Molding machine cylinder and its production method
10300527 ยท 2019-05-28
Assignee
Inventors
Cpc classification
C22C19/007
CHEMISTRY; METALLURGY
C22C19/056
CHEMISTRY; METALLURGY
B22D21/005
PERFORMING OPERATIONS; TRANSPORTING
B22D23/06
PERFORMING OPERATIONS; TRANSPORTING
B22F1/00
PERFORMING OPERATIONS; TRANSPORTING
B22F2302/45
PERFORMING OPERATIONS; TRANSPORTING
B22D21/06
PERFORMING OPERATIONS; TRANSPORTING
B22D13/02
PERFORMING OPERATIONS; TRANSPORTING
B29C33/38
PERFORMING OPERATIONS; TRANSPORTING
B22F2304/10
PERFORMING OPERATIONS; TRANSPORTING
B22D19/08
PERFORMING OPERATIONS; TRANSPORTING
International classification
B22D13/02
PERFORMING OPERATIONS; TRANSPORTING
B29C33/38
PERFORMING OPERATIONS; TRANSPORTING
B22F1/00
PERFORMING OPERATIONS; TRANSPORTING
B22D23/06
PERFORMING OPERATIONS; TRANSPORTING
B22D21/06
PERFORMING OPERATIONS; TRANSPORTING
B22D21/00
PERFORMING OPERATIONS; TRANSPORTING
C22C32/00
CHEMISTRY; METALLURGY
Abstract
A molding machine cylinder comprising a lining layer having a structure comprising 20-50% by area of tungsten carbide particles and 1-10% by area of tungsten-based metal carboboride particles in a nickel-based alloy matrix, and containing 1-7.5% by mass of Fe, can be produced by a centrifugal casting method comprising a first step of heating at higher than 1140 C. and lower than 1200 C., and a second step of heating at 1080-1140 C. after melting the raw material powder.
Claims
1. A method for producing a molding machine cylinder comprising a lining layer having a structure comprising 20-50% by area of tungsten carbide particles and 1-10% by area of tungsten-based metal carboboride particles in a nickel-based alloy matrix, the % by area being based on a cross section of the lining layer, and containing 1-7.5% by mass of Fe, comprising the steps of charging a raw material for the lining layer into a steel cylinder, said raw material comprising 40-70 parts by mass of nickel-based alloy powder containing 1-5% by mass of B, and 60-30 parts by mass of tungsten carbide powder; melting said raw material for the lining layer while rotating said cylinder at 5-30 rpm; increasing the number of rotation of said cylinder for centrifugal casting, to form a centrifugally cast layer comprising an outside lining layer and an inside particle-lack layer on an inner surface of said cylinder; and removing said particle-lack layer by machining; said raw material for the lining layer being melted by a first step of heating at higher than 1140 C. and lower than 1200 C., and a second step of heating at 1080-1140 C. after said first heating step.
2. The method for producing a molding machine cylinder according to claim 1, wherein said alloy powder comprises 0.01-1% by mass of C, 1-5% by mass of B, 2-20% by mass of Cr, 0.2-5% by mass of Si, 0.2-5% by mass of Mn, 2-30% by mass of Co, 0-5% by mass of Cu, and 0-1% by mass of Fe, the balance being nickel and inevitable impurities.
3. The method for producing a molding machine cylinder according to claim 1, wherein said alloy powder has an average particle size of 20-300 m.
4. The method for producing a molding machine cylinder according to claim 1, wherein said tungsten carbide powder has an average particle size of 1.5-15 m.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
(2)
(3)
(4)
DESCRIPTION OF THE PREFERRED EMBODIMENTS
(5) The embodiments of the present invention will be explained in detail below without intention of restricting the present invention thereto. Proper modifications and improvements may be added based on the common knowledge of those skilled in the art, within a range not deviating from the technical idea of the present invention.
(6) As shown in
(7) [1] Molding Machine Cylinder
(8) (A) Composition of Lining Layer
(9) Because the lining layer 4 has a structure in which tungsten carbide particles and tungsten-based metal carboboride particles are dispersed in a nickel-based alloy matrix, the composition of the entire lining layer 4 differs from the matrix composition. In order that the lining layer 4 exhibits excellent wear resistance and corrosion resistance with chipping suppressed during machining, the lining layer 4 preferably has the following composition (average composition including both matrix and hard particles).
