WO1994005732A2 - Carbon blacks - Google Patents
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- WO1994005732A2 WO1994005732A2 PCT/US1993/008129 US9308129W WO9405732A2 WO 1994005732 A2 WO1994005732 A2 WO 1994005732A2 US 9308129 W US9308129 W US 9308129W WO 9405732 A2 WO9405732 A2 WO 9405732A2
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- WIPO (PCT)
- Prior art keywords
- carbon black
- carbon blacks
- epdm
- carbon
- blacks
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/44—Carbon
- C09C1/48—Carbon black
- C09C1/50—Furnace black ; Preparation thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/62—Submicrometer sized, i.e. from 0.1-1 micrometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/19—Oil-absorption capacity, e.g. DBP values
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/22—Rheological behaviour as dispersion, e.g. viscosity, sedimentation stability
Definitions
- the present invention relates to new carbon blacks which are suitable for various applications and particularly well suited for use in plastic and rubber compositions.
- Carbon blacks may be utilized as pigments, fillers, reinforcing agents, and for a variety of other applications. They are widely used in the preparation of rubber compositions and plastic compositions where it is desirable to achieve an optimal combination of compound processing characteristics and physical properties of fabricated parts.
- Carbon blacks are generally characterized on the basis of their properties including, but not limited to, their surface areas, surface chemistry, aggregate sizes, and particle sizes.
- I 2 No. iodine adsorption number
- DBP dibutyl phthalate adsorption
- TINT Tint value
- Dst Dst
- Dmode Dst/Dmode
- the first class of carbon blacks has an Iodine adsorption number (I 2 No.) of 17-23 mg/g (milligrams I 2 per gram carbon black) and a DBP (dibutyl phthalate value) of 115-150 cc/lOOg (cubic centimeters of dibutyl phthalate per 100 grams carbon black) .
- this class of carbon blacks is characterized by having an I 2 No. of about 20 mg/g.
- the second class of carbon blacks has an I 2 No. of 10-19 mg/g and a DBP of 70-95 cc/lOOg.
- the third class of carbon blacks has an I 2 No. of 12-20 mg/g and a DBP of 34-65 cc/lOOg.
- this class of carbon blacks is characterized by having an I 2 No. of 14-18 mg/g and a DBP of 36-55 cc/lOOg, and more preferably a DBP of either 36-42 cc/lOOg or 45-55 cc/lOOg.
- the fourth class of carbon blacks has an I 2 No. of 28-43 mg/g, and a DBP of 28-47 cc/lOOg.
- this class of carbon blacks is characterized by having an I 2 No. of 30- 42mg/g.
- the fifth class of carbon blacks has an I 2 No. of 8-32 mg/g / a DBP of 28-150 cc/lOOg and an M-Ratio of 1.25-2.00.
- the sixth class of carbon blacks has an I 2 No. of 33-70 mg/g, a DBP of 28-60 cc/lOOg and an M-Ratio of 1.25-2.00.
- the seventh class of carbon blacks has an I 2 No. of 42-50 mg/g, a DBP of 61-105 cc/lOOg and an M-Ratio of 1.25-2.00.
- the eighth class of carbon blacks has an I 2 No. of 51-62 mg/g, a DBP of 61-125 cc/lOOg and an M-Ratio of 1.25-2.00.
- the ninth class of carbon blacks has an I 2 No. of 63-70 mg/g, a DBP of 61-105 cc/lOOg and an M-Ratio of 1.25-2.00.
- the carbon blacks of the present invention may be produced in a furnace carbon black reactor having a combustion zone, a transition zone, and a reaction zone.
- a carbon black yielding feedstock is injected into a hot combustion gas stream.
- the resultant mixture of hot combustion gases and feedstock passes into the reaction zone.
- Pyrolysis of the carbon black yielding feedstock is stopped by quenching the mixture after the carbon blacks of the present invention have been formed.
- pyrolysis is stopped by injecting a quenching fluid.
