冷冻取芯过程煤样温度变化特性研究

为探究冷冻取芯过程煤样温度变化特性,基于模拟试验的相似性,自主设计冷冻取芯模拟测试试验装置,选取榆家梁矿、首山一矿、六龙煤矿、九里山矿4个矿区不同变质程度煤样,用以测定瓦斯吸附平衡压力为0、1.0、2.0、3.0 MPa下冷冻取芯过程煤样的温度实时变化数据,并统计分析各条件下的数据。研究结果表明:冷冻取芯技术的冷冻效果与煤变质程度及瓦斯吸附平衡压力呈正相关关系;冷冻取芯对含瓦斯煤冷冻效果优于不含瓦斯煤;冷冻取芯对高变质煤冷冻效果优于低变质煤;冷冻取芯过程中,煤样温度随时间变化曲线符合指数函数关系。     

改变垫水层沸点的薄层扬沸实验研究

扬沸是油池火灾的一种特殊现象,燃料和垫水层交界面的过热温度和沸腾状态是决定扬沸是否发生以及发生时间的最主要因素,过热温度由沸点决定。在垫水层中添加氯化钠能够改变垫水层的沸点,从而改变交界面的过热温度。在垫水层添加氯化钠使其成为饱和氯化钠水溶液,对此条件下的油池火燃烧进行实验探究,以验证前人关于扬沸临界条件的研究结果,并为扬沸防治提供思路。垫水层改变为饱和氯化钠溶液后,柴油实验组均没有发生扬沸,且观察到火焰温度和热辐射强度的下降。表明此方法可以有效抑制扬沸的发生。     

基于压力与温度对损失瓦斯量影响试验研究*

为研究取芯管取芯过程中压力与温度对损失瓦斯量的影响,以及t法的偏差,利用自主研发的取芯管取芯过程模拟测试装置,基于模拟试验的相似性,开展不同加热功率下取芯过程模拟试验与室温（30 ℃）对比,以及变温条件下不同吸附压力取芯过程模拟试验。结果表明:前30 min煤芯瓦斯解吸曲线符合Qt=a+b/［1+(t/t0)c］。吸附压力一定时,取芯过程模拟测试的煤芯瓦斯解吸率均大于室温下的对比测试,3~16 min（退钻过程）温度对损失量的影响大于0~3 min（取芯过程）;随着加热功率的增加,煤芯瓦斯解吸量增大,煤芯损失瓦斯量的模拟值亦增大;t法推算值与模拟值的绝对误差随加热功率的增大而增大,相对误差在65.08%~70.79%;加热功率一定时,随着吸附压力的增加,煤芯瓦斯解吸量愈大,煤芯损失瓦斯量t法推算值增大,模拟值亦增大;t法推算值与模拟值的绝对误差随吸附压力的增大而增大,相对误差在68.21%~72.13%。     

不同粒径易自燃煤常温氧化实验研究*

为探究易自燃煤在常温条件下的氧化特性,自行设计煤常温封闭氧化实验装置,采用实验研究与回归分析2种方法,分析易自燃煤发生氧化反应的气体变化过程,探究3种粒径煤样在20 ℃有限空间内的耗氧与产气特征。结果表明:易自燃煤样在16 d常温封闭氧化过程中,容器内O2体积浓度呈指数衰减、CO和CO2体积浓度呈指数增长的变化规律;在0.06~0.83 mm范围内,粒径越大,易自燃煤耗氧速率越大,CO和CO2产生速率则先增大后减小;介于中间的粒径为0.13~0.25 mm易自燃煤氧化反应最强烈,更容易发生氧化。研究结果对揭示生产环境温度下煤粒粒径对煤自燃的影响有一定的意义。     

温度作用下混凝土拼接桥梁拼接缝界面剪应力研究*

为探究拼宽混凝土桥梁在温度效应下连接缝位置产生的界面剪应力问题,考虑施工过程中现浇拼接缝混凝土各项参数的变化,以某高速公路拼接桥梁为研究对象,基于初等梁理论提出1种考虑纵向温度应力的拼宽桥梁界面剪应力力学模型。结果表明:拼接缝混凝土弹性模量的改变对拼接缝界面剪应力的数值和分布形态影响较小;新梁和旧梁的线膨胀系数差异越大拼接缝界面剪应力越大;研究得到不同拼宽宽度下拼宽桥界面局部剪切柔度修订值的变化规律,并拟合变化公式。     

