Synergistic effect of modified anhydrous magnesium carbonate and hexaphenoxycyclotriphosphazene on flame retardancy of ethylene-vinyl acetate copolymer.

Ethylene-vinyl acetate copolymer (EVA) is widely used in various applications; however, its flammability limits its application in wire and cable industries. In this study, 3-methacryloxypropyltrimethoxysilane (KH570) was successfully grafted onto the surface of anhydrous magnesium carbonate (AMC) by alkali activation treatment. The KH570 modified AMC (AMC@KH570) was then introduced into the EVA matrix along with hexaphenoxycyclotriphosphazene (HPCTP) to assess their effects on the flame retardancy and mechanical properties of EVA composites. The results illustrate a significant synergistic effect in enhancing the flame retardancy of EVA composites by using AMC@KH570 and HPCTP, and the limiting oxygen index (LOI) and vertical burning test (UL-94) of EVA filled with 5 wt% HPCTP and 45 wt% AMC@KH570 (mAMC/H-45-5) reached 27.6% and V-0, respectively. The flame retardant mechanism was investigated by thermogravimetric/infrared (TG-IR) spectroscopy and residual carbon composition analysis. The results show that the thermal decomposition of AMC@KH570 and HPCTP consists of gas dilution, free radical quenching, and catalytic carbonization. Furthermore, KH570 works as a bridge to improve the compatibility of AMC and EVA matrix, which offsets the mechanical loss of EVA to some extent. The present research provides a new path to modify AMC and fabricate EVA composites with excellent flame retardant properties.

Preparation and characterization of polydopamine and n-butyl methacrylate copolymer coatings on titanium-nickel alloy stents.

Cardiovascular diseases pose a significant global health threat, and stents play a crucial role in managing these diseases. However, challenges exist with respect to the poor adhesion of stent coatings. Cardiac stents are often composed of titanium-nickel (TiNi) alloys as the metallic component and poly(n-butyl methacrylate) (PBMA) as the coating. The poor adhesion of PBMA to TiNi alloy surface may cause detachment and subsequent thrombosis post-implantation. This study utilizes Reversible Addition-Fragmentation Chain Transfer (RAFT) polymerization to synthesize a novel block copolymer, PBMA-b-PVP, composed of PBMA and poly(N-vinylpyrrolidone) (PVP). TiNi alloy surfaces are functionalized with polydopamine (PDA) to enhance polymer coating adhesion. PBMA-b-PVP exhibits a remarkable improvement in adhesion from class 5 to class 0 and high coating stability after a 15 days immersion in a phosphate buffer solution. The corrosion current density is reduced by 44% with the incorporation of PDA into PBMA-b-PVP coatings, suggesting high corrosion resistance. PDA-functionalized coatings promote cell viability without cytotoxicity, suggesting high biocompatibility. This study provides a robust strategy for preparing stent coatings with high adhesion, corrosion resistance, and biocompatibility.

Hierarchical Porous Carbon Based on Waste Quinoa Straw for High-Performance Supercapacitors.

This work presents a novel porous activated carbon electrode based on quinoa straw (QSC), which is derived from the Qinghai-Tibet Plateau. The QSC is prepared through simple precarbonization and potassium carbonate (K2CO3) activation processes and is intended for use in supercapacitors. The QSC-3 exhibits a high specific capacitance of 469.5 F g-1 at a current density of 0.5 A g-1, as well as a high specific surface area of 1802 m2 g-1. Additionally, symmetrical supercapacitors assembled using QSC-3 samples demonstrate a superior energy power density. In a 3 M KOH electrolyte, the energy density can reach 15.0 Wh kg-1 at a power density of 689.7 W kg-1. In a 1 M Na2SO4 electrolyte, the power density reaches 999.00 W kg-1, and the energy density is 39.68 Wh kg-1. Furthermore, the device shows excellent cycle life in both 3 M KOH and 1 M Na2SO4 electrolytes, with capacitance retentions of 97.55% and 96.20% after 10 000 cycles, respectively. This study provides an excellent example of utilizing waste quinoa straw to achieve low-cost, high-performance supercapacitor electrode material for sustainable electrochemical energy storage systems.

Controlled delivery of 5-fluorouracil from monodisperse chitosan microspheres prepared by emulsion crosslinking.

