The present invention relates to a method of making a hypereutectoid, head-hardened steel rail. The present invention further relates to the hypereutectoid, head-hardened steel rail.
United States railroads, especially the Class 1 railroads (BN, UP, CSX, NS, CP and CN) are demanding higher hardness levels and deeper hardness in the head of railroad rail for improved in-track life (higher hardness gives better wear resistance). The American Railway Engineering and Maintenance-of-Way Association (AREMA) is one of the recognized organizations for promulgating rail specifications in North America. There are three types of AREMA rail steel based on minimum properties: standard strength, intermediate strength, and high strength. The minimum properties for each steel type are set forth in the table below:
The hardness is specified in the rail head only. The above properties as reported and measured herein are tested according to AREMA standards set forth in AREMA Part 2, Manufacture of Rail (2007). To meet the AREMA standards of high strength, the rail must have a fully pearlitic microstructure with substantially no untempered martensite allowed. Generally, the elongation should be 10% or higher for high strength rail steel, although a relatively small number (e.g., about 5 percent) of rails may have an elongation less than 10% but no lower than 9%.
The most difficult grade to produce is the high strength grade. Some rail producers strive to achieve the required properties of high strength steel through accelerated cooling of the rail directly in-line after the rolling mill. Other producers reheat the rail from ambient temperature and then apply accelerated cooling (an off-line process). The process of cooling the rail is called head hardening. In the United States, the currently practiced cooling processes use either water sprays to cool the rail or high volume air manifolds. In all the head hardening processes the rail is cooled at a moderate cooling rate to form a fine pearlitic microstructure and to avoid the formation of untempered martensite which is not allowed by AREMA.
In addition to accelerated cooling to develop a fine pearlite interlamellar spacing, it is known to add alloying elements to the rail steel to increase hardness. Traditionally for the past decade, it has been known in the United States to use high strength head-hardened steel containing 0.80-0.84 wt % C, 0.80-1.1 wt % Mn, 0.20-0.40 wt % Si and 0.20-0.25 wt % Cr. The high carbon level of 0.80-0.84 wt % provides the pearlitic microstructure and at this carbon level the steel is at or slightly above the eutectoid point of the iron-carbon binary phase diagram. Carbon is essential because the pearlitic microstructure that develops contains about 12 wt % iron carbide (cementite) in the form of platelets imbedded alongside platelets of ferrite (forming a lamellar morphology). The cementite platelets provide hardness and wear resistance.
It has long been known that further increases in carbon can provide increased hardness of pearlite as the volume fraction of the hard cementite phase increases. When steel has a carbon level that is above the eutectoid point, however, cementite may form on the prior austenitic grain boundaries. This form of cementite is called proeutectoid cementite and the steel is referred to as hypereutectoid steel. Reduced ductility may occur in hypereutectoid steels if a continuous proeutectoid cementite network develops on the prior austenitic grain boundaries, rendering the steel brittle and unacceptable as a railroad rail.
A first aspect of the invention provides a method of making a hypereutectoid, head-hardened steel rail featuring head hardening a steel rail having a composition containing at least 0.86-1.00 wt % carbon, 0.40-0.75 wt % manganese, 0.40-1.00 wt % silicon, 0.05-0.15 wt % vanadium, 0.015-0.030 wt % titanium, and sufficient nitrogen to react with the titanium to form titanium nitrides. The head hardening is conducted at a cooling rate that, if plotted on a graph with xy-coordinates with the x-axis representing cooling time in seconds and the y-axis representing temperature in Celsius of the surface of the head of the steel rail, is maintained in a region between an upper cooling rate boundary plot defined by an upper line connecting xy-coordinates (0 s, 775° C.), (20 s, 670° C.), and (110 s, 550° C.) and a lower cooling rate boundary plot defined by a lower line connecting xy-coordinates (0 s, 750° C.), (20 s, 610° C.), and (110 s, 500° C.).
