WO2012034404A1 - Gypsum whisker, enhanced mineral wool sound-absorbing plate containing the same and preparation method thereof - Google Patents
Gypsum whisker, enhanced mineral wool sound-absorbing plate containing the same and preparation method thereof Download PDFInfo
- Publication number
- WO2012034404A1 WO2012034404A1 PCT/CN2011/073950 CN2011073950W WO2012034404A1 WO 2012034404 A1 WO2012034404 A1 WO 2012034404A1 CN 2011073950 W CN2011073950 W CN 2011073950W WO 2012034404 A1 WO2012034404 A1 WO 2012034404A1
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- WIPO (PCT)
- Prior art keywords
- parts
- gypsum
- mineral wool
- weight
- gypsum whisker
- Prior art date
Links
- 239000010440 gypsum Substances 0.000 title claims abstract description 71
- 229910052602 gypsum Inorganic materials 0.000 title claims abstract description 71
- 239000011490 mineral wool Substances 0.000 title claims abstract description 39
- 238000002360 preparation method Methods 0.000 title abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 22
- 238000001035 drying Methods 0.000 claims abstract description 9
- 229960000892 attapulgite Drugs 0.000 claims abstract description 8
- 239000004927 clay Substances 0.000 claims abstract description 8
- 229910052625 palygorskite Inorganic materials 0.000 claims abstract description 8
- 239000012188 paraffin wax Substances 0.000 claims abstract description 8
- 229920002401 polyacrylamide Polymers 0.000 claims abstract description 8
- 229920000881 Modified starch Polymers 0.000 claims abstract description 7
- 239000004368 Modified starch Substances 0.000 claims abstract description 7
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims abstract description 7
- 235000019426 modified starch Nutrition 0.000 claims abstract description 7
- 239000002002 slurry Substances 0.000 claims description 22
- 229920000742 Cotton Polymers 0.000 claims description 21
- 238000006243 chemical reaction Methods 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 12
- 239000013078 crystal Substances 0.000 claims description 11
- 239000000047 product Substances 0.000 claims description 10
- 239000007787 solid Substances 0.000 claims description 10
- 238000003756 stirring Methods 0.000 claims description 10
- 239000003381 stabilizer Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 238000001027 hydrothermal synthesis Methods 0.000 claims description 5
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 239000002893 slag Substances 0.000 claims description 4
- 238000005520 cutting process Methods 0.000 claims description 3
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 3
- 239000002994 raw material Substances 0.000 claims description 3
- 239000011780 sodium chloride Substances 0.000 claims description 3
- 239000005995 Aluminium silicate Substances 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 claims description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 2
- 229910000323 aluminium silicate Inorganic materials 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 235000006408 oxalic acid Nutrition 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000001509 sodium citrate Substances 0.000 claims description 2
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 claims description 2
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 claims description 2
- 229940082004 sodium laurate Drugs 0.000 claims description 2
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 claims description 2
- 238000005406 washing Methods 0.000 claims description 2
- PZZYQPZGQPZBDN-UHFFFAOYSA-N aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 claims 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 claims 1
- 229940116315 oxalic acid Drugs 0.000 claims 1
- 229960001790 sodium citrate Drugs 0.000 claims 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 claims 1
- 229940080350 sodium stearate Drugs 0.000 claims 1
- 229940045136 urea Drugs 0.000 claims 1
- 238000005452 bending Methods 0.000 abstract description 6
- 239000012535 impurity Substances 0.000 abstract description 4
- 239000002440 industrial waste Substances 0.000 abstract description 4
- 239000000126 substance Substances 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 230000007797 corrosion Effects 0.000 abstract description 2
- 238000005260 corrosion Methods 0.000 abstract description 2
- 230000007423 decrease Effects 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- 230000002194 synthesizing effect Effects 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 12
- 238000006477 desulfuration reaction Methods 0.000 description 7
- 230000023556 desulfurization Effects 0.000 description 7
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000003546 flue gas Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 235000019738 Limestone Nutrition 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 235000011132 calcium sulphate Nutrition 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000006028 limestone Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001175 calcium sulphate Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000003009 desulfurizing effect Effects 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000010437 gem Substances 0.000 description 1
- 229910001751 gemstone Inorganic materials 0.000 description 1
- 239000011799 hole material Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04B—GENERAL BUILDING CONSTRUCTIONS; WALLS, e.g. PARTITIONS; ROOFS; FLOORS; CEILINGS; INSULATION OR OTHER PROTECTION OF BUILDINGS
- E04B1/00—Constructions in general; Structures which are not restricted either to walls, e.g. partitions, or floors or ceilings or roofs
- E04B1/62—Insulation or other protection; Elements or use of specified material therefor
- E04B1/74—Heat, sound or noise insulation, absorption, or reflection; Other building methods affording favourable thermal or acoustical conditions, e.g. accumulating of heat within walls
- E04B1/82—Heat, sound or noise insulation, absorption, or reflection; Other building methods affording favourable thermal or acoustical conditions, e.g. accumulating of heat within walls specifically with respect to sound only
- E04B1/84—Sound-absorbing elements
- E04B1/86—Sound-absorbing elements slab-shaped
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B14/38—Fibrous materials; Whiskers
- C04B14/383—Whiskers
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B26/00—Compositions of mortars, concrete or artificial stone, containing only organic binders, e.g. polymer or resin concrete
- C04B26/02—Macromolecular compounds
- C04B26/28—Polysaccharides or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/52—Sound-insulating materials
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04B—GENERAL BUILDING CONSTRUCTIONS; WALLS, e.g. PARTITIONS; ROOFS; FLOORS; CEILINGS; INSULATION OR OTHER PROTECTION OF BUILDINGS
- E04B1/00—Constructions in general; Structures which are not restricted either to walls, e.g. partitions, or floors or ceilings or roofs
- E04B1/62—Insulation or other protection; Elements or use of specified material therefor
- E04B1/74—Heat, sound or noise insulation, absorption, or reflection; Other building methods affording favourable thermal or acoustical conditions, e.g. accumulating of heat within walls
- E04B2001/742—Use of special materials; Materials having special structures or shape
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/91—Use of waste materials as fillers for mortars or concrete
Definitions
- Gypsum whisker reinforced mineral wool sound absorbing plate containing the gypsum whisker and preparation method thereof
- the invention relates to a building decoration material and a preparation method thereof, in particular to a gypsum whisker, a reinforced mineral wool sound absorbing plate containing the gypsum whisker and a preparation method thereof.
