
Accordingly, with respect to Figure 2, we have shown a simple and accurate method both of monitoring the final product and of controlling the rate of addition of additive B to the mixing vessel to the end that the desired amount is quickly added without danger of adding excessive and uneconomical amounts to the mixture.
While the invention has been described in connection with present, preferred embodiments thereof, it is to be understood that this description is illustrative only and is not intended to limit the invention.
We claim:
l. In a system for continuously blending a lubricating oil stock with an additive, in combination, a source of oil stock A, a source of oil stock B, a storage vessel containing an additive A, a storage vessel containing an additive B which has an infrared absorption band within the 5.5 to 6.1 micron region, means defining a mixing zone, valved conduits connecting said sources and the storage vessel for additive A, respectively, to said mixing zone, rate of flow controllers operatively connected to the respective valves to maintain preset rates of ow through the conduits controlled thereby, a line connecting said storage vessel for additive B to said mixing zone, a valve in said line, a rate of iiow controller operatively connected to "said valve to maintain a preset rate of flow of additive B tolsaid mixing zone, said controller having a settable yele- 6 ment arranged to vary the rate of flow of said additive B, said mixing zone incorporating a homogenizer to secure an intimate mixture of said cil stocks and said additives, an infrared analyzer having Aa `sample cell, means for continuously .passing a sample of material from said mixing zone through said cell, means for passing a twin beam of infrared radiation through said cellr and the material included therein, a lter in one beam to attenuate radiation Within `the 5.5 to 6.1 micron region, radiation detector means, and a shaft rotatable by said detector means in accordance with the amount of additive B ,present lin the sample material, a contact member driven by said shaft. a pair of xed contacts spaced from said contact member whereby rotation of said shaft a predetermined amount in one direction closes a circuit between one fixed contact and said movable contact member while rotation of the `shaft a predetermined amount Vin 'the opposite direction closes a circuit between said movable Contact member and the other fixed contact, an adjusting member connected to 4said settable element, a solenoid arranged to effect stepwise movement of said adjusting member in one direction, a second solenoid arranged to effect stepwise movement of said adjusting member in the other direction, said solenoids being connected to circuit, respectively, with said iixed contacts, `a current source, a time delay `relay having an operating winding and a set of normally closed contacts, and means` for completing both solenoid ,circuits through said movable contact member the operating winding and contacts of said relay, and said current source.
2,. In a system lfor .effecting batch blending of a lubricating oil stock, a mixing tank, an agitator therein, a source of a lubricating oil stock A and a source of a lubricating oil stock B, a sotirce of an additive A, valved conduits connecting the respective sources to said mixing tank, a source of an additive B having an infrared absorption band within the 5.5 to 6.1 micron region, a valved line connecting said source of additive B to said mixing tank, a rate of flow controller operatively connected to said valve and arranged t-o maintain a controlled rate of ow through said line, said controller having a settable element to vary said rate of flow, an infrared analyzer sensitive to radiation within the 5.5 to 6.1 micron region, said analyzer having a sampling device connected to said mixing tank, and said analyzer having a rotatable shaft, the angular position of which is representative of the concentration of additive B in the blending vessel, a cam fixed on said shaft, mechanism actuated by said cam to adjust said settable element, said cam having a iiat part arranged to maintain a high rate of ilow of additive B to the blending vessel when its concentration is substantially below a predetermined value, an angular portion arranged to decrease the rate of tiow of additive B as the predetermined concentration is approached, and a second at portion arranged to shut off the flow of additive B when the concentration thereof reaches said predetermined value.
3. The method of preparing a lubricating oil stock which comprises adding a material containing carboxylic groups as an additive to a lubricating oil stock, intermixing said additive and said stock, passing a beam of infrared radiation through a sample of the intermixed material, producing an electrical output representative of the portion of radiation in the wave length of range of 5.5 to 6.1 microns passing through said sample, said output being proportional to the amount of said additive in said stock, and regulating the relative amounts of additive and stock fed to the admixing step in accordance with said output so as to maintain a ixed concentration of additive in said stock.
4. The method of blending an additive into a lubricating oil stock which comprises introducing a stream of lubricating oil stock and a stream of lubricating oil additives into a mixing zone, continuously withdrawing a sample of the additive-lubricating oil mixture from the mixing zone, passing a beam of infrared radiation through the vwithdrawn sample, producing an output representative of the intensity of said beam after it has passed through said sample, and regulating the rate of flow of one of said streams to the mixing zone in accordance with said output to maintain said -output at a constant predetermined value.
5. The method of blending an additive into a lubrieating oil stock which comprises introducing a plurality of streams of diierent lubricating oil stocks and a stream of lubricating oil additive into a mixing zone, continuously withdrawing a sample of the additive-lubricating oil mixture from the mixing zone, passing a beam of infrared radiation through the withdrawn sample, producing an output representative of the intensity of said beam after it has passed through said sample, and regulating the rate of ow of said additive stream to the mixing zone in accordance with said output to maintain said output at -a constant predetermined value.
6. The method of continuously blending an additive into a lubricating oil which comprises passing a stream of an oil stock A, a stream of an oil stock B, a stream of an additive A and a stream of an -additive B into a mixing zone, said additive B having an infrared absorption band within the 5.5 to 6.1 micron region, maintaining a conw stant rate of flow of said oil stock A, oil stock B, and said additive A into the mixing zone, homogenizing the mixture of oil stocks and additive within the mixing zone, continuously withdrawing a sample of homogenized material from the mixing zone, passing a beam of infrared radiation through the withdrawn sample, ltering the radiation to provide an output substantially representative of energy within said 5.5 to 6.1 micron region and substantially unaffected by radiation outside said region, and controlling the rate of ow of said additive B into the mixing zone in accordance with said output to maintain said output and thus the concentration of additive B at a constant predetermined value.
