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In this paper, a mathematical ordinary differential tumor-immune model is proposed based on an immune checkpoint inhibitor, which is an innovative method for tumor immunotherapies. Two important factors in tumor-immune response are the programmed cell death protein 1 (PD-1) and its ligand PD-L1. The model consists of three populations: tumor cells, activated T cells and anti-PD-1. By analyzing the dynamics of the model, it is found that there is always a unique tumor-free equilibrium and at most two tumor interior equilibria. The nonexistence of nontrivial positive periodic orbits is established by using the new Dulac function, and then a global dynamics of the model is obtained. The conclusions of our analysis show that increasing the possibility of T cells killing tumor cells (p), early detection of tumor cells, or the use of PD-1 inhibitors to activate T cells are effective in eliminating tumor cells. [ABSTRACT FROM AUTHOR]

Catalytic hydrogenation of nitriles represents an efficient and sustainable one‐step synthesis of valuable bulk and fine chemicals. We report herein a molecular cobalt electrocatalyst for selective hydrogenative coupling of nitriles with amines using protons as the hydrogen source. The key to success for this reductive reaction is the use of an electrocatalytic approach for efficient cobalt‐hydride generation through a sequence of cathodic reduction and protonation. As only electrons (e−) and protons (H+) as the redox equivalent and hydrogen source, this general electrohydrogenation protocol is showcased by highly selective and straightforward synthesis of various functionalized and structurally diverse amines, as well as deuterium isotope labeling applications. Mechanistic studies reveal that the electrogenerated cobalt‐hydride transfer to nitrile process is the rate‐determining step. [ABSTRACT FROM AUTHOR]

Catalytic hydrogenation of nitriles represents an efficient and sustainable one‐step synthesis of valuable bulk and fine chemicals. We report herein a molecular cobalt electrocatalyst for selective hydrogenative coupling of nitriles with amines using protons as the hydrogen source. The key to success for this reductive reaction is the use of an electrocatalytic approach for efficient cobalt‐hydride generation through a sequence of cathodic reduction and protonation. As only electrons (e−) and protons (H+) as the redox equivalent and hydrogen source, this general electrohydrogenation protocol is showcased by highly selective and straightforward synthesis of various functionalized and structurally diverse amines, as well as deuterium isotope labeling applications. Mechanistic studies reveal that the electrogenerated cobalt‐hydride transfer to nitrile process is the rate‐determining step. [ABSTRACT FROM AUTHOR]

A metal-free porphyrin T4PP with a pyridine group is proposed as a new electrode for lithium/sodium-based dual-ion batteries (LDIBs/SDIBs). The electrochemical performance and reaction mechanism of T4PP are explored thoroughly. The extended porphyrin conjugated structure by the pyridine groups enables an excellent cycle life (5000 cycles) and a high-power density (18.7 kW kg−1). A hybrid charge-storage mechanism with the contribution of both cations and anions benefits fast charge transfer. [ABSTRACT FROM AUTHOR]

Introduction: High blood pressure is one of the main modifiable risk factors for dementia. However, it remains unclear whether lowering the blood pressure effectively prevents cognitive impairment. Our objective was to explore the association between the prevalence, medication adherence and control of hypertension and mild cognitive impairment (MCI) among elderly individuals in northern China. Methods: A two-stage clustering sampling method was used, and 9036 participants aged ≥ 65 years were included in the analysis. The Mini-Mental State Examination and activities of daily living were used to assess participants' cognitive function. Demographic characteristics (gender, age, marital status, education level, occupation), history and duration of hypertension, use of antihypertensive medications (AHMs) and its control effect were obtained. Results: The prevalence of MCI in all participants was 18.1%, and the prevalence of MCI was significantly higher in hypertensive subjects than in normotensive subjects (19.7% vs 16.2%, P < 0.01). Furthermore, in hypertensive patients, the prevalence of MCI was lower in those with good adherence (17.3%) than in those with poor adherence (23.7%, P < 0.01) and lower in those controlled (16.5%) than in those with uncontrolled adherence (20.8%, P < 0.01). In univariate analyses, being female gender, increased age, agriculture occupation, unmarried and widow, less than primary school and middle school were associated with MCI prevalence. The assessment of the hypertensive patients revealed the adjusted OR (95% CI) of having MCI in those with poor adherence to AHMs was 1.32 (1.14– 1.54) compared with those having good adherence. Conclusion: There is an association between the prevalence of hypertension, adherence to AHMs and MCI, suggesting that hypertensives should be screened for MCI to provide improved diagnoses and optimal therapeutics for cognitive decline prevention, especially in poor AHM adherence. [ABSTRACT FROM AUTHOR]

