US3404093A - Fluorescent composition for magnetic particle inspection - Google Patents
Fluorescent composition for magnetic particle inspection Download PDFInfo
- Publication number
- US3404093A US3404093A US443705A US44370565A US3404093A US 3404093 A US3404093 A US 3404093A US 443705 A US443705 A US 443705A US 44370565 A US44370565 A US 44370565A US 3404093 A US3404093 A US 3404093A
- Authority
- US
- United States
- Prior art keywords
- fluorescent
- magnetic
- resin
- water
- particles
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000006249 magnetic particle Substances 0.000 title description 36
- 239000000203 mixture Substances 0.000 title description 36
- 238000007689 inspection Methods 0.000 title description 9
- 229920005989 resin Polymers 0.000 description 27
- 239000011347 resin Substances 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- 239000003605 opacifier Substances 0.000 description 23
- 229920005992 thermoplastic resin Polymers 0.000 description 22
- 239000002245 particle Substances 0.000 description 21
- 238000000576 coating method Methods 0.000 description 20
- 238000000034 method Methods 0.000 description 20
- 239000007850 fluorescent dye Substances 0.000 description 19
- 239000011248 coating agent Substances 0.000 description 18
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 17
- 239000000243 solution Substances 0.000 description 14
- 239000011162 core material Substances 0.000 description 12
- 239000003960 organic solvent Substances 0.000 description 12
- 239000000975 dye Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 230000005291 magnetic effect Effects 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- 239000007900 aqueous suspension Substances 0.000 description 8
- 239000006185 dispersion Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000000049 pigment Substances 0.000 description 8
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthene Chemical compound C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 238000013019 agitation Methods 0.000 description 6
- 239000000696 magnetic material Substances 0.000 description 6
- 239000006247 magnetic powder Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- -1 xylene red Naphthalimides Chemical class 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 230000001464 adherent effect Effects 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000012065 filter cake Substances 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 239000013557 residual solvent Substances 0.000 description 3
- DXWHZJXKTHGHQF-UHFFFAOYSA-N 2-butyl-6-(butylamino)benzo[de]isoquinoline-1,3-dione Chemical compound O=C1N(CCCC)C(=O)C2=CC=CC3=C2C1=CC=C3NCCCC DXWHZJXKTHGHQF-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- IHBCFWWEZXPPLG-UHFFFAOYSA-N [Ca].[Zn] Chemical compound [Ca].[Zn] IHBCFWWEZXPPLG-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 235000001671 coumarin Nutrition 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 2
- 125000003914 fluoranthenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC=C4C1=C23)* 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 235000021286 stilbenes Nutrition 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- MXODCLTZTIFYDV-UHFFFAOYSA-L zinc;1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound [Zn+2].C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C([O-])=O.C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C([O-])=O MXODCLTZTIFYDV-UHFFFAOYSA-L 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- XNMAQDVPSHMBPO-UHFFFAOYSA-N 1-methylpyrrolidin-2-one;propan-2-one Chemical compound CC(C)=O.CN1CCCC1=O XNMAQDVPSHMBPO-UHFFFAOYSA-N 0.000 description 1
- SQAINHDHICKHLX-UHFFFAOYSA-N 1-naphthaldehyde Chemical compound C1=CC=C2C(C=O)=CC=CC2=C1 SQAINHDHICKHLX-UHFFFAOYSA-N 0.000 description 1
- JVCMLZFTHRTGDS-UHFFFAOYSA-N C=O.C(C1=CC=CC=C1)S(=O)(=O)N.N1=C(N)N=C(N)N=C1N Chemical compound C=O.C(C1=CC=CC=C1)S(=O)(=O)N.N1=C(N)N=C(N)N=C1N JVCMLZFTHRTGDS-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical group [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000005577 anthracene group Chemical group 0.000 description 1
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical compound C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229960000956 coumarin Drugs 0.000 description 1
- 150000004775 coumarins Chemical class 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 229940113088 dimethylacetamide Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- VYXSBFYARXAAKO-UHFFFAOYSA-N ethyl 2-[3-(ethylamino)-6-ethylimino-2,7-dimethylxanthen-9-yl]benzoate;hydron;chloride Chemical compound [Cl-].C1=2C=C(C)C(NCC)=CC=2OC2=CC(=[NH+]CC)C(C)=CC2=C1C1=CC=CC=C1C(=O)OCC VYXSBFYARXAAKO-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 239000003302 ferromagnetic material Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- TWKNNWSZHUMEEH-UHFFFAOYSA-N formaldehyde triazine-4-sulfonamide Chemical compound C=O.N1=NN=C(C=C1)S(=O)(=O)N TWKNNWSZHUMEEH-UHFFFAOYSA-N 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- QJKBHDRXPAOHSY-UHFFFAOYSA-N morpholine;pyridine Chemical compound C1COCCN1.C1=CC=NC=C1 QJKBHDRXPAOHSY-UHFFFAOYSA-N 0.000 description 1
- LSQODMMMSXHVCN-UHFFFAOYSA-N ovalene Chemical compound C1=C(C2=C34)C=CC3=CC=C(C=C3C5=C6C(C=C3)=CC=C3C6=C6C(C=C3)=C3)C4=C5C6=C2C3=C1 LSQODMMMSXHVCN-UHFFFAOYSA-N 0.000 description 1
- GUVXZFRDPCKWEM-UHFFFAOYSA-N pentalene Chemical compound C1=CC2=CC=CC2=C1 GUVXZFRDPCKWEM-UHFFFAOYSA-N 0.000 description 1
- BHDZLFBQVBBVDL-UHFFFAOYSA-N piperidine;pyrazine Chemical compound C1CCNCC1.C1=CN=CC=N1 BHDZLFBQVBBVDL-UHFFFAOYSA-N 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 150000003732 xanthenes Chemical class 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- 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
- G01N21/84—Systems specially adapted for particular applications
- G01N21/88—Investigating the presence of flaws or contamination
