Deformation behavior of high performance fiber reinforced cementitious composite prepared with asphalt emulsion

A novel engineered cementitious composite(ECC) was prepared with the complex binder of Portland cement and asphalt emulsion.By adjusting the amount of asphalt emulsion,different mixture proportions were adopted in experiments,including four-point bending test,compressive test,and scanning electric microscopy(SEM).The SEM observation was conducted to evaluate the contribution of polyvinyl alcohol(PVA) fiber and asphalt emulsion to the composite toughening mechanism.The tests results show that the most remarkable deflection-hardening behavior and saturated multiple cracking are achieved when the content of asphalt emulsion is 10%.However,excessive content of asphalt emulsion causes severe damages on the deformation behavior as well as loss in compressive strength of the mixture.SEM observation indicates that the influence of asphalt emulsion on the fiber/matrix interfacial property changes the dominant fiber failure type from rupture into pull-out mode,and thus causes beneficial effects for strain-hardening behavior.

Properties and Microstructure of Polymer Emulsions Modifi ed Fibers Reinforced Cementitious Composites

The synthesis and characterization of a new class of cementitious composites filled with polymer emulsions were investigated, and their superior mechanical strength and durability properties compared to composites devoid of fi llers were reported. Polymer emulsions were utilized to mechanically reinforce the composite and bridge the cement, fly ash, aggregate and fibers. The results reveal that the epoxy emulsion and poly（ethylene-co-vinyl acetate） emulsion markedly enhance the mechanical and durability properties of cemetitious composites. The fi bers can be pulled out in the form of slip-hardening and the abrasion phenomenon can be observed clearly on the surface of the fibers. The hydration extent of cement is higher than that of the pristine composites. The polymer modified cementitious composites designed on micromechanics, have fl exibility and plasticity which could be applied for a novel form of multifunctional materials with a range of pipeline coatings applications.

Application and Properties of Organic Emulsion Coated Phosphogypsum in Aluminous Rock Based Mineral Polymer Composite

A polarizing microscope,X-ray diffraction(XRD),fourier transform infrared spectrometer(FTIR),scanning electron microscope and energy dispersive spectrometer(SEM-EDS),X-ray photoelectron spectroscopy(XPS),and micro computed tomography(Micro CT)were used to investigate the relation between the structure and properties of the composite.Meanwhile,the physical properties,mechanical properties and strength mechanism were researched.The experimental results show that the structure and morphology of coated phosphogypsum remain intact in the composite,which shows good compatibility and forms a clear interface layer of transition zone between the coated phosphogypsum and the matrix,conforming to the structure of particle reinforced inorganic composites.The emulsion coated phosphogypsum has a certain strengthening effect on the aluminous rock mineral polymer composite.The compressive strength of the composite can reach 16.5 MPa when the amount of coated phosphogypsum is 40%,and the apparent density is 1.75 g·cm^(-3),which is significantly lower than that of common concrete;the thermal stability of the composite is also improved to a certain extent.Some certain chemical reactions occur in the process of forming the matrix of aluminous rock mineral polymer materials,with a structure of three-dimensional network.The research will provide a new way for the comprehensive utilization of phosphogypsum and low-grade aluminous rock.

Preparation of Composite Particles by Forming Pickering Emulsion Followed by Drying-In-Liquid and Effect of Stepwise Addition of Solid Powder on Structure of Composite Particles

It was tried to prepare composite particles made of polymer and two kinds of solid powders by forming Pickeringemulsion followed by the drying-in-liquid method and to investigate how the stepwise addition of solid powders affected the contained ratio and adhesion ratio of solid powders and the structure of composite particles. Limonene oil dissolving expanded polystyrene and ethylene glycol were adopted as the dispersed phase and the continuous phase, respectively. Magnetite and titanium dioxide were used as solid powders. Magnetite was added before or after formation of the (O/W) dispersion. Titanium dioxide was added at the various elapsed times from addition of magnetite. Titanium dioxide adhered only on the surface of composite particles irrespective of addition time. At the earlier addition of both solid powders, the surface-covering type composite particles were prepared. At the latter addition of titanium dioxide, a part of magnetite adhered on the surface and the remainder was dispersed into composite particle.