According to a second aspect of the invention, a method of making a hypereutectoid, head-hardened steel rail is provided. The method features head hardening a steel rail having a composition containing at least 0.86-1.00 wt % carbon, 0.40-0.75 wt % manganese, 0.40-1.00 wt % silicon, 0.05-0.15 wt % vanadium, 0.015-0.030 wt % titanium, and sufficient nitrogen to react with the titanium to form titanium nitride. The head hardening is conducted at a cooling rate that, if plotted on a graph with xy-coordinates with the x-axis representing cooling time in seconds and the y-axis representing temperature in Celsius of the surface of the head of the steel rail, is maintained in a region between an upper cooling rate boundary plot defined by an upper line connecting xy-coordinates (0 s, 775° C.), (20 s, 670° C.), and (110 s, 550° C.) and a lower cooling rate boundary plot defined by a lower line connecting xy-coordinates (0 s, 750° C.), (20 s, 610° C.), and (110 s, 500° C.). The cooling rate from 0 second to 20 seconds plotted on the graph has an average within a range of 5-10° C./s, and the cooling rate from 20 seconds to 110 seconds plotted on the graph is greater than a comparable air cooling rate.
A third aspect of the invention provides a method of making a hypereutectoid, head-hardened steel rail. According to this aspect, a steel rail composition is formed at a temperature of about 1600° C. to about 1650° C. by sequentially adding manganese, silicon, carbon, aluminum, followed by titanium and vanadium in any order or combination to form a steel rail composition containing at least 0.86-1.00 wt % carbon, 0.40-0.75 wt % manganese, 0.40-1.00 wt % silicon, 0.05-0.15 wt % vanadium, 0.015-0.030 wt % titanium, and sufficient nitrogen to react with the titanium to form titanium nitride. The steel rail is then head hardened at a cooling rate that, if plotted on a graph with xy-coordinates with the x-axis representing cooling time in seconds and the y-axis representing temperature in Celsius of the surface of the head of the steel rail, is maintained in a region between an upper cooling rate boundary plot defined by an upper line connecting xy-coordinates (0 s, 775° C.), (20 s, 670° C.), and (110 s, 550° C.) and a lower cooling rate boundary plot defined by a lower line connecting xy-coordinates (0 s, 750° C.), (20 s, 610° C.), and (110 s, 500° C.).
Other aspects of the invention, including apparatus, systems, articles, compositions, methods, and the like which constitute part of the invention, will become more apparent upon reading the following detailed description of the exemplary embodiments and viewing the drawings.
The accompanying drawings are incorporated in and constitute a part of the specification. The drawings, together with the general description given above and the detailed description of the exemplary embodiments and methods given below, serve to explain the principles of the invention. In such drawings:
Reference will now be made in detail to exemplary embodiments and methods of the invention as illustrated in the accompanying drawings, in which like reference characters designate like or corresponding parts throughout the drawings. It should be noted, however, that the invention in its broader aspects is not limited to the specific details, representative articles and methods, and illustrative examples shown and described in connection with the exemplary embodiments and methods.
Exemplary embodiments of the invention relate to a hypereutectoid rail composition containing relatively high levels of silicon and vanadium. In production, the rail may be accelerated-cooled to achieve high hardness, yield and tensile strength significantly beyond the current AREMA specification for high strength rail. The exemplary steel compositions exhibit one or more of four different but interrelated characteristics. In particularly exemplary embodiments, the four characteristics are all concurrently possessed by the steel to yield the properties shown and explained below. These four concurrent characteristics are:
(1) Increased hardness over the conventional head-hardened C—Mn—Si rail steel through the higher carbon and silicon levels and the addition of vanadium. It is believed that the carbon increases the volume percentage of hard cementite, the silicon hardens the ferrite phase in the pearlite through solid solution strengthening, and vanadium provides precipitation hardening of the pearlitic ferrite phase through the formation of vanadium carbides.
