• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:

    公开号:AT509990A4
    申请号:T0211610
    申请日:2010-12-22
    公开日:2012-01-15
    发明作者:
    申请人:Asamer Basaltic Fibers Gmbh；
    IPC主号:
    专利说明:

    25 16:06:09 22-12-2010 5/20
    * · »·« 4 «» «· * 4 -1 -
    The invention relates to basalt fibers comprising the elements Si, Al, Fe, Mn, Ti, Ca, Mg, K, Na and O, wherein the Si central atom is surrounded by four oxygen atoms and the other elements are also surrounded by oxygen atoms in different coordination or at least coupled to oxygen atoms and form further structural Einheften and a method for producing the Basaltfasem invention.
    Basalt fibers are thin fibers of basalt and belong to the category of mineral fibers (MMF - man made mineral fibers). They are made from a liquid basalt melt at about 1400 ° C. The fiber has a greenish-brown color. The composition of the melt influences the physical properties of the basalt fiber. Unlike carbon fiber or aramid fiber, the basalt fiber is not stretched but, like the glass fiber, amorphous. Basalt fibers are used as reinforcing fibers in fiber-plastic composites or as heat protection material. The physical properties and thus the fields of application are similar to those of glass fiber. However, they are thicker than glass fiber and very brittle in the form of insulating ones. However, one has to distinguish clearly between basalt wool and endiosbasalt fiber. Endless basalt fibers are harmless to health and are mainly used in composite applications (lightweight construction in cars and commercial vehicles). With new technologies, however, even the finest fibers with a thickness of less than 0.01 mm can be produced and processed into fabric.
    The benefits of basalt fiber are in a wider temperature range (- 260 ° C to + 700 eC), a 20% to 30% higher modulus of elasticity than that of the E-Gias fiber and reaching the level of aramid fibers, a higher thermal and electrical conductivity Compared to E-glass, this can result in faster injection molding cycle times.
    N2007 / 10BOQ 22/12 2010 MI 16:03 [SE / EM NR 8051] @ 005 16:06:23 22-12-2010 6/20 25 16:06:23 22-12-2010 6/20 25
    -2-
    Basalt fibers are used for reinforcement, such as cement or concrete. They must have a high tensile strength and high chemical resistance in order to compete with the known from the prior art alkali-resistant glass fibers, which are, however, very expensive and expensive to manufacture, and aramid or Kohlenstofffa-sem.
    The object of the present invention is therefore to provide a basalt fiber with improved tensile strength.
    The object of the invention is in each case independent by a basalt fiber comprising the elements Si, Al, Fe, Mn, Ti, Ca, Mg, K, Na and O, wherein the Si central atom is surrounded by four oxygen atoms and the other elements also of oxygen atoms surrounded in different coordination or at least coupled to oxygen atoms and form further structural units, wherein preorientierte or oriented molecular structures, in particular domains, in an otherwise X-ray amorphous structure and a method for producing the Basaitfasern invention, wherein the raw material comprising 30% to 70% basalt and / or diabase, 8% to 40% quartz component, in particular quartz sand, and 5% to 30% slag, in particular blast furnace slag, is ground to particles, are made from the particles molded body, already pass through a temperature range before melting, in which the components of the raw material react with each other and new mine form ralphasen and molecular structures, and are melted in a melting furnace, the melt is fed through a feeder channel via a flow feeder the bushing and basaic fibers are pulled, optionally sizing, and subsequently optionally supplied to the winder. Advantageously, it turns out that a high tensile strength can be achieved. As a result of the preoriented or oriented molecular structures, in particular domains, the mechanical strength of the basalt fiber is substantially greater than that of the starting basalt. The continuous basalt fiber according to the invention is further distinguished by optimized chemical-thermal properties, in particular by high temperature resistance, high tear strength, high chemical resistance, especially in alkaline pH ranges, very good insulating and elongation properties and good recyclability.
