Preparation and Performance of Organically Modified Montmorillonite Composite Separation Membrane

A new composite separation membrane was developed by using organically modified montmorillonite(OMMT)as an additive.The effects of OMMT on the modification and properties of PVDF composite membranes were investigated.It is found that different kinds and amounts of OMMT into the casting solution can obviously change the pure water flux,separation performance and hydrophilicity of composite membrane in varying degrees.When the TA/PDA-MMT was 0.5 wt%,the pure water flux of the membrane reached the maximum,which was 584.7 L/(m^(2)·h),about 6 times that of the original membrane.The OMMT/PVDF composite membrane had good hydrophilicity and stability in the treatment of oily wastewater.The development of novel OMMT/PVDF composite membrane will provide a new idea for solving the problem of oily wastewater treatment.

Study of Rice Husks and Expanded Polystyrene Composites for Construction Applications

In the current context of environmental challenges, this study focuses on developing innovative and eco-friendly composites using rice husk and recycled expanded polystyrene. This dual-responsibility approach valorizes a by-product like rice husk, often considered waste, and reuses polystyrene, a plastic waste, thereby contributing to CO2 emission reduction and effective waste management. The manufacturing process involves dissolving recycled polystyrene into a solvent to create a binder, which is then mixed with rice husk and cold-compacted into composite materials. The study examines the impact of two particle sizes (fine and coarse) and different proportions of recycled polystyrene binder. The results show significant variations in the mechanical characteristics of the composites, with Modulus of Rupture (MOR) values varying from 2.41 to 3.47 MPa, Modulus of Elasticity (MOE) ranging from 223.41 to 1497.2 MPa, and Stiffness Coefficient (K) from 5.04 to 33.96 N/mm. These characteristics demonstrate that these composites are appropriate for various construction applications, including interior decoration, panel claddings, and potentially for furniture and door manufacturing when combined with appropriate coatings. This study not only highlights the recycling of agricultural and plastic waste but also provides a localized approach to addressing global climate change challenges through the adoption of sustainable building materials.

Photocatalytic remediation ofγ-hexachlorocyclohexane contaminated soils using TiO_2 and montmorillonite composite photocatalyst

TiO2 and montmorillonite composite photocatalysts were prepared and applied in degrading γ-hexachlorocyclohexane （γ-HCH） in soils. After being spiked with γ-HCH, soil samples loaded with the composite photocatalysts were exposed to UV-light irradiation. The results indicated that the photocatalytic activities of the composite photocatalysts varied with the content of TiO2 in the order of 10%〈70%〈50% 〈30%, Moreover, the photocatalytic activity of the composite photocatalysts with TiO2 content 30% was higher than that of the pure P25 with the same mass of TiO2. The strong adsorption capacity of the composite photocatalysts and quantum size effect may contribute to its increased photocatalytic activities. In addition, effect of dosage of composite photocatalysts and soil pH on γ-HCH photodegradation was investigated. Pentachlorocyclohexene, trichlorocyclohexene, and dichlorobenzene were detected as photodegradation intermediates, which were gradually degraded with the photodegradation evolution.

Fabrication of Fluorescent Porphyrin/Polystyrene Composite Nanospheres by Electrospinning

Fluorescent polystyrene（PS）/porphyrin（TPPA） composite nanospheres were successfully fabricated by electrospinning. The SEM images clearly show that owing to adding TPPA in PS, the averaged diameter of the composite nanospheres became smaller, from 1500 to 580 nm. Fourier-transform infrared（FTIR） spectra determined the chemical composition of the resulting PS/TPPA composite nanospheres. The photoluminescent（PL） spectral analysis indicates that the peak position of the composite nanospheres in either solid state or water is identical to that of pure TPPA, at about 652 nm, and is still unchangeable when they are left for at least 20 d, indicating the stable photoluminescent property of the fluorescent composite nanospheres.