- G01N21/91—Investigating the presence of flaws or contamination using penetration of dyes, e.g. fluorescent ink
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/72—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating magnetic variables
- G01N27/82—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating magnetic variables for investigating the presence of flaws
- G01N27/83—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating magnetic variables for investigating the presence of flaws by investigating stray magnetic fields
- G01N27/84—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating magnetic variables for investigating the presence of flaws by investigating stray magnetic fields by applying magnetic powder or magnetic ink
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/90—Magnetic feature
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/913—Material designed to be responsive to temperature, light, moisture
Definitions
- a fluorescent magnetic material for use in non-destructive methods of testing ferromagnetic work pieces comprising discrete magnetic particles coated with a thermoplastic resin containing a fluorescent dye, preferably in combination with an opacifier having a cascading effect in combination with said dye, the coated particles having an average particle size preferably of not over about 5 microns maximum dimension.
- the method of coating includes dissolving a thermoplastic resin and a fluoragent in a water-miscible organic solvent to form a solution thereof, separately forming a water dispersion of highly divided magnetic particles, and then adding the solution to the water dispersion with thorough mixing until the resin and fluoragent are thrown out of solution, whereby the magnetic particles become coated with a sticky, adherent coating of the resin and fluoragent.
- the water dispersion of magnetic particles is formed under conditions of high shear.
- thermoplastic resin which is preferably a melamine-toluene sulfonamide-formaldehyde resin, is insoluble in water and therefore precipitates out upon dilution of the resin-fluoragent solution with the water of the water dispersion magnetic particles.
- This invention relates to a fluorescent composition for magnetic particle inspection and to a method of making the same.
- Non-destructive methods of testing structures of ferromagnetic material (herein sometimes referred to as test pieces, or work pieces), by the use of fluorescent magnetic particles have been described in Patents Nos. 2,267,999, 2,936,287 and others. Such methods involve the inspection of the test piece in the substantial absence of visible light but under filtered ultraviolet light, usually referred to as Black Light.
- fluorescent magnetic particles as compared with magnetic particles having only their natural visible coloration, is that there is a greatly increased contrast between the fluorescent magnetic particles and the background of the test piece, thereby giving a greatly increased sensitivity in the inspection of the surface for indications of surface discontinuities, flaws and the like.
- thermoplastic resinous fluorescent coating is applied to the magnetic cores, as the initial, uncoated magnetic particles are termed herein.
- a solvent is used for dissolving the thermoplastic resin that is relatively miscible with water and that can be removed from the coatings after application to the magnetic cores by the simple step of suspending and agitating the coated particles in water. This step simultaneously effects the precipitation on the cores of the resin in a sticky form. Such stickiness is due to the presence of solvent in the resin coating and become less as the solvent is leached out into the Water. Any residual traces of solvent in the coated particles are removed by washing, after which the coated particles are dried and ground.
- Thermoplastic resins are chosen that have softening points of at least C. or over, so that there is no tendency of the resincoated particles to become agglomerated in the grinding thereof due to the generation of heat in the grinding operation.
- thermoplastic resin and the fluoragents may be dissolved separately in the water-miscible solvent to be used, or the resin and the fluoragents may first be combined into a pigment form, in accordance with the method described in Patent No. 2,938,873, or by any suitable method.
- thermoplastic resin and the fluoragents are separately dissolved in the solvent or a pre-formed pigment consisting essentially of the thermoplastic resin and the fluoragents in a solv-ated state in the resin, the result is the same. Since, however, fluorescent thermoplastic resin pigments are available on the market that are suitable for use in accordance with my invention, it is usually less expensive and less trouble to use the available fluorescent thermoplastic resin pigments than to prepare them sepaparately.
- fluoragent is used herein to designate a substance that is capable of emitting visible light under invisible fluorescigenous radiation, such as Black Light.
- two or more fluoragents are used in the resinous coating for the magnetic cores in making my fluorescent composition.
- At least one of the fluoragents used is a fluorescent dye capable by itself of emitting visible light when subjected to fluorescigenous radiation to exhibit a color brightness that is more than twice that which would be due to reflectance alone, as in the case of a visible dye.
- the other of the plurality of fluoragents may be also a fluorescent dye, recognized as such, or it may be a substance having a different absorption-emission curve from that of the principal fluorescent dye and capable of exhibiting a cascading effect therewith.
- cascading is used in the sense in which it is used in Patent No. 2,920,203, and for a further explanation of the term reference is made to that patent.