- Mineral wool board is a new type of building material. It has excellent fireproof, waterproof, moisture proof, soundproofing, heat insulation and easy deep processing. It is widely used in decorative ceilings of public buildings at home and abroad, and can also be used in industry. Factory buildings, high-end residences and high-rise buildings.
- Mineral wool boards generally contain a variety of fillers to enhance physical properties.
- Gypsum whiskers are non-toxic and harmless. They have the advantages of high strength, good toughness, high temperature resistance, chemical resistance and easy surface treatment. Therefore, they can be used as medium-strength fillers.
- Gypsum whiskers can be made from desulfurized gypsum.
- Desulfurization gypsum is an industrial by-product gypsum obtained by desulfurizing and purifying flue gas generated after combustion of a sulfur-containing fuel (coal, oil, etc.), and is obtained by reacting S0 2 in flue gas with limestone CaC0 3 . Its main component is CaS0 4 .23 ⁇ 40, and a small amount of CaC0 3 and CaS0 3 as well as some impurities such as fly ash, organic carbon, calcium carbonate, aluminum oxide, silicon oxide and iron oxide.
- the purity of the desulfurized gypsum varies greatly depending on the desulfurization process and the purity of the limestone feedstock.
- the purity of the desulfurized gypsum is a key factor affecting the synthesis of gypsum whiskers. If the gypsum contains more impurities, it will cause the whiskers to grow without orientation. Therefore, the preparation of gypsum whiskers is usually in the form of gypsum having a very high level of gypsum, such as the method of CN 200810011193.5 (the method of "preparation of calcium sulfate whiskers using flue gas desulfurization gypsum"). The content of calcium sulphate is higher than 90%. However, the desulfurization process in China is relatively backward, and the purity of desulfurization gypsum is generally between 75% and 90%. Therefore, the existing gypsum whisker preparation process is not applicable to the purity of the current desulfurization gypsum in China.
- a first object of the present invention is to provide a gypsum whisker which can be prepared using desilsil gypsum having a purity of between 75% and 90%.
- a second object of the present invention is to provide a reinforced cotton wool sound absorbing plate which is added to the reinforced cotton wool sound absorbing panel to improve the strength of the mineral wool sound absorbing panel.
- a third object of the present invention is to provide a method of preparing the above-described reinforced mineral wool sound absorbing panel.
- the present invention relates to a gypsum whisker which is obtained by the following steps:
- Step 1 Mixing the desulfurized gypsum with a purity of 75% to 90% with water to form a slurry having a solid content of 2% to 15%;
- Step 2 adding dilute acid to the slurry prepared in step 1, filtering and washing, and then adding dilute acid to adjust the pH of the slurry to 1 to 5, the solid content is 2% to 15%, and then the The slurry is placed in an autoclave, and oxygen is introduced at a temperature of 50 to 90 ° C and a stirring speed of 50 rpm to 300 rpm, and the reaction is stopped after 5 to 30 minutes;
- Step 3 After adding a crystal stabilizer to the autoclave, the autoclave is sealed, and the temperature is maintained at a temperature of 110 160 ° C and a stirring speed of 50 rpm to 300 rpm. 600 minutes for the hydrothermal synthesis reaction, and then the reaction product is filtered and washed;
- Step 4 The washed product is dried at 110 to 600 ° C for 2 to 5 hours to obtain the gypsum whisker.
- the prepared gypsum whiskers have a diameter of 0.1 to 4 ⁇ m and an aspect ratio of 30 to 150.
- the pH value of the slurry in step 2 is preferably 2 to 3, and the gemstone whiskers prepared in the range have a relatively large aspect ratio and a better performance.
- the crystal stabilizer of step 3 is selected from the group consisting of magnesium chloride, sodium tripolyphosphate, ethylenediaminetetraacetic acid (EDTA), sodium chloride, aluminum silicate, sodium oleate, sodium stearate, and dodecylbenzene. Sodium, oxalic acid, urea, sodium laurate, sodium citrate, and combinations thereof, the crystal form stabilizer is present in an amount of from 0.01% to 2% by weight.
- the invention also relates to an enhanced mineral wool sound absorbing panel comprising the following components in a weight ratio: mineral wool: 100 parts
- Attapulgite clay 10 ⁇ 16 parts Modified starch:
- Emulsified paraffin Aluminium silicate: 0.4-0.7 parts
- the mineral wool is granular cotton made from industrial waste residue, blast furnace slag.
- the invention also relates to a method for preparing a reinforced cotton sound absorbing panel, comprising the following steps: Step 1: weighing 100 parts by weight of mineral wool, 10-16 parts by weight of attapulgite clay, 5-9 parts by weight Starch starch, 0.6 to 1.0 part by weight of polyacrylamide, 0.5 to 0.7 part by weight of emulsified paraffin, 0.4 0.7 part by weight of aluminum sulfate, and 2 to 30 parts by weight of the above-mentioned gypsum whisker, and the above raw materials are stirred and mixed. Mixture;
- Step 2 The mixture is formed by a wet process, and cut into a plate by a cutter;
- Step 3 The plate is dried, the drying temperature is 230-285 ° C, and the drying time is 2 hours.
- Step 4 cutting the dried plate according to specifications, and performing surface finishing to obtain the enhanced mineral wool sound absorbing plate.
- the mineral wool is granular cotton made from industrial waste residue, blast furnace slag.
- the wet drawing process in the step 2 is carried out in a web forming machine, and after forming, it is preferably cut into a plate by high pressure water in a cutting machine; the drying temperature in the step 3 is preferably 260 ° C;
- the surface finishing method of the board in 4 is the same as the existing surface finishing method of the mineral wool board.