- the rubbers and plastics for which the novel carbon blacks of this invention are effective include natural and synthetic rubbers and plastics.
- amounts of the carbon black product ranging from about 10 to about 300 parts by weight can be used for each 100 parts by weight of rubber or plastic.
- rubbers or plastics suitable for use with the present invention are natural rubber, synthetic rubber and their derivatives such as chlorinated rubber; copolymers of from about 10 to about 70 percent by weight of styrene and from about 90 to about 30 percent by weight of butadiene such as copolymer of 19 parts styrene and 81 parts butadiene, a copolymer of 30 parts styrene and 70 parts butadiene, a copolymer of 43 parts styrene and 57 parts butadiene and a copolymer of 50 parts styrene and 50 parts butadiene; polymers and copolymers of conjugated dienes such as polybutadiene, polyisoprene, polychloroprene, and the like, and copolymers of such conjugated dienes with an ethylenic group-containing monomer copolymerizable therewith such as styrene, methyl styrene, chlorostyren
- An advantage of the carbon blacks of the present invention is that the carbon blacks are useful for incorporation into natural rubbers, synthetic rubbers, plastics or blends thereof for industrial applications, particularly where compound processing and part performance characteristics are important.
- a further advantage of the carbon blacks of the present invention is that certain of the carbon blacks of the present invention will replace blends of carbon blacks in applications that currently require the use of blends of carbon blacks to achieve desired performance characteristics.
- Figure 1 is a cross-sectional view of a portion of one type of furnace carbon black reactor which may be utilized to produce the carbon blacks of the present invention.
- Figure 2 is a sample histogram of the weight fraction of the aggregates of a carbon black sample versus the Stokes Diameter in a given sample.
- the carbon blacks of the present invention may be produced in a modular, also referred to as "staged", furnace carbon black reactor.
- a section of a typical modular furnace carbon black reactor which may be utilized to produce the carbon black of the present invention is depicted in Figure 1.
- Other details of a typical modular furnace carbon black reactor may be found, for example, in the description contained in U.S. Patent No. 3,922,335, the disclosure of which is herein incorporated by reference.
- a carbon black reactor particularly well-suited for the production of the carbon blacks of the present invention is described in commonly assigned U.S. patent application serial number 07/818,943, filed January 10, 1992, the disclosure of which is hereby incorporated by reference.
- the carbon blacks of the Examples described herein were made by the process described in the 943 application.
- the '943 application describes a process for producing carbon blacks wherein auxiliary hydrocarbon is added to the reaction zone of a multistage reactor and the primary combustion and overall combustion of the reaction are adjusted so that the SSI of the process is less than zero.
- the SSI of the process may be determined by the following relationships:
- the "auxiliary hydrocarbon” comprises hydrogen or any hydrocarbon having a molar hydrogen-to-carbon ratio greater than the molar hydrogen-to-carbon ratio of the feedstock.
- the carbon blacks of the present invention may be produced in a furnace carbon black reactor 2, having a combustion zone 10, which has a zone of converging diameter 11, transition zone 12, entry section 18, and reaction zone 19.
- the diameter of the combustion zone 10, up to the point where the zone of converging diameter 11 begins, is shown as D-l; the diameter of zone 12, as D-2; the diameters of the stepped entry section, 18, as D-4, D-5, D-6, and D-7; and the diameter of zone 19, as D-3.
- the length of the combustion zone 10, up to the point where the zone of converging diameter 11 begins, is shown as L-l; the length of the zone of converging diameter is shown as L-2; the length of the transition zone is shown as L-3; and the lengths of the steps in the reactor entry section, 18, as L-4, L-5, L-6 and L-7.
- hot combustion gases are generated in combustion zone 10, by contacting a liquid or gaseous fuel with a suitable oxidant stream such as air, oxygen, mixtures of air and oxygen or the like.