- a substance may be used that is not usually termed a fluorescent dye, but which exhibits the property of absorption of rays in the ultraviolet region, with emission of additional visible light over and above what would be reflected if the substance were subjected to visible light radiation only.
- the term opacifier has been applied to this second, or additional, fluoragent, since it has the property of being relatively opague to ultraviolet light, that is, capable of absorbing ultraviolet light and re-emitting light rays in the visible range.
- the proportions of components of the fluorescent composition of my invention are relatively critical within rather broad limits, variations in proportions are entirely dependent upon the results sought to be achieved.
- equal parts by weight of the magnetic core material and of the coating material may be used, but the proportion may be varied between two parts of the core material to one part of the coating material and one part of the core material to one and one-half parts of the coating material, by weight.
- the amount of fluoragents in the coating composition should not exceed that which is capable of being entirely dissolved, or solvated, in the resin.
- fluoragents In general, from 0.5 to 5.0% of fluoragents may be used based upon the weight of the thermoplastic resin in the coating composition, with the op'acifier, if one is used, present in the proper proportion to give a maximum cascading effect with the fluorescent dye used as the principal fluorescent color.
- Example I (General) Formula: Parts by weight Magnetic powder 100. Resin-fluorescent dye-opacifier mixture 70 to 100. Organic solvent 300 or q.s. to dissolve mixture. Water 3400.
- the magnetic powder is added to water, in the proportion of 100 parts of magnetic powder to 3400 parts of water, in a colloid mill.
- the filter cake from the press filter is added, along with Water, to a ball mill wherein the size of the particles of coated magnetic material is reduced to an average of not over 5 microns.
- the ball-milled mass is then filtered to separate the ground powder and the latter dried in a low temperature oven.
- the resulting dried powder comprises discrete magnetic particles coated with an adherent solvent-free resin film having solvated therein a fluorescent dye and an opacifier having a cascading effect with respect to said dye.
- the cascading effect results in an enhanced fluorescent brightness of color.
- test wheel is a steel wheel that is circumferentially magnetized and provided with a plurality of transverse holes (bores) positioned at progressively greater distances radially inwardly of the periphery of the wheel to simulate defects in a workpiece.
- An acceptable fluorescent magnetic particle finds up to about 7 indications on such a wheel;
- Items 4 and 5 show that the fluorescent composition of my invention is not well adapted for use in oily vehicles often used for suspending magnetic particles but is especially well adapted for suspension in water as a water suspension for magnetic particle testing.
- thermoplastic resins that can be used in Example I are the following:
- Amino-triazine-sulfonamide-aldehyde resins specifically, melamine sulfonamide-formaldehyde; benzoguanaminesulfonamide-formaldehyde and other thermoplastic resins of Patent No. 2,938,873.
- Polystyrene resins Water-white or transparent.
- Zinc resinates i.e., zincor zinc-calcium resinates that are permanently refusible and have melting points of above about C. (capillary tube).
- suitable fluorescent dyes the following are named:
- Rhodamines xanthenes
- rhodamine B Extra e.g., rhodamine B Extra
- rhodamine 6 GDN Extra rhodamine 6 GDN Extra
- xylene red Naphthalimides e.g. brilliant yellow (6 G base)
- (4 N- butylamino) 1,8 naphthal N-butylimide Coumarins e.g. dimethyl amino coumarin; 4 methyl 7 diethyl amino coumarin Stilbenes; e.g. p, p di [p" (p" amino benzoylamino) benzoylamino] stilbene 0,0 di ⁇ sodium sulfonate] Fluorols (General Aniline & Chemical Co.); e.g. Fluorol 7GA, Fluorol SGA.
- Suitable opacifiers e.g. 2 hydroxy 1, naphthaldazine
- suitable opacifiers the following are named:
- Multi-ring benzenoid hydrocarbons e.g. anthracene (C H 2) C6H4) py (CISHIO) fluoranthene (C H Fused polycyclic hydrocarbons Pentalene Ovalene
- C H Fused polycyclic hydrocarbons Pentalene Ovalene In general, all materials that fluoresce blue-white and cascade the fluorescent dyes have proven satisfactory. There are thirty five of these materials, the structural formulae of which are listed in the Chemical Rubber Handbook, 45th Edition, pp. O-11 and C-12.
- Suitable water-miscible organic solvents are the following:
- Example II (Specific) Formula: Parts by weight Magnetic powder, as a mixture of gamma Fe O synthetic and natural magnetite, Fe (average particle size less than 6 microns) 25 Resin, melamine-sulfonamide-aldehyde- 20 Fluorescent dye, Fluorol 7GA 1 Opacifier, fiuoranthene 4 Organic solvent, dimethyl formamide 75 Water 750-1000
- a thermoplastic zincor zinc-calcium resinate such as described in Patents Nos. 2,346,992 and 2,346,993, respectively, can be substituted, without change in the other components for the amounts of the resin components given in said example.
- a zinc resinate is available on the market under the trademark Zitro of Heyden Newport Chemical Company, a division of Tennessee Gas Transmission Company.
- Procedure-The resin, dye and opacifier are dissolved in the dimethyl formamide to form a solution thereof.