- the preparation method of the reinforced cotton wool sound absorbing panel of the invention further comprises the step of packaging, that is, the finished product is qualified and packaged into the warehouse.
- gypsum whiskers are prepared from the desulfurized gypsum having a lower purity, and the strength of the mineral wool sound absorbing plate is enhanced by adding gypsum whiskers.
- the gypsum whisker prepared by the invention has the advantages of high strength, good toughness, high temperature resistance, chemical resistance, etc. It is a fine single crystal, the internal structure is very complete, and the highly ordered atomic arrangement makes it almost free of any common materials. Defects such as holes, impurities, and particle interfaces, the intensity is close to the theoretical value of the crystal - the intensity of the inter-atomic bond.
- the mineral wool of the present invention is sucked After the soundboard is added to the prepared gypsum whiskers, the bending failure load is increased by 10 to 30%.
- the present invention can fully utilize the desulfurization gypsum with a purity of 75% to 90%, and not only fully utilizes the industrially desulfurized gypsum to realize waste recycling, but also greatly reduces the production cost.
- Figure 1 is a flow chart of a method for preparing gypsum whiskers of the present invention
- FIG. 2 is a flow chart of a method for preparing a reinforced cotton wool sound absorbing panel of the present invention. Preferred embodiment of the invention
- Gypsum whisker preparation was carried out in accordance with the flow chart shown in Fig. 1, and each of the materials in the following examples was commercially available.
- Step 1 Mix 75% of the desulfurized gypsum with water to make a slurry with a solid content of 15%.
- Step 2 Add dilute sulfuric acid to the slurry prepared in step 1, filter and wash, then add dilute sulfuric acid to adjust the pH of the slurry to 1 and the solid content to 15%, and then put the slurry into the autoclave.
- Oxygen was introduced at a temperature of 90 ° C and a stirring speed of 300 rpm, and the reaction was stopped after 30 minutes of reaction.
- Step 3 After adding a crystal stabilizer (1.5% by weight of EDTA and 0.5% by weight of sodium sulphate) to the autoclave, close the inlet and outlet to make the high pressure The reaction vessel was sealed. Then, the mixture was kept at a temperature of 160 ° C and a stirring speed of 50 rpm for 600 minutes to carry out a hydrothermal synthesis reaction, and then the reaction product was filtered and washed.
- a crystal stabilizer (1.5% by weight of EDTA and 0.5% by weight of sodium sulphate
- Step 4 The washed product was dried at 110 ° C for 5 hours to obtain a gypsum whisker product ⁇ .
- Example 2 Step 1 The desulfurized gypsum with a purity of 90% was uniformly mixed with water to prepare a slurry having a solid content of 2%.
- Step 2 Add dilute sulfuric acid to the slurry prepared in step 1, filter and wash, then add dilute sulfuric acid to adjust the pH of the slurry to 5, the solid content is 2%, and then put the slurry into the high pressure reaction kettle.
- Oxygen was introduced at a temperature of 50 ° C and a stirring speed of 50 rpm, and oxygen was stopped after 5 minutes of reaction.
- Step 3 After adding a crystal stabilizer (0.01% by weight of magnesium chloride) to the autoclave, close the inlet and outlet to seal the high pressure reactor. Then, the mixture was kept at a temperature of 110 ° C and a stirring speed of 300 rpm for 240 minutes to carry out a hydrothermal synthesis reaction, and then the reaction product was filtered and washed.
- a crystal stabilizer 0.01% by weight of magnesium chloride
- Step 4 The washed product was dried at 300 ° C for 3 hours to obtain a gypsum whisker product ⁇ .
- Step 1 Mix 85% of the desulfurized gypsum with water to make a slurry with a solid content of 8%.
- Step 2 Add dilute sulfuric acid to the slurry prepared in step 1, filter and wash, then add dilute sulfuric acid to adjust the pH of the slurry to 4, the solid content is 8%, and then put the slurry into the high pressure reaction kettle. Oxygen was introduced at a temperature of 75 ° C and a stirring speed of 200 rpm, and the reaction was stopped after 15 minutes.
- Step 3 After adding a crystal stabilizer (0.3% by weight of sodium chloride) to the autoclave, close the inlet and outlet to seal the high pressure reactor. Then, the mixture was kept at a temperature of 130 ° C and a stirring speed of 150 rpm for 30 minutes to carry out a hydrothermal synthesis reaction, and then the reaction product was filtered and washed.
- a crystal stabilizer (0.3% by weight of sodium chloride)
- Step 4 The washed product was dried at 600 ° C for 2 hours to obtain a gypsum whisker product.
- the gypsum whiskers prepared in the above examples have a diameter of 0.1 to 4 ⁇ m and a length to diameter ratio of 30 to 150. Enhance the preparation of mineral wool sound absorbing panels:
- Step 1 Weigh 100 parts by weight of mineral wool, 10 parts by weight of attapulgite clay, 5 parts by weight of modified starch, 0.6 parts by weight of polyacrylamide, 0.5 parts by weight of emulsified paraffin, 0.4 parts by weight of aluminum sulfate, And gypsum whiskers prepared in Example 1 in the preparation of the above gypsum whiskers in an amount of 12 parts by weight.
- the above raw materials are mixed with water, and thoroughly mixed in a batching mixer to prepare a mixture, and the mixture is output to a returning machine.
- Step 2 The above mixture is formed in a web forming machine by a wet process, and cut into sheets by high pressure water.
- Step 3 The plate is conveyed to a drying kiln through a distributor and dried at a temperature of about 260 ° C for about 2 hours.
- Step 4 Cut the dried plate into 600cm X 600cm size and finish the surface.
- the surface is processed in the same way as the existing mineral wool board surface.
- Step 5 The finished board is made into a 12mm thick reinforced cotton wool sound absorbing board, and the finished product is inspected and packaged.
- each component is weighed according to the following ratio: 100 parts by weight of mineral wool, 14 parts by weight of attapulgite clay, 8 parts by weight of modified starch, 0.9 parts by weight of polyacrylamide, 0.6 weight.
