Patent Application
20120149271
1. Field of the Invention
The present invention relates to a mat material and an exhaust gas processing apparatus.
2. Discussion of the Background
For the past century and continuing, the number of automobiles is drastically rising. In proportion to this rise, the amount of exhaust gas released from internal combustion engines of the automobiles is rapidly increasing. Since various substances contained in the exhaust gas (particularly, exhaust gas of diesel engines) lead to air pollution and the like, the exhaust gas containing such substances has a serious effect on the global environment.
Under such circumstances, various exhaust gas processing apparatuses have been proposed and put to actual use. A typical exhaust gas processing apparatus has a tubular member (casing) disposed at the midstream of an exhaust pipe that is connected to an exhaust gas manifold of the engine, and an exhaust gas processing body accommodated within the tubular casing. The exhaust gas processing body has an inlet and an outlet for the exhaust gas, and a large number of fine-sized pores are provided within the exhaust gas processing body. Examples of the exhaust gas processing body include catalyst carriers, and exhaust gas filters such as Diesel Particulate Filters (DPFs). In the case of the DPF, for example, when the exhaust gas enters from the inlet of the exhaust gas processing body and exits from the outlet of the exhaust gas processing body within the casing, particles are trapped on walls surrounding the pores to thereby remove the particles from the exhaust gas.
A retaining seal member is provided between the exhaust gas processing body and the casing. The retaining seal member prevents damage caused by the contact between the exhaust gas processing body and the casing when the vehicle or the like moves, and prevents the exhaust gas from leaking from a gap between the casing and the exhaust gas processing body. Further, the retaining seal member also prevents the exhaust gas processing body from falling off from the casing due to the exhaust gas pressure. On the other hand, the exhaust gas processing body is required to maintain a relatively high temperature in order to maintain its reaction, and the retaining seal member is required to be heat resistant. In order to satisfy these requirements, the retaining seal member may be made of a mat material which includes inorganic fiber such as alumina fiber.
The mat material is wound on at least a portion of an outer peripheral surface of the exhaust gas processing body, excluding the inlet and outlet, and is integrally fixed to the exhaust gas processing body by taping or the like in order to function as the retaining seal member. Thereafter, the exhaust gas processing body, having the mat material integrally fixed thereon as the retaining seal member, is press-fit within the casing to form the exhaust gas processing apparatus.
Typically, the mat material contains, for example, an inorganic fiber (e.g., alumina fiber) and an organic binder and is manufactured by a needling method, a paper-making process, or the like. Recently, a mat material using glass fiber (e.g., e-glass) is proposed to be used instead of a mat material using alumina fiber for the purpose of, for example, cost reduction (see, for example, Japanese National Publication of International Patent Application No. 2006-516043).
According to one aspect of the present invention, a mat material comprises a glass fiber. The glass fiber comprises 52 to 62% by weight of SiO2, 9 to 17% by weight of Al2O3, 17 to 27% by weight of CaO, 0 to 9% by weight of MgO, 0 to 4% by weight of TiO2, 0 to 5% by weight of ZnO, substantially no B2O3, and 0 to 2% by weight of a total sum of Na2O+K2O. The mat material is interposed between an upper base and a lower base. A surface pressure of the mat material is 100 kPa or more when a temperature of the upper base and a temperature of the lower base reaches 700° C. and 400° C., respectively, in a case of increasing the temperature of the upper base at a temperature increase rate of 15° C./minute at a same time of increasing the temperature of the lower base at a temperature increase rate of 8.6° C./minute where GBD (Gap Bolt Density)=0.35 g/cm3.
According to another aspect of the present invention, an exhaust gas processing apparatus comprises an exhaust gas processing body, a retaining seal member, and a cylindrical member. The exhaust gas processing body includes two openings through which an exhaust gas flows. The retaining seal member is wound around at least a part of an outer peripheral surface of the exhaust gas processing body except for the openings. The cylindrical member accommodates the exhaust gas processing body around which the retaining seal member is wound. The retaining seal member includes the mat materials.
A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings.
