Prosecution Insights
Last updated: April 19, 2026
Application No. 17/906,805

HYDROGEN STORAGE DEVICE

Non-Final OA §103§112
Filed
Sep 20, 2022
Examiner
PEREZ, JELITZA M
Art Unit
1774
Tech Center
1700 — Chemical & Materials Engineering
Assignee
H2Go Power Ltd.
OA Round
1 (Non-Final)
75%
Grant Probability
Favorable
1-2
OA Rounds
2y 5m
To Grant
99%
With Interview

Examiner Intelligence

Grants 75% — above average
75%
Career Allow Rate
436 granted / 580 resolved
+10.2% vs TC avg
Strong +29% interview lift
Without
With
+28.9%
Interview Lift
resolved cases with interview
Typical timeline
2y 5m
Avg Prosecution
34 currently pending
Career history
614
Total Applications
across all art units

Statute-Specific Performance

§103
45.4%
+5.4% vs TC avg
§102
20.4%
-19.6% vs TC avg
§112
21.1%
-18.9% vs TC avg
Black line = Tech Center average estimate • Based on career data from 580 resolved cases

Office Action

§103 §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 . Election/Restrictions Applicant's election with traverse of Group I, Claims 1-24 in the reply filed on September 5, 2025 is acknowledged. Upon reconsideration, the examiner found that the requirement for restriction is improper. Therefore, the requirement for restriction is withdrawn and Groups I and II have been rejoined. Claim Objections Claims 3 and 11 are objected to because of the following informalities: Incorrect spelling. Claim 3 recites: “…wherein the thermally conducting network comprises fluidically interconnected passageways within the arms and/or nodes thereof, for flow therethough of a fluid.” The correct word should be “therethrough”. Claim 11 recites: “…wherein the LOHC comprises and/or is a compound selected from a group consisting of: N-ethylcarbazole (NEC), monobenzyltoluene (MBT), dibenzyltoluene (DBT), 1,2- dihydro-1,2-azaborine (AB), toluene (TOL), naphthalene (NAP), benzene, phenanthrene, pyrene, pyridine, chinoline, flurene, carbazole, methanol, formic acid, phenazine, ammonia, and mixtures thereof.” The correct compound is “fluorene”. For purposes of examination, examiner will interpret claim 11 as reciting: “…wherein the LOHC comprises and/or is a compound selected from a group consisting of: N-ethylcarbazole (NEC), monobenzyltoluene (MBT), dibenzyltoluene (DBT), 1,2- dihydro-1,2-azaborine (AB), toluene (TOL), naphthalene (NAP), benzene, phenanthrene, pyrene, pyridine, chinoline, fluorene, carbazole, methanol, formic acid, phenazine, ammonia, and mixtures thereof. Claim 8 is objected to because of the following informalities: Missing preposition. Claim 8 recites: “…wherein the first heater is arranged heat the hydrogen storage material to a temperature in a range of from 50 to 400ºC.” Preposition “to” is missing after the word “arranged”. For purposes of examination, examiner will interpret claim 8 as reciting: “…wherein the first heater is arranged to heat the hydrogen storage material to a temperature in a range of from 50 to 400ºC.” Appropriate correction is required. 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. The following is a quotation of 35 U.S.C. 112(b): (b) CONCLUSION.—The specification shall conclude with one or more claims particularly pointing out and distinctly claiming the subject matter which the inventor or a joint inventor regards as the invention. The following is a quotation of 35 U.S.C. 112 (pre-AIA ), second paragraph: The specification shall conclude with one or more claims particularly pointing out and distinctly claiming the subject matter which the applicant regards as his invention. Claim 4 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 4 recites: “The hydrogen storage device according to claim 1, wherein the thermally conducting network comprises a LOHC hydrogenation and/or dehydrogenation catalyst, provided on and/or in a surface thereof.” This limitation is redundant and therefore fails to further limit the subject matter of claim 1. Applicant may cancel the claim, amend the claim to place the claim in proper dependent form, rewrite the claim in independent form, or present a sufficient showing that the dependent claim complies with the statutory requirements. Claims 7 and 10 are rejected under 35 U.S.C. 112(b) or 35 U.S.C. 112 (pre-AIA ), second paragraph, as being indefinite for failing to particularly point out and distinctly claim the subject matter which the inventor or a joint inventor (or for applications subject to pre-AIA 35 U.S.C. 112, the applicant), regards as the invention. Claim 7 recites: “…wherein the first heater is arranged to provide a heat output in a range from 0.1MWm-3 to 50MWm-3, preferably in a range from 1MWm-3 to 25MWm-3, more preferably in a range from 