In this work, we developed a type of shape-stabilized phase change materials (SSPCMs) based on carbonized melamine foam/graphene aerogel (CMGA) as a supporting material and polyethylene glycol (PEG) as a phase change material. PEG@CMGA SSPCMs were prepared by fabricating a series of CMGA double skeleton with different carbonization temperatures using freeze-drying and high-temperature carbonization, followed by vacuum impregnation of PEG into the CMGA double skeleton. The morphological structure, thermal storage property, shape stability, thermal conductivity, and solar/electric conversion behavior of the fabricated SSPCMs are investigated. The results showed that PEG@CMGA SSPCMs exhibited excellent shape stability, high latent thermal storage capacity of 181.2 J/g, thermal cycling stability, enhanced thermal conductivity with 387% higher than that of pure PEG, solar-to-thermal energy conversion capability with high efficiency of 91.7% and electric-to-thermal energy conversion capability with high efficiency of 87.3%. The results of this work provide a strategy for the design and development of high performance, multiple energy conversion forms of SSPCMs for promising applications in solar energy utilization, energy-efficient buildings, and heat preservation. [Display omitted] • CMGA double skeleton with excellent mechanical property is constructed by in situ self-assembly and carbonization. • The composite phase change materials possess excellent energy storage properties and high thermal conductivity. • PEG@CMGA 1600 SSPCMs achieve efficient solar-to-thermal conversion efficiency of 91.7%. • PEG@CMGA 1600 SSPCMs exhibit electric-to-thermal energy conversion capability with high efficiency of 87.3%. [ABSTRACT FROM AUTHOR]

• Ethynyl functionalized porphyrins are proposed as cathodes for organic batteries. • In-situ electropolymerization of porphyrin renders its highly stable structure. • Cation and anion are alternatively interacted with porphyrin for charge storage. • Excellent cycling stability up to 5000 cycles is achieved for porphyrin cathode. Organic materials, featuring low cost, structural diversity, and environmental friendliness, have emerged as promising electrode materials for rechargeable batteries in recent years. However, they suffer from unstable cycling performance due to their high solubility in liquid electrolytes. Herein, we demonstrated a novel functionalized porphyrin [5,15-bis(ethynyl)- porphinato]copper(II) (CuDEP) as the stable organic cathode for organic alkali metal batteries. Owing to the in-situ electropolymerization and multiple electron transfer capability, CuDEP showed highly reversible capacity, long-term cycling stability (106 mAh/g at 1 A/g after 5000 cycles), and superior rate performance in organic lithium battery. N atoms act the charge storage sites where both cations and anions are alternatively stored during the charge and discharge. In organic sodium and potassium batteries, CuDEP cathode also demonstrated stable cycling and high rate capability. This result suggests that ethynyl group functionalized small porphyrin molecule would be a promising cathode for long-term organic alkali metal batteries for green and stable energy storage. [ABSTRACT FROM AUTHOR]

• MF/GA double-skeleton with excellent mechanical property is constructed by in situ self-assembly method. • Dual-skeleton based MF/GA@PEG SSPCMs possess superior shape memory property and solar-thermal conversion ability. • Anti-leakage mechanism of MF/GA@PEG SSPCMs is proposed. • This design strategy provides a new application of MF/GA@PEG SSPCMs in microelectronic devices. Polyethylene glycol (PEG) is widely used for thermal energy storage, but its practical application is limited by its strong rigidity, poor shape stability. In this work, a kind of melamine foam/graphene aerogel (MF/GA) double-skeleton was prepared, then PEG was stably encapsulated into MF/GA by vacuum melt impregnation method to obtain MF/GA@PEG shape-stabilized phase change materials (SSPCMs). Structural characterization and performance tests were performed on MF/GA@PEG SSPCMs, including morphological observation, latent heat, thermal conductivity, shape stability, and photothermal conversion capability. The experimental results show that the MF/GA@PEG SSPCMs show high energy storage density (168.3 J/g), good shape stability, shape memory performance and excellent solar-thermal energy conversion capability with a high efficiency of 84.8%, the thermal conductivity of MF/GA@PEG SSPCMs is 161% higher than that of pure PEG. The MF/GA@PEG SSPCMs with comprehensive properties have promising application in solar-thermal energy storage and thermal management in microelectronic devices. [Display omitted] [ABSTRACT FROM AUTHOR]

