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acetic peroxide相关的网络例句

查询词典 acetic peroxide

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

The vinegar ' inoculates the acetic acid fungus , and the acetic acid fungus will oxidize the alcohol into the acetic acid, will establish the acidity in accordance with the working condition again, general acidity of acetic acid 2.0-3.0 about for pH, when reach this value in acidity, need to utilize the sterilization project to kill the acetic acid fungus , otherwise the acidity may be sourer and sourer !

醋」是接种醋酸菌,而醋酸菌会将酒精氧化成醋酸,再依生产条件设定酸度,一般醋酸的酸度为pH为2.0-3.0左右,当酸度达到此值时,便需利用杀菌工程将醋酸菌杀灭,不然酸度可能会愈来愈酸!

A novel method for determination of benzoyl peroxide with spectrophotometry was developed. Inclusion ratio of β cyclodextrin to dibenzoy peroxide and benzoic acid is obtained with spectrophotometry.The mechanism of the inclusion was studied,too. The results showed that β-CD react with dibenzoyl peroxide to form a 1:1 or 2:1 host-guest complex, with the apparent formation constants of 5.0× 10~2and 2.5× 10~4 , respectively.β-CD reacts with benzoic acid to form a 1:1 host-guest complex with the apparent formation constant of 6.9 × 10~2 after the dibenzoyl peroxide was reduced by hydroxyl ammonium chloride.

建立了用β环糊精测定过氧化苯甲酰的分光光度法,并测定了β环糊精与过氧化苯甲酰和苯甲酸的包结比,随着β-CD浓度的增大,可与BPO分别形成1:1或2:1的包容络合物,包结常数分别为5.0×10~2和2.5×10~4,与苯甲酸形成1:1的包容络合物,包结常数为6.9×10~2;由于包结物的吸光度值比过氧化苯甲酰的吸光度值大大增加,建立了一种当β-CD存在下,在水溶液中测定过氧化苯甲酰的方法。

The results show that:First, concentration of hydrogen peroxide have the most obvious influence to oil yield and carbon black yield,with the increase of concentration of hydrogen peroxide the oil yield first increase then decrease,when concentration of hydrogen peroxide is 8.19% or so,the oil yield reach to the biggest value, and with the increase of concentration of hydrogen peroxide carbon black yield decrese;Then,reaction time have more obvious influence to oil yield and carbon black yield,oil yield increase but carbon black yield decrease with the increase of reaction time;Thirdly,reaction tempreture have some influence to oil yield and carbon black yield,samely,oil yield increase but carbon black yield decrease with the increase of reaction tempreture;Finally,reaction pressure does almost no influence on oil yield and carbon black yield.

研究结果表明:过氧化氢质量浓度对产油率和炭黑产率的影响最为显著,产油率随过氧化氢质量浓度的提高先提高后降低,在过氧化氢质量浓度为8.19%左右时达到最大值,炭黑产率随过氧化氢质量浓度的提高而降低;反应时间对产油率和炭黑产率的影响也比较显著,产油率随反应时间的增加而提高,炭黑产率随反应时间的增加而降低;反应温度对产油率和炭黑产率也有一定的影响,产油率随反应温度的提高而相应地提高,炭黑产率随反应温度的提高而降低;在本文实验范围内,反应压力对产油率和炭黑产率基本上没有影响。

Propagules and buds of Elodea nuttallii and Potamogeton crispus were exposed to acetic acid concentrations from 1 to 16 mmol/L for 3 or 6 days, and then they were subsequently cultured in absence of acetic acid. Results showed P. crispus was more tolerant to acetic acid than E. nuttallii. At acetic acid concentration of 1 mmol/L, E.