The embodiments will now be described with reference to the accompanying drawings, wherein like reference numerals designate corresponding or identical elements throughout the various drawings.
According to an embodiment of the present invention, there can be obtained a mat material having high initial retaining force and a relatively satisfactory retaining force even after repeatedly receiving load from compression and decompression even where the mat material includes glass fiber.
As illustrated in
When using the mat material 30 as a retaining seal member 24, the longitudinal direction along the long side, that is, the direction X, corresponds to the winding direction in which the retaining seal member 24 (or mat material 30) is wound on an exhaust gas processing body 20 which is illustrated in
The mat material may be a mat material including an inorganic fiber (e.g., alumina fiber) and an organic binder. Glass fiber such as e-glass is recently proposed to be used as the inorganic fiber for the purpose of, for example, cost reduction. Here, “e-glass” refers to a generic term of the glass including the composition indicated in the column “COMPOSITION OF E-GLASS” of Table 1.
That is, the e-glass is a glass includes 52 to 62% by weight of SiO2, 12 to 16% by weight of Al2O3, 16 to 25% by weight of CaO, 0 wt % to 5 wt % by weight of MgO, 5 wt % to 10 wt % by weight of B2O3, 0 to 1.5% by weight of TiO2, or 0 to 2% by weight a total sum of Na2O+K2O.
However, with a mat material using a glass fiber such as e-glass, there is a problem of having low initial retaining force compared to a mat material using an alumina fiber.
Further, the exhaust gas processing body inside the exhaust gas processing apparatus repeatedly receives cycles of expansion and contraction along with the increase and the decrease of temperature due to the flow or stop of exhaust gas. Accordingly, the retaining seal member repeatedly receives load of compression and decompression in correspondence with the behavior (expansion and contraction) of the exhaust gas processing body during use. However, with a mat material using glass fiber such as e-glass, the retaining force of the mat material significantly decreases if the cycles of compression and decompression are repeated.
Accordingly, in a case where a mat material using glass fiber such as e-glass is used for a retaining seal member, the lack of initial retaining force of the mat material and/or chronological decrease of the retaining force of the mat material may cause the exhaust gas processing body being held by the mat material to fall off.
Under such circumstance, the inventor of the present application has dedicated himself/herself to research and development. As a result, it has been found that there can be obtained a mat material having significantly high initial retaining force and being capable of maintaining a comparatively satisfactory retaining force even where load is repeatedly received from compression and decompression when a glass fiber having a specific composition and characteristic is used. This has lead to the embodiments of the present invention.
In other words, with the embodiments of the present invention, there is provided a mat material including a glass fiber, wherein the glass fiber includes 52 to 62% by weight of SiO2, 9 to 17% by weight of Al2O3, 17 to 27% by weight of CaO, 0 to 9% by weight of MgO, 0 to 4% by weight of TiO2, and 0 to 5% by weight of ZnO, wherein the glass fiber includes substantially no B2O3, wherein the glass fiber includes 0 to 2% by weight of a total sum of Na2O+K2O, wherein the mat material is interposed between an upper base and a lower base, wherein a surface pressure is 100 kPa or more when a temperature of the upper base and a temperature of the lower base reaches 700° C. and 400° C., respectively, in a case of increasing the temperature of the upper base at a temperature increase rate of 15° C./minute at the same time of increasing the temperature of the lower base at a temperature increase rate of 8.6° C./minute where GBD (Gap Bolt Density)=0.35 g/cm3.
The method of measuring the surface pressure of the mat material is described in detail in the following embodiments.
The column “COMPOSITION OF GLASS FIBER OF PRESENT INVENTION” of the below-described Table 1 indicates the composition of the glass fiber included in the mat material according to an embodiment of the present invention. Further, the glass fiber includes 52-62% by weight of SiO2, 9-17% by weight of AlO3, 17-27% by weight of CaO, 0-9% by weight of MgO, 0-4% by weight of TiO2, and 0-5% by weight of ZnO. Further, the glass fiber includes substantially no B2O3. Further, the glass fiber includes 0-2% by weight of the total sum of Na2O+K2O. Unlike e-glass, the glass fiber used for the mat material according to an embodiment of the present invention has a feature of having substantially no B2O3. Typically, B2O3 is considered as having the role of lowering the softening point of glass fiber. Because B2O3 is excluded from the glass fiber according to an embodiment of the present invention, the lowering of the softening point of the glass fiber can be prevented. Further, this increases the strength of glass fiber in a high temperature.