Shape-stabilized phase change material (SSPCM) are widely used as energy storage materials due to its advantages of easy preparation and adjustable scale. But the thermal conductivity enhancement of SSPCM still need to be further studied to improve the energy storage efficiency. In this work, silicone rubber (SR)/paraffin@SiO 2 (Pn@SiO 2)/graphene nanoplates (GNPs) shape-stabilized phase change materials (SPG) with different GNPs content were prepared. Pn@SiO 2 and GNPs can be homogeneously dispersed in the SR matrix due to the enhanced interfacial compatibility between Pn@SiO 2 and SR. The leakage rate of SPG composites was as low as 0.25% due to the protection of SiO 2 shell, SR matrix and GNPs. The SPG composites had excellent thermal storage properties, with the enthalpy about 50 J·g−1. The thermal conductivity of SPG composites was improved with the content of GNPs, the thermal conductivity of SPG reach 0.989 W·m−1·K−1 at a GNPs content of 10 phr. The low hardness of SPG composites above the phase change temperature can provide a more cohesive surface when applied to heat dissipation. The heat dissipation of the SPG composites in electric devices was simulated and demonstrated that the addition of GNPs made the heat dissipation rate of the SPG composites increased significantly. Therefore, the SPG composites can be applied in thermal energy storage and heat dissipation of electronic devices. [Display omitted] • The thermal conductivity enhancement of SSPCM was further discussed. • The interfacial compatibility of components in the SSPCM was enhanced by the rational strategy. • The leakage-prevention performance of SSPCM was improved with the multiple protection. • The thermal conductivity of SSPCM reach 0.989 W·m−1·K−1 due to the well-dispersed GNPs and Pn@SiO 2 in SR. • Numerical simulation was used to predict the thermal performance of SPG composites. [ABSTRACT FROM AUTHOR]

Inorganic hydrated salts possess high latent heat of phase transition and are promising phase change materials (PCMs). However, the issues of supercooling, low thermal conductivity, susceptibility to leakage, and phase separation significantly impediment the practical applications of inorganic hydrated salts. In this study, it is proposed to decrease the inorganic hydrated salt supercooling degree by increasing the surface roughness of the porous material and to load the nucleating agent silver (Ag) onto polydopamine (PDA) modified melamine foam (MF) by electroless plating to obtain 3D porous Ag foams, which are then utilized as support materials. The results demonstrated that the 3D porous Ag foam compounded with barium hydroxide octahydrate (BHO) can ameliorate the shortcomings of leakage and reduce the supercooling degree in the cooling process. The composite not only exhibits high enthalpy of over 248.5 J/g and high thermal conductivity of 1.82 W·m−1·K−1 but also has a low supercooling degree of 0.21 ℃. Furthermore, the composites exhibited superior shape stability and thermal cycling stability. This study provides an effective method for reducing the supercooling degree of inorganic hydration salts. [Display omitted] [ABSTRACT FROM AUTHOR]

Microencapsulation of paraffin with melamine formaldehyde shell (Pn@MF) shows the drawbacks of low thermal conductivity. Hence, we constructed SiO2 shells on Pn@MF phase change microcapsules by interfacial polycondensation to obtain Pn@MF@SiO2 double‐shelled microcapsules. The effect of tetraethoxysilane (TEOS) contents on the performance of Pn@MF@SiO2 was discussed in detail. As the TEOS contents increased, the thermal conductivity of Pn@MF@SiO2 gradually increased, reaching up to 0.376 W m−1 K−1. The Pn@MF@SiO2 have exhibited superior leakage‐proof properties and thermal reliability through double‐shelled protection, and the highest reduction in leakage rate reached 45.06 % compared to Pn@MF microcapsules. The Pn@MF@SiO2‐3 with the lowest enthalpy still exhibit a latent heat storage capacity of more than 176 J/g, which displayed outstanding latent heat storage/release capability and good anti‐permeable property. [ABSTRACT FROM AUTHOR]