(10) (1) C: 1.5-4% by Mass
(11) C is combined with W to form tungsten carbide particles and tungsten-based metal carboboride particles. When C is less than 1.5% by mass, tungsten carbide particles and metal carboboride particles are insufficiently formed, failing to obtain sufficient wear resistance. On the other hand, when C exceeds 4% by mass, the lining layer 4 becomes brittle, resulting in low machinability. The C content is preferably 2-3.5% by mass.
(12) (2) B: 0.5-3.5% by Mass
(13) B is an element constituting metal carboboride particles, contributing to increasing wear resistance and stabilizing the thickness of the particle-lack layer. When B is less than 0.5% by mass, this effect is not obtained sufficiently. On the other hand, when B exceeds 3.5% by mass, the lining layer 4 becomes brittle, resulting in low machinability. The B content is preferably 1-2.5% by mass.
(14) (3) W: 25-60% by Mass
(15) W is combined not only with C to form tungsten carbide particles, but also with B and C to form tungsten-based metal carboboride particles. When W is less than 25% by mass, tungsten carbide particles and metal carboboride particles are insufficiently formed, failing to obtain sufficient wear resistance and to sufficiently stabilize the thickness of the particle-lack layer. On the other hand, when W exceeds 60% by mass, the lining layer 4 becomes brittle, resulting in low machinability. The W content is preferably 35-50% by mass.
(16) (4) Nickel: Balance
(17) Ni is a main element constituting the matrix. The matrix containing 20% or more by mass of Ni exhibits excellent corrosion resistance. The Ni content is preferably 25% or more by mass, more preferably 30% or more by mass.
(18) The lining layer 4 properly contains the following elements, depending on the application and usage of the molding machine cylinder 1.
(19) (5) Co: 1-15% by Mass
(20) Like Ni, Co has a function of imparting corrosion resistance to the lining layer 4, and is dissolved in the matrix to improve the strength. When Co is less than 1% by mass, these effects are not obtained sufficiently. On the other hand, when Co exceeds 15% by mass, these effects are saturated, economically disadvantageous. The Co content is more preferably 2-10% by mass.
(21) (6) Cr: 1-10% by Mass
(22) Cr is mainly dissolved in the matrix to increase the strength, and forms chromium-based metal carboboride particles. When Cr is less than 1% by mass, the strength-improving effect is unlikely obtained. On the other hand, when Cr exceeds 10% by mass, excessive chromium-based metal carboboride particles are formed, resulting in a brittle lining layer 4. The Cr content is more preferably 2-8% by mass. The amount of chromium-based metal carboboride particles formed may be less than 1% by area of the lining layer 4.
(23) (7) Fe: 1-7.5% by Mass
(24) Fe is dissolved in the matrix, contributing to improving adhesion to the cylinder. At least part of Fe comes from the steel cylinder fused by centrifugal casting. When Fe is less than 1% by mass, sufficient adhesion to the cylinder is not obtained. On the other hand, more than 7.5% by mass of Fe provides low corrosion resistance. The Fe content is more preferably 1-7% by mass. The most preferable upper limit of the Fe content is 6% by mass.
(25) (8) Si: 0.1-3% by Mass
(26) Si is dissolved in the matrix of the lining layer 4, increasing hardness, and thus improving wear resistance. When Si is less than 0.1% by mass, this effect is insufficient. On the other hand, when Si exceeds 3% by mass, the lining layer 4 becomes brittle. The Si content is more preferably 0.5-2.5% by mass.
(27) (9) Mn: 0.1-2% by Mass
(28) 0.1% or more by mass of Mn exhibits a sufficient effect of removing foreign matter such as oxides, etc. However, when Mn exceeds 2% by mass, the corrosion resistance of the lining layer 4 is undesirably deteriorated. The Mn content is more preferably 0.2-1% by mass.
(29) (10) Cu: 0-5% by Mass
(30) Cu is dissolved in the matrix of the lining layer 4 to improve the strength. When it exceeds 5% by mass, the corrosion resistance of the lining layer 4 is deteriorated. The Cu content is more preferably 0-3% by mass.
