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The results showed that the effect of the electrostatic field is very different from the traditional electrically assisted photocatalysis.

结果表明,静电场对光催化的影响与通常的电助光催化不同,电场强度越高,光催化效率反而降低。

The degradation experiments of benzamide by photocatalysis and electrically assisted photocatalysis demonstrated that the extra electric field had the obvious assistant effect on photocatalysis and the benzamide degradation rate by EAP was much higher than that by photocatalysis. When the electrode potential of photocatalyst was -0.05V/SCE, the removal efficiency of benzamide could be 95% in 120min.

苯甲酰胺降解试验表明,外加电场对光催化氧化技术具有较强的辅助作用,电助光催化氧化技术的处理效率远远高于光催化氧化技术,当施加的电极电位为-0.05V时,苯甲酰胺在120min时的去除率可达95%。

Study K2-xLa2Ti3-xVxO10 serves as smooth activator to be more than 290 Nm ray radiation to fall in wavelengh, splitting decomposition aquatic product gives birth to hydric smooth catalysis active, discuss V5+ to adulterate the influence of active of smooth catalysis of K2La2Ti3O10 of mine of calcic to layer shape titanium.

探究K2-xLa2Ti3-xVxO10作为光催化剂在波长大于290 nm光辐射下,裂解水产生氢气的光催化活性,并讨论V5+掺杂对层状钙钛矿K2La2Ti3O10光催化活性的影响。

MIPC was photocatalytically transformed to 3,4-dihydroxyl hypnone, 2-iso-butyl phenol and acetic acid, and mineralized ultimately in oxygenated TiO2 slurries. The photocatalytic degradation processed according to first order kinetics with the apparent rate constant depending on initial concentration, light intensity and the amount of catalyst. The amount of catalyst had an optimum value (0.5g/L). The apparent rate was inversely proportional to square root of the initial concentration approximately.

MIPC能被光催化转化成3,4-二羟基苯乙酮、2-异丁基苯酚和乙酸等产物并最终被矿化,MIPC的光催化反应过程符合一级动力学规律,其表观速率常数与MIPC的起始浓度、TiO2量和光强等因素有关,MIPC降解的反应速率与入射光强成正比,与MIPC初始浓度的平方根成反比。

The phosphotungstic acid was used to degrade the methyl orange solution with ultraviolet radiation.

以磷钨酸为光催化剂,在紫外灯照射下,对甲基橙溶液进行光催化降解,考察了几种阴阳离子对磷钨酸光催化降解甲基橙溶液的影响。

The result of the test showed that the fed quantity of TiO2 was 1.25 mg/mL,the photocatalytic degradation of the pyridine was in conformity with the first order kinetic equation,the feeding of 0.2%H2O2 obviously increased the degradation rate of the pyridine and the nitrogen in the pyridine converted into ammonia nitrogen;the pearlite-loaded TiO2 had the same catalytic effect as that of powered TiO2 and was easy to recover and reutilize.

以钛酸四丁酯水解法制备TiO2,采用溶胶一凝胶法在膨胀珍珠岩上负载TiO2,在UV-TiO2体系中对水中吡啶进行光催化降解,结果表明:TiO2加入量为1.25mg/mL,吡啶的光催化降解符合一级动力学方程,加入0.2%H2O2可明显加快吡啶的降解速度,吡啶中氮转化为氨氮,珍珠岩负载型TiO2与粉末TiO2具有相同的催化效能,且便于回收和重复使用。

Photocatalytic activity of the catalyst was investigated for microwave assisted photocataqlytic degradation of acid mordant red B dye in aqueous solution.

通过可溶性染料酸性媒介红 B的微波辅助光催化氧化反应,考察了其光催化活性;并研究了复合催化剂的煅烧温度、铈掺杂量和涂覆次数等对催化活性的影响。

The result show that the N elements curbed the transition from anatase phase to rutile phase , Doped-N was in the structure of the TiO2 as the form of Ti-O-N and formed a new bond energy level;N-doped changed the paramagnetic of the characteristics. The paramagnetic resonance spectrum of TiO2 showed anisotropic and showed hyperfine splitting, The Lande factor of Ti3 + combined with the N is 1.956. UV-Vis absorption spectra showed that the photocatalytic ability of photocatalyst TiO2-xNx to expand to the visible region, the sample (3.84wt %) has the highest photo catalytic activity, the adsorption edge extend to 520nm and degradation is 55.54% under the visible light for 1.5h.

研究结果显示,N元素抑制了锐钛矿相向金红石相的转变,阻止了晶粒的长大,掺杂的N元素以O-Ti-N的形式存在于光催化剂结构中,形成了新的能级结构;N掺杂改变了催化剂的顺磁特征,使TiO2的顺磁共振谱线呈现各向异性,发生了超精细分裂,其中g2=1.956,是与N结合的Ti3+的朗德因子;紫外可见光吸收谱表明,催化剂TiO2-xNx的光响应能力拓展到可见光区,光吸收带发生红移;光催化测试结果显示,掺杂量为3.84的TiO2-xNx在可见光区的响应能力最高,吸收波长延伸至520nm,其光催化活性最大,1.5h降解率达到55.54%。

The effect of several ions on photocatalytic degradation of methyl orange solution was investigated in detail.

以磷钨酸为光催化剂,在紫外灯照射下,对甲基橙溶液进行光催化降解,考察了几种阴阳离子对磷钨酸光催化降解甲基橙溶液的影响。

The research indicated that the nano TiO_2/mineral composite photocatalyst had the best effect on the treatment of wastewater of azo dye.

研究认为,纳米TiO_2/矿物复合光催化材料,对含偶氮染料云母珠光颜料工业废水的光催化效果最好。

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