- fuels suitable for use in contacting the oxidant stream in combustion zone 10 to generate the hot combustion gases are any of the readily combustible gas, vapor, or liquid streams such as natural gas, hydrogen, carbon monoxide, methane, acetylene, alcohol, or kerosene. It is generally preferred, however, to utilize fuels having a high content of carbon-containing /05732 _ g _
- the ratio of air to natural gas utilized to produce the carbon blacks of the present invention may preferably be from about 10:1 to about 100:1.
- the oxidant stream may be preheated.
- the hot combustion gas stream flows downstream from zones 10 and 11 into zones 12, 18, and 19.
- the direction of the flow of hot combustion gases is shown in the figure by the arrow.
- Carbon black-yielding feedstock 30 is introduced at point 32 (located in zone 12), and/or at point 70 (located in zone 11).
- Suitable for use herein as carbon black-yielding hydrocarbon feedstocks which are readily volatilizable under the conditions of the reaction, are unsaturated hydrocarbons such as acetylene; olefins such as ethylene, propylene, butylene; aromatics such as benzene, toluene and xylene; certain saturated hydrocarbons; and other hydrocarbons such as kerosenes, naphthalenes, terpenes, ethylene tars, aromatic cycle stocks and the like.
- unsaturated hydrocarbons such as acetylene; olefins such as ethylene, propylene, butylene; aromatics such as benzene, toluene and xylene; certain saturated hydrocarbons; and other hydrocarbons such as kerosenes, naphthalenes, terpenes, ethylene tars, aromatic cycle stocks and the like.
- carbon black-yielding feedstock 30 is injected in the form of a plurality of streams which penetrate into the interior regions of the hot combustion gas stream to insure a high rate of mixing and shearing of the carbon black-yielding feedstock by the hot combustion gases so as to rapidly and completely decompose and convert the feedstock to carbon black.
- Auxiliary hydrocarbon is introduced at point 70 through probe 72 or through auxiliary hydrocarbon passages 75 in the walls which form the boundaries of zone 12 of the carbon black forming process or through auxiliary hydrocarbon passages 76 in the walls which form the boundaries of zones 18 and/or 19 of the carbon black forming process.
- the auxiliary hydrocarbon may be introduced at any location between the point immediately after the initial combustion reaction of the first-stage fuel and the point immediately before the end of formation of carbon black provided that unreacted auxiliary hydrocarbon eventually enters the reaction zone.
- auxiliary hydrocarbon was introduced through either three or four orifices in the same axial plane as the carbon black yielding feedstock streams.
- the orifices are arranged in an alternating pattern, one feedstock, the next auxiliary hydrocarbon, spaced evenly around the outer periphery of section 12.
- this is merely exemplary and is not intended to be limiting of the methods usable for introducing auxiliary hydrocarbon.
- Quench 60 located at point 62, injecting quenching fluid 50, which may be water, is utilized to stop chemical reaction when carbon blacks are formed.
- Point 62 may be determined in any manner known to the art for selecting the position of a quench to stop pyrolysis.
- One method for determining the position of the quench to stop pyrolysis is by determining the point at which an acceptable toluene extract level for the carbon black is reached. Toluene extract level may be measured by using ASTM Test D1618-83 "Carbon Black Extractables - Toluene Discoloration".
- Q is the distance from the beginning of zone 18 to quench point 62, and will vary according to the position of Quench 60.
- the cooled gases pass downstream into any conventional cooling and separating means whereby the carbon blacks are recovered.
- the separation of the carbon black from the gas stream is readily accomplished by conventional means such as a precipitator, cyclone separator or bag filter. This separation may be followed by pelletizing using, for example, a wet pelletizer.
- Iodine adsorption number of the carbon blacks was determined according to ASTM Test Procedure D 1510. Tinting strength (Tint) of the carbon blacks was determined according to ASTM Test Procedure D3265-85a.
- the DBP (dibutyl phthalate value) of the carbon blacks was determined according to the procedure set forth in ASTM D3493-86.
