• 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:
    An inorganic-organic combined material constituted of co-hardened inorganic and organic components is prepared by mixing a polyvalent metal salt of phosphoric acid, a hardening agent and a thermosetting resin curable with an acid catalyst and subjecting the resultant mixture to co- hardening, optionally in the presence of a blowing agent. This material has excellent nonflammability and water resistance as well as in other properties such as mechanical strength. In particular, expanded products having cell walls made of this material are suitable for various purposes, e.g. construction materials and lagging materials.
    公开号:SU1020007A3
    申请号:SU782700103
    申请日:1978-12-27
    公开日:1983-05-23
    发明作者:Есино Акира；Вакабаяси Цунео；Ивами Исаму
    申请人:Асахи-Дау Лимитед (Фирма)；
    IPC主号:
    专利说明:

    ts9
    LTD
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    Isolation refers to the preparation of a spongy material obtained on the basis of an organic / nerganic binder, and can be used in various industrial areas as a heat insulating refractory material. A known method for producing inorganic-organic foam by mixing thermosetting. resins with a foaming agent, an acidic catalyst and a salt of phosphoric acid. As the salt of phosphoric acid, the reaction product of m-oxide (midium oxide) and orthophosphonic acid is used with the ratio of metal ion to phosphorus ION, O, and the ratio of metal d ome to ph ора ohr atom, equal to О D1. Upon receipt of the foam, non-organic components are dispersed in a powder form into the walls of the components consisting of organic components. As a result, the resulting material is characterized by low compressive strength, increased moisture absorption and combustibility. The object of the invention is to increase the compressive strength, reduce the flammability and moisture absorption of the material. . Said object is achieved in that in the preparation of organic-neooganichesko .penomateriala by mixing thermosetting resin with vspenivayuschegotverzhdayuschim agent, an acid catalyst and a salt of phosphoric acid as termore su- resin isprlzuyut aqueous urea resins or phenol-formaldehyde resin or melamine resin, and the salt phosphoric acid, apply the hardened product of the reaction of phosphoric acid with luminium hydroxide and zinc oxide or primary aluminum phosphate, or the reaction product of phosphate fororic acid with aluminum hydroxide, magnesium oxide, zinc oxide, napti giprookigyu with a ratio of metal ion and phosphorus ion (E) equal to., and at a ratio of the atom metal and phosphorus atom (M / P). equal 1: 6-3 : 2, The cell walls of the resulting foam consist of inorganic and organic components, as a result of which the strength characteristics of the material are improved, the water absorption and combustibility are reduced. In the examples, thermal conductivity is measured by ASTMC518. The oxygen index is measured using the ON-1 flammability tester (manufactured by Suga Testing Machinery Company Limited) using a test strip of H mm x 5 mm x 100 mm. PRI me R I. Content of components, parts by weight; Phosphoric acid (75% aqueous solution) 160 Aluminum oxide 20 Oxide, zinc 35 These components are mixed to carry out the reaction, as a result of which a transparent viscous coating is obtained, having an E-value of 0.4 and an M / P-value of O, 5 B. A liquid solution having 30 parts by weight is also prepared. molten oxide in magnesium, divided into 50 veg .. h. an aqueous solution of urea resin (solids content. Both solutions are mixed together and mixed. The mixture is placed in a molding frame measuring 2 cm x 2 cm x 10. After 6 hours, curing is considered complete upon receipt of a block of cured product having an E-value O , 8 and M / P-value of 1.5. The resulting product is translucent and has a specific weight of 1.9 ~ compressive strength of 650 kg / cm and an oxygen index of 90 or more. P RIM ep 2. Component content, parts by weight : Phosphoric acid (75% aqueous solution) In Aluminum oxide 10 Zinc oxide 17.5 U The mixed components were mixed for the reaction, resulting in a clear, viscous solution having an E-value, O, 4, and a M / P value of 0.56. A liquid solution is also prepared, containing 15 parts by weight of fully cured magnesium oxide, distributed in 00 weight, including carbamide resin, which is used in example 1.
    Both solutions are mixed together, mixed and fed to a 2 cm x X 2 cm X 10 cm molding frame. The molded product is considered full-length hardened after 6 hours to form an aperture block with an E value of 0.8 and M / P-value 1.5, containing 100 v. & C. hardened solar product (| humoric acid and 350 parts by weight of hardened carbamide resin product. This deviated product is semi-transparent and has a very high weight of 1, 5, compressive strength 1050 g / cm and oxygen index 55 , 0.
    Comparative Example 1. Content of components, weight. h .:.
    VOD1. "And solution
    carbamide resin (solids content 70) .500 Anhydrous Calcium Sulphate Powder LLP 10 weight percent is added to the liquid solution prepared by mixing these components. including 10 -nog water solution of phosphoric acid. The rubber mixture is fed to a molding frame measuring 2 cm x 2 cm x 10 cm. After 3 hours, complete curing is achieved.
    A cured product thus prepared containing
    too anhydrous calcium sulphate powder and 350 wt. The cured carbamide resin product has a specific gravity of 5, a compressive strength of 850 kg / cm and an oxygen index of 25.0.
    Froze Content of components, weight .4 .: phosphoric acid
    751st water growth-1bO
    thief;
    Aluminum hydroxide .20 Zinc oxide 35 These components are mixed to obtain a clear viscous solution, which has an E-value of Q, kk and M / Pc. A value of 0.5b.