The mat material of according to an embodiment of the present invention includes a feature of having a significantly high initial retaining force. Further, the mat material according to an embodiment of the present invention can prevent the retaining force from decreasing even in an environment of repeatedly receiving load from compression and decompression in a high temperature. Further, the mat material according to an embodiment of the present invention can exhibit a steady holding force for a long period.
In the mat material according to an embodiment of the present invention, the composition of the glass fiber particularly is preferred to include 59-62% by weight of SiO2, 12-15% by weight of Al2O3, 20-24% by weight of CaO, 1-4% by weight of MgO, 0-0.9% by weight of TiO2, include substantially no ZnO, and include 0-1% by weight of the total sum of Na2O+K2O (hereinafter also referred to as “first glass fiber composition”).
Alternatively, the composition of the glass fiber is preferred to include 56-62% by weight of SiO2, 9-15% by weight of Al2O3, 17-25% by weight of CaO, 0-5% by weight of MgO, 0-4% by weight of TiO2, and 0-5% by weight of ZnO, and have 0-1% by weight of the total sum of Na2O+K2O (hereinafter also referred to as “second glass fiber composition”).
The first and the second glass fiber compositions of according to an embodiment of the present invention are indicated together in the below-described Table 1.
In addition to including glass fiber, the mat material 30 of according to an embodiment of the present invention may also include an organic binder.
For example, an epoxy resin, an acrylic resin, a rubber resin, or a styrene resin may be used as the organic binder. The amount of organic binder contained in the mat material (weight of organic binder relative to the total weight of the mat material) is preferably, for example, 1-10% by weight. However, in a case of using an exhaust gas processing apparatus including the mat material, the organic binder impregnated in the mat material becomes one of the causes for increasing the amount of organic components discharged from the exhaust gas processing apparatus. Therefore, the amount of organic binder contained in the mat material is preferred to be as low as possible. For example, the organic binder does not need to be impregnated in the mat material.
The mat material according to the embodiment of the present invention may include an expansive material. It is preferable for the expansive material to have a characteristic of expanding in a range from 400° C. to 800° C.
For example, vermiculite, bentonite, bronze mica, perlite, expandable graphite, and expandable fluoro-mica may be used as the expansive material.
In a case where the expansive material is used, the mat material 30 expands in a temperature ranging from 400° C. to 800° C. Accordingly, the retaining force of the mat material 30 can be improved even in a high temperature range (above 700° C.) in which the strength of the glass fiber decreases.
The additive amount of the expansive material is not limited in particular. For example, it is preferable for the additive amount of the expansive material to range from 10%-50% by weight with respect to the entire weight of the mat material 30.
The mat material 30 according to an embodiment of the present invention can be used as, for example, a retaining seal member of the exhaust gas processing apparatus 10.
The exhaust gas processing apparatus 10 includes an exhaust gas processing body 20 that is wound around an outer peripheral surface of the retaining seal member 24, a casing 12 accommodating the exhaust gas processing body 20, an inlet pipe (for exhaust gas) 2 connected to the inlet side of the casing 12, and an outlet pipe (for exhaust gas) 4 connected to the outlet side of the casing 12. The inlet pipe 2 has a tapered shape with a diameter which increases towards the position where the inlet pipe 2 connects to the casing 12. The outlet pipe 4 has a tapered shape with a diameter which increases towards the position where the outlet pipe 4 connects to the casing 12. In this example of
The retaining seal member 24 is formed by the mat material 12 including the above-described glass fiber. Accordingly, the retaining seal member 24 has a satisfactory retaining force with respect to the exhaust gas processing boy at an initial stage. Further, in the above-described exhaust gas processing apparatus 10, the decreasing rate of retaining force of the retaining seal member 24 can be significantly restrained even where load from compression and decompression is repeatedly applied to the retaining seal member 24 in correspondence with the flowing and stopping of the exhaust gas. Therefore, the exhaust gas processing body 20 can be prevented from deviating or falling off from a predetermined position after a long period of use. Thereby, the reliability of the exhaust gas processing apparatus 10 is improved.
