Preparation and properties of polymer-encapsulated phthalocyanine blue pigment via emulsion polymerization

Polymer-encapsulated phthalocyanine blue pigment dispersion was prepared with a polymerizable dispersant by emulsion polymerization method, and the effect of preparation conditions on the particle size of dispersion was investigated. Dynamic light scattering measurement demonstrated that allyloxy nonyl-phenoxypropanolpolyoxyethyleneetherammonium sulfonate (ANPS) was suitable for phthalocyanine blue pigment modification. The polymer-encapsulated phthalocyanine blue pigment dispersion with the small particles was obtained when the mass ratio of ANPS to phthalocyanine blue pigment, styrene (St) to phthalocyanine blue pigment, and ammonium persulfate (APS) to St was about 0.2, 0.2, and 0.01, respectively. Transmission electron microscopy (TEM), Fourier transforms infrared spectra (FTIR) and thermogravimetric analyses (TGA) provided supporting evidences for the encapsulation of phthalocyanine blue pigment with the formed copolymer. The polymer-encapsulated phthalocyanine blue pigment dispersion showed excellent stabilities to freeze–thaw treatment and centrifugal force.     

Oxidative polymerization of 3,4-ethylenedioxythiophene using transition-metal tetrasulfonated phthalocyanine

A method for the synthesis of water-soluble polyethylenedioxythiophene (PEDOT) by using transition-metal tetrasulfonated phthalocyanine (TSPc) and hydrogen peroxide as effective catalysts in the presence of sulfonated polystyrene (SPS) is reported. The reactions were carried out with different catalysts, such as iron, cobalt and manganese phthalocyanine. Metallophthalocyanines have shown good activities for polymerization, although they degraded easily under oxidizing conditions. In order to determine the role of pH during the polymerization, the reaction was carried out under different pH conditions 2, 2.5 and 3 and the best results were obtained at pH 2. The conductivity of our product was obtained and compared with similar commercial material. PEDOT was characterized by UV–vis and FT-IR spectroscopies and also cyclic voltammetry. Cyclic voltammetry (CV) demonstrated that the synthesized polymer has convenient electroactivity.     

Synthesis and characterization of ethylene-xylene-based polysulfide block-copolymers using the interfacial polymerization method

Copolymers of linear and aromatic polysulfide blocks are synthesized using interfacial polymerization of dichloro-xylene-based aromatic and ethylene-dichloride-based non-aromatic organic monomers. Synthesized copolymers consist of poly(ethylene sulfide) as well as ploy (xylene sulfide) blocks. Fascinating properties of linear and aromatic polysulfide species are gathered in the structure of synthesized polysulfide copolymers. Ethylene dichloride and α,α′-dichloro-p-xylene are used as the non-aromatic and aromatic organic monomers, respectively. To investigate the influences of sulfur contents in the backbone of the polymer on the thermal stability of synthesized copolymers, poly(ethylene-xylene disulfide) (PEXDS), poly(ethylene-xylene trisulfide) (PEXTRS) and poly(ethylene-xylene tetrasulfide) (PEXTS) copolymers are synthesized using, respectively, sodium disulfide, sodium trisulfide and sodium tetrasulfide, as aqueous monomers. Compared to both linear and nonlinear homopolymers, synthesized copolymers exhibit improved thermal stability. Moreover, the thermal degradation temperatures of synthesized copolymers improve by decreasing the number of sulfur atoms in the backbone of copolymers. These results reveal that thermal degradation of polysulfide copolymers can be tailored by controlling the polysulfide chain’s sulfur contents. Structural characteristics of synthesized polysulfide copolymers are also investigated using Fourier transform infrared spectroscopy, proton nuclear magnetic resonance spectroscopy and X-ray diffraction analysis.     

