子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 自固化性铸型造型用粘结剂组合物及使用其的铸型的制造方法 | CN201280042567.4 | 2012-08-31 | CN103764312B | 2016-05-04 | 岩本亮司; 吉田昭 |
| 一种自固化性铸型造型用粘结剂组合物，其含有呋喃树脂和离子化合物，所述离子化合物含有选自亚硫酸氢离子、亚硫酸离子、焦亚硫酸离子、硫代硫酸离子、连多硫酸离子及连二亚硫酸离子中的1种以上的阴离子，所述阴离子的含量相对于所述呋喃树脂有效成分100重量份为0.006～0.60重量份，并且所述自固化性铸型造型用粘结剂组合物在25℃下的pH为6以下。上述离子化合物中的阳离子优选为选自化学元素周期表第1族、第2族及第12族的元素中的金属离子。另外，上述离子化合物中的阴离子优选为选自硫代硫酸离子、亚硫酸氢离子及亚硫酸离子中的1种以上。 | ||||||
| 2 | 自固化性铸型造型用粘结剂组合物及使用其的铸型的制造方法 | CN201280042567.4 | 2012-08-31 | CN103764312A | 2014-04-30 | 岩本亮司; 吉田昭 |
| 一种自固化性铸型造型用粘结剂组合物，其含有呋喃树脂和离子化合物，所述离子化合物含有选自亚硫酸氢离子、亚硫酸离子、焦亚硫酸离子、硫代硫酸离子、连多硫酸离子及连二亚硫酸离子中的1种以上的阴离子，所述阴离子的含量相对于所述呋喃树脂有效成分100重量份为0.006～0.60重量份，并且所述自固化性铸型造型用粘结剂组合物在25℃下的pH为6以下。上述离子化合物中的阳离子优选为选自化学元素周期表第1族、第2族及第12族的元素中的金属离子。另外，上述离子化合物中的阴离子优选为选自硫代硫酸离子、亚硫酸氢离子及亚硫酸离子中的1种以上。 | ||||||
| 3 | Oxazolidine curing agent for joining wood article with a resorcinol resin | JP2000509758 | 1998-08-14 | JP2001515109A | 2001-09-18 | ゴーミング ウー， |
| (57)【要約】 【課題】 木質物品の接合用接着剤としてレソルシノール樹脂又はタンニン樹脂と組合せて用いる改良されたオキサゾリン系硬化剤を提供する。 【解決手段】 好ましくはオキサゾリンを粒状シリカと合体し、樹脂をＮａＯＨ等の塩基と合体する。 この硬化剤に基づく接着剤は木質部品の接着に用いて室温で２４時間硬化後に湿強度要件をパスする。 この硬化剤組成物は保存安定性があり使用前の適宜の時点でつくることができ、それ故接着剤の使用直前に硬化剤をつくる必要がない。 ホルムアルデヒドがないのでホルムアルデヒド又はパラホルムアルデヒドを取扱う際の安全上の問題もない。 この硬化剤は適度のゲル時間又は作業時間をもたらす。 この樹脂は室温で硬化できるのでオーブン加熱を必要とせず、硬化時間を短縮できる。 放射線で樹脂を硬化する場合は暴露時間を短縮できる。 | ||||||
| 4 | 自硬性鋳型造型用粘結剤組成物 | JP2012190042 | 2012-08-30 | JP5986457B2 | 2016-09-06 | 岩本 亮司; 吉田 昭 |
| 5 | RESIST UNDERLAYER FILM-FORMING COMPOSITION CONTAINING NOVOLAC RESIN TO WHICH AROMATIC VINYL COMPOUND IS ADDED | US15127889 | 2015-03-17 | US20170097568A1 | 2017-04-06 | Takafumi ENDO; Keisuke HASHIMOTO; Hirokazu NISHIMAKI; Rikimaru SAKAMOTO |
| A resist underlayer film-forming composition has high solubility in a solvent used at a lithography process for exhibiting good coating film forming properties and able to decrease a sublime generated during formation of a film. A resist underlayer film-forming composition having a novolac resin having a structure group (C) obtained by a reaction of an aromatic ring structure of an aromatic ring-containing compound (A) with a vinyl group of an aromatic vinyl compound (B). The aromatic vinyl compound (B) is represented by Formula (1), and is specifically styrene, 2-vinylnaphthalene, 4-tert-butylstyrene, or 4-tert-butoxystyrene. The structure group (C) is represented by Formula (2). The aromatic ring-containing compound (A) is an aromatic amine compound or a phenolic hydroxy group-containing compound. The novolac resin is a resin produced by a reaction of the aromatic amine compound or the phenolic hydroxy group-containing compound with aldehyde or ketone. | ||||||
| 6 | CEMENTITIOUS STRUCTURE COMPONENTS | US14197961 | 2014-03-05 | US20140182220A1 | 2014-07-03 | Christopher M. Hunt |
| Processes, machines, articles of manufacture and compositions of matter required to construct a habitable structure comprised of a cementitious product, preferably autoclaved aerated concrete (“AAC”), formed in unique blocks, panels and beams. This results in an extremely environmentally friendly habitable dwelling, residential or commercial, which, due to the resultant synergy of embodiments, when compared to a similar structure employing prior art and/or current industry's standard materials and methods of construction, is structurally superior and simultaneously yields substantial savings in labor, time and costs. | ||||||
| 7 | Autoclaved aerated concrete structure components | US11982455 | 2007-10-31 | US08720133B1 | 2014-05-13 | Christopher M. Hunt |
| Processes, machines, articles of manufacture and compositions of matter required to construct a habitable structure comprised of a cementitious product, preferably autoclaved aerated concrete (“AAC”), formed in unique blocks, panels and beams. This results in an extremely environmentally friendly habitable dwelling, residential or commercial, which, due to the resultant synergy of embodiments, when compared to a similar structure employing prior art and/or current industry's standard materials and methods of construction, is structurally superior and simultaneously yields substantial savings in labor, time and costs. | ||||||