Next, an example of a method for manufacturing a mat material according to an embodiment of the present invention is described with reference to
The method for manufacturing the mat material according to an embodiment of the present invention includes:
(A) a step of preparing a glass fiber including the above-described composition (S110);
(B) a step of fabricating a laminate sheet using the glass fiber (S120); and
(C) a step of forming a mat material with a needling process from the laminate sheet (S130).
In this method, the mat material is fabricated by using a so-called “needling process”. The needling process is a generic term of a method for manufacturing a mat material whereby a needle is pushed in and pulled out of a laminate sheet including an inorganic fiber.
Next, each of the steps is described in detail.
In step S110, a glass fiber including the above-described composition is prepared. The length of the glass fiber is not limited in particular. However, the glass fiber is preferred to be comparatively long so that fibers can be easily interlaced during a subsequent needling process. The “average length” of the glass fiber preferably ranges from 5 mm to 100 mm (e.g., 50 mm). The “average length” is the average entire length of 100 randomly extracted fibers.
The diameter of the glass fiber is not limited in particular. However, the average diameter of the glass fiber is preferred to range from, for example, 9 μm to 13 μm (e.g., 11 μm). The “average diameter” is the average diameter of 300 randomly extracted fibers being measured with a SEM (Scanning Electron Microscope).
Then, an opening process using the above-described glass fiber is performed. Thereby, a cotton-like laminate sheet can be formed. The opening process may be performed by, for example, a carding process. With this process, a laminate sheet is formed by forming bonded fabrics (referred to as a “web”) and laminating many of the bonded fabrics.
Then, a mat material is formed by performing the “needling process” on the laminate sheet.
In a normal case of performing the needling process, a needling apparatus is used.
Normally, the needling apparatus includes a needle board capable of reciprocating in a direction in which a needle is pushed in and pulled out (normally, in a vertical direction) and a pair of support plates (one provided on the front side of the laminate sheet and the other provided on the rear side of the laminate sheet). Many needles (e.g., density of 25-5000 needles per 100 cm2) are attached to the needle board so that the needles can be pushed in and pulled out with respect to the laminate sheet. Each of the support plates has many through-holes for the needles. Accordingly, in a state where the pair of support plates is pressed against both sides of the laminate sheet, the needle board is moved toward and away with respect to the laminate sheet. Thereby, needles can be pushed in and pulled out with respect to the laminate sheet. Thus, a mat material having interlaced glass fibers can be obtained.
Further, in another embodiment, the needling apparatus may include 2 sets of needle boards. Each needle board includes a support plate. Each set of needle boards is mounted to the front and rear surfaces of the laminate sheet, and the support plate bounds the laminate sheet from both sides of the laminate sheet. The needles are arranged so that the positions of the needles of one of the needle boards do not overlap with those of the needles of the other of the needle boards during a needling process. Further, taking the needle arrangement of both sets of needle boards into consideration, many through-holes are provided in the corresponding support plates so that the needles do not contact the support plates in a case where the needling process is performed on both sides of the laminate sheet. By using such needling apparatus, the needling process may be performed on both sides of the laminate sheet with 2 sets of needling boards where the laminate sheet is sandwiched by the 2 sets of support plates from both sides. By performing the needling process with the above-described method, process time can be reduced.
Then, a thermal process is performed on the glass fiber. The temperature of the thermal process preferably ranges from, for example, 600° C., to 800° C., (e.g., 700° C.). The time of the thermal process preferably ranges from, for example, 10 minutes to 24 hours (e.g., 20 minutes).