- the preparation procedure was the same as in Example 1, and a 12 mm thick reinforced cotton wool sound absorbing panel was obtained.
- each component is weighed according to the following ratio: 100 parts by weight of mineral wool, 16 parts by weight of attapulgite clay, 9 parts by weight of modified starch, 1.0 part by weight of polyacrylamide, 0.7 weight Parts of emulsifying paraffin, 0.7 parts by weight of aluminum sulfate, and 2 parts by weight of gypsum whiskers prepared in Example 1 in the preparation of the above gypsum whiskers.
- the preparation procedure was the same as in Example 1, and a 12 mm thick increase was obtained. Strong mineral wool sound absorption board finished.
- the reinforced cotton wool sound absorbing plate prepared by the invention has light weight, good sound insulation effect, and the physical and mechanical properties of the reinforced cotton sound absorbing plate are significantly improved compared with the traditional mineral wool sound absorbing plate.
- the bending damage load of the reinforced cotton wool sound absorbing plate prepared in Example 1 is increased by about 30%, and the bending damage load of the reinforced cotton wool sound absorbing plate obtained in Embodiment 2 is increased by about 18%, and the embodiment 3 is The bending damage load of the enhanced mineral wool sound absorbing panel is increased by about 10%.
- the gypsum whiskers prepared by the invention have the advantages of high strength, good toughness, high temperature resistance and chemical corrosion resistance, and can be added as fillers to the mineral wool sound absorbing panels to improve the strength of the mineral wool sound absorbing panels.
- the reinforced cotton wool sound absorbing panels prepared by the invention have significantly improved physical and mechanical properties, especially bending damage loads, and are therefore more suitable for decorative ceilings of public buildings, industrial plants, high-grade residences and high-rise buildings.
- the building's decorative building materials are also provided.
- the invention fully utilizes industrial waste and greatly reduces production costs.
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Abstract
Description
一种石膏晶须, 含有所述石膏晶须的增强矿棉吸声板及其制备方法 Gypsum whisker, reinforced mineral wool sound absorbing plate containing the gypsum whisker and preparation method thereof
技术领域 Technical field
本发明涉及建筑装饰材料及其制备方法, 具体的说, 涉及一种石膏晶须, 含有所述石膏晶须的增强矿棉吸声板及其制备方法。 The invention relates to a building decoration material and a preparation method thereof, in particular to a gypsum whisker, a reinforced mineral wool sound absorbing plate containing the gypsum whisker and a preparation method thereof.
背景技术 Background technique
矿棉板是一种新型建筑材料, 其因具有优良的防火、 防水、 防潮、 隔音、 隔热、 易深加工等性能, ^以在国内外被广泛用于公共建筑的装饰吊顶, 也 可用于工业厂房、 高级住宅和高层建筑。 Mineral wool board is a new type of building material. It has excellent fireproof, waterproof, moisture proof, soundproofing, heat insulation and easy deep processing. It is widely used in decorative ceilings of public buildings at home and abroad, and can also be used in industry. Factory buildings, high-end residences and high-rise buildings.
矿棉板一般包含有多种填充剂用以提高物理性能。 石膏晶须无毒无害, 具有强度高、 韧性好、 耐高温、 抗化学腐蚀、 易进行表面处理等优点, 因而 可用作中等强度的填充剂。 Mineral wool boards generally contain a variety of fillers to enhance physical properties. Gypsum whiskers are non-toxic and harmless. They have the advantages of high strength, good toughness, high temperature resistance, chemical resistance and easy surface treatment. Therefore, they can be used as medium-strength fillers.
石膏晶须可由脱硫石膏制得。 脱硫石膏是对含硫燃料(煤、 油等)燃烧 后产生的烟气进行脱硫净化处理得到的工业副产石膏, 是由烟气中的 S02和 石灰石 CaC03发生反应而得的。 其主要成分是 CaS04.2¾0, 还有少量的 CaC03和 CaS03以及一些粉煤灰、 有机碳、 碳酸钙、 氧化铝、 氧化硅、 氧化 铁等杂质。 根据脱硫工艺和石灰石原料纯度的不同, 脱硫石膏的纯度也有很 大差别。 而脱硫石膏的纯度是影响石膏晶须能否合成的关键因素。 如果石膏 中含有较多杂质, 就会导致晶须无法定向生长。 因此, 目前石膏晶须的制备 通常釆用品位极高的石膏, 如 CN 200810011193.5号专利 (名称为 "利用烟 气脱硫石膏制备硫酸钙晶须的方法" ) 中要求制备石膏晶须的脱硫石膏中二 水石克酸钙的含量高于 90%。 然而, 我国脱硫工艺相对落后, 脱硫石膏的纯度 一般在 75% ~ 90%之间, 因此, 现有的石膏晶须制备工艺对于我国目前的脱 硫石膏纯度是不适用的。 Gypsum whiskers can be made from desulfurized gypsum. Desulfurization gypsum is an industrial by-product gypsum obtained by desulfurizing and purifying flue gas generated after combustion of a sulfur-containing fuel (coal, oil, etc.), and is obtained by reacting S0 2 in flue gas with limestone CaC0 3 . Its main component is CaS0 4 .23⁄40, and a small amount of CaC0 3 and CaS0 3 as well as some impurities such as fly ash, organic carbon, calcium carbonate, aluminum oxide, silicon oxide and iron oxide. The purity of the desulfurized gypsum varies greatly depending on the desulfurization process and the purity of the limestone feedstock. The purity of the desulfurized gypsum is a key factor affecting the synthesis of gypsum whiskers. If the gypsum contains more impurities, it will cause the whiskers to grow without orientation. Therefore, the preparation of gypsum whiskers is usually in the form of gypsum having a very high level of gypsum, such as the method of CN 200810011193.5 (the method of "preparation of calcium sulfate whiskers using flue gas desulfurization gypsum"). The content of calcium sulphate is higher than 90%. However, the desulfurization process in China is relatively backward, and the purity of desulfurization gypsum is generally between 75% and 90%. Therefore, the existing gypsum whisker preparation process is not applicable to the purity of the current desulfurization gypsum in China.
