IPCI

 

International Polyol Chemicals, Inc.

  PO BOX 190 - Blue River, OR 97413 - (541) 822-8400

 

 

 

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IPCI TECHNOLOGY

1.  IPCI HYDROGENATION

A variety of methods have been developed for the conversion of sugars to sugar alcohols, including treatment with sodium amalgam, enzymatic conversions, fermentation, electrolytic reduction and catalytic hydrogenation.  Thermal catalytic hydrogenation is, by far, the technology most widely used for sugar alcohol production.  The IPCI hydrogenation technology is applicable to manufacture of most of the commercial sugar alcohols.

The basic chemistry for hydrogenation of a sugar to a sugar alcohol is according to the following equation:

The most common sugar alcohol, sorbitol, is commercially produced in large volume today using batch processes, and, typically, a Raney nickel catalyst usually prepared fresh for each batch.   A few continuous sorbitol processes have been developed, and plants built - but we believe most, if not all, have been abandoned in favor of the better established batch process.

IPCI's hydrogenation process to produce sorbitol or other sugar alcohols is characterized by: 

·        Continuous process

·        Uses a robust, high activity, supported nickel catalyst

·        Typical glucose conversion >98.5%

·        Produces specification sorbitol from a glucose feed

·        Can utilize invert sugar (glucose and fructose) to produce mannitol and sorbitol

·        Flexible Reactor System designs

 

2.   IPCI HYDROGENOLYSIS

Hydrogenolysis is a term describing chemical reactions in which hydrogen is used to break molecular bonds in larger organic molecules in order to provide smaller, higher value or more useful molecules.  Hydrogenolysis reactions are usually conducted over a catalyst of some type, and at an elevated temperature (typically for carbohydrates, 100 to 300 oC) and high hydrogen pressures (typically 70 to 300 atmospheres).  In glycols and carbohydrates it is known that both C-C and C-O bonds can be broken by hydrogenolysis or hydrocracking, as it is sometimes called.

In contrast to the case for hydrogenation of carbohydrates, the chemistry of hydrogenolysis of the sugar alcohols (alditols) is complex, not well understood, and variable with even small changes in the catalyst system or the process conditions - particularly the reaction temperature.  It is therefore difficult to describe the exact process chemistry taking place.  In fact, there appears to be a chain or series of reactions, where primary reaction products are further hydrocracked to smaller molecule polyols and alcohols in secondary and tertiary reactions.

 Theoretically, the primary reaction is a hydrogen splitting of the alditol molecule at the center C-C bond to produce glycerin, or propylene glycol and water.  However, there seems to be no proof that these reactions occur completely, since it is almost always the case that both glycerin and propylene glycol are produced in alditol hydrocracking. Following are the simple chemical equations for formation of glycerin and propylene glycol from sorbitol or mannitol:   

It has been shown conclusively that glycerin will hydrocrack to propylene glycol, as in (3): 

Smaller molecule compounds such as EG, the 1-3 carbon alcohols and the butanediols could be formed from various alditol cracking schemes, but it seems more likely that they are produced from glycerin hydrocracking under more severe process conditions (although the butanediols are more likely formed by a 4 - 2 split of the alditol carbon chain, together with EG or ethanol).   In any case, it is typical of hydrogenolysis of sugar alcohols to produce several polyol and specialty chemical products.

 We believe that other than the IPCI hydrogenolysis technology, no commercial process is available to use for producing polyols from sugar alcohols. 

The IPCI hydrogenolysis process is characterized by:

·        Use of reliable, long-lived (> ~1600 hour life test with no degradation) supported nickel catalyst

·        Produces primarily propylene glycol, ethylene glycol and glycerin

·        Water solvent system

·        High conversion to polyols

·        Provisions for recycle of unreacted sorbitol and unwanted byproducts

·        Proven separation system for isolation of the individual polyol products

·        Ability to adjust product slate, and to produce and separate selected byproducts such as the butanediols, isosorbide and THF glycol

·        Flexible in feedstock as to using either single or multiple component sugar alcohols


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