2.5MWm-3 to 10MWm-3. The term “preferably” is considered indefinite because it this is a relative term and it is unclear as to what the meets and bounds of the claim is. For purposes of examination, examiner will interpret claim 7 as reciting: “…wherein the first heater is arranged to provide a heat output in a range from 0.1MWm-3 to 50MWm-3. Claim 10 recites: “…wherein the LOHC comprises and/or is a saturated cycloalkene…” This limitation is considered indefinite because it is unclear as to what applicant refers to. A cycloalkene is inherently unsaturated because it contains at least one carbon-carbon double bond in their ring, while a saturated cyclic compound (e.g. cycloalkanes) have only single bonds. Therefore, the term saturated cycloalkene would be contradictory. 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. The factual inquiries for establishing a background for determining obviousness under 35 U.S.C. 103 are summarized as follows: 1. Determining the scope and contents of the prior art. 2. Ascertaining the differences between the prior art and the claims at issue. 3. Resolving the level of ordinary skill in the pertinent art. 4. Considering objective evidence present in the application indicating obviousness or nonobviousness. Claims 1, 3-11, 13, 15-17, 20, 23-24 and 26 are rejected under 35 U.S.C. 103 as being unpatentable over Ishikawa et al. (US Pat. Pub. No. 2011/0005473, hereinafter Ishikawa). In regards to Claim 1, Ishikawa discloses a hydrogen storage device (#40) comprising: a first vessel (#41, #51), having a first fluid inlet (#42) and/or a first fluid outlet (#43), having therein a thermally conducting network (#52) thermally coupled to a first heater (see figures 7 and 8a-8b and paragraphs [0084] and [0147]-[0150]; Ishikawa discloses a hydrogen supply device #41, i.e. first vessel, using hydrogen separation tubes #52, i.e. thermally conducting network, which comprise multiple reaction tubes provided inside the hydrogen supply device #41 and each reaction tube #52 is filled with a catalyst layer #56, and the catalyst can be heated by a heater, i.e. first heater, provided on the outer wall of the hydrogen supply device #40, i.e. thermally conducting network is thermally coupled to a first heater.); wherein the first vessel (#41, #51) is arranged to receive therein a hydrogen storage material (fuel) in thermal contact, at least in part, with the thermally conducting network (#52) (see figures 7 and 8a-8b and paragraphs [0048], [0112], [0149] and [0151]); wherein the thermally conducting network (#52, #70, #73) has a lattice geometry, a gyroidal geometry and/or a fractal geometry in two and/or three dimensions, comprising a plurality of nodes, having thermally conducting arms (catalyst plates) therebetween, with voids (#53) between the arms (see figures 8a-8b and 10a-10b and paragraphs [0148]-[0150] and [0159]); wherein the hydrogen storage material comprises and/or is a liquid organic hydrogen carrier (LOHC) (see paragraph [0008]-[0009], [0048], [0082] and [0112]); and wherein the thermally conducting network (#52) comprises a LOHC hydrogenation and/or dehydrogenation catalyst provided on and/or in a surface thereof (see paragraphs [0084]-[0091], [0094] and [0147]-[0150]). In regards to Claim 3, Ishikawa discloses wherein the thermally conducting network (#52) comprises fluidically interconnected passageways within the arms and/or nodes thereof, for flow therethrough of a fluid (see figures 8a-8b and 10a-10b and paragraphs [0148]-[0150] and [0159]). In regards to Claim 4, Ishikawa discloses wherein the thermally conducting network (#52) comprises a LOHC hydrogenation and/or dehydrogenation catalyst, provided on and/or a in a surface thereof (see paragraphs [0048], [0084]-[0091], [0094] and [0147]-[0150]). In regards to Claim 5, Ishikawa discloses the hydrogen storage device as recited in claim 1. Although Ishikawa does not explicitly disclose wherein the thermally conducting network has a porosity in a range of from 50% to 99% by volume of the thermally conducting network, adjusting the porosity of the thermally conducting network to an optimum range, such as from 50% to 99% by volume of the thermally conducting network as claimed, is within one skilled in the art through routine experimentation, in order to obtain a desired end-result, such as for improved hydrogen storage, and is considered prima facie obvious, absent evidence to the criticality or new or unexpected results. See MPEP 2144.05. In regards to Claim 6, Ishikawa discloses the hydrogen storage device as recited in claim 1. Although Ishikawa does not explicitly disclose wherein the thermally conducting network has a