This work aims to determine the optimal conditions for emulsion cross-linking of chitosan (CHS) with various molecular weights using glutaraldehyde as a cross-linking agent to produce 5-fluorouracil-loaded CHS microspheres (5-FU/CHS). Their drug loading and encapsulation efficiencies are found to be in the range of 3.87-12.35% and 20.13-70.45%, respectively. The dynamic light scattering results show that 5-FU/CHS microspheres are micron-sized with a uniform size distribution, and the scanning electron microscopy results show that they are spherical. The results of thermogravimetric analysis, X-ray diffraction, and Fourier transform infrared spectroscopy demonstrate that 5-FU is successfully incorporated into the microspheres. The in vitro release tests show that 5-FU/CHS have a prolonged, pH-responsive release pattern of 5-FU, and the cumulative release rate under acidic condition is much larger than that under neutral conditions. The drug release kinetic analysis further demonstrates that the release of 5-FU can be well described by the Fickian diffusion model.

Facile preparation of carbon nitride by binary eutectic KNO3/KCl molten salt and its photocatalytic performance evaluation.

Graphitic carbon nitride (g-C3N4) has been widely investigated and applied in photocatalysis, but it always suffers from unsatisfactory photocatalytic activity performance. In this study, a facile molten salt-assisted heat-treated g-C3N4via binary eutectic KNO3/KCl was successfully developed. Based on this assumption, the heat treatment temperature has been successfully lowered to 350 °C to modulate and optimize the carbon nitride structure. The obtained target photocatalysts were characterized using various characterization methods (scanning electron microscope (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS), Fourier transform infrared spectroscopy (FT-IR), photoluminescence (PL) and transient photocurrents), confirming the practicability of the proposed strategy. The presence of doped K+ ions and the introduction of cyano groups into the main structure can strengthen the photo-induced electron-hole separation and migration ability, suppressing their recombination. Consequently, the much-enhanced photocatalytic activity of the obtained target catalyst was achieved and demonstrated through comprehensive tests such as photocatalytic degradation of organic dyes, photocatalytic degradation of pesticides, photocatalytic degradation of organic flotation reagent, and photocatalytic hydrogen production. Among these, g-CN-A-PN/PC-T350 exhibited the highest photocatalytic activity and the highest recycling usage stability compared with the pure sample. In addition, a possible mechanism for photocatalytic degradation of organic compounds and photocatalytic H2 evolution was obtained based on comprehensive experimental analysis. Our finding provides a promising way for g-C3N4 to manipulate the photocatalytic activity simply by introducing eutectic KNO3/KCl in the preparation process and provides a comprehensive understanding of the roles of molten salt.

Effect of Different Compatibilizers on the Mechanical, Flame Retardant, and Rheological Properties of Highly Filled Linear Low-Density Polyethylene/Magnesium Hydroxide Composites.

Maleic anhydride-modified homopolymerized polypropylene (PP-g-MAH) and maleic anhydride-modified polyolefin elastomer (POE-g-MAH) were used as bulking agents to improve the poor processing and mechanical properties of highly filled composites due to high filler content. In this study, a series of linear low-density polyethylene (LLDPE)/magnesium hydroxide (MH) composites were prepared by the melt blending method, and the effects of the compatibilizer on the mechanical properties, flame retardancy, and rheological behavior of the composites were investigated. The addition of the compatibilizer decreased the limiting oxygen index (LOI) values of the composites, but they were all greater than 30.00%, which belonged to the flame retardant grade. Mechanical property tests showed that the addition of the compatibilizer significantly increased the tensile and impact strengths of the LLDPE/60MH (MH addition of 60 wt%) composites. Specifically, the addition of 5 wt% POE-g-MAH increased 154.07% and 415.47% compared to the LLDPE/60MH composites, respectively. The rotational rheology test showed that the addition of the compatibilizer could effectively improve the processing flow properties of the composites. However, due to the hydrocarbon structure of the compatibilizer, its flame retardant properties were adversely affected. This study provides a strategy that can improve the processing and mechanical properties of highly filled composites.

Effect of Functionalized Polyethylene Wax on the Melt Processing and Properties of Highly Filled Magnesium Hydroxide/Linear Low-Density Polyethylene Composites.