Finally, the mat material manufactured in the above-described manner is cut (a shape having a recess and a protrusion on the end surfaces of a rectangular solid as illustrated in
Next, another example of a method for manufacturing a mat material according to an embodiment of the present invention is described with reference to
The method for manufacturing the mat material according to an embodiment of the present invention includes:
(A) a step of preparing a glass fiber including the above-described composition (S210);
(B) a step of preparing a slurry using the glass fiber (S220); and
(C) a step of forming a mat material with a paper-making process from the slurry (S230).
In this method, the mat material is fabricated by using a so-called “paper-making process”. The paper-making process refers to a method for manufacturing a mat material whereby a slurry of an inorganic fiber is filled into a paper-making die, and the paper-making die is absorbed and dehydrated.
Next, each of the steps is described in detail.
Because the step of preparing the glass fiber is substantially the same as step S110 of the needling process, further description of the step of preparing the glass fiber is omitted.
It is to be noted that, the glass fiber is preferred to be comparatively short in a case of the paper-making process. It is to be noted that the “average length” of the glass fiber is preferred to range from, for example, 1 mm to 10 mm (e.g., 3 mm). Although the diameter of the glass fiber is not limited in particular, the “average diameter” is preferred to range from, for example, 9 μm to 13 μm (e.g., 11 μm).
Then, a slurry is prepared with the glass fiber obtained in Step S210 by using the following method.
First, a predetermined amount of glass fiber and an organic binder are mixed inside water. Further, an inorganic binder and/or a flocculant may be added to the mixture. Further, a material including the above-described expansive material may also be added.
For example, an alumina sol and a silica sol are used as the inorganic binder. Further, latex or the like may be used as the organic binder. The amount of organic binder contained in the mixture is preferred to be 20 wt %. In a case where the amount of organic binder contained in the mixture is greater than 20 wt %, the amount of organic components discharged from the exhaust gas processing apparatus increases significantly.
Then, the obtained mixture is agitated inside a mixer (e.g., paper-making apparatus), to thereby prepare a slurry having its fibers opened. Normally, the agitation is preferred to be performed for approximately 20 to 120 seconds.
Then, a mat material is manufactured with the obtained slurry by using the paper-making process.
First, a slurry is guided into, for example, a molding die having fine holes formed at a bottom thereof. Further, a raw material mat having a predetermined shape is obtained by absorbing moisture with an absorbing apparatus or the like from a lower side of the molding die, and performing a dehydration process.
Then, a mat material is obtained by compressing the raw material mat with a pressing apparatus and heating/drying the raw material mat at a predetermined temperature. The compression process is preferred to be performed so that the sheet density after the compression process becomes approximately 0.10 g/cm3 to 0.40 g/cm3. For example, the heating/drying process is preferred to be performed by having the raw material mat placed inside a thermal processing apparatus (e.g., oven) at a temperature of 90° C., to 180° C., for approximately 5 to 60 minutes.
Effects according to an embodiment of the present invention are described with reference to the following examples.
First, a commercially available glass fiber having an average diameter of 11 μm φ is prepared. The nominal composition of this glass fiber is indicated in the column “composition of first glass fiber” of Table 1. More specifically, this glass fiber includes 59 to 62% by weight of SiO2, 12 to 15% by weight of Al2O3, 20 to 24% by weight of CaO, 1 to 4% by weight of MgO, and 0 to 0.9% by weight of TiO2, includes substantially no ZnO, and includes 0-1% by weight of a total sum of Na2O and K2O. It is to be noted that this glass fiber includes substantially no B2O3.
The glass fiber was cut so that the average fiber length is 3 mm. Further, the glass fiber was used after maintaining the glass fiber at a temperature of 700° C., for 20 minutes.
Then, 30 g of the glass fiber was placed inside a mixer containing 6 l of water, agitated for 1 minute. Thereby, fibers of the glass fiber were opened. Then, latex 3.5 g (solid content 50%), alumina sol 1.2 g (solid content 20%), and flocculant 30 g (solid content 0.5%) are added to the water containing the glass fiber after having its fibers opened. The water is further agitated for 1 minute. Thereby, a slurry is prepared.
