Diffusion of some dyes in aqueous polymer solutions

The diffusion of both Direct Blue 76 and acid orange dyes in aqueous dilute polymer solutions was studied using the capillary method. The polymer systems studied included dilute solutions of carboxymethyl cellulose, polyethylene oxide and polyacrylamide. It was found that the diffusion coefficients of the two dyestuffs in carboxymethyl cellulose solutions are higher than that in pure water, while in polyacrylamide solutions the values of the coefficients are lower than that in pure water. In case of polyethylene oxide solutions, the diffusion coefficient of Direct Blue 76 was found to be lower than that in pure water, whereas that of acid orange was found to be higher than that in pure water. The diffusion coefficients of both dyes were found to decrease with increasing polymer concentration in the case of polyethylene oxide and polyacrylamide, whereas in the case of carboxymethyl cellulose the diffusion coefficients increased with polymer concentration. With change of temperature, the diffusion coefficients of both dyes in the three polymer solutions were found to obey the Arrhenius equation. The activation energy for diffusion of the two dyes was calculated in pure water, as well as in the different polymer solutions.     

天然高分子亲水性凝胶材料在竹醋液中 溶胀度的初步研究

测定了壳聚糖、黄原胶、海藻酸钠3种天然高分子亲水性凝胶材料在竹醋液中的溶胀度。探讨了温度、pH值对其溶胀度和溶胀速率的影响。结果表明在20~40℃ 范围内,3种凝胶的溶胀度和溶胀速率随着温度的升高而增加;在不同pH值的竹醋液中,壳聚糖和黄原胶的溶胀速率十分相近,而且黄原胶比壳聚糖更稳定。     

Diffusion in aqueous polymer solutions

The diffusion of Direct Blue 76 dye in aqueous dilute polymer solutions was studied using the capillary method. The polymer systems studied included dilute solution of carboxymethyl cellulose, poly(ethylene oxide), and polyacrylamide. It was found that the diffusion coefficient of Direct Blue 76 in carboxymethyl cellulose is higher than that in pure water, while in polyacrylamide and poly(ethylene oxide) solutions the value is lower than that in pure water. The diffusion coefficient of Direct Blue was found to decrease with increasing polymer concentration in case of poly(ethylene oxide) and polyacrylamide, while in case of carboxymethyl cellulose the diffusion coefficient increases with polymer concentration. The effect of temperature on the diffusion coefficient of Direct Blue 76 in the three polymers was found to obey the Arrhenius equation. The activation energy for diffusion of Direct Blue 76 in water, poly(ethylene oxide), polyacrylamide, and carboxymethyl cellulose was found to be 4.38, 7.7, 5.44, and 5 kcal, respectively, for polymer concentration of 0.25 g/l.     

Measurement of shear-dependent intrinsic viscosities of carboxymethyl cellulose and xanthan gum suspensions

A rotational rheometer with cone and plate fixtures was used to measure the intrinsic viscosities of aqueous suspensions of xanthan gum and carboxymethyl cellulose (CMC). The reduced viscosities or hydrodynamic volumes of CMC suspensions increased with dilution. However, the reduced viscosities of xanthan gum suspensions decreased with dilution within the concentration range of 0.1–0.06% and increased with dilution within the concentration range of 0.04–0.01%. When the gums were suspended and diluted with 0.06 M sodium acetate, the reduced viscosities of all the xanthan gum and CMC suspensions decreased upon dilution. The intrinsic viscosities of xanthan gum and CMC suspensions decreased with increasing the shear rate, showing a dependence of hydrodynamic volume on shear rate.     

Some properties of xanthan gum in aqueous solutions: effect of temperature and pH

The properties of xanthan gum (XG) aqueous solutions were investigated by using viscometric, electrokinetic and surface tension measurements. The effects of polymer concentration, temperature and pH on the viscosity of the XG solutions were evaluated and discussed. Zeta potential data determined for XG solutions in water in the temperature range of 15–45 °C corroborated with the results obtained from the viscometric investigations suggest the occurence of conformational changes above 36 °C. The activation energy of flow and that associated with the electrophoretic migration of the charged particles were estimated for XG solutions in water. In acid medium, xanthan gum determines a slight decrease of the surface tension of pure water at all investigated temperatures.     

