Prosecution Insights
Last updated: April 19, 2026
Application No. 16/383,035

METHOD FOR MANUFACTURING A SPECIAL EFFECT PIGMENT

Final Rejection §103
Filed
Apr 12, 2019
Examiner
PENNY, TABATHA L
Art Unit
1712
Tech Center
1700 — Chemical & Materials Engineering
Assignee
VIAVI SOLUTIONS INC.
OA Round
8 (Final)
46%
Grant Probability
Moderate
9-10
OA Rounds
4y 1m
To Grant
68%
With Interview

Examiner Intelligence

Grants 46% of resolved cases
46%
Career Allow Rate
260 granted / 566 resolved
-19.1% vs TC avg
Strong +22% interview lift
Without
With
+22.4%
Interview Lift
resolved cases with interview
Typical timeline
4y 1m
Avg Prosecution
30 currently pending
Career history
596
Total Applications
across all art units

Statute-Specific Performance

§101
0.2%
-39.8% vs TC avg
§103
59.9%
+19.9% vs TC avg
§102
7.6%
-32.4% vs TC avg
§112
26.4%
-13.6% vs TC avg
Black line = Tech Center average estimate • Based on career data from 566 resolved cases

Office Action

§103
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 § 103 The text of those sections of Title 35, U.S. Code not included in this action can be found in a prior Office action. Claims 1-4, 10, 12-13, 15-17, 19, and 21-26 are rejected under 35 U.S.C. 103 as being unpatentable over Auweter (US 20030177943) in view of Henglein (US 20090264575) and Trummer (US 20080249209). Regarding Claims 1, 19, and 24-26, Auweter teaches a method of making pigments, comprising: forming a first slurry including a first solvent, a substrate, and a polymer (Example 5, THF, polycarbonate and Primacor 59801, and Pigment Blue); forming a first functional solvent including a second solvent and a functional component (Example 5, water and fluorosurfactant); and combining the first slurry and the functional solvent so that the substrate is encapsulated by the polymer to form a first coating (Example 5, abstract). Auweter teaches the first and first functional solvents are miscible ([0010]). Auweter teaches the pigments are special effect pigments (metal effect pigments, pearl luster pigments, interference pigments, [0027-0028]; optical properties, such as the refractive index, of the particles can be optimized to the end use [0095]). Auweter does not explicitly teach the first slurry including a colorant wherein the first coating is a colored coating comprising the polymer and the colorant; however, Henglein teaches polymer coating pigment particles to produce colored effect pigments ([0081]) wherein the polymer coating includes a colorant additive pigment (Henglein, Claims 1, 4-5, 35, and 37). Henglein teaches inorganic and organic pigments, titanium dioxide, and iron oxide ([0081]). It would have been prima facie obvious to one of ordinary skill in the art at the time of the invention to modify the method of Auweter to include a colorant additive in the coating solution and coating, as suggested in Henglein, in order to obtain a resultant pigment particle having a desired color for the end use application. Auweter teaches different solvents, polymers, and colorants. Auweter does not explicitly teach repeating the process to form a second coating; however, Trummer teaches metallic effect pigments having multiple coating layers of different compositions ([0124-0129]). It would have been prima facie obvious to one of ordinary skill in the art at the time of the invention to modify the method of Auweter to include multiple layers, as taught in Trummer, because metallic effect pigments having multiple coating layers are known in the art and one of ordinary skill in the art would have had a reasonable expectation of predictably achieving coated pigments of Auweter having desirable end properties with multiple layers as suggested by Trummer. Auweter teaches metal effect pigments ([0028]). Auweter is silent as to the composition of the metal effect pigments; therefore, one of ordinary skill in the art would have been motivated to look to related art to determine suitable compositions for the metal effect pigments. Trummer teaches metallic effect pigments being platelet shaped aluminum or copper ([0107-0108]). It would have been prima facie obvious to one of ordinary skill in the art to modify the metal effect pigments of Auweter to be metallic effect pigments, as taught in Trummer, because they are known pigments in the art and one of ordinary skill in the art would have had a reasonable expectation of predictably achieving the coated pigments of Auweter with a pigment as taught in Trummer. Regarding Claim 2, Auweter teaches the polymer provided as a solution of the polymer in a first solvent selected depending on the solubility of the polymer used ([0010-0013]). Regarding Claim 3-4 and 22-23, Auweter teaches acetates, acetones, ketones, glycol, glycol derivatives, alcohols, esters, and heterocyclic solvents ([0013]). Regarding Claim 10, Auweter teaches the polymer is insoluble in the water ([0010]). Regarding Claims 12, Auweter teaches embodiments where both the first and second solvent are organic solvents ([0016]). Auweter teaches examples of solvents including acetones and cyclohexane ([0013-0016]). Auweter teaches the second solvent selected so that the polymer is insoluble in the second solvent and the second solvent is miscible with the first solvent ([0010]). It would have been prima facie obvious to one of ordinary skill in the art at the time of the invention to select the second solvent of Auweter to be acetones or cyclohexanes, as suggested in Auweter, in order to achieve a mixture of first and second organic solvents wherein the second solvent is miscible with the first solvent and does not dissolve the polymer. Regarding Claim 13, Auweter teaches