Synthesis and Characterization of Poly(St-co-BA) Latex with an Organic-Inorganic Hybrid Compound as Emulsifier

A poly (St-co-BA) latex was successfully synthesized by using an organic-inorganic hybrid compound (OIHC), an aliphatic carboxylate sodium/nano-silica composite, as the emulsifier, and investigated by particle size analyzer, transmission electron microscope (TEM), optical contact angle measurement (OCA) and dynamic mechanical analyzer (DMA). It was found that the protective agent, sodium polyacrylate (PA),could obviously improve the polymerization stability and the functional monomer, glycidyl methacrylate (GMA), could enhance the store stability of the latex. The particle size of poly(St-co-BA) latex decreased and then leveled off as OIHC content increased. TEM shows that the prepared polymers were actually organic-inorganic nanocomposites, and these films have better waterproof property than those prepared by traditional poly(St-co-BA) latex or organic silicone modified poly(St-co-BA) latex. The nanocomposite polymer has much higher glass transition temperature than organic silicone modified poly(St-co-BA) polymer containing the same organic silicone content.

3D direct writing and micro detonation of CL-20 based explosive ink containing O/W emulsion binder

The booming development of DIW technology present an unprecedented prospect in energetic materials field and has attracted great interest due to its relative simplicity and high flexibility of manufacturing.Herein,a novel CL-20 based explosive ink formulation have been developed successfully for MEMS initiation systems via DIW technology.We designed PVA/GAP into an oil-in-water(O/W)emulsion,in the way that the aqueous solution of PVA as water phase,the ethyl acetate solution of GAP as oil phase,the combination of Tween 80 and SDS as emulsifier,BPS as a curing agent of GAP.The ideal formulation with good shear-thinning rheology properties and clear gel point was prepared using only 10 wt%emulsion.The dual-cured network formed during the curing process made the printed sample have good mechanical properties.The printed samples had satisfactory molding effect without cracks or fractures,the crystal form of CL-20 not changed and the thermal stability have improved.Deposition of explosive inks via DIW in micro-scale grooves had excellent detonation performances,which critical detonation size was 1×0.045 mm,detonation velocity was 7129 m/s and when the corner reaching 150°can still detonated stably.This study may open new avenues for developing binder systems in explosive ink formulations.

Synthesis of nano-CaCO_3 composite particles and their application

Nano-calcium carbonate composite particles were synthesized by the soapless emulsion polymerization technique of double monomers. The composite particles formation mechanism was investigated. The effects of composite particles on the mechanical properties of nano-CaCO3-ABS （acrylonitrile-butadiene-styrene copolymer） composite material were studied. It was validated that the composite particles are made up of the nano-calcium carbonate cores and the shells of alternating copolymers of butyl acrylate （BA） and styrene （St）. The shells are chemically grafted and physically wrapped on the surface of nano-calcium carbonate particles. When the composite particles were filled in ABS matrix, the CaCO3 particles are homogeneously dispersed in the composite material as nanoscales. The impact strength of the composite material is obviously enhanced after filling appropriate amounts of composite particles. It can be concluded that the soapless emulsion polymerization of double monomers is an effective method for nano-CaCO3 surface treatment. 2008 University of Science and Technology Beijing. All rights reserved.