Intercalation Assembly, Characterization and Luminescent Properties of Novel Supramolecular Composite Materials, Tb(Ⅲ) Complex with Tetrapodal Ligand-Montmorillonite

Two kinds of Tb（ Ⅲ ） complexes with tetrapodal ligand, [TbL（NO3）]^3＋ and [TbL]^3＋ （L： 1,1, 1＇, 1＇-tera （ 2-pyridinecarboxylester ）-di （ trimethylpropane）） were intercalated into the interlayer space of montmorillonite （MT） by ion exchange and coordination reaction of L with the Tb^3＋ ion existing in the interlayer space of Tb-MT respectively. The obtained luminescent supramolecular composite materials, [ TbL （NO3） ]^2＋-MT and [TbL]^3＋-MT were characterized by elemental analysis, XRD, FT-IR, UV-vis and thermal analysis. At the same time, the luminescent properties of the materials were also studied. The results show that the intercalated materials with regular layered structure, good thermal stability and the interlayer spacing （d001） approximates to the size of the complex ions which are located in the interlayer space of MT in the form of a monolayer.

Chlorinated butyl rubber/two-step modified montmorillonite nanocomposites:Mechanical and damping properties

Montmorillonite(MMT) was modified by ultrasound and castor oil quaternary ammonium salt intercalation method to prepare a new type of organic montmorillonite(OMMT). The surface structure, particle morphology, interlayer distance, and thermal behavior of the samples obtained were characterized. The modified OMMT was then added to chlorinated butyl rubber(CIIR) by mechanical blending, and a composite material with excellent damping properties was obtained. The mechanical experiment results of CIIR nanocomposites showed that the addition of OMMT improved their tensile strength, hardness,and stress relaxation rate. Compared with pure CIIR, when the content of OMMT was 5 phr(part per hundred of rubber), the tensile strength of the nanocomposite was increased by 677% and the elongation at break was also increased by 105.4%. The enhancement of this performance was mainly due to the dispersion of the nanosheets in CIIR rubber and the chemical interaction between the organoclay and the polymer matrix, which was confirmed by morphology and spectral analysis. OMMT also endowed a positive effect on the damping properties of CIIR nanocomposites. After adding 5 phr of OMMT, the nanocomposite owned the best damping performance, and the damping factor, tanδmax, was 37.9% higher than that of pure CIIR. Therefore, the good damping and mechanical properties of these CIIR nanocomposites provided some novel and promising methods for preparing high-damping rubber in a wide temperature range.

Application of Polymerizable Surfactant in the Preparation of Polystyrene/Nano-Fe_3O_4 Composite

Monooctadecyl maleate, as a polymerizable surfactant, was synthesized by the mono-esterification of maleic anhydride and octadecanol, and was utilized to surface-modify nano-Fe3O4 particles. A polymerizable magnetic fluid was obtained by directly dispersing modified nano-Fe3O4 particles into styrene monomer, and the polystyrene/nano-Fe3O4 composite was prepared through free radical polymerization of polymerizable magnetic fluid. The structure and dispersion status in different dispersion phases of modified nano-Fe3O4 particles were studied by Fourier transform infrared （FTIR） spectrometry, X-ray diffraction （XRD） and transmission electron microscopy （TEM）, respectively. The experimental results show that the nano-Fe3O4 particles modified by monooctadecyl maleate with the size of about 7-10 nm can be uniformly dispersed into styrene and fixed in the composite during the procedure of polymerization. Thermogravimetric analysis （TGA） and vibrating sample magnetometry （VSM） indicate that the thermal stability of polystyrene/nano-Fe3O4 composite is improved compared to that of pure polystyrene, and the composite is a sort of superparamagnetic materials.

Dynamic Mechanical and Thermal Properties of Cross-linked Polystyrene/Glass Fiber Composites

Cross-linked polystyrene/glass fiber composites were fabricated using cross-linked polystyrene （CLPS） as matrix and E-glass fiber as the reinforcement. Surfaces of E-glass fibers were modified by vinyl triethoxysilane （VTES）, vinyl trimethoxysilane （VTMS） and γ-methacryloylpropyl trimethoxysilane （MPS）. The treated glass fibers were analyzed by fourier transform infrared spectroscopy （FTIR）. Dynamic mechanical thermal analysis （DMTA） and thermo-gravimetric analysis （TGA） were employed to investigate the effect of glass fibers surface modification on viscoelastic behavior and thermal properties. The morphology of fracture surfaces of various composites was observed by scanning electron microscopy （SEM）. The results revealed that these coupling agents were connected to the surfaces of the fibers by chemical bonding. Dynamic mechanical properties as well as thermal stability of the composites were improved considerablely, but to varying degrees depending on the fiber modification. The diversities of improvement of properties were attributed to the different interfacial adhesion between CLPS matrix and the glass fibers.