Then, the slurry is injected to a paper-making apparatus, and moisture is filtered by the paper-making apparatus. Thereby, a raw material mat is obtained. The raw material mat is maintained at 105° C. and dried in a state compressed by a pressing apparatus. Thereby, a mat material having a sheet density of approximately 0.14 g/cm3 is obtained.
Then, the mat material is cut into a predetermined size, to thereby obtain a sample of the mat material (hereinafter referred to as sample of first example).
The mat material of example 2 is manufactured with the same method as that of example 1. In example 2, a commercially available glass fiber (having an average diameter 1 μmφ) having a nominal composition indicated in the column “composition of second glass fiber” of the above-described Table 1 is used as the glass fiber in example 2. More specifically, the composition of the glass fiber includes 56 to 62% by weight of SiO2, 9 to 15% by weight of Al2O2, 17 to 25% by weight of CaO, 0 to 5% by weight of MgO, 0 to 4% by weight of TiO2, 0 to 5% by weight of ZnO and includes 0 to 1% by weight the total sum of Na2O and K2O. Further, the glass fiber was cut so that the average fiber length is 3 mm. Further, the glass fiber was used after maintaining the glass fiber at a temperature of 700° C., for 20 minutes.
A mat material according to comparative example 1 is manufactured with the same method as that of example 1. In the comparative example 1, a commercially available e-glass fiber (typical e-glass) (having an average diameter 11 μm φ) was used as the glass fiber. Further, the glass fiber was cut so that the average fiber length is 3 mm. Further, the glass fiber was used after maintaining the glass fiber at a temperature of 700° C., for 20 minutes.
The nominal composition of the used e-glass fiber is indicated in the above-described Table 1. More specifically, the glass fiber includes 52 to 62% by weight of SiO2, 12 to 16% by weight of Al2O2, 16 to 25% by weight of CaO, 0 to 5% by weight of MgO, 5 to 10% by weight of B2O2, 0 to 1.5% by weight of TiO2, and includes 0 to 2% by weight of a total sum of Na2O and K2O.
In order to evaluate the retaining force of the mat material in a high temperature, an initial surface pressure evaluation test was performed using each sample.
The evaluation test was performed by using the testing apparatus illustrated in
The testing apparatus 600 illustrated in
By using the testing apparatus 600, the retaining force (surface pressure) of each sample is measured according to the following procedures.
First, any of the above-described samples 650 (56.42 mm φ) is placed on the top surface of the lower base 610 of the testing apparatus 600. Then, the upper base 620 is lowered by lowering the support member 640. The upper base 620 is lowered until the apparent density GBD (Gap Bolt Density) of the sample 650 becomes 0.35 g/cm3. It is to be noted that GBD is an index value calculated by (mass of sample 650/area of sample 650/thickness of sample 650).
Then, the heaters inside the lower and the upper bases 610, 620 were heated so that the temperature of the lower base 610 becomes 400° C. and the temperature of the upper base 620 becomes 700° C. (i.e. so that the temperature at the lower side of the sample 650 becomes 400° C. and the temperature of the upper side of the sample 650 becomes 700° C.) while the apparent density GBD is maintained at 0.35 g/cm3. The temperature increase rate of the lower base 610 was set to 8.6° C./minute, and the temperature increase rate of the upper base 620 was set to 15° C./minute.
When the temperature of the lower and the upper bases 610, 620 becomes 400° C. and 700° C., respectively, the load on the sample 650 is measured with a load cell. The measuring is performed at least within 5 minutes after the temperatures of the lower and the upper bases 610, 620 are increased to predetermined temperatures. The maximum value obtained is assumed as the initial surface pressure of the sample 650.
According to these results, it is understood that the initial surface pressure (P0) of the sample of comparative example 1 is approximately 80 kPa whereas the initial surface pressure (P0) of examples 1 and 2 is over 100 kPa.
Based on the above, it was confirmed that the mat material according to an embodiment of the present invention has a significantly high initial retaining force compared to a conventional mat material using e-glass.
Next, a high temperature cycle test was performed on each of the samples of examples 1, 2, and comparative example 1 for understanding the changes of retaining force after repeatedly applying load of compression and decompression to mat material.
