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《中南林业科技大学学报(自然科学版)》2017,(2)
不施加任何胶黏剂,通过添加阻燃剂聚磷酸铵(APP)制造阻燃无胶高密度蔗渣碎料板。探讨APP含量对板材物理力学性能的影响,并利用热重分析和锥形量热分析对阻燃板材进行燃烧性能的表征。结果表明:APP的加入使板材强度有所下降,但板材强度仍能满足室内结构用板的标准要求;APP有效地抑制了蔗渣的受热分解,促进成炭;APP有效抑制了阻燃板燃烧时的热释放和烟释放。 相似文献
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为解决醛系合成树脂胶黏剂甲醛释放、热稳定性差和阻燃效果较差的难题,探讨了一种功能叠加型无机镁质胶黏剂的制备技术,以期替代醛类合成树脂胶黏剂在木材工业上的使用。本研究中镁质胶黏剂的优化配方为n(MgO)/n(MgCl_2)=6,n(H_2O)/n(MgCl_2)=16,胶合板制备工艺为施胶量700 g/m~2(双面),冷压时间28 h,养护时间15 d。试验结果显示,养护天数对镁质胶黏剂制备胶合板胶合强度的影响最显著。当养护天数为3~19 d时,胶合板的干、湿胶合强度均呈现先增大后下降的趋势,13 d时干、湿胶合强度均达到峰值,干、湿胶合强度分别为1.40和1.08 MPa。通过对胶合板剪切破坏界面进行扫描电镜观察发现,镁质胶黏剂渗透到木材孔隙中形成了胶钉,产生了机械咬合结构。利用热重分析仪和锥形量热仪等对镁质胶黏剂的热稳定性和燃烧性能进行了测试,结果表明,镁质胶黏剂在本研究温度范围(30~800℃)内的总质量损失率为48%。在50 k W/m~2的热辐射功率下,镁质胶黏剂制备胶合板的平均热释放速率(HRR)为35.84 k W/m~2,总热释放量(THR)为20.97MJ/m~2。与普通酚醛树脂胶黏剂相比,镁质胶黏剂具有较好的热稳定性和阻燃性能。 相似文献
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以脱脂大豆粉为原料制备大豆蛋白基胶黏剂(豆胶,S),以普通甲醛制备的酚醛树脂(PF_1)和高浓度甲醛制备的酚醛树脂(PF_2)为交联剂,使用前将两者直接混合得酚醛树脂改性豆胶(PF_1/S、PF_2/S)。利用差示扫描量热(DSC)、红外光谱(FT-IR)、动态热机械性能(DMA)和核磁共振碳谱(~(13) C NMR)分析对产品性能进行了测试与表征。结果表明:等物质的量之比条件下,高浓度甲醛较之普通甲醛制备的酚醛树脂改性豆胶胶合板干、湿剪切强度分别提高4.3%和11.6%,并且强度稳定性好;动态DSC分析表明,PF_2可以降低豆胶体系的固化温度和活化能,与豆胶的交联反应较容易;~(13) C NMR分析表明,PF_2体系羟甲基达88.73%,明显高于PF_1的80.91%;FT-IR分析证实酚醛树脂与豆胶中的氨基发生反应,并且PF_2反应效率更高;DMA分析表明,PF_2/S能够改善胶合产品的力学性能和热稳定性,降低豆胶的固化反应起始温度,提高固化反应速率。 相似文献
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研制了一种适合“热进-热出”工艺的中温固化水溶性酚醛树脂,该酚醛树脂是在传统的水溶性酚醛树脂合成工艺的基础上,加入一定量的间苯二酚和尿素制成。它可以在115℃时快速固化,降低了酚醛树脂胶的固化温度,缩短了固化时间。采用该酚醛树脂制造的竹胶板能够满足国标要求。 相似文献
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采用聚磷酸铵(APP)作为阻燃剂,对竹/聚丙烯纤维复合毡增强酚醛树脂基复合材料进行阻燃改性,研究阻燃剂的添加对复合材料力学、阻燃和导热性能的影响。当复合材料中添加25%APP时,力学性能测试结果表明,该复合材料的静曲强度和内结合强度分别降低了18.49%和62.86%,而隔热效果基本不变。采用扫描电子显微镜对复合材料内部进行表征,结果表明,APP的添加会破坏酚醛树脂的固化能力,导致力学性能的下降。采用锥形量热仪和极限氧指数仪对复合材料的阻燃性能进行分析,结果表明,添加APP后,复合材料的热释放速率和总热释放量分别降低了50.62%和50.82%,而极限氧指数则达到29.7,阻燃性能得到了明显改善。采用导热系数测定仪对阻燃前后复合材料的隔热效果进行表征,结果表明,APP的添加对复合材料保温效果没有影响。 相似文献
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以硅酸钠、硅酸铝、氧化镁和硅烷偶联剂为原料,制备胶合板用硅镁系硅酸盐无机胶黏剂。采用单因素试验和正交试验考察了主要成分用量对胶黏剂的胶合性能的影响,并采用锥形量热分析技术和热重法分别测试其阻燃抑烟性能以及耐热性能。结果表明,当硅酸钠的质量分数为92.5%,硅酸铝的质量分数为4.7%,氧化镁的质量分数为2.8%,硅烷偶联剂的百分比含量为0.6%(相对于硅酸钠的质量而言)时,改性胶黏剂的综合性能最好,其胶合强度达到0.85MPa,阻燃抑烟性能效果显著,热释放总量和热释放速率明显降低。 相似文献
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研制了一种刨花板用阻燃酚醛树脂胶 ,并对制板工艺进行了优化。经测定 ,制成的刨花板的物理力学性能达到刨花板国家标准 GB/ T4 897- 92中 A类板优等品的性能指标要求 ;氧指数值达到热固性树脂装饰层压板标准 GB7911.6 -87规定的要求 (>37) 相似文献
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Fengqiang Wang Zhijun Zhang Qingwen Wang Jiayin Tang 《Frontiers of Forestry in China》2008,3(4):487-492
An intumescent waterborne amino-resin fire-retardant coating for wood (C) was synthesized and its fire-retardant and smoke-suppressant
properties were investigated. The main film-builder of C was urea-formaldehyde resin blended with polyvinyl acetate resin.