- the magnetic powder is separately milled in water to a particle size of less than microns, if necessary.
- the separately formed resin-solvent-dye-solution is then added to the water suspension of the magnetic powder in the mill, and agitation is continued until a sample removed from the mill, after washing with Water and drying, shows maximum fluorescent brightness.
- the entire mass is then dumped, filtered, and the filter cake washed and dried.
- the resulting particles comprise the magnetic cores and resinous coatings in approximately equal proportions by weight.
- the final fluorescent composition prepared as described above, can be made into a concentrated aqueous paste of the fluorescent magnetic particles for dilution when used,
- the usual concentration is approximately oz. of the fluorescent composition per gal. of water, but the concentration can vary between and ,4 oz. per gal.
- My fluorescent composition has the advantage of being physically resistant to fragmentation during agitation and circulation of the water suspension of the fluorescent magnetic particles and also resistant to bleeding of color into the water of the suspension. Additionally, because of the cascading effect, the composition has as good, if not better, brightness than heretofore known fluorescent magnetic particle compositions. In general, it is less expensive to manufacture and presents fewer manufacturing problems, especially when a pre-formed resin-dye-opacifier, such as a daylight fluorescent color pigment, is used.
- thermoplastic resin and fluoragent dissolving a thermoplastic resin and a fluoragent in a water-miscible organic solvent to form a solution of said resin and fluoragent
- said water dispersion of magnetic particles is formed under conditions of high shear.
- said opacifier is a multi-ring benzenoid hydrocarbon having absorption in the ultraviolet range and having a cascading effect upon the fluorescent dye. 4.
- the method of making a fluorescent magnetic material which comprises the steps of dissolving a mixture of a water insoluble thermoplastic resin, a fluorescent dye and an opacifier having a cascading effect with respect to said dye in a watermiscible organic solvent to form a solution of said mixture,
- said organic solvent is dimethyl-sulfoxid'e.
- thermoplastic resin is a triazine-sulfonamideformaldehyde resin.
- thermoplastic resin is a zinc resinate.
- thermoplastic resin is a melamine-sulfonamideformaldehyde condensation product
- said organic solvent is dimethyl formamide
- said dye is a naphthalimide
- said opacifier is fiuoroanthene.
- a composition of matter comprising discrete magnetic particles coated with a thermoplastic resin containing a fluorescent dye and an opacifier selected from the group consisting of fluorescent multi-ring benzenoid hydrocarbons, pyrene, fluoranthene and fluorescent fused polycyclic hydrocarbons, said opacifier having a cascading effect in combination with said dye, said coated particles having an average particle size of not over about 5 microns.
- thermoplastic resin is a triazine-sulfonamide-formaldehyde resin.
- composition as defined in claim 12, wherein said opacifier is fiuoranthene.
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Description
United States Patent 3,404,093 FLUORESCENT COMPOSITION FOR MAGNETIC PARTICLE INSPECTION Paul Kenneth Borrows, Chicago, Ill., assignor to Magnallux Corporation, Chicago, Ill., a corporation of Delaware No Drawing. Filed Mar. 29, 1965, Ser. No. 443,705 17 Claims. (Cl. 252-6252) ABSTRACT OF THE DISCLOSURE A fluorescent magnetic material for use in non-destructive methods of testing ferromagnetic work pieces, comprising discrete magnetic particles coated with a thermoplastic resin containing a fluorescent dye, preferably in combination with an opacifier having a cascading effect in combination with said dye, the coated particles having an average particle size preferably of not over about 5 microns maximum dimension. The method of coating includes dissolving a thermoplastic resin and a fluoragent in a water-miscible organic solvent to form a solution thereof, separately forming a water dispersion of highly divided magnetic particles, and then adding the solution to the water dispersion with thorough mixing until the resin and fluoragent are thrown out of solution, whereby the magnetic particles become coated with a sticky, adherent coating of the resin and fluoragent. The water dispersion of magnetic particles is formed under conditions of high shear. The thermoplastic resin, which is preferably a melamine-toluene sulfonamide-formaldehyde resin, is insoluble in water and therefore precipitates out upon dilution of the resin-fluoragent solution with the water of the water dispersion magnetic particles.
This invention relates to a fluorescent composition for magnetic particle inspection and to a method of making the same.
Non-destructive methods of testing structures of ferromagnetic material (herein sometimes referred to as test pieces, or work pieces), by the use of fluorescent magnetic particles have been described in Patents Nos. 2,267,999, 2,936,287 and others. Such methods involve the inspection of the test piece in the substantial absence of visible light but under filtered ultraviolet light, usually referred to as Black Light. One of the advantages of using fluorescent magnetic particles, as compared with magnetic particles having only their natural visible coloration, is that there is a greatly increased contrast between the fluorescent magnetic particles and the background of the test piece, thereby giving a greatly increased sensitivity in the inspection of the surface for indications of surface discontinuities, flaws and the like.
