Office Action Predictor
Last updated: April 17, 2026
Application No. 18/343,405

NANO-LITER PHOTOIONIZATION MASS SPECTROMETRY ION SOURCE DEVICE AND OPERATION METHOD THEREOF

Non-Final OA §103
Filed
Jun 28, 2023
Examiner
STOFFA, WYATT A
Art Unit
2881
Tech Center
2800 — Semiconductors & Electrical Systems
Assignee
national institute of metrology china
OA Round
1 (Non-Final)
80%
Grant Probability
Favorable
1-2
OA Rounds
2y 5m
To Grant
99%
With Interview

Examiner Intelligence

Grants 80% — above average
80%
Career Allow Rate
803 granted / 1003 resolved
+12.1% vs TC avg
Strong +22% interview lift
Without
With
+22.5%
Interview Lift
resolved cases with interview
Typical timeline
2y 5m
Avg Prosecution
81 currently pending
Career history
1084
Total Applications
across all art units

Statute-Specific Performance

§101
2.3%
-37.7% vs TC avg
§103
37.3%
-2.7% vs TC avg
§102
23.2%
-16.8% vs TC avg
§112
29.7%
-10.3% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1003 resolved cases

Office Action

§103
DETAILED ACTION Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . Election/Restrictions Claims 9-20 are withdrawn from further consideration pursuant to 37 CFR 1.142(b) as being drawn to a nonelected invention, there being no allowable generic or linking claim. Election was made without traverse in the reply filed on 10/17/25. Claim Rejections - 35 USC § 103 In the event the determination of the status of the application as subject to AIA 35 U.S.C. 102 and 103 (or as subject to pre-AIA 35 U.S.C. 102 and 103) is incorrect, any correction of the statutory basis (i.e., changing from AIA to pre-AIA ) for the rejection will not be considered a new ground of rejection if the prior art relied upon, and the rationale supporting the rejection, would be the same under either status. The following is a quotation of 35 U.S.C. 103 which forms the basis for all obviousness rejections set forth in this Office action: A patent for a claimed invention may not be obtained, notwithstanding that the claimed invention is not identically disclosed as set forth in section 102, if the differences between the claimed invention and the prior art are such that the claimed invention as a whole would have been obvious before the effective filing date of the claimed invention to a person having ordinary skill in the art to which the claimed invention pertains. Patentability shall not be negated by the manner in which the invention was made. This application currently names joint inventors. In considering patentability of the claims the examiner presumes that the subject matter of the various claims was commonly owned as of the effective filing date of the claimed invention(s) absent any evidence to the contrary. Applicant is advised of the obligation under 37 CFR 1.56 to point out the inventor and effective filing dates of each claim that was not commonly owned as of the effective filing date of the later invention in order for the examiner to consider the applicability of 35 U.S.C. 102(b)(2)(C) for any potential 35 U.S.C. 102(a)(2) prior art against the later invention. Claims 1 and 6-8 rejected under 35 U.S.C. 103 as being unpatentable over CN 115910744 A [Huang], the translation of which is attached, in view of Van Berkel, Gary J., Keiji G. Asano, and Paul D. Schnier. "Electrochemical processes in a wire-in-a-capillary bulk-loaded, nano-electrospray emitter." Journal of the American Society for Mass Spectrometry 12.7 (2001): 853-862 [hereinafter Van Berkel]. Regarding Claim 1: Huang teaches a nano-liter photoionization mass spectrometry ion source device (as shown in Fig. 2), comprising: a nano-tip, configured to load a sample solution, thus achieving a nano-electrospray process (Fig. 2 (1), claim 9); and a UV lamp (Fig. 2 (8)), configured to emit a high-energy ultraviolet photon to be combined with a gaseous molecule obtained by vaporizing the sample solution, thus achieving a photoionization process (claim 7). However, Huang fails to teach a metal electrode, inserted into the nano-tip to contact with the sample solution directly, thus providing a high-voltage electric field for the nano-electrospray. Van Berkel teaches a nano-electrospray ion source (abstract) comprising a borosilicate glass capillary with a platinum electrode inserted therein. Section: Off-line Optical Monitoring of the Nano-ES Emitters, para 1; Fig. 1. It would have been obvious to one of ordinary skill in the art before the effective time of filing to replace the generic nano-electrospray tip of Huang with the wire in capillary geometry taught by Van Berkel since