(31) (B) Composition of Lining Layer Matrix
(32) After metal carboboride particles are precipitated, the matrix of the lining layer 4 preferably contains 50% or more by mass of nickel. The matrix may contain Co, Cr, Si, C, B, Mn, W, Fe, Cu, etc., in addition to Ni. The matrix of the lining layer 4 has a preferred composition comprising 50-75% by mass of Ni, 2-30% by mass of Co, 2-20% by mass of Cr, 0.2-5% by mass of Si, 0.05-1% by mass of C, 0.5-3% by mass of B, 1-5% by mass of W, 0.2-5% by mass of Mn, 2-15% by mass of Fe, and 0-10% by mass of Cu, the balance being inevitable impurities. Fe is more preferably 2-10% by mass.
(33) (C) Hard Particles
(34) (1) Tungsten Carbide Particles
(35) The nickel-based alloy matrix of the lining layer 4 has a structure in which 20-50% by area of tungsten carbide particles and 1-10% by area of tungsten-based metal carboboride particles are dispersed. 1-10% by area of metal carboboride particles can suppress the aggregation of tungsten carbide, making the particle-lack layer 5 in the centrifugally cast layer 3 thinner, and stably controlling the thickness of the particle-lack layer 5. Accordingly, the centrifugally cast layer 3 needs not be cut deep, resulting in a high material yield.
(36) When tungsten carbide particles are less than 20% by area, the lining layer 4 does not have sufficient wear resistance. On the other hand, when tungsten carbide particles exceed 50% by area, the lining layer 4 becomes brittle, resulting in low machinability. Accordingly, the amount of tungsten carbide particles is 20-50% by area, preferably 25-40% by area. The % by area of tungsten carbide particles is determined by measuring the area of tungsten carbide particles whose maximum diameters are 1 m or more in a photograph of a cross section of the lining layer 4 [photograph (magnification: 1000 times) mapping-analyzed by EPMA to identify a matrix, tungsten carbide particles and metal carboboride particles] by image analysis, and dividing it by the entire area of the cross section. The image analysis was conducted by image analysis software (Image-Pro Plus ver. 6.3 available from Media Cybernetics) on a photograph of a cross section of the lining layer 4.
(37) The tungsten carbide particles preferably have an average particle size of 1.5-15 m. The average particle size is determined by number-averaging the maximum diameters of tungsten carbide particles. When the average particle size of tungsten carbide particles is less than 1.5 m, the lining layer 4 has low wear resistance. On the other hand, when the average particle size of tungsten carbide particles exceeds 15 m, tungsten carbide particles are likely detached and chipped when inner corners of the cylinder 2 are machined, resulting in reduced machinability. The average particle size of tungsten carbide particles is more preferably 2-10 m, further preferably 2-8 m.
(38) (2) Metal Carboboride Particles
(39) Metal carboboride particles having more affinity than tungsten boride (WB) particles to the matrix have higher adhesion strength to the matrix, avoiding the deterioration of wear resistance by detaching. The metal carboboride particles also suppress the aggregation and segregation of tungsten carbide particles, contributing to providing the lining layer 4 with more uniform wear resistance. Further, by suppressing the aggregation and segregation of tungsten carbide particles, the thickness of the particle-lack layer 5 in the centrifugally cast layer 3 can be stably controlled.
(40) When the metal carboboride particles are less than 1% by area, tungsten carbide particles are aggregated in the lining layer 4, failing to stably control the thickness of the particle-lack layer. On the other hand, when metal carboboride particles exceed 10% by area, the metal carboboride particles likely become larger, resulting in more chipping during machining, and thus lower machinability. Accordingly, the amount of metal carboboride particles is 1-10% by area, preferably 1-5% by area, more preferably 1.5-4% by area. To suppress the aggregation of tungsten carbide particles, an area ratio of metal carboboride particles/tungsten carbide particles is preferably 0.05-0.2, more preferably 0.07-0.12. The % by area of metal carboboride particles is determined by measuring the area of metal carboboride particles whose maximum diameters are 0.5 m or more in a photograph of a cross section of the lining layer 4 by image analysis, and dividing it by the entire area of the cross section. The image analysis was conducted by image analysis software (Image-Pro Plus ver. 6.3 available from Media Cybernetics) on a photograph of a cross section of the lining layer 4 (photograph mapping-analyzed by EPMA to identify a matrix, tungsten carbide particles and metal carboboride particles).
