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Found results for
patents
1.
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IMPACT COPOLYMERS HAVING IMPROVED PROPERTIES
Application Number |
US2008005293 |
Publication Number |
2008/136932 |
Status |
In Force |
Filing Date |
2008-04-24 |
Publication Date |
2008-11-13 |
Owner |
SUNOCO, INC. (R & M) (USA)
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Inventor |
- Doufas, Antonios, K.
- Salek, Jeffrey, S.
- Andrekanic, Ronald, A.
- Thurston, William, C.
- Rice, Leon, M.
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Abstract
Improvements in the aesthetic appearance and performance properties of heterophasic polymers is obtained through the breaking up and dispersion of large gels. According to the current invention, a novel process is provided for filtration of heterophasic polymers using a fiber metal felt (FMF) media. Molded articles made from impact copolymers prepared according to the present invention have improved appearance and fracture mechanics relative to impact copolymers produced according to prior art methods.
IPC Classes ?
- D01D 1/10 - Filtering or de-aerating the spinning solution or melt
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2.
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RESIN COMPOSITIONS FOR PRODUCING BIAXIALLY ORIENTED POLYPROPYLENE FILMS
Application Number |
US2008002955 |
Publication Number |
2008/112116 |
Status |
In Force |
Filing Date |
2008-03-06 |
Publication Date |
2008-09-18 |
Owner |
SUNOCO, INC. (R & M) (USA)
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Inventor |
- Kim, Sehyun
- Stephans, Michael, Robert
- Avolio, John
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Abstract
Polypropylene resin compositions are provided that are useful in the production of biaxially oriented polypropylene films (BOPPs). The resins of the present invention are blends of high crystalline (low solubles) polypropylene homopolymer and an ethylene/propylene random copolymer (RCP). These blends can be used to replace standard high solubles BOPP grade polypropylene homopolymers. In addition, the use of high crystalline polypropylene homopolymers in the blends imparts improved stiffness to the finished films while maintaining good processability of the blends.
IPC Classes ?
- B32B 27/00 - Layered products essentially comprising synthetic resin
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3.
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HIGH CRYSTALLINITY, HIGH MELT FLOW RATE POLYPROPYLENE
Application Number |
US2007012868 |
Publication Number |
2007/140019 |
Status |
In Force |
Filing Date |
2007-05-30 |
Publication Date |
2007-12-06 |
Owner |
SUNOCO, INC. (R & M) (USA)
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Inventor |
- Meverden, Craig
- Schnitgen, Andrew
- Kim, Sehyun
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Abstract
High melt flow rate high crystallinity polypropylene homopolymer are produced in a bulk polymerization process using a Ziegler-Natta catalyst containing a combination of two internal electron donors and selected external donors. The high melt flow rate, high crystallinity polypropylene homopolymers produced according to the current invention display improved flexural modulus and tensile yield stress when nucleated.
IPC Classes ?
- C08F 110/06 - Propene
- C08F 2/02 - Polymerisation in bulk
- C08F 4/656 - Pretreating with metals or metal-containing compounds with silicon or compounds thereof
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4.
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PROCESS FOR RECOVERY OF CUMENE HYDROPEROXIDE DECOMPOSITION PRODUCTS BY DISTILLATION
Application Number |
US2006043848 |
Publication Number |
2007/058962 |
Status |
In Force |
Filing Date |
2006-11-10 |
Publication Date |
2007-05-24 |
Owner |
SUNOCO, INC. (R & M) (USA)
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Inventor |
- Keenan, Scott, R.
- Harach, Amber, R.
- Skipworth, James, G.
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Abstract
Products from the decomposition of cuniene hydroperoxide (CHP) are recovered by distillation. The majority of the undesirable by-product acetol (hydroxyacetone) is removed from the phenol stream by distillation wherein the majority of the acetol is carried with an overheads stream comprising acetone, cumene and alphamethylstyrene (AMS). Acetol is subsequently separated from acetone by distillation wherein acetone is taken as an overheads stream and acetol remains with a bottoms stream comprising cumene, AMS and phenol. The acetol, along with residual phenol, is extracted from the cumene and AMS by counter-current washing with an aqueous alkali metal hydroxide. The phenol stream is then distilled to separate phenol from cumene, alphamethylstyrene and higher boiling compounds. The phenol, containing only a small amount of acetol, can then be treated to remove methylbenzofuran by treatment with an acidic resin or solid superacid catalyst without formation of significant amounts of additional methylbenzofuran.
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