界面聚合技术制备分离膜的研究进展

界面聚合技术具有许多优良性能,如反应条件温和、可控性强、可以实现自封闭和自终止等,被广泛应用于分离膜制备中。本文阐述了界面聚合技术的原理,详细介绍了界面聚合在膜分离中的应用情况,包括纳滤膜、反渗透膜和气体分离膜,并综述了界面聚合技术在微胶囊、导电聚合物、纤维材料等方面的应用现状。最后,对界面聚合技术制备分离膜的研究前景进行了展望。     

Characterization of synthesized poly(aryldisulfide) through interfacial polymerization using phase-transfer catalyst

A new polysulfide polymer was synthesized from 1,4-bis(chloromethyl)-benzene and sodium disulfide by an interfacial polycondensation technique in the presence of tetrabutyl ammonium bromide, methyltributyl ammonium chloride and benzyl triethyl ammonium chloride as phase-transfer catalysts (PTC). The effect of PTC on the kinetics of polymerization was investigated. Structures of this aromatic polysulfide were confirmed through elemental analyses, attenuated total reflectance Fourier transform infrared spectroscopy, Raman spectroscopy, an X-ray diffraction technique, and a nuclear magnetic resonance spectroscopy method. The thermal behavior of this polymer was also characterized by differential scanning calorimetry and thermogravimetric analysis. The solubility of prepared polymer was critically dependent on the identity of the solvent.     

Optimization of microencapsulation of silane coupling agent by spray drying using response surface methodology

A microcapsule containing a silane coupling agent was prepared by spray drying. The optimal encapsulating condition was determined by employing a response surface methodology with a central composite design. The effect of emulsion’s solid content and oil concentration, inlet air temperature, and atomizer speed on properties of microcapsule were investigated. The resulting microcapsule containing silane coupling agent and possessing an unbroken surface and a good shape under optimized conditions exhibited an encapsulation efficiency of 82.7%, average size of 21.3?µm, and moisture content of 0.93%. The experimental results agree well with the model prediction, with a relative error below 5.0%.     

Examples of interference and the color pigment mixtures green with red and red with green

In industrial paint formulations, interference pigments are usually mixed with color pigments. Transparent interference pigments mix together according to the laws of additive mixing and color pigments to the laws of subtractive mixing. The behavior of both types differs depending on whether similar colors such as pearl green and green or contrasting colors such as pearl green and red are mixed. In this article examples of these differences for color measurement are discussed, along with showing the resulting charts. © 2001 Wiley Periodicals, Inc. Col Res Appl, 27, 276–281, 2002; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/col.10063     

Separation performance of thin-film composite nanofiltration membrane through interfacial polymerization using different amine monomers

Four kinds of thin-film composite (TFC) membranes were prepared via interfacial polymerization using diethylenetriamine (DETA), triethylenetetramine (TETA), tetraethylenepentamine (TEPA) and piperazidine (PIP) as water-soluble monomer, and trimesoyl chloride (TMC) as organic-soluble monomer. The surface chemical features of the resultant membranes were confirmed by contact angle measurement and Fourier transform infrared spectroscopy (FTIR). The membrane morphology and surface charges were investigated through Scanning electronic microscopy (SEM) and Zeta potential, respectively. Salt rejection was used to evaluate the separation performance of the four kinds of TFC membranes. The results showed that all the four kinds of TFC membranes exhibited typical negatively charged nanofiltration membrane characteristics. The salt rejections followed the sequence: Na₂SO₄ > MgSO₄ > MgCl₂ and the rejection of Na₂SO₄ was all over 80%. It was also found that the solubility of water-soluble monomer in organic solvent played an important role in manipulating the membrane structure, charge properties and thus the separation performance.     

硅铬绿色料煅烧温度及保温时间的研究

采用固相法合成硅铬绿色料并对色料进行了XRD测试,讨论了煅烧温度和保温时间对色料呈色的影响,确定了比较适合的煅烧温度和保温时间。     

The effects of Al and Ba on the colour performance of chromic oxide green pigment

On the basis of the novel hydrogen reduction of chromite ore, an activated sintering method was devised to prepare chromic oxide green pigment. Using XRD, SEM, EDX, ICP-AES, UV and reflectance colorimetry it was found that the colour performance of the synthesized pigment was markedly improved by adding Al and Ba, which resulted in the formation of an Al₂O₃–Cr₂O₃ solid solution and a secondary BaCr₂O₄ phase, respectively, within the pigment. The colour performance of the chromic oxide green pigment doped with 0.1% Al and 0.55% Ba conformed to commercial pigment standards.     