(41) The metal carboboride particles preferably comprise 65-85% by mass of W, 0.5-6% by mass of B, 0.5-4% by mass of C, and 1-20% by mass of Ni. W is a main element constituting metal carboboride particles, forming carboboride with C and B in the above ranges. W is more preferably 70-80% by mass, B is more preferably 2-5% by mass, and C is more preferably 1-3% by mass. The metal carboboride particles may contain trace amounts of metal components such as Fe, Cr, Co, etc., in addition to W and Ni.
(42) When the metal carboboride particles contain 1% or more by mass of Ni, sufficient affinity for the matrix is obtained, with excellent adhesion to the matrix, resulting in less decrease in wear resistance by detaching. When Ni exceeds 20% by mass, metal carboboride particles have reduced hardness, resulting in low wear resistance. The Ni content in metal carboboride particles is more preferably 2-15% by mass.
(43) The metal carboboride particles preferably have an average particle size of 0.5-5 m. The average particle size is determined by number-averaging the maximum diameters of metal carboboride particles. When the average particle size of metal carboboride particles is 0.5 m or more, the aggregation of tungsten carbide particles can be suppressed, thereby stabilizing the thickness of the particle-lack layer. However, when the average particle size of metal carboboride particles exceeds 5 m, the lining layer 4 becomes brittle. The average particle size of metal carboboride particles is more preferably 1-3 m. The average particle size of metal carboboride particles is preferably smaller than that of tungsten carbide particles. Specifically, an average particle size ratio of metal carboboride particles to tungsten carbide particles is preferably 0.2-0.5.
(44) [2] Production Method of Cylinder for Molding Machine
(45) (A) Raw Material Powder
(46) (1) Alloy Powder
(47) The alloy powder is made of a Ni-based alloy containing at least 1-5% by mass of B. B lowers the melting point of the alloy powder to increase the fluidity of an alloy melt, and forms metal carboboride particles to improve the wear resistance and stabilize the thickness of the particle-lack layer 5. When B is less than 1% by mass, these effects are not obtained sufficiently. On the other hand, when B exceeds 5% by mass, the lining layer 4 becomes brittle. The B content is preferably 2-4% by mass. The Ni content in the Ni-based alloy is preferably 50% or more by mass. The alloy powder preferably contains 0.01-1% by mass of C, 2-20% by mass of Cr, 0.2-5% by mass of Si, 0.2-5% by mass of Mn, and 2-30% by mass of Co. The alloy powder may further contain 0-1% by mass of Fe, and 0-5% by mass of Cu.
(48) The average particle size of the alloy powder is preferably 20-300 m. When the average particle size of the alloy powder is less than 20 m, the alloy powder has a large specific surface area, likely suffering surface oxidation during production and heating. On the other hand, when the average particle size of the alloy powder exceeds 300 m, the tungsten carbide powder and the alloy powder exhibit large fluidity difference due to their particle size difference, so that both powders may be separated when the cylinder is rotated. The average particle size of the alloy powder is more preferably 50-200 m. The average particle size was measured by a laser diffraction particle size analyzer (Microtrac).
(49) (2) Tungsten Carbide Powder
(50) The tungsten carbide powder preferably has an average particle size of 1.5-15 m. When the average particle size of tungsten carbide powder exceeds 15 m, tungsten carbide particles contained in the lining layer 4 have too large particle sizes, likely detached during machining. On the other hand, when the average particle size of tungsten carbide powder is less than 1.5 m, the wear resistance of the lining layer 4 is not sufficiently improved. The average particle size of tungsten carbide powder is more preferably 7-15 m, most preferably 7-12 m. The average particle size was measured by a laser diffraction particle size analyzer (Microtrac). Also, fine tungsten carbide powder is preferably contained in a proper amount, because part of their surfaces are easily melted during heating (in the first heating step described below) before centrifugal casting, contributing to the precipitation of metal carboboride in centrifugal casting. The tungsten carbide powder preferably has a particle size distribution that particle sizes of 6 m or less are 0.2-20% by weight.