Heretofore used fluorescent compositions, however, have been relatively expensive and diflicult to manufacture. In order for the fluorescent composition to be satisfactory for use in magnetic particle inspection methods the composition must possess a high order of visible brightness when viewed under Black Light and the particles making up the fluorescent composition must be relatively resistant to physical change as a result of rubbing forces tending to separate the fluorescent coating from the magnetic particles, during, for instance, the agitation of baths containing suspensions of such fluorescent-coated magnetic particles. Also, there is the problem of separation of the fluorescent pigment coating from the magnetic particle during grinding of the composition to obtain the very fine particle size desired in the finished product.
It is therefore an important object of the present invention to provide an improved method of bonding a fluo- 3,404,093 Patented Oct. 1, 1968 rescent coating to magnetic particles so as to increase the resistance of the particles to separation of the coating from the particles during grinding thereof and during use of the composition when suspended in liquids subjected to severe agitation in agitated and circulated systems.
It is a further important object of this invention to provide fluorescent compositions for magnetic particle inspection that have increased fluorescent brightness and therefore a higher degree of visibility; that permit of a wider choice of colors at lower cost and with greater ease of manufacture.
Other and further important objects of this invention will become apparent from the following description and appended claims.
In the method of making fluorescent compositions according to my present invention, a thermoplastic resinous fluorescent coating is applied to the magnetic cores, as the initial, uncoated magnetic particles are termed herein. In forming the coating, a solvent is used for dissolving the thermoplastic resin that is relatively miscible with water and that can be removed from the coatings after application to the magnetic cores by the simple step of suspending and agitating the coated particles in water. This step simultaneously effects the precipitation on the cores of the resin in a sticky form. Such stickiness is due to the presence of solvent in the resin coating and become less as the solvent is leached out into the Water. Any residual traces of solvent in the coated particles are removed by washing, after which the coated particles are dried and ground. The removal of the residual solvent from the coated particles leaves the resin coating of the particles firmly adherent to the magnetic cores as a relatively hard and high melting point, solvent-free resin. Thermoplastic resins are chosen that have softening points of at least C. or over, so that there is no tendency of the resincoated particles to become agglomerated in the grinding thereof due to the generation of heat in the grinding operation.
In the coating of the magnetic cores the thermoplastic resin and the fluoragents may be dissolved separately in the water-miscible solvent to be used, or the resin and the fluoragents may first be combined into a pigment form, in accordance with the method described in Patent No. 2,938,873, or by any suitable method. Whether the thermoplastic resin and the fluoragents are separately dissolved in the solvent or a pre-formed pigment consisting essentially of the thermoplastic resin and the fluoragents in a solv-ated state in the resin, the result is the same. Since, however, fluorescent thermoplastic resin pigments are available on the market that are suitable for use in accordance with my invention, it is usually less expensive and less trouble to use the available fluorescent thermoplastic resin pigments than to prepare them sepaparately.
The term fluoragent is used herein to designate a substance that is capable of emitting visible light under invisible fluorescigenous radiation, such as Black Light. Preferably, two or more fluoragents are used in the resinous coating for the magnetic cores in making my fluorescent composition. At least one of the fluoragents used is a fluorescent dye capable by itself of emitting visible light when subjected to fluorescigenous radiation to exhibit a color brightness that is more than twice that which would be due to reflectance alone, as in the case of a visible dye. The other of the plurality of fluoragents may be also a fluorescent dye, recognized as such, or it may be a substance having a different absorption-emission curve from that of the principal fluorescent dye and capable of exhibiting a cascading effect therewith. The term cascading is used in the sense in which it is used in Patent No. 2,920,203, and for a further explanation of the term reference is made to that patent.
Instead of using a second, or additional fluorescent dye to obtain the cascading eflect desired, a substance may be used that is not usually termed a fluorescent dye, but which exhibits the property of absorption of rays in the ultraviolet region, with emission of additional visible light over and above what would be reflected if the substance were subjected to visible light radiation only. The term opacifier has been applied to this second, or additional, fluoragent, since it has the property of being relatively opague to ultraviolet light, that is, capable of absorbing ultraviolet light and re-emitting light rays in the visible range.
While the proportions of components of the fluorescent composition of my invention are relatively critical within rather broad limits, variations in proportions are entirely dependent upon the results sought to be achieved. In general, equal parts by weight of the magnetic core material and of the coating material may be used, but the proportion may be varied between two parts of the core material to one part of the coating material and one part of the core material to one and one-half parts of the coating material, by weight. The amount of fluoragents in the coating composition should not exceed that which is capable of being entirely dissolved, or solvated, in the resin. In general, from 0.5 to 5.0% of fluoragents may be used based upon the weight of the thermoplastic resin in the coating composition, with the op'acifier, if one is used, present in the proper proportion to give a maximum cascading effect with the fluorescent dye used as the principal fluorescent color.
The following examples, giving general and specific formulae and procedures, will serve as illustrations of how my invention can be practiced to best advantage. It will be understood, however, that the examples are by way of illustration only and are not by way of limitation upon the scope of my invention.
Example I (General) Formula: Parts by weight Magnetic powder 100. Resin-fluorescent dye-opacifier mixture 70 to 100. Organic solvent 300 or q.s. to dissolve mixture. Water 3400.
Procedure:
(1) The resin, fluorescent dye and opacifier, either as separate components or as an admixture in which the fluorescent dye and opacifier are present in solvated state in the resin, are dissolved in the organic solvent to form a solution thereof.