- the cetyl-trimethyl ammonium bromide absorption value (CTAB) of the carbon blacks was determined according to ASTM Test Procedure D3765-85.
- Dmode, and Dst of the carbon blacks were determined from a histogram of the weight fraction of carbon black versus the Stokes diameter of the carbon black aggregates, as shown in Figure 2.
- the data used to generate the histogram are determined by the use of a disk centrifuge such as the one manufactured by Joyce Loebl Co. Ltd. of Tyne and Wear, United Kingdom.
- the following procedure is a modification of the procedure described in the instruction manual of the Joyce Loebl disk centrifuge file reference DCF 4.008 published on February 1, 1985, the teachings of which are hereby incorporated by reference, and was used in determining the data.
- the procedure is as follows.
- NONIDET P-40 is a registered trademark for a surfactant manufactured and sold by Shell Chemical Co.
- the resulting suspension is dispersed by means of ultrasonic energy for 15 minutes using Sonifier Model No. W 385, manufactured and sold by Heat Systems Ultrasonics Inc., Farmingdale, New York.
- the volume of spin fluid which in this instance is 10 cc of water;
- the density of the spin fluid which in this instance is 0.9975 g/cc at 23 degrees C;
- the disk speed which in this instance is 8000 rpm;
- the data sampling interval which in this instance is 1 second.
- the disk centrifuge is operated at 8000 rpm while the stroboscope is operating. 10 cc of distilled water are injected into the spinning disk as the spin fluid. The turbidity level is set to 0; and 1 cc of the solution of 10% absolute ethanol and 90% distilled water is injected as a buffer liquid. The cut and boost buttons of the disk centrifuge are then operated to produce a smooth concentration gradient between the spin fluid and the buffer liquid and the gradient is monitored visually. When the gradient becomes smooth such that there is no distinguishable boundary between the two fluids, 0.5 cc of the dispersed carbon black in aqueous ethanol solution is injected into the spinning disk and data collection is started immediately. If streaming occurs the run is aborted.
- the disk is spun for 20 minutes following the injection of the dispersed carbon black in aqueous ethanol solution. Following the 20 minutes of spinning, the disk is stopped, the temperature of the spin fluid is measured, and the average of the temperature of the spin fluid measured at the beginning of the run and the temperature of the spin fluid measured at the end of the run is entered into the computer which records the data from the disk centrifuge.
- the data is analyzed according to the standard Stokes equation and is presented using the following definitions:
- Carbon black aggregate a discrete, rigid colloidal entity that is the smallest dispersible unit; it is composed of extensively coalesced particles;
- Stokes diameter the diameter of a sphere which sediments in a viscous medium in a centrifugal or gravitational field according to the Stokes equation.
- a non-spherical object such as a carbon black aggregate, may also be represented in terms of the Stokes diameter if it is considered as behaving as a smooth, rigid sphere of the same density, and rate of sedimentation as the object.
- the customary units are expressed in nanometer diameters.
- Mode (D ode for reporting purposes) The Stokes diameter at the point of the peak (Point A of Figure 2 herein) of the distribution curve for Stokes diameter.
- Median Stokes diameter - (Dst for reporting purposes) the point on the distribution curve of Stokes diameter where 50% by weight of the sample is either larger or smaller. It therefore represents the median value of the determination.
- the modulus, tensile and elongation of the EPDM compositions were measured by the procedure set forth in ASTM
- Rebound data for the EPDM compositions was determined according to the procedure set forth in ASTM D1054, utilizing a ZWICK Rebound Resilience Tester, Model 5109, manufactured by
- the Compression set of the EPDM compositions was determined according to the procedure set forth in ASTM D395, wherein the composition was tested at 150 B F for 70 hours.
- the extrusion shrinkage of the EPDM compositions was determined by the procedure set forth in ASTM D-3674 The extrusion shrinkage was measured on the BRABENDER extruder at 100 a C and 50 rpm using a 5 mm diameter die. 4/05732 _ l3 _
- Mixing energy is the total amount of energy put into the compositions which is determined by integrating the mixing torque curve over the course of the mixing cycle, described hereinafter.
