Prosecution Insights
Last updated: August 06, 2026
Application No. 18/681,287

ANAEROBIC ADHESIVE COMPOSITION

Non-Final OA §102
Filed
Feb 05, 2024
Priority
Aug 11, 2021 — JP 2021-131256 +1 more
Examiner
EGWIM, KELECHI CHIDI
Art Unit
1762
Tech Center
1700 — Chemical & Materials Engineering
Assignee
Okura Industrial Co. Ltd.
OA Round
1 (Non-Final)
70%
Grant Probability
Favorable
1-2
OA Rounds
7m
Est. Remaining
84%
With Interview

Examiner Intelligence

Grants 70% — above average
70%
Career Allowance Rate
557 granted / 797 resolved
+4.9% vs TC avg
Moderate +14% lift
Without
With
+13.9%
Interview Lift
resolved cases with interview
Typical timeline
3y 1m
Avg Prosecution
41 currently pending
Career history
846
Total Applications
across all art units

Statute-Specific Performance

§101
1.5%
-38.5% vs TC avg
§103
27.3%
-12.7% vs TC avg
§102
47.7%
+7.7% vs TC avg
§112
20.1%
-19.9% vs TC avg
Black line = Tech Center average estimate • Based on career data from 797 resolved cases

Office Action

§102
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. (a)(2) the claimed invention was described in a patent issued under section 151, or in an application for patent published or deemed published under section 122(b), in which the patent or application, as the case may be, names another inventor and was effectively filed before the effective filing date of the claimed invention. Claim(s) 1 and 2 is/are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Kobayashi et al. (JP S51129438). In table 1, Kobayashi et al. teaches an anaerobic adhesive composition comprising a meth)acrylic monomer (MMA, HEMA), an organic peroxide (cumene hydroperoxide), a curing accelerator (thioamide compound), and an isoparaffin wax. The composition encompasses 100 parts by mass of the (meth)acrylic monomer, 7 parts by mass of the organic peroxide, 0.08 parts by mass of the curing accelerator, and 0.35 parts by mass of isoparaffin wax. Thus, the requirements for rejection under 35 U.S.C. 102(a)(1) are met. Claim(s) 1 and 2 is/are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Tang et al. (CN 106590513). In example 4, Tang et al. teaches an anaerobic adhesive composition comprising a (meth)acrylic monomer (100 parts), an organic peroxide (cumene peroxide 1.35 parts), a curing accelerator (dimethyl-p toluidine 1.35 parts), an isoparaffin liquid wax (1.35 parts), and silica (38.1 parts). Thus, the requirements for rejection under 35 U.S.C. 102(a)(1) are met. Claim(s) 1 and 2 is/are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Kimura et al. (JP 59051902). In claim 1, Kimura et al. teaches an anaerobically curable composition comprising a radical-polymerizable acrylate monomer and/or methacrylate monomer, an organic peroxide polymerization initiator and a halogenated paraffin. In the upper right column, line 13 top. 5, upper left column, line 8, Kimura et al. teaches an anaerobically curable composition which exhibits good adhesion to an oily surface of a bolt or nut and which is obtained by subjecting 152 g of tetrahydrophthalic anhydride, 212 g of diethylene glycol and 172 g of methacrylic acid to an esterification reaction while heating to reflux to obtain a polyester polymethacrylate-containing anaerobic monomer mixture, and then mixing 80 parts of the obtained polyester polymethacrylate-containing anaerobic monomer mixture, 20 parts of a chlorinated paraffin (Empara 40), 1 part of cumene hydroperoxide, 0.5 parts of N,N-dimethylaniline and 0.5 parts of o-sulfobenzimide (example 1 etc.). Here, the Empara 40 disclosed in Kimura et al. is obtained from a paraffin wax, and because paraffin wax contains a small amount of isoparaffin (generally