specific surface area in a range from 0.1m-1 to 100m-1, Ishikawa discloses substantially the same hydrogen storage device and having substantially similar thermally conducting network as claimed by the applicant. Therefore, it is reasonably expected, absent evidence to the contrary, that Ishikawa’s thermally conducting network will have a specific surface area in a range as claimed by the applicant, as it has been held that when the structure recited in the reference is substantially identical to that of the claims, claimed functions are considered prima facie obvious, and also it has been held that chemical compositions and its properties are inseparable. See MPEP 2112.01. In regards to Claim 7, Ishikawa discloses the hydrogen storage device as recited in claim 1. Although Ishikawa does not explicitly disclose that the first heater is arranged to provide a heat output in a range from 0.1MWm-3 to 50MWm-3, Ishikawa discloses substantially the same hydrogen storage device with substantially similar first heater as claimed by the applicant. Therefore, it is reasonably expected, absent evidence to the contrary, that Ishikawa’s heater will be reasonably capable of functioning in the same manner as claimed, as it has been held that when the structure recited in the reference is substantially identical to that of the claims, claimed functions are considered prima facie obvious. See MPEP 2112.01. In regards to Claim 8, Ishikawa discloses wherein the first heater is arranged to heat the hydrogen storage material to a temperature in a range of from 50 to 400ºC (see paragraph [0150]; Ishikawa discloses wherein the catalyst can be heated by a heater provided on the outer wall of the hydrogen supply device (#41, #51). The produced hydrogen from methylcyclohexane by the hydrogen supply devices of figure 8 and hydrogen gas of 250 liters per minute was obtained at 250ºC. In view of this, it is considered reasonably obvious, absent evidence to the contrary, that the first heater heats the hydrogen storage material to a temperature of 250ºC, which falls inside the claimed range of from 50 to 400ºC, thereby making the claimed range prima facie obvious. See MPEP 2144.05.). In regards to Claim 9, Ishikawa discloses further comprising a pump (#45 booster pump) arranged to flow the hydrogen storage material through the first vessel (#41, #51) (see figure 7 and paragraphs [0082] and [0147]).’ In regards to Claim 10, Ishikawa discloses wherein the LOHC comprises and/or is an aromatic, heterocyclic aromatic and/or a mixture thereof (see paragraphs [0048] and [0112]). In regards to Claim 11, Ishikawa discloses wherein the LOHC comprises and/or is a compound selected from a group consisting of: N-ethylcarbazole (NEC), monobenzyltoluene (MBT), dibenzyltoluene (DBT), 1,2- dihydro-1,2-azaborine (AB), toluene (TOL), naphthalene (NAP), benzene, phenanthrene, pyrene, pyridine, chinoline, flurene, carbazole, methanol, formic acid, phenazine, ammonia, and mixtures thereof (see paragraphs [0048] and [0112]). In regards to Claim 13, Ishikawa discloses the hydrogen storage device as recited in claim 1. Although Ishikawa does not explicitly disclose having a hydrogen storage density of at least 0.01wt% of the hydrogen storage material, Ishikawa discloses substantially the same hydrogen storage device as claimed by the applicant. Therefore, it is reasonably expected, absent evidence to the contrary, that Ishikawa’s hydrogen storage device will function in the same manner as claimed, as it has been held that when the structure recited in the reference is substantially identical to that of the claims, claimed functions are considered prima facie obvious. See MPEP 2112.01. In regards to Claim 15, Ishikawa discloses the hydrogen storage device as recited in claim 1. Although Ishikawa is silent in regards to wherein an effective density of the lattice geometry is uniform in a first dimension and non-uniform in mutually orthogonal second and third dimensions, adjusting/changing the shape of the lattice geometry to have an effective density of the lattice geometry be uniform in a first dimension and non-uniform in mutually orthogonal second and third dimensions is a mere engineering design choice in order to obtain a desired end-result, such as for improved hydrogen generation and is considered prima facie obvious, absent evidence to the criticality or new or unexpected results. See MPEP 2144.04. In regards to Claim 16, Ishikawa discloses the hydrogen storage device as recited in claim 1. Although Ishikawa is silent in regards to wherein the lattice geometry is Bravais lattice, a monoclinic lattice, an orthorhombic lattice, a tetragonal lattice, a