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ÔÚK.R. SeddonΪInorganic Liquids in Synthesis (Second Edition)Ò»ÊéдµÄÐòÑÔÖУ¬ËûдµÀ£º"How many papers within this annual flood of reviews say anything critical, useful, or interesting? How many add value to a list of abstracts which can be generated in five minutes using SciFinder ot the ISI Web of Knowledge? How many of them can themselves be categorised as garbage? It is the twenty-first century----if a review is just an uncritical list of papers and data, what is its value?"µ±È»Ëû»¹Ð´Á˺ܶàÀàËÆµÄ¡°»µ»°¡±£¬¶ÁÆðÀ´ÁîÎҷdz£Ê泩¡£¶Áµ½ÕâÐòÑÔ£¬ÎÒµÄÄÔº£ÖÐÏëÏó³öÒ»¸ö´óºú×ÓÀÏÍ·ÔÚÅØÏø¡¢³âÔð±ðÈË·¢±íÀ¬»øÎÄÕ¡£

ÏÖÔںܶà¸ãÄÉÃ׺ÍÄÉÃ×´ß»¯µÄÈ˶¼¿ñ´µ×Ô¼ºµÄ´ß»¯¼ÁÈçºÎÈçºÎÓÐÓᣵ«ÊÇÊÂʵÉϺܶàÄÉÃ×´ß»¯¼ÁÖ»ÊÇÎüÒýÑÛÇò£¬ËüÃǵÄÖÆ±¸·Ç³£·±Ëö£¬ÎÞ·¨¹¤Òµ»¯¡£¸üºÎ¿öºÜ¶àÎÄÕ±¨µÀµÄÄÉÃ×нṹ´ß»¯¼ÁµÄЧ¹û±ÈÆÕͨÉÌÆ·»¯´ß»¯¼Á¶¼²î£¬ÄÇôµÇɽºÎ±Ø¿¸×Å´¬ÄØ£¿ÔÚÎÒдµÄһƪ¹ØÓڻƽð´ß»¯¼Á×ÛÊöGold Nanoparticles as Chemical Catalysts, in: Nanomaterials: Inorganic and Bioinorganic Perspectives, C.M. Lukehart, R.A. Scott (eds.), John Wiley & Sons, Chichester, 2009ÖУ¬ÎÒÔںܳ¤µÄ½áβ²¿·ÖдÁËÈçÏÂÎÄ×Ö£º

One valid question is whether the gold catalysts synthesized by advanced, demanding, and often tedious, synthetic methods or using unique nanostructured supports (e.g., nanotubes and nanobelts) are better than those synthesized via conventional methods or using commercialized supports. As commented in a recent book,12 ¡°Many methods of preparation have been used, but one wonders why some people have laboured to develop very sophisticated methods while others have been content with a much simpler method, apparently giving the same result, namely, the desired small gold particles.¡± The answer to that question is certainly ambiguous. On the one hand, modern nanotechnology can indeed help with the design of many gold catalysts with improved catalytic performance that can not be achieved by using conventional methods. On the other hand, one can find many publications focusing on the synthesis part, with the catalytic performance not reported or very low.12 One pitfall may be that some gold catalysts may contain residual capping agents and/or organic fragments. These organic fragments, if not sufficiently removed by special treatments, may poison CO oxidation, although gold catalysts with organic fragments may still show some activity in certain organic reactions. This point was sometimes overlooked, and thus undermining the real performance of these advanced gold catalysts. How to properly remove the organic fragments while avoiding the sintering of gold nanoparticles is a challenge. Even if this challenge is overcome, many factors still have to be considered before there can be large-scale utilization of gold catalysts synthesized by advanced technology.