The high temperature cycle test was performed with the following procedures by using the above-described testing apparatus illustrated in
First, any one of the above-described samples 650 (56.42 mm Φ) is placed on the top surface of the lower base 610 of the testing apparatus 600. Then, the upper base 620 is lowered by lowering the support member 640. The upper base 620 is lowered until the apparent density GBD of the sample 650 becomes 0.38 g/cm3.
Then, the heaters inside the lower and the upper bases 610, 620 were heated so that the temperature of the lower base 610 becomes 400° C., and the temperature of the upper base 620 becomes 700° C. (i.e. so that the temperature at the lower side of the sample 650 becomes 400° C. and the temperature of the upper side of the sample 650 becomes 700° C.) while the apparent density GBD is maintained at 0.35 g/cm3. The temperature increase rate of the lower base 610 was set to 8.6° C./minute, and the temperature increase rate of the upper base 620 was set to 15° C./minute.
In the heating, the upper base 620 is gradually heated, and the compression of the sample 650 is gradually relieved so that the apparent density GBD of the sample becomes 0.35 g/cm3 when the sample 650 is heated to the above-described predetermined temperatures.
For 5 minutes, the sample 650 is maintained in a state where the temperature of the lower and the upper bases 610, 620 is 400° C. and 700° C., respectively, while the apparent density GBD of the sample is maintained to 0.35 g/cm3. Then, the upper base 620 is lowered until the apparent density GBD of the sample becomes 0.38 g/cm3. Upon reaching such state, the upper base 620 is immediately raised. Here, the upper base 620 is raised until the apparent density GBD becomes 0.35 g/cm3. When reaching this state, the load applied to the sample 650 is measured with a load cell. The measured load is assumed as the surface pressure (P1) (unit kPa) after 1 cycle.
This operation is repeated 1000 times. Until the apparent density GBD of the sample becomes 0.35 g/cm3 for the 1000th time, the load (P1000) at the time of raising the upper base 620 is measured with the load cell.
Based on the obtained results, the retaining force decrease rate of the sample was calculated by the following expression:
Retaining force decrease rate D (%)={(P1−P1000)/(P1)}×100 Expression (1)
Table 2 indicates the surface pressure P1 after 1 cycle and the surface pressure P1000 after 1000 cycles as measured by the high temperature cycle test, and the retaining force decrease rate D (%) of each sample.
Further,
According to these results, it is understood that examples 1 and 2 have a surface pressure which is larger than that of comparative example 1 after 1000 cycles (P1000) and exhibit a retaining force decrease rate that is significantly low. Particularly, in a case of the sample of example 1, the surface pressure after 1000 cycles (P1000), was approximately 70 kPa. This value is equivalent to a value (45 kPa to 70 kPa) obtained from a typical mat material using an inorganic fiber as alumina fiber.
According to the foregoing test results, it is confirmed that a significantly high initial retaining force can be obtained by using the mat material according to an embodiment of the present invention compared to using a conventional mat material using e-glass. Further, it is confirmed that the mat material according to an embodiment of the present invention can maintain a comparatively satisfactory retaining force even after repeatedly receiving load from compression/decompression.
A commercially available glass fiber having an average diameter of 11 μm Φ and a commercially available vermiculite (manufactured by AVI (Australian Vermiculite Industries), Grade 1) were prepared.
The nominal composition of glass fiber is indicated in column “composition of first glass fiber” of the above-described Table 1. The glass fiber includes substantially no B2O3.
The glass fiber was cut so that the average fiber length is 3 mm. Further, the glass fiber was used after being maintained at a temperature of 740° C. for 10 minutes and then being cooled to 650° C. at a rate of 10° C./minute.
The vermiculite was used after being added to water of 500 ml and being crushed for 1 minute with a mixer (manufactured by TESCOM & Co. Ltd, type TMD1000E5).
Then, the glass fiber 24.7 g and the vermiculite 6.4 g were placed inside a mixer, agitated for 1 minute, to thereby obtained opened fibers. Then, a slurry was prepared by adding latex 3.5 g (solid content 50%), alumina sol 1.2 g (solid content 20%), and an aggregate 30 g (solid content 0.5%) were to water containing the glass fiber having opened fibers and stirring the mixture for 1 minute.