- Cure characteristics of the EPDM compositions were measured using a Monsanto MDR curemeter maintained at 160 B C.
- the tests were conducted according to the instructions furnished with the Monsanto MDR curemeter.
- Composition resistivity was measured on plaque samples 2 inches wide by 6 inches long by 0.085 inch thick.
- the plaques were painted on both ends with a half inch width of silver paint.
- the sample was conditioned to produce a stable reading by cycling from room temperature to 100 ⁇ C and back to room temperature, followed by aging at 90 s C for 24 hours.
- the stabilized resistivity was measured at the end of the aging cycle, and once again after the sample was allowed to cool back to room temperature.
- Examples of the novel carbon blacks of the present invention were prepared in a reactor generally described herein, and as depicted in Figure l, utilizing the reactor conditions and geometry set forth in Table 3.
- the fuel utilized in the combustion reaction was natural gas.
- the auxiliary hydrocarbon used was also natural gas.
- the liquid feedstock utilized had the properties indicated in Table 2 below:
- the carbon blacks of the present invention produced in example runs 1-8 were incorporated into EPDM (ethylene- propylene diene polymethylene) compositions and compared to EPDM compositions incorporating the four control carbon blacks.
- the EPDM compositions were prepared utilizing each of the carbon black samples in an amount of 200 parts by weight in the EPDM Composition Formulation shown below in Table 6. Table 6 - EPDM COMPOSITION FORMULATION
- EPDM - EXXON VISTALON ® 5600 manufactured and sold by EXXON Corporation, Houston, Texas;
- Sunpar 2280 A trade arked oil manufactured and sold by
- Butyl Zimate - A trademarked zinc dibutyldithiocarbamate manufactured and sold by R. T. Vanderbilt
- Methyl Zimate A trademarked zinc dimethyldithiocarbamate manufactured and sold by R. T. Vanderbilt Co. ;
- Sulfasan R - A trademarked 4,4 -dithiodimorpholine, manufactured and sold by Monsanto Co., St.
- the EPDM compositions were produced as follows.
- EPDM was added to the mixer and mixed for approximately 30 seconds.
- the carbon black containing EPDM mixture was mixed for approximately 4 1/2 minutes and then the curing agents, TMTDS, Butyl Zimate, Methyl Zimate, Sulfur and Sulfasan R, were added to the mixture.
- the batch composition was then discharged from the mixer and analyzed by the techniques described herein.
- EPDM compositions incorporating the control carbon blacks A-D were also evaluated according to the procedures described herein. The results are set forth in Tables 8-13 below, where comparisons between EPDM compositions containing carbon blacks of the present invention and EPDM compositions containing the most appropriate control carbon black are made.
- the EPDM composition incorporating the carbon black of the present invention has lower viscosity and lower mixing energy than the EPDM composition incorporating the control carbon black. This indicates that EPDM compositions incorporating the carbon black of the present invention will have improved processibility in comparison with EPDM compositions incorporating the control carbon black.
- EPDM composition incorporating the carbon black of the present invention has a higher extrusion rate than the EPDM compositions incorporating the control carbon black.
- EPDM compositions incorporating the carbon blacks of the present invention may be extruded at higher throughputs than EPDM compositions incorporating the control carbon blacks.
- the EPDM composition incorporating the carbon black of the present invention also has a lower extrusion shrinkage and therefore will have better dimensional control during the extrusion operation than the EPDM compositions incorporating the control carbon blacks.
- the EPDM composition incorporating the carbon black of the present invention has good overall physical properties. Additionally, the carbon blacks of the present invention have a unique combination of surface area and structure that results in the carbon blacks being useful in preparing EPDM compositions that are to be UHF cured. It should be clearly understood that the forms of the present invention herein described are illustrative only and are not intended to limit the scope of the invention.