The goal of the study was to confirm whether preoperative controlling nutritional status (CONUT) was a prognostic factor in early-stage cervical cancer patients with high-risk factors after surgery and postoperative concurrent chemoradiotherapy (CCRT). Between 2004 and 2015, a total of 698 patients who were treated with surgery and postoperative CCRT were included in this retrospective study. The prescribed dose for postoperative radiotherapy was 45–50.4 Gy in 25–28 fractions and the concurrent chemotherapy regimen contained cisplatin or paclitaxel. Based on the receiver operating characteristic (ROC) analysis, the patients were classified into low (<3) and high (≥3) CONUT groups. Of all study patients, 471 (67.5%) patients were included in the low CONUT group. The low CONUT group had significantly better 5-year disease-free survival (DFS) and overall survival (OS) than the high CONUT group (p<0.001 and p = 0.001, respectively). A high CONUT score was significantly associated with lymph node metastasis, parametrial invasion, and poorer nutritional status, including lower body mass index (BMI) and lower prognostic nutritional index (PNI) score (p<0.05, respectively). The CONUT score was an independent predictor of DFS and OS in multivariate analysis. Notably, the CONUT score still efficiently stratified DFS in the high PNI score group (P = 0.001). The preoperative high CONUT scores indicated poor prognosis for early-stage cervical cancer patients with high-risk factors treated with surgery and postoperative CCRT. In clinical practice, patients with high CONUT score should be considered to receive consolidation chemotherapy. • Controlling nutritional status (CONUT) score was underutilized in early-stage cervical cancer with high-risk factors. • The preoperative CONUT score was a useful marker for predicting prognosis. • The high CONUT score predicted poor prognosis for early-stage cervical cancer patients with high-risk factors. • Patients with high CONUT score should be considered to receive consolidation chemotherapy after adjuvant therapy. [ABSTRACT FROM AUTHOR]

Meconopsis integrifolia (Maxim.) Franch. is used extensively in traditional Tibetan medicine for its potent anti‐inflammatory properties. In this study, six cyclooxygenase‐2 (COX‐2) inhibitors were purified from M. integrifolia using high‐speed counter‐current chromatography guided by ultrafiltration liquid chromatography (ultrafiltration‐LC). First, ultrafiltration‐LC was performed to profile the COX‐2 inhibitors in M. integrifolia. The reflux extraction conditions were further optimized using response surface methodology, and the results showed that the targeted COX‐2 inhibitors could be well enriched under the optimized extraction conditions. Then the six target COX‐2 inhibitors were separated by high‐speed countercurrent chromatography with a solvent system composed of ethyl acetate/n‐butanol/water (4:1:4, v/v/v. Finally, the six COX‐2 inhibitors, including 21.2 mg of 8‐hydroxyluteolin 7‐sophoroside, 29.6 mg of 8‐hydroxyluteolin 7‐[6′''‐acetylallosyl‐(1→2)‐glucoside], 42.5 mg of Sinocrassoside D3, 54.1 mg of Hypolaetin 7‐[6′′′‐acetylallosyll‐(l→2)‐3′′‐acetylglucoside, 30.6 mg of Hypolaetin 7‐[6′′′‐acetylallosyll‐(l→2)‐6′′‐acetylglucoside and 17.8 mg of Hypolaetin were obtained from 500 mg of sample. Their structures were elucidated by 1H‐NMR spectroscopy. This study reveals that ultrafiltration‐LC combined with high‐speed counter‐current chromatography is a robust and efficient strategy for target‐guided isolation and purification of bioactive molecules. It also enhances the scientific understanding of the anti‐inflammatory properties of M. integrifolia but also paves the way for its further medicinal applications. [ABSTRACT FROM AUTHOR]

Urtica laetevirens Maxim. is used extensively in traditional Chinese medicine (TCM) for its potent antioxidative properties. In this study, three antioxidants were purified from U. laetevirens. using HSCCC guided by online DPPH-HPLC analysis. Firstly, the online DPPH-HPLC analysis was performed to profile out the antioxidant active molecules in U. laetevirens. The ultrasonic-assisted extraction conditions were optimized by response surface methodology and the results showed the targeted antioxidant active molecules could be well enriched under the optimized extraction conditions. Then, the antioxidant active molecules were separated by high-speed countercurrent chromatography ethyl acetate/n-butanol/water (2:3:5, v/v/v) as the solvent system. Finally, the three targets including 16.8 mg of Isovitexin, 9.8 mg of Isoorientin, and 26.7 mg of Apigenin-6,8-di-C-β-d-glucopyranoside were obtained from 100 mg of sample. Their structures were identified by 1H NMR spectroscopy. [ABSTRACT FROM AUTHOR]

A series of paraffin@poly(methyl methacrylate) phase‐change microcapsules (Pn@PMMA) were synthesized by suspension polymerization. The prepared Pn@PMMA had excellent latent heat storage and release properties (ΔHm=183.2 J/g, ΔHc=181.9 J/g), excellent thermal stability and cycle durability of at least 100 cycles. The effects of emulsifier type, cross‐linking agent content and core/shell mass ratio on structure and properties of Pn@PMMA were investigated by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT‐IR) and differential scanning calorimetry (DSC). The morphology of Pn@PMMA exhibited spherical profile with styrene‐maleic anhydride (SMA) as emulsifier and the agglomeration was significantly reduced. The enthalpy of the microcapsules was significantly improved with the addition of crosslinker. The anti‐permeability of Pn@PMMA subsequently further improved with continued increasing amount of cross‐linker. Besides, the enthalpy and anti‐leaking property of the microcapsules progressively reduced with the core/shell mass ratio decreased, while the thermal conductivity gradually increased. Therefore, the results showed that the Pn@PMMA with the enthalpy of 183.2 J/g and the leakage rate of 4.72 %, which displayed a high thermal reliability potential for thermal energy storage and temperature regulation. [ABSTRACT FROM AUTHOR]

