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硝酸钠

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The lipolytic and proteolytic activities of the 8 strains by the special Media were studied. It showed that Staphylococcus warneri, Staphylococcus saprophyticus and Lactobacillus plantarum had the proteolytic activity.

其中,松鼠葡萄球菌、木糖葡萄球菌和腐生葡萄球菌的耐盐性最强,在NaCl浓度为15%时,仍能生长;乳酸菌中,戊糖片球菌的耐盐性要高于植物乳杆菌。8株优势菌对亚硝酸盐均不敏感,在亚硝酸钠浓度为0.15%时,生长良好。

MethodsIn the solvent of 1 mol/L NaOH, using the reaction of the water-soluble phenolic acidity in Radix Salviae Miltiorrhizae and the NaNO_2-Al(NO_3)_3, the total components of water-soluble phenolic acidity in Radix Salviae Miltiorrhizae injections and drip solution(calculated with protocatechualdehyde) were determined by colorimetric s...

方法利用丹参中水溶性酚酸类成分与亚硝酸钠和硝酸铝溶液在碱性条件下的显色反应,比色法测定该两种制剂中水溶性酚酸的总量。结果原儿茶醛在3.336~14.46mg/L范围内呈良好的线性关系,回归方程为:A=0.02777C+0.01279(r=0.9996),加样平均回收率为100.8%,RSD为0.96%。结论该法简便快速,结果准确,重现性好,可用于该制剂的质量控制。

The floatation separation behaviuor of Pd (superscript 2+) by KBr-cetyl pyridinium bromide system in the presence of NaNO3 and the conditions for the separation of Pd (superscript 2+) from other metal ions were studied.

研究了硝酸钠存在下,溴化十六烷基吡啶-溴化钾体系浮选分离钯的行为及与一些金属离子分离的条件。

The floatation rate of Pd (superscript 2+) reaches 100% when the concentrations of NaNO3, KBr and cetyl pyridinium bromide in solution are 0.05 g/mL, 3.0×10^(-2) mol/L, 5.0×10^(-4) mol/L(pH 4.0), respectively. Pd (superscript 2+) could be separated from Ru (superscript 3+), Al (superscript 3+), Cr (superscript 3+), Ni (superscript 2+), Ga (superscript 3+), Fe (superscript 3+) and Zn (superscript 2+) by floatation quantiatively. A method of flotation separation and enrichment of Pd (superscript 2+) was established.

当溶液中硝酸钠、溴化钾、溴化十六烷基吡啶的浓度分别为0.05 g/mL,3.0×10^(-2)mol/L,5.0×10^(-4)mol/L,在pH 4.0时,Pd(上标 2+)的浮选率达到100%,Pd(上标 2+)可与Ru(上标 3+),Al(上标 3+),Cr(上标 3+),Ni(上标 2+),Ga(上标 3+),Fe(上标 3+),Zn(上标 2+)定量分离,据此建立了浮选分离和富集Pd(上标 2+)的新方法。

Comparison of inhibitors for anti-polymerization of isoprene, such as NaNO2, p-tert-butylcatechol, N-methyl pyrrolidone and paradioxybenzene, was carried out using polymer segregation process and the results showed that TBC was the best one.

采用聚合物离析法比较了亚硝酸钠(NaNO2)、对叔丁基邻苯二酚、N-甲基吡咯烷酮、对苯二酚对异戊二烯的阻聚效果,发现TBC阻聚效果最好。

METHODS Ammonium sulfamate and 1 mol·L -1 hydrochloric acid were added to the benzalkonium bromide solution,which was a reference solution.

取浓度相同的两份苯扎溴铵消毒液,一份加入氨基磺酸铵和 1mol·L-1盐酸作为参比液,在 35 4 6nm测定亚硝酸钠的ΔA。

The surface of natural scale graphite was modified by wet chemical method using sulfanilic acid and sodium nitrite as raw materials,which could remarkably elevate the hydrophilicity of natural scale graphite.

以对氨基苯磺酸、亚硝酸钠为原料,对天然石墨鳞片表面进行了接枝改性处理,显著提高了天然石墨鳞片的亲水性。

A model system simulated the stomach conditions (pH 3.13-3.28, 37℃) was used to study the blocking effect of the Chinese gooseberry juice on the morpholine nitrosation.

在37℃,pH3.13-3.28,吗啉及亚硝酸钠浓度各为2.0mM,经0.5、1.0及2.0小时,其阻断率分别为98.54%,96.43%及97.99%;此结果优于柠檬汁,后者阻断率分别为84.55%,34.79%及37.43%;并优于含同样量的抗坏血酸溶液,其结果分别为97.56%、89.48%及65.62%。

Methods: 2ethyl aniline was used as starting material of the synthesis and was processed by acetic anhydride acylation, strong nitric acid nitraction at low temperature, and desacyl synthesis to produce 2ethyl5nitro aniline. The product was then synthesized to 3methyl6nitro1Hindazole by using ringclosing reaction in the presence of NaNO2, and then ethylated to obtain 2,3diethyl6 nitro2Hindazole. The latter compound was then reduced by SnCl2/Hcl to get target compound 2,3diethyl6nitro2Hindazole.

以2乙基苯胺为原料经醋酐酰化、浓硝酸低温硝化及去酰基保护合成2乙基5硝基苯胺,后用亚硝酸钠关环得3甲基6硝基1H吲唑,经硫酸二甲酯甲基化得2,3二甲基6硝基2H吲唑,最后用氯化亚锡将其还原得到目标产物,通过1H NMR确定结构与目标产物一致。

Methods: 2-ethyl aniline was used as starting material of the synthesis and was processed by acetic anhydride acylation, strong nitric acid nitraction at low temperature, and desacyl synthesis to produce 2-ethyl-5-nitro aniline. The product was then synthesized to 3-methyl-6-nitro-lH-indazole by using ring-closing reaction in the presence of NaNO2, and then ethylated to obtain 2, 3-diethyl-6- nitro-2H-indazole. The latter compound was then reduced by SnC12/Hcl to get target compound 2, 3-diethyl-6-nitro-2H-indazole.

以2-乙基苯胺为原料经醋酐酰化、浓硝酸低温硝化及去酰基保护合成2-乙基-5-硝基苯胺,后用亚硝酸钠关环得3-甲基-6-硝基-1H-吲唑,经硫酸二甲酯甲基化得2,3-二甲基-6-硝基-2H-吲唑,最后用氯化亚锡将其还原得到目标产物,通过1HNMR确定结构与目标产物一致。

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