界面聚合在渗透汽化膜分离领域的应用进展

蒸馏、萃取等传统分离方法能耗高,污染环境,而渗透汽化由于低能耗、高效、环保等优势,为共沸物、近沸点混合物的分离提供了新的思路,但渗透汽化膜制备过程中面临的最大问题是获得性能优异且稳定的膜材料。在众多制备方法中,界面聚合法具有反应活性高、常温下生成膜层稳定、制备活性层致密等特点而备受关注。通过对界面聚合过程的调控,可以优化活性层,从而制备出兼具高通量和高选择性的渗透汽化膜。本文综述了界面聚合的原理、在渗透汽化膜制备方面的优势和近年来国内外的研究进展,详细阐述了复合膜制备过程中底膜的选择与改性、界面聚合条件的调控对渗透汽化膜结构和分离性能的影响机制,并对界面聚合制备渗透汽化膜所面临的问题及前景进行了总结与展望。     

Unraveling the film-formation kinetics of interfacial polymerization via low coherence interferometry

Interfacial polymerization (IP) is one of the most important methods for fabricating thin film composite (TFC) membranes. Understanding the film-formation mechanisms is of great value for developing membranes with enhanced performance. This work proposed a novel method to in situ characterize the film-formation kinetics via low coherence interferometry (LCI). The polyamide film formed at the liquid–substrate interface was scanned in real time; the polymerization induced significant variations in the optical properties around the reaction zone. After mitigating the effects of the perturbed interface, the surface-averaged intensity profiles provide a solid basis for analyzing the film-formation kinetics at various depths. In particular, the effects of the monomer concentrations were investigated to reveal the asymmetric growth and development of irregular substructures. All the characterization results confirm that the LCI-based characterization is a powerful tool for studying the structural evolution of the IP layer and thereby providing deeper insights for optimizing TFC membranes.     

The behavior of interfacial polycondensation on synthesizing of poly(amic-ester)s: homogeneity of the interfacial films

Summary The behavior in interfacial polycondensation of 4,4-methylenedianiline (MDA) or 4,4-oxydianiline (ODA) in water with dimethoxycarbonylterephthaloyl chloride (DCMTC) in dichloromethane with benzyltriethylammonium chloride (BTEAC) as the catalyst was examined with a Raman imaging microscope, and scanning electron microscope.The surfaces of the polymers adjacent to the water phase had higher average molecular weight than the surfaces of the polymers adjacent to the organic phase. Moreover, the morphology of the films also changed from dense to porous along the thickness direction of the films. To obtain an interfacial film more homogeneous in morphology and molecular weight, the reaction time of interfacial condensation should not exceed 5 minutes in this system. The interfacial films were anisotropic. The chain axis of the poly(amic-ester)s mainly oriented perpendicularly to the interface in the direction of membrane growth.     

The microencapsulation of terbinafine via in situ polymerization of melamine‐formaldehyde and their application to cotton fabric

In this study an antifungal pharmaceutical agent, terbinafine, was microencapsulated by using in situ polymerization. The polymerization was carried out at four mole ratio level and preparations were applied to the 100% cotton fabric. X‐ray diffractometry, DSC, FTIR, BET, contact angle measurements, particle size distribution and imaging techniques were performed. Best results were obtained in the case of 8 : 1 mole ratio. Strength of microcapsule applied fabrics to washing and fungus were also determined. After 25 washing cycle, microcapsules were still in the fabric and had antifungal properties against A. niger. Antifungal strength against T. rubrum was observed up to 15 washing cycles. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Preparation and electrochemical performances of porous polypyrrole film by interfacial polymerization

In this study, porous polypyrrole (PPy) film was synthesized by facile interfacial polymerization using ionic liquid as oxidant. The morphology of PPys changed from dense microspherical/nanospherical agglomerated structure to porous structure with the increasing concentration of the oxidant. The magnetic ionic liquid, 1‐butyl‐3‐methylimidazolium tetrachloroferrate (Bmim[FeCl₄]), played a major role of oxidant when the concentration was lower than 0.075M. As the concentration increased to 0.075M, the π–π interactions between pyrrole cations and iminazole ring of Bmim[FeCl₄], as evidenced by Fourier transform infrared spectrometer results, may affect the packing of PPy chains and subsequently cause the formation of porous structure of PPys. Electrochemical performances showed that PPy with porous structure displayed the highest specific capacitance of 170 F/g at a current density of 2 A/g in 1M H₂SO₄ solution and a good capacitive behavior, which has potential application as supercapacitor materials. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Reducing active layer thickness of polyamide composite membranes using a covalent organic framework interlayer in interfacial polymerization