hexagonal lattice or a cubic lattice, changing the shape of the lattice geometry is a mere engineering design choice in order to obtain a desired end-result, as is considered prima facie obvious, absent evidence to the criticality or new or unexpected results. See MPEP 2144.04. In regards to Claim 17, Ishikawa discloses the hydrogen storage device as recited in claim 1. Although Ishikawa is silent in regards to wherein the thermally conductive arms have a cross sectional dimension in a range from 0.1mm to 10mm, adjusting the arms of the cross sectional dimension to an optimum value is within one skilled in the art through routine experimentation, in order to obtain a desired end-result, such as for improved hydrogen generation and storage, and is considered prima facie obvious, absent evidence to the criticality or new or unexpected results. See MPEP2144.05. In regards to Claim 20, Ishikawa discloses wherein the thermally conducting network (#52) partially fills an internal volume of the first vessel, of at least 50% by volume of the first vessel (#41, #51), thereby defining an unfilled volume (see figures 8a-8b and 10a-10b and paragraphs [0148]-[0150]). In regards to Claim 23, Ishikawa discloses wherein the hydrogen storage device (#40) comprises thermal insulation (#54), configured to thermally insulate the first vessel (#41, #51) (see figure 8a and paragraph [0148]). In regards to Claim 24, Ishikawa discloses wherein the first vessel comprises a set of expansion tanks (#41, #48), including a first expansion tank (#41) and a second expansion tank (348), wherein the first expansion tank (#41) and the second expansion tank (#48) are mutually fluidically coupled (see figure 7 and paragraph [0147]). In regards to Claim 26, Ishikawa discloses a method of providing hydrogen comprising releasing hydrogen gas from a hydrogen storage device (#40) according to claim 1, comprising heating the thermally conducting network (#52) using the first heater (see figure 7 and 8a-8b and paragraphs [0147]-[0150]). Claim 12 is rejected under 35 U.S.C. 103 as being unpatentable over Ishikawa in view of Milstein et al. (US Pat. Pub. No. 2022/0024758, with an effective filing date of February 6, 2020, hereinafter Milstein). In regards to Claim 12, Ishikawa discloses the hydrogen storage device as recited in claim 1, but fails to disclose wherein the hydrogen storage material comprises a dopant, is provided in a solvent, or both. However, Milstein teaches a system, process and a method of storing hydrogen and releasing it on demand, comprising and making use of N-heterocycles as liquid organic hydrogen carriers (LOHCs) (see paragraph [0035]). The system for storing hydrogen and releasing it on demand comprises a transition metal catalyst, which is used for both hydrogen loading (hydrogenation) and hydrogen discharging (dehydrogenation) processes (see paragraph [0069]). In some embodiments, the system and method further comprises at least one organic solvent, such as benzene, toluene, p-xylene, cyclohexane and combinations thereof (see paragraph [0074]). Milstein further teaches in a working example for dehydrogenation of 2-methylpiperidine, i.e. LOHC, to 2-picoline in a solvent: In a glovebox, catalyst, t-BuOK (0.2mmol), 2-methylpiperidine (1mmol) and solvent (1ml) were added to a Schlenk tube for hydrogen release (see paragraphs [0110]-[0111]). It would have been obvious by one of ordinary skill in the art before the effective filing date of the applicant’s invention to modify the hydrogen storage device as disclosed by Ishikawa by having the hydrogen storage material to further comprise a dopant, is provided in a solvent, or both, as claimed by the applicant, with a reasonable expectation of success as Milstein teaches a system, process and a method of storing hydrogen and releasing it on demand, comprising and making use of N-heterocycles as liquid organic hydrogen carriers (LOHCs), wherein the system for storing hydrogen and releasing it on demand comprises a transition metal catalyst, which is used for both hydrogen loading (hydrogenation) and hydrogen discharging (dehydrogenation) processes (see paragraph [0069]), whereby in some embodiments, the system and method further comprises at least one organic solvent, such as benzene, toluene, p-xylene, cyclohexane and combinations thereof, such that in a working example for dehydrogenation of 2-methylpiperidine, i.e. LOHC, to 2-picoline in a solvent, a solvent is added to 2-methylpiperidine and disposed in a Schlenk tube along with a catalyst and t-BuOK for hydrogen release (see paragraphs [0110]-[0111]). Claims 2, 14, 18-19, 21-23 and 25 are rejected under 35 U.S.C. 103 as being