Prosecution Insights
Last updated: April 19, 2026
Application No. 18/006,834

ADDITIVE MANUFACTURING COMPOSITION FOR 3-D PRINTED OBJECT

Non-Final OA §102§112
Filed
Jan 25, 2023
Examiner
MCCLENDON, SANZA L
Art Unit
1765
Tech Center
1700 — Chemical & Materials Engineering
Assignee
Mitsubishi Chemical UK Limited
OA Round
1 (Non-Final)
81%
Grant Probability
Favorable
1-2
OA Rounds
2y 11m
To Grant
91%
With Interview

Examiner Intelligence

Grants 81% — above average
81%
Career Allow Rate
978 granted / 1213 resolved
+15.6% vs TC avg
Moderate +10% lift
Without
With
+10.4%
Interview Lift
resolved cases with interview
Typical timeline
2y 11m
Avg Prosecution
37 currently pending
Career history
1250
Total Applications
across all art units

Statute-Specific Performance

§101
0.2%
-39.8% vs TC avg
§103
38.1%
-1.9% vs TC avg
§102
32.4%
-7.6% vs TC avg
§112
17.2%
-22.8% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1213 resolved cases

Office Action

§102 §112
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 . Claim Rejections - 35 USC § 102 The following is a quotation of the appropriate paragraphs of 35 U.S.C. 102 that form the basis for the rejections under this section made in this Office action: A person shall be entitled to a patent unless – (a)(1) the claimed invention was patented, described in a printed publication, or in public use, on sale, or otherwise available to the public before the effective filing date of the claimed invention. Claim(s) 1-2, 11, 13, 17, 22, 25-31, 34 and 41 is/are rejected under 35 U.S.C. 102(a1) as being anticipated by Kotani et al (US 201/0147776). Kotani sets forth methods for producing photocured three-dimensional objects which includes ejecting and applying droplets of a photocurable resin composition (A) having a viscosity o 20 mPa*s to 500 Pa*s at 23 deg. C—see abstract. Said photocurable resin composition (A) comprises (I) a photocurable resin; (II) at least one of a photoinitiator; and (III) at least one diluent monomer, wherein said photocurable resin composition may optionally comprise a filler; plasticizer; if necessary, a solvent; thixotropic additives; and other additives—see [0055]; [0067]; [0080]; [0083]; [0084]; [0086]; [0088]; [0090]; and [0091]. Said photocurable resin (A) has a photocrosslinkable group in the molecule [0056], wherein Souda teaches said resin (A) may be selected from a (meth) acrylic (meth) acrylate resin [0060]. The photoinitiator is set forth as usable alone or in combination. Additionally, said photoinitiator may be used in combination with an amine (sensitizer)—see [0073]. The diluent monomer may be used alone or in combination, as well as, being selected from monofunctional and/or polyfunctional (meth) acrylate monomers—see [0081]. Per synthesis example 3, Souda explicitly sets forth obtaining a photocurable resin (A) which is an acrylic copolymer comprising the reaction product of n-butyl acrylate/ethyl acrylate/methoxyethyl acrylate having acryloyl groups [P3] and a number-average molecular weight of 35,000. The ratio of the n-butyl acrylate/ethyl acrylate/methoxyethyl acrylate copolymer components is 73/25/0—see [0164] and [0165]. Per formulation example 3, Souda explicitly sets forth a resin composition comprising 100 parts of photocurable resin [P3]; 3 parts Irganox 1010 (antioxidant); 50 parts of acrylolmorpholine (reactive diluent); 10 parts of methoxy-polyethylene glycol acrylate (reactive diluent); 1-part trimethylolpropane triacrylate (reactive diluent having crosslinkable groups); 2.5 parts of the photoinitiator (OXE-01); and 0.01 part of RDW-R13 (a polymerizable dye)—see [0186]. Regarding claims 1-2, 22, 29, 31, and 34: The composition of example 3 is deemed to anticipate the composition of claim 1, wherein [P3] has ethyl (meth)acrylate residues; the trimethylolpropane triacrylate corresponds to applicants crosslinker having at least two terminal groups capable of polymerization; the acrylolmorpholine has a viscosity of 9-12 mPa*s at room temperature (liquid reactive diluent); and methoxy-polyethylene glycol acrylate has a viscosity of25 mPa*s at room temperature (liquid reactive diluent); and the OXE-01 is a photoinitiator. The formulation of example 3 has a viscosity of 7.8 Pa*s (7800 cP) at room temperature. Souda sets forth curing by exposure to UV radiation having a wavelength of 365 nm after jetting and curing layer by layer to form a shaped object—see [0188]. Regarding claim 11. The reactive diluent in formulation example 3 comprises a combination of monomer. Regarding claim 13: Souda sets forth the use of trimethylolpropane triacrylate in formula example 3—see example 3. Regarding claim 17: The photoinitiator is initiated by ultraviolet (UV) radiation—see [0188]. Regarding claim 25 and 27: The trimethylolpropane triacrylate has a viscosity 70-80 mPa*s at room temperature (liquid diluent corresponding to applicants crosslinker); the acrylolmorpholine has a viscosity of 9-12 mPa*s at room temperature (liquid reactive diluent); and methoxy-polyethylene glycol acrylate has a viscosity of 25 mPa*s at room temperature. Thus claim 25 is anticipated. Both reactive diluents (acrylolmorpholine and methoxy-polyethylene glycol acrylate) has a viscosity lower than the trimethylolpropane triacrylate. Thus claim 27 is anticipated. Regarding claim 26, 28, and 30: Souda sets forth all components in the formulation of example 3 are all dissolved in the mixture [0186] and is jetted at 60 deg. C (ejection temperature) in the form of droplets using a stereolithographic process—see [0188]. Thus claim 26 is anticipated. Regarding claim 41: The trimethylolpropane triacrylate comprises three reactive terminal alkyl acrylate groups. Claim Rejections - 35 USC § 112 The following is a quotation of 35 U.S.C. 112(d): (d) REFERENCE IN DEPENDENT FORMS. —Subject to subsection (e), a claim in dependent form shall contain a reference to a claim previously set forth and then specify a further limitation of the subject matter claimed. A claim in dependent form shall be construed to incorporate by reference all the limitations of the claim to which it refers. The following is a quotation of pre-AIA 35 U.S.C. 112, fourth paragraph: Subject to the following paragraph [i.e., the fifth paragraph of pre-AIA 35 U.S.C. 112], a claim in dependent form shall contain a reference to a claim previously set forth and then specify a further limitation of the subject matter claimed. A claim in dependent form shall be construed to incorporate by reference all the limitations of the claim to which it refers. Claim 13 is rejected under 35 U.S.C. 112(d) or pre-AIA 35 U.S.C. 112, 4th paragraph, as being of improper dependent form for failing to further limit the subject matter of the claim upon which it depends, or for failing to include all the limitations of the claim upon which it depends. Claim 13 sets forth the limitation “the primary monomer” in line 2. Claim 1 does not set forth a limitation for a primary monomer. Applicant may cancel the claim(s), amend the claim(s) to place the claim(s) in proper dependent form, rewrite the claim(s) in independent form, or present a sufficient showing that the dependent claim(s) complies with the statutory requirements. Allowable Subject Matter Claims 3, 6-7, 9 and 32-33 are objected to as being dependent upon a rejected base claim, but would be allowable if rewritten in independent form including all of the limitations of the base claim and any intervening claims. Souda does not provide any guidance on the amount of ethyl (meth) acrylate used to obtain the acrylic copolymer. Souda is silent with regard to a crosslinker in an amount of 5 to 94 wt.% of the resin composition. Souda does not set forth the type or compounds found in claims 7 and 9 as crosslinking monomer/components. And Souda is silent with regard to the flexural strength and/or the flexural modulus of the cured photocurable resin compositions. Conclusion Any inquiry concerning this communication or earlier communications from the examiner should be directed to SANZA L MCCLENDON whose telephone number is (571)272-1074. The examiner can normally be reached 8-5. 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, Heidi Riviere-Kelley can be reached at 571-270-1831. 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. /SANZA L. McCLENDON/Primary Examiner, Art Unit 1765 SMc
Read full office action