(2) Suppression of harmful continuous proeutectoid cementite networks on the prior austenite grain boundaries. Without suppression of the proeutectoid cementite, the steel will exhibit diminished ductility and toughness. Higher levels of silicon alter the activity of carbon in austenite and thereby suppress proeutectoid cementite from forming at the boundaries. It is believed that the vanadium addition through its combination with carbon alters the morphology of proeutectoid cementite to produce discrete particles instead of continuous networks. The suppression of pro eutectoid cementite networks is also affected by a high cooling rate during transformation from austenite.
(3) Elimination of soft ferrite from forming at the rail surface during decarburization. High temperature heating practices can naturally create oxidizing conditions that cause decarburization. The higher carbon level of exemplified steel described herein is sufficient to allow decarburization to take place but insufficient to cause enough carbon loss to allow the steel to become hypoeutectoid where soft pro eutectoid ferrite forms.
(4) Prevention of heat transfer instability and lower transformation products. By shifting the pearlite transformation to shorter times, a higher cooling rate can be employed without generating undesirable heat transfer instability and bainitic/martensitic microstructures. Lowering the manganese level to within the levels discussed herein achieves this shift.
Generally, in exemplary embodiments a new hypereutectoid rail composition is provided that comprises, consists essentially of, and/or consists of the elements and weight concentrations set forth below in Table 1:
The above formulation may be modified to provide carbon in a range of 0.90-1.00 wt %.
Carbon is essential to achieve AREMA high strength rail properties. Carbon combines with iron to form iron carbide (cementite). The iron carbide contributes to high hardness and imparts high strength to rail steel. With high carbon content (above about 0.8 wt % C, optionally above 0.9 wt %) a higher volume fraction of iron carbide (cementite) continues to form above that of conventional eutectoid (pearlitic) steel. One way to utilize the higher carbon content in the new steel is by accelerated cooling (head hardening) and suppressing the formation of harmful proeutectoid cementite networks on austenite grain boundaries. As discussed below, the higher carbon level also avoids the formation of soft ferrite at the rail surface by normal decarburization. In other words, the steel has sufficient carbon to prevent the surface of the steel from becoming hypoeutectoid. Carbon levels greater than 1 wt % can create undesirable cementite networks.
Manganese is a deoxidizer of the liquid steel and is added to tie-up sulfur in the form of manganese sulfides, thus preventing the formation of iron sulfides that are brittle and deleterious to hot ductility. Manganese also contributes to hardness and strength of the pearlite by retarding the pearlite transformation nucleation, thereby lowering the transformation temperature and deceasing interlamellar pearlite spacing. High levels of manganese (e.g., above 1%) can generate undesirable internal segregation during solidification and microstructures that degrade properties. In exemplary embodiments, manganese is lowered from a conventional head-hardened steel composition level to shift the “nose” of the continuous cooling transformation (CCT) diagram to shorter times. Referring to
Silicon is another deoxidizer of the liquid steel and is a powerful solid solution strengthener of the ferrite phase in the pearlite (silicon does not combine with cementite). Silicon also suppresses the formation of continuous proeutectoid cementite networks on the prior austenite grain boundaries by altering the activity of carbon in the austenite. Silicon is preferably present at a level of at least about 0.4 wt % to prevent network formation, and at a level not greater than 1.0 wt % to avoid embrittlement during hot rolling.
Chromium provides solid solution strengthening in both the ferrite and cementite phases of pearlite.
Vanadium combines with excess carbon to form vanadium carbide (carbonitride) during transformation for improving hardness and strengthening the ferrite phase in pearlite. The vanadium effectively competes with the iron for carbon, thereby preventing the formation of continuous cementite networks. The vanadium carbide refines the austenitic grain size, and acts to break-up the formation continuous pro eutectoid cementite networks at austenite grain boundaries, particularly in the presence of the levels of silicon practiced by the exemplary embodiments of the invention. Vanadium levels below 0.05 wt % produce insufficient vanadium carbide precipitate to suppress the continuous cementite networks. Levels above 0.15 wt % can be harmful to the elongation properties of the steel.
