可酸化的

The results indicate that the optimized sulfonylation reaction time is 4 h, the materiel rate of chlorosulfonic acid and 2-chloroimidazo[1,2-α]pyridine is 1.2 : 1, with ethylamine the yield increasing from 15.4% to above 70%; the optimized ammonolysis reaction time is 3 h and the reaction temperature is 27℃, with the acetonitrile yield increasing from 60.1% to above 79.6%.

实验结果表明，磺酰化反应的最佳反应时间为4 h，氯磺酸与2-氯咪唑并[1，-α]吡啶的用量比为1.2：1，加入三乙胺可将收率由15.4%提高到70%以上；氨解反应的最佳反应时间为3 h，反应温度为27 ℃，加入乙腈可将收率由60.1%提高到79.6%；方案经改进后，总反应时间缩短3 h，收率提高了5.5%。

The results indicate that improving temperature to reflux, using low polarity solvent as dispersion medium and proper molar ratio of tetrabutyl titanate to stearic acid can bring out good modification. The function of tetrabutyl titanate is to react with the surface hydroxyl groups and adsorbed H2O on the powder particles to produce new binding sites such as M—O—Ti—OC4H9and M—O—Ti—OH, which can easily react with the carboxylic acid. As temperature increases from room temperature to reflux temperature, the reactions between RCOO- and Ti change from coordinate bonds to covalent bonds, which makes the carbon chains of stearic acids more strongly bound with the powder particles surface.

研究结果表明，提高处理温度、适当增加复合改性剂中硬脂酸的量并选用极性弱的有机溶剂可达到比较理想的改性效果；钛酸四丁酯的作用是与粉体粒子表面的羟基以及吸附水反应产生偶联点，如M—O—Ti—OH，这些偶联点易于与羧酸反应；在低温时RCOO-与偶联点的Ti之间以配合物的形式发生作用，在回流温度下处理时，主要发生酯化反应，使硬脂酸更牢固地嫁接到粉体粒子表面，改性效果更好。

Through lots of tests, the new technology of preparing the polymeric ferric aluminum silicate sulfate by using the waste-acid of Ti02-industriy and the coal fly ash has been designed. The highest Al-acid stripping rate can be achieved by the waste sulfate acid under boiling degree for 1. 5h when the mass ratio between NaCl and Coal Fly ash is 0. 05:1, as well as that between Coal Fly ash and Waste Acid ratio is 1:10. By means of the oxidation-polymerized reaction under 40-50*C and normal pressure, using NaNCkas catalyst and air as oxidation, the polymeric ferric aluminum sulfate can be obtained. The poly-silicic acid is polymerized with soluble glass in the optimum conditions of pH=5-6 and the concentration of Si02 is about 3%. The inorganic high molecule coagulant of PFASS is synthesized with the poly-silicic acid into the solution of polymeric ferric aluminum sulfate.

本论文通过大量的试验，研究开发出了用粉煤灰及钛白废酸制取聚合硫酸硅酸铁铝的新工艺，其最佳工艺条件为：于沸点温度，以NaCl为助溶剂(NaCl与粉煤灰质量比为0.05：1)，以钛白废酸浸取粉煤灰(固液比为1：10)中的铝1.5小时，最大浸取率可达40％；经过滤洗涤后，调节滤液pH至2.0左右，以NANO_2为催化剂(NaNO_2用量为滤液中FeSO_4·7H_2O量的3％)，空气为氧化剂，于40-50℃进行常压催化氧化反应，制取聚合硫酸铁铝，催化氧化时间为2小时；将工业水玻璃稀释至3％左右，调节其pH于5-6，室温下制备活性聚硅酸；将活性聚硅酸与聚合硫酸铁铝按照一定比例复合，经熟化，即制得新型无机高分子混凝剂PFASS。

The results show that the sulfonation degree of the final pmducts under the condition of temperature 80~90℃, pH≥11 and reaction time 80-90 min is higher than that under other conditions.

研究表明，在pH＞11.5，温度为80~90℃和合适的时间内可以获得高磺化程度的三聚氰胺磺酸盐；在摩尔比F/M=4.0和S/M=1.0的反应体系中，磺化可同时发生在仲氮和叔氮原子上，两种结构之比约为2：1。

The spectra of X-ray diffract revealed that its crystal is B type and the value is about 18%, far lower than that of ordinary maize starch. With the method of chemistry modification, we modified the amylose starch with acetates. The result showed that the best reaction condition was at the ratio of 1:5.3 (glucose: acerbity), with MSA 1.5% catalyzer, at 75℃ for 3 h.

利用化学改性法对高直链玉米淀粉进行醋酸酯化改性，最佳反应条件为，淀粉葡萄糖基与酸的质量比1：5.3、催化剂甲磺酸用量为体系的1.5%、反应温度75℃、反应时间3 h，在此条件下可制备取代度为2.84的醋酸酯淀粉，比普通玉米淀粉高0.78。

Solid superacids SO~2-_4/TiO_2-Al_2O_3 were prepared and used to catalyze the esterfication of iso-octyl alcohol and by-products in oxidization reaction of durene,which were pretreated before esterifying reaction.