Prosecution Timeline

Jan 25, 2023
Application Filed
Jul 10, 2023
Response after Non-Final Action
Sep 24, 2025
Non-Final Rejection — §102, §112 (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12600819
A COMPOSITION FOR FAST-CURED THERMOSETS CONTAINING AMINES, THIOLS AND UNSATURATED MOLECULES
2y 5m to grant Granted Apr 14, 2026
Patent 12600820
PHOTOCURABLE COMPOSITION WITH HIGH SILICON CONTENT
2y 5m to grant Granted Apr 14, 2026
Patent 12600817
DEVICES AND METHODS FOR ANALYZING BIOLOGICAL SAMPLES
2y 5m to grant Granted Apr 14, 2026
Patent 12590211
COMPOSITIONS AND METHODS OF MAKING A GREEN BODY OR A PRINTED ARTICLE USING THE SAME
2y 5m to grant Granted Mar 31, 2026
Patent 12583789
COMPOSITION FOR FORMING COATING LAYER OF OPTICAL FIBER AND CURED LAYER THEREOF, OPTICAL FIBER HAVING CURED LAYER, AND USE THEREOF
2y 5m to grant Granted Mar 24, 2026
Study what changed to get past this examiner. Based on 5 most recent grants.

AI Strategy Recommendation

Get an AI-powered prosecution strategy using examiner precedents, rejection analysis, and claim mapping.
Powered by AI — typically takes 5-10 seconds

Prosecution Projections

1-2
Expected OA Rounds
81%
Grant Probability
91%
With Interview (+10.4%)
2y 11m
Median Time to Grant
Low
PTA Risk
Based on 1213 resolved cases by this examiner. Grant probability derived from career allow rate.

Sign in with your work email

Enter your email to receive a magic link. No password needed.

Personal email addresses (Gmail, Yahoo, etc.) are not accepted.

Free tier: 3 strategy analyses per month