溴化十六烷基三甲基铵胶束高效液相色谱的研究和应用

研究了苯、苯胺、苯酚和甲苯在以溴化十六烷基三甲基铵(CTAB)水溶液为移动相,YWG-NH_2为固定相时的保留行为。当柱温为45℃、移动相组成为5%正丙醇(或9%乙醇)的0.03mol/L CTAB 时,苯、苯胺、苯酚和甲苯分离最佳。还计算了溶质传质过程的焓值及其在水、胶束、固定相间的分配系数。     

氧化铁生产废液的治理和利用

氧化铁生产产生的含铁硫酸铵废液和洗涤废水中含有铁、硫酸根、铵等离子。采用化学沉淀、过滤、蒸发等方法处理该废水可回收废水中的硫酸铵、氧化铁、处理后的废水可回用于生产。     

2-羟丙基三甲基氯化铵壳聚糖的制备及其表征

以脱乙酰度为90%的壳聚糖(CTS)为原料,异丙醇为溶剂,w(NaOH)=40 0%的水溶液为催化剂,3 氯 2 羟丙基三甲基氯化铵(CTA)为改性剂,在m(NaOH)∶m(CTS)=1 0∶1 0,m(CTA)∶m(CTS)=4 0∶1 0,反应温度65 0℃下制备了2 羟丙基三甲基氯化铵壳聚糖(HTCC)。实验结果表明,在反应时间达到或超过9 0h时,得到的HTCC产品的接枝度超过90 0%,在pH=6 7～7 0的水中可完全溶解形成w(HTCC)=3 0%的溶液。IR和1HNMR的结果表明,接枝反应主要发生在CTS的氨基上。     

国外过氧化氢在化学合成中应用研究进展

介绍了近期国外过氧化氢在部分化学品合成中应用研究新进展 ,产品包括过碳酸钠、过碳酰胺、4Na2 SO4·2H2 O2 ·NaCl加合物、叔胺氧化物、水合肼、二羟基苯、季铵盐过氧化氢和甲乙酮肟。内容涉及产品质量 (纯度、安定性、溶解速率、外观等 )、产品收率、催化剂、工艺过程等方面改进。主要介绍专利技术。     

造纸黑液制水煤浆添加剂成浆性能的研究

针对淮化德士古气化炉所用的义马煤和鲁南化肥厂使用的配煤 ,进行了造纸黑液制添加剂实验室和工业制浆性能的考察。结果表明 ,其在工业应用中的添加量范围在 1.2 %～ 1.6 % (浆基 ,添加剂含固量 2 0 % ) ,对义马煤和鲁南配煤分别可以制出浓度在 6 4 .5 %和 6 9%之间 ,稳定性能良好 ,满足工业生产要求的水煤浆     

肥料磷铵溶解净化法的研究

在湿法磷酸净化中,氨化对多种杂质有沉淀去除作用,由此提出了肥料磷铵溶解净化法,用于制备生产各种精细磷化工产品的优质磷源,过滤所得残渣可返回肥料系统,不造成磷损失。以粉状磷酸一铵为原料,考察了不同温度、固液比、搅拌时间和搅拌速度对溶解浸出法溶出率、溶出液中P2O5含量的影响。通过单因子试验和正交试验,筛选出了适宜的工艺条件为:溶解温度70℃,固液比0.7,搅拌时间8min,中速搅拌,溶出率和溶出液中P2O5质量分数分别达67.04%和19.78%,铁和氟的去除率分别达99%和97%以上。     

Crystallography and equilibrium solubility for ammonium and potassium orthophosphites and hypophosphites

The composition and solubility properties of eight ammonium and potassium orthophosphites and hypophosphites were determined to evaluate the potential of these classes of materials for increasing the plant nutrient content of liquid fertilizers. Phase relationships for the systems (NH₄)₂O-P₂O₃-H₂O, K₂O-P₂O₃-H₂O, (NH₄)₂O-P₂O-H₂O, and K₂O-P₂O-H₂O were determined along with the crystallographic properties (X-ray and optical) of the solid phases. Toxicity and phosphite response was tested in greenhouse experiments for the compounds.     