The poor processing and rheological properties of highly filled composites caused by the high loading of fillers can be improved with the use of maleic anhydride grafted polyethylene wax (PEWM) as compatibilizer and lubricant. In this study, two PEWMs with different molecular weights were synthesized by melt grafting, and their compositions and grafting degrees were characterized by Fourier transform infrared (FTIR) spectroscopy and acid-base titration. Subsequently, magnesium hydroxide (MH)/linear low-density polyethylene (LLDPE) composites with 60 wt% of MH were prepared using polyethylene wax (PEW) and PEWM, respectively. The equilibrium torque and melt flow index tests indicate that the processability and fluidity of MH/MAPP/LLDPE composites are significantly improved with the addition of PEWM. The addition of PEWM with a lower molecular weight leads to a substantial reduction in viscosity. The mechanical properties are also increased. The limiting oxygen index (LOI) test and cone calorimeter test (CCT) show that both PEW and PEWM have adverse effects on flame retardancy. This study provides a strategy to simultaneously improve the processability and mechanical properties of highly filled composites.

Preparation and Characterization of a Novel Sulfonated Titanium Oxide Incorporated Chitosan Nanocomposite Membranes for Fuel Cell Application.

In this study, nano-TiO2 sulfonated with 1,3-propane sultone (STiO2) was incorporated into the chitosan (CS) matrix for the preparation of CS/STiO2 nanocomposite membranes for fuel cell applications. The grafting of sulfonic acid (-SO3H) groups was confirmed by Fourier transform infrared spectroscopy, thermogravimetric analysis and energy-dispersive X-ray spectroscopy. The physicochemical properties of these prepared membranes, such as water uptake, swelling ratio, thermal and mechanical stability, ion exchange capacity and proton conductivity, were determined. The proton conducting groups on the surface of nano-TiO2 can form continuous proton conducting pathways along the CS/STiO2 interface and thus improve the proton conductivity of CS/STiO2 nanocomposite membranes. The CS/STiO2 nanocomposite membrane with 5 wt% of sulfonated TiO2 showed a proton conductivity (0.035 S·cm-1) equal to that of commercial Nafion 117 membrane (0.033 S·cm-1). The thermal and mechanical stability of the nanocomposite membranes were improved because the interfacial interaction between the -SO3H group of TiO2 and the -NH2 group of CS can restrict the mobility of CS chains to enhance the thermal and mechanical stability of the nanocomposite membranes. These CS/STiO2 nanocomposite membranes have promising applications in proton exchange membrane fuel cells.

A dual polymer composite of poly(3-hexylthiophene) and poly(3,4-ethylenedioxythiophene) hybrid surface heterojunction with g-C3N4 for enhanced photocatalytic hydrogen evolution.

A surface heterojunction catalyst of g-C3N4-PEDOT/P3HT with P3HT and PEDOT as the polymer sensitizer and hole transport pathway is successfully prepared. The as constructed g-C3N4-PEDOT/P3HT composite exhibits a photocatalyst H2 evolution rate up to 427703.3 µmol h-1 g-1 which is 1059 times higher than that of g-C3N4, 118 times higher than that of g-C3N4-PEDOT with ascorbic acid as sacrificial reagents. What's more, the g-C3N4-PEDOT/P3HT can even show an obviously enhanced photocatalytic H2 evolution rate which is 6.1 times higher than that of pure g-C3N4 in pure water without any sacrificial reagent. Combining the experimental results and molecular dynamic (MD) simulation results, a possible mechanism can be drawn that the existed PEDOT possesses relatively higher hole mobility and can be used as a hole conductor between g-C3N4 and P3HT. Then, the photogenerated holes migration can be accelerated by PEDOT from the VB of g-C3N4 to the VB of P3HT. All those factors may benefit the synergy among g-C3N4, PEDOT and P3HT, which finally facilitates the rapid migration of photoinduced electron-hole pairs and eventually improves the photocatalytic H2 activity process of g-C3N4-PEDOT/P3HT with visible light. The present work may provide useful insights for designing a surface heterojunction composite photocatalyst with high photocatalytic activity for H2 production.

Effect of Modified Cardanol as Secondary Plasticizer on Thermal and Mechanical Properties of Soft Polyvinyl Chloride.

This study represents the first attempt to prepare a novel cardanol-based plasticizer. Modified cardanol (MC, i.e., phosphorylated cardanol) containing nitrogen and phosphoric acid groups was synthesized and then incorporated into polyvinyl chloride (PVC) as the secondary plasticizer for partial substitution of dioctyl phthalate (DOP). The molecular structure of MC was characterized by Fourier transform infrared spectroscopy, 1H nuclear magnetic resonance (NMR), and 31P NMR spectroscopy. The thermal degradation behavior, mechanical performance, and compatibility of MC were also investigated. The substitution of DOP with MC enables PVC blends to have higher thermal stability, tensile strength, and leaching resistance. The tensile strength is increased from 17.7 MPa for DOP/PVC blend (MC-0) to 25.7 MPa for MC/PVC blend (MC-4), and the elongation at break is increased from 256 to 432%, respectively. The microstructure of the tensile fractured surface was studied by scanning electron microscopy. The results show that the addition of MC allows PVC blends to have well-balanced properties of flexibility and strength and excellent migration resistance.

