Determining fatigue threshold of elastomers through an elastic limit strain point.

Determining the fatigue threshold of elastomers is particularly important to predict their durability and lifespan. However, there has been almost no effective approach to calculate this threshold fast and accurately so far. To realize rapid fatigue performance testing, in this paper, a new method is proposed to calculate the fatigue threshold through the elastic limit strain point of elastomers that can be obtained from the continuous Mullins test. Compared with the traditional binary method to predict fatigue threshold, this method significantly reduces the time required for fatigue testing of elastomers, which can save approximately 2-3 sampling points in the fatigue test, i.e. a time savings of around 40%. Our method also proved to be effective for the elastomers at 0 °C. Additionally, a dual-network elastomer was synthesized using the interpenetrating network method, exhibiting improved elasticity (2.1 MPa and 3.1 MPa), toughness (1423 J m-2 and 2100 J m-2), and higher fatigue threshold (125 J m-2 and 385 J m-2) at 0 °C and room temperature. This material presents great application potential in marine anti-fouling.

Study on Capillary Water Absorption of Waterborne-Polyurethane-Modified Recycled Coarse Aggregate Concrete.

The reuse of construction and demolition waste as a substitute for natural coarse aggregate in the production of recycled concrete has been widely used. In order to study the capillary water absorption performance of waterborne-polyurethane-modified recycled aggregate concrete (WPUMRC), the effects of different curing systems, polymer-cement ratios, and waterborne polyurethane addition methods on the cumulative water absorption and the rate of capillary water absorption of WPUMRC were analyzed, and through MIP tests, the micro modification mechanism of waterborne polyurethane in recycled concrete was analyzed. The results indicate that the optimal curing system for both DC (waterborne polyurethane is added separately from water) and HC (waterborne polyurethane is mixed with some effective water and then added) is the 14 d standard curing-14 d indoor natural drying curing system. Waterborne polyurethane can fill the pores and micro-cracks inside WPUMRC or interweave with the hydration products of cement to form a spatial network structure, reducing the porosity, and thereby improving the capillary water absorption performance of WPUMRC. Based on the MIP test results, the grey correlation method was used to establish the relationship between capillary water absorption and the pore structure of WPUMRC under the optimal curing system. In addition, the prediction model of capillary water absorption in recycled concrete was established according to the test results, which can be used to predict WPUMRC's capillary water absorption performance.

Anti-reflection metallic anode-enhanced performance of organic solar cells via cross coupling between Fabry-Perot cavity modes and microcavity modes.

An effective anti-reflection metallic anode with the structure of glass/dielectric2 /Ag (D1D2M) is demonstrated both in small-molecule (SM) and conjugated polymer (CP) organic solar cells (OSCs). The anti-reflection mechanism is investigated by the finite-difference time-domain numerical calculation method and the experimental method. By tuning the refractive index and the thickness of the D2 layer, the reflection light is confined in the Fabry-Perot (F-P) cavity modes, which effectively enhances the transmittance of the D1D2M anode in the wavelength range of 420 nm-800 nm. Compared with the conventional glass/Ag (D1M) anode, the experimental transmittance of the D1D2M anode is enhanced by 33.24% at a wavelength of 550 nm. By replacing the D1M anode with the D1D2M anode in the OSCs, the F-P cavity modes cross couple with the microcavity modes in the active layers. As a result, the absorption intensity is obviously increasing in a wide angle range (0≤θ≤85∘) in the wavelength ranges of 475 nm-650 nm and 540 nm-720 nm for the SM and CP OSCs, respectively. The short circuit current density and power conversion efficiency of the SM OSC is increased by 25.07% and 27.23%, respectively.

Instant, Tough, Noncovalent Adhesion.

