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sodium hydroxide相关的网络例句

查询词典 sodium hydroxide

与 sodium hydroxide 相关的网络例句 [注:此内容来源于网络,仅供参考]

The solution is Cap.59 out of monlchamus, emulsibility deink de-fluxing COTS use gasoline, 5% aqueous solution of sodium hydroxide and pumice mixed abrosive, at the same time on the roll is also the processing to be done.

处置方法是铲掉乳化不朱,不兵脱不朱胶辊用汽油洗不污,用5%的氢氧化钠火溶液与浮石粉搀和打磨,同时差金属辊也给怠工相答办理。

Spiral Spirobifluorene acetylated is oxidated by m-chloroperoxybenzoic acid and hydrolyzed by sodium hydroxide ,obtaining 2,2 '- dihydroxy -9,9'- spiral Spirobifluorene .Through nitrification,Reduced by hydrazine hydrate, we may get the 2,2 '- diamino -9,9'- spiral Spirobifluorene which are characterizated by IR, 1H-NMR !

L-酒石酸和乙醇酯化得到酒石酸二乙酯,将保护羧基保护起来,然后用碘甲烷在2,3-位上两个甲基,得到2,3-二甲氧基-酒石酸二乙酯,再用氢氧化钠将其水解,得到2,3-二甲氧基-酒石酸,用五氯化磷将羧基酰化,得到2,3-二甲氧基- 1,4-丁二酰氯,经过与二环己胺反应,得到拆分配体2,3-二甲氧基–N,N,N',N'-四环己丁二酰胺。

Aromatic dinitro compounds were reduced irrespective of the presence or absence of β-CD in sodium hydroxide solution, which revealed particularity of aromatic dinitro compounds.These reactions have advantages below over past research results of aromatic nitro compounds:(1) The synthetic method using water as the reaction medium may

这些反应与过去人们对硝基化合物反应的研究结果相比,具有以下优点:(1)反应在水介质中进行,避免使用辅助有机溶剂和金属催化剂,是环境友好的清洁反应,比较符合绿色化学的发展要求;(2)反应中所用的β-环糊精无毒,价廉,易得

The research results obtained showed that, sulphonating extent of synthetic starch xanthate was high, under room temperature, time 120 minutes, mol ratio of starch, sodium hydroxide and disulphide being 10 : 4 : 3, It was to say that sulphur content and supplent extent were high.

研究结果表明,原料配比为:淀粉:NaOH:CS_2为10:4:3,反应温度为室温,黄化反应时间为120min,合成DX的黄原酸化程度高,即产品含硫量和取代度高。

Thiol groups were good to be used in functionalizing gold nanoparticles, and ester bond formation and breakage played the major role in this research. Thioctic acid and 11-mercapto-1-undecanol were used to functionalize the gold nanoparticles and form ester bond by using the carboxylic acid group on thioctic acid and the hydroxyl group on 11-mercapto-1-undecanol. Concentrated sulfuric acid was used to be the catalyst in this reaction, and sodium hydroxide was added for the proceeding of the reverse reaction.

硫醇官能基在金奈米粒子的修饰有很好的效果,利用带有硫醇官能基之tioctic acid 与11-mercapto-1-undecanol (11-MUDO)分子修饰在金奈米粒子上,并使TA上之羧基和11-MUDO上之羟基脱水生成酯化键,浓硫酸则是反应中的催化剂,而氢氧化钠则可促使系统进行逆反应。

Purine derivatives was confected tosolution of 3*10~(-5) g/mL by sodium hydroxide solution(1 weight% in water), and thenmeasured the diameter of fungistatic circle.

将实验所得嘌呤化合物溶解于质量浓度为1%的氢氧化钠水溶液中,通过测量抑菌圈直径的大小来测试了所有所得嘌呤衍生物的抑菌活性。

Furoin was synthesized from furol with VB1 as the catalyst,which was then reacted with acetyl chloride, lauroyl chloride ,benzoyl chloride,α-furoyl chloride and 3-α-furyl acryloyl chloride,respectively;corresponding monoester compounds of furoin were synthesized in THF in the presence of sodium hydroxide under reflux.

以糠醛为基础原料,经维生素B1催化合成糠偶姻,再由糠偶姻分别和乙酰氯、月桂酰氯、苯甲酰氯、α-呋喃甲酰氯和3-α-呋喃烯丙酰氯反应,在NaOH/无水THF体系中,于水浴回流条件下合成了相对应的糠偶姻单酯类化合物。

Furyl 3 buten 2 one is synthesized from furfural and acetone in water sodium hydroxide medium.

以呋喃醛为原料,在水-氢氧化钠体系中合成了糠叉丙酮,探讨了丙酮用量,氢氧化钠浓度对反应的影

Glyoxylic acid was prepared by reaction of sodium hydroxide surplus with methyl dichloroacetate in methanol solution via neutralization of filtrate with 50 percentage sulfuric acid to pH 2~3 and hydrolyzation after separation of salts.

二氯乙酸甲酯和过量的氢氧化钠在甲醇溶液中反应,滤出氯化钠后,直接加入适量的 5 0 %的硫酸调 pH值为 2~ 3,滤出硫酸钠,蒸馏回收甲醇,水解、浓缩,得到不含乙二醛的 4 0 %乙醛酸溶液。

The molecular sieve is prepared in the steps: at the room temperature, hexadecyl trimethyl ammonium bromide is mixed and dissolved with the sodium hydroxide, and is added with TEOS in dropping way, and simultaneously added with Me metal salt water solution and lanthanum nitrate solution in dropping way; the pH value of the mixed solution is adjusted by acetic acid to be 10 to 11, and is mixed for 1 to 2 hours after being stabilized; the sol is moved into a polyfluortetraethylene bottle to be heated and crystallized for 2 days in the oven at the temperature of 100 DEG C; after filtering, washing and drying for nights, and being calcined in a muffle at the temperature of 550 DEG C for 3 to 7 hours, the dual-metal-atom improved MCM-41 mesoporous molecular sieve is obtained.

该分子筛的制备为室温下,将十六烷基三甲基溴化铵和氢氧化钠混合溶解,搅拌并滴加入TEOS,同时滴加入Me金属盐水溶液和硝酸镧溶液并搅拌,用乙酸调节pH值至10~11,稳定后搅拌1~2小时,溶胶转入聚四氟乙烯瓶中在100℃下烘箱水热晶化2天,经过滤、洗涤、干燥过夜,马弗炉550℃焙烧3-7h,得双金属原子改性MCM-41介孔分子筛产品。

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