approximately 10% or more), it is considered that the adhesive composition disclosed in Kimura et al. contains an isoparaffin wax. Thus, the requirements for rejection under 35 U.S.C. 102(a)(1) are met. Claim(s) 1 and 2 is/are rejected under 35 U.S.C. 102(a)(1)/(a)(2) as being anticipated by Nakano et al. (USPN 4,174,311). In claim 1, Nakano et al. teach a hardenable composition that contains (1) an acrylate and/or methacrylate monomer, (2) diisopropylbenzene dihydroperoxide as a hardener, and (3) a hardening (curing) accelerator; wherein the composition is suitable for use as an adhesive.(See col. 1, lines 13-16) In col. 3, lines 36-62, col. 4, lines 10-30, col. 4, lines 37-42, examples and claims, Nakano et al. teaches mixing 840 g of methyl methacrylate, 840 g of 2-hydroxymethyl methacrylate, 6 g of paraffin wax having a melting point of 56°C and 320 g of an NBR (Nippol 1072), and then mixing 100 parts of this mixture with 0.5 parts of hydroquinone and 6 parts of diisopropylbenzene dihydroperoxide to obtain an agent A, separately adding 6 parts of ethylene thiourea (a hardening accelerator) to 100 parts of this mixture to obtain an agent B, and then combining the obtained agents A and B (example 2 etc.). Here, because paraffin wax contains a small amount of isoparaffin, it is considered that the adhesive composition disclosed in Nakano et al. contains an isoparaffin wax. Thus, the requirements for rejection under 35 U.S.C. 102(a)(1)/(a)(2) are met. Claim(s) 1-3 is/are rejected under 35 U.S.C. 102(a)(1) as being anticipated by (GB 1,083,486). In example 2, GB 1,083,486 teaches an anaerobic adhesive composition comprising a (meth)acrylic monomer (MMA, butylacrylate 100 parts), an organic peroxide (benzoylperoxide 5.5 parts), a curing accelerator (dimethyl-p toluidine 1.5 parts), and an isoparaffin wax (2.5 parts) and silica (AEROSIL 12.5 parts). The basic, untreated form of AEROSIL® which is furned silica is hydrophilic due to the presence of silanol (Si-OH) groups on its surface. Thus, the requirements for rejection under 35 U.S.C. 102(a)(1) are met. Claim(s) 1-3 is/are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Yagi (JP 10017780). In claim 4, Yagi teaches a curable adhesive comprising mainly a resin composition comprising a compound (A1) containing an acid anhydride group and a compound (B) that forms at least one of a primary amino group, a secondary amino group or ammonia by reacting with water. In addition, Yagi teaches a silica powder and a colloidal silica powder as examples of a filler (¶ 155). In ¶’s 11, 134, 136, 151, 154, 155, 159, 165, 176, 181, 182, and 254-257, Yagi teaches a curable adhesive obtained by melting 20 parts by weight of a paraffin wax (SP-0145) and 40 parts by weight of a rosin ester (Ester Gum HS), mixing these with 40 parts by weight of an ethylene-vinyl acetate copolymer resin (Evaflex #220) to obtain a thermoplastic resin 1, and then mixing 25 parts of an acrylic resin 1 (an epoxy-modified bisphenol F type diacrylate, Kayarad R-712), 50 parts of calcium carbonate as a filler, 75 parts of the obtained thermoplastic resin 1, 2 parts of a polymerization modifier 1 (cumene hydroperoxide), 1 part of a silane compound 1 (vinyltrimethoxysilane; KBM 1003), 1 part of a silane compound 2 (y-glycidoxypropyltrimethoxysilane; KBM 403) and 6 parts of a ketimine 1 (H-2) ( example 50 etc.). Here, because paraffin wax contains a small amount of isoparaffin, it is considered that the adhesive composition disclosed in Yagi contains an isoparaffin wax. Thus, the requirements for rejection under 35 U.S.C. 102(a)(1) are met. Claim(s) 1-3 is/are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Kobayashi