Preparation of Flame-Retardant Rigid Polyurethane Foams by Combining Modified Melamine-Formaldehyde Resin and Phosphorus Flame Retardants.

In this work, ethylene glycol-modified melamine-formaldehyde resin (EMF) was synthesized from ethylene glycol, paraformaldehyde, and melamine, and then rigid polyurethane foams (RPUFs) were prepared using EMF, polyols and polyisocyanate. The effects of ammonium polyphosphate (APP) and dimethyl methylphosphonate (DMMP) on the flame retardancy, mechanical properties, thermal stability, and morphology of the prepared RPUFs were studied. It is shown that the flame-retardant performance of EMF-filled RPUFs can be enhanced by the addition of APP and DMMP. Thus, APP and DMMP can synergistically improve the flame retardancy of RPUFs. APP has good smoke suppression, while DMMP can increase the total smoke production and CO/CO2 weight ratio during the combustion of RPUFs.

A nanofiltration membrane prepared by PDA-C3N4 for removal of divalent ions.

In this study, a positively charged nanofiltration (NF) membrane was prepared by interfacial polymerization for separation of divalent cations, whereby a nanomaterial (modified graphitic carbon nitride (g-C3N4) with poly(dopamine), PDA-C3N4) was incorporated into the active layer of the NF membrane. PDA-C3N4 sheets were synthesized from g-C3N4 sheets prepared by thermal oxidation of melamine, and the preparation conditions of NF membrane were also optimized. The results show that the roughness of PDA-C3N4 embedded NF membrane decreases, and the hydrophilicity and the permeation increase. The membrane also shows high rejection for divalent cations (Mg2+, Ca2+, Ba2+, Cu2+ and Zn2+) but low rejection (36.8%) for monovalent cation (Li+), as well as good fouling resistance performance. The fabricated membrane has the potential for treatment of industrial wastewater.

Effects of α-zirconium phosphate and zirconium organophosphonate on the thermal, mechanical and flame retardant properties of intumescent flame retardant high density polyethylene composites.

The combination of synergistic agents with intumescent flame retardants (IFRs) is an excellent strategy for the development of high-performance flame retardant composites. Zirconium-based compounds are multifunctional materials with applications in various fields. In this study, zirconium-based compounds were synthesized and then combined with an IFR composed of ammonium polyphosphate (APP) and tris (2-hydroxyethyl) isocyanurate (THEIC) to prepare flame retardant high density polyethylene (HDPE) composites. α-Zirconium phosphate (α-ZrP) and two organic-inorganic hybrids (zirconium organophosphonate), Zr-ATMP and Zr-PA, were prepared using amino tri (methylene phosphonic acid) (ATMP) and phytic acid (PA), respectively, and their thermal, mechanical and flame retardant properties were characterized by thermogravimetric analysis, tensile test, limiting oxygen index (LOI) measurement and cone calorimetry test. The results showed that the LOI value of HD/IFR/Zr-ATMP composite reached a maximum of 26.2% using 25 wt% of flame retardant containing 3 wt% of Zr-ATMP. Of the three zirconium-based compounds, Zr-ATMP and α-ZrP can reduce the peak heat release rate compared with the composite containing only IFR. However, zirconium-based compounds showed no significant improvement of tensile strength.

Multistage Polymerization Design for g-C3N4 Nanosheets with Enhanced Photocatalytic Activity by Modifying the Polymerization Process of Melamine.

