Thermosetting resin modified asphalt:A comprehensive review

Thermosetting resins have advantages such as high strength,corrosion resistance,and aging resistance,and have excellent prospects for practical application as asphalt modifiers.In order to promote the research of thermosetting resin modified asphalt,to provide direction for its further research,this paper reviews the research progress of thermosetting resin modified asphalt in recent years.The material composition,modification mechanism,and curing behavior of epoxy asphalt,thermosetting polyurethane modified asphalt,unsaturated polyester modified asphalt,and other thermosetting resin modified asphalts are overviewed.Different types of thermosetting resin modified asphalt have different performances,the performance advantages of different thermosetting resin modified asphalts are summarized.At the same time,the existing problems in thermosetting resin modified asphalt and further research directions are provided.Encouraging researchers to produce thermosetting resin modified asphalts using waste or bio-based materials,and to study the recycling technologies and life cycle assessment of thermosetting resin modified asphalt.This paper provides a reference for the study of thermosetting resin modified asphalt.

Flame Retardants Nanocomposites-Synergistic Effect of Combination Conventional Retardants with Nanofillers of the Flammability of Thermoset Resins

The consumption ofthermoset resins as building polymers is approximately over one million tone word wide. The thermoset resins are proven construction materials for the technical and highly demanding applications of the transportation, electrical and building part industry. Heat stability, high thermal, low shrinkage, excellent mechanical properties are typical for their type of polymers. Above applications in addition to the mechanical properties also require good flame retardants of the materials. Undertaken activities refer to official draft, laws and legal recommendations in UE states. This paper presents positive effect of reduced flammability of thermoset resins （unsaturated polyester and epoxy resins） thanks to the use of nanocomposites containing multi-ingredient halogen-flee flame retardants which combine conventional phosphorus/nitrogen modifiers interacting with nanofillers （oMMT （organomodified montmorillonite）, EG （expandable graphite）, graphene, GO （graphene oxide）, nSi （nanosilica））.

Kinetic Laws of Heating Initiated Reactions for Materials in Aerospace Applications

Cure and decomposition reaction kinetics of typical organic materials in aerospace applications are introduced.From the data of dynamic differential scanning calorimetry(DSC)experiments,and based on changes of the peak temperatures(T_(p))with different heating rates(β),a linear equation,T_(p)=T_(1)+△Tlnβ,has been obtained more reasonably.The above equation can be used to explain some laws of higher or lower of apparent activation energies(E_(a)),by which the apparent activation energy(E_(a))is nearly equal to RT^(2)_(1)/△T.A number of kinetic investigations of typical thermosetting resins and energetic materials in aerospace applications were chosen to validate the above equations.

Thermal Polymerization of Cyanate Ester-Benzoxazine:Study of a Functional Model Compound

A novel benzoxazine(BOZ)monomer is synthesized by a pot method with solvent-free to blend with cyanate ester(CE).A soluble intermediate is obtained after being cured for 20 h at 80℃.The two model compound and the blends are analyzed with the infrared radiation(IR),nuclear magnetic resonance(NMR)spectroscopy,and differential scanning calorimetry(DSC).The results show that an intermediate of the iminocarbonate and BOZ structures is formed by the ring-open BOZ reacting with the cyanate groups and ring-unopened BOZ.Moreover,rearrangement and ring-opening occur in the postcure of the intermediate to form the alkyl isocyanurate structure with polybenzoxazine.

Preparation of Poly(phosphoric acid piperazine) and Its Application as an Effective Flame Retardant for Epoxy Resin

A phosphorus-nitrogen containing flame retardant additive of poly（phosphoric acid piperazine）, defined as PPAP, was synthesized by the salt-forming reaction between anhydrous piperazine and phosphoric acid, and the dehydration polymerization under heating in nitrogen atmosphere. Its chemical structure was well characterized by Fourier transform infrared（FTIR） spectroscopy, ^（13）C and ^（31）P solid-state nuclear magnetic resonance measurements. The synthesized PPAP and curing agent m-phenylenediamine were blended into epoxy resin（EP） to prepare flame retardant EP thermosets. The effects of PPAP on the fire retardancy and thermal degradation behavior of cured EP/PPAP composites were investigated by limiting oxygen index（LOI）, vertical burning（UL-94）, thermogravimetric analysis/infrared spectrometry（TG-IR） and cone calorimeter tests. The morphologies and chemical compositions of char residues for cured epoxy resin were investigated by scanning electron microscopy（SEM） and X-ray photoelectron spectroscopy（XPS）, respectively. The results demonstrated that the flame retardant EP thermosets successfully passed UL-94 V-0 flammability rating and the LOI value was as high as 30.8% when incorporating 5 wt% PPAP into the EP thermosets. The TGA results indicated that the synthesized PPAP flame retardant additive possessed high thermal stability and excellent charring capability. Meanwhile, the incorporation of PPAP stimulated the epoxy resin matrix to decompose and charring ahead of time due to its catalytic decomposition effect, which led to a higher char yield at high temperature. The morphological structures and the analysis results of XPS for char residues of EP thermosets revealed that the introduction of PPAP benefited the formation of a sufficient, more compact and homogeneous char layer containing phosphorus-nitrogen flame retardant elements on the material surface during combustion. The formed char layer with high quality effectively prevented the heat transmission and diffusion, limited the production of combustible gases, and inhibited the emission of smoke, leading to the reduction of heat and smoke release.

Recent Advance in Low-Dielectric-Constant Organosilicon Polymers

Comprehensive Summary,Low dielectric(low-k)organosilicon polymers have received extensive interests from industry and academia due to good electrical insulation,high temperature resistance,flame retardancy and hydrophobicity.These attractive properties enable them to be utilized as low-k materials in fabrication of electronic devices in high-frequency communication technology.This review summarizes recent progress in developing low-k organosilicon polymers,including the synthetic methods and properties of different organosilicon polymers classified according to the chemical structures.It may provide some inspiration to design new low-k organosilicon polymers for application in the.

Scalable Synthesis of Hierarchical Antimony/Carbon Micro-/Nanohybrid Lithium/Sodium-Ion Battery Anodes Based on Dimethacrylate Monomer

A facile scalable synthesis of hierarchical Sb/C micro-/nanohybrid has been addressed in this work, which possesses the advantages of both micrometer and nanometer scale structures as lithium-ion battery anode. Difunctional methacrylate monomers are used as solvent and carbon source as well. Liquid precursor of antimony（III） n-butoxide is dissolved in the resin monomer solution, and further incorporated into the cross-linking polymer network via photo polymerization. Through calcination in argon/hydrogen atmosphere, antimony nanoparticles are in situ formed by carbothermal reduction, and homogeneously embedded in the in situ formed micrometer sized carbon matrix. The morphology, structure, crys- tallinity, spatial dispersion, composition, and electrochemical performance of the Sb/C micro-/nanohybrid are systemati- cally investigated. The cyclic and rate performance of the Sb/C micro-/nanohybrid anode have been effectively improved compared to the pure carbon anode. A reversible capacity of 362 mAh g-1 is achieved with a reasonable mass loading density after 300 cycles at 66 mA g-1, corresponding to capacity retention of 79%. With reducing mass loading density, the reversible capacity reaches 793 mAh g-1 after 100 cycles. Moreover, the electrochemical performance of Sb/C micro-/nanohybrid as sodium-ion battery anode is also investigated in this study.