(51) (3) Formulation
(52) A raw material for the lining layer comprises 40-70 parts by mass of the alloy powder and 60-30 parts by mass of the tungsten carbide powder. When the alloy powder is more than 70 parts by mass (the tungsten carbide powder is less than 30 parts by mass), the lining layer 4 does not have sufficient wear resistance. On the other hand, when the alloy powder is less than 40 parts by mass (the tungsten carbide powder is more than 60 parts by mass), the lining layer 4 has too high hardness. More preferably, the alloy powder is 40-60 parts by mass, and the tungsten carbide powder is 60-40 parts by mass.
(53) (4) Melting
(54) A mixed powder of the alloy powder and the tungsten carbide powder (raw material for the lining layer) is charged into a cylinder 2 made of steel such as SCM440, etc., and melted while rotating the cylinder 2 at 5-30 rpm. The heating step of the raw material for the lining layer comprises a first step of heating at higher than 1140 C. and lower than 1200 C., and a second step of heating at 1080-1140 C. after the first heating step.
(55) (a) First Heating Step
(56) By heating the raw material for the lining layer at a relatively high temperature of higher than 1140 C. and lower than 1200 C., part of surfaces of tungsten carbide particles are sufficiently melted in an alloy melt. A heating temperature of 1140 C. or lower does not sufficiently melt tungsten carbide, while a heating temperature of 1200 C. or higher erodes the steel cylinder too much, resulting in too high concentration of iron in the lining layer 4. The heating temperature in the first heating step is preferably 1150-1190 C. The heating time in the first heating step may be about 10-60 minutes. Because the heating temperature is sufficiently high in the first heating step, alloy oxides inevitably generated are melted and segregated on the inside during centrifugal casting, so that they do not remain in the lining layer 4.
(57) (b) Second Heating Step
(58) With as relatively low a heating temperature as 1080-1140 C., part of surfaces of tungsten carbide particles are further melted in the alloy melt while suppressing the erosion of the cylinder 2, causing sufficient reactions of W, B and C in the alloy melt to precipitate tungsten-based metal carboboride. The heating time in the second heating step is as relatively long as 60-120 minutes, to sufficiently precipitate metal carboboride. Because the second heating step is conducted for a relatively long period of time, the upper limit of the heating temperature should be 1140 C. or lower to suppress the erosion of the cylinder 2. The upper limit of the heating temperature is preferably 1135 C. When the heating temperature is lower than 1080 C., the alloy melt has low fluidity, resulting in a reduced stirring effect by rotation, failing to sufficiently obtain metal carboboride particles. The lower limit of the heating temperature is preferably 1100 C.
(59) (c) Rotation Speed of Cylinder
(60) With the cylinder 2 rotated at as relatively low a speed as 5-30 rpm in the first and second heating steps, the melting of tungsten carbide and the precipitation of metal carboboride are accelerated by stirring the alloy melt, while suppressing the erosion of an inner surface of the cylinder 2, and the temperature of the alloy melt is made uniform, resulting in uniformly precipitated metal carboboride particles. When the number of rotation of the cylinder 2 is less than 5 rpm, a stirring function is insufficient, failing to uniformly precipitate a sufficient amount of metal carboboride particles. On the other hand, the number of rotation of the cylinder 2 exceeding 30 rpm provides an excessive stirring function, likely making metal carboboride particles too large. The preferred number of rotation of the cylinder 2 is 5-15 rpm.
(61) (5) Centrifugal Casting
(62) After tungsten-based metal carboboride particles are precipitated while melting part of surfaces of tungsten carbide particles, the cylinder 2 is rotated at a high speed exceeding 1000 rpm (for example, 1200-2500 rpm) to carry out centrifugal casting. Because heating is not conducted during the centrifugal casting, the alloy melt is gradually cooled, so that metal carboboride particles are further precipitated. Thus formed is a centrifugally cast layer 3 composed of an outside lining layer 4 having many tungsten carbide particles and metal carboboride particles dispersed, and an inside particle-lack layer 5 containing less tungsten carbide particles and metal carboboride particles.