The storage of latent heat using phase change materials (PCM) is an effective method of energy storage. In this study, silicone rubber (SR)/graphene nanoplates (GNPs)/paraffin@SiO2 phase change microcapsules (Pn@SiO2) shape-stabilized phase change materials (SSPCM) with high thermal conductivity, low leakage rate and tunable thermal management capability are prepared by method of add phase change microcapsules and thermal conductivity enhancer graphene nanoplates. The effects of Pn@SiO2 content on properties of the SR/GNPs/Pn@SiO2 (SGP) composites were investigated by scanning electron microscopy, X-ray diffraction, differential scanning calorimetry. The results show that the enthalpy of phase change composites can be adjusted from 25.6 to 78.56 J·g−1 by changing the addition amount of Pn@SiO2 microcapsules. Moreover, the effect of GNPs on the thermal conductivity of SR matrix is greater than that of Pn@SiO2 on SR, as a consequence, the thermal conductivity of SGP composites decreases with the increase of Pn@SiO2. In addition, the thermal conductivity of SGP phase change composites can also reach 0.567 W·m−1K−1 after the addition of microcapsules, which dramatically shortens the response time of the material in the application. In summary, SGP composites have promising applications in the field of thermal storage. [ABSTRACT FROM AUTHOR]

A series of paraffin (Pn)@silica (SiO2) microencapsulated phase change materials (MEPCM) were synthesized by sol‐gel process using tetraethyl orthosilicate (TEOS) and silane coupling agent as precursors. The morphology and chemical compositions of Pn@SiO2 microcapsules were characterized by SEM and FT‐IR, and thermal energy storage capacity was tested by DSC. The results showed that the Pn@SiO2 microcapsules modified with 3‐methacryloxypropyltrimethoxysilane (MPS) had a desirable phase transition enthalpy (184.12 J/g). Meanwhile, the contact angle and leakage rate of Pn@SiO2 microcapsules were analyzed, and the data indicated the contact angle of Pn@SiO2 microcapsules was significantly improved and the leakage rate of Pn@SiO2 microcapsules was reduced to different degrees by modification with silane coupling agents. The main reason is that the modification of silane coupling agents improves the wettability of silica on the surface of paraffin wax, which makes the aggregation of silica on the surface of paraffin more efficient. Among them, the Pn@SiO2 microcapsules modified by MPS showed the most significant reduction in leakage rate, which was reduced from 8.38 % to 1.24 %. Pn@SiO2 microcapsules modified by MPS not only showed outstanding latent heat‐storage/release capability with a high capacity but also exhibited good shape stability, high thermal stability and excellent phase‐change reliability and durability. [ABSTRACT FROM AUTHOR]

In this paper, a series of silicone rubber (SR)/thermochromic microcapsules (TC@MF)/cuprous oxide (Cu 2 O) flexible phase change composites (STC) with multi-colors and reversible thermochromic were prepared. In this composite, SR was used as polymer matrix and TC@MF with phase change enthalpy of 193 J/g was used as functional filler. Moreover, different contents of Cu 2 O were introduced to change color of composites and improve thermal conductivity and photothermal conversion. The STC composites could undergo reversible color changes from blue-violet to red with a color change temperature of approximately 52 °C. And it exhibited excellent leakage resistance with the leakage rate of STC-2 as low as 0.41%. The thermal conductivity of the STC-3 composite reached 0.33 W m−1 K−1 at Cu 2 O content of 9 phr. The STC composites were applied to dissipate heat from the battery and the maximum surface temperature was only 49.0 °C at 9.8 A discharge rate which represented 24.03 % reduction in surface temperature compared to the bare battery. This work offers an effective route for preparation of battery thermal regulation materials based on thermochromic microcapsules, which has significant potential for application in the field of battery thermal management. [Display omitted] • Cu 2 O can enhance the thermal conductivity and photothermal conversion of the composites. • TC@MF and Cu 2 O were cleverly utilized to synergistically improve the safety of the thermal management materials. • The composites exhibited excellent reversible thermochromic capacities with blue-violet to red transformation. • The composites showed efficient battery thermal management capacity. [ABSTRACT FROM AUTHOR]

