The Filtration Properties of Atropa belladonna Plant Cell Suspensions; Effects of Hydrodynamic Shear and Elevated Carbon Dioxide Levels on Culture and Filtration Parameters

The filtration properties of Atropa belladonna plant cell suspensions cultured at different bioreactor stirrer speeds and gas-phase carbon dioxide levels were measured. Cell cake compressibility did not vary significantly with culture time, shear intensity or carbon dioxide concentration. Average cell cake permeability decreased by c. 70% with increasing stirrer speeds between 400 and 1000 rpm, and could be correlated with concomitant reductions in cell aggregate size. Permeability was more responsible than other culture parameters, such as growth, cell membrane integrity and protein release, to levels of hydrodynamic energy dissipation in the range 10⁶–10⁹ J m⁻³. Cell cake permeability was significantly affected by carbon dioxide levels of 10 and 15%, but not 2%. Average permeability at 15% CO₂ was reduced by c. 50% compared with the air-sparged control culture, even though aggregate size, morphological characteristics and filtered cake compressibility were unaltered. A distinctive pattern of permeability change over the course of the cultures was observed when the reactor conditions were not inhibitory to growth; however, this pattern was destroyed at medium-to-high shear levels and high carbon dioxide concentrations. © 1997 SCI.     

Viscoelastic and adhesive properties of single‐component thermo‐resistant acrylic pressure sensitive adhesives

Poly(butyl acrylate‐vinyl acetate‐acrylic acid) based acrylic pressure sensitive adhesives (PSAs) were synthesized by solution polymerization for the fabrication of high performance pressure sensitive adhesive tapes. The synthesized PSAs have high shear strength and can be peeled off substrate without residues on the substrate at temperature up to 150°C. The PSAs synthesized in the present work are single‐component crosslinked and they can be used directly once synthesized, which is convenient for real applications compared to commercial multi‐component adhesives. The results demonstrated that the viscosity of the PSAs remained stable during prolonged storage. The effects of the preparation conditions such as initiator concentration, cross‐linker amount, organosiloxane monomer amount and tackifier resin on the polymer properties, such as glass transition temperature (T_g), molecular weight (M_w), surface energy and shear modulus, were studied, and the dependence of the adhesive properties on the polymer properties were also investigated. Crosslinking reactions showed a great improvement in the shear strength at high temperature. The addition of tackifier resin made peel strength increase compared to original PSAs because of the improvement of the adhesion strength. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40086.     

Balance of mechanical and electrical performance in polyimide/nano titanium dioxide prepared by an in‐sol method

Hybrid polyimide (PI)/titanium dioxide (TiO₂) films were prepared by in situ polymerization and sol–gel and in‐sol methods (where in‐sol method indicates that in situ polymerization and the sol–gel method were used in the same samples). The mechanical and electrical properties were found to be sensitive to the processing methods and the dispersion of nano titanium dioxide (nano‐TiO₂) in the PI matrix. For the PI/TiO₂ films prepared by the in situ polymerization method, their tensile strength increased with increasing TiO_{2‐in situ} (“TiO_{2‐in situ}” is “the TiO₂ nano‐particles prepared by in situ polymerization method”) concentration. However, the optimal corona lifetime of the PI/TiO₂ films was 15 min at 20 kHz and 2 kV because of poor dispersion. For the PI/TiO₂ films prepared by the sol–gel method, the corona lifetime reached 113 min because of superior dispersion and a tensile strength of about 19.63 MPa. A balance of mechanical and electrical performances was achieved with the in‐sol method. The corona‐resistant life of the PI/TiO₂ films was 43 min, which was about six times longer than that of the neat PI. Their tensile strength was 83.5 MPa; these films showed no decrease in this value compared with the pure PI films. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44666.     

Development of new hybrid ultrafiltration membranes by entanglement of macromolecular PPSU‐SO3H chains: Preparation,morphologies, mechanical strength,and fouling resistant properties

