GB740560A - Improvements in hydrogenation of monosaccharides - Google Patents

Improvements in hydrogenation of monosaccharides

Info

Publication number
GB740560A
GB740560A GB7169/53A GB716953A GB740560A GB 740560 A GB740560 A GB 740560A GB 7169/53 A GB7169/53 A GB 7169/53A GB 716953 A GB716953 A GB 716953A GB 740560 A GB740560 A GB 740560A
Authority
GB
United Kingdom
Prior art keywords
glucose
invert sugar
preferred
hydrogenation
hydroxide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB7169/53A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Atlas Powder Co
Original Assignee
Atlas Powder Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Atlas Powder Co filed Critical Atlas Powder Co
Publication of GB740560A publication Critical patent/GB740560A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23GCOCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
    • A23G3/00Sweetmeats; Confectionery; Marzipan; Coated or filled products
    • A23G3/34Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
    • A23G3/36Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds
    • A23G3/42Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds characterised by the carbohydrates used, e.g. polysaccharides

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

<PICT:0740560/IV(a)/1> Non-gelling, non-crystallizing high-viscosity polyol compositions are made by introducing a monosaccharide and an alkali metal or an alkaline earth metal hydroxide into water to form a mixture containing from 40 to 70 per cent by weight of monosaccharide and from 0.15 to 0.4 hydroxyl equivalents of hydroxide per litre; heating the resulting mixture to 40-80 DEG , preferably 50-65 DEG C.; maintaining the mixture at the said temperature for a time corresponding to a time-temperature point within the polygon ABCDE; adjusting the pH of the resulting solution to a value of from 7 to 5.0, preferably 7-6; and hydrogenating the resulting solution in the presence of a hydrogenation catalyst, at a temperature of 120-170 DEG C., preferably 140-160 DEG C., and a hydrogen pressure above 500, preferably 1500-2000, pounds per square inch. Glucose, invert sugar, fructose, mannose and xylose are specified saccharides, glucose and invert sugar being preferred. Readily crystallizable products such as mannitol may be removed and the composition mainly comprising sorbitol is obtained non-gelling and non-crystallizing by limitation of the quantity of sorbitol in the syrup (determined by means of a pyridine-sorbitol complex) so that its pyridine number is not substantially above 60, such limitation being effected by working within the conditions of the polygon. Neutralization before hydrogenation may be effected by means of acids or by ion-exchange materials. Reduced supported nickel hydrogenation catalysts are preferred. Hydrogenation may be effected as in Specification 721,260. Calcium hydroxide is the preferred hydroxide and preferably not over 0.3 hydroxyl equivalents are used per litre. With invert sugar limits imposed by ABCGF are preferred and with glucose those set by AHCDE. Particularly preferred for invert sugar are temperatures of 60-65 DEG C. for about 6 hours and for glucose 50-55 DEG C. for about 16 hours. Examples illustrate the conversion of glucose and invert sugar into humectant polyol syrups, alkali treatment being with sodium, barium or calcium hydroxides, any mannitol obtained in the processes being removed after crystallization.
GB7169/53A 1952-04-03 1953-03-16 Improvements in hydrogenation of monosaccharides Expired GB740560A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US740560XA 1952-04-03 1952-04-03

Publications (1)

Publication Number Publication Date
GB740560A true GB740560A (en) 1955-11-16

Family

ID=22117425

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7169/53A Expired GB740560A (en) 1952-04-03 1953-03-16 Improvements in hydrogenation of monosaccharides

Country Status (1)

Country Link
GB (1) GB740560A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0809444A1 (en) * 1993-12-29 1997-12-03 Wm. Wrigley Jr. Company Liquid sorbitol/mannitol/glycerin blend and compositions containing same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0809444A1 (en) * 1993-12-29 1997-12-03 Wm. Wrigley Jr. Company Liquid sorbitol/mannitol/glycerin blend and compositions containing same
EP0809444A4 (en) * 1993-12-29 1998-04-15 Wrigley W M Jun Co Liquid sorbitol/mannitol/glycerin blend and compositions containing same

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