基于动态硼酸酯键改性黄原胶的性能

基于苯硼酸聚合物可以与存在于黄原胶糖环单元结构中的伯、仲醇羟基通过硼酸酯键形成动态共价微交联结构的性质对黄原胶进行改性。以偶氮二异丁基脒二盐酸盐（AIBA）为引发剂，通过水相自由基聚合，制备了不同共聚比的丙烯酰胺（AM）、N-(3-二甲氨基丙基)丙烯酰胺（DMAPAM）和3-丙烯酰胺基苯硼酸（AMBB）的三元共聚物P(AM-co-DMAPAM-co-AMBB)。通过1H NMR、FTIR、元素分析和光散射对聚合物结构及相对分子质量进行了表征，并对其与黄原胶复配体系的增黏性、流变性、抗老化性及抗干扰性进行了评价。结果表明：P(AM-co-DMAPAM-co-AMBB)与黄原胶复配后对黄原胶溶液具有明显的增黏性，其中苯硼酸单体的摩尔比为1.0 mol%的聚合物对黄原胶溶液的增黏幅度达43.8%，在8074 mg/L的矿化水中增黏幅度高达56.4%，且复配体系具有良好的抗老化降解性，对乙二醇和1,3-丙二醇具有较强的抗干扰性。     

Temperature-induced thickening of sodium carboxymethylcellulose and poly(N-isopropylacrylamide) physical blends in aqueous solution

This study describes the synthesis of poly(N-isopropylacrylamide) (PNIPAM) via free radical polymerization, the preparation of physical blends containing sodium carboxymethylcellulose (CMC) and PNIPAM in aqueous solution, at total polymer concentrations of 2 and 6?g/L in different compositions, and applies rheology to investigate interactions between PNIPAM and CMC compared to pure polymers, in aqueous solution. Rheological measurements indicated thermothickening behavior for the 50?% PNIPAM–50?% CMC physical blend in aqueous solution, at 6?g/L, as viscosity rose when temperature was increased to a range of 25–40?°C. Similar thermothickening behavior was observed for the 25?% CMC–75?% PNIPAM physical blend in solution, at a total polymer concentration of 2?g/L. These results provide new information for preparing physical blends in aqueous solutions exhibiting thermothickening behavior, indicating that this behavior depends on total polymer concentration and composition of the mixture.     

Gas hold-up and oxygen transfer in three-phase external-loop airlift bioreactors: Non-Newtonian fermentation broths

The effects of solids loading on gas hold-up and oxygen transfer in external-loop airlift bioreactors with non-Newtonian fermentation media are discussed. Experiments were performed in two model external-loop airlift bioreactors with aqueous solutions of carboxymethyl cellulose (CMC) and xanthan gum representing non-Newtonian flows. Low-density plastic particles of 1030 and 1300 kg m⁻³ were used and the solids loading was varied in the range 0–20% (v/v). For the inelastic non-Newtonian CMC aqueous solutions, the presence of low-density solid particles slightly increased the riser gas hold-up, ϕ_gr, but decreased the volumetric mass transfer coefficient, k_La. On the other hand, ϕ_gr decreased but k_La increased with solids loading in the viscoelastic non-Newtonian xanthan gum aqueous solution. The extent of these effects depended on non-Newtonian flow behavior. Theoretical models of riser gas hold-up and volumetric mass transfer coefficient have been developed. The capability of the proposed models was examined using the present experimental data obtained in the model external-loop airlift bioreactors and the available data in the literature. The data were successfully correlated by the proposed correlations except the results for k_La coefficient in the xanthan gum solution.     

