Sabic Innovative Plastics IP B.v.

General Electric Company

Sabic Global Technologies B.v.

Kiran Arunkumar Puthamane

Shantaram Narayan Naik

Robert Russell Gallucci

Gary Charles Davis

Philippe Schottland

Eugene Pauling Boden

Arunkumar Natarajan

Adil Minoo Dhalla

Vandita Pai-Paranjape

Ganapati Shankarling

Meerakani Sait

Krishnamoorthy Sivakumar

Mahesh Chaudhari

Rahul R Khanwelkar

Martin Alexander Zuideveld

Jan Henk Kamps

Mark Allen Cheverton

Pradeep Jeevaji Nadkarni

Yogendrasinh Bharatsinh Chauhan

Sriramakrishna Maruvada

Venkata Ramanarayanan Ganapathy Bhotla

Edward Joseph Nesakumar

Sumeet Jain

Girish Mariswamy Chandra

Vinodkumar Vasudevan

Dafne Lise Steinfort

Minor Senthil Kumar

Mudubagilu Udaya Kumar

Navinchandra Asthana

Ruud Van Der Heijden

Elena Uliyanchenko

Anika Meppelder

Michael T Takemori

Yogendrasinh Bharatsing Chauhan

Sivukumar Krishnamoorthy

Rahul Ravindra Khanwelkar

A process for preparing a procatalyst for polymerization of olefins, comprising contacting a magnesium-containing support with a halogen-containing titanium compound, and an internal electron donor according to Formula (I), said process comprising the steps of: i) contacting a compound RMgXwith an alkoxy- or aryloxy-containing silane compound to give a first intermediate reaction product, being a solid Mg(OR)X, ii) optionally contacting the solid Mg(OR)X-x obtained in step ii) with at least one activating compound selected from the group formed by activating electron donors and metal alkoxide compounds of formula M(OR)(OR)or M(OR)(R), to obtain a second intermediate product; iii) contacting the first or second intermediate reaction product, obtained respectively in step i) or ii), with a halogen-containing Ti-compound and said compound represented Formula (I), as the internal electron donor.

Process for polymerization of polypropylene using ziegler-natta procatalyst with novel 1,3-diether internal donors

Disclosed herein are phenylindane dicarboxylic acid (PIDA) monomers, polymer compositions comprising the PIDA monomers, and methods of preparing PIDA monomers. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure.

Dicarboxylic acid monomers and methods of making and using the same

An article comprising the compound of Formula (I): 

Authenticatable articles and methods therefor

A composition comprising compound of formula I, a process for preparing the composition comprising compound of formula I, methods of authentication for an article comprising compound of formula I or compound of formula II, authentication technology for polymer based articles comprising compound of formula I or formula II, methods of facilitating such authentication and method of making articles capable of authentication.

Composition, method of authenticating, methods of making authenticatable compositions, authenticatable articles made there from

Disclosed are compositions comprising at least one [benzo[4,5]imidazo(heterocycle)] compound, said [benzo[4,5]imidazo(heterocycle)] compound selected from the group consisting of structures I and II, wherein Rand Rare independently selected from the group consisting of a hydrogen atom, electron withdrawing group, organic group, divalent 1,2-cycloalkylidene group, or combinations thereof; 'q' is independently an integer from 1-4, L is a linking group, and 'r' is independently 0 or 1; said at least one [benzo[4,5]imidazo(heterocycle)] compound being present at a concentration sufficient to cause said composition to exhibit upon exposure to an excitation radiation having a wavelength of from about 330 nanometers to about 390 nanometers, a maximum fluorescence emission wavelength of greater than or equal to about 470 nanometers; and a Stokes shift of greater than or equal to about 80 nanometers; wherein the wavelengths are measured in bisphenol A polycarbonate matrix.

Chemical compositions for authenticatable polymers and articles, and authentication methods thereof

An article comprising the compound of Formula (I) wherein X is hydrogen or a radical of Formula (II), Rindependently at each occurrence is a C-Caliphatic radical, a C-Ccycloaliphatic radical, or a C-Caromatic radical; R, R, Rand Rare independently at each occurrence a halogen, a nitro group, a cyano group, a hydroxy group, a C-Caliphatic radical, a C-Ccycloaliphatic radical, or a C-Caromatic radical; and 'n', 'q', and &#x201c;p&#x201d; are each independently integers having a value of 0 to 3, and &#x201c;m&#x201d; is an integer having a value of 0 to 4.

Articles comprising benzopyran colorants, method of manufacture, and method of use

A compound of Formula (I) wherein X is hydrogen or a radical of Formula (II), Rindependently at each occurrence is a C&#x2013;Caliphatic radical, a C&#x2013;Ccycloaliphatic radical, or a C&#x2013;Caromatic radical; R, R, Rand Rare independently at each occurrence a halogen, a nitro group, a cyano group, a hydroxy group, a C&#x2013;Caliphatic radical, a C&#x2013;Ccycloaliphatic radical, or a C&#x2013;Caromatic radical; and 'n', 'q', and &#x201c;p&#x201d; are each independently integers having a value of 0 to 3, and &#x201c;m&#x201d; is an integer having a value of 0 to 4.

Benzopyran colorants, method of manufacture, and method of use

Disclosed are compositions comprising at least one [benzo[4,5]imidazo(heterocycle)] compound, said [benzo[4,5]imidazo(heterocycle)] compound selected from the group consisting of structures I and II, wherein Rand Rare independently selected from the group consisting of a hydrogen atom, electron withdrawing group, organic group, divalent 1,2-cycloalkylidene group, or combinations thereof; 'q' is independently an integer from 1&#x2013;4, L is a linking group, and 'r' is independently 0 or 1; said at least one [benzo[4,5]imidazo(heterocycle)] compound being present at a concentration sufficient to cause said composition to exhibit upon exposure to an excitation radiation having a wavelength of from about 330 nanometers to about 390 nanometers, a maximum fluorescence emission wavelength of greater than or equal to about 470 nanometers; and a Stokes shift of greater than or equal to about 80 nanometers; wherein the wavelengths are measured in bisphenol A polycarbonate matrix.

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Karnataka, India

Kiran Arunkumar Puthamane