    Preferably, the structural units form a close-ordering, wherein the atomic and molecular distances and angles between the positively charged central atom and the surrounding negatively charged oxygen atoms are irregular and the precursor N20Q7 / 10900 22/12 2010 MI 16:03 [SE / EM NR 8051] 0006 16:06:41 22-12-2010 7/20 25 16:06:41 22-12-2010 7/20 25
    Thus, a higher tensile strength, in particular higher than that of E glass, can be achieved.
    The preoriented or oriented molecular structures, in particular domains, can exhibit a rearrangement of chain and / or ribbon molecules similar to the pyroxene structure, which in turn explains the high tensile strength. In addition, the basalt fiber according to the invention is UV-resistant, non-toxic and behaves chemically completely inert.
    Advantageously, the proportion of chain molecules similar to the pyroxene structure is selected from a range with a lower limit of 20% and an upper limit of 80%, whereby the improved values for the tensile strength are achieved and thus the possibilities of using the basalt fiber according to the invention are increased.
    The modulus of elasticity of the basalt fiber has a value with a lower limit of 60000 MPa and an upper limit of 150000 MPa, whereby a high rigidity is achieved and in particular improves the suitability of the basalt fiber for reinforcing purposes.
    Preferably, the tensile strength of the basalt fiber has a value with a lower limit of 1500 MPa and an upper limit of 8000 MPa, whereby the mechanical load for the basalt fiber can be very large without cracking.
    The value for the density is selected from a range with a lower limit of 2.0 g / cm 3 and an upper limit of 3.0 g / cm 3, especially 2.3 g / cm 3, advantageously with little increase in density Tensile strength and rigidity can be significantly increased. In one embodiment variant, the shaped bodies are melted in a melting tank, the melt is fed through a feeder channel via a flow feeder, in particular into the melt, to the bushing and the basalt fibers are drawn and subsequently fed to the winder, whereby an already established production method for the production of the Basalt fiber according to the invention can be used and thus the cost of the evaluation of a completely new manufacturing process can be saved. It is only necessary to adapt the process parameters.
    The moldings are subjected to a temperature range of from room temperature to 1200 ° C. before melting, which on the one hand enables better physical properties, such as higher abrasion resistance and lower flaking, and on the other hand, to be achieved. N2007 / 10900 22/12 2010 MI 16:03 [SE / EM NR 8051] @ 007 16:06:58 22-12-2010 8/20 25 • P «· · -4-space requirements for storage for drying are eliminated. Furthermore, the basalt and / or diabase, quartz component, in particular quartz sand, and the slag, in particular blast furnace slag, can react with one another and form new mineral phases and molecular structures. The new mineral phases thus formed melt completely in the melting furnace, whereby previously existing molecular structures are retained or are formed again during cooling. The material remembers its previous condition.
    For a better understanding of the invention, this will be explained in more detail with reference to the following figures.
    Each shows in a highly schematically simplified representation:
    Fig. 1 X-ray diffraction diagram of a basalt fiber according to the invention;
    FIG. 2 shows an X-ray diffraction diagram of the basalt fiber according to the invention at different temperatures; FIG.
    Fig. 3 X-ray diffraction diagram of a mineral fiber (glass fiber) of the prior art at different temperatures.
    By way of introduction, it should be noted that in the differently described embodiments, like parts are given the same designations, and the disclosures contained throughout the specification can be applied analogously to like parts with designations. Also, the location information chosen in the description, such as top, bottom, side, etc. related to the directly described embodiment and are to be transferred to a new position analogously to a new position. Furthermore, individual features or combinations of features from the different exemplary embodiments shown and described can also represent independent, inventive or inventive solutions. All statements on ranges of values in the description of the present invention should be understood to include any and all sub-ranges thereof, e.g. the indication 1 to 10 should be understood to include all sub-ranges, starting from the lower limit 1 and the upper limit 10, i. all subregions begin with a lower limit of 1 or greater and end at an upper limit of 10 or less, e.g. 1 to 1.7, or 3.2 to 8.1 or 5.5 to 10. N2007 / 10800 22/12 2010 MI 16:03 [SE / EMN 80511 0008 16:07:13 22-12-2010 9 / 20 25 · f > · F * I · * * 4 * • * »·» • · * · »·
    5
    The basalt fiber according to the invention, which comprises the elements Si, Al, Fe, Mn, Ti, Ca, Mg, K, Na, O and optionally B, P, S, Cr, Zr and Li, forms structural units and has oriented or preoriented molecular structures , in particular domains, in an otherwise X-ray amorphous structure. The oriented regions are in the form of chain and / or ribbon molecules similar to a pyroxene structure such as ortho and clinopyroxenes. In the Klinopyroxenen are mainly Augit and Diopside.
