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catsupport

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Thank you for submitting your manuscript for publication in The Journal of Physical Chemistry. It has been examined by expert reviewers whose reviews are enclosed. After careful consideration of their comments (and my own evaluation of the manuscript), I am unable to accept the manuscript for publication in The Journal of Physical Chemistry.

While your work appears to have been carried out with care, unfortunately, we are unable to accept all of the sound work submitted to the journal. We appreciate your choice of The Journal of Physical Chemistry as a possible forum for presentation of your work.

With sincere regards,

Prof. Catherine Murphy
Senior Editor
The Journal of Physical Chemistry
Phone: 803-777-4332
Fax: 202-513-8768
Editor Email: jphyschem@chem.sc.edu


Reviewer: 1

Recommendation: This paper is not recommended because it does not provide new physical insights.

Comments:
This work mainly contains two sections: xx synthesis and characterization, and the investigation on the catalytic activity of as-prepared xx toward the degradation of  xx in aqueous solution in the presence of H2O2. The first part of the work was studied systematically and the related resulted was characterized by a range of techniques, however, as far as the method is concerned, the novelty is limited. The investigation on the catalytic activity of xx toward the degradation of xx is interesting, however, the evidence for chemical oxidation degradation of Xx by H2O2 in the presence of xx is not convincing. The morphology of xx can not change substantially after absorbing XO, furthermore, the sulfur element can also not be detected by EDS as S on the surface is limited. The statement ¡°which indicating no Xx molecule on the surface of the xx¡± is not accurate due to the fact that xx have high absorption ability, if IR measurement was performed, the characteristic peaks of XO could be observed. Based on above reasons, I do not recommend this Ms published in The Journal of Physical Chemistry. Some other comments are demonstrated as follows:
1.Page 21 line 32, ¡°Figure 2. (A), (B), (c), (D);¡± should be ¡°Figure 2. (a), (b), (c) and (d)¡±, authors should use them unitedly in the whole Ms.
2.Page 11, line 24, ¡°It is well know¡± should be ¡°It is well known¡±
3.I don¡¯t agree with the authors¡¯ statement that the xx.
4.Page 14, line 22, ¡°SEM and EDS were used to obverse the surface¡± should be ¡°SEM and EDS were used to observe the surface¡±




Reviewer: 2

Recommendation: This paper is probably publishable, but should be reviewed again in revised form before it is accepted.

Comments:
The authors report that xx are synthesized and their catalytic degradation properties are also desirable. These results are interesting in the paper, but the following points should be considered by the authors.
1. Considering main feature of the produced structure is ¡°xx¡± and it affects the xx properties and catalytic effects of sample, a test to measure the specific area of samples may be necessary, and the distribution of the pore size is also interesting.
2. Page 8, Lines 14-17. ¡°¡­the
3. Page 14, Lines 42-50. There are not experimental data support the The final sentence in the Conclusions. Thus I suggest the authors delete it.
4. Page 4, ¡°However, to the best of the authors¡¯ knowledge, there are few reports on the synthesis of xx.¡± The authors should delete it because the xx have been synthesized by a different method from the author¡¯s.

In addition, ¡°NaAc¡± in the Abstract may be replaced with ¡°sodium acetate¡±; Ref. 58 is not correct.

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visitor958

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"as far as the method is concerned, the novelty is limited. The investigation on the catalytic activity of xx toward the degradation of xx is interesting, however, the evidence for chemical oxidation degradation of Xx by H2O2 in the presence of xx is not convincing. The morphology of xx can not change substantially after absorbing XO, furthermore, the sulfur element can also not be detected by EDS as S on the surface is limited. The statement ¡°which indicating no Xx molecule on the surface of the xx¡± is not accurate due to the fact that xx have high absorption ability, if IR measurement was performed, the characteristic peaks of XO could be observed. "
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Originally posted by catsupport at 2010-11-06 10:45:05:
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Thank you for submitting your manuscript for publication in The Journal of  ...

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