Physical and Mechanical Properties of Eco-Friendly Composites Made from Wood Dust and Recycled Polystyrene

The development of alternative wood composites based on the use of waste or recycled materials can be beneficial due to over exploitation of natural resources.Under this frame,an option for the successful utilization of waste polystyrene which avoids environmental problems that formaldehyde adhesives cause and also reduces waste dis-posal,is its potential application as a binder for the production of value-added environmentally friendly and low cost wood composites.Two types of panel were successfully made,consisting of wood dust and two recycled poly-styrene contents,namely,15%and 30%.Both physical properties,water absorption and thickness swelling,and mechanical properties,modulus of rupture,shear strength parallel in the plane of the board and glue line shear strength,were significantly improved as the recycled polystyrene content increased from 15%to 30%.Water absorption and thickness swelling after 24 h immersion in water were improved by 165%and 750%as the recycled polystyrene content increased from 15%to 30%.The magnitude of the improvement in mechanical properties however,was less pronounced than of the physical properties since modulus of rupture,shear strength parallel in the plane of the board and glue line shear strength were increased by 43.6%,50%and 61.5%,respec-tively.The low viscosity of the recycled polystyrene caused more mobility inside the panel matrix and therefore,an improved penetration took place into adequate depth of the compressed dust particles.It is concluded that boards can be successfully produced using these waste raw materials,wood dust and recycled polystyrene in organic solvent as a binder,and therefore it can reduce waste disposal and provide cleaner production for the development of wood-based boards.

Determination of Triclocarban, Triclosan and Methyl-Triclosan in Environmental Water by Silicon Dioxide/Polystyrene Composite Microspheres Solid-Phase Extraction Combined with HPLC-ESI-MS

This paper developed a sensitive and efficient analytical method for triclocarban (TCC), triclosan (TCS) and Methyl-triclosan (MTCS) determination in environmental water, which involves enrichment by using silicon dioxide/polystyrene composite microspheres solid-phase extraction and detection with HPLC-ESI-MS. The influence of several operational parameters, including the eluant and its volume, the flow rate and acidity of water sample were investigated and optimized. Under the optimum conditions, the limits of detection were 1.0 ng/L, 2.5 and 4.5 ng/L for TCC, TCS, and MTCS, respectively. The linearity of the method was observed in the range of 5-2000 ng/L, with correlation coefficients (r2) >.99. The spiked recoveries of TCC, TCS and MTCS in water sampleswereachieved in the range of 89.5% -96.8% with RSD below 5.7%. The proposed method has been successfully applied to analyze real water samples and satisfactory results were achieved.

Synthesis of zinc oxide–montmorillonite composite and its effect on the removal of aqueous lead ions

Lead adsorption of zinc oxide-coated ACOR montmorillonite was investigated in batches and under reducing conditions at ambient temperature. The presence of zinc oxide coating significantly enhanced the adsorption of Pb^(2+) ions by ACOR montmorillonite. Characterization of adsorbents involved the use of X-ray diffraction, sodium saturation techniques, coulter laser analysis, scanning electron microscopy, and electron dispersive spectroscopy.Synthesis involved the trimetric process, activation of the ACOR montmorillonite and reacting of the same with zinc nitrate to produce a zinc oxide composite solid at 450 °C.The reaction mechanism indicated less than one proton coefficient, and higher mass transfer rates, when compared with bare montmorillonite. Intraparticle diffusion was higher than the value recorded for the bare montmorillonite. Reactions based on initial Pb^(2+) concentration indicated that coated montmorillonite gradually became saturated as the concentration was increased. Reactions based on solid concentration demonstrated a complex change in the capacity of adsorption over different Pb^(2+) concentrations(10–40 mg L^(-1)) and solid concentrations(2–10 g L^(-1)). The specific surface area reduction, particle size increase, mineral aggregation, and concentration gradient effect controlled the complex changes in adsorption.