Water-Based Processing of Fiberboard of Acrylic Resin Composites Reinforced With Cellulose Wood Pulp and Cellulose Nanofibrils

Despite the great potential of cellulose wood pulp and cellulose nanofibrils as reinforcing filler in thermoplastics,its use is limited due to its tendency to form agglomerates and due to its high hydrophilic character.Here we describe fiberboard composites with high contents of wood pulp or cellulose nanofibrils,and a resin of poly(styrene-methyl-methacrylate-acrylic acid)used as water-based emulsion.Cellulose wood pulp and cellulose nanofibrils were used directly in the form of water suspensions.The method is based on the flocculation of the polymer emulsion followed by agglomeration of a mixture of the polymer emulsion and cellulose suspension,leading to the co-precipitation of the composite material,which can be easily separated from the water phase.Composites with acrylic polymer/cellulose fibers in the proportions of 75:25,50:50 and 25:75 wt%were prepared.Composites were characterized by scanning electron microscopy(SEM),Fourier transform infrared spectroscopy(FTIR),thermogravimetric analysis(TGA),dynamic mechanical analysis(DMA)and water absorption tests.SEM analysis revealed a very good dispersion of the fibers without evidence of agglomeration,which led to superior mechanical properties.These results showed the effectiveness of the methodology and the potential of cellulose wood pulp and CNF as reinforcement fillers in fiberboard composites and any other high fiber-content materials.

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.

THE EFFECT OF MONOMERS FEEDING METHODS ON EMULSION COPOLYMERIZATION OF VINYLIDENE CHLORIDE AND ACRYLATES

The emulsion copolymerization of vinylidene chloride (VDC) with methyl-methacrylate(MMA) and acrylonitrile (AN) was carried out by batch, seeded batch and semicontinuous pro-cesses,respectively. Significant differences were found in the physical and mechanical propertiesof the latexes and films, depending on the methods of monomer feeding. The results both intheory and experiments demonstrated that the copolymer composition and the length of the VDC sequences in the copolymer could be controlled by the modes of monomer feeding process.

Advances in controlled-release fertilizer encapsulated by organic-inorganic composite membranes

Heavy use of conventional fertilizers can lead to negative environmental concerns.Controlled-release fertilizers(CRFs)can effectively reduce the amounts of fertilizers used,improve the availability of fer-tilizers,and which is conducive to the protection of the ecological environment and sustainable devel-opment of agriculture.Therefore,it is imperative to develop and use CRFs as an alternative to traditional fertilizers.This review aims to present the classification,raw material composition,benefits,release process,release mode,and manufacturing methods of fertilizers coated with organic-inorganic com-posite membranes(OICMs)in order to provide an overall update and summarize CRFs encapsulated by OICMs and provide an insight for future trends in the field of fertilizers.It is expected that utilizing CRFs encapsulated by OICMs and their characteristics for agricultural applications can provide innovative ideas and suggestions for developing novel CRFs suitable for modern and sustainable agriculture.

Rheological properties of magnetorheological fluid prepared by gelatincarbonyl iron composite particles

Gelatincarbonyl iron composite particle was prepared by micro emulsion method. The analysis of scanning electron microscope(SEM) shows that the ultrafine particles are spheroids coated by gelatin, and the average sizes of particles are 310μm. The specific saturation magnetization σ_s is 130.9A·m2/kg, coercivity H_c is 0.823A/m, and residual magnetism r is 4.98Am2/kg for the composite particles. It is shown that the particles possess properties of soft magnetic. The yield stress of magnetorheological fluid(MRF) with composite particle reaches 70kPa at 0.5T magnetic induction. Magnetorheological effects are superior in lower magnetic field intensity and the subsidence stability of the MRF is excellent compared with pure carbonyl iron powder.

Aqueous-Phase Sorption Behaviors of Cs⁺, Co²⁺, Sr²⁺and Cd²⁺ions on some Composite Ion Exchangers

A two new hybrid “organic-inorganic” composite ion exchangers (SAM and FAM), was synthesized by the combination of inorganic ion exchanger tin (IV) silicate and tin (IV) antimonate respectively with organic polymer polyacrylamide (PAm). The sorption isotherms for Cs+, Co2+, Sr2+ and Cd2+ ions on composite ion exchanger were investigated in the range (0.0005 - 0.01M) at different reaction temperature (30℃, 45℃ and 60℃ ± 1℃). The sorption data were subjected to different sorption isotherms and the results verified that Langmuir isotherm is the best model to be applied, and the monolayer sorption capacity were calculated and was found to increase as the reaction temperature increases.