The present work focuses on the preparation of Polyphenylsulfone (PPSU) membranes with enhanced antifouling surfaces through an incorporation of sulfonated Polyphenylsulfone (PPSU‐SO₃H), which acts as both, surface modifying agent and macromolecular additive. Initially, Sulfonated polyphenylsulfone (PPSU‐SO₃H) was synthesized by using chlosulfonic acid via bulk modification method. The degree of sulfonation (DS, %) of PPSU‐SO₃H was calculated by using NMR (nuclear magnetic resonance).The phase inversion technique was used to prepare all asymmetric membranes by allowing the PPSU‐SO₃H (different wt %) to entangle with the PPSU membrane matrix. All prepared membranes were characterized by using scanning electron microscope (SEM), X‐ray diffraction analysis (XRD), contact angle analysis (CA), mechanical strength analysis, molecular weight cut off (MWCO), porosity (%), mean pore size, and BSA adsorption studies. The performance efficiency of the membranes was evaluated by using BSA protein as a model foulant in terms of permeability, rejection (SR %), R_m (hydraulic resistance), R_c (cake layer resistance), R_p (pore plugging resistance), R_r (reversible fouling), R_ir (irreversible fouling), and FRR (flux recovery ratio). © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41986.     

Interforce initiated by magnetic nanoparticles for reducing internal concentration polarization in CTA forward osmosis membrane

The interforce between the magnetic composite forward osmosis (FO) membranes and the magnetic draw solution was proposed to reduce the internal concentration polarization (ICP) of FO process, and realized the synergetic permeability improvement of resultant FO membranes. The key factor was the successful fabrication of the Fe₃O₄ magnetic nanoparticles (MNPs) with small‐size and narrow distribution via co‐precipitation method. The cellulose triacetate (CTA) magnetic composite FO membranes were fabricated using Fe₃O₄ as additive via in situ interfacial polymerization, and named CTA‐Fe₃O₄. Dynamic light scattering (DLS) and zeta results showed that the coated sodium oleate on the MNPs explained their reducing aggregation and the stability of various pHs. The MNPs' surface segregation during demixing process resulted in the improvement of hydrophilicity, Fe content and roughness of resultant CTA‐Fe₃O₄ composite FO membranes. Furthermore, the in situ interfacial polymerization resulted in the formation of the polyamide selective layer, and the CTA‐Fe₃O₄ membrane's N content was 11.02% to 11.12%. The permeability properties (FO and pressure retarded osmosis modules) were characterized using 1.0M NaCl and 100 mg/L Fe₃O₄ as draw solutions, respectively. The results indicated that the higher concentration of MNPs supplied more interforce and better FO permeability properties. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44852.     

Effect of Cake Compression on the Performance of Centrifugal Dewatering

The effect of cake compression on the centrifugal dewatering is investigated under various rotating speeds and different kinds of cakes. A numerical method is proposed to estimate the capillary pressure and cake permeability under various cake saturations. The most dewatering in this study are operated at the funicular state of cake. The cake permeability decreases, while the capillary pressure increases rapidly, with the decrease of cake saturation during a centrifugal dewatering. The cake saturation can also be simulated once the relations among capillary pressure, cake permeability, and cake saturation are known. The deviations between simulated saturations and experimental data for compressible talc cakes are less than 2%. The centrifugal dewatering of compressible cake includes two mechanisms, the water squeeze due to cake compression and the centrifugal drainage due to pressure difference. The role of cake compression is dominant at the initial 500 s of the dewatering period, and these two factors are almost equal in magnitude as well as in importance when the cake approaches its equilibrium saturation. The porosity and compressibility of cake play the major roles in determining the equilibrium cake saturation. The equilibrium saturation of the compressible talc cake with a lower porosity is much higher than that of incompressible Al₂O₃ cake under a fixed rotating speed. An increase in rotating speed (centrifugal effect) results in a lower equilibrium cake saturation for either compressible or incompressible cakes; however, the increase in rotating speed is more efficient for an incompressible cake in the centrifugal dewatering.     

Adsorption behavior and effectiveness of poly(N,N‐dimethylacrylamide‐co‐Ca 2‐acrylamido‐2‐methylpropanesulfonate) as cement fluid loss additive in the presence of acetone‐formaldehyde‐sulfite dispersant

A copolymer of N,N‐dimethylacrylamide and Calcium 2‐acrylamido‐2‐methylpropanesulfonate was synthesized by free‐radical copolymerization. Its performance as anionic fluid loss additive (FLA) was studied by measuring static filtration properties of oil well cement slurries at 27°C and 70 bar pressure, respectively. It was found that cement filter cake permeability and API fluid loss decrease with increasing FLA dosage. Filtrate analysis revealed a linear correlation between fluid loss and the amount of FLA adsorbed on the cement surface. FLA adsorption on cement was determined by total organic carbon (TOC) analysis in cement filtrate and confirmed by ζ‐potential measurement. According to environmental scanning electron microscopy (ESEM) investigations, FLA does not alter the filter cake structure. In the presence of an anionic acetone–formaldehyde–sulfite (AFS) polycondensate dispersant, fluid loss control from FLA decreased and cement filter cake permeability increased because AFS reduces the amount of FLA adsorbed. In comparison to FLA, AFS shows stronger adsorption on the cement surface and succeeds in the competition with FLA. The different adsorption behavior of the two polymers is the reason for limited compatibility of this admixture com bination. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4341–4347, 2006     