Titanium combines with nitrogen to form titanium nitride precipitates that pin the austenite grain boundaries during heating and rolling of the steel thereby preventing excessive austenitic grain growth. This grain refinement is important to restricting austenite grain growth during heating and rolling of the rails at finishing temperatures above 900° C. Grain refinement provides a good combination of ductility and strength. Titanium levels above 0.015 wt % are favorable to tensile elongation, producing elongation values over 10%, such as 10-12%. Titanium levels below 0.015 wt % can reduce the elongation average to below 10%. Titanium levels above 0.030 wt % can produce large potentially harmful TiN particles.
Nitrogen is important to combine with the titanium to form TiN precipitates. A naturally occurring amount of nitrogen impurity is typically present in the electric furnace melting process. It may be desirable to add additional nitrogen to the composition to bring the nitrogen level to above 0.0050 wt %, which is typically a sufficient nitrogen level to allow nitrogen to combine with titanium to form titanium nitride precipitates. Generally, nitrogen levels higher than 0.0150 wt % are not necessary.
Processing and Head Hardening
Generally, steelmaking may be performed in a temperature range sufficiently high to maintain the steel in a molten stage. For example, the temperature may be in a range of about 1600° C. to about 1650° C. The alloying elements may be added to molten steel in any particular order, although it is desirable to arrange the addition sequence to protect certain elements such as titanium and vanadium from oxidation. According to one exemplary embodiment, manganese is added first as ferromanganese for deoxidizing the liquid steel. Next, silicon is added in the form of ferrosilicon for further deoxidizing the liquid steel. Carbon is then added, followed by aluminum for further deoxidation. Vanadium and titanium are added in the penultimate and final steps, respectively. After the alloying elements are added, the steel may be vacuum degassed to further remove oxygen and other potentially harmful gases, such as hydrogen.
Once degassed, the liquid steel may be cast into blooms (e.g., 370 mm×600 mm) in a three-strand continuous casting machine. The casting speed may be set at, for example, under 0.46 m/s. During casting, the liquid steel is protected from oxygen (air) by shrouding that involves ceramic tubes extending from the bottom of the ladle into the tundish (a holding vessel that distributes the molten steel into the three molds below) and the bottom of the tundish into each mold. The liquid steel may be electromagnetically stirred while in the casting mold to enhance homogenization and thus minimize alloy segregation.
After casting, the cast blooms are heated to about 1220° C. and rolled into a “rolled” bloom in a plurality (e.g., 15) of passes on a blooming mill. The rolled blooms are placed “hot” into a reheat furnace and re-heated to 1220° C. to provide a uniform rail rolling temperature. After descaling, the rolled bloom may be rolled into rail in multiple (e.g., 10) passes on a roughing mill, intermediate roughing mill and a finishing mill. The finishing temperature desirably is about 1040° C. The rolled rail may be descaled again at about 900° C. to obtain uniform secondary oxide on the rail prior to head hardening. The rail may be air cooled to about 775° C.-750° C.
The rail is subjected to an in-line, head-hardening cooling process using a water-spray system. An exemplary cooling apparatus is shown in
According to an implementation, the in-line, head-hardening cooling involves an accelerated first stage from an initial temperature in a range of about 775° C.-750° C. to an intermediate temperature in a range of about 670° C.-610° C. Depending on the line speed and size of the cooling apparatus, the spray nozzles may be positioned, for example, over the first 25 meters of the cooling apparatus. The water flow rate may be varied in the cooling apparatus to optimize heat removal and to develop the proper pearlite microstructure and hardness. Generally, the accelerated first stage is conducted to maintain the rail head surface temperature within the boundaries identified in
Pursuant to this implementation, the in-line, head-hardening cooling then involves a gradual second stage from about the intermediate temperature in the range of 670-610° C. to a temperature in a range of about 550-500° C., as further illustrated in the graph of
During the first stage of cooling in accordance with an exemplary embodiment, water at a temperature of for example, about 10° C. to about 15° C. is sprayed on the top head surface 12, both side head surfaces 16 and both web surfaces 20 at a total water flow rate of about 20 to about 30 m3/hr on the top head surface, about 20 to about 30 m3/hr total on both on the side head surfaces and about 10 to about 20 m3/hr total on both the web surfaces. In the illustrated embodiment, the first stage of cooing may take place in the first 25 meter section of the 100-meter long head-hardening device.