the functional component includes a surfactant ([0134]). Regarding Claims 15-16, Auweter teaches continuously mixing the aqueous phase with the solvent phase and teaches the substrate being encapsulated (Example 5, abstract). Auweter teaches the first and second solvents being miscible ([0010]) and the polymer directly precipitates when its solubility is exceeded during the mixing of the solvents ([0097]). Auweter does not explicitly teach in the mixing the first slurry breaking into droplets dispersed in the functional solvent or the first solvent being drawn into the functional solvent to dry the polymer into a coating; however, Where the claimed and prior art products are identical or substantially identical in structure or composition, or are produced by identical or substantially identical processes, a prima facie case of inherency has been established, In re Best, 195 USPQ 430, 433 (CCPA 1977). With regard to the limitation that the mixing breaks the first slurry into droplets dispersed in the functional solvent and draws the first solvent into the functional solvent, when the structure recited in the prior art is substantially identical to that of the claims, the claimed properties or function are presumed inherent. MPEP 2112. In this situation, the prior art exemplifies the applicant's claimed materials and method, so the claimed function relating to mixing of the materials are present in the prior art. Absent an objective evidentiary showing to the contrary, the addition of the physical properties to the claim language fail to provide patentable distinction over the prior art of record. Regarding Claim 17, Auweter teaches mixing continuously 209 grams (2+1+200+5+0.5+0.5) at a rate of 72 g/min with 2000.66 grams (0.66+2000) at a rate of 500 g/min, i.e. combining for a time of about 4 minutes. Regarding Claim 21, Auweter teaches the first and second solvent is acetates, acetones, ketones, glycol, glycol derivatives, alcohols, esters, and heterocyclic solvents ([0013]). Auweter teaches the second solvent is water ([0015]). Auweter teaches the pigment particles present in the solution of first and/or second solvent prior to mixing ([0011]), i.e. the first and second solvent are interchangeable. Claim(s) 7 is rejected under 35 U.S.C. 103 as being unpatentable over Auweter (US 20030177943) in view of Henglein (US 20090264575) and Trummer (US 20080249209) as applied to claims 1-4, 10, 12-13, 15-17, 19, and 21-26 above, and further in view of Bartsch (US 3669922). Regarding Claim 7, Auweter teaches wherein the polymer includes polystyrene, polyvinyl acetate, polymethyl methacrylate, and mixtures thereof ([0119]). Auweter does not explicitly teach cellulose acetate butyrate; however, Bartsch teaches polymer-pigment particles wherein cellulose acetate butyrate is recognized as an equivalent polymer to those of Auweter (col. 4 ln. 68-col. 5 ln. 24). It would have been prima facie obvious to one of ordinary skill in the art at the time of the invention to modify the polymer of Auweter to include cellulose acetate butyrate, as taught in Bartsch, because it is a known polymer for colored particles in the art and one of ordinary skill in the art would have had a reasonable expectation of predictably achieving the particles of Auweter with cellulose acetate butyrate, as in Bartsch. Claim(s) 14 is rejected under 35 U.S.C. 103 as being unpatentable over Auweter (US 20030177943) in view of Henglein (US 20090264575) and Trummer (US 20080249209) as applied to 1-4, 10, 12-13, 15-17, 19, and 21-26, and further in view of Corwin (Corwin, Introductory Chemistry: Concepts and Critical Thinking, Worked Example Exercise 14.1-14.11, 6th Edition, Pearson Education, 2011, pg. 1-17). Regarding Claim 14, Auweter teaches dissolving the surfactant in the water (Example 5). Auweter does not explicitly teach the dissolving including agitating; however, stirring increases the rate that solvent molecules come in contact with solute (Corwin, 14.5). It would have been prima facie obvious to one of ordinary skill in the art at the time of the invention to modify the method of Auweter to include stirring, as taught in Corwin, in order to achieve an increased rate of dissolving. Claim(s) 27 is rejected under 35 U.S.C. 103 as being unpatentable over Auweter (US 20030177943) in view of Henglein (US 20090264575), Trummer (US 20080249209), and Bartsch (US 3669922) as applied to claim 7 above, and further in view of Horiguchi (US 4171987). Regarding Claim 27, Bartsch teaches polymer-pigment particles wherein cellulose acetate butyrate is recognized as an equivalent polymer to those of Auweter (col. 4 ln. 68-col. 5 ln. 24), as discussed above. Auweter teaches the first and second solvent is acetates, acetones, ketones, glycol, glycol derivatives, alcohols, esters, and heterocyclic solvents ([0013]). Auweter teaches the second solvent is water ([0015]). The combined references do not explicitly teach the first solvent is methyl isobutyl ketone and the second solvent is heptane; however, Horiguchi teaches a method of coating a cellulose ester solution wherein methyl isobutyl ketone is a known ketone solvent for cellulose acetate butyrate and heptane is a known alternative to water as a non-solvent for cellulose acetate butyrate (col. 2 ln. 20-45, col. 3 ln. 14-25). It would have been prima facie obvious to one of ordinary skill in the art at the time of the invention to modify the method of the combined references to include a methyl isobutyl ketone first solvent and heptane second solvent, as suggested by Horiguchi, because they are a known solvent/non-solvent in the art and one of ordinary skill in the art would have