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The main part of our previous short communication26 focused on the in-depth characterization of ... alloy NPs and an ...... catalyst prepared under optimal conditions, whereas the influences of synthesis parameters on the resulting products, the synthesis mechanism, the critical roles of pretreatment conditions and catalyst compositions in determining catalytic performance, as well as the contribution of the work to the fields of bimetallic materials synthesis and gold catalysis were not reported or elaborated in detail. Therefore, we expand on these aspects more explicitly in the current paper. There are two significant aspects of the work described in this paper. First, the synthesis of size-controlled and homogeneous ... alloy NPs has been found to be extremely evasive to date.15 Hence, the low-temperature solution-phase synthesis of ... alloy NPs with well controlled shape and sizes should be an important progress that may inspire subsequent bimetallic materials synthesis. Second, catalysis by gold nanoparticles has been intensively studied recently,28-33 but the use of alloy NPs as precursors to design advanced catalysts with multiple components (i.e., active metal, metal oxide modifier/promoter, solid support) and tailored interfacial structures has been rarely reported. Hence, this work may be of interest to both materials scientists and those working in the area of catalyst design.

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View Letter
Date: Jun 30, 2007
To:***. cc: ***. From:  ***
Subject: Your Submission
Ms. Ref. No.:  ***
Title:***
****

Dear ****,
Reviewers have now commented on your paper. You will see that they are advising that you revise your manuscript. If you are prepared to undertake the work required, I would be pleased to reconsider my decision.  

For your guidance, reviewers' comments are appended below.

If you decide to revise the work, please submit a list of changes or a rebuttal against each point which is being raised when you submit the revised manuscript.

To submit a revision, please go to ***and login as an Author.
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On your Main Menu page is a folder entitled "Submissions Needing Revision". You will find your submission record there.
Yours sincerely, ***  Editor *****

Reviewers' comments:
Reviewer #1: You can find 1.reviewer comments as follows:

1- Authors were used "UV curing mechanism" of ** in the manuscript title, but there are not any originalities of the suggested mechanism.

2- The aim of the research is not clear. Is it search for UV curing mechanism of ** or initiate of the curing reaction without initiator?  

3- Although the title of manuscript had been focused on curing mechanism, there were many details about the mechanical properties (especially pencil hardness) of the films. I suggest that the changing title of the manuscript according to this direction.

4- What is the exact time of UV curing? It must be given to emphasize the differences reaction time with and without photoinitiator. It is not enough to write "several minutes" in many places in the manuscript.  

5- In section 3.1: sentences 2 and 3 must be removed from the manuscript. The determination of molecular weights for crosslinked materials is impossible, and the solubility of these materials is also impossible any kind of solvents, because of crosslinking structure. I am sure the author's know this general information for these materials, so no need to write this section.

6- There is a contradiction between section 3.3 and Table 2. The oxygen content had increased slightly with the irradiation time according to Table 2. But in section 3.3. had written "The oxygen content did not increase with the irradiation time; this proved that the mechanism, different from the polymerization¡­¡­..". This sentence or data in table 2 must be checked again and changed or corrected related parts.

7- The title of y axis must be added in Figure 1.

8- There are several writing mistakes in the manuscript. They are listed below.
In Abstract section: 13.lines:     UV curing
                : didn't and wasn't must be corrected did not and was not
In Introduction Part 5. lines: with must be separated 0-3 olefins,¡­¡­..
In section 2.2.2 line 2: GY.UV2kW/ ??
In section 2.3, 2. lines     : The IR spectra was
         4. lines: elements must be changed as percentage
In Reference section     Ref. 2:  Press must be corrected as capital letter
              Ref. 4: Polym. must be corrected as capital letter
                 Some of author's names must be written as full name(s) of author(s).  
              Ref. 6: J. of ¡­¡­..
              Ref. 13: The name of journal must be written short form.         
              And must be removed from Ref. 10,15, 17, and 20.  

As a result, the manuscript is suitable publication for **** after major revision.