unpatentable over Ishikawa in view of Hamed et al. (US Pat. Pub. No. 2021/0180837, with a PCT publication date of December 19, 2019, hereinafter Hamed). In regards to Claim 2, Ishikawa discloses the hydrogen storage device as recited in claim 1. Ishikawa further discloses wherein the hydrogen storage device is arrangeable in a first arrangement wherein the thermally conducting network (#52) is within the first vessel (#41, #51) (see figures 7 and 8a-8b). Ishikawa fails to disclose a second arrangement wherein the thermally conducting network is outside the first vessel, and wherein the first vessel comprises a circumferential releasable joint. However, Hamed teaches a hydrogen storage device comprising a hollow metal cylindrical vessel (#1) having a fluid inlet (#8), a fluid outlet (#9), and an aluminum fractal structure (#4), i.e. thermally conducting network, thermally coupled to a heater (#6). The vessel (#1) is arranged to receive a hydrogen storage material (#5) in thermal contact with the thermally conducting network (#4) (see figure 1 and abstract). The hydrogen storage device further comprises two metallic end-caps (#2) which forms a hydrogen gas containment volume along with the hollow metal cylindrical vessel (#1). Inside this volume, the aluminum fractal structure (#4), i.e. thermally conducting network, is introduced, i.e. first arrangement wherein the thermally conducting network is within the first vessel. The end-caps (#2) are held in place and form a seal through a thread and O-ring arrangement (#3), i.e. circumferential releasable joint. The end-caps (#2) can be removed for easy access to the hydrogen containment volume (see figure 1 and paragraph [0046]). Although Hamed does not explicitly disclose a second arrangement wherein the thermally conducting network is outside the first vessel, it is considered reasonably obvious, absent evidence to the contrary, that a second arrangement where the thermally conducting network is outside the first vessel is obviously present at some point since Hamed clearly teaches that the end-caps can be removed for access to the hydrogen containment volume and the aluminum fractal structure is placed within the hydrogen containment volume of the hollow metal cylindrical vessel. It would have been obvious by one of ordinary skill in the art before the effective filing date of the applicant’s invention to modify the hydrogen storage device as disclosed by Ishikawa by having the hydrogen storage device to be also arrangeable in a second arrangement wherein the thermally conducting network is outside the first vessel, and wherein the first vessel comprises a circumferential releasable joint, as claimed by the applicant, with a reasonable expectation of success, as Hamed teaches a hydrogen storage device comprising a vessel having a fluid inlet, a fluid outlet, and a thermally conducting network thermally coupled to a heater, wherein the vessel is arranged to receive a hydrogen storage material in thermal contact with the thermally conducting network, wherein the hydrogen storage device further comprises two metallic end-caps which forms a hydrogen gas containment volume along with the hollow metal cylindrical vessel, whereby inside this volume, the aluminum fractal structure, i.e. thermally conducting network, is introduced, i.e. first arrangement wherein the thermally conducting network is within the first vessel, the end-caps are held in place and form a seal through a thread and O-ring arrangement, i.e. circumferential releasable joint, and the end-caps can be removed for easy access to the hydrogen containment volume, thereby improving the ease of maintenance and replacement of the thermally conducting network within the vessel (see figure 1 and paragraph [0046]). In regards to Claim 14, Ishikawa discloses the hydrogen storage device as recited in claim 1, but fails to disclose wherein the fractal geometry is selected from a group consisting of: a Quadratic Koch Island, a Quadratic Koch surface, a Von Koch surface, a Koch Snowflake, a Sierpinski carpet, a Sierpinski tetrahedron, a Mandelbox, a Mandelbulb, a Dodecahedron fractal, a Icosahedron fractal, a Octahedron fractal, a Menger sponge, a Jerusalem cube, and a 3D H-fractal. However, Hamed teaches a hydrogen storage device comprising a vessel (#1) having a fluid inlet (#8), a fluid outlet (#9), and a thermally conducting network (#4) thermally coupled to a heater (#6). The vessel (#1) is arranged to receive a hydrogen storage material (#5) in thermal contact with the thermally conducting network (#4) (see figure 1 and abstract). The thermally conducting network (#4) has a fractal geometry in two or three