Noncovalent adhesion has long been developed for numerous applications, including pressure-sensitive adhesives, wound closure, and drug delivery. Recent advances highlight an urgent need: a general principle to guide the development of instant, tough, noncovalent adhesion. Here, we show that noncovalent adhesion can be both instant and tough by separately selecting two types of noncovalent bonds for distinct functions: tougheners and interlinks. We demonstrate the principle using a hydrogel with a covalent polymer network and noncovalent tougheners, adhering another material through noncovalent interlinks. The adhesion is instant if the interlinks form fast. When an external force separates the adhesion, the covalent polymer network transmits the force through the bulk of the hydrogel to the front of the separation. The adhesion is tough if the interlinks are strong enough for many tougheners to unzip. Our best result achieves adhesion energy above 750 J/m2 within seconds. The adhesion detaches in response to a cue, such as a change in pH or temperature. We identify several topologies of noncovalent adhesion and demonstrate them in the form of tape, powder, brush, solution, and interpolymer complex. The abundant diversity of noncovalent bonds offers enormous design space to create instant, tough, noncovalent adhesion for engineering and medicine.

Stretchable materials of high toughness and low hysteresis.

In materials of all types, hysteresis and toughness are usually correlated. For example, a highly stretchable elastomer or hydrogel of a single polymer network has low hysteresis and low toughness. The single network is commonly toughened by introducing sacrificial bonds, but breaking and possibly reforming the sacrificial bonds causes pronounced hysteresis. In this paper, we describe a principle of stretchable materials that disrupt the toughness-hysteresis correlation, achieving both high toughness and low hysteresis. We demonstrate the principle by fabricating a composite of two constituents: a matrix of low elastic modulus, and fibers of high elastic modulus, with strong adhesion between the matrix and the fibers, but with no sacrificial bonds. Both constituents have low hysteresis (5%) and low toughness (300 J/m2), whereas the composite retains the low hysteresis but achieves high toughness (10,000 J/m2). Both constituents are prone to fatigue fracture, whereas the composite is highly fatigue resistant. We conduct experiment and computation to ascertain that the large modulus contrast alleviates stress concentration at the crack front, and that strong adhesion binds the fibers and the matrix and suppresses sliding between them. Stretchable materials of high toughness and low hysteresis provide opportunities to the creation of high-cycle and low-dissipation soft robots and soft human-machine interfaces.

Characterization of gastric cancer models from different cell lines orthotopically constructed using improved implantation techniques.

AIM: To develop orthotopic gastric cancer mouse models from different cell lines and characterize the tumor features to assist further in preclinical trials and clinical treatment strategies. METHODS: Human gastric cancer SGC-7901 and BGC-823 cell suspensions were injected subcutaneously into nude mice to develop solid tumors, and tumor tissue pieces were then implanted under the serous coat of the stomach. An autopsy was performed on all animals of the SGC-7901 and BGC-823 models to observe the primary tumor growth and metastases using pathological and immunohistochemical methods. RESULTS: Both models showed large tumors in situ resulting in pressure and infiltration of the adjacent organs. The gastric cavity became smaller, along with stenosis of the cardia or pylorus. There were biological and statistical differences between the two models. The metastasis rate in involved organs (lymph nodes, kidney, spleen, testis) was significantly higher in the BGC-823 model compared to the SGC-7901 model (P < 0.05 or P < 0.01). The median survival of the BGC-823 model was shorter than that of SGC-7901 (23 d vs 84 d, P < 0.05). Histopathologically, the primary tumor and metastatic lesions of the two models showed obvious atypia and mucus in the cytoplasm. Compared with the SGC-7901 model, BGC-823 appeared more poorly differentiated (absence of adenoid structure), had a smaller volume, and richer capillary structure. Immunohistochemical staining revealed cytokeratin 20 and epithelial membrane antigen expression was positive in the SGC-7901 tumors, while negative in BGC-823 ones. CONCLUSION: Models using the SGC-7901 and BGC-823 cell lines were established which could function in gastric cancer research on carcinogenesis mechanism and drug discovery. The two models showed different tumor behavior and the latter was more malignant than the former.