Then, a raw material mat was obtained by introducing the slurry into a paper-making machine and filtering its moisture. Then, the raw material mat was dried by being maintained at 105° C. in a state being compressed by a pressing machine. Thereby, a mat material having a sheet density of 0.14 g/cm3 was obtained.
Then, a sample of the mat material (hereinafter referred to as “sample according to example 3”) was obtained by cutting the mat material to a predetermined size. It is to be noted that the amount of vermiculite contained in the mat material is 25 wt %.
A mat material according to comparative example 2 is manufactured by the same method as that of example 3. However, with comparative example 2, a commercially available e-glass (typical e-glass) (average diameter 11 μm Φ) was used as the glass fiber.
A high temperature surface pressure evaluation test was performed on both samples for evaluating the retaining force of the mat material according to example 3 and the comparative example 2 at a high temperature. The testing method is the same as that of the above-described column “initial surface pressure evaluation test”. However, the initial apparent density GBD was set to 0.40 g/cm3. The upper base 620 was heated from room temperature to 800° C., and the lower base 610 was heated from room temperature to 456° C. The temperature increase rate of the upper base 620 was 15° C./minute, and the temperature increase rate of the lower base 610 was 8.6° C./minute.
As illustrating in the drawing, in a case where the mat material of example 3 having an expansive material added thereto is in a range of 500° C. to 800° C., an improvement of surface pressure was observed by the addition of expansive material.
According to the results, it was shown that the initial surface pressure of mat material can be further improved by adding an expansive material to the mat material according to an embodiment of the present invention, particularly in a range of 500° C., to 800° C.
In the case of comparative example where a typical e-glass is used as the glass fiber, improvement of initial surface pressure by the addition of expansive material was observed in a range of 500° C., to 700° C. Nevertheless, a sufficient initial surface pressure could not be attained in other temperature ranges.
The mat material according to an embodiment of the present invention can be applied to a retaining seal member of an exhaust gas processing apparatus used in a vehicle or the like.
According to the above-described embodiment of the present invention, even in a case of a mat material including glass fiber, there can be provided a mat material that can attain high initial retaining force and maintain a comparatively satisfactory retaining force even after repeatedly receiving load from compression and decompression. Further, according to the above-described embodiment of the present invention, there can be provided an exhaust gas processing apparatus that uses the mat material as a retaining seal member.
Further, the present invention is not limited to these embodiments, but various variations and modifications may be made without departing from the scope of the present invention.
According to the embodiment of the present invention, there is provided a mat material including a glass fiber, wherein the glass fiber includes 52 to 62% by weight of SiO2, 9 to 17% by weight of Al2O3, 17 to 27% by weight of CaO, 0 to 9% by weight of MgO, 0 to 4% by weight of TiO2, and 0 to 5% by weight of ZnO, wherein the glass fiber includes substantially no B2O3, wherein the glass fiber includes 0 to 2% by weight of a total sum of Na2O+K2O, wherein the mat material is interposed between an upper base and a lower base, wherein a surface pressure is 100 kPa or more when a temperature of the upper base and a temperature of the lower base reaches 700° C. and 400° C., respectively, in a case of increasing the temperature of the upper base at a temperature increase rate of 15° C./minute at the same time of increasing the temperature of the lower base at a temperature increase rate of 8.6° C./minute where GBD (Gap Bolt Density)=0.35 g/cm3.
Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2009-156538 | Jul 2009 | JP | national |
| 2010-070705 | Mar 2010 | JP | national |
The present application is a U.S. continuation application filed under 35 USC 111(a) claiming benefit under 35 USC 120 and 365(c) of PCT Application No. PCT/JP2010/061118, filed Jun. 30, 2010, which claims priority to Japanese Patent Application Nos. 2009-156538 and 2010-070705, filed on Jul. 1, 2009 and Mar. 25, 2010, respectively. The foregoing applications are hereby incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/JP2010/061118 | Jun 2010 | US |
| Child | 13339416 | US |