(63) (6) Removal of Particle-Lack Layer
(64) Because the particle-lack layer 5 has a stable thickness in the centrifugally cast layer 3 formed by the method of the present invention, the centrifugally cast layer 3 may be removed in small thickness by machining. If the particle-lack layer 5 had uneven thickness, removal would have to be conducted exceeding the particle-lack layer 5 to a relatively thick part of the lining layer 4 for safety margin, failing to obtain a lining layer 4 having sufficient thickness. Thus, the molding machine cylinder 1 comprising a lining layer 4 containing 20-50% by area of tungsten carbide particles and 1-10% by area of tungsten-based metal carboboride particles dispersed in a nickel-based alloy matrix, is obtained.
(65) The present invention will be explained in more detail with Examples below, without intention of restricting the present invention thereto.
Examples 1-3, Reference Examples 1 and 2, and Comparative Examples 1-3
(66) Each alloy powder having a composition shown in Table 1 was produced by a gas atomizing method, and classified by a sieve to have an average particle size shown in Table 2. Each alloy powder was dry-mixed with tungsten carbide powder having purity of 99% or more and an average particle size shown in Table 2. Table 2 shows the amounts of alloy powder and tungsten carbide powder in each raw material for the lining layer.
(67) TABLE-US-00001 TABLE 1 Composition (% by mass) of Alloy Powder No. B C Cr Fe Si Mn Co Cu Ni Example 1 3.1 0.05 8.3 3.6 1.1 8.1 Balance Example 2 2.6 0.12 12.5 0.1 3.6 1.1 18.5 2.5 Balance Example 3 3.1 0.05 8.3 3.6 1.1 8.1 Balance Ref. Ex. 1 3.8 0.08 15.8 4.9 3.6 1.1 35.0 5.2 Balance Ref. Ex. 2 3.1 0.05 8.3 3.6 1.1 8.1 Balance Com. Ex. 1 3.1 0.05 8.3 3.6 1.1 8.1 Balance Com. Ex. 2 3.1 0.05 8.3 3.6 1.1 8.1 Balance Com. Ex. 3 3.1 0.05 8.3 3.6 1.1 8.1 Balance
(68) TABLE-US-00002 TABLE 2 Alloy Powder Tungsten Carbide Powder Average Amount Average Amount Particle Size (parts by Particle Size (parts by No. (m) mass) (m) mass) Example 1 110 60 5.0 40 Example 2 46 70 13.9 30 Example 3 117 60 8.8 40 Ref. Ex. 1 60 75 9.0 25 Ref. Ex. 2 110 60 5.0 40 Com. Ex. 1 110 60 5.0 40 Com. Ex. 2 110 85 5.0 15 Com. Ex. 3 110 60 200 40
(69) Each raw material for the lining layer was charged in an amount of forming as thick a centrifugally cast layer as 4 mm into a cylinder of 250 mm in outer diameter, 94 mm in inner diameter and 2500 mm in length made of machine-structural alloy steel (SCM440), and steel lids were welded to both end openings of the cylinder for sealing. This cylinder was put in a furnace having a rotation mechanism, to carry out the first and second heating steps while rotating the cylinder under the conditions shown in Table 3.
(70) TABLE-US-00003 TABLE 3 First Heating Step Second Heating Step Heating Heating Number of Temper- Heating Temper- Heating Rotation ature Time ature Time No. (rpm) ( C.) (minute) ( C.) (minute) Example 1 6 1160 30 1120 60 Example 2 20 1180 30 1130 90 Example 3 10 1180 30 1140 90 Ref. Ex. 1 20 1180 30 1130 60 Ref. Ex. 2 6 1180 90 Com. Ex. 1 0 1150 30 Com. Ex. 2 10 1160 30 1120 60 Com. Ex. 3 60 1160 30 1120 60
(71) After the second heating step, each cylinder was taken out of the furnace, and placed on a centrifugal casting apparatus. A centrifugally cast layer having a thickness of 4 mm was formed by a centrifugal casting method by rotating the cylinder at a gravitational acceleration of 80 G (1230 rpm) on an inner surface of the cylinder, until the temperature was lowered to 700 C. After cooling to room temperature, two disc-shaped samples as thick as 20 mm were cut out of the cylinder at each center position separated 100 mm from each end.