研究了暴露于不同浓度的乙酸溶液后伊乐藻和菹草无性繁殖体的萌发和幼芽的生长状况。1mmol/L的乙酸能显著抑制伊乐藻幼芽的生长(P.05),但对其繁殖体的萌发无明显影响。

The models of auricular edema in mice by dimethyl benzene and increased permeability of celiac blood capillary by acetic acid were studied,the results showed that the petroleum ether and acetic ester fraction of fermentation product of Calvatia gigantea could inhibit ear edema;acetic ester and n-Butanol fraction of fermentation product could reduce the permeability of celiac blood capillary by acetic acid.

大秃马勃Calvatia gigantea发酵液的石油醚、乙酸乙酯和正丁醇提取物进行二甲苯诱导小鼠耳廓急性炎症和醋酸所致小鼠腹腔毛细血管通透性实验,结果表明大秃马勃Calvatia gigantea发酵液石油醚提取物处理组、乙酸乙酯提取物处理组对二甲苯诱导小鼠耳肿胀具有明显的抑制作用;大秃马勃Calvatia gigantea发酵液乙酸乙酯提取物处理组、正丁醇提取物处理组对醋酸所致小鼠腹腔毛细血管通透性具有明显的抑制作用。

The results show that the decalescence of catalyst bed affects the process of hydrogen peroxide catalytic decomposition greatly. If the catalyst bed is preheated or made up of materials with low thermal conductivity, that influence can be depressed. At the same time, the response characteristic of catalyst bed and the efficiency of catalytic decomposition can be improved. The low frequency pressure instability of catalyst bed occurs because of the coupling of catalytic decomposition and supplying. The decomposition plane pushes all the way through the catalyst bed during pressure oscillations, causing unreacted liquid hydrogen peroxide to be exhausted from the bed and leading to the appearance of liquid hydrogen peroxide channeling. Consequently, how to prevent or at least limit this channeling is the key to eliminate the pressure instability of catalyst bed. It was found that adding clapboard to the catalyst bed can depress the pressure instability efficiently.

结果表明催化剂床及催化剂的吸热对过氧化氢分解过程影响很大,对催化剂床进行预热或采用热导率低的材料制造催化剂床等措施,可以降低催化剂床壁面吸热对催化分解过程的影响,提高催化剂床的响应特性和催化分解效率;催化剂床的低频不稳定是催化分解过程与供应系统耦合产生的,催化剂床气体界面的波动过程中,液体过氧化氢穿透催化剂床形成过氧化氢液体通道,过氧化氢液体通道的产生和扩大是催化剂床不稳定的主要原因,也是消除催化剂床不稳定的关键,试验中在催化剂床内加入分流板成功地抑制了催化剂床的低频不稳定。

The results show that a little amount of heteropolymolybdovanadophosphate can remarkably speed the degradation, the best conditions of the oxidative degradation of chitosan with hydrogen peroxide catalized by heteropolymolybdovanadophosphate in homogeneous condition are as follows: the ratio of catalyst and chitosan is 1 to 10, concentration of hydrogen peroxide is 0.15%, the temperature is 80℃, reaction time is 2h. 0.2g chitosan was degraded under the best condition and the molecular weight by viscometry was degraded from 1460000 to 7812. then water-soluble chitosan was obtained by this method; The heterogeneous method is a high efficient way, the best condition of this method are as follows: the ratio of catalyst and chitosan is 2 to 100, the volume of 30% hydrogen peroxide is about 3mL, the temperature is 90℃, reaction time is 5min~30min.

研究结果表明,适量磷钼钒的存在可显著加速壳聚糖的降解,磷钼钒催化过氧化氢均相氧化降解壳聚糖的适宜反应条件是:催化剂与壳聚糖的质量比为1∶10、过氧化氢百分浓度为0.15%、反应温度为80℃、反应时间为2h,在此条件下对0.2g溶解在100 mL 0.5%稀醋酸中的壳聚糖进行降解,可使壳聚糖的粘均分子量由原来的146万下降到七千多(7812),成为水溶性低分子量壳聚糖,从而达到应用的要求;在异相条件下以磷钼钒为催化剂催化过氧化氢氧化降解壳聚糖是一种高效快速的方法,此法降解壳聚糖的最佳反应条件是:催化剂与壳聚糖的质量比为2∶100;30%过氧化氢的用量为3mL左右;反应温度为90℃、反应时间为5min~30min。