Thermodynamic and structural properties of polystyrene/C60 composites: A molecular dynamics study

To tailor properties of polymer composites are very important for their applications.Very small concentrations of nanoparticles can significantly alter their physical characteristics.In this work,molecular dynamics simulations are performed to study the thermodynamic and structural properties of polystyrene/C60(PS/C60)composites.The calculated densities,glass transition temperatures,and coefficient of thermal expansion of the bulk PS are in agreement with the experimental data available,implying that our calculations are reasonable.We find that the glass transition temperature Tg increases accordingly with an added concentration of C60 for PS/C60 composites.However,the self-diffusion coefficient D decreases with increase of addition of C60.For the volumetric coefficients of thermal expansion(CTE)of bulk PS and PS/C60 composites,it can be seen that the CTE increases with increasing content of C60 above Tg(rubbery region).However,the CTE decreases with increasing content of C60 below Tg(glassy region).

STUDIES ON POLYSILOXANE-POLYSTYRENE COMPOSITE LATEXES

Polysiloxane-polystyrene composite latexes were prepared by two-stage emulsionpolymerization. Polymerization of styrene in swollen polysiloxane latex particles were studied.Formation of simple polystyrene particle in the 2nd-stage polymerization depends on the particlesize of the lst-stage latex and the polymerization temperature. Polystyrene domains in thevulcanizates reinforce the silicone rubbers effectively.

PREPARATION,CHARACTERIZATION AND ELECTROCHEMICAL PROPERTIES OF POLYPYRROLE-POLYSTYRENE SULFONIC ACID COMPOSITE FILM

Polypyrrole-polystyrene sulfonic acid(PPy-PSSA)composite films have been electrosynthesized in an aqueoussolution of PSSA.The electro-active films exhibit cation exchange during the redox process.Infrared,Raman and energy-dispersive spectroscopic results demonstrated that the polyanion of PSS^- is co-deposited into the PPy matrix and couldn't bestripped fiom the film extensively by dedoping.The doping level together with dipolaron content of the PPy-PSSAcomposite film increases during electrochemical polymerization process.SEM images revealed that the composite film hassmooth and compact morphology and AFM pictures suggested that PPy chains are possibly grown perpendicular to theelectrode surface.TGA tests indicated that the composite films has much better thermal stability than that of pure PPy.Furthermore,electrochemical studies showed that the relaxation process at certain holding potential has great effect on theshape of the cyclic voltammetric curves of PPy-PSSA composite film.The composite film exhibits cation and anionexchange during the redox process after undergoing the relaxation step.It is more difficult for divalent anion to enter thepolymer matrix than a univalent ion,and a large cation such as(CH_3CH_2CH_2CH_2)_4N^+ cannot be involved in the ionexchange process.

Influence of a Mineral Filler on the Fire Behaviour and Mechanical Properties of a Wood Waste Composite Material Stabilized with Expanded Polystyrene

The use of vegetable fibers composites in structures sometimes presents significant fires risks because of their high flammability. This work aims to study the impact of the addition of mineral filler (clay) on the fire behaviour of wood-polystyrene composites and their mechanical properties. Thus, composites containing 25% of expanded polystyrene binder have been produced. On this base material, proportions of clay ranging from 0% to 15% were gradually added. These samples were elaborated by compaction and for some them, submitted to thermoforming after drying. Both kinds of sample were subjected to flame persistence test;flexural strength and compressive strength test were also measured. The results show that composites without mineral filler ignite continuously until the total consumption and when the mineral filler content increases the combustion time decreases. The addition of the mineral filler allows these composites to pass from class M3 of moderately flammable combustible materials to class M2 of hardly flammable materials, according to the M classification of construction and furnishing materials. The measurement of the mechanical properties shows that the strengths increase when the filler content goes from 0% to 10% and then decrease. This leads to set the optimum content of mineral filler around 10%.