Preparation of Chitosan/Poly(L-Lactide) Porous Composite Scaffolds

This research investigates the formation of chitosan/poly （L-lactide） （CS/PLLA） porous composite scaffold using a novel emulsion freeze-drying technique. First, an oil in-water （O/W） emulsification system was used in the presence of surfactant Tween-80, in which CS solution was used as the water phase and PLLA solution was used as the oil phase. The emulsion was observed by inverted microscope （× 200）. The emulsion droplet was spherical and uniform in size. FT-IR analysis revealed that there were hydrogen bonding interactions between CS and PLLA components. The microstructure and physical properties of the scaffolds were also analyzed. The SEM results showed that composite scaffolds formed well interconnected pore structure and homogenous distribution of CS and PLLA. When the content of PLLA reached 50%, the porosity of CS/PLLA composite scaffolds were between 83 %-91% and density in the range of 0.047 to 0.11 g/era3. The porosity showed a slight decrease and the density increased with the increase of PLLA dose. The compressive strength increased from 0.32 to 0.43 MPa, while the compressive modulus increased from 1.99 to 3.91 MPa as the PLLA contents increased from 10% to 50%.

Preparation of polyacrylamide/silica composite capsules by inverse Pickering emulsion polymerization

Polyacrylamide/silica （PAM/SiO2） composite capsules were synthesized by inverse Pickering emulsion polymerization. Silica nanoparticles modified with methacryloxypropyltrimethoxysilane （MPS） were used as a stabilizer. Transmission electron microscopy （TEM）, scanning electron microscopy （SEM）. Fourier transform infrared （FTIR） spectroscopy, and thermal gravimetric analysis （TGA） were used to characterize the morphology and composition of the composite capsules. SEM and TEM images showed that capsules consisted of a particle shell and a polymer inner layer. The capsule size depends on the nanoparticle concentration in the continuous phase. The composite rigidity largely depends on the acrylamide concentration. FTIR and TGA results indicated the existence of polyacrylamide and SiO2 in the composite particles. Aqueous Hg（ll） removal testing by the PAM/SiO2 composite capsules indicated promising potential for removing heavy metal ions from wastewater.

Recent Advances and Progress for the Fabrication and Surface Modification of AIE-active Organic-inorganic Luminescent Composites

Organic dyes based hybrid organic-inorganic luminescent nanomaterials with high quantum efficiency, good physical or chemical stability, and favorable biocompatibility, have attracted growing attention recently because of their important applications in the areas of biomedical imaging, chemical sensors, and light-emitting diodes(LEDs). Nevertheless, conventional fluorescence molecules suffer from aggregation-caused quenching(ACQ) when they are doped into inorganic nanomaterials. Aggregation-induced emission(AIE) is an abnormal and intriguing fluorescent phenomenon that has aroused increasing interest for various applications especially in biomedical fields. Compared with conventional organic dyes, the AIE-active molecules will emit more intense fluorescence in their aggregates or solid states. It provides an elegant route to overcome the drawbacks of conventional organic molecules. Over the past few decades, the fabrication and surface modification of various organic-inorganic luminescent composites doped with AIE-active molecules have been reported. Therefore, it is highly desirable to summarize these advances. In this review, recent advances and progress in constructing various AIEgens-doped organic-inorganic hybrid nanocomposites and their subsequent surface modification were summarized. We hope this review could further promote the research of AIE-active functional materials.

