Hydrophobic starches

Curcumin Hydrophobically modified starch Hydrophobic interaction Increased of dispersibility in water and anticarcinogenic activity [174]... 

Keywords Biopolymers, superhydrophobic, cellulose, starch, hydrophobic cellulose, nanofibers. 

Grafting hydrocarbon chains to make starch hydrophobic... 

For practical uses see - anionic starches, car-boxymethyl starch, - cationic starches, - cross-linked starches, - hydrophobic starches, - oxidized starches, - starch industrial applications. 

Cyclodextrins are macrocyclic compounds comprised of D-glucose bonded through 1,4-a-linkages and produced enzymatically from starch. The greek letter which proceeds the name indicates the number of glucose units incorporated in the CD (eg, a = 6, /5 = 7, 7 = 8, etc). Cyclodextrins are toroidal shaped molecules with a relatively hydrophobic internal cavity (Fig. 6). The exterior is relatively hydrophilic because of the presence of the primary and secondary hydroxyls. The primary C-6 hydroxyls are free to rotate and can partially block the CD cavity from one end. The mouth of the opposite end of the CD cavity is encircled by the C-2 and C-3 secondary hydroxyls. The restricted conformational freedom and orientation of these secondary hydroxyls is thought to be responsible for the chiral recognition inherent in these molecules (77). 

Ghdants are needed to faciUtate the flow of granulation from the hopper. Lubricants ensure the release of the compressed mass from the punch surfaces and the release/ejection of the tablet from the die. Combinations of siUcas, com starch, talc (qv), magnesium stearate, and high molecular weight poly(ethylene glycols) are used. Most lubricants are hydrophobic and may slow down disintegration and dmg dissolution. 

A similar procedure was adopted for synthesis of nanoparticles of cellulose (CelNPs). The polysaccharide nanoparticles were derivatised under ambient conditions to obtain nanosized hydrophobic derivatives. The challenge here is to maintain the nanosize even after derivatisation due to which less vigorous conditions are preferred. A schematic synthesis of acetyl and isocyanate modified derivatives of starch nanoparticles (SNPs) is shown in scheme 3. The organic modification was confirmed from X-ray diffraction (XRD) pattern which revealed that A- style crystallinity of starch nanoparticles (SNPs) was destroyed and new peaks emerged on derivatisation. FT-IR spectra of acetylated derivatives however showed the presence of peak at 3400 cm- due to -OH stretching indicating that the substitution is not complete. 

Carboxymethylcellulose, polyethylene glycol Combination of a cellulose ether with clay Amide-modified carboxyl-containing polysaccharide Sodium aluminate and magnesium oxide Thermally stable hydroxyethylcellulose 30% ammonium or sodium thiosulfate and 20% hydroxyethylcellulose (HEC) Acrylic acid copolymer and oxyalkylene with hydrophobic group Copolymers acrylamide-acrylate and vinyl sulfonate-vinylamide Cationic polygalactomannans and anionic xanthan gum Copolymer from vinyl urethanes and acrylic acid or alkyl acrylates 2-Nitroalkyl ether-modified starch Polymer of glucuronic acid... 

In addition to the bio degradability of PHAs, they have another important feature, which is their hydrophobicity. This makes PHAs superior to their biodegradable competitors like starch and proteins in moisture resistance, despite the higher price of PHAs [18]. Apart from the unique combination of biodegradability and hydrophobicity, PHAs have other interesting and useful material characteristics. The combination of the various special material properties should be kept in mind for application development. 

Gels used for the stationary phase can be hydrophilic, for separations in aqueous and other polar solvents, or hydrophobic, for use in non-polar or weakly-polar solvents. Agar, starch, polyacrylamide and cross-linked dextrans possess hydroxyl or amide groups and are thus hydrophilic. They swell... 

Instead, native starch has been oxidized with H202 in the presence of soluble organometallic complexes to meet specific hydrophilic/hydrophobic properties needed for end-products to be used in paper, paint and cosmetic industries [79-... 

Modification of Starch and Other Saccharides by Crafting Hydrophobic Chains... 

To prepare more hydrophobic starches for specific applications, the partial substitution of starch with acetate, hydroxypropyl, alkylsiliconate or fatty-acid ester groups has been described in the literature. A new route, however, consists of grafting octadienyl chains by butadiene telomerization (Scheme 3.9) [79, 82, 83], The reaction was catalyzed by hydrosoluble palladium-catalytic systems prepared from palladium diacetate and trisodium tris(m-sulfonatophenyl)phosphine (TPPTS). 

The transposition of this reaction to starch [79, 83] was challenging because this substrate is insoluble in water at room temperature and gelatinizes above ca. 70 °C. The DS should be kept low enough because modified starch should not be too hydrophobic, and for obvious economic reasons the catalyst/starch ratio should be kept low. Figure 3.4 shows that the DS depends upon the amount... 

In the homogenous mixture of Starch and Polyvinyl alcohol (PVA), 30 % of plasticizer was mixed to make Pure blend. Then 10 % cellulose was mixed into above mixture followed by removal of extra water gave Cellulose-Reinforced starch-PVA blends. The different proportions of Fly ash were mixed into mixture of Cellulose-Reinforced starch-PVA blends to get various fly ash inserted Cellulose-Reinforced starch-PVA blends. Solubility, swelling behaviour and water absorption studies of Fly ash blends were measured at different time intervals at relative humidity of 50-55%. The insertion of Cellulose into starch-PVA blend decreases the solubility of blends due to the hydrophobicity of cellulose, but the solubility further increases by insertion of Fly ash into starch-PVA matrix that indicating the mechanical stability enhancement of blends. The water absorption behaviour of fly ash blends increases rapidly upto 150 min and then no change. The optimum concentration of Fly ash into Cellulose-Reinforced starch-PVA blend was 4%. 

Starch-plastic composites contain a mixture of two very different types of materials (/) hydrophobic, petrochemical-derived polymers (PE, EAA) known to be highly resistant to degradation by living organisms, and (i7) a hydrophilic, natural polymer (starch) that is easily broken down by a wide array of organisms. In the process developed by Otey (3), these fundamentally incompatible materials are forced into an intimate mixture during production of the plastic film. Since... 

Blends of starch and a hydrophobic polymer make it possible to overcome the disadvantages described above. Starch compounds with Ecoflex are used to enhance hydrophobicity as well as the mechanical and thermal properties of compounded products. To obtain high quality film products, the starch has to be treated before being blended with Ecoflex . The crystalline structure of starch granules has to be destroyed because starch granules are as large as the film thickness of typical film applications and would therefore reduce the mechanical properties of the films. 

Polymerization in P-cyclodextrin (CD) complexes with monomer offers a route to polymerization, as well as other organic reactions, in water without the need for organic solvents [Ritter and Tabatabai, 2002]. P-Cyclodextrins are toms-shaped, cyclic oligosaccharides obtained by degradation of starch. The hydroxyl groups of the glucose repeat unit of CD are located on the outer surface. This makes the outer surface hydrophilic, whereas the inner surface and cavity are hydrophobic. Water-insoluble monomers become solubilized in water when mixed with CD or CD derivatives because the monomers are absorbed into the cavity. This allows polymerization in aqueous, not organic media, with water-soluble initiators. 

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