dimensions. It has been found that the fractal geometry provides an especially high surface area to volume ratio, which enables especially efficient heat transfer to and from the hydrogen storage material. The fractal geometry may be selected from a 3D H-fractal, a Quadratic Koch Island, a Quadratic Koch surface, a Von Koch surface, a Koch Snowflake, a Sierpinski carpet, a Sierpinski tetrahedron, a Mandelbox, a Mandelbulb, a Dodecahedron fractal, a Icosahedron fractal, a Octahedron fractal, a Menger sponge and a Jerusalem cube (see paragraph [0033]). It would have been obvious by one of ordinary skill in the art before the effective filing date of the applicant’s invention to modify the hydrogen storage device as disclosed by Ishikawa by substituting a known thermally conducting network for another known thermally conducting network such as a thermal conducting network having a fractal geometry such as a Quadratic Koch Island, a Quadratic Koch surface, a Von Koch surface, a Koch Snowflake, a Sierpinski carpet, a Sierpinski tetrahedron, a Mandelbox, a Mandelbulb, a Dodecahedron fractal, a Icosahedron fractal, a Octahedron fractal, a Menger sponge, a Jerusalem cube and a 3D H-fractal geometry, as claimed by the applicant, with a reasonable expectation of success, as Hamed teaches a hydrogen storage device comprising a vessel having a fluid inlet, a fluid outlet, and a thermally conducting network thermally coupled to a heater, wherein the vessel is arranged to receive a hydrogen storage material in thermal contact with the thermally conducting network, whereby the thermally conducting network has a fractal geometry in two or three dimensions such as a 3D H-fractal, a Quadratic Koch Island, a Quadratic Koch surface, a Von Koch surface, a Koch Snowflake, a Sierpinski carpet, a Sierpinski tetrahedron, a Mandelbox, a Mandelbulb, a Dodecahedron fractal, a Icosahedron fractal, a Octahedron fractal, a Menger sponge and a Jerusalem cube, since it has been found that the fractal geometry provides an especially high surface area to volume ratio, which enables especially efficient heat transfer to and from the hydrogen storage material (see paragraph [0033]). In regards to Claim 18, Ishikawa discloses the hydrogen storage device as recited in claim 1, but fails to disclose wherein the thermally conducting network is formed, at least in part, by additive manufacturing and/or by casting. However, Hamed teaches a hydrogen storage device comprising a vessel (#1) having a fluid inlet (#8), a fluid outlet (#9), and a thermally conducting network (#4) thermally coupled to a heater (#6). The vessel (#1) is arranged to receive a hydrogen storage material (#5) in thermal contact with the thermally conducting network (#4) (see figure 1 and abstract). The thermally conducting network (#4) has a fractal geometry in two or three dimensions. It has been found that the fractal geometry provides an especially high surface area to volume ratio, which enables especially efficient heat transfer to and from the hydrogen storage material. The thermally conducting network (#4) is produced by 3D printing since it allows for the fabrication of especially complex shapes with fine control and in three dimensions, or it can alternatively be formed by casting (see paragraphs [0024]-[0025] and [0033]). It would have been obvious by one of ordinary skill in the art before the effective filing date of the applicant’s invention to modify the hydrogen storage device as disclosed by Ishikawa by forming the thermally conducting network by additive manufacturing and/or by casting, as claimed by the applicant, with a reasonable expectation of success, as Hamed teaches a hydrogen storage device comprising a vessel having a fluid inlet, a fluid outlet, and a thermally conducting network thermally coupled to a heater, wherein the vessel is arranged to receive a hydrogen storage material in thermal contact with the thermally conducting network, whereby the thermally conducting network has a fractal geometry in two or three dimensions and the thermally conducting network (#4) is produced by 3D printing since it allows for the fabrication of especially complex shapes with fine control and in three dimensions, or it can alternatively be formed by casting (see paragraphs [0024]-[0025] and [0033]). In regards to Claim 19, Ishikawa discloses the hydrogen storage device as recited in claim 1, but fails to disclose further comprising a thermally-conducting foam attached and/or attachable to the thermally conducting network. However, Hamed teaches a hydrogen storage device comprising a vessel (#1) having a fluid inlet (#8), a fluid outlet (#9), and a thermally conducting