During the second stage of cooling in accordance with an exemplary embodiment, water at a temperature of about 10° C. to about 15° C. is sprayed on the rail in three progressively decreasing flow rates on the top surface of the rail head 12. In the second 25-meter section of the head hardening device, water flow is applied on the top head surface at a flow rate of about 25 to about 35 m3/hr. In the third 25 meter-section, water flow is applied on the top head surface at a flow rate of about 12 to about 18 m3/hr. In the fourth 25-meter section, water flow is applied on the top head surface at a flow rate of about 10 to about 15 m3/hr. In these three sections about 20 to about 30 m3/hr of water flow is applied on both the side head surfaces and about 10 to about 20 m3/hr on both the web surfaces. The second stage of cooling gradually and precisely balances the extent of recalescence with the formation of a fine interlamellar spacing of the pearlite. The travel velocity of the rail in both stages may be, for example, about 0.65 to about 0.85 meter/s.
Temperature measurements are taken at the top head surface of the rail passing through the cooling apparatus. This dual stage cooling process provides a fully pearlitic microstructure without the formation of harmful continuous proeutectoid cementite networks that otherwise tend to form when rails are air-cooled or accelerated cooled at an insufficiently high rate. This dual stage cooling process provides precise control of heat extraction to prevent the heat of transformation (recalescence) from allowing the pearlite to coarsen during transformation and produce lower hardness.
Production Trials: Three full-scale samples of exemplary compositions were produced into 136RE (136 pounds per yard) rail. A conventional comparative high strength rail composition (Comparative Composition A) processed the same day as the exemplary compositions (Inventive Compositions 1, 2 and 3) are compared below. The actual chemical compositions (in weight percentages) are listed in Table 2 below:
The compositions were produced in a 140-ton DC electric arc melting furnace with tap temperatures of 1610° C. to 1640° C. followed by treatment in an AC ladle treatment furnace (for alloy additions) and tank degassing (to remove dissolved gasses). The compositions were continuous cast into blooms of cross section 370 mm×600 mm, cut to length (˜5 m) and reheated in a furnace. After heating to 1220° C., each bloom was rolled on a blooming mill to a smaller bloom cross section of 190 mm×280 mm then sheared to length to provide for a single rail. The rolled blooms were reheated to a rolling temperature (1230° C.) in a batch-type reheat furnace then rolled to a 27 meter-long rail (5 passes in a roughing mill, 3 passes in an intermediate roughing mill and 2 passes in a finishing mill). Temperature after the final rolling pass ranged from 1000-1050° C. In all trials the AREMA 136RE (136 pounds per yard) section was produced. Just after rolling, a rail end was cut with a hot saw and that cut-end of the rail entered the head-hardening machine approximately 8 minutes later at a temperature of 750-775° C. The head hardening machine was 99 meters long and consisted of 67 water spray modules with each module having 3 top head spray nozzles, 4 side head spray nozzles, and 4 web spray nozzles. There were also separate foot spray nozzles. The rail passed through these nozzle arrays in 120-150 seconds at a travel velocity of 0.65 to 0.85 m/s. The rail exited the machine with surface temperatures below 450° C. The process was thus controlled by the amount of water flow, the entry temperature and the speed of the rail as described above. Single wave length infrared pyrometers were mounted outside and inside the machine to measure rail head surface temperature at distances of approximately 0, 15, 29, 42, 56, 80 and 102 m from the machine entry pyrometer (see
Properties. An important mechanical property of railway rail is the hardness of the head. The higher the hardness, the better the wear resistance and the longer the service life of the rail in use as track.