(72) Composition/structure-observing samples of about 20 mm20 mm20 mm were cut out of each disc-shaped sample from an inner surface of its circular hole circumferentially every 90, and mirror-polished. The thickness of a particle-lack layer in a centrifugally cast layer of each sample was measured by a scanning electron microscope, to determine its minimum and maximum. Table 8 shows a thickness range of the particle-lack layer.
(73) The particle-lack layer 5 was removed from each composition/structure-observing sample to analyze components in the lining layer 4. Table 4 shows the composition of the lining layer 4 (average composition including all of an alloy matrix, tungsten carbide and metal carboboride).
(74) TABLE-US-00004 TABLE 4 Composition (% by mass) of Lining Layer No. C B W Cr Fe Si Mn Co Cu Ni Example 1 2.8 1.5 42.0 3.6 4.1 1.1 0.5 4.8 Balance Example 2 2.6 1.6 36.3 8.4 6.6 1.9 0.5 10.8 2.7 Balance Example 3 3.2 1.2 52.7 3.1 7.2 0.9 0.4 4.1 Balance Ref. Ex. 1 2.6 1.6 36.3 8.4 8.3 1.9 0.5 21.6 2.7 Balance Ref. Ex. 2 3.2 1.2 55.7 3.1 12.1 0.9 0.4 4.1 Balance Com. Ex. 1 4.1 1.3 55.4 2.6 0.5 1.3 0.3 3.9 Balance Com. Ex. 2 1.4 1.8 23.0 4.6 5.8 1.5 0.9 7.3 Balance Com. Ex. 3 2.7 1.5 41.9 3.9 3.6 0.9 0.6 3.5 Balance
(75) The metal composition of a matrix in each composition/structure-observing sample was analyzed by EDX. Table 5 shows the composition of detectable metal elements in the matrix. Table 6 shows the area percentages and average particle sizes of tungsten carbide particles and metal carboboride particles, and Table 7 shows the composition of metal carboboride particles measured by EPMA.
(76) TABLE-US-00005 TABLE 5 Composition (% by mass) of Matrix No. Ni W Cr Fe Mn Co Cu Example 1 71.3 2.1 5.9 6.7 0.8 9.5 Example 2 51.7 4.9 10.8 8.9 0.8 15.3 4.2 Example 3 68.9 1.7 4.8 14.3 0.5 5.8 Ref. Ex. 1 24.5 4.9 13.8 11.1 0.8 36.1 4.2 Ref. Ex. 2 55.6 1.7 4.8 27.2 0.5 5.8 Com. Ex. 1 70.1 1.9 6.3 6.5 0.7 10.4 Com. Ex. 2 71.6 0.9 7.1 6.9 1.4 11.6 Com. Ex. 3 68.9 1.6 6.1 6.1 0.8 9.8
(77) TABLE-US-00006 TABLE 6 Tungsten Carbide Metal Carboboride Particles Particles Average Average % Particle Size % Particle Size No. by area (m) by area (m) Example 1 35.2 4.2 6.5 2.2 Example 2 26.7 6.4 2.3 1.1 Example 3 33.8 3.6 2.6 1.6 Ref. Ex. 1 26.1 18.4 16.9 7.5 Ref. Ex. 2 51.9 8.6 3.2 0.7 Com. Ex. 1 38.8 21.0 0.1 0.2 Com. Ex. 2 17.4 4.2 2.4 2.2 Com. Ex. 3 38.6 190.0 25.7 12.3
(78) TABLE-US-00007 TABLE 7 Composition (% by mass) of Metal Carboboride Particles No. C B W Ni Example 1 1.8 3.0 76.4 9.9 Example 2 1.6 3.2 71.6 5.2 Example 3 1.8 2.9 75.2 7.8 Ref. Ex. 1 1.6 3.2 71.6 2.6 Ref. Ex. 2 1.8 2.9 75.2 7.8 Com. Ex. 1 0.3 3.2 70.4 8.1 Com. Ex. 2 1.7 2.8 55.2 27.1 Com. Ex. 3 1.9 3.5 76.2 13.5
(79) As shown in
(80) TABLE-US-00008 TABLE 8 Thickness (mm) Centri- Particle- fugally Lack Wear Corrosion No. Cast Layer Layer (mg) Machinability Resistance Example 1 4 0.7-0.9 2.5 Good Good Example 2 4 0.9-1.1 3.4 Good Good Example 3 4 1.2-1.5 2.0 Good Good Ref. Ex. 1 4 1.5-1.6 3.6 Good Fair Ref. Ex. 2 4 1.6-1.9 2.2 Good Poor Com. Ex. 1 4 2.2-2.9 2.3 Poor Good Com. Ex. 2 4 1.4-1.9 12.5 Good Good Com. Ex. 3 4 1.1-1.5 2.7 Poor Good