    To this solution add 100 weight, h. carbamide resin (solid content 7.0) for a more viscous, clear solution. Directly following
    By this, 70 parts by weight of powdered basic magnesium carbonate is added to the solution, which is to be completely mixed with the solution. Foaming begins immediately after the mixture has completely hardened for 6 hours. E-value after expansion and curing should be equal to 0.8, and M / G-value 1.5.
    This spongy product should have a bulk density of 0.09, an average diameter of 1.9 and a thermal conductivity of 0.035 kcal / m.
    PRI me R s 4, i) and with and in and those ly p e m R u s. 2.3. Analogously to Example 1, with the exception that the amount of the urea solution aqueous solution varies according to Table 1.
    Each of the obtained spongy products has the properties listed in table 2. , Example, 6.7 and with and in and t eli y syshp p. I mery, 5. Prepare solutions of phosphoric acid, having the compositions given in the table.
    Two solutions, namely: each of the phosphate salt solutions, which has the specified composition, and a 200-u carbamide resin solution (solid particle content 701) ,. having fully dispersed 50 weight parts. aluminum silicate, .0 ve of magnesium oxide and 15 weight.h. the pentane distributed therein is mixed together and left to stand. The results are summarized in table.
    Comparative Example 6. Similarly to Example 3, except that instead of 70% of basic magnesium carbonate, 5 parts by weight are added. The resulting spongy and cured product has an E-value of 0.6 and a M / P value of O, .86.
    The resulting spongy product is very hygroscopic and gives an acidic reaction even after 8 h.
    PRI me R 8. Content of components, parts:
    Aluminum primary phosphate (50% aqueous solution, E-value 0.33, M / P-value 0.33) 150 Resol-type phenolic resin (80% aqueous solution) Aluminum powder After mixing these components, the mixture is kept at 80 for 30 minutes while drying with hot air. After curing, the sponge product has an E-value of 1.0 ,. M / P is a value of 1.0 and the specific gravity is O ,, 08. This spongy product remains in an electric oven, installed for 1 hour. After calcination, the spongy discoloration product is in the dark, but its original cellular structure is preserved. Substantial example, Contents of components. weight. including: Resole-type phenolic resin (80% aqueous solution) 125 Aluminum tertiary phosphate powder 95 Pentane 5 To the solution, mixed with the indicated components, add 20 parts by weight. A 10% aqueous solution of phosphoric acid in which 2.0 parts by weight is dissolved. p-toluene sulfurous acid. The mixture is left to stand at. After 1 minute, foaming begins. generation of heat, which leads to the formation of a spongy product having a specific weight of 0.12. This sponge product is left in the electric furnace installed at 1 hour. After calcination, only the powdered carbonated product is retained. Example 9. The content of components, weight, h .; Phosphoric acid (75% aqueous solution) 1bS Aluminum hydroxide 20 Zinc oxide20 These components are mixed to obtain a clear and viscous solution. After additional addition of 1.0 parts by weight. laurylamine as a water repellent and weight parts. paper pulp as a reinforcing material to a solution of 100 weight, h. an aqueous solution of melamine resin, which is diluted with 20 wt. hours, powdered metallic aluminum is added to the mixture. After complete mixing, the mixture is left to dry with a hot air of 100 ° C, the homogeneous mixture set for 30 minutes. The resulting sponge product has a specific gravity of 0.16 and is also endowed with the property of complete water repellency.
    X Content of carbamide resin: hard carbamide resin (parts by weight) per 100 parts by weight solidified phosphoric acid salt.
    Table 2
    Table3
    权利要求:
    Claims (1)
    [1]
    METHOD FOR PRODUCING INORGANIC-ORGANIC QMATE RIAL FOAM by mixing a thermosetting agent with a curing agent, an acidic catalyst and phosphorus acid salt, characterized in that, in order to increase the compressive strength, reduce the combustibility and moisture absorption of foam An aqueous solution of a urea resin or phenol-formaldehyde resin or melamine resin is used as the thermoactive resin, and a cured reaction product of phosphoric acid with aluminum hydroxide is used as the phosphoric acid salt. zinc oxide or primary aluminum phosphate, or the reaction product of phosphoric acid with aluminum hydroxide, magnesium oxide, zinc oxide, sodium hydroxide with a metal ion to phosphorus ion ratio of 1: 9-3: 4, and a metal atom to atom ratio phosphorus equal to 1: 6-3: 2.
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    同族专利:
    公开号 | 公开日
    GB2011926A|1979-07-18|
    FR2413440A1|1979-07-27|
    DE2856137B2|1981-06-19|
    JPS5488925A|1979-07-14|
    FR2413440B1|1983-12-09|
    DE2856137C3|1982-03-25|
    GB2011926B|1982-08-25|
    DE2856137A1|1979-06-28|
    JPS5835532B2|1983-08-03|
    CA1108349A|1981-09-01|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    JPS606035U|1983-06-27|1985-01-17|
    JPS606032U|1983-06-27|1985-01-17|
    JP2901537B2|1995-09-27|1999-06-07|三洋化成工業株式会社|Inorganic-organic composite foam and method for producing the same|
    GB2505974B|2012-09-18|2016-11-02|Kingspan HoldingsLtd|Phenolic foam|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    JP15654777A|JPS5835532B2|1977-12-27|1977-12-27|
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