(2) The magnetic powder is added to water, in the proportion of 100 parts of magnetic powder to 3400 parts of water, in a colloid mill.
(3) The colloid mill is run at V3 its rated speed for 15 minutes during which time the mill clearance is reduced from 0.020" to 0.005".
(4) Clearance is then increased to 0.030" and solution (1) is dumped in.
(5) The colloid mill is run for an additional period of 15 minutes at the same speed.
(6) The contents of the colloid mill are drained out and the dispersion run into a filter press, wherein the press cake is washed with clear water to remove all residual organic solvent from the filter cake.
(7) The filter cake from the press filter is added, along with Water, to a ball mill wherein the size of the particles of coated magnetic material is reduced to an average of not over 5 microns.
(8) The ball-milled mass is then filtered to separate the ground powder and the latter dried in a low temperature oven.
The resulting dried powder comprises discrete magnetic particles coated with an adherent solvent-free resin film having solvated therein a fluorescent dye and an opacifier having a cascading effect with respect to said dye. The cascading effect results in an enhanced fluorescent brightness of color.
The coated magnetic material prepared in accordance with my invention has the following properties and characteristics:
(1) A brightness on a Fischer spectrophotometer twice, and usually two and one-half times, the brightness under filtered ultra-violet light (black light) of the fluorescent dye, by itself, used in the material;
(2) A capability to find at least 10 and usually 15 indications on a test wheel. The test wheel is a steel wheel that is circumferentially magnetized and provided with a plurality of transverse holes (bores) positioned at progressively greater distances radially inwardly of the periphery of the wheel to simulate defects in a workpiece. An acceptable fluorescent magnetic particle finds up to about 7 indications on such a wheel;
(3) A magnetic reading of 30, and usually about 40. Such magnetic reading is determined with the powder as the core in an electromagnetic coupling having a unity reading with air only as the core;
(4) Very poor oil durability in terms of mechanical stability against attrition or loss in weight of the individual particles when agitated in oil; but
(5) Good water durability or resistance to physical change and dye or opacifier when agitated in water containing a wetting agent as the bath.
Items 4 and 5 show that the fluorescent composition of my invention is not well adapted for use in oily vehicles often used for suspending magnetic particles but is especially well adapted for suspension in water as a water suspension for magnetic particle testing.
Suitable thermoplastic resins that can be used in Example I are the following:
Amino-triazine-sulfonamide-aldehyde resins specifically, melamine sulfonamide-formaldehyde; benzoguanaminesulfonamide-formaldehyde and other thermoplastic resins of Patent No. 2,938,873.
Polystyrene resins, Water-white or transparent.
Terpene resins.
Zinc resinates, i.e., zincor zinc-calcium resinates that are permanently refusible and have melting points of above about C. (capillary tube). As examples of suitable fluorescent dyes, the following are named:
Rhodamines (xanthenes); e.g., rhodamine B Extra; rhodamine 6 GDN Extra; xylene red Naphthalimides; e.g. brilliant yellow (6 G base); (4 N- butylamino) 1,8 naphthal N-butylimide Coumarins; e.g. dimethyl amino coumarin; 4 methyl 7 diethyl amino coumarin Stilbenes; e.g. p, p di [p" (p" amino benzoylamino) benzoylamino] stilbene 0,0 di {sodium sulfonate] Fluorols (General Aniline & Chemical Co.); e.g. Fluorol 7GA, Fluorol SGA.
Azines; e.g. 2 hydroxy 1, naphthaldazine As examples of suitable opacifiers, the following are named:
Multi-ring benzenoid hydrocarbons; e.g. anthracene (C H 2) C6H4) py (CISHIO) fluoranthene (C H Fused polycyclic hydrocarbons Pentalene Ovalene In general, all materials that fluoresce blue-white and cascade the fluorescent dyes have proven satisfactory. There are thirty five of these materials, the structural formulae of which are listed in the Chemical Rubber Handbook, 45th Edition, pp. O-11 and C-12.
Examples of suitable water-miscible organic solvents are the following:
N,N-dimethyl formamide (DMF) Dimethyl sulfoxide (DMSO) N-methyl-2-pyrrolidone Acetone (dimethyl ketone) Pyrazine Piperidine Diox-ane Morpholine Pyridine Azedine Dimethyl acetamide Any of the foregoing components can be substituted for the corresponding generally named components of the Formula of Example I in like amounts to those therein specified with generally satisfactory results.
Example II (Specific) Formula: Parts by weight Magnetic powder, as a mixture of gamma Fe O synthetic and natural magnetite, Fe (average particle size less than 6 microns) 25 Resin, melamine-sulfonamide-aldehyde- 20 Fluorescent dye, Fluorol 7GA 1 Opacifier, fiuoranthene 4 Organic solvent, dimethyl formamide 75 Water 750-1000 In place of the melamine-sulfonamide-formaldehyde resin in Example II, a thermoplastic zincor zinc-calcium resinate such as described in Patents Nos. 2,346,992 and 2,346,993, respectively, can be substituted, without change in the other components for the amounts of the resin components given in said example. A zinc resinate is available on the market under the trademark Zitro of Heyden Newport Chemical Company, a division of Tennessee Gas Transmission Company.