Simple Summary: Cancer metastasis is still the main cause of cancer-related mortality. Peritoneal metastases are the first presentation of advanced ovarian cancer, and metastatic cancer cells tend to disseminate trans-peritoneally in the peritoneal cavity. Hypoxia is a critical factor in governing transcoelomic metastases of ovarian cancer. Therefore, targeting hypoxia appears to be a promising approach to arrest cancer metastasis. In the present work, we identified that BCL2A1, a BCL2 family member, is significantly induced by hypoxia and other physiological stresses by NF-κB signaling and followed by a gradual degradation. The upregulated BLC2A1 has been shown to enhance ovarian cancer survival, tumor growth, and tumor dissemination by suppressing intrinsic cell apoptosis. These data indicate BCL2A1 is an early response factor in the stressed tumor microenvironment, and targeting BCL2A1 may be a potential therapeutic approach in eradicating peritoneal metastases of ovarian cancer. Emerging evidence indicates that hypoxia plays a critical role in governing the transcoelomic metastasis of ovarian cancer. Hence, targeting hypoxia may be a promising approach to prevent the metastasis of ovarian cancer. Here, we report that BCL2A1, a BCL2 family member, acts as a hypoxia-inducible gene for promoting tumor progression in ovarian cancer peritoneal metastases. We demonstrated that BCL2A1 was induced not only by hypoxia but also other physiological stresses through NF-κB signaling and then was gradually reduced by the ubiquitin-proteasome pathway in ascites-derived ovarian cancer cells. The upregulated BCL2A1 was frequently found in advanced metastatic ovarian cancer cells, suggesting its clinical relevance in ovarian cancer metastatic progression. Functionally, BCL2A1 enhanced the foci formation ability of ovarian cancer cells in a stress-conditioned medium, colony formation in an ex vivo omental tumor model, and tumor dissemination in vivo. Under stress conditions, BCL2A1 accumulated and colocalized with mitochondria to suppress intrinsic cell apoptosis by interacting with the BH3-only subfamily BCL2 members HRK/BAD/BID in ovarian cancer cells. These findings indicate that BCL2A1 is an early response factor that maintains the survival of ovarian cancer cells in the harsh tumor microenvironment. [ABSTRACT FROM AUTHOR]

Summary: A series of paraffin (Pa)@silicon dioxide (SiO2) microcapsules with different core/shell ratios were constructed by interfacial‐polycondensation of tetraethoxysilane (TEOS) and γ‐Methacryloxypropyltrimethoxysilane (MPS), and then were embedded in addition‐cure liquid silicone rubber (ALSR) to fabricate ALSR/Pa@SiO2 phase‐change composites. The SiO2 shell can avoid the leakage of Pa. Meanwhile, the in‐situ modification of the SiO2 shell by MPS can enhance the interface bonding between Pa@SiO2 and ALSR, because the C═C bond introduced by MPS on the SiO2 shell can participate in the curing reaction of ALSR. The study explored the effects of the core/shell ratio on the Pa@SiO2 microcapsules and ALSR/Pa@SiO2 composites. Differential scanning calorimetry analysis demonstrated that ALSR/Pa@SiO2 composites have dependable thermal energy storage capability which can reach to 90.7 J g−1 and phase‐change enthalpy of the composites increase with the core/shell ratio. The ALSR/Pa@SiO2 composites were found as form‐stable phase‐change materials with low leakage rate, which is attributed to the protection of both SiO2 shell and ALSR matrix. Due to the chemical interfacial interaction, the composites displayed improved mechanical strength. The composites can be used for thermal management and temperature regulation as an electronic packaging material. [ABSTRACT FROM AUTHOR]