Polyamide(PA)-based thin-film composite membranes exhibit enormous potential in water purification, owing to their facile fabrication, decent performance and desirable stability. However, the thick PA active layer with high transport resistance from the conventional interfacial polymerization hampers their applications. The controllable fabrication of a thin PA active layer is essential for high separation efficiency but still challenging. Herein,a covalent organic framework TpPa-1 interlayer was firstly deposited on a polyethersulfone(PES) substrate to reduce the thickness of PA active layer in interfacial polymerization. The abundant pores of TpPa-1 increase the local concentration of amine monomers by adsorbing piperazine molecules, while hydrogen bonds between hydrophilic groups of TpPa-1 and piperazine molecules slow down their diffusion rate. Arising from those synergetic effects, the PA active layer is effectively reduced from 200 nm to 120 nm. By optimizing TpPa-1 interlayer and PA active layer, the water flux of resultant membranes can reach 171.35 L·m~(-2)·h~(-1)·MPa~(-1), which increased by 125.4% compared with PA/PES membranes, while the rejection rates of sodium sulfate and dyes solution remained more than 90% and 99%, respectively. Our strategy may stimulate rational design of ultrathin PA-based nanofiltration membranes with high performances.     

Enhanced desalination performance and arsenate removal using semi-aromatic polyamide-based pervaporation membranes by modifying with amino-acids via interfacial polymerization

In this study, the semi-aromatic polyamide membranes were synthesized by the interfacial polymerization between piperazine (PIP) monomers in the water phase and Benzene-1,3,5-tricarbonyl chloride in the organic phase. To further modify the semi-aromatic pervaporation membrane, the two amino acids, glycine, and l -lysine, were mixed with PIP monomers for interfacial polymerization. The morphology and physicochemical properties of the synthesized membranes were analyzed using Fourier transform infrared (FTIR), field emission scanning electron microscope (FE-SEM), atomic force microscope (AFM), and contact angle measurements. The results show that the semi-aromatic polyamide membranes modified by the two amino acids possess a higher hydrophilic surface and lower thickness compared to the unmodified membrane. Additionally, the permeation flux of the semi-aromatic polyamide membranes was improved by 18.6% and 38.5% as modified with glycine and l -lysine, respectively, at the operating temperature of 70°C when the rejection of both NaCl and arsenic are higher than 99.8%. Furthermore, the operating temperature significantly influenced the permeation flux, while the salt rejections were insignificantly affected. The permeation flux increases by 3.2- and 4.0-folds for glycine and lysine-modified membranes, respectively, when elevating the feed temperature from 40°C to 70°C. The highest permeation flux of 29.5 kg m⁻² h⁻¹ with a 5 wt% NaCl rejection of 99.8% was obtained at 70°C by using 0.3 wt% l -lysine modified polyamide (PA) membrane. For elimination of 1.5 mg L⁻¹ As solution at the feed temperature of 70°C, such l -lysine modified PA membrane exhibited the permeation flux of 30.5 kg m⁻² h⁻¹ and As rejection of 99.6%, respectively. This work provides a cost-saving, facile, and eco-friendly preparation method for effectively improving the permeation flux while not sacrificing the high rejection of salts of the modified membranes.     

药物微胶囊技术及其应用

详细介绍了药物微胶囊的组成、制备技术，并讨论了其应用现状与发展趋势。     

Design and regulation of the surface and interfacial behavior of protein molecules

Surface and interfacial behavior of protein molecules are crucial for the protein function involved in many biochemical processes and biomedical products such as enzyme design, bio-separation, drug design and delivery. This article is devoted to an overview of design and regulation of the surface and interfacial behavior of protein molecules. The improvement of enzyme surface such as the directed evolution and the rational design of enzymes is introduced at first, followed by the rational design of protein interface for the protein assembly. Thereafter, the design of micro-environment and ligands are described as two examples for the design guided by protein surface. Then the design of protein surface and interface with the help of artificial intelligence will be discussed.