Reviewer #2: There are some important details missing in the paper:
- How were the samples prepared on the glass slide from xylene solution (vacuum,
time, temperature, final film thickness)?
- What was the temperature of the films during the UV irradiation?
- For comparison of hardness measurements, what is the hardness of fully cured
*** film when ***-catalyzed polymerization is used?
- Are the results of Elemental analysis in Table 2 average from more measurements?
How can be explained the increase in carbon content after irradiation?
- What is the lifetime of *** radicals observed by ESR spectroscopy?
I recommend the paper for publication after clarification of missing details.
¿´µ½ÍËÐÞÐÅ֮ʱ£¬ÎÒ»¹²»¶®¡°major revision¡±ÊǶàôÑÏÖØµÄÒ»¸ö´Ê£¬µ«Ö»ÊǾõµÃ£¬Ã»ÓÐÌá³ö¶àÉÙÓï·¨ÉϵĴíÎó£¬ÎÒ»¹ÊÇÓе㿪ÐÄ£¬±Ï¾¹´Óд¡¢¸Äµ½Í¶£¬¶¼ÊÇÎÒÒ»¸öÈËÍê³ÉµÄѽ¡£µ«ÎÒÖªµÀÇ°ÃæÈý¸öÎÊÌâÊÇÖÂÃüÖ®´¦£¬¡± no any originalities¡±, ¡°The aim of the research is not clear¡±.
µÚ¶þÌìÔÚʵÑéÊÒһλÄêÇáµÄÀÏʦ˵£¬¸øÁË¡°major revision¡±£¬Ã»Ï£Íû ÁË£¬ÄãҪôÊDz¹³äÊý¾Ý£¬ÒªÃ´ÊǸÄͶ¡£ÎÒÏëÎҵĴ¦Å®×÷¾ÍÕâÑùÍêÁË£¿ºóÃæÀ´µ½Ð¡Ä¾³æÀïÓÖÕÒµ½ÁË×ÔÐÅ£¬²»¼ÇµÃÊÇÄĸöÌû×ÓÀÓÐһλ³æÓÑ˵¹ý£¬Èç¹û¸øÁË¡°major revision¡±»ò¡°miner revision¡±, ¾Í¿ÉÒÔ×øÏÂÀ´ºÈ±­¿§·ÈÁË£¬Õâ¸öʱºò¿ÉÒÔССÇìףһϡ£ÓÚÊǾÍÔÚµ¼Ê¦µÄÖ¸µ¼Ï£¬×Ô¼ºÒ»ÌõÌõµÄ¸øÓè»Ø´ð£¬ÓÐµÄ»Ø´ð»¹±È½ÏÆ«¼¤£¬ÌýÁËÄêÇáÀÏʦÄǶλ°£¬ÎÒÒ²²»±§Ê²Ã´Ï£ÍûÁË¡£Ò»ÖܺóÐ޸ĸåͶ³ö£¬ÓÉËûÈ¥°É£¬×Ô¼º×öºÃÁ˾ͿÉÒÔÁË£¬½Ó²»½ÓÊÕÖ÷±àµÄÊ¡£Ã»Ïëµ½8ÔÂ15½ÓÊÕÁË£¬ÏÂÃæÊǽÓÊÕÐÅ£º

View Letter

Date: Aug 15, 2007  To: **cc: **  From: **
Subject: Your Submission  
Ms. Ref. No.:  ***R1
Title: ****     £¬****
Dear ***,

I am pleased to confirm that your paper "****" has been accepted for publication in ***.

Comments from the Editor and Reviewers can be found below.

Thank you for submitting your work to this journal.

With kind regards,

***
Editor
***

Comments from the Editors and Reviewers:

Reviewer #1:
The manuscript ***R1 entitled "**" by *** has been carefully reviewed.

These authors have been made all of related corrections and changes according to referee's comments. As a result, the manuscript is suitable publication for *** without revision.

Additionally, the author's letter made me very happy especially the author's thinking on referee's comments. All suggestions of referee's considered by authors. They I also would like to thank you and these authors.
Õâ¸öÆÀίµÄ×îºóÒ»¶Î»°£¬Ê¹ÎÒ±ÈÎÄÕ±»½ÓÊÕ»¹¿ªÐÄ£¬ÒòΪÎÒµÄÐ޸ĸåÄÜÈÃËû¡± very happy¡±.

Reviewer #2: I recommend the paper for publication after the revision.