Graphene-like g-C3N4 nanosheets (NSs) have been successfully synthesized with a modified polymerization process of melamine by cocondensation with volatile salts. Volatile ammonium salts such as urea-NH4Cl/(NH4)2SO4/(NH4)3PO4 were added with melamine to modulate the thermodynamic process during polymerization and optimize the structure formation in situ. The surface area, surface structure, and surface charge state of the obtained g-C3N4 NSs could be controlled by simply adjusting the mass ratio of the melamine/volatile ammonium salt. As a consequence, the g-C3N4 NSs exhibited much higher activity than bulk g-C3N4 for the photocatalytic degradation of target pollutants (rhodamine B, methylene blue, and methyl orange), and it also exhibited greater hydrogen evolution under visible light irradiation with an optimal melamine/volatile ammonium salt ratio. The as-prepared g-C3N4 NSs with melamine-urea-NH4Cl showed the highest visible light photocatalytic H2 production activity of 1853.8 µmol·h-1·g-1, which is 9.4 times higher than that of bulk g-C3N4 from melamine. The present study reveals that the synergistic effect of the enhanced surface area, surface structure, and surface charge state is the key for the enhancement of photocatalytic degradation and hydrogen evolution, which could be controlled by the proposed strategy. The result is a good explanation for the hypothesis that adding properly selected monomers can truly regulate the polymerization process of melamine, which is beneficial for obtaining g-C3N4 NSs without molecular self-assembly. Considering the inexpensive feedstocks used, a simple synthetic controlling method provides an opportunity for the rational design and synthesis, making it decidedly appealing for large-scale production of highly photocatalytic, visible-sensitizable, metal-free g-C3N4 photocatalysts.

In situ green oxidation synthesis of Ti3+ and N self-doped SrTiO x N y nanoparticles with enhanced photocatalytic activity under visible light.

A simple in situ green oxidation synthesis route was developed to prepare Ti3+ and N self-doped SrTiO x N y nanoparticles using TiN and H2O2 as precursors. X-ray diffraction (XRD), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) were used to characterize the crystallinity, structure and morphology. X-ray photoelectron spectroscopy (XPS) tests confirmed the presence of Ti3+ and N in the prepared SrTiO x N y nanoparticles. The resultant nanoparticles were shown to have strong absorption from 400 to 800 nm using UV-vis diffuse reflectance spectroscopy (UV-vis DRS). The formation mechanism of the Ti3+ and N self-doped SrTiO x N y nanoparticles was also discussed. Under visible light irradiation, the obtained Ti3+ and N self-doped samples showed higher photocatalytic activity for the degradation of the model wastewater, methylene blue (MB) solution. The most active sample T-130-Vac, obtained at 130 °C under vacuum, showed a 9.5-fold enhancement in the visible light decomposition of MB in comparison to the commercial catalyst nano-SrTiO3. The sample also showed a relatively high cycling stability for photocatalytic activity.

Preparation and fire behavior of rigid polyurethane foams synthesized from modified urea-melamine-formaldehyde resins.

In this study, a series of ethylene glycol modified urea-melamine-formaldehyde resins (EUMFs) were synthesized from urea, melamine, paraformaldehyde and ethylene glycol, and then incorporated into rigid polyurethane foams (RPUFs) as a reactive-type liquid flame retardant. The structure of EUMFs was characterized by Fourier transform infrared spectrometry; the morphology of the foams was characterized by scanning electron microscopy; and the thermal degradation and fire behavior of RPUFs were characterized by limiting oxygen index (LOI), cone calorimetry test and thermogravimetry analysis. The results show that the incorporation of EUMFs results in an increase in thermal stability, smoke suppression and LOI of RPUFs. As the melamine loading in EUMFs increases, the peak heat release rate and the total heat release of RPUFs decrease significantly, but the LOI increases slightly. Compared with the original foam, the cells of RPUFs become less regular with nonuniform diameters. In general, EUMFs show excellent flame retardancy and smoke suppression for RPUFs.

Multiple gold nanorods@hierarchically porous silica nanospheres for efficient multi-drug delivery and photothermal therapy.

Gold-based nanocomposites have attracted intensive attention due to their unique optical properties and great potential in biomedical applications. Herein, we report a simple route for the synthesis of multiple gold nanorods encapsulated, hierarchically porous silica nanospheres (MGNRs@HPSNs) based on the cooperative self-assembly of amphiphilic block copolymer polystyrene-b-poly (acrylic acid) (PS-b-PAA), cetyl trimethyl ammonium bromide (CTAB), gold nanorods and the organosilane of tetraethyl orthosilicate (TEOS) in an oil/water system. Multiple gold nanorods have been loaded successfully into the interior of the hierarchically porous silica nanospheres, which consist of large, interconnected pores of 13.2 nm throughout the whole sphere and small pores of 2.7 nm in the silica framework. Moreover, the loading amount (or number) of gold nanorods in the silica matrix can be tuned by simply changing the initial concentration of preformed gold nanorods. Due to the presence of the hierarchically porous structure, the PEGylated MGNRs@HPSNs display high loading capability for both small anti-tumor drugs (i.e., doxorubicin hydrochloride, 69.2 ± 7.2 mg g-1) and bio-macromolecules (i.e., bovine serum albumin, 248.1 ± 12.3 mg g-1). More importantly, MGNRs@HPSNs present better photothermal effect than that of hierarchically porous silica nanoparticles containing less (one or two) gold nanorods at the same Au concentration. It is thus demonstrated that MGNRs@HPSNs can not only act as promising drug/protein nanocarriers, but also can be used as photoabsorbers for photothermal tumor therapy under NIR laser irradiation.