Synthesis of submicron-sized composite particles with unique morphology by emulsifier-free seeded emulsion copolymerization

Polystyrene （PSt） microspheres with diameter of 375 nm to be used as the seeds for seeded emulsion polymerization were prepared via emulsion polymerization using potassium persulfate （KPS） as initiator in ethanol-water mixed solvents. Emulsifier-free seeded emulsion copolymerization of styrene （St） with acrylonitrile （AN） was carried out in the presence of poly（ethylene glycol） monomethoxymonomethacrylate （PEGm） macromonomer as reactive stabilizer and 2,2＇-azobisisobutyronitrile （AIBN） as initiator to obtain submicron-sized PEGm graft poly（styrene-coacrylonitrile） （PEGm-g-PSAN） composite particles with unique morphology. Scanning electron microscopy （SEM） indicated that St and AN together contributed to forming the unusual morphology. The concentration of St and AN, total monomer concentration, initiator type and the monomer adding method remarkably affected the morphology of the composite polymer particles.

醋酸纤维素水性高分子/SiO_(2)纳米复合皮革涂饰剂的制备

以A50为亲水剂,通过转换反应位点和反应官能团,调节分子链软硬段比例,引入纳米SiO_(2)提升乳液涂膜综合性能,制备WSCDA/SiO_(2)纳米复合乳液。结果表明,亲水剂A50用量为10.8%(质量分数),复合乳液及涂膜性能最优。最优条件下合成的复合乳液的平均粒径为109.5nm,粒径分布均匀,涂膜表面致密光滑,柔韧性、附着力、耐水性、耐黄变性、机械性能和热稳定性良好。WSCDA/SiO_(2)纳米复合乳液成膜时,在涂膜表面形成许多小“乳突”,产生荷叶效应,提高涂膜耐水、耐介质及耐黄变等性能。

咖啡酸-葡聚糖-肌原纤维蛋白酶解物乳液稳定性的研究

为了探究咖啡酸(Caffeic Acid,CA)、葡聚糖(Dextran,DEX)复合修饰联合胰蛋白酶不完全酶解对于肌原纤维蛋白(Myofibrillar Protein,MP)乳化特性的提升效果,以CA-DEX-MP复合酶解物为乳液稳定剂制备乳液,优化稳定剂的添加剂量,并以原始MP和MP酶解物稳定的乳液为对照,评估乳液在不同环境刺激下的稳定性。结果表明,CA-DEX-MP酶解物添加量为3 wt.%时乳液具有较低的颗粒粒径(390.26 nm)、电位(-23.6 mV)和较高的界面蛋白吸附量(11.22 mg/mL),且均匀分布;流变性研究表明,该乳液体系显示出显著低于原始MP乳液的表观粘度,可有效避免乳液的相分离现象。3 wt.%CA-DEX-MP复合酶解物乳液在不同温度、酸碱、盐离子强度和28 d贮藏期下均表现出较优的稳定性,可实现乳液的稳定。最终结果表明,乳液稳定剂为3 wt.%CA-DEX-MP复合酶解物时,乳液拥有最高的稳定性。该研究可为肌原纤维蛋白在新型食品乳液稳定剂开发中的应用提供理论支撑和方法学指引。

复合二氧化钛的制备及在装饰原纸中的应用

采用乳液法制备二氧化钛(TiO_(2))/滑石粉复合填料,并将其应用在装饰原纸中。结合油包水型(W/O)乳液的拟三元相图,寻找合适的乳液体系,并利用响应曲面试验对TiO_(2)/滑石粉复合填料的制备工艺进行优化。结果表明,环己烷比正庚烷更适合作为油相,正丁醇的用量影响着乳液的稳定性;复合填料制备的最优工艺为:Tween80/正丁醇的质量比为1∶1,乳化剂/环己烷的质量比为4∶6,水/环己烷的质量比为1∶3,滑石粉/钛酸四丁酯(TBT)质量比为1∶4,在此条件下制备的复合填料加填在装饰原纸中,得到的不透明度为97.0%,白度为84.0%ISO。通过扫描电子显微镜(SEM)、X射线能谱仪(EDS)及X射线衍射(XRD)分析方法对复合填料进行表征,结果显示,滑石粉表面包覆了一层致密均匀的TiO_(2),其晶型结构为锐钛矿型。