铝电解电容器用新型宽温高压工作电解液

采用异癸二酸铵为主溶质,乙二醇和γ-丁内酯为复合溶剂,制备新型宽温(-40~105℃)、高压(400 V)铝电解电容器工作电解液,并检测了该电解液和用该电解液生产的电解电容器的性能。测试结果表明,该工作电解液25℃时电导率达到1.6 mS/cm,闪火电压为480 V,-40℃下未见晶体析出;CD 110/400 V铝电解电容器试样的漏电流≤10μA,损耗0.03,容量变化率只有-3%。经过105℃高温贮存250 h后各项电气性能不仅优于国家标准,而且能达到严格的企业标准。     

Heat-release mechanism in ammonium dinitramide flame

To verify the adequacy of various models of heat release in ammonium dinitramide flame to real processes, chemical processes in products of thermal decomposition at a pressure of 10 torr and in ammonium dinitramide [ADN; NH₄N(NO₂)₂] flame at a pressure of 0.4 to 60 atm are numerically simulated. The calculations are performed on the basis of a detailed kinetic mechanism and boundary conditions correlated with experimental data, thermodynamic properties, and chemical composition of ADN. The kinetic mechanism includes submechanisms that describe high-temperature chemical processes in NH₃/N₂O/NO/NO₂/HNO₂/HNO₃ and NH₃/HN(NO₂)₂ mixtures, and the global stages of aerosol decomposition. Based on calculated and experimental data, the role of dinitraminic acid HN(NO₂)₂, aerosols, and ADN vapor in heat release in the ADN flame zone adjacent to the burning surface is estimated. The calculations predict that the main source of heat release in the cold flame zone at p ≥ 3 atm is dinitraminic acid incoming through the channel of dissociative evaporation ADN_liq → NH₃ + HN(NO₂)₂ from the burning surface. In the high-temperature flame zone, heat release is caused by the reaction that occurs in the NH₃/N₂O/NO/NO₂/HNO₂/HNO₃ mixture. At moderate pressures, the high-temperature and low-temperature zones are separated by an induction zone. The stage governing production of the OH radical, which plays an important role in combustion, in the induction zone is the reaction HNO₃ + M → OH + NO₂ + M. Because of a high activation energy of the stage, small temperature perturbations in the induction zone at low pressures lead to a finite change in the stand-off distance between the high-temperature flame zone and the burning surface. Therefore, small temperature perturbations in the induction zone, which are caused by admixtures in the sample or by heat transfer between the reacting gas and the ambient medium, may be responsible for disagreement between various experimental data and between experimental and calculated data on the stand-off distance between the high-temperature flame zone and the burning surface. In numerical calculations, the position of the high-temperature zone is effectively controlled by varying rate constants of elementary stages within admissible limits. __________ Translated from Fizika Goreniya i Vzryva, Vol. 43, No. 5, pp. 64–76, September–October, 2007.     

Mussoorrie rock phosphate-pyrite mixture as phosphate fertilizer

Mussoorrie rock phosphate (MRP), MRP + pyrite (25% by weight), diammonium phosphate (DAP), ammonium polyphosphate (APP) and nitrophosphate (NP) were compared in a field experiment as fertilizers for wheat. At 20 kg P ha^–1, MRP was only 6 per cent as effective as DAP. However, when it was mixed with pyrite, the efficiency of MRP increased to 64 per cent at 20 kg P ha^–1 compared with 97 per cent at 40 kg P ha^–1. The P requirement for a targeted yield for 4.5 t ha^–1 decreased from 39.4 kg P ha^–1 as MRP to 23.7 kg P ha^–1 as MRP + pyrite. Of the other P fertilizers studied, NP was as effective as DAP, whereas APP was 9 to 37 per cent more effective than DAP. However, the P requirement as DAP, NP and APP for a targeted yield of 4.5 t ha^–1 was similar (11 ± 0.5 kg P ha^–1).