A110－1－H／A110－1型氨合成催化剂在双筐并流合成塔中的使用

在双筐并流氨合成塔中使用了Ａ１１０－１－Ｈ／Ａ１１０－１型氨合成催化剂，使用寿命达１７４０天，累计产氨４３８３７８ｔ．该催化剂组合具有低温活性好、易还原、高催化活性、高抗毒能力、良好的热稳定性与破碎强度等优点．     

A QM/MM study of the catalytic mechanism of aspartate ammonia lyase

Aspartate ammonia lyase (Asp) is one of three types of ammonia lyases specific for aspartate or its derivatives as substrates, which catalyzes the reversible reaction of l-aspartate to yield fumarate and ammonia. In this paper, the catalytic mechanism of Asp has been studied by using combined quantum-mechanical/molecular-mechanical (QM/MM) approach. The calculation results indicate that the overall reaction only contains two elementary steps. The first step is the abstraction of C_β proton of l-aspartate by Ser318, which is calculated to be rate limiting. The second step is the cleavage of C_αN bond of l-aspartate to form fumarate and ammonia. Ser318 functions as the catalytic base, whereas His188 is a dispensable residue, but its protonation state can influence the active site structure and the existing form of leaving amino group, thereby influences the activity of the enzyme, which can well explain the pH dependence of enzymatic activity. Mutation of His188 to Ala only changes the active site structure and slightly elongates the distance of C_β proton of substrate with Ser318, causing the enzyme to remain significant but reduced activity.     

Determination of dinitrogen emission and retention in floodwater and porewater of a lowland rice field fertilized with15N-urea

This paper reports a study on the distribution of dinitrogen between the atmosphere, floodwater and porewater of the soil in a flooded rice field after addition of¹⁵N-labelled urea into the floodwater.Microplots (0.086 m²) were established in a rice field near Griffith, N.S.W., and labelled urea (80 kg N ha^–1 containing 79.25 atoms %¹⁵N) was added to the floodwater when the rice was at the panicle initiation stage. Emission of nitrous oxide and dinitrogen was measured directly during the day and overnight, using a cover collection method and gas chromatographic and mass spectrometric analytical methods. Ammonia volatilization was calculated with a bulk aerodynamic method from measurements of wind speed and floodwater pH, temperature and ammoniacal nitrogen concentration. Seven days after urea application the¹⁵N₂ content of the floodwater and soil porewater was determined and total fertilizer nitrogen loss was calculated from an isotopic balance.Throughout the experimental period gas fluxes were low; nitrous oxide, ammonia and dinitrogen flux densities were less than 5, 170 and 720 g N ha^–1 d^–1, respectively. The greatest dinitrogen flux density was observed two days after urea addition and this declined to ~ 100 g ha^–1 d^–1 after seven days.The data indicate that, of the urea nitrogen added, 0.02% was lost to the atmosphere as nitrous oxide, 0.9% was lost by ammonia volatilization, and 3.6% was lost as dinitrogen gas during the 7 days of measurement. At the end of this period 0.028% and 0.002% of the added nitrogen was retained as dinitrogen gas in the floodwater and soil porewater respectively. Recovery of the¹⁵N applied as nitrogen gases, plant uptake, and soil and floodwater constituents totaled about 94% of the nitrogen added.     