| 8 | Aldehyde-polyamine or aldehyde-polyamine- aromatic compound condensation resin adsorbent for heavy metals and heavy metallic compounds | US42468073 | 1973-12-14 | US3892709A | 1975-07-01 | ODA NAKAAKI; IWASA SHOZO; IDOHARA MITSURU; HORIE YOSHIO; FUKUI TAKEO; TAKASAKA NAOMICHI |
| This invention relates to novel aldehyde-polyamine or aldehydepolyamine-aromatic comdensation resin adsorbents for heavy metals and heavy metallic compounds.
|
||||||
| 9 | Process for the preparation of finely divided,insoluble and infusible melamine-formaldehyde condensation products | US51996366 | 1966-01-11 | US3428607A | 1969-02-18 | RENNER ALFRED |
| Infusible and insoluble melamine-formaldehyde condensation products having a mean particle size <1m are prepared by reacting an aqueous solution of melamine and formaldehyde or an aqueous solution of a melamine-formaldehyde precondensate, in the presence of a protective colloid in the pH range 6 to 8 until a solid phase is formed. Reaction is preferably carried out at elevated temperature, e.g. at the boiling point of the solution. 1.5 to 6 mols. of HCHO may be used per mol. of melamine. Other aminoplast forming compounds (e.g. urea and its derivatives and other amino-triazines) may also be present. Examples of protective colloids are starch, tragacanth, gelatine, agar,-agar, polyvinyl alcohol, the sodium salt of carboxmethylcellulose and a hydrolysed polymer of maleic anhydride and styrene. The amount of protective colloid used may be 0.1 to 10% by wt. based on the total amount of aqueous reaction mixture. The starting solution may contain from 5 to 25% by wt. of resin-forming constituents. The precipitation reaction may be carried out at the boiling point of the reaction mixture. | ||||||
| 10 | OXAZOLIDINE-BASED HARDENERS FOR CURING RESORCINOL RESINS IN THE BONDING OF WOOD ARTICLES | EP98913071.1 | 1998-03-25 | EP0973640B1 | 2007-09-05 | WU, Gaoming |
| An improved oxazolidine-based hardener to be used with a resorcinol resin or a tannin resin as the adhesive for the bonding of wood articles. Preferably, an oxazolidine is combined with a base such as NaOH and a powdered absorbent such as wheat flour. The adhesive based on the improved hardener can be used to glue wood particles to pass wet strength requirements after the glue is cured at room temperature for under 24 hours. The improved hardener composition is storage stable; it can be prepared anytime before its use, thus eliminating the need to prepare a hardener immediately prior to the glue use. Since it is formaldehyde-free, it eliminates the safety issues associated with handling formaldehyde or paraformaldehyde. Also, the hardener provides flexible gel time or working time. Since the resins can be cured at room temperature, heating in an oven is not needed but could be used to reduce curing time. If radio frequencies are used to cure the resins, the exposure time can be reduced. | ||||||
| 11 | OXAZOLIDINE-BASED HARDENERS FOR CURING RESORCINOL RESINS IN THE BONDING OF WOOD ARTICLES | EP98913071 | 1998-03-25 | EP0973640A4 | 2000-06-28 | WU GAOMING |
| An improved oxazolidine-based hardener to be used with a resorcinol resin or a tannin resin as the adhesive for the bonding of wood articles. Preferably, an oxazolidine is combined with a base such as NaOH and a powdered absorbent such as wheat flour. The adhesive based on the improved hardener can be used to glue wood particles to pass wet strength requirements after the glue is cured at room temperature for under 24 hours. The improved hardener composition is storage stable; it can be prepared anytime before its use, thus eliminating the need to prepare a hardener immediately prior to the glue use. Since it is formaldehyde-free, it eliminates the safety issues associated with handling formaldehyde or paraformaldehyde. Also, the hardener provides flexible gel time or working time. Since the resins can be cured at room temperature, heating in an oven is not needed but could be used to reduce curing time. If radio frequencies are used to cure the resins, the exposure time can be reduced. | ||||||