Physical absorption of oxygen in laminar falling films of dilute polymeric aqueous solutions

Diffusion coefficients of oxygen in three dilute polymeric aqueous solutions (sodium carboxymethyl cellulose, hydroxyethyl cellulose,polyvinyl alcohol) were measured under flowing conditions, and the influence of shear rate on diffusivity was investigated. The rheological properties of the three polymeric solutions were determined using a Couette-Hatschek viscometer. The absorption experiment was made in a wetted-wall column which was made of a stainless steel tube, and was 16.5mm, 55mm in outside diameter and effective height respectively. The concentration of the physically absorbed oxygen was measured using Winkler titration method. Diffusivity enhancement was observed in the sodium CMC which was the most viscous of solutions experimented with in this study.     

Synthesis, characterization and drug release properties of thermosensitive poly(N-isopropylacrylamide) microgels

Nanocomposite membranes (NCMs) were prepared by using the solution casting technique by incorporating the different amounts like 6, 8, 10 wt.% of Preyssler type heteropolyacid nanoparticles to the sodium alginate. Prepared NCMs were utilized for the sorption and permeation studies for the aqueous isopropanol solutions at different concentrations. Sorption experiment enabled the study of interactions between the components of the mixture and the polymer. Flory-Huggins interaction parameters between the permeating molecules and polymer and solubility parameters were determined to explain the sorption behavior of the NCMs. Permeation properties of the NCMs were tested by applying them for pervaporation dehydration of IPA at different concentrations. Different PV parameters like separation factor, flux, Permeance and selectivity were calculated to explain the permeation behavior of the NCMs. In this study, increased sorption, permeation and selectivity was observed for the NCMs than pristine sodium alginate membrane, indicating that NCMs are efficient for PV dehydration of the IPA. Solution-diffusion model was adopted to study the mass transfer through the membrane by calculating the diffusion coefficients.     

Diffusion of electrolytes in dilute polymer solutions

The diffusion of sodium chloride in dilute solutions of carboxymethylcellulose (CMC) was studied using the porous frit technique. It was found that at relatively low CMC concentrations the diffusivity of sodium chloride (D) is higher than that in water (D₀); with increasing CMC concentration, the diffusivity decreases gradually and reaches a value lower than that in water. The relation between the diffusivity (D) and CMC concentration (C_p) was represented by the equation D = a – bC_p. The effect of temperature on the diffusivity of sodium chloride in CMC solutions was found to obey the Arrhenius equation with an activation energy of 2230 cal/mol.     

Isothermal titration calorimetry, transmission electron microscopy, and field emission scanning electron microscopy of a main-chain viologen polymer containing bromide as counterions

The interaction of a main-chain viologen polymer containing bromide as counterions with water and aqueous potassium bromide over a broad range of concentrations was studied with isothermal titration calorimetry. The dilution process of this polymer was endothermic as opposed to flexible poly(sodium acrylate) and poly(sodium styrenesulfonate). This result may be related to the different mechanism of hydration of pyridinium and bromide groups in the main chain. It also exhibited aggregation phenomenon in both water and aqueous potassium bromide solutions as detected by transmission electron microscopy like other flexible and rigid-rod polyelectrolytes. As the polymer concentrations in aqueous solutions increase, the aggregated polymer exhibited more defined ordered structures than random structures observed at low polymer concentrations. Field emission scanning electron microscopy also revealed the effect of variation of concentration of aqueous potassium bromide on the morphology of the polymer matrix. At increasing concentrations of aqueous potassium bromide, the polymer structures became more ordered than those in low concentrations.     

Some Characteristics of Stirred Vessel Flows of Dilute Polymer Solutions Powered by a Hyperboloid Impeller

Measurements of the power consumption and mean and turbulent velocities in the wall jet of a stirred vessel flow, powered by a hyperboloid impeller, were carried out. The fluids were aqueous solutions of tylose, CMC and xanthan gum (XG), at weight concentrations ranging from 0.1% to 0.6%, which exhibited varying degrees of shear‐thinning and viscoelasticity. The hyperboloid impeller parameter k of Metzner and Otto (1957) was found to be equal to 27.2 ±4. In the Reynolds number range of 10³ to 3 × 10⁴ the mixing power was reduced for all non‐Newtonian fluids, but never by more than 13%. The flows of the 0.2% CMC and 0.2% XG solutions were found to be less turbulent than those of water, especially for the latter fluid where a reduction in axial rms in excess of 50% was found in the wall jet. This was attributed to elasticity effects and especially to the high zero shear viscosity of the latter fluid.     