因此, 有必要提供一种新工艺制备的石膏晶须, 以及含有所述石膏晶须 的增强矿棉吸声板及其制备方法。 发明内容 Therefore, it is necessary to provide a gypsum whisker prepared by a new process, and a reinforced mineral wool sound absorbing plate containing the gypsum whisker and a preparation method thereof. Summary of the invention
本发明的第一目的是提供一种石膏晶须, 其可利用纯度在 75% ~ 90%之 间的脱石克石膏制备而成。 A first object of the present invention is to provide a gypsum whisker which can be prepared using desilsil gypsum having a purity of between 75% and 90%.
本发明的第二目的是提供一种增强矿棉吸声板, 所述石膏晶须添加在该 增强矿棉吸声板中, 提高了矿棉吸声板的强度。 A second object of the present invention is to provide a reinforced cotton wool sound absorbing plate which is added to the reinforced cotton wool sound absorbing panel to improve the strength of the mineral wool sound absorbing panel.
本发明的第三目的是提供上述增强矿棉吸声板的制备方法。 A third object of the present invention is to provide a method of preparing the above-described reinforced mineral wool sound absorbing panel.
本发明涉及一种石膏晶须, 其是通过以下步骤制得的: The present invention relates to a gypsum whisker which is obtained by the following steps:
步骤 1 : 将纯度为 75% ~ 90%的脱硫石膏与水混合均匀, 制成固含量为 2%~15%的料浆; Step 1: Mixing the desulfurized gypsum with a purity of 75% to 90% with water to form a slurry having a solid content of 2% to 15%;
步骤 2: 在步骤 1制得的料浆中加入稀 酸, 过滤洗涤, 再加入稀^ 酸 以调整所述料浆的 pH值为 1~5 , 固含量为 2%~15%, 然后将所述料浆放入高 压反应釜中, 在温度为 50~90°C和搅拌速度为 50转 /分钟〜 300转 /分钟的条件 下通入氧气, 反应 5-30分钟后停止通入氧气; Step 2: adding dilute acid to the slurry prepared in step 1, filtering and washing, and then adding dilute acid to adjust the pH of the slurry to 1 to 5, the solid content is 2% to 15%, and then the The slurry is placed in an autoclave, and oxygen is introduced at a temperature of 50 to 90 ° C and a stirring speed of 50 rpm to 300 rpm, and the reaction is stopped after 5 to 30 minutes;
步骤 3: 在所述高压反应釜中加入晶型稳定剂后, 密闭所述高压反应釜, 在温度为 110 160 °C和搅拌速度为 50 转 /分钟〜 300 转 /分钟的条件下保温 30~600分钟, 以进行水热合成反应, 然后将反应产物过滤洗涤; Step 3: After adding a crystal stabilizer to the autoclave, the autoclave is sealed, and the temperature is maintained at a temperature of 110 160 ° C and a stirring speed of 50 rpm to 300 rpm. 600 minutes for the hydrothermal synthesis reaction, and then the reaction product is filtered and washed;
步骤 4: 将洗涤后的产物在 110~600°C的条件下烘干 2~5小时, 即得到所 述石膏晶须。 Step 4: The washed product is dried at 110 to 600 ° C for 2 to 5 hours to obtain the gypsum whisker.
优选地, 制得的石膏晶须的直径为 0.1~4 μπι, 长径比为 30~150。 Preferably, the prepared gypsum whiskers have a diameter of 0.1 to 4 μm and an aspect ratio of 30 to 150.
其中, 步骤 2所述料浆的 ρΗ值优选为 2~3 , 此范围内的 ρΗ值条件所制 得的石膏晶须的长径比相对更大, 性能更好。 步骤 3所述晶型稳定剂选自氯 化镁、 三聚磷酸钠、 乙二胺四乙酸(EDTA ) 、 氯化钠、 石克酸铝、 油酸钠、 硬 脂酸钠、 十二烷基苯横酸钠、 草酸、 尿素、 月桂酸钠、 柠檬酸钠及其组合, 所述晶型稳定剂的重量百分含量为 0.01%-2%。 Wherein, the pH value of the slurry in step 2 is preferably 2 to 3, and the gemstone whiskers prepared in the range have a relatively large aspect ratio and a better performance. The crystal stabilizer of step 3 is selected from the group consisting of magnesium chloride, sodium tripolyphosphate, ethylenediaminetetraacetic acid (EDTA), sodium chloride, aluminum silicate, sodium oleate, sodium stearate, and dodecylbenzene. Sodium, oxalic acid, urea, sodium laurate, sodium citrate, and combinations thereof, the crystal form stabilizer is present in an amount of from 0.01% to 2% by weight.
本发明还涉及一种增强矿棉吸声板, 其包括以下重量配比的各组分: 矿棉: 100份 The invention also relates to an enhanced mineral wool sound absorbing panel comprising the following components in a weight ratio: mineral wool: 100 parts
凹凸棒粘土: 10~16份 改性淀粉: Attapulgite clay: 10~16 parts Modified starch:
聚丙烯酰胺: 0.6-1.0 Polyacrylamide: 0.6-1.0
乳化石蜡: 石克酸铝: 0.4-0.7份 Emulsified paraffin: Aluminium silicate: 0.4-0.7 parts
上述石膏晶须: 2~30份。 The above gypsum whiskers: 2~30 parts.