Abstract
Description
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Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU9401197A HU221383B1 (en) | 1992-08-27 | 1993-08-27 | Carbon blacks and preparations incorporating carbon blacks |
EP06119269A EP1788038B1 (en) | 1992-08-27 | 1993-08-27 | Carbon blacks |
EP93920405A EP0609433B2 (en) | 1992-08-27 | 1993-08-27 | Carbon blacks |
KR1019940701376A KR100296566B1 (en) | 1992-08-27 | 1993-08-27 | Carbon black |
PL303409A PL191404B1 (en) | 1992-08-27 | 1993-08-27 | Carbon black comprising rubber and plastic compositions |
DE69327226T DE69327226D1 (en) | 1992-08-27 | 1993-08-27 | Russian |
BR9305623A BR9305623A (en) | 1992-08-27 | 1993-08-27 | Carbon black and composition of matter |
AU50960/93A AU673855B2 (en) | 1992-08-27 | 1993-08-27 | Carbon blacks |
JP50735694A JP3213908B2 (en) | 1992-08-27 | 1993-08-27 | Carbon black |
UA94005503A UA39863C2 (en) | 1992-08-27 | 1993-08-27 | CARBON CARBON / OPTIONS / AND COMPOSITION CONTAINING CARBON CARBON |
HK98119166A HK1016417A1 (en) | 1992-08-27 | 1998-12-28 | Carbon blacks |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US93579492A | 1992-08-27 | 1992-08-27 | |
US07/935,794 | 1992-08-27 | ||
US8188193A | 1993-06-25 | 1993-06-25 | |
US08/081,881 | 1993-06-25 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO1994005732A2 true WO1994005732A2 (en) | 1994-03-17 |
WO1994005732A3 WO1994005732A3 (en) | 1994-07-21 |
Family
ID=26766084
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1993/008129 WO1994005732A2 (en) | 1992-08-27 | 1993-08-27 | Carbon blacks |
Country Status (17)
Country | Link |
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US (1) | US5456750A (en) |
EP (3) | EP0911371B1 (en) |
JP (1) | JP3213908B2 (en) |
KR (1) | KR100296566B1 (en) |
CN (1) | CN1052253C (en) |
AU (1) | AU673855B2 (en) |
BR (1) | BR9305623A (en) |
CA (1) | CA2121693A1 (en) |
CZ (1) | CZ284059B6 (en) |
DE (2) | DE69334319D1 (en) |
ES (1) | ES2141773T5 (en) |
HK (1) | HK1016417A1 (en) |
HU (1) | HU221383B1 (en) |
RU (1) | RU2118974C1 (en) |
SG (1) | SG49945A1 (en) |
UA (1) | UA39863C2 (en) |
WO (1) | WO1994005732A2 (en) |
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- 1993-08-27 EP EP98122661A patent/EP0911371B1/en not_active Expired - Lifetime
- 1993-08-27 DE DE69334319T patent/DE69334319D1/en not_active Expired - Lifetime
- 1993-08-27 DE DE69327226T patent/DE69327226D1/en not_active Expired - Lifetime
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- 1993-08-27 CZ CZ94983A patent/CZ284059B6/en not_active IP Right Cessation
- 1993-08-27 EP EP93920405A patent/EP0609433B2/en not_active Expired - Lifetime
- 1993-08-27 AU AU50960/93A patent/AU673855B2/en not_active Ceased
- 1993-08-27 ES ES93920405T patent/ES2141773T5/en not_active Expired - Lifetime
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Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
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US5688317A (en) * | 1992-08-27 | 1997-11-18 | Cabot Corporation | Carbon blacks |