Effect of nutrient seed coating on the emergence of wheat and oats

A series of experiments was conducted under controlled soil moisture and temperature conditions in a growth chamber to examine the effect of a range of nutrient seed coatings on the emergence to wheat (Triticum aestivum L. cv. Kite) and oats (Avena sativa L. cv. Blackbutt) sown in a coarse sandy loam soil. Final emergence of oats was not reduced by a coating containing 10 kg P ha^–1 (as monocalcium phosphate [MCP]) whereas the same coating reduced wheat emergence by 15%. The emergence of both wheat and oats was severely reduced by urea coatings (supplying 10 kg N ha^–1) to 33 and 13% respectively; this injury was lessened markedly by the inclusion of phenyl phosphorodiamidate (PPD) in the urea coatings at 1% (w/w) (emergence increased to 66 and 56% respectively).Low soil moisture (67% of field capacity [FC]) resulted in almost no emergence of wheat coated with urea (± bentonites of different pH). In soil at FC, the addition of bentonite of pH 5 (B5) to urea coatings permitted greater emergence (54%) than when bentonite of pH 9 (B9) was added (32%) which, in turn, permitted greater emergence than urea coating alone (10%). When PPD and bentonite (B5 or B9) were combined either singly or together with urea in seed coatings, PPD was more effective than either of the bentonites in reducing injury and masked the slight positive effect of B5.Coatings containing various combinations of N and P sources (at 3.6 and at 8 kg ha^–1 respectively) all reduced the emergence of wheat compared to raw seed (91% emergence). When applied alone, MCP was least damaging (74%); the combination of MCP with ammonium sulfate (AS) caused somewhat more injury (68%) whilst combination with calcium nitrate (CN) caused most injury (29%). In contrast, CN alone caused relatively little damage (73%) whilst AS alone was more damaging (50%). There was no significant regression found between percentage emergence and either the calculated partial salt index or the pH of the nutrient coatings. Further work is needed to examine the mechanisms of injury due to nutrient seed coatings so that safe but effective formulations can be developed.     

Ammonia Decomposition on Ir(100): From Ultrahigh Vacuum to Elevated Pressures

Ammonia decomposition on Ir(100) has been studied over the pressure range from ultrahigh vacuum to 1.5 Torr and at temperatures ranging from 200 to 800 K. The kinetics of the ammonia decomposition reaction was monitored by total pressure change. The apparent activation energy obtained in this study (84 kJ/mol) is in excellent agreement with our previous studies using supported Ir catalysts (Ir/Al₂O₃ 82 kJ/mol). Partial pressure dependence studies of the reaction rate yielded a positive order (0.9±0.1) with respect to ammonia and negative order (–0.7 ±0.1) with respect to hydrogen. Temperature-programmed desorption data from clean and hydrogen co-adsorbed Ir(100) surfaces indicate that ammonia undergoes facile decomposition on both these surfaces. Recombinative desorption of N₂ is the rate-determining step with a desorption activation energy of 63 kJ/mol. Co-adsorption data also indicate that the observed negative order with respect to hydrogen pressure is due to enhancement of the reverse reaction (NH _x + H NH _x+1, x=0–2) in the presence of excess H atoms on the surface.     

现有合成氨厂建设8万吨/年硫酸钾及4万吨/年纯碱装置的可行性

本文试图论述现有合成氨厂改变产品结构,采取以生产化肥为主,联产化工产品。通过对钾芒硝法工艺及联碱工艺技术路线的选择,技术经济分析,以期提高化肥厂的经济效益。     

优质饮用水直接进户试验研究

针对目前上海市自来水水质存在的不足,试验了三种水质深度处理工艺。试验证明,该三种工艺对浊度、色度、耗氧量、余氯、氨等指标均有明显的去除效果。在其它水质指标方面,符合建设部2002年“水质目标”及欧盟水质标准的要求,最后确定了一种工艺用于小区供水。     

小型合成氨厂节气节能工艺评价 (Ⅷ)换热式转化深冷净化工艺

作者对“换热式转化深冷净化工艺”用于改造以间歇蒸汽转化工艺生产合成氨小厂的工艺流程、主要原料消耗、技术经济指标和风险性进行了研究、计算、分析和比较,为国内105家以天然气为原料的小型合成氨厂节气节能改造的方案选择提供依据。     

合成气中氨含量测定方法的改进

用快速测定仪测定气体中的氨含量，采气量为50ml，可准确测出高含量氨体积百分比含量为80%-100%和低含量氨体积百分比含量为1%-20%的样气，该仪器结构简单，易于制造，测定过程简单，结果准确，一目了然。     

新型CO耐硫变换催化剂QDB-04的开发及应用

介绍了新型CO耐硫变换催化剂QDB-04的性能特点及工业应用情况，对Shell粉煤气化煤气第一变换炉反应深度的问题及控制第一变换炉“床层飞温”的办法进行了讨论，提出了ODB-04催化剂应用于低水气比Shell粉煤气化制氨变换工艺的设计方案。