乌鲁木齐市供热现状调查分析

通过调查，分析了供热方式与环境质量的关系，比对了集中供热与分散供热环境效益和经济效益。到本世纪末可实现供热规化后，使城市热化率达到２０％。市内大气环境质量将有较大改善。     

一种采用可控复合技术的新型升温炉

在普通电加热炉的基础上,通过配备液化燃烧器加热装置,开发了一种可同时实施自动控制电加热和燃气加热复合升温的新型装配式试验炉。试验测试表明,该新型复合式升温方法能够很好地模拟ISO-834标准升(降)温曲线,同时具有电炉安全可靠、测控精度高、操作简便、无污染,以及液化气火焰升温快、容易控制并可真实模拟火灾的优点,因而具有良好的试验效果和经济效果,是一种实用的结构抗火试验设施。     

混凝土高温爆裂性能影响因素及预防措施综述

对混凝土高温爆裂成因进行总结,综述高温下混凝土内部蒸汽压力的测试手段、降低混凝土内部蒸汽压力方法、提高混凝土在高温中的抗高温爆裂性能的方法,以及总结了升温速率对混凝土高温爆裂的影响,并提出了几种预防混凝土高温爆裂的措施,为混凝土高温爆裂研究提供依据。     

分析样品处理中的红外线快速加热技术

本文研究了红外线快速加热样品处理工艺,红外线由钨灯产生,酸性悬浊液样品盛在玻璃容器中.该工艺的主要优点是结构简单、费用低.另外,稀酸溶液不到60s中就可加热到需要温度,且整个过程不到5min.该工艺适用于痕量分析,最初的研究是测定牛肝、苹果叶等原料中的Cu、Fe、Mn含量.结果可以达到95%的置信水平.在未经任何预处理或仅做冷冻干燥情况下,可测定铜和锰的含量,证实与用常规的微波辅助法结果一致.     

湿热法处理实现厨余垃圾饲料化的研究

探索了湿热法工艺处理厨余垃圾并将其饲料化的可行性。实验表明,湿热法处理可以在满足消毒杀菌的同时,降低厨余原料中的高油脂含量和高含盐量,调节营养成分,实现物化性状的均一。经湿热法处理后的厨余垃圾的饲用价值得到明显改善,可作为良好的饲料原料,同时可回收利用油脂。总之,湿热法工艺可实现厨余垃圾的无害化、减量化和资源化处理,对于消除环境污染、缓解我国饲料原料紧张及资源回收利用等方面有着显著的环境效益、社会效益和经济效益,具有重要的现实意义。     

焦炉加热过程中热力型氮氧化物的生成及影响因素研究

以武钢焦化公司6 m、7 m、7.63 m 3种炉型焦炉为对象,研究了焦炉加热过程中热力型氮氧化物的生成规律和影响因素。结果表明,焦炉氮氧化物排放量与炉型、空气过剩系数以及立火道温度有着直接的关系。7 m、7.63 m焦炉的氮氧化物排放量平均值均在210 ppm以下,6 m焦炉氮氧化物排放量平均值在400 ppm以上。6 m焦炉废气中NOx排放量明显高于7 m和7.63 m焦炉,这是由于7 m和7.63 m焦炉采用了分段加热方式,可以有效控制在焦炉加热过程中热力型NOx的生成,有利于减少最终烟气中NOx的浓度。     

微波加热再生废弃的净化石油化工废水活性炭

为了对石油化工废水净化处理后的废弃活性炭实现循环利用,提出了在无保护气体和活化气体条件下进行微波加热的方法。主要评估了再生温度和再生时间对再生活性炭的吸附性能和得率的影响。结果表明,在再生温度为600℃,再生时间为15 min时,活性炭的碘吸附能力达到最大值971 mg/g,得率为82.36%。再生活性炭比表面积高达1 028 m2/g,总孔体积为1.23 mL/g,平均孔径为4.89 nm。通过废弃活性炭和再生活性炭进行了SEM对比分析,再生活性炭表面杂质减少,孔隙数量明显增多。     

Modelling of a downdraft gasifier fed by agricultural residues

A non-stoichiometric model for a downdraft gasifier was developed in order to simulate the overall gasification process. Mass and energy balances of the gasifier were calculated and the composition of produced syngas was predicted. The capacity of the modeled gasifier was assumed to be 0.5 MW, with an Equivalence Ratio (EQ) of 0.45. The model incorporates the chemical reactions and species involved, while it starts by selecting all species containing C, H, and O, or any other dominant elements. Olive wood, miscanthus and cardoon were tested in the formulated model for a temperature range of 800-1200 °C, in order to examine the syngas composition and the moisture impact on the supplied fuel. Model results were then used in order to design an olive wood gasification reactor.     

湿煤堆自热过程的非稳态数学模拟

利用简化的自热过程一维数学模型,分析煤堆内水分变化及迁移对煤堆自热所能达到的最高温度的影响。分析结果表明：当煤堆内水蒸气达到饱和时,预计的煤堆最高温度将低于９０℃;而当煤堆中气流的相对湿度减小时,预计的煤堆最高温度将会超过１００℃。结果还表明,把气流相对湿度与煤堆含水量之间的平衡关系引入自热过程的非稳态数学模型,不仅是可行的,而且能够更客观地描述实际煤堆的自热过程。     

Transformations in carbon and nitrogen-forms in peat subjected to progressive thermal stress as revealed by analytical pyrolysis

To study the characteristic N-forms of humic-type materials, samples of sapric peat from Galicia (northern Spain) were heated at 350 °C for 60, 90, 120, 150 and 180 s, and studied by Curie-point Py-GC/MS, solid-state CPMAS ¹³C-NMR and ¹⁵N-NMR spectroscopies. NMR analysis of the peat samples in the progressive heating stages showed the concentration of heterocyclic N-forms, the maximum structural transition amide-to-heterocyclic forms being observed in samples heated for 120 s (56% heterocyclic N and 34% aromatic C). Under more drastic conditions all N-forms were depleted. Correlation between spectroscopic and pyrolytic data betrayed specific pyrolytic markers for the different N-forms. The intensity of the ¹⁵N-NMR amide peak tended to be positively correlated to the yield of indoles, imidazoles and pyrazoles, and negatively correlated to those of benzonitriles and pyrazines. Analytical pyrolysis also showed a progressive enrichment in lipids and alkyl macromolecules with increasing heating intensity, and a decrease in lignin-derived, polysaccharide-derived and N-containing compounds. The relative abundance of non-methoxyphenolic aromatic compounds did not change. The N-compounds in peat samples unheated or heated for 60–90 s released methylpyrazole, dimethylpyrroline, methyldiphenylindole and pyrazole, whereas peat samples heated for 120 s mainly yielded methylpyrazine and methyldiphenylindole. Dimethylpyrroline and pyrazine prevailed in samples heated for 150 s, whereas samples heated for 180 s yielded mainly pyrrole. Pyrolysis data presented low possibilities for forecasting the extent of the O-alkyl domain, but reflected quantitatively the transformations in the lignin-like moiety. Both techniques coincide in pointing out the accumulation of a recalcitrant alkyl domain possibly derived from abiotic condensations or inherited lipid biomacromolecules.