Procedure-The resin, dye and opacifier are dissolved in the dimethyl formamide to form a solution thereof. The magnetic powder is separately milled in water to a particle size of less than microns, if necessary. The separately formed resin-solvent-dye-solution is then added to the water suspension of the magnetic powder in the mill, and agitation is continued until a sample removed from the mill, after washing with Water and drying, shows maximum fluorescent brightness. The entire mass is then dumped, filtered, and the filter cake washed and dried. The resulting particles comprise the magnetic cores and resinous coatings in approximately equal proportions by weight.
The final fluorescent composition, prepared as described above, can be made into a concentrated aqueous paste of the fluorescent magnetic particles for dilution when used,
or can be sold as a dry powder for use in magnetic particle testing or for other purposes, such as for magnetic inks to identify checking accounts and the like. When made into a water suspension for magnetic particle inspection of magnetizable test pieces for surface discontinuities, the usual concentration is approximately oz. of the fluorescent composition per gal. of water, but the concentration can vary between and ,4 oz. per gal.
My fluorescent composition has the advantage of being physically resistant to fragmentation during agitation and circulation of the water suspension of the fluorescent magnetic particles and also resistant to bleeding of color into the water of the suspension. Additionally, because of the cascading effect, the composition has as good, if not better, brightness than heretofore known fluorescent magnetic particle compositions. In general, it is less expensive to manufacture and presents fewer manufacturing problems, especially when a pre-formed resin-dye-opacifier, such as a daylight fluorescent color pigment, is used. Prior to my discovery of the feasibility of using organic solvents that have solvent action toward all of the thermoplastic resins, fluorescent dyes and opacifiers used in making my fluorescent composition and that are miscible with water, no method was available to the best of my knowledge, for making a satisfactory fluorescent composition for magnetic particle inspection from the individual components, or from already formed daylight fluorescent resinous pigments.
The latter pigments are available on the market under the proprietary names, Day-G10, of Switzer Brothers, Inc., and Hy Viz, of Lawter Chemical Co.
It will be understood that modifications and variations may be elfected without departing from the scope of the novel concepts of the present invention.
I claim as my invention:
1. The method of making a fluorescent magnetic material in particulate form, which comprises:
dissolving a thermoplastic resin and a fluoragent in a water-miscible organic solvent to form a solution of said resin and fluoragent,
separately forming a water dispersion of finely divided magnetic particles, and
adding said solution to said water dispersion with thorough mixing until said resin and fluoragent are thrown out of solution,
whereby said magnetic particles become coated with a sticky, adherent coating of said resin and fluoragent.
2. The method as defined in claim 1, wherein said fluoragent is initially in a solvated state in said resin, and
said water dispersion of magnetic particles is formed under conditions of high shear.
3. The method as defined in claim 1, wherein said fluoragent includes a dye and opacifier, and
said opacifier is a multi-ring benzenoid hydrocarbon having absorption in the ultraviolet range and having a cascading effect upon the fluorescent dye. 4. The method of making a fluorescent magnetic material which comprises the steps of dissolving a mixture of a water insoluble thermoplastic resin, a fluorescent dye and an opacifier having a cascading effect with respect to said dye in a watermiscible organic solvent to form a solution of said mixture,
separately forming a water suspension of dispersed finely ground particles of magnetic material of an average particle size less than 5 microns, adding with agitation said solution of said mixture to said suspension in such proportions of said solution and said Water suspension as to elfect a precipitation of said mixture upon said magnetic particles to coat the same while said mixture is in a sticky, adhesive condition due to the presence of residual solvent therein, and
continuing agitation until the coating of said particles and the removal of said residual solvent from said coating have been substantially completed,
whereby there results a mass of discrete magnetic particles coated with a substantially solvent-free resin containing said fluorescent dye and opacifier and having a brightness exceeding that due to the fluorescent brightness of said dye alone.
5. The method as defined in claim 4, wherein said organic solvent is dimethyl formamide.
6. The method as defined in claim 4, wherein,
said organic solvent is dimethyl-sulfoxid'e.
7. The method as defined in claim 4, wherein said thermoplastic resin is a triazine-sulfonamideformaldehyde resin.
8. The method as defined in claim 4, wherein said thermoplastic resin is a zinc resinate.
9. The method as defined in claim 4, wherein said opacifier is fluoranthene.
10. The method as defined in claim 4, wherein said opacifier is anthracene.
11. The method as defined in claim 4, wherein said thermoplastic resin is a melamine-sulfonamideformaldehyde condensation product,
said organic solvent is dimethyl formamide,
said dye is a naphthalimide, and
said opacifier is fiuoroanthene.
12. A composition of matter comprising discrete magnetic particles coated with a thermoplastic resin containing a fluorescent dye and an opacifier selected from the group consisting of fluorescent multi-ring benzenoid hydrocarbons, pyrene, fluoranthene and fluorescent fused polycyclic hydrocarbons, said opacifier having a cascading effect in combination with said dye, said coated particles having an average particle size of not over about 5 microns.