Background: In contrast to stable genetic events, epigenetic changes are highly plastic and play crucial roles in tumor evolution and development. Epithelial ovarian cancer (EOC) is a highly heterogeneous disease that is generally associated with poor prognosis and treatment failure. Profiling epigenome-wide DNA methylation status is therefore essential to better characterize the impact of epigenetic alterations on the heterogeneity of EOC. Methods: An epigenome-wide association study was conducted to evaluate global DNA methylation in a retrospective cohort of 80 mixed subtypes of primary ovarian cancers and 30 patients with high-grade serous ovarian carcinoma (HGSOC). Three demethylating agents, azacytidine, decitabine, and thioguanine, were tested their anti-cancer and anti-chemoresistant effects on HGSOC cells. Results: Global DNA hypermethylation was significantly associated with high-grade tumors, platinum resistance, and poor prognosis. We determined that 9313 differentially methylated probes (DMPs) were enriched in their relative gene regions of 4938 genes involved in small GTPases and were significantly correlated with the PI3K-AKT, MAPK, RAS, and WNT oncogenic pathways. On the other hand, global DNA hypermethylation was preferentially associated with recurrent HGSOC. A total of 2969 DMPs corresponding to 1471 genes were involved in olfactory transduction, and calcium and cAMP signaling. Co-treatment with demethylating agents showed significant growth retardation in ovarian cancer cells through differential inductions, such as cell apoptosis by azacytidine or G2/M cell cycle arrest by decitabine and thioguanine. Notably, azacytidine and decitabine, though not thioguanine, synergistically enhanced cisplatin-mediated cytotoxicity in HGSOC cells. Conclusions: This study demonstrates the significant association of global hypermethylation with poor prognosis and drug resistance in high-grade EOC and highlights the potential of demethylating agents in cancer treatment. [ABSTRACT FROM AUTHOR]

The application of graphene aerogel fabricated by reduction self-assembly and ice template methods is limited due to the difficulties in shape control and poor compression resistance. Here, a series of polyvinyl alcohol/graphene aerogels (PGA) were prepared by the chemical crosslinking and freeze-drying method, in which (3-Aminopropyl) diethoxymethylsilane (APDEMS) used as cross-linking agent and reducing agent, reduce graphene oxide (rGO) and polyvinyl alcohol (PVA) as supporting structural materials. The crosslinking effect and PVA enhancement effect achieved the shape control of aerogels and enhanced the compression resistance. When the content of graphene oxide is 50 mg, the obtained PGA5 hybrid aerogel has better compression-resilience properties with compressive strength of 6.26 KPa at 50 % compression. Then, PGA@PEG shape-stabilized phase change materials (SSPCMs) were prepared by loading PEG into PGA by vacuum impregnation. PGA5@PEG prepared with PGA5, had significant thermal conductivity of 0.481 W m−1 K−1, excellent energy storage performance (phase change enthalpy of 178.6 J/g) and good thermal cycling stability. Moreover, PGA5@PEG had high solar-thermal conversion efficiency of 86.9 %. Accordingly, we designed a solar-thermal water system to broaden the application of SSPCMs in the field of solar-thermal energy conversion. During the 2-h heating process, the PGA5@PEG-water system can rapidly reach a maximum temperature of 57.3 °C, higher than the pure water system (40.4 °C). PGA@PEG SSPCMs would be very promising as latent heat storage/release units for applications in solar energy storage and conversion. [Display omitted] • PGA with excellent compression-resilience properties are fabricated by chemical cross-linking. • Efficient solar-to-thermal energy conversion and storage are realized. • This design strategy provides a new idea for the application of PGA@PEG SSPCMs in solar-thermal water systems. [ABSTRACT FROM AUTHOR]

Hydrated salt phase change materials (PCMs) have the advantages of high energy storage density and low cost, and have great application prospects in the field of phase change energy storage. However, the problems of supercooling, phase separation and leakage of hydrated salt PCMs limit their further applications. In this work, we designed and fabricated Cu-coated melamine foam (MF)/barium hydroxide octahydrate (BHO) shape-stabilized phase change materials (SSPCMs) with low supercooling. MF was used as supporting material and Cu as a nucleating agent and thermal conductivity enhancer by loading it onto MF via electroless plating. BHO was then encapsulated into the MF@Cu skeleton through vacuum impregnation to obtain BHO@MF@Cu SSPCMs. The results demonstrated that BHO@MF@Cu SSPCMs not only present very low supercooling degree of 0.12 °C and high thermal energy capacity of 247 J/g, but maintained a latent heat of phase transition of 229.3 J/g with little change in enthalpy after 100 thermal cycles. Moreover, compared to BHO, SSPCMs exhibited high thermal conductivity of 1.687 W m−1 K−1, excellent shape stability, and thermal cycling stability. In summary, BHO@MF@Cu SSPCMs with low supercooling degree were prepared by electroless plating and vacuum impregnation in this study, which provides a new strategy to reduce the supercooling degree of hydrated salt PCMs. [Display omitted] [ABSTRACT FROM AUTHOR]