Synthesis of a New Titanate Coupling Agent for the Modification of Calcium Sulfate Whisker in Poly(Vinyl Chloride) Composite.

A new titanate coupling agent synthesized from polyethylene glycol (PEG), isooctyl alcohol, and phosphorus pentoxide (P2O5) was used for the modification of calcium sulfate whiskers (CSWs) and the preparation of high-performance CSW/poly(vinyl chloride) (PVC) composites. The titanate coupling agent (sTi) and the modified CSWs (sTi-CSW) were characterized by Fourier transform infrared (FTIR) spectroscopy, and the mechanical, dynamic mechanical, and heat resistant properties and thermostability of sTi-CSW/PVC and CSW/PVC composites were compared. The results show that sTi-CSW/PVC composite with 10 wt. % whisker content has the best performance, and its tensile strength, Young's modulus, elongation at break, break strength, and impact strength are 67.2 MPa, 1926 MPa, 233%, 51.1 MPa, and 12.75 KJ·m-2, with an increase of 20.9%, 11.5%, 145.3%, 24.6%, and 65.4% compared to that of CSW/PVC composite at the same whisker content. As the whisker content increases, the storage modulus increases, the Vicat softening temperature decreases slightly, and the glass transition temperature increases at first and then decreases.

Mechanical Properties and Morphologies of Carboxyl-Terminated Butadiene Acrylonitrile Liquid Rubber/Epoxy Blends Compatibilized by Pre-Crosslinking.

In order to enhance the compatibilization and interfacial adhesion between epoxy and liquid carboxyl-terminated butadiene acrylonitrile (CTBN) rubber, an initiator was introduced into the mixture and heated to initiate the cross-linking reaction of CTBN. After the addition of curing agents, the CTBN/epoxy blends with a localized interpenetrating network structure were prepared. The mechanical properties and morphologies of pre-crosslinked and non-crosslinked CTBN/epoxy blends were investigated. The results show that the tensile strength, elongation at break and impact strength of pre-crosslinked CTBN/epoxy blends are significantly higher than those of non-crosslinked CTBN/epoxy blends, which is primarily due to the enhanced interfacial strength caused by the chemical bond between the two phases and the localized interpenetrating network structure. Both pre-crosslinked and non-crosslinked CTBN/epoxy blends show a bimodal distribution of micron- and nano-sized rubber particles. However, pre-crosslinked CTBN/epoxy blends have smaller micron-sized rubber particles and larger nano-sized rubber particles than non-crosslinked CTBN/epoxy blends. The dynamic mechanical analysis shows that the storage modulus of pre-crosslinked CTBN/epoxy blends is higher than that of non-crosslinked CTBN/epoxy blends. The glass transition temperature of the CTBN phase in pre-crosslinked CTBN/epoxy blends increases slightly compared with the CTBN/epoxy system. The pre-crosslinking of rubber is a promising method for compatibilization and controlling the morphology of rubber-modified epoxy materials.

Dioxins contamination in the feed additive (feed grade cupric sulfate) tied to chlorine industry.

The sources of polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs) found in animal feed additive (feed grade cupric sulfate, CuSO4) were investigated and traced back to the formation of chlorinated organic compounds in the chlor-alkali industry. PCDD/Fs could be transported through the supply chain: hydrochloric acid (HCl) by-produced during formation of chlorinated organic compounds in chlor-alkali industry → spent acid etching solution (acid-SES) generated in printed circuit board production → industrial cupric salt → CuSO4 in animal feed, and finally enter the food chain. The concentration ranges in HCl and acid-SES were similar, of which the level in acid-SES was also consistent with that in various cupric salt products including CuSO4 based on Cu element content. PCDD/Fs also showed very similar congener profiles in all the sample types. This indicates a probable direct transport pathway of PCDD/Fs into the food chain, which may eventually be exposed to humans through consumption. To date this is the first study in China that systematically reports on the PCDD/Fs transport from industrial pollution sources to industrial processes and finally enters the human food chain.