Biological degradable polymers on a basis of renewable raw materials, such as polysaccharides, represent promising alternatives to synthetic polymers used as flocculant or stabilizing agents. Polysaccharides derived from potato starch and chitosan have been modified with benzyl- and the first one with additionally cationic hydroxypropyl-trimethylammonium groups of different degrees of substitution (DS). The aim of this work was to characterize the solution properties of these novel amphiphilic polysaccharides concerning the impact of their DS on charge density, particle size, dynamic surface tension and viscosity behaviour. The work is further focused on investigations on flocculation properties of these amphiphilic polyelectrolytes in dispersions of kaolin and silica to identify the interplay between charge density and hydrophobicity. Flocculation efficiency has been evaluated via joint analysis of charge density measurements (using polyelectrolyte titration), turbidity and TOC measurements, as well as dynamic surface tension measurements applying the drop profile analysis. Particle sizes and particle size distributions have been determined by dynamic light scattering and laser diffraction methods. In addition, these amphiphilic starch derivatives have been used to remove substances which impact negatively the paper production process when using recycled paper, so called stickies. Model suspensions have been studied using a multitude of different measurement techniques with the aim to predict a “sticky potential” and to reduce containing dissolved and colloidal substances such as micro stickies. The surface activity and viscometric behaviour have been studied of solely cationic and moderately and highly substituted, amphiphilic polysaccharides in salt-free and 0.05 M NaCl aqueous solution. For the first time dynamic surface tension measurement results have been correlated with particle sizes and apparent charge density. Rheological investigation of large concentration ranges (0.01–20 g/L) was used to discuss Huggins plots and typical polyelectrolyte behaviour for all polysaccharide derivatives could be found. Overlap concentration and, in dilute aqueous solution, intrinsic viscosity could be determined. For polysaccharide solution in dilute regime semi-empirical equations of Rao and Wolf have been applied, making it possible to get insights to polyelectrolyte conformation in dependence on the DS of both substituents. It is shown that for intrinsic viscosity a change of the impact of both substituents takes place when having derivatives with enhanced hydrophobicity. Data evaluation via the ratio of both DS values had been successfully utilized and thus, the applied method has been identified as being a promising tool to compare a multitude of starch derivatives with substituents of different polarity in various degrees of substitution to get tendencies regarding overall hydrophobicity. Moderate hydrophobic substitution was found to lead to a decrease of the efficient flocculant dose and to an increase of the flocculation window width. Amphiphilic starch derivatives with high DS of hydrophobic moieties showing strong hydrophobic association are effective only at significantly higher doses, but in a broader concentration range compared to cationic starch of the same DS. Joint analysis of adsorption isotherms and flocculation test data has revealed, that the surface coverage required to induce phase separation ranges between 10 and 25 % and is minimal for amphiphilic starch derivatives. This gave the evidence of the complex mechanism of flocculation via combination of electrostatic “charge patch” interactions and bridging. Concerning sticky reduction experiments by systematically studying the interactions between the novel amphiphilic starch derivatives and the model suspension it turned out, that dynamic surface tension is a very suitable property to characterize the surface active compounds in the model suspension giving additional information about the sticky potential of waste water, e.g. white water, being a new and sensitive method to describe the parameter “hydrophobicity”. Moderate cationic and hydrophobic starch derivatives have been proved to be the most effective ones for sticky removal.

Biological degradable polymers on a basis of renewable raw materials, such as polysaccharides, represent promising alternatives to synthetic polymers used as flocculant or stabilizing agents. Polysaccharides derived from potato starch and chitosan have been modified with benzyl- and the first one with additionally cationic hydroxypropyl-trimethylammonium groups of different degrees of substitution (DS). The aim of this work was to characterize the solution properties of these novel amphiphilic polysaccharides concerning the impact of their DS on charge density, particle size, dynamic surface tension and viscosity behaviour. The work is further focused on investigations on flocculation properties of these amphiphilic polyelectrolytes in dispersions of kaolin and silica to identify the interplay between charge density and hydrophobicity. Flocculation efficiency has been evaluated via joint analysis of charge density measurements (using polyelectrolyte titration), turbidity and TOC measurements, as well as dynamic surface tension measurements applying the drop profile analysis. Particle sizes and particle size distributions have been determined by dynamic light scattering and laser diffraction methods. In addition, these amphiphilic starch derivatives have been used to remove substances which impact negatively the paper production process when using recycled paper, so called stickies. Model suspensions have been studied using