    The structural units form a close arrangement, whereby the atomic and molecular distances and angles between positively charged central atom and the surrounding negatively charged oxygen atoms are irregular and the oriented or pre-oriented (semicrystalline) molecular structures, in particular domains, form a noncrystalline Femorder.
    The close order of the melt is made up of structural units that also characterize the structure of the corresponding amorphous phases. The basic building block for the melt for the production of basalt fibers is the [SiOJ4 tetrahedron. The oxygen that forms two adjacent [SiCXt] 4 " Tetrahedron is referred to as bridging oxygen or bridging oxygen. By incorporating alkali and alkaline earth oxides, which act as network conversion oxides (Na20, K2Ot20 etc.) and intermediate oxides (such as the divalent metals or metal oxides such as CaO, MgO, BaO, FeO, etc.), the network becomes depolymerized the opposite effect is caused by the additional presence of aluminum in the network. The [SiOJ4 tetrahedron is a nearly rigid unit regardless of the degree of polymerization. The changes in the structure are determined by the bond angles Si-O-St (bridge angle) and bond lengths Si-O (bridge oxygen).
    The basalt fiber according to the invention is characterized by a 30% to 40% higher tensile strength compared to previous basalt fibers. This is achieved by precursors or the formation of new pre-oriented molecular structures, in particular with a chain or band structure. The higher tensile strength is achieved by the non-crystalline arrangement of the molecules.
    The basalt fibers consist mainly of consumed Si04 tetrahedra. By thermal treatment, chain and / or ribbon molecules form similar to a pyroxene structure. Taking into account the temperature- and time-dependent homogeneous and heterogeneous nuclei · N2007 / 10900 22/12 2010 MI 16:03 [SE / EM NR 8051] 0009 16:07:30 22-12-2010 10/20 25 -6 and crystal formation mechanisms, partial crystallinity can also be achieved via controlled nucleation and crystal growth cycles.
    A possible production variant for the basalt fiber according to the invention comprises a pretreatment of the raw material before it enters the melting furnace. The raw material, in particular rock, is ground during the pretreatment, then moldings are formed and finally the moldings undergo a temperature treatment selected from a range of room temperature to 1200 ° C, wherein in this process step in a pre-reaction already structures are formed, the precursor for the preoriented or oriented (semicrystalline) molecular structures, in particular domains, are. By compacting into shaped bodies, the individual particles are so close to each other that they can react faster than in comparison to loose particles, where there are cavities between them. In addition, a pre-reaction already takes place before the complete melting of the starting materials in the melting furnace, resulting in higher strengths than in conventional glass and basalt-based materials.
    The chain and / or ribbon molecular structure is already present in the melt at about 1500 ° C and forms in the course of the Abkühtvorganges, the path of the melt, on. The path of the melt comprises the following steps: a) partial melt during the loading, Vonwärm- and Aufschmelzvorganges; b) perfect melt in the furnace at about 1500 "C or higher; c) Melt flow in the feeder channel - > less than 1500 ° or lower than in the melting furnace; d) further cooling takes place in the flow feeder, which corresponds to the limit of platinum or platinum alloying stress; e) in the bushing or nozzle a further cooling to about 1250- 1350 ° C; f) during the fiber drawing process and optionally sizing a cooling of 1250- 1350 ° C to temperatures below 100 ° C is performed.