ʧ°ÜµÄ½Ìѵ£º
     ºóÃæµÄ¹¤×÷×öÁËһЩÊý¾Ý£¬×Ô¼º¾õµÃ±ÈÉϴεϹºÃһЩ£¬ÓÖÊÇÇ°Ãæ¹¤×÷µÄ½øÒ»²½·¢Õ¹£¬ÏëÔÙÊÔÊÔͬһÆÚ¿¯£¬Õâ´ÎÎÒÃÇÀϰåÍÐÁ˹ØÏµ£¬ÍâÎĸå¼þ¸øÁ˱±»¯ËùµÄÅ£ÈËÐ޸Ĺý¡£µ«ÎÒ×Ô¼º¾ÍûÓÐÏóµÚÒ»´ÎÄÇÑù£¬×Ô¼º¸ÄÄÇô¶à´ÎÁË¡£07Äê10Ô³õͶ¸å£¬11ÔÂ18ºÅËÍÉó£¬2ÔÂ22ºÅдÁ˴߸åÐÅ£¬3ÔÂ9ºÅ´ò¿ª²é¿´Í¶¸å״̬²é¿´ÀïÃæ£¬·¢ÏÖµ½ÁË×îºóÒ»²½È¥ÁË£¬Ö÷±àϾö¶¨ÁË¡£ÐÄÀïÏëÖ±½ÓÊÕ¿ÉÄÜÐÔ²»´ó£¬¿Ï¶¨ÊǾÜÁË£¬´ò¿ªÒ»¿´¹ûÈ»¡°reject¡±ÁË¡£±¨¸æµ¼Ê¦£¬Ô­À´¶¼ÊÇÒòΪһЩϸ½ÚÎÊÌâ±»¾Ü£¬ÓеãÓôÃÆ¡£ÈçÏ£º
View Letter

Date: Mar 09, 2008  
To: ****  
cc:****
From: **  
Subject: Your Submission  
Ms. Ref. No.: ***
Title: ***      *****

Dear ***,

Reviewers' comments on your work have now been received.  You will see that there are so many critical points in your experiment before publication of your work.  Therefore I must terminate our process with " reject".
I will recommend you to submit it again after your consideration.

For your guidance, I append the reviewers' comments below.

Thank you for giving us the opportunity to consider your work.

Yours sincerely,
****
Editor
***
Ò»¿´Ö»ÓÐÒ»¸öÉó¸åÈ˵ÄÒâ¼û£¬ÊDz»ÊÇÎÒ´ßµÃÌ«¼±ÁË£¿ÔÙϸ¿´Éó¸åÈ˵ÄÒâ¼û£¬¸üÊÇÓôÃÆÁË¡£¶¼ÊÇһЩϸ½ÚÐÔµÄÎÊÌ⣬¾ÍÖ±½Ó¾ÜÁË£¬²»¸ø¸ÄµÄ»ú»á£¿ÔÚÿһ¸öÎÊÌâÖÐÎÒÓÐ˵Ã÷¡£µ±È»Èç¹ûÊǸøÖ÷±à¿´²»ÄÜÈçϽâÊÍÁË£¡¹þ¡­¡­

Reviewers' comments:


Reviewer #1: There are some critical details missing in the experimental part of the paper:
On p. 4 - How is ** soluble in absolute ethanol? What was the particle size after **?£¨ÔõôÈܽâµÄ£¬ÎÒ¿ÉÒÔ˵Ã÷Çå³þÂ
On p. 4 - What and when happened to ethanol from solution as the samples were UV irradiated? Was any left in the films?£¨¾Æ¾«ÊÇ·ñ»¹ÔÚĤÉÏÃæ£¬ÔõôÑùÁË£¬ÓжàÉÙ£¿Éó¸åÈËÊDz»ÊÇÍ¿ÁÏÀàµÄר¼Ò£¿³£Ê¶Ñ½£¬Í¿ÁϸÉÁË£¬ÈܼÃÊǻӷ¢ÁË£©
On p. 4 - How were powders prepared from the films?£¨Ä¤ÔõôÑù¸ã³É·ÛÄ©£¿Õâ¸ö»¹ÄÑÂ𣿣©
On p. 4 - In preparation of £¨**£© are missing details - amounts, time, temperature, particle size ...
£¨ÊµÑéÓÃÁ¿£¬Î¶ȣ¬Á£¾¶´óС£¿ÎÄÖж¼Ð´Çå³þÁËѽ£©
On p. 6 - What is JCPDS No. ***?£¨Õâ¸öJadeÖеÄPDFÊý¾Ý£¬ÊÇÁò»¯ïÓ¾§Ð͵ÄÒ»ÖÖ£¬ËµÁò»¯ïÓÊÇÁ¢·½¾§Ïµ¡£ÁíÓÐACSÉÏһƪÎÄÏ×ÀïҲ˵Á¢·½¾§ÏµµÄ¸ÃÄÉÃ׿ÉÒÔ´ÓÕâÀï±È½ÏµÃ³ö£¬¿É¼û¸ÃÉó¸åÈ˸ù±¾Ã»Ê²Ã´Ë®Æ½£¬×Ô¼º²»ÖªµÀ£¬Á¬²éÒ²²»È¥²é£¬ÎÊÕâôµÍ¼¶µÄÎÊÌ⣡¹þ¡­¡­£©
On p. 6 - In addition to 14.1 and 185.6 nm particle size it would be desirable to compare those values with particle size of *** from Figure 3c.£¨Äã¿´Õâ²»ÊÇÁ£¾¶´óСÂð£¿ËûÃ÷Ã÷¿´µ½Á˵ġ££©
On p. 7 - Figure 3a is showing that the ***particles are in big clusters and not "homogeneously dispersed".£¨Í¼ÐκÍACSµÄһƪ¸ß¼¶±ðµÄÎÄÏ×¼«ËÆ£¬ÉÏÃæÒ²ÊÇ˵"homogeneously dispersed".£©
On p. 8 - Can be the Figure 3b enlarged? It looks that the *** particles are irregular and not "spherical".£¨ÎÒÃDzâÊÔʱ¿´µ½µÄ±ß½ç¶¼ºÜÇåÎú£¬¿ÉÄÜÊÇÒÇÆ÷²»ÏȽø£¬Í¼Æ¬Ï´³öÀ´ÓеãÄ£ºý£¬¿ÉÒÔÓÃÏȽøµÄÒÇÆ÷ÖØ²âTEMÂ
On p. 8 - It would be desirable to have unmodified **** included in the Figure 4 for comparison of thermal stability.£¨Õâ¸öÊý¾Ý²â¹ý£¬¼Ó½øÈ¥²»¾Í¿ÉÒÔÁË£©
     ÎÒ×¼±¸¹ý¼¸ÌìÔÙдÐÅÈ¥Ö÷±àÄDZç½âһϡ£°ÑÕâЩÎÊÌⶼ˵Ã÷Çå³þ£¬¿´¿´Çé¿ö»áÔõôÑù¡£¹þ¡­¡­
×îºóË͸÷λ³æÓÑËĸö×Ö£º×ÔÐÅ£¬ÑϽ÷£¡
×£¸÷λ³æÓѺÃÔË¡£²¢»¶Ó­Óв»Í¬¼û½âµÄ³æÒ»Æð½»Á÷¡£ÒÔÏÂÊÇÎÒ¸öÈ˵ÄһЩ¿´·¨¼°¾­Àú£º

1. д×÷ǰ´óÁ¿ÔĶÁÒÔÓ¢ÓïΪĸÓïµÄÎÄÏ×£¬³ä·ÖÁ˽â×Ô¼ºµÄ¿ÎÌâÄÚÈÝ£¬ÕÒ³ö×Ô¼ºµÄÄ¿±êÆÚ¿¯£¬ÕÆÎÕÓ¢Óï¿Æ¼¼ÂÛÎĵıí´ï·½Ê½¡£
2.д×÷ʱһ¶¨ÒªÓÐÕë¶ÔÐÔ¡£ÔÚ×Ô¼ºµÄÄ¿±êÆÚ¿¯ÖвéÔÄÏà¹ØÎÄÏ×£¬Ñϸñ°´ÕÕ×î½üµÄ¸ñʽд£¬²ÎÕÕ¸ÃÆÚ¿¯ÖÐÂÛÎĵĽṹ˼·À´²¼ÖÃ×Ô¼ºµÄÂÛÎÄ£¬±ÜÃâ·¸È絥λ¡¢Í¼±íµÈ·½ÃæµÄµÍ¼¶´íÎó¡£
3. ÎÄÏ×ÒýÓþ¡Á¿¶àµÄÒýÓñ¾ÆÚ¿¯¼°Ó°ÏìÒò×Ó¸ßÓÚ±¾ÆÚ¿¯µÄÎÄÏס£
4. ÍËÐÞʱ¶ÔÉó¸åÈ˵ÄÒâ¼ûÒªÖðÒ»»Ø´ð¡£³ýÁËдÇåÐÞ¸ÄÄÚÈÝÍ⣬»¹ÓÐһЩ»°ÊDZØÐëҪдµÄ¡£¶ÔÉó¸åÈ˵ÄÒâ¼ûÌá³ö²»Í¬µÄ¿´·¨Ò²Ó¦¸Ã½²¾¿Ò»¶¨µÄ¼¼ÇÉ¡£

