The present invention relates to optionally substituted 1,3-dimethoxypropanes and 3-methoxypropylamines, and more particularly to their use as internal donors in Ziegler-Natta catalysts to obtain polymers with desirable properties. The present disclosure further concerns Ziegler-Natta catalyst components comprising said optionally substituted 1,3-dimethoxypropanes and 3-methoxypropylamines, and Ziegler-Natta catalysts for olefin polymerization comprising said Ziegler-Natta catalyst components, as well as a method for preparing the same and their use in providing polyolefins.

The present invention relates to optionally substituted 1,3-dimethoxypropanes and 3-methoxypropylamines, and more particularly to their use as internal donors in Ziegler-Natta catalysts to obtain polymers with desirable properties. The present disclosure further concerns Ziegler-Natta catalyst components comprising said optionally substituted 1,3-dimethoxypropanes and 3-methoxypropylamines, and Ziegler-Natta catalysts for olefin polymerization comprising said Ziegler-Natta catalyst components, as well as a method for preparing the same and their use in providing polyolefins.

Embodiments of the present disclosure are directed towards methods of etherification including modifying a zeolite catalyst with phosphorus to provide a phosphorus modified zeolite catalyst; and contacting the phosphorus modified zeolite catalyst with an olefin and an alcohol to produce a monoalkyl ether.

Embodiments of the present disclosure are directed towards methods of etherification including modifying a zeolite catalyst with phosphorus to provide a phosphorus modified zeolite catalyst; and contacting the phosphorus modified zeolite catalyst with an olefin and an alcohol to produce a monoalkyl ether.

The present invention relates to an integrated process that allows the production of tert-butyl ethers of glycerol, used as a high boiling point solvent (HBPS) in paint formulations (water-based) and cleaning products, or a stream of isooctenes to be used as an octane in the gasoline pool, in a simple way, just directing the flow through the areas necessary for the conversion and separation of the process and using the same equipment, aiming at gains in process yield (maximization of glycerol and isobutene conversions) and minimizing investment and operating costs. In view of this, there is a unit flexibility in producing different high added value products.

The present invention relates to an integrated process that allows the production of tert-butyl ethers of glycerol, used as a high boiling point solvent (HBPS) in paint formulations (water-based) and cleaning products, or a stream of isooctenes to be used as an octane in the gasoline pool, in a simple way, just directing the flow through the areas necessary for the conversion and separation of the process and using the same equipment, aiming at gains in process yield (maximization of glycerol and isobutene conversions) and minimizing investment and operating costs. In view of this, there is a unit flexibility in producing different high added value products.

Described herein are compounds according to general formula (I)

R.sup.1—CHR.sup.2—CH.sub.2—O-(AO).sub.x—CH.sub.2—CH(OH)—R.sup.3  (I).

Also described herein are a process to make the compounds according to general formula (I), and a method of using the compounds according to general formula (I) in a composition for automatic dishwashing.

A method of etherifying glycols or other diols by employing renewable reagents is disclosed. In particular, the method involves contacting a diol with an alkylating agent in an alcoholic solvent, catalyzed with a catalyst (carbonic acid) generated in situ (from CO.sub.2). The mono- and di-ether products can serve as valued precursors to an array of renewable surfactants, dispersants, and lubricants, among others.

A method of etherifying glycols or other diols by employing renewable reagents is disclosed. In particular, the method involves contacting a diol with an alkylating agent in an alcoholic solvent, catalyzed with a catalyst (carbonic acid) generated in situ (from CO.sub.2). The mono- and di-ether products can serve as valued precursors to an array of renewable surfactants, dispersants, and lubricants, among others.

Disclosed is a method for preparing a double end capped glycol ether, the method comprising: introducing into a reactor a raw material comprising a glycol monoether and a monohydric alcohol ether, and enabling the raw material to contact and react with an acidic molecular sieve catalyst to generate a double end capped glycol ether, a reaction temperature being 50-300° C., a reaction pressure being 0.1-15 MPa, a WHSV of the glycol monoether in the raw material being 0.01-15.0 h.sup.−1, and a mole ratio of the monohydric alcohol ether to the glycol monoether in the raw material being 1-100:1. The method of the present invention enables a long single-pass lifespan of the catalyst and repeated regeneration, has a high yield and selectivity of a target product, low energy consumption during separation of the product, a high economic value of a by-product, and is flexible in production scale and application.