a multitude of different measurement techniques with the aim to predict a “sticky potential” and to reduce containing dissolved and colloidal substances such as micro stickies. The surface activity and viscometric behaviour have been studied of solely cationic and moderately and highly substituted, amphiphilic polysaccharides in salt-free and 0.05 M NaCl aqueous solution. For the first time dynamic surface tension measurement results have been correlated with particle sizes and apparent charge density. Rheological investigation of large concentration ranges (0.01–20 g/L) was used to discuss Huggins plots and typical polyelectrolyte behaviour for all polysaccharide derivatives could be found. Overlap concentration and, in dilute aqueous solution, intrinsic viscosity could be determined. For polysaccharide solution in dilute regime semi-empirical equations of Rao and Wolf have been applied, making it possible to get insights to polyelectrolyte conformation in dependence on the DS of both substituents. It is shown that for intrinsic viscosity a change of the impact of both substituents takes place when having derivatives with enhanced hydrophobicity. Data evaluation via the ratio of both DS values had been successfully utilized and thus, the applied method has been identified as being a promising tool to compare a multitude of starch derivatives with substituents of different polarity in various degrees of substitution to get tendencies regarding overall hydrophobicity. Moderate hydrophobic substitution was found to lead to a decrease of the efficient flocculant dose and to an increase of the flocculation window width. Amphiphilic starch derivatives with high DS of hydrophobic moieties showing strong hydrophobic association are effective only at significantly higher doses, but in a broader concentration range compared to cationic starch of the same DS. Joint analysis of adsorption isotherms and flocculation test data has revealed, that the surface coverage required to induce phase separation ranges between 10 and 25 % and is minimal for amphiphilic starch derivatives. This gave the evidence of the complex mechanism of flocculation via combination of electrostatic “charge patch” interactions and bridging. Concerning sticky reduction experiments by systematically studying the interactions between the novel amphiphilic starch derivatives and the model suspension it turned out, that dynamic surface tension is a very suitable property to characterize the surface active compounds in the model suspension giving additional information about the sticky potential of waste water, e.g. white water, being a new and sensitive method to describe the parameter “hydrophobicity”. Moderate cationic and hydrophobic starch derivatives have been proved to be the most effective ones for sticky removal.

Nowadays, natural polymeric materials extracted from plants are the new alternatives for synthetic chemicals in water and wastewater treatment. The aim of this study is to evaluate the ability of Cassia fistula seed gum (CFG) as a coagulant aid with PAC in the treatment of textile wastewater. Jartest experiments were carried out to identify the optimal parameters of coagulation-flocculation for removing color and COD in synthesis wastewater containing Methyl blue and RB21 dyes, including pH, settling time, PAC dose, the optimal CFG dosage in comparing with the cationic polymer. After that, actual textile wastewater was treated by using PAC, PAC plus cationic polymer, and PAC plus CFG for evaluating the role of CFG. CFG supplementation has assisted the process effects at nearly 98% color, 85% COD for RB21 and 90% color, 70% COD for MB at the best dose of CFG 0.15 mL and 0.1 mL, respectively. The optimized parameters for the coagulation of real textile wastewater using PAC were pH = 6 and dose = 0.6 mL can removal 66% of color. By adding CFG to PAC, the efficient of treatment was increased about 70% even at the lower dosage of PAC and CFG (0.5 mL for each reagent). The yield of combining PAC and polymer was a little bit lower than PAC and CFG, for instant 68% color was decreased at the same condition. These achievements demonstrated a workable substitute of natural products such as Cassis fistula seed gum for synthetic chemical products in coagulation-flocculation process. / Hiện nay các loại vật liệu sinh học chiết xuất từ thực vật đang được nghiên cứu ứng dụng trong xử lý nước và nước thải thay cho các chất hóa học. Mục tiêu của nghiên cứu này là đánh giá hiệu quả của việc sử dụng gum được chiết xuất từ hạt cây Muồng Hoàng Yến (MHY) làm chất trợ keo tụ trong xử lý nước thải dệt nhuộm. Thí nghiệm Jartest được tiến hành nhằm xác định các điều kiện tối ưu cho quá trình xử lý nước thải tổng hợp chứa thuốc nhuộm Methyle Blue (MB) và RB21 bao gồm pH, thời gian lắng, liều PAC, liều gum MHY và liều polymer. Sau đó tiến hành xử lý nước thải thật với các điều kiện thích hợp đã xác định nhằm đánh giá vai trò của gum MHY. Gum MHY làm tăng hiệu quả của quá trình xử lý, đạt gần 98% đối với độ màu, 85% COD đối với RB21, 90% độ màu và 70% COD đối với MB với liều lượng tương ứng là 0,15 mL và 0,1 mL. Các thông số tối ưu cho quá trình xử lý trên mẫu nước thải thật là pH = 6, liều PAC = 0.6 mL có thể làm giảm 66% độ màu. Bổ sung gum MHY làm chất trợ keo tụ giúp gia tăng hiệu quả xử lý màu lên 70% dù với liều lượng rất thấp là 0,5 mL. Hiệu suất xử lý khi sử dụng kết hợp PAC và polymer thấp hơn trong trường hợp sử dụng PAC và gum MHY, cụ thể khoảng 68% độ màu được xử lý ở cùng một điều kiện. Những kết quả này cho thấy tiềm năng của việc sử dụng các vật liệu gum tự nhiên nhằm thay thế cho các hợp chất hóa học trong các quá trình keo tụ tạo bông để xử lý nước thải.