had a reasonable expectation of predictably achieving the particles of the combined references with solvent/non-solvent as in Horiguchi. Response to Arguments Applicant’s arguments, see amendment to Claim 7, filed 7/28/2025, with respect to the previous prior art rejection(s) of claim(s) have been fully considered and are persuasive. Therefore, the rejection has been withdrawn. However, upon further consideration, a new ground(s) of rejection is made as discussed above. Applicant's other arguments filed 7/28/2025 have been fully considered but they are not persuasive. Applicant argues Auweter teaches the polymer to modify the surfaces of the pigment particles and there is no teaching of suggestion in Auweter of using a second colorant combined in the polymer coating. In response to applicant's arguments against the references individually, one cannot show nonobviousness by attacking references individually where the rejections are based on combinations of references. See In re Keller, 642 F.2d 413, 208 USPQ 871 (CCPA 1981); In re Merck & Co., 800 F.2d 1091, 231 USPQ 375 (Fed. Cir. 1986). A colorant combined in the polymer coating is suggested by Henglein. Applicant argues the teachings of Auweter make the use of a second coating unpredictable because the pigment substrate serves as a seed onto which the polymer is precipitated. In response to applicant’s argument, Auweter teaches various organic and inorganic cores suitable for use with the invention and Trummer teaches metallic effect pigments having multiple coating layers of different compositions applied by solution coating methods ([0124-0129]). One of ordinary skill in the art considering the teachings of Auweter and Trummer would have had a reasonable expectation of predictability in modifying the solution based method of Auweter to include a repeated coating process and multiple layers. Applicant argues the process of Henglein is a very different mechanism than Auweter. Applicant argues the ability to use a separate colorant in the coatings of Henglein is not predictive of the ability to use a colorant in the liquid solvent precipitated coatings of Auweter. In response to Applicant’s argument, Henglein and Auweter both teach methods for applying a polymer coating layer onto a pigment particle. Contrary to Applicant’s argument, both Auweter and Henglein teach solution precipitated coatings and there is no suggestion in the art that a colorant would not be suitable for use in a solution precipitated coating. Applicant argues the rejection ignores the express teachings of Auweter that the pigment serves as a seed and that the polymer enrobed pigment particles will generally contain only one pigment particles as core. Applicant argues one of ordinary skill in the art would not expect the encapsulating coating used to enrobe a single finished pigment particle of Auweter to include pigments other than the single pigment that is being enrobed and would have been dissuaded from attempting to combine the colorants of Henglein into the polymer coatings of Auweter because Auweter teaches the process results in a single pigment being enrobed. In response to Applicant’s arguments, the coated pigments of Henglein and Auweter are both enveloped with polymer for the purpose of improved stability. Applicant argues that one of ordinary skill in the art would not combine the pigments of Henglein in the polymer coatings of Auweter; however, Henglein teaches the pigment colorant in a polymer coating on a pigment core particle. Henglein ([0143]) and Auweter ([0142]) both teach the product pigments useful in printing ink applications. Contrary to Applicant’s argument, there is no teaching or suggestion in the references that a colorant included in the polymer coating would be unpredictable. Auweter teaches mixtures of coating materials used wherein thermal, mechanical, and optical properties of the particles can be optimized to the end use. Including a pigment colorant as one of the coating materials of Auweter would predictably allow for additional modification of the optical properties of the product particles for end use optimization. Applicant argues Corwin does not overcome the above-described deficiencies; however, this is not convincing as discussed above. Conclusion Applicant's amendment necessitated the new ground(s) of rejection presented in this Office action. Accordingly, THIS ACTION IS MADE FINAL. See MPEP § 706.07(a). Applicant is reminded of the extension of time policy as set forth in 37 CFR 1.136(a). A shortened statutory period for reply to this final action is set to expire THREE MONTHS from the mailing date of this action. In the event a first reply is filed within TWO MONTHS of the mailing date of this final action and the advisory action is not mailed until after the end of the THREE-MONTH shortened statutory period, then the shortened statutory period will expire on the date the advisory action is mailed, and any nonprovisional extension fee (37 CFR 1.17(a)) pursuant to 37 CFR 1.136(a) will be calculated from the mailing date of the advisory action. In no event, however, will the statutory period for reply expire later than SIX MONTHS from the mailing date of this final action. Any inquiry concerning this communication or earlier communications from the examiner should be directed to TABATHA L PENNY whose telephone number is (571)270-5512. The examiner can normally be reached M-F 8:00-5:00. 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, Michael Cleveland can be reached on 5712721418. 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. /TABATHA L PENNY/Primary Examiner, Art Unit 1712
Read full office action