US6797763B2 (en) | 1992-08-27 | 2004-09-28 | Bin Chung | Carbon black containing EPDM compositions having either a high gloss or a textured matte finish |
WO1995023196A1 (en) * | 1994-02-25 | 1995-08-31 | Cabot Corporation | Carbon blacks |
US5426147A (en) * | 1994-05-03 | 1995-06-20 | Cabot Corporation | Low permeability rubber compositions |
WO1995029953A1 (en) * | 1994-05-03 | 1995-11-09 | Cabot Corporation | Low permeabilitly rubber compositions |
AU681960B2 (en) * | 1994-05-03 | 1997-09-11 | Cabot Corporation | Low permeabilitly rubber compositions |
CN1097609C (en) * | 1994-05-03 | 2003-01-01 | 卡伯特公司 | Low permeabilitly rubber compositions |
KR100377074B1 (en) * | 1994-05-03 | 2003-06-09 | 캐보트 코포레이션 | Low Permeability Rubber Composition |
EP1233042A3 (en) * | 2001-02-16 | 2003-10-01 | Degussa AG | Carbon black, method for producing the same and use thereof |
US6762236B2 (en) | 2001-02-16 | 2004-07-13 | Degussa Ag | Carbon black, process for its production and its use |
EP1233042A2 (en) * | 2001-02-16 | 2002-08-21 | Degussa AG | Carbon black, method for producing the same and use thereof |
KR100815066B1 (en) * | 2001-02-16 | 2008-03-19 | 에보니크 데구사 게엠베하 | Carbon black, process for its production and its use |
CZ302574B6 (en) * | 2001-02-16 | 2011-07-20 | Evonik Carbon Black Gmbh | Carbon black, process of its preparation, use and rubber mixtures |
US8003069B2 (en) | 2003-09-04 | 2011-08-23 | Evonik Carbon Black Gmbh | Carbon black, method for the production of carbon black or other flame aerosols, and device for carrying out said method |
EP2094511A1 (en) * | 2006-11-13 | 2009-09-02 | Société de Technologie MICHELIN | Elastomer compositions with carbon black |
EP2094511A4 (en) * | 2006-11-13 | 2015-04-15 | Michelin & Cie | Elastomer compositions with carbon black |
JP2015155552A (en) * | 2007-04-24 | 2015-08-27 | キャボット コーポレイションCabot Corporation | Low structure carbon black and method of making the same |
Also Published As
Publication number | Publication date |
---|---|
AU5096093A (en) | 1994-03-29 |
JP3213908B2 (en) | 2001-10-02 |
EP0911371B1 (en) | 2010-02-03 |
KR100296566B1 (en) | 2001-12-01 |
ES2141773T3 (en) | 2000-04-01 |
EP0609433A1 (en) | 1994-08-10 |
HU221383B1 (en) | 2002-09-28 |
CN1084533A (en) | 1994-03-30 |
CA2121693A1 (en) | 1994-03-17 |
EP0609433B1 (en) | 1999-12-08 |
CZ98394A3 (en) | 1994-07-13 |
HU9401197D0 (en) | 1994-07-28 |
EP0609433B2 (en) | 2010-11-10 |
HK1016417A1 (en) | 1999-10-29 |
RU2118974C1 (en) | 1998-09-20 |
CZ284059B6 (en) | 1998-08-12 |
JPH07500631A (en) | 1995-01-19 |
EP1788038A2 (en) | 2007-05-23 |
EP0911371A1 (en) | 1999-04-28 |
WO1994005732A3 (en) | 1994-07-21 |
RU94022962A (en) | 1996-05-20 |
EP1788038B1 (en) | 2012-02-29 |
CN1052253C (en) | 2000-05-10 |
ES2141773T5 (en) | 2011-04-05 |
BR9305623A (en) | 1995-03-07 |
DE69327226D1 (en) | 2000-01-13 |
EP1788038A3 (en) | 2010-11-10 |
DE69334319D1 (en) | 2010-03-25 |
UA39863C2 (en) | 2001-07-16 |
AU673855B2 (en) | 1996-11-28 |
US5456750A (en) | 1995-10-10 |
HUT71052A (en) | 1995-11-28 |
SG49945A1 (en) | 1998-06-15 |
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