Gas-liauid mass transfer in non-newtonian fluids in a tank stirred with a helical ribbon screw impeller

Oxygen transfer in aqueous solutions of CMC, xanthan gum, and polyacrylamide in a vessel equipped with a helical ribbon screw impeller and a multi-orifice ring sparger was studied. The K_La values obtained were comparable to those reported for radial flow impellers, but they are more representative of the oxygen transfer in the bulk of the liquid because of a more homogeneous mixing and absence of dead zones. Dimensionless correlations including the effect of the physical properties of the fluids, and those of operating conditions were developed. A dimensionless correlation for each fluid is proposed.     

STUDIES OF MIXING IN A CONCENTRIC TUBE AIR-LIFT REACTOR CONTAINING XANTHAN GUM BY MEANS OF AN IMPROVED FLOW FOLLOWER

The influence of a pseudoplastic non-Newtonian fluid upon the hydrodynamic performance and mixing parameters of a concentric tube air-lift fermenter has been studied using a range of dilute xanthan gum solutions (0-0.5% weight by volume). Liquid circulation times vary in a complex pattern with increasing gum concentration. At low concentrations, circulation was more; rapid due to drag reduction whilst at the highest concentrations circulation times were increased. The column voidage decreased with increasing gum concentration and bubbly flow in the riser was replaced by slug flow. For all gum concentrations the effective dispersion coefficient for a single passage around the loop was increased relative to tap water. An improved radio-pill flow follower system for hydrodynamic studies is described.     

The usability of (sodium alginate/acrylamide) semi-interpenetrating polymer networks on removal of some textile dyes

In this study, (sodium alginate/acrylamide) interpenetrating polymer networks ((NaAlg/AAm)IPN) have been prepared at definite composition. The aqueous solution of 3% (w/v) sodium alginate and 50% (w/v) acrylamide was irradiated with ⁶⁰Co-γ rays at a dose rate of 0.07 kGy/h up to 5 kGy. The percent conversion was determined gravimetrically and 100% gelation was achieved at 5 kGy dose. To understand whether the semi-interpenetrating polymer network of sodium alginate is performed, Fourier Transform Infrared (FTIR) spectra of polyacrylamide (PAAm), sodium alginate, and the semi-interpenetrating polymer network were recorded. It is found that the FTIR spectra of PAAm, NaAlg, and the semi-interpenetrating polymer network are different. The thermograms of PAAm, sodium alginate, and the semi-interpenetrating polymer network were recorded for investigating their thermal character. (NaAlg/AAm)IPN hydrogels were immersed to swell in a solution of pH 7, at a temperature of 25°C. The swelling results at pH 7.0 indicated that (NaAlg/AAm)IPN hydrogel, containing 3% NaAlg showed maximum % swelling in water but swelling increased in the order of water > Magenta > Methylene Blue > Safranine-O > Methyl Violet. Diffusion of water and aqueous solution of dyes within (NaAlg/AAm)IPN hydrogels was found to be of Fickian character at the initial stage of swelling with regard to values calculated for diffusion coefficient of (NaAlg/AAm)IPN hydrogels in water and aqueous solution of dyes. Some diffusion parameters were calculated from swelling of (NaAlg/AAm)IPN in water and dyes and their adsorption isotherms were plotted. In the adsorption experiments, the efficiency of (NaAlg/AAm)IPN hydrogels to adsorb Magenta, Safranine-O, Methylene Blue, and Methyl Violet dyes from water was studied. (NaAlg/AAm)IPN hydrogels showed different adsorption for different aqueous solution of dyes at pH 7.0. Adsorption isotherms were constructed for (NaAlg/AAm)IPN-dye systems. S type adsorption in the Giles classification system was found. Thermal and spectroscopic characterization of semi-interpenetrating polymer network of sodium alginate and acrylamide and dye adsorbed semi-interpenetrating polymer network of sodium alginate and acrylamide was recorded. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Residual temperature dependence of normalized diffusion of polystyrene latex in aqueous solvents

