AHP/碱木质素聚氨酯泡沫的阻燃性能

对精制后的碱木质素进行羟甲基化改性,再利用改性后的羟甲基化碱木质素部分替代聚醚多元醇,采用一步发泡法与聚合MDI制备了羟甲基化木质素基聚氨酯泡沫材料。将次磷酸铝(AHP)作为阻燃剂添加到泡沫中制备了阻燃碱木质素聚氨酯泡沫,通过极限氧指数(LOI)测试分析了羟甲基化木质素基阻燃聚氨酯泡沫的阻燃性能。利用热重分析(TG)和扫描电子显微镜(SEM)分别研究制得泡沫的热降解行为、成炭性能和残炭形貌。实验结果表明,当羟甲基化碱木质素替代聚醚多元醇的量为60%,次磷酸铝的添加量为30%时,碱木质素聚氨酯泡沫材料的极限氧指数(LOI)值达到了27.5%。因此,羟甲基化碱木质素和次磷酸铝使泡沫在燃烧时能更好的形成炭层,从而有效地隔绝空气,降低热传递,提高了材料的阻燃性能。     

电子装备测试性融合评估方法

测试性是装备通用质量特性之一，其设计水平直接影响了装备保障效能的发挥，如何更加真实的评估装备的测试性水平是当前研究的热点。在研制阶段装备实物测试性试验数据数量少、获取难、费用高，可认为是“小子样”数据，为了更加全面客观地评价装备的测试性水平，需要充分利用测试性仿真试验获取仿真数据进行融合评估。进行测试性仿真试验时，研究电子装备的仿真模型、故障模型、仿真故障注入方法，获取测试性仿真数据；在此基础上，将仿真试验数据作为验前信息并进行的处理，结合“小子样”装备实物试验数据，采用贝叶斯方法进行测试性试验数据的融合来评估装备的测试性水平，提高评估结果的客观性和可信度。通过案例分析，验证了测试性融合评估方法的有效性。     

Improving the flame retardancy of polypropylene foam with piperazine pyrophosphate via multilayering coextrusion of film/foam composites

A series of 16-layer polypropylene/flame retardant (PP/FR) film/foam composite structures were produced by microlayer coextrusion. A highly branched PP was used in the foam layers to increase strain hardening and cell stability, while the PP used in the film layers was a high shear viscosity grade to confine bubble growth. In addition to improved tensile properties, the PP/FR composite film/foams exhibited five times the compression modulus of PP/FR composite foams at each FR loading level. The thermal stabilities of the composites were investigated, exhibiting three step decompositions. The FR particles were effective in decreasing flammability by forming intumescent char. The PP/FR-film/foam-20 showed self-extinguishing behavior in a modified vertical burn test, while the PP/FR-foam-20 sample continued to burn. Cone calorimetry demonstrated that PP/FR film/foams had lower heat release than PP/FR foams due to the unique alternating film/foam structure of PP/FR film/foams. Scanning electron microscopy imaging of the residual chars from fire testing that the PP/FR composite film/foams showed a more continuous protective char surface when compared with PP/FR composite foams at each FR concentration. The combined data indicate that the formation of a surface film on top of a foam ensures a robust intumescent fire protective barrier for partly foamed materials and shows a new way toward lightweight materials with improved fire safety performance. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48552.     

Impact of flat roof–integrated solar photovoltaic installation mode on building fire safety

This paper quantifies experimentally the fire‐induced reradiation to roof surface created by flame extension on the back of the flat roof–integrated photovoltaic (PV) array. A gas burner underneath the tilted PV panels was employed as the fire source. The effects of the PV tilt angle, distance from PV panel to roof, and fire heat release rate (HRR) were investigated. The flame extension geometries and flame reradiation heat flux distribution were recorded. The results show that the flame extension length and vertical thickness (ie, the vertical distance from the back surface of the PV panel to the extension flame profile) are reduced with the increase of PV tilt angle and panel‐roof distance but are increased with increases in the fire HRR. A unified nondimensional HRR coupled with all these factors is proposed to quantify the flame extension geometry. Furthermore, a general equation based on the physical relationship between flame radiation and flame geometry is developed to characterize the distribution of reradiation heat flux on the roof surface with the nondimensional local flame thickness. Finally, suggestions regarding PV installations on flat roofs and the selection of roofing materials are given to decrease the possibility of flame propagation underneath the PV arrays.     