Prosecution Timeline

Apr 12, 2019
Application Filed
Mar 11, 2022
Non-Final Rejection — §103
Jun 14, 2022
Response Filed
Aug 30, 2022
Final Rejection — §103
Oct 26, 2022
Response after Non-Final Action
Dec 06, 2022
Request for Continued Examination
Dec 09, 2022
Response after Non-Final Action
Apr 04, 2023
Non-Final Rejection — §103
Jun 30, 2023
Response Filed
Oct 03, 2023
Final Rejection — §103
Jan 10, 2024
Request for Continued Examination
Jan 11, 2024
Response after Non-Final Action
Feb 21, 2024
Non-Final Rejection — §103
Jun 17, 2024
Response Filed
Sep 03, 2024
Final Rejection — §103
Nov 14, 2024
Request for Continued Examination
Nov 15, 2024
Response after Non-Final Action
Apr 23, 2025
Non-Final Rejection — §103
Jul 28, 2025
Response Filed
Oct 23, 2025
Final Rejection — §103 (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12601862
LAMELLAR PARTICLES AND METHODS OF MANUFACTURE
2y 5m to grant Granted Apr 14, 2026
Patent 12599962
SYSTEM AND METHOD FOR TREATING ADDITIVE POWDER
2y 5m to grant Granted Apr 14, 2026
Patent 12580176
STRUCTURED COMPOSITE MATERIALS
2y 5m to grant Granted Mar 17, 2026
Patent 12576429
METHOD OF WETTING LOW SURFACE ENERGY SUBSTRATE AND A SYSTEM THEREFOR
2y 5m to grant Granted Mar 17, 2026
Patent 12576427
APPARATUS AND METHODS USING COATINGS FOR METAL APPLICATIONS
2y 5m to grant Granted Mar 17, 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

9-10
Expected OA Rounds
46%
Grant Probability
68%
With Interview (+22.4%)
4y 1m
Median Time to Grant
High
PTA Risk
Based on 566 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