混凝土箱梁水化热温度损伤安全评价模型研究

目前混凝土箱梁0#块在施工过程中出现水化热温度冲击和裂缝现象,严重影响混凝土箱梁结构早期强度的形成以及结构的安全性能.综合考虑混凝土水化热温度荷载和弹模的时变效应,给出时域损伤函数;根据变权分析原理,确定敏感损伤和累积损伤,建立混凝土水化热温度损伤安全评价模型;对混凝土箱梁0#块水化热温度损伤进行三维数值仿真,总结水化热温度损伤时变效应规律,对早期含水化热温度损伤参数的混凝土箱梁结构安全性能进行分析评价.结果表明:混凝土水化热反应速率、水化热温差峰值与损伤速率敏感度、累积损伤敏感度同步.温差峰值过大、水化热反应速率过快,敏感损伤度和累积损伤度增大,安全指标降低,易形成温冲,产生裂缝,导致整体破坏.通过时域损伤函数和安全评价模型可及时分析计算混凝土箱梁0#块的安全指标,指导混凝土箱梁0#块安全施工.     

浙江某农场土壤和沟渠沉积物对氨氮的吸附研究

通过静态吸附实验,研究农田土壤及沟渠沉积物对氨氮的吸附作用.实验表明,水相氨氮浓度为5～100 mg/L时,风干农田土壤、风干沟渠沉积物及新鲜沟渠沉积物3种吸附剂的吸附等温线均呈良好线性关系,并符合Freundlich吸附模式;农田土壤与沟渠沉积物的氨氮背景含量分别为12 mg·kg^-1和92 mg·kg^-1,并且农田土壤对氨氮的吸附系数为8.21,而风干沟渠沉积物与新鲜沟渠沉积物吸附系数分别为5.42与6.84,因此,土壤的吸附能力要大于沟渠沉积物,后两者的吸附能力相近.对3种吸附剂吸附机制的讨论表明,吸附特性与界面性质相关,实验氨氮浓度范围内吸附作用主要为离子交换.相同实验条件下,当初始氨氮浓度较大时,随温度升高,3种吸附剂对氨氮的平衡吸附量减小,对氨氮的吸附为弱放热过程.     

Production and application of a novel bioflocculant by multiple-microorganism consortia using brewery wastewater as carbon source

The flocculating activity of a novel bioflocculant MMF1 produced by multiple-microorganism consortia MM1 was investigated. MM1 was composed of strain BAFRT4 identified as Staphylococcus sp. and strain CYGS1 identified as Pseudomonas sp. The flocculating activity of MMF1 isolated from the screening medium was 82.9%, which is remarkably higher than that of the bioflocculant produced by either of the strains under the same condition. Brewery wastewater was also used as the carbon source for MM1, and the cost-effective production medium for MM1 mainly comprised 1.0 L brewery water （chemical oxygen demand （COD） 5000 mg/L）, 0.5 g/L urea, 0.5 g/L yeast extract, and 0.2 g/L （NH4）2SO4. The optimal conditions for the production of MMF1 was inoculum size 2%, initial pH 6.0, cultivating temperature 30℃, and shaking speed 160 r/min, under which the flocculating activity of the MMF1 reached 96.8%. Fifteen grams of purified bioflocculant could be recovered from 1.0 L of fermentation broth. MMF1 was identified as a macromolecular substance containing both protein and polysaccharide. It showed good flocculating performance in treating indigotin printing and dyeing wastewater, and the maximal removal efficiencies of COD and chroma were 79.2% and 86.5%, respectively.     

Temperature dependence of the absolute rate constant for the reaction of ozone with dimethyl sulfide

Absolute rate constants for the reaction of ozone with dimethyl sulfide (DMS) were measured in a 200-L Teflon chamber over the temperature range of 283-353 K. Measurements were carried out using DMS in large excess over ozone of 10 to 1 or greater. Over the indicated temperature range,the data could be fit to the simple Arrhenius expression as KDMS = (9.96±3.61)×10-11exp(-(7309.7±1098.2)/T)cm3/(molecule·s). A compared investigation of the reaction between ozone and ethene had a kc2H4 value of(1.35±0.11)×10-18 cm3/(molecule·s) at room temperature.     

Remove cooking fume using catalytic combustion over Pt/La-Al2O3

Five monolithic catalysts with low noble metal content were prepared by irnmerge method （Pt/γ=Al2O3, Pt/La-Al2O3, Pt/YSZ-AI203, Pt＋Pd/La-Al2O3 and Pd/La-Al2O3） and their activity measurements were carried out in a conventional fixed-bed flow reactor. The results show that La-Al2O3 can promote activity of the prepared catalysts and can decrease the complete conversion temperature of cooking fume. The Pt/La-Al2O3 catalyst has the highest activity and can be applied in wide range of gas hourly space velocity （GHSV）. Some characterizations （XRD, TPR） were carried out with the objective to explain differences in catalytic behaviors. The prepared catalyst showed a great potential for application.