Ultrafine modified hydromagnesite composite powder, and preparation method and application thereof
US-2024409748-A1 · Dec 12, 2024 · US
US9522990B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9522990-B2 |
| Application number | US-201314438046-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 24, 2013 |
| Priority date | Oct 26, 2012 |
| Publication date | Dec 20, 2016 |
| Grant date | Dec 20, 2016 |
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A modified carbon black comprising carbon black and at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II), in which the content of the at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II) relative to 100 parts by weight of carbon black is 0.1 to 50 parts by weight.
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The invention claimed is: 1. A modified carbon black comprising carbon black and at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II), wherein a content of the at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II) relative to 100 parts by weight of carbon black is 0.1 to 50 parts by weight: wherein P 1 and P 2 each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, or P 1 and P 2 are combined with each other to represent an alkanediyl group having 2 to 6 carbon atoms; m represents an integer of 2 to 9; M n+ represents H + or an n-valent metal cation; and n represents an integer of 1 to 3; wherein R 1 represents an alkanediyl group having 1 to 12 carbon atoms and optionally having a substituent, a cycloalkanediyl group having 3 to 12 carbon atoms and optionally having a substituent, or a *—B 1 —Ar—B 2 —* group wherein * represents a bond, B 1 represents a single bond or an alkanediyl group having 1 to 12 carbon atoms, B 2 represents a single bond or an alkanediyl group having 1 to 12 carbon atoms, and Ar represents a divalent aromatic hydrocarbon group having 6 to 12 carbon atoms and optionally having a substituent; R 2 and R 3 each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 12 carbon atoms, a hydroxy group or an alkoxy group having 1 to 6 carbon atoms, or R 2 and R 3 are combined with each other to represent an alkanediyl group having 2 to 12 carbon atoms; R 4 represents a hydroxy group, an alkoxy group having 1 to 6 carbon atoms, an aryloxy group having 6 to 12 carbon atoms, an arylalkoxy group having 7 to 15 carbon atoms, an amino group having 0 to 12 carbon atoms or —O − (Y n+ ) 1/n wherein Y n+ represents an n-valent cation and n represents 1 or 2; and X 2 represents —NH— or —O—. 2. The modified carbon black according to claim 1 , wherein the at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II) is a compound represented by formula (I), a nitrogen-element content is 0.01 to 10 wt %, and a sulfur-element content is 0.04 to 13.5 wt %. 3. The modified carbon black according to claim 1 , obtained by mixing carbon black and at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II). 4. The modified carbon black according to claim 1 , obtained by mixing carbon black and at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II) in the presence of a solvent and taking out a solid substance from the obtained mixture. 5. The modified carbon black according to claim 4 , wherein the solvent is water. 6. The modified carbon black according to claim 1 , wherein the at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II) is a compound represented by formula (I-1): 7. The modified carbon black according to claim 1 , wherein the modified carbon black is in a granular form. 8. The modified carbon black according to claim 1 , obtained by mixing carbon black and an aqueous solution of at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II), and granulating followed by drying. 9. The modified carbon black according to claim 1 , obtained by mixing carbon black and water, granulating, thereafter adding an aqueous solution of at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II) and drying. 10. A method for producing a modified carbon black comprising mixing carbon black and at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II): wherein P 1 and P 2 each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, or P 1 and P 2 are combined with each other to represent an alkanediyl group having 2 to 6 carbon atoms; m represents an integer of 2 to 9; M n+ represents H + or an n-valent metal cation; and n represents an integer of 1 to 3; wherein R 1 represents an alkanediyl group having 1 to 12 carbon atoms and optionally having a substituent, a cycloalkanediyl group having 3 to 12 carbon atoms and optionally having a substituent, or a *—B 1 —Ar—B 2 —* group wherein * represents a bond, B 1 represents a single bond or an alkanediyl group having 1 to 12 carbon atoms, B 2 represents a single bond or an alkanediyl group having 1 to 12 carbon atoms, and Ar represents a divalent aromatic hydrocarbon group having 6 to 12 carbon atoms and optionally having a substituent; R 2 and R 3 each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 12 carbon atoms, a hydroxy group or an alkoxy group having 1 to 6 carbon atoms, or R 2 and R 3 are combined with each other to represent an alkanediyl group having 2 to 12 carbon atoms; R 4 represents a hydroxy group, an alkoxy group having 1 to 6 carbon atoms, an aryloxy group having 6 to 12 carbon atoms, an arylalkoxy group having 7 to 15 carbon atoms, an amino group having 0 to 12 carbon atoms or —O − (Y n+ ) 1/n wherein Y n+ represents an n-valent cation and n represents 1 or 2; and X 2 represents —NH— or —O—. 11. The method for producing a modified carbon black according to claim 10 , comprising mixing carbon black and at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II) in the presence of a solvent and taking out a solid substance from the obtained mixture. 12. The method for producing a modified carbon black according to claim 11 , wherein the solvent is water. 13. The method for producing a modified carbon black according to claim 10 , comprising mixing carbon black and an aqueous solution of at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II), and granulating followed by drying. 14. The method for producing a modified carbon black according to claim 10 , comprising mixing carbon black and water, granulating, thereafter adding an aqueous solution of at least one compound selected from the group consisting of a compound represented by formula (I) and a compound represented by formula (II) and drying.
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