(81) The particle-lack layer 5 was removed by grinding from the centrifugally cast layer 3 of each cylinder after the disc-shaped sample was cut out. An inner-surface corner portion of each cylinder was cut by turning with a CBN tool, to evaluate machinability with the detaching and chipping of tungsten carbide particles and metal carboboride particles from the lining layer 4, by the following standard. The results are shown in Table 8.
(82) Good: Detaching and chipping did not occur.
(83) Poor: Detaching or chipping occurred.
(84) A corrosion resistance-evaluating sample of 1.5 mm in thickness, 4.0 mm in width and 10 mm in length was cut out of the lining layer 4. Each sample was immersed in an 18-% hydrochloric acid solution at 50 C. for 24 hours, to evaluate corrosion resistance with a weight reduction ratio by immersion by the following standard. The results are shown in Table 8.
(85) Good: The weight reduction ratio was less than 7%.
(86) Fair: The weight reduction ratio was 7% or more and less than 15%.
(87) Poor: The weight reduction ratio was 15% or more.
(88) When each centrifugally cast layer 3 of Examples 1-3 was cut to the depth of 2 mm, the particle-lack layer 5 was completely removed, so that the lining layer 4 was exposed to the entire inner surface of the cylinder. Thereafter, the outer periphery and ends, etc. of the cylinder 2 were machined to produce a molding machine cylinder 1. When injection molding was conducted using the molding machine cylinder 1 of Example 1, it was confirmed that the lining layer 4 had good wear resistance and corrosion resistance.
(89) On the other hand, when the centrifugally cast layer 3 of Comparative Example 1 was cut to the depth of 2 mm, a too thick particle-lack layer 5 was not completely removed, failing to have a lining layer 4 on the entire inner surface of the cylinder.
(90) When each centrifugally cast layer of Reference Examples 1 and 2 and Comparative Example 2 was cut to the depth of 2 mm, the particle-lack layer 5 was completely removed to expose a lining layer 4. A molding machine cylinder 1 was then produced by machining. However, when injection molding was conducted using the molding machine cylinder 1 of Reference Example 1, the lining layer 4 was slightly poor in corrosion resistance because the matrix had a relatively small Ni content. When injection molding was conducted using the molding machine cylinder 1 of Reference Example 2, the lining layer 4 did not exhibit sufficient corrosion resistance because the lining layer had a large Fe content. When injection molding was conducted using the molding machine cylinder 1 of Comparative Example 2, the lining layer 4 was prematurely worn because of too small an area ratio of tungsten carbide particles, failing to exhibit sufficient wear resistance.
(91) As is clear from Table 8, the thickness differences between the maximum and minimum (unevenness) of the particle-lack layers 5 in Examples 1-3 were within a range of 0.1-0.3 mm. On the other hand, the thickness unevenness of the particle-lack layers 5 in Comparative Examples 1-3 was as large as 0.4-0.7 mm. This indicates that in Examples 1-3, the thickness of the particle-lack layer 5 is stably controlled.
DESCRIPTION OF REFERENCE NUMERALS
(92) 1: Molding machine cylinder 2: Cylinder 3: Centrifugally cast layer 4: Lining layer 5: Particle-lack layer 6: Hollow portion 11: Sandpaper 12: Substrate of test piece 13: Lining layer of test piece