Study on downward flame spread over extruded polystyrene foam in a vertical channel: Influence of opening area

Experimental methods and theoretical analysis are employed to investigate effects of channel opening area on downward flame spread characteristics of extruded polystyrene (XPS) thermal insulation materials on building facade. The average flame height first drops and then rises as dimensionless opening area (the ratio of sidewall opening area to sidewall area, ie, S^*) increases. As S^* rises, both the average and maximum temperature of the curtain wall decrease, and the decreasing of the average temperature is linear. XPS surface temperature history can be divided into four stages, ie, inapparent rising stage (preheating), significant rising stage (melting), dropping stage (pyrolysis), and rerising stage (ignition). The preheating length first rises and then drops as S^* increases. The XPS flame spreads steadily at the early period while acceleration occurs at the later period. For different opening areas, the difference in spread distance history is not apparent in the early stage while this difference is significant in the later stage. The flame spread rate (V_f) first increases and then decreases as S^* rises. A downward flame spread model for XPS in vertical channel with openings is built. The varied trend of V_f predicted using this model corresponds to the experimental result.     

Vinyl-functionalized polyborosiloxane for improving mechanical and flame-retardancy performances of silicone rubber foam composites

In this work, we first synthesized vinyl-terminated polyborosiloxane (pBS) filler, and then incorporated it into silicone rubber foam (SRF) matrix to prepare composite materials through a simple chemical dehydrogenative foaming method under ambient conditions. The pBS filler with reactive groups could form physical and chemical crosslinking networks in SRF, leading to an excellent dispersion level of pBS in the SRF matrix. Moreover, the inserted pBS could remarkably improve the mechanical and flame-retardancy properties of SRF-pBS composites. Intriguingly, the SRF-pBS6 foam containing 6 wt% of pBS possessed a uniform porous structure and balanced mechanical properties (σ_b = 65.4 kPa, ε_b = 56.7%, compression stress 97.1 kPa), thermal conductivity (0.102 W (m K)^?1), limiting oxygen index (29.8%) and UL-94 rating (V-0) among the prepared foams. In addition, the incorporated pBS (6 wt%) could synergistically catalyze the formation of a silicon–boron strengthened ceramic-like protective layer under fire and was capable of suppressing heat and smoke production in the SRF-pBS6 foam. The present work provides a promising way for developing high mechanical and flame-retardant polymeric foam materials with good thermal insulation. © 2021 Society of Industrial Chemistry.     

Synthesis of a novel DOPO‐based polyphosphoramide with high char yield and its application in flame‐retardant epoxy resins

A novel and highly effective flame retardant (FR), DOPO‐TPMP oligomer, was synthesized by a simple condensation of 4‐(hydroxymethyl)‐2,6,7‐trioxa‐1‐phosphabicyclo[2.2.2]octane‐1‐oxide and phosphorus oxychloride followed by a polycondensation reaction with 6‐(2,5‐dihydroxyphenyl)‐6H‐dibenzo[c,e][1,2]oxaphosphinine‐6‐oxide. The chemical structure of DOPO‐TPMP was well characterized using Fourier transform infrared and NMR spectra. DOPO‐TPMP was used as an additive‐type FR for epoxy resin (EP). The FR properties of the resultant EP composites were investigated by limiting oxygen index (LOI) test, UL‐94 vertical burning test and cone calorimeter measurements. Specifically, the EP composite containing 10.0% DOPO‐TPMP achieved a LOI value of 36.1%, V‐0 rating in the UL‐94 test and a 58% reduction in peak heat release rate. Further mechanism analysis attributed the enhanced flame retardancy to the increased char yield on the addition of DOPO‐TPMP. © 2019 Society of Chemical Industry     

Numerical investigation of the effects of H2/CO/syngas additions on laminar premixed combustion characteristics of NH3/air flame

Co-firing NH₃ with H₂/CO/syngas (SYN) is a promising method to overcome the low reactivity of NH₃/air flame. Hence, this study aims to systematically investigate the laminar premixed combustion characteristics of NH₃/air flame with various H₂/CO/SYN addition loadings (0–40%) using chemical kinetics simulation. The numerical results were obtained based on the Han mechanism which can provide accurate predictions of laminar burning velocities. Results showed that H₂ has the greatest effects on increasing laminar burning velocities and net heat release rates of NH₃/air flame, followed by SYN and CO. CO has the most significant effects on improving NH₃/air adiabatic flame temperatures. The H₂/CO/SYN additions can accelerate NH₃ decomposition rates and promote the generation of H and NH₂ radicals. Furthermore, there is an evident positive linear correlation between the laminar burning velocities and the peak mole fraction of H + NH₂ radicals. The reaction NH₂ + NH <=> N₂H₂ + H and NH₂ + NO <=> NNH + OH have remarkable positive effects on NH₃ combustion. The mole fraction of OH × NH₂ radicals positively affects the net heat release rates. Finally, it was discovered that H radicals play an important role in the generation of NO. The H₂/CO/SYN additions can reduce the hydrodynamic and diffusional-thermal instabilities of NH₃/air flame. The NH₃ reaction pathways for NH₃–H₂/CO/SYN-air flames can be categorized mainly into NH₃–NH₂–NH–N–N₂, NH₃–NH₂–HNO–NO(?N₂O)–N₂ and NH₃–NH₂(?N₂H₂)–NNH–N₂. CO has the greatest influence on the proportions of three NH₃ reaction routes.