Development of a Composite Material Based on Wood Waste Stabilized with Recycled Expanded Polystyrene

Environmental pollution is a whole world concern. One of the causes of that pollution is the proliferation of plastic waste. Among these wastes there is expanded polystyrene (EPS), mainly from packaging. This study aims to valorize EPS waste by developing a composite material from EPS waste and wood waste. For this purpose, a resin made of EPS has been elaborated by dissolving EPS in acetone. That resin was used as a binder in volume proportions of 15%, 20%, 25% and 30% to stabilize the samples. Some of them were thermoformed. The method of elaboration was based on a device consisting of an extruder for mixing the constituents, and a manual press for shaping and compacting the samples. Analyses show that the drying time depends on the composition of the mixture. Increasing the resin content leads to reduce water absorption and porosity of the samples;it also contributes to homogenize the internal structure of the samples. However, for the same resin contents, the thermoformed samples are less porous;they have more homogeneous internal structure;and absorb less water than non-thermoformed samples.

Preparation and Properties of TiO_2/Montmorillonite Nano-Composite with Different TiO_2

The hydrated-titanium-oxide/montmorillonite composite samples were prepared using a hydrolysation- intercalation composite method by controlling the amount of TiOSO4·2H2O. The TiO2/montmorillonite composite samples were got after calculated at 700℃ and 1100 ℃. The results show that: when the value of Ti/montmorillonite is 12.5 mmol/g, the c axis of hydrated-titanium-oxide/ montmorillonite composite sample began to disorder, moreover, the crystal size of anatase is just 13.4nm in the TiO2/montmorillonite composite sample calculated at 700 ℃, and after calculated at 1100 ℃, the crystal size of anatase is 55.8 nm, and the relative content of anatase reaches the highest (55.7%). Compared with pure TiO2 nano-particle sample, TiO2/montmorillonite composite sample has a higher phase transition temperature from anatase phase to rutile phase and smaller crystal size of TiO2. Montmorillonite structure layer has a significant blocking effect on TiO2 phase transformation and grain growth, and the blocking effect reaches saturation when the value of Ti/montmorillonite is 12.5 mmol/g.

Wettability Control between Oleophobic/Superhydrophilic and Superoleophilic/Superhydrophobic Characteristics on the Modified Surface Treated with Fluoroalkyl End-Capped Oligomers/Micro-Sized Polystyrene Particle Composites

Fluoroalkyl end-capped vinyltrimethoxysilane-N,N-dimethylacrylamide cooligomer [RF-(CH2-CHSi(OMe)3)x-(CH2-CHC(=O)NMe2)y-RF;RF = CF(CF3)OC3F7: RF-(VM)x-(DMAA)y-RF] was synthesized by reaction of fluoroalkanoyl peroxide [RF-C(=O)O-O(O=)C-RF] with vinyltrimethoxysilane (VM) and N,N-dimethylacrylamide (DMAA). The modified glass surface treated with the cooligomeric nanoparticles [RF-(VM-SiO3/2)x-(DMAA)y-RF] prepared under the sol-gel reaction of the cooligomer under alkaline conditions was found to exhibit an oleophobic/superhydrophilic property, although the corresponding fluorinated homooligomeric nanoparticles [RF-(VM-SiO3/2)n-RF] afforded an oleophobic/hydrophobic property on the modified surface under similar conditions. RF-(VM-SiO3/2)n-RF/RF-(VM-SiO3/2)x-(DMAA)y-RF/PSt (micro-sized polystyrene particles) composites, which were prepared by the sol-gel reactions of the corresponding homooligomer and cooligomer in the presence of PSt particle under alkaline conditions, provided an oleophobic/superhydrophilic property on the modified surface. However, it was demonstrated that the surface wettability on the modified surface treated with the RF-(VM-SiO3/2)n-RF/RF-(VM-SiO3/2)x-(DMAA)y-RF/PSt composites changes dramatically from oleophobic/superhydrophilic to superoleophilic/superhydrophilic and superoleophilic/superhydrophobic characteristics, increasing with greater feed ratios (mg/mg) of the RF-(VM)n-RF homooligomer in homooligomer/cooligomer from 0 to 100 in the preparation of the composites. Such controlled surfac

STUDY OF COMPOSITE BY MELTING INTERCALATION OF POLYACRYLAMIDE IN MONTMORILLONITE

The synthesis of polyacrylamide (PAM)-montmorillinote composite by direct melting intercalation of polymer powders is studied using XRD, IR and DSC. The results show that melt PAM can intercalate into montmorillonite layer. The layered distance(d//0//0//1) of montmorillonite increases, and the melt absorption peak of PAM in layer has eliminated. (Author abstract) 8 Refs.