    Upon heat treatment of the basalt fiber according to the invention, new mineral formations with crystallinity and partial crystallinity occur. In particular, clino- and orthopyroxes are newly formed or amplified in an X-ray diffractometric analysis. There is thus an increase in crystallinity. In addition, plagioclase still occurs.
    An X-ray diffractogram of a basalt fiber according to the invention is shown in FIG. 1. The measurement parameters for the preparation of the X-ray diffractogram are: Radiation source: Ν2007Π0900 22/12 2010 MI 16:03 (SE / EM NR 8051] S) 010 16:07:47 22-12- 2010 η / 20 25 -7-
    Cu Κ alpha, at a temperature of 25 ° C, in an angular range of 2-theta 5 ". The one-square peaks indicate anorthite Ca (Al 2 Si 2 O 8), triclinic - a 8.16400 - b 12.89000 - c 14.21400 - □ 93.220 - □ 115.9 □ 91.13; the peaks with a rhombus show kiinopyroxen Ca 0.970 Co 0.030 (Mg 0.831 Co 0.169) (Si 2 O 6), monoclinic - a 9.7527 - b 8.9261 - c 5.2486 - □ 90 - □ 105.856 - □ 90; and the peaks with a circle indicate orthopyroxenes Mg1,12 Fe0,88 Si2 O6, orthorhombic - a 18,224 - b 8,775 - c 5,179 - □ 90 - □ 90 - o 90.
    Fig. 2 shows an X-ray diffractogram of the fiber according to the invention, wherein the curves from bottom to top show an analysis of the continuous basalt fiber at a heat treatment of 800 aC, 900 ° C and 1000 ° C. From the Si04 tetrahedra distorted at the beginning in the preorientation phase, regular tetrahedra, complex silicates and regular mineral structures, in particular pyroxenes, are formed depending on time and temperature, whereby the crystallinity in the fibers also increases.
    In prior art comparative fibers (glass fibers), the crystallinity in the temperature field under study increases much less than in the basalt fiber of the invention. Fig. 3 shows an X-ray diffraction diagram of a prior art mineral fiber (glass fiber) at different temperatures, showing first from bottom to top the untreated fiber, followed by a heat treatment of 800 ° C, 900 ** C and 1000 ° C.
    The strength of the preorientation, ie the proportion of the chain molecular structure similar to the pyroxene structure, is selected from a range with a lower limit of 20% and an upper limit of 80%, preferably 40% to 60%, in particular 45% to 55%, wherein by a longer heat treatment and a higher temperature increased mineral formation, in particular pyroxene formation takes place. The fiber diameter also plays a role. Thus, thinner fibers with the same duration and temperature treatment have a higher proportion of pyroxene than thicker endless basalt fibers.
    The basalt fibers according to the invention have a diameter selected from a range with a lower limit of 5 μm and an upper limit of 40 μm, preferably from 7 μm to 25 μm, in particular from 9 μm to 16 μm.
    The mix and regrind of the raw material can be based on approx. 50% basalt, approx. 20% blast furnace slag, approx. 30% quartz sand and clay. In alternative embodiments, the starting material may also only basalt, or only selected additives such as only N2007 / 10900 22/12 2010 MI 16:03 [SE / EM NR 8051] ®011 16:08:04 22-12-2010 12/20 25 16:08:04 22-12-2010 12/20 25
    • · ι * - '• · -8-
    Blast furnace slag, quartz sand or clay. It is also possible to add further substances to the starting material. Further compositions which likewise form the basis for sasalt fibers according to the invention are disclosed in the Applicant's patent application "Raw Material for the Production of Basaite Fibers" of 23.12.2010, the content of which also applies here. The moldings can be produced by means of different methods, these also being disclosed in a patent application of the applicant "pretreatment of raw material for the production of basalt fibers" of 23.12.2010 and thus also belong to the content of this application.
    The moldings pass through a temperature range from room temperature to 1200 ° C for a period of 2 to 15 minutes before melting. Preferably, the temperatures are about 300 ° C ± 50eC.
