A novel process has been developed, that enable the production of carboxymethylated starches (CMS) with substitution degrees up to 1.5 and yields of more than 70 percent. Different starches have been used, including native and waxy potatoe starches, corn and wheat starches and high amylose. The novel patented carboxymethylation method is based on a heterogeneous process using free monochloro-acetic acid as the etherification agent, and appropriate election of the reaction conditions such as water concentration, molar relations of the reagents, reaction time, and reaction temperature, prevent the common lumping of the reaction mixtures. With the obtained CMSs clear aqueous solutions are formed, that exhibit a broad viscosity range, high gel ...
In this study, carboxymethyl starch (CMS) was synthesized by reacting native sago starch with sodium...
The objective of this dissertation was to study the use of reactive extrusion for the chemical modif...
DE 10129312 A UPAB: 20030731 NOVELTY - Optionally protected alkyl isocyanates are used in a method f...
Carboxymethyl starches (CMS) with a degree of substitution (DS) in the range of 0.5 to 1.5 and reage...
A process design for the continuous production of highly substituted granular carboxymethyl starch (...
Modified starch is synthesized to change the physical and chemical properties, one of which is solub...
Carboxymethylation of cassava starch was carried out in three different reaction media: iso-propanol...
Chemically modified sago starch into carboxymethyl sago starch (CMSS) was done by using carboxymethy...
The carboxymethylation of cassava starch using sodium monochloroacetate (SMCA) as an etherification ...
The carboxymethylation of cassava starch using sodium monochloroacetate (SMCA) as an etherification ...
AbstractA pregelatinized starch (PGS) was derivatized with sodium chloroacetate (SCA) in alcoholic m...
Abstract In this study, sago starch was modified in order to enhance its physicochemical properties....
This paper describes the impact of carboxymethyl starch preparation conditions on physicochemical pr...
Carboxymethyl starch was synthesized by the esterification of starch with monochloroacetic acid in e...
In this study, sago starch was modified in order to enhance its physicochemical properties. Carboxym...
In this study, carboxymethyl starch (CMS) was synthesized by reacting native sago starch with sodium...
The objective of this dissertation was to study the use of reactive extrusion for the chemical modif...
DE 10129312 A UPAB: 20030731 NOVELTY - Optionally protected alkyl isocyanates are used in a method f...
Carboxymethyl starches (CMS) with a degree of substitution (DS) in the range of 0.5 to 1.5 and reage...
A process design for the continuous production of highly substituted granular carboxymethyl starch (...
Modified starch is synthesized to change the physical and chemical properties, one of which is solub...
Carboxymethylation of cassava starch was carried out in three different reaction media: iso-propanol...
Chemically modified sago starch into carboxymethyl sago starch (CMSS) was done by using carboxymethy...
The carboxymethylation of cassava starch using sodium monochloroacetate (SMCA) as an etherification ...
The carboxymethylation of cassava starch using sodium monochloroacetate (SMCA) as an etherification ...
AbstractA pregelatinized starch (PGS) was derivatized with sodium chloroacetate (SCA) in alcoholic m...
Abstract In this study, sago starch was modified in order to enhance its physicochemical properties....
This paper describes the impact of carboxymethyl starch preparation conditions on physicochemical pr...
Carboxymethyl starch was synthesized by the esterification of starch with monochloroacetic acid in e...
In this study, sago starch was modified in order to enhance its physicochemical properties. Carboxym...
In this study, carboxymethyl starch (CMS) was synthesized by reacting native sago starch with sodium...
The objective of this dissertation was to study the use of reactive extrusion for the chemical modif...
DE 10129312 A UPAB: 20030731 NOVELTY - Optionally protected alkyl isocyanates are used in a method f...