Process for preparing blends of trans-1,4-polybutadiene and syndiotactic 1,2-polybutadiene
US-10035908-B1 · Jul 31, 2018 · US
US10711075B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10711075-B2 |
| Application number | US-201816033810-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 12, 2018 |
| Priority date | Jul 21, 2017 |
| Publication date | Jul 14, 2020 |
| Grant date | Jul 14, 2020 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Provided is a method of preparing a rubber composition, which includes (a) reacting a conjugated diene-based monomer with one or more of compounds in the presence of a first catalyst; (b) adding a conjugated diene-based monomer to a product of the step (a) and inducing a reaction; and (c) adding a second catalyst and a conjugated diene-based monomer to a product of the step (b) and inducing a reaction.
Opening claim text (preview).
What is claimed is: 1. A method of preparing a rubber composition, comprising: (a) reacting a conjugated diene-based monomer with one or more of compounds represented by the following Chemical Formulas 1 and 2 in the presence of a first catalyst; (b) adding a conjugated diene-based monomer to a product of the step (a) and inducing a reaction; and (c) adding a second catalyst and a conjugated diene-based monomer to a product of the step (b) and inducing a reaction: (R 1 ) m —Z 1 C≡C n Z 2 —(R 2 ) o <Chemical Formula 1> (R 1 ) m —Z 1 -A 1 C≡C n A 2 -Z 2 —(R 2 ) o <Chemical Formula 2> wherein R 1 and R 2 each are a C1 to C20 alkyl, aryl, or alkoxy group, —NR′R″, —SiR′R″R″′, or hydrogen, wherein R′, R″, and R′″ each are a C1 to C20 alkyl, aryl, or alkoxy group, or hydrogen, m and o each are an integer of 0 to 3, Z 1 and Z 2 each are silicon, tin, nitrogen, oxygen, sulfur, phosphorus, carbon, or hydrogen, A 1 and A 2 each are a C1 to C20 alkylene or arylene group, and n is an integer of 1 to 20. 2. The method of claim 1 , wherein the first catalyst is a neodymium-based catalyst prepared from a monomeric neodymium salt compound. 3. The method of claim 2 , wherein the monomeric neodymium salt compound is one or more selected from the group consisting of neodymium hexanoate, neodymium heptanoate, neodymium octanoate, neodymium octoate, neodymium naphthenate, neodymium stearate, neodymium versatate, neodymium bis(2-ethylhexyl) phosphate, neodymium bis(1-methylheptyl) phosphate, neodymium (mono-2-ethylhexyl-2-ethylhexyl) phosphonate, and neodymium bis(2-ethylhexyl) phosphite. 4. The method of claim 2 , wherein, in the step (a), a molar ratio of the monomeric neodymium salt compound and the conjugated diene-based monomer is 1:5 to 30. 5. The method of claim 2 , wherein, in the step (a), a molar ratio of the monomeric neodymium salt compound and each of the compounds represented by Chemical Formulas 1 and 2 is 1:1 to 10. 6. The method of claim 1 , wherein each of the reacted and added conjugated diene-based monomer is one or more selected from the group consisting of 1,3-butadiene, isoprene, 2,3-dimethyl-1,3-butadiene, 2,3-dimethylbutadiene, 2-phenyl-1,3-butadiene, 2-chloro-1,3-butadiene, 1,3-pentadiene, 2-methyl-1,3-pentadiene, 3-methyl-1,3-pentadiene, 4-methyl-1,3-pentadiene, 1,3-hexadiene, 2-ethyl-1,3-butadiene, 2,4-hexadiene, and cyclo-1,3-hexadiene. 7. The method of claim 1 , wherein the second catalyst includes an organoaluminum compound, a phosphorus compound, and a transition metal complex. 8. The method of claim 7 , wherein the second catalyst includes 15 to 40 equivalents of the organoaluminum compound and 1 to 15 equivalents of the phosphorus compound with respect to 1 equivalent of the transition metal complex. 9. The method of claim 7 , wherein the organoaluminum compound is one or more selected from the group consisting of trimethylaluminum, triethylaluminum, tripropylaluminum, tributylaluminum, triisobutylaluminum, trihexylaluminum, and diisobutylaluminum hydride. 10. The method of claim 7 , wherein the phosphorus compound is a phosphite, a phosphate, or a mixture thereof. 11. The method of claim 7 , wherein the transition metal complex is an iron carboxylate or an iron acetylacetonate. 12. The method of claim 1 , wherein the steps (a) to (c) are carried out in situ. 13. The method of claim 1 , wherein a product of the step (c) includes 60 to 90 wt % of an end-modified conjugated diene-based polymer and 10 to 40 wt % of syndiotactic 1,2-polybutadiene.
Iron group metals, platinum group metals or compounds thereof · CPC title
rare earths being present, e.g. triethylaluminium + neodymium octanoate · CPC title
on to polymers of conjugated dienes · CPC title
Organic solvent · CPC title
Compositions of natural rubber · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.