| 12 | Kondensationsprodukte aus Phenolmonosulfonsäuren, Dihydroxydiphenylsulfonen, Harnstoff und Formaldehyd | EP91107074.6 | 1991-05-02 | EP0459168A2 | 1991-12-04 | Graf, Hermann, Dr.; Stuebinger, Adolf, Dr.; Lorenz, Klaus, Dr.; Schaffer, Ortwin, Dr.; Stork, Karl, Dr. |
Kondensationsprodukte aus Phenolmonosulfonsäuren, Dihydroxydiphenylsulfonen, Harnstoff und Formaldehyd, die dadurch erhältlich sind, daß man
|
||||||
| 13 | Memory cells and devices | US15611732 | 2017-06-01 | US10115785B1 | 2018-10-30 | Jin Wu; Lin Ma |
| Disclosed are memory cells that include a mixture of an acrylic polyol, an alkylene urea-glyoxal resin, and an acid catalyst, and memory devices that contain a plurality of memory cells. | ||||||
| 14 | Binder composition for making self-hardening foundry molds, and method of producing foundry mold using the same | US14342183 | 2012-08-31 | US09943903B2 | 2018-04-17 | Ryoji Iwamoto; Akira Yoshida |
| The present invention relates to a binder composition for making self-hardening foundry molds that is capable of improving the hardening speed of the molds and the strength of the molds, and is excellent in storage stability; and a method for producing a foundry mold, using this composition. The binder composition for making self-hardening foundry molds of the present invention is a binder composition for making self-hardening foundry molds, comprising a furan resin and an ion compound, wherein the ion compound contains at least one anion selected from the group consisting of a hydrogensulfite ion, a sulfite ion, a pyrosulfite ion, a thiosulfate ion, a thionate ion, and a dithionite ion; the content of the anion is from 0.006 to 0.60 parts by weight for 100 parts by weight of the furan resin; and the composition has a pH of 6 or less at 25° C. | ||||||
| 15 | BINDER COMPOSITION FOR MAKING SELF-HARDENING FOUNDRY MOLDS, AND METHOD OF PRODUCING FOUNDRY MOLD USING THE SAME | US14342183 | 2012-08-31 | US20140296372A1 | 2014-10-02 | Ryoji Iwamoto; Akira Yoshida |
| The present invention relates to a binder composition for making self-hardening foundry molds that is capable of improving the hardening speed of the molds and the strength of the molds, and is excellent in storage stability; and a method for producing a foundry mold, using this composition. The binder composition for making self-hardening foundry molds of the present invention is a binder composition for making self-hardening foundry molds, comprising a furan resin and an ion compound, wherein the ion compound contains at least one anion selected from the group consisting of a hydrogensulfite ion, a sulfite ion, a pyrosulfite ion, a thiosulfate ion, a thionate ion, and a dithionite ion; the content of the anion is from 0.006 to 0.60 parts by weight for 100 parts by weight of the furan resin; and the composition has a pH of 6 or less at 25° C. | ||||||
| 16 | Non-formaldehyde reinforced thermoset plastic composites | US10261070 | 2002-09-30 | US20040036056A1 | 2004-02-26 | Lawrence E. Shea; Frank Ghiorso |
| The invention relates to composition for crosslinking phenol-formaldehyde, phenol-resorcinol-formaldehyde, resorcinol-formaldehyde, tannin-formaldehyde, and similar thermosetting resins with a reactant nitroparaffin derivative, a pH adjuster, a viscosity controller, a polymerization shortstop, and water for use in Reinforced Thermal Plastic (RTP) Composite applications. | ||||||
| 17 | Oxazolidine-based hardeners for the room temperature cure of resorcinol resins in the bonding of wood articles--II | US915522 | 1997-08-15 | US5912317A | 1999-06-15 | Gaoming Wu |