The intumescent fire-retardant system of C consisted of guanylurea phosphate (GUP), ammonium polyphosphate (APP), pentaerythritol
(PER) and melamine (MEL). Specimens of plywood painted, respectively, with a commercial intumescent fire-retardant coating
(A), a synthesized coating (C), and the main film-builder of coating C (B), as well as an unpainted plywood (S-JHB), were
analyzed by cone calorimetry (CONE). The results show a marked decrease in the heat release rate (HRR) and the total heat
release (THR), an increased mass of residual char (Mass), a marked postponement in time to ignition (TTI) and a reduced carbon
monoxide production rate (P
CO). The smoke production rate (SPR) and total smoke production (TSP) of the plywood painted with coating C were observed with
the CONE test. The overall fire-retardant and smoke-suppressant performance of the synthesized coating C was much better than
that of the commercial coating A. The thermo-gravimetric analysis (TGA) results of coating C and its film-builder B indicated
that the thermal degradation process of B was slowed down by the addition of the intumescent fire-retardant system; the increase
in the amount of charring of coating C was considerable.
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Translated from Scientia Silvae Sinicae, 2007, 43(12): 117–121 [译自: 林业科学] 相似文献
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Guangjie Zhao Wensheng Luo T. Furuno Qiang Ren Erni Ma 《Frontiers of Forestry in China》2007,2(2):231-236
In order to investigate the pyrolytic characteristics of the burning residue of fire-retardant wood, a multifunctional fire-resistance
test oven aimed at simulating the course of a fire was used to burn fire-retardant wood and untreated wood. Samples at different
distances from the combustion surface were obtained and a thermogravimetric analysis (TG) was applied to test the prrolytic
process of the burning residue in an atmosphere of nitrogen. The results showed that: 1) there was little difference between
fire-retardant wood and its residue in the initial temperature of thermal degradation. The initial temperature of thermal
degradation of the combustion layer in untreated wood was higher than that in the no burning wood sample; 2) the temperature
of the flame retardant in fire-retardant wood was 200°C in the differential thermogravimetry (DTG). The peak belonging to
the flame retardant tended to dissipate during the time of burning; 3) for the burning residue of fire-retardant wood, the
peak belonging to hemicellulose near 230°C in the DTG disappeared and there was a gentle shoulder from 210 to 240°C; 4) the
temperature of the main peaks of the fire-retardant wood and its burning residue in DTG was 100°C lower than that of the untreated
wood and its burning residue. The rate of weight loss also decreased sharply; 5) the residual weight of fire-retardant wood
at 600°C clearly increased compared with that of untreated wood. Residual weight of the burning residue increased markedly
as the heating temperature increased when burning; 6) there was a considerable difference with respect to the thermal degradation
temperature of the no burning sample and the burning residue between fire-retardant wood and untreated wood.
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Translated from Journal of Beijing Forestry University, 2006, 28(3): 133–138 [译自: 北京林业大学学报] 相似文献
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Curing kinetics of phenol formaldehyde resin and wood-resin interactions in the presence of wood substrates 总被引:1,自引:0,他引:1
The curing kinetics of resol PF resin and resin–wood interactions in the presence of wood substrates have been studied by differential scanning calorimetry (DSC) and Fourier transform infrared (FTIR) spectroscopy. The activation energy of cure of PF resin generally increases when PF resin is mixed with wood, mainly due to the decrease of the pH values resulting from the presence of wood. However, wood decreases the curing enthalpy of PF resin through diffusion and the change in the phase of the curing system, which suggests that the curing reactions reached a lower final degree of conversion for the mixtures of PF resin with wood than for the PF resin alone. Moreover, DSC curves and the variation of activation energy with conversion indicate that wood accelerates the addition reactions and retards condensation ones during the curing process of PF resin with wood. The study also revealed that almost no chemical reactions occur between PF resin and wood, but the secondary force interactions of hydroxyl groups between PF resin and wood have been detected. These most significant secondary forces can catalyze the self-condensation reactions of PF resin, although their effect is not vital on the curing kinetics of PF resin. 相似文献
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