Patent classifications
B01J27/135
Chiral auxiliaries and uses thereof
The present invention relates to chiral auxiliaries and the syntheses thereof and uses thereof.
Chiral auxiliaries and uses thereof
The present invention relates to chiral auxiliaries and the syntheses thereof and uses thereof.
Catalyst for producing light aromatics with heavy aromatics, method for preparing the catalyst, and use thereof
A catalyst for producing light aromatics with heavy aromatics, a method for preparing the catalyst, and a use thereof are disclosed. The catalyst comprises a carrier, component (1), and component (2), wherein component (1) comprises one metal element or more metal elements selected from a group consisting of Pt, Pd, Ir, and Rh, and component (2) comprises one metal element or more metal elements selected from a group consisting of IA group, IIA group, IIIA group, IVA group, IB group, IIB group, IIIB group, IVB group, VB group, VIB group, VIIB group, La group, and VIII group other than Pt, Pd, Ir, and Rh. The catalyst can be used for producing light aromatics with heavy aromatics, whereby heavy aromatics hydrogenation selectivity and light aromatics yield can be improved.
HIGHLY ACTIVE, ROBUST AND VERSATILE MULTIFUNCTIONAL, FULLY NON-NOBLE METALS BASED ELECTRO-CATALYST COMPOSITIONS AND METHODS OF MAKING FOR ENERGY CONVERSION AND STORAGE
The invention provides noble metal-free electro-catalyst compositions for use in acidic media, e.g., acidic electrolyte. The noble metal-free electro-catalyst compositions include non-noble metal absent of noble metal. The non-noble metal is non-noble metal oxide, and typically in the form of any configuration of a solid or hollow nano-material, e.g., nano-particles, a nanocrystalline thin film, nanorods, nanoshells, nanoflakes, nanotubes, nanoplates, nanospheres and nanowhiskers or combinations of myriad nanoscale architecture embodiments. Optionally, the noble metal-free electro-catalyst compositions include dopant, such as, but not limited to halogen. Acidic media includes oxygen reduction reaction (ORR) in proton exchange membrane (PEM) fuel cells, and direct methanol fuel cells and oxygen evolution reaction (OER) in PEM-based water electrolysis and metal air batteries, and hydrogen generation from solar energy and electricity-driven water splitting.
Polypropylenes and Methods for Making Them
A polypropylene comprising a xylene soluble fraction of 1.5 wt % by weight of the polymer and soluble fraction or less, wherein the polypropylene has a melt flow rate within a range from 50 g/10 min to 500 g/10 min and a flexural modulus within a range from 1780 MPa to 2200 MPa. The polypropylene is preferably made from contacting propylene with a solid magnesium/titanium catalyst component that has been washed at least once with a solvent having a desirable solubility parameter.
Polypropylenes and Methods for Making Them
A polypropylene comprising a xylene soluble fraction of 1.5 wt % by weight of the polymer and soluble fraction or less, wherein the polypropylene has a melt flow rate within a range from 50 g/10 min to 500 g/10 min and a flexural modulus within a range from 1780 MPa to 2200 MPa. The polypropylene is preferably made from contacting propylene with a solid magnesium/titanium catalyst component that has been washed at least once with a solvent having a desirable solubility parameter.
METHOD FOR MANUFACTURING DIARYLMETHANE COMPOUND
An object is to provide a method for producing a compound which is useful as a synthetic intermediate for an active pharmaceutical ingredient of an antidiabetic drug or the like in an industrially inexpensive and efficient manner, and the present invention can achieve the object by reducing a compound (2) represented by the following formula (2):
##STR00001## wherein R.sub.1, Ar, n and X are as mentioned herein in the presence of a titanium compound by using a reducing agent to produce a compound (1) represented by the following formula (1):
##STR00002## wherein R.sub.1, Ar and n are the same as defined above.
METHOD FOR MANUFACTURING DIARYLMETHANE COMPOUND
An object is to provide a method for producing a compound which is useful as a synthetic intermediate for an active pharmaceutical ingredient of an antidiabetic drug or the like in an industrially inexpensive and efficient manner, and the present invention can achieve the object by reducing a compound (2) represented by the following formula (2):
##STR00001## wherein R.sub.1, Ar, n and X are as mentioned herein in the presence of a titanium compound by using a reducing agent to produce a compound (1) represented by the following formula (1):
##STR00002## wherein R.sub.1, Ar and n are the same as defined above.
Bulk transient materials made of cyclic poly(phthalaldehyde)
The present disclosure provides a composition of matter comprising purified cyclic poly(phthalaldehyde) (cPPA) and a plasticizer. The composition enables thermal processing and molding in bulk quantities, and is designed to degrade when contacted by an acid or exposed to a high enough temperature. Photodegradable cPPA containing a photooxidant is disclosed. Methods of making and recycling the composition of matter are also provided.
SYNTHESIS OF CYANURATE AND MULTIFUNCTIONAL ALCOHOL-BASED POLYETHER ACRYLATE FOR UV CURABLE MATERIALS
Polyether (meth)acrylates based on cyanuric acid or substituted cyanuric acid and multifunctional alcohol, which optionally include triethanolamine units, have wide applications in UV curable adhesives, coatings, inks, sealants, paints or 3D printing. These polyether acrylates have rigid cyanurate structure endowing the material with extra strength and thermal stability. Furthermore, triethanolamine unit, when present, endows the material with anti-oxygen inhibition property in UV curing process. These polyether (meth)acrylates have low viscosity and high reactivity towards UV curing. The cured resins have high resilience and strength. The process of making the polyether (meth)acrylates includes the synthesis of trifunctional polyether polyols through controlled polymerization of propylene oxide using multifunctional alcohol (such as glycerol and sucrose), cyanuric acid or substituted cyanuric acid, and optionally triethanolamine, in the presence of a catalyst, followed by the synthesis of polyether (meth)acrylates through transesterification or through direct esterification of the trifunctional polyether polyols.