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The company has two production¨×biopsy device, the three modified PTT and PTT fibers,¨×fiber production line, a set of three monomers (isophthalic acid, 5 - sodium) production unit, a four-monomer production line with annual production of 15,000 tons slice¨×composite and PTT fibers, staple¨×compound, PTT modified fiber 15,000 tons and 1,000 tons of the four monomers, three monomers 1200 tons, brominated flame retardants EPS with the capacity of 3000 tons .

公司拥有两套波斯伦切片生产装置,三条PTT及改性PTT纤维、波斯伦纤维生产线,一套三单体(间苯二甲酸,5-磺酸钠)生产装置,一套四单体生产线,具有年生产波斯伦复合切片15000吨和PTT纤维、波斯伦复合短纤、PTT改性纤维15000吨及四单体1000吨,三单体1200吨、溴系EPS用阻燃剂3000吨的能力。

Fourteen new pyrethroids containing isoxazole were designed and synthesized from 4-isopropyl-3-substituted phenyl-5-hydroxyl isoxazoles as major material, whose structures were also characterized by IR, 1H NMR and elemental analysis.

以4-异丙基-3-取代苯基-5-羟基异噁唑和3-苯氧基苄基溴为原料,三乙胺为缚酸剂,设计并合成了14个未见报道的4-异丙基-3-取代苯基-5-异噁唑基-(3'-苯氧基)苄基醚。通过红外光谱、核磁共振、元素分析等手段,确证了它们的化学结构。

The results show that the optimal parameters of esterification are as follows: 4% of SO42-/ZrO2, molar ratio of methanol to litsea cubeba kernel oil 101, 68 ℃ of reaction temperature and 4 h of reaction time, the acid value decreases to 2.52 mg/g. Compared with the traditional acidic-catalyzed method, this method has the advantages of no acid proof equipment, easy to recycle catalyst and no acidic waste water emission. The optimal parameters of transesterification are as follows: 25 ℃ of reaction temperature, 0.5% of hexadecyl-trimethyl-ammonium bromide, 1% of NaOH, molar ratio of methanol to the oil 61 and 15 min of reaction time. The ester exchanging rate is 97.6%. This method adopts phase transfer catalyst and produces industry prospect, which has many advantages such as energy-saving and time-saving under room temperature.

研究结果表明,固体酸SO42-/ZrO2催化酯化反应的最佳条件为:油重4%的SO42-/ZrO2,醇油摩尔比为101,温度为68 ℃,反应时间为4 h,原油酸值降到2.52 mg/g;该法相对浓硫酸催化酯化法具有不需耐酸设备、催化剂易回收、无废水排放等优点;相转移催化酯交换反应的最佳条件为:温度为 25 ℃,0.5%的十六烷基三甲基溴化铵,油重1%的NaOH,醇油摩尔比为61,反应15 min,原油酯交换率达到97.6%;采用相转移催化技术,反应在常温下进行,大大减少了能耗,缩短了反应时间,具有的产业化前景。

This investigation was prepared MCM-41 catalyst films on silicon wafer in ammonia media, using tetraethyl orthosilicate as a precursor and cetyltrimethylammonium bromide as a surfactant.

中文摘要本研究以四乙基氧矽溶液为矽酸盐的来源,溴化十六烷基三甲基铵盐为界面活性剂,在氨水的环境下,制备MCM-41触媒薄膜於矽晶片上。

The synthetic route starts from penicillin G, peroxyacetic acid(8.5%) as Oxidizing Agent to get penicillin G sulfoxide; esterifided with p-nitrobenzyl bromine to synthesize penicillin G sulfoxide ester; we synthesize 3-exomethylenecepham sulfoxide ester with phthalimide potassium and 4A molecular sieve as acid scavenger to open the ring, SnCl_4 as catalyzation to close the ring. The yield is over 60%.

本研究采用的合成路线为:以青霉素G钾盐为原料,选用工业过氧化氢制备的过氧乙酸(22.3%)稀释至8.5%为氧化剂,氧化得青霉素亚砜;采用对硝基溴苄为酯化试剂,制备青霉素亚砜酯;以NCP(N-氯代邻苯二甲酰亚胺)为开环试剂,酞酰亚胺钾和4A型分子筛为酸清除剂,顺利开环;再经无水SnCl_4催化闭环得3-环外亚甲基头孢亚砜酯,最终产率在60%以上。

Improved synthesis of 2-(4-bromomethylphenyl)propionic acid,the key intermediate for loxoprofen sodium,was investigated.

对洛索洛芬钠的关键中间体2-(4-溴甲基苯基)丙酸的合成工艺进行了改进研究。

Aim To investigate a new synthetic method of 2-(4-bromomethylpheny1)propionic acid,the key intermediate of loxoprofen sodium.

摘要目的研究消炎镇痛药洛索洛芬钠的关键中间体2-4-溴甲基)苯基丙酸的合成新方法。

Results and conclusion The structure of 2-(4-bromomethylphenyl) propionic acid was identified by 1H-NMR, FT-IR and MS analysis. The target compound was prepared in an overall yield of 38%.

结果与结论关键中间体2-(4-溴甲基)苯基丙酸的结构经1H-NMR、FT-IR、MS谱确证,目标化合物的总收率为38%。

Results and conclusion The structure of 2-(4-bromomethylpheny1)propionic acid was identified by1H-NMR, FT-IR and MS analysis. The target compound was prepared in an overall yield of 38%.

结果与结论关键中间体2-4-溴甲基)苯基丙酸的结构经1H-NMR、FT-IR、MS谱确证,目标化合物的总收率为38%。

A HPLC method for determination of phenylephrine hydrochloride, paracetamol, caffeine anhydrous ,salicylamide and brompheniramine maleate in Liufenkamin tablets was established.

建立了HPLC法测定柳酚咖敏片中盐酸去氧肾上腺素、对乙酰氨基酚、无水咖啡因、水杨酰胺、马来酸溴苯那敏的含量。

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