The head-hardened steel rails of the exemplary compositions have higher hardness than the conventional comparative composition head-hardened steel rail. It is also seen in
In marked contrast, the Inventive Compositions 1 and 2 provided steel of hypereutectoid composition (specifically about 0.10% C higher than the conventional steel) and the loss of carbon at the surface from decarburization did not shift the surface layers below the eutectoid point. Thus, the surface layers of the rail head were still hypereutectoid and there was a complete absence of soft ferrite. This explains the hardness profile of the exemplary steel compositions. In order to determine the actual carbon content at the eutectoid point for the embodied steel, modeling was performed using ThermoCalc (TCW) software. (www.thermocalc.com). The model shows a slice of the iron-carbon diagram as influenced by the alloying elements deliberately added to the exemplary steel samples. The result is shown for Inventive Composition 2 (Table 2) where it can be seen that the eutectoid point is at 0.679 wt % C, well below the actual carbon content of 0.94 wt % C.
Inventive Compositions 1 and 2 and the Comparative Composition A were subject to similar heating and cooling (head-hardening) processes. As shown in
The accelerating cooling stages for the above examples will now be described in further detail. In the case of Inventive Composition 2, a rail was cut with the hot saw to provide a control sample (Comparative Rail Example A in Table 3 below) in an air-cooled condition. The remaining rail (Inventive Rail Example 1 in Table 3 below) was head-hardened in accordance with an embodiment of the invention. Rockwell-C hardness measurements taken at 3.175 mm (⅛″) depth increments along the centerline from the top surface of the rail head are compared.
The tensile properties are compared in Table 4 below:
The above data of Table 4 demonstrates that accelerated cooling contributes to achieving improved hardness properties compared to an air-cooled comparative example.
The rail enters the head hardening machine at a specific temperature (Te=entry temperature) and passes through four independent water spray sections each 25 meters long (see
Inventive Rail Example 3 (Cooling Inside the Upper/Lower Limits).
Comparative Rail Examples B and C (Cooling Outside the Upper/Lower Limits).
The resulting steel rail head of Comparative Rail Example B (
The steel rail head of Comparative Rail Example C (
Unless stated otherwise, all percentages mentioned herein are by weight.
The foregoing detailed description of the certain exemplary embodiments of the invention has been provided for the purpose of explaining the principles of the invention and its practical application, thereby enabling others skilled in the art to understand the invention for various embodiments and with various modifications as are suited to the particular use contemplated. This description is not intended to be exhaustive or to limit the invention to the precise embodiments disclosed. Although only a few embodiments have been disclosed in detail above, other embodiments are possible and the inventors intend these to be encompassed within this specification and the scope of the appended claims. The specification describes specific examples to accomplish a more general goal that may be accomplished in another way. Modifications and equivalents will be apparent to practitioners skilled in this art having reference to this specification, and are encompassed within the spirit and scope of the appended claims and their appropriate equivalents. This disclosure is intended to be exemplary, and the claims are intended to cover any modification or alternative which might be predictable to a person having ordinary skill in the art.
Only those claims which use the words “means for” are to be interpreted under 35 USC 112, sixth paragraph. Moreover, no limitations from the specification are to be read into any claims, unless those limitations are expressly included in the claims.