such an arrangement proves more robust and reliable, per Van Berkel pg 853, column 2. Regarding Claim 6: The above modified invention teaches the nano-liter photoionization mass spectrometry ion source device according to claim 1, wherein the nano-tip is made of a borosilicate glass. Van Berkel Section: Off-line Optical Monitoring of the Nano-ES Emitters, para 1. Regarding Claim 7: The above modified invention teaches the nano-liter photoionization mass spectrometry ion source device according to claim 1, wherein the metal electrode is an inert metal material. Van Berkel Section: Off-line Optical Monitoring of the Nano-ES Emitters, para 1 - Platinum. Regarding Claim 8: The above modified invention teaches the nano-liter photoionization mass spectrometry ion source device according to claim 7, wherein the inert metal material is a platinum wire. Van Berkel Section: Off-line Optical Monitoring of the Nano-ES Emitters, para 1 - Platinum. Claims 2-5 rejected under 35 U.S.C. 103 as being unpatentable over CN 115910744 A [Huang], the translation of which is attached, in view of Van Berkel, Gary J., Keiji G. Asano, and Paul D. Schnier. "Electrochemical processes in a wire-in-a-capillary bulk-loaded, nano-electrospray emitter." Journal of the American Society for Mass Spectrometry 12.7 (2001): 853-862 [hereinafter Van Berkel] as applied to claim 1, and further in view of US 6,653,626 B2 [Fischer]. Regarding Claim 2: The above modified invention teaches the nano-liter photoionization mass spectrometry ion source device according to claim 1, but fails to teach that device further comprises a square chamber, wherein an end portion of the nano-tip and the UV lamp are located inside the square chamber, and the square chamber is filled with an inert shielding gas to reduce an effect of oxygen from the air on photoionization. Fischer teaches a photoionization source (abstract) wherein the sample emission structure (Fig. 7 (310)) and the UV lamp (Fig. 7 (350)) are placed in a square chamber (Fig. 7 (12)), and the square chamber is filled with an inert shielding gas to reduce an effect of oxygen from the air on photoionization (13:30-47). It would have been obvious to one of ordinary skill in the art before the effective time of filing to incorporate the above noted box and nitrogen gas of Fischer into the modified invention. One would have been motivated to do so in order to contain noxious vapors and improve the effectiveness of the UV lamp. Fischer 6:8-15, 13:30-47. Regarding Claim 3: The above modified invention teaches the nano-liter photoionization mass spectrometry ion source device according to claim 2, wherein the inert shielding gas is nitrogen. Fischer 13:30-47. Regarding Claim 4: The above modified invention teaches the nano-liter photoionization mass spectrometry ion source device according to claim 2, wherein a gas inlet and a gas outlet are formed on opposite sides of the square chamber for entry and exhaust of the inert shielding gas, respectively. Fischer – note the inlet (351) is on the opposite side from the outlet (vacuum system associated with 222a). Regarding Claim 5: The above modified invention teaches the nano-liter photoionization mass spectrometry ion source device according to claim 4, wherein a dopant inlet is formed on a side of the gas inlet on the square chamber. Fischer demonstrates a solute (301) being introduced on a side of the gas inlet. Conclusion Any inquiry concerning this communication or earlier communications from the examiner should be directed to WYATT A STOFFA whose telephone number is (571)270-1782. The examiner can normally be reached M-F 0700-1600 EST. Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, ROBERT KIM can be reached at 571 272 2293. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. WYATT STOFFA Primary Examiner Art Unit 2881 /WYATT A STOFFA/Primary Examiner, Art Unit 2881
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Prosecution Timeline

Jun 28, 2023
Application Filed
Nov 19, 2025
Non-Final Rejection — §103
Mar 26, 2026
Response after Non-Final Action
Mar 26, 2026
Response Filed

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Study what changed to get past this examiner. Based on 5 most recent grants.

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Prosecution Projections

1-2
Expected OA Rounds
80%
Grant Probability
99%
With Interview (+22.5%)
2y 5m
Median Time to Grant
Low
PTA Risk
Based on 1003 resolved cases by this examiner. Grant probability derived from career allow rate.

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