et al. (JP 2008174707). In claim 1, Kobayashi et al. teaches a curable composition which comprises: one or more organic peroxides (a); a curing accelerator (b) that reacts with the organic peroxide(s) and accelerates polymerization of a monomer; a monofunctional (meth)acrylate (c); and a polyfunctional (meth)acrylate (d), wherein the organic peroxide (a) is included in a microcapsule. In ¶’s 15, 16, 23, 24 and 37-48, Kobayashi et al. teaches a curable composition obtained by mixing 10 parts by mass of microcapsules (containing 30 mass% of Percumyl H80, which contains 80% of cumene hydroperoxide), 0.5 parts by mass of vanadyl acetylacetonate, 15 parts by mass of methacrylic acid, 45 parts by mass of dicyclopentenyloxyethyl methacrylate, 25 parts by mass of polyethylene oxide (10 mol)-modified bisphenol A dimethacrylate, 5 parts by mass of an NBR, 15 parts by mass of an MBS, 0.5 parts by mass of Aerosil (R-974), 3 parts by mass of polyethylene oxide (2 mol)-modified bisphenol A dimethacrylate, 3 parts by mass of trimethylolpropane trimethacrylate, 1.5 parts by mass of (2-hydroxyethyl)methacrylic acid phosphate, 0.5 parts by mass of paraffin wax, 0.2 parts by mass of phenothiazine and 2 parts by mass of benzotriazole (example 1 etc.). In ¶ 65, Kobayashi et al. teaches an anaerobic (meth)acrylic monomer and is obtained using an organic peroxide that is the same as one used in examples in the present application, and is therefore considered to correspond to an anaerobic adhesive. In addition, because paraffin wax contains a small amount of isoparaffin, it is considered that the curable composition disclosed in Kobayashi et al. contains an isoparaffin wax. Furthermore, Kobayashi et al. teaches a microcrystalline wax as an example of a paraffin (¶ 65), and because microcrystalline waxes contain approximately 50% of isoparaffin, it can be said that Kobayashi et al. containing an isoparaffin wax. Thus, the requirements for rejection under 35 U.S.C. 102(a)(1) are met. Claim(s) 1-3 is/are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Asaho et al. (JP 2003105044). In claim 1, ¶’s 6, 11, 15, 18, 19, 23-26, and 28, Asaho et al. discloses a curable resin composition which contains: (1) 100 parts by mass of a polymerizable vinyl monomer comprising 30-60 mass% of methyl methacrylate (a), 20-40 mass% of 2-hydroxyethyl methacrylate (b) and 20-40 mass% of 2,2-bis( 4-(methacryloxyethoxy)phenyl) propane (c); (2) 1-10 parts by mass of a polymerization initiator comprising cumene hydroperoxide; (3) 0.1-1.0 parts by mass of a polymerization accelerator comprising vanadyl acetylacetonate; ( 4) a total of 10-30 parts by mass of an acrylonitrile-butadiene rubber and a methyl methacrylate-butadiene-styrene copolymer; and (5) 100-300 parts by mass of a silica powder having an average particle diameter of 10-50 μm. In ¶’s 6, 11, 15, 18, 19, 23-26, and 28, Asaho et al. teaches mixing 40 parts of methyl methacrylate, 30 parts of 2-hydroxyethyl methacrylate, 30 parts of dicyclopentenyloxyethyl methacrylate, 0.4 parts of vanadyl acetylacetonate, 6 parts of an acrylonitrile-butadiene rubber, 9 parts of a methyl methacrylate-butadiene-styrene copolymer, 150 parts of a silica powder, 5 parts of a phosphate, 0.5 parts of paraffin wax and 0.3 parts of hydroquinone monomethyl ether to obtain a second agent, and then mixing the obtained first and second agents (example 1 etc.). In ¶ 23, Asaho et al. teaches the curable composition containing an anaerobic (meth)acrylic monomer and is obtained using an organic peroxide that is the same as one used in examples in the present application, and is therefore considered to correspond to an anaerobic adhesive. Because