network (#4) thermally coupled to a heater (#6). The vessel (#1) is arranged to receive a hydrogen storage material (#5) in thermal contact with the thermally conducting network (#4) (see figure 1 and abstract). The thermally conducting network (#4) has a fractal geometry in two or three dimensions. A metal foam may be attached to the thermally conducting network (#4) since it has been found that a metal foam can aid heat transfer to and from the hydrogen storage material (see paragraphs [0026] and [0033]). It would have been obvious by one of ordinary skill in the art before the effective filing date of the applicant’s invention to modify the hydrogen storage device as disclosed by Ishikawa by including a thermally-conducting foam attached and/or attachable to the thermally conducting network, as claimed by the applicant, with a reasonable expectation of success, as Hamed teaches a hydrogen storage device comprising a vessel having a fluid inlet, a fluid outlet, and a thermally conducting network thermally coupled to a heater, wherein the vessel is arranged to receive a hydrogen storage material in thermal contact with the thermally conducting network, whereby the thermally conducting network has a fractal geometry in two or three dimensions, and a metal foal may be attached to the thermally conducting network, as it has been found that a metal foam can aid heat transfer to and from the hydrogen storage material (see paragraphs [0026] and [0033]). In regards to Claim 21, Ishikawa discloses the hydrogen storage device as recited in claim 1, but fails to disclose wherein the first heater comprises a Joule heater, a recirculating heater and/or a hydrogen catalytic combustor and the hydrogen storage device is arranged to interchangeably receive the Joule heater and the recirculating heater therein and/or thereon. However, Hamed teaches a hydrogen storage device comprising a vessel (#1) having a fluid inlet (#8), a fluid outlet (#9), and a thermally conducting network (#4) thermally coupled to a heater (#6). The vessel (#1) is arranged to receive a hydrogen storage material (#5) in thermal contact with the thermally conducting network (#4) (see figure 1 and abstract). The thermally conducting network (#4) has a fractal geometry in two or three dimensions. The heater can make use of Joule heating, i.e. heater comprises a Joule heater and the hydrogen storage device is arranged to interchangeably receive the Joule heater and the recirculating heater therein and/or thereon (see paragraphs [0019]-[0020] and [0033]). It would have been obvious by one of ordinary skill in the art before the effective filing date of the applicant’s invention to modify the hydrogen storage device as disclosed by Ishikawa by substituting a known heater for another known heater such as the first heat to comprise a Joule heater, a recirculating heater and/or a hydrogen catalytic combustor and the hydrogen storage device is arranged to interchangeably receive the Joule heater and the recirculating heater therein and/or thereon, as claimed by the applicant, with a reasonable expectation of success, as Hamed teaches a hydrogen storage device comprising a vessel having a fluid inlet, a fluid outlet, and a thermally conducting network thermally coupled to a heater, wherein the vessel is arranged to receive a hydrogen storage material in thermal contact with the thermally conducting network, whereby the thermally conducting network has a fractal geometry in two or three dimensions, and the heater can make use of Joule heating, i.e. heater comprises a Joule heater and the hydrogen storage device is arranged to interchangeably receive the Joule heater and the recirculating heater therein and/or thereon (see paragraphs [0019]-[0020]). In regards to Claim 22, Ishikawa discloses the hydrogen storage device as recited in claim 1, but fails to disclose wherein the hydrogen storage device comprises a heat exchanger configured to exchange heat from and/or the LOHC. However, Hamed teaches a hydrogen storage device comprising a vessel (#1) having a fluid inlet (#8), a fluid outlet (#9), and a thermally conducting network (#4) thermally coupled to a heater (#6). The vessel (#1) is arranged to receive a hydrogen storage material (#5) in thermal contact with the thermally conducting network (#4) (see figure 1 and abstract). The thermally conducting network (#4) has a fractal geometry in two or three dimensions. The heater is a thermoelectric heater and/or cooler which can enable heat to be removed from the hydrogen storage material during the hydrogen storage phase, and heat to be supplied to the hydrogen storage material during hydrogen release (see