优选地, 所述矿棉是以工业废渣——高炉矿渣为原料制成的粒状棉。 本发明还涉及一种增强矿棉吸声板的制备方法, 其包括以下步骤: 步骤 1 : 称量 100重量份的矿棉、 10~16重量份的凹凸棒粘土、 5~9重量 份的改性淀粉、 0.6~1.0 重量份的聚丙烯酰胺、 0.5~0.7 重量份的乳化石蜡、 0.4 0.7重量份的硫酸铝, 以及 2~30重量份的上述的石膏晶须, 将上述原料 搅拌混合制成混合料; Preferably, the mineral wool is granular cotton made from industrial waste residue, blast furnace slag. The invention also relates to a method for preparing a reinforced cotton sound absorbing panel, comprising the following steps: Step 1: weighing 100 parts by weight of mineral wool, 10-16 parts by weight of attapulgite clay, 5-9 parts by weight Starch starch, 0.6 to 1.0 part by weight of polyacrylamide, 0.5 to 0.7 part by weight of emulsified paraffin, 0.4 0.7 part by weight of aluminum sulfate, and 2 to 30 parts by weight of the above-mentioned gypsum whisker, and the above raw materials are stirred and mixed. Mixture;
步骤 2: 将所述混合料经湿法抄取工艺成型, 并经切割机切割成板; 步骤 3: 将所述板烘干, 烘干温度为 230~285 °C , 烘干时间为 2小时; 步骤 4: 将烘干后的所述板按规格切割, 并进行表面精加工后即得所述 增强矿棉吸声板。 Step 2: The mixture is formed by a wet process, and cut into a plate by a cutter; Step 3: The plate is dried, the drying temperature is 230-285 ° C, and the drying time is 2 hours. Step 4: cutting the dried plate according to specifications, and performing surface finishing to obtain the enhanced mineral wool sound absorbing plate.
优选地, 所述矿棉是以工业废渣——高炉矿渣为原料制成的粒状棉。 其中, 步骤 2中所述湿法抄取工艺是在成网机中进行的, 成型后优选在 切割机中经高压水切成板; 步骤 3中所述烘干温度优选为 260 °C ; 步骤 4中 所述板的表面精加工方法与现有的矿棉板表面精加工方法相同。 Preferably, the mineral wool is granular cotton made from industrial waste residue, blast furnace slag. Wherein the wet drawing process in the step 2 is carried out in a web forming machine, and after forming, it is preferably cut into a plate by high pressure water in a cutting machine; the drying temperature in the step 3 is preferably 260 ° C; The surface finishing method of the board in 4 is the same as the existing surface finishing method of the mineral wool board.
本发明的增强矿棉吸声板的制备方法还包括包装的步骤, 即将成品检验 合格后包装入库。 The preparation method of the reinforced cotton wool sound absorbing panel of the invention further comprises the step of packaging, that is, the finished product is qualified and packaged into the warehouse.
本发明具有以下优点: The invention has the following advantages:
本发明釆用纯度较低的脱硫石膏制备出石膏晶须, 并通过添加石膏晶须 增强了矿棉吸声板的强度。 本发明制备的石膏晶须具有强度高、 韧性好、 耐 高温、 抗化学腐蚀等优点, 它作为细微的单晶体, 内部结构十分完整, 高度 有序的原子排列, 使它几乎不存在任何普通材料的空穴、 杂质、 颗粒界面等 缺陷, 强度接近晶体理论值一一原子间价键的强度。 因此, 本发明的矿棉吸 声板在加入所制得的石膏晶须后, 弯曲破坏载荷提高了 10~30%。 此外, 本发 明能够充分利用纯度在 75% ~ 90%的脱硫石膏, 不仅充分利用了工业废弃的 脱硫石膏, 实现废物再利用, 而且大大降低了生产成本。 附图概述 In the present invention, gypsum whiskers are prepared from the desulfurized gypsum having a lower purity, and the strength of the mineral wool sound absorbing plate is enhanced by adding gypsum whiskers. The gypsum whisker prepared by the invention has the advantages of high strength, good toughness, high temperature resistance, chemical resistance, etc. It is a fine single crystal, the internal structure is very complete, and the highly ordered atomic arrangement makes it almost free of any common materials. Defects such as holes, impurities, and particle interfaces, the intensity is close to the theoretical value of the crystal - the intensity of the inter-atomic bond. Therefore, the mineral wool of the present invention is sucked After the soundboard is added to the prepared gypsum whiskers, the bending failure load is increased by 10 to 30%. In addition, the present invention can fully utilize the desulfurization gypsum with a purity of 75% to 90%, and not only fully utilizes the industrially desulfurized gypsum to realize waste recycling, but also greatly reduces the production cost. BRIEF abstract
下面结合附图对本发明的实施方式作进一步说明: The embodiments of the present invention are further described below in conjunction with the accompanying drawings:
图 1为本发明的石膏晶须的制备方法的流程图; Figure 1 is a flow chart of a method for preparing gypsum whiskers of the present invention;
图 2为本发明的增强矿棉吸声板的制备方法的流程图。 本发明的较佳实施方式 2 is a flow chart of a method for preparing a reinforced cotton wool sound absorbing panel of the present invention. Preferred embodiment of the invention
石膏晶须的制备: Preparation of gypsum whiskers:
按照图 1所示的流程图进行石膏晶须制备, 下述实施例中的各原料均可 由市售获得。 Gypsum whisker preparation was carried out in accordance with the flow chart shown in Fig. 1, and each of the materials in the following examples was commercially available.
实施例 1 Example 1
步骤 1 : 将纯度为 75%的脱硫石膏与水混合均匀, 制成固含量为 15%的 料浆。 Step 1: Mix 75% of the desulfurized gypsum with water to make a slurry with a solid content of 15%.
步骤 2: 在步骤 1制得的料浆中加入稀硫酸, 过滤洗涤, 再加入稀硫酸 以调整料浆的 pH值为 1 , 固含量为 15%, 然后将料浆放入高压反应釜中, 在 温度为 90°C和搅拌速度为 300转 /分钟的条件下通入氧气, 反应 30分钟后停 止通入氧气。 Step 2: Add dilute sulfuric acid to the slurry prepared in step 1, filter and wash, then add dilute sulfuric acid to adjust the pH of the slurry to 1 and the solid content to 15%, and then put the slurry into the autoclave. Oxygen was introduced at a temperature of 90 ° C and a stirring speed of 300 rpm, and the reaction was stopped after 30 minutes of reaction.