paraffin wax contains a small amount of isoparaffin, it is considered that the curable composition disclosed in Asaho et al. contains an isoparaffin wax. Furthermore, Asaho et al. discloses a microcrystalline wax as an example of a paraffin (¶ 23), and because microcrystalline waxes contain approximately 50% of isoparaffin, it can be said that Asaho et al. contains an isoparaffin wax. Thus, the requirements for rejection under 35 U.S.C. 102(a)(1) are met. Claim(s) 1-3 is/are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Sudo et al. (JP 2002308944). In claim 1, Sudo et al. teaches a curable resin composition which contains a polymerizable vinyl monomer, has a static viscosity of 110,000 mPa or less at 20 rpm, and has a thixotropic factor, which is obtained by dividing the static viscosity at 2 rpm by the static viscosity at 20 rpm, of 1.7 or more. In ¶’s 5-9, 31-38, 43 and 44, Sudo et al. teaches an adhesive composition obtained by mixing 40.0 parts of phenoxyethyl methacrylate, 20.0 parts of 2-hydroxypropyl methacrylate, 30.0 parts of 2-hydroxyethyl methacrylate, 10.0 parts of 2,2-bis( 4-methacryloxypolyethoxyphenyl)propane, 13.0 parts of an acrylonitrile-butadiene rubber, 30.0 parts of a crystalline silica powder, 5.0 parts of a colloidal fine silica powder, 1.0 parts of paraffin and 0.2 parts of hydroquinone monomethyl ether to obtain a first agent, separately mixing 40.0 parts of phenoxyethyl methacrylate, 20.0 parts of 2-hydroxypropyl methacrylate, 30.0 parts of 2-hydroxyethyl methacrylate, 10.0 parts of 2,2-bis( 4-methacryloxypolyethoxyphenyl)propane, 13.0 parts of an acrylonitrile-butadiene rubber, 0.5 parts of vanadyl acetylacetonate, 30.0 parts of a crystalline silica powder, 5.0 parts of a colloidal fine silica powder, 2.0 parts of acid phosphoxyethyl methacrylate, 1.0 parts of paraffin and 0.2 parts of hydroquinone monomethyl ether to obtain a second agent, and then mixing equal quantities of the obtained first and second agents (example 2-4, etc.). In ¶ 43, Sudo et al. reach the curable resin composition containing an anaerobic (meth)acrylic monomer and is obtained using an organic peroxide that is the same as one used in examples in the present application, and is therefore considered to correspond to an anaerobic adhesive. In addition, because paraffin wax contains a small amount of isoparaffin, it is considered that the curable composition disclosed in Sudo et al. contains an isoparaffin wax. Furthermore, Sudo et al. discloses a microcrystalline wax as an example of a paraffin (and because microcrystalline waxes contain approximately 50% of isoparaffin, it can be said that Sudo et al. contains an isoparaffin wax. See ¶ 43). Thus, the requirements for rejection under 35 U.S.C. 102(a)(1) are met. Any inquiry concerning this communication or earlier communications from the examiner should be directed to KELECHI CHIDI EGWIM whose telephone number is (571)272-1099. The examiner can normally be reached M-Th 9-7. 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 Jones can be reached at (571) 270-7733. 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. /KELECHI C EGWIM/Primary Examiner, Art Unit 1762 KCE
Read full office action

Prosecution Timeline

Feb 05, 2024
Application Filed
Jun 24, 2026
Non-Final Rejection mailed — §102 (current)

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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
70%
Grant Probability
84%
With Interview (+13.9%)
3y 1m (~7m remaining)
Median Time to Grant
Low
PTA Risk
Based on 797 resolved cases by this examiner. Grant probability derived from career allowance rate.

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