13. A composition as defined in claim 12, wherein the thermoplastic resin is a triazine-sulfonamide-formaldehyde resin.
14. A composition as defined in claim 12, wherein said opacifier is fiuoranthene.
15. A composition as defined in claim 12, wherein said magnetic particles comprise a mixture of gamma Fe O and natural magnetite, Fe O said thermoplastic resin is a melamine-sulfonamide-formaldehyde resin and said opacifier is fluoranthene.
16. An aqueous suspension of the composition as defined in claim 12.
17. An aqueous suspension of the composition as defined in claim 15.
References Cited UNITED STATES PATENTS 2,809,954 lO/l957 Kazenas 252-301.2 2,920,203 1/ 1960 SWitZer et a1 252-3012 2,936,287 5/1960 Kazenas 252-6252 3,242,051 3/ 1966 Hiestand et a1. 3,265,629 8/ 1966 Jensen.
TOBIAS E. LEVOW, Primary Examiner.
ROBERT D. EDMONDS, Assistant Examiner.
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US443705A US3404093A (en) | 1965-03-29 | 1965-03-29 | Fluorescent composition for magnetic particle inspection |
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US443705A US3404093A (en) | 1965-03-29 | 1965-03-29 | Fluorescent composition for magnetic particle inspection |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3485758A (en) * | 1967-06-27 | 1969-12-23 | Magnaflux Corp | Method of making fluorescent magnetic particles |
US4273671A (en) * | 1979-09-18 | 1981-06-16 | The United States Of America As Represented By The Secretary Of The Air Force | Fluorescent detection of flaws |
US4331871A (en) * | 1979-09-18 | 1982-05-25 | The United States Of America As Represented By The Secretary Of The Air Force | Fluorescent detection of flaws |
US4361806A (en) * | 1980-07-07 | 1982-11-30 | Magnaflux Corporation | Method using aqueous emulsion having magnetizable particles for detecting flaws in magnetizable workpieces |
US4433289A (en) * | 1981-01-15 | 1984-02-21 | Magnaflux Corporation | Method for inspecting steel billets with a dry mixture of magnetic particles and a water soluble carrier solid |
US4724094A (en) * | 1985-02-07 | 1988-02-09 | Magnaflux Corporation | Fluorescent magnetic composition and method of making and using same |
US6528165B2 (en) * | 1999-08-17 | 2003-03-04 | Luminex Corporation | Encapsulation of discrete quanta of fluorescent particles |
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US2809954A (en) * | 1954-01-26 | 1957-10-15 | Switzer Brothers Inc | Thermoplastic melamine-sulfonamideformaldehyde resinous materials and process for making same |
US2920203A (en) * | 1955-09-21 | 1960-01-05 | Switzer Brothers Inc | Fluorescent penetrant inspection materials and methods |
US2936287A (en) * | 1956-08-01 | 1960-05-10 | John D Steele | Magnetic particles |
US3242051A (en) * | 1958-12-22 | 1966-03-22 | Ncr Co | Coating by phase separation |
US3265629A (en) * | 1958-12-22 | 1966-08-09 | Ncr Co | Coating by phase separation |
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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US2809954A (en) * | 1954-01-26 | 1957-10-15 | Switzer Brothers Inc | Thermoplastic melamine-sulfonamideformaldehyde resinous materials and process for making same |
US2920203A (en) * | 1955-09-21 | 1960-01-05 | Switzer Brothers Inc | Fluorescent penetrant inspection materials and methods |
US2936287A (en) * | 1956-08-01 | 1960-05-10 | John D Steele | Magnetic particles |
US3242051A (en) * | 1958-12-22 | 1966-03-22 | Ncr Co | Coating by phase separation |
US3265629A (en) * | 1958-12-22 | 1966-08-09 | Ncr Co | Coating by phase separation |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3485758A (en) * | 1967-06-27 | 1969-12-23 | Magnaflux Corp | Method of making fluorescent magnetic particles |
US4273671A (en) * | 1979-09-18 | 1981-06-16 | The United States Of America As Represented By The Secretary Of The Air Force | Fluorescent detection of flaws |
US4331871A (en) * | 1979-09-18 | 1982-05-25 | The United States Of America As Represented By The Secretary Of The Air Force | Fluorescent detection of flaws |
US4361806A (en) * | 1980-07-07 | 1982-11-30 | Magnaflux Corporation | Method using aqueous emulsion having magnetizable particles for detecting flaws in magnetizable workpieces |
US4433289A (en) * | 1981-01-15 | 1984-02-21 | Magnaflux Corporation | Method for inspecting steel billets with a dry mixture of magnetic particles and a water soluble carrier solid |
US4724094A (en) * | 1985-02-07 | 1988-02-09 | Magnaflux Corporation | Fluorescent magnetic composition and method of making and using same |
US6528165B2 (en) * | 1999-08-17 | 2003-03-04 | Luminex Corporation | Encapsulation of discrete quanta of fluorescent particles |
US20030132538A1 (en) * | 1999-08-17 | 2003-07-17 | Luminex Corporation | Encapsulation of discrete quanta of fluorescent particles |
US6905766B2 (en) | 1999-08-17 | 2005-06-14 | Luminex Corporation | Encapsulation of discrete quanta of fluorescent particles |
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