考察了催化剂用量、异辛醇与混合酸的质量比、反应时间等因素对酯化反应的影响，确定了较佳的反应工艺条件：m∶m∶m=0.01∶3.18∶1，反应时间为3 h，在此反应条件下预处理后的混合酸转化率可达到99.9%。

Through salification, esterification, hydrogenation, condensation, oxidation and halogenation etc.,LA can produce useful chemicals and new polymer materials.

同时它具有良好的反应活性，通过成盐、酯化、加氢、缩合、氧化和卤化等化学反应，可制得各种各样有用的化合物和新型高分子材料，因此乙酰丙酸有望成为一个基于生物质资源的新平台化合物。

In the case of decorative zinc electroplatings, a further enhancement of the appearance of such substrates in addition to the corrosion resistance imparted is achieved by the passivate film which ranges from a clear bright to a light blue bright appearance simulating that of a chromium deposit or alternatively, a clear light-yellow appearance simulating that obtained by use of prior art hexavalent chromium solutions.

可选择的治疗方法，可进一步遏制卤化物包括氟离子、氯化物和溴化物离子进一步增加了硬度钝化膜以及一个或多个兼容为实现高效润湿剂接触基板对待。现在的发明特别地可适用但是不限制在碱而产生酸非氰化物的锌的治疗使电解沉积传授对被对待的基体改良的腐蚀抵抗和装饰的外表。

The mainly conclusions in our research are as flowing: tungsten trioxide powders with 100 nm primary particle are obtained by spray drying,calcination and wet milling process, and an average size of quadric particle composed of agglomerated particles is 0.64 μm; tungtsen powders with 39 nm grain size and 60 -100 nm primary particle are produced directly from previous tungsten trioxide using one step reduction in hydrogen at 700℃, and an average size of quadric particle of tungsten powder is 2.91 μm; tungsten trioxide and copper tungstate compound powders with 100 nm - 200 nm primary particle are produced using ammonia metatungsten and copper nitrate as raw materials by spray drying,calcination and wet milling process;the compound powders are transformed completely into tungsten and copper compound powders by reduction in hydrogen at 700℃,in which tungsten grain size is 59 nm and copper grain size is 51 nm; primary particle size of compound powders is 80 - 120 nm,and an average size of agglomerated quadric particle is 1.86 μm; tungsten nitride powders with 35 nm grain size are prepared from tungsten trioxide powders by nitrogen treatment thoroughly in pure ammonia at 650℃, and an average size of agglomerated quadric particle is 0.64 μm in normal temperature.

研究结果表明：采用喷雾干燥—焙烧—球磨工艺可以制备出粒度约为100nm的WO_3粉体，它们在团聚后形成的二次颗粒平均粒度为0.64μm；采用一步直接氢还原方法可在700℃下从上述WO_3粉体制备出晶粒尺寸为39nm的、一次颗粒粒度为60-100nm的W粉体，其二次颗粒的平均粒度为2.91μm；以偏钨酸铵、硝酸铜为原料，采用喷雾干燥—焙烧—球磨工艺可制备出一次粒度为100-200nm的WO_3和CuWO_4混合粉体；采用氢还原工艺可在700℃下将这种粉体完全转变为W、Cu复合粉体，其中W的平均晶粒粒尺寸为59nm，Cu的平均晶粒尺寸为51nm；复合粉体的一次颗粒尺寸为80-120nm，在常温下团聚后形成的二次平均粒度为1.86μm；采用纯氨氮化工艺可以在650℃下由WO_3粉体制得WN，其晶粒尺度为35nm，在常温下团聚后的二次平均粒度为6.4μm。

In this report, half-esterification between these pendent hydroxyl groups of hydroxyl-PU and maleic anhydride could lead to new pendent groups, carboxylic groups. These highly polar carboxylic groups in the side chain of PU could play the role of internal emulsifier. They had self-dissociation ability in the water or were neutralized first by appropriate amount of base. Then, PU bearing carboxylic group could dispersed steadily in the water, named aqueous-based polyurethane dispersion.

在本论文中，利用原来亲油性Hydroxyl PU主链段上悬挂的羟基经由与琥珀酸酐的半酯化(Half-esterification Reaction)反应后，使PU在侧链上悬挂具有强极性的羧酸基，其可作为聚胺酯分子中的内乳化剂，羧酸基能在水相中自身解离产生离子或加入适量碱使之中合，使聚氨酯高分子能够稳定分散於水中，即所谓水性PU分散液(Aqueous-based Polyurethane Dispersion)。

For a big chunk of credit-card losses; the number of filings (and thus charge-off rates) would be rising again, whether

年美国个人破产法的一个改动使得破产登记急速下降，而后引起了信用卡大规模的亏损。

Eph. 4:23 And that you be renewed in the spirit of your mind

弗四23 而在你们心思的灵里得以更新