The so-called anomalous dependence of diffusion of polystyrene latex⁴ was examined in detail using quasi-elastic light scattering. The normalized diffusion coefficients showed a residual decrease with increasing temperature for solutions in water, 0.1 M phosphate buffers, methanol and 0.1 M sodium carbonate but not in dilute solutions of dimethyl ketone, Triton X-100, some salt solutions and pure ethanol. Using sensitive analyses for multi-exponential fits to the data, it was shown that the presence or absence of the dependence was not affected by possible low levels of aggregation of the latex. These results are interpreted as reflecting an increased solvation of the charge groups on the latex with rising temperature.     

STUDIES OF MIXING IN A CONCENTRIC TUBE AIR-LIFT REACTOR CONTAINING XANTHAN GUM BY MEANS OF AN IMPROVED FLOW FOLLOWER

The influence of a pseudoplastic non-Newtonian fluid upon the hydrodynamic performance and mixing parameters of a concentric tube air-lift fermenter has been studied using a range of dilute xanthan gum solutions (0-0.5% weight by volume). Liquid circulation times vary in a complex pattern with increasing gum concentration. At low concentrations, circulation was more; rapid due to drag reduction whilst at the highest concentrations circulation times were increased. The column voidage decreased with increasing gum concentration and bubbly flow in the riser was replaced by slug flow. For all gum concentrations the effective dispersion coefficient for a single passage around the loop was increased relative to tap water. An improved radio-pill flow follower system for hydrodynamic studies is described.     

Stability and rheological study of sodium carboxymethyl cellulose and alginate suspensions as binders for lithium ion batteries

Currently, the most widely used binder in batteries is polyvinylidene fluoride with N‐methyl‐2‐pyrrolidone used as a solvent. This solvent is flammable and toxic. Here, we focus on the suitability of using water‐soluble sodium alginate (Na‐alginate) and sodium carboxymethyl cellulose (Na‐CMC) as alternative biobased binder materials for the anodes of lithium ion batteries. It reduces the environmental impact of current manufacturing processes. However, control of the rheological characteristics of the binder whilst containing active and conductive additives is key for optimized processing. Here, we perform stability and rheological measurements of Na‐alginate and Na‐CMC solutions containing varying amounts of graphite and carbon black used as active and conductive materials, respectively. Compared with the benchmark Na‐CMC, the degree of flocculation shows that for the same concentration of binder in water, Na‐alginate suspensions are more stable. The rheology measurements show that Na‐alginate slurries have a higher viscosity than Na‐CMC at a shear rate of 50 s^?1 with that for a 1.5% of Na‐alginate binder being 1.26 Pa s while for Na‐CMC it was for 0.20 Pa s. The loss factor was lower for Na‐Alginate, between 2 and 3 against between 2.9 and 3.3 for Na‐CMC, showing a more developed network structure. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46217.     

Experimental investigations of non‐Newtonian/Newtonian liquid‐liquid flows in microchannels

The plug flow of a non‐Newtonian and a Newtonian liquid was experimentally investigated in a quartz microchannel (200‐µm internal diameter). Two aqueous glycerol solutions containing xanthan gum at 1000 and 2000 ppm were the non‐Newtonian fluids and 0.0046 Pa s silicone oil was the Newtonian phase forming the dispersed plugs. Two‐color particle image velocimetry was used to obtain the hydrodynamic characteristics and the velocity profiles in both phases under different fluid flow rates. The experimental results revealed that the increase in xanthan gum concentration produced longer, bullet‐shaped plugs, and increased the thickness of the film surrounding them. From the shear rate and viscosity profiles, it was found that the polymer solution was in the shear‐thinning region while the viscosity was higher in the middle of the channel compared to the region close to the wall. Circulation times in the aqueous phase increased with the concentration of xanthan gum. © 2017 The Authors AIChE Journal published by Wiley Periodicals, Inc. on behalf of American Institute of Chemical Engineers AIChE J, 63: 3599–3609, 2017