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乙基化

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CA-CTSs including N,O-carboxymethyl chitosan,N,O-1-carboxyethyl chitosan (N,O-1-CEC),N,O-2-carboxyethyl chltosan(N,O-2-CEC),N-carboxymethyl chitosan and N-1-carboxyethyl chitosan(N-1-CEC) are quaternized using active quaternary salts prepared in laboratory.5 series including 25 kinds amphoteric chitosans characterized with polymeric ampholyte,in which 24 kinds are synthesized firstly,are obtained, 2-Hydroxypropyl dimethylbenzyl ammonium N,O-(1-carboxyethyl) chitosan chloride (GDMBA-N,O-1-CEC) is hydrolyzed into serial low molecular weight GDMBA-N, O-1-CEC with acid as catalyst and microwave as assistant instrumentality innovately.

以合成的活性季铵盐改性了N,O-羧甲基壳聚糖、N,O-1-羧乙基壳聚糖(N,O-1-CEC)、N,O-2-羧乙基壳聚糖(N,O-2-CEC)、N-羧甲基壳聚糖和N-1-羧乙基壳聚糖(N-1-CEC)等羧烷基壳聚糖,得到5个系列25种具有两性高分子电解质特征的新季铵化羧烷基壳聚糖,其中24种为首次合成;创新提出以微波辅助酸催化的方法催化2-羟丙基二甲基苄基-N,O-(1-羧乙基)壳聚糖氯化铵(GDMBA-N,O-1-CEC)水解,得到了低分子量的GDMBA-N,O-1-CEC。

FTIR,X-ray,TMA and SEM were used to study and characterize the microview struc-ture and thermoplasticity of cyanoethylated wood.

利用FTIR、X-ray、TMA、SEM等对氰乙基化木材的微观结构和热塑性进行了研究和表征。

Wood ; Cyanoethylation ; Chemical modification ; Thermoplasticity

木材;氰乙基化;化学改性;热塑性

The 6- cyano-1, 1 (1, 3- dioxypropylidene)-7-(carbomethoxyl group- methyl - 5- oxo-Delt6 (8)- tetrahydrochysene indolizine and haloethane reacts with each other for ethylization with existence of alkali and organic solution with or without phase transversion catalyst, and produces mentioned product.

本发明在相转移催化剂或无相转移催化剂存在下,6-氰基-1,1-(1,3-亚丙二氧基)-7-(甲氧羰基-甲基-5-氧代-Δ6(8)-四氢中氮茚类化合物与卤代乙烷在碱和有机溶剂的存在下进行乙基化反应即得6-氰基-1,1-(1,3-亚丙二氧基)-7-1′-(烷氧羰基-丙基-5-氧代-Δ6(8)-四氢中氮茚类化合物。

In this Ph. D. dissertation, reverse microemulsion method was fully used infabricating and modifying polyacrylamide with functional and high-relative moleculeweight. The copolymerization of 2-acrylamide-2-methylpxopanesulfonic acid, fluorescent monomer 4-methoxy-N-(2-N\', N\'-dimethylamino ethyl)naphthalimide alkyl chloride quaternary ammonium salt, fluorescentmonomer 4-(N\'-methyl-1-piperazinylallyl)-N-butyl-naphthalimide chloride quaternaryammonium salt, Cationic monomer dimethylethylammonium bromide and hydrophobical monomer octadecylacrylate with acrylamide and properties of the copolymers werestudied. The interaction between five polymers and Al_2O_3(012) crystal surface have beensimulated by Materials Studio 3.0 program package, binding energies and non-bondinteraction energies and deformation energies have also been acquired.

本文以制备具有较高相对分子质量和功能型PAM为研究目的,将反相微乳液法运用到其制备及改性的有关环节,通过反相微乳液聚合工艺,将几种改性功能单体2-丙烯酰胺基-2-甲基-丙磺酸、荧光单体2-(4-甲氧基-1,8-萘二甲酰亚胺基)-乙基二甲基烯丙基氯化铵、荧光单体4-(N'-甲基-1-哌嗪基)-N-丁基-1,8-萘烯丙氯季铵盐、阳离子单体丙烯酰氧乙基-二甲基-乙基溴化铵和疏水单体丙烯酸十八酯与AM共聚,制备AMPS改性PAM、荧光示踪型PAM、阳离子单体DMB改性PAM和OA改性PAM等四类不同功能单体改性PAM,并研究其应用性能。

Total mercury and methyl mercury concentrations were analyzed by cold vapor atomic fluorescence spectrometry and aqueous phase ethylation,GC separation,and CVAFS detection.

2006年1~12月,每月采集乌江流域梯级水库入出库河流水样,用两次金汞齐-冷原子荧光光谱法和蒸馏-乙基化结合GCCVAFS法测定了水中总汞和甲基汞的浓度。

Three cationic surfactants, N -dodecyl- N -(2-hydroxyethyl)- N , N -dimethylammonium bromide, N -tetradecyl- N -(2-hydroxyethyl)- N , N -dimethylammonium bromide and N -cetyl- N -(2-hydroxyethyl)- N , N - dimethylammonium bromide have been synthesized.

合成了 N -十二烷基- N -(2-羟乙基)- N , N -二甲基溴化铵、 N -十四烷基- N -(2-羟乙基)- N , N -二甲基溴化铵和 N -十六烷基- N -(2-羟乙基)- N , N -二甲基溴化铵等3个季铵盐阳离子表面活性剂。

The ethylated wood of weight percent gain about 6-23 can resoluted at 80℃ in bisphenolA-ethyl acetate solution. In the presence of NaOH, these solution can reacted with epichlorohydrin toproduce new epoxy resin adhesive with wood as backbone.

发现增重率6~23的乙基化木材可在温和条件(80℃)下溶解于双酚A-乙酸乙酯溶液中,形成的溶液可用于制备以木材主成份为骨架的新型环氧树脂胶粘剂。

Ethylated wood ; Bisphenol A ; Epoxy resin ; Adhesive

乙基化木材;双酚A ;环氧树脂;胶粘剂

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。

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