    The process according to the invention comprises the following process steps: a) the shaped bodies are melted in a melting trough, b) the melt is heated by a Feeder kana! fed via a flow feeder the nozzle or bushing, where the basalt fibers are drawn and optionally c) sizing and d) fed subsequently to the winder. The heat-treated moldings are placed in a melting tank, where an oven temperature of up to 1750 ° C prevails and the melting temperature is up to 1600 "C. There is a cavity pressure of 0.5 to 3 mmWS (1mmWS = 0.09807 mbar). For heating, preferably two burners with gas / Oz feed are used. In the feeder channel prevails an oven temperature to 1550 ° C and a melt bath temperature to 1500 ° C, which is produced by 9 burners with gas / Oz heating. In the feeder channel, the temperature is always lower than in the melting furnace. The flow feeder has a diameter of about 15 to 23 mm and has a temperature up to 1450 ° C. It achieves an output of up to 80 kg / h per spinning station. In Bushing with up to 2000 tips, the temperature is up to 1500 ° C and it is also the performance of up to 80 kg / h per spinning position achieved. The Basaitfasem be cooled considerably. Subsequently, a sizing of the continuous basalt fiber can be done. The winder can have a capacity of 0 to 3600 m / min.
    It is also possible to use other methods such as the previously described method for producing the inventive endless batt fiber with improved tensile strength.
    The exemplary embodiments show possible embodiments of the basalt fiber, it being noted at this point that the invention is not limited to the specifically illustrated embodiments of the same, but rather also various combina- N2007 / 10900 22/12 2010 HI 16:03 [SE / EM NO 8051] @ 012 16:08:22 22-12-2010 13/20 25 • * · -0-ons of the individual design variants are possible with each other and this variati onsmöglichkeit due to the doctrine of technical action by representational invention in the skills of this on technical expert. So are all conceivable embodiments, which are possible by combinations of individual details of the illustrated and described embodiment variant, includes the scope of protection.
    The task underlying the independent inventive solutions can be taken from the description. N2007 / 10900 22/12 2010 MI 16:03 [SE / EM NR 8051] @ 013
    权利要求:
    Claims (9)
    [1]
    16:08:28 22-12-2010 14/20 25 * «» · · «

    1. Basalt fiber comprising the elements Si, Al, Fe, Mn, Ti, Ca, Mg, K, Na and O, wherein the Si central atom is surrounded by four oxygen atoms, and the other elements also of oxygen atoms in various Coordination surrounded or at least coupled to oxygen atoms and form further structural units, characterized in that pre-oriented or oriented molecular structures, in particular domains, are present in an otherwise X-ray amorphous structure.
    [2]
    2. Basalt fiber according to claim 1, characterized in that the structural units ausbllden a Nahordnung, wherein the atomic and mofekularen distances and angles between positively charged central atom and the surrounding negatively charged oxygen atoms are irregular and the pre-oriented or oriented Mo lekülstrukturen, in particular domains, form a non-crystalline femoral order.
    [3]
    3. basalt fiber according to claim 2, characterized in that the preoriented or oriented molecular structures, in particular domains, a Femordnung of chain and / or band molecules similar to a pyroxene structure.
    [4]
    The basalt fiber according to claim 3, characterized in that the proportion of the chain molecules similar to the pyroxene structure is selected from a range having a lower limit of 20% and an upper limit of 60%.
    [5]
    5. basalt fiber according to any one of claims 1 to 4, characterized in that the modulus of elasticity of the basalt fiber has a value with a lower limit of 60,000 MPa and an upper limit of 150,000 MPa.
    [6]
    6. Basaitfaser according to any one of claims 1 to 5, characterized in that the tensile strength of the basalt fiber has a value with a lower limit of 1500 MPa and an upper limit of 6000 MPa. N2007 / 10900 22/12 2010 MI 16:03 [SE / EM NR 80511 0014 16:08:41 22-12-2010 15/20 25 16:08:41 22-12-2010 15/20 25 • * • ♦ * «« «· · * *« * * «* · *« «« * Β «· *« ··· * »· * ·« ·· «·· -2-
    [7]
    7. Basalt fiber according to any one of claims 1 to 6, characterized in that the density has a value with a lower limit of 2.0 g / cm3 and an upper limit of 3.0 g / cm3.
