求高手帮忙翻译

The photoactivity of titania-coated NiFe2O4 particles was
measured by decomposing C16H18N3ClS•4H2O (methylene
blue tetrahydrate, Yakuri Pure Chemicals Co. Ltd., 95%)
[20] in a semi-circulation batch reactor of annular shape. The
prepared titania-coated NiFe2O4particles were dispersed in
760 mL of purified water and sonicated for 30 min. The cat-
alyst loading was 0.26 g L−1 and the initial concentration of
MB was 10 ppm. The diameter and length of the used UV
lamp (15 W, Black light, (1.5–5) × 1016protons s−1cm−3)
were 25.5 and 350 mm, respectively. The wavelength of
the lamp was in the range from 300 to 400 nm. The con-
centration of MB was monitored by UV-Vis spectroscopy
(Model-SpectraView 2000, K-MAC) as a function of reac-
tion time. The photoactivity of a commercial titania sample
(Degussa P-25) was also tested as a reference to evaluate
the photoactivity of the prepared catalysts for the decompo-
sition of MB.

3. Results and discussion
with applied magnetic field was measured by VSM (vibrat-
ing sample magnetometer, Model VSM-5, Toel Kogyo Co.
Ltd.). The prepared NiFe2O4particles show typical ferro-
magnetic hysteresis and the saturated magnetization value is
proportional to the amount of NiFe2O4 in the titania-coated
NiFe2O4 particles. This linearity is a strong indication
that the coating of titania or silica does not influence the
magnetic property.
Figs. 3 and 4 are XRD patterns of titania-coated NiFe2O4
and titania–silica layer-coated NiFe2O4particles. All peaks
are clearly assigned to either the anatase phase of titania or
NiFe2O4. There are no peaks for impurities in the interface
between titania and NiFe2O4, even at 900 ◦C. The silica
exists as an amorphous phase because of the relatively low
temperature of the second reactor. From the XRD data, the
crystallite size of titania was calculated by using the Debye
and Scherrer equations [21] and is plotted in Fig. 5. The
crystallite size of the coated titania is increased with an
increased amount of injected TTIP and is decreased with
an increased amount of silica precursor. The silica layer
between titania and NiFe2O4 hindered the titania crystal
growth while the ethyl alcohol that was added to dilute
TEOS retarded the growth of the titania particles. The crys-
tallite size is increased with increased TTIP and slightly
decreased with increased temperature in the second reactor.
These dependencies on the concentration and temperature
correspond with those in the gas phase formation of titania
particles by TTIP decomposition. This observation implies
that the coating mechanism is similar to that in the gas phase
decomposition of TTIP [22]. This hypothesis is supported
by the TEM micrograph of the coated particles presented
in Fig. 8, which shows that the coated layer is a collection
of particles, and is not a film.

我在金山词霸上翻译的读不下去

这个photoactivity titania-coated的NiFe2O4粒子
C16H18N3ClS测量4H2O(亚•分解
蓝色的tetrahydrate Yakuri纯化学品公司,。有限公司、95%)。
(二)在一个semi-circulation间歇式反应器的形状。这个
titania-coated NiFe2O4particles准备的人也都四散了
曼梯·里的水,purified铸件sonicated为30分钟。猫-
alyst加载−1号信用证,非甾体类抗炎药的初始浓度的影响
10兆/。圆的直径和长度的紫外线
灯(15 / W,黑色亮光,(1.5 - 5)×1016protons s−)厘米−
被25.5%,350毫米,分别。光的波长
灯是在这个范围从300至400海里。评估-
centration症的紫外-可见分光光度法进行了
(Model-SpectraView 2000年,K-MAC)作为一种可行的功能
兴时间。这个photoactivity对商业二氧化钛样品
P-25)(德测试作为参考来评估
这个photoactivity催化剂的准备的decompo -
sition的目录。

3。结果与讨论
与应用磁field向量空间模型进行了研究,()
VSM-5 ing样品,Toel仪、模型Kogyo有限责任公司。
有限公司)。典型的准备NiFe2O4particles铁磁-
磁滞环和饱和磁化值
NiFe2O4成正比的titania-coated
NiFe2O4颗粒。这是一个强烈的暗示。线性
提泰妮娅:硅涂料或不influence了
磁性特性。
无花果。3和4是x射线衍射模式的titania-coated NiFe2O4
layer-coated NiFe2O4particles和titania-silica。所有的山峰上
显然是指定或anatase阶段的二氧化钛或吗
NiFe2O4。有任何严重的杂质的接口
提泰妮娅和NiFe2O4之间,甚至在900◦C。这个二氧化硅
作为一种无定形的时期,因为存在的相对较低
第二个反应器温度。从x射线数据,
提泰妮娅晶粒度的计算采用Debye
和Scherrer方程(21)和曲线在图5。这个
提泰妮娅晶粒度的增加与一个
TTIP注入量增加,减少
增加的数量的二氧化硅前兆。在硅层
提泰妮娅和NiFe2O4之间的提泰妮娅:水晶
经济增长,同时乙醇被加到稀释
正硅酸乙酯弱智生长的二氧化钛粒子。这个crys -
tallite尺寸增加TTIP和轻微增加
温度下降,增加了在第二次核反应堆。
这些连接的浓度和温度
与那些在气相形成的二氧化钛
通过TTIP粒子分解。这个观察意味
那个涂料机制类似于在气相
TTIP分解(22)。这个假设是支持的
由TEM显微颗粒的涂层
图8,显示出该涂一层是收藏
颗粒,并不是一个film。

第一段 punch switch 冲打开关 seting this swith to on produces a dynamic drum sound while increasing the perceived power of the sound. 将该开关设置为“开启”，产生动态鼓声，同时增大感受到的声音功率。 switch this on whenever needed. 在任何需要的时刻开启该开关。 * the effect of this function is applied to the device connected to v-drums/ch1. *该功能的效果应用于连接到v-drums/ch1的装置。 第二段 this switches the range of sound output from the main unit. 这切换来自主单元的声音输出范围。 subwoofer:only sounds in the low-frequency range are output.when used together with the satellite speakers,this mode produces a drum sound with great presence, this is optimal when v-drums stands are used. subwoofer：仅低频范围的声音被输出。当与卫星式扬声器一起使用时，该模式产生具有强烈在场感的鼓声。当v-drums停顿被使用时，这是最优的。 full range:this provides powerful,full-range sound,from low frequencies on up to the high end.this also enables the unit to be used for smaller ensemble performances as a main speaker for the v-drums. full range：这从低频一直到高频端产生强大的全程声音。这也使得该单元也可以作为v-drums的主扬声器而用于较小的合唱性能。 this does not affect the sounds output from the speaker out,headphones,and line out outputs. 这不影响从speaker out、头戴式耳机和line out输出的声音输出。

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