Serial observations on an orthotopic gastric cancer model constructed using improved implantation technique.

AIM: To establish a gastric cancer nude-mouse model with improved orthotopic implantation and investigate its biological characteristics at different time points. METHODS: Human gastric cancer SGC-7901 cell suspensions were injected subcutaneously into a nude mouse to develop solid tumors, and the tumor tissue pieces were implanted under the serous coat. The nude mice were then euthanized in group every two weeks to observe the primary tumor growth and metastases. RESULTS: Within 2-4 wk, there were no obvious changes about the primary tumor in stomach. At the sixth week, the primary tumor began to grow fast, resulting in incrassation of the gastric wall and stenosis of the gastric cavity, and metastases into the liver and lymph nodes were detected. The tumor, which compressed the adjacent organs, gradually became bigger and bigger followed by stenosis or vanishment of the gastric cavity from 8 to 12 wk. There were massive metastases, and the rate of metastasis was 58% in lymph nodes, 78% in liver, 39% in kidney, and 81% in peritoneum or septum. CONCLUSION: A gastric cancer model is established, which can simulate the clinical tumor behavior and provide experimental carrier for clinical trials of gastric cancer treatment.

Analysis of biliary epithelial-mesenchymal transition in portal tract fibrogenesis in biliary atresia.

BACKGROUND: The cellular origin of myofibroblast in the liver fibrosis remains unclear. This study was designed to investigate whether biliary epithelial cells (BECs) undergoing epithelial-mesenchymal transition (EMT) might be found in patients with biliary atresia, thereby serving as a source of fibrotic myofibroblasts. METHODS: Liver sections from patients with biliary atresia were evaluated to detect antigen for the BECs marker 4 and cytokeratin-7 (CK-7), proteins (fibroblast-specific protein 1, also known S100A4; the collagen chaperone heat shock protein 47, HSP47) characteristically expressed by cells undergoing EMT, as well as myofibroblasts marker a-smooth muscle actin (a-SMA). RESULTS: Normal bile ducts BECs could express CK-7 and low levels of a-SMA; they did not express S100A4 and HSP47. However, BECs from biliary atresia resulted in increased expression of a-SMA, S100A4, with concurrent transition to a fibroblast-like morphology and decreased expression of AK-7. Furthermore, BECs in biliary atresia were associated with significant bile ductular proliferation and coexpressed both epithelial and mesenchymal markers. CONCLUSIONS: From significant histologic evidence, the BECs forming small- and medium-sized bile ducts undergoing EMT may account for prominent bile ductular proliferation and directly contribute to fibrogenesis in BA.

Prognostic value of hedgehog signal component expressions in hepatoblastoma patients.

OBJECTIVE: Activation of hedgehog (Hh) pathway has been implicated in the development of human malignancies. Hh as well as related downstream target genes has been extensively studied in many kinds of malignant tumours for clinical diagnostic or prognostic utilities. This study aimed at investigating whether Hh molecules provides a molecular marker of hepatoblastoma malignancy. METHODS: We obtained tissue sections from 32 patients with hepatoblastoma as well as cholestasis and normal control. Immunohistochemical analysis were performed to determine Hh signal components in human hepatoblastoma. The prognostic significance of single expression of Hh signal components were evaluated using Cox proportional hazards regression models and Kaplan-Meier survival analysis for statistical analysis. RESULTS: Expression of Hh signal components showed an increase in hepatoblastoma compared with cholestasis and normal tissues. There was a positive correlation between Smo or Gli1 expression and tumor clinicopathological features, such as histological type, tumor grade, tumor size and clinical stage. Both Smo or Gli1 protein high expression was significantly associated with poor prognosis by univariate analyses and multivariate analyses. CONCLUSIONS: Abnormal Hh signaling activation plays important roles in the malignant potential of hepatoblastoma. Gli1 expression is an independent prognostic marker.