In the three systems, system realizes the crosslinking of PVC bases on the peroxide crosslinking mechanism, the tensile strength of crosslinked PVC has been improved somewhat, the IR spectrum of gel demonstrates that there are characteristic absorption peaks of n-alcohol that belongs to ethanol amine and benzenoid group. From the analysis of gel structure , deduces that the mechanism of crosslinking reaction: under the initiations of peroxide and high temperature, PVC yields macromolecules free radicals, at the same time , styrene"s polymerization and grafting onto PVC takes place, at last the system forms crosslinking structure through coupling between radicals; confirms that triethanol amine can absorb HC1 produced by degradation of PVC, so improves the crosslinking efficiency of peroxide, decreases the HCl"s promotion for PVC"s degradation; deduces that triethanol amine can activate the PVC macromolecules and prolong the free radicals" life-time of PVC macromolecules; the effect to the PVC macromolecule makes styrenes graft reaction easy, and thus improves the crosslinking efficiency.

三种体系中三乙醇胺/过氧化二异丙苯/苯乙烯体系基于过氧化物交联机理实现了聚氯乙烯的交联,聚氯乙烯交联后拉伸强度有一定提高,凝胶红外光谱分析证实了凝胶结构中含有乙醇胺的伯醇基团特征吸收和苯环的特征吸收,由凝胶结构分析,推断出交联反应的机理:聚氯乙烯在过氧化物和热作用下产生大分子自由基,苯乙烯在过氧化物和大分子自由基的作用下发生聚合和接枝反应,最终通过自由基之间的偶合产生交联;证实三乙醇胺可以吸收聚氯乙烯分解产生的HCl,提高了过氧化物的交联效率,消弱了HCl对聚氯乙烯降解的促进作用;推断三乙醇胺可以活化聚氯乙烯大分子并有可能使聚氯乙烯大分子自由基存在的时间得以延长,对聚氯乙烯大分子的作用使苯乙烯的接枝反应易于发生,从而提高了交联效率。

The experimental results indicated that under the steady operating conditions, the ignition timing of the base fuel (PRF90-90% iso-octane+10% n- heptane), which is equivalent to RON 90, delayed and the peak value of the heat release rate was low compared to the base fuel with single additive (Ditert-butyl peroxide-DTBP, Dicumyl peroxide-DCP, Tert-butyl hydroperoxide-TBHP, Tert-butyl cumyl peroxide -TBCP or Cumene hydroperoxide-CPO) which advanced ignition timing and increased the peak of the heat release rate obviously.

试验结果分析表明,在HCCI发动机燃烧稳定工况下,没有添加剂的基础燃料记作PRF90(为90%异辛烷与10%正庚烷的混合,相当于90号汽油)着火滞后,燃烧放热率峰值低,而混有单一添加剂(Ditert-butyl peroxide-DTBP、Dicumyl peroxide-DCP、Tert-butyl hydroperoxide-TBHP、Tert-butyl cumyl peroxide-TBCP或Cumene hydroperoxide-CPO)的基础燃料则着火明显提前,燃烧放热峰值升高。

Abnormal phenomenon of BOD5 measurement of hydrogen peroxide bleaching wastewater was discussed and it was caused by the oxygen generated from decomposition of residual hydrogen peroxide in wastewater. Sodium sulfite is proposed to use for deoxidizing the residual hydrogen peroxide and the abnormal phenomenon can be eliminated effectively.

摘 要:探讨了H2O2漂白废水BOD5测定过程中的异常现象,发现废水中残余H2O2分解产生氧气是导致BOD5测定产生异常的原因,提出了加入亚硫酸钠(Na2SO3)还原废水中的残余H2O2的方法,可有效消除BOD5测定过程中的异常现象。

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