    [8]
    8. A process for producing a basaitic fiber according to any one of claims 1 to 7, characterized in that raw material comprising 30% to 70% basalt and / or diabase, B% to 40% quartz component, in particular quartz sand, and 5% to 30% slag, In particular, blast furnace slag is ground to particles, moldings are produced from the particles, the moldings already undergo a temperature range before melting, in which the components of the raw material react with each other and form new mineral phases and molecular structures, and melted in a melting furnace, the melt fed through a feeder channel via a flow feeder to the nozzle or bushing and basalt fibers are pulled, if necessary, a sizing takes place, and subsequently optionally fed to the winder.
    [9]
    9. The method according to claim 8, characterized in that the Formköiper undergo a temperature range from room temperature to 1200 ° C before melting. Asamer Basaltic Fibers GmbH by lawyers

    Partner Rechtsanwalt GmbH N2007 / 10900 22/12 2010 MI 16:03 [SE / EM NR 8051] @ 015
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    同族专利:
    公开号 | 公开日
    HUE028356T2|2016-12-28|
    EP2655277A2|2013-10-30|
    WO2012088561A2|2012-07-05|
    PL2655277T3|2017-08-31|
    ES2583366T3|2016-09-20|
    AT509990B1|2012-01-15|
    EP2655277B1|2016-04-20|
    WO2012088561A9|2012-08-30|
    WO2012088561A3|2012-10-18|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    DE2652149A1|1976-11-16|1978-05-18|Corning Glass Works|Alkali-resistant glass fibres - contg. tholeiitic basalt and zirconia and useful for reinforcing cements|
    DE2909148A1|1978-03-09|1979-09-20|Univ Washington|PROCESS FOR IMPROVING THE TENSILE PROPERTIES OF BASALT FIBERS|WO2012083334A3|2010-12-22|2012-09-07|Asamer Basaltic Fibers Gmbh|Raw material for producing basalt fibres|US3557575A|1969-02-04|1971-01-26|Corning Glass Works|Process for forming a basaltic glass-ceramic product|
    US4199336A|1978-09-25|1980-04-22|Corning Glass Works|Method for making basalt glass ceramic fibers|
    GB9412007D0|1994-06-15|1994-08-03|Rockwell International A S|Production of mineral fibres|
    AT509991B1|2010-12-22|2012-01-15|Asamer Basaltic Fibers Gmbh|RAW MATERIAL FOR THE MANUFACTURE OF BASALT FIBERS|CN111393030A|2020-02-21|2020-07-10|西格马高温科技集团有限公司|High-density mineral cotton fiberboard for replacing blockboard and preparation method thereof|
    法律状态:
    2016-06-15| PC| Change of the owner|Owner name: ASA.TEC GMBH, AT Effective date: 20160415 |
    2021-08-15| MM01| Lapse because of not paying annual fees|Effective date: 20201222 |
    优先权:
    申请号 | 申请日 | 专利标题
    AT0211610A|AT509990B1|2010-12-22|2010-12-22|BASALT FIBER|AT0211610A| AT509990B1|2010-12-22|2010-12-22|BASALT FIBER|
    PL11819046T| PL2655277T3|2010-12-22|2011-12-21|Continuous basalt fibres|
    ES11819046.1T| ES2583366T3|2010-12-22|2011-12-21|Continuous basalt fiber|
    PCT/AT2011/050053| WO2012088561A2|2010-12-22|2011-12-21|Basalt fibres|
    HUE11819046A| HUE028356T2|2010-12-22|2011-12-21|Continuous basalt fibres|
    EP11819046.1A| EP2655277B1|2010-12-22|2011-12-21|Continuous basalt fibres|
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