This application is a continuation of application Ser. No. 13/584,145 filed Aug. 13, 2012, now U.S. Pat. No. 8,721,807, which is a continuation of application Ser. No. 12/794,191 filed Jun. 4, 2010, now U.S. Pat. No. 8,241,442, which claims the benefit of priority under 35 U.S.C. §119(e) of provisional application 61/286,264 filed on Dec. 14, 2009, the complete disclosures of which are incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
4486248 | Ackert | Dec 1984 | A |
4838963 | Huchtemann | Jun 1989 | A |
5658400 | Uchino et al. | Aug 1997 | A |
5762723 | Ueda et al. | Jun 1998 | A |
5830286 | Ueda et al. | Nov 1998 | A |
7217329 | Cordova | May 2007 | B2 |
7288159 | Cordova | Oct 2007 | B2 |
RE40263 | Ueda et al. | Apr 2008 | E |
RE41033 | Ueda et al. | Dec 2009 | E |
8241442 | Bramfitt et al. | Aug 2012 | B2 |
8721807 | Bramfitt et al. | May 2014 | B2 |
20040187981 | Ueda et al. | Sep 2004 | A1 |
20070181231 | Ueda et al. | Aug 2007 | A1 |
20080011393 | Ueda et al. | Jan 2008 | A1 |
20090314049 | Ueda et al. | Dec 2009 | A1 |
Number | Date | Country |
---|---|---|
1793403 | Jun 2006 | CN |
2196552 | Jun 2010 | EP |
2161831 | Jan 1986 | GB |
11092867 | Apr 1999 | JP |
2000178690 | Jun 2000 | JP |
2000219939 | Aug 2000 | JP |
2000226637 | Aug 2000 | JP |
2000345296 | Dec 2000 | JP |
2005146346 | Jun 2005 | JP |
2005171326 | Jun 2005 | JP |
2005171327 | Jun 2005 | JP |
2007291413 | Nov 2007 | JP |
2007291418 | Nov 2007 | JP |
94019951 | Apr 1996 | RU |
2113511 | Jun 1998 | RU |
87084 | Jun 2009 | UA |
Entry |
---|
Decision on Grant from corresponding RU Application No. 2012130024/02; Oct. 23, 2015; 6 pages. |
Thermo-Calc Software brochure(2009), 2 pages. |
Arema, Arema Manual for Railway Engineering, Part 2, Manufacture of Rail, 2007, pp. 4-2-1 to 4-2-15. |
Pavlov, “Production of Wear-Resistant Rail”, Steel in Translation, 2007, pp. 836-838, vol. 37, No. 10. |
Ueda et al, “Application of Hypereutectoid Steel to Heavy Haul Track Rail”, Thermomechanical Processing and Mechanical Properties of Hypereutectoid Steels and Cast Irons, The Minerals, Metals & Materials Socitey, 1997, pp. 161-174. |
Han, “Effects of vanadium additions on microstructure and hardness of hypereutectoid pearlitic steels”, Materials Science and Engineering A190, 1995, pp. 207-214. |
Pan et al, “Production of Wear-Resistant Rails at the NTMK”, 1994 Rail Steels Symposium Proceedings, pp. 19-22. |
Han et al, “Pearlite Phase Transformation in Si and V Steel”, Metallurgical and Materials Transactions A, Jul. 1995, vol. 26A, pp. 1617-1631. |
Uchino et al, “Development of Hypereutectoid Steel Rail for Heavy Haul Railways”, 99th MWSP Conf. Proc., ISS, 1998, vol. 35, pp. 1047-1055. |
Fletcher et al, “Fast-welding chromium-molybdenum-vanadium extra-high strength rail steels”, Vanadium in Rail Steels, Proceeding of Seminar, Nov. 8, 1979, pp. 41-47. |
Han et al, “Optimization of Mechanical Properties of High-Carbon Pearlitic Steels with Si and V Additions”, Metallurgical and Materials Transactions A, vol. 32A, Jun. 2001, pp. 1313-1324. |
Machine-English translation of Japanese Patent No. 2000-345296, Ueda Masaharau et al, Dec. 12, 2000. |
State Intellectual Property Office of the People's Republic of China, English Translation of Search Report issued for Application No. 201080062517.3 filed Dec. 14, 2010. |
Number | Date | Country | |
---|---|---|---|
20140246130 A1 | Sep 2014 | US |
Number | Date | Country | |
---|---|---|---|
61286264 | Dec 2009 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 13584145 | Aug 2012 | US |
Child | 14276061 | US | |
Parent | 12794191 | Jun 2010 | US |
Child | 13584145 | US |