paragraphs [0021] and [0033]). This is considered equivalent to wherein the hydrogen storage device comprises a heat exchanger configured to exchange heat from and/or the hydrogen storage material, as claimed by the applicant. It would have been obvious by one of ordinary skill in the at before the effective filing date of the applicant’s invention to modify the hydrogen storage device as disclosed by Ishikawa by having the hydrogen storage device to comprise a heat exchanger configured to exchange heat from and/or the LOHC, as claimed by the applicant, with a reasonable expectation of success, as Hamed teaches a hydrogen storage device comprising a vessel having a fluid inlet, a fluid outlet, and a thermally conducting network thermally coupled to a heater, wherein the vessel is arranged to receive a hydrogen storage material in thermal contact with the thermally conducting network, whereby the thermally conducting network has a fractal geometry in two or three dimensions, and the heater is a thermoelectric heater and/or cooler which can enable heat to be removed from the hydrogen storage material during the hydrogen storage phase, and heat to be supplied to the hydrogen storage material during hydrogen release (see paragraphs [0021] and [0033]). In regards to Claim 25, Ishikawa discloses the hydrogen storage device (#40) as recited in claim 1 and heating the thermally conducting network (#52) using the first heater (see figures 7 and 8a-8b and paragraphs [0084] and [0147]-[0150]; Ishikawa discloses a hydrogen supply device #41, i.e. first vessel, using hydrogen separation tubes #52, i.e. thermally conducting network, which comprise multiple reaction tubes provided inside the hydrogen supply device #41 and each reaction tube #52 is filled with a catalyst layer #56, and the catalyst can be heated by a heater, i.e. first heater, provided on the outer wall of the hydrogen supply device #40, i.e. thermally conducting network is thermally coupled to a first heater.). Ishikawa fails to disclose a method of storing hydrogen comprising passing hydrogen gas into the hydrogen storage device. However, Hamed teaches a method of storing hydrogen and a hydrogen storage device comprising a vessel (#1) having a fluid inlet (#8), a fluid outlet (#9), and a thermally conducting network (#4) thermally coupled to a heater (#6). The vessel (#1) is arranged to receive a hydrogen storage material (#5) in thermal contact with the thermally conducting network (#4) (see figure 1 and abstract). The thermally conducting network (#4) has a fractal geometry in two or three dimensions (see paragraph [0033]). The fluid inlet #8 located through the lid and fractal act as a hydrogen gas inlet, which passes hydrogen gas into the hydrogen storage device (see paragraphs [0039], [0042] and [0050] and claim 12). It would have been obvious by one of ordinary skill in the art before the effective filing date of the applicant’s invention to modify the hydrogen storage device as disclosed by Ishikawa by having a method of storing hydrogen comprising passing hydrogen gas into the hydrogen storage device, as claimed by the applicant, with a reasonable expectation of success, as Hamed teaches a hydrogen storage device comprising a vessel having a fluid inlet, a fluid outlet, and a thermally conducting network thermally coupled to a heater, wherein the vessel is arranged to receive a hydrogen storage material in thermal contact with the thermally conducting network, whereby the thermally conducting network has a fractal geometry in two or three dimensions, and the fluid inlet #8 located through the lid and fractal act as a hydrogen gas inlet, which passes hydrogen gas into the hydrogen storage device, thereby improving the absorption of hydrogen within the hydrogen storage device (see paragraphs [0039], [0042] and [0050] and claim 12). Conclusion Any inquiry concerning this communication or earlier communications from the examiner should be directed to JELITZA M PEREZ whose telephone number is (571)272-8139. The examiner can normally be reached Monday-Friday 9:00am-6:00pm. 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, Claire Wang can be reached at (571) 270-1051. 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. /JELITZA M PEREZ/Primary Examiner, Art Unit 1774
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Prosecution Timeline

Sep 20, 2022
Application Filed
Sep 22, 2022
Response after Non-Final Action
Jan 14, 2026
Non-Final Rejection — §103, §112 (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
75%
Grant Probability
99%
With Interview (+28.9%)
2y 5m
Median Time to Grant
Low
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