A series of reversibly thermochromic phase-change microcapsules (TC@MF), demonstrating excellent energy storage and release properties, were synthesized using melamine formaldehyde resin (MF) encapsulated ternary complex consisting of crystal violet lactone (CVL), 2,2-Di-(4-hydroxyphenyl) propane (BPA), and n-hexadecanol. The microstructure, chemical composition, thermal storage capacity, thermal cycling durability, discoloration effect, and thermal regulation performance of TC@MF with different core contents were investigated in detail. With core contents gradually increasing, the chromatic aberration values (ΔE) value of TC@MF increased from 38.23 to 71.69, the melting enthalpy (ΔH m) gradually increased from 180.2 J/g to 218.6 J/g while the leak-proof performance decreased gradually. The TC@MF-2 with the best comprehensive performance has exhibited superior latent heat storage (ΔH m = 192.2 J/g), high chromatic aberration values (ΔE = 57.31), and well leak-proof properties (5.61 %). Furthermore, the thermal performance, morphology, and reversible color reliability of TC@MF-2 remained stable through 100 thermal heating and cooling cycles, demonstrating excellent thermal cycling stability. In summary, such multifunctional microcapsules can directly reflect the energy saturation and depletion states in phase change material applications through color changes. That might be conducive to expanding the value of its practical application in the field of latent heat energy storage, including smart fabrics or fibers, commodity packaging, thermal sensors, reversible thermochromic coatings and solar energy storage, and so on. [Display omitted] [ABSTRACT FROM AUTHOR]

• Charge storage performance of functionalized porphyrin complexes is regulated by electron-donating/withdrawing groups. • Strong electron withdrawing effect of chlorine functionalized groups enables higher reversible capacity. • Extremely cycling stability up to 2000 cycles with capacity retention more than 80% is achieved. • Multiple electrons transfer mechanism in porphyrin electrode is evidenced. Organic electrode materials exhibit wide application prospects in the electrochemical energy storage devices, owing to their adjustable structure, low cost and environmental friendliness. Though organic electrode materials delivered high theoretical energy density, but suffer from low electronic conductivity and high solubility. In order to decrease the solubility and regulate redox potential of the porphyrin molecule, electron-donating group and electron-withdrawing group were functionalized on bipolar porphyrin complex. Herein, we report two novel cathodes of [5,15-bis(ethynyl)-10,20-bis(5-methylthienyl) porphinato] copper(II) (CuDETMP) and [5,15-bis(ethynyl)-10,20-bis(5-chlorothienyl)porphinato]copper(II) (CuDETCP). Strong electron withdrawing effect of chlorine functionalized groups enables higher reversible capacity (≈125 mAh/g vs 100 mAh/g at 1 A/g), while with electron donating group of CuDETMP showed stable cycling capability. Extremely cycling stability up to 2000 cycles with capacity retention more than 80% was achieved in both electrodes. Compared to CuDETMP, higher capacity of CuDETCP benefits from reaction between chlorine atoms and Li cations, which can be a partially reversible process lead to degraded capacity. Nevertheless, CuDETMP and CuDETCP can deliver reversible capacity and provide multiple-redox sites enabling high energy density in respective proper voltage ranges. Through comparison towards physical and electrochemical properties of two molecules, mechanism between substituent and electrochemical performance was clarified. This work not only elaborates the significant correlation between different substituents and electrochemical performance, but also provides a novel strategy to tunable molecular design of organic electrode materials for high-energy rechargeable organic lithium batteries. [ABSTRACT FROM AUTHOR]

[Display omitted] • Thiophene functionalized porphyrin is proposed as new cathode for organic-sodium batteries. • In-situ polymerization strategy renders excellent cycling stability (11000 cycles). • High energy (508 Wh kg−1) and power density (18 KW kg−1) are achieved as well. • Nitrogen and Sulfur atoms are active sites for charge storage. Organic-sodium batteries have attracted extensive attention due to the abundance of sodium resource and the molecular tunability of organic materials. However, the dissolution of organic materials in electrolytes and low electronic conductivity limit its development. Here, a porphyrin complex of [5,15-di(thiophen-2-yl) porphinato] M(II) (MTP, M = Cu, Ni) is proposed as highly stable cathode material for organic-sodium batteries. Benefiting from the multiple electron transfer of metal porphyrin complex and in-situ polymerization of thiophene groups of porphyrin complex in initial cycles, the CuTP cathode delivers a reversible capacity of 203 mAh/g at 100 mA g−1 and long-term cycling stability up to 11,000 cycles at a high current density of 5 A/g owing to the enhanced conjugated structure induced by in situ polymerization process. A specific energy density of 508 Wh kg−1 and a power density of 18 KW kg−1 are achieved for metal porphyrin-based cathode. The charge storage sites and in-situ polymerization mechanism of MTP cathode are systematically evaluated by both experimental and simulated studies. This study would provide a new strategy to address the dissolution issue of organic cathode and improve cycling stability of the organic-sodium batteries. [ABSTRACT FROM AUTHOR]