步骤 3:在高压反应釜中加入晶型稳定剂(重量百分含量为 1.5%的 EDTA 和重量百分含量为 0.5%的三聚碑酸钠)后, 关闭进气口、 出气口, 使高压反 应釜密闭。然后在温度为 160°C和搅拌速度为 50转 /分钟的条件下保温 600分 钟, 以进行水热合成反应, 然后将反应产物过滤洗涤。 Step 3: After adding a crystal stabilizer (1.5% by weight of EDTA and 0.5% by weight of sodium sulphate) to the autoclave, close the inlet and outlet to make the high pressure The reaction vessel was sealed. Then, the mixture was kept at a temperature of 160 ° C and a stirring speed of 50 rpm for 600 minutes to carry out a hydrothermal synthesis reaction, and then the reaction product was filtered and washed.
步骤 4: 将洗涤后的产物在 110°C的条件下烘干 5小时, 得到石膏晶须产 口 σ。 Step 4: The washed product was dried at 110 ° C for 5 hours to obtain a gypsum whisker product σ.
实施例 2 步骤 1 : 将纯度为 90%的脱硫石膏与水混合均匀, 制成固含量为 2%的料 浆。 Example 2 Step 1: The desulfurized gypsum with a purity of 90% was uniformly mixed with water to prepare a slurry having a solid content of 2%.
步骤 2: 在步骤 1制得的料浆中加入稀硫酸, 过滤洗涤, 再加入稀硫酸 以调整料浆的 pH值为 5 , 固含量为 2%, 然后将料浆放入高压反应釜中, 在 温度为 50°C和搅拌速度为 50转 /分钟的条件下通入氧气, 反应 5分钟后停止 通入氧气。 Step 2: Add dilute sulfuric acid to the slurry prepared in step 1, filter and wash, then add dilute sulfuric acid to adjust the pH of the slurry to 5, the solid content is 2%, and then put the slurry into the high pressure reaction kettle. Oxygen was introduced at a temperature of 50 ° C and a stirring speed of 50 rpm, and oxygen was stopped after 5 minutes of reaction.
步骤 3: 在高压反应釜中加入晶型稳定剂(重量百分含量为 0.01%的氯化 镁)后, 关闭进气口、 出气口, 使高压反应釜密闭。 然后在温度为 110°C和 搅拌速度为 300转 /分钟的条件下保温 240分钟, 以进行水热合成反应, 然后 将反应产物过滤洗涤。 Step 3: After adding a crystal stabilizer (0.01% by weight of magnesium chloride) to the autoclave, close the inlet and outlet to seal the high pressure reactor. Then, the mixture was kept at a temperature of 110 ° C and a stirring speed of 300 rpm for 240 minutes to carry out a hydrothermal synthesis reaction, and then the reaction product was filtered and washed.
步骤 4: 将洗涤后的产物在 300°C的条件下烘干 3小时, 得到石膏晶须产 口 σ。 Step 4: The washed product was dried at 300 ° C for 3 hours to obtain a gypsum whisker product σ.
实施例 3 Example 3
步骤 1 : 将纯度为 85%的脱硫石膏与水混合均匀, 制成固含量为 8%的料 浆。 Step 1: Mix 85% of the desulfurized gypsum with water to make a slurry with a solid content of 8%.
步骤 2: 在步骤 1制得的料浆中加入稀硫酸, 过滤洗涤, 再加入稀硫酸 以调整料浆的 pH值为 4, 固含量为 8%, 然后将料浆放入高压反应釜中, 在 温度为 75°C和搅拌速度为 200转 /分钟的条件下通入氧气, 反应 15分钟后停 止通入氧气。 Step 2: Add dilute sulfuric acid to the slurry prepared in step 1, filter and wash, then add dilute sulfuric acid to adjust the pH of the slurry to 4, the solid content is 8%, and then put the slurry into the high pressure reaction kettle. Oxygen was introduced at a temperature of 75 ° C and a stirring speed of 200 rpm, and the reaction was stopped after 15 minutes.
步骤 3: 在高压反应釜中加入晶型稳定剂 (重量百分含量为 0.3%的氯化 钠)后, 关闭进气口、 出气口, 使高压反应釜密闭。 然后在温度为 130°C和 搅拌速度为 150转 /分钟的条件下保温 30分钟, 以进行水热合成反应, 然后 将反应产物过滤洗涤。 Step 3: After adding a crystal stabilizer (0.3% by weight of sodium chloride) to the autoclave, close the inlet and outlet to seal the high pressure reactor. Then, the mixture was kept at a temperature of 130 ° C and a stirring speed of 150 rpm for 30 minutes to carry out a hydrothermal synthesis reaction, and then the reaction product was filtered and washed.
步骤 4: 将洗涤后的产物在 600°C的条件下烘干 2小时, 得到石膏晶须产 品。 Step 4: The washed product was dried at 600 ° C for 2 hours to obtain a gypsum whisker product.
经测试, 上述实施例制备得到的石膏晶须直径为 0.1~4μπι, 长径比为 30~150。 增强矿棉吸声板的制备: The gypsum whiskers prepared in the above examples have a diameter of 0.1 to 4 μm and a length to diameter ratio of 30 to 150. Enhance the preparation of mineral wool sound absorbing panels:
按照图 2所示的流程图进行增强矿棉吸声板的制备, 下述实施例中的各 原料均可由市售获得。 实施例 1 The preparation of the reinforced cotton wool sound absorbing panel was carried out in accordance with the flow chart shown in Fig. 2, and each of the materials in the following examples was commercially available. Example 1
步骤 1 : 称量 100重量份的矿棉、 10重量份的凹凸棒粘土、 5重量份的 改性淀粉、 0.6重量份的聚丙烯酰胺、 0.5重量份的乳化石蜡、 0.4重量份的硫 酸铝, 以及 12重量份的上述石膏晶须的制备中实施例 1制得的石膏晶须。 将 上述原料与水混合, 并在配料搅拌机中充分搅拌制成混合料, 并将混合料输 出到回料机。 Step 1: Weigh 100 parts by weight of mineral wool, 10 parts by weight of attapulgite clay, 5 parts by weight of modified starch, 0.6 parts by weight of polyacrylamide, 0.5 parts by weight of emulsified paraffin, 0.4 parts by weight of aluminum sulfate, And gypsum whiskers prepared in Example 1 in the preparation of the above gypsum whiskers in an amount of 12 parts by weight. The above raw materials are mixed with water, and thoroughly mixed in a batching mixer to prepare a mixture, and the mixture is output to a returning machine.