| An improved oxazolidine-based hardener to be used with a resorcinol resin or a tannin resin as the adhesive for the bonding of wood articles. Preferably, an oxazolidine is combined with particulate silica, and the resin is combined with a base such as NaOH. The adhesive based on the improved hardener can be used to glue wood particles to pass wet strength requirements after the glue is cured at room temperature for under 24 hours. The improved hardener composition is storage stable; it can be prepared anytime before its use and, thus, eliminate the need to prepare a hardener immediately prior to the glue use. Since it is formaldehyde-free; it eliminates the safety issues associated with handling formaldehyde or paraformaldehyde. Also, the hardener provides flexible gel time or working time. Since the resins can be cured at room temperature, heating in an oven is not needed but could be used to reduce curing time. If radio frequencies are used to cure the resins, the exposure time can be reduced. | ||||||
| 18 | Benzylic ether phenolic resole resins and their uses | US684800 | 1996-07-17 | US5908914A | 1999-06-01 | Thomas Edward Dando; William Rexford Dunnavant; Robert Bernard Fechter; Heimo Josef Langer |
| This invention relates to benzylic ether phenolic resole resins prepared in a sealed reaction vessel and their uses. The benzylic ether phenolic resole resins are prepared by heating phenol and an aldehyde in a sealed reaction vessel in the presence of a divalent metal catalyst without removing water generated by the reaction until an appropriate endpoint for the resin is reached. The benzylic ether phenolic resole resins produced by the process are preferably free or essentially free of unreacted formaldehyde and can be used in the resin component of phenolic-urethane foundry binders to make foundry cores and/or molds by the cold-box and no-bake processes. The cores and/or molds are used for making metal castings. | ||||||
| 19 | Oxazolidine-based hardeners for the room temperature cure of resorcinol resins in the bonding of wood articles | US825870 | 1997-04-02 | US5858553A | 1999-01-12 | Gaoming Wu |
| An improved oxazolidine-based hardener to be used with a resorcinol resin or a tannin resin as the adhesive for the bonding of wood articles. Preferably, an oxazolidine is combined with a base such as NaOH and a powdered absorbent such as wheat flour. The adhesive based on the improved hardener can be used to glue wood particles to pass wet strength requirements after the glue is cured at room temperature for under 24 hours. The improved hardener composition is storage stable; it can be prepared anytime before its use, thus eliminating the need to prepare a hardener immediately prior to the glue use. Since it is formaldehyde-free; it eliminates the safety issues associated with handling formaldehyde or paraformaldehyde. Also, the hardener provides flexible gel time or working time. Since the resins can be cured at room temperature, heating in an oven is not needed but could be used to reduce curing time. If radio frequencies are used to cure the resins, the exposure time can be reduced. | ||||||
| 20 | Products of the condensation of phenolmonosulfonic acids, dihydroxydiphenyl sulfones, urea and formaldehyde | US696912 | 1991-05-08 | US5155164A | 1992-10-13 | Hermann Graf; Adolf Stuebinger; Klaus Lorenz; Ortwin Schaffer; Karl Stork |
| Products of the condensation of phenolmonosulfonic acids, dihydroxydiphenyl sulfones, urea and formaldehyde can be obtained by(A) preparing a homogeneous reaction mixture in sulfuric acid from the phenolmonosulfonic acid and dihydroxydiphenyl sulfone in the molar ratio of from 3:1 to 10:1, with the proviso that the water content of the mixture is not more than 10% of the total weight of the components, and the mixture contains from 0.3 to 1.5 moles of sulfuric acid per mole of dihydroxydiphenyl sulfone, at from 100.degree. to 180.degree. C.,(B) subsequently, at from 40.degree. to 90.degree. C., carrying out a precondensation with 1 to 2 moles of formaldehyde and 0.5 to 1.5 moles of urea per mole of phenol units present in aqueous medium,(C) partially neutralizing the reaction mixture,(D) adding to the partially neutralized reaction mixture 0 to 0.5 mole of phenol per mole of phenol units present and then 0.1 to 0.8 mole of formaldehyde per mole of phenol units then present,(E) further condensing at from 40.degree. to 90.degree. C.,(F) shifting the pH of the reaction mixture into the neutral range and(G) subsequently acidifying with a weak acid. | ||||||
QQ群二维码
意见反馈
意见反馈