Ê×ÏÈ£¬Òª¶ÔÉó¸åÈ˱íʾ¸Ðл£¡
¡°We appreciate you and the reviewer¡¯s comments and revision suggestions about our manuscript. Some corrections and/or responses reviewer¡¯s comments are illustrated as follows: ¡±

ÓÐЩÉó¸åÈ˵Äcomments»á±È½Ï¼áÈñ£¬Ò²²»ÓýôÕÅ£¬¿ÉÄÜÊÇËû¶ÔÄã×öµÄÄÚÈÝÊDz»Ì«Ê죬ÏëºÃÓ¦¶Ô´ëÊ©¡£ÈçÎÒÕë¶ÔµÚÒ»¸öÉó¸åÈ˵ĵÚÒ»µãnot any originalities ÊÇÈçÏ»شðµÄ£º
¡°1.The laccase¨Ccatalyzed and aerobic oxidative polymerization of*****
require a long period and special conditions, and this strictly restricts the
applications of lacquer. When *** films 50¦Ìm thick on glass substrates
were placed in the air about 55~60% relative humidity at 20¡æ~26¡æ, 48h later, the hardness of the ** films was 2B, and 15d later, it was 4H. The yield of ** adds up to about 90% in the world, and the processing industry of ** in China is pervasive. However, how to make ** drying fast is
still a difficult problem in this field. In our manuscript an efficient method
(UV irradiation) was reported to cure *** rapidly within 2min (the hardness
of the films is 4H) without any photoinitiator. There is no previous literature
which has reported this research, so it is very important in this field. We think this is the originality in this field.¡±
ÎÒ×öµÄÊÇÍ¿ÁÏ·½ÃæµÄ£¬ÒÔǰĤµÄ×ÔÈ»¸ÉÔï Òª15ÌìÓ²¶È²Å´ï4H£¬¶øÎÒ²ÉÓÃз½·¨Ö»2min¾Í¿ÉÒÔ´ï4H,ͬʱ˵Ã÷ÎÒ¹úÕâ·½ÃæÔÚÊÀ½çÉϵÄÓ°Ïì¼°µØÎ»¡°The yield of ** adds up to about 90% in the world, and the processing industry of ** in China is pervasive. ¡±

Èç¹ûÉó¸åÈËÌáµÄÒâ¼ûÄãÔÝʱÎÞ·¨»Ø´ð»ò×öµ½£¨±ÈÈ磬ҪÄãÔö¼ÓʵÑé»ò¸Ä½øÊµÑéµÈ£©£¨ÕâÑùÐèҪʱ¼ä£¬Ò²ÐíÎÒÃǵÈ×ÅÕâÆªÎÄÕ±ÏÒµ£©£¬¿ÉίÍñµÄ¾Ü¾ø¡£

ÈçÎÒ¶Ô¡°What is the lifetime of *** radicals ¡±£¨ÎÊ×ÔÓÉ»ùÊÙÃü£¬ÎÒû×ö¹ý£©¡£
ÎÒÊÇÈçÏ»شðµÄ£º¡°¡­¡­¡­¡­¡­¡­As to the lifetime of *** radicals,
I think it is not very important to our research, so we are sorry to
tell you that we have not measured it so far.¡±

×îºó˵Ã÷¡°Please don¡¯t hesitate to contact me
if you have any other questions about our manuscript.¡±


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