7. A method of batch blending a lubricating stock which comprises feeding predetermined amounts of a lubricating oil stock A, a lubricating oil stock B, and an additive A to a mixing zone, agitating the mixture in the mixing zone, withdrawing a sample of material from the mixing zone, passing a beam of infrared radiation through the sample, filtering the radiation so as to produce an output sensitive to radiation within the 5.5 to 6.1 micron region and substantially insensitive to radiation outside said region, adding an additive B having an infrared absorption band within the 5.5 to 6.1 micron region to the mixing tank, controlling the rate of ow of said additive B in accordance with said output to cause said additive B to ow into the mixing tank until said output reaches a predetermined value, and thereupon terminating the flow of said additive B to the mixing tank.
References Cited in the le of this patent UNITED STATES PATENTS 2,015,056 Barnes Sept. 24, 1935 2,203,980 Burt June 11, 1940 2,386,831 Wright Oct. 16, 1945 2,518,307 Groebe Aug. 8, 1950 2,579,825 Hutchins Dec. 25, 1951 2,621,297 Obermaier Dec. 7, 1952 2,673,297 Miller Mar. 23, 1954 2,685,649 Miller Aug. 3, 1954
Claims (1)
1. IN A SYSTEM FOR CONTINUOUSLY BLENDING A LUBRICATING OIL STOCK WITH AN ADDITIVE, IN COMBINATION, A SOURCE OF OIL STOCK A, A SOURCE OF OIL STOCK B, A STORAGE VESSEL CONTAINING AN ADDITIVE A, A STORAGE VESSEL CONTAINING AN ADDITIVE B WHICH HAS AN INFRARED ABSORPTION BAND WITHIN THE 5.5 TO 6.1 MICRON REGION, MEANS DEFINING A MIXING ZONE, VALVED CONDUITS CONNECTING SAID SOURCES AND THE STORAGE VESSEL FOR ADDITIVE A, RESPECTIVELY, TO SAID MIXING ZONE, RATE OF FLOW CONTROLLERS OPERATIVELY CONNECTED TO THE RESPECTIVE VALVES TO MAINTAIN PRESET RATES OF FLOW THROUGH THE CONDUITS CONTROLLED THEREBY, A LINE CONNECTING SAID STORAGE VESSEL FOR ADDITIVE B TO SAID MIXING ZONE, A VALVE IN SAID LINE, A RATE OF FLOW CONTROLLER OPERATIVELY CONNECTED TO SAID VALVE TO MAINTAIN A PRESET RATE OF FLOW OF ADDITIVE B TO SAID MIXING ZONE, SAID CONTROLLER HAVING A SETTABLE ELEMENT ARRANGED TO VARY THE RATE OF FLOW OF SAID ADDITIVE B, SAID MIXING ZONE INCORPORATING A HOMOGENIZER TO SECURE AN INTIMATE MIXTURE OF SAID OIL STOCKS AND SAID ADDITIVES, AN INFRARED ANALYZER HAVING A SAMPLE CELL, MEANS FOR CONTINUOUSLY PASSING A SAMPLE OF MATERIAL FROM SAID MIXING ZONE THROUGH SAID CELL, MEANS FOR PASSING A TWIN BEAM OF INFRARED RADIATION THROUGH SAID CELL AND THE MATERIAL INCLUDED THEREIN, A FILTER IN ONE BEAM TO ATTENUATE RADIATION WITHIN THE 5.5 TO 6.1 MICRON REGION, RADIATION DETECTOR MEANS, AND A SHAFT ROTATABLE BY SAID DETECTOR MEANS IN ACCORDANCE WITH THE AMOUNT OF ADDITIVE B PRESENT IN THE SAMPLE MATERIAL, A CONTACT MEMBER DRIVEN BY SAID SHAFT, A PAIR OF FIXED CONTACTS SPACED FROM SAID CONTACT MEMBER WHEREBY ROTATION OF SAID SHAFT A PREDETERMINED AMOUNT IN ONE DIRECTION CLOSES A CIRCUIT BETWEEN ONE FIXED CONTACT AND SAID MOVABLE CONTACT MEMBER WHILE ROTATION OF THE SHAFT A PREDETERMINED AMOUNT IN THE OPPOSITE DIRECTION CLOSES A CIRCUIT BETWEEN SAID MOVABLE CONTACT MEMBER AND THE OTHER FIXED CONTACT, AN ADJUSTING MEMBER CONNECTED TO SAID SETTABLE ELEMENT, A SOLENOID ARRANGED TO EFFECT STEPWISE MOVEMENT OF SAID ADJUSTING MEMBER IN ONE DIRECTION, A SECOND SOLENOID ARRANGED TO EFFECT STEPWISE MOVEMENT OF SAID ADJUSTING MEMBER IN THE OTHER DIRECTION, SAID SOLENOIDS BEING CONNECTED TO CIRCUIT, RESPECTIVELY, WITH SAID FIXED CONTACTS, A CURRENT SOURCE, A TIME DELAY RELAY HAVING AN OPERATING WINDING AND A SET OF NORMALLY CLOSED CONTACTS, AND MEANS FOR COMPLETING BOTH SOLENOID CIRCUITS THROUGH SAID MOVABLE CONTACT MEMBER THE OPERATING WINDING AND CONTACTS OF SAID RELAY, AND SAID CURRENT SOURCE.
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WO2020094258A1 (en) * | 2018-11-05 | 2020-05-14 | Brillux Gmbh & Co. Kg | Process for preserving a dispersion in a metering apparatus and metering apparatus |
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