步骤 2: 将上述混合料在成网机中经湿法抄取工艺成型, 并经高压水切 成板。 Step 2: The above mixture is formed in a web forming machine by a wet process, and cut into sheets by high pressure water.
步骤 3: 将上述板通过分配机输送至干燥窑, 在 260°C左右的温度下烘干 2小时左右。 Step 3: The plate is conveyed to a drying kiln through a distributor and dried at a temperature of about 260 ° C for about 2 hours.
步骤 4: 将烘干后的板按规格切割成 600cm X 600cm大小, 并进行表面精 加工, 表面 ^"加工方法与现有的矿棉板表面 ^"加工方法相同。 Step 4: Cut the dried plate into 600cm X 600cm size and finish the surface. The surface is processed in the same way as the existing mineral wool board surface.
步骤 5: 将精加工后的板制成 12mm厚的增强矿棉吸声板成品, 将成品 检验合格后包装入库。 Step 5: The finished board is made into a 12mm thick reinforced cotton wool sound absorbing board, and the finished product is inspected and packaged.
实施例 2 Example 2
本实施例中, 按照如下配比称取各组分: 称量 100重量份的矿棉、 14重 量份的凹凸棒粘土、 8重量份的改性淀粉、 0.9重量份的聚丙烯酰胺、 0.6重 量份的乳化石蜡、 0.6重量份的硫酸铝, 以及 30重量份的上述石膏晶须的制 备中实施例 1制得的石膏晶须。 制备流程与实施例 1相同, 制得 12mm厚的 增强矿棉吸声板成品。 In this embodiment, each component is weighed according to the following ratio: 100 parts by weight of mineral wool, 14 parts by weight of attapulgite clay, 8 parts by weight of modified starch, 0.9 parts by weight of polyacrylamide, 0.6 weight. Parts of emulsifying paraffin, 0.6 parts by weight of aluminum sulfate, and 30 parts by weight of gypsum whiskers prepared in Example 1 in the preparation of the above gypsum whiskers. The preparation procedure was the same as in Example 1, and a 12 mm thick reinforced cotton wool sound absorbing panel was obtained.
实施例 3 Example 3
本实施例中, 按照如下配比称取各组分: 称量 100重量份的矿棉、 16重 量份的凹凸棒粘土、 9重量份的改性淀粉、 1.0重量份的聚丙烯酰胺、 0.7重 量份的乳化石蜡、 0.7重量份的硫酸铝, 以及 2重量份的上述石膏晶须的制备 中实施例 1制得的石膏晶须。 制备流程与实施例 1相同, 制得 12mm厚的增 强矿棉吸声板成品。 In this embodiment, each component is weighed according to the following ratio: 100 parts by weight of mineral wool, 16 parts by weight of attapulgite clay, 9 parts by weight of modified starch, 1.0 part by weight of polyacrylamide, 0.7 weight Parts of emulsifying paraffin, 0.7 parts by weight of aluminum sulfate, and 2 parts by weight of gypsum whiskers prepared in Example 1 in the preparation of the above gypsum whiskers. The preparation procedure was the same as in Example 1, and a 12 mm thick increase was obtained. Strong mineral wool sound absorption board finished.
对上述实施例 1〜实施例 3所制得的增强矿棉吸声板分别进行物理性能测 试, 测试结果如下表 1所示。 The reinforced cotton wool sound absorbing panels prepared in the above Examples 1 to 3 were respectively subjected to physical property tests, and the test results are shown in Table 1 below.
表 1 增强矿棉吸声板性能评价 Table 1 Performance Evaluation of Enhanced Mineral Wool Acoustic Panel
如表 1所示, 本发明制备的增强矿棉吸声板质量轻, 隔音隔热效果良好, 且与传统矿棉吸声板相比, 其物理力学性能显著提高。 其中, 实施例 1制得 的增强矿棉吸声板的弯曲破坏载荷提高了约 30%, 实施例 2制得的增强矿棉 吸声板的弯曲破坏载荷提高了约 18%, 实施例 3制得的增强矿棉吸声板的弯 曲破坏载荷提高了约 10%。 As shown in Table 1, the reinforced cotton wool sound absorbing plate prepared by the invention has light weight, good sound insulation effect, and the physical and mechanical properties of the reinforced cotton sound absorbing plate are significantly improved compared with the traditional mineral wool sound absorbing plate. The bending damage load of the reinforced cotton wool sound absorbing plate prepared in Example 1 is increased by about 30%, and the bending damage load of the reinforced cotton wool sound absorbing plate obtained in Embodiment 2 is increased by about 18%, and the embodiment 3 is The bending damage load of the enhanced mineral wool sound absorbing panel is increased by about 10%.
工业实用性 本发明制备的石膏晶须具有强度高、 韧性好、 耐高温、 抗化学腐蚀等优 点, 可作为填料添加于矿棉吸声板中来提高矿棉吸声板的强度。 Industrial Applicability The gypsum whiskers prepared by the invention have the advantages of high strength, good toughness, high temperature resistance and chemical corrosion resistance, and can be added as fillers to the mineral wool sound absorbing panels to improve the strength of the mineral wool sound absorbing panels.
本发明制备的增强矿棉吸声板与传统矿棉吸声板相比, 其物理力学性能 特别是弯曲破坏载荷显著提高, 因而更加适用于公共建筑的装饰吊顶, 以及 工业厂房、 高级住宅和高层建筑的装饰建材中。 Compared with the traditional mineral wool sound absorbing panels, the reinforced cotton wool sound absorbing panels prepared by the invention have significantly improved physical and mechanical properties, especially bending damage loads, and are therefore more suitable for decorative ceilings of public buildings, industrial plants, high-grade residences and high-rise buildings. The building's decorative building materials.
本发明充分利用了工业废弃物, 大大降低了生产成本。 The invention fully utilizes industrial waste and greatly reduces production costs.
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