Gravitational drainage of compressible organic materials

A model was developed to simulate drainage of compressible particle suspensions, and study how cake compression and volumetric load influence the process. The input parameters were settling velocity, cake resistance and compressibility. These parameters were found using a new experimental method. Dextran‐MnO₂ particle suspensions were drained as these resemble organic waste slurries with respect to settling and compressibility. It was demonstrated that cake compressibility must be taken into account to obtain adequate simulations. This implies that pressurized filtration resistances cannot be used for drainage simulations. In the filtration step, a distinct increase of dry matter from top to bottom of the cake was observed. During the subsequent consolidation, the cake compressed and a uniform dry matter profile was found. The final dry matter content of the cake increased with feed concentration and volumetric load. The drainage time increased proportionally with feed concentration and, more importantly, proportionally with squared volumetric load. © 2010 American Institute of Chemical Engineers AIChE J, 2010     

Injection of saline solutions to improve the electro-osmotic pressure and consolidation of foundation soil

Injection of saline solutions can enhance the effect of electro-osmotic pressure. This study considers the consolidation and stability of foundation soil for building construction. Kaolinite (KGa-1) and Taipei silty clay were subjected to zeta potential (ZP), electro-osmosis and laboratory vane shear tests with injection of saline solutions. The ZP values decrease (i.e., less negative potential) with increased cationic valences and concentrations. The increased electro-osmotic permeability from injecting CaCl₂ (1 N, EOC5) solution is about 172% higher than that without injection due to an increase of drained water from the cathode and the resulting increase of undrained shear strength. Average undrained shear strength for injecting CaCl₂ solution over a period of 7 days is about 4 to 5 times greater than that without injection during electro-osmosis tests. Electro-osmosis tests with injection of saline solutions reveal that the increase of undrained soil shear strength (ΔS_u) is proportional to the ZP tests.     

Physical and mechanical properties of Al(OH)3/polypropylene composites modified by in situ‐functionalized polypropylene

Al(OH)₃/polypropylene (PP) composites modified by in situ‐functionalized polypropylene (FPP) were prepared by a one‐step melt‐extrusion process. The effect of in situ FPP on the crystallization and melting behavior, melt‐flow index, limiting oxygen index, thermal degradation, mechanical properties, and fracture morphology of Al(OH)₃/PP composites was studied. Formation of in situ FPP resulted in a decreased crystallization temperature and melting point of PP in the composites, an increased melt‐flow index, and improved tensile and flexural strengths of Al(OH)₃/PP composites, whereas the thermal degradation behavior and limiting oxygen index was not been influenced. The impact strength of the Al(OH)₃/PP composites modified by in situ FPP depended upon the content of the initiator, dicumyl peroxide, and the monomer, acrylic acid. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2850–2857, 2002; DOI 10.1002/app.10269     

A simple and effective model for cross‐flow microfiltration and ultrafiltration

A semi‐theoretical unsteady‐state model for the flux in cross‐flow microfiltration and ultrafiltration has been developed. The model predicts fouling behaviour for a wide range of particle sizes and foulant concentrations. The developed model uses only two coefficients, k₁ and k₂, incorporating both the influences of the cake formation and the shear cleaning of the membrane, to describe flux decline. These two parameters were found to be almost independent of the operating conditions. The model provides both a fundamental understanding of the key physical phenomena governing flux decline and a rational basis for the design of an improved and modified cross flow filters.     

Improving mechanical properties of poly(vinyl chloride) by doping with organically functionalized reactive nanosilica

Nanosilica particles are functionalized by in situ surface‐modification with trimethyl silane and vinyl silane. Resultant reactive nanosilica (coded as RNS) contains double bonds and possesses good compatibility with vinyl chloride (VC) and polyvinyl chloride (PVC). This makes it feasible for RNS to copolymerize with VC generating RNS/PVC composites via in situ suspension polymerization. As‐prepared RNS/PVC composite resins are analyzed by means of FTIR. The tensile strength and impact strength of compression‐molded RNS/PVC composites are measured and compared with that of compression‐molded PVC composites doped with dispersible nano‐SiO₂ particles (abridged as DNS) surface‐modified with trimethyl silane alone. Moreover, the thermal stability of compression‐molded RNS/PVC and DNS/PVC composites is evaluated by thermogravimetric analysis. It has been found that RNS/PVC composites possess greatly increased impact strength and tensile strength than PVC matrix, while DNS/PVC composites possess higher impact strength than PVC matrix but almost the same tensile strength as the PVC matrix. This implies that DNS is less effective than RNS in improving the mechanical strength of PVC matrix. Particularly, RNS/PVC composites prepared by in situ suspension polymerization have much higher mechanical strength than RNS/PVC composites prepared by melt‐blending, even when their nanosilica content is only 1/10 of that of the melt‐blended ones. Besides, in situ polymerized RNS/PVC and DNS/PVC composites have better thermal stability than melt‐blended nanosilica/PVC composites. Hopefully, this strategy, may be extended to fabricating various novel high‐performance polymer‐matrix composites doped with organically functionalized nanoparticles like RNS. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Novel in situ carbon nanofiber/polydimethylsiloxane nanocomposites: Synthesis,morphology, and physico‐mechanical properties

A series of carbon nanofiber (CNF)/polydimethylsiloxane (PDMS)‐based nanocomposites was prepared by anionic ring opening polymerization of octamethylcyclotetrasiloxane (D₄) in presence of pristine CNF and amine‐modified CNF. A detailed study of morphology–property relationship of the nanocomposites was carried out in order to understand the effect of chemical modification and loading of filler on property enhancement of the nanocomposites. An elaborate comparison of structure and properties was carried out for the nanocomposites prepared by in situ and conventional ex situ methods. Pronounced improvement in degree of dispersion of the fillers in the matrix on amine modification of CNFs was reflected in mechanical properties of the modified nanocomposites. Maximum upliftment in mechanical properties was observed for in situ prepared amine modified CNF/hydroxyl PDMS nanocomposites. For 8 phr filler loading, tensile strength increased by 370%, while tensile modulus showed an increase of 515% compared with the virgin elastomer. Furthermore, in situ prepared unmodified CNF/hydroxyl PDMS nanocomposites showed an increase of 141°C in temperature of maximum degradation (T_max) for 8 phr CNF loading. These results were correlated with the morphological analysis through transmission electron microscopic studies. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

In situ emulsion polymerization and characterization of PVAc nanocomposites including colloidal silica nanoparticles for wood specimens bonding

Polyvinyl acetate (PVAc) nanocomposites for wood adhesives containing different amounts of colloidal silica nanoparticles (CSNs) were synthesized via in situ one-step emulsion polymerization. The adhesion strength of wood specimens bonded by PVAc nanocomposites was investigated by the tensile test. Thermal properties of PVAc nanocomposites were also characterized by differential scanning calorimetry and thermogravimetric analysis. Rheological and morphological properties of the PVAc nanocomposites were investigated using rheometric mechanical spectrometry and field emission scanning electron microscopy (FESEM), respectively. The obtaining results showed that the shear strength of PVAc nanocomposite including 1 wt. % CSNs has the highest shear and tensile strength about 4.7 and 3.2 MPa, respectively. A small increment of T_g (~3 °C) and considerable increment of the ash content proved the enhancement of PVAc thermal characterization in the presence of CSNs. FESEM results showed uniform dispersion of nanoparticles throughout the PVAc matrix due to using the in situ emulsion polymerization process. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48570.     

Improvement of SiC–Si/MAS Interface in the Joints via In Situ Synthesizing SiC Nanowires

Improving the SiC–Si/MAS interface is essential for enhancing the SiC–Si/MAS joint strength. In this work, well‐dispersed SiC nanowires (NWs) were in situ synthesized at the SiC–Si/MAS interface in the joints as the anchors, which made the fracture feature of the joints change from SiC–Si/MAS interface fracture to MAS fracture, resulting in an obvious improvement of the shear strength. The results showed that the average shear strength of the joints was increased by 49% by in situ synthesizing SiC NWs, which was primarily attributed to the excellent interface anchoring effects of SiC NWs involving the interfacial bonding anchoring between SiC NWs and SiC–Si layer and the mechanical interlocking anchoring between SiC NWs with the junctions and the surrounding grains. This study may provide new insight into the anchoring mechanisms and suggest a new design methodology for nanowire joints, leading to improved joint strength.     

Unified model for the prediction of consecutive solid–liquid filtration and expression at the constant pressure

Unified nonlinear model is proposed for the prediction of consecutive solid–liquid filtration and expression at the constant pressure. This model is based on the Darcy–Terzaghi filtration-consolidation equations modified to consider power-law pressure dependence of the specific cake resistance, and transforming Darcy law to the linear form. The model considers nonuniform structure of compressible filter cakes obtained by filtration and following expression. The profiles of local compressive pressure and local cake characteristics are simulated and compared for different moderately and highly compressible filter cakes (H.K. kaolin, CaCO₃, silica, activated sludge) based on the analytical and numerical solutions of the model. It is shown that the behavior of solid–liquid expression depends from the initial structure of compressed materials. Consolidation ratio U of the filter cakes with initially nonuniform structure formed by filtration differs from that of semi-solid materials with initially uniform structure. Different methods of determination of consolidation coefficient are analyzed and compared for nonuniformly structured filter cakes.     

Toughening polylactide with epoxidized styrene–butadiene impact resin: Mechanical,morphological, and rheological characterization

Styrene–butadiene impact resin (SBC) was chosen as the toughening agent to improve the tensile toughness of polylactide (PLA). Epoxidized SBC (ESBC) with different epoxidation degree were prepared by epoxidation using in situ peroxoformic acid method and a series of PLA/SBC(ESBC) blends were prepared by melt blending. The elongation at break of the PLA/ESBC blends was greatly improved, which was reflected in the slight decrease in the tensile strength and tensile modulus. Moreover, the tensile strength and tensile modulus were not significantly affected by the epoxidation degree of ESBC. For example, the incorporation of ESBC28.8% (30 wt %) to PLA caused an obvious increment of elongation at break from 3.5% of pure PLA to 305.0%, while the tensile modulus and tensile strength decreased to 80 and 78% of pure PLA, respectively. Scanning electron microscopy observations of cryo‐fractured surface morphology and particle size analysis demonstrated that the compatibility of the PLA/ESBC blends was improved significantly compared to PLA/SBC blend. PLA/ESBC(70/30) blends exhibited shear‐thinning behavior over the range of the studied shear rate. With an increase in shear rate, the non‐Newtonian index of the blends decreased gradually. Furthermore, the flow behavior of PLA/ESBC(70/30) blends was more sensitive to the shear rate than pure PLA. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46058.     

Preparation and characterization of acrylic latex/nano‐SiO2 composites

Acrylic/nano‐silica composite latexes were prepared by blending via high shear stirring (SS) or ball milling (BM) and in situ polymerization (IS). For comparison, composites filled with micro‐silica were also prepared. The mechanical and optical properties of the polymers formed by the composite latex filled with nano‐ or micro‐silica were investigated using an Instron testing machine, by dynamic mechanical analysis, ultraviolet–visible spectrophotometry and transmission electron micrography. The results showed that SS and BM methods could obtain better nanocomposite latex and polymers than the IS method, characterized by better dispersion of nanoparticles, higher tensile strength and T_g for SS and BM than for IS. The increase in absorbance and reduction in transmittance of UV (290–400 nm wavelength) were observed as nano‐silica content increased, whereas the UV absorbance or transmittance basically were kept unchanged for the composites filled with micro‐silica. © 2002 Society of Chemical Industry     

Preparation and property investigation of crosslinked alginate/silicon dioxide nanocomposite films

Crosslinked nanocomposite films of sodium alginate (SA) and silicon dioxide (SiO₂) with different SiO₂ loading values were prepared by in situ synthesis. Biocomposite films were produced by solution casting and solvent evaporation with glycerol as the plasticizer and calcium chloride as the crosslinking agent. The effects of the addition of nano silicon dioxide (nano‐SiO₂) in SA on the microstructural, physical, mechanical, and optical properties of the nanocomposite films were characterized. The results show that nano‐SiO₂ was dispersed homogeneously in the SA matrix; it thereby formed a strong interfacial interaction between the nano‐SiO₂ particles and the matrix. The transparency of the bionanocomposite films was enhanced. Thermogravimetric analysis also revealed that nano‐SiO₂ improved the thermal stability of the SA films. The incorporation of SiO₂ further reduced the water vapor permeability and swelling degree and significantly increased the tensile strength and elongation, which are parameters important for packaging industries. Finally, the lower light transmission of UV light from 200 to 250